CHEBI:66296 - rediocide G

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ChEBI Name rediocide G
ChEBI ID CHEBI:66296
Definition A diterpenoid of the class of daphnane-type terpenes. Isolated from Trigonostemon reidioides, it exhibits cytotoxicity against various cancer cell lines.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C46H54O13
Net Charge 0
Average Mass 814.91320
Monoisotopic Mass 814.35644
InChI InChI=1S/C46H54O13/c1-25-22-32-43(52)35(25)55-33(48)17-11-10-16-31(54-39(49)29-12-6-4-7-13-29)28-20-18-27(19-21-28)23-41(3,51)45(53)36-26(2)44(32)34(37-42(24-47,56-37)40(43)50)38(45)58-46(57-36,59-44)30-14-8-5-9-15-30/h4-17,25-28,31-32,34-38,40,47,50-53H,18-24H2,1-3H3/b16-10-,17-11+/t25-,26+,27?,28?,31-,32+,34-,35-,36-,37-,38+,40+,41+,42-,43+,44-,45-,46-/m0/s1
InChIKey VAEBJJRRTFBWLJ-JKUKCDQCSA-N
SMILES [H][C@@]12C[C@H](C)[C@@H]3OC(=O)\C=C\C=C/[C@H](OC(=O)c4ccccc4)C4CCC(CC4)C[C@@](C)(O)[C@]4(O)[C@H]5O[C@]6(O[C@@H]4[C@]([H])([C@@H]4O[C@]4(CO)[C@@H](O)[C@@]13O)[C@]2(O6)[C@@H]5C)c1ccccc1
Metabolite of Species Details
Trigonostemon reidioides (IPNI:358060-1) Found in root (BTO:0001188). See: PubMed
Roles Classification
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing rediocide G (CHEBI:66296) has role antineoplastic agent (CHEBI:35610)
rediocide G (CHEBI:66296) has role metabolite (CHEBI:25212)
rediocide G (CHEBI:66296) is a benzoate ester (CHEBI:36054)
rediocide G (CHEBI:66296) is a diterpenoid (CHEBI:23849)
rediocide G (CHEBI:66296) is a epoxide (CHEBI:32955)
rediocide G (CHEBI:66296) is a ortho ester (CHEBI:71989)
rediocide G (CHEBI:66296) is a terpene lactone (CHEBI:37668)
Registry Number Type Source
20035836 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
16204992 PubMed citation Europe PMC
Last Modified
22 April 2013