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Ethyl 1-(4-Fluorobenzyl)-2-methyl-5-(3-(piperidin-1-yl)propoxy)-1H-indole-3-carboxylate ID: ALA3775789
Chembl Id: CHEMBL3775789
PubChem CID: 127033557
Max Phase: Preclinical
Molecular Formula: C27H33FN2O3
Molecular Weight: 452.57
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: CCOC(=O)c1c(C)n(Cc2ccc(F)cc2)c2ccc(OCCCN3CCCCC3)cc12
Standard InChI: InChI=1S/C27H33FN2O3/c1-3-32-27(31)26-20(2)30(19-21-8-10-22(28)11-9-21)25-13-12-23(18-24(25)26)33-17-7-16-29-14-5-4-6-15-29/h8-13,18H,3-7,14-17,19H2,1-2H3
Standard InChI Key: CUOLUMWSTSHDGE-UHFFFAOYSA-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: 452.57Molecular Weight (Monoisotopic): 452.2475AlogP: 5.57#Rotatable Bonds: 9Polar Surface Area: 43.70Molecular Species: BASEHBA: 5HBD: ┄#RO5 Violations: 1HBA (Lipinski): 5HBD (Lipinski): ┄#RO5 Violations (Lipinski): 1CX Acidic pKa: ┄CX Basic pKa: 9.20CX LogP: 5.49CX LogD: 3.69Aromatic Rings: 3Heavy Atoms: 33QED Weighted: 0.31Np Likeness Score: -1.47
References 1. Lepri S, Buonerba F, Goracci L, Velilla I, Ruzziconi R, Schindler BD, Seo SM, Kaatz GW, Cruciani G.. (2016) Indole Based Weapons to Fight Antibiotic Resistance: A Structure-Activity Relationship Study., 59 (3): [PMID:26757340 ] [10.1021/acs.jmedchem.5b01219 ]