(Q27149418)

Vestitol (English)

8 October 2016

2 references

inferred from InChIKey

based on heuristic

inferred from InChI

chemical formula

C₁₆H₁₆O₄

1 reference

Vestitol (English)

8 October 2016

COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O

1 reference

Vestitol (English)

8 October 2016

COC1=CC(=C(C=C1)[C@H]2CC3=C(C=C(C=C3)O)OC2)O

1 reference

Vestitol (English)

8 October 2016

Dalbergia candenatensis

1 reference

Traditional medicinal plants of Thailand, VIII. Isoflavonoids of Dalbergia candenatensis.

Wisteria brachybotrys

2 references

Isoflavones from the gall and wood of Wisteria brachybotrys

Anti-tumor promoting activities of isoflavonoids from Wistaria brachybotrys

Dalbergia parviflora

1 reference

Flavonoids from the heartwood of the Thai medicinal plant Dalbergia parviflora and their effects on estrogenic-responsive human breast cancer cells

Dalbergia sissoo

1 reference

Nitric oxide production inhibitory activity of flavonoids contained in trunk exudates of Dalbergia sissoo

Glycyrrhiza pallidiflora

2 references

Flavonoids and isoflavonoids of chemotaxonomic significance from Glycyrrhiza pallidiflora (Leguminosae)

Flavonoids and isoflavonoids of chemotaxonomic significance from Glycyrrhiza pallidiflora (Leguminosae)

Medicago rugosa

1 reference

A New isoflavanone phytoalexin from Medicago rugosa

Endosamara racemosa

2 references

An isoflavan from Millettia racemosa

An isoflavan from Millettia racemosa

Centrolobium tomentosum

2 references

Diarylheptanoids and isoflavonoids from Centrolobium species

Diarylheptanoids and isoflavonoids from Centrolobium species

Gliricidia sepium

3 references

Studies on the constituents of Gliricidia sepium (Leguminosae) leaves and roots: isolation and structure elucidation of new triterpenoid saponins and aromatic compounds

Studies on the constituents of Gliricidia sepium (Leguminosae) leaves and roots: isolation and structure elucidation of new triterpenoid saponins and aromatic compounds

New 12a-hydroxyrotenoids from gliricidia sepium bark

Glycyrrhiza uralensis

3 references

Anti-Helicobacter pylori flavonoids from licorice extract

Preliminary evaluation of antinephritis and radical scavenging activities of glabridin from Glycyrrhiza glabra.

Isoflavonoids and coumarins from Glycyrrhiza uralensis: antibacterial activity against oral pathogens and conversion of isoflavans into isoflavan-quinones during purification

Hedysarum polybotrys

2 references

Studies on the constituents of Hedysarum polybotrys Hand.-Mazz.

Studies on the constituents of Hedysarum polybotrys Hand.-Mazz.

Pterocarpus soyauxii

1 reference

Flavonoid analogues from Pterocarpus species

Cadophora gregata

1 reference

Antifungal stress compounds from adzuki bean, Vigna angularis, treated with Cephalosporium gregatum.

Dalbergia odorifera

3 references

Inhibitors of prostaglandin biosynthesis from Dalbergia odorifera

Inhibitors of prostaglandin biosynthesis from Dalbergia odorifera.

Isoflavan and related compounds from Dalbergia odorifera. I.

liquorice

1 reference

Phenolics from Glycyrrhiza glabra roots and their PPAR-gamma ligand-binding activity

Hedysarum theinum

1 reference

Components of the ethylacetate extract of Hedysarum theinum roots

Lotus angustissimus

1 reference

Isolation of a new isoflavan phytoalexin from two Lotus species

Lotus edulis

1 reference

Isolation of a new isoflavan phytoalexin from two Lotus species

Lotus corniculatus

1 reference

Vestitol as a chemical barrier against intrusion of parasitic plant Striga hermonthica into Lotus japonicus roots

Maackia amurensis

1 reference

Polyphenols from Maackia amurensis Root Bark

Vigna angularis

1 reference

Antifungal stress compounds from adzuki bean, Vigna angularis, treated with Cephalosporium gregatum.

Cyclolobium brasiliense

1 reference

Isoflavonoids from Cyclolobium species

Cyclolobium claussenii

1 reference

Isoflavonoids from Cyclolobium species

Identifiers

InChI

InChI=1S/C16H16O4/c1-19-13-4-5-14(15(18)8-13)11-6-10-2-3-12(17)7-16(10)20-9-11/h2-5,7-8,11,17-18H,6,9H2,1H3/t11-/m0/s1

1 reference

XRVFNNUXNVWYTI-NSHDSACASA-N

Vestitol (English)

8 October 2016

2 references

Vestitol (English)

8 October 2016

ChEBI release 2020-09-01

2 references

(-)-vestitol (English)

XRVFNNUXNVWYTI-NSHDSACASA-N

8 October 2016

InChIKey

10 April 2021

https://commonchemistry.cas.org/detail?cas_rn=35878-41-2

1 reference

(3R)-3-(2-Hydroxy-4-methoxyphenyl)-7-chromanol (English)

8 October 2016

1 reference

Vestitol (English)

8 October 2016

Reaxys registry number

6068457

1 reference

(-)-vestitol (English)

8 October 2016

ChEBI ID

80392

mapping relation type

1 reference

(-)-vestitol (English)

8 October 2016

1 reference

CHEMBL479145 (English)

8 October 2016

1 reference

1 reference

Global Substance Registration System

(-)-vestitol (English)

8 October 2016

1 reference

UNII

9JHS2AVR43

VESTITOL, (-)- (English)

8 October 2016

1 reference

(-)-vestitol (English)