Interesting facts
Interesting Facts about 2-[[(4R)-4-[(3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,7,12-trihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoyl]amino]ethanesulfonic acid
This compound is a fascinating example of a complex molecule that plays a role in biological systems. Here are some interesting highlights:
- Structural Complexity: Its multi-ring structure, enhanced by various hydroxy and pentanoyl groups, demonstrates the intricate design often found in natural compounds.
- Biological Significance: This compound may be involved in vital biochemical pathways, illustrating the connection between intricate chemistry and life processes.
- Synthesis Challenges: The synthesis of such a complex molecule presents unique challenges, often requiring multiple steps and careful optimization of reaction conditions.
- Potential Applications: Compounds of this type are often researched for their therapeutic potential, particularly in fields such as endocrinology and oncology, where specific biochemical interactions can be crucial.
- Natural Occurrence: Many similar compounds are derived from natural sources, highlighting the chemical diversity found in nature. This leads scientists to explore biodiversity for novel compounds.
The study of such compounds gives insight not only into their chemical properties but also into how they can inspire new scientific discoveries and innovations. In the words of famous chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." This compound is undoubtedly a testament to the creativity and complexity present in the field of chemistry!
Synonyms
TAUROCHOLIC ACID
Taurocholate
81-24-3
Cholaic acid
Cholyltaurine
N-Choloyltaurine
Cholic acid taurine conjugate
Taurine, N-choloyl-
Acidum cholatauricum
Taurine Cholate
HSDB 832
Choloyl-taurine
3alpha,7alpha,12alpha-Trihydroxy-5beta-cholanic acid 24-taurine
EINECS 201-336-2
NSC 25505
Ethanesulfonic acid, 2-(((3alpha,5beta,7alpha,12alpha)-3,7,12-trihydroxy-24-oxocholan-24-yl)amino)-
CHEBI:28865
5E090O0G3Z
NSC25505
2-(((3alpha,5beta,7alpha,12alpha)-3,7,12-Trihydroxy-24-oxocholan-24-yl)amino)ethanesulfonic acid
2-((3-alpha,7-alpha,12-alpha-Trihydroxy-24-oxo-5-be ta-cholan-24-yl)amino)ethanesulfonic acid
NSC-25505
TAUROCHOLIC ACID [MI]
TAUROCHOLIC ACID [HSDB]
DTXSID00883259
N-choloyl-taurine
N-(3Alpha,7Alpha,12Alpha-trihydroxy-5Beta-cholan-24-oyl)-taurine
3.BETA.-HYDROXYDINOR-5-CHOLENIC ACID
2-[(3alpha,7alpha,12alpha-trihydroxy-24-oxo-5beta-cholan-24-yl)amino]ethanesulfonic acid
2-(((3alpha,5beta,7alpha,12alpha)-3,7,12-Trihydroxy-24-oxocholan-24-yl)amino)ethanesulphonic acid
2-[[(4R)-4-[(3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,7,12-trihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoyl]amino]ethanesulfonic acid
Ethanesulfonic acid, 2-[[(3.alpha.,5.beta.,7.alpha.,12.alpha.)-3,7,12-trihydroxy-24-oxocholan-24-yl]amino]-
ethanesulfonic acid, 2-[[(3alpha,5beta,7alpha,12alpha)-3,7,12-trihydroxy-24-oxocholan-24-yl]amino]-
Sodium taurocholate hydrate
2-(((3.ALPHA.,5.BETA.,7.ALPHA.,12.ALPHA.)-3,7,12-TRIHYDROXY-24-OXOCHOLAN-24-YL)AMINO)ETHANESULFONIC ACID
[3H]-taurocholate
[3H]taurocholic acid
[3H]-taurocholic acid
UNII-5E090O0G3Z
tauro-cholic acid
2-((3alpha,7alpha,12alpha-trihydroxy-24-oxo-5beta-cholan-24-yl)amino)ethanesulfonic acid
2-(4-((5R,7S,9R,16S)-5,9,16-trihydroxy-2,15-dimethyltetracyclo(8.7.0.02,7.011,15)heptadecan-14-yl)pentanamido)ethane-1-sulfonic acid
2-[(4R)-4-[(1S,2S,5R,7S,9R,10R,11S,14R,15R,16S)-5,9,16-trihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanamido]ethane-1-sulfonic acid
2-{[(3Alpha,5beta,7alpha,12alpha)-3,7,12-trihydroxy-24-oxocholan-24-yl]amino}ethanesulfonic acid
2-{4-[(5R,7S,9R,16S)-5,9,16-trihydroxy-2,15-dimethyltetracyclo[8.7.0.02,7.011,15]heptadecan-14-yl]pentanamido}ethane-1-sulfonic acid
3alpha,7alpha,12alpha-Trihydroxy-5beta-cholan-24-oic acid N-(2-sulfoethyl)amide
Spectrum5_002015
bmse000927
SCHEMBL3705
Taurocholic acid (Standard)
BIDD:PXR0195
Taurine, N-choloyl-(8CI)
CHEMBL224867
GTPL4546
GTPL4547
HY-B1788R
MSK2582
WBWWGRHZICKQGZ-HZAMXZRMSA-N
DTXCID601022803
HMS2090N18
HY-B1788
BDBM50375594
LMST05040001
AKOS030242840
DB04348
MS-29575
3BETA-HYDROXYDINOR-5-CHOLENIC ACID
CS-0013819
NS00002884
G12125
AB01275537-01
EN300-19734139
SR-05000001533
3a,7a,12a-Trihydroxy-5b-cholanic acid-24-taurine
Q2659931
SR-05000001533-1
BRD-K81062487-001-05-8
WLN: L E5 B666TJ A1 DQ E1 FY1&2VM2SWQ KQ OQ
3.alpha.,12.alpha.-Trihydroxy-5.beta.-cholanic acid 24-taurine
2-[(3.alpha.,12.alpha.-Trihydroxy-24-oxo-5.beta.-cholan-24-yl)amino]ethanesulfonic acid
2-[(4R)-4-[(1R,3aS,3bR,4R,5aS,7R,9aS,9bS,11S,11aR)-4,7,11-trihydroxy-9a,11a-dimethyl-hexadecahydro-1H-cyclopenta[a]phenanthren-1-yl]pentanamido]ethane-1-sulfonic acid
2-{[(3beta,5beta,7alpha,12alpha,14beta,17alpha)-3,7,12-trihydroxy-24-oxocholan-24-yl]amino}ethanesulfonic acid
Ethanesulfonic acid,5.beta.,7.alpha.,12.alpha.)-3,7,12-trihydroxy-24-oxocholan-24-yl]amino]-
Solubility of 2-[[(4R)-4-[(3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,7,12-trihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoyl]amino]ethanesulfonic acid
The solubility of this complex compound is influenced by several factors. Due to its intricate and large structure, it tends to exhibit limited solubility in non-polar solvents, primarily existing in:
In terms of specific values, the precise solubility may vary, but in general, compounds with a high degree of hydroxylation and the sulfonic acid moiety tend to favor solubility in polar environments. To quote a common guideline, *“Like dissolves like”*—indicative of how similar polarities will enhance solubility interactions.
Ultimately, determining the solubility in practical applications would require empirical testing, taking into consideration variables such as temperature and pH, which can alter the solubility profile significantly.