(trans)-N-(3-(7-(3-Acrylamido-4-methylphenylamino)-1-methyl-2-oxo-1,2-dihydropyrimido[4,5-d]pyrimidin-3(4H)-yl)-4-methylphenyl)-4-isopropylcyclohexanecarboxamide

ID: ALA4086774

PubChem CID: 137641775

Max Phase: Preclinical

Molecular Formula: C34H41N7O3

Molecular Weight: 595.75

Molecule Type: Small molecule

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  C=CC(=O)Nc1cc(Nc2ncc3c(n2)N(C)C(=O)N(c2cc(NC(=O)[C@H]4CC[C@H](C(C)C)CC4)ccc2C)C3)ccc1C

Standard InChI:  InChI=1S/C34H41N7O3/c1-7-30(42)38-28-16-26(14-8-21(28)4)37-33-35-18-25-19-41(34(44)40(6)31(25)39-33)29-17-27(15-9-22(29)5)36-32(43)24-12-10-23(11-13-24)20(2)3/h7-9,14-18,20,23-24H,1,10-13,19H2,2-6H3,(H,36,43)(H,38,42)(H,35,37,39)/t23-,24-

Standard InChI Key:  BMTSNXMAAOHQMW-RQNOJGIXSA-N

Molfile:  

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M  END

Alternative Forms

  1. Parent:

    ALA4086774

    ---

Associated Targets(Human)

BMX Tchem Tyrosine-protein kinase BMX (1995 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

BaF3 (4657 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 595.75Molecular Weight (Monoisotopic): 595.3271AlogP: 6.94#Rotatable Bonds: 8
Polar Surface Area: 119.56Molecular Species: NEUTRALHBA: 6HBD: 3
#RO5 Violations: 2HBA (Lipinski): 10HBD (Lipinski): 3#RO5 Violations (Lipinski): 2
CX Acidic pKa: 13.08CX Basic pKa: 1.69CX LogP: 6.78CX LogD: 6.78
Aromatic Rings: 3Heavy Atoms: 44QED Weighted: 0.24Np Likeness Score: -1.17

References

1. Liang X, Lv F, Wang B, Yu K, Wu H, Qi Z, Jiang Z, Chen C, Wang A, Miao W, Wang W, Hu Z, Liu J, Liu X, Zhao Z, Wang L, Zhang S, Ye Z, Wang C, Ren T, Wang Y, Liu Q, Liu J..  (2017)  Discovery of 2-((3-Acrylamido-4-methylphenyl)amino)-N-(2-methyl-5-(3,4,5-trimethoxybenzamido)phenyl)-4-(methylamino)pyrimidine-5-carboxamide (CHMFL-BMX-078) as a Highly Potent and Selective Type II Irreversible Bone Marrow Kinase in the X Chromosome (BMX) Kinase Inhibitor.,  60  (5): [PMID:28140585] [10.1021/acs.jmedchem.6b01413]

Source