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Details

Stereochemistry ABSOLUTE
Molecular Formula C6H11NO2
Molecular Weight 129.157
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METHYL L-PROLINATE

SMILES

COC(=O)[C@@H]1CCCN1

InChI

InChIKey=BLWYXBNNBYXPPL-YFKPBYRVSA-N
InChI=1S/C6H11NO2/c1-9-6(8)5-3-2-4-7-5/h5,7H,2-4H2,1H3/t5-/m0/s1

HIDE SMILES / InChI

Molecular Formula C6H11NO2
Molecular Weight 129.157
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Immense essence of excellence: marine microbial bioactive compounds.
2010-10-15
A solution NMR investigation into the murine amelogenin splice-variant LRAP (Leucine-Rich Amelogenin Protein).
2010-09
Dynamic kinetic resolution of N-benzoyl-DL-amino acids via peptide bond forming reactions.
2010-04
(3R,8aS)-3-Ethyl-perhydro-pyrrolo[1,2-a]pyrazine-1,4-dione.
2010-01-23
Systematic study of the structures of potassiated tertiary amino acids: salt bridge structures dominate.
2009-08-27
Kinetic determination of potassium affinities by IRMPD: elucidation of precursor ion structures.
2009-07-09
Highly efficient formal synthesis of cephalotaxine, using the Stevens rearrangement--acid lactonization sequence as a key transformation.
2009-03-06
Viridamides A and B, lipodepsipeptides with antiprotozoal activity from the marine cyanobacterium Oscillatoria nigro-viridis.
2008-09
Formation of strecker aldehydes from polyphenol-derived quinones and alpha-amino acids in a nonenzymic model system.
2006-03-08
Variable tolerance of wetland tree species to combined salinity and waterlogging is related to regulation of ion uptake and production of organic solutes.
2006
An efficient, PIFA mediated approach to benzo-, naphtho-, and heterocycle-fused pyrrolo[2,1-c][1,4]diazepines. An advantageous access to the antitumor antibiotic DC-81.
2005-03-18
Structures of cationized proline analogues: evidence for the zwitterionic form.
2005-03-10
Stereoselective synthesis of a potent thrombin inhibitor by a novel P2-P3 lactone ring opening.
2004-05-28
Inclusion complexes of 2-chloroethylnitrososulfamides (CENS) with beta-cyclodextrin.
2004-01
Formation and stability of the enolates of N-protonated proline methyl ester and proline zwitterion in aqueous solution: a nonenzymatic model for the first step in the racemization of proline catalyzed by proline racemase.
2003-07-15
Alkali metal ion binding to amino acids versus their methyl esters: affinity trends and structural changes in the gas phase.
2002-03-15
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:24:52 GMT 2025
Edited
by admin
on Mon Mar 31 22:24:52 GMT 2025
Record UNII
0II79F4L0K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
METHYL L-PROLINATE
Systematic Name English
METHYL PROLINE, (-)-
Preferred Name English
(S)-PYRROLIDINE-2-CARBOXYLIC ACID METHYL ESTER
Systematic Name English
METHYL (2S)-2-PYRROLIDINECARBOXYLATE
Systematic Name English
METHYL (S)-PROLINATE
Systematic Name English
PROLINE, METHYL ESTER, L-
Systematic Name English
METHYL PROLINE, (S)-
Common Name English
L-PROLINE, METHYL ESTER
Systematic Name English
METHYL PROLINATE
Systematic Name English
(-)-L-PROLINE METHYL ESTER
Systematic Name English
METHYL L-PROLINE
Systematic Name English
METHYL (S)-PYRROLIDINE-2-CARBOXYLATE
Systematic Name English
(S)-PROLINE METHYL ESTER
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
219-932-6
Created by admin on Mon Mar 31 22:24:52 GMT 2025 , Edited by admin on Mon Mar 31 22:24:52 GMT 2025
PRIMARY
PUBCHEM
853477
Created by admin on Mon Mar 31 22:24:52 GMT 2025 , Edited by admin on Mon Mar 31 22:24:52 GMT 2025
PRIMARY
FDA UNII
0II79F4L0K
Created by admin on Mon Mar 31 22:24:52 GMT 2025 , Edited by admin on Mon Mar 31 22:24:52 GMT 2025
PRIMARY
EPA CompTox
DTXSID401311462
Created by admin on Mon Mar 31 22:24:52 GMT 2025 , Edited by admin on Mon Mar 31 22:24:52 GMT 2025
PRIMARY
CAS
2577-48-2
Created by admin on Mon Mar 31 22:24:52 GMT 2025 , Edited by admin on Mon Mar 31 22:24:52 GMT 2025
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER