Interesting facts
Interesting Facts about (2S,3S,4S)-3-(carboxymethyl)-4-isopropenyl-pyrrolidine-2-carboxylic acid
This fascinating compound is a member of the family of amino acids and has garnered attention in various scientific fields. Its unique structure features a pyrrolidine ring, which is a five-membered saturated ring containing nitrogen. Here are some compelling aspects of this compound:
- Biological Relevance: This compound plays a significant role in biological processes and has been studied for its potential impact on metabolic pathways, particularly in relation to amino acid biosynthesis.
- Potential Applications: Due to its structural characteristics, it may have applications in the pharmaceutical industry, especially in the design of new drugs targeting various diseases.
- Chirality: The presence of multiple stereocenters (indicated by the S configurations) introduces significant chirality, which is crucial in biological systems where often only one enantiomer is bioactive.
- Research Interest: Scientists are continuously searching for innovative methods to synthesize such compounds more efficiently, leading to advancements in organic chemistry.
- Interdisciplinary Connections: This compound connects various fields, including organic chemistry, biochemistry, and pharmacology, demonstrating the interdisciplinary nature of modern scientific research.
"Understanding the nuances of compounds like (2S,3S,4S)-3-(carboxymethyl)-4-isopropenyl-pyrrolidine-2-carboxylic acid can unlock new avenues in drug discovery and development."
In summary, the exploration of (2S,3S,4S)-3-(carboxymethyl)-4-isopropenyl-pyrrolidine-2-carboxylic acid represents a captivating intersection of chemistry and biology, offering potential insights into the molecular foundations of life and innovative solutions in medicine.
Synonyms
kainic acid
487-79-6
Digenin
Digenic acid
Helminal
Kainate
L-alpha-Kainic acid
Acide kainique
Acido kainico
alpha-Kainic acid
Digensaeure
Kainsaeure
Acidum kainicum
(2S,3S,4S)-3-(Carboxymethyl)-4-(prop-1-en-2-yl)pyrrolidine-2-carboxylic acid
alpha- Kainic acid
3-Pyrrolidineacetic acid, 2-carboxy-4-(1-methylethenyl)-, (2S,3S,4S)-
CHEMBL275040
SIV03811UC
DTXSID7040526
CHEBI:31746
2-Carboxy-4-isopropenyl-3-pyrrolidineacetic acid
3-Pyrrolidineacetic acid, 2-carboxy-4-isopropenyl-
(2S,3S,4S)-3-(carboxymethyl)-4-prop-1-en-2-ylpyrrolidine-2-carboxylic acid
NSC136038
NSC-759587
3-(Carboxymethyl)-4-isopropenylproline
NCGC00024504-05
(3S,4R)-3-(carboxymethyl)-4-(prop-1-en-2-yl)-L-proline
2-Carboxy-3-carboxymethyl-4-isopropenylpyrrolidine
NSC 136038
(2S-(2alpha,3beta,4beta))-2-carboxy-4-(1-methylethenyl)-3-pyrrolidineacetic acid
(-)-A-KAINIC ACID
DTXCID5020526
(3S,4S)-3-(carboxymethyl)-4-prop-1-en-2-yl-L-proline
Kainic acid [INN:JAN]
4071-38-9
CAS-487-79-6
Acide kainique [INN-French]
Acido kainico [INN-Spanish]
Acidum kainicum [INN-Latin]
SR-01000075454
BRN 0086660
UNII-SIV03811UC
kainic-acid
DL-Kainic acid
NSC-136038
KAI
1p1n
KAINIC ACID [MI]
WRW5P6M3EM
Biomol-NT_000217
KAINIC ACID [INN]
UPCMLD-DP146
Kainic acid, (+/-)-
3-Pyrrolidineacetic acid, 2-carboxy-4-(1-methylethenyl)-, (2S-(2alpha,3beta,4beta))-
Lopac0_000656
SCHEMBL15777
4-22-00-01523 (Beilstein Handbook Reference)
MLS001074661
KAINIC ACID [WHO-DD]
BPBio1_001306
(-)-(.alpha.)-Kainic Acid
UPCMLD-DP146:001
UPCMLD-DP146:002
HMS2233K05
HMS3262C13
HMS3266C11
HMS3411A21
HMS3675A21
AAA48779
EX-A8001
HY-N2309
Tox21_110905
Tox21_500656
BDBM50002369
Kainic Acid - CAS 487-79-6
AKOS024456995
Tox21_110905_1
CCG-204742
LP00656
SDCCGSBI-0050635.P002
3-Pyrrolidineacetic acid, 2-carboxy-4-(1-methylethenyl)-, (2S-(2-alpha,3-beta,4-beta))-
NCGC00024504-02
NCGC00024504-03
NCGC00024504-04
NCGC00024504-06
NCGC00024504-07
NCGC00024504-08
NCGC00024504-09
NCGC00024504-15
NCGC00261341-01
DA-64702
SMR000471885
CS-0020451
EU-0100656
NS00075498
K 0250
Q390239
SR-01000597728
SR-01000075454-1
SR-01000075454-5
SR-01000075454-6
SR-01000075454-7
SR-01000597728-1
BRD-K52459018-001-09-1
rel-(3R,4R)-3-(carboxymethyl)-4-isopropenyl-D-proline
2S-CARBOXY-4S-(1-METHYLETHENYL)-3S-PYRROLDINEACETIC ACID
L-proline, 3-(carboxymethyl)-4-(1-methylethenyl)-, (3S,4S)-
3-Pyrrolidineacetic acid, 2-carboxy-4-(1-methylethenyl)-, (2R,3R,4R)-rel-
(2S-(2.ALPHA.,3.BETA.,4.BETA.))-2-CARBOXY-4-(1-METHYLETHENYL)-3-PYRROLIDINEACETIC ACID
InChI=1/C10H15NO4/c1-5(2)7-4-11-9(10(14)15)6(7)3-8(12)13/h6-7,9,11H,1,3-4H2,2H3,(H,12,13)(H,14,15)/t6-,7+,9-/m0/s
Solubility Characteristics
The solubility of (2S,3S,4S)-3-(carboxymethyl)-4-isopropenyl-pyrrolidine-2-carboxylic acid is a fascinating subject due to its multi-functional characteristics. This compound contains multiple carboxylic acid groups, which significantly influence its solubility in various solvents.
Key Factors Affecting Solubility:
In typical scenarios, you can expect:
In summary, the solubility profile of this compound portrays a balance between its polar and non-polar regions, making it an interesting subject for studies focusing on drug formulation and biochemical interactions.