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| Product | Description | |
|---|---|---|
| Vildagliptin Impurity 45 | Vildagliptin Impurity 45. Uses: For analytical and research use. CAS No. 2401-64-1. Molecular formula: C5H6Cl2N4. Mole weight: 193.03. Catalog: APB2401641. |  |
| Vildagliptin Impurity 48 | Vildagliptin Impurity 48. Uses: For analytical and research use. CAS No. 1846606-32-3. Molecular formula: C7H10N2O3. Mole weight: 170.17. Catalog: APB1846606323. | |
| Vildagliptin Impurity 49 | Vildagliptin Impurity 49. Uses: For analytical and research use. Alternative Names: (2S,2'S)-1,1'-acetylbis(pyrrolidine-2-carbonitrile). CAS No. 2253194-13-5. Molecular formula: C12H16N4O. Mole weight: 232.28. Catalog: APB2253194135. | |
| Vildagliptin Impurity 5 | Vildagliptin Impurity 5. Uses: For analytical and research use. CAS No. 1844894-70-7. Molecular formula: C17H24N2O3. Mole weight: 304.39. Catalog: APB1844894707. | |
| Vildagliptin Impurity 50 | Vildagliptin Impurity 50. Uses: For analytical and research use. Alternative Names: (S)-1-(2-iodoacetyl)pyrrolidine-2-carbonitrile. CAS No. 1811569-16-0. Molecular formula: C7H9ION2. Mole weight: 264.06. Catalog: APB1811569160. | |
| Vildagliptin Impurity 53 | Vildagliptin Impurity 53. Uses: For analytical and research use. CAS No. 700376-84-7. Molecular formula: C7H10N2O. Mole weight: 138.17. Catalog: APB700376847. | |
| Vildagliptin Impurity 54 | Vildagliptin Impurity 54. Uses: For analytical and research use. CAS No. 7531-52-4. Molecular formula: C5H10N2O. Mole weight: 114.15. Catalog: APB7531524. | |
| Vildagliptin Impurity 56 | Vildagliptin Impurity 56. Uses: For analytical and research use. Alternative Names: (S)-1-(2-chloroacetyl)-N-(2-((S)-2-cyanopyrrolidin-1-yl)-2-oxoethyl)pyrrolidine-2-carboxamide. Molecular formula: C14H19ClN4O3. Mole weight: 326.78. Catalog: APB01847. | |
| Vildagliptin Impurity 56 | Vildagliptin Impurity 56. Uses: For analytical and research use. CAS No. 2253194-12-4. Molecular formula: C12H18N4O2. Mole weight: 250.3. Catalog: APB2253194124. | |
| Vildagliptin Impurity 57 | Vildagliptin Impurity 57. Uses: For analytical and research use. CAS No. 913980-23-1. Molecular formula: C7H12ClN3O. Mole weight: 189.64. Catalog: APB913980231. | |
| Vildagliptin Impurity 57 (4-Methylbenzenesulfonate) | Vildagliptin Impurity 57 (4-Methylbenzenesulfonate). Uses: For analytical and research use. Alternative Names: (S)-1-(2-aminoacetyl)pyrrolidine-2-carbonitrile 4-methylbenzenesulfonate. Molecular formula: C7H11N3O·C7H8O3S. Mole weight: 325.38. Catalog: APB01846. | |
| Vildagliptin Impurity 58 | Vildagliptin Impurity 58. Uses: For analytical and research use. Molecular formula: C10H16N2O2. Mole weight: 196.25. Catalog: APB10055. | |
| Vildagliptin Impurity 59 | Vildagliptin Impurity 59. Uses: For analytical and research use. Molecular formula: C14H19ClN4O3. Mole weight: 326.78. Catalog: APB10056. | |
| Vildagliptin Impurity 59 | Vildagliptin Impurity 59. Uses: For analytical and research use. Alternative Names: (1R,3S,5r,7r)-5-aminoadamantane-1,3-diol. CAS No. 1382839-19-1. Molecular formula: C10H17NO2. Mole weight: 183.25. Catalog: APB1382839191. | |
| Vildagliptin Impurity 6 | Vildagliptin Impurity 6. Uses: For analytical and research use. CAS No. 1846606-31-2. Molecular formula: C17H23N3O2. Mole weight: 301.39. Catalog: APB1846606312. | |
| Vildagliptin Impurity 60 | Vildagliptin Impurity 60. Uses: For analytical and research use. Molecular formula: C17H24ClN3O2. Mole weight: 337.85. Catalog: APB10058. | |
| Vildagliptin Impurity 61 | Vildagliptin Impurity 61. Uses: For analytical and research use. Molecular formula: C17H23N3O2. Mole weight: 301.39. Catalog: APB10059. | |
| Vildagliptin Impurity 62 | Vildagliptin Impurity 62. Uses: For analytical and research use. Molecular formula: C17H23N3O3. Mole weight: 317.39. Catalog: APB10057. | |
| Vildagliptin Impurity 63 | Vildagliptin Impurity 63. Uses: For analytical and research use. CAS No. 702-82-9. Molecular formula: C10H17NO. Mole weight: 167.25. Catalog: APB702829. | |
| Vildagliptin Impurity 64 | Vildagliptin Impurity 64. Uses: For analytical and research use. Molecular formula: C17H25N3O3. Mole weight: 319.41. Catalog: APB10061. | |
| Vildagliptin Impurity 65 | Vildagliptin Impurity 65. Uses: For analytical and research use. Molecular formula: C17H25N3O3. Mole weight: 319.41. Catalog: APB10060. | |
| Vildagliptin Impurity 66 | Vildagliptin Impurity 66. Uses: For analytical and research use. Alternative Names: (S)-1-(2-(((1r,3R,5R,7S)-3-hydroxyadamantan-1-yl)(nitroso)amino)acetyl)pyrrolidine-2-carboxylic acid. Molecular formula: C17H25N3O5. Mole weight: 351.40. Catalog: APB01845. | |
| Vildagliptin Impurity 66 | Vildagliptin Impurity 66. Uses: For analytical and research use. CAS No. 79108-51-3. Molecular formula: C5H9N3O2. Mole weight: 143.15. Catalog: APB79108513. | |
| Vildagliptin Impurity 7 | Vildagliptin Impurity 7. Uses: For analytical and research use. CAS No. 565452-98-4. Molecular formula: C7H9ClN2O. Mole weight: 172.61. Catalog: APB565452984. | |
| Vildagliptin Impurity 8 | Vildagliptin Impurity 8. Uses: For analytical and research use. CAS No. 741657-02-3. Molecular formula: C17H25N3O. Mole weight: 287.41. Catalog: APB741657023. | |
| Vildagliptin Impurity 9 | Vildagliptin Impurity 9. Uses: For analytical and research use. CAS No. 2246354-69-6. Molecular formula: C17H23N3O2. Mole weight: 301.38. Catalog: APB2246354696. | |
| Vildagliptin Impurity C | Vildagliptin Impurity C. Uses: For analytical and research use. Alternative Names: (S)-1-(2-(((1r,3R,5R,7S)-3-hydroxyadamantan-1-yl)amino)acetyl)pyrrolidine-2-carboxamide. CAS No. 565453-39-6. Molecular formula: C17H27N3O3. Mole weight: 321.41. Catalog: APB565453396. | |
| Vildagliptin Impurity D | Vildagliptin Impurity D. Uses: For analytical and research use. Alternative Names: 1789703-37-2(free base); 2-((1r,3s,5R,7S)-3-hydroxyadamantan-1-yl)-1-iminohexahydropyrrolo[1,2-a]pyrazin-4(1H)-one hydrochloride. Molecular formula: C17H25N3O2·HCl. Mole weight: 339.86. Catalog: APB01851. | |
| Vildagliptin Impurity E | Vildagliptin Impurity E. Uses: For analytical and research use. Alternative Names: 2-((1r,3s,5R,7S)-3-hydroxyadamantan-1-yl)hexahydropyrrolo[1,2-a]pyrazine-1,4-dione. CAS No. 1789703-36-1. Molecular formula: C17H24N2O3. Mole weight: 304.38. Catalog: APB1789703361. | |
| Vildagliptin Impurity ZA5 | Vildagliptin Impurity ZA5. Uses: For analytical and research use. Alternative Names: (1r,3R,5R,7S,Z)-N-(2-((S)-2-cyanopyrrolidin-1-yl)-2-oxoethylidene)-3-hydroxyadamantan-1-amine oxide. Molecular formula: C17H23N3O3. Mole weight: 317.38. Catalog: APB01849. | |
| Vildagliptin Oxidation Impurity | Vildagliptin Oxidation Impurity. Uses: For analytical and research use. Alternative Names: 2-((S)-2-cyanopyrrolidin-1-yl)-N-(3-hydroxyadamantan-1-yl)-2-oxoacetamide. Molecular formula: C17H23N3O3. Mole weight: 317.38. Catalog: APB01844. | |
| 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. |  |
| 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. Category: Signaling pathways. 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 is a non-brain-penetrant, selective norepinephrine transporter (NET) inhibitor (IC50= 0.26 μM) and 5-HT receptor modulator. Viloxazine antagonizes 5-HT2B receptors (Ki=4.2 μM) and agonizes 5-HT2C receptors (EC50= 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. Category: Signaling pathways. Alternative Names: Viloxazin; Emovit. CAS No. 46817-91-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W380450. | |
| Viltolarsen | Viltolarsen (NS-065/NCNP-01) is a phosphorodiamidate morpholino antisense oligonucleotide. Viltolarsen 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 has the potential for Duchenne muscular dystrophy (DMD) research[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: NS-065/NCNP-01. CAS No. 2055732-84-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-132586. | |
| 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-IN-1 | Vimentin-IN-1 is a FiVe1 derivative, an orally active and selective anticancer agent. FiVe1 binds type III intermediate filament protein vimentin (VIM), to induce hyperphosphorylation of Ser56, resulting selective disruption of mitosis and multinucleation in transformed VIM-expressing mesenchymal cancer cells. Vimentin-IN-1 shows better oral bioavailability and pharmacokinetic profiles than FiVe1[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2319587-80-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-151424. | |
| Vimirogant hydrochloride | Vimirogant (VTP-43742) hydrochloride is a potent, selective, and orally active RORγt inhibitor (Ki=3.5 nM; IC50=17 nM). Vimirogant hydrochloride exhibits >1000-fold selectivity versus the RORα and RORβ isotypes. Vimirogant hydrochloride inhibits Th17 differentiation and IL-17A secretion from mouse splenocytes (IC50=57 nM) without affecting Th1, Th2, or Treg cell differentiation. Vimirogant hydrochloride has the potential for autoimmune disorders research[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: VTP-43742 hydrochloride. CAS No. 1802678-42-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-103637A. | |
| Vimnerixin | Vimnerixin (AZD4721) is the potent and orally active antagonist of acidic CXC chemokine receptor 2 (CXCR2). Vimnerixin has the potential for the research of inflammatory disease[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AZD4721; RIST4721. CAS No. 1418112-77-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-145640. | |
| Vimseltinib | Vimseltinib (DCC-3014) is a c-FMS (CSF-IR) and c-Kit dual inhibitor extracted from patent WO2014145025A2, Compound Example 10, has IC50s of <0.01 μM and 0.1-1 μM, respectively[1]. Vimseltinib has certain oral bioavailability[2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: DCC-3014. CAS No. 1628606-05-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-136256. | |
| 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 | Vinaxanthone (SM-345431) is a potent and selective semaphorin3A, phospholipase C (PLC) and FabI inhibitor, with IC50s of 0.1-0.2 μM and 0.9 mM for semaphorin3A and FabI. Vinaxanthone inhibits the substrate (t-o-NAC thioester) and the cofactor (NADPH) with Kis of 3.1 μM and 1.0 μM, respectively. Vinaxanthone can be used to handle infections caused by multidrug-resistant pathogens[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: SM-345431. CAS No. 133293-89-7. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg. Product ID: HY-N9480. | |
| 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. Group: Biochemicals. Grades: Plant Grade. CAS No. 865-21-4. Pack Sizes: 20mg. US Biological Life Sciences. | Worldwide |
| 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-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. 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. Alternative Names: VLB, Vincaleukoblastine sulfate salt. CAS No. 143-67-9. Purity: >80.0%. Product ID: FFC-AR-143679. Molecular formula: C46H60N4O13S. Mole weight: 909.05. IUPAC Name: methyl (1R,9R,10S,11R,12R,19R)-11-acetyloxy-12-ethyl-4-[(13S,15R,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. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| 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: Scientific research. Category: Signaling pathways. Alternative Names: Vincaleukoblastine sulfate salt. CAS No. 143-67-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 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 |
| 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. Category: Signaling pathways. CAS No. 1617-90-9. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 500 mg; 1 g. Product ID: HY-B1021. | |
| Vincamine | Vincamine. Alternative Names: 14,15-Dihydro-14-hydroxyeburnamenine-14-carboxylic acid methyl ester. CAS No. 1617-90-9. Purity: >98.0%. Product ID: FFC-AR-1617909. Molecular formula: C21H26N2O3. Mole weight: 354.44. IUPAC Name: methyl (15S,17S,19S)-15-ethyl-17-hydroxy-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraene-17-carboxylate. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Vincetoxicoside B | Vincetoxicoside B. Group: Biochemicals. CAS No. 22007-72-3. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Vincosamide | Vincosamide, an alkaloid from Psychotria leiocarpa extract, inhibits the acetylcholinesterase (AChE) activity with anti-inflammatory activity[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 23141-27-7. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N1089. | |
| 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 | Vincristine (Leurocristine; NSC-67574; 22-Oxovincaleukoblastine) is a microtubule inhibitor that disrupts microtubule polymerization by binding to β-tubulin (with a Ki of 85 nM in bovine), arrests the cell cycle and induces apoptosis. Vincristine inhibits cell replication, tumor blood flow and the proliferation of various cancer cells, while triggering effects such as oxidative stress, inflammation, calcium overload, epithelial-mesenchymal transition and peripheral neuropathic pain. Vincristine upregulates the expression of various transporters and nuclear receptors, and enriches gastric cancer stem-like cells. Vincristine is used in research related to various tumors including acute lymphoblastic leukemia, lymphoma, melanoma, gastric cancer, solid tumors and sarcomas[1][2][3][4][5][6][7][8]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Leurocristine; NSC-67574; 22-Oxovincaleukoblastine. CAS No. 57-22-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0488A. | |
| 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 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 |
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