4-(3'-Chloro-4'-hydroxy-5'-nitro-3-biphenyl)-5-phenylisoxazole-3-carboxylic Acid

ID: ALA4215472

Chembl Id: CHEMBL4215472

PubChem CID: 145972554

Max Phase: Preclinical

Molecular Formula: C22H13ClN2O6

Molecular Weight: 436.81

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  O=C(O)c1noc(-c2ccccc2)c1-c1cccc(-c2cc(Cl)c(O)c([N+](=O)[O-])c2)c1

Standard InChI:  InChI=1S/C22H13ClN2O6/c23-16-10-15(11-17(20(16)26)25(29)30)13-7-4-8-14(9-13)18-19(22(27)28)24-31-21(18)12-5-2-1-3-6-12/h1-11,26H,(H,27,28)

Standard InChI Key:  SPIZPABAPBQRSM-UHFFFAOYSA-N

Alternative Forms

1. Parent:

   

   ALA4215472

   ---

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: 436.81

Molecular Weight (Monoisotopic): 436.0462

AlogP: 5.64

#Rotatable Bonds: 5

Polar Surface Area: 126.70

Molecular Species: ACID

HBA: 6

HBD: 2

#RO5 Violations: 1

HBA (Lipinski): 8

HBD (Lipinski): 2

#RO5 Violations (Lipinski): 1

CX Acidic pKa: 3.84

CX Basic pKa: ┄

CX LogP: 5.48

CX LogD: 0.55

Aromatic Rings: 4

Heavy Atoms: 31

QED Weighted: 0.31

Np Likeness Score: -0.75

References

1. Vickers CF, Silva APG, Chakraborty A, Fernandez P, Kurepina N, Saville C, Naranjo Y, Pons M, Schnettger LS, Gutierrez MG, Park S, Kreiswith BN, Perlin DS, Thomas EJ, Cavet JS, Tabernero L..  (2018)  Structure-Based Design of MptpB Inhibitors That Reduce Multidrug-Resistant Mycobacterium tuberculosis Survival and Infection Burden in Vivo.,  61  (18): [PMID:30153005] [10.1021/acs.jmedchem.8b00832]

Source

Source(1):

• Scientific Literature