(Q27108480)

Trifolirhizin (English)

(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[[(1R,12R)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-16-yl]oxy]oxane-3,4,5-triol

5 October 2016

stereoisomer of

2 references

inferred from InChIKey

(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[[(1S,12S)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-16-yl]oxy]oxane-3,4,5-triol

2 references

inferred from InChIKey

(2S,3R,4R,5S,6R)-2-(hydroxymethyl)-6-[[(1R,12R)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-16-yl]oxy]oxane-3,4,5-triol

1 reference

(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(1R,12R)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-16-yl]oxy]oxane-3,4,5-triol

1 reference

chemical formula

C₂₂H₂₂O₁₀

1 reference

Trifolirhizin (English)

5 October 2016

canonical SMILES

C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6

1 reference

Trifolirhizin (English)

5 October 2016

isomeric SMILES

C1[C@@H]2[C@H](C3=C(O1)C=C(C=C3)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6

1 reference

Phenolic compounds of Ononis arvensis. III

Trifolirhizin (English)

5 October 2016

1 reference

Cicer mogoltavicum

1 reference

Isoflavonoids ofCiver mogoltavicum

Maackia amurensis

1 reference

A prenylated flavanone from roots of Maackia amurensis subsp. Buergeri

Euchresta formosana

3 references

Cytotoxic coumaronochromones from the roots of Euchresta formosana.

Cytotoxic coumaronochromones from the roots of Euchresta formosana.

Antiplatelet and Anti-HIV Constituents from Euchresta Formosana

Glycyrrhiza pallidiflora

3 references

Flavonoids from Glycyrrhiza pallidiflora hairy root cultures

Flavonoids from Glycyrrhiza pallidiflora hairy root cultures

Flavonoids from Glycyrrhiza pallidiflora hairy root cultures

Cicer judaicum

2 references

Isoflavenes from the roots of Cicer judaicum

Isoflavenes from the roots of Cicer judaicum

Ononis natrix

1 reference

Resorcinol Derivatives and Flavonoids ofOnonisnatrixSubspeciesramosissima

Ononis vaginalis

1 reference

Phenolic constituents of Ononis vaginalis roots

Sophora alopecuroides

3 references

Structures of two new flavanones fromVexibia alopecuroides

Flavonoids ofVexibia 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

Trifolium pratense

1 reference

Trifolirhizin and maackiain in red clover: changes in Fusarium roseum “Avenaceum”-infected roots and in vitro effects on the pathogen

Styphnolobium japonicum

1 reference

A new isoflavone glycoside from the stem bark of Sophora japonica

Sophora flavescens

10 references

Monoamine oxidase inhibitory components from the roots of Sophora flavescens

A new prenylated flavonol from the roots of Sophora flavescens

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

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

Prenylated Flavanone Production in Callus Cultures of Sophoraßavescens var. angustifolia

Inhibitory effects of kurarinol, kuraridinol, and trifolirhizin from Sophora flavescens on tyrosinase and melanin synthesis

A New Prenylated Flavanonol from the Roots of Sophora flavescens

Ononis spinosa

1 reference

Isolation of Trifolirhizin from Ononis spinosa L

Sophora flavescens var. flavescens

1 reference

Localization of Prenylated Flavonoids in Sophora flavescens var. angustifolia Plants

Sophora tonkinensis var. tonkinensis

1 reference

A new pterocarpan, (-)-maackiain sulfate, from the roots of Sophora subprostrata

Identifiers

InChI

InChI=1S/C22H22O10/c23-6-17-18(24)19(25)20(26)22(32-17)30-9-1-2-10-13(3-9)27-7-12-11-4-15-16(29-8-28-15)5-14(11)31-21(10)12/h1-5,12,17-26H,6-8H2/t12-,17+,18+,19-,20+,21-,22+/m0/s1

1 reference

Trifolirhizin (English)

VGSYCWGXBYZLLE-QEEQPWONSA-N

5 October 2016

InChIKey

2 references

Trifolirhizin (English)

5 October 2016

ChEBI release 2020-09-01

2 references

Trifolirhizin (English)

VGSYCWGXBYZLLE-QEEQPWONSA-N

5 October 2016

InChIKey

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=6807-83-6

1 reference

(6aR,12aR)-6a,12a-Dihydro-6H-[1,3]dioxolo[5,6][1]benzofuro[3,2-c]chromen-3-yl beta-D-glucopyranoside (English)

5 October 2016

1 reference

Trifolirhizin (English)

5 October 2016

ChEBI ID

9714

mapping relation type

1 reference

Trifolirhizin (English)

5 October 2016

1 reference

splash10-0udi-0920000000-5d15bcf978390bbdb00b

TRIFOLIRHIZIN (English)

5 October 2016

1 reference

0 references

DSSTox substance ID

DTXSID70987516

0 references

DSSTOX compound identifier

DTXCID501414675

0 references

EC number

804-190-3

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.230.928

27 December 2018

ECHA Substance Infocard ID

[No public or meaningful name is available] (English)

quotation

CAS no.: 6807-83-6 (English)

100.230.928

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.230.928

27 December 2018

Human Metabolome Database ID

[No public or meaningful name is available] (English)

quotation

CAS no.: 6807-83-6 (English)

HMDB0303946

1 reference

inferred from InChIKey

1 reference

Trifolirhizin (English)

5 October 2016

0 references

1 reference

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

Trifolirhizin (English)

5 October 2016

1 reference