DPR

D-PROLINE

Created: 1999-07-08
Last modified:  2023-11-03

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Chemical Details

Formal Charge0
Atom Count17
Chiral Atom Count1
Bond Count17
Aromatic Bond Count0
2D diagram of DPR

Chemical Component Summary

NameD-PROLINE
Systematic Name (OpenEye OEToolkits)(2R)-pyrrolidine-2-carboxylic acid
FormulaC5 H9 N O2
Molecular Weight115.13
TypeD-PEPTIDE LINKING

Chemical Descriptors

TypeProgram Version Descriptor
SMILESACDLabs12.01O=C(O)C1NCCC1
SMILESCACTVS3.370OC(=O)[CH]1CCCN1
SMILESOpenEye OEToolkits1.7.0C1CC(NC1)C(=O)O
Canonical SMILESCACTVS3.370 OC(=O)[C@H]1CCCN1
Canonical SMILESOpenEye OEToolkits1.7.0 C1C[C@@H](NC1)C(=O)O
InChIInChI1.03 InChI=1S/C5H9NO2/c7-5(8)4-2-1-3-6-4/h4,6H,1-3H2,(H,7,8)/t4-/m1/s1
InChIKeyInChI1.03 ONIBWKKTOPOVIA-SCSAIBSYSA-N

Drug Info: DrugBank

DrugBank IDDB02853 
NameD-Proline
Groups experimental
DescriptionD-proline is an isomer of the naturally occurring amino acid, L-Proline. D-amino acids have been found in relatively high abundance in human plasma and saliva [A19262]. These amino acids may be of bacterial origin, but there is also evidence that they are endogenously produced through amino acid racemase activity [A19263].
Synonyms
  • D-Proline
  • (2R)-pyrrolidine-2-carboxylic acid
  • DPR
  • (R)-2-Carboxypyrrolidine
  • (R)-pyrrolidine-2-carboxylic acid
CAS number344-25-2

Drug Targets

NameTarget SequencePharmacological ActionActions
Proton-coupled amino acid transporter 1MSTQRLRNEDYHDYSSTDVSPEESPSEGLNNLSSPGSYQRFGQSNSTTWF...unknown
Drug Info/Drug Targets: DrugBank 3.0: a comprehensive resource for 'omics' research on drugs. Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS. Nucleic Acids Res. 2011 Jan; 39 (Database issue):D1035-41. | PMID:21059682

Related Resource References

Resource NameReference
PubChem 8988, 6971012
ChEMBL CHEMBL80257
ChEBI CHEBI:16313, CHEBI:57726
CCDC/CSD HUDRAC