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(Q72497912)
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oplopanone
chemical compound
(-)-Oplopanone
10alpha-Hydroxyoplopan-4-one
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Statements
instance of
type of chemical entity
0 references
subclass of
7-Acetyl-2-hydroxy-2-methyl-5-isopropylbicyclo[4.3.0]nonane
1 reference
based on heuristic
inferred from SMILES
chemical structure
Oplopanone.svg
330 × 375; 10 KB
0 references
mass
238.193280072
dalton
1 reference
based on heuristic
inferred from SMILES
stereoisomer of
1-[(1S,3aR,4R,7S,7aR)-4-hydroxy-4-methyl-7-propan-2-yl-1,2,3,3a,5,6,7,7a-octahydroinden-1-yl]ethanone
2 references
based on heuristic
inferred from InChIKey
based on heuristic
inferred from InChI
1-[[(1R,3abeta,7aalpha)-Octahydro-4beta-hydroxy-4-methyl-7alpha-isopropyl-1H-inden]-1-yl]ethanone
2 references
based on heuristic
inferred from InChIKey
based on heuristic
inferred from InChI
1-[(1S,3aS,4R,7S,7aR)-4-hydroxy-4-methyl-7-propan-2-yl-1,2,3,3a,5,6,7,7a-octahydroinden-1-yl]ethanone
2 references
based on heuristic
inferred from InChIKey
based on heuristic
inferred from InChI
1-[4-Hydroxy-4-methyl-7-(propan-2-yl)octahydro-1H-inden-1-yl]ethan-1-one
2 references
based on heuristic
inferred from InChIKey
based on heuristic
inferred from InChI
1-[(1R,3aS,4S,7R,7aS)-4-hydroxy-4-methyl-7-propan-2-yl-1,2,3,3a,5,6,7,7a-octahydroinden-1-yl]ethanone
1 reference
based on heuristic
inferred from InChI
chemical formula
C₁₅H₂₆O₂
0 references
canonical SMILES
O=C(C)C1CCC2C1C(CCC2(O)C)C(C)C
0 references
isomeric SMILES
CC(C)[C@@H]1CC[C@@]([C@H]2[C@H]1[C@H](CC2)C(=O)C)(C)O
0 references
found in taxon
Juniperus sabina
3 references
stated in
Terpenoids from Juniperus sabina
stated in
Two diterpenoids from leaves of juniperus sabina
stated in
Two diterpenoids from leaves of juniperus sabina
Teucrium leucocladum
1 reference
stated in
Chemical analysis and biological activities of the essential oil of Teucrium leucocladum Boiss. (Lamiaceae)
Teucrium polium
1 reference
stated in
Biofilm blocking sesquiterpenes from Teucrium polium
Teucrium ramosissimum
3 references
stated in
Sesquiterpenoids from Teucrium ramosissimum
stated in
Sesquiterpenoids from Teucrium ramosissimum
stated in
Sesquiterpenoids from Teucrium ramosissimum
Agastache rugosa
1 reference
stated in
Volatile Constituents ofAgastache rugosa
Artemisia campestris
1 reference
stated in
2-Methyl-2-hydroxymethylchromenes from Artemisia campestris subsp. glutinosa
Calendula officinalis
1 reference
stated in
Oxygen-Containing Terpene Derivatives from Calendula officinalis
Chamaecyparis formosensis
2 references
stated in
Terpenes and lignans from leaves of Chamaecyparis formosensis
stated in
Terpenes and lignans from leaves of Chamaecyparis formosensis
Chamaecyparis lawsoniana
1 reference
stated in
Volatile Fractions ofChamaecyparis lawsoniana(A. Murray) Parl, andChamaecyparis pisifera(Sieb. et Zucc.) Endl. var.filifera.Identification of Oplopanonyl Acetate
Chamaecyparis pisifera
1 reference
stated in
Volatile Fractions ofChamaecyparis lawsoniana(A. Murray) Parl, andChamaecyparis pisifera(Sieb. et Zucc.) Endl. var.filifera.Identification of Oplopanonyl Acetate
Chrysanthemum indicum
4 references
stated in
Medicinal flowers. I. Aldose reductase inhibitors and three new eudesmane-type sesquiterpenes, kikkanols A, B, and C, from the flowers of Chrysanthemum indicum L
stated in
Medicinal flowers. II. Inhibitors of nitric oxide production and absolute stereostructures of five new germacrane-type sesquiterpenes, kikkanols D, D monoacetate, E, F, and F monoacetate from the flowers of Chrysanthemum indicum L
stated in
Medicinal flowers. I. Aldose reductase inhibitors and three new eudesmane-type sesquiterpenes, kikkanols A, B, and C, from the flowers of Chrysanthemum indicum L
stated in
Medicinal flowers. II. Inhibitors of nitric oxide production and absolute stereostructures of five new germacrane-type sesquiterpenes, kikkanols D, D monoacetate, E, F, and F monoacetate from the flowers of Chrysanthemum indicum L
Commiphora guidottii
1 reference
stated in
Minor components with smooth muscle relaxing properties from scented myrrh (Commiphora guidotti)
Cryptomeria japonica
2 references
stated in
Sesquiterpenes from leaves of Cryptomeria japonica
stated in
Sesquiterpenes from leaves of Cryptomeria japonica
Disynaphia multicrenulata
1 reference
stated in
Sesquiterpene lactones and other constituents of Disynaphia multicrenulata from Argentina
Hedychium gardnerianum
1 reference
stated in
A new xanthone fromHedychium gardnerianum
Homalomena aromatica
2 references
stated in
Sesquiterpenoids from the roots of Homalomena aromatica
stated in
Sesquiterpenoids from the roots of Homalomena aromatica
Isocoma coronopifolia
1 reference
stated in
A nor-diterpene and other constituents from Isocoma coronopifolia
Juniperus communis
1 reference
stated in
Structure Elucidation of Germacrane Alcohols from Juniperus communis subsp. Hemisphaerica
Juniperus thurifera
1 reference
stated in
Terpenoids from leaves of Juniperus thurifera
Larix kaempferi
2 references
stated in
Abietane diterpene acids and other constituents from the leaves of Larix kaempferi
stated in
Abietane diterpene acids and other constituents from the leaves of Larix kaempferi
Liatris microcephala
2 references
stated in
Sesquiterpene alcohols and triterpenoids from Liatris microcephala
stated in
Sesquiterpene alcohols and triterpenoids from Liatris microcephala
Magnolia biondii
2 references
stated in
Sesquiterpene components from the flower buds ofMagnolia fargesii
stated in
Scopoletin from the flower buds of Magnolia fargesii inhibits protein glycation, aldose reductase, and cataractogenesis ex vivo
Ocotea porosa
1 reference
stated in
Phenylpropanoid-catechins from bark of Ocotea porosa
Pallenis spinosa
1 reference
stated in
Sesquiterpenoids from Pallenis spinosa
Pseudobrickellia brasiliensis
2 references
stated in
A hydroxygermacrene and other constituents from Pseudobrickellia brasiliensis
stated in
A hydroxygermacrene and other constituents from Pseudobrickellia brasiliensis
Pulicaria paludosa
1 reference
stated in
Sesquiterpenoids and phenolics of Pulicaria paludosa
Raulinoa echinata
2 references
stated in
Chemistry and bioactivity of Raulinoa echinata Cowan, an endemic Brazilian Rutaceae species
stated in
Chemistry and bioactivity of Raulinoa echinata Cowan, an endemic Brazilian Rutaceae species
Renealmia cincinnata
1 reference
stated in
Anti-plasmodial sesquiterpenoids from the African Reneilmia cincinnata
Santolina rosmarinifolia
2 references
stated in
Components from Santolina rosmarinifolia, subspecies rosmarinifolia and canescens
stated in
Components from Santolina rosmarinifolia, subspecies rosmarinifolia and canescens
Schefflera taiwaniana
2 references
stated in
Cytotoxic Components from the Leaves ofSchefflera Taiwaniana
stated in
Cytotoxic Components from the Leaves ofSchefflera Taiwaniana
Senecio adenophyllus
1 reference
stated in
Eremophilane, germacrane and shikimic acid derivatives from chilean Senecio species
Aldama tucumanensis
2 references
stated in
Terpenoid constituents of Viguiera tucumanensis
stated in
Antifeedant activity of metabolites from Viguiera tucumanensis.
Sinacalia tangutica
1 reference
stated in
Terpenoids from the Flower ofCacalia Tangutica
Casearia sylvestris
1 reference
stated in
New clerodane diterpenoids from Casearia sylvestris.
Laurencia subopposita
1 reference
stated in
Metabolites of the red alga Laurencia subopposita
Petasites tatewakianus
1 reference
stated in
Sesquiterpenoids from Petasites tatewakianus
Jacobaea argunensis
1 reference
stated in
Sesquiterpenoids from Senecio argunensis
Jacobaea erucifolia
1 reference
stated in
Sesquiterpenoids from Senecio argunensis
Senecio microglossus
1 reference
stated in
Two sesquiterpenes from Senecio species
Acorus calamus
1 reference
stated in
Chemical composition of the essential oil and supercritical CO2 extract of Commiphora myrrha (Nees) Engl. and of Acorus calamus L.
Magnolia
1 reference
stated in
Lignans and sesquiterpenes from Magnolia praecocissima
Aldama tukumanensis
2 references
stated in
Antifeedant activity of metabolites from Viguiera tucumanensis.
stated in
Terpenoid constituents of Viguiera tucumanensis
Identifiers
InChI
InChI=1S/C15H26O2/c1-9(2)11-7-8-15(4,17)13-6-5-12(10(3)16)14(11)13/h9,11-14,17H,5-8H2,1-4H3/t11-,12+,13+,14+,15+/m0/s1
0 references
InChIKey
WLXJHVQYKOJBBN-NJVJYBDUSA-N
0 references
CAS Registry Number
1911-78-0
1 reference
InChIKey
WLXJHVQYKOJBBN-NJVJYBDUSA-N
stated in
CAS Common Chemistry
retrieved
9 April 2021
reference URL
https://commonchemistry.cas.org/detail?cas_rn=1911-78-0
PubChem CID
10466745
1 reference
matched by identifier from
InChIKey
InChIKey
WLXJHVQYKOJBBN-NJVJYBDUSA-N
UniChem compound ID
32039509
1 reference
stated in
UniChem
DSSTox substance ID
DTXSID80172633
1 reference
matched by identifier from
InChIKey
InChIKey
WLXJHVQYKOJBBN-NJVJYBDUSA-N
DSSTOX compound identifier
DTXCID0095124
0 references
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