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irinotecan hydrochloride (anhydrous)

PropertiesImageOccurences in reactions
MNX_IDMNXM739798Image of MNXM739798
#reac
in my sandbox 0
in MNXref (generic)1
in models (compartimentalized) 0
formulaC33H39ClN4O6
charge0
mass622.25581
referencechebi:5971
InChIKeyGURKHSYORGJETM-WAQYZQTGSA-N
InChIInChI=1S/C33H38N4O6.ClH/c1-3-22-23-16-21(43-32(40)36-14-10-20(11-15-36)35-12-6-5-7-13-35)8-9-27(23)34-29-24(22)18-37-28(29)17-26-25(30(37)38)19-42-31(39)33(26,41)4-2;/h8-9,16-17,20,41H,3-7,10-15,18-19H2,1-2H3;1H/t33-;/m0./s1
SMILESCCc1c2c(nc3ccc(OC(=O)N4CCC(N5CCCCC5)CC4)cc13)-c1cc3c(c(=O)n1C2)COC(=O)[C@]3(O)CC.Cl
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 Deprecated MNXref IDs graph
Similar chemical compounds in external resources
IdentifierDescription
CHEBI:5971
chebi:5971 		irinotecan hydrochloride (anhydrous)
(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 [1,4'-bipiperidine]-1'-carboxylate hydrochloride
1-[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]piperidin-1-ium chloride
7-Ethyl-10-(4-(1-piperidino)-1-piperidino)carbonyloxy camptothecin hydrochloride
CPT 11
CPT-11
Camptothecin 11 hydrochloride
Irinotecan HCl
Irinotecan hydrochloride
U 101440E
irinotecan monohydrochloride
seed.compound:cpd08152
seedM:cpd08152 		CPT-11
CPT 11
Irinotecan hydrochloride
sabiork.compound:27732
sabiorkM:27732 		Irinotecan
CPT 11
CPT-11
Irinotecan hydrochloride
seedM:M_cpd08152 secondary/obsolete/fantasy identifier