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| Product | Description | |
|---|---|---|
| Verinurad Impurity17 | Verinurad Impurity17. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1877347-77-7. Molecular Formula: C20H10D6N2O2S. Mole Weight: 354.46. Catalog: APB1877347777. |  |
| Verinurad Impurity2 | Verinurad Impurity2. Uses: For analytical and research use. Group: Impurity standards. CAS No. 313391-86-5. Molecular Formula: C20H14N2O2S. Mole Weight: 346.4. Catalog: APB313391865. | |
| Verinurad Impurity3 | Verinurad Impurity3. Uses: For analytical and research use. Group: Impurity standards. CAS No. 310456-47-4. Molecular Formula: C14H10N2O2S. Mole Weight: 270.31. Catalog: APB310456474. | |
| Verinurad Impurity4 | Verinurad Impurity4. Uses: For analytical and research use. Group: Impurity standards. CAS No. 125305-75-1. Molecular Formula: C9H11NO2S. Mole Weight: 197.25. Catalog: APB125305751. | |
| Verinurad Impurity5 | Verinurad Impurity5. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1016858-18-6. Molecular Formula: C8H6N2O2S. Mole Weight: 194.21. Catalog: APB1016858186. | |
| Verinurad Impurity6 | Verinurad Impurity6. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1352792-73-4. Molecular Formula: C18H12N2O2S. Mole Weight: 320.37. Catalog: APB1352792734. | |
| Verinurad Impurity7 | Verinurad Impurity7. Uses: For analytical and research use. Group: Impurity standards. CAS No. 445391-28-6. Molecular Formula: C14H11N3O2S. Mole Weight: 285.32. Catalog: APB445391286. | |
| Verinurad Impurity8 | Verinurad Impurity8. Uses: For analytical and research use. Group: Impurity standards. CAS No. 329903-73-3. Molecular Formula: C15H12N2O2S. Mole Weight: 284.33. Catalog: APB329903733. | |
| Verinurad Impurity9 | Verinurad Impurity9. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1019535-82-0. Molecular Formula: C10H9NO2S. Mole Weight: 207.25. Catalog: APB1019535820. | |
| Verlamelin | It is a depsipeptide antibiotic produced by the strain of Fungi MF 4683. It has anti-fungal activity against plant pathogens. Synonyms: MSD-A-43F; Verlamelin; A-43F; Antibiotic MSD-A-43F; Antibiotic A-43F; Cyclo[D-Tyr-5-L-Val-oxytetradecanoyl-D-aThr-D-Ala-L-Pro-L-Glu(NH2)-]. CAS No. 74758-64-8. Molecular formula: C45H71N7O11. Mole weight: 886.09. |  |
| Verlamelin A | Verlamelin A is a cyclic lipodepsipeptide produced by the strain of entomopathogenic fungus Lecanicillium sp. HF627. Synonyms: Verlamelin. CAS No. 1619244-34-6. Molecular formula: C45H71N7O11. Mole weight: 886.08. | |
| Verlukast | A receptor antagonist for the treatment of respiratory diseases. Group: Biochemicals. Alternative Names: 3- [ [ (R) - [3- [ (1E) -2- (7-Chloro-2-quinolinyl) ethenyl] phenyl] [ [3- (dimethylamino) -3-oxopropyl] thio] methyl] thio] -propanoic Acid; L 668019; MK 679; R-(-)-MK 571. Grades: Highly Purified. CAS No. 120443-16-5. Pack Sizes: 5mg, 10mg. US Biological Life Sciences. |  Worldwide |
| Verlukast | Heterocyclic Organic Compound. Alternative Names: 3-[[ (R) -[3-[ (1E) -2- (7-Chloro-2-quinolinyl) ethenyl]phenyl][[3- (dimethylamino) -3-oxopropyl]thio]methyl]thio]-propanoic Acid; L 668019; MK 679; R-(-)-MK 571. CAS No. 120443-16-5. Molecular formula: C26H27ClN2O3S2. Mole weight: 515.09. Catalog: ACM120443165. |  |
| Verlukast | This active molecular is a R-enantiomer of MK-571 which is a selective LTD4 receptor antagonist. Verlukast showed [3H]leukotriene D4 binding in guinea-pig with IC50 value of 3.1+/-0.5nM, in human lung homogenates with IC50 value of 8.0+/-3.0nM and in dimethyl sulfoxide differentiated U937 cell membrane preparations with IC50 value of 10.7+/-1.6nM. Verlukast was in clinical development for the treatment of respiratory diseases but was discontinued for treatment of Asthma. Uses: The treatment of respiratory diseases. Synonyms: 3-[[(R)-[3-[(1E)-2-(7-Chloro-2-quinolinyl)ethenyl]phenyl][[3-(dimethylamino)-3-oxopropyl]thio]methyl]thio]-propanoic Acid; L 668,019; L 668019; L-668,019; MK 0679; MK 679; MK-679; R-(-)-MK 571. Grades: 95%. CAS No. 120443-16-5. Molecular formula: C26H27ClN2O3S2. Mole weight: 515.09. | |
| Verlukast-d6 | A receptor antagonist for the treatment of respiratory diseases. Group: Biochemicals. Alternative Names: 3- [ [ (R) - [3- [ (1E) -2- (7-Chloro-2-quinolinyl) ethenyl] phenyl] [ [3- (di (methyl-d3) amino) -3-oxopropyl] thio] methyl] thio] -propanoic Acid; L 668019-d6; MK 679-d6; R-(-)-MK 571-d6. Grades: Highly Purified. CAS No. 153698-86-3. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Vermiculine | Vermiculine is produced by the strain of Pen. vermiculatum CCM-F-2. It has anti-protozoal and anti-tumor effects, and it also has a less potent effect against gram-positive bacteria. Synonyms: Vermiculin; NSC657321; (-)-Vermiculine; 1,11-diene-2,5,10,13-tetrone,8,16-bis(2-oxopropyl)-, (3E,8S,11E,16S)-. CAS No. 37244-00-1. Molecular formula: C20H24O8. Mole weight: 392.40. | |
| Vermisporin | Other Alkaloids. CAS No. 122301-98-8. Mole weight: 415.6. Purity: 95%+. Catalog: ACM122301988. | |
| Vermistatin | It is a new metabolite from mine-dwelling Penicillium vermiculatum. It is an antibiotic with cytotoxic effects. Synonyms: (R,E)-4,6-dimethoxy-3-(4-oxo-6-(prop-1-en-1-yl)-4H-pyran-3-yl)isobenzofuran-1(3H)-one; Fijiensin; (-)-Fijiensin; NSC 656107; 1(3H)-Isobenzofuranone, 4,6-dimethoxy-3-(4-oxo-6-(1-propenyl)-4H-pyran-3-yl)-, (R)-; 5-(4,6-Dimethoxy-3R-phthalidy)-2-(1E)-propenyl-4H-pyran-4-one. CAS No. 72669-21-7. Molecular formula: C18H16O6. Mole weight: 328.32. | |
| Vernakalant | Vernakalant is an drug under regulatory for the treatment for conversion of atrial fibrillation. It blocks atrial potassium channels, thereby prolonging repolarization. It differs from typical class III agents and is more effective at high heart rates. It also slightly blocks the hERG potassium channel, leading to a prolonged QT interval. It also blocks atrial sodium channels. It was initially developed by Cardiome Pharma, and the intravenous formulation was bought for further development by Merck in April 2009. In September 2012, Merck terminated its agreements with Cardiome and has consequently returned all rights of the drug back to Cardiome. The drug (under brand name Brinavess) was approved in Europe on 1 September 2010. An oral formulation underwent Phase II clinical trials between 2005 and 2008. Uses: Vernakalant is an drug under regulatory for the treatment for conversion of atrial fibrillation. it blocks atrial potassium channels, thereby prolonging repolarization. it also slightly blocks the herg potassium channel, leading to a prolonged qt interval. it also blocks atrial sodium channels. Synonyms: Brinavess; RSD1235; (3R) -1-[ (1R, 2R) -2-[2- (3, 4-dimethoxyphenyl) ethoxy]cyclohexyl]pyrrolidin-3-ol. Grades: 95%. CAS No. 794466-70-9. Molecular formula: C20H31NO4. Mole weight: 349.47. | |
| Vernakalant ((3R,1'R,2'R)-Isomer) HCl | Vernakalant hydrochloride, also known as RSD1235, is a novel, relatively atrial-selective antiarrhythmic drug which can terminate acute atrial fibrillation (AF) in humans at 2 to 5 mg/kg. It belongs mixed ion channel blocker. It may be more atrial-selective than available agents in treatment of antiarrhythmic. It blocks atrial potassium channels, thereby prolonging repolarization. It also blocks atrial sodium channels. It also slightly blocks the hERG potassium channel, leading to a prolonged QT interval, which may theoretically increase the risk of ventricular tachycardia, though this does not seem to be clinically relevant. It is more effective at high heart rates. It wa...ks atrial potassium channels, thereby prolonging repolarization. it also blocks atrial sodium channels. it also slightly blocks the herg potassium channel, leading to a prolonged qt interval, which may theoretically increase the risk of ventricular tachycardia, though this does not seem to be clinically relevant. it is more effective at high heart rates. Synonyms: RSD1235, RSD-1235, RSD 1235, Vernakalant HCl, Kynapid, Brinavess; D06665;(3R)-1-[(1R,2R)-2-[2-(3,4-Dimethoxyphenyl)ethoxy]cyclohexyl]-3-pyrrolidinol monohydrochloride;RSD 1235 hydrochloride;Vernakalant ((3R,1'R,2'R)-Isomer) HCl. Grades: 98%. CAS No. 748810-28-8. Molecular formula: C20H32NO4Cl. Mole weight: 385.93. | |
| Vernakalant Hydrochloride | Vernakalant hydrochloride is a mixed voltage- and frequency-dependent Na + and atria-preferred K + channel blocker. IC 50 for block by Vernakalant of wild-type and mutant Kv1.5 channels Fractional block is 13.35±0.93 μM, 0.61±0.03 μM, and 1.63±0.09 μM for Kv1.5 channel wt , Kv1.5 channel I508F , Kv1.5 channel T479A , respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: RSD1235 hydrochloride. CAS No. 748810-28-8. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14183. |  |
| Vernakalant Impurity 1 ((3S,1'S,2'S)-Isomer) HCl | An impurity of Vernakalant. Vernakalant is a medication used for the treatment of acute conversion of atrial fibrillation. Vernakalant blocks cardiac transient outward potassium current with increased potency as the heart rate increases. CAS No. 795282-00-7. Molecular formula: C20H31NO4. HCl. Mole weight: 385.93. | |
| Vernakalant Impurity 2 ((3S,1'R,2'R)-Isomer) HCl | An impurity of Vernakalant. Vernakalant is a medication used for the treatment of acute conversion of atrial fibrillation. Vernakalant blocks cardiac transient outward potassium current with increased potency as the heart rate increases. CAS No. 795281-99-1. Molecular formula: C20H31NO4. HCl. Mole weight: 385.93. | |
| Vernakalant Impurity 3 ((3S,1'R,2'S)-Isomer) | An impurity of Vernakalant. Vernakalant is a medication used for the treatment of acute conversion of atrial fibrillation. Vernakalant blocks cardiac transient outward potassium current with increased potency as the heart rate increases. CAS No. 795282-30-3. Molecular formula: C20H31NO4. Mole weight: 349.47. | |
| Vernakalant Impurity 4 ((3S,1'S,2'R)-Isomer) | An impurity of Vernakalant. Vernakalant is a medication used for the treatment of acute conversion of atrial fibrillation. Vernakalant blocks cardiac transient outward potassium current with increased potency as the heart rate increases. CAS No. 795282-28-9. Molecular formula: C20H31NO4. Mole weight: 349.47. | |
| Vernakalant Impurity 5 ((3R,1'S,2'S)-Isomer) HCl | An impurity of Vernakalant. Vernakalant is a medication used for the treatment of acute conversion of atrial fibrillation. Vernakalant blocks cardiac transient outward potassium current with increased potency as the heart rate increases. CAS No. 795281-93-5. Molecular formula: C20H31NO4. HCl. Mole weight: 385.93. | |
| Vernakalant Impurity 7 ((3R,1'R,2'S)-Isomer) | An impurity of Vernakalant. Vernakalant is a medication used for the treatment of acute conversion of atrial fibrillation. Vernakalant blocks cardiac transient outward potassium current with increased potency as the heart rate increases. CAS No. 795282-29-0. Molecular formula: C20H31NO4. Mole weight: 349.47. | |
| Vernakalant Impurity 8 ((3R,1'S,2'R)-Isomer) | An impurity of Vernakalant. Vernakalant is a medication used for the treatment of acute conversion of atrial fibrillation. Vernakalant blocks cardiac transient outward potassium current with increased potency as the heart rate increases. CAS No. 795282-27-8. Molecular formula: C20H31NO4. Mole weight: 349.47. | |
| Vernaldehyde ® | Vernaldehyde ®. CAS No. 66327-54-6. Kosher: Y. VIGON Item # 500415. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. |  America & Internationally |
| Vernamycin B | Vernamycin B is originally isolated from Str. loidensis. Vernamycin B has an antimicrobial effect, but is less effective against gram-negative bacteria and mycobacteria. CAS No. 9040-14-6. Molecular formula: C62H85N7O16S. Mole weight: 1216.44. | |
| Verofylline | Verofylline is used as a methylxanthine bronchodilator. Uses: Verofylline is used as a methylxanthine bronchodilator. Synonyms: CK 0383; CK0383; CK-0383; Verofilina; Verofyllinum; 3,7-Dihydro-1,8-dimethyl-3-(2-methylbutyl)-1H-purine-2,6-dione. Grades: 98%. CAS No. 66172-75-6. Molecular formula: C12H18N4O2. Mole weight: 250.30. | |
| Verosudil | Verosudil is a selective Rho-kinase inhibitor originated by Aerie Pharmaceuticals. In Jun 2013, Phase-II for Ocular hypertension in USA was discontinued. In Sep 2013, Phase-II for Glaucoma in USA was discontinued. Uses: Glaucoma; ocular hypertension. Synonyms: AR 12286; AR12286; AR-12286; rac-(2R)-2-(dimethylamino)-N-(1-oxo- 1,2-dihydroisoquinolin-6-yl)-2-(thiophen-3-yl)acetamide. Grades: 98%. CAS No. 1414854-42-4. Molecular formula: C17H17N3O2S. Mole weight: 327.41. | |
| Verrucarin A | Verrucarin A (Muconomycin A), a Type D macrocyclic mycotoxin derived from the pathogen fungus Myrothecium verrucaria , is an inhibitor of protein synthesis. Verrucarin A inhibits growth of leukemia cell lines and activates caspases and apoptosis and inflammatory signaling in macrophages. Verrucarin A effectively increased the phosphorylation of p38 MAPK and diminished the phosphorylation of ERK/Akt. Verrucarin A caused cell cycle deregulation through the induction of p21 and p53 [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Muconomycin A. CAS No. 3148-9-2. Pack Sizes: 1 mg; 5 mg. Product ID: HY-107426. | |
| Verrucarin A | It is produced by the strain of Myrothecium verrucaria NRRL 3003. Verrucarin A has the effect of anti-Gram-negative bacteria and fungi, inhibiting Newcastle disease virus, tobacco Mosaic virus, and S-37 sarcoma and Yoshida sarcoma in animals. Synonyms: Muconomycin A; Antibiotic 379Y; VER A; (4S, 5R, 10E, 12Z, 16R, 16aS, 17S, 18R, 19aR, 23aR)-4-hydroxy-5, 16a, 21-trimethyl-4, 5, 6, 7, 16, 16a, 22, 23-octahydro-3H, 18H, 19aH-spiro[16, 18-methano[1, 6, 12]trioxacyclooctadecino[3, 4-d]chromene-17, 2'-oxirane]-3, 9, 14-trione; NSC 126728. Grades: 95%. CAS No. 3148-9-2. Molecular formula: C27H34O9. Mole weight: 502.55. | |
| Verrucarin B | It is produced by the strain of Myrothecium verrucaria NRRL 3003. Verrucarin B has an effect on Ascites carcinoma, also has a weak inhibitory effect on fungi. Synonyms: (2'S,3'R)-2'-Deoxy-2',3'-oxyverrucarin A. CAS No. 2290-11-1. Molecular formula: C27H32O9. Mole weight: 500.54. | |
| Verrucarin J | Verrucarin J is produced by the strain of Myrothecium verrucaria NRRL 3003. The ED50 of Verrucarin J on giant cell tumor P-815 cells was about 0.001 μg/mL. Uses: For research used only. Synonyms: Muconomycin B; 2',3'-Didehydro-2'-deoxyverrucarin A; Verrucarin A, 2',?3'-didehydro-2'-deoxy-, (2'E)?-; Verrucrin J; Verrucosporin J. Grades: ≥98%. CAS No. 4643-58-7. Molecular formula: C27H32O8. Mole weight: 484.54. | |
| Verrucarin K | Verrucarin K is produced by the strain of Myrothecium verrucaria NRRL 3003. The ED50 of Verrucarin K on giant cell tumor P-815 cells was about 0.001 μg/mL. Synonyms: BRN 1276841; Verrucarin A, 12,13-deepoxy-12,13-didehydro-. CAS No. 63739-93-5. Molecular formula: C27H34O8. Mole weight: 486.55. | |
| Verrucofortine | A diketopiperazine alkaloid derived from tryptophan and leucine. It is a fungal metabolite isolated from penicillium verrucosum. It exhibits no apparent toxicity in mice even at high doses in vivo. Synonyms: Fructigenine B; Verrucosine; Verrucozine; (-)-Verrucofortine; (3S-(3alpha,5aalpha,10balpha,11abeta))-6-Acetyl-10b-(1,1-dimethyl-2-propenyl)-6,10b,11,11a-tetrahydro-3-(2-methylpropyl)-2H-pyrazino(1',2':1,5)pyrrolo(2,3-b)indole-1,4-(3H,5aH)-dione; (3S,5aR,10bR,11aS)-6-acetyl-10b-(1,1-dimethyl-2-propen-1-yl)-6,10b,11,11a-tetrahydro-3-(2-methylpropyl)-2H-pyrazino[1',2':1,5]pyrrolo[2,3-b]indole-1,4(3H,5aH)-dione. Grades: >99% by HPLC. CAS No. 113706-21-1. Molecular formula: C24H31N3O3. Mole weight: 409.52. | |
| Verrucofortine | Heterocyclic Organic Compound. Alternative Names: Fructigenine B. CAS No. 113706-21-1. Molecular formula: C24H31N3O3. Mole weight: 409.5. Appearance: Pale yellow residue. Purity: 95%+. IUPACName: Verrucofortine. Canonical SMILES: CC (C)CC1C (=O)N2C (CC3 (C2N (C4=CC=CC=C43)C (=O)C)C (C) (C)C=C)C (=O)N1. Density: 1.21g/cm³. Catalog: ACM113706211. | |
| Verrucofortine (Fructigenine B, Verrucosine, Verrucozine) | Verrucofortine is an alkaloidal diketopiperazine derived from tryptophan and leucine isolated from Penicillium species. There are no reports of intensive investigation of verrucofortine. In vivo, mice showed no apparent toxic effects at high doses. Group: Biochemicals. Alternative Names: Fructigenine B, Verrucosine, Verrucozine. Grades: Highly Purified. CAS No. 113706-21-1. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Verruculogen | Verruculogen is a tremorgenic mycotoxin isolated from penicillium verruculosu. It can inhibit the K+ channel activated by ca2+, and is a cell cycle inhibitor that prevents M phase division. Synonyms: TR 1 toxin. Grades: >95% by HPLC. CAS No. 12771-72-1. Molecular formula: C27H33N3O7. Mole weight: 511.57. | |
| Verruculogen | Verruculogen is a tremorgenic mycotoxin first isolated from Penicillium verruculosum in 1972 and the structure resolved as an indole alkaloid in 1974. Subsequent investigations have shown that verruculogen is produced by several species of Penicillium and Aspergillus and its presence is a useful taxonomic phenotypic marker. The tremorgenic action of verruculogen is complex but is associated with increases in spontaneous glutamate and aspartate release, decreases in GABA levels and, at toxic doses, an increase in the number and decrease in the affinity of DHP receptors in rat cortex. In in vitro guinea pig ileum preparations, verruculogen causes an increase in contractile responses due to electrical field stimulation, attributed to enhancement of acetylcholine from presynaptic nerve terminals. Verruculogen also inhibits Ca2+-activated K+ channels and is a cell cycle inhibitor blocking division at the M phase. Group: Biochemicals. Grades: Highly Purified. CAS No. 12771-72-1. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Verruculogen (NA 209A, TR 1) | Fumitremorgin-type alkaloid. Tremorgenic neurotoxic mycotoxin. Selective blocker of KCa1.1 (high-conductance Ca2+-activated K+; BK; maxi-K) channels. Decreases GABA levels in CNS. Increases spontaneous glutamate and aspartate release. At toxic doses, increases the number and decreases the affinity of DHP receptors in rat cortex. Cell cycle inhibitor at the M phase. Inhibits calmodulin and PKC activity. Has apoptotic effects on human T lymphocytes. Stimulates the growth of seedling roots of buckwheat. Group: Biochemicals. Alternative Names: (5R, 10S, 10aR) -1, 10, 10a, 14, 14aS, 15bS-hexahydro-10, 10a-dihydroxy-7-methoxy-2, 2-dimethyl-5- (2-methyl-1-propen-1-yl) -5H, 12H-3, 4-dioxa-5a, 11a, 15a-triazacyclooct [lm]indeno [5, 6-b]fluorene-11, 15 (2H, 13H) -dione. Grades: Highly Purified. CAS No. 12771-72-1. Pack Sizes: 1mg, 5mg. Molecular Formula: C27H33N3O7. US Biological Life Sciences. | Worldwide |
| verruculogen prenyltransferase | Found in a number of fungi. Catalyses the last step in the biosynthetic pathway of the indole alkaloid fumitremorgin A. The enzyme from the fungus Neosartorya fischeri is also active with fumitremorgin B and 12α,13α-dihydroxyfumitremorgin C. Group: Enzymes. Synonyms: FtmPT3. Enzyme Commission Number: EC 2.5.1.107. 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-2723; verruculogen prenyltransferase; EC 2.5.1.107; FtmPT3. Cat No: EXWM-2723. |  |
| verruculogen synthase | Requires Fe2+ and ascorbate. Found in the fungus Aspergillus fumigatus. Both atoms of a dioxygen molecule are incorporated into verruculogen. Involved in the biosynthetic pathways of several indole alkaloids such as fumitremorgin A. Group: Enzymes. Synonyms: fmtF (gene name); FmtOx1. Enzyme Commission Number: EC 1.14.11.38. 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-0656; verruculogen synthase; EC 1.14.11.38; fmtF (gene name); FmtOx1. Cat No: EXWM-0656. | |
| Versamid 754 | Heterocyclic Organic Compound. Alternative Names: Dimer acid polyamide, Versamid 140, Versamid 754, Versamid 900, Ethylenediamine - linoleic acid dimer polymer, Poly(ethylenedilinoleamide), AC1O5V7Z, EINECS 276-685-7, Ethylenediamine, linoleic acid dimer polymer, Ethylenediamine - linoleic acid dimer copolymer, Linoleic acid dimer - ethylenediamine copolymer, ethane-1,2-diamine; (9Z,12Z)-octadeca-9,12-dienoic acid, 1,2-Ethanediamine, polymer with (9Z,12Z)-9,12-octadecadienoic acid dimer, 1,2-Ethanediamine, polymer with (Z,Z)-9,12-octadecadienoic acid dimer, 9,12-Octadecadienoic acid (Z,Z)-, dimer, polymer with 1,2-ethanediamine, 9,12-Octadecadienoic acid (9Z,12Z)-, dimer, polymer with 1,2-ethanediamine, 9,12-Octadecadienoic acid (9Z,12Z)-, dimer, reaction products with ethylenediamine, 9,12-Octadecadienoic acid (Z,Z)-, dimer, reaction products with ethylenediamine, 11098-02-5, 12624-35-0. CAS No. 12624-35-0. Molecular formula: C38H72N2O4. Mole weight: 620.9893. Purity: 0.96. IUPACName: ethane-1,2-diamine;(9Z,12Z)-octadeca-9,12-dienoic acid. Canonical SMILES: CCCCCC=CCC=CCCCCCCCC(=O)O. CCCCCC=CCC=CCCCCCCCC(=O)O. C(CN)N. Density: g/cm³. ECNumber: 276-685-7. Catalog: ACM12624350. | |
| versatile peroxidase | A hemoprotein. This ligninolytic peroxidase combines the substrate-specificity characteristics of the two other ligninolytic peroxidases, EC 1.11.1.13, manganese peroxidase and EC 1.11.1.14, lignin peroxidase. Unlike these two enzymes, it is also able to oxidize phenols, hydroquinones and both low- and high-redox-potential dyes, due to a hybrid molecular architecture that involves multiple binding sites for substrates. Group: Enzymes. Synonyms: VP; hybrid peroxidase; polyvalent peroxidase; reactive-black-5:hydrogen-peroxide oxidoreductase. Enzyme Commission Number: EC 1.11.1.16. CAS No. 42613-30-9, 114995-15-2. Versatile Peroxidase. 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-0497; versatile peroxidase; EC 1.11.1.16; 42613-30-9, 114995-15-2; VP; hybrid peroxidase; polyvalent peroxidase; reactive-black-5:hydrogen-peroxide oxidoreductase. Cat No: EXWM-0497. | |
| Versicolin | Versicolin is originally isolated from Asp. versicolor. It only has antibacterial effect on filamentous fungi, and has no inhibitory effect on yeast-like fungi and bacteria. Synonyms: 2,3,6-Trihydroxytoluene; Toluene-2,3,6-triol; BRN 2249549; 1-methyl-2,3,6-trihydroxybenzene. CAS No. 4389-44-0. Molecular formula: C7H8O3. Mole weight: 140.14. | |
| Versicolorin A | Versicolorin A is a quinone antibiotic produced by the strain of Asp. versicolor. It has the effect of anti-tuberculosis Mycobacterium H37RV and other mycobacteria. Synonyms: Z-(-)-4,6,8-Trihydroxy-3a,12a-dihydroanthra(2,3-b)furo(3,2-d)furan-5,10-dione; NSC 274542; (3aS,12aR)-4,6,8-trihydroxy-3a,12a-dihydroanthra[2,3-b]furo[3,2-d]furan-5,10-dione. Grades: 98%. CAS No. 6807-96-1. Molecular formula: C18H10O7. Mole weight: 338.27. | |
| Versicolorin A | Versicolorin A. Uses: For analytical and research use. Group: Impurity standards. CAS No. 6807-96-1. Molecular Formula: C18H10O7. Mole Weight: 338.27. Catalog: APB6807961. | |
| Versicolorin B | Versicolorin B is a quinone antibiotic produced by the strain of Asp. versicolor. It has the effect of anti-tuberculosis Mycobacterium H37RV and other mycobacteria. Synonyms: (3aS,12aR)-4,6,8-trihydroxy-2,3,3a,12a-tetrahydroanthra[2,3-b]furo[3,2-d]furan-5,10-dione; Anthra(2,3-b)furo(3,2-d)furan-5,10-dione, 2,3,3a,12a-tetrahydro-4,6,8-trihydroxy-, cis-(+-)-. CAS No. 4331-22-0. Molecular formula: C18H12O7. Mole weight: 340.28. | |
| versicolorin B synthase | Isolated from the aflatoxin-producing mold Aspergillus parasiticus. Involved in aflatoxin biosynthesis. Group: Enzymes. Synonyms: versiconal cyclase; VBS. Enzyme Commission Number: EC 4.2.1.143. 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-4984; versicolorin B synthase; EC 4.2.1.143; versiconal cyclase; VBS. Cat No: EXWM-4984. | |
| versiconal hemiacetal acetate esterase | Isolated from the mold Aspergillus parasiticus. Involved in a metabolic grid that leads to aflatoxin biosynthesis. Group: Enzymes. Synonyms: VHA esterase. Enzyme Commission Number: EC 3.1.1.94. 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-3523; versiconal hemiacetal acetate esterase; EC 3.1.1.94; VHA esterase. Cat No: EXWM-3523. | |
| versiconal hemiacetal acetate reductase | Isolated from the mold Aspergillus parasiticus. Involved in a metabolic grid that leads to aflatoxin biosynthesis. Group: Enzymes. Synonyms: VHA reductase; VHA reductase I; VHA reductase II; vrdA (gene name). Enzyme Commission Number: EC 1.1.1.353. 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-0269; versiconal hemiacetal acetate reductase; EC 1.1.1.353; VHA reductase; VHA reductase I; VHA reductase II; vrdA (gene name). Cat No: EXWM-0269. | |
| Vertenex | Vertenex (Para Butyl Cyclohexyl Acetate). CAS No. 32210-23-4. VIGON Item # 501612. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. | America & Internationally |
| Verteporfin | Verteporfin Inhibitor. Uses: Scientific use. Product Category: T3112. CAS No. 129497-78-5. |  |
| Verteporfin | Verteporfin is a potent second-generation photosensitizing agent derived from porphyrin. It is used as a photosensitizer for photodynamic therapy to eliminate abnormal blood vessels in the eye that are associated with conditions such as macular degeneration. Verteporfin also suppresses the formation of autophagosome via targeting p62, which binds both polyubiquitinated proteins destined for degradation and LC3 on autophagosomal membranes. Synonyms: CL 318952; SC 95659; CL318952; SC95659; CL-318952; SC-95659; BPD-MA-A1; (4R,4aS)-rel-18-ethenyl-4,4a-dihydro-3,4-3,4-bis(methoxycarbonyl)-4a,8,14,19-tetramethyl-24H,26H-benzo[b]porphine-9,13-dipropanoic acid, monomethyl ester. Grades: 95%. CAS No. 129497-78-5. Molecular formula: C41H42N4O8. Mole weight: 718.81. | |
| Verteporfin | Verteporfin (CL 318952) is a photosensitizer for photodynamic therapy to eliminate the abnormal blood vessels in the eye associated with conditions such as age-related macular degeneration. Verteporfin is a YAP inhibitor which disrupts YAP-TEAD interactions. Verteporfin induces cell apoptosis [1]. Verteporfinis an autophagy inhibitor that blocks autophagy at an early stage by inhibiting autophagosome formation [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CL 318952. CAS No. 129497-78-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B0146. | |
| Verteporfin | Verteporfin (CL 318952) is a photosensitizer for photodynamic therapy to eliminate the abnormal blood vessels in the eye associated with conditions such as age-related macular degeneration. Verteporfin is a YAP inhibitor which disrupts YAP-TEAD interactions. Verteporfin induces cell apoptosis. Verteporfinis an autophagy inhibitor that blocks autophagy at an early stage by inhibiting autophagosome formation. Group: Inhibitors. Alternative Names: Verteprofin; Verteporphin; trans-3,4-Dicarboxy-4,4a-dihydro-4a,8,14,19-tetramethyl-18-vinyl-23H,25H-benzo(b)porphine-9,13-dipropionic acid 3,4,9-trimethyl ester; Visudyne; VERTEPORFIN (200 MG). CAS No. 129497-78-5. Molecular formula: C41H42N4O8. Mole weight: 1437.61. Appearance: Powder. Purity: 0.95. IUPACName: Verteporfin. Canonical SMILES: C[C@]1 (/C2=C/C (N3)=C4C)C (C (/C=C (C (C)=C/5C=C)\NC5=C/C6=N/C (C (CCC (OC)=O)=C6C)=C\C3=C4CCC (O)=O)=N2)=CC=C (C (OC)=O)[C@H]1C (OC)=O. C[C@]7 (/C8=C/C (N9)=C%10C)C (C (/C=C (C (C)=C/%11C=C)\NC%11=C/C%12=N/C (C (CCC (O)=O)=C%12C)=C\C9=C%10CCC (OC)=O)=N8)=CC=C (C (OC)=O)[C@H]7C (OC)=O. Catalog: ACM129497785-1. | |
| Verteporfin | Verteporfin. Group: Biochemicals. Alternative Names: CL 318952; Visudyne; (4R,4aS)-rel-24H,26H-Benzo[b]porphine-9,13-dipropanoic acid, 18-ethenyl-4,4a-dihydro-3,4-bis(methoxycarbonyl)-4a,8,14,19-tetramethyl-monomethyl Ester. Grades: Highly Purified. CAS No. 129497-78-5. Pack Sizes: 10mg. Molecular Formula: C41H44N4O9, Molecular Weight: 736.81. US Biological Life Sciences. | Worldwide |
| Verticillatine | Verticillatine is a chemical compound that belongs to the family of biphenyls. It has been found to have anti-inflammatory effects and haemodynamic effects, as well as the ability to reduce blood pressure. Verticillatine has also been shown to reduce pain in anesthetized rats. This may be due to its ability to modulate the body's inflammatory response or its effect on the haemodynamic system (e.g., by affecting vasodilation). The chemical structure of verticillatine is similar to that of other biphenyls, which are used in industrial processes as models for other molecules. Verticillatine has been shown to react with acid catalysts and is capable of forming conjugates with amino acids and sugars. Group: Other alkaloids. CAS No. 10247-54-8. Molecular formula: C25H27NO5. Mole weight: 421.49 g/mol. Canonical SMILES: COc1ccc2[C@@H]3C[C@H] (C[C@H]4CCCCN34)OC (=O)\C=C/c5ccc (O)c (c5)c2c1O. Catalog: ACM10247548. | |
| Verticillin A | Verticillin A is originally isolated from Verticillium sp. Tm-759. It has the effect of anti-gram-positive bacteria, mycobacterium and protozoa, and has the inhibitory effect on the cancer of Ascites. Synonyms: (6S,6'S)-19,19'-Dideoxy-6,6'-dihydroxychetocin. CAS No. 32164-16-2. Molecular formula: C30H28N6O6S4. Mole weight: 696.84. | |
| Verticillin B | Verticillin B is originally isolated from Verticillium sp. Tm-759. It has the effect of anti-gram-positive bacteria, mycobacterium and protozoa, and has the inhibitory effect on the cancer of Ascites. Synonyms: (6S,6'S)-19-Deoxy-6,6'-dihydroxychetocin. CAS No. 52212-86-9. Molecular formula: C30H28N6O7S4. Mole weight: 712.84. | |
| Verticillin C | Verticillin C is originally isolated from Verticillium sp. Tm-759. It has the effect of anti-gram-positive bacteria, mycobacterium and protozoa, and has the inhibitory effect on the cancer of Ascites. Synonyms: Verticillin C. Grades: 95%. CAS No. 51798-48-2. Molecular formula: C30H28N6O7S5. Mole weight: 744.90. | |
| Vertimycin | It is a cyclopentane derivative of antibiotic produced by the strain of Streptoverticillium sp. JA 4498. It has anti-gram-positive bacteria and fungal effects. It has weak effect on Ehrlich ascites cancer cells in vitro. Synonyms: Cyclopentanone, 2-(2-hydroxyethoxy)-5-(hydroxymethyl)-; 1-Ethylenodiolo-3-methylolo-cyclopentanone-2; 1-(Aethylendiol-1,2)-methylol-3-cyclopentanon-2. CAS No. 14477-60-2. Molecular formula: C8H14O4. Mole weight: 174.19. | |
| Vertisporin | It is an antibiotic produced by the strain of Verticimonosporium diffractum TM-2098 and TM-2492. It has the effect against a few fungal. It is cytotoxic to HeLa cells with ED50 of 0.001 μg/mL. Synonyms: Spiro[4H-3a, 22-(epoxyethano)-10, 12-methano-17H, 18H-furo[2', 3':10, 11][1, 6]dioxacyclohexadecino[3, 4-d][1]benzopyran-11(12H), 2'-oxirane]-8, 20(5H, 22aH)-dione, 2, 3, 10, 10a, 13a, 16-hexahydro-2, 3-dihydroxy-10a, 15-dimethyl-, (2R, 2'S, 3R, 3aR, 6Z, 10R, 10aS, 12R, 13aR, 17aR, 21E, 21bR)-. CAS No. 57100-32-0. Molecular formula: C29H36O10. Mole weight: 544.59. | |
| Verubecestat | Verubecestat (MK-8931) is an orally active, high-affinity BACE1 and BACE2 inhibitor with K i values of 2.2 nM and 0.38 nM. Verubecestat effectively reduces Aβ40 and has the potential for Alzheimer's Disease [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MK-8931. CAS No. 1286770-55-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16759. | |
| Verubecestat | Verubecestat, an iminothiadiazine dioxide compound, is an oral BACE1 inhibitor originated by Merck & Co. It can bind significantly to β-secretase. Verubecestat has the potent effect to treat Alzheimer's disease and is currently in Phase III clinical trials. Uses: Alzheimer's disease. Synonyms: N-[3-[(5R)-3-amino-2,5-dimethyl-1,1-dioxo-6H-1,2,4-thiadiazin-5-yl]-4-fluorophenyl]-5-fluoropyridine-2-carboxamide; J1I0P6WT7T; Verubecestat; UNII-J1I0P6WT7T; J1I0P6WT7T; 1286770-55-5; Verubecestat [USAN]; Verubecestat (USAN/INN); GTPL8699; CHEMBL3301601; SCHEMBL10328722; SCHEMBL17507398; BDBM143220; example 25 (US8940748); SCH-900931; D10739; US8940748, 25; 2-Pyridinecarboxamide, N-(3-((5R)-3-amino-5,6-dihydro-2,5-dimethyl-1,1-dioxido-2H-1,2,4-thiadiazin-5-yl)-4-fluorophenyl)-5-fluoro-; N-(3-((5R)-3-amino-2,5-dimethyl-1,1-dioxo-1,2,5,6-tetrahydro-1lambda6,2,4-thiadiazin-5-yl)-4-fluorophenyl)-5-fluoropyridine-2-carboxamide; N-(3-((5R)-3-amino-2,5-dimethyl-1,1-dioxo-5,6-dihydro-2H-1lambda6,2,4-thiadiazin-5-yl)-4-fluorophenyl)-5-fluoropyridine-2-carboxamide; N-[3-[(5R)-3-amino-2,5-dimethyl-1,1-dioxo-6H-1,2,4-thiadiazin-5-yl]-4-fluorophenyl]-5-fluoropyridine-2-carboxamide. Grades: 98%. CAS No. 1286770-55-5. Molecular formula: C17H17F2N5O3S. Mole weight: 409.41. | |
| Verubecestat TFA | Verubecestat, also known as MK-8931 or SCH 900931, is a potent and selective beta-secretase inhibitor, and BACE1 protein inhibitor or Beta-site APP-cleaving enzyme 1 inhibitor. Verubecestat is a promising novel therapeutic drug candidate in Alzheimer's disease. Verubecestat reduced Aβ cerebral spinal fluids (CSF) levels up to 92% and was well tolerated by patients. Group: Inhibitors. Alternative Names: MK-8931; MK 8931; MK8931; MK-8931-009; SCH 900931; SCH-900931; SCH900931; Verubecestat TFA. CAS No. 2095432-65-6. Molecular formula: C19H18F5N5O5S. Mole weight: 523.44. Appearance: White to off-white solid powder. Purity: >98%. IUPACName: (R)-N-(3-(3-amino-2,5-dimethyl-1,1-dioxido-5,6-dihydro-2H-1,2,4-thiadiazin-5-yl)-4-fluorophenyl)-5-fluoropicolinamide trifluoroacetic acid. Canonical SMILES: O=C (NC1=CC=C (F)C ([C@@] (C2) (C)N=C (N)N (C)S2 (=O)=O)=C1)C3=NC=C (F)C=C3. O=C (O)C (F) (F)F. Catalog: ACM2095432656. | |
| Verubulin | Verubulin, also known as MPC-6827, is quinazoline derivative with potential dual antineoplastic activities. Verubulin hydrochloride binds to and inhibits tubulin polymerization and interrupts microtubule formation, resulting in disruption of mitotic spindle assembly, cell cycle arrest in the G2/M phase, and cell death. This agent is not a substrate for several subtypes of multidrug resistance ABC transporters, such as P-glycoprotein, multidrug resistance-associated protein 1 (MRP1), and breast cancer resistance protein 1 (BCRP1); therefore, it may be useful for treating multidrug resistant (MDR) tumors that express these transporters. In addition, as a vascular disrupting agent (VDA), MPC-6827 appears to disrupt tumor microvasculature specifically, which may result in acute ischemia and massive tumor cell death. Synonyms: MPC6827; MPC-6827; MPC 6827; MX128495; MX-128495; MX 128495; EP90745; EP-90745;EP 90745; Verubulin; trade name: Azixa. Grades: ≥98%. CAS No. 827031-83-4. Molecular formula: C21H25BrN3O9P. Mole weight: 279.34. | |
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