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3β,12-dihydroxy-13-methyl-5,8,11,13-podocarpatetraene-7-one |
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CHEBI:65781 |
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3beta,12-dihydroxy-13-methyl-5,8,11,13-podocarpatetraene-7-one |
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A diterpenoid that is podocarpa-5,8,11,13-tetraen-7-one substituted by hydroxy groups at positions 3 and 12 and a methyl group at position 13 (the 3β stereoisomer). Isolated from Securinega suffruticosa, it exhibits antineoplastic activity. |
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![](images/goldenstar.gif) ![](images/goldenstar.gif)
This entity has been manually annotated by the ChEBI Team.
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Molfile
XML
SDF
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InChI=1S/C18H22O3/c1- 10- 7- 11- 12(8- 13(10) 19) 18(4) 6- 5- 16(21) 17(2,3) 15(18) 9- 14(11) 20/h7- 9,16,19,21H,5- 6H2,1- 4H3/t16- ,18+/m0/s1 |
XKTPGZPMUGPQQP-FUHWJXTLSA-N |
Cc1cc2C(=O)C=C3C(C)(C)[C@@H](O)CC[C@]3(C)c2cc1O |
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Securinega suffruticosa
(NCBI:txid544674)
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Found in
callus
(BTO:0001010).
See:
PubMed
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metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
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antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
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View more via ChEBI Ontology
Outgoing
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3β,12-dihydroxy-13-methyl-5,8,11,13-podocarpatetraene-7-one
(CHEBI:65781)
has role
antineoplastic agent
(CHEBI:35610)
3β,12-dihydroxy-13-methyl-5,8,11,13-podocarpatetraene-7-one
(CHEBI:65781)
has role
metabolite
(CHEBI:25212)
3β,12-dihydroxy-13-methyl-5,8,11,13-podocarpatetraene-7-one
(CHEBI:65781)
is a
aromatic ketone
(CHEBI:76224)
3β,12-dihydroxy-13-methyl-5,8,11,13-podocarpatetraene-7-one
(CHEBI:65781)
is a
carbotricyclic compound
(CHEBI:38032)
3β,12-dihydroxy-13-methyl-5,8,11,13-podocarpatetraene-7-one
(CHEBI:65781)
is a
diterpenoid
(CHEBI:23849)
3β,12-dihydroxy-13-methyl-5,8,11,13-podocarpatetraene-7-one
(CHEBI:65781)
is a
enone
(CHEBI:51689)
3β,12-dihydroxy-13-methyl-5,8,11,13-podocarpatetraene-7-one
(CHEBI:65781)
is a
phenols
(CHEBI:33853)
3β,12-dihydroxy-13-methyl-5,8,11,13-podocarpatetraene-7-one
(CHEBI:65781)
is a
secondary alcohol
(CHEBI:35681)
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(3β)-3,12-dihydroxy-13-methylpodocarpa-5,8,11,13-tetraen-7-one
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10278373
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Reaxys Registry Number
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Reaxys
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16327202
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PubMed citation
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Europe PMC
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