N-(2-(2-acrylamidoacetamido)pyrimidin-5-yl)-3-methyl-5-(3-methylbenzamido)benzamide

ID: ALA5288995

Chembl Id: CHEMBL5288995

Max Phase: Preclinical

Molecular Formula: C25H24N6O4

Molecular Weight: 472.51

Associated Items:

Names and Identifiers

Canonical SMILES:  C=CC(=O)NCC(=O)Nc1ncc(NC(=O)c2cc(C)cc(NC(=O)c3cccc(C)c3)c2)cn1

Standard InChI:  InChI=1S/C25H24N6O4/c1-4-21(32)26-14-22(33)31-25-27-12-20(13-28-25)30-24(35)18-9-16(3)10-19(11-18)29-23(34)17-7-5-6-15(2)8-17/h4-13H,1,14H2,2-3H3,(H,26,32)(H,29,34)(H,30,35)(H,27,28,31,33)

Standard InChI Key:  FJZGMVSVUJSVBF-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA5288995

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Associated Targets(Human)

BTK Tclin Tyrosine-protein kinase BTK (8973 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OCI-Ly7 (35 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: 472.51Molecular Weight (Monoisotopic): 472.1859AlogP: 2.84#Rotatable Bonds: 8
Polar Surface Area: 142.18Molecular Species: NEUTRALHBA: 6HBD: 4
#RO5 Violations: HBA (Lipinski): 10HBD (Lipinski): 4#RO5 Violations (Lipinski):
CX Acidic pKa: 10.90CX Basic pKa: 0.93CX LogP: 2.83CX LogD: 2.83
Aromatic Rings: 3Heavy Atoms: 35QED Weighted: 0.37Np Likeness Score: -1.44

References

1. Liu XJ, Xu-Liu, Pang XJ, -Ying Yuan X, Yu GX, Li YR, Guan YF, Zhang YB, Song J, Zhang QR, Zhang SY..  (2021)  Progress in the development of small molecular inhibitors of the Bruton's tyrosine kinase (BTK) as a promising cancer therapy.,  47  [PMID:34479103] [10.1016/j.bmc.2021.116358]

Source