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| Product | Description | |
|---|---|---|
| Vildagliptin | Glyptins are class of oral anti-hyperglycemic agents that inhibit dipeptidyl peptidase 4 (DPP-4), which can act as a serine exopeptidase. Aside from there use in type 2 diabetes, gliptins have positive cardiovascular and anti-inflammtatory effects. Antidiabetic. Uses: Dipeptidyl-peptidase iv inhibitors. Synonyms: LAF237; LAF 237; LAF-237; Galvus; NVP-LAF 237; Zomelis; Xiliarx; Jalra; DSP 7238; DSP-7238; DSP7238; Vildagliptin; Zomelis. Grade: 98%. CAS No. 274901-16-5. Molecular formula: C17H25N3O2. Mole weight: 303.406. |  |
| 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 | Vildagliptin is a cyanopyrrolidine-based, orally bioavailable inhibitor of dipeptidyl peptidase 4 (DPP-4), with hypoglycemic activity. Vildagliptin's cyano moiety undergoes hydrolysis and this inactive metabolite is excreted mainly via the urine. Alternative Names: Galvus. Xiliarx. Jalra. CAS No. 274901-16-5. Product ID: API274901165. Molecular formula: C17H25N3O2. Mole weight: 303.4. EINECS: 630-410-0. SMILES: C1C[C@H](N(C1)C(=O)CNC23CC4CC(C2)CC(C4)(C3)O)C#N. Appearance: White solid. Category: Anti-Acid APIs. |  |
| 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 | ?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 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-[d6] | Vildagliptin-[d6] is the labeled analogue 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 D6; Vildagliptin-d6; (2S)-1-[[(3-Hydroxytricyclo[3.3.1.13,7]dec-1-yl)amino]acetyl]-pyrrolidine-2-carbonitrile-3,3,4,4,5,5-d6; (S)-1-[2-[(3-Hydroxyadamant-1-yl)amino]acetyl]pyrrolidine-2-carbonitrile-3,3,4,4,5,5-d6; Vidagliptin-d6; Xiliarx-d6. Grade: >95%. CAS No. 2747956-23-4. Molecular formula: C17H19N3O2D6. Mole weight: 309.44. | |
| Vildagliptin-[d7] | Vildagliptin-[d7] is the labelled analogue of Vildagliptin, a DPP-4 inhibitor used as an anti-diabetic drug. Synonyms: Vildagliptin D7. Grade: 98% by HPLC; 98% atom D. CAS No. 1133208-42-0. Molecular formula: C17H18D7N3O2. Mole weight: 310.4. | |
| 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 ( (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. | |
| Villosin | Villosin is a natural diterpenoid isolated from the herbs of Hedychium coronarium. For its potent cytotoxic activity with IC(50) of 0.40 microM, villosin may be used as a potential lead molecule for antitumor therapeutic development. Uses: Anti-tumor. Synonyms: 8(17),11,13-Labdatrien-16,15-olide. Grade: >98%. CAS No. 160598-92-5. Molecular formula: C20H28O2. Mole weight: 300.4. | |
| 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 Antibody [B13H12] | Vimentin Antibody [B13H12]. Group: Antibodies. Pack Sizes: 20ul. Product ID: F0166. Storage Conditions: -20°C (avoid freeze-thaw cycles), 2 years. |  United States; Europe |
| Vimentin Antibody [N21E20] | Vimentin Antibody [N21E20]. Group: Antibodies. Pack Sizes: 20uL. Product ID: F2517. Storage Conditions: -20°C (avoid freeze-thaw cycles), 2 years. | United States; Europe |
| 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 (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 |
| Vina-ginsenoside R4 | Formula: Group: Biochemicals. Grades: Plant Grade. CAS No. 156009-80-2. Pack Sizes: 5mg, 10mg. US Biological Life Sciences. | Worldwide |
| Vina-ginsenoside R8 | Formula: Group: Biochemicals. Grades: Plant Grade. CAS No. 156042-22-7. Pack Sizes: 5mg, 10mg. US Biological Life Sciences. | Worldwide |
| Vinaxanthone | It is a semaphorin inhibitor produced by the strain of Penicillinm sp. SPF-3059. It inhibits Semaphorin with IC50 of 0.1 μg/mL. Synonyms: Antibiotic 411F; Antibiotic Ro-09-1450; 9H-Xanthene-1-carboxylic acid, 5,7-diacetyl-6-(5-carboxy-6,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl)-2,3-dihydroxy-9-oxo-. CAS No. 133293-89-7. Molecular formula: C28H16O14. Mole weight: 576.42. | |
| Vinblastine | Vinblastine, an inhibitor of nAChR, is a natural alkaloid isolated from the plant Vinca rosea Linn. It binds to tubulin and inhibits microtubule formation, leading to disruption of mitotic spindle assembly and arrest of tumor cells in the M-phase of the cell cycle. It may also interfere with the metabolism of amino acids, cyclic AMP, and glutathione. It is used to treat malignant lymphoma. Uses: Antitumor. Synonyms: [3aR-[3aa,4b,5b,5ab,9(3R*,5S*,7R*,9S*),10bR*,13aa]]-Methyl 4-(acetyloxy)-3a-ethyl-9-[5-ethyl-1,4,5,6,7,8,9,10-octahydro-5-hydroxy-9-(methoxycarbonyl)-2H-3,7-methanoazacycloundecino[5,4-b]indol-9-yl]-3a,4,5,5a,6,11,12,13a-octahydro-5-hydroxy-8-methoxy-6-methyl-1H-indolizino[8,1-cd]carbazole-5-carboxylate; 1H-Indolizino[8,1-cd]carbazole, vincaleukoblastine deriv.; 1H-Indolizino(8,1-cd)carbazole-5-carboxylic acid, 4-(acetyloxy)-3a-ethyl-9-(5-ethyl-1,4,5,6,7,8,9,10-octahydro-5-hydroxy-9-(methoxycarbonyl)-2H-3,7-methanoazacycloundecino(5,4-b)indol-9-yl)-3a,4,5,5a,6,11,12,13a-octahydro-5-hydroxy-8-methoxy-6-methyl-, methyl ester, (3aR-(3aα,4β,5β,5aβ,9(3R*,5S*,7R*,9S*),10bR*,13aα))-; Rozevin; (+)-Vinblastine; Vincaleukoblastine. Grade: >98%. CAS No. 865-21-4. Molecular formula: C46H58N4O9. Mole weight: 810.97. | |
| Vinblastine | Vinblastine. Group: Biochemicals. Grades: Plant Grade. CAS No. 865-21-4. Pack Sizes: 20mg. US Biological Life Sciences. | Worldwide |
| Vinblastine-d3 | Labeled Vinblastine. Antitumor alkaloid isolated from periwinkle, Vinca rosea Linn., Apocynaceae; inhibits microtubule assembly. An antineoplastic. Group: Biochemicals. Alternative Names: Vincaleukoblastine. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Vinblastine-d5-methylchloride Iodide | Vinblastine-d5-methylchloride Iodide is the labeled analogue of Vinblastine-methylchloride Iodide (V314010), an adduct of Vinblastine (V314000), an antitumor alkaloid isolated from periwinkle, Vinca rosea Linn., Apocynaceae; inhibits microtubule assembly. An antineoplastic. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 10mg. Molecular Formula: C47H55D5ClIN4O9, Molecular Weight: 992.39. US Biological Life Sciences. | Worldwide |
| Vinblastine sulfate | Vinblastine sulfate is a cytotoxic alkaloid used against various cancer types. Vinblastine sulfate inhibits the formation of microtubule and suppresses nAChR with an IC50 of 8.9 μM. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (3S)-3-Phenylisoserine hydrochloride. Product Category: Inhibitors. Appearance: White powder. CAS No. 143-67-9. Molecular formula: C46H60N4O13S. Mole weight: 909.05. Purity: 0.98. IUPACName: Methyl (1R,9R,10S,11R,12R,19R)-11-acetyloxy-12-ethyl-4-[(13S,15S,17S)-17-ethyl-17-hydroxy-13-methoxycarbonyl-1,11-diazatetracyclo[13.3.1.04,12.05,10]nonadeca-4(12),5,7,9-tetraen-13-yl]-10-hydroxy-5-methoxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraene-10-carboxylate;sulfuric acid. Canonical SMILES: CC[C@@]1(C[C@@H]2C[C@@](C3=C(CCN(C2)C1)C4=CC=CC=C4N3)(C5=C(C=C6C(=C5)[C@]78CCN9[C@H]7[C@@](C=CC9)([C@H]([C@@]([C@@H]8N6C)(C(=O)OC)O)OC(=O)C)CC)OC)C(=O)OC)O.OS(=O)(=O)O. Product ID: ACM143679. Alfa Chemistry ISO 9001:2015 Certified. | |
| Vinblastine sulfate | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardseuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: Vinblastine sulfate, methyl (3aR,4R,5S,5aR,10bR,13aR)-4-(acetyloxy)-3a-ethyl-9-[(5S,7R,9S)5-ethyl-5-hydroxy-9-(methoxycarbonyl)-1,4,5,6,7,8,9,10-octahydro-2H-3,7-methanoazacycloundecino[5,4-b]indol-9-yl]-5-hydroxy-8-methoxy-6-methyl-3a,4,5,5a,6,11,12,13a-octahydro-1H-indolizino[8,1-cd]carbazole-5-carboxylate sulfate. | |
| Vinblastine sulfate | Vinblastine sulfate. Group: Biochemicals. Alternative Names: Vincaleukoblastine. Grades: Highly Purified. CAS No. 143-67-9. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C46H60N4O13S. US Biological Life Sciences. | Worldwide |
| Vinblastine sulfate | Vinblastine sulfate is a cytotoxic alkaloid used against various cancer types. Vinblastine sulfate inhibits the formation of microtubule and suppresses nAChR with an IC 50 of 8.9 μM. Uses: Scientific research. Group: Natural products. Alternative Names: Vincaleukoblastine sulfate salt. CAS No. 143-67-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-13780. | |
| Vinblastine Sulfate (29060-LE, Exal, Velban, Velbe,) | An antineoplastic. Group: Biochemicals. Alternative Names: 29060-LE, Exal, Velban, Velbe. Grades: Highly Purified. CAS No. 143-67-9. Pack Sizes: 20mg. US Biological Life Sciences. | Worldwide |
| Vinburnine | Vincamone is a vinca alkaloid and a metabolite of vincamine, is a vasodilator. Uses: Scientific research. Group: Natural products. Alternative Names: (-)-Eburnamonine; (-)-Vincamone. CAS No. 4880-88-0. Pack Sizes: 10 mM * 1 mL; 100 mg; 200 mg. Product ID: HY-B1180. | |
| Vincadifformine | Vincadifformine. Group: Biochemicals. Grades: Highly Purified. CAS No. 15539-10-3. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. Molecular Formula: C21H26N2O2. US Biological Life Sciences. | Worldwide |
| Vincamine | Vincamine. Group: Biochemicals. Grades: Plant Grade. CAS No. 1617-90-9. Pack Sizes: 20mg. Molecular Formula: C21H26N2O3, Molecular Weight: 354.44. US Biological Life Sciences. | Worldwide |
| Vincamine | Vincamine is a monoterpenoid indole alkaloid extracted from the Madagascar periwinkle. Vincamine is a peripheral vasodilator and exerts a selective vasoregulator action on the brain microcapilar circulation [1]. Vincamine is a GPR40 agonist and acts as a β-cell protector by ameliorating β-cell dysfunction and promoting glucose-stimulated insulin secretion (GSIS). Vincamine improves glucose homeostasis in vivo , and has the potential for the type 2 diabetes mellitus (T2DM) research [2]. Uses: Scientific research. Group: Natural products. CAS No. 1617-90-9. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B1021. | |
| Vincamine | analytical standard. Group: Herbal medicinal products standardseuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: Perval, 1H-Indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine eburnamenine-14-carboxylic acid deriv., Equipur, Oxygeron, Minorine, Vincafolina, Vincagil, Novicet, Angiopac, Ocu-vinc, Vinvasaunier, Vincafor,Vincamine, Devinkan, (+)-Vincamine, Minorin, (3alpha,14beta,16alpha)-14,15-Dihydro-14-hydroxyeburnamenine-14-carboxylic acid methyl ester, (+)-cis-Vincamine, Tripervan, Vincadar, Vincapront, Vincimax, Pervincamine, Devincan, Pervone, Vinodrel Retard, Sostenil, Vincapan, cis-Vincamine, NSC 91998, Vincafarm, Vincamin, Vincamidol, Vincalen, Arteriovinca, Vraap, Methyl vincaminate. | |
| Vincamine | analytical standard. Uses: For analytical and research use. Group: Herbal medicinal products standards; european pharmacopoeia (ph. eur.); pharmaceutical toxicology; pharmacopoeial standards. Alternative Names: Perval, 1H-Indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine eburnamenine-14-carboxylic acid deriv., Equipur, Oxygeron, Minorine, Vincafolina, Vincagil, Novicet, Angiopac, Ocu-vinc, Vinvasaunier, Vincafor,Vincamine, Devinkan, (+)-Vincamine, Minorin, (3alpha,14beta,16alpha)-14,15-Dihydro-14-hydroxyeburnamenine-14-carboxylic acid methyl ester, (+)-cis-Vincamine, Tripervan, Vincadar, Vincapront, Vincimax, Pervincamine, Devincan, Pervone, Vinodrel Retard, Sostenil, Vincapan, cis-Vincamine, NSC 91998, Vincafarm, Vincamin, Vincamidol, Vincalen, Arteriovinca, Vraap, Methyl vincaminate. Grades: analytical standard. CAS No. 1617-90-9. Pack Sizes: 50MG. IUPAC Name: (3?,14?,16?)-14,15-Dihydro-14-hydroxyeburnamenine-14-carboxylic acid methyl ester. Molecular formula: C21H26N2O3. Mole weight: 354.44. EC Number: 216-576-3. Catalog: APS1617909. Assay: ?97.0%. SMILES: CC[C@@]12CCCN3CCc4c([C@H]13)n(c5ccccc45)[C@](O)(C2)C(=O)OC. Format: Neat. | |
| Vincetoxicoside B | Vincetoxicoside B. Group: Biochemicals. CAS No. 22007-72-3. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Vincristine | Vincristine. Group: Biochemicals. Grades: Plant Grade. CAS No. 57-22-7. Pack Sizes: 20mg. US Biological Life Sciences. | Worldwide |
| Vincristine | Vincristine. CAS No: 57-22-7 |  Sarchem Laboratories New Jersey NJ |
| Vincristine Chloromethiodide | Vincristine Chloromethiodide is an impurity of Vincristine (V314250), An antitumor alkaloid isolated from Vinca rosea Linn. An antineoplastic. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg, 50mg. Molecular Formula: C47H58ClIN4O10, Molecular Weight: 1001.34. US Biological Life Sciences. | Worldwide |
| Vincristine Chloromethiodide-d5 | Vincristine Chloromethiodide-d5 is the labeled analogue of Vincristine Chloromethiodide (V314230), an impurity of Vincristine (V314250), An antitumor alkaloid isolated from Vinca rosea Linn. An antineoplastic. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 10mg. Molecular Formula: C47H53D5ClIN4O10, Molecular Weight: 1006.37. US Biological Life Sciences. | Worldwide |
| Vincristine-D3 | Vincristine-D3. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1246817-09-3. Molecular formula: C46H53D3N4O10. Mole weight: 827.99. Catalog: APB1246817093. | |
| Vincristine-d3 Sulfate | Labelled Vincristine. An antitumor alkaloid isolated from Vinca rosea Linn. An antineoplastic. Group: Biochemicals. Alternative Names: 22-Oxovincaleukoblastine-d3 Sulfate. Grades: Highly Purified. CAS No. 1217854-24-4. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Vincristine-d6 Sulfate | Vincristine-d6 Sulfate. Group: Biochemicals. Alternative Names: 22-Oxovincaleukoblastine-d6 Sulfate. Grades: Highly Purified. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Vincristine Impurity 4 | Vincristine Impurity 4. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1246812-06-5. Molecular formula: C46H56N4O11. Mole weight: 840.97. Catalog: APB1246812065. | |
| Vincristine (Leurocristine) Sulfate | Vincristine sulfate is an inhibitor of polymerization of microtubules by binding to tubulin with IC50 of 32 μM in a cell-free assay. Vincristine sulfate induces apoptosis. Group: Inhibitors. Alternative Names: Leurocristine sulfate, NSC-67574 sulfate, 22-Oxovincaleukoblastine sulfate. CAS No. 2068-78-2. Pack Sizes: 10mg. Product ID: S1241. Formula: C46H58N4O14S. Smiles: CCC1(CC2CC(C3=C(CCN(C2)C1)C4=CC=CC=C4N3)(C5=C(C=C6C(=C5)C78CCN9C7C(C=CC9)(C(C(C8N6C=O)(C(=O)OC)O)OC(=O)C)CC)OC)C(=O)OC)O.OS(=O)(=O)O. Storage Conditions: 2 years -80 in solvent. | United States; Europe |
| Vincristine M1 | Vincristine M1. CAS No: 910580-56-2 | Sarchem Laboratories New Jersey NJ |
| Vincristine N-Oxide | Potential treatment for hyperproliferative disorders. Group: Biochemicals. Alternative Names: 22-Oxo-vincaleukoblastine 6'-Oxide. Grades: Highly Purified. CAS No. 947527-73-3. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Vincristine sulfate | Vincristine sulfate is an antitumor vinca alkaloid which inhibits microtubule formation in mitotic spindle, resulting in an arrest of dividing cells at the metaphase stage. It binds to microtubule with a K i of 85 nM. Uses: Scientific research. Group: Natural products. Alternative Names: Leurocristine sulfate; NSC-67574 sulfate; 22-Oxovincaleukoblastine sulfate. CAS No. 2068-78-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-N0488. | |
| Vincristine sulfate | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardschiral moleculeseuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: Methyl (3aR,4R,5S,5aR,10bR,13aR)-4-(acetyloxy)-3a-ethyl-9-[(5S,7R,9S)-5-ethyl-5-hydroxy-9-(methoxycarbonyl)-1,4,5,6,7,8,9,10-octahydro-2H-3,7-methanoazacycloundecino[5,4-b]indol-9-yl]-6-formyl-5-hydroxy-8-methoxy-3a,4,5,5a,6,11,12,13a-octahydro-1H-indolizino[8,1-cd]carbazole-5-carboxylate sulfate,Vincristine sulfate. | |
| Vincristine Sulfate | An antitumor alkaloid isolated from Vinca rosea Linn. An antineoplastic. Group: Biochemicals. Grades: Highly Purified. CAS No. 2068-78-2. Pack Sizes: 10mg, 25mg, 50mg, 100mg. Molecular Formula: C??H??N?O??S. US Biological Life Sciences. | Worldwide |
| Vincristine sulfate (assay) | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Vincristine Sulfate Liposome | Vincristine sulfate is in the vinca alkaloid family that exerts its cell cycle-specific antitumor effects by affecting spindle microtubule formation through inhibition of microtubule protein polymerization. This product is a PEGylated pre-formulated liposome with vincristine sulfate. It is only for research purposes. Group: Drug-loaded liposome. |  |
| Vincristine sulfate salt | 95.0-105.0% (HPLC), powder. Group: Fluorescence/luminescence spectroscopy. | |
| Vinculin (10-19) | Vinculin (10-19) is a 22-residue peptide of Vinculin. Vinculin is a cytoskeletal protein that plays an important role in the regulation of focal adhesions and embryonic development. It can be used in Ovarian carcinoma research. | |
| Vinculin Antibody [M20M17] | Vinculin Antibody [M20M17]. Group: Antibodies. Pack Sizes: 20ul. Product ID: F0110. Storage Conditions: -20°C (avoid freeze-thaw cycles), 2 years. | United States; Europe |
| Vindesine | Vindesine. Group: Biochemicals. Grades: Highly Purified. CAS No. 53643-48-4. Pack Sizes: 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| Vindesine sulfate | Vindesine sulfate is a potent tubulin inhibitor with an K i of 0.110 μM. Vindesine sulfate shows anti-proliferation effect in vitro. Vindesine sulfate shows antitumor effect in vivo [1]. Uses: Scientific research. Group: Natural products. CAS No. 59917-39-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-129071. | |
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