3-O-Methyl Estradiol-d3

Product Name 3-O-Methyl Estradiol-d3
Alternate Names Estradiol Stable Isotopes, Stable Isotopes of Estradiol
CAT No. CS-T-80068
CAS No. 57983-88-7
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Estradiol
Smileys CC12CCC3C(CCC4=C3C=CC(OC)=C4)C1CC([2H])([2H])[C@@]2([2H])O
Canonical Smiles CC12CCC3C(C1CCC2O)CCC4=C3C=CC(=C4)OC
InchIKey ULAADVBNYHGIBP-NQZLLTOTSA-N
Inchl InChI=1S/C19H26O2/c1-19-10-9-15-14-6-4-13(21-2)11-12(14)3-5-16(15)17(19)7-8-18(19)20/h4,6,11,15-18,20H,3,5,7-10H2,1-2H3/t15-,16-,17+,18+,19+/m1/s1/i8D2,18D
IUPAC (8R,9S,13S,14S,17S)-16,16,17-trideuterio-3-methoxy-13-methyl-6,7,8,9,11,12,14,15-octahydrocyclopenta[a]phenanthren-17-ol
Controlled No
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3-O-Methyl Estradiol-d3 is a stable isotopic form of 3-O-Methyl Estradiol, which is a synthetic derivative of Estradiol. It is a potent estrogen and a selective agonist of the estrogen receptor. Its chemical formula is C21H21D3O3. The compound is commonly used in research studies to investigate the binding and activation of the estrogen receptor, as well as the effects of estrogen on various physiological processes. It is also used in drug development for the treatment of menopausal symptoms, hormonal imbalances, and cancer. 3-O-Methyl Estradiol-d3 is administered orally or through injection, and its dosage varies depending on the intended use. It has a half-life of approximately 13 hours and is rapidly metabolized in the liver. The metabolites of the compound are excreted in the urine and feces. The compound has been found to have potential side effects, including nausea, vomiting, headaches, and breast tenderness. It may also increase the risk of uterine and breast cancer in some women. Therefore, it is important to use 3-O-Methyl Estradiol-d3 under the guidance of a qualified healthcare professional. In summary, 3-O-Methyl Estradiol-d3 is a potent estrogen that is widely used in research and drug development. Its chemical properties and physiological effects make it a valuable tool in understanding the role of estrogen in the body and developing effective treatments for various conditions.

Related Compounds

Ethinylestradiol sulfate-D4 | Estradiol Sulphate D4 sodium | Estradiol 17-Valerate-d9 | Ethynyl Estradiol-13C2 | Estradiol D4 | Estradiol 17-Palmitate-d31 | Sodium 17 β-Estradiol 3-Sulfate D4 | Ethinylestradiol -D4 | Ethynyl Estradiol-2,4,9,6,6,16,16- D7 | Estradiol-13C6 |

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