4-Chloro-N-{3-[1-(2-hydroxyethyl)-1H-indol-5-yl]-1H-indazol-5-yl}benzamide

ID: ALA4474297

Chembl Id: CHEMBL4474297

PubChem CID: 155536980

Max Phase: Preclinical

Molecular Formula: C24H19ClN4O2

Molecular Weight: 430.90

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  O=C(Nc1ccc2[nH]nc(-c3ccc4c(ccn4CCO)c3)c2c1)c1ccc(Cl)cc1

Standard InChI:  InChI=1S/C24H19ClN4O2/c25-18-4-1-15(2-5-18)24(31)26-19-6-7-21-20(14-19)23(28-27-21)17-3-8-22-16(13-17)9-10-29(22)11-12-30/h1-10,13-14,30H,11-12H2,(H,26,31)(H,27,28)

Standard InChI Key:  ZRMNMJGTFRPZSF-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA4474297

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Associated Targets(non-human)

Tlr4 Toll-like receptor 4/Ly96 (54 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Peritoneal macrophage (1554 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 430.90Molecular Weight (Monoisotopic): 430.1197AlogP: 5.08#Rotatable Bonds: 5
Polar Surface Area: 82.94Molecular Species: NEUTRALHBA: 4HBD: 3
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.83CX Basic pKa: 1.73CX LogP: 4.66CX LogD: 4.66
Aromatic Rings: 5Heavy Atoms: 31QED Weighted: 0.36Np Likeness Score: -1.67

References

1. Liu Z, Chen L, Yu P, Zhang Y, Fang B, Wu C, Luo W, Chen X, Li C, Liang G..  (2019)  Discovery of 3-(Indol-5-yl)-indazole Derivatives as Novel Myeloid Differentiation Protein 2/Toll-like Receptor 4 Antagonists for Treatment of Acute Lung Injury.,  62  (11): [PMID:30998353] [10.1021/acs.jmedchem.9b00316]

Source