(Q105290095)

English

Bavachinin

chemical compound

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Statements

type of chemical entity

0 references

6C-substituted flavanone

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8C-prenylflavanone

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6C-prenylflavanone

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338.151809184 dalton

1 reference

based on heuristic

inferred from SMILES

chemical formula

C₂₁H₂₂O₄

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canonical SMILES

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

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isomeric SMILES

COc1cc2c(cc1CC=C(C)C)C(=O)C[C@@H](c1ccc(O)cc1)O2

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Cullen corylifolia

5 references

Prenylflavones from Psoralea corylifolia inhibit nitric oxide synthase expression through the inhibition of I-kappaB-alpha degradation in activated microglial cells

Bioactive constituents from Chinese natural medicines. XX. Inhibitors of antigen-induced degranulation in RBL-2H3 cells from the seeds of Psoralea corylifolia.

Antibacterial prenylflavone derivatives from Psoralea corylifolia, and their structure-activity relationship study

Fingerprint analysis of Psoralea corylifolia L. by HPLC and LC-MS.

Characterization of Compounds in Psoralea corylifolia Using High-Performance Liquid Chromatography Diode Array Detection, Time-of-Flight Mass Spectrometry and Quadrupole Ion Trap Mass Spectrometry

Cullen corylifolium

5 references

Prenylflavones from Psoralea corylifolia inhibit nitric oxide synthase expression through the inhibition of I-kappaB-alpha degradation in activated microglial cells

Bioactive constituents from Chinese natural medicines. XX. Inhibitors of antigen-induced degranulation in RBL-2H3 cells from the seeds of Psoralea corylifolia.

Antibacterial prenylflavone derivatives from Psoralea corylifolia, and their structure-activity relationship study

Fingerprint analysis of Psoralea corylifolia L. by HPLC and LC-MS.

Characterization of Compounds in Psoralea corylifolia Using High-Performance Liquid Chromatography Diode Array Detection, Time-of-Flight Mass Spectrometry and Quadrupole Ion Trap Mass Spectrometry

Identifiers

InChI=1S/C21H22O4/c1-13(2)4-5-15-10-17-18(23)11-20(14-6-8-16(22)9-7-14)25-21(17)12-19(15)24-3/h4,6-10,12,20,22H,5,11H2,1-3H3/t20-/m0/s1

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VOCGSQHKPZSIKB-FQEVSTJZSA-N

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CAS Registry Number

1 reference

CAS (formerly Chemical Abstracts Service)

25 January 2022

2 references

17 September 2022

based on heuristic

inferred from InChIKey

matched by identifier from

VOCGSQHKPZSIKB-FQEVSTJZSA-N

mapping relation type

2 references

ChEBI release 2022-06-13

matched by identifier from

International Chemical Identifier

InChI=1S/C21H22O4/c1-13(2)4-5-15-10-17-18(23)11-20(14-6-8-16(22)9-7-14)25-21(17)12-19(15)24-3/h4,6-10,12,20,22H,5,11H2,1-3H3/t20-/m0/s1

UniChem compound ID

1 reference

1 reference

matched by identifier from

VOCGSQHKPZSIKB-FQEVSTJZSA-N

Probes And Drugs ID

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