5-CHLORO-2-(5-METHYLTHIOPHEN-2-YL)BENZO[D]OXAZOLE

ID: ALA2259987

Max Phase: Preclinical

Molecular Formula: C12H8ClNOS

Molecular Weight: 249.72

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1ccc(-c2nc3cc(Cl)ccc3o2)s1

Standard InChI:  InChI=1S/C12H8ClNOS/c1-7-2-5-11(16-7)12-14-9-6-8(13)3-4-10(9)15-12/h2-6H,1H3

Standard InChI Key:  SYXAXNWEMZBDQC-UHFFFAOYSA-N

Associated Targets(non-human)

Pseudomonas putida 467 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Escherichia coli 133304 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Geobacillus stearothermophilus 181 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Bacillus subtilis 32866 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Aspergillus niger 16508 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Aspergillus flavus 8875 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 249.72Molecular Weight (Monoisotopic): 249.0015AlogP: 4.52#Rotatable Bonds: 1
Polar Surface Area: 26.03Molecular Species: NEUTRALHBA: 3HBD: 0
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 4.37CX LogD: 4.37
Aromatic Rings: 3Heavy Atoms: 16QED Weighted: 0.63Np Likeness Score: -2.13

References

1. Kumar R, Nair RR, Dhiman SS, Sharma J, Prakash O.  (2010)  Iodine (III)-mediated synthesis of some 2-aryl/hetarylbenzoxazoles as antibacterial/antifungal agents,  19  (6): [10.1007/s00044-009-9211-y]

Source