(6S)-dehydrovomifoliol (Q27106358)

Gene Ontology release 2020-05-02

Rhea release 113

mass

222.125594±0 dalton

1 reference

Dehydrovomifoliol (English)

5 October 2016

stereoisomer of

(6R)-dehydrovomifoliol

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

chemical formula

C₁₃H₁₈O₃

1 reference

Dehydrovomifoliol (English)

5 October 2016

canonical SMILES

CC1=CC(=O)CC(C1(C=CC(=O)C)O)(C)C

1 reference

Dehydrovomifoliol (English)

5 October 2016

isomeric SMILES

CC1=CC(=O)CC([C@]1(/C=C/C(=O)C)O)(C)C

1 reference

Glycosidically bound aroma compounds in the fruits of Prunus species: apricot (P. armeniaca, L.), peach (P. persica, L.), yellow plum (P. domestica, L. ssp. syriaca)

Dehydrovomifoliol (English)

5 October 2016

1 reference

peach

1 reference

Glycosidically bound aroma compounds in the fruits of Prunus species: apricot (P. armeniaca, L.), peach (P. persica, L.), yellow plum (P. domestica, L. ssp. syriaca)

Prunus domestica

1 reference

Glycosidically bound aroma compounds in the fruits of Prunus species: apricot (P. armeniaca, L.), peach (P. persica, L.), yellow plum (P. domestica, L. ssp. syriaca)

Buphthalmum salicifolium

2 references

Flavonoid glucosides and dicaffeoylquinic acids from flowerheads of Buphthalmum salicifolium1Dedicated to Professor Dr. G. Willuhn, Institute of Pharmaceutical Biology, Heinrich-Heine-Universität on the occasion of his 65th birthday.1

Flavonoid glucosides and dicaffeoylquinic acids from flowerheads of Buphthalmum salicifolium1Dedicated to Professor Dr. G. Willuhn, Institute of Pharmaceutical Biology, Heinrich-Heine-Universität on the occasion of his 65th birthday.1

Cucumis sativus

3 references

Two new megastigmanes from the leaves of Cucumis sativus

Inhibitory effect of Cucumis sativus on melanin production in melanoma B16 cells by downregulation of tyrosinase expression

Two new megastigmanes from the leaves of Cucumis sativus

Dictyopteris divaricata

1 reference

Cadinane sesquiterpenes from the brown alga Dictyopteris divaricata

Euphorbia helioscopia

3 references

Cytotoxic diterpenoids from Euphorbia helioscopia

Cytotoxic macrocyclic diterpenoids from Euphorbia helioscopia

Cytotoxic diterpenoids from Euphorbia helioscopia

Rhaphidophora decursiva

2 references

Antimalarial compounds from Rhaphidophora decursiva

Antimalarial compounds from Rhaphidophora decursiva

Salvia chinensis

2 references

New germacrane sesquiterpenes from Salvia chinensis

New germacrane sesquiterpenes from Salvia chinensis

Stachys byzantina

2 references

Iridoid glycoside constituents of Stachys lanata

Iridoid glycoside constituents of Stachys lanata

Mantisalca salmantica

1 reference

Norisoprenoids from Centaurea aspera and C. salmantica

common sunflower

2 references

Allelochemicals from sunflower leaves cv. Peredovick

Bioactive norsesquiterpenes from Helianthus annuus with potential allelopathic activity

Helianthus heterophyllus

1 reference

Heliangolides, kauranes and other constituents of Helianthus heterophyllus

Houttuynia cordata

2 references

The constituents and their bioactivities of Houttuynia cordata

The constituents and their bioactivities of Houttuynia cordata

Phaseolus vulgaris

1 reference

Glycinoeclepins, Natural Hatching Stimuli for the Soybean Cyst Nematode,Heterodera Glycines. I. Isolation

Salvia divinorum

2 references

Neo-clerodane Diterpenes from the Hallucinogenic SageSalvia divinorum.

Neo-clerodane diterpenes from the hallucinogenic sage Salvia divinorum

Solanum lyratum

2 references

Two new sesquiterpenoids from Solanum lyratum with cytotoxic activities.

Two new sesquiterpenoids from Solanum lyratum with cytotoxic activities.

Vitis vinifera

3 references

Glycosidically Bound Norisoprenoids from Vitis vinifera cv. Riesling Leaves

Free and Bound Volatile Secondary Metabolites of Vitis Vhifera Grape cv. Sauvignon Blanc

3-oxo-α-ionol, vomifoliol and roseoside in Vitis vinifera fruit

Chenopodium album

2 references

Isolation and Phytotoxicity of Apocarotenoids fromChenopodiumalbum

Isolation and Phytotoxicity of Apocarotenoids fromChenopodiumalbum

Epimedium grandiflorum var. koreanum

1 reference

2-Phenoxychromones and prenylflavonoids from Epimedium koreanum and their inhibitory effects on LPS-induced nitric oxide and interleukin-1β production

Nelumbo nucifera

1 reference

Chemical constituents from Nelumbo nucifera leaves and their anti-obesity effects

Sanicula lamelligera

1 reference

Sesquiterpene and norsesquiterpene derivatives from Sanicula lamelligera and their biological evaluation

Dendrobium loddigesii

1 reference

New phenanthrenes and stilbenes from Dendrobium loddigesii

Euphorbia lagascae

1 reference

Lagaspholones A and B: two new jatropholane-type diterpenes from Euphorbia lagascae

Physalis peruviana

1 reference

Two New Withanolides fromPhysalis peruviana

Piper lolot

1 reference

Isolation and identification of antiplatelet aggregatory principles from the leaves of Piper lolot.

Piper sarmentosum

1 reference

Isolation and identification of antiplatelet aggregatory principles from the leaves of Piper lolot.

Psychotria correae

1 reference

Alkaloids and other compounds from Psychotria correae

Tridax procumbens

1 reference

Chemical-constituent diversity of Tridax procumbens

Tripterygium regelii

1 reference

The genus Tripterygium: A phytochemistry and pharmacological review

Chamaecyparis formosensis

1 reference

New Terpenoids from Chamaecyparis formosensis (Cupressaceae) Leaves with Modulatory Activity on Matrix Metalloproteases 2 and 9.

Pontederia africana

1 reference

One Alkenylphenol and Steroids from the Aquatic PlantMonochoria Vaginalis

Palicourea correae

1 reference

Alkaloids and other compounds from Psychotria correae

Tripterygium wilfordii

1 reference

The genus Tripterygium: A phytochemistry and pharmacological review

Stachys palaestina

1 reference

Iridoid glycoside constituents of Stachys lanata

Identifiers

InChI

InChI=1S/C13H18O3/c1-9-7-11(15)8-12(3,4)13(9,16)6-5-10(2)14/h5-7,16H,8H2,1-4H3/b6-5+/t13-/m1/s1

1 reference

Dehydrovomifoliol (English)

JJRYPZMXNLLZFH-URWSZGRFSA-N

5 October 2016

InChIKey

2 references

Dehydrovomifoliol (English)

5 October 2016

ChEBI release 2020-09-01

1 reference

(6S)-dehydrovomifoliol (English)

5 October 2016

1 reference

(6S)-dehydrovomifoliol (English)

5 October 2016

1 reference

Dehydrovomifoliol (English)

5 October 2016

Reaxys registry number

2050827

1 reference

(6S)-dehydrovomifoliol (English)

5 October 2016

ChEBI ID

4372

mapping relation type

1 reference

(6S)-dehydrovomifoliol (English)

5 October 2016

1 reference

Human Metabolome Database ID

CHEMBL461278 (English)

5 October 2016

1 reference

HMDB0302822

1 reference

based on heuristic

inferred from InChIKey

1 reference

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

(6S)-dehydrovomifoliol (English)

5 October 2016

1 reference