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> ChEBI Ontology
CHEBI:167548 - ophiobolin C
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ChEBI Name
ophiobolin C
ChEBI ID
CHEBI:167548
Definition
A sesterterpenoid that is ophiobolane with a hydroxy group at position 3, oxo group at positions 5, formyl group at position 7, and double bonds at positions 7-8 and 19-20.
Stars
This entity has been manually annotated by the ChEBI Team.
Submitter
Kristian Axelsen
Supplier Information
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Roles Classification
Biological Role
(s):
apoptosis inducer
Any substance that induces the process of apoptosis (programmed cell death) in multi-celled organisms.
Aspergillus metabolite
Any fungal metabolite produced during a metabolic reaction in the mould,
Aspergillus
.
chemokine receptor 5 antagonist
An antogonist that blocks chemokine receptor 5 (CCR5).
fungal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
Application
(s):
antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
nematicide
A substance used to destroy pests of the phylum
Nematoda
(roundworms).
Related Structures
ophiobolin C is a
Structural Derivative
of
ophiobolane
Mass : 346.63274
Formula : C25H46
sesterterpene
Definition : A C
25
terpene.
terpene
Definition : A hydrocarbon of biological origin having carbon skeleton formally derived from isoprene [CH
2
2
C(CH
3
)CH
2
CH
2
].
Graph View
Tree View
CHEBI:24431 chemical entity
CHEBI:23367 molecular entity
CHEBI:33579 main group molecular entity
CHEBI:33675 p-block molecular entity
CHEBI:33582 carbon group molecular entity
CHEBI:50860 organic molecular entity
CHEBI:33285 heteroorganic entity
CHEBI:36962 organochalcogen compound
CHEBI:36963 organooxygen compound
CHEBI:36586 carbonyl compound
CHEBI:17478 aldehyde
CHEBI:51718 α,β-unsaturated aldehyde
CHEBI:51688 enal
CHEBI:167548 ophiobolin C
CHEBI:17087 ketone
CHEBI:3992 cyclic ketone
CHEBI:167548 ophiobolin C
CHEBI:72695 organic molecule
CHEBI:36587 organic oxo compound
CHEBI:36586 carbonyl compound
CHEBI:17478 aldehyde
CHEBI:51718 α,β-unsaturated aldehyde
CHEBI:51688 enal
CHEBI:167548 ophiobolin C
CHEBI:17087 ketone
CHEBI:3992 cyclic ketone
CHEBI:167548 ophiobolin C
CHEBI:33832 organic cyclic compound
CHEBI:51958 organic polycyclic compound
CHEBI:51959 organic tricyclic compound
CHEBI:38032 carbotricyclic compound
CHEBI:167548 ophiobolin C
CHEBI:33598 carbocyclic compound
CHEBI:35294 carbopolycyclic compound
CHEBI:38032 carbotricyclic compound
CHEBI:167548 ophiobolin C
CHEBI:33245 organic fundamental parent
CHEBI:24632 hydrocarbon
CHEBI:35186 terpene
CHEBI:35192 sesterterpene
CHEBI:36552 ophiobolane
CHEBI:167548 ophiobolin C
CHEBI:35507 natural product fundamental parent
CHEBI:35662 terpenoid fundamental parent
CHEBI:36552 ophiobolane
CHEBI:167548 ophiobolin C
CHEBI:18059 lipid
CHEBI:24913 isoprenoid
CHEBI:35186 terpene
CHEBI:35192 sesterterpene
CHEBI:36552 ophiobolane
CHEBI:167548 ophiobolin C
CHEBI:26873 terpenoid
CHEBI:26660 sesterterpenoid
CHEBI:167548 ophiobolin C
CHEBI:24913 isoprenoid
CHEBI:35186 terpene
CHEBI:35192 sesterterpene
CHEBI:36552 ophiobolane
CHEBI:167548 ophiobolin C
CHEBI:26873 terpenoid
CHEBI:26660 sesterterpenoid
CHEBI:167548 ophiobolin C
CHEBI:33822 organic hydroxy compound
CHEBI:30879 alcohol
CHEBI:26878 tertiary alcohol
CHEBI:167548 ophiobolin C
CHEBI:78840 olefinic compound
CHEBI:51688 enal
CHEBI:167548 ophiobolin C
CHEBI:167548 ophiobolin C
CHEBI:33304 chalcogen molecular entity
CHEBI:36962 organochalcogen compound
CHEBI:36963 organooxygen compound
CHEBI:36586 carbonyl compound
CHEBI:17478 aldehyde
CHEBI:51718 α,β-unsaturated aldehyde
CHEBI:51688 enal
CHEBI:167548 ophiobolin C
CHEBI:17087 ketone
CHEBI:3992 cyclic ketone
CHEBI:167548 ophiobolin C
CHEBI:25806 oxygen molecular entity
CHEBI:36963 organooxygen compound
CHEBI:36586 carbonyl compound
CHEBI:17478 aldehyde
CHEBI:51718 α,β-unsaturated aldehyde
CHEBI:51688 enal
CHEBI:167548 ophiobolin C
CHEBI:17087 ketone
CHEBI:3992 cyclic ketone
CHEBI:167548 ophiobolin C
CHEBI:24651 hydroxides
CHEBI:33822 organic hydroxy compound
CHEBI:30879 alcohol
CHEBI:26878 tertiary alcohol
CHEBI:167548 ophiobolin C
CHEBI:33674 s-block molecular entity
CHEBI:33608 hydrogen molecular entity
CHEBI:33692 hydrides
CHEBI:37175 organic hydride
CHEBI:33245 organic fundamental parent
CHEBI:24632 hydrocarbon
CHEBI:35186 terpene
CHEBI:35192 sesterterpene
CHEBI:36552 ophiobolane
CHEBI:167548 ophiobolin C
CHEBI:35507 natural product fundamental parent
CHEBI:35662 terpenoid fundamental parent
CHEBI:36552 ophiobolane
CHEBI:167548 ophiobolin C
CHEBI:24651 hydroxides
CHEBI:33822 organic hydroxy compound
CHEBI:30879 alcohol
CHEBI:26878 tertiary alcohol
CHEBI:167548 ophiobolin C
CHEBI:36357 polyatomic entity
CHEBI:37577 heteroatomic molecular entity
CHEBI:33692 hydrides
CHEBI:37175 organic hydride
CHEBI:33245 organic fundamental parent
CHEBI:24632 hydrocarbon
CHEBI:35186 terpene
CHEBI:35192 sesterterpene
CHEBI:36552 ophiobolane
CHEBI:167548 ophiobolin C
CHEBI:35507 natural product fundamental parent
CHEBI:35662 terpenoid fundamental parent
CHEBI:36552 ophiobolane
CHEBI:167548 ophiobolin C
CHEBI:24651 hydroxides
CHEBI:33822 organic hydroxy compound
CHEBI:30879 alcohol
CHEBI:26878 tertiary alcohol
CHEBI:167548 ophiobolin C
CHEBI:25367 molecule
CHEBI:72695 organic molecule
CHEBI:36587 organic oxo compound
CHEBI:36586 carbonyl compound
CHEBI:17478 aldehyde
CHEBI:51718 α,β-unsaturated aldehyde
CHEBI:51688 enal
CHEBI:167548 ophiobolin C
CHEBI:17087 ketone
CHEBI:3992 cyclic ketone
CHEBI:167548 ophiobolin C
CHEBI:33832 organic cyclic compound
CHEBI:51958 organic polycyclic compound
CHEBI:51959 organic tricyclic compound
CHEBI:38032 carbotricyclic compound
CHEBI:167548 ophiobolin C
CHEBI:33598 carbocyclic compound
CHEBI:35294 carbopolycyclic compound
CHEBI:38032 carbotricyclic compound
CHEBI:167548 ophiobolin C
CHEBI:33595 cyclic compound
CHEBI:33832 organic cyclic compound
CHEBI:51958 organic polycyclic compound
CHEBI:51959 organic tricyclic compound
CHEBI:38032 carbotricyclic compound
CHEBI:167548 ophiobolin C
CHEBI:33598 carbocyclic compound
CHEBI:35294 carbopolycyclic compound
CHEBI:38032 carbotricyclic compound
CHEBI:167548 ophiobolin C
CHEBI:33635 polycyclic compound
CHEBI:51958 organic polycyclic compound
CHEBI:51959 organic tricyclic compound
CHEBI:38032 carbotricyclic compound
CHEBI:167548 ophiobolin C
CHEBI:35295 homopolycyclic compound
CHEBI:35294 carbopolycyclic compound
CHEBI:38032 carbotricyclic compound
CHEBI:167548 ophiobolin C
CHEBI:33597 homocyclic compound
CHEBI:33598 carbocyclic compound
CHEBI:35294 carbopolycyclic compound
CHEBI:38032 carbotricyclic compound
CHEBI:167548 ophiobolin C
CHEBI:35295 homopolycyclic compound
CHEBI:35294 carbopolycyclic compound
CHEBI:38032 carbotricyclic compound
CHEBI:167548 ophiobolin C
CHEBI:50906 role
CHEBI:24432 biological role
CHEBI:52206 biochemical role
CHEBI:25212 metabolite
CHEBI:75763 eukaryotic metabolite
CHEBI:76946 fungal metabolite
CHEBI:76956
Aspergillus
metabolite
CHEBI:167548 ophiobolin C
CHEBI:167548 ophiobolin C
CHEBI:68495 apoptosis inducer
CHEBI:167548 ophiobolin C
CHEBI:52210 pharmacological role
CHEBI:48706 antagonist
CHEBI:63673 chemokine receptor 5 antagonist
CHEBI:167548 ophiobolin C
CHEBI:33232 application
CHEBI:52217 pharmaceutical
CHEBI:23888 drug
CHEBI:35610 antineoplastic agent
CHEBI:167548 ophiobolin C
CHEBI:25944 pesticide
CHEBI:25491 nematicide
CHEBI:167548 ophiobolin C
Relationship Types
is a
has part
is conjugate base of
is conjugate acid of
is tautomer of
is enantiomer of
has functional parent
has parent hydride
is substituent group from
has role
Status
Checked
Unchecked