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Details

Stereochemistry ACHIRAL
Molecular Formula C17H14O6
Molecular Weight 314.2895
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of JARANOL

SMILES

COC1=CC2=C(C(=O)C(OC)=C(O2)C3=CC=C(O)C=C3)C(O)=C1

InChI

InChIKey=BJBUTJQYZDYRMJ-UHFFFAOYSA-N
InChI=1S/C17H14O6/c1-21-11-7-12(19)14-13(8-11)23-16(17(22-2)15(14)20)9-3-5-10(18)6-4-9/h3-8,18-19H,1-2H3

HIDE SMILES / InChI

Molecular Formula C17H14O6
Molecular Weight 314.2895
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Phytoconstituents from Alpinia purpurata and their in vitro inhibitory activity against Mycobacterium tuberculosis.
2010-10
2-Arylbenzofuran neolignans from the bark of Nectandra purpurascens (Lauraceae).
2010-07
Secondary metabolites from Tectona philippinensis.
2008-06-15
Flavonoids with anti-inflammatory and antinociceptive activity from Cistus laurifolius L. leaves through bioassay-guided procedures.
2007-07-25
New dihydrochalcones and anti-platelet aggregation constituents from the leaves of Muntingia calabura.
2007-06
Prostaglandin inhibitory and antioxidant components of Cistus laurifolius, a Turkish medicinal plant.
2006-12-06
Antioxidant and alpha-amylase inhibitory compounds from aerial parts of Varthemia iphionoides Boiss.
2006-09
Effect of Cistus laurifolius L. leaf extracts and flavonoids on acetaminophen-induced hepatotoxicity in mice.
2006-02-20
Inhibition of mouth skeletal muscle relaxation by flavonoids of Cistus ladanifer L.: a plant defense mechanism against herbivores.
2004-06
[Studies on chemical constituents of sini tang].
2004-05
[Studies on chemical constituents in bud of Artemisia scoparia (III)].
2004-05
Antimycobacterial flavones from Haplopappus sonorensis.
2003-04
Cytotoxic activity of low molecular weight polyphenols against human oral tumor cell lines.
2000-08-23
Substance Class Chemical
Created
by admin
on Mon Mar 31 20:13:10 GMT 2025
Edited
by admin
on Mon Mar 31 20:13:10 GMT 2025
Record UNII
5FAQ11412T
Record Status Validated (UNII)
Record Version
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Name Type Language
3,7-DI-O-METHYL KAEMPFEROL
Preferred Name English
JARANOL
Common Name English
KAEMPFEROL 3,7-O-DIMETHYL ETHER
Common Name English
KAEMPFEROL 3,7-DIMETHYL ETHER
Common Name English
4',5-DIHYDROXY-3,7-DIMETHOXYFLAVONE
Systematic Name English
KUMATAKENIN
Common Name English
5,4'-DIHYDROXY-3,7-DIMETHOXYFLAVONE
Systematic Name English
KAMATAKENIN
Common Name English
KUMATAKENIN A
Common Name English
4H-1-BENZOPYRAN-4-ONE, 5-HYDROXY-2-(4-HYDROXYPHENYL)-3,7-DIMETHOXY-
Systematic Name English
3,7-DIMETHYLKAEMPFEROL
Common Name English
FLAVONE, 4',5-DIHYDROXY-3,7-DIMETHOXY-
Systematic Name English
KUMATAKILLIN
Common Name English
Code System Code Type Description
PUBCHEM
5318869
Created by admin on Mon Mar 31 20:13:11 GMT 2025 , Edited by admin on Mon Mar 31 20:13:11 GMT 2025
PRIMARY
EPA CompTox
DTXSID90186645
Created by admin on Mon Mar 31 20:13:11 GMT 2025 , Edited by admin on Mon Mar 31 20:13:11 GMT 2025
PRIMARY
CAS
3301-49-3
Created by admin on Mon Mar 31 20:13:11 GMT 2025 , Edited by admin on Mon Mar 31 20:13:11 GMT 2025
PRIMARY
WIKIPEDIA
KUMATAKENIN
Created by admin on Mon Mar 31 20:13:11 GMT 2025 , Edited by admin on Mon Mar 31 20:13:11 GMT 2025
PRIMARY
FDA UNII
5FAQ11412T
Created by admin on Mon Mar 31 20:13:11 GMT 2025 , Edited by admin on Mon Mar 31 20:13:11 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
PARENT -> CONSTITUENT ALWAYS PRESENT
JARANOL was tested for antithrombotic activity.