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tert-Butyl (4-(5-carbamoyl-2-(1-ethyl-3-methyl-1H-pyrazole-5-carboxamido)-1Hbenzo[d]imidazol-1-yl)butyl)carbamate ID: ALA5205725
PubChem CID: 131997673
Max Phase: Preclinical
Molecular Formula: C24H33N7O4
Molecular Weight: 483.57
Associated Items:
Names and Identifiers Canonical SMILES: CCn1nc(C)cc1C(=O)Nc1nc2cc(C(N)=O)ccc2n1CCCCNC(=O)OC(C)(C)C
Standard InChI: InChI=1S/C24H33N7O4/c1-6-31-19(13-15(2)29-31)21(33)28-22-27-17-14-16(20(25)32)9-10-18(17)30(22)12-8-7-11-26-23(34)35-24(3,4)5/h9-10,13-14H,6-8,11-12H2,1-5H3,(H2,25,32)(H,26,34)(H,27,28,33)
Standard InChI Key: MPJIVKZUCVOHHJ-UHFFFAOYSA-N
Molfile:
RDKit 2D
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-2.7578 0.7913 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.5526 0.5783 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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29 30 2 0
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31 32 1 0
32 33 1 0
32 34 1 0
32 35 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: 483.57Molecular Weight (Monoisotopic): 483.2594AlogP: 3.22#Rotatable Bonds: 9Polar Surface Area: 146.16Molecular Species: NEUTRALHBA: 8HBD: 3#RO5 Violations: ┄HBA (Lipinski): 11HBD (Lipinski): 4#RO5 Violations (Lipinski): 1CX Acidic pKa: 13.47CX Basic pKa: 1.96CX LogP: 2.22CX LogD: 2.22Aromatic Rings: 3Heavy Atoms: 35QED Weighted: 0.40Np Likeness Score: -1.93
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 ]