ID: ALA3401288

Max Phase: Preclinical

Molecular Formula: C28H26N6O2S

Molecular Weight: 510.62

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1c(NC(=O)c2cc3c(s2)CCCC3)cccc1-c1cn(C)c(=O)c(Nc2ccn3ccnc3c2)n1

Standard InChI:  InChI=1S/C28H26N6O2S/c1-17-20(7-5-8-21(17)32-27(35)24-14-18-6-3-4-9-23(18)37-24)22-16-33(2)28(36)26(31-22)30-19-10-12-34-13-11-29-25(34)15-19/h5,7-8,10-16H,3-4,6,9H2,1-2H3,(H,30,31)(H,32,35)

Standard InChI Key:  VYGROVXFZCNUMO-UHFFFAOYSA-N

Associated Targets(Human)

Tyrosine-protein kinase BTK 8973 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Tyrosine-protein kinase BTK 130 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

Properties

Molecular Weight: 510.62Molecular Weight (Monoisotopic): 510.1838AlogP: 5.34#Rotatable Bonds: 5
Polar Surface Area: 93.32Molecular Species: NEUTRALHBA: 8HBD: 2
#RO5 Violations: 2HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 6.26CX LogP: 4.42CX LogD: 4.39
Aromatic Rings: 5Heavy Atoms: 37QED Weighted: 0.33Np Likeness Score: -1.74

References

1. Young WB, Barbosa J, Blomgren P, Bremer MC, Crawford JJ, Dambach D, Gallion S, Hymowitz SG, Kropf JE, Lee SH, Liu L, Lubach JW, Macaluso J, Maciejewski P, Maurer B, Mitchell SA, Ortwine DF, Di Paolo J, Reif K, Scheerens H, Schmitt A, Sowell CG, Wang X, Wong H, Xiong JM, Xu J, Zhao Z, Currie KS..  (2015)  Potent and selective Bruton's tyrosine kinase inhibitors: discovery of GDC-0834.,  25  (6): [PMID:25701252] [10.1016/j.bmcl.2015.01.032]

Source