(Q27095092)

(2S)-7-hydroxyflavanone (English)

19 October 2016

stereoisomer of

(2R)-7-hydroxyflavanone

1 reference

based on heuristic

inferred from InChI

chemical formula

C₁₅H₁₂O₃

1 reference

(2S)-7-hydroxyflavanone (English)

20 November 2016

canonical SMILES

C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3

1 reference

(2S)-7-hydroxyflavanone (English)

20 November 2016

isomeric SMILES

C1[C@H](OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3

1 reference

(2S)-7-hydroxyflavanone (English)

20 November 2016

found in taxon

Pterocarpus marsupium

1 reference

Constituents of Pterocarpus marsupium

Virgilia oroboides

1 reference

Flavonoids and isoflavonoids from the heartwood ofVirgilia oroboides

Virola surinamensis

2 references

Antifungal constituents from roots of Virolasurinamensis

Antifungal constituents from roots of Virolasurinamensis

Vachellia vernicosa

1 reference

Flavonoids from the exudate of Acacia neovernicosa

Ceratiola ericoides

1 reference

Ceratiolin and other flavonoids from Ceratiola ericoides

Crinum asiaticum

1 reference

Chemical constituents of Crinum asiaticum L. var. sinicum Baker and their cytotoxic activities

Cryptocarya chinensis

1 reference

Cytotoxic flavonoids from the leaves of Cryptocarya chinensis

Dalbergia cochinchinensis

1 reference

Phenolic constituents from Dalbergia cochinchinensis

Dalbergia sissoo

1 reference

Nitric oxide production inhibitory activity of flavonoids contained in trunk exudates of Dalbergia sissoo

Dracaena cinnabari

1 reference

Flavonoids of dragon's blood from Dracaena cinnabari

Muntingia calabura

2 references

Cytotoxic chalcones and flavonoids from the leaves of Muntingia calabura

Activity-guided isolation of the chemical constituents of Muntingia calabura using a quinone reductase induction assay.

Oxytropis falcata

1 reference

Flavonoids in the Poisonous Plant Oxytropis falcata

Zuccagnia punctata

2 references

Argentinean propolis from Zuccagnia punctata Cav. (Caesalpinieae) exudates: phytochemical characterization and antifungal activity.

Antifungal chalcones and new caffeic acid esters from Zuccagnia punctata acting against soybean infecting fungi.

Propolis

2 references

Cytotoxic constituents from Brazilian red propolis and their structure-activity relationship.

Constituents of Brazilian red propolis and their preferential cytotoxic activity against human pancreatic PANC-1 cancer cell line in nutrient-deprived condition.

Identifiers

InChI

InChI=1S/C15H12O3/c16-11-6-7-12-13(17)9-14(18-15(12)8-11)10-4-2-1-3-5-10/h1-8,14,16H,9H2/t14-/m0/s1

1 reference

(2S)-7-hydroxyflavanone (English)

20 November 2016

2 references

(2S)-7-hydroxyflavanone (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

2545-13-3

2 references

Global Substance Registration System

UNII

MF98742K2H

(S)-7-hydroxyflavanone (English)

20 November 2016

https://commonchemistry.cas.org/detail?cas_rn=2545-13-3

9 April 2021

1 reference

(2S)-7-Hydroxy-2-phenyl-2,3-dihydro-4H-chromen-4-one (English)

20 November 2016

2 references

(2S)-7-hydroxyflavanone (English)

20 November 2016

Reaxys registry number

7134185

1 reference

(2S)-7-hydroxyflavanone (English)

19 October 2016

ChEBI ID

41888

mapping relation type

2 references

CHEMBL402744 (English)

20 November 2016

International Chemical Identifier

InChI

InChI=1S/C15H12O3/c16-11-6-7-12-13(17)9-14(18-15(12)8-11)10-4-2-1-3-5-10/h1-8,14,16H,9H2/t14-/m0/s1

1 reference

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

CHEMBL402744 (English)

20 November 2016

1 reference

2 references

DSSTOX compound identifier

DTXCID60302052

0 references

DrugBank ID

DB04274

1 reference

UNII

MF98742K2H

2 references

Global Substance Registration System

UNII

MF98742K2H

(S)-7-hydroxyflavanone (English)

20 November 2016

0 references

0 references

1 reference

1FM8 (English)