(Q104399815)

English

(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

chemical compound

In more languages

Statements

type of chemical entity

0 references

Sophoraflavone G

1 reference

based on heuristic

inferred from SMILES

424.188588616 dalton

1 reference

based on heuristic

inferred from SMILES

stereoisomer of

sophoraflavanone G

2 references

based on heuristic

inferred from InChIKey

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

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canonical SMILES

O=C1C2=C(O)C=C(O)C(=C2OC(C3=CC=C(O)C=C3O)C1)CC(C(=C)C)CC=C(C)C

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isomeric SMILES

C=C(C)[C@@H](CC=C(C)C)Cc1c(O)cc(O)c2c1O[C@H](c1ccc(O)cc1O)CC2=O

0 references

Sophora flavescens

7 references

Flavonoids in Sophora Species

Inhibition of adenosine 3',5'-cyclic monophosphate phosphodiesterase by components of Sophora flavescens Aiton

BACE1 inhibitory effects of lavandulyl flavanones from Sophora flavescens

Cytotoxic lavandulyl flavanones from Sophora flavescens

Antibacterial and antiandrogen flavonoids from Sophora flavescens

A novel flavonoid from Sophora flavescens

Inhibition of adenosine 3',5'-cyclic monophosphate phosphodiesterase by components of Sophora flavescens Aiton

Sophora alopecuroides

1 reference

Six flavonostilbenes and a flavanone in roots of Sophora alopecuroides

1 reference

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

Sophora moorcroftiana

1 reference

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.

Identifiers

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-/m0/s1

0 references

XRYVAQQLDYTHCL-WNSKOXEYSA-N

0 references

1 reference

17 September 2022

based on heuristic

inferred from InChIKey

UniChem compound ID

1 reference

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