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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H16N2O4
Molecular Weight 348.352
Optical Activity ( + )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CAMPTOTHECIN

SMILES

CC[C@@]1(O)C(=O)OCC2=C1C=C3N(CC4=C3N=C5C=CC=CC5=C4)C2=O

InChI

InChIKey=VSJKWCGYPAHWDS-FQEVSTJZSA-N
InChI=1S/C20H16N2O4/c1-2-20(25)14-8-16-17-12(7-11-5-3-4-6-15(11)21-17)9-22(16)18(23)13(14)10-26-19(20)24/h3-8,25H,2,9-10H2,1H3/t20-/m0/s1

HIDE SMILES / InChI

Molecular Formula C20H16N2O4
Molecular Weight 348.352
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:45:30 UTC 2023
Edited
by admin
on Fri Dec 15 15:45:30 UTC 2023
Record UNII
XT3Z54Z28A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CAMPTOTHECIN
MI   WHO-DD  
Common Name English
Camptothecin [WHO-DD]
Common Name English
(+)-CAMPTOTHECIN
Common Name English
NSC-94600
Code English
CAMPTOTHECINE
Common Name English
1H-PYRANO(3',4':6,7)INDOLIZINO(1,2-B)QUINOLINE-3,14(4H,12H)-DIONE, 4-ETHYL-4-HYDROXY-, (4S)-
Systematic Name English
TOPOTECAN RELATED COMPOUND C [USP-RS]
Common Name English
TOPOTECAN RELATED COMPOUND C
USP-RS  
Common Name English
CAMPTOTHECIN [MI]
Common Name English
(4S)-4-ETHYL-4-HYDROXY-1H-PYRANO(3',4':6,7)INDOLIZINO(1,2-B)QUINOLINE-3,14(4H,12H)-DIONE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C1904
Created by admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
Code System Code Type Description
PUBCHEM
24360
Created by admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
PRIMARY
NCI_THESAURUS
C338
Created by admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
PRIMARY
EVMPD
SUB25812
Created by admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
PRIMARY
EPA CompTox
DTXSID0030956
Created by admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
PRIMARY
DRUG BANK
DB04690
Created by admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
PRIMARY
CHEBI
27656
Created by admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
PRIMARY
NSC
94600
Created by admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
PRIMARY
RS_ITEM_NUM
1672280
Created by admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
PRIMARY
MESH
D002166
Created by admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
PRIMARY
MERCK INDEX
m3007
Created by admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
PRIMARY Merck Index
SMS_ID
100000089959
Created by admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
PRIMARY
CAS
7689-03-4
Created by admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
PRIMARY
WIKIPEDIA
CAMPTOTHECIN
Created by admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
PRIMARY
FDA UNII
XT3Z54Z28A
Created by admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
DERIVATIVE -> PARENT
TRANSPORTER -> SUBSTRATE
Down-regulation of ABCB5αresulted in a gain of drug sensitivity to camptothecin 10-OH, 5-fluorouracil, and mitoxantrone.
CONJUGATE->CONJUGATE COMPONENT
DERIVATIVE -> PARENT
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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ACTIVE MOIETY