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| Product | Description | |
|---|---|---|
| APHA Compound 8 | APHA Compound 8 is a synthetic HDAC (histone deacetylase) inhibitor, which is in the same structural class as SAHA. The IC50 for mouse HDAC1 is 0.5 μM. It induces histone hyperacetylation, growth inhibition, and terminal cell differentiation. Synonyms: MC-1353; MC1353; MC 1353; APHA-8; APHA Compound 8; Aroyl pyrrole hydroxy amide #8; APHA 8; APHA8. Grades: ≥98%. CAS No. 676599-90-9. Molecular formula: C16H16N2O3. Mole weight: 284.3. |  |
| C-phycocyanin from aphanoteca*halophytica | Heterocyclic Organic Compound. CAS No. 11016-15-2. Catalog: ACM11016152. |  |
| 2-Methylbutyl acetate | 2-Methylbutyl acetate. CAS No. 624-41-9. Pack Sizes: 1 kg in glass bottle. Product ID: CDC10-0170. Molecular formula: CH3CO2CH2CH(CH3)C2H5. Category: Flavoring Chemical Agents. Product Keywords: Cosmetic Ingredients; Flavoring Chemical Agents; 2-Methylbutyl acetate; CDC10-0170; 624-41-9; CH3CO2CH2CH(CH3)C2H5; 210-843-8; MFCD00040494; 624-41-9. Grade: Fragrance grade. Purity: 99%, FG. Color: APHA: ≤100. EC Number: 210-843-8. Physical State: neat. Quality Level: 400. Application: flavors and fragrances. Boiling Point: 138 °C/741 mmHg (lit.). Melting Point: -74.65°C (estimate). Density: 0.876 g/mL at 25 °C (lit.). Product Description: 2-Methylbutyl acetate is one of the key volatile aroma compounds that contribute to the characteristic aroma of apples of different varieties such as royal gala apple and Fiji apples. It also occurs naturally in pear and banana. |  |
| glycine/sarcosine N-methyltransferase | Cells of the oxygen-evolving halotolerant cyanobacterium Aphanocthece halophytica synthesize betaine from glycine by a three-step methylation process. This is the first enzyme and it leads to the formation of either sarcosine or N,N-dimethylglycine, which is further methylated to yield betaine (N,N,N-trimethylglycine) by the action of EC 2.1.1.157, sarcosine/dimethylglycine N-methyltransferase. Differs from EC 2.1.1.20, glycine N-methyltransferase, as it can further methylate the product of the first reaction. Acetate, dimethylglycine and S-adenosyl-L-homocysteine can inhibit the reaction. Group: Enzymes. Synonyms: ApGSMT; glycine-sarcosine methyltransferase; GSMT; GMT; glycine sarcosine N-methyltransferase; S-adenosyl-L-methionine:sarcosine N-methyltransferase. Enzyme Commission Number: EC 2.1.1.156. CAS No. 294210-82-5. 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-1752; glycine/sarcosine N-methyltransferase; EC 2.1.1.156; 294210-82-5; ApGSMT; glycine-sarcosine methyltransferase; GSMT; GMT; glycine sarcosine N-methyltransferase; S-adenosyl-L-methionine:sarcosine N-methyltransferase. Cat No: EXWM-1752. |  |
| Kanosamine hydrochloride | Kanosamine hydrochloride is an antibiotic which inhibits the growth of plant-pathogenic oomycetes, certain fungi and a few bacterial species. Kanosamine inhibits Phytophthora medicaginis M2913 and Aphanomyces euteiches WI-98 with MIC s of 25 and 60 μg/mL, respectively. Uses: Scientific research. Group: Signaling pathways. CAS No. 57649-10-2. Pack Sizes: 1 mg; 5 mg. Product ID: HY-112176. |  |
| Linuron-d6 | Labeled analog of a restricted use pesticide. Group: Biochemicals. Alternative Names: N'-(3,4-Dichlorophenyl)-N-methoxy-N-methyl-urea-d6; 1-(3,4-Dichlorophenyl)-3-methoxy-3-methylurea-d6; Afalon-d6; Afalon Inuron-d6; Alfalon-d6; Alfalone-d6; Aphalon-d6; Cephalon-d6; Du Pont 326-d6; Du Pont Herbicide 326-d6; Herbicide 326-d6; Linex-d6; Linurex-d6; Liron-d6; Lorex-d6; Lorox-d6; Methoxydiuron-d6. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| Native Streptomyces griseus Chitosanase | Chitosanase catalyzes the endohydrolysis of β (1,4) linkages between N-acetyl-D-glucosamine and D-glucosamine residues in partially deacetylated chitosan. Chitosanase from Streptomyces griseus is capable of hydrolyzing both chitosan and carboxymethyl cellulose. It is used for the lysis of cell walls of fungi belonging to the group Mucorales. It is found in several types of microorganisms. Applications: Chitosanase from streptomyces griseus has been used in a study to assess the effect of chitin sources on production of chitinase and chitosanase. chitosanase from streptomyces griseus has also been used in a study to investigate the effective production of chitinase an...cete aphanomyces euteiches, a major parasite of legume plants. it has also been used for the enzymatic hydrolysis of the fully de-n-acetylated chitosan to get chitosan oligomer mixtures during the preparation of biocompatible chitosan-alginate gel. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Enzyme Commission Number: EC 3.2.1.132. CAS No. 51570-20-8. Chitosanase. Activity: >50 units/mg protein (Bradford). Storage: -20°C. Form: Lyophilized powder containing potassium phosphate buffer salts. Source: Streptomyces griseus. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Cat No: NATE-0125. | |
| Nitritocobalamin | Nitritocobalamin is a useful synthetic intermediate in the synthesis of Hydroxocobalamin Acetate; a physiological analog of vitamin B12 where the CN group is replaced with OH. Exists in aqueous solution as an equilibrium mixture of the hydroxy isomer and the ionic aqua isomer (aquacobalamin). Precursor of the coenzymes methylcobalamin and cobamamide. Coordination Compound. Vitamin (hematopoietic). Group: Biochemicals. Alternative Names: Co-(nitrito-κO)-cobinamide Dihydrogen Phosphate (Ester) Inner Salt 3-Ester with (5,6-Dimethyl-1-alpha-D-ribofuranosyl-1H-benzimidazole-κN3), Nitrocobalamin; Vitamin B12c; Cobinamide, hydroxide nitrite (salt), dihydrogen phosphate (ester), inner salt, 3-ester with 5, 6-di methyl -1-alpha-D-ribofuranosyl benzimidazole, Cobinamide, nitrite (salt), dihydrogen phosphate (ester), inner salt, 3-ester with 5,6-dimethyl-1-alpha-D-ribofuranosyl-1H-benzimidazole, Cobinamide, nitrite phosphate, 3-ester with 5, 6-di methyl -1-apha-D-ribofuranosyl benzimidazole, inner salt. Grades: Highly Purified. CAS No. 20623-13-6. Pack Sizes: 10mg, 25mg, 50mg. Molecular Formula: C62H88CoN14O16P. US Biological Life Sciences. | Worldwide |
| Parathion | Parathion. Group: Biochemicals. Alternative Names: Parathion A; Parathion-ethyl; Penncap E; RB; Rhodiasol; Rhodiatox; Selephos; Super Rodiatox; Thiomex; Thiophos; Thiophos 3422; Vitrex; AAT; AATP; Alkron; Alleron; American Cyanamid 3422; Aphamite; Aralo; BAY 1605; Bayer E-605; Bladan F; DNTP; Diethyl 4-nitrophenyl phosphorothioate; Diethyl p-nitrophenyl phosphorothionate; Diethyl p-Nitrophenyl Thionophosphate; Diethyl parathion; E 605; E 605F; E 605FT20; ENT 15108; Ecatox 20; Ekatox; Ekatox 20; Ethyl parathion; Etilon; Folidol; Folidol E; Folidol E-605; Folidol oil; Fosferno; Fostox; Galpar; Gearphos; Lirothion; NIUIF 100; NSC 8933; Niran; Nitrostigmine; Nourithion; O,O-Diethyl O-(4-nitrophenyl) phosphorothioate; O,O-Diethyl O-(p-nitrophenyl) phosphorothioate; O,O-Diethyl O-p-nitrophenyl thiophosphate; Oleofos 20; Oleoparathene; Oleoparathion; Pacol; Paramar 50; Paraphos; Parathene; O,O-Diethyl O-(p-Nitrophenyl) Ester Phosphorothioic Acid; OO-Diethyl O-(4-Nitrophenyl) Ester Phosphorothioic Acid. Grades: Highly Purified. CAS No. 56-38-2. Pack Sizes: 500mg. Molecular Formula: C10H14NO5PS, Molecular Weight: 291.26. US Biological Life Sciences. | Worldwide |
| Parathion-d10 | Parathion-d10. Group: Biochemicals. Alternative Names: Parathion A-d10; Parathion-ethyl-d10; Penncap E-d10; RB-d10; Rhodiasol-d10; Rhodiatox-d10; Selephos-d10; Super Rodiatox-d10; Thiomex-d10; Thiophos-d10; Thiophos 3422-d10; Vitrex-d10; AAT-d10; AATP-d10; Alkron-d10; Alleron-d10; American Cyanamid 3422-d10; Aphamite-d10; Aralo-d10; BAY 1605-d10; Bayer E-605-d10; Bladan F-d10; DNTP-d10; Diethyl 4-nitrophenyl phosphorothioate-d10; Diethyl p-nitrophenyl phosphorothionate-d10; Diethyl p-Nitrophenyl Thionophosphate-d10; Diethyl parathion-d10; E 605-d10; E 605F-d10; E 605FT20-d10; ENT 15108-d10; Ecatox 20-d10; Ekatox-d10; Ekatox 20-d10; Ethyl parathion-d10; Etilon-d10; Folidol-d10; Folidol E-d10; Folidol E-605-d10; Folidol oil-d10; Fosferno-d10; Fostox-d10; Galpar-d10; Gearphos-d10; Lirothion-d10; NIUIF 100-d10; NSC 8933-d10; Niran-d10; Nitrostigmine-d10; Nourithion-d10; O,O-Diethyl O-(4-nitrophenyl) phosphorothioate-d10; O,O-Diethyl O-(p-nitrophenyl) phosphorothioate-d10; O,O-Diethyl O-p-nitrophenyl thiophosphate-d10; Oleofos 20-d10; Oleoparathene-d10; Oleoparathion-d10; Pacol-d10; Paramar 50-d10; Paraphos-d10; Parathene-d10; O,O-Diethyl O-(p-Nitrophenyl) Ester Phosphorothioic Acid-d10; OO-Diethyl O-(4-Nitrophenyl) Ester Phosphorothioic Acid-d10. Grades: Highly Purified. Pack Sizes: 2.5mg. Molecular Formula: C10H4D10NO5PS, Molecular Weight: 301.32. US Biological Life Sciences. | Worldwide |
| Prazosin Hydrochloride | Prazosin Hydrochloride (Terazosin EP Impurity K) is an antihypertensive. α1-Adrenergic blocker. Prazosin hydrochloride, a quinazole derivative, is a very potent and highly selective antagonist for apha-1-adrenoceptors (affinity for alpha-1 is about 1000-fold greater than for alpha-2 receptors). Mainly used as a clinic vasodilator for blood pressure control without increasing the heart rate or significantly impairing sympathetic functions. Has also been used clinically to treat anxiety, PTSD, and panic disorder. An excellent candidate for research studying brain functions mediated through alpha-1-adrenergic receptors, such as reward, pleasure, aggression, fear, anxiety, and addiction. Group: Biochemicals. Alternative Names: [4-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-1-piperazinyl]-2-furanylmethanone Hydrochloride; 1- (4-Amino-6, 7-dimethoxy-2-quinazolinyl) -4- (2-furanylcarbonxyl) piperazine Hydrochloride; Adversuten; Adverszuten; Alpress LP; Furazosin; Lentopres; NSC 292810; Peripress; Terazosin EP Impurity K. Grades: Highly Purified. CAS No. 19237-84-4. Pack Sizes: 100mg, 250mg, 500mg. Molecular Formula: C??H??ClN?O?, Molecular Weight: 419.86r. US Biological Life Sciences. | Worldwide |
| sarcosine/dimethylglycine N-methyltransferase | Cells of the oxygen-evolving halotolerant cyanobacterium Aphanocthece halophytica synthesize betaine from glycine by a three-step methylation process. The first enzyme, EC 2.1.1.156, glycine/sarcosine N-methyltransferase, leads to the formation of either sarcosine or N,N-dimethylglycine, which is further methylated to yield betaine (N,N,N-trimethylglycine) by the action of this enzyme. Both of these enzymes can catalyse the formation of N,N-dimethylglycine from sarcosine. The reactions are strongly inhibited by S-adenosyl-L-homocysteine. Group: Enzymes. Synonyms: ApDMT; sarcosine-dimethylglycine methyltransferase; SDMT; sarcosine dimethylglycine N-methyltransferase; S-adenosyl-L-methionine:N,N-dimethylglycine N-methyltransferase. Enzyme Commission Number: EC 2.1.1.157. 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-1753; sarcosine/dimethylglycine N-methyltransferase; EC 2.1.1.157; ApDMT; sarcosine-dimethylglycine methyltransferase; SDMT; sarcosine dimethylglycine N-methyltransferase; S-adenosyl-L-methionine:N,N-dimethylglycine N-methyltransferase. Cat No: EXWM-1753. | |
| WF14865A | WF14865A is a cathepsins B and L inhibitor with IC50 of 8.4 X 10(-9) and 6.6 X 10(-8) mol/L, respectively. It is produced by Aphanoascus fulvescens. Synonyms: WF-14865A. Molecular formula: C16H25N5O5. Mole weight: 367.4. | |
| WF14865B | WF14865B is a cathepsins B and L inhibitor with IC50 of 1.3 X 10(-8) and 7.2 X 10(-8) mol/L, respectively. It is produced by Aphanoascus fulvescens. Synonyms: WF-14865B. Molecular formula: C17H27N5O5. Mole weight: 381.43. | |
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