(Q82123192)

1,4a-dimethyl-6-methylidene-5-(3-methylpenta-2,4-dienyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid

inferred from SMILES

1 reference

inferred from SMILES

mass

302.2245802 dalton

1 reference

2 references

(1S,4aS,5R,8aS)-1,4a-dimethyl-6-methylidene-5-[(2Z)-3-methylpenta-2,4-dienyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid

2 references

(9R,10S,12E)-Labda-8(20),12,14-trien-19-oic acid

2 references

(1S,4aR,5R,8aS)-1,4a-dimethyl-6-methylidene-5-[(2E)-3-methylpenta-2,4-dienyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid

2 references

(1R,4aR,5R,8aR)-1,4a-dimethyl-6-methylidene-5-(3-methylpenta-2,4-dienyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid

2 references

(1S,4aR,5R,8aR)-1,4a-dimethyl-6-methylidene-5-[(2E)-3-methylpenta-2,4-dienyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid

2 references

(1S,4aR,5R,8aR)-1,4a-dimethyl-6-methylidene-5-(3-methylpenta-2,4-dienyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid

2 references

(1R,4aR,5R,8aS)-1,4a-dimethyl-6-methylidene-5-[(2E)-3-methylpenta-2,4-dienyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid

1 reference

(1S,4aR,5S,8aS)-1,4a-dimethyl-6-methylidene-5-[(2E)-3-methylpenta-2,4-dienyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid

1 reference

(1R,4aR,5S,8aR)-1,4a-dimethyl-6-methylidene-5-[(2Z)-3-methylpenta-2,4-dienyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid

1 reference

(1S,4aS,5S,8aS)-1,4a-dimethyl-6-methylidene-5-[(2Z)-3-methylpenta-2,4-dienyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid

1 reference

(1S,4aS,5R,8aR)-1,4a-dimethyl-6-methylidene-5-[(2Z)-3-methylpenta-2,4-dienyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid

1 reference

(1S,4aR,5S,8aR)-1,4a-dimethyl-6-methylidene-5-(3-methylpenta-2,4-dienyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid

1 reference

(1S,4aS,5S,8aR)-1,4a-dimethyl-6-methylidene-5-[(2E)-3-methylpenta-2,4-dienyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid

1 reference

(1S,4aR,5S,8aS)-1,4a-dimethyl-6-methylidene-5-[(2Z)-3-methylpenta-2,4-dienyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid

1 reference

(1R,4aR,5S,8aR)-1,4a-dimethyl-6-methylidene-5-[(2E)-3-methylpenta-2,4-dien-1-yl]-hexahydro-2H-naphthalene-1-carboxylic acid

1 reference

1 reference

C₂₀H₃₀O₂

0 references

canonical SMILES

O=C(O)C1(C)CCCC2(C)C(C(=C)CCC12)CC=C(C=C)C

0 references

isomeric SMILES

C/C(=C\C[C@H]1C(=C)CC[C@@H]2[C@@]1(CCC[C@]2(C)C(=O)O)C)/C=C

0 references

found in taxon

Juniperus sabina

1 reference

Terpenoids from Juniperus sabina

Juniperus communis

4 references

Antimycobacterial terpenoids from Juniperus communis L. (Cuppressaceae).

Diterpene acids from Juniperus communis subsp. Hemisphaerica

Diterpene acids from Juniperus communis subsp. Hemisphaerica

New natural diterpene acids from Juniperus communis

Juniperus

1 reference

Oxygenated Diterpenes and Other Constituents from Moroccan Juniperus phoenicea and Juniperus thurifera Var. africana

Apis mellifera

1 reference

Terpenes with antimicrobial activity from Cretan propolis

Araucaria angustifolia

1 reference

Phenylpropanoid derivatives and biflavones at different stages of differentiation and development of Araucaria angustifolia.

Chamaecyparis formosensis

1 reference

Terpenes and lignans from leaves of Chamaecyparis formosensis

Chamaecyparis obtusa

1 reference

Abietane-type and labdane-type diterpenoids from the cones ofChamaecyparis obtusa

Cryptomeria japonica

3 references

Diterpenoids from leaves of Cryptomeria japonica

Diterpenoids from leaves of Cryptomeria japonica

Anti-inflammatory constituents of topically applied crude drugs. II. Constituents and anti-inflammatory effect of Cryptomeria japonica D. Don

Entada abyssinica

3 references

A Diterpene, a Flavonol Glycoside, and a Phytosterol Glycoside from Securidaca longipedunculata and Entada abyssinica

A Bioactive Diterpene from Entada Abyssinica

A Diterpene, a Flavonol Glycoside, and a Phytosterol Glycoside from Securidaca longipedunculata and Entada abyssinica

Juniperus chinensis

2 references

Terpenes from heartwood of Juniperus chinensis

Terpenes from heartwood of Juniperus chinensis

Juniperus formosana

2 references

Dehydroabietane diterpenes from Juniperus formosana hay. var. concolor hay

Dehydroabietane diterpenes from Juniperus formosana hay. var. concolor hay

Juniperus procera

1 reference

Further antibacterial diterpenes from the bark and leaves ofJuniperus procera hochst. ex Endl

Libocedrus bidwillii

1 reference

Antitumour lignans and cytotoxic resin acids from a New Zealand gymnosperm, Libocedrus plumosa

Calocedrus formosana

3 references

Terpenoids from leaves of Calocedrus formosana

Cytotoxic Constituents of the Leaves ofCalocedrus Formosana

Terpenoids from leaves of Calocedrus formosana

Pinus luchuensis

3 references

Potential antitumor-promoting diterpenes from the cones of Pinus luchuensis

Potential antitumor-promoting diterpenes from the cones of Pinus luchuensis

Potential antitumor-promoting diterpenes from the cones of Pinus luchuensis

Porella navicularis

2 references

ChemInform Abstract: Pinguisane Sesquiterpenes from the Liverwort Porella navicularis.

Pinguisane sesquiterpenes from the liverwort porella Navicularisfn2fn2Dedicated to Prof. T. Eicher on the occasion of his 65th birthday.fn3fn3Publication No. 124 of Arbeitskreis Chemie und Biologie der Hoose.

Sciadopitys verticillata

2 references

Diterpenes from the seed of Sciadopitys verticillata

Diterpenes from the seed of Sciadopitys verticillata

Thuja standishii

3 references

Anti-tumor promoting diterpenes from the stem bark of Thuja standishii (Cupressaceae).

Aromatase inhibitory activities of standishinal and the diterpenoids from the bark of Thuja standishii

Anti-tumor promoting diterpenes from the stem bark of Thuja standishii (Cupressaceae).

Agathis australis

1 reference

The Chemistry of the Order Araucariales. Part 4. The Bled Resins of Agathis australis.

Chamaecyparis lawsoniana

1 reference

Antibacterials and modulators of bacterial resistance from the immature cones of Chamaecyparis lawsoniana

Chromolaena collina

1 reference

A labdane derivative from Chromolaena collina and a p-hydroxyacetophenone derivative. From Stomatanthes corumbensis

Juniperus horizontalis

1 reference

THE CHEMICAL COMPOSITION OF THE WOOD AND BARK EXTRACTIVES OF JUNIPERUS HORIZONTALIS MOENCH

Juniperus rigida

1 reference

A new lignan glycoside from Juniperus rigida

Phyllocladus trichomanoides

1 reference

Chemistry of the Podocarpaceae. LVI. Resin acids from Phyllocladus trichomanoides

Pseudotsuga sinensis var. sinensis

1 reference

Terpenoids and flavonoids from Pseudotsuga wilsoniana

Fokienia hodginsii

1 reference

Diterpenoids from the twigs and leaves of Fokienia hodginsii

Pinus strobus

1 reference

Diterpene resin acids from the needle oleoresin of pinus strobus

Torreya nucifera

1 reference

18-Oxoferruginol from the leaf of Torreya nucifera

Larix gmelinii var. gmelinii

1 reference

Chemical composition of the oleoresin of Larix dahurica

Larix gmelinii

1 reference

Chemical composition of the oleoresin of Larix dahurica

Platycladus orientalis

3 references

15-Hydroxypinusolidic Acid, a New Diterpene from the Pericarp of Platycladus orientalis Franco

Chemical Constituents of the Pericarp ofPlatycladus orientalis

Terpenoids from the seed of platycladus orientalis

Callitris columellaris

1 reference

Natural and thermal isomers of methyl trans-communate

Identifiers

InChI

InChI=1S/C20H30O2/c1-6-14(2)8-10-16-15(3)9-11-17-19(16,4)12-7-13-20(17,5)18(21)22/h6,8,16-17H,1,3,7,9-13H2,2,4-5H3,(H,21,22)/b14-8+/t16-,17+,19+,20-/m0/s1

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DSSTOX compound identifier

DTXCID10299483

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UNII

SER34Y2ER9

1 reference

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