(Q27135170)

inferred from SMILES

mass

438.204±0 dalton

1 reference

leachianone A (English)

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

7 October 2016

stereoisomer of

2 references

inferred from InChIKey

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

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₂₆H₃₀O₆

1 reference

leachianone A (English)

7 October 2016

canonical SMILES

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

1 reference

leachianone A (English)

7 October 2016

isomeric SMILES

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

1 reference

Anti-allergic prenylated flavonoids from the roots of Sophora flavescens

leachianone A (English)

7 October 2016

10 references

Two New Lavandulyl Flavonoids from Sophora flavescens

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

Cytotoxic lavandulyl flavanones from Sophora flavescens

Binding of flavonoids from Sophora flavescens to the rat uterine estrogen receptor

BACE1 inhibitory effects of lavandulyl flavanones from Sophora flavescens

Cytotoxic lavandulyl flavanones from Sophora flavescens

Antibacterial and antiandrogen flavonoids from Sophora flavescens

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

Vasorelaxant prenylated flavonoids from the roots of Sophora flavescens

Sophora alopecuroides

3 references

Six flavonostilbenes and a flavanone in roots of Sophora alopecuroides

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

Sophora davidii

2 references

Stilbene oligomers in roots of Sophora davidii

Stilbene oligomers in roots of Sophora davidii

Sophora leachiana

2 references

Two flavanones in Sophora leachiano and some related structures

Two flavanones in Sophora leachiano and some related structures

Sophora stenophylla

2 references

Phenolic Compounds Isolated from the Roots of Sophora stenophylla.

Phenolic Compounds Isolated from the Roots of Sophora stenophylla.

Sophora

1 reference

Leachianone A as a potential anti-cancer drug by induction of apoptosis in human hepatoma HepG2 cells.

Identifiers

InChI

InChI=1S/C26H30O6/c1-14(2)6-7-16(15(3)4)10-19-20(28)12-21(29)25-22(30)13-24(32-26(19)25)18-9-8-17(27)11-23(18)31-5/h6,8-9,11-12,16,24,27-29H,3,7,10,13H2,1-2,4-5H3/t16-,24+/m1/s1

1 reference

leachianone A (English)

YLTPWCZXKJSORQ-GYCJOSAFSA-N

7 October 2016

InChIKey

2 references

leachianone A (English)

7 October 2016

ChEBI release 2020-09-01

CAS Registry Number

97938-31-3

1 reference

CAS (formerly Chemical Abstracts Service)

25 January 2022

1 reference

(2S)-5,7-Dihydroxy-2-(4-hydroxy-2-methoxyphenyl)-8-[(2R)-2-isopropenyl-5-methyl-4-hexen-1-yl]-2,3-dihydro-4H-chromen-4-one (English)

7 October 2016

2 references

leachianone A (English)

matched by identifier from

7 October 2016

InChIKey

YLTPWCZXKJSORQ-GYCJOSAFSA-N

Reaxys registry number

8594952

1 reference

leachianone A (English)

7 October 2016

ChEBI ID

66559

mapping relation type

2 references

leachianone A (English)

matched by identifier from

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C26H30O6/c1-14(2)6-7-16(15(3)4)10-19-20(28)12-21(29)25-22(30)13-24(32-26(19)25)18-9-8-17(27)11-23(18)31-5/h6,8-9,11-12,16,24,27-29H,3,7,10,13H2,1-2,4-5H3/t16-,24+/m1/s1

1 reference