Find where to buy products from suppliers in the USA, including: distributors, industrial manufacturers in America, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the American suppliers website for prices, SDS or more information. You can also view suppliers in Australia, NZ or the UK.
| Product | Description | |
|---|---|---|
| Direct Red 224 | Direct Red 224. Group: Biochemicals. Grades: Highly Purified. CAS No. 12222-48-9. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. US Biological Life Sciences. |  Worldwide |
| Direct Red 224 | Heterocyclic Organic Compound. Alternative Names: Direct Red 224;Direct red F2G. CAS No. 12222-48-9. Catalog: ACM12222489. |  |
| Direct Red 227 | Direct Dyes. Alternative Names: Light Rose FR;Ambidirect Rose FR;Best Direct Light Rose FR;Direct Fast Red FR;Everdirect Light Rose FR;Intralite Fast Rose LRK;Nippon Kagaku Direct Paper Pink BL;Optisal Red 7B. CAS No. 12222-51-4. Molecular formula: C60H46N16O22S6.6Na. Catalog: ACM12222514. | |
| Direct Red 254 | Direct Red 254. Uses: It is applicable to cotton, rayon and linen. Group: Dyes (technical grade). CAS No. 64683-40-5. Catalog: AP64683405. |  |
| Direct Red 28 | Direct Red 28. Group: Biochemicals. Grades: Highly Purified. CAS No. 573-58-0. Pack Sizes: 500g, 1kg, 2kg, 5kg, 10kg. US Biological Life Sciences. | Worldwide |
| Direct Red 31, Technical grade Dye content | Direct Red 31, Technical grade Dye content. Group: Biochemicals. Grades: Purified. CAS No. 5001-72-9. Pack Sizes: 500mg, 1g. US Biological Life Sciences. | Worldwide |
| Direct Red 79, Technical grade Dye contents | Direct Red 79, Technical grade Dye contents. Group: Biochemicals. Grades: Purified. CAS No. 1937-34-4. Pack Sizes: 2g, 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
| Direct Red 80 | Direct Red 80. Group: Biochemicals. Grades: Highly Purified. CAS No. 2610-10-8. Pack Sizes: 50g, 100g, 250g, 500g, 1kg. US Biological Life Sciences. | Worldwide |
| Direct Red 80 | Direct Red 80 (Sirius Red) is a polyazo dye used principally in staining methods for collagen and amyloid. Direct Red 80 does not release benzidine upon degradation and is safer than many traditional direct dyes [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Sirius Red. CAS No. 2610-10-8. Pack Sizes: 1 g. Product ID: HY-D0333. |  |
| Direct Red 81 | Heterocyclic Organic Compound. CAS No. 12237-71-7. Catalog: ACM12237717. | |
| Direct Red 83:1 | Direct Red 83:1. Uses: It is applicable to cotton, rayon and linen, with good light fastness. Group: Dyes (technical grade). CAS No. 90880-77-6. Catalog: AP90880776. | |
| Benzopurpurin 4B (Direct Red 2, CI 23500) | Benzopurpurine 4B is a biological stain and pH indicator for pH 1.3 to 4.2. Group: Biochemicals. Alternative Names: C.I. Direct Red 2; C.I. Direct Red 2, Disodium Salt; Amanil Purpurine 4B; Atul Direct Red 4B; Azamin 4B; Azocard Red 4B; Bencidal Purple 4B; Benzanil Purpurine 4B; Benzopurpurin 4B; Benzopurpurin B; Benzopurpurine 4BKX; Benzopurpurine 4BX; Brasilamina Red 4B; C.I. 23500; Calcomine Red 4BX; Chrome Leather Red 4B; Cotton Red 4B; Diacotton Benzopurpurine 4B; Diamine Purpurine 4B; Diaphtamine; Diazamine Purpurine 4B; Diazine Red 4B; Diazol Purpurine 4B; Diphenyl Red 4B; Diphenyl Red 4BS; Direct Purpurine 4B; Direct Purpurine M 4B; Direct Red 2; Direct Red 4A; Direct Red 4B; Direct Red DCB; Direct Scarlet 4BE; Eclipse Red; Erie Benzo 4BP; Erie Red 4B; Fast Scarlet; Hispamin Red 4B; Kayaku Benzopurpurine 4B; Mitsui Benzopurpurine 4BX; Paper Red 4BS; Phenamine Purpurine 4B; Purpurin 4B; Purpurine. Grades: Molecular Biology Grade. CAS No. 992-59-6. Pack Sizes: 25g, 100g, 250g. Molecular Formula: C34H28N6O6S2 2Na, Molecular Weight: 726.73. US Biological Life Sciences. | Worldwide |
| Benzopurpurin 4B (Direct Red 2, CI 23500, 3,3'-Dimethylbiphenyl-4,4'-bis-2-aminonaphthylazo-6-sulfonate) | Benzopurpurin 4B (Direct Red 2, CI 23500, 3,3'-Dimethylbiphenyl-4,4'-bis-2-aminonaphthylazo-6-sulfonate). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 25g, 100g, 250g, 1Kg. US Biological Life Sciences. | Worldwide |
| Direct fast red BNL | Heterocyclic Organic Compound. Alternative Names: DirectfastredBNL;C.I. Direct Red 89;Direct Fast Red BNLL;Kayarus Supra Scarlet BNL;Sumilight Supra Scarlet BNS. CAS No. 12217-67-3. Catalog: ACM12217673. | |
| 10% β carotene direct pressed powder(With modified starch) | Free flowing dark red uniform particles with a slight odor and some white starch particles visible. Product ID: PE-0660. Category: Filler Excipients. Product Keywords: Other Filler Excipients; 10% β carotene direct pressed powder(With modified starch); PE-0660; Filler Excipients;. Grade: Food Grade. Solubility: Form a stable orange dispersion in warm water. Applications: Due to its good fluidity, especially suitable for direct pressing and hard capsule filling of multivitamin and mineral tablets. |  |
| 10% lycopene powder(With fish gelatin) | Free flowing dark red uniform particles with a slight odor and some white starch particles visible. Product ID: PE-0662. Category: Filler Excipients. Product Keywords: Other Filler Excipients; 10% lycopene powder(With fish gelatin); PE-0662; Filler Excipients;. Grade: Food Grade. Solubility: Form a stable red dispersion in warm water. Applications: Due to its good fluidity, it is especially suitable for direct pressing and hard capsule filling of tomato red tablets, multivitamin and mineral tablets. | |
| 1, 1'-Bis (dicyclohexylphosphino)ferrocene | Ligand for palladium-catalyzed synthesis of oxindoles by amide ?-arylation. Ligand for palladium-catalyzed alkoxycarbonylation of aryl chlorides. Ligand for ruthenium-catalyzed alcohol-allene C-C coupling reaction via hydrohydroxyalkylation of 1,1-disubstituted allenes employing alcohols. Ligand for nickel-catalyzed cross-coupling reaction of arylboronic acids with aryl carbonates. Ligand for palladium-catalyzed regiodivergent hydroesterification of aryl olefins with phenyl formate to form linear structured phenyl arylpropanoates. Ligand for palladium-catalyzed direct borylation of benzyl alcohol and its analogues in the absence of bases. Group: Organic phosphine compounds. Alternative Names: 1,1-Bis(dicyclohexylphosphino)ferrocene; 1,1-Bis(Dicyclohexylphosphino)Ferrocene; 1,1-BIS(DICYCLOHEXYLPHOSPHINO)FERROCENE. CAS No. 146960-90-9. Molecular formula: C34H52FeP2. Mole weight: 578.57. Appearance: Orange-red powder. Purity: 0.98. IUPACName: dicyclohexyl(cyclopentyl)phosphane; iron. Canonical SMILES: C1CCC (CC1)P (C2CCCCC2)[C]3[CH][CH][CH][CH]3. C1CCC (CC1)P (C2CCCCC2)[C]3[CH][CH][CH][CH]3. [Fe]. Catalog: ACM146960909. | |
| 1,2,3,4,5,6-Hexabromocyclohexane | Potently and directly inhibits JAK2 tyrosine kinase autophosphorylation, specifically inhibiting ligand-dependent JAK2 activation. A 16-hour treatment with 1uM of compound reduces JAK2 tyrosine autophosphorylation levels to ~ 50% while 50uM elimates nearly all JAK2 activity. Non-cytotoxic at 100uM. Group: Biochemicals. Grades: Purified. CAS No. 1837-91-8. Pack Sizes: 50mg. Molecular Formula: C6H6Br6. US Biological Life Sciences. | Worldwide |
| 1,2-dehydroreticulinium reductase (NADPH) | Reduces the 1,2-dehydroreticulinium ion to (R)-reticuline, which is a direct precursor of morphinan alkaloids in the poppy plant. The enzyme does not catalyse the reverse reaction to any significant extent under physiological conditions. Group: Enzymes. Synonyms: 1,2-dehydroreticulinium ion reductase. Enzyme Commission Number: EC 1.5.1.27. CAS No. 130590-58-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1509; 1,2-dehydroreticulinium reductase (NADPH); EC 1.5.1.27; 130590-58-8; 1,2-dehydroreticulinium ion reductase. Cat No: EXWM-1509. |  |
| 1,6-Hexanediol | 1,6-Hexanediol is a saturated straight-chain diol, colorless liquid at room temperature, soluble in water. Industrially, 1,6-hexanediol can be synthesized by hydrogenation of adipic acid or its esters. It is usually prepared in the laboratory by the reduction of adipic acid with lithium aluminum hydride. Uses: 1,6-hexanediol can be used for a variety of s such as: a structure-directing agent for the synthesis of zsm-5 zeolite a solvent for titanium tetraisopropoxide to form titanium oxide (tio2) nanocrystals a phase change material in combination with lauric acid for thermal energy storage s. Group: 3d printing materials monomers. Alternative Names: Hexamethylene glycol. CAS No. 629-11-8. Pack Sizes: Packaging 50 g in poly bottle. Product ID: hexane-1,6-diol. Molecular formula: 118.17. Mole weight: HO(CH2)6OH. OCCCCCCO. 1S/C6H14O2/c7-5-3-1-2-4-6-8/h7-8H, 1-6H2. XXMIOPMDWAUFGU-UHFFFAOYSA-N. ≥ 97%. |  |
| 1,6-Hexanediol | 1,6-Hexanediol is a saturated straight-chain diol, colorless liquid at room temperature, soluble in water. Industrially, 1,6-hexanediol can be synthesized by hydrogenation of adipic acid or its esters. It is usually prepared in the laboratory by the reduction of adipic acid with lithium aluminum hydride. Uses: 1,6-hexanediol can be used for a variety of s such as: a structure-directing agent for the synthesis of zsm-5 zeolite a solvent for titanium tetraisopropoxide to form titanium oxide (tio2) nanocrystals a phase change material in combination with lauric acid for thermal energy storage s. Group: Diol monomers. Alternative Names: 1,6-Dihydroxyhexane; Hexamethylene Glycol; 1,6-Hexylene Glycol. CAS No. 629-11-8. Molecular formula: C6H14O2. Mole weight: 118.18 g/mol. Appearance: White to Almost White Powder to Lump. Purity: 97.0%(GC). IUPACName: hexane-1,6-diol. Canonical SMILES: OCCCCCCO. Density: 0.96. ECNumber: 211-074-0. Catalog: ACM-MO-629118. | |
| 17b-Hydroxysteroid Dehydrogenase Type-3 Inhibitor (17b-HSD3 Inhibitor, 5-(3-Bromo-4-hydroxybenzylidene)-3-(4-methoxyphenyl)-2-thioxothiazolidin-4-one) | A cell-permeable benzylidine-thioxothiazolidinone compound that blocks the steroidogenesis of testosterone by directly inhibiting 17b-HSD3- (17b-hydroxysteroid dehydrogenase type 3) catalyzed, NADPH-dependent, reduction of delta4-dione C17 ketone in a delta4-dione- (4-androstene-3,17-dione) competitive, highly potent (IC50=0.6, 6.0, and 40nM, respectively, against momoset, human, and mouse 17b-HSD3 activity in testes homogenate), and selective manner, displaying no activity against 17b-HSD1 and 17b-HSD2 activity. Poor pharmacokinetic properties limit its use to culture treatments and cell-free assays only. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| 17-PA | Selective antagonist of neurosteroid potentiation and direct gating of GABAA receptors. Selectively reduces the effects of 5α-reduced steroids compared to 5 β-reduced steroids and displays no effect on potentiation evoked by barbiturates and benzodiazepines. Attenuates 3α,5α-THP-induced loss of righting reflex and total sleep time following i.c.v administration in rats. Group: Biochemicals. Grades: Highly Purified. CAS No. 694438-95-4. Pack Sizes: 10mg, 50mg. Molecular Formula: C25H34O. US Biological Life Sciences. | Worldwide |
| 1-Chloro-6-iodohexane | 1-Chloro-6-iodohexane is used in studies to demonstrate the direct reduction of 1-Bromo-6-chlorohexane/1-Chloro-6-iodohexane at silver cathodes in Dimethylformamide. Group: Biochemicals. Grades: Highly Purified. CAS No. 34683-73-3. Pack Sizes: 1g, 5g. Molecular Formula: C6H12ClI. US Biological Life Sciences. | Worldwide |
| 20% β carotene direct pressed powder(With fish gelatin) | Free flowing dark red uniform particles with a slight odor and some white starch particles visible. Product ID: PE-0661. Category: Filler Excipients. Product Keywords: Other Filler Excipients; 20% β carotene direct pressed powder(With fish gelatin); PE-0661; Filler Excipients;. Grade: Food Grade. Solubility: Form a stable orange dispersion in warm water. Applications: Due to its good fluidity, especially suitable for direct pressing and hard capsule filling of multivitamin and mineral tablets. | |
| 2,3-bis-O-geranylgeranyl-sn-glycerol 1-phosphate reductase [NAD(P)H] | A flavoprotein (FAD). The enzyme from the archaeon Thermoplasma acidophilum is involved in the biosynthesis of membrane lipids. In vivo the reaction occurs in the reverse direction with the formation of 2,3-bis-O-phytanyl-sn-glycerol 1-phosphate. cf. EC 1.3.7.11, 2,3-bis-O-geranylgeranyl-sn-glycero-phospholipid reductase. Group: Enzymes. Synonyms: digeranylgeranylglycerophospholipid reductase; Ta0516m (gene name); DGGGPL reductase; 2,3-digeranylgeranylglycerophospholipid reductase. Enzyme Commission Number: EC 1.3.1.101. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1273; 2,3-bis-O-geranylgeranyl-sn-glycerol 1-phosphate reductase [NAD(P)H]; EC 1.3.1.101; digeranylgeranylglycerophospholipid reductase; Ta0516m (gene name); DGGGPL reductase; 2,3-digeranylgeranylglycerophospholipid reductase. Cat No: EXWM-1273. | |
| 24-hydroxycholesterol 7α-hydroxylase | A P450 heme-thiolate protein that is found in liver microsomes and in ciliary non-pigmented epithelium. The enzyme is specific for (24S)-cholest-5-ene-3β,24-diol, which is formed mostly in the brain by EC 1.14.14.25, cholesterol 24-hydroxylase. The direct electron donor to the enzyme is EC 1.6.2.4, NADPH-hemoprotein reductase. Group: Enzymes. Synonyms: 24-hydroxycholesterol 7α-monooxygenase; CYP39A1; CYP39A1 oxysterol 7α-hydroxylase. Enzyme Commission Number: EC 1.14.14.26. CAS No. 288309-90-0. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0923; 24-hydroxycholesterol 7α-hydroxylase; EC 1.14.14.26; 288309-90-0; 24-hydroxycholesterol 7α-monooxygenase; CYP39A1; CYP39A1 oxysterol 7α-hydroxylase. Cat No: EXWM-0923. | |
| 25/26-hydroxycholesterol 7α-hydroxylase | A P-450 (heme-thiolate) protein. Unlike EC 1.14.14.26, 24-hydroxycholesterol 7α-monooxygenase, which is specific for its oxysterol substrate, this enzyme can also metabolize the oxysterols 24,25-epoxycholesterol, 22-hydroxycholesterol and 24-hydroxycholesterol, but to a lesser extent. The direct electron donor to the enzyme is EC 1.6.2.4, NADPH-hemoprotein reductase. Group: Enzymes. Synonyms: 25-hydroxycholesterol 7α-monooxygenase; CYP7B1; CYP7B1 oxysterol 7α-hydroxylase; 27-hydroxycholesterol 7-monooxygenase; 27-hydroxycholesterol 7α-hydroxylase; cholest-5-ene-3β,25-diol,NADPH:oxygen oxidoreductase (7α-hydroxylating); 25-hydroxycholesterol 7α-hydroxylase. Enzyme Commission Number: EC 1.14.14.29. CAS No. 149316-80-3. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0926; 25/26-hydroxycholesterol 7α-hydroxylase; EC 1.14.14.29; 149316-80-3; 25-hydroxycholesterol 7α-monooxygenase; CYP7B1; CYP7B1 oxysterol 7α-hydroxylase; 27-hydroxycholesterol 7-monooxygenase; 27-hydroxycholesterol 7α-hydroxylase; cholest-5-ene-3β,25-diol,NADPH:oxygen oxidoreductase (7α-hydroxylating); 25-hydroxycholesterol 7α-hydroxylase. Cat No: EXWM-0926. | |
| 2,5-diamino-6-(ribosylamino)-4(3H)-pyrimidinone 5'-phosphate reductase | The reaction proceeds in the opposite direction. A step in riboflavin biosynthesis, NADPH and NADH function equally well as reductant. Differs from EC 1.1.1.193 [5-amino-6-(5-phosphoribosylamino)uracil reductase] since it does not catalyse the reduction of 5-amino-6-ribosylaminopyrimidine-2,4(1H,3H)-dione 5'-phosphate. Group: Enzymes. Synonyms: 2,5-diamino-6-ribosylamino-4(3H)-pyrimidinone 5'-phosphate reductase; MjaRED; MJ0671 (gene name). Enzyme Commission Number: EC 1.1.1.302. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0213; 2,5-diamino-6-(ribosylamino)-4(3H)-pyrimidinone 5'-phosphate reductase; EC 1.1.1.302; 2,5-diamino-6-ribosylamino-4(3H)-pyrimidinone 5'-phosphate reductase; MjaRED; MJ0671 (gene name). Cat No: EXWM-0213. | |
| 2,5-didehydrogluconate reductase (2-dehydro-L-gulonate-forming) | The enzyme is involved in ketogluconate metabolism, and catalyses the reaction in vivo in the reverse direction to that shown. It is used in the commercial microbial production of ascorbate. cf. EC 1.1.1.274, 2,5-didehydrogluconate reductase (2-dehydro-D-gluconate-forming). Group: Enzymes. Synonyms: 2,5-diketo-D-gluconate-reductase (ambiguous); YqhE reductase; dkgA (gene name); dkgB (gene name). Enzyme Commission Number: EC 1.1.1.346. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0261; 2,5-didehydrogluconate reductase (2-dehydro-L-gulonate-forming); EC 1.1.1.346; 2,5-diketo-D-gluconate-reductase (ambiguous); YqhE reductase; dkgA (gene name); dkgB (gene name). Cat No: EXWM-0261. | |
| 2-enoate reductase | An iron-sulfur-flavoprotein (FAD). Acts (in the reverse direction) on a wide range of alkyl and aryl αβ-unsaturated carboxylate ions; but-2-enoate was the best substrate tested. Group: Enzymes. Synonyms: enoate reductase. Enzyme Commission Number: EC 1.3.1.31. CAS No. 70712-51-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1304; 2-enoate reductase; EC 1.3.1.31; 70712-51-5; enoate reductase. Cat No: EXWM-1304. | |
| 2-methylene-furan-3-one reductase | In the fruit-ripening process of strawberry (Fragaria x ananassa) the reaction is catalysed in the reverse direction from that shown. 4-hydroxy-2,5-dimethylfuran-3(2H)-one is one of the major aroma compounds in the fruits. The enzyme has also been detected in tomato (Solanum lycopersicum) fruits. NADPH is the preferred cofactor. Group: Enzymes. Synonyms: FaEO; SIEO; enone oxidoreductase. Enzyme Commission Number: EC 1.3.1.105. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1277; 2-methylene-furan-3-one reductase; EC 1.3.1.105; FaEO; SIEO; enone oxidoreductase. Cat No: EXWM-1277. | |
| 3β-hydroxycholanate 3-dehydrogenase (NAD+) | This bacterial enzyme is involved, along with EC 1.1.1.52, 3α-hydroxycholanate dehydrogenase (NAD+), or EC 1.1.1.392, 3α-hydroxycholanate dehydrogenase (NADP+), in the modification of secondary bile acids to form 3β-bile acids (also known as iso-bile acids). The enzyme catalyses the reaction in the reduction direction in vivo. Also acts on related 3-oxo bile acids. cf. EC 1.1.1.393, 3β-hydroxycholanate 3-dehydrogenase (NADP+). Group: Enzymes. Synonyms: 3β-hydroxysteroid dehydrogenase. Enzyme Commission Number: EC 1.1.1.391. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0311; 3β-hydroxycholanate 3-dehydrogenase (NAD+); EC 1.1.1.391; 3β-hydroxysteroid dehydrogenase. Cat No: EXWM-0311. | |
| 3β-hydroxycholanate 3-dehydrogenase (NADP+) | This bacterial enzyme is involved, along with EC 1.1.1.52, 3α-hydroxycholanate dehydrogenase (NAD+), or EC 1.1.1.392, 3α-hydroxycholanate dehydrogenase (NADP+), in the modification of secondary bile acids to form 3β-bile acids (also known as iso-bile acids). The enzyme catalyses the reaction in the reduction direction in vivo. Also acts on related 3-oxo bile acids. cf. EC 1.1.1.391, 3β-hydroxycholanate 3-dehydrogenase (NAD+). Group: Enzymes. Synonyms: 3β-hydroxysteroid dehydrogenase (ambiguous). Enzyme Commission Number: EC 1.1.1.393. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0313; 3β-hydroxycholanate 3-dehydrogenase (NADP+); EC 1.1.1.393; 3β-hydroxysteroid dehydrogenase (ambiguous). Cat No: EXWM-0313. | |
| 3β-hydroxysteroid 3-dehydrogenase | The enzyme acts on multiple 3β-hydroxysteroids. Participates in the biosynthesis of zemosterol and cholesterol, where it catalyses the reaction in the opposite direction to that shown. The mammalian enzyme is bifunctional and also catalyses EC 1.1.1.62, 17β-estradiol 17-dehydrogenase. Group: Enzymes. Synonyms: 3-keto-steroid reductase; 3-KSR; HSD17B7 (gene name); ERG27 (gene name). Enzyme Commission Number: EC 1.1.1.270. CAS No. 42616-29-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0177; 3β-hydroxysteroid 3-dehydrogenase; EC 1.1.1.270; 42616-29-5; 3-keto-steroid reductase; 3-KSR; HSD17B7 (gene name); ERG27 (gene name). Cat No: EXWM-0177. | |
| 4-hydroxy-3-methylbut-2-en-1-yl diphosphate reductase | An iron-sulfur protein that contains either a [3Fe-4S] or a [4Fe-4S] cluster. This enzyme forms a system with a ferredoxin or a flavodoxin and an NAD(P)H-dependent reductase. This is the last enzyme in the non-mevalonate pathway for isoprenoid biosynthesis. This pathway, also known as the 1-deoxy-D-xylulose 5-phosphate (DOXP) or as the 2-C-methyl-D-erythritol-4-phosphate (MEP) pathway, is found in most bacteria and in plant chloroplasts. The enzyme acts in the reverse direction, producing a 5:1 mixture of isopentenyl diphosphate and dimethylallyl diphosphate. Group: Enzymes. Synonyms: isopentenyl-diphosphate:NADP+ oxidoreductase; LytB; (E)-4-hydroxy-3-methylbut-2-en-1-yl diphosphate reductase; HMBPP reductase; IspH; LytB/IspH. Enzyme Commission Number: EC 1.17.7.4. CAS No. 512789-14-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1099; 4-hydroxy-3-methylbut-2-en-1-yl diphosphate reductase; EC 1.17.7.4; 512789-14-9; isopentenyl-diphosphate:NADP+ oxidoreductase; LytB; (E)-4-hydroxy-3-methylbut-2-en-1-yl diphosphate reductase; HMBPP reductase; IspH; LytB/IspH. Cat No: EXWM-1099. | |
| (5-formylfuran-3-yl)methyl phosphate synthase | The enzyme catalyses the reaction in the direction of producing (5-formylfuran-3-yl)methyl phosphate, an intermediate in the biosynthesis of methanofuran. The sequence of events starts with the removal of a phosphate group, followed by aldol condensation and cyclization. Methanofuran is a carbon-carrier cofactor involved in the first step of the methanogenic reduction of carbon dioxide by methanogenic archaea. Group: Enzymes. Synonyms: mfnB (gene name); 4-HFC-P synthase; 4-(hydroxymethyl)-2-furaldehyde phosphate synthase. Enzyme Commission Number: EC 4.2.3.153. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5168; (5-formylfuran-3-yl)methyl phosphate synthase; EC 4.2.3.153; mfnB (gene name); 4-HFC-P synthase; 4-(hydroxymethyl)-2-furaldehyde phosphate synthase. Cat No: EXWM-5168. | |
| Acid Cellulase for Textile | This product is a kind of acid cellulase by fermentation of nonpathogenic microbe. It can be used for cellulose fabrics bio-polishing. Be applied to woven fabric, knitted fabric and can get better effect on cotton fabric, cotton/polyester blends, flax, ramie. After the use of this acid cellulase, the fuzziness and the pilling is reduced, the feeling of fabric is more softer and smoother and the color is more lustrous. The dosage of this product is based on dilution, and the processing time is 30-90 minutes. The bach ratio is 5:1~20:1. Group: Enzymes. Synonyms: endo-1,4-β-D-glucanase; β-1,4-glucanase; β-1,4-endoglucan hydrolase; celluase A; cellulosin AP; endoglucanase D; alkali cellulase; cellulase A 3; celludextrinase; 9.5 cell. Enzyme Commission Number: EC 3.2.1.4. CAS No. 9012-54-8. Cellulase. Activity: 3,500 Unit/ml. Appearance: brownish(Color can vary from batch to batch, color intensity is not an indication of enzyme activity), liquid. Storage: Avoid direct sunlight and store at cool and dry place. endo-1,4-β-D-glucanase; β-1,4-glucanase; β-1,4-endoglucan hydrolase; celluase A; cellulosin AP; endoglucanase D; alkali cellulase; cellulase A 3; celludextrinase; 9.5 cellulase; avicelase; pancellase SS; 1,4-(1,3; 1,4)-β-D-glucan 4-glucanohydrolase; EC 3.2.1.4. Pack: 20kg barrel, 200kg plastic drum. Cat No: NATE-1749. | |
| acrylyl-CoA reductase (NADH) | Contains FAD. The reaction is catalysed in the opposite direction to that shown. The enzyme from the bacterium Clostridium propionicum is a complex that includes an electron-transfer flavoprotein (ETF). The ETF is reduced by NADH and transfers the electrons to the active site. Catalyses a step in a pathway for L-alanine fermentation to propanoate. cf. EC 1.3.1.84, acrylyl-CoA reductase (NADPH). Group: Enzymes. Enzyme Commission Number: EC 1.3.1.95. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1365; acrylyl-CoA reductase (NADH); EC 1.3.1.95. Cat No: EXWM-1365. | |
| AD-mix-α | AD-mix-α is a mixture of organic compounds, commonly used to distinguish and identify asymmetric carbon atoms in chiral compounds. It consists of compounds containing catalytically active metals and chiral ligands. AD-mix-α is widely used in various organic synthesis reactions, such as hydrogenation, addition, and carbonylation reactions, to increase yield and reduce the formation of side reaction products. Although it has no direct application in the medical field, it plays an important role in the pharmaceutical industry and chemical research. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 153130-59-7. Pack Sizes: 1 g; 5 g. Product ID: HY-24312. | |
| African Mango Seed Extract | African Mango Seed Extract. Applications: Used for health care products, dietary supplements, weight loss, reducing blood lipids. Group: Others. Synonyms: African Mango Seed Extract; 9005-80-5; Irvingia GabonensisSeed. CAS No. 9005-80-5. Purity: 20% Phytoprotein By KJELDAHL, 10:1 By TLC. Appearance: Light yellow fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Seed. Species: Irvingia GabonensisSeed. African Mango Seed Extract; 9005-80-5; Irvingia GabonensisSeed; plant extract. Pack: 20KG-25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-103. | |
| AKR1C1 Inhibitor, 5-PBSA | A cell-permeable salicylic acid compound that acts as a highly potent, active-site directed and substrate competitive AKR1C1 inhibitor (Ki=4nM) with moderate to excellent selectivity over AKR1C2, AKR1C3 and AKR1C4 (Ki=0.087, 4.2 and 18.2uM, respectively). Shown to inhibit the metabolism of progesterone by AKR1C1 (IC50=460nM in AKR1C1 overexpressing BAECs).CAS No.4906-68-7. Group: Biochemicals. Alternative Names: Aldo-Keto Reductase family 1 member C1 Inhibitor, 5-PBSA, 3-Bromo-5-phenylsalicylic acid, 20α-Hydroxysteroid Dehydrogenase Inhibitor, 5-PBSA. Grades: Highly Purified. CAS No. 4906-68-7. Pack Sizes: 25mg. Molecular Formula: C??H?BrO?. US Biological Life Sciences. | Worldwide |
| Akt Inhibitor XIX, 3CAI (2-Chloro-1-(1H-indol-3-yl)-ethanone, 3-Chloroacetyl-indole) | A cell-permeable chloroacetyl-indole compound that inhibits Akt1 and Akt2 kinase activity (IC50 <1uM) by directly targeting Akt PH domain, exhibiting little or much reduced activity against a panel of 84 other kinases. Effectively inhibits Akt-mediated downstream effector proteins phosphorylation in a time-dependent manner, resulting in effective apoptosis induction in HCT116 and HT29 cultures (by 55% and 60%, respectively; 4uM for 4 days). Reported to retard HCT116-derived tumor growth in mice (EC50=30mg/kg; 5 times/wk for 3 wks via p.o.) in vivo. Group: Biochemicals. Grades: Highly Purified. CAS No. 28755-03-5. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| Alkaline Phosphatase Mutein from Bovine, Recombinant | Part of marker enzyme portfolio. In addition to the AP Mutein, recombinant the lyophilizate contains a mixture of proteins from the Pichia system supporting the interference elimination. AP Mutein is lyophilized from a solution containing in NaCl, 0.2 mol/l; ZnCl2, 0.1 mmol/l; Tea, 30 mmol/l; MgCl2, 1 mmol/l; raffinose, 50% (w/v); pH approximately 7.6. Production is done according to the procedures of the active enzyme. Rely on the special design for reducing alkaline phosphatase-related assay interference interactions. Applications: Use alkaline phosphatase mutein (ap mutein) to eliminate human serum derived ap directed assay interferences. Group: Enzymes. Synonyms: ALKP; ALPase; Alk Phos; Alkaline phosphomonoesterase; Glycerophosphatase; Phosphomonoesterase. CAS No. 9001-78-9. ALP. Activity: <10 U/mg protein. Stability: At +2 to +8°C within specification range for 24 months. Appearance: White to yellowish lyophilizate. Source: Pichia pastoris. Species: Calf intestine. Alkaline phosphatase; ALP; ALKP; ALPase; Alk Phos; EC 3.1.3.1; Alkaline phosphomonoesterase; Glycerophosphatase; Phosphomonoesterase. Cat No: NATE-0992. | |
| all-trans-retinol 13,14-reductase | The reaction is only known to occur in the opposite direction to that given above, with the enzyme being specific for all-trans-retinol as substrate. Neither all-trans-retinoic acid nor 9-cis, 11-cis or 13-cis-retinol isomers are substrates. May play a role in the metabolism of vitamin A. Group: Enzymes. Synonyms: retinol saturase; RetSat; (13,14)-all-trans-retinol saturase; all-trans-retinol:all-trans-13,14-dihydroretinol saturase. Enzyme Commission Number: EC 1.3.99.23. CAS No. 879291-21-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1425; all-trans-retinol 13,14-reductase; EC 1.3.99.23; 879291-21-1; retinol saturase; RetSat; (13,14)-all-trans-retinol saturase; all-trans-retinol:all-trans-13,14-dihydroretinol saturase. Cat No: EXWM-1425. | |
| AMG-8718 | This active molecular is a potent BACE1 inhibitor that is a potential target for the treatment of Alzheimer's disease. AMG-8718 produced significantly reductions of CSF and brain Aβ levels in animal models. It also exhibited reduced potential for QTc elongation in a cardiovascular safety model. BACE1 inhibition has direct efficacy in the Alzheimer's disease pathology but it does not affect viability largely. Uses: The treatment of alzheimer's disease. Synonyms: AMG8718; AMG 8718; AMG-8718. (4S)-7'-(2-fluoropyridin-3-yl)-3'-[2-(3-methyloxetan-3-yl)ethynyl]spiro[5H-1,3-oxazole-4,5'-chromeno[2,3-b]pyridine]-2-amine. Grades: 98%. CAS No. 1215868-94-2. Molecular formula: C25H19FN4O3. Mole weight: 442.45. |  |
| Amlodipine Maleate | Amlodipine Maleate is an impurity of Amlodipine. Amlodipine is a long-acting dihydropyridine L-type calcium channel blocker. Amlodipine is used to lower blood pressure and prevent chest pain. Uses: Amlodipine maleate is a peripheral arterial vasodilator that acts directly on vascular smooth muscle to cause a reduction in peripheral vascular resistance and reduction in blood pressure. Synonyms: 3-Ethyl 5-methyl (+-)-2-((2-aminoethoxy)methyl)-4-(o-chlorophenyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylate, maleate (1:1). Grades: >95%. CAS No. 88150-47-4. Molecular formula: C20H25ClN2O5.C4H4O4. Mole weight: 524.95. | |
| Anamorelin Fumarate | Anamorelin hydrochloride is the orally bioavailable hydrochloride salt of a synthetic, small-molecule ghrelin mimetic with appetite-stimulating and anabolic activities. Anamorelin binds to and stimulates the growth hormone secretagogue receptor (GHSR) centrally, thereby mimicking the appetite-stimulating and growth hormone-releasing effects of grhelin. Stimulation of GHSR may also reduce the production of the pro-inflammatory cytokines TNF-alpha and interleukin-6, which may play a direct role in cancer-related loss of appetite. Synonyms: RC-1291 Fumarate; ONO-7643 Fumarate; RC1291 Fumarate; ONO7643 Fumarate; RC 1291 Fumarate; ONO 7643 Fumarate. Grades: >98%. CAS No. 339539-92-3. Molecular formula: C35H46N6O7. Mole weight: 662.78. | |
| Anisodamine | Anisodamine, an anticholinergic drug, has antishock effect, which is intimately linked to alpha7nAChR-dependent anti-inflammatory pathway. Anisodamine demonstrates a direct cardiac depressive action at the myocyte level, which may be related to, at least in part, NO production and cholinoceptor antagonism, it causes the changes of structure and function in the transmembrane domain of the Ca(2+)-ATPase from sarcoplasmic reticulum. Anisodamine, a vasoactive drug, can abate endogenous endotoxaemia subsequent to splanchnic vasoconstriction due to hypovolaemia, it alleviates inflammatory damage by significantly reducing the expressions of VEGF and ICAM-1, and shows significant protective effects in an animal model of infusion phlebitis. Anisodamine also inhibits shiga toxin type 2-mediated tumor necrosis factor-alpha production in vitro and in vivo. Group: Biochemicals. Grades: Plant Grade. CAS No. 55869-99-3. Pack Sizes: 100mg. Molecular Formula: C17H23NO4, Molecular Weight: 305.374. US Biological Life Sciences. | Worldwide |
| Arbutin | Arbutin is a natural active substance derived from green plants. It combines the "green plant, safe and reliable" and "high-efficiency discoloration" into a skin decolorizing component, which can quickly penetrate into the skin without affecting cell proliferation. At the same time, it can effectively inhibit the activity of tyrosinase in the skin, block the formation of melanin, and directly combine with tyrosinase to accelerate the decompositio;n and excretion of melanin, thereby reducing skin pigmentation, eliminating pigmentation and Freckles, and do not produce toxic, irritating, sensitizing and other side effects on melanocytes, as well as bactericidal and anti-inflammatory effects. Group: Material of cosmetics. Alternative Names: 4-Hydroxyphenyl-beta-D-glucopyranosid. CAS No. 497-76-7. Molecular formula: C12H16O7. Mole weight: 272.25. Appearance: Solid. Purity: 0.98. IUPACName: (2R,3S,4S,5R,6S)-2-(Hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol. Canonical SMILES: C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O. Density: 1.3582 g/cm³. ECNumber: 207-850-3. Catalog: ACM497767. | |
| aromatase | A cytochrome P-450. The enzyme catalyses three sequential hydroxylations of the androgens androst-4-ene-3,17-dione and testosterone, resulting in their aromatization and forming the estrogens estrone and 17β-estradiol, respectively. The direct electron donor to the enzyme is EC 1.6.2.4, NADPH-hemoprotein reductase. Group: Enzymes. Synonyms: CYP19A1 (gene name); estrogen synthetase (incorrect). Enzyme Commission Number: EC 1.14.14.14. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0911; aromatase; EC 1.14.14.14; CYP19A1 (gene name); estrogen synthetase (incorrect). Cat No: EXWM-0911. | |
| Azido-PEG3-amine | A PEG derivative, which contains a free amine that can be conjugated to biological molecules directly by an amide linkage (or via the corresponding isothiocyanate) and an azide that can be reduced to an amine for conjugation to other molecules. PEG derivatives are water soluble. Bifunctional water soluble compounds with flexible dimensions allow for conjugation of small molecules to proteins or molecular probes. 1-amino-11-azido-3,6,9-trioxaundecane can be reacted with small organic molecules for the synthesis of heterobifunctional compounds. It has been used to synthesize a mannose-fluorescein conjugate for the study of cell-surface mannose-specific lectins. Synonyms: Azide-PEG4-Amine;1-Amino-11-azido-3,6,9-trioxaundecane; Amino-PEG3-C2-Azido; 1-[2-(2-aminoethoxy)ethoxy]-2-(2-azidoethoxy)ethane; N3-PEG3-CH2CH2NH2; Ethanamine, 2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]-; 11-Azido-3,6,9-trioxaundecan-1-amine; 2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)ethan-1-amine. Grades: ≥95%. CAS No. 134179-38-7. Molecular formula: C8H18N4O3. Mole weight: 218.25. | |
| azobenzene reductase | The reaction occurs in the reverse direction to that shown above. Other azo dyes, such as Methyl Red, Rocceline, Solar Orange and Sumifix Black B can also be reduced. Group: Enzymes. Synonyms: new coccine (NC)-reductase; NC-reductase; azo-dye reductase; orange II azoreductase; NAD(P)H:1-(4'-sulfophenylazo)-2-naphthol oxidoreductase; orange I azoreductase; azo reductase; azoreductase; nicotinamide adenine dinucleotide (phosphate) azoreductase; NADPH2-dependent azoreductase; dimethylaminobenzene reductase; p-dimethylaminoazobenzene azoreductase; dibromoprop. Enzyme Commission Number: EC 1.7.1.6. CAS No. 9029-31-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1613; azobenzene reductase; EC 1.7.1.6; 9029-31-6; new coccine (NC)-reductase; NC-reductase; azo-dye reductase; orange II azoreductase; NAD(P)H:1-(4'-sulfophenylazo)-2-naphthol oxidoreductase; orange I azoreductase; azo reductase; azoreductase; nicotinamide adenine dinucleotide (phosphate) azoreductase; NADPH2-dependent azoreductase; dimethylaminobenzene reductase; p-dimethylaminoazobenzene azoreductase; dibromopropylaminophenylazobenzoic azoreductase; N,N-dimethyl-4-phenylazoaniline azoreductase; p-aminoazobenzene reductase; methyl red azoreductase; NADPH2:4-(dimethylamino)azobenzene oxidoreductase. Cat No: EXWM-1613. | |
| Betahistine | Betahistine is a H1 receptor agonist, which serves as a vasodilator. It is used in Meniere disease and in vascular headaches but may exacerbate bronchial asthma and peptic ulcers. It is an antivertigo drug first used for treating vertigo. It is also commonly used for patients with balance disorders. It is believed to act by reducing the asymmetrical functioning of sensory vestibular organs as well as by increasing vestibulocochlear blood flow. It also acts as a histamine H3-receptor antagonist which causes an increased output of histamine from histaminergic nerve endings which can further increase the direct H1-agonist activity. It has been listed. Uses: Betahistine is used in meniere disease and in vascular headaches. it is an antivertigo drug first used for treating vertigo. it is also commonly used for patients with balance disorders. Synonyms: N-methyl-2-pyridin-2-ylethanamine. Grades: 98 %. CAS No. 5638-76-6. Molecular formula: C8H12N2. Mole weight: 136.19. | |
| betaine reductase | The reaction is observed only in the direction of betaine reduction. The enzyme from Eubacterium acidaminophilum consists of subunits A, B and C. Subunit B contains selenocysteine and a pyruvoyl group, and is responsible for betaine binding and trimethylamine release. Subunit A, which also contains selenocysteine, is reduced by thioredoxin, and is needed to convert the carboxymethyl group into a ketene equivalent, in turn used by subunit C to produce acetyl phosphate. Only subunit B distinguishes this enzyme from EC 1.21.4.2 (glycine reductase) and EC 1.21.4.3 (sarcosine reductase). Group: Enzymes. Synonyms: acetyl-phosphate trimethylamine:thioredoxin disulfide oxidoreductase (N,N,N-trimethylglycine-forming). Enzyme Commission Number: EC 1.21.4.4. CAS No. 125752-87-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1259; betaine reductase; EC 1.21.4.4; 125752-87-6; acetyl-phosphate trimethylamine:thioredoxin disulfide oxidoreductase (N,N,N-trimethylglycine-forming). Cat No: EXWM-1259. | |
| Biotin hydrazide | Biotin hydrazide is a biotinyl derivative that can be used as a probe for the determination of protein carbonylation, which is a component of several diseases. Protein carbonylation, an irreversible post translational modification (PTM), is caused by attack of reactive oxygen species (ROS), numerous lipid oxidation products (such as α,β-unsaturated γ-hydroxyalkenals), or nonemzymatic glycation resulting in the loss of protein function. Biotin hydrazide is a preferred carbonyl-reactive probe for its direct reaction and chemistry and no requirement of additional catalysts or reducing agents. Biotin hydrazide exclusively and readily derivatizes carbonyl groups at pH 5.5, which facilitates its use to measure carbonylated proteins in biological samples. Group: Heterocyclic organic compound. Alternative Names: (+)-Biotin Hydrazide; Biotin-Hz; Hydrazide Biotin; Biotine Hydrazide. CAS No. 66640-86-6. Molecular formula: C10H18N4O2S. Mole weight: 258.3 g/mol. Appearance: white or slightly yellow powder. Purity: 0.98. IUPACName: 5-[(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanehydrazide. Canonical SMILES: C1C2C(C(S1)CCCCC(=O)NN)NC(=O)N2. Density: 1.243 g/cm³. ECNumber: 613-970-0. Catalog: ACM66640866. | |
| Bitter Orange Extract | Bitter Orange Extract. Applications: Used for health care products, dietary supplements, reducing cholesterol. Group: Others. Synonyms: Bitter Orange Extract; Citrus aurantium L. Purity: 4-10:1 By TLC. Appearance: Brown yellow fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Fruit. Species: Citrus aurantium L. Bitter Orange Extract; Citrus aurantium L.; plant extract. Pack: 20KG-25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-106. | |
| Bivalirudin | Bivalirudin is a specific and reversible direct thrombin inhibitor (DTI). It is a synthetic congener of the naturally occurring drug hirudin. It is a DTI that overcomes many limitations seen with indirect thrombin inhibitors, such as heparin. It is a short, synthetic peptide that is potent, highly specific, and a reversible inhibitor of thrombin. It inhibits both circulating and clot-bound thrombin, while also inhibiting thrombin-mediated platelet activation and aggregation. It has a quick onset of action and a short half-life. It does not bind to plasma proteins (other than thrombin) or to red blood cells. Therefore, it has a predictable antithrombotic response. It does not require a binding cofactor such as antithrombin and does not activate platelets. Synonyms: Hirulog; Hirulog I; Angiomax; Hirulog-1; Hirulog1; Hirulog 1; BG8967; BG 8967; BG-8967; LS-172701; LS172701; LS 172701. Grades: > 95%. CAS No. 128270-60-0. Molecular formula: C98H138N24O33. Mole weight: 2180.32. | |
| Bivatuzumab | Bivatuzumab (Anti-CD44 Recombinant Antibody; BIWA 4) is a humanized monoclonal antibody directed against CD44v6. CD44v6 could acts as a sarcoma target for CAR-redirected CIK cells [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: BIWA 4; Anti-CD44 Recombinant Antibody. CAS No. 214559-60-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99281. | |
| Black Raspberry Extract | Black Raspberry Extract. Applications: Used for health care products, dietary supplements. Group: Others. Synonyms: Black Raspberry Extract; Rubus occidentalis L. Purity: 5%-10%Anthocyanidins, 5%-20% Proanthocyanidins, 4-50:1. Appearance: Red brown fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Fruit. Species: Rubus occidentalis L. Black Raspberry Extract; Rubus occidentalis L; plant extract. Pack: 25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-190. | |
| BRD32048 | The ETV1 transcription factor is phosphorylated downstream of MAPK signaling and is acetylated at lysines 33 and 116 by the histone acetyltransferase p300. BRD32048 is an inhibitor of the ETV1 transcription factor oncoprotein. BRD32048 binds ETV1 directly, modulating both ETV1-mediated transcriptional activity and invasion of ETV1-driven cancer cells. BRD32048 is a substituted [1,3,5]triazine derivative that inhibits ETV1 transcriptional activity by binding to ETV1 with KD of 17.1 μM, which reduces p300-dependent acetylation and stability of ETV1. Synonyms: BRD-32048; BRD 32048. Grades: ≥98%. CAS No. 433694-46-3. Molecular formula: C16H22N6O. Mole weight: 314.4. | |
| Camostat Mesylate | Orally active, non-peptide proteolitic enzyme inhibitor with anti-trypsin and anti-plasmin activities, related structurally to gabexate. Protease inhibitor. Camostat mesilate is a serine protease inhibitor that inhibits plasmin, kallikrein, thrombin as well as trypsin, which attenuates pancreatic fibrosis. It reduces weight gain and improves metabolism in obese rodent models. It is in clinical use (in Japan) for pancreatitis. Camostat has been found to inhibit influenza virus replication in human tracheal epithelial cells and is also a direct prostasin inhibitor which may be useful in reducing sodium transport in cystic fibrosis. Additionally it has been shown to reduce infection of Calu-3 lung cells by SARS-CoV-2 (the coronavirus responsible for COVID-19) via inhibition of the serine protease TMPRSS2 required for viral spike protein priming. Group: Biochemicals. Alternative Names: 4- [ [4- [ (Aminoiminomethyl) amino] benzoyl] oxy] benzeneacetic Acid 2-(Dimethylamino)-2-oxoethyl Ester Methanesulfonate; FOY 305; FOY-S 980; Foipan. Grades: Highly Purified. CAS No. 59721-29-8. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C??H??N?O?S. US Biological Life Sciences. | Worldwide |
| carboxylate reductase | A tungsten protein. Methyl viologen can act as acceptor. In the reverse direction, non-activated acids are reduced by reduced viologens to aldehydes, but not to the corresponding alcohols. Group: Enzymes. Synonyms: aldehyde:(acceptor) oxidoreductase. Enzyme Commission Number: EC 1.2.99.6. CAS No. 125008-36-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1234; carboxylate reductase; EC 1.2.99.6; 125008-36-8; aldehyde:(acceptor) oxidoreductase. Cat No: EXWM-1234. | |
| carboxynorspermidine synthase | The reaction takes place in the opposite direction. Part of a bacterial polyamine biosynthesis pathway. L-aspartate 4-semialdehyde and propane-1,3-diamine/putrescine form a Schiff base that is reduced to form carboxynorspermidine / carboxyspermidine, respectively. The enzyme from the bacterium Vibrio cholerae is essential for biofilm formation. The enzyme from Campylobacter jejuni only produces carboxyspermidine in vivo even though it also can produce carboxynorspermidine in vitro. Group: Enzymes. Synonyms: carboxynorspermidine dehydrogenase; carboxyspermidine dehydrogenase; CASDH; CANSDH; VC1624 (gene name). Enzyme Commission Number: EC 1.5.1.43. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1524; carboxynorspermidine synthase; EC 1.5.1.43; carboxynorspermidine dehydrogenase; carboxyspermidine dehydrogenase; CASDH; CANSDH; VC1624 (gene name). Cat No: EXWM-1524. | |
| Catnip Extract | Catnip Extract. Applications: Catnip is most used in connection with anxiety, insomnia, and nervousness. sedative. lessen migraine headaches to relieve stomach complaints such as colic, cramps, gas, and indigestion reduce swelling associated. Group: Others. Synonyms: Catnip Extract; Nepeta cataria. Purity: 5-10:1 By TLC. Appearance: Brown yellow fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Leaf. Species: Nepeta cataria. Catnip Extract; Nepeta cataria; plant extract. Pack: 25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-165. | |
| CBF beta-Runx1 Inhibitor II, Ro5-3335 ([7-chloro-5-(2-pyrryl)-3H-1,4 benzodiazapin-2-(H)-one], Ro53335, CBFalpha-CBFbeta Inhibitor II) | A cell-permeable benzodiazepine that suppresses CBFalpha/Runx1-CBFbeta transactivation activity (25uM; 293-0 cells) via direct bindings to both subunits of the heterodimeric transcription factor complex. Shown to inhibit oncogenic fusion CBFB-MYH11-, TEL-RUNX1-, and RUNX1-ETO-, dependent leukemia cells proliferation (IC50 = 1.1 to 21.7uM) in vitro and more effectively reduce peripheral blood c-kit+ population (300mg/kg/d via animal feed) than Cytarabine in a murine Cbfb-MYH11 leukemia model in vivo. Comparing to CBFbeta-Runx1 Inhibitor I, Ro5-3335 modulates the Runx1-CBFbeta heterodimer formation without completely disrupting the subunits interaction. Group: Biochemicals. Grades: Highly Purified. CAS No. 30195-30-3. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Cetostearyl Alcohol | Cetostearyl alcohol occurs as white or cream-colored unctuous masses, flakes, pellets or granules. It has a faint, characteristic sweet odor. On heating, cetostearyl alcohol melts to a clear, colorless or pale yellow-colored liquid free of suspended matter. Synonyms: Alcohol cetylicus et stearylicus; cetearyl alcohol; cetyl stearyl alcohol; Crodacol CS90; Lanette O; Speziol C16-18 Pharma; Tego Alkanol 1618; Tego Alkanol 6855. CAS No. 8005-44-5. Product ID: PE-0531. Category: Emollient; Emulsifying Agents; Viscosity-increasing Agents. Product Keywords: Excipients for Liquid Dosage Form; Emulsifier Excipients; PE-0531; Cetostearyl Alcohol; Emollient; Emulsifying Agents; Viscosity-increasing Agents; ; 8005-44-5. UNII: 2DMT128M1S. Chemical Name: Cetostearyl alcohol. Grade: Pharmceutical Excipients. Administration route: Oral; topical; vaginal. Dosage Form: Oral tablets; topical emulsions, lotions, ointments; vaginal suppositories. Stability and Storage Conditions: Cetostearyl alcohol is stable under normal storage conditions. Cetostearyl alcohol should be stored in a well-closed container in a cool, dry place. Source and Preparation: Cetostearyl alcohol is prepared by the reduction of the appropriate fatty acids from vegetable and animal sources. Cetostearyl alcohol can also be prepared directly from hydrocarbon sources. Applications: Cetostearyl alcohol is used in cosmetics and topical pharmaceutical preparations. | |
| chlorite O2-lyase | Reaction occurs in the reverse direction in chlorate- and perchlorate-reducing bacteria. There is no activity when chlorite is replaced by hydrogen peroxide, perchlorate, chlorate or nitrite. The term chlorite dismutase is misleading as the reaction does not involve dismutation/disproportionation. Contains iron and protoheme IX. Group: Enzymes. Enzyme Commission Number: EC 1.13.11.49. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0567; chlorite O2-lyase; EC 1.13.11.49. Cat No: EXWM-0567. | |
| Chloro(1,5-cyclooctadiene)iridium(I) dimer | 1. Precursor to catalysts for the asymmetric hydrogenation of tri- and tetrasubstituted olefins. 2. Precursor to catalyst for enantioselective reduction of imines. 3. Precursor to catalyst for allylic alkylation. 4. Precursor to catalyst for allylic amination and etherification. 5. Precursor to catalyst for the reaction of aroyl chlorides with internal alkynes to produce substituted naphthalenes and anthracenes. 6. Ir-catalyzed addition of acid chlorides to terminal alkynes. 7. Intramolecular hydroamination of unactivated alkenes with secondary alkyl- and arylamines. 8. Enantioselective [2+2] cycloaddition. 9. Silyl-directed, Ir-catalyzed ortho-borylation of arenes. 10. Ir-catalyzed cross-coupling of styrene derivatives with allylic carbonates. 11. Transfer hydrogenative C-C coupling. Group: Iridium series of catalysts. Alternative Names: Bis(1,5-cyclooctadiene)diiridium(I) dichloride. CAS No. 12112-67-3. Molecular formula: C16H24Cl2Ir2. Mole weight: 671.71. Appearance: Red brown powder. Purity: 0.99. IUPACName: (1Z,5Z)-cycloocta-1,5-diene;iridium;dichloride. Canonical SMILES: C1CC=CCCC=C1. C1CC=CCCC=C1. [Cl-]. [Cl-]. [Ir]. [Ir]. ECNumber: 235-170-7. Catalog: ACM12112673-4. | |
| cholesterol 24-hydroxylase | A P-450 heme-thiolate protein. The enzyme can also produce 25-hydroxycholesterol. In addition, it can further hydroxylate the product to 24,25-dihydroxycholesterol and 24,27-dihydroxycholesterol. This reaction is the first step in the enzymic degradation of cholesterol in the brain as hydroxycholesterol can pass the blood-brain barrier whereas cholesterol cannot. The direct electron donor to the enzyme is EC 1.6.2.4, NADPH-hemoprotein reductase. Group: Enzymes. Synonyms: cholesterol 24-monooxygenase; CYP46; CYP46A1; cholesterol 24S-hydroxylase; cytochrome P450 46A1. Enzyme Commission Number: EC 1.14.14.25. CAS No. 50812-30-1, 213327-78-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0922; cholesterol 24-hydroxylase; EC 1.14.14.25; 50812-30-1, 213327-78-7; cholesterol 24-monooxygenase; CYP46; CYP46A1; cholesterol 24S-hydroxylase; cytochrome P450 46A1. Cat No: EXWM-0922. | |
Our database is helping our users find suppliers everyday.
