(Q27134672)

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

Kurarinone (English)

7 October 2016

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₆H₃₀O₆

1 reference

Kurarinone (English)

7 October 2016

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

1 reference

Kurarinone (English)

7 October 2016

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

1 reference

Acyl secoiridoids and antifungal constituents from Gentiana macrophylla.

Kurarinone (English)

7 October 2016

2 references

Acyl secoiridoids and antifungal constituents from Gentiana macrophylla.

Sophora flavescens

23 references

Cytotoxic lavandulyl flavanones from Sophora flavescens

BACE1 inhibitory effects of lavandulyl flavanones from Sophora flavescens

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

Cytotoxic lavandulyl flavanones from Sophora flavescens

Tyrosinase inhibitory prenylated flavonoids from Sophora flavescens

Antibacterial and antiandrogen flavonoids from Sophora flavescens.

Estrogenic and anticarcinogenic properties of kurarinone, a lavandulyl flavanone from the roots of Sophora flavescens.

In vitro sortase A inhibitory and antimicrobial activity of flavonoids isolated from the roots of Sophora flavescens.

Identification and characterization of antioxidants from Sophora flavescens.

A novel flavonoid from Sophora flavescens

Na+-glucose cotransporter (SGLT) inhibitory flavonoids from the roots of Sophora flavescens

In vitro inhibition of diacylglycerol acyltransferase by prenylflavonoids from Sophora flavescens

Kurarinol, tyrosinase inhibitor isolated from the root of Sophora flavescens

A new flavonoid from Sophora flavescens Ait.

A new prenylated flavanone from the roots of Sophora flavescens

Activity of Ku Shen compounds againstStaphylococcus aureus andStreptococcus mutans

In vitro antitumour activity of flavonoids from Sophora flavescens

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

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

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

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

Vasodilatory active principles of Sophora flavescens root

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

Albizia julibrissin

1 reference

Isolation of flavonoids and a cerebroside from the stem bark of Albizzia julibrissin

Identifiers

InChI

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

1 reference

LTTQKYMNTNISSZ-MWTRTKDXSA-N

Kurarinone (English)

7 October 2016

2 references

Kurarinone (English)

7 October 2016

ChEBI release 2020-09-01

CAS Registry Number

34981-26-5

1 reference

CAS (formerly Chemical Abstracts Service)

25 January 2022

1 reference

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

7 October 2016

1 reference

Kurarinone (English)

retrieved

7 October 2016

Reaxys registry number

9739392

1 reference

(2S)-(-)-kurarinone (English)

retrieved

7 October 2016

ChEBI ID

66150

mapping relation type

1 reference

(2S)-(-)-kurarinone (English)

7 October 2016

1 reference

0 references

1 reference