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(S)-2-((S)-2-amino-5-guanidinopentanamido)-3-(pyridin-3-yl)propanoic acid ID: ALA4206914
Chembl Id: CHEMBL4206914
PubChem CID: 145977667
Max Phase: Preclinical
Molecular Formula: C14H22N6O3
Molecular Weight: 322.37
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: N=C(N)NCCC[C@H](N)C(=O)N[C@@H](Cc1cccnc1)C(=O)O
Standard InChI: InChI=1S/C14H22N6O3/c15-10(4-2-6-19-14(16)17)12(21)20-11(13(22)23)7-9-3-1-5-18-8-9/h1,3,5,8,10-11H,2,4,6-7,15H2,(H,20,21)(H,22,23)(H4,16,17,19)/t10-,11-/m0/s1
Standard InChI Key: WILPEDDCPARJQX-QWRGUYRKSA-N
Associated Targets(non-human) Molecule Features Natural Product: NoOral: 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: 322.37Molecular Weight (Monoisotopic): 322.1753AlogP: -1.22#Rotatable Bonds: 9Polar Surface Area: 167.21Molecular Species: ZWITTERIONHBA: 5HBD: 6#RO5 Violations: 1HBA (Lipinski): 9HBD (Lipinski): 8#RO5 Violations (Lipinski): 1CX Acidic pKa: 3.70CX Basic pKa: 12.02CX LogP: -3.24CX LogD: -3.98Aromatic Rings: 1Heavy Atoms: 23QED Weighted: 0.19Np Likeness Score: 0.11
References 1. Fernandez Diaz-Rullo F, Zamberlan F, Mewis RE, Fekete M, Broche L, Cheyne LA, Dall'Angelo S, Duckett SB, Dawson D, Zanda M.. (2017) Synthesis and hyperpolarisation of eNOS substrates for quantification of NO production by 1H NMR spectroscopy., 25 (10): [PMID:28365086 ] [10.1016/j.bmc.2017.03.041 ]