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(Q75052923)
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Cyclonerodiol
bioactive natural product
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Statements
instance of
type of chemical entity
0 references
subclass of
3-(2-Hydroxy-6-methylhept-5-en-2-yl)-1,2-dimethylcyclopentan-1-ol
1 reference
based on heuristic
inferred from SMILES
mass
240.208930136
dalton
1 reference
based on heuristic
inferred from SMILES
stereoisomer of
(1R,2S,3R)-3-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-1,2-dimethylcyclopentan-1-ol
2 references
based on heuristic
inferred from InChIKey
based on heuristic
inferred from InChI
(1R,2S,3S)-3-[(2R)-2-hydroxy-6-methylhept-5-en-2-yl]-1,2-dimethylcyclopentan-1-ol
1 reference
based on heuristic
inferred from InChI
chemical formula
C₁₅H₂₈O₂
0 references
canonical SMILES
OC1(C)CCC(C1C)C(O)(C)CCC=C(C)C
0 references
isomeric SMILES
CC(C)=CCC[C@@](C)(O)[C@@H]1CC[C@@](C)(O)[C@H]1C
0 references
found in taxon
Trichoderma harzianum
1 reference
stated in
Antifungal metabolites from Trichoderma harzianum
Botrytis
3 references
stated in
Bromomyrothenone B and botrytinone, cyclopentenone derivatives from a marine isolate of the fungus botrytis.
stated in
Bromomyrothenone B and botrytinone, cyclopentenone derivatives from a marine isolate of the fungus botrytis.
stated in
Bromomyrothenone B and Botrytinone, Cyclopentenone Derivatives from a Marine Isolate of the Fungus Botrytis
Myrothecium
1 reference
stated in
Myrothenones A and B, cyclopentenone derivatives with tyrosinase inhibitory activity from the marine-derived fungus Myrothecium sp.
Fusarium fujikuroi
5 references
stated in
Characterization of cyclonerodiol isolated from corn infested byfusarium moniliforme sheld.: One- and two-dimensional1H and13C NMR study
stated in
Fusarin C and 8Z-fusarin C from Gibberella fujikuroi
stated in
Characterization of cyclonerodiol isolated from corn infested byfusarium moniliforme sheld.: One- and two-dimensional1H and13C NMR study
stated in
Conversion of farnesyl and nerolidyl pyrophosphate to cyclonerodiol by a cell-free extract from Gibberella fujikuroi
stated in
The microbiological production of analogues of mould metabolites. Part 2. Production of 9α-fluorogibberellin A4, 9α-fluorogibberellin A14, and other fluoroterpenoids by Gibberella fujikuroi
Trichoderma koningii
2 references
stated in
Studies on Metabolites of Mycoparasitic Fungi. III. New Sesquiterpene Alcohol from Trichoderma koningii.
stated in
Cyclonerodiol from a novel source, Trichoderma koningii: Plant growth regulatory activity.
Trichoderma polysporum
1 reference
stated in
Fungal metabolites. II. Structural elucidation of minor metabolites, valinotricin, cyclonerodiol oxide, and epicyclonerodiol oxide, from Trichoderma polysporum.
Gibberella fujikuroi
1 reference
stated in
Fusarin C and 8Z-fusarin C from Gibberella fujikuroi
Identifiers
InChI
InChI=1S/C15H28O2/c1-11(2)7-6-9-15(5,17)13-8-10-14(4,16)12(13)3/h7,12-13,16-17H,6,8-10H2,1-5H3/t12-,13+,14+,15+/m0/s1
0 references
InChIKey
ZBJPVPFEDGYYBD-GBJTYRQASA-N
0 references
CAS Registry Number
28834-06-2
0 references
PubChem CID
168840
2 references
stated in
PubChem
PubChem CID
168840
language of work or name
English
matched by identifier from
InChIKey
InChIKey
ZBJPVPFEDGYYBD-GBJTYRQASA-N
ChEBI ID
197613
mapping relation type
exact match
1 reference
matched by identifier from
International Chemical Identifier
InChI
InChI=1S/C15H28O2/c1-11(2)7-6-9-15(5,17)13-8-10-14(4,16)12(13)3/h7,12-13,16-17H,6,8-10H2,1-5H3/t12-,13+,14+,15+/m0/s1
UniChem compound ID
7290124
1 reference
stated in
UniChem
DSSTox substance ID
DTXSID80183022
1 reference
matched by identifier from
InChIKey
InChIKey
ZBJPVPFEDGYYBD-GBJTYRQASA-N
DSSTOX compound identifier
DTXCID90105513
0 references
UNII
4ZP8FLH4RC
1 reference
matched by identifier from
InChIKey
InChIKey
ZBJPVPFEDGYYBD-GBJTYRQASA-N
Natural Product Atlas ID
NPA000091
2 references
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
ZBJPVPFEDGYYBD-GBJTYRQASA-N
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