5-[(2-chlorophenyl)sulfanyl]-2-{6-[(2-cyclopropylethyl)amino]pyridin-2-yl}-6'-[(3,4-difluorophenyl)amino]-4-hydroxy-1,2,3,6-tetrahydro-[2,2'-bipyridin]-6-one

ID: ALA5171701

Chembl Id: CHEMBL5171701

PubChem CID: 168269890

Max Phase: Preclinical

Molecular Formula: C32H28ClF2N5O2S

Molecular Weight: 620.12

Names and Identifiers

Canonical SMILES:  O=C1NC(c2cccc(NCCC3CC3)n2)(c2cccc(Nc3ccc(F)c(F)c3)n2)CC(O)=C1Sc1ccccc1Cl

Standard InChI:  InChI=1S/C32H28ClF2N5O2S/c33-21-5-1-2-6-25(21)43-30-24(41)18-32(40-31(30)42,26-7-3-9-28(38-26)36-16-15-19-11-12-19)27-8-4-10-29(39-27)37-20-13-14-22(34)23(35)17-20/h1-10,13-14,17,19,41H,11-12,15-16,18H2,(H,36,38)(H,37,39)(H,40,42)

Standard InChI Key:  XJPQZHPKRRVQMS-UHFFFAOYSA-N

Alternative Forms

1. Parent:

   

   ALA5171701

   ---

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

Calculated Properties

Molecular Weight: 620.12

Molecular Weight (Monoisotopic): 619.1620

AlogP: 7.69

#Rotatable Bonds: 10

Polar Surface Area: 99.17

Molecular Species: ACID

HBA: 7

HBD: 4

#RO5 Violations: 2

HBA (Lipinski): 7

HBD (Lipinski): 4

#RO5 Violations (Lipinski): 2

CX Acidic pKa: 4.89

CX Basic pKa: 6.26

CX LogP: 5.83

CX LogD: 4.87

Aromatic Rings: 4

Heavy Atoms: 43

QED Weighted: 0.14

Np Likeness Score: -1.11

References

1. Wei B, Robarge K, Labadie SS, Chen J, Corson LB, DiPasquale A, Dragovich PS, Eigenbrot C, Evangelista M, Fauber BP, Hitz A, Hong R, Lai KW, Liu W, Ma S, Malek S, O'Brien T, Pang J, Peterson D, Salphati L, Sampath D, Sideris S, Ultsch M, Xu Z, Yen I, Yu D, Yue Q, Zhou A, Purkey HE..  (2022)  Structure-based optimization of hydroxylactam as potent, cell-active inhibitors of lactate dehydrogenase.,  59  [PMID:35065235] [10.1016/j.bmcl.2022.128576]

2. Wei B, Robarge K, Labadie SS, Chen J, Corson LB, DiPasquale A, Dragovich PS, Eigenbrot C, Evangelista M, Fauber BP, Hitz A, Hong R, Lai KW, Liu W, Ma S, Malek S, O'Brien T, Pang J, Peterson D, Salphati L, Sampath D, Sideris S, Ultsch M, Xu Z, Yen I, Yu D, Yue Q, Zhou A, Purkey HE..  (2022)  Structure-based optimization of hydroxylactam as potent, cell-active inhibitors of lactate dehydrogenase.,  59  [PMID:35065235] [10.1016/j.bmcl.2022.128576]

Source

Source(1):

• Scientific Literature