Interesting facts
Interesting Facts about (2S,4aS,6aR,6aS,6bR,8aR,10S,12aS,14bR)-10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-13-oxo-3,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picene-2-carboxylic acid
This compound, often referred to in shorthand as a complex polycyclic carboxylic acid, is notable for its intricate structure and diverse chemical properties. Here are some captivating insights regarding this fascinating molecule:
- Structural Complexity: The compound features a multi-ring structure that reflects its classification as a polycyclic compound. This complexity gives rise to unique spatial arrangements and reactivities.
- Natural Occurrence: Similar compounds can often be found in nature, particularly in various plant species. These compounds play essential roles in ecological interactions, such as attracting pollinators.
- Biological Activity: Given its functional groups, this compound may exhibit diverse biological activities, which could be pivotal in pharmacological research, especially for its potential medicinal properties.
- Synthesis and Applications: The synthesis of such complex compounds often involves advanced synthetic techniques and may lead to applications in organic materials, as they can be incorporated into various products ranging from cosmetics to pharmaceuticals.
- Chirality: The presence of multiple stereocenters makes this compound a chiral molecule. Chiral compounds often have different biological actions or pharmacokinetics depending on their stereochemistry, highlighting the importance of understanding chirality in drug design.
In conclusion, the thorough study of (2S,4aS,6aR,6aS,6bR,8aR,10S,12aS,14bR)-10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-13-oxo-3,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picene-2-carboxylic acid not only broadens our understanding of organic chemistry but also enriches our exploration of potential applications in biotechnology and material science. As research continues, we may uncover further secrets held within its structure.
Synonyms
enoxolone
471-53-4
Glycyrrhetic acid
GLYCYRRHETINIC ACID
Uralenic acid
18-beta-Glycyrrhetinic acid
18beta-Glycyrrhetinic acid
Rhetinic Acid
Enoxolona
Biosone
alpha-Glycyrrhetinic acid
Enoxolonum
Jintan
3beta-Hydroxy-11-oxoolean-12-en-30-oic acid
18-beta-Glycyrrhetic acid
CCRIS 3962
18beta-Glycyrrhetic acid
EINECS 207-444-6
UNII-P540XA09DR
NSC 35347
NSC-35347
3-Glycyrrhetinic acid
BRN 2229654
P540XA09DR
DTXSID9020669
CHEBI:30853
3-beta-Hydroxy-11-oxoolean-12-en-30-oic acid
beta-Glycyrrhetinic acid
DTXCID50669
4-10-00-03775 (Beilstein Handbook Reference)
Olean-12-en-30-oic acid, 3beta-hydroxy-11-oxo-
Olean-12-en-30-oic acid, 3-beta-hydroxy-11-oxo-
(3beta,20beta)-3-Hydroxy-11-oxo-olean-12-en-29-oic acid
Glyciram
ENOXOLONE (MART.)
ENOXOLONE [MART.]
ENOXOLONE (EP IMPURITY)
ENOXOLONE [EP IMPURITY]
ENOXOLONE (EP MONOGRAPH)
ENOXOLONE [EP MONOGRAPH]
Acid, Rhetinic
Acid, Uralenic
Acid, Glycyrrhetic
Acid, Glycyrrhetinic
Hidermart
D03AX10
(3beta,20beta)-3-Hydroxy-11-oxoolean-12-en-29-oic acid
15301-63-0
207-444-6
Glycyrrhetin
18|A-Glycyrrhetinic acid
Arthrodont
18 beta-Glycyrrhetintic Acid
MFCD00003706
Glycyrrhetinate
Glycyrrhetinic acid [JAN]
MLS000028748
CHEMBL230006
Enoxolone (INN)
(2S,4aS,6aR,6aS,6bR,8aR,10S,12aS,14bR)-10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-13-oxo-3,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picene-2-carboxylic acid
NCGC00017244-03
SMR000058239
ENOXOLONE [INN]
Glycyrrhetinic acid (JAN)
(3beta,5beta,14beta)-3-Hydroxy-11-Oxoolean-12-En-29-Oic Acid
3beta-Hydroxy-11-oxo-18beta,20beta-olean-12-en-29-oic acid
Enoxolonum [INN-Latin]
Enoxolona [INN-Spanish]
GlycyrrhetinicAcid
Enoxolone [INN:BAN:DCF]
CAS-471-53-4
18b-Glycyrrhetinic acid
SR-01000721867
Enoloxone
Enoxolone (Glycyrrhetinic acid)
NSC-35350
18|A-Glycyrrhetinic acid (Standard)
Hidermart (TN)
NCGC00181115-01
CBW
18-Glycyrrhetinic acid
ENOXOLONE [MI]
Enoxolone (Glycyrrhetin)
Opera_ID_1048
ENOXOLONE [WHO-DD]
SCHEMBL18540
(2S,4aS,6aS,6bR,8aR,10S,12aS,12bR,14bR)-10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-13-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-2-carboxylic acid
MLS001146949
MLS002207101
Enoxolone, Glycyrrhetinic acid
(3beta)-3-hydroxy-11-oxoolean-12-en-30-oic acid
18 beta -Glycyrrhetinic Acid
BX-1
GTPL11264
HY-N0180R
STX-352
CHEBI: 30853
MPDGHEJMBKOTSU-YKLVYJNSSA-N
18beta-Glycyrrhetinic acid, 97%
HMS2233P23
HY-N0180
MSK40366
Tox21_110804
Tox21_112726
Tox21_200799
BDBM50233538
s2296
AKOS015960428
AKOS016036757
HMDB: 0011628
AC-1925
AC-8906
CCG-208506
CS-W020624
DB13089
FG09301
GM-1658
KS-1262
LMPR0106150014
Enoxolone 100 microg/mL in Acetonitrile
Glycyrrhetin ;18beta Glycyrrhetinic acid
NCGC00017244-04
NCGC00017244-06
NCGC00017244-16
NCGC00017244-20
NCGC00142473-03
NCGC00258353-01
(5S,8S,15S,18S,1R,2R,10R,14R,20R)-18-hydroxy-1,2,5,8,15,19,19-heptamethyl-13-o xopentacyclo[12.8.0.0<2,11>.0<5,10>.0<15,20>]docos-11-ene-8-carboxylic acid
107420-91-7
1ST40366
G0149
NS00000590
3beta-hydroxy-11-oxoolean-12-en-29-oic acid
C02283
D00156
S00284
Enoxolone (synonym: 18ss--Glycyrrhetinic acid)
18beta-Glycyrrhetinic acid, purum, >=97.0% (T)
Q5948038
SR-01000721867-3
SR-01000721867-4
SR-01000721867-5
SR-01000721867-6
BRD-K96137854-001-17-1
3ss-Hydroxy-11-oxo-18ss,20ss-olean-12-en-29-oic acid
Enoxolone, European Pharmacopoeia (EP) Reference Standard
3-b-Hydroxy-11-oxo-18b,20b-olean-12-en-29-oic acid;Enoxolone
(2S,4aS,6aR,6aS,6bR,8aR,10S,12aS,14bR)-10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-13-oxo-3,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picene-2-carboxylicacid
Enoxolone; 18beta-Glycyrrhetinic acid; 3?-Hydroxy-11-oxo-18?,20?-olean-12-en-29-oic acid
Solubility of (2S,4aS,6aR,6aS,6bR,8aR,10S,12aS,14bR)-10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-13-oxo-3,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picene-2-carboxylic acid
The solubility of organic compounds can be influenced by several factors, particularly their molecular structure and functional groups. For the compound in question, certain aspects are crucial to determining its solubility:
Thus, it can be anticipated that this compound exhibits limited solubility in water due to its bulky hydrophobic structure yet may be soluble in organic solvents due to the presence of the polar carboxylic acid moiety. Overall, the dual characteristics reinforce the idea that understanding solubility often necessitates careful consideration of both polar and non-polar interactions.