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| Product | Description | |
|---|---|---|
| HAE | HAE is a 3-amino acid peptide which consists of histidine, alanine and glutamate. Uses: Scientific research. Group: Peptides. CAS No. 64111-99-5. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P1232. |  |
| HAEGTFT | HAEGTFT is the first N-terminal 1-7 residues of GLP-1 peptide. Uses: Scientific research. Group: Peptides. CAS No. 926018-95-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P1228. | |
| HAEGTFT acetate | HAEGTFT acetate is the 1-7 residues of the first N-terminal of glucagon-like peptide-1 (GLP-1). Synonyms: H-His-Ala-Glu-Gly-Thr-Phe-Thr-OH.CH3CO2H; L-histidyl-L-alanyl-L-alpha-glutamyl-glycyl-L-threonyl-L-phenylalanyl-L-threonine acetic acid. Grades: ≥95%. Molecular formula: C35H51N9O14. Mole weight: 821.84. |  |
| HAEGTFTSDVSSYLE | HAEGTFTSDVSSYLE is a polypeptide from patent CN 102920658 B. GLP-I analog contains the sequence. Uses: Scientific research. Group: Peptides. CAS No. 926018-57-7. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P1445. | |
| HAEGT TFA | HAEGT TFA is the 1-5 residues of the first N-terminal of glucagon-like peptide-1 (GLP-1). Synonyms: H-His-Ala-Glu-Gly-Thr-OH.TFA; L-histidyl-L-alanyl-L-alpha-glutamyl-glycyl-L-threonine trifluoroacetic acid. Grades: ≥95%. Molecular formula: C22H32F3N7O11. Mole weight: 627.53. | |
| Hae III | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA in 1 hour at 37°C in a total reaction volume of 50 μl. Applications: After 20-fold overdigestion with enzyme more than 90% of the dna fragments can be ligated and recut. Group: Restriction Enzymes. Purity: 2000U; 10000U. GG↑CC CC↓GG. Activity: 10000; 50000u.a./ml. Appearance: 10 X SE-buffer G. Storage: -20°C. Form: Liquid. Source: An E.coli strain, that carries the cloned Hae III gene from Haemophilus aegyptius. Pack: 10 mM Tris-HCl (pH 7.5); 100 mM NaCl; 0.1 mM EDTA; 1 mM DTT; 200 μg/ml BSA; 50% glycerol. Cat No: ET-1116RE. |  |
| Haemanthamine | Haemanthamine is a crinine-type alkaloid isolated from the Amaryllidaceae plants with potent anticancer activity. Haemanthamine targets ribosomal that inhibits protein biosynthesis during the elongation stage of translation. Haemanthamine has pro-apoptotic, antioxidant, antiviral, antimalarial and anticonvulsant activities. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3-Epicrinamine. Product Category: Inhibitors. Appearance: Solid. CAS No. 466-75-1. Molecular formula: C17H19NO4. Mole weight: 301.34. Purity: 90%+. Canonical SMILES: O[C@@H](C1)[C@@]2(C=C3)C4=CC(OCO5)=C5C=C4C[N@@]1[C@@]2([H])C[C@@H]3OC. Product ID: ACM466751. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Haematocin | It is produced by the strain of Nectria haematococca Berk. et Br. (880701a-1). It can inhibit the germination of Pyricularia oryzae spore. 500 μg/mL of Haematocin culture 5h may inhibit 97.5% spore germination, but has no effect below 30 μg/mL. Synonyms: 6H,13H-pyrazino[1,2-a,4,5-a']diindole-6,13-dione,4,11-bis(acetyloxy)-4,4a,6a,7,11,11a,13a,14-octahydro-6a,13a-bis(methylthio)-,(4S,4aS,6aS,11S,11aS,13aR)-(9Cl). CAS No. 262425-39-8. Molecular formula: C24H26N2O6S2. Mole weight: 502.60. | |
| Haematommic acid | It is a metabolite of manglicolous lichen Roccella montagnei and Ramalina leiodea. Synonyms: Benzoic acid, 3-formyl-2,4-dihydroxy-6-methyl-; Hamatommsaure; 3-Formylorsellinic acid; 2-Hydroxy-3-(hydroxymethylene)-6-methyl-4-oxo-3,4-dihydrobenzoic acid. CAS No. 479-25-4. Molecular formula: C9H8O5. Mole weight: 196.16. | |
| Haematoxylin | 6,6a,7,11b-tetrahydroindeno[2,1-c]chromene-3,4,6a,8,9-pentaol hematoxylin, Natural Black 1, C.I. 75290. CAS No. 517-28-2. Product ID: 8-04279. Molecular formula: C16H14O6. Mole weight: 302.28. |  |
| Haematoxylin (C.I. 75290) | 25g Pack Size. Group: Stains & Indicators. Formula: C16H14O6. CAS No. 517-28-2. Prepack ID 29628570-25g. Molecular Weight 302.28. See USA prepack pricing. |  |
| 4-O-Methylhaematommic acid | 4-O-Methylhaematommic acid is a derivative of Haematommic acid, which is a metabolite of manglicolous lichen Roccella montagnei and Ramalina leiodea. Molecular formula: C10H10O5. Mole weight: 210.18. | |
| Algae Haematococcus pluvialis | Solid. Group: Organic light-emitting diode (oled) materials. CAS No. 472-61-7. Product ID: (6S)-6-hydroxy-3-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(4S)-4-hydroxy-2,6,6-trimethyl-3-oxocyclohexen-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-2,4,4-trimethylcyclohex-2-en-1-one. Molecular formula: 596.8g/mol. Mole weight: C40H52O4. CC1=C (C (CC (C1=O)O) (C)C)C=CC (=CC=CC (=CC=CC=C (C)C=CC=C (C)C=CC2=C (C (=O)C (CC2 (C)C)O)C)C)C. InChI=1S/C40H52O4/c1-27 (17-13-19-29 (3)21-23-33-31 (5)37 (43)35 (41)25-39 (33, 7)8)15-11-12-16-28 (2)18-14-20-30 (4)22-24-34-32 (6)38 (44)36 (42)26-40 (34, 9)10/h11-24, 35-36, 41-42H, 25-26H2, 1-10H3/b12-11+, 17-13+, 18-14+, 23-21+, 24-22+, 27-15+, 28-16+, 29-19+, 30-20+/t35-, 36-/m0/s1. MQZIGYBFDRPAKN-UWFIBFSHSA-N. |  |
| Astaxanthin esters from Haematococcus pluvialis | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. |  |
| Ethyl 4-O-methylhaematommate | Ethyl 4-O-methylhaematommate is a derivative of Haematomma, which is a genus of crustose lichens. Synonyms: Benzoic acid, 3-formyl-2-hydroxy-4-methoxy-6-methyl-, ethyl ester; ethyl 2-hydroxy-3-formyl-4-methoxy-6-methylbenzoate; 3-Formyl-2-hydroxy-4-methoxy-6-methylbenzoic acid ethyl ester. CAS No. 38629-37-7. Molecular formula: C12H14O5. Mole weight: 238.24. | |
| Methyl haematommate | Methyl haematommate is an antifungal agent isolated from Stereocaulon ramulosum. Synonyms: Methyl 3-formylorsellinate; Isophthalaldehydic acid, 2,4-dihydroxy-6-methyl-, methyl ester (6CI,7CI). CAS No. 34874-90-3. Molecular formula: C10H10O5. Mole weight: 210.18. | |
| pBR322/BsuR I (HaeIII) | pBR322/BsuR I (HaeIII). The bsur i digest of pbr322 dna yields 22 fragments suitable for use as molecular weight standards for agarose and polyacrylamide gel electrophoresis. Group: Markers & Ladders. Storage: Store at -20 ?. Cat No: MK-2025. | |
| 15(S)-HETE ethanolamide | Arachidonoyl ethanolamide (AEA) was the first endogenous cannabinoid (CB) to be isolated and characterized as an agonist acting on the same receptors (CB1 and CB2) as THC. 15(S)-HETE ethanolamide is less potent than AEA at the CB1 receptor (Ki of 600 versus 90 nM). 15(S)-HETE ethanolamide also inhibits fatty acid amide hydrolase. Synonyms: 15(S)-hydroxy-N-(2-hydroxyethyl)-5Z,8Z,11Z,13E-eicosatetraenamide; 15(S)-HAEA. Grades: >98%. CAS No. 161744-53-2. Molecular formula: C22H37NO3. Mole weight: 363.5. | |
| 2-Hydrazinobenzothiazole | 2-Hydrazinobenzothiazole is a potent IDO1 inhibitor with an IC 50 of 8 μM. 2-hydrazinobenzothiazole interacts with the IDO1 haem through hydrazine. 2-hydrazinobenzothiazole has the potential for immune system related diseases research [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 615-21-4. Pack Sizes: 10 mM * 1 mL; 5 g. Product ID: HY-78699. | |
| 4-Diazo-3-methoxy-2,5-cyclohexadien-1-one | It is produced by the strain of Penicillum funiculosum. It has favourable anti-anaerobe activity. MIC: 0.4μg/mL for Clostridium and Bacterioids, 0.2μg/mL for Haemophilus, <0.05μg/mL for Clostridium and digestive Streptococcus. And it has a weak antibacterial effect on aerobic bacteria. Synonyms: 2,5-Cyclohexadien-1-one,4-diazo-3-methoxy-; 4-diazonio-3-methoxyphenolate; SQ 30957. CAS No. 105114-23-6. Molecular formula: C7H6N2O2. Mole weight: 150.13. | |
| AGN 194310 | A high affinity pan-RAR antagonist (AGN194310, K(d) for binding to RARs=2-5 nM) inhibited colony formation (by 50%) by all three lines at 16-34 nM, and led to a transient accumulation of flask-cultured cells in G1 followed by apoptosis. AGN194310 is 12-22 fold more potent than all-trans retinoic acid (ATRA) against cell lines and also more potent in inhibiting the growth of primary prostate carcinoma cells. The administration of all-trans retinoic acid to VAD mice resulted in a transient reduction in NF-kappaB activity and, conversely, a single dose of the RAR-pan-antagonist, AGN 194310, administered to control mice, led to a marked, transient induction of whole-body luminescence. Mice were treated with AGN194310, a synthetic retinoid that antagonises the physiological function of the three RAR isotypes (alpha, beta, gamma) but does not interact with RXRs. Analyses of the granulocytic lineage using Gr-1, c-Kit and CD11b antibodies, demonstrated that granulocyte numbers were strikingly increased across haemopoietic compartments in all AGN194310-treated mice. A significant increase in the frequency of progenitor cells containing granulocytes was observed in the bone marrow of mice following treatment with AGN194310. Synonyms: AGN194310; AGN-194310; VTP194310; VTP 194310; VTP-194310. Grades: >98%. CAS No. 229961-45-9. Molecular formula: C28H24O2S. Mole weight: 424.55. | |
| Albitiazolium bromide | Albitiazolium bromide is a choline analogue acts as a cholinergic receptor antagonists, inhibits choline transport into Plasmodium-infected erythrocytes, thus preventing parasite PC biosynthesis, and also to interact with plasmodial haemoglobin degradation in the food vacuole. Uses: Cholinergic receptor antagonists. Synonyms: SAR97276; SAR-97276; SAR 97276; Albitiazolium bromide1,12-bis[4-Methyl-5-(2-hydroxyethyl)thiazol-3-ium-3-yl]dodecane dibromide; 2-[3-[12-[5-(2-hydroxyethyl)-4-methyl-1,3-thiazol-3-ium-3-yl]dodecyl]-4-methyl-1,3-thiazol-3-ium-5-yl]ethanol;dibromide. Grades: ≥95%. CAS No. 321915-72-4. Molecular formula: C24H42Br2N2O2S2. Mole weight: 614.54. | |
| Anionic peptide SAAP | Anionic peptide SAAP is an antimicrobial peptide produced by Pasteurella haemolytica. It has antibacterial activity. Synonyms: Asp-Asp-Asp-Asp-Asp-Asp. Grades: >95%. Molecular formula: C24H32N6O19. Mole weight: 708.54. | |
| Antibacterial protein 1 | Antibacterial protein 1 is an antimicrobial peptide produced by Staphylococcus haemolyticus. It has antibacterial activity. It has hemolytic activity and also inhibits the growth of gonococci. Synonyms: Antibacterial protein1; GGI-1; Gonococcal growth inhibitor 1; Ac-Met-Gln-Lys-Leu-Ala-Glu-Ala-Ile-Ala-Ala-Ala-Val-Ser-Ala-Gly-Gln-Asp-Lys-Asp-Trp-Gly-Lys-Met-Gly-Thr-Ser-Ile-Val-Gly-Ile-Val-Glu-Asn-Gly-Ile-Thr-Val-Leu-Gly-Lys-Ile-Phe-Gly-Phe-CONH2. Grades: >85%. | |
| Antibacterial protein 1 homolog | Antibacterial protein 1 homolog is an antimicrobial peptide found in Staphylococcus haemolyticus (strain JCSC1435). It has antibacterial activity. Synonyms: SH1741 Antibacterial protein 1 homolog; Met-Gln-Lys-Leu-Ala-Glu-Ala-Ile-Ala-Ala-Ala-Val-Gln-Ala-Gly-Gln-Asp-Lys-Asp-Trp-Gly-Lys-Met-Gly-Thr-Ser-Ile-Val-Gly-Ile-Val-Glu-Asn-Gly-Ile-Ser-Val-Leu-Gly-Lys-Ile-Phe-Gly-Phe. Grades: >85%. | |
| Antibacterial protein 2 | Antibacterial protein 2 is an antimicrobial peptide found in Staphylococcus haemolyticus. It has antibacterial activity. Synonyms: Gonococcal growth inhibitor II; Met-Glu-Lys-Ile-Ala-Asn-Ala-Val-Lys-Ser-Ala-Ile-Glu-Ala-Gly-Gln-Asn-Gln-Asp-Trp-Thr-Lys-Leu-Gly-Thr-Ser-Ile-Leu-Asp-Ile-Val-Ser-Asn-Gly-Val-Thr-Glu-Leu-Ser-Lys-Ile-Phe-Gly-Phe. Grades: >85%. | |
| Antibacterial protein 3 | Antibacterial protein 3 is an antimicrobial peptide found in Staphylococcus haemolyticus (strain JCSC1435). It has antibacterial activity. Synonyms: Gonococcal growth inhibitor III; Met-Ser-Lys-Leu-Val-Gln-Ala-Ile-Ser-Asp-Ala-Val-Gln-Ala-Gln-Gln-Asn-Gln-Asp-Trp-Ala-Lys-Leu-Gly-Thr-Ser-Ile-Val-Gly-Ile-Val-Glu-Asn-Gly-Val-Gly-Ile-Leu-Gly-Lys-Leu-Phe-Gly-Phe. Grades: >85%. | |
| Antibacterial protein 3 homolog | Antibacterial protein 3 homolog is an antimicrobial peptide found in Staphylococcus haemolyticus (strain JCSC1435). It has antibacterial activity. Synonyms: Antibacterial protein 3 homolog (SH1743); Met-Ser-Lys-Leu-Val-Gln-Ala-Ile-Ser-Asp-Ala-Val-Gln-Ala-Gly-Gln-Asn-Gln-Asp-Trp-Ala-Lys-Leu-Gly-Thr-Ser-Ile-Val-Gly-Ile-Val-Glu-Asn-Gly-Val-Gly-Ile-Leu-Gly-Lys-Leu-Phe-Gly-Phe. Grades: >85%. | |
| Asiatic acid | Asiatic acid, a pentacyclic triterpene found in Centella asiatica ( Centella asiatica ), has anticancer activity. Asiatic acid induces apoptosis in melanoma cells and has barrier protective effects on human aortic endothelial cells (HAEC). Asiatic acid also has anti-inflammatory activity and inhibits tumor necrosis factor (TNF)-α-induced endothelial barrier dysfunction. Asiatic acid also inhibits NLRP3 inflammasome activation and NF-κB pathway, effectively inhibits inflammation in rats, and has neuroprotective effects in rat spinal cord injury (SCI) model [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Natural products. CAS No. 464-92-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-N0194. | |
| Astaxanthin | Astaxanthin. Synonyms: 3,3'-DIHYDROXY-B,B-CAROTENE-4,4'-DIONE;3,3-DIHYDROXY-B,B-CAROTENE-4,4-DIONE;3,3'-DIHYDROXY-BETA,BETA-CAROTENE-4,4'-DIONE;ASTAXANTHIN;AXN;Astazine 5%;(3S,3S)-3,3-Dihydroxy-.beta.. beta.-carotene-4,4-dione;HAEMATOCOCCUS PLUVIALIS. CAS No. 472-61-7. Pack Sizes: 1 kg. Product ID: CDF4-0145. Molecular formula: C40H52O4. Category: Nutrients. Product Keywords: Food Ingredients; Nutrients; Astaxanthin; CDF4-0145; 472-61-7; C40H52O4; 207-451-4; 472-61-7. Purity: 0.99. Color: pink to very dark purple. EC Number: 207-451-4. Physical State: Powder. Solubility: DMSO: soluble1mg/mL (warmed). Storage: -20°C. Boiling Point: 568.55°C (rough estimate). Melting Point: 215-216 °C. Density: 0.9980 (rough estimate). Product Description: all-trans-Astaxanthin is a ketocarotenoid, most commonly identified in marine and aquatic animals, including krill, wild salmon, rainbow trout, microalgae, shells of lobster, shrimp, seafood products, etc. It is biologically known as a vitamin A precursor, and exhibits strong antioxidant property, much higher compared to vitamin E and β-carotene. Its role in food and the medicinal industry is also well-defined. |  |
| Astaxanthin microencapsulated powder | Astaxanthin microencapsulated powder. Synonyms: 3, 3'-DIHYDROXY-B, B-CAROTENE-4, 4'-DIONE;3, 3-DIHYDROXY-B, B-CAROTENE-4, 4-DIONE;3, 3'-DIHYDROXY-BETA, BETA-CAROTENE-4, 4'Chemicalbook-DIONE;ASTAXANTHIN;AXN;Astazine5%;(3S, 3S)-3, 3-Dihydroxy-.beta.. beta.-carotene-4,4-dione;HAEMATOCOCCUSPLUVIALIS. Product ID: CDF4-0194. Molecular formula: NA. Category: Antioxidant; nutrient supplements. Product Keywords: Food Ingredients; Nutrients; CDF4-0194; Astaxanthin microencapsulated powder; Antioxidant; nutrient supplements. Appearance: pink to very dark purple powder. Chemical Name: 3, 3'-DIHYDROXY-B, B-CAROTENE-4, 4'-DIONE;3, 3-DIHYDROXY-B, B-CAROTENE-4, 4-DIONE;3, 3'-DIHYDROXY-BETA, BETA-CAROTENE-4, 4'Chemicalbook-DIONE;ASTAXANTHIN;AXN;Astazine5%;(3S, 3S)-3, 3-Dihydroxy-.beta.. beta.-carotene-4,4-dione;HAEMATOCOCCUSPLUVIALIS. Color: pink to very dark purple. Physical State: powder. Source and Preparation: Shrimp, crab, fish. Solubility: DMSO: soluble1mg/mL (warmed). Storage: -20°C. Applications: Dietary supplements, nutritional supplements, cosmetic raw materials, etc. Boiling Point: 568.55°C (rough estimate). Melting Point: 215-216 °C. Density: 0.9980 (rough estimate). | |
| Benzylpenicillin | It is produced by the strain of Penicillum sp. Penicillin has a strong antibacterial effect on gram-positive bacteria, Neisseria, Haemophilus, anaerobes (except fragile bacilli), spirochetes and actinomycetes, but no effect on mycobacterium tuberculosis, rickettsia, fungi, protozoa and virus. Synonyms: penicillin g; Benzylpenicillinic acid; Pencillin G. Molecular formula: C16H18N2O4S. Mole weight: 334.39. | |
| Berotralstat dihydrochloride | Berotralstat dihydrochloride is a low toxicity, effective, highly specific, second-generation, synthetic and orally active plasma kallikrein inhibitor used for the research of hereditary angioedema (HAE) attacks. Berotralstat dihydrochloride works by blocking the enzymatic activity of plasma kallikrein in releasing bradykinin, the major biologic peptide that promotes swelling and pain associated with attacks of HAE [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BCX7353 dihydrochloride. CAS No. 1809010-52-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109127A. | |
| Bikaverin | Antibiotic. Antiprotozoal. Antifungal. Anticancer. ATP synthesis inhibitior. Haemolytic agent. Antioomycete. Spermidine-induced autoactivation inhibitor. Plasma hyaluronan-binding protein (PHBP) inhibitor (active form). Group: Biochemicals. Alternative Names: NSC 215139, BRN 0358013, Lycopersin, Mycogonin, Passiflorin. Grades: Highly Purified. CAS No. 33390-21-5. Pack Sizes: 250ug, 1mg. Molecular Formula: C20H14O8. US Biological Life Sciences. |  Worldwide |
| Bilirubin | Bilirubin (formerly referred to as haematoidin) is a yellow compound that occurs in the normal catabolic pathway that breaks down heme in vertebrates. This catabolism is a necessary process in the bodys clearance of waste products that arise from the destruction of aged red blood cells. First the hemoglobin gets stripped of the heme molecule which thereafter passes through various processes of porphyrin catabolism, depending on the part of the body in which the breakdown occurs. For example, the molecules excreted in the urine differ from those in the feces. The production of biliverdin from heme is the first major step in the catabolic pathway, after which the enzyme biliverdin reductase performs the second step, producing bilirubin from biliverdin.Bilirubin is excreted in bile and urine, and elevated levels may indicate certain diseases. It is responsible for the yellow color of bruises and the yellow discoloration in jaundice. Its subsequent breakdown products, such as stercobilin, cause the brown color of feces. A different breakdown product, urobilin, is the main component of the straw-yellow color in urine.It has also been found in plants. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Cholerythrin. Product Category: Heterocyclic Organic Compound. Appearance: Solid. CAS No. 635-65-4. Molecular formula: C33H36N4O6. Mole weight: 584.66. Purity: 0.98. IUPACName: 3-[2-[[3-(2-Car | |
| Bletilla Extract | Bletilla Extract. Applications: Use for stop bleeding by astringency, relieving swelling and promoting tissue regeneration. treat haematenesis and tomachache; and with dondey-hide gelatin, dried rehmannia root, biota tops.treat diabrotic skin sorebe. Group: Others. Synonyms: Bletilla Extract; Bletilla striata (Thunb.ex A.Murray)Rchb.f. Purity: 10:1 by TLC. Appearance: Brown yellow fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Root. Species: Bletilla striata (Thunb.ex A.Murray)Rchb.f. Bletilla Extract; Bletilla striata (Thunb.ex A.Murray)Rchb.f.; plant extract. Pack: 25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-196. | |
| BMS-520 | This active molecular is a selective S1P1 receptor agonist that originated by Bristol-Myers Squibb. BMS-520 shows really good efficacy in animal models of arthritis as well as in a mouse EAE (experimental autoimmune encephalomyelitis) model of multiple sclerosis. Agonism of S1P1 has been known to play an important role in lymphocyte trafficking from the thymus and secondary lymphoid organs, resulting in immunosuppression. Uses: Haematological malignancies; solid tumours. Synonyms: BMS-520; BMS 520; BMS520. 1-(4-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)benzyl)azetidine-3-carboxylic acid. Grades: 98%. CAS No. 1236188-38-7. Molecular formula: C23H17F3N4O4. Mole weight: 470.41. | |
| Brilacidin | Brilacidin (PMX 30063) is an anti-infective antimicrobial with MIC90s of 1 and 8 μg/mL for Gram-positive bacteria Streptococcus pneumonia and Streptococcus viridans , and MIC90 of 8 and 4 μg/mL for Gram-negative bacteria Haemophilus influenza and Pseudomonas aeruginosa. Brilacidin is a defensin mimetic antibiotic compound [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PMX 30063. CAS No. 1224095-98-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-19892. | |
| Cadrofloxacin | Cadrofloxacin, also known as Caderofloxacin and CS-940, is a novel fluoroquinolone antibacterial. The activities of CS-940 against gram-positive cocci and gram-negative rods, including methicillin-susceptible Staphylococcus aureus and penicillin-resistant Streptococcus pneumoniae, were comparable to those of tosufloxacin, with MICs at which 90% of the strains were inhibited (MIC90s) of 0.5 microg/ml or less. Against methicillin-resistant S. aureus, CS-940 was as active as tosufloxacin, with a MIC90 of 16 microg/ml. The efficacy of CS-940 against murine respiratory infections due to S. pneumoniae or Haemophilus influenzae was better than those of tosufloxacin and sparfloxacin. The efficacy of oral doses of CS-940 reflected not only potent in vitro activity but also a high transmigration ratio from the bloodstream to lung tissues. Uses: Designed for use in research and industrial production. Additional or Alternative Names: CS-940; CS 940; CS940; Cadrofloxacin; Caderofloxacin; Cadrofloxacin hydrochloride; Cadrofloxacin HCl. Product Category: Others. Appearance: Solid powder. CAS No. 153808-85-6. Molecular formula: C19H20F3N3O4. Mole weight: 411.38. Purity: >98%. IUPACName: (S)-1-cyclopropyl-8-(difluoromethoxy)-6-fluoro-7-(3-methylpiperazin-1-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid. Canonical SMILES: O=C(C1=CN(C2CC2)C3=C(C=C(F)C(N4C[C@H](C)NCC4)=C3OC(F)F)C1=O)O. Density: 1.458g/cm³. Product ID: ACM153808856. Alfa Chem | |
| Caffeoyltryptophan | Caffeoyltryptophan is a competitive PTP1B inhibitor, with an IC 50 of 16.99 μM. Caffeoyltryptophan can also inhibit α-glucosidase , linoleic acid peroxidation and haemolysis. Caffeoyltryptophan can be used for the research of type 2 diabetes [1]. Uses: Scientific research. Group: Natural products. CAS No. 109163-69-1. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N10002. | |
| Carbazochrome | Carbazochrome is a capillary stabiliser and used for the research of haemorrhage. Carbazochrome is an antihemorrhagic agent [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 69-81-8. Pack Sizes: 10 mM * 1 mL; 100 mg; 250 mg. Product ID: HY-B1587. | |
| Cefixime trihydrate | A broad spectrum third generation cephalosporin targeting a wide range of gram-positive and gram-negative organisms. It is especially useful against pathogens responsible for causing ear, nose, and throat infections such as haemophilus influenzae and moraxella. Synonyms: [6R-[6α , 7β (Z)]]-7-[[ (2-Amino-4-thiazolyl)[ (carboxymethoxy)imino]acetyl]amino]-3-ethenyl-8-oxo-5-Thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid Trihydrate; (E)-cefixime trihydrate; Ytterbium(III) Ionophore I. Grades: ≥97%. CAS No. 125110-14-7. Molecular formula: C16H15N5O7S2.3H2O. Mole weight: 507.50. | |
| Cefmenoxime hydrochloride | Cefmenoxime hydrochloride is a third-generation cephalosporin antibiotic with strong antimicrobial activities against Streptococcus pneumoniae, Haemophilus influenzae and Moraxella subgenus Branhamella catarrhalis that were 3 major aerobic bacteria from sinusitis. It is administered intravenously or intramuscularly. It is active against most common gram-positive and gram-negative microorganisms, It is a potent inhibitor of Enterobacteriaceae and is highly resistant to hydrolysis by beta-lactamases. It has a high rate of efficacy in many types of infection and to date no severe side effects have been noted. Uses: Cefmenoxime hydrochloride is active against most common gram-positive and gram-negative microorganisms, it is a potent inhibitor of enterobacteriaceae and is highly resistant to hydrolysis by beta-lactamases. Synonyms: Cefmenoxime Hydrochloride; SCE 1365 hydrochloride; AB 50912 hemihydrochloride; EINECS 278-299-4; Cefmenoxime hemihydrochloride; Cefmenoxime HCl; SCE1365; Hydrochloride, Cefmenoxime; SCE 1365; SCE-1365;VA10523; A838501;7-[[2-(2-amino-4-thiazolyl)-2-methoxyimino-1-oxoethyl]amino]-3-[[(1-methyl-5-tetrazolyl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid hydrochloride;8-[2-(2-amino-1,3-thiazol-4-yl)-2-methoxyimino-acetyl]amino-4-[(1-methyltetrazol-5-yl)sulfanylmethyl]-7-oxo-2-thia-6-azabicyclo[4.2.0]oct-4-ene-5-carboxylic acid hydrochloride (2:1);Cefmenoxime hemihydrochloride;SCE-1365 hemihydrochloride. Grades: 98%. CAS No. 75738-58-8. Molecular formula: C32H35ClN18O10S6. Mole weight: 1059.58. | |
| Cefquinome sulfate | Cefquinome is a fourth-generation cephalosporin with pharmacological and antibacterial properties valuable in the treatment of coliform mastitis and other infections. Cefquinome sulfate is used in the treatment of infections caused by pathogens such as S. aureus, E. coli, Streptococcus, P. multocida and A. pleuropneumoniae. It can be used to treat respiratory infections in pigs, cattle and sheep caused by sensitive bacteria, dairy cow mastitis and sow agalactia syndrome, and can prevent piglet diarrhea, Haemophilus parasuis and streptococcus disease. Synonyms: Quinolinium, 1-[[(6R,7R)-7-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]-5,6,7,8-tetrahydro-, sulfate (1:1); Quinolinium, 1-[[ (6R, 7R)-7-[[ (2Z)- (2-amino-4-thiazolyl) (methoxyimino)acetyl]amino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-en-3-yl]methyl]-5, 6, 7, 8-tetrahydro-, sulfate (1:1); Quinolinium, 1-[[7-[[ (2-amino-4-thiazolyl) (methoxyimino)acetyl]amino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-en-3-yl]methyl]-5, 6, 7, 8-tetrahydro-, [6R-[6α,7β(Z)]]-, sulfate (1:1); Cefquinome sulphate; HR 111V sulfate. Grades: ≥98%. CAS No. 118443-89-3. Molecular formula: C23H27N6O9S3. Mole weight: 626.68. | |
| Centhaquin | Centhaquine (Centhaquin; PMZ-2010) is a novel agent has the potential for treatment of haemorrhagic shock. Centhaquine (Centhaquin; PMZ-2010) can augment cardiac output, reduce systemic vascular resistance in haemorrhagic models [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Centhaquine; PMZ-2010. CAS No. 57961-90-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-106690. | |
| Chloramphenicol succinate sodium | Chloramphenicol succinate sodium is a proagent of Chloramphenicol, with Haemotoxicity. Chloramphenicol succinate is a competitive substrate and inhibitor of succinate dehydrogenase (SDH) that is the possible reason for its toxicity [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 982-57-0. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-N7114A. | |
| Chuangxinmycin | Chuangxinmycin is produced by the strain of Actinoplanes jinanensis. It has activities against Staphylococcus aureus, Haemophilus influenzae, Escherichia coli and Shigella laminae. Synonyms: Chuanghsinmycin; (-)-chuangxinmycin; cis-(-)-3,5-Dihydro-3-methyl-2H-thiopyrano(4,3,2-cd)indole-2-carboxylic acid. CAS No. 63339-68-4. Molecular formula: C12H11NO2S. Mole weight: 233.29. | |
| Chymotrypsin | Chymotrypsin is a proteolytic enzyme. It can priority hydrolyze tyrosine containing l-isomer, phenylalanine and the peptide bond of tryptophan, the best effective condition is pH 8.0. Its activity can be restrained by heavy metal or natural trypsin inhibitor in some degrees. Applications: Practically used to heal cicatrisation caused by injuries, inflammation and it is also used for avoiding part dropsy, blood-gathering, haematoma caused by wrick, breast dropsy after operation, tympanitis and rhinitis brief introduction of production: the high purity chymotrypsin is extracted from bovine or porcine pancreas and purified by affinity chromatography in order to avoid being polluted by other protease. Group: Enzymes. Synonyms: Chymotrypsin; Alpha-chymotrypsin; Chymotrypsin A; Chymotrypsin B. CAS No. 9004-7-3. Chymotrypsin. Appearance: inquire. Chymotrypsin; Alpha-chymotrypsin; Chymotrypsin A; Chymotrypsin B. Pack: inquire. Cat No: BIO-1012. | |
| Ciprofloxacin HCI | Ciprofloxacin hydrochloride is the hydrochloride of ciprofloxacin, which belongs to the second generation of synthetic quinolone antibacterial drugs. It has broad spectrum antibacterial activity and good bactericidal effect. Its antibacterial activity against almost all bacteria is 2 ~ 4 times stronger than that of norfloxacin and enoxacin. It has antibacterial effect on enterobacter, Pseudomonas aeruginosa, Haemophilus influenzae, gonococcus, Streptococcus, Legionella and Staphylococcus aureus. CAS No. 93107-08-5. Product ID: PAP-0062. Molecular formula: C17H18FN3O3.HCl. Category: Antibiotic. Product Keywords: Antibacterial, Anti-inflammatory and Antiviral Series; Ciprofloxacin HCI; PAP-0062; Antibiotic; C17H18FN3O3.HCl; 93107-08-5. Appearance: Crystalline Solid. Standard: USP/EP. Grade: CEP/ISO. Color: White or yellowish. Physical State: crystalline powder. Solubility: insoluble in EtOH; ≥33.87 mg/mL in H2O; ≥9.34 mg/mL in DMSO with ultrasonic. Storage: Sealed in dry,Room Temperature. Applications: It has a broad spectrum and efficient antibacterial effect, a wide range of treatment, good oral absorption, low toxicity, and is mainly used in the treatment of urinary tract infection, biliary tract infection and intestinal infection. Melting Point: >300 ºC. | |
| Clazosentan | Clazosentan, also called as AXV 034, Ro 61-1790 or VML 588, a novel endothelin A antagonist, improves cerebral blood flow and behavior after traumatic brain injury. In 2016 Actelion plans two phase III trials of Clazosentan for Cerebral vasospasm (in patients with aneurysmal subarachnoid haemorrhage) in Japan. Synonyms: N-[6-(2-hydroxyethoxy)-5-(2-methoxyphenoxy)-2-[2-(2H-tetrazol-5-yl)pyridin-4-yl]pyrimidin-4-yl]-5-methylpyridine-2-sulfonamideAXV034; AXV-034; AXV 034; AXV 034343; AXV-034343; AXV-343434; Ro 61-1790; Ro-61-1790; VML 588; VML-588; VML 588; Clazosentan. Grades: 95%. CAS No. 180384-56-9. Molecular formula: C25H23N9O6S. Mole weight: 577.57. | |
| Clindamycin | Clindamycin is an orally active and broad-spectrum bacteriostatic lincosamide antibiotic. Clindamycin can inhibit bacterial protein synthesis , possessing the ability to suppress the expression of virulence factors in Staphylococcus aureus at sub-inhibitory concentrations (sub-MICs). Clindamycin resistance results from enzymatic methylation of the antibiotic binding site in the 50S ribosomal subunit (23S rRNA). Clindamycin decreases the production of Panton-Valentine leucocidin (PVL), toxic-shock-staphylococcal toxin (TSST-1) or alpha-haemolysin (Hla). Clindamycin also can be used for researching malaria [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 18323-44-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-B1455. | |
| Clindamycin | Clindamycin is an orally active and broad-spectrum bacteriostatic lincosamide antibiotic. Clindamycin can inhibit bacterial protein synthesis, possessing the ability to suppress the expression of virulence factors in Staphylococcus aureus at sub-inhibitory concentrations (sub-MICs). Clindamycin resistance results from enzymatic methylation of the antibiotic binding site in the 50S ribosomal subunit (23S rRNA). Clindamycin decreases the production of Panton-Valentine leucocidin (PVL), toxic-shock-staphylococcal toxin (TSST-1) or alpha-haemolysin (Hla). Clindamycin also can be used for researching malaria. Uses: Designed for use in research and industrial production. Additional or Alternative Names: L-threo-alpha-D-galacto-Octopyranoside, methyl 7-chloro-6,7,8-trideoxy-6-(((1-methyl-4-propyl-2-pyrrolidinyl)carbonyl)amino)-1-thio-, (2S-trans)-. Product Category: Inhibitors. CAS No. 18323-44-9. Molecular formula: C18H33ClN2O5S. Mole weight: 424.98. Product ID: ACM18323449. Alfa Chemistry ISO 9001:2015 Certified. | |
| Clonidine Hydrochloride | α2-Adrenergic agonist. Antihypertensive; analgesic for neuropathic pain. Group: Biochemicals. Alternative Names: N-(2,6-Dichlorophenyl)-4,5-dihydro-1H-imidazol-2-amine Hydrochloride; 2-(2,6-Dichloroanilino)-2-imidazoline Hydrochloride; Atensina; Capresin; Catapres; Haemiton; Hemiton; Isoglaucon; Katapresan; Neuclon; Normopresan; ST 155. Grades: Highly Purified. CAS No. 4205-91-8. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
| Clonidine Hydrochloride | Clonidine HCl is a direct-acting α2 adrenergic agonist with an ED50 of 0.02±0.01 mg/kg. Uses: Sympatholytics. Synonyms: N-(2,6-Dichlorophenyl)-4,5-dihydro-1H-imidazol-2-amine Hydrochloride; 2-(2,6-Dichloroanilino)-2-imidazoline Hydrochloride; Atensina; Capresin; Catapres; Haemiton; Hemiton; Isoglaucon; Katapresan; Neuclon; Normopresan; ST 155. Grades: >98%. CAS No. 4205-91-8. Molecular formula: C9H9Cl2N3.HCl. Mole weight: 266.5. | |
| Concizumab | Concizumab is an anti-TFPI monoclonal antibody (IgG4 type) that binds to the Kunitz-type protease inhibitor (KPI) 2 structural domain of TFPI , thereby blocking the interaction of this structural domain with the FXa active site. Concizumab can be used in the study of haemophilia [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: NN 7415; mAb 2021; Anti-TFPI Recombinant Antibody. CAS No. 1312299-39-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99283. | |
| Congo red | Congo red. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Congazone sodium; Congo red; Haemomedical; Solucongo; Haemonorm; DIRECT RED 28; sodium salt of benzidinediazobis-1-naphthylamine-4-sulfonic acid; Benzo Congo Red; disodium,4-amino-3-[[4-[4-[(1-amino-4-sulfonatonaphthalen-2-yl)diazenyl]phenyl]phenyl]diazen. Product Category: Heterocyclic Organic Compound. Appearance: brown-red powder. CAS No. 573-58-6. Molecular formula: C32H22N6Na2O6S2. Mole weight: 696.663. Purity: 0.96. IUPACName: Congo Red. Density: 1. Product ID: ACM573586. Alfa Chemistry ISO 9001:2015 Certified. | |
| Congo Red | Congo Red is an acid secondary azo dye. It is a VGlut inhibitor and could decrease synaptic transmission in the dentate gyrus. It is an amyloid fibril-binding dye. It can be used to diagnose amyloidosis and used as a diagnostic test for the presence of amyloid in tissue sections. It inhibits the pancreatic islet cell toxicity of diabetes-associated amylin. Its excitation wavelength is 497 nm. It is also a general tissue stain for use as a cytoplasmic counterstain. It is also used in testing for hydrochloric acid in gastric contents and used to stain β sheet aggregates. Synonyms: 1-Naphthalenesulfonic acid, 3,3'-[[1,1'-biphenyl]-4,4'-diylbis(2,1-diazenediyl)]bis[4-amino-, sodium salt (1:2); 1-Naphthalenesulfonic acid, 3,3'-[[1,1'-biphenyl]-4,4'-diylbis(azo)]bis[4-amino-, disodium salt; C.I. Direct Red 28, disodium salt; Atlantic Congo Red; Atul Congo Red; Azocard Red Congo; Benzo Congo Red; Brasilamina Congo 4B; C.I. 22120; C.I. Direct Red 28; Congo red disodium salt; Cotton Red L; Diacotton Congo Red; Direct Congo Red; Erie Congo 4B; Haemomedical; Haemonorm; Hemorrhagyl; Kayaku Congo Red; Mitsui Congo Red; Peeramine Congo Red; Red K (dye); Solucongo; Sugai Congo Red; Tertrodirect Red C; Trisulfon Congo Red; Vondacel Red CL. Grades: ≥98% by HPLC. CAS No. 573-58-0. Molecular formula: C32H22N6Na2O6S2. Mole weight: 696.66. | |
| Contortin | It was the first intestinal antigen of the sheep parasite Haemonchus contortus and was used to induce significant levels of protection when inoculated in lambs. Synonyms: 1,1'-(2,2'-dihydroxy-4,4',6,6'-tetramethoxy-5,5'-dimethyl-[1,1'-biphenyl]-3,3'-diyl)bis(ethan-1-one); Ethanone, 1,1'-(2,2'-dihydroxy-4,4',6,6'-tetramethoxy-5,5'-dimethyl(1,1'-biphenyl)-3,3'-diyl)bis-. CAS No. 91925-83-6. Molecular formula: C22H26O8. Mole weight: 418.44. | |
| coproporphyrinogen oxidase | Coproporphyrinogen oxidase, the sixth enzyme of the haem biosynthetic pathway, converts coproporphyrinogen III to protoporphyrinogen IX through two sequential steps of oxidative decarboxylation. Group: Enzymes. Synonyms: coproporphyrinogen III oxidase; coproporphyrinogenase. Enzyme Commission Number: EC 1.3.3.3. CAS No. 9076-84-0. 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-1377; coproporphyrinogen oxidase; EC 1.3.3.3; 9076-84-0; coproporphyrinogen III oxidase; coproporphyrinogenase. Cat No: EXWM-1377. | |
| CP-10 | CP-10 is a PROTAC connected by ligands for Cereblon and CDK , with highly selective, specific, and remarkable CDK6 degradation ( DC 50 =2.1 nM). It inhibits proliferation of several haematopoietic cancer cells with impressive potency including multiple myeloma, and can still degrades mutated and overexpressed CDK6 [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2366268-80-4. Pack Sizes: 1 mg; 5 mg; 10 mg; 50 mg. Product ID: HY-125835. | |
| Debio 0932 | Debio 0932, also known as CUDC-305, is a novel Hsp90 inhibitor with strong affinity for Hsp90 alpha/beta, high oral bioavailability and potent anti-proliferative activity against a broad range of cancer cell lines (with a mean IC50 of 220 nmol/L), including many non-small cell lung cancer (NSCLC) cell lines which are resistant to standard-of-care (SOC) agents. Debio 0932 potently inhibits tumour growth in subcutaneous xenograft models of a number of solid and haematological malignancies, including models of NSCLC which harbour mutations conferring acquired or primary erlotinib resistance. Furthermore, Debio 0932 is able to extend animal survival in models of brain metastasis due to its ability to cross the blood-brain barrier, and it enhances the activity of several standard-of-care agents in animal models of cancer. Synonyms: Debio0932; Debio 0932; CUDC-305; CUDC305; CUDC 305. Grades: >98%. CAS No. 1061318-81-7. Molecular formula: C22H30N6O2S. Mole weight: 442.58. | |
| Deoxyfusarubin | Deoxyfusarubin is produced by the strain of Nectria haematococca. Synonyms: 3,4-dihydro-3,9-dihydroxy-7-methoxy-3-methyl-1H-naphtho(2,3-c)pyran-5,10-dione. CAS No. 132899-05-9. Molecular formula: C15H14O6. Mole weight: 290.27. | |
| diaminobutyrate decarboxylase | A pyridoxal-phosphate protein that requires a divalent cation for activity. N4-Acetyl-L-2,4-diaminobutanoate, 2,3-diaminopropanoate, ornithine and lysine are not substrates. Found in the proteobacteria Haemophilus influenzae and Acinetobacter baumannii. In the latter, this enzyme is cotranscribed with the dat gene that encodes EC 2.6.1.76, diaminobutyrate-2-oxoglutarate transaminase, which can supply the substrate for this enzyme. Group: Enzymes. Synonyms: DABA DC; L-2,4-diaminobutyrate decarboxylase; L-2,4-diaminobutanoate carboxy-lyase. Enzyme Commission Number: EC 4.1.1.86. 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-4835; diaminobutyrate decarboxylase; EC 4.1.1.86; DABA DC; L-2,4-diaminobutyrate decarboxylase; L-2,4-diaminobutanoate carboxy-lyase. Cat No: EXWM-4835. | |
| Diflomotecan | Diflomotecan is an E-ring modified camptothecin analogue, which possesses greater lactone stability in plasma compared with other topoisomerase I inhibitors. Diflomotecan is also a 10,11-difluoro-homocamptothecin, represents a new promising class of topoisomerase I inhibitors with enhanced plasma stability and superior preclinical anti-tumour activity as compared to the established camptothecins, irinotecan and topotecan. Diflomotecan was the first homocamptothecin to enter clinical studies. Phase I data are summarized for both the intravenous and oral schedules. The toxicity is primarily haematological while no severe gastrointestinal toxicity has been observed in contrast to other topoisomerase I inhibitors. Diflomotecan has a high oral bioavailability (72 - 95%) and the oral day 1 - 5 every 3 weeks regimen is recommended for Phase II testing because it is relatively well tolerated, convenient and mimics protracted exposure. Synonyms: BN 80915; 3H,15H-Oxepino[3',4':6,7]indolizino[1,2-b]quinoline-3,15-dione, 5-ethyl-9,10-difluoro-1,4,5,13-tetrahydro-5-hydroxy-, (5R)-; (5R)-5-Ethyl-9,10-difluoro-1,4,5,13-tetrahydro-5-hydroxy-3H,15H-oxepino[3',4':6,7]indolizino[1,2-b]quinoline-3,15-dione; (R)-5-Ethyl-9, 10-difluoro-5-hydroxy-4, 5-dihydrooxepino[3', 4':6, 7]indolizino[1, 2-b]quinoline-3, 15(1H, 13H)-dione. Grades: ≥95%. CAS No. 220997-97-7. Molecular formula: C21H16F2N2O4. Mole weight: 398.36. | |
| Dihydronovobiocin | Dihydronovobiocin is a derivative of novobiocin. It is active against the bacteria S. aureus, S. haemolyticus, D. pneumoniae, S. typhosa, K. pneumoniae, and P. multocida (MICs = 0.6, 2, 0.6, 10, 10, and 3 μg/ml, respectively). Dihydronovobiocin inhibits DNA gyrase subunit B with an IC50 value of 64.5 nM. Synonyms: N-[7-[[3O-(aminocarbonyl)-6-deoxy-5C-methyl-4O-methyl-α-L-lyxo-hexopyranosyl]oxy]-4-hydroxy-8-methyl-2-oxo-2H-1benzopyran-3-yl]-4-hydroxy-3-(3-methylbutyl)-benzamide. Grades: >95% by HPLC. CAS No. 29826-16-2. Molecular formula: C31H38N2O11. Mole weight: 614.64. | |
| Eculizumab | Eculizumab (Anti-Human C5, Humanized Antibody) is a long-acting humanized monoclonal antibody targeted against complement C5. Eculizumab inhibits the cleavage of C5 into C5a and C5b and hence inhibits deployment of the terminal complement system including the formation of membrane attack complex (MAC). Eculizumab has the potential for haemolysis research [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: Anti-Human C5, Humanized Antibody. CAS No. 219685-50-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P9914. | |
| Efaproxiral | Efaproxiral is a haemoglobin (Hb) synthetic allosteric modifier, decreases Hb-oxygen (O2) binding affinity and enhances oxygenation of hypoxic tumours during radiation therapy [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: RSR13. CAS No. 131179-95-8. Pack Sizes: 10 mM * 1 mL; 50 mg. Product ID: HY-13619. | |
| Efaproxiral sodium | Efaproxiral sodium (RSR13 sodium) is a synthetic allosteric modifier of haemoglobin (Hb), decreases Hb-oxygen (O2) binding affinity and enhances oxygenation of hypoxic tumours during radiation therapy. Uses: Scientific research. Group: Signaling pathways. Alternative Names: RSR13 sodium. CAS No. 170787-99-2. Pack Sizes: 10 mM * 1 mL; 50 mg. Product ID: HY-13619A. | |
| Empagliflozin | Potent, selective and competitive inhibitor of sodium-glucose cotransporter SGLT2, which is implicated in renal glucose reabsorption. The compound increases urinary glucose excretion, helps decrease hyperglyceamia and maintains glucose homeostasis in diabetic individuals. It has been associated with weight loss, lower blood pressure and decreased glycated haemoglobin. Animal studies suggest that empagliflozin preserves regeneration of β-cells in pancreatic Langerhans islets. Group: Biochemicals. Alternative Names: (1S) -1, 5-Anhydro-1-C- [4-chloro-3- [ [4- [ [ (3S) -tetrahydro-3-furanyl] oxy] phenyl] methyl] phenyl] -D-glucitol. Grades: Highly Purified. CAS No. 864070-44-0. Pack Sizes: 5g, 10g, 25g. Molecular Formula: C23H27ClO7, Molecular Weight: 450.91. US Biological Life Sciences. | Worldwide |
| Erythromycin lactobionate | Erythromycin lactobionate is a soluble salt of erythromycin that is a macrolide antibiotic which inhibits bacterial protein synthesis by targeting the 50S ribosomal subunit, blocking the progression of nascent polypeptide chains. Erythromycin is effective against a host of bacterial genera, including Streptococcus, Staphylococcus, and Haemophilus. Synonyms: Erythromycin 4-O-β-D-galactopyranosyl-D-gluconate. CAS No. 3847-29-8. Molecular formula: C49H89NO25. Mole weight: 1092.22. | |
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