DPR
D-PROLINE
Created: | 1999-07-08 |
Last modified: | 2023-11-03 |
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Chemical Details | |
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Formal Charge | 0 |
Atom Count | 17 |
Chiral Atom Count | 1 |
Bond Count | 17 |
Aromatic Bond Count | 0 |
Chemical Component Summary | |
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Name | D-PROLINE |
Systematic Name (OpenEye OEToolkits) | (2R)-pyrrolidine-2-carboxylic acid |
Formula | C5 H9 N O2 |
Molecular Weight | 115.13 |
Type | D-PEPTIDE LINKING |
Chemical Descriptors | |||
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Type | Program | Version | Descriptor |
SMILES | ACDLabs | 12.01 | O=C(O)C1NCCC1 |
SMILES | CACTVS | 3.370 | OC(=O)[CH]1CCCN1 |
SMILES | OpenEye OEToolkits | 1.7.0 | C1CC(NC1)C(=O)O |
Canonical SMILES | CACTVS | 3.370 | OC(=O)[C@H]1CCCN1 |
Canonical SMILES | OpenEye OEToolkits | 1.7.0 | C1C[C@@H](NC1)C(=O)O |
InChI | InChI | 1.03 | InChI=1S/C5H9NO2/c7-5(8)4-2-1-3-6-4/h4,6H,1-3H2,(H,7,8)/t4-/m1/s1 |
InChIKey | InChI | 1.03 | ONIBWKKTOPOVIA-SCSAIBSYSA-N |
Drug Info: DrugBank
DrugBank ID | DB02853 |
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Name | D-Proline |
Groups | experimental |
Description | D-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 |
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CAS number | 344-25-2 |
Drug Targets
Name | Target Sequence | Pharmacological Action | Actions |
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Proton-coupled amino acid transporter 1 | MSTQRLRNEDYHDYSSTDVSPEESPSEGLNNLSSPGSYQRFGQSNSTTWF... | 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 Name | Reference |
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PubChem | 8988, 6971012 |
ChEMBL | CHEMBL80257 |
ChEBI | CHEBI:16313, CHEBI:57726 |
CCDC/CSD | HUDRAC |