(Q27123466)

isopimarinol (English)

1-Phenanthrenemethanol, 7-ethenyl-1,2,3,4,4a,4b,5,6,7,8,10,10a-dodecahydro-1,4a,7-trimethyl-, (1S,4aR,4bS,7S,10aR)-

6 October 2016

stereoisomer of

2 references

inferred from InChIKey

9beta-pimara-7,15-dien-19-ol

2 references

inferred from InChIKey

[(1R,4aR,4bS,7R,10aR)-7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-1-yl]methanol

1 reference

[(1S,4aS,4bS,7S,10aS)-7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-1-yl]methanol

1 reference

chemical formula

C₂₀H₃₂O

1 reference

isopimarinol (English)

6 October 2016

canonical SMILES

CC1(CCC2C(=CCC3C2(CCCC3(C)CO)C)C1)C=C

1 reference

isopimarinol (English)

6 October 2016

isomeric SMILES

C[C@@]1(CC[C@H]2C(=CC[C@@H]3[C@@]2(CCC[C@@]3(C)CO)C)C1)C=C

1 reference

Terpenoids of the oleoresins ofPicea orientalis andAbies normanniana growing in the Caucasus

isopimarinol (English)

6 October 2016

1 reference

Pinus sibirica

1 reference

Group composition of the oleoresin of the Siberian Stone Pine

Larix kaempferi

1 reference

Terpenoids of the oleoresin ofLarix leptolepis

Abies firma

1 reference

Terpenoids from seeds of Abies firma

Callicarpa japonica

1 reference

Phytotoxicity and volatile constituents from leaves of Callicarpa japonica Thunb

Cryptomeria japonica

1 reference

Diterpenoids from leaves of Cryptomeria japonica

Larix gmelinii

1 reference

Neutral compounds of the extractive substances of larix gmelini

Nepeta tuberosa

1 reference

Diterpenoids from Nepeta tuberosa subsp. reticulata

Pinus densiflora

1 reference

Terpenoids ofPinus funebris

Pinus brutia var. pityusa

1 reference

Terpenoids of the oleoresins ofPinus pityusa andP. eldarica

Pinus pumila

1 reference

Terpenoids of the oleoresin of Pinus pumila

Pinus sylvestris

1 reference

3?-Hydroxy-trans-biformene and its acetate and other diterpene alcohols fromPinus sylvestris shoots

Prumnopitys andina

1 reference

EXTRACTABLE COMPOUNDS OF NATIVE TREES CHEMICAL AND BIOLOGICAL STUDY I: Bark of Prumnopytis andina (Podocarpaceae) and Austrocedrus chilensis (Cupressaceae)

Taiwania cryptomerioides

1 reference

Comparison of the Antifungal Activity of Cadinane Skeletal Sesquiterpenoids from Taiwania (Taiwania cryptomerioides Hayata) Heartwood

Halocarpus bidwillii

1 reference

Diterpenes of Dacrydium bidwillii

Juniperus thurifera

1 reference

Oxygenated diterpenes and other constituents from Moroccan Juniperus phoenicea and Juniperus thurifera var. africana.

Prumnopitys ferruginea

1 reference

Diterpenes of Podocarpus ferrugineus bark

Trichilia heudelotii

1 reference

Antimicrobial activity of Trichilia heudelotti leaves.

Trichilia monadelpha

1 reference

Antimicrobial activity of Trichilia heudelotti leaves.

Identifiers

InChI

InChI=1S/C20H32O/c1-5-18(2)12-9-16-15(13-18)7-8-17-19(3,14-21)10-6-11-20(16,17)4/h5,7,16-17,21H,1,6,8-14H2,2-4H3/t16-,17-,18-,19-,20+/m0/s1

1 reference

isopimarinol (English)

DUEINKIQNGZKPL-VYJAJWGXSA-N

6 October 2016

InChIKey

2 references

isopimarinol (English)

6 October 2016

ChEBI release 2020-09-01

1 reference

isopimara-7,15-dienol (English)

6 October 2016

1 reference

iso-Pimarinol (English)

6 October 2016

1 reference

isopimarinol (English)

6 October 2016

Reaxys registry number

2132408

1 reference

isopimara-7,15-dienol (English)

6 October 2016

ChEBI ID

52484

mapping relation type

1 reference

DSSTOX compound identifier

isopimara-7,15-dienol (English)

6 October 2016

1 reference

0 references

0 references

1 reference

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

isopimara-7,15-dienol (English)

6 October 2016

1 reference