N-(3-(4-(4-(1-(3,3-dimethylbutanoyl)piperidin-4-yloxy)-3-methylphenylamino)quinazolin-6-yl)prop-2-ynyl)-2-methoxyacetamide

ID: ALA230575

Chembl Id: CHEMBL230575

PubChem CID: 44426260

Max Phase: Preclinical

Molecular Formula: C32H39N5O4

Molecular Weight: 557.70

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  COCC(=O)NCC#Cc1ccc2ncnc(Nc3ccc(OC4CCN(C(=O)CC(C)(C)C)CC4)c(C)c3)c2c1

Standard InChI:  InChI=1S/C32H39N5O4/c1-22-17-24(9-11-28(22)41-25-12-15-37(16-13-25)30(39)19-32(2,3)4)36-31-26-18-23(8-10-27(26)34-21-35-31)7-6-14-33-29(38)20-40-5/h8-11,17-18,21,25H,12-16,19-20H2,1-5H3,(H,33,38)(H,34,35,36)

Standard InChI Key:  WYWVXEDYXGGHGR-UHFFFAOYSA-N

Alternative Forms

1. Parent:

   

   ALA230575

   N-(3-(4-(4-(1-(3,3-dimethylbutanoyl)piperidin-4-yloxy)-3-methylphenylamino)quinazolin-6-yl)prop-2-ynyl)-2-methoxyacetamide

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Small molecule

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 557.70

Molecular Weight (Monoisotopic): 557.3002

AlogP: 4.60

#Rotatable Bonds: 8

Polar Surface Area: 105.68

Molecular Species: NEUTRAL

HBA: 7

HBD: 2

#RO5 Violations: 1

HBA (Lipinski): 9

HBD (Lipinski): 2

#RO5 Violations (Lipinski): 1

CX Acidic pKa: 12.12

CX Basic pKa: 4.07

CX LogP: 4.05

CX LogD: 4.05

Aromatic Rings: 3

Heavy Atoms: 41

QED Weighted: 0.39

Np Likeness Score: -1.31

References

1. Lippa B, Kauffman GS, Arcari J, Kwan T, Chen J, Hungerford W, Bhattacharya S, Zhao X, Williams C, Xiao J, Pustilnik L, Su C, Moyer JD, Ma L, Campbell M, Steyn S..  (2007)  The discovery of highly selective erbB2 (Her2) inhibitors for the treatment of cancer.,  17  (11): [PMID:17398092] [10.1016/j.bmcl.2007.03.046]

Source

Source(1):

• Scientific Literature