Product Name :
2-Hydroxy Estrone (CAS 362-06-1)
Synonym :
Catecholestrone
Application :
2-Hydroxy Estrone is an estradiol metabolite
CAS:
362-06-1
Purity:
Molecular Weight:
286.37
Formula :
C18H22O3
Physical state:
Solid
solubility :
Soluble in DMSO and Methanol
Shipping Condition :
Store at 4° C
Melting point:
199-201°C (lit.)
SMILES:
C[C@]12CC[C@H]3[C@H]([C@@H]1CCC2=O)CCC4=CC(=C(C=C34)O)O
References:
:Reproducibility over time of measurements of androgens, estrogens and hydroxy estrogens in urine samples from post-menopausal women. | Rinaldi, S., et al.1251013-26-9 Order 2003.Ursocholic acid site Eur J Epidemiol. 18: 417-24. PMID: 12889688Estrogen metabolites in the release of inflammatory mediators from human amnion-derived cells. | Pavan, B., et al. 2011. Life Sci. 88: 551-8. PMID: 21277863Total dietary fat and omega-3 fatty acids have modest effects on urinary sex hormones in postmenopausal women. | Young, LR., et al. 2013. Nutr Metab (Lond). 10: 36. PMID: 23618064Covalent binding to proteins of reactive intermediates resulting from prostaglandin H synthase-catalyzed oxidation of stilbene and steroid estrogens.PMID:33712925 | Freyberger, A. and Degen, GH. 1989. J Biochem Toxicol. 4: 95-103. PMID: 2512390Novel and potent biological antioxidants on membrane phospholipid peroxidation: 2-hydroxy estrone and 2-hydroxy estradiol. | Nakano, M., et al. 1987. Biochem Biophys Res Commun. 142: 919-24. PMID: 3827906Estrogen 2-, 4-, 6- or 16-hydroxylation by human follicles shown by gas chromatography-mass spectrometry associated with stable isotope dilution. | Dehennin, L., et al. 1984. J Steroid Biochem. 20: 465-71. PMID: 6708529Role of catechol estrogens in activation of lordosis in female rats and guinea pigs. | Marrone, BL., et al. 1977. Pharmacol Biochem Behav. 7: 13-7. PMID: 905327