CAS 1150-90-9

Estra-1,3,5(10),16-tetraen-3-ol

Description:

Estra-1,3,5(10),16-tetraen-3-ol, with the CAS number 1150-90-9, is a steroidal compound that belongs to the class of estrogens. It features a tetracyclic structure typical of steroid hormones, characterized by a series of double bonds and a hydroxyl group (-OH) at the C-3 position. This compound is known for its biological activity, particularly in relation to estrogenic effects, which can influence various physiological processes, including reproductive functions and secondary sexual characteristics. Estra-1,3,5(10),16-tetraen-3-ol is often studied in the context of hormone replacement therapies and its potential implications in endocrine-related conditions. Its solubility properties typically indicate moderate solubility in organic solvents, while its stability can be affected by environmental factors such as light and temperature. As with many steroid compounds, it may exhibit a range of pharmacological activities, making it a subject of interest in both medicinal chemistry and endocrinology research.

Formula: C₁₈H₂₂O

InChI: InChI=1S/C18H22O/c1-18-9-2-3-17(18)16-6-4-12-11-13(19)5-7-14(12)15(16)8-10-18/h2,5,7,9,11,15-17,19H,3-4,6,8,10H2,1H3/t15-,16-,17+,18+/m1/s1

InChI key: InChIKey=CRMOMCHYBNOFIV-BDXSIMOUSA-N

SMILES: C[C@@]12[C@]([C@]3([C@@](C=4C(CC3)=CC(O)=CC4)(CC1)[H])[H])(CC=C2)[H]

Synonyms:

• (8S,9S,13S,14S)-13-methyl-6,7,8,9,11,12,14,15-octahydrocyclopenta[a]ph enanthren-3-ol
• Compound 742
• Estra-1,3,5(10),16-Tetraen-3-Ol

Estra-1,3,5(10),16-tetraen-3-ol

CAS: 1150-90-9

Formula: C₁₈H₂₂O

Purity: 95%

Color and Shape: Solid

Molecular weight: 254.3667

Ref: IN-DA000FL8

Estratetraenol

CAS: 1150-90-9

Estratetraenol is a synthetic estrogen that has the same structure as 17β-estradiol, but with three additional hydroxyl groups. It is used in research to study the effects of estrogens on humans and animals. Estratetraenol has been shown to activate the cell membrane receptors, which leads to a physiological response. This drug also causes an increase in oxygen consumption and inhibits ovulation. Estratetraenol binds to estrogen receptor cells and is metabolized by chemical substances in the liver into 17β-estradiol, which is then excreted by the kidneys. The drug does not bind to other types of receptor cells in humans or animals, such as those for progesterone or testosterone.

Formula: C₁₈H₂₂O

Purity: Min. 98 Area-%

Color and Shape: Powder

Molecular weight: 254.37 g/mol

Ref: 3D-FE22835

Estratetraenol

Controlled Product

CAS: 1150-90-9

Applications A steroid produced by females having pheromone activities.
References Kotiyan, P., et al.: J. Pharm. Biomed. Anal., 22, 667 (2000), Bensafi, M., et al.: Behaviour. Brain Res., 152, 11 (2004), Zhu, B., et al.: Endocrinol., 147, 4132 (2006), Bellavance, E., et al.: J. Med. Chem., 52, 7488 (2009),

Formula: C₁₈H₂₂O

Color and Shape: Neat

Molecular weight: 254.37

Ref: TR-E888940

Estratetraenol

CAS: 1150-90-9

Formula: C₁₈H₂₂O

Molecular weight: 254.4

Ref: ST-EA-CP-E28025