2-(1-Ethyl-3-methyl-1H-pyrazole-5-carboxamido)-7-(3-(1-ethyl-3-methyl-1H-pyrazole-5-carboxamido)propoxy)-1-methyl-1H-benzo[d]imidazole-5-carboxamide

ID: ALA5176115

PubChem CID: 168276131

Max Phase: Preclinical

Molecular Formula: C26H33N9O4

Molecular Weight: 535.61

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  CCn1nc(C)cc1C(=O)NCCCOc1cc(C(N)=O)cc2nc(NC(=O)c3cc(C)nn3CC)n(C)c12

Standard InChI:  InChI=1S/C26H33N9O4/c1-6-34-19(11-15(3)31-34)24(37)28-9-8-10-39-21-14-17(23(27)36)13-18-22(21)33(5)26(29-18)30-25(38)20-12-16(4)32-35(20)7-2/h11-14H,6-10H2,1-5H3,(H2,27,36)(H,28,37)(H,29,30,38)

Standard InChI Key:  SZRWWBFZIKGCGY-UHFFFAOYSA-N

Molfile:  

 
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M  END

Alternative Forms

  1. Parent:

    ALA5176115

    ---

Associated Targets(Human)

STING1 Tchem Stimulator of interferon genes protein (1885 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THP1-Dual (100 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 535.61Molecular Weight (Monoisotopic): 535.2656AlogP: 2.17#Rotatable Bonds: 11
Polar Surface Area: 163.98Molecular Species: NEUTRALHBA: 10HBD: 3
#RO5 Violations: 1HBA (Lipinski): 13HBD (Lipinski): 4#RO5 Violations (Lipinski): 2
CX Acidic pKa: 13.34CX Basic pKa: 2.10CX LogP: 0.56CX LogD: 0.56
Aromatic Rings: 4Heavy Atoms: 39QED Weighted: 0.25Np Likeness Score: -1.37

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]

Source