Interesting facts
Interesting Facts About (8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13,17-trimethyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-one
This fascinating compound is a steroid hormone with a complex structure that demonstrates the intricate relationships between molecular configuration and biological activity. Here are some engaging insights about this compound:
- Steroidal Framework: The structure of this compound reveals a steroidal framework, which is essential in many biological processes. Steroids play crucial roles in bodily functions, including metabolism, inflammation, and immune responses.
- Chirality: The presence of multiple chiral centers makes this compound optically active. Chirality is fundamental in chemistry as it can significantly affect the biological activity and interactions of molecules within living organisms.
- Biological Significance: Compounds that share similar frameworks often exhibit activities related to hormone regulation, growth, and development. For instance, the hydroxyl group in this compound could potentially facilitate interaction with hormone receptors, indicating its importance in endocrinology.
- Natural Occurrence: Steroidal compounds like this one are often found in various plants and animals, contributing to their physiological processes and helping in biological communication.
- Research Potential: Ongoing studies on similar compounds continue to reveal potential therapeutic applications, including the development of synthetic analogs for therapeutic use, which might lead to innovative treatments and medications.
As scientists explore the vast realm of organic compounds, they uncover the delicate balance between structure and function, and this compound serves as an intriguing example of nature's complexity and ingenuity.
Synonyms
METHANDROSTENOLONE
Metandienone
Methandienone
72-63-9
Dianabol
Nerobol
Metanabol
Metandienonum
Methandrolone
Metandienon
Metandrostenolon
Metandrostenolone
Anabolin
Andoredan
Dianabole
Encephan
Metastenol
Nerobolettes
Perbolin
Protobolin
Stenolon
Stenolone
Abirol
Danabol
Geabol
Naposim
Crein
Dehydromethyltestosterone
Anabolicum Medivet
Methylandrostenolone
Metandienona
Methandienonum
1-Dehydromethyltestosterone
Compound 17309
Methandrostenolonum
Ciba 17309-ba
NSC-42722
1,2-Dehydro-17-methyltestosterone
A1-Dehydromethyltesterone
17beta-Hydroxy-17-methylandrosta-1,4-dien-3-one
Ciba 17309 BA
delta'-17-Methyltestosterone
Metandienonum [Latin]
Testosterone, 1-dehydro-17-methyl-
1-Dehydro-17alpha-methyltestosterone
17alpha-Methyl-1-dehydrotestosterone
1-Dehydro-17-alpha-methyltestosterone
17-alpha-Methyl-1-dehydrotestosterone
TMV 17
COZ1R7EOCC
UNII-COZ1R7EOCC
HSDB 3360
delta(1)-17alpha-Methyltestosterone
delta-1,17-alpha-Methyltestosterone
EINECS 200-787-2
NSC 42722
Metandienone [INN]
DTXSID2023276
delta(sup 1)-17-alpha-Methyltestosterone
17-beta-Hydroxy-17-alpha-methylandrostra-1,4-dien-3-one
Androsta-1,4-dien-3-one, 17-beta-hydroxy-17-alpha-methyl-
Androsta-1,4-dien-3-one, 17-hydroxy-17-methyl-, (17beta)-
17-beta-hydroxy-17-methyl-androsta-1,4-dien-3-one
Sterolon
17alpha-Methyl-17beta-hydroxyandrosta-1,4-dien-3-one
Androsta-1,4-dien-3-one, 17beta-hydroxy-17-methyl-
17-alpha-Methyl-17-beta-hydroxy-1,4-androstadien-3-one
DTXCID203276
1-Dehydro-17-methyltestosterone
NSC42722
Metandienone (INN)
(8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13,17-trimethyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-one
MA
Metandienonum (Latin)
NCGC00159415-02
NCGC00159415-04
1-Dehydro-17-.alpha.-methyltestosterone
Androsta-1,4-diene-3-one, 17-hydroxy-17-methyl-, (17beta)-
Androsta-1,4-dien-3-one, 17-hydroxy-17-methyl-, (17-beta)-
METHANDIENONE (MART.)
METHANDIENONE [MART.]
(17beta)-17-hydroxy-17-methylandrosta-1,4-dien-3-one
.delta.'-17-Methyltestosterone
Metandienona [Spanish]
Methandrostenolone [USP]
Metandrostenolone [DCIT]
Metandienonum [INN-Latin]
1-Dehydro-17.alpha.-methyltestosterone
17.alpha.-Methyl-1-dehydrotestosterone
CAS-72-63-9
MA (VAN)
Metandienona [INN-Spanish]
.DELTA.1-17.alpha.-Methyltestosterone
Androsta-1, 17.beta.-hydroxy-17-methyl-
Androsta-1, 17.beta.-hydroxy-17.alpha.-methyl-
Androsta-1, 17-hydroxy-17-methyl-, (17.beta.)-
17-.beta.-hydroxy-17-methyl-androsta-1,4-dien-3-one
Methandrostenolone (1.0 mg/mL in 1,2-Dimethoxyethane)
Methandrostenolone (Metandienone)
17-.beta.-Hydroxy-17-.alpha.-methylandrostra-1,4-dien-3-one
Androsta-1,4-diene-3-one, 17-hydroxy-17-methyl-, (17.beta.)-
17-Hydroxy-17-methylandrosta-1,4-dien-3-one
Androsta-1,4-dien-3-one, 17-hydroxy-17-methyl-, (17b)-
DIANABOL (TN)
METANDIENONE [WHO-DD]
SCHEMBL140928
Androsta-1,4-dien-3-one, 17-hydroxy-17-methyl-, (17.alpha.)-
METHANDROSTENOLONE [MI]
CHEBI:6810
CHEMBL1418176
METHANDROSTENOLONE [HSDB]
METHANDROSTENOLONE [VANDF]
MSK2297
1-Dehydro-17-methyl-Testosterone
Methandienone, 1mg/ml in Methanol
BCP10774
NSC51180
Tox21_111647
1, 2-Dehydro-17-methyltestosterone
BBL029917
LMST02020013
NSC-51180
s4796
STK801870
AKOS005267170
Tox21_111647_1
CCG-267474
DB13586
17-.alpha.-Methyl-1-dehydrotestosterone
NCGC00159415-03
NCGC00159415-05
17alpha-methyl-Androsta-1,4-dien-3-one
laquo deltaRaquo '-17-Methyltestosterone
VS-09501
.delta.-1,17-.alpha.-Methyltestosterone
17-alpha-Methylandrostra-1,4-dien-3-one
NS00010330
laquo deltaRaquo 1-17alpha-Methyltestosterone
D00389
AB01332687-02
Methandrostenolone 100 microg/mL in Acetonitrile
17-Hydroxy-17-methylandrosta-1,4-dien-3-one #
Q417194
17beta-hydroxy-17-methyl-Androsta-1,4-dien-3-one
laquo deltaRaquo (Sup1)-17alpha-Methyltestosterone
Androsta-1,4-dien-3-one, 17alpha-methyltestosterone
17beta-Hydroxy-17-methylandrosta-1,4-dien-3-one, 98%
17beta-hydroxy-17alpha-methyl-Androsta-1,4-dien-3-one
17beta-Hydroxy-17alpha-methylandrosta-1,4-dien-3-one
17-Hydroxy-17-methyl-(17beta)-Androsta-1,4-dien-3-one
17-Hydroxy-17-methyl-(17beta)-Androsta-1,4-diene-3-one
Androsta-1,4-dien-3-one, 17.alpha.-hydroxy-17-methyl-
17BETA-17-HYDROXY-17-METHYLANDROSTA-1,4-DIEN-3-ONE
17-Hydroxy-17-methylandrosta-1,4-dien-3-one (ACD/Name 4.0)
17beta-Hydroxy-17-methylandrosta-1,4-dien-3-one, >=99.0% (HPLC)
17beta-Hydroxy-17-methylandrosta-1,4-dien-3-one, analytical standard
(1S,3aS,3bR,9aR,9bS,11aS)-1-hydroxy-1,9a,11a-trimethyl-1H,2H,3H,3aH,3bH,4H,5H,7H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-7-one
(8R,10R,13S,17S)-17-Hydroxy-10,13,17-trimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-cyclopenta[a]phenanthren-3-one
(9S,10R,13S,14S,17S)-17-hydroxy-10,13,17-trimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-3-one
200-787-2
Solubility of (8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13,17-trimethyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-one
The solubility of the compound with the molecular formula C18H22O2 reveals several intriguing characteristics:
As a rule of thumb, “like dissolves like” applies here, meaning that polar compounds will generally not dissolve well in non-polar media, and vice versa. It's crucial to take these factors into account when considering the solubility profile of this particular compound. Thus, for practical applications and formulation strategies, understanding the solubility in various solvents is essential for effective use and manipulation.