ID: ALA3393628

Max Phase: Preclinical

Molecular Formula: C22H12Cl4N2O6

Molecular Weight: 542.16

Molecule Type: Small molecule

Representations

Canonical SMILES:  O=C(c1ccc(O)cc1O)c1[nH]c(Cl)c(Cl)c1-n1c(C(=O)c2ccc(O)cc2O)cc(Cl)c1Cl

Standard InChI:  InChI=1S/C22H12Cl4N2O6/c23-12-7-13(19(33)10-3-1-8(29)5-14(10)31)28(22(12)26)18-16(24)21(25)27-17(18)20(34)11-4-2-9(30)6-15(11)32/h1-7,27,29-32H

Standard InChI Key:  GJVYKJZHPIQLTD-UHFFFAOYSA-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: 542.16

Molecular Weight (Monoisotopic): 539.9449

AlogP: 5.70

#Rotatable Bonds: 5

Polar Surface Area: 135.78

Molecular Species: NEUTRAL

HBA: 7

HBD: 5

#RO5 Violations: 2

HBA (Lipinski): 8

HBD (Lipinski): 5

#RO5 Violations (Lipinski): 2

CX Acidic pKa: 6.70

CX Basic pKa:

CX LogP: 6.71

CX LogD: 5.60

Aromatic Rings: 4

Heavy Atoms: 34

QED Weighted: 0.21

Np Likeness Score: 0.07

References

1. Li R, Cheng C, Balasis ME, Liu Y, Garner TP, Daniel KG, Li J, Qin Y, Gavathiotis E, Sebti SM..  (2015)  Design, synthesis and evaluation of marinopyrrole derivatives as selective inhibitors of Mcl-1 binding to pro-apoptotic Bim and dual Mcl-1/Bcl-xL inhibitors.,  90  [PMID:25437618] [10.1016/j.ejmech.2014.11.035]

Source

Source(1):

• Scientific Literature