(+)-4-epi-cryptomeridiol (Q27138813)

eudesmane-4beta,11-diol (English)

(1S,4aR,7R,8aR)-7-(1-hydroxy-1-methyl-ethyl)-1,4a-dimethyl-decalin-1-ol

7 October 2016

stereoisomer of

2 references

inferred from InChIKey

(1S,4aS,7R,8aS)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-octahydronaphthalen-1-ol

2 references

inferred from InChIKey

(1R,8aalpha)-1,4abeta-Dimethyl-7alpha-(1-hydroxy-1-methylethyl)decahydronaphthalen-1-ol

2 references

inferred from InChIKey

(1R,4aS,7R,8aS)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol

1 reference

1 reference

(+)-5-Epieudesmane-4alpha,11-diol

1 reference

(1S,4aR,7R,8aS)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol

1 reference

chemical formula

C₁₅H₂₈O₂

1 reference

eudesmane-4beta,11-diol (English)

7 October 2016

canonical SMILES

CC12CCCC(C1CC(CC2)C(C)(C)O)(C)O

1 reference

eudesmane-4beta,11-diol (English)

7 October 2016

isomeric SMILES

C[C@@]12CCC[C@]([C@H]1C[C@H](CC2)C(C)(C)O)(C)O

1 reference

2-Methyl-2-hydroxymethylchromenes from Artemisia campestris subsp. glutinosa

eudesmane-4beta,11-diol (English)

7 October 2016

1 reference

Magnolia ovata

1 reference

Cytotoxic Components from Stem Bark ofMagnolia obovata

Magnolia obovata

1 reference

Cytotoxic Components from Stem Bark ofMagnolia obovata

Artemisia argyi

1 reference

Eudesmanolides and Other Constituents from Artemisia argyi

Sphaeranthus indicus

1 reference

7-Hydroxyeudesmanolides from Sphaeranthus indicus

Carissa edulis

1 reference

Sesquiterpenes from carissa edulis

Carissa spinarum

1 reference

Sesquiterpenes from carissa edulis

Chamaecyparis formosensis

1 reference

Terpenes and lignans from leaves of Chamaecyparis formosensis

Dysphania graveolens

1 reference

Flavonoids and terpenoids of Chenopodium graveolens

Cryptomeria japonica

1 reference

Sesquiterpenes from leaves of Cryptomeria japonica

Cymbopogon parkeri

1 reference

Constituents of Plants Growing in Qatar IX. The Antispasmodic Components of Cymbopogon parkeri Stapf. Parkeri Stapf

Juniperus thurifera

1 reference

Terpenoids from leaves of Juniperus thurifera

Neolitsea hiiranensis

1 reference

Chemical Constituents from the Roots ofNeolitsea hiiranensis

Ratibida mexicana

1 reference

Biochemically active sesquiterpene lactones from Ratibida mexicana.

Santolina rosmarinifolia

1 reference

Bioactive sesquiterpenes from Santolina rosmarinifolia subsp. Canescens. A conformational analysis of the germacrane ring

Chamaecyparis obtusa

1 reference

Neurite outgrowth-promoting active constituents of the Japanese cypress (Chamaecyparis obtusa).

Laggera crispata

1 reference

Eudesmane sesquiterpenes from Laggera pterodonta

Laggera pterodonta

1 reference

Eudesmane sesquiterpenes from Laggera pterodonta

Citrus hystrix

1 reference

Citrusosides A-D and furanocoumarins with cholinesterase inhibitory activity from the fruit peels of Citrus hystrix

Identifiers

InChI

InChI=1S/C15H28O2/c1-13(2,16)11-6-9-14(3)7-5-8-15(4,17)12(14)10-11/h11-12,16-17H,5-10H2,1-4H3/t11-,12-,14-,15-/m0/s1

1 reference

eudesmane-4beta,11-diol (English)

LKKDASYGWYYFIK-JURCDPSOSA-N

7 October 2016

InChIKey

2 references

eudesmane-4beta,11-diol (English)

7 October 2016

ChEBI release 2020-09-01

1 reference

(1S,4aS,7S,8aS)-7-(2-Hydroxy-2-propanyl)-1,4a-dimethyldecahydro-1-naphthalenol (English)

7 October 2016

1 reference

eudesmane-4beta,11-diol (English)

7 October 2016

ChEBI ID

70477

mapping relation type

2 references

(+)-4-epi-cryptomeridiol (English)