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(2S,3R)-3-hydroxypiperidine-2-carboxylic acid ID: ALA403077
Chembl Id: CHEMBL403077
Cas Number: 194297-98-8
PubChem CID: 10855598
Max Phase: Preclinical
Molecular Formula: C6H11NO3
Molecular Weight: 145.16
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Synonyms: (2S,3R)-3-Hydroxypipecolic Acid | (2S,3R)-3-hydroxypiperidine-2-carboxylic acid|112241-70-0|194297-98-8|(2S,3R)-3-Hydroxypipecolic Acid|2-Piperidinecarboxylicacid,3-hydroxy-,(2R,3S)-rel-(9CI)|2-Piperidinecarboxylicacid, 3-hydroxy-, (2S,3R)-|2-Piperidinecarboxylicacid,3-hydroxy-,(2S,3R)-(9CI)|CHEMBL403077|SCHEMBL2964298|FDMYUQHVJYNDLI-UHNVWZDZSA-N|EN300-701253|2-Piperidinecarboxylic acid,3-hydroxy-,(2S,3R)-|rac-(2R,3S)-3-hydroxypiperidine-2-carboxylic acid
Canonical SMILES: O=C(O)[C@H]1NCCC[C@H]1O
Standard InChI: InChI=1S/C6H11NO3/c8-4-2-1-3-7-5(4)6(9)10/h4-5,7-8H,1-3H2,(H,9,10)/t4-,5+/m1/s1
Standard InChI Key: FDMYUQHVJYNDLI-UHNVWZDZSA-N
Associated Targets(Human) Associated Targets(non-human) Molecule Features Natural Product: YesOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 145.16Molecular Weight (Monoisotopic): 145.0739AlogP: -0.82#Rotatable Bonds: 1Polar Surface Area: 69.56Molecular Species: ZWITTERIONHBA: 3HBD: 3#RO5 Violations: ┄HBA (Lipinski): 4HBD (Lipinski): 3#RO5 Violations (Lipinski): ┄CX Acidic pKa: 1.75CX Basic pKa: 9.79CX LogP: -3.20CX LogD: -3.20Aromatic Rings: ┄Heavy Atoms: 10QED Weighted: 0.45Np Likeness Score: 1.60
References 1. Ohara C, Takahashi R, Miyagawa T, Yoshimura Y, Kato A, Adachi I, Takahata H.. (2008) Synthesis of all stereoisomers of 3-hydroxypipecolic acid and 3-hydroxy-4,5-dehydropipecolic acid and their evaluation as glycosidase inhibitors., 18 (6): [PMID:18296050 ] [10.1016/j.bmcl.2008.02.028 ] 2. Yoshimura Y, Ohara C, Imahori T, Saito Y, Kato A, Miyauchi S, Adachi I, Takahata H.. (2008) Synthesis of both enantiomers of hydroxypipecolic acid derivatives equivalent to 5-azapyranuronic acids and evaluation of their inhibitory activities against glycosidases., 16 (17): [PMID:18703340 ] [10.1016/j.bmc.2008.06.016 ]