Interesting facts
Interesting Facts About 17-ethynyl-17-hydroxy-13-methyl-1,2,6,7,8,9,10,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-one
This compound belongs to the class of steroids, and its structural complexity provides intriguing insights into its properties and potential applications. Here are some notable facts:
- Steroid Nature: As a modified steroid, it features unique functional groups that influence its biological activity.
- Potential Uses: Compounds like this are often researched for their potential pharmaceutical applications, including hormonal therapies and anti-cancer treatments.
- Synthesis: The synthetic pathways to create such specific compounds often involve intricate multi-step reactions, showcasing the elegance and complexity of organic chemistry.
- Biological Impact: Modifications such as ethynyl and hydroxyl groups can significantly alter how the compound interacts with biological systems, increasing potency or changing the mechanism of action.
- Research Interest: The study of such compounds is essential in medicinal chemistry, as researchers aim to discover new drugs with improved efficacy and fewer side effects.
In conclusion, 17-ethynyl-17-hydroxy-13-methyl-1,2,6,7,8,9,10,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-one embodies the profound link between organic chemistry and biological functions. Its intricate structure not only represents a remarkable achievement in synthetic chemistry but also holds promise for advancements in medical science.
Synonyms
Minovlar
(17beta)-17-ethynyl-17-hydroxyestr-4-en-3-one
17.alpha.-Ethinyl-19-nortestosterone
17.alpha.-Ethynyl-19-nortestosterone
19-Nor-17.alpha.-ethynyltestosterone
Nor-Q.D.
17.alpha.-Ethynyl-4-estren-17-ol-3-one
17.alpha.-Ethynyl-17-hydroxy-4-estren-3-one
17.alpha.-Ethinylestra-4-en-17.beta.-ol-3-one
17.beta.-Hydroxy-19-norpregn-4-en-20-yn-3-one
Estr-4-en-3-one, 17.alpha.-ethynyl-17-hydroxy-
17.alpha.-Ethynyl-17.beta.-hydroxyestr-4-en-3-one
17-Hydroxy-19-nor-17.alpha.-pregn-4-en-20-yn-3-one
19-nor-17.alpha.-Ethynylandrosten-17.beta.-ol-3-one
17.alpha.-Ethynyl-19-nor-4-androsten-17.beta.-ol-3-one
17.alpha.-Ethynyl-19-norandrost-4-en-17.beta.-ol-3-one
19-Nor-17.alpha.-pregn-4-en-20-yn-3-one, 17-hydroxy-
17.alpha.-Ethynyl-17.beta.-hydroxy-19-norandrost-4-en-3-one
19-nor-17.alpha.-Ethynyl-17.beta.-hydroxy-4-androsten-3-one
17.alpha.-Ethinyl-17.beta.-hydroxy-.delta.(sup:4)-estren-3-one
component of Noriday
Oprea1_606355
19-Norpregn-4-en-20-yn-3-one, 17-hydroxy-, (17.alpha.)-
SCHEMBL5021649
CHEMBL4579631
DTXSID60859071
VIKNJXKGJWUCNN-UHFFFAOYSA-N
BBL012124
STK730956
AKOS005524503
AKOS037478319
NCGC00263506-02
17-ethynyl-17-hydroxy-13-methyl-1,2,6,7,8,9,10,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-one
AB01325874-02
WLN: L E5 B666 OV MUTJ E FQ F1UU1 -A&F
1aEthynyla1ahydroxya11aamethyla1H,2H,3H,3aH,3bH,4H,5H,7H,8H,9H,9aH,9bH,10H,11H,11aHacyclopenta[a]phenanthrena7aone
Solubility of 17-ethynyl-17-hydroxy-13-methyl-1,2,6,7,8,9,10,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-one
The solubility of the compound 17-ethynyl-17-hydroxy-13-methyl-1,2,6,7,8,9,10,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-one (C20H24O2) can be characterized as follows:
In summary, while the compound shows promising solubility in general organic solvents, its hydrophobic nature limits its solubility in polar solvents, making its applications in aqueous systems somewhat challenging. As a result, understanding the solubility profile is crucial for further applications and studies involving this compound.