(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

Alternative Forms

  1. Parent:

    ALA3357203

    ---

Associated Targets(non-human)

NA Neuraminidase (159 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NA Neuraminidase (94 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 456.59Molecular Weight (Monoisotopic): 456.2737AlogP: 2.88#Rotatable Bonds: 11
Polar 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: 0.74
Aromatic 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]

Source