Camptothecin

GPTKB entity

Statements (52)
Predicate Object
gptkbp:instanceOf natural product
alkaloid
topoisomerase inhibitor
gptkbp:ATCCode L01XX17
gptkbp:CASNumber 7689-03-4
gptkbp:category alkaloid
antineoplastic agent
lactone
quinoline
plant alkaloid
gptkbp:chemicalFormula C20H16N2O4
gptkbp:color yellow
gptkbp:discoveredBy gptkb:Mansukh_C._Wani
Monica M. Wall
Wallace H. Bollinger
gptkbp:discoveredIn 1966
gptkbp:foundIn gptkb:Camptotheca_acuminata
https://www.w3.org/2000/01/rdf-schema#label Camptothecin
gptkbp:IUPACName (S)-4-ethyl-4-hydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione
gptkbp:mechanismOfAction inhibits DNA topoisomerase I
gptkbp:meltingPoint 267–269 °C
gptkbp:molecularWeight 348.36 g/mol
gptkbp:notableDerivative gptkb:irinotecan
gptkb:topotecan
gptkbp:predecessor gptkb:SN-38
gptkb:irinotecan
gptkb:topotecan
BMS-184476
BMS-275183
S-9
TAS-103
belotecan
diflomotecan
exatecan
gimatecan
lurtotecan
namitecan
rubitecan
gptkbp:PubChem_CID gptkb:CHEMBL418
24360
gptkbp:sideEffect nausea
vomiting
diarrhea
myelosuppression
gptkbp:solubility poorly soluble in water
gptkbp:source gptkb:Camptotheca_acuminata
gptkbp:structureType pentacyclic quinoline alkaloid
gptkbp:toxicity high
gptkbp:UNII 8M8G366C5K
gptkbp:usedAs anticancer agent
gptkbp:bfsParent gptkb:Mansukh_C._Wani
gptkbp:bfsLayer 6