(4,4',5,5'-Tetrachloro-1'H-1,3'-bipyrrole-2,2'-diyl)bis((2-hydroxy-4-(1-octyl-1H-1,2,3-triazol-5-yl)phenyl)methanone)

ID: ALA3393641

Chembl Id: CHEMBL3393641

PubChem CID: 118725574

Max Phase: Preclinical

Molecular Formula: C41H44Cl4N8O4

Molecular Weight: 854.67

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  CCCCCCCCn1cc(-c2ccc(C(=O)c3[nH]c(Cl)c(Cl)c3-n3c(C(=O)c4ccc(-c5cn(CCCCCCC)nn5)cc4O)cc(Cl)c3Cl)c(O)c2)nn1

Standard InChI:  InChI=1S/C41H44Cl4N8O4/c1-3-5-7-9-11-13-19-52-24-31(48-50-52)26-15-17-28(34(55)21-26)39(57)36-37(35(43)40(44)46-36)53-32(22-29(42)41(53)45)38(56)27-16-14-25(20-33(27)54)30-23-51(49-47-30)18-12-10-8-6-4-2/h14-17,20-24,46,54-55H,3-13,18-19H2,1-2H3

Standard InChI Key:  SXPUMGCDHXYDMQ-UHFFFAOYSA-N

Alternative Forms

1. Parent:

   

   ALA3393641

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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: 854.67

Molecular Weight (Monoisotopic): 852.2240

AlogP: 11.14

#Rotatable Bonds: 20

Polar Surface Area: 156.74

Molecular Species: ACID

HBA: 11

HBD: 3

#RO5 Violations: 3

HBA (Lipinski): 12

HBD (Lipinski): 3

#RO5 Violations (Lipinski): 3

CX Acidic pKa: 6.32

CX Basic pKa: 0.13

CX LogP: 13.23

CX LogD: 11.57

Aromatic Rings: 6

Heavy Atoms: 57

QED Weighted: 0.05

Np Likeness Score: -0.40

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