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tert-Butyl (4-(5-carbamoyl-2-(1-isopropyl-3-methyl-1H-pyrazole-5-carboxamido)-1H-benzo[d]imidazol-1-yl)butyl)carbamate ID: ALA5195810
PubChem CID: 165146907
Max Phase: Preclinical
Molecular Formula: C25H35N7O4
Molecular Weight: 497.60
Associated Items:
Names and Identifiers Canonical SMILES: Cc1cc(C(=O)Nc2nc3cc(C(N)=O)ccc3n2CCCCNC(=O)OC(C)(C)C)n(C(C)C)n1
Standard InChI: InChI=1S/C25H35N7O4/c1-15(2)32-20(13-16(3)30-32)22(34)29-23-28-18-14-17(21(26)33)9-10-19(18)31(23)12-8-7-11-27-24(35)36-25(4,5)6/h9-10,13-15H,7-8,11-12H2,1-6H3,(H2,26,33)(H,27,35)(H,28,29,34)
Standard InChI Key: CUMSUNXHURJHIP-UHFFFAOYSA-N
Molfile:
RDKit 2D
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3.0384 1.2365 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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29 30 1 0
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14 33 1 0
16 34 1 0
34 35 1 0
34 36 1 0
M END Associated Targets(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: 497.60Molecular Weight (Monoisotopic): 497.2751AlogP: 3.78#Rotatable Bonds: 9Polar Surface Area: 146.16Molecular Species: NEUTRALHBA: 8HBD: 3#RO5 Violations: ┄HBA (Lipinski): 11HBD (Lipinski): 4#RO5 Violations (Lipinski): 1CX Acidic pKa: 13.46CX Basic pKa: 1.93CX LogP: 2.64CX LogD: 2.64Aromatic Rings: 3Heavy Atoms: 36QED Weighted: 0.38Np Likeness Score: -1.78
References 1. Jeon MJ, Lee H, Lee J, Baek SY, Lee D, Jo S, Lee JY, Kang M, Jung HR, Han SB, Kim NJ, Lee S, Kim H.. (2022) Development of Potent Immune Modulators Targeting Stimulator of Interferon Genes Receptor., 65 (7.0): [PMID:35315650 ] [10.1021/acs.jmedchem.1c01795 ]