ID: ALA5198937

Max Phase: Preclinical

Molecular Formula: C28H28Cl2FNO4

Molecular Weight: 532.44

Representations

Canonical SMILES:  Cc1cc(C(=O)O)ccc1CN1CCC[C@H](O[C@H](CO)c2cc(Cl)cc(Cl)c2)[C@@H]1c1ccc(F)cc1

Standard InChI:  InChI=1S/C28H28Cl2FNO4/c1-17-11-19(28(34)35)4-5-20(17)15-32-10-2-3-25(27(32)18-6-8-24(31)9-7-18)36-26(16-33)21-12-22(29)14-23(30)13-21/h4-9,11-14,25-27,33H,2-3,10,15-16H2,1H3,(H,34,35)/t25-,26+,27-/m0/s1

Standard InChI Key:  LXHHWDWGDGHYRC-VJGNERBWSA-N

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type:

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Properties

Molecular Weight: 532.44

Molecular Weight (Monoisotopic): 531.1379

AlogP: 6.60

#Rotatable Bonds: 8

Polar Surface Area: 70.00

Molecular Species: ACID

HBA: 4

HBD: 2

#RO5 Violations: 2

HBA (Lipinski): 5

HBD (Lipinski): 2

#RO5 Violations (Lipinski): 2

CX Acidic pKa: 3.72

CX Basic pKa: 8.05

CX LogP: 4.02

CX LogD: 3.95

Aromatic Rings: 3

Heavy Atoms: 36

QED Weighted: 0.34

Np Likeness Score: -0.55

References

1. Mak VW, Patel AM, Yen R, Hanisak J, Lim YH, Bao J, Zheng R, Seganish WM, Yu Y, Healy DR, Ogawa A, Ren Z, Soriano A, Ermakov GP, Beaumont M, Metwally E, Cheng AC, Verras A, Fischmann T, Zebisch M, Silvestre HL, McEwan PA, Barker J, Rearden P, Greshock TJ..  (2022)  Optimization and Mechanistic Investigations of Novel Allosteric Activators of PKG1α.,  65  (15.0): [PMID:35878399] [10.1021/acs.jmedchem.1c02109]

Source

Source(1):

• Scientific Literature