
CAS 190710-79-3: N-DESMETHYL TOPOTECAN
Formula:C22H21N3O5
InChI:InChI=1/C22H21N3O5/c1-3-22(29)15-7-17-19-11(9-25(17)20(27)14(15)10-30-21(22)28)6-12-13(8-23-2)18(26)5-4-16(12)24-19/h4-7,23,26,29H,3,8-10H2,1-2H3/t22-/m0/s1
SMILES:CC[C@@]1(c2cc3c4c(cc5c(CNC)c(ccc5n4)O)Cn3c(=O)c2COC1=O)O
Synonyms:- (4S)-4-Ethyl-4,9-dihydroxy-10-[(methylamino)methyl]-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione
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Found 4 products.
1H-Pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione, 4-ethyl-4,9-dihydroxy-10-[(methylamino)methyl]-, (4S)-
CAS:Formula:C22H21N3O5Color and Shape:SolidMolecular weight:407.4192N-Desmethyl topotecan
CAS:Topotecan is a camptothecin derivative that inhibits topoisomerase I, which is an enzyme that maintains the integrity of DNA. It binds to DNA and prevents the separation of two strands, leading to cell death by inhibiting protein synthesis. Topotecan has been shown to be effective in the treatment of primary brain tumors and solid tumours, as well as urinary tract cancers. Side effects include drug interactions and concomitant use with other anticancer drugs. Topotecan has a carboxylate group at one end of its molecule that can bind to tissue samples such as liver tissue or urine samples from patients with bladder cancer. This allows for chromatographic separation, which can be used to measure drug levels in tissues or urine samples.Formula:C22H21N3O5Purity:Min. 95%Molecular weight:407.42 g/molRef: 3D-FD21332
Discontinued productN-Desmethyl Topotecan
CAS:Stability Unstable in Solution Applications A metabolite of Topotecan. References Herben, V., et al.: Anti-Cancer Drugs, 9, 411 (1998), Hsiang, Y., et al.: Cancer Res., 48, 1722 (1988), Hertzberg, R., et al.: J. Med. Chem., 32, 715 (1989), Beijnen, J., et al.: J. Pharm. Biomed. Anal., 8, 789 (1990),Formula:C22H21N3O5Color and Shape:NeatMolecular weight:407.42