CHEBI:9050 - sciadopitysin

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ChEBI Name sciadopitysin
ChEBI ID CHEBI:9050
Definition A biflavonoid that is a 7, 4', 4'''-trimethyl ether derivative of amentoflavone.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C33H24O10
Net Charge 0
Average Mass 580.53770
Monoisotopic Mass 580.13695
InChI InChI=1S/C33H24O10/c1-39-18-7-4-16(5-8-18)27-15-25(38)32-23(36)13-22(35)30(33(32)43-27)20-10-17(6-9-26(20)41-3)28-14-24(37)31-21(34)11-19(40-2)12-29(31)42-28/h4-15,34-36H,1-3H3
InChIKey YCXRBCHEOFVYEN-UHFFFAOYSA-N
SMILES COc1ccc(cc1)-c1cc(=O)c2c(O)cc(O)c(-c3cc(ccc3OC)-c3cc(=O)c4c(O)cc(OC)cc4o3)c2o1
Roles Classification
Application(s): bone density conservation agent
An agent that inhibits bone resorption and/or favor bone mineralization and bone regeneration. Used to heal bone fractures and to treat bone diseases such as osteopenia and osteoporosis.
platelet aggregation inhibitor
A drug or agent which antagonizes or impairs any mechanism leading to blood platelet aggregation, whether during the phases of activation and shape change or following the dense-granule release reaction and stimulation of the prostaglandin-thromboxane system.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing sciadopitysin (CHEBI:9050) has functional parent amentoflavone (CHEBI:2631)
sciadopitysin (CHEBI:9050) has role bone density conservation agent (CHEBI:50646)
sciadopitysin (CHEBI:9050) has role platelet aggregation inhibitor (CHEBI:50427)
sciadopitysin (CHEBI:9050) is a biflavonoid (CHEBI:50128)
sciadopitysin (CHEBI:9050) is a hydroxyflavone (CHEBI:24698)
sciadopitysin (CHEBI:9050) is a methoxyflavone (CHEBI:25241)
sciadopitysin (CHEBI:9050) is a ring assembly (CHEBI:36820)
IUPAC Name
5,7-dihydroxy-8-[5-(5-hydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2-methoxyphenyl]-2-(4-methoxyphenyl)-4H-chromen-4-one
Synonyms Sources
5,7-dihydroxy-8-(5-(5-hydroxy-7-methoxy-4-oxo-4H-1- benzopyran-2-yl)-2-methoxyphenyl)-2-(4-methoxyphenyl)-4- benzopyrone ChEBI
Amentoflavone-7,4',4'''-trimethyl ether ChemIDplus
Sciadopitysin KEGG COMPOUND
Manual Xrefs Databases
C00001098 KNApSAcK
C10182 KEGG COMPOUND
LMPK12040006 LIPID MAPS
NZ563818 Patent
View more database links
Registry Numbers Types Sources
381493 Reaxys Registry Number Reaxys
521-34-6 CAS Registry Number KEGG COMPOUND
521-34-6 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
16574412 PubMed citation Europe PMC
16644528 PubMed citation Europe PMC
22981471 PubMed citation Europe PMC
345599 Chinese Abstracts citation Europe PMC
7623623 PubMed citation Europe PMC
Last Modified
28 July 2014