The store will not work correctly when cookies are disabled.
JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.
Ethyl 1-(3-Methoxybenzyl)-2-methyl-5-(3-(piperidin-1-yl)-propoxy)-1H-indole-3-carboxylate ID: ALA3774891
Chembl Id: CHEMBL3774891
PubChem CID: 127033276
Max Phase: Preclinical
Molecular Formula: C28H36N2O4
Molecular Weight: 464.61
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: CCOC(=O)c1c(C)n(Cc2cccc(OC)c2)c2ccc(OCCCN3CCCCC3)cc12
Standard InChI: InChI=1S/C28H36N2O4/c1-4-33-28(31)27-21(2)30(20-22-10-8-11-23(18-22)32-3)26-13-12-24(19-25(26)27)34-17-9-16-29-14-6-5-7-15-29/h8,10-13,18-19H,4-7,9,14-17,20H2,1-3H3
Standard InChI Key: XZKRNSBNHHHWQW-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: 464.61Molecular Weight (Monoisotopic): 464.2675AlogP: 5.44#Rotatable Bonds: 10Polar Surface Area: 52.93Molecular Species: BASEHBA: 6HBD: ┄#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): ┄#RO5 Violations (Lipinski): 1CX Acidic pKa: ┄CX Basic pKa: 9.20CX LogP: 5.19CX LogD: 3.39Aromatic Rings: 3Heavy Atoms: 34QED Weighted: 0.30Np Likeness Score: -1.31
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 ]