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| Product | Description | |
|---|---|---|
| Vigabatrin Related Compound B | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. |  |
| Vigabatrin Related Compound E | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Vigabatrin solution | 1.0 mg/mL in methanol, ampule of 1 mL, certified reference material. Group: Certified reference materials (crms). | |
| Vilagletistat | ZED-1227 is a specific and orally active transglutaminase 2 (TG2) inhibitor, with an IC50 of 45 nM. ZED-1227 can block inflammation-induced TG2 expression and activity. ZED-1227 can be used for the research of celiac disease (CeD)[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ZED-1227. CAS No. 1542132-88-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-19359. |  |
| Vilanterol | Vilanterol (GW642444) is a long-acting β 2 -adrenoceptor (β 2 -AR) agonist with 24 h activity. The pEC 50 s for β 2 -AR,β 1 -AR and β 3 -AR is 10.37±0.05, 6.98±0.03 and 7.36±0.03, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GW642444. CAS No. 503068-34-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14300. | |
| Vilanterol Impurity 1 | An impurity of Vilanterol. Vilanterol is a relatively selective, long-acting β2-adrenergic agonist as a bronchodilator used for the treatment of COPD and asthma. Synonyms: (1R) -2-[[6-[2-[ (2, 6-Dichlorobenzyl) oxy]ethoxy]hexyl]amino]-1- (2, 2-dimethyl-4H-1, 3-benzodioxin-6-yl) ethanol; (α R) -α -[[[6-[2-[ (2, 6-Dichlorophenyl) methoxy]ethoxy]hexyl]amino]methyl]-2, 2-dimethyl-4H-1, 3-benzodioxin-6-methanol. CAS No. 503068-37-9. Molecular formula: C27H37Cl2NO5. Mole weight: 526.51. |  |
| Vilanterol Impurity 10 | An impurity of Vilanterol. Vilanterol is a relatively selective, long-acting β2-adrenergic agonist as a bronchodilator used for the treatment of COPD and asthma. Synonyms: (R) -5- (2- ( (6- (2- ( (2, 6-Dichlorobenzyl) oxy) ethoxy) hexyl) amino) -1-hydroxyethyl) -2-hydroxybenzaldehyde. Molecular formula: C24H31Cl2NO5. Mole weight: 484.42. | |
| Vilanterol Impurity 11 | An impurity of Vilanterol. Vilanterol is a relatively selective, long-acting β2-adrenergic agonist as a bronchodilator used for the treatment of COPD and asthma. Synonyms: 2- ( ( (6- (2- ( (2, 6-Dichlorobenzyl) oxy) ethoxy) hexyl) ( (R) -2-hydroxy-2- (4-hydroxy-3- (hydroxymethyl) phenyl) ethyl) amino) methyl) -4- ( (R) -2- ( (6- (2- ( (2, 6-dichlorobenzyl) oxy) ethoxy) hexyl) amino) -1-hydroxyethyl) phenol. Molecular formula: C48H64Cl4N2O9. Mole weight: 954.87. | |
| Vilanterol Impurity 12 | An impurity of Vilanterol. Vilanterol is a relatively selective, long-acting β2-adrenergic agonist as a bronchodilator used for the treatment of COPD and asthma. Synonyms: (R) -4- (2- ( (6- (2- ( (2, 6-Dichlorobenzyl) oxy) ethoxy) hexyl) amino) -1-hydroxyethyl) -2- (ethoxymethyl) phenol. Molecular formula: C26H37Cl2NO5. Mole weight: 514.49. | |
| Vilanterol Impurity 19 | Vilanterol Impurity 19. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1027529-99-2. Molecular formula: C13H15NO4. Mole weight: 249.27. Catalog: APB1027529992. | |
| Vilanterol Impurity 2 | An impurity of Vilanterol. Vilanterol is a relatively selective, long-acting β2-adrenergic agonist as a bronchodilator used for the treatment of COPD and asthma. Synonyms: (R)-1-(2,6-Dichlorophenyl)-21-(4-hydroxy-3-(hydroxymethyl)phenyl)-2,5,12-trioxa-19-azahenicosan-21-ol 2,2,2-Triphenylacetate. Molecular formula: C30H45Cl2NO6. C20H16O2. Mole weight: 874.95. | |
| Vilanterol Impurity 3 | An impurity of Vilanterol. Vilanterol is a relatively selective, long-acting β2-adrenergic agonist as a bronchodilator used for the treatment of COPD and asthma. Synonyms: (R) -4- (2- ( (5- (2- ( (2, 6-Dichlorobenzyl) oxy) ethoxy) pentyl) amino) -1-hydroxyethyl) -2- (hydroxymethyl) phenol 2,2,2-Triphenylacetate. Molecular formula: C23H31Cl2NO5. C20H16O2. Mole weight: 760.76. | |
| Vilanterol Impurity 37 | Vilanterol Impurity 37. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1026253-66-6. Molecular formula: C17H23NO5. Mole weight: 321.37. Catalog: APB1026253666. | |
| Vilanterol Impurity 4 | An impurity of Vilanterol. Vilanterol is a relatively selective, long-acting β2-adrenergic agonist as a bronchodilator used for the treatment of COPD and asthma. Synonyms: (R)-4-(2-((6-(Hex-5-en-1-yloxy)hexyl)amino)-1-hydroxyethyl)-2-(hydroxymethyl)phenol 2,2,2-Triphenylacetate. Molecular formula: C21H35NO4. C20H16O2. Mole weight: 653.87. | |
| Vilanterol Impurity 5 | An impurity of Vilanterol. Vilanterol is a relatively selective, long-acting β2-adrenergic agonist as a bronchodilator used for the treatment of COPD and asthma. Synonyms: (R)-4-(2-((6-((2,6-dichlorobenzyl)oxy)hexyl)amino)-1-hydroxyethyl)-2-(hydroxymethyl)phenol 2,2,2-Triphenylacetate. Molecular formula: C22H29Cl2NO4. C20H16O2. Mole weight: 730.74. | |
| Vilanterol Impurity 6 | An impurity of Vilanterol. Vilanterol is a relatively selective, long-acting β2-adrenergic agonist as a bronchodilator used for the treatment of COPD and asthma. Synonyms: (R) -4- (2- ( (6- (2- ( (2, 4-Dichlorobenzyl) oxy) ethoxy) hexyl) amino) -1-hydroxyethyl) -2- (hydroxymethyl) phenol 2,2,2-Triphenylacetate. Molecular formula: C23H31Cl2NO5. C20H16O2. Mole weight: 760.76. | |
| Vilanterol Impurity 7 | An impurity of Vilanterol. Vilanterol is a relatively selective, long-acting β2-adrenergic agonist as a bronchodilator used for the treatment of COPD and asthma. Synonyms: (R) -4- (2- ( (6- (2- ( (2, 5-Dichlorobenzyl) oxy) ethoxy) hexyl) amino) -1-hydroxyethyl) -2- (hydroxymethyl) phenol 2,2,2-Triphenylacetate. Molecular formula: C23H31Cl2NO5. C20H16O2. Mole weight: 760.76. | |
| Vilanterol Impurity 8 (S-isomer) | An impurity of Vilanterol. Vilanterol is a relatively selective, long-acting β2-adrenergic agonist as a bronchodilator used for the treatment of COPD and asthma. Synonyms: (S) -4- (2- ( (6- (2- ( (2, 6-dichlorobenzyl) oxy) ethoxy) hexyl) amino) -1-hydroxyethyl) -2- (hydroxymethyl) phenol 2,2,2-Triphenylacetate. Molecular formula: C24H33Cl2NO5.C20H16O2. Mole weight: 774.77. | |
| Vilanterol Impurity 9 | An impurity of Vilanterol. Vilanterol is a relatively selective, long-acting β2-adrenergic agonist as a bronchodilator used for the treatment of COPD and asthma. Synonyms: 4,4'-((1R,1'R)-((Oxybis(hexane-6,1-diyl))bis(azanediyl))bis(1-hydroxyethane-2,1-diyl))bis(2-(hydroxymethyl)phenol) 2,2,2-Triphenylacetate. Molecular formula: C30H48N2O7. C20H16O2. Mole weight: 837.08. | |
| Vilanterol trifenatate | Vilanterol trifenatate (GW642444 trifenatate) is a long-acting β 2 -adrenoceptor (β 2 -AR) agonist with inherent 24-hour activity. The pEC 50 s for β 2 -AR, β 1 -AR and β 3 -AR are 10.37, 6.98 and 7.36, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GW642444 trifenatate. CAS No. 503070-58-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14300A. | |
| Vilanterol Trifenatate | Vilanterol, also known as GW-642444, is a long-acting beta-2 agonist drug, which in May 2013 was approved in combination with fluticasone furoate for sale as Breo Ellipta by GlaxoSmithKline for the treatment of chronic obstructive pulmonary disease (COPD). Synonyms: (R) -4- (2- ( (6- (2- ( (2, 6-dichlorobenzyl) oxy) ethoxy) hexyl) amino) -1-hydroxyethyl) -2- (hydroxymethyl) phenol 2,2,2-triphenylacetate; GW-642444; GW642444; GW-642444; GW 642444X; Vilanterol; Vilanterol trifenatate. Grades: 98%. CAS No. 503070-58-4. Molecular formula: C24H33Cl2NO5.C20H16O2. Mole weight: 774.776. | |
| Vilaprisan | Vilaprisan is a selective oral progesterone receptor antagonist under the development of Bayer HealthCare Pharmaceuticals. BAY 1002670 showed a marked dose-dependent reduction of fibroid tumour weight gain of 95% at a dose of 3 mg/kg/day (P < 0.005) in a human fibroid xenograft model. Now clinical trials Phase III for Endometriosis and Uterine leiomyoma was on-going. Synonyms: BAY1002670; BAY-1002670; BAY 1002670; BAY-10-02670; BAY10-02670; BAY 10-02670. Grades: 98%. CAS No. 1262108-14-4. Molecular formula: C27H29F5O4S. Mole weight: 544.58. | |
| Vilaprisan | Vilaprisan is a selective progesterone receptor modulator (SPRM), which targets progesterone receptors. Vilaprisan can inhibit cell proliferation and stimulate apoptosis. Vilaprisan has oral efficacy and anti-proliferative activity against uterine leiomyoma (UF [1] ). Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAY 1002670. CAS No. 1262108-14-4. Pack Sizes: 1 mg; 5 mg. Product ID: HY-16775. | |
| Vilastobart | Vilastobart is an anti- CTLA4 human IgG1 κ monoclonal antibody [1]. Recommend Isotype Controls: Human IgG1 kappa, Isotype Control (HY-P99001). Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2760549-50-4. Pack Sizes: 1 mg. Product ID: HY-P990775. | |
| Vilazodone | Vilazodone (EMD 68843; SB 659746A) is a potent, selective and orally active serotonin reuptake inhibitor (SSRI) and partial 5-HT 1 A receptor agonist. Vilazodone exhibits antidepressant efficacy in vivo can be used for the research of major depressive disorder (MDD) and affective disorders [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EMD 68843; SB659746A. CAS No. 163521-12-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-14262. | |
| Vilazodone | It is a combined serotonin specific reuptake inhibitor (SSRI) and 5-HT1A receptor partial agonist currently under clinical evaluation for the treatment of major depression. Group: Biochemicals. Alternative Names: 5-[4-[4-(5-Cyano-1H-indol-3-yl)butyl]-1-piperazinyl]-2-benzofurancarboxamide; EMD 515259. Grades: Highly Purified. CAS No. 163521-12-8. Pack Sizes: 5mg. US Biological Life Sciences. |  Worldwide |
| Vilazodone | Vilazodone (EMD 68843; SB 659746A) is a combined serotonin specific reuptake inhibitor (SSRI) and 5-HT1A receptor partial agonist currently under clinical evaluation for the treatment of major depression. Uses: Antidepressant. Synonyms: EMD 68843; SB 659746A; EMD-68843; EMD68843; SB-659746A; SB659746A. Grades: 0.98. CAS No. 163521-12-8. Molecular formula: C26H27N5O2. Mole weight: 441.52. | |
| Vilazodone Carboxy Acid | Vilazodone Carboxy Acid is an intermediate in the synthesis of the antidepressant Vilazodone. Synonyms: 5-[4-[4-(5-Cyano-1H-indol-3-yl)butyl]-1-piperazinyl]-2-benzofurancarboxylic Acid. CAS No. 163521-19-5. Molecular formula: C26H26N4O3. Mole weight: 442.52. | |
| Vilazodone Carboxylic Acid | Vilazodone Carboxylic Acid. Uses: For analytical and research use. Group: Impurity standards. CAS No. 163521-19-5. Pack Sizes: 2.5MG. IUPAC Name: 5-[4-[4-(5-cyano-1H-indol-3-yl)butyl]piperazin-1-yl]-1-benzofuran-2-carboxylic acid. Molecular formula: C26H26N4O3. Mole weight: 442.51. Catalog: APS163521195. SMILES: OC(=O)c1oc2ccc(cc2c1)N3CCN(CCCCc4c[nH]c5ccc(cc45)C#N)CC3. Format: Neat. Shipping: Room Temperature. | |
| Vilazodone-d4. | Vilazodone-d4. Group: Biochemicals. Alternative Names: 5-[4-[4-(5-Cyano-1H-indol-3-yl)butyl]-1-(piperazinyl-d8)]-2-benzofurancarboxamide-d4; EMD 515259-d4. Grades: Highly Purified. Pack Sizes: 500ug. Molecular Formula: C26H23D4N5O2, Molecular Weight: 445.55. US Biological Life Sciences. | Worldwide |
| Vilazodone-D4 hydrochloride solution | 100 ?g/mL in methanol (as free base), ampule of 1 mL, certified reference material. Group: Certified reference materials (crms). | |
| Vilazodone Dimer Impurity | An impurity of Vilazodone. Vilazodone is a serotonin specific reuptake inhibitor (SSRI) and 5-HT1A receptor partial agonist that is used for the treatment of major depressive disorder. Synonyms: N-5-(2-Carbamoyl) Benzofuranyl Vilazodone. Molecular formula: C35H32N6O4. Mole weight: 600.68. | |
| Vilazodone Hydrochloride | Vilazodone Hydrochloride (EMD 68843 Hydrochloride) is a serotonin transporter (SER) inhibitor and 5-HT 1A receptor partial agonist. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EMD 68843 Hydrochloride; SB659746A Hydrochloride. CAS No. 163521-08-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-14261. | |
| Vilazodone Impurity 23 | An impurity of Vilazodone. Vilazodone is a serotonin specific reuptake inhibitor (SSRI) and 5-HT1A receptor partial agonist that is used for the treatment of major depressive disorder. Synonyms: 3-(4-chlorobutanoyl)-1-(4-(5-cyano-1H-indol-3-yl)-4-oxobutyl)-1H-indole-5-carbonitrile. Molecular formula: C26H21ClN4O2. Mole weight: 456.94. | |
| Vilazodone Impurity C | Vilazodone Impurity C is a metabolite of Vilazodone. Vilazodone is a serotonin specific reuptake inhibitor (SSRI) and 5-HT1A receptor partial agonist that is used for the treatment of major depressive disorder. Synonyms: Vilazodone N-Oxide; 5-[4-[4-(5-Cyano-1H-indol-3-yl)butyl]-4-oxido-1-piperazinyl]-2-benzofurancarboxamide. CAS No. 1622425-52-8. Molecular formula: C26H27N5O3. Mole weight: 457.54. | |
| Vilazodone impurity II | An impurity of Vilazodone. Vilazodone is a serotonin specific reuptake inhibitor (SSRI) and 5-HT1A receptor partial agonist that is used for the treatment of major depressive disorder. Synonyms: ethyl 5-(4-(4-(5-cyano-1H-indol-3-yl)butyl)piperazin-1-yl)benzofuran-2-carboxylate hydrochloride. Molecular formula: C28H30N4O3.HCl. Mole weight: 507.04. | |
| Vildagliptin | Vildagliptin (LAF237) is a potent, stable, selective dipeptidyl peptidase IV (DPP-IV) inhibitor with an IC50 of 3.5 nM in human Caco-2 cells. Vildagliptin possesses excellent oral bioavailability and potent antihyperglycemic activity. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Unii-I6B4B2U96p; Laf 237; Galvus. Product Category: Inhibitors. Appearance: white crystalline powder. CAS No. 274901-16-5. Molecular formula: C17H25N3O2. Mole weight: 303.4. Purity: 0.98. IUPACName: (2S)-1-[2-[(3-hydroxy-1-adamantyl)amino]acetyl]pyrrolidine-2-carbonitrile. Canonical SMILES: C1CC(N(C1)C(=O)CNC23CC4CC(C2)CC(C4)(C3)O)C#N. Density: 1.27 g/cm³. Product ID: ACM274901165. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Vildagliptin | Vildagliptin (LAF237) is a potent, stable, selective dipeptidyl peptidase IV ( DPP-IV ) inhibitor with an IC 50 of 3.5 nM in human Caco-2 cells. Vildagliptin possesses excellent oral bioavailability and potent antihyperglycemic activity [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LAF237; NVP-LAF 237. CAS No. 274901-16-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-14291. | |
| Vildagliptin | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopyapi standardschiral moleculespharmaceutical toxicology. Alternative Names: NVP-LAF 237,(2S)-1-[2-[(3-Hydroxytricyclo[3.3.1.13,7]dec-1-yl)amino]acetyl]-2-pyrrolidinecarbonitrile, 2-Pyrrolidinecarbonitrile, 1-[[(3-hydroxytricyclo[3.3.1.13,7]dec-1-yl)amino]acetyl]-, (2S)- (9CI), Vildagliptin, (S)-1-[2-[(3-Hydroxyadamant-1-yl)amino]acetyl]pyrrolidine-2-carbonitrile, DSP 7238, Galvus, Equa, LAF 237. | |
| Vildagliptin | It is a new oral anti-hyperglycemic agent of a new dipeptidyl peptidase-IV (DPP-IV) inhibitor class of drugs. Antidiabetic. Group: Biochemicals. Grades: Highly Purified. CAS No. 274901-16-5. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Vildagliptin Carboxylic Acid Lithium Salt Hydrate | The major metabolite of Vildagliptin. Group: Biochemicals. Alternative Names: N-(3-Hydroxytricyclo[3. 3. 1. 13, 7]dec-1-yl)glycyl-. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Vildagliptin Carboxylic Acid Metabolite | Vildagliptin Carboxylic Acid Metabolite is a major metabolite of vildagliptin. Synonyms: N-(3-Hydroxytricyclo[3.3.1.1~3,7~]decan-1-yl)glycyl-L-proline. CAS No. 565453-40-9. Molecular formula: C17H26N2O4. Mole weight: 322.405. | |
| Vildagliptin Impurity 1 | Vildagliptin Impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1036959-27-9. Molecular formula: C17H25N3O2. Mole weight: 303.41. Catalog: APB1036959279. | |
| Vildagliptin Impurity 2 | Vildagliptin Impurity 2. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1036959-23-5. Molecular formula: C24H33N5O3. Mole weight: 439.56. Catalog: APB1036959235. | |
| Vildagliptin Impurity 22 | Vildagliptin Impurity 22. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1032564-18-3. Molecular formula: C12H19NO3. Mole weight: 225.29. Catalog: APB1032564183. | |
| Vildagliptin Impurity 26 | Vildagliptin Impurity 26. Uses: For analytical and research use. Group: Impurity standards. CAS No. 108-80-5. Molecular formula: C3H3N3O3. Mole weight: 129.08. Catalog: APB108805. | |
| Vildagliptin Impurity 3 Trifluoroacetate | An impurity of Vildagliptin. Vildagliptin is a new dipeptidyl peptidase-4 (DPP-4) inhibitor that is used as an anti-hyperglycemic agent. Vildagliptin could reduce hyperglycemia in type 2 diabetes mellitus via the suppressive effect of inactivation of GLP-1 and GIP by DPP-4. Synonyms: Vildagliptin Carboxy Acid Metabolite Trifluoroacetate. CAS No. 565453-41-0. Molecular formula: C17H26N2O4. C2HF3O2. Mole weight: 436.43. | |
| Vildagliptin Impurity A | An impurity of Vildagliptin. Vildagliptin is a new dipeptidyl peptidase-4 (DPP-4) inhibitor that is used as an anti-hyperglycemic agent. Vildagliptin could reduce hyperglycemia in type 2 diabetes mellitus via the suppressive effect of inactivation of GLP-1 and GIP by DPP-4. CAS No. 565453-39-6. Molecular formula: C17H27N3O3. Mole weight: 321.4. | |
| Vildagliptin Impurity B | An impurity of Vildagliptin. Vildagliptin is a new dipeptidyl peptidase-4 (DPP-4) inhibitor that is used as an anti-hyperglycemic agent. Vildagliptin could reduce hyperglycemia in type 2 diabetes mellitus via the suppressive effect of inactivation of GLP-1 and GIP by DPP-4. Synonyms: Vildagliptin Impurity 2; (2S,2'S)-1,1'-[[(3-Hydroxytricyclo[3.3.1.13,7]dec-1-yl)imino]bis(1-oxo-2,1-ethanediyl)]bis-2-pyrrolidinecarbonitrile. CAS No. 1036959-23-5. Molecular formula: C24H33N5O3. Mole weight: 439.56. | |
| Vildagliptin Impurity C | Molecular formula: C17H24N2O3. | |
| Vildagliptin Impurity E hydrochloride | An impurity of Vildagliptin, an anti-hyperglycemic agent of the dipeptidyl peptidase-4 (DPP-4) inhibitor class. Synonyms: Vildagliptin Impurity E HCl; 2-(3-Hydroxyadamantan-1-yl)-1-iminohexahydropyrrolo[1,2-a]pyrazin-4(1H)-one hydrochloride. Molecular formula: C17H25N3O2.HCl. Mole weight: 339.87. | |
| Vildagliptin Related Compound A | An impurity of Vildagliptin. Vildagliptin is a new dipeptidyl peptidase-4 (DPP-4) inhibitor that is used as an anti-hyperglycemic agent. Vildagliptin could reduce hyperglycemia in type 2 diabetes mellitus via the suppressive effect of inactivation of GLP-1 and GIP by DPP-4. Synonyms: Vildagliptin Imp.A; 2-Pyrrolidinecarbonitrile, 1-[2-(tricyclo[3.3.1.13,7]dec-1-ylamino)acetyl]-, (2S)-; Vildagliptin Deshydroxy Impurity; (S)-1-(2-((3R,5R,7R)-adamantan-1-ylamino)acetyl)pyrrolidine-2-carbonitrile. CAS No. 741657-02-3. Molecular formula: C17H25N3O. Mole weight: 287.4. | |
| Vildagliptin ( (S) -1-[N- (3-hydroxy-1-adamantyl) glycyl]pyrrolidine-2-carbonitrile) | An antidiabetic agent. A potent inhibitor of dipeptidyl peptidase IV (DPP IV), an enzyme that breaks down Glucagon-like peptide 1 (GLP-1). By delaying the degradation of GLP-1, vildagliptin extends the action of insulin while also suppressing the release of glucagon. This leads to a reduction in elevated blood glucose levels (hyperglycemia), which is a characteristic feature of type 2 diabetes. Group: Biochemicals. Grades: Highly Purified. CAS No. 274901-16-5. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Vilella's Reagent | Good for ferrite-carbide structures (tempered martensite) in iron and steel. Group: Etchants. |  |
| Villocarine A | Villocarine A is a natural vasorelaxant indole alkaloid [1]. Uses: Scientific research. Group: Natural products. CAS No. 1319743-81-1. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N11478. | |
| Vilobelimab | Vilobelimab (CaCP-29, IFX-1) is a monoclonal anti- C5a antibody to the allergen C5a, a pro-inflammatory complement division product that plays a central role in mediating organ dysfunction. Vilobelimab acts as a C5a inhibitor, inhibiting neutrophil activation, chemotaxis, and reducing inflammatory signalling, and may be used in studies related to sepsis, COVID-19, etc [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: CaCP-29, IFX-1. CAS No. 2250440-41-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99520. | |
| Viloxazine | Viloxazine (Viloxazin) is a norepinephrine reuptake inhibitor, also a potent 5-HT 2C agonist and 5-HT 2B antagonist with an EC 50 of 32 μM and an IC 50 of 27 μM for 5-HT 2C and 5-HT 2B , respectively. The mechanism of action of Viloxazine predominantly involves serotonergic and noradrenergic pathways. Viloxazine can be used for researching depression [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Viloxazin; Emovit. CAS No. 46817-91-8. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W380450. | |
| Viloxazine hydrochloride | Viloxazine hydrochloride is a non-brain-penetrant, selective norepinephrine transporter (NET) inhibitor ( IC 50 =0.26 μM) and 5-HT receptor modulator. Viloxazine antagonizes 5-HT2B receptors ( K i =4.2 μM) and agonizes 5-HT2C receptors ( EC 50 =32 μM), respectively, and enhances 5-HT neurotransmission by modulating 5-HT2B/C receptors. Viloxazine also competitively inhibits NET from increasing NE and DA levels in the synaptic cleft, and can be used in the study of attention deficit hyperactivity disorder (ADHD) [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Viloxazin hydrochloride; Emovit hydrochloride. CAS No. 35604-67-2. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-125784. | |
| Viltolarsen sodium | Viltolarsen (NS-065/NCNP-01) sodium is a phosphorodiamidate morpholino antisense oligonucleotide. Viltolarsen sodium binds to exon 53 of the dystrophin mRNA precursor and restores the amino acid open-reading frame by skipping exon 53, resulting in the production of a shortened dystrophin protein that contains essential functional portions. Viltolarsen sodium has the potential for Duchenne muscular dystrophy (DMD) research[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NS-065/NCNP-01 sodium. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-132586A. | |
| Vimentin (177-185) | Vimentin (177-185) is a 9-amino acid peptide of Vimentin which is a type III intermediate filament (IF) protein that is expressed in mesenchymal cells. It can be used in Ovarian carcinoma research. | |
| Vimentin (226-234) | Vimentin (226-234) is a 9-amino acid peptide of Vimentin which is a type III intermediate filament (IF) protein that is expressed in mesenchymal cells. It can be used in Ovarian carcinoma research. | |
| Vimentin (402-413) | Vimentin (402-413) is a 12-amino acid peptide of Vimentin which is a type III intermediate filament (IF) protein that is expressed in mesenchymal cells. It can be used in Ovarian carcinoma research. | |
| Vimentin from bovine lens | lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| Vimentin, His tagged human | recombinant, expressed in E. coli, ?90% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| Vimseltinib | Vimseltinib is a selective dual inhibitor of CSF-1R (c-FMS) and c-Kit. Vimseltinib has been used in the research of tenosynovial giant cell tumor (TGCT). Synonyms: DCC-3014; DCC 3014; DCC3014. CAS No. 1628606-05-2. Molecular formula: C23H25N7O2. Mole weight: 431.49. | |
| Vimseltinib | Vimseltinib (DCC-3014) is a c-FMS ( CSF-IR ) and c-Kit dual inhibitor extracted from patent WO2014145025A2, Compound Example 10, has IC 50 s of <0.01 μM and 0.1-1 μM, respectively [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: DCC-3014. CAS No. 1628606-05-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-136256. | |
| Vinaginsenoside-r3 | Vinaginsenoside-r3. Uses: Designed for use in research and industrial production. Additional or Alternative Names: VINAGINSENOSIDE-R3. Product Category: Heterocyclic Organic Compound. CAS No. 156012-92-9. Molecular formula: C48H82O17. Mole weight: 931.159. Product ID: ACM156012929. Alfa Chemistry ISO 9001:2015 Certified. Categories: Vinaginsenoside R3. | |
| Vina-ginsenoside R3 | Formula: Group: Biochemicals. Grades: Plant Grade. CAS No. 156012-92-9. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Vinaginsenoside R3 | Vinaginsenoside R3 is a saponin composition of roots of Panax ginseng. Ginsengs have been not only used as therapeutic agents with tonic, sedative, anti-fatigue, and anti-gastric ulcer effect but also marketed as dietary supplements and raw materials of health food. Vinaginsenoside R3 is the first naturally occurring glycoside of dammarenediol 2. Synonyms: β-D-Glucopyranoside, (3β)?-20-(β-D-glucopyranosyloxy)?dammar-24-en-3-yl 2-O-β-D-glucopyranosyl-;(3β)-20-(β-D-Glucopyranosyloxy)dammar-24-en-3-yl 2-O-β-D-glucopyranosyl-β-D-glucopyranoside. Grades: > 98%. CAS No. 156012-92-9. Molecular formula: C48H82O17. Mole weight: 931.15. | |
| Vina-ginsenoside R4 | Vina-ginsenoside R4 is a triterpenoid vina-ginsenoside standard extracted from Panax ginseng. Panax ginseng is a familiar herbal medicine which has been used as a tonic, sedative, anti-fatigue, or anti-gastric ulcer drug, and also has antidiabetic and antitumor activities. More than 40 ginsenosides have been identified, isolated and characterised till now. Synonyms: β-D-Glucopyranoside, (3β,?6α,?12β)?-20-(β-D-glucopyranosyloxy)?-6,?12-dihydroxydammar-24-en-3-yl 2-O-β-D-glucopyranosyl-. Grades: > 98%. CAS No. 156009-80-2. Molecular formula: C48H82O19. Mole weight: 963.15. | |
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