CAS 23360-92-1: Leurosine
Formula:C46H56N4O9
InChI:InChI=1S/C46H56N4O9/c1-8-42-16-12-18-50-20-17-44(37(42)50)30-21-31(34(55-5)22-33(30)48(4)38(44)46(54,41(53)57-7)39(42)58-26(3)51)45(40(52)56-6)23-27-24-49(25-43(9-2)36(27)59-43)19-15-29-28-13-10-11-14-32(28)47-35(29)45/h10-14,16,21-22,27,36-39,47,54H,8-9,15,17-20,23-25H2,1-7H3/t27-,36+,37-,38+,39+,42+,43-,44+,45-,46-/m0/s1
InChI key:InChIKey=LPGWZGMPDKDHEP-NVDFJPPOSA-N
SMILES:C(C)[C@@]12[C@]3([C@@]4([C@]([C@](C(OC)=O)(O)[C@@H]1OC(C)=O)(N(C)C=5C4=CC(=C(OC)C5)[C@]6(C(OC)=O)C7=C(C=8C(N7)=CC=CC8)CC[N@@]9C[C@](C6)([C@@]%10([C@@](CC)(O%10)C9)[H])[H])[H])CCN3CC=C2)[H]
Synonyms:- (2alpha,2'beta,3alpha,3'beta,4alpha,5beta,19beta)-O~3~',3'-cyclovincaleukoblastine
- (3′α,4′α)-4′-Deoxy-3′,4′-epoxyvincaleukoblastine
- 1H-Indolizino[8,1-cd]carbazole, vincaleukoblastine deriv.
- 2H-3,13-Methanooxireno[9,10]azacycloundecino[5,4-b]indole, vincaleukoblastine deriv.
- Amotin
- Amotin [Russian]
- Brn 0079636
- Hsdb 3506
- Leurosine
- NSC 528004
- Vincaleukoblastine, 4'-deoxy-3',4'-epoxy-, (3'alpha,4'alpha)-
- See more synonyms
Sort by
Found 6 products.
Vinleurosine
CAS:Vinleurosine can partially inhibit the energy dependent transport of alpha-aminoisobutyric acid in Ehrlich ascites tumor cells.Formula:C46H56N4O9Purity:98%Color and Shape:SolidMolecular weight:808.973Leurosine
CAS:Leurosine is a vinca alkaloid, which is a type of plant-derived compound with pharmacological significance. It is sourced from the periwinkle plant, Vinca minor, and is part of a larger class of naturally occurring compounds known for their antineoplastic properties. Its mode of action primarily involves the inhibition of microtubule formation in mitotic spindle fibers, thereby arresting the cell cycle at the metaphase stage. This mechanism disrupts cellular division, making leurosine effective in halting the proliferation of cancer cells. In terms of applications, leurosine is used in oncology research to explore potential treatments for various types of cancer. Its ability to disrupt cell division has made it a compound of interest in the study of tumor reduction and cancer management. Scientists leverage leurosine primarily in experimental settings to further understand its efficacy and potential integration into chemotherapeutic regimens. Further exploration into its action and broader applications continues to be a significant focus in cancer research, contributing to the development of advanced antineoplastic strategies.Formula:C46H56N4O9Purity:Min. 95%Molecular weight:809 g/mol
