(Q7563137)

(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one

Vexibinol (English)

6 October 2016

1 reference

based on heuristic

inferred from InChI

(2R)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₅H₂₈O₆

1 reference

Vexibinol (English)

6 October 2016

CC(=CCC(CC1=C(C=C(C2=C1OC(CC2=O)C3=C(C=C(C=C3)O)O)O)O)C(=C)C)C

1 reference

Vexibinol (English)

6 October 2016

CC(=CC[C@H](CC1=C(C=C(C2=C1O[C@@H](CC2=O)C3=C(C=C(C=C3)O)O)O)O)C(=C)C)C

1 reference

Three flavanones with a lavandulyl group in the roots of Sophora exigua

Vexibinol (English)

6 October 2016

5 references

Inhibition of the growth of cariogenic bacteria in vitro by plant flavanones

Antibacterial activity of flavanone isolated fromSophora exigua against methicillin-resistantStaphylococcus aureus and its combination with antibiotics

Occurrence of prenylated flavonoids and oligostilbenes and its significance for chemotaxonomy of genus Sophora (Leguminosae)

Reduction of membrane fluidity by antibacterial sophoraflavanone G isolated from Sophora exigua

Sophora leachiana

2 references

Occurrence of prenylated flavonoids and oligostilbenes and its significance for chemotaxonomy of genus Sophora (Leguminosae)

Two flavanones in Sophora leachiano and some related structures

Sophora moorcroftiana

3 references

Occurrence of prenylated flavonoids and oligostilbenes and its significance for chemotaxonomy of genus Sophora (Leguminosae)

Studies on the constituents of Sophora species. XXII. Constituents of the root of Sophora moorcroftiana BENTH. ex BAKER.(1).

Studies on the constituents of Sophora species. XXII. Constituents of the root of Sophora moorcroftiana BENTH. ex BAKER.(1).

Sophora stenophylla

1 reference

Phenolic Compounds Isolated from the Roots of Sophora stenophylla.

Sophora pachycarpa

1 reference

Flavonoids from Sophora griffithii and Goebelia pachycarpa

Sophora flavescens

20 references

Two New Lavandulyl Flavonoids from Sophora flavescens

Anti-allergic prenylated flavonoids from the roots of Sophora flavescens

Re-evaluation of the antioxidant prenylated flavonoids from the roots of Sophora flavescens

A novel flavonoid from Sophora flavescens

Efficient production and capture of 8-prenylnaringenin and leachianone G-biosynthetic intermediates of sophoraflavanone G--by the addition of cork tissue to cell suspension cultures of Sophora flavescens

Studies on the Constituents of Sophora flavescens AIT. IV

Activity of Ku Shen compounds againstStaphylococcus aureus andStreptococcus mutans

Determination of isoprenyl and lavandulyl positions of flavonoids fromSophora flavescens by NMR experiment

A cytotoxic constituent fromSophora flavescens

Occurrence of prenylated flavonoids and oligostilbenes and its significance for chemotaxonomy of genus Sophora (Leguminosae)

Tyrosinase inhibitory prenylated flavonoids from Sophora flavescens

Prenylated flavonoids from the roots of Sophora flavescens with tyrosinase inhibitory activity

Antiulcer action of Sophora flavescens root and an active constituent. I

Vasodilatory active principles of Sophora flavescens root

Origin of two isoprenoid units in a lavandulyl moiety of sophoraflavanone G from Sophora flavescens cultured cells

Lavandulylflavonoids: a new class of in vitro apoptogenic agents from Sophora flavescens

Cytotoxic lavandulyl flavanones from Sophora flavescens

Identification and characterization of antioxidants from Sophora flavescens.

A new flavonoid from Sophora flavescens Ait.

The structure of kushenol M fromSophora flavescens

Sophora alopecuroides

5 references

Six flavonostilbenes and a flavanone in roots of Sophora alopecuroides

Occurrence of prenylated flavonoids and oligostilbenes and its significance for chemotaxonomy of genus Sophora (Leguminosae)

Structures of two new flavanones fromVexibia alopecuroides

Chemical constituents isolated from the Mongolian medicinal plant Sophora alopecuroides L. and their inhibitory effects on LPS-induced nitric oxide production in RAW 264.7 macrophages

Sophoraflavanone G from Sophora alopecuroides inhibits lipopolysaccharide-induced inflammation in RAW264.7 cells by targeting PI3K/Akt, JAK/STAT and Nrf2/HO-1 pathways.

Sophora flavescens var. flavescens

1 reference

Localization of Prenylated Flavonoids in Sophora flavescens var. angustifolia Plants

Sophora davidii

1 reference

Stilbene oligomers in roots of Sophora davidii

1 reference

Identifiers

InChI

InChI=1S/C25H28O6/c1-13(2)5-6-15(14(3)4)9-18-20(28)11-21(29)24-22(30)12-23(31-25(18)24)17-8-7-16(26)10-19(17)27/h5,7-8,10-11,15,23,26-29H,3,6,9,12H2,1-2,4H3/t15-,23+/m1/s1

1 reference

Vexibinol (English)

6 October 2016

2 references

Vexibinol (English)

6 October 2016

ChEBI release 2020-09-01

2 references

sophoraflavanone G (English)

6 October 2016

https://commonchemistry.cas.org/detail?cas_rn=97938-30-2

10 April 2021

1 reference

Sophoraflavanone G (English)

6 October 2016

2 references

Vexibinol (English)

6 October 2016

Reaxys registry number

8594725

1 reference

sophoraflavanone G (English)

6 October 2016

ChEBI ID

50209

mapping relation type

2 references

sophoraflavanone G (English)

6 October 2016

International Chemical Identifier

InChI

InChI=1S/C25H28O6/c1-13(2)5-6-15(14(3)4)9-18-20(28)11-21(29)24-22(30)12-23(31-25(18)24)17-8-7-16(26)10-19(17)27/h5,7-8,10-11,15,23,26-29H,3,6,9,12H2,1-2,4H3/t15-,23+/m1/s1

1 reference

SOPHORAFLAVANONE G (English)

6 October 2016

2 references

inferred from InChIKey

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

1 reference

2 references

DSSTOX compound identifier

0 references

0 references

1 reference