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Flavonoids

Polyphenolic organic compounds that have 15 carbons with the general structure of two phenyl rings and a heterocyclic ring, or a ring with two or more atoms. Flavonoids are a class of polyphenolic plant and fungus secondary metabolites.
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1

7-Hydroxyflavanone 98.0+%, TCI America™

CAS: 6515-36-2 Molecular Formula: C15H12O3 Molecular Weight (g/mol): 240.258 MDL Number: MFCD00017487 InChI Key: SWAJPHCXKPCPQZ-UHFFFAOYSA-N Synonym: 7-hydroxyflavanone,7-hydroxy-2-phenylchroman-4-one,chembl97542,7-hydroxy-2-phenyl-4-chromanone,7-hydroxy-2-phenyl-2,3-dihydro-4h-chromen-4-one,2,3-dihydro-7-hydroxy-2-phenyl-4h-1-benzopyran-4-one,4h-1-benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-phenyl,7-hydroxy-flavanone,d05zpo PubChem CID: 1890 ChEBI: CHEBI:34483 IUPAC Name: 7-hydroxy-2-phenyl-2,3-dihydrochromen-4-one SMILES: C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3

PubChem CID 1890
CAS 6515-36-2
Molecular Weight (g/mol) 240.258
ChEBI CHEBI:34483
MDL Number MFCD00017487
SMILES C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3
Synonym 7-hydroxyflavanone,7-hydroxy-2-phenylchroman-4-one,chembl97542,7-hydroxy-2-phenyl-4-chromanone,7-hydroxy-2-phenyl-2,3-dihydro-4h-chromen-4-one,2,3-dihydro-7-hydroxy-2-phenyl-4h-1-benzopyran-4-one,4h-1-benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-phenyl,7-hydroxy-flavanone,d05zpo
IUPAC Name 7-hydroxy-2-phenyl-2,3-dihydrochromen-4-one
InChI Key SWAJPHCXKPCPQZ-UHFFFAOYSA-N
Molecular Formula C15H12O3
2

eMolecules​ 7-Hydroxyflavanone | 6515-36-2 | MFCD00017487 | 5g

Combi-Blocks, Inc. | 7-Hydroxyflavanone | 5g | 603145398 | QC-9267 | 98.000 | 6515-36-2 | MFCD00017487 | 240.258 | C15H12O3

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3

Medchemexpress LLC 4H-1-benzopyran-4-one, 5,7-dihydroxy-2-(4-hydroxyphenyl)- | 520-36-5 | 270.24 | 200 MG
SDP

Apigenin (4',5,7-Trihydroxyflavone) is a competitive CYP2C9 inhibitor with a Ki of 2 μM. It inhibits cytochrome P450 2C9 (CYP2C9) with a Ki of 2 μM in the CYP2C9 RECO system, a purified, reconstituted enzyme system. This natural flavonoid possesses broad biological properties including antioxidative, anti-inflammatory, anticancer, and neuroprotective effects.

  • Inhibits cell proliferation
  • Suppresses clone formation of SGC-7901 cells
  • Alleviates Adriamycin-induced myocardial injury
  • Reduces serum aspartate amino transferase (AST) release
  • Reduces serum lactate dehydrogenase (LDH) release
  • Reduces serum creatine kinase (CK) contents

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4

Accela Chembio Inc 5 | 7-dihydroxy-2-(4-hydroxyphenyl)-4h-chromen-4-one | 5g | 520-36-5 | MFCD00006831 | 97+% | Shelf Life: 900 Days | Nitrogen Or Argon/store In Freezer(-20) Upon Receipt
SDP

5 | 7-dihydroxy-2-(4-hydroxyphenyl)-4h-chromen-4-one | 5g | 520-36-5 | MFCD00006831 | 97+% | Shelf Life: 900 Days | Nitrogen Or Argon/store In Freezer(-20) Upon Receipt

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