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| Product | Description | |
|---|---|---|
| Violacein | It is a nitrogenous heterocyclic indole antibiotic produced by the strain of Chromobacterium violaceum. It has anti-gram-positive bacteria, fungi and protozoa effects. The serum has an effect on its activity. Synonyms: (3E)-3-[5-(5-Hydroxy-1H-indol-3-yl)-2-oxo-1,2-dihydro-3H-pyrrol-3-yliden]-1,3-dihydro-2H-indol-2-one; 2H-Indol-2-one, 3-[1,2-dihydro-5-(5-hydroxy-1H-indol-3-yl)-2-oxo-3H-pyrrol-3-ylidene]-1,3-dihydro-, (3E)-. Grades: ≥ 95% (violacein and deoxyviolacein)?Violacein ≥ 80%. CAS No. 548-54-9. Molecular formula: C20H13N3O3. Mole weight: 343.34. |  |
| Violacein from Janthinobacterium lividum | >98% (violacein (minimum 85% violacein) and deoxyviolacein, HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| violacein synthase | The enzyme, characterized from the bacterium Chromobacterium violaceum, participates in the biosynthesis of the violet pigment violacein. The products, violaceinate and deoxyviolaceinate, undergo non-enzymic autooxidation into violacein and deoxyviolacein, respectively. Group: Enzymes. Synonyms: proviolaceinate monooxygenase; vioC (gene name). Enzyme Commission Number: EC 1.14.13.224. 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-0827; violacein synthase; EC 1.14.13.224; proviolaceinate monooxygenase; vioC (gene name). Cat No: EXWM-0827. |  |
| Violaceol I | Violaceol I is an aromatic ether in which the ether functionality links two 2,3-dihydroxy-5-methylphenyl groups. Fungal metabolite isolated inter alia from Aspergillus spp. It has a role as a mycotoxin and a metabolite. It is a member of catechols and an aromatic ether. Synonyms: violaceol i; violaceol-I; NSC-330927; 3,3'-Oxybis(5-methyl-1,2-benzenediol). Grades: ≥95%. CAS No. 68027-81-6. Molecular formula: C14H14O5. Mole weight: 262.26. | |
| Violaceol II | It is a mycotoxin isolated from Emericella violacea and Aspergillus spp. It has weak activity against Gram-positive bacteria, Gram-negative bacteria, fungi and yeast. Synonyms: violacerol-II; 3-(2,6-dihydroxy-4-methylphenoxy)-5-methylbenzene-1,2-diol; 5-methyl-2-[5-methyl-2,3-bis(oxidanyl)phenoxy]benzene-1,3-diol; 2-(2,3-dihydroxy-5-methyl-phenoxy)-5-methyl-resorcinol. CAS No. 81827-49-8. Molecular formula: C14H14O5. Mole weight: 262.26. | |
| Violacin A | Violacin A is an antibacterial peptide isolated from Viola odorata. It has low hemolytic activity. Synonyms: cyclo[Ala-Ile-Ser-Cys(1)-Gly-Glu-Thr-Cys(2)-Phe-Lys-Phe-Lys-Cys(3)-Tyr-Thr-Pro-Arg-Cys(1)-Ser-Cys(2)-Ser-Tyr-Pro-Val-Cys(3)-Lys-Ser]; SAISCGETCFKFKCYTPRCSCSYPVCK. Molecular formula: C129H191N33O37S6. Mole weight: 2988.5. | |
| Violanone | Violanone, an isoflavanone compound, can inhibit tubulin polymerization. Violanone also exhibits larvicidal activity against A. aegypti. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. CAS No. 52250-38-1. Molecular formula: C17H16O6. Mole weight: 316.31. Canonical SMILES: O=C1C2=CC=C(C=C2OCC1C3=CC=C(C(O)=C3OC)OC)O. Product ID: ACM52250381. Alfa Chemistry ISO 9001:2015 Certified. Categories: Viola-Jones object detection framework. |  |
| Violanthin | Violanthin is a flavonoid showing antioxidant and antibacterial activities. Synonyms: Violanthin; 40581-17-7; C10196; 5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]chromen-4-one5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3S,4R,5R,6R)-3,4,5-trihydroxy -6-(hydroxymethyl)oxan-2-yl]-8-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-me thyl-oxan-2-yl]chromen-4-one. Grades: 0.98. CAS No. 40581-17-7. Molecular formula: C27H30O14. Mole weight: 578.5. | |
| Violanthrone 79 | Violanthrone 79. Group: Biochemicals. Alternative Names: 16, 17-Bis (octyloxy) anthra [9, 1, 2-cde]benzo [rst]pentaphene-5, 10-dione. Grades: Highly Purified. CAS No. 85652-50-2. Pack Sizes: 100mg. Molecular Formula: C50H48O4, Molecular Weight: 712.91. US Biological Life Sciences. |  Worldwide |
| Violanthrone-79 | Violanthrone-79. Group: other materials. CAS No. 85652-50-2. Product ID: 30, 34-dioctoxynonacyclo[18.10.2.22, 5.03, 16.04, 13.06, 11.017, 31.022, 27.028, 32]tetratriaconta-1(30), 2(34), 3(16), 4(13), 5(33), 6, 8, 10, 14, 17(31), 18, 20(32), 22, 24, 26, 28-hexadecaene-12, 21-dione. Molecular formula: 712.9g/mol. Mole weight: C50H48O4. CCCCCCCCOC1=C2C3=C (C=CC4=C3C (=C1)C5=CC=CC=C5C4=O)C6=C7C2=C (C=C8C7=C (C=C6)C (=O)C9=CC=CC=C98)OCCCCCCCC. InChI= 1S / C50H48O4 / c1-3-5-7-9-11-17-27-53-41-29-39-31-19 -13-15-21-35 (31) 49 (51) 37-25-23-33-34-24-26-38-44-40 (32-20-14-16-22-36 (32) 50 (38) 52) 30-42 (54-28-18-12-10-8-6-4-2) 48 (46 (34) 44) 47 (41) 45 (33) 4 3 (37) 39 / h13-16, 19-26, 29-30H, 3-12, 17-18, 27-28H2, 1-2H3. LLPQZABTDLOYAL-UHFFFAOYSA-N. |  |
| Violaxanthin | analytical standard. Group: Colorant standards. | |
| violaxanthin de-epoxidase | Along with EC 1.14.13.90, zeaxanthin epoxidase, this enzyme forms part of the xanthophyll (or violaxanthin) cycle for controlling the concentration of zeaxanthin in chloroplasts. It is activated by a low pH of the thylakoid lumen (produced by high light intensity). Zeaxanthin induces the dissipation of excitation energy in the chlorophyll of the light-harvesting protein complex of photosystem II. In higher plants the enzyme reacts with all-trans-diepoxides, such as violaxanthin, and all-trans-monoepoxides, but in the alga Mantoniella squamata, only the diepoxides are good substrates. Group: Enzymes. Synonyms: VDE. Enzyme Commission Number: EC 1.23.5.1. CAS No. 57534-73-3. 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-1269; violaxanthin de-epoxidase; EC 1.23.5.1; 57534-73-3; VDE. Cat No: EXWM-1269. | |
| Violaxanthin (Mixture of Diastereomers) | Violaxanthin is a carotenoid found in prickly pear fruit. Group: Biochemicals. Alternative Names: 5,6,5,6-Tetrahydrozeaxanthin 5,6:5,6-diepoxide; (1R, 1R, 3S, 3S)-6, 6-((3E, 5E, 7E, 9E, 11E, 13E, 15E)-3, 7, 12, 16-Tetramethyloctadeca-1, 3, 5, 7, 9, 11, 13, 15, 17-nonaene-1, 18-diyl)bis(1, 5, 5-trimethyl-7-oxabicyclo[4. 1. 0]heptan-3-ol). Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Violettyne MIP | Violettyne MIP. CAS No. 166432-52-6. VIGON Item # 502849. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. |  America & Internationally |
| Violuric acid | Violuric acid is a redox mediator used in the laccase system. The violuric acid assay is a method to ascertain that the high-redox potential of laccase is not lost during directed evolution [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 87-39-8. Pack Sizes: 1 g; 5 g; 10 g. Product ID: HY-W097009. |  |
| Viomellein (BRN4630536) | Genotoxic mycotoxin. Antibacterial (Gram-positive) and insecticidal. Group: Biochemicals. Grades: Highly Purified. CAS No. 55625-78-0. Pack Sizes: 500ug, 1mg. US Biological Life Sciences. | Worldwide |
| Viomycin | Tuberactinomycin B is a member of the tuberactinomycin family of antibiotics used for the treatment of multidrug-resistant tuberculosis. Tuberactinomycin B inhibits group I intron splicing and prokaryotic protein synthesis, and freezes bacterial ribosomes in either the pre-or post-translational state. Uses: The treatment of multidrug-resistant tuberculosis. Synonyms: Tuberactinomycin B; Celiomycin; Florimycin; Viomicina; Viomycine; Viomycinum. CAS No. 32988-50-4. Molecular formula: C25H43N13O10. Mole weight: 685.69. | |
| viomycin kinase | Acts also on capreomycins. A serine residue in the peptide antibiotics acts as phosphate-acceptor. Group: Enzymes. Synonyms: viomycin phosphotransferase; capreomycin phosphotransferase. Enzyme Commission Number: EC 2.7.1.103. CAS No. 77000-11-4. 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-2950; viomycin kinase; EC 2.7.1.103; 77000-11-4; viomycin phosphotransferase; capreomycin phosphotransferase. Cat No: EXWM-2950. | |
| Viomycin sulfate | It is a peptide antibiotic produced by the strain of Str. puniceus 1314-5 and Str. floridae A5014. It has broad-spectrum antibacterial and strong anti-mycobacterium effect. 1-10 μg/mL of Viomycin can inhibit the growth of most tuberculosis bacilli, the main effect is to inhibit the protein synthesis of bacteria, but bacteria are prone to develop drug resistance. In clinical application, it is only used as a second-line drug to treat tuberculosis. Synonyms: Tuberactinomycin B sulfate salt; celicomycin-sulfate; florimycin sulfate; Vinacetin A sulfate; hexanamide, 3,6-diamino-N-[(3S,6Z,9S,12S,15S)-6-[[(aminocarbonyl)amino]methylene]-3-[(4R,6S)-2-amino-3,4,5,6-tetrahydro-6-hydroxy-4-pyrimidinyl]-9,12-bis(hydroxymethyl)-2,5,8,11,14-pentaoxo-1,4,7,10,13-pentaazacyclohexadec-15-yl]-, (3S)-, sulfate (1:1) (salt). CAS No. 37883-00-4. Molecular formula: C25H43N13O10.H2O4S. Mole weight: 783.77. | |
| Viomycin trihydrochloride | It is a peptide antibiotic produced by the strain of Str. puniceus 1314-5 and Str. floridae A5014. It has broad-spectrum antibacterial and strong anti-mycobacterium effect. 1-10 μg/mL of Viomycin can inhibit the growth of most tuberculosis bacilli, the main effect is to inhibit the protein synthesis of bacteria, but bacteria are prone to develop drug resistance. In clinical application, it is only used as a second-line drug to treat tuberculosis. Synonyms: Florimycin trihydrochloride; Viomycinum trihydrochloride; Vinacetin A trihydrochloride; Hexanamide, 3,6-diamino-N-[(3S,6Z,9S,12S,15S)-6-[[(aminocarbonyl)amino]methylene]-3-[(4R,6S)-2-amino-1,4,5,6-tetrahydro-6-hydroxy-4-pyrimidinyl]-9,12-bis(hydroxymethyl)-2,5,8,11,14-pentaoxo-1,4,7,10,1 3-pentaazacyclohexadec-15-yl]-, (3S)-, hydrochloride (1:3). CAS No. 39750-31-7. Molecular formula: C25H43N13O10.3HCl. Mole weight: 795.07. | |
| Vioxanthin | Vioxanthin is an antibiotic produced by Malbranchea pulchella var. sulfurea. It is active against gram-positive bacteria and bacteroides fragilis. Synonyms: Tf-26Vx. CAS No. 15447-05-9. Molecular formula: C30H26O10. Mole weight: 546.5. | |
| Vioxx | Vioxx. Group: Biochemicals. Alternative Names: 4-[4- (Methylsulfonyl) phenyl]-3-phenyl-2 (5H) -furanone. Grades: Highly Purified. CAS No. 162011-90-7. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C17H14O4S. US Biological Life Sciences. | Worldwide |
| Vioxx-d5 (Major) | A selective labeled cyclooxygenase-2 (COX-2) inhibitor. Use as an anti-inflammatory, analgesic. Group: Biochemicals. Alternative Names: 4-[4- (Methylsulfonyl) phenyl]-3- (phenyl-d5) -. Grades: Highly Purified. CAS No. 544684-93-7. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Vioxx (Rofecoxib, MK-0966, 4-[4-(methylsulfonyl)-phenyl]-3-phenyl-2(5H)-furanone) | A selective cyclooxygenase-2 (COX-2) inhibitor. Use as an anti-inflammatory. Group: Biochemicals. Alternative Names: Rofecoxib, MK-0966, 4-[4-(methylsulfonyl)-phenyl]-3-phenyl-2(5H)-furanone. Grades: Highly Purified. CAS No. 162011-90-7. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Vip | Vip. Uses: Designed for use in research and industrial production. Additional or Alternative Names: VASOACTIVE INTESTINAL PEPTIDE (HUMAN, BOVINE, PORCINE, RAT);VASOACTIVE INTESTINAL PEPTIDE (HUMAN, PORCINE);VASOACTIVE INTESTINAL PEPTIDE, HUMAN, PORCINE, AND RAT;VASOACTIVE INTESTINAL PEPTIDE (HUMAN, PORCINE) (BOVINE, RAT, CANINE);VASOACTIVE INTESTINAL PEPTIDE HUMAN, PORCINE, RAT;VASOACTIVE INTESTINAL PEPTIDE, HUMAN, PORCINE, RAT, OVINE;VASOACTIVE INTESTINAL PEPTIDE, PORCINE;VASOACTIVE INTESTINAL PEPTIDE. Product Category: Heterocyclic Organic Compound. Appearance: powder. CAS No. 40077-57-4. Molecular formula: C147H238N44O42S. Mole weight: 3325.8. Product ID: ACM40077574. Alfa Chemistry ISO 9001:2015 Certified. | |
| Vip(4-28)(human,bovine,porcine,rat) | Vip(4-28)(human,bovine,porcine,rat). Uses: Designed for use in research and industrial production. Additional or Alternative Names: AVIPTADIL (4-28);H-ALA-VAL-PHE-THR-ASP-ASN-TYR-THR-ARG-LEU-ARG-LYS-GLN-MET-ALA-VAL-LYS-LYS-TYR-LEU-ASN-SER-ILE-LEU-ASN-NH2;VIP (4-28) (HUMAN, BOVINE, PORCINE, RAT). Product Category: Heterocyclic Organic Compound. CAS No. 64326-02-9. Molecular formula: C134H221N39O36S. Product ID: ACM64326029. Alfa Chemistry ISO 9001:2015 Certified. | |
| VIP (6-28) (human, rat, porcine, bovine) | VIP (6-28) (human, rat, porcine, bovine) is an effective antagonist of the actions of exogenous vasoactive intestinal peptide (VIP) on cAMP. Synonyms: Aviptadil (6-28); Vasoactive Intestinal Peptide (6-28). CAS No. 69698-54-0. Molecular formula: C126H207N37O34S. Mole weight: 2816.28. | |
| Vipadenant | Vipadenant is an adenosine A2 receptor antagonists used as an immunosuppressant. Synonyms: BG-14; CEB-4520; V2006; VER-11135; VER-A00-11; VER-A00049; VER-ADO-49; VR-2006. CAS No. 442908-10-3. Molecular formula: C16H15N7O. Mole weight: 321.34. | |
| VIP Antagonist | VIP antagonist, a hybrid of neurotensin (6-11) and VIP (7-28), is a competitive antagonist of VIP-binding to glial cells. In rats with reduced masculine potency, it significantly inhibits VIP-stimulated sexual behavior. It antagonizes VIP receptors on non-small cell lung cancer cells, thereby inhibiting tumor growth in vivo and in vitro. Synonyms: [Lys1,Pro2,5,Arg3,4,Tyr6]VIP, human, porcine, rat, ovine; H-Lys-Pro-Arg-Arg-Pro-Tyr-Thr-Asp-Asn-Tyr-Thr-Arg-Leu-Arg-Lys-Gln-Met-Ala-Val-Lys-Lys-Tyr-Leu-Asn-Ser-Ile-Leu-Asn-NH2; L-lysyl-L-prolyl-L-arginyl-L-arginyl-L-prolyl-L-tyrosyl-L-threonyl-L-alpha-aspartyl-L-asparagyl-L-tyrosyl-L-threonyl-L-arginyl-L-leucyl-L-arginyl-L-lysyl-L-glutaminyl-L-methionyl-L-alanyl-L-valyl-L-lysyl-L-lysyl-L-tyrosyl-L-leucyl-L-asparagyl-L-seryl-L-isoleucyl-L-leucyl-L-asparaginamide; [Lys1,Pro2,5,Arg3,4,Tyr6]-Vasoactive Intestinal Peptide human, porcine, rat. Grades: 95%. CAS No. 125093-93-8. Molecular formula: C154H257N49O40S. Mole weight: 3467.06. | |
| VIP (guinea pig) | VIP (guinea pig) is a neuropeptide that plays a role in neurotransmission, smooth muscle relaxation and has trophic and mitogenic actions. CAS No. 96886-24-7. Molecular formula: C147H239N43O42S2. Mole weight: 3346. | |
| VIP(Guinea pig) | VIP Guinea pig (Vasoactive intestinal peptide), a trophic and mitogenic factor, stimulates growth in whole cultured embryos. VIP Guinea pig functions as a simple gastrointestinal hormone and suggest a possible neurotransmitter function [1] [2]. Uses: Scientific research. Group: Peptides. Alternative Names: Vasoactive Intestinal Peptide, guinea pig. CAS No. 96886-24-7. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P1015. | |
| Viphi A | Viphi A is a cytotoxic cyclic peptide isolated from Viola philippica, which shows cytotoxic activity to cancer cell lines MM96L, HeLa and BGC-823. Synonyms: Gly-Ser-Ile-Pro-Cys-Gly-Glu-Ser-Cys-Val-Phe-Ile-Pro-Cys-Ile-Ser-Ser-Val-Ile-Gly-Cys-Ala-Cys-Lys-Ser-Lys-Val-Cys-Tyr-Lys-Asn. Mole weight: 3170. | |
| Viphi D | Viphi D is a cytotoxic cyclic peptide isolated from Viola philippica, which shows cytotoxic activity to cancer cell lines MM96L, HeLa and BGC-823. Synonyms: Gly-Ile-Pro-Cys-Gly-Glu-Ser-Cys-Val-Phe-Ile-Pro-Cys-Ile-Ser-Ser-Val-Ile-Gly-Cys-Ser-Cys-Ser-Ser-Lys-Val-Cys-Tyr-Arg-Asn. Mole weight: 3086.3. | |
| Viphi E | Viphi E is a cytotoxic cyclic peptide isolated from Viola philippica, which shows cytotoxic activity to cancer cell lines MM96L, HeLa and BGC-823. Synonyms: Gly-Ser-Ile-Pro-Cys-Gly-Glu-Ser-Cys-Val-Phe-Ile-Pro-Cys-Ile-Ser-Ala-Val-Ile-Gly-Cys-Ser-Cys-Ser-Asn-Lys-Val-Cys-Tyr-Lys-Asn. Mole weight: 3456.24. | |
| Viphi F | Viphi F is a cytotoxic cyclic peptide isolated from Viola philippica, which shows cytotoxic activity to cancer cell lines MM96L, HeLa and BGC-823. Synonyms: Gly-Ser-Ile-Pro-Cys-Gly-Glu-Ser-Cys-Val-Phe-Ile-Pro-Cys-Ile-Ser-Ala-Ile-Ile-Gly-Cys-Ser-Cys-Ser-Ser-Lys-Val-Cys-Tyr-Lys-Asn. Mole weight: 3143.3. | |
| Viphi G | Viphi G is a cytotoxic cyclic peptide isolated from Viola philippica, which shows cytotoxic activity to cancer cell lines MM96L, HeLa and BGC-823. Synonyms: Gly-Ser-Ile-Pro-Cys-Gly-Glu-Ser-Cys-Val-Phe-Ile-Pro-Cys-Ile-Ser-Ala-Ile-Ile-Gly-Cys-Ser-Cys-Ser-Asn-Lys-Val-Cys-Tyr-Lys-Asn. Mole weight: 3170.36. | |
| VIPhyb | VIPhyb (compound VIPhyb) is a vasoactive intestinal polypeptide (VIP) receptor antagonist that can be used in the study of cancers such as non-small cell lung cancer (NSCLC)[1]. Uses: Scientific research. Group: Peptides. CAS No. 125093-93-8. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-P5005. | |
| Vipivotide tetraxetan | Vipivotide tetraxetan (PSMA-617) is a high potent prostate-specific membrane antigen (PSMA) inhibitor, with a K i of 0.37 nM. Vipivotide tetraxetan (PSMA-617) is designed consisting of three components: the pharmacophore Glutamate-urea-Lysine, the chelator DOTA able to complex both 68Ga or 177Lu, and a linker connecting these two entities. Glutamate-urea-Lysine is the selective pharmacophore to bind to prostate specific membrane antigen. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PSMA-617. CAS No. 1702967-37-0. Pack Sizes: 10 mM * 1 mL; 1 mg; 2 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-117410. | |
| Vipoglanstat | Vipoglanstat (BI 1029539), a carboxamide, is a potent and selective, non-peptide and orally active small molecular inhibitor of human prostaglandin E synthase 1 (mPGES-1). Vipoglanstat also has anti-inflammatory activity[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BI 1029539; GS-248; OX-MPI. CAS No. 1360622-01-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-147416. | |
| Viramidine Hydrochloride | Taribavirin hydrochloride is an orally active inosine monophosphate dehydrogenase inhibitor, has activity against a wide range of viruses, especially the hepatitis C virus and influenza virus. Taribavirin hydrochloride is a Ribavirin prodrug, is designed to concentrate within the liver to target HCV-infected hepatocytes while minimizing distribution within red blood cells (RBCs) and the development of hemolytic anemia. Uses: Antiviral agents. Synonyms: 1-β-D-Ribofuranosyl-1H-1,2,4-triazole-3-carboximidamide Monohydrochloride; AVS 206; ICN 3142; Ribamidine Hydrochloride; Taribavirin Hydrochloride. Grades: 98%. CAS No. 40372-00-7. Molecular formula: C8H14ClN5O4. Mole weight: 279.68. | |
| Viramidine Hydrochloride | Viramidine Hydrochloride. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1-β-D-Ribofuranosyl-1H-1,2,4-triazole-3-carboximidamide Monohydrochloride. Appearance: White Solid. CAS No. 40372-00-7. Molecular formula: C8H14ClN5O4. Mole weight: 279.68. Purity: 0.98. Product ID: ACM40372007. Alfa Chemistry ISO 9001:2015 Certified. Categories: Taribavirin hydrochloride. | |
| Viranamycin A | It is produced by the strain of Str. sp. CH 41. It can inhibit the growth of murine leukemia cell P388 with IC50 of 5.8 ng/mL, and it can also inhibit KB human multi-squamous cell carcinoma cells with IC50 of 6.4 ng/mL. Synonyms: Concanamycin A, 23-O-(3-carboxy-1-oxo-2-propenyl)-23-O-de[4-O-(aminocarbonyl)-2,6-dideoxy-b-D-arabino-hexopyranosyl]-25-de(1-propenyl)-25-methyl-. CAS No. 139595-03-2. Molecular formula: C41H64O13. Mole weight: 764.94. | |
| Viranamycin B | It is produced by the strain of Str. sp. CH 41. It can inhibit the growth of murine leukemia cell P388 with IC50 of 2.8 ng/mL, and it can also inhibit KB human multi-squamous cell carcinoma cells with IC50 of 1.9 ng/mL. Synonyms: Concanamycin A, 25-de(1-propenyl)-25-methyl-. CAS No. 139595-04-3. Molecular formula: C44H73NO14. Mole weight: 840.05. | |
| Virantmycin | Virantmycin. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Virantmycin, NSC 374127, CID100206, NSC374127, LS-141710, 6-Quinolinecarboxylic acid, 1,2,3,4-tetrahydro-3-chloro-2-(3,4-dimethyl-3-pentenyl)-2-(methoxymethyl)-, (2S-trans)-, 6-Quinolinecarboxylic acid, 3-chloro-2-(3,4-dimethyl-3-pentenyl)-1,2,3,4-tetrahydro-2-(methoxymethyl)-, 76417-04-4. Product Category: Heterocyclic Organic Compound. CAS No. 76417-04-4. Molecular formula: C19H26ClNO3. Mole weight: 351.867640 [g/mol]. Purity: 0.96. IUPACName: 3-chloro-2-(3,4-dimethylpent-3-enyl)-2-(methoxymethyl)-3,4-dihydro-1H-quinoline-6-carboxylic acid. Product ID: ACM76417044. Alfa Chemistry ISO 9001:2015 Certified. | |
| Virantmycin | It is produced by the strain of Str. nitrosporeus AM-2722. It has antiviral effect. It inhibits four RNA viruses and four DNA viruses with MIC (μg/mL) of 0.008-0.04 and 0.005-0.03, respectively. It has weak antifungal effect. Synonyms: 6-Quinolinecarboxylic acid, 3-chloro-2-(3,4-dimethyl-3-penten-1-yl)-1,2,3,4-tetrahydro-2-(methoxymethyl)-, (2R,3R)-; NSC 374127; 6-Quinolinecarboxylic acid, 3-chloro-2-(3,4-dimethyl-3-pentenyl)-1,2,3,4-tetrahydro-2-(methoxymethyl)-, (2R-cis)-; (-)-Virantmycin. Grades: 99%. CAS No. 76417-04-4. Molecular formula: C19H26C1NO3. Mole weight: 351.87. | |
| VIRE_HELVI Virescein | VIRE_HELVI Virescein is an antibacterial peptide isolated from Helioth is virescens. Synonyms: Virescein (Insects, animals); Gly-Lys-Ile-Pro-Ile-Gly-Ala-Ile-Lys-Lys-Ala-Gly-Lys-Ala-Ile-Gly-Lys-Gly-Leu-Arg-Ala-Val-Asn-Ile-Ala-Ser-Thr-Ala-His-Asp-Val-Tyr-Thr-Phe-Phe-Lys-Pro-Lys-Lys-Arg-His. Molecular formula: C202H336N60O49. Mole weight: 4389.26. | |
| Virensic acid | It is a lichen acid with enzyme inhibitory potential. Synonyms: 11H-Dibenzo[b,e][1,4]dioxepin-7-carboxylic acid, 4-formyl-3,8-dihydroxy-1,6,9-trimethyl-11-oxo-; 10-formyl-3,9-dihydroxy-1,4,7-trimethyl-6-oxobenzo[b][1,4]benzodioxepine-2-carboxylic acid; Granulatine; NSC 685587. CAS No. 668-14-4. Molecular formula: C18H14O8. Mole weight: 358.30. | |
| Viresin | Viresin is an antibacterial protein isolated from immune hemolymph of Helioth is virescens pupae. Viresin showed antibacterial activity against several Gram-negative bacteria including E. cloacae but not against Gram-positive bacteria. Synonyms: Tyr-Asp-Asn-Val-Asn-Leu-Asp-Glu-Ile-Leu-Ala-Asn-Asp-Arg-Leu-Leu-Val-Pro-Tyr-Ile-Lys-Cys-Leu-Leu-Asp-Glu-Gly-Lys-Lys-Ala-Pro-Asp-Ala-Lys-Glu-Leu-Lys-Glu-His-Ile-ArgX-Ala-Leu. Molecular formula: C221H361N59O66S. Mole weight: 5062.06. | |
| Virgaureagenin G | Virgaureagenin G. Group: Biochemicals. CAS No. 22338-71-2. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Virginiamycin | Virginiamycin. Uses: For analytical and research use. Group: Pharma & vet compounds & metabolites; pharma & vet compounds & metabolites; chiral molecules. Alternative Names: Pyostacin, Stafac, Eskalin 500, Streptogramin, Stafac 500, Livelong, Eskalin V,Mikamycin, Stafac 20, Stapyocine, Virgimycin, Pyostacine, Lactrol. CAS No. 11006-76-1. Molecular formula: C43H49N7O10+C28H35N3O7. Mole weight: 1349.51. Catalog: APS11006761. SMILES: CCC1C(=O)N2CCCC2C(=O)N(C(C(=O)N3CCC(=O)CC3C(=O)NC(C(=O)OC(C(C(=O)N1)NC(=O)C4=C(C=CC=N4)O)C)C5=CC=CC=C5)CC6=CC=CC=C6)C.CC1C=CC(=O)NCC=CC(=CC(CC(=O)CC2=NC(=CO2)C(=O)N3CCC=C3C(=O)OC1C(C)C)O)C. Format: Neat. | |
| Virginiamycin | Virginiamycin complex contains two streptogramin antibiotics, virginiamycin M1 (75%) and virginiamycin S1 (25%). It is an antibiotic used primarily in the treatment of staphylococcal infections, and to a less extent streptococcal infections. Uses: Anti-bacterial agents. Synonyms: Pristinamycin. CAS No. 11006-76-1. Molecular formula: C71H84N10O17. Mole weight: 1349.48. | |
| Virginiamycin B | Virginiamycin B is a depsipeptide antibiotic co-produced with ostreogrycin A and used as a synergistic mixture. Virginiamycin B, also known as ostreogrycin B and streptogramin B among other synonyms, was discovered independently and named by several groups leading to considerable confusion in the literature. Viriginiamycin B acts as a synergist binding to the conformational change in the peptidyl transferase centre of the 50S ribosome induced by ostreogrycin A. Group: Biochemicals. Grades: Highly Purified. CAS No. 3131-3-1. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Virginiamycin B | Pristinamycin IA is an ester peptide antibiotic produced by Str. pristinaespiralis 5647 (NRRL 2958). Activity against gram-positive bacteria. Synonyms: Ostreogrycin B, Pristinamycin IA, Streptogramin B, Syncothrecin B1, Synergistin B, Vernamycin Balpha, Virginiamycin 1A, NSC 125176, 14725-1, PA 114B, RP 12535. Grades: ≥ 95%. CAS No. 3131-3-1. Molecular formula: C45H54N8O10. Mole weight: 866.96. | |
| Virginiamycin Complex | Virginiamycin complex is defined as a mixture of 75% virginamycin M1 (ostreogrycin A) and 25% virginiamycin S1 and the less abundant S analogs. As the two major components have quite different solubilities these proportions are not readily achieved or used. The individual components are isolated and re-combined to provide the defined components of virginiamycin complex. The structure composition of the complex is important as Virginiamycin S1 acts a synergist, binding to the conformational change of the peptidyl transferase center of the 50S ribosome induced by ostreogrycin A. Group: Biochemicals. Alternative Names: Cebin V, Eskalin V, Eskamicin, Stafac, Stephylomycin, Mikamycin, Ostreogrycin, Patricin, Pristinamycin, Streptogramin, Vernamycin. Grades: Highly Purified. CAS No. 11006-76-1. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Virginiamycin M1 | Virginiamycin M1. Uses: For analytical and research use. Group: Pharma & vet compounds & metabolites; pharma & vet compounds & metabolites. Alternative Names: NSC 87432, (3R,4R,5E,10E,12E,14S)-8,9,14,15,24,25-Hexahydro-14-hydroxy-4,12-dimethyl-3-(1-methylethyl)-3H-21,18-nitrilo-1H,22H-pyrrolo[2,1-c][1,8,4,19]dioxadiazacyclotetracosine-1,7,16,22(4H,17H)-tetrone, Factor M, RP 12536, [3R-(3R*,4R*,5E,10E,12E,14S*)]-8,9,14,15,24,25-Hexahydro-14-hydroxy-4,12-dimethyl-3-(1-methylethyl)-3H-21,18-nitrilo-1H,22H-pyrrolo[2,1-c][1,8,4,19]dioxadiazacyclotetracosine-1,7,16,22(4H,17H)-tetrone, NSC 244426, Ostreogrycin A (7CI), PA 114A, Virginiamycin M1, Mikamycin A (6CI,8CI), Antibiotic PA 114A1, Pristinamycin IIA,3H-21,18-Nitrilo-1H,22H-pyrrolo[2,1-c][1,8,4,19]dioxadiazacyclotetracosine-1,7,16,22(4H,17H)-tetrone, 8,9,14,15,24,25-hexahydro-14-hydroxy-4,12-dimethyl-3-(1-methylethyl)-, (3R,4R,5E,10E,12E,14S)-, Staphylomycin M1, Pristinamycin II, Factor M (antibiotic), Antibiotic PA 114A, Streptogramin A, Vernamycin A. CAS No. 21411-53-0. Molecular formula: C28H35N3O7. Mole weight: 525.59. Catalog: APS21411530A. SMILES: CC(C)[C@H]1OC(=O)C2=CCCN2C(=O)c3coc(CC(=O)C[C@H](O)\C=C(/C)\C=C\CNC(=O)\C=C\[C@H]1C)n3. Format: Neat. | |
| Virginiamycin M1 | Virginiamycin M1 (Pristinamycin IIA; Ostreogrycin A), produced by Streptomyces virginiae , is an polyunsaturated macrocyclic lactone antibiotic and acts as a component of Virginiamycin (HY-112665) [1]. Virginiamycin M1 alone is against Staphylococcus aureus with a MIC of 0.25 μg/mL. Uses: Scientific research. Group: Natural products. Alternative Names: Pristinamycin IIA; Ostreogrycin A. CAS No. 21411-53-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N6686. | |
| Virginiamycin M1 | Macrolactone antibiotic. Antibacterial; growth promotant. Group: Biochemicals. Grades: Highly Purified. CAS No. 21411-53-0. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Virginiamycin S1 | It is a depsipeptide antibiotic produced by the strain of Str. virginiae and Str. virginiae var. sp. It has anti-gram-positive bacteria and mycobacterium effects, and the antibacterial activity of component M of Virginiamycin against cocci is stronger than component S, while the activity is stronger than component M. Synonyms: Staphylomycin S; Staphylomycin S1; Antibiotic 1754Z3B; Virginiamycin factor S; NSC177858; Stephylomycin; Eskamicin; Cebin V; Factor S; Glycine, N-[(3-hydroxy-2-pyridinyl)carbonyl]-L-threonyl-D-2-aminobutanoyl-L-prolyl-N-methyl-L-phenylalanyl-4-oxo-L-2-piperidinecarbonyl-L-2-phenyl-, r-lactone. Grades: >99% by HPLC. CAS No. 23152-29-6. Molecular formula: C43H49N7O10. Mole weight: 823.89. | |
| Virginiamycin S1 | Virginiamycin S1 is a main component of virginiamycin preparations. Virginiamycin S1 is one of a family of depsipeptide antibiotic co-produced with ostreogrycin A and used as a synergistic mixture. Virginiamycin S1 also known as Staphylomycin S and Factor S, among other synonyms were discovered independently and named by several groups leading to considerable confusion in the literature. Virginiamycin S1 acts a synergist binding to the conformational change induced by ostreogrycin A of the peptidyl transferase centre of the 50S ribosome. Virginiamycin S1 differs from virginiamycin B in lacking the dimethylamino moiety on the phenyl ring. Group: Biochemicals. Alternative Names: Staphylomycin S, PA 114B2, Antibiotic 899, Antibiotic PA 114B2, Antibiotic 1745Z3B, Factor S. Grades: Highly Purified. CAS No. 23152-29-6. Pack Sizes: 5mg. Molecular Formula: C43H49N7O10, Molecular Weight: 823.89. US Biological Life Sciences. | Worldwide |
| Virginiamycin S2 | It is a depsipeptide antibiotic produced by the strain of Str. virginiae and Str. virginiae var. sp. It has anti-gram-positive bacteria and mycobacterium effects, and the antibacterial activity of component M of Virginiamycin against cocci is stronger than component S, while the activity is stronger than component M. Synonyms: Staphylomycin-S2; 4-L-Phenylalanine-5-(cis-4-hydroxy-L-2-piperidinecarboxylic acid)virginiamycin S1; N-[(3-Hydroxy-2-pyridinyl)carbonyl]cyclo[L-Thr*-D-Abu-L-Pro-L-Phe-[(4R)-4-hydroxy-L-pipecoloyl]-L-phenyl-Gly-]; N-[(3-Hydroxy-2-pyridyl)carbonyl]-cyclo[L-Thr*-D-Abu-L-Pro-L-Phe-4β-hydroxy-L-Hpr-L-phenyl-Gly-]. CAS No. 33477-38-2. Molecular formula: C42H49N7O10. Mole weight: 811.88. | |
| Virginiamycin S3 | It is a depsipeptide antibiotic produced by the strain of Str. virginiae and Str. virginiae var. sp. It has anti-gram-positive bacteria and mycobacterium effects, and the antibacterial activity of component M of Virginiamycin against cocci is stronger than component S, while the activity is stronger than component M. Synonyms: Staphylomycin S3; Virginiamycin S1, 5-(5-hydroxy-4-oxo-L-2-piperidinecarboxylic acid)-; N-[(3-Hydroxy-2-pyridinyl)carbonyl]cyclo[L-Thr*-D-Abu-L-Pro-N-methyl-L-Phe-4-oxo-5-hydroxy-L-pipecoloyl-L-phenyl-Gly-]. CAS No. 33477-39-3. Molecular formula: C43H49N7O11. Mole weight: 839.89. | |
| Viridicatin | It is a quinoline aromatic antibiotic produced by the strain of Pen. viridicatum, Pen. cyclopium SM-72 and Pen. puberulum. It has anti-gram-positive bacteria and mycobacteria effects. Synonyms: 2,3-dihydroxy-4-phenylquinoline; 2(1H)-Quinolinone, 3-hydroxy-4-phenyl-. Grades: >99% by HPLC. CAS No. 129-24-8. Molecular formula: C15H11NO2. Mole weight: 237.25. | |
| Viridicatin | Viridicatin is a fungal metabolite produced by several species of Penicillium and formed by the rearrangement of the benzodiazepine, cyclopenin. Viridicatin exhibits potent selective activity against Mycobacterium tuberculosis but is inactive against most other bacteria. Group: Biochemicals. Alternative Names: 2,3-dihydroxy-4-phenylquinoline. Grades: Highly Purified. CAS No. 129-24-8. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Viridicatol | Viridicatol is a fungal metabolite found in various Penicillium species as well as Phoma. It suppresses the expression of COX-2 and inducible nitric oxide synthase (iNOS) and inhibits production of nitric oxide and prostaglandin E2 (PGE2) in LPS-stimulated RAW 264.7 and BV2 cells. Synonyms: 2(1H)-Quinolinone, 3-hydroxy-4-(3-hydroxyphenyl)-; Carbostyril, 3-hydroxy-4-(m-hydroxyphenyl)-; 3-hydroxy-4-(3-hydroxyphenyl)carbostyril; 4-(3-Hydroxyphenyl)-2,3-quinolinediol. Grades: ≥95%. CAS No. 14484-44-7. Molecular formula: C15H11NO3. Mole weight: 253.25. | |
| Viridicatumtoxin | A tetracycline-like metabolite produced by several species of penicillium. It causes myocardial deterioration, renal tubule necrosis and spleen atrophy. It is a mycotoxin and a potent antibacterial with activity against S. Aureus including MRSA and QRSA strains. Synonyms: NSC 159628; viridicatumtoxin A; (1R,7'aR,11'aR,12'R)-rel-(-)-7',7'a,8',11',11'a,12'-hexahydro-5',6',7'a,10',11'a,12'-hexahydroxy-3'-methoxy-2,6,6-trimethyl-7',8'-dioxo-spiro[2-cyclohexene-1,2'(1'H)-cyclopenta[de]naphthacene]-9'-carboxamide; (2'α, 7'aβ, 11'aβ, 12'β)-(-)-7', 7'a, 8', 11', 11'a, 12'-Hexahydro-5', 6', 7'a, 10', 11'a, 12'-hexahydroxy-3'-methoxy-2, 6, 6-trimethyl-7', 8'-dioxo-spiro[2-cyclohexene-1, 2'(1'H)-cyclopenta[de]naphthacene]-9'-carboxamide. Grades: >98% by HPLC. CAS No. 39277-41-3. Molecular formula: C30H31NO10. Mole weight: 565.57. | |
| viridiflorene synthase | Viridiflorene is the only product of this enzyme from Solanum lycopersicum. Group: Enzymes. Synonyms: TPS31. Enzyme Commission Number: EC 4.2.3.88. 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-5251; viridiflorene synthase; EC 4.2.3.88; TPS31. Cat No: EXWM-5251. | |
| Viridiflorol | analytical standard. Group: Flavor and fragrance standards. | |
| Viridin | It is a steroidal antibiotic produced by the strain of Gliocladium virens. It has anti-fungal and gram-positive bacterial effects. Synonyms: (1S-(1alpha,2alpha,11balpha))-1,7,8,11b-Tetrahydro-1-hydroxy-2-methoxy-11b-methylcyclopenta(7,8)phenanthro(10,1-bc)furan-3,6,9(2H)-trione; 18-Norandrosta-5,8,11,13-tetraeno(6,5,4-bc)furan-3,7,17-trione, 1-hydroxy-2-methoxy-, (1beta,2beta)-; Cyclopenta(7,8)phenanthro(10,1-bc)furan-3,6,9(2H)-trione, 1,7,8,11b-tetrahydro-1-hydroxy-2-methoxy-11b-methyl-, (1S,2R,11bS)-. CAS No. 3306-52-3. Molecular formula: C20H16O6. Mole weight: 352.34. | |
| Viridiol | Viridiol is a steroid antibiotic metabolized from viridin. Viridiol acts as a PI3K inhibitor. Synonyms: NSC 658706. Grades: ≥95%. CAS No. 23820-80-6. Molecular formula: C20H18O6. Mole weight: 354.4. | |
| Viridiol | Viridiol, a fungal metabolite from Trichodernza viride, shows antifungal activity. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Cyclopenta(7,8)phenanthro(10,1-bc)furan-6,9-dione, 1,2,3,7,8,11b-hexahydro-1,3-dihydroxy-2-methoxy-, (1S-(1alpha,2alpha,3alpha,11balpha))-. Product Category: Inhibitors. CAS No. 23820-80-6. Molecular formula: C20H18O6. Mole weight: 354.35. Canonical SMILES: C[C@]12C3=C(OC=C3[C@H]([C@H]([C@H]2O)OC)O)C(C4=C(CCC5=O)C5=CC=C41)=O. Product ID: ACM23820806. Alfa Chemistry ISO 9001:2015 Certified. Categories: Viridiplantae. | |
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