| Weight | 268.224 g/mol |
|---|---|
| Formula | C15H8O5 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 4 |
| Rotatable Bonds | 0 |
COUMESTROL (479-13-0)
Score:
#1546 in Biochemistry
,
#3574 in Biology
,
#4487 in Chemistry
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- Isotope Dilution Gas ChromatographicMass Spectrometric Method for the Determination of Isoflavonoids, Coumestrol, and Lignans in Food Samples (Analytical Biochemistry, 1996)
- Coumestrol, a new estrogen isolated from forage crops. (Science, 1957)
- Regulation of estrogen receptor beta mRNA in the brain: opposite effects of 17-estradiol and the phytoestrogen, coumestrol (Molecular Brain Research, 1999)
- THE INTERACTION IN THE IMMATURE MOUSE OF POTENT OESTROGENS WITH COUMESTROL, GENISTEIN AND OTHER UTERO-VAGINOTROPHIC COMPOUNDS OF LOW POTENCY (Journal of Endocrinology, 1966)
- AFFINITY OF RABBIT UTERINE OESTRADIOL RECEPTOR FOR PHYTO-OESTROGENS AND ITS USE IN A COMPETITIVE PROTEIN-BINDING RADIOASSAY FOR PLASMA COUMESTROL (Reproduction, 1972)
- An efficient synthesis of coumestrol and coumestans by iodocyclization and pd-catalyzed intramolecular lactonization (Journal of Organic Chemistry, 2005)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C(C=C1O)OC3=C2C(=O)OC4=C3C=CC(=C4)O
-
InChIKeyZZIALNLLNHEQPJ-UHFFFAOYSA-N
- Pubchem - COUMESTROL
- Wikipedia - coumestrol
Coumestrol is a natural organic compound in the class of phytochemicals known as coumestans. Coumestrol was first identified as a compound with estrogenic properties by E. M.
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