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(3R,4R,5S)-N-(3-(1H-indol-2-yl)propoxy)-4-acetamido-5-amino-3-(pentan-3-yloxy)cyclohex-1-enecarboxamide ID: ALA3357203
Chembl Id: CHEMBL3357203
PubChem CID: 118722033
Max Phase: Preclinical
Molecular Formula: C25H36N4O4
Molecular Weight: 456.59
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: CCC(CC)O[C@@H]1C=C(C(=O)NOCCCc2cc3ccccc3[nH]2)C[C@H](N)[C@H]1NC(C)=O
Standard InChI: InChI=1S/C25H36N4O4/c1-4-20(5-2)33-23-15-18(14-21(26)24(23)27-16(3)30)25(31)29-32-12-8-10-19-13-17-9-6-7-11-22(17)28-19/h6-7,9,11,13,15,20-21,23-24,28H,4-5,8,10,12,14,26H2,1-3H3,(H,27,30)(H,29,31)/t21-,23+,24+/m0/s1
Standard InChI Key: NVEHHLIUGKSLBV-QPTUXGOLSA-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: 456.59Molecular Weight (Monoisotopic): 456.2737AlogP: 2.88#Rotatable Bonds: 11Polar Surface Area: 118.47Molecular Species: BASEHBA: 5HBD: 4#RO5 Violations: ┄HBA (Lipinski): 8HBD (Lipinski): 5#RO5 Violations (Lipinski): ┄CX Acidic pKa: 8.50CX Basic pKa: 9.34CX LogP: 1.67CX LogD: 0.74Aromatic Rings: 2Heavy Atoms: 33QED Weighted: 0.31Np Likeness Score: 0.33
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 ]