![5-{[1-({[(4S)-4,11-diethyl-4-hydroxy-3,14-dioxo-3,4,12,14-tetrahydro-1H-pyrano[3',4':6,7]indolizin…](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F292383-5-1-4s-411-diethyl-4-hydroxy-314-dioxo-341214-tetrahydro-1h-pyrano-3-4-67-indolizino-12-b-quinolin-9-yl-oxy-carbonyl-piperidin-4-yl-amino-pentanoic-acid.webp&w=3840&q=75)
CAS 181467-56-1: 5-{[1-({[(4S)-4,11-diethyl-4-hydroxy-3,14-dioxo-3,4,12,14-tetrahydro-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-9-yl]oxy}carbonyl)piperidin-4-yl]amino}pentanoic acid
Formula:C33H38N4O8
InChI:InChI=1/C33H38N4O8/c1-3-21-22-15-20(45-32(42)36-13-10-19(11-14-36)34-12-6-5-7-28(38)39)8-9-26(22)35-29-23(21)17-37-27(29)16-25-24(30(37)40)18-44-31(41)33(25,43)4-2/h8-9,15-16,19,34,43H,3-7,10-14,17-18H2,1-2H3,(H,38,39)/t33-/m0/s1
SMILES:CCc1c2cc(ccc2nc2c1Cn1c2cc2c(COC(=O)[C@@]2(CC)O)c1=O)OC(=O)N1CCC(CC1)NCCCCC(=O)O
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Found 5 products.
7-Ethyl-10-(4-N-aminopentanoic acid)-1-piperidino)carbonyloxycamptothecin
CAS:Controlled ProductApplications A major metabolite of Irinotecan. References Canal, P., et al.: J. Clin. Oncol., 14, 2688 (1996), Haaz, M., et al.: Cancer Res., 58, 468 (1998), Kehrer, D., et al.: Clin. Cancer Res., 6, 3451 (2000), Hanioka, N., et al.: Xenobiotica, 31, 687 (2001), Satoh, T., et al.: Drug Metab. Dispos., 30, 488 (2002),Formula:C33H38N4O8Color and Shape:Light YellowMolecular weight:618.67681-Piperidinecarboxylic acid, 4-[(4-carboxybutyl)amino]-, (4S)-4,11-diethyl-3,4,12,14-tetrahydro-4-hydroxy-3,14-dioxo-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-9-yl ester
CAS:Formula:C33H38N4O8Purity:99.59%Color and Shape:SolidMolecular weight:618.67687-Ethyl-10-(4-N-aminopentanoic acid)-1-piperidino)carbonyloxycamptothecin
CAS:7-Ethyl-10-(4-N-aminopentanoic acid)-1-piperidino)carbonyloxycamptothecin (APC) is a potent inhibitor of secretory phospholipase A2, which has been shown to be involved in the pathogenesis of several diseases. APC also inhibits the production of β-catenin and has been shown to inhibit tumor growth in vivo. Furthermore, APC has been shown to have anti-cancer properties against squamous carcinoma cells and may be an effective chemotherapeutic agent for this type of cancer. The mechanism of action for APC is not well understood, but it may involve inhibition of DNA polymerase α or δ, or binding to the ribosomal protein S6 kinase 1.Formula:C33H38N4O8Purity:Min. 95%Molecular weight:618.68 g/molRef: 3D-FE23086
Discontinued productRPR121056
CAS:RPR121056 is a Irinotecan metabolite, which is generated by CYP3A4. Irinotecan is an antineoplastic agent that inhibits topoisomerase type I.Formula:C33H38N4O8Purity:98%Color and Shape:SolidMolecular weight:618.68