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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H16N2O5
Molecular Weight 364.3514
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 10-HYDROXYCAMPTOTHECIN

SMILES

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

InChI

InChIKey=HAWSQZCWOQZXHI-FQEVSTJZSA-N
InChI=1S/C20H16N2O5/c1-2-20(26)14-7-16-17-11(5-10-6-12(23)3-4-15(10)21-17)8-22(16)18(24)13(14)9-27-19(20)25/h3-7,23,26H,2,8-9H2,1H3/t20-/m0/s1

HIDE SMILES / InChI

Molecular Formula C20H16N2O5
Molecular Weight 364.3514
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 19:22:01 UTC 2023
Edited
by admin
on Fri Dec 15 19:22:01 UTC 2023
Record UNII
9Z01632KRV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
10-HYDROXYCAMPTOTHECIN
Common Name English
(S)-10-HYDROXYCAMPTOTHECIN
Common Name English
10-HCPT
Common Name English
(+)-10-HYDROXYCAMPTOTHECIN
Common Name English
10-Hydroxycamptothecin [WHO-DD]
Common Name English
1H-PYRANO(3',4':6,7)INDOLIZINO(1,2-B)QUINOLINE-3,14(4H,12H)-DIONE, 4-ETHYL-4,9-DIHYDROXY-, (4S)-
Systematic Name English
HYDROXYCAMPTOTHECIN
Common Name English
NSC-107124
Code English
IRINOTECAN RELATED COMPOUND A [USP-RS]
Common Name English
IRINOTECAN RELATED COMPOUND A
USP-RS  
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID00941444
Created by admin on Fri Dec 15 19:22:01 UTC 2023 , Edited by admin on Fri Dec 15 19:22:01 UTC 2023
PRIMARY
SMS_ID
100000087613
Created by admin on Fri Dec 15 19:22:01 UTC 2023 , Edited by admin on Fri Dec 15 19:22:01 UTC 2023
PRIMARY
CAS
19685-09-7
Created by admin on Fri Dec 15 19:22:01 UTC 2023 , Edited by admin on Fri Dec 15 19:22:01 UTC 2023
PRIMARY
FDA UNII
9Z01632KRV
Created by admin on Fri Dec 15 19:22:01 UTC 2023 , Edited by admin on Fri Dec 15 19:22:01 UTC 2023
PRIMARY
RS_ITEM_NUM
1347610
Created by admin on Fri Dec 15 19:22:01 UTC 2023 , Edited by admin on Fri Dec 15 19:22:01 UTC 2023
PRIMARY
EVMPD
SUB23339
Created by admin on Fri Dec 15 19:22:01 UTC 2023 , Edited by admin on Fri Dec 15 19:22:01 UTC 2023
PRIMARY
PUBCHEM
97226
Created by admin on Fri Dec 15 19:22:01 UTC 2023 , Edited by admin on Fri Dec 15 19:22:01 UTC 2023
PRIMARY
NSC
107124
Created by admin on Fri Dec 15 19:22:01 UTC 2023 , Edited by admin on Fri Dec 15 19:22:01 UTC 2023
PRIMARY
DRUG BANK
DB12385
Created by admin on Fri Dec 15 19:22:01 UTC 2023 , Edited by admin on Fri Dec 15 19:22:01 UTC 2023
PRIMARY
Related Record Type Details
TRANSPORTER -> SUBSTRATE
Down-regulation of ABCB5αresulted in a gain of drug sensitivity to camptothecin 10-OH, 5-fluorouracil, and mitoxantrone.
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP