| Weight | 270.24 g/mol |
|---|---|
| Formula | C15H10O5 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 1 |
apigenin (520-36-5)
Score:
#428 in Biochemistry
,
#1431 in Biology
,
#1676 in Chemistry
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- Flavonoid (Myricetin, Quercetin, Kaempferol, Luteolin, and Apigenin) Content of Edible Tropical Plants (Journal of Agricultural and Food Chemistry, 2001)
- Suppression of inducible cyclooxygenase and inducible nitric oxide synthase by apigenin and related flavonoids in mouse macrophages (Carcinogenesis, 1999)
- Induction of apoptosis by apigenin and related flavonoids through cytochrome c release and activation of caspase-9 and caspase-3 in leukaemia HL-60 cells (European Journal of Cancer, 1999)
- FLAVONOIDS APIGENIN AND QUERCETIN INHIBIT MELANOMA GROWTH AND METASTATIC POTENTIAL (International Journal of Cancer, 2000)
- Apigenin and cancer chemoprevention: Progress, potential and promise (Review) (International Journal of Oncology, 2007)
- Apigenin: A Promising Molecule for Cancer Prevention (Pharmaceutical Research, 2010)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O
-
InChIKeyKZNIFHPLKGYRTM-UHFFFAOYSA-N
- Pubchem - apigenin
- Wikipedia - apigenin
Apigenin (4,5,7-trihydroxyflavone), found in many plants, is a natural product belonging to the flavone class that is the aglycone of several naturally occurring glycosides. It is a yellow crystalline solid that has been used to dye wool.
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