ID: ALA4214491

Max Phase: Preclinical

Molecular Formula: C19H17ClFN3O

Molecular Weight: 357.82

Molecule Type: Small molecule

Representations

Canonical SMILES:  CC(C)(C)c1ccc(C(=O)/C(C#N)=N/Nc2ccc(F)c(Cl)c2)cc1

Standard InChI:  InChI=1S/C19H17ClFN3O/c1-19(2,3)13-6-4-12(5-7-13)18(25)17(11-22)24-23-14-8-9-16(21)15(20)10-14/h4-10,23H,1-3H3/b24-17+

Standard InChI Key:  QPNPMAJDUMICKQ-JJIBRWJFSA-N

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

Properties

Molecular Weight: 357.82

Molecular Weight (Monoisotopic): 357.1044

AlogP: 4.95

#Rotatable Bonds: 4

Polar Surface Area: 65.25

Molecular Species: ACID

HBA: 4

HBD: 1

#RO5 Violations: 0

HBA (Lipinski): 4

HBD (Lipinski): 1

#RO5 Violations (Lipinski): 0

CX Acidic pKa: 6.09

CX Basic pKa:

CX LogP: 6.41

CX LogD: 5.22

Aromatic Rings: 2

Heavy Atoms: 25

QED Weighted: 0.48

Np Likeness Score: -1.81

References

1. Liu Z, Zhu Y, Chen H, Wang P, Mei FC, Ye N, Cheng X, Zhou J..  (2017)  Structure-activity relationships of 2-substituted phenyl-N-phenyl-2-oxoacetohydrazonoyl cyanides as novel antagonists of exchange proteins directly activated by cAMP (EPACs).,  27  (23): [PMID:29100797] [10.1016/j.bmcl.2017.10.056]

Source

Source(1):

• Scientific Literature