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ID: ALA4848715
Max Phase: Preclinical
Molecular Formula: C26H36INO4
Molecular Weight: 426.58
Molecule Type: Unknown
Associated Items:
Representations Canonical SMILES: COc1c2c(cc3c1C(CC(=O)/C=C/C1C(C)=CCCC1(C)C)[N+](C)(C)CC3)OCO2.[I-]
Standard InChI: InChI=1S/C26H36NO4.HI/c1-17-8-7-12-26(2,3)20(17)10-9-19(28)15-21-23-18(11-13-27(21,4)5)14-22-24(25(23)29-6)31-16-30-22;/h8-10,14,20-21H,7,11-13,15-16H2,1-6H3;1H/q+1;/p-1/b10-9+;
Standard InChI Key: FBJIMHZEFFXCFU-RRABGKBLSA-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: 426.58Molecular Weight (Monoisotopic): 426.2639AlogP: 5.00#Rotatable Bonds: 5Polar 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: 0.58CX LogD: 0.58Aromatic Rings: 1Heavy Atoms: 31QED Weighted: 0.38Np Likeness Score: 1.99
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 ]