N-(2-(2-(dimethylamino)ethylsulfonyl)-4-methoxy-5-(4-(1-methyl-1H-indol-3-yl)pyrimidin-2-ylamino)phenyl)acrylamide

ID: ALA4592472

Chembl Id: CHEMBL4592472

PubChem CID: 155568841

Max Phase: Preclinical

Molecular Formula: C27H30N6O4S

Molecular Weight: 534.64

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  C=CC(=O)Nc1cc(Nc2nccc(-c3cn(C)c4ccccc34)n2)c(OC)cc1S(=O)(=O)CCN(C)C

Standard InChI:  InChI=1S/C27H30N6O4S/c1-6-26(34)29-22-15-21(24(37-5)16-25(22)38(35,36)14-13-32(2)3)31-27-28-12-11-20(30-27)19-17-33(4)23-10-8-7-9-18(19)23/h6-12,15-17H,1,13-14H2,2-5H3,(H,29,34)(H,28,30,31)

Standard InChI Key:  UZTKORAJTJRUTJ-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA4592472

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Associated Targets(Human)

EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H1975 (4994 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PC-9 (1037 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H292 (733 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: 534.64Molecular Weight (Monoisotopic): 534.2049AlogP: 3.85#Rotatable Bonds: 10
Polar Surface Area: 118.45Molecular Species: NEUTRALHBA: 9HBD: 2
#RO5 Violations: 1HBA (Lipinski): 10HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 10.83CX Basic pKa: 6.25CX LogP: 4.02CX LogD: 3.99
Aromatic Rings: 4Heavy Atoms: 38QED Weighted: 0.29Np Likeness Score: -1.17

References

1. An B, Pan T, Hu J, Pang Y, Huang L, Chan ASC, Li X, Yan J..  (2019)  The discovery of a potent and selective third-generation EGFR kinase inhibitor as a therapy for EGFR L858R/T790M double mutant non-small cell lung cancer.,  183  [PMID:31581004] [10.1016/j.ejmech.2019.111709]

Source