ID: ALA4779833

Max Phase: Preclinical

Molecular Formula: C14H10Cl2N2O4

Molecular Weight: 341.15

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  O=C(Nc1ccc(Cl)c(Cl)c1)Nc1ccc(O)c(C(=O)O)c1

Standard InChI:  InChI=1S/C14H10Cl2N2O4/c15-10-3-1-8(6-11(10)16)18-14(22)17-7-2-4-12(19)9(5-7)13(20)21/h1-6,19H,(H,20,21)(H2,17,18,22)

Standard InChI Key:  FMTGIWPRRZNPAR-UHFFFAOYSA-N

Associated Targets(non-human)

O-acetylserine sulfhydrylase 237 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

S-sulfocysteine synthase 20 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 341.15Molecular Weight (Monoisotopic): 340.0018AlogP: 4.04#Rotatable Bonds: 3
Polar Surface Area: 98.66Molecular Species: ACIDHBA: 3HBD: 4
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 2.61CX Basic pKa: CX LogP: 4.33CX LogD: 0.82
Aromatic Rings: 2Heavy Atoms: 22QED Weighted: 0.63Np Likeness Score: -1.11

References

1. Brunner K,Maric S,Reshma RS,Almqvist H,Seashore-Ludlow B,Gustavsson AL,Poyraz Ö,Yogeeswari P,Lundbäck T,Vallin M,Sriram D,Schnell R,Schneider G.  (2016)  Inhibitors of the Cysteine Synthase CysM with Antibacterial Potency against Dormant Mycobacterium tuberculosis.,  59  (14): [PMID:27379713] [10.1021/acs.jmedchem.6b00674]
2. Brunner K, Steiner EM, Reshma RS, Sriram D, Schnell R, Schneider G..  (2017)  Profiling of in vitro activities of urea-based inhibitors against cysteine synthases from Mycobacterium tuberculosis.,  27  (19): [PMID:28882483] [10.1016/j.bmcl.2017.08.039]

Source