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(19S)-10,19-diethyl-19-hydroxy-14,18-dioxo-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4,6,8,10,15(20)-heptaen-7-yl 4-aminopiperidine-1-carboxylate
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ChemBase ID:
168410
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Molecular Formular:
C28H30N4O6
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Molecular Mass:
518.561
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Monoisotopic Mass:
518.2165347
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SMILES and InChIs
SMILES:
NC1CCN(CC1)C(=O)Oc1ccc2c(c1)c(c1c(n2)c2n(C1)c(=O)c1c(c2)[C@](C(=O)OC1)(CC)O)CC
Canonical SMILES:
CC[C@@]1(O)C(=O)OCc2c1cc1c3nc4ccc(cc4c(c3Cn1c2=O)CC)OC(=O)N1CCC(CC1)N
InChI:
InChI=1S/C28H30N4O6/c1-3-17-18-11-16(38-27(35)31-9-7-15(29)8-10-31)5-6-22(18)30-24-19(17)13-32-23(24)12-21-20(25(32)33)14-37-26(34)28(21,36)4-2/h5-6,11-12,15,36H,3-4,7-10,13-14,29H2,1-2H3/t28-/m0/s1
InChIKey:
APWFTHDYKJHNEV-NDEPHWFRSA-N
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Cite this record
CBID:168410 http://www.chembase.cn/molecule-168410.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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(19S)-10,19-diethyl-19-hydroxy-14,18-dioxo-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4,6,8,10,15(20)-heptaen-7-yl 4-aminopiperidine-1-carboxylate
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IUPAC Traditional name
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(19S)-10,19-diethyl-19-hydroxy-14,18-dioxo-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4,6,8,10,15(20)-heptaen-7-yl 4-aminopiperidine-1-carboxylate
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Synonyms
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4-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 1-Piperidinecarboxylic Acid Ester
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RPR 132595A
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NPC (metabolite)
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7-Ethyl-10-(4-amino-1-piperidino)carbonyloxycamptothecin
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CAS Number
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PubChem SID
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PubChem CID
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
Data Source
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Data ID
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Price
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TRC
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CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
Acid pKa
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11.716885
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H Acceptors
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6
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H Donor
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2
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LogD (pH = 5.5)
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-1.9158231
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LogD (pH = 7.4)
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-1.3383697
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Log P
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0.99369514
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Molar Refractivity
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139.119 cm3
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Polarizability
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54.53705 Å3
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Polar Surface Area
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135.29 Å2
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Rotatable Bonds
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4
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Lipinski's Rule of Five
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false
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DETAILS
DETAILS
TRC
REFERENCES
REFERENCES
From Suppliers
Google Scholar
PubMed
Google Books
- • Canal, P., et al.: J. Clin. Oncol., 14, 2688 (1996)
- • Haaz, M., et al.: Cancer Res., 58, 468 (1996)
- • Kehrer, D., et al.: Clin. Cancer Res., 6, 3451 (1996)
- • Hanioka, N., et al.: Xenobiotica, 31, 687 (1996)
- • Satoh, T., et al.: Drug Metab. Dispos., 30, 488 (2
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PATENTS
PATENTS
PubChem Patent
Google Patent