Interesting facts
Interesting Facts about (17-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl) N,N-bis(2-chloroethyl)carbamate
This intriguing compound is notable for its dual functionality, combining elements of both a steroid and a carbamate. Here are some engaging insights into its characteristics and applications:
- Diverse Applications: Its structure allows it to be studied for potential applications in pharmacology, especially in cancer therapeutics due to its steroid-like backbone.
- Synthetic Compound: The synthesis of this compound is a fascinating endeavor, often involving multistep organic reactions that demonstrate advanced techniques in organic chemistry.
- Chloroethyl Group: The presence of the N,N-bis(2-chloroethyl) groups is particularly interesting, as chloroethyl moieties are known for their reactivity and role in alkylating agents used in chemotherapy.
- Biological Activity: Compounds like this one are researched for their potential biological activity, which may involve interactions with steroid receptors, influencing cell growth and differentiation.
- Historical Context: Compounds of this type have historical significance in the study of hormones and their analogs, shedding light on the intricate pathways of endocrine activity.
In summary, this compound serves as a prime example of how complex organic structures can lead to significant implications in both chemistry and medicine. The blend of its steroid-like features with the reactive chloroethyl segments opens up avenues for exploration in drug design and biological research.
Synonyms
(17-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl) N,N-bis(2-chloroethyl)carbamate
LEO 275
17-Hydroxyestra-1,3,5(10)-trien-3-yl bis(2-chloroethyl)carbamate
MLS002701936
17.beta.-Estradiol 3-(bis(2-chloroethyl)carbamate)
CHEMBL290686
SCHEMBL14031683
DTXSID30859780
FRPJXPJMRWBBIH-UHFFFAOYSA-N
SMR001565519
NS00004873
Estradiol {3-[bis(2-chloroethyl)carbamate]}
Estradiol, {3-[bis(2-chloroethyl)carbamate]}
17.Beta.-Estradiol {3-[bis(2-chloroethyl)carbamate]}
17-Hydroxyestra-1,3,5(10)-trien-3-yl bis(2-chloroethyl)carbamate, (17.beta.)-
Carbamic acid, bis(2-chloroethyl)-, 17.beta.-hydroxyestra-1,3,5(10)-trien-3-yl ester
Estra-1,3,5(10)-triene-3, 17-diol, {3-[bis(2-chloroethyl)carbamate],} (17.beta.)-
Estra-1,3,5(10)-triene-3,17-diol (17.beta.)-, {3-[bis(2-chloroethyl)carbamate]}
Estra-1,3,5(10)-triene-3,17-diol (17.beta.)-, 3-[bis(2-chloroethyl)carbamate]
Estra-1,3,5(10)-triene-3,17-diol, 3-(bis(2-chloroethyl)carbamate), (17.beta.)-
Solubility of (17-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl) N,N-bis(2-chloroethyl)carbamate
The solubility of the compound (17-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl) N,N-bis(2-chloroethyl)carbamate can be influenced by several factors, including its molecular structure and environmental conditions. Generally, this compound may exhibit varied solubility properties based on the following considerations:
Factors Affecting Solubility:
In general, this compound may be expected to have limited solubility in water due to its hydrophobic characteristics, whereas non-polar solvents could facilitate better dissolving properties. As always, specific experimental data is vital to accurately determine the solubility profile of such complex compounds.
In summary, while general predictions can be made about the solubility of this carbamate compound, precise solubility metrics should be evaluated under controlled laboratory conditions to understand its behavior fully.