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| Product | Description | |
|---|---|---|
| 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. |  |
| Viltolarsen sodium | Viltolarsen sodium. |  |
| 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. | |
| Viminol | Viminol is an opioid analgesic that has both antitussive (cough suppressing) and analgesic (pain reducing) effects. Alternative Names: Dividol; 1-(o-Chlorobenzyl)-α-((di-sec-butylamino)methyl)pyrrole-2-methanol; 1-(α-(N-o-Chlorobenzyl)pyrryl)-2-di-sec-butylaminoethanol; 1H-Pyrrole-2-methanol, α-((bis(1-methylpropyl)amino)methyl)-1-((2-chlorophenyl)methyl)-; α-[[bis(1-methylpropyl)amino]methyl]-1-[(2-chlorophenyl)methyl]-1H-pyrrole-2-methanol; 1-[1-(2-Chlorobenzyl)-1H-pyrrol-2-yl]-2-(di-sec-butylamino)ethanol; Viminolo; Diviminol; Z 424. Grades: ≥95%. CAS No. 21363-18-8. Molecular formula: C21H31ClN2O. Mole weight: 362.94. | |
| 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 |
| 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. Alternative Names: 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 | Formula: Group: Biochemicals. Grades: Plant Grade. CAS No. 156009-80-2. Pack Sizes: 5mg, 10mg. US Biological Life Sciences. | Worldwide |
| 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. Alternative Names: 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. | |
| Vina-ginsenoside R8 | Formula: Group: Biochemicals. Grades: Plant Grade. CAS No. 156042-22-7. Pack Sizes: 5mg, 10mg. US Biological Life Sciences. | Worldwide |
| Vinaginsenoside R8 | Vinaginsenoside R8 has the side chain with a migrated double bond on introduction of OH at C-25. Most of the known saponins have been isolated from other Panax spp., though gypenoside XVII and hemsloside Ma3 were not previously isolated from Araliaceae but from Cucurbitaceous plants. Alternative Names: β-D-Glucopyranoside, (3β,12β,23E)-20-(β-D-glucopyranosyloxy)-12,25-dihydroxydammar-23-en-3-yl 2-O-β-D-glucopyranosyl-. Grades: > 98%. CAS No. 156042-22-7. Molecular formula: C48H82O19. Mole weight: 963.15. | |
| 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. Alternative Names: 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. Alternative Names: [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. Grades: >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 Impurity C | An impurity of Vinblastine. Vinblastine, isolated from Vinca rosea Linn., is an antitumor agent that is used for the treatment of kinds of cancers, including Hodgkin's lymphoma, non-small cell lung cancer, bladder cancer, brain cancer, melanoma, and testicular cancer. It binds tubulin and inhibits the assembly of microtubules. Alternative Names: N-Desmethyl Vinblastine; 1-Demethyl-vincaleukoblastine; N-Deformylleurocristine; N-Deformylvincristine. CAS No. 18172-50-4. Molecular formula: C45H56N4O9. Mole weight: 796.97. | |
| Vinblastine sulfate | Vinblastine sulfate, also called cellblastin, derived from C. roseus, as a microtubule disrupter and antineoplastic agent, it binds tubulin and disrupts microtubule assembly and proper formation of the mitotic spindle, which leads to the assembly of microtubules and causing M phase-specific cell cycle arrest. Uses: Anticancer. Alternative Names: cell pharm Brand of Vinblastine Sulfate; cellblastin; EG Labo Brand of Vinblastine Sulfate; Faulding Brand of Vinblastine Sulfate; Gastrozepin Brand of Vinblastine Sulfate; Gry Brand of Vinblastine Sulfate; Hexal Brand of Vinblastine Sulfate; Lemblastine; Lemery Brand of Vinblastine Sulfate; Lilly Brand of Vinblastine Sulfate; Sulfate, Vinblastine; Velban; Velbe; Vinblastin Hexal; Vinblastina Lilly; Vinblastine; Vinblastine Sulfate; Vinblastinsulfat-Gry; Vincaleukoblastine; Vinblastine sulfate; 143-67-9; C46H58N4O9H2SO4. Grades: >98%. CAS No. 143-67-9. Molecular formula: C46H58N4O9.H2SO4. Mole weight: 909.06. | |
| 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 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 | 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 (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, naturally occurs from herbal constituent of Catharanthus roseus (L.) G. Don.The contractile and relaxant actions of Vincamine and vinpocetine on the guinea pig trachealis may be due to the generation of prostaglandins and to changes in the memb. Alternative Names: (3aS,5S,11S)-3a-Ethyl-5-hydroxy-1,2,3,3a,4,5,10,11b-octahydro-11H-5a,11a-diaza-benzo[cd]fluoranthene-5-carboxylic acid methyl ester Cerebroxine Devincan Pervincamine Vincamine Vincapront Vincimax. Grades: >98%. CAS No. 1617-90-9. Molecular formula: C21H26N2O3. Mole weight: 354.44. | |
| 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 |
| Vincetoxicoside B | Vincetoxicoside B is a natural compound isolated from Polygonum paleaceum Wall. It exhibits antifungal activity. Uses: Pharmacological experiment, content determination, identification, active filter. Alternative Names: 3,5-Dihydroxy-2-(3,4-dihydroxyphenyl)-7-(α-L-rhamnopyranosyloxy)-4H-1-benzopyran-4-one; 7-(α-L-Rhamnopyranosyloxy)-2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-4H-1-benzopyran-4-one; 7-(α-L-Rhamnopyranosyloxy)-3,5-dihydroxy-2-(3,4-dihydroxyphenyl)-4H-1-benzopyran-4-one; Quercetin 7-rhamnoside; Vincetoxicoside B; Quercetin-7- O-α-L-rhaMnoside. Grades: >98%. CAS No. 22007-72-3. Molecular formula: C21H20O11. Mole weight: 448.38. | |
| Vinclozolin | Vinclozolin is a dicarboximide fungicide. Alternative Names: Ronilan; Vinclozoline; Ornalin. CAS No. 50471-44-8. Molecular formula: C12H9Cl2NO3. Mole weight: 286.11. | |
| 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 (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 | Vincristine. CAS No: 57-22-7 |  Sarchem Laboratories New Jersey NJ |
| Vincristine | Vincristine. Group: Biochemicals. Grades: Plant Grade. CAS No. 57-22-7. Pack Sizes: 20mg. US Biological Life Sciences. | Worldwide |
| 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 |
| 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 EP Impurity A | Vincristine EP Impurity A. Uses: For analytical and research use. Molecular formula: C46H56N4O11. Mole weight: 840.97. Catalog: APB10879. |  |
| Vincristine EP Impurity B | Vincristine EP Impurity B. Uses: For analytical and research use. CAS No. 68135-16-0. Molecular formula: C46H56N4O9. Mole weight: 808.97. Catalog: APB68135160. | |
| Vincristine EP Impurity C | Vincristine EP Impurity C. Uses: For analytical and research use. CAS No. 18172-50-4. Molecular formula: C45H56N4O9. Mole weight: 796.96. Catalog: APB18172504. | |
| Vincristine EP Impurity D | Vincristine EP Impurity D. Uses: For analytical and research use. CAS No. 3704-1-6. Molecular formula: C44H54N4O9. Mole weight: 782.94. Catalog: APB3704016. | |
| Vincristine EP Impurity E | Vincristine EP Impurity E. Uses: For analytical and research use. CAS No. 3352-69-0. Molecular formula: C44H56N4O8. Mole weight: 768.95. Catalog: APB3352690. | |
| Vincristine EP Impurity F (Vinorelbine EP Impurity E) | Vincristine EP Impurity F (Vinorelbine EP Impurity E). Uses: For analytical and research use. CAS No. 23360-92-1. Molecular formula: C46H56N4O9. Mole weight: 808.97. Catalog: APB23360921. | |
| Vincristine EP Impurity F (Vinorelbine EP Impurity E) Sulfate | Vincristine EP Impurity F (Vinorelbine EP Impurity E) Sulfate. Uses: For analytical and research use. CAS No. 54081-68-4. Molecular formula: C46H58N4O13S. Mole weight: 907.05. Catalog: APB54081684. | |
| Vincristine EP Impurity G | Vincristine EP Impurity G. Uses: For analytical and research use. CAS No. 54022-49-0. Molecular formula: C46H54N4O10. Mole weight: 822.96. Catalog: APB54022490. | |
| Vincristine EP Impurity H (vinblastine) | Vincristine EP Impurity H (vinblastine). Uses: For analytical and research use. CAS No. 865-21-4. Molecular formula: C46H58N4O9. Mole weight: 810.99. Catalog: APB865214. | |
| Vincristine EP Impurity H (vinblastine) Sulfate | Vincristine EP Impurity H (vinblastine) Sulfate. Uses: For analytical and research use. CAS No. 143-67-9. Molecular formula: C46H60N4O13S. Mole weight: 909.06. Catalog: APB143679. | |
| Vincristine Impurity 2 | Vincristine Impurity 2. Uses: For analytical and research use. CAS No. 910580-56-2. Molecular formula: C45H54N4O10. Mole weight: 810.95. Catalog: APB910580562. | |
| Vincristine Impurity 3 | Vincristine Impurity 3. Uses: For analytical and research use. Molecular formula: C90H110N8O20. Mole weight: 1623.91. Catalog: APB10880. | |
| Vincristine Impurity 4 | Vincristine Impurity 4. Uses: For analytical and research use. CAS No. 1246812-06-5. Molecular formula: C46H56N4O11. Mole weight: 840.97. Catalog: APB1246812065. | |
| Vincristine Impurity 5 | Vincristine Impurity 5. Uses: For analytical and research use. CAS No. 55855-88-4. Molecular formula: C44H56N4O7. Mole weight: 752.95. Catalog: APB55855884. | |
| Vincristine Impurity 6 | Vincristine Impurity 6. Uses: For analytical and research use. Molecular formula: C46H56N4O11. Mole weight: 840.97. Catalog: APB10913. | |
| 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 (Leurocristine; NSC-67574; 22-Oxovincaleukoblastine) sulfate 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 sulfate 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 sulfate upregulates the expression of various transporters and nuclear receptors, and enriches gastric cancer stem-like cells. Vincristine sulfate 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 sulfate; NSC-67574 sulfate; 22-Oxovincaleukoblastine sulfate. CAS No. 2068-78-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-N0488. | |
| Vincristine sulfate | Vincristine sulfate. Alternative Names: 22-Oxovincaleukoblastine sulfate. CAS No. 2068-78-2. Purity: >95.0%. Product ID: FFC-AR-2068782. Molecular formula: C46H58N4O14S. Mole weight: 923.04. IUPAC Name: 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]-8-formyl-10-hydroxy-5-methoxy-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. | |
| Vincristine Sulfate | Vincristine is an inhibitor of polymerization of microtubules by binding to tubulin with IC50 of 32 μM. Uses: Anti-cancer. Alternative Names: Leurocristine. Grades: >98%. CAS No. 2068-78-2. Molecular formula: C46H58N4O14S. Mole weight: 923.04. | |
| 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 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. |  |
| 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 |
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