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| Product | Description | |
|---|---|---|
| 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 | 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 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 | 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 |
| 4-Desacetyl Vinblastine Methosulfate | A pro-drug of Vinblastine. Group: Biochemicals. Alternative Names: O4-Deacetyl-vincaleukoblastine Methosulfate; 4-Deacetylvinblastine Methosulfate; Deacetylvinblastine Methosulfate. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Anhydro Vinblastine-d3 Disulfate Salt | Anhydrovinblastine. Group: Biochemicals. Alternative Names: 3', 4'-Dide hydro-4'-deoxyvincaleukoblastin e-d3 Disulfate Salt; (+)-Anhydrovinblastine-d3 Disulfate Salt; 3',4'-Anhydrovinblastine-d3 Disulfate Salt; 3',4'-Dehydroisoleurosine-d3 Disulfate Salt; 3',4'-Dehydrovinblastine-d3 Disulfate Salt; 3',4'-Didehydroisoleurosine-d3 Disulfate Salt; An hydrovincaleukoblas tine-d3 Disulfate Salt; F 81097-d3 Disulfate Salt. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Anhydro Vinblastine Disulfate Salt | Anhydrovinblastine. Group: Biochemicals. Alternative Names: 3', 4'-Dide hydro-4'-deoxyvincaleukoblastin e Disulfate Salt; (+)-Anhydrovinblastine Disulfate Salt; 3',4'-Anhydrovinblastine Disulfate Salt; 3',4'-Dehydroisoleurosine Disulfate Salt; 3',4'-Dehydrovinblastine Disulfate Salt; 3',4'-Didehydroisoleurosine Disulfate Salt; An hydrovincaleukoblas tine Disulfate Salt; F 81097 Disulfate Salt. Grades: Highly Purified. CAS No. 81165-17-5. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| N-Desmethyl vinblastine | N-Desmethyl vinblastine. Group: Biochemicals. Alternative Names: 1-Demethyl-vincaleukoblastine; N-Deformylleurocristine; N-Deformylvincristine. Grades: Highly Purified. CAS No. 18172-50-4. Pack Sizes: 1mg, 2mg, 5mg, 10mg. Molecular Formula: C45H56N4O9. US Biological Life Sciences. | Worldwide |
| N-Desmethyl Vinblastine | N-Desmethyl Vinblastine. Uses: For analytical and research use. Group: Impurity standards. CAS No. 18172-50-4. Molecular formula: C45H56N4O9. Mole weight: 796.95. Catalog: APS18172504. SMILES: CC[C@]1(O)C[C@@H]2CN(CCc3c([nH]c4ccccc34)[C@@](C2)(C(=O)OC)c5cc6c(N[C@H]7[C@](O)([C@H](OC(=O)C)[C@]8(CC)C=CCN9CC[C@]67[C@H]89)C(=O)OC)cc5OC)C1. Format: Neat. | |
| N-Desmethyl Vinblastine, protocol with the exact weight | N-Desmethyl Vinblastine, protocol with the exact weight. Uses: For analytical and research use. Group: Impurity standards. CAS No. 18172-50-4. Pack Sizes: 10MG. Molecular formula: C45H56N4O9. Mole weight: 796.95. Catalog: APS18172504A. SMILES: CC[C@]1(O)C[C@@H]2CN(CCc3c([nH]c4ccccc34)[C@@](C2)(C(=O)OC)c5cc6c(N[C@H]7[C@](O)([C@H](OC(=O)C)[C@]8(CC)C=CCN9CC[C@]67[C@H]89)C(=O)OC)cc5OC)C1. Format: Neat. | |
| 19'-Oxovincaleukoblastine-d3 Sulfate | 19'-Oxovincaleukoblastine-d3 Sulfate is the labeled analogue of 19'-Oxovincaleukoblastine Sulfate (O867210), a metabolite of Vinblastine Sulfate (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: C46H53D3N4O10. x(H2O4S), Molecular Weight: 827.989808. US Biological Life Sciences. | Worldwide |
| 19'-Oxovincaleukoblastine Sulfate | 19'-Oxovincaleukoblastine Sulfate is a metabolite of Vinblastine Sulfate (V314000), an antitumor alkaloid isolated from periwinkle, Vinca rosea Linn., Apocynaceae; inhibits microtubule assembly. An antineoplastic. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg, 50mg. Molecular Formula: C46H56N4O10. x(H2O4S), Molecular Weight: 824.969807999999. US Biological Life Sciences. | Worldwide |
| 3',4'-Anhydro Vincristine Ditartrate | A derivative of Vinblastine, an antitumor alkaloid. Group: Biochemicals. Alternative Names: 3',4'-Didehydro-4'-deoxy-22-oxo-vincaleukoblastine Ditartrate; 3',4'-Anhydroleurocristine Ditartrate; 3',4'-Anhydrovincristine Ditartrate; Anhydroleurocristine Ditartrate; Anhydrovincristine Ditartrate. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| ALB-109564 | ALB 109564(a) is a semi-synthetic derivative of the vinka alkaloid vinblastine with potential antineoplastic activity. Tubulin inhibitor ALB 109564(a) binds to tubulin monomers and inhibits microtubule formation, resulting in disruption of mitotic spindle assembly and arrest of tumor cells in the G2/M phase of the cell cycle. Synonyms: ALB-109564; ALB 109564; ALB109564; ALB 109564(a); Vincaleukoblastine, 12'-(methylthio)-, hydrochloride (1:2). CAS No. 854756-74-4. Molecular formula: C47H60N4O9S. Mole weight: 857.07. | |
| Ansamitocin P3 | Ansamitocin P-3 is a metabolite of Ansamitocin which is a new maytansinoid antitumor antibiotic. Fungal metabolite with antineoplastic, antimitotic activity. Binds to tubulin and inhibits vinblastine-induced spiral formation. Group: Biochemicals. Alternative Names: 3-O-De[2-(acetylmethylamino)-1-oxopropyl]-3-O-(1-oxobutyl)-maytansine; 4, 24-Dioxa-9, 22-diazatetracyclo[19. 3. 1. 110, 14. 03, 5]hexacosane, maytansine deriv.; Ansamitocin P 3; Antibiotic C 15003P3; Maytansinol Butyrate. Grades: Purified. CAS No. 66547-09-9. Pack Sizes: 25mg, 50mg, 100mg, 250mg. Molecular Formula: C32H43CIN2O9, Molecular Weight: 635.14. US Biological Life Sciences. | Worldwide |
| Catharanthine-d3 | Isotope labeled precursor of Vinblastine-type alkaloids. Group: Biochemicals. Alternative Names: (2α,5 β,6α,18 β)-3,4-Didehydro-ibogamine-18-carboxylic Acid Methyl-d3 Ester; (+)-3,4-Didehydrocoronaridine-d3; (+)-Catharanthine-d3; Catharanthin-d3. Grades: Highly Purified. CAS No. 133146-02-8. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Catharanthine-[d3] | Catharanthine-[d3] is the labelled analogue of Catharanthine, which inhibits nicotinic receptor-mediated diaphragm contractions. Uses: Isotope labelled precursor of vinblastine-type alkaloids. Synonyms: Catharanthine D3; (2α,5β,6α,18β)-3,4-Didehydro-ibogamine-18-carboxylic Acid Methyl-d3 Ester; (+)-3,4-Didehydrocoronaridine-d3; (+)-Catharanthine-d3; Catharanthin-d3. Grade: ≥98%. CAS No. 133146-02-8. Molecular formula: C21H21D3N2O2. Mole weight: 339.45. | |
| Catharanthine Tartrate | Precursor of Vinblastine-type alkaloids. Group: Biochemicals. Alternative Names: (2α,5 β,6α,18 β)-3,4-Didehydro-ibogamine-18-carboxylic Acid Methyl Ester Tartrate ; (+)-3,4-Didehydrocoronaridine Tartrate; (+)-Catharanthine Tartrate; Catharanthin Tartrate. Grades: Highly Purified. CAS No. 4168-17-6. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Cevipabulin | Cevipabulin (TTI-237) is an oral, microtubule-active antitumor compound and inhibits the binding of [ 3 H] vinblastine to tubulin, with an IC 50 of 18-40 nM for cytotoxicity in human tumor cell line [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TTI-237. CAS No. 849550-05-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14949. | |
| Cevipabulin fumarate | Cevipabulin fumarate is a microtubule-active antitumor compound and inhibits the binding of [3H] vinblastine to tubulin (IC50: 18-40 nM in the human tumor cell line). Synonyms: TTI-237 fumarate. Grade: 99%. CAS No. 849550-67-0. Molecular formula: C22H22ClF5N6O5. Mole weight: 580.89. | |
| cis-Diamineplatinum(II) dichloride | cis-Diamineplatinum(II) dichloride. Uses: Cisplatin is a cytostatic agent and it is used to treat various cancer types, including cancer of ovary, testis, lung, head, neck, bladder, neuroblastoma, and nephroblastoma, and hodgkin's disease and non-hodgkin lymphoma.cddp, also referred to as cisplatinum or cisplatin, is a yellow powder and has found widespread use a chemotherapeutic agent.cisplatin, combined with bleomycin and vinblastine or etoposide, produces cures in most patients with metastatic testicular cancer or germ cell cancer of the ovary. cisplatin also shows some activity against carcinomas of the head and neck, bladder, cervix, prostate, and lung. Group: Salt. Alternative Names: cis-Dichlorodiammine platinum(II). CAS No. 15663-27-1. Molecular formula: 300.05. Mole weight: Pt(NH3)2Cl2. Pt ≥65.0%. |  |
| DM4-SPDB | DM4 with a reactive linker SPDB, which can react with antibody to make antibody drug conjugate. DM4 can bind to tubulin at or near the vinblastine-binding site. Synonyms: (1S,2R,3S,5S,6S,16E,18E,20R,21S)-11-Chloro-21-hydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8,23-dioxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.110,14.03,5]hexacosa-10(26),11,13,16,18-pentaen-6-yl (2 S)-2-{[4-({4-[(2,5-dioxo-1-pyrrolidinyl)oxy]-4-oxobutyl}disulfanyl)-4-methylpentanoyl](methyl)amino}propanoate (non-preferred name); DM4 SPDB. Grade: ≥98%. CAS No. 1626359-62-3. Molecular formula: C46H63ClN4O14S2. Mole weight: 995.59. | |
| DM4-SPDP | DM4 with a reactive linker SPDP, which can react with antibody to make antibody drug conjugate. DM4 can bind to tubulin at or near the vinblastine-binding site. Synonyms: Maytansinoid DM4- succinimidyl 3-(2-pyridyldithio)propionate; DM4 SPDP. Grade: ≥98%. CAS No. 2245698-48-8. Molecular formula: C45H61ClN4O14S2. Mole weight: 981.57. | |
| Licochalcone A | Licochalcone A is a chalconoid, a type of natural phenols. It can be isolated from root of Glycyrrhiza glabra (liquorice) or Glycyrrhiza inflata. It is a potent membrane-active agent that transforms normal erythrocytes into echinocytes. It exhibits potent antimalarial activity and might be developed into a new antimalarial drug. It had anti-tumor activity in all cell lines tested and enhanced the effect of paclitaxel and vinblastine chemotherapy. Synonyms: 4,4'-Dihydroxy-3-α,α-dimethylallyl-6-methoxychalcone; 7-Dimethoxycoumarin; 3-Dimethylallyl-4,4'-dihydroxy-6-methoxychalcone; (E)-3-[5-(1,1-Dimethyl-2-propenyl)-4-hydroxy-2-methoxyphenyl]-1-(4-hydroxyphenyl)-2-propen-1-one; (2E)-3-[5-(1,1-Dimethyl-2-propen-1-yl)-4-hydroxy-2-methoxyphenyl]-1-(4-hydroxyphenyl)-2-propen-1-one; 2-Propen-1-one, 3-[5-(1,1-dimethyl-2-propenyl)-4-hydroxy-2-methoxyphenyl]-1-(4-hydroxyphenyl)-, (2E)-; 2-Propen-1-one, 3-[5-(1,1-dimethyl-2-propenyl)-4-hydroxy-2-methoxyphenyl]-1-(4-hydroxyphenyl)-, (E)-. Grade: >98%. CAS No. 58749-22-7. Molecular formula: C21H22O4. Mole weight: 338.40. | |
| ODORINE | Odorine isolated from the herbs of Aglaia odorata. It inhibits the growth of the vinblastine-resistant KB cells by enhancing the anticancer activity of vinblastine. Uses: Anti-carcinogenic effect. Synonyms: (S)-2-Methyl-N-[(2R)-1-[(E)-1-oxo-3-phenyl-2-propenyl]pyrrolidin-2-yl]butanamide. Grade: 0.95. CAS No. 72755-20-5. Molecular formula: C18H24N2O2. Mole weight: 300.4. | |
| Phomopsin A | It is an acidic 13-membered cyclic hexapeptide-like metabolite with three unusual amino acids. It is a potent mycotoxin produced by the fungus, phomopsis leptostromiformis. It is an important bioprobe for understanding cellular structural proteins. It selectively binds to the dimeric tubulin at the overlap of vinblastine and maytansine, inhibits the formation of the microtubule spindle to block cell division. Synonyms: 2-Oxa-5,8-diazabicyclo[10.3.1]hexadecane, cyclic peptide deriv.; (2E)-(βS)-3-chloro-β,5-dihydroxy-N-methyl-L-tyrosyl-3,4-didehydro-L-valyl-3-hydroxy-L-isoleucyl-3,4-didehydro-L-prolyl-(2E)-2,3-didehydroisoleucyl-2,3-didehydro-aspartic acid, cyclic (15→3)-ether; NSC 381839; PMSA; Phomopsin. Grade: >98% by HPLC. CAS No. 64925-80-0. Molecular formula: C36H45ClN6O12. Mole weight: 789.23. | |
| Phomopsin A | Phomopsin A is an acidic 13-membered cyclic hexapeptide-like metabolite with three unusual amino acids linked in an "ansa" macrocycle with a three amino acid "tail", terminating in a dicarboxylic acid. Phomopsin A is a potent mycotoxin produced by the fungus Phomopsis leptostromiformis and is the causative agent of lupinosis in livestock fed infected lupins. Phomopsin A is an important bioprobe for understanding cellular structural proteins. It acts by selectively binding to dimeric tubulin, inhibiting the formation of the microtubule spindle to block cell division. Phomopsin A binds to tubulin at a site overlapping that of vinblastine and maytansine. Uniquely, phomopsin A protects tubulin from decay. Group: Biochemicals. Alternative Names: 2-Oxa-5, 8-diazabicyclo[10. 3. 1]hexadecane, cyclic peptide deriv.; 3-Chloro-erythro- β,5-dihydroxy-N-methyl-L-tyrosyl-3,4-didehydro-L-valyl-3-hydroxy-L-isoleucyl-3,4-didehydro-L-prolyl-(E)-2,3-didehydroisoleucyl-(E)-2,3-didehydroaspartic acid cyclic (15?3)-ether; NSC 381839. Grades: Highly Purified. CAS No. 64925-80-0. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Secologanin | Secologanin, a secoiridoid glucoside, is a pivotal terpenoid intermediate in the biosynthesis of biologically active monoterpenoid indole alkaloids such as reserpine, ajmaline, and vinblastine. Secologanin synthase (cytochrome P450 isoform CYP72A1) catalyzes the oxidative cleavage of loganin into Secologanin [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 19351-63-4. Pack Sizes: 1 mg. Product ID: HY-125598. | |
| sulfo-SPDB-DM4 | DM4 with a reactive linker sulfo-SPDB, which can react with antibody to make antibody drug conjugate. DM4 can bind to tubulin at or near the vinblastine-binding site. Synonyms: Maytansinoid DM4- succinimidyl 4-(N-maleimidomethyl)cyclohexane-3-sulfo-carboxylate. Grade: ≥98%. CAS No. 1626359-59-8. Molecular formula: C46H63ClN4O17S3. Mole weight: 1075.66. | |
| Taltobulin | Taltobulin, also known as HTI-286 and SPA-110, is a fully synthetic analog of the natural tripeptide hemiasterlin, inhibits tubulin polymerization and circumvents transport-based resistance to taxanes. HTI-286 was a potent inhibitor of proliferation (mean IC50 = 2.5 ± 2.1 nm in 18 human tumor cell lines) and had substantially less interaction with multidrug resistance protein (P-glycoprotein) than currently used antimicrotubule agents, including paclitaxel, docetaxel, vinorelbine, or vinblastine. Uses: Adcs cytotoxin. Synonyms: HTI-286; HTI286; HTI 286; SPA-110; SPA-110; SPA110; SPA 110; N,beta,beta-Trimethyl-L-phenylalanyl-N-[(1S,2E)-3-carboxy-1-(1-methylethyl)-2-butenyl]-N,3-dimethyl-L-valinamide. Grade: ≥98.0% (HPLC). CAS No. 228266-40-8. Molecular formula: C27H43N3O4. Mole weight: 473.32. | |
| Tanshinone IIB | Tanshinone IIB isolated from the roots of Salvia miltiorrhiza. It inhibits the uptake of digoxin and vinblastine in membrane vesicles containing PgP or MRP1, moderately stimulates PgP ATPase activity. Uses: Neuro-protective; antioxidant. Synonyms: (S)-6-(HydroxyMethyl)-1,6-diMethyl-6,7,8,9-tetrahydrophenanthro[1,2-b]furan-10,11-dione. Grade: 0.97. CAS No. 17397-93-2. Molecular formula: C19H18O4. Mole weight: 310.4. | |
| Vindesine Sulfate Salt (LY-099094, Eldisine, Fildesin) | Synthetic derivative of the dimeric Catharanthus alkaloid vinblastine. Antineoplastic. Group: Biochemicals. Alternative Names: LY-099094; Eldisine; Fildesin. Grades: Highly Purified. CAS No. 59917-39-4. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
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