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Bacillimidazole H ID: ALA5284127
Chembl Id: CHEMBL5284127
Max Phase: Preclinical
Molecular Formula: C29H35N4+
Molecular Weight: 439.63
Associated Items:
Names and Identifiers Canonical SMILES: Cc1c(C)[n+](CCc2c[nH]c3ccccc23)c(CC(C)C)n1CCc1c[nH]c2ccccc12
Standard InChI: InChI=1S/C29H35N4/c1-20(2)17-29-32(15-13-23-18-30-27-11-7-5-9-25(23)27)21(3)22(4)33(29)16-14-24-19-31-28-12-8-6-10-26(24)28/h5-12,18-20,30-31H,13-17H2,1-4H3/q+1
Standard InChI Key: IXCFQGVSEKBUGS-UHFFFAOYSA-N
Associated Targets(Human) Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Topical: 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: 439.63Molecular Weight (Monoisotopic): 439.2856AlogP: 6.04#Rotatable Bonds: 8Polar Surface Area: 40.39Molecular Species: NEUTRALHBA: 1HBD: 2#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 1CX Acidic pKa: ┄CX Basic pKa: ┄CX LogP: 1.69CX LogD: 1.69Aromatic Rings: 5Heavy Atoms: 33QED Weighted: 0.28Np Likeness Score: -0.17
References 1. Ham SL, Lee TH, Kim KJ, Kim JH, Hwang SJ, Lee SH, Yu JS, Kim KH, Lee HJ, Lee W, Kim CS.. (2023) Discovery and Biosynthesis of Imidazolium Antibiotics from the Probiotic Bacillus licheniformis ., 86 (4): [PMID:36921254 ] [10.1021/acs.jnatprod.2c01032 ]