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Tectochrysin - 10mM in DMSO, high purity , CAS No.520-28-5
Basic Description
Synonyms
Tectochrysin | 520-28-5 | 5-Hydroxy-7-methoxyflavone | 5-Hydroxy-7-methoxy-2-phenyl-4H-chromen-4-one | Techtochrysin | 7-Methoxy-5-hydroxyflavone | 7-O-METHYLCHRYSIN | Techtochrysine | 4H-1-Benzopyran-4-one, 5-hydroxy-7-methoxy-2-phenyl- | 5-hydroxy-7-methoxy-2-phenylchrom
Specifications & Purity
10mM in DMSO
Biochemical and Physiological Mechanisms
Tectochrysin (Techtochrysin, NSC 80687) is one of the major flavonoids of Alpinia oxyphylla Miquel. Tectochrysin significantly increases the expression of DR3, DR4 and Fas and inhibits activity of NF-κB. Tectochrysin induces apoptotic cell death.
Storage Temp
Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description
Information
Tectochrysin Tectochrysin (Techtochrysin, NSC 80687) is one of the major flavonoids of Alpinia oxyphylla Miquel . Tectochrysin significantly increases the expression of DR3 , DR4 and Fas and inhibits activity of NF-κB . Tectochrysin induces apoptotic cell death.
Targets
NF-κB
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Flavonoids
Subclass
O-methylated flavonoids
Intermediate Tree Nodes
Not available
Direct Parent
7-O-methylated flavonoids
Alternative Parents
Flavones 5-hydroxyflavonoids Chromones Anisoles Pyranones and derivatives Alkyl aryl ethers 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Benzene and substituted derivatives Vinylogous acids Heteroaromatic compounds Oxacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
7-methoxyflavonoid-skeleton - 5-hydroxyflavonoid - Flavone - Hydroxyflavonoid - Chromone - Benzopyran - 1-benzopyran - Anisole - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Pyranone - Monocyclic benzene moiety - Pyran - Benzenoid - Heteroaromatic compound - Vinylogous acid - Oxacycle - Ether - Organoheterocyclic compound - Organic oxygen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 7-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone.
External Descriptors
Flavones and Flavonols
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Product Properties
ALogP
2.878
HBD Count
1
Rotatable Bond
2
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
IUPAC Name
5-hydroxy-7-methoxy-2-phenylchromen-4-one
INCHI
InChI=1S/C16H12O4/c1-19-11-7-12(17)16-13(18)9-14(20-15(16)8-11)10-5-3-2-4-6-10/h2-9,17H,1H3
InChIKey
IRZVHDLBAYNPCT-UHFFFAOYSA-N
Smiles
COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O
Isomeric SMILES
COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O
PubChem CID
5281954
Molecular Weight
268.26
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
DMSO(mg / mL) Max Solubility
7
DMSO(mM) Max Solubility
26.0940878252442
Water(mg / mL) Max Solubility
-1
Molecular Weight
268.260 g/mol
XLogP3
2.400
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
2
Exact Mass
268.074 Da
Monoisotopic Mass
268.074 Da
Topological Polar Surface Area
55.800 Ų
Heavy Atom Count
20
Formal Charge
0
Complexity
397.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
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