(Q27110176)

(1S,4S,5R,9S,10S,13R)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carbaldehyde

Kaurenal (English)

5 October 2016

2 references

1 reference

(1R,4R,5S,9R,10S,13S)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carbaldehyde

2 references

(1S,4R,5R,9S,10R,13R)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carbaldehyde

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₂₀H₃₀O

1 reference

Kaurenal (English)

5 October 2016

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

1 reference

Kaurenal (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)C=O

1 reference

Sesqui- and diterpenes from Baccharis species

Kaurenal (English)

5 October 2016

1 reference

Disynaphia multicrenulata

1 reference

Heliangolides and germacrolides from Disynaphia multicrenulata

common sunflower

1 reference

Neutral Diterpenoids of Helianthus annuus

Lasianthea fruticosa

1 reference

Kaurene derivatives from Lasianthea fruticosa, revision of stereochemistry of related compounds

Montanoa tomentosa

2 references

Two further 6,12-cis-germacranolides from Montanoa tomentosa subsp. xanthiifolia

Two further 6,12-cis-germacranolides from Montanoa tomentosa subsp. xanthiifolia

Oyedaea verbesinoides

3 references

Melampolides from Oyedaea verbesinoides

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

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

Perymenium klattianum

1 reference

Germacranolides from Perymenium klattianum and Perymeniopsis ovalifolia

Smallanthus glabratus

1 reference

Homogeranyl nerol derivatives and a melampolide from Smallanthus glabratus

Wedelia bishoplecta

1 reference

A highly oxygenated germacrane fromAspilia eenii and constituents from otherAspilia species

Wedelia ovalifolia

1 reference

A highly oxygenated germacrane fromAspilia eenii and constituents from otherAspilia species

Baccharis minutiflora

1 reference

Baccharis ramosissima

1 reference

Baccharis retusa

1 reference

Baccharis rhomboidalis

1 reference

Baccharis truncata

1 reference

Casearia corymbosa

1 reference

Clerodane diterpenes from Casearia corymbosa stem bark

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

Ichthyothere terminalis

1 reference

New melampolides, kaurene derivatives and other constituents from Ichthyothere species

Mikania arrojadoi

1 reference

An epoxygermacranolide and further constituents from Mikania species

Smallanthus fruticosus

1 reference

Neue melampolide aus Smallanthus fruticosus

Solidago nemoralis

1 reference

Sesquiterpene and diterpene derivatives from Solidago species

Steiractinia sodiroi

1 reference

Neue eudesmanolide aus Steiractinia mollis

Espeletia guacharaca

1 reference

Tricyclic sesquiterpenes and further diterpenes from Espeletiopsis species

Arabidopsis thaliana

1 reference

Arabidopsis ent-kaurene oxidase catalyzes three steps of gibberellin biosynthesis

Cucurbita

1 reference

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

Helichrysum nudifolium

1 reference

An anomalous sesquiterpene from Helichrysum davyi

Identifiers

InChI

InChI=1S/C20H30O/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/h13,15-17H,1,4-12H2,2-3H3/t15-,16-,17+,18+,19-,20-/m1/s1

1 reference

JCAVDWHQNFTFBW-XRNRSJMDSA-N

Kaurenal (English)

5 October 2016

2 references

Kaurenal (English)

5 October 2016

ChEBI release 2020-09-01

1 reference

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

5 October 2016

1 reference

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

5 October 2016

1 reference

Kaurenal (English)

5 October 2016

mapping relation type

1 reference

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

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

5 October 2016

1 reference

1 reference

DSSTOX compound identifier

DTXCID60283190

0 references

Human Metabolome Database ID

HMDB0036728

1 reference

KNApSAcK ID

C00055814

1 reference

1 reference