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(3R,4R,5S)-4-acetamido-5-amino-N-(benzyloxy)-3-(pentan-3-yloxy)cyclohex-1-enecarboxamide ID: ALA3357202
Chembl Id: CHEMBL3357202
PubChem CID: 118722032
Max Phase: Preclinical
Molecular Formula: C21H31N3O4
Molecular Weight: 389.50
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: CCC(CC)O[C@@H]1C=C(C(=O)NOCc2ccccc2)C[C@H](N)[C@H]1NC(C)=O
Standard InChI: InChI=1S/C21H31N3O4/c1-4-17(5-2)28-19-12-16(11-18(22)20(19)23-14(3)25)21(26)24-27-13-15-9-7-6-8-10-15/h6-10,12,17-20H,4-5,11,13,22H2,1-3H3,(H,23,25)(H,24,26)/t18-,19+,20+/m0/s1
Standard InChI Key: CNTAQJJKIIBOQW-XUVXKRRUSA-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: 389.50Molecular Weight (Monoisotopic): 389.2315AlogP: 1.97#Rotatable Bonds: 9Polar Surface Area: 102.68Molecular Species: BASEHBA: 5HBD: 3#RO5 Violations: ┄HBA (Lipinski): 7HBD (Lipinski): 4#RO5 Violations (Lipinski): ┄CX Acidic pKa: 8.36CX Basic pKa: 9.30CX LogP: 1.02CX LogD: 0.19Aromatic Rings: 1Heavy Atoms: 28QED Weighted: 0.56Np Likeness Score: 0.40
References 1. Hong BT, Chen CL, Fang JM, Tsai KC, Wang SY, Huang WI, Cheng YS, Wong CH.. (2014) Oseltamivir hydroxamate and acyl sulfonamide derivatives as influenza neuraminidase inhibitors., 22 (23): [PMID:25456388 ] [10.1016/j.bmc.2014.10.005 ]