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Details

Stereochemistry ACHIRAL
Molecular Formula C25H24O6
Molecular Weight 420.4545
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of POMIFERIN

SMILES

CC(C)=CCC1=C2OC(C)(C)C=CC2=C3OC=C(C(=O)C3=C1O)C4=CC(O)=C(O)C=C4

InChI

InChIKey=GHCZYXUOYFOXIP-UHFFFAOYSA-N
InChI=1S/C25H24O6/c1-13(2)5-7-15-21(28)20-22(29)17(14-6-8-18(26)19(27)11-14)12-30-24(20)16-9-10-25(3,4)31-23(15)16/h5-6,8-12,26-28H,7H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C25H24O6
Molecular Weight 420.4545
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
1.0 µM [IC50]
Target ID: P00915
Gene ID: 759.0
Gene Symbol: CA1
Target Organism: Homo sapiens (Human)
471.0 µM [Ki]
Target ID: P00918
Gene ID: 760.0
Gene Symbol: CA2
Target Organism: Homo sapiens (Human)
235.7 µM [Ki]
PubMed

PubMed

TitleDatePubMed
Pomiferin.
2003 Mar
Antioxidant isoflavones in Osage orange, Maclura pomifera (Raf.) Schneid.
2003 Oct 22
Antioxidative and EROD activities of osajin and pomiferin.
2004 Mar
Proteomic profiling of cholangiocarcinoma cell line treated with pomiferin from Derris malaccensis.
2005 Nov
Effects of prenylated isoflavones osajin and pomiferin in premedication on heart ischemia-reperfusion.
2006 Jul
[Protective effects of the flavonoids osajin and pomiferin on heart ischemia-reperfusion].
2006 Jul
Outlook on Thailand's genomics and computational biology research and development.
2008 Jul 25
Cholinesterase inhibitory effects of the extracts and compounds of Maclura pomifera (Rafin.) Schneider.
2009 Aug
Examining the genomic influence of skin antioxidants in vitro.
2010
Isolation, structure, and bioactivities of abiesadines A-Y, 25 new diterpenes from Abies georgei Orr.
2010 Jan 15
Effect of pomiferin administration on kidney ischaemia-reperfusion injury in rats.
2010 Jun
Involvement of 1,25D3-MARRS (membrane associated, rapid response steroid-binding), a novel vitamin D receptor, in growth inhibition of breast cancer cells.
2010 Mar 10
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:44:11 GMT 2023
Edited
by admin
on Fri Dec 15 19:44:11 GMT 2023
Record UNII
74YIS40APM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
POMIFERIN
INCI  
INCI  
Official Name English
4H,8H-BENZO(1,2-B:3,4-B')DIPYRAN-4-ONE, 3-(3,4-DIHYDROXYPHENYL)-5-HYDROXY-8,8-DIMETHYL-6-(3-METHYL-2-BUTENYL)-
Systematic Name English
POMIFERIN [INCI]
Common Name English
3'-HYDROXYOSAJIN
Common Name English
4H,8H-BENZO(1,2-B:3,4-B')DIPYRAN-4-ONE, 3-(3,4-DIHYDROXYPHENYL)-5-HYDROXY-8,8-DIMETHYL-6-(3-METHYL-2-BUTEN-1-YL)-
Systematic Name English
NSC-5113
Code English
Code System Code Type Description
FDA UNII
74YIS40APM
Created by admin on Fri Dec 15 19:44:11 GMT 2023 , Edited by admin on Fri Dec 15 19:44:11 GMT 2023
PRIMARY
PUBCHEM
4871
Created by admin on Fri Dec 15 19:44:11 GMT 2023 , Edited by admin on Fri Dec 15 19:44:11 GMT 2023
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DAILYMED
74YIS40APM
Created by admin on Fri Dec 15 19:44:11 GMT 2023 , Edited by admin on Fri Dec 15 19:44:11 GMT 2023
PRIMARY
MESH
C474837
Created by admin on Fri Dec 15 19:44:11 GMT 2023 , Edited by admin on Fri Dec 15 19:44:11 GMT 2023
PRIMARY
CAS
572-03-2
Created by admin on Fri Dec 15 19:44:11 GMT 2023 , Edited by admin on Fri Dec 15 19:44:11 GMT 2023
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WIKIPEDIA
Pomiferin
Created by admin on Fri Dec 15 19:44:11 GMT 2023 , Edited by admin on Fri Dec 15 19:44:11 GMT 2023
PRIMARY
NSC
5113
Created by admin on Fri Dec 15 19:44:11 GMT 2023 , Edited by admin on Fri Dec 15 19:44:11 GMT 2023
PRIMARY
RXCUI
2593691
Created by admin on Fri Dec 15 19:44:11 GMT 2023 , Edited by admin on Fri Dec 15 19:44:11 GMT 2023
PRIMARY
EPA CompTox
DTXSID00205831
Created by admin on Fri Dec 15 19:44:11 GMT 2023 , Edited by admin on Fri Dec 15 19:44:11 GMT 2023
PRIMARY