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ID: ALA4860268
Max Phase: Preclinical
Molecular Formula: C25H32INO4
Molecular Weight: 410.53
Molecule Type: Unknown
Associated Items:
Representations Canonical SMILES: COc1c2c(cc3c1C(CC(=O)c1ccc(CC(C)C)cc1)[N+](C)(C)CC3)OCO2.[I-]
Standard InChI: InChI=1S/C25H32NO4.HI/c1-16(2)12-17-6-8-18(9-7-17)21(27)14-20-23-19(10-11-26(20,3)4)13-22-24(25(23)28-5)30-15-29-22;/h6-9,13,16,20H,10-12,14-15H2,1-5H3;1H/q+1;/p-1
Standard InChI Key: WUWXOGZFWFWPGC-UHFFFAOYSA-M
Associated Targets(Human) Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: UnknownTopical: 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
Properties Molecular Weight: 410.53Molecular Weight (Monoisotopic): 410.2326AlogP: 4.57#Rotatable Bonds: 6Polar Surface Area: 44.76Molecular Species: NEUTRALHBA: 4HBD: 0#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 0CX Acidic pKa: CX Basic pKa: CX LogP: 0.48CX LogD: 0.48Aromatic Rings: 2Heavy Atoms: 30QED Weighted: 0.52Np Likeness Score: 0.88
References 1. Ivanenkov YA, Yu Filyaeva K, Matniyazov RT, Baymiev AK, Baymiev AK, Vladimirova AA, Yamidanov RS, Mavzyutov AR, Zileeva ZR, Zainullina LF, Vakhitova JV, Marina VI, Terentiev VA, Osterman IA, Kartsev VG, Bezrukov DS, Dontsova OA.. (2021) Antibacterial activity of noscapine analogs., 43 [PMID:33892103 ] [10.1016/j.bmcl.2021.128055 ]