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Bacillimidazole G ID: ALA5281606
Chembl Id: CHEMBL5281606
Max Phase: Preclinical
Molecular Formula: C28H33N4+
Molecular Weight: 425.60
Associated Items:
Names and Identifiers Canonical SMILES: CCCc1n(CCc2c[nH]c3ccccc23)c(C)c(C)[n+]1CCc1c[nH]c2ccccc12
Standard InChI: InChI=1S/C28H33N4/c1-4-9-28-31(16-14-22-18-29-26-12-7-5-10-24(22)26)20(2)21(3)32(28)17-15-23-19-30-27-13-8-6-11-25(23)27/h5-8,10-13,18-19,29-30H,4,9,14-17H2,1-3H3/q+1
Standard InChI Key: CELKXWDQNLWDDM-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: 425.60Molecular Weight (Monoisotopic): 425.2700AlogP: 5.79#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: 1.40CX LogD: 1.40Aromatic Rings: 5Heavy Atoms: 32QED Weighted: 0.30Np Likeness Score: -0.20
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 ]