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(3R,4R,5S)-4-acetamido-5-guanidino-N-methoxy-3-(pentan-3-yloxy)cyclohex-1-enecarboxamide ID: ALA3357204
Chembl Id: CHEMBL3357204
PubChem CID: 118722034
Max Phase: Preclinical
Molecular Formula: C16H29N5O4
Molecular Weight: 355.44
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: CCC(CC)O[C@@H]1C=C(C(=O)NOC)C[C@H](NC(=N)N)[C@H]1NC(C)=O
Standard InChI: InChI=1S/C16H29N5O4/c1-5-11(6-2)25-13-8-10(15(23)21-24-4)7-12(20-16(17)18)14(13)19-9(3)22/h8,11-14H,5-7H2,1-4H3,(H,19,22)(H,21,23)(H4,17,18,20)/t12-,13+,14+/m0/s1
Standard InChI Key: HHWJNIXDCNTTTC-BFHYXJOUSA-N
Associated Targets(Human) 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: 355.44Molecular Weight (Monoisotopic): 355.2220AlogP: -0.08#Rotatable Bonds: 8Polar Surface Area: 138.56Molecular Species: BASEHBA: 5HBD: 5#RO5 Violations: ┄HBA (Lipinski): 9HBD (Lipinski): 6#RO5 Violations (Lipinski): 1CX Acidic pKa: 8.79CX Basic pKa: 11.88CX LogP: -0.63CX LogD: -1.94Aromatic Rings: ┄Heavy Atoms: 25QED Weighted: 0.23Np Likeness Score: 0.54
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 ]