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Camptotheca acuminata
(NCBI:txid16922)
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Found in
xylem
(BTO:0001468).
Previous component: wood;
See:
PubMed
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Fusarium solani
(NCBI:txid169388)
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Endophytic fungus isolated from inner bark of Camptotheca acuminata
of strain
INFU/Ca/KF/3
See:
PubMed
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genotoxin
A role played by a chemical compound to induce direct or indirect DNA damage. Such damage can potentially lead to the formation of a malignant tumour, but DNA damage does not lead inevitably to the creation of cancerous cells.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
EC 5.99.1.2 (DNA topoisomerase) inhibitor
A topoisomerase inhibitor that inhibits the bacterial enzymes of the DNA topoisomerases, Type I class (EC 5.99.1.2) that catalyze ATP-independent breakage of one of the two strands of DNA, passage of the unbroken strand through the break, and rejoining of the broken strand. These bacterial enzymes reduce the topological stress in the DNA structure by relaxing negatively, but not positively, supercoiled DNA.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via alkaloid )
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antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
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(4S)- 4-ethyl-4-hydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione
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(+)-camptothecin
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DrugBank
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(+)-camptothecine
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DrugBank
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(S)-(+)-camptothecin
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DrugBank
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20(S)-camptothecine
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ChemIDplus
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21,22-Secocamptothecin-21-oic acid lactone
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ChemIDplus
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Camptothecin
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KEGG COMPOUND
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Camptothecine
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ChemIDplus
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CPT
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DrugBank
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D-camptothecin
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DrugBank
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6075662
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Reaxys Registry Number
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Reaxys
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6075662
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Beilstein Registry Number
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Beilstein
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7689-03-4
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CAS Registry Number
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ChemIDplus
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