Navigation

name Structure Reference Source Properties Activities Metabolism

4-hydroxyproline

AlkaPlorer ID: AK003363

Synonym: '4-Hydroxyproline', 'cis-4-Hydroxy-L-Proline', '51-35-4', 'Hydroxyproline', 'L-Hydroxyproline', '(2S)-4-hydroxypyrrolidine-2-carboxylic acid', '4-Hydroxy-L-proline', '49761-17-3', 'cis-4-Hydroxy-D-proline', '4-hydroxy-L-proline', '618-27-9', 'trans-4-Hydroxy-L-proline', '3398-22-9', 'L-threo-4-hydroxyproline', 'Hydroxy-L-proline', '(2S,4R)-4-hydroxy-2-pyrrolidinecarboxylic acid', 'L-4-Hydroxyproline', 'Hyp', 'trans-4-Hydroxyproline', '618-28-0', 'cis-4-hydroxy-D-proline', 'trans-L-Hydroxyproline', 'trans-Hydroxyproline', 'Hypro', '4Hyp', '(2S,4R)-trans-4-hydroxyproline', '2584-71-6', 'trans-4-hydroxy-L-proline', 'delta-hydroxyproline', 'hydroxy-L-proline'

IUPAC Name: (2R,4S)-4-hydroxypyrrolidine-2-carboxylic acid

Structure

SMILES: O=C(O)[C@H]1C[C@H](O)CN1

copy

InChI: InChI=1S/C5H9NO3/c7-3-1-4(5(8)9)6-2-3/h3-4,6-7H,1-2H2,(H,8,9)/t3-,4+/m0/s1

copy

InChIKey: PMMYEEVYMWASQN-IUYQGCFVSA-N

copy

Source

Species Genus Family Order Class Phylum Kingdom Domain
Antirrhinum majus Antirrhinum Plantaginaceae Lamiales Magnoliopsida Streptophyta Viridiplantae Eukaryota

Properties Information

Molecule Weight: 131.131

TPSA？: 69.56

MolLogP？: -1.2062

Number of H-Donors: 3

Number of H-Acceptors: 3

RingCount: 1

Activities Information

Organism Target Name Standard Type Standard Value Standard Units doi

Metabolism Information

AKRT ID Reaction Reaction Link ID
AKRT023055 O=C(O)[C@@H]1C[C@H](O)CN1>>O=C(O)[C@H]1C[C@H](O)CN1 None
AKRT023059 O=C(O)[C@@H]1C[C@H](O[C@H]2O[C@@H](CO)[C@H](O)[C@H]2O[C@H]2O[C@@H](CO)[C@H](O)[C@H]2O)CN1>>O=C(O)[C@H]1C[C@H](O)CN1 enzymemap_60301
AKRT023060 O=C(O)[C@@H]1C[C@H](O[C@H]2O[C@@H](CO)[C@H](O)[C@H]2O[C@H]2O[C@@H](CO)[C@H](O)[C@H]2O)CN1>>O=C(O)[C@H]1C[C@H](O)CN1.OC[C@@H]1O[C@H](O[C@H]2[C@@H](O)O[C@@H](CO)[C@@H]2O)[C@H](O)[C@H]1O None
AKRT023112 O=C(O)[C@H]1C[C@@H](O[C@H]2O[C@@H](CO)[C@H](O)[C@@H]2O)CN1>>O=C(O)[C@H]1C[C@H](O)CN1 enzymemap_60301
AKRT023113 O=C(O)[C@H]1C[C@@H](O[C@H]2O[C@@H](CO)[C@H](O)[C@@H]2O)CN1>>O=C(O)[C@H]1C[C@H](O)CN1.OC[C@@H]1O[C@H](O)[C@@H](O)[C@H]1O None
AKRT023114 O=C(O)[C@H]1C[C@H](O)CN1>>O=C(O)[C@@H]1C[C@H](O)CN1 None