Kaur-16-en-18-ol (Q27110177)

inferred from SMILES

mass

288.245316 dalton

1 reference

[(1S,4S,5R,9S,10S,13R)-5,9-dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methanol

Kaurenol (English)

5 October 2016

2 references

inferred from InChIKey

[(1S,4R,5R,9S,10R,13R)-5,9-dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methanol

inferred from InChI

2 references

inferred from InChIKey

2 references

inferred from InChIKey

1 reference

C₂₀H₃₂O

1 reference

Kaurenol (English)

5 October 2016

CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)CO

1 reference

Kaurenol (English)

5 October 2016

C[C@]1(CCC[C@@]2([C@@H]1CC[C@]34[C@H]2CC[C@H](C3)C(=C)C4)C)CO

1 reference

Arabidopsis ent-kaurene oxidase catalyzes three steps of gibberellin biosynthesis

Kaurenol (English)

5 October 2016

1 reference

Calocephalus knappii

2 references

Kaurane and beyerane derivatives from Calocephalus knappii

Kaurane and beyerane derivatives from Calocephalus knappii

Perymenium featherstonei

1 reference

4α,15-Dihydroencelin and related sesquiterpene acids from perymenium featherstonei

Abrotanella nivigena

1 reference

Isolation of ent-16-Kauren-19-oic Acid and ent-16-Kauren-19-ol from Abrotanella nivigena Muell

Annona glabra

1 reference

Bioactive kaurane diterpenoids from Annona glabra.

Wedelia bishoplecta

1 reference

A highly oxygenated germacrane fromAspilia eenii and constituents from otherAspilia species

Baccharis minutiflora

1 reference

Diterpenes from Baccharis species

Baccharis quitensis

1 reference

Diterpenes from Baccharis species

Bruguiera gymnorhiza

1 reference

New diterpenoids from the marine mangrove Bruguiera gymnorrhiza

Bruguiera gymnorrhiza

1 reference

New diterpenoids from the marine mangrove Bruguiera gymnorrhiza

Disynaphia multicrenulata

1 reference

Heliangolides and germacrolides from Disynaphia multicrenulata

Espeletia grandiflora

1 reference

Kauranoid dieterpenes in Espeletia grandiflora

Espeletiopsis guacharaca

1 reference

Tricyclic sesquiterpenes and further diterpenes from Espeletiopsis species

Goyazianthus tetrastichus

1 reference

Kolavenol derivatives from goyazianthus tetrastichus

Helichrysum aureum

1 reference

Twenty-one acylphloroglucinol derivatives and further constituents from south african Helichrysum species

Helichrysum nudifolium var. nudifolium

1 reference

An anomalous sesquiterpene from Helichrysum davyi

Ichthyothere terminalis

1 reference

New melampolides, kaurene derivatives and other constituents from Ichthyothere species

Libanothamnus banksiifolius

1 reference

Neue sesquiterpene und norditerpene aus vertretern der gattung Libanothamnus

Mikania arrojadoi

1 reference

An epoxygermacranolide and further constituents from Mikania species

Mikania haenkeana

1 reference

A cadinanolide and other sesquiterpene lactones from Mikania haenkeana

Mikania vitifolia

1 reference

Kaurene diterpenes from Mikania vitifolia

Oyedaea verbesinoides

1 reference

Studies of ent-kaurane diterpenes from Oyedaea verbesinoides for their inhibitory activity on vascular smooth muscle contraction

Sagittaria trifolia

1 reference

Absolute Stereostructures of Trifoliones A, B, C, and D, New Biologically Active Diterpenes from the Tuber of Sagittaria trifolia L

Smallanthus fruticosus

1 reference

Neue melampolide aus Smallanthus fruticosus

Steiractinia sodiroi

1 reference

Neue eudesmanolide aus Steiractinia mollis

Stevia lucida

1 reference

An ent-kaurenolide from Stevia lucida

Tripterygium doianum

1 reference

Kaurane and abietane diterpenoids from Tripterygium doianum (Celastraceae).

Wedelia hookeriana

1 reference

Eudesmanolides and kaurene derivatives from Wedelia hookeriana

Xylopia frutescens

1 reference

Frutoic acid, a dimeric kaurane diterpene from Xylopia frutescens

Espeletia guacharaca

1 reference

Tricyclic sesquiterpenes and further diterpenes from Espeletiopsis species

Sagittaria sagittifolia

1 reference

Absolute Stereostructures of Trifoliones A, B, C, and D, New Biologically Active Diterpenes from the Tuber of Sagittaria trifolia L

Cucurbita

1 reference

The Biosynthesis of Gibberellin Precursors in a Cell-free System from Cucurbita Pepo L.

Identifiers

InChI

InChI=1S/C20H32O/c1-14-11-20-10-7-16-18(2,13-21)8-4-9-19(16,3)17(20)6-5-15(14)12-20/h15-17,21H,1,4-13H2,2-3H3/t15-,16-,17 ,18 ,19-,20-/m1/s1

1 reference

TUJQVRFWMWRMIO-XRNRSJMDSA-N

Kaurenol (English)

5 October 2016

2 references

Kaurenol (English)

5 October 2016

ChEBI release 2020-09-01

1 reference

Kaur-16-en-18-ol (English)

5 October 2016

1 reference

(5beta,8alpha,9beta,10alpha,13alpha)-Kaur-16-en-18-ol (English)

5 October 2016

2 references

matched by identifier from

Kaurenol (English)

retrieved

5 October 2016

InChIKey

TUJQVRFWMWRMIO-XRNRSJMDSA-N

ChEBI ID

29611

mapping relation type

2 references

matched by identifier from

Kaur-16-en-18-ol (English)

retrieved

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C20H32O/c1-14-11-20-10-7-16-18(2,13-21)8-4-9-19(16,3)17(20)6-5-15(14)12-20/h15-17,21H,1,4-13H2,2-3H3/t15-,16-,17 ,18 ,19-,20-/m1/s1

1 reference

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

CHEMBL590263 (English)

5 October 2016

1 reference

2 references

matched by identifier from

InChIKey

TUJQVRFWMWRMIO-XRNRSJMDSA-N

DSSTOX compound identifier

0 references

1 reference

Kaur-16-en-18-ol (English)

5 October 2016

1 reference