For research use only. Not for therapeutic Use.
Estrone(Cat No.:A000974)is a naturally occurring estrogen steroid hormone with the molecular formula C18H22O2. It is one of the three main estrogens in the human body, alongside estradiol and estriol, and is primarily produced in the ovaries, adipose tissue, and adrenal glands. Estrone plays a key role in the development and maintenance of female reproductive tissues and secondary sexual characteristics. It is less potent than estradiol but becomes the predominant estrogen after menopause. Estrone is used in hormone replacement therapy and can be administered orally or transdermally. Excess levels may be associated with certain cancers.
CAS Number | 53-16-7 |
Synonyms | 53-16-7; Folliculin; OESTRONE; Theelin; Estrovarin |
Molecular Formula | C18H22O2 |
Purity | ≥95% |
Target | Metabolic Enzyme/Protease |
Solubility | >9.8mg/mL in DMSO |
Storage | -20°C |
IUPAC Name | (8R,9S,13S,14S)-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-one |
InChI | InChI=1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16,19H,2,4,6-9H2,1H3/t14-,15-,16+,18+/m1/s1 |
InChIKey | DNXHEGUUPJUMQT-CBZIJGRNSA-N |
SMILES | C[C@]12CC[C@H]3[C@H]([C@@H]1CCC2=O)CCC4=C3C=CC(=C4)O |
Reference | 1: Snoj T, Zuzek MC, Cebulj-Kadunc N, Majdic G. Short communication: Heat 2: Trifunović J, Borčić V, Vukmirović S, Mikov M. Structural insights into <br> 4: Ruksrithong C, Phattarapattamawong S. Removals of estrone and 17β-estradiol by <br> 6: Song H, Wang Y, Zhang L, Tian L, Luo J, Zhao N, Han Y, Zhao F, Ying X, Li Y. 7: Feifarek DJ, Shappell NW, Schoenfuss HL. Do environmental factors affect male 8: Sornalingam K, McDonagh A, Zhou JL, Johir MAH, Ahmed MB. Photocatalysis of 9: Shappell NW, Feifarek DJ, Rearick DC, Bartell SE, Schoenfuss HL. Do 10: Otsuka M, Kadokawa H. GPR30 mediates estrone, estriol, and estradiol to |
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