N-[(5-Chloro-2-thienyl)methyl]-[3-methoxy-4-(5-oxazolyl)phenyl]amine

ID: ALA2435800

Chembl Id: CHEMBL2435800

PubChem CID: 73349419

Max Phase: Preclinical

Molecular Formula: C15H13ClN2O2S

Molecular Weight: 320.80

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1cc(NCc2ccc(Cl)s2)ccc1-c1cnco1

Standard InChI:  InChI=1S/C15H13ClN2O2S/c1-19-13-6-10(18-7-11-3-5-15(16)21-11)2-4-12(13)14-8-17-9-20-14/h2-6,8-9,18H,7H2,1H3

Standard InChI Key:  XBWUBORBRAUTNJ-UHFFFAOYSA-N

Associated Targets(non-human)

Coxsackievirus B6 (58 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Coxsackievirus B3 (1096 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Vero (26788 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hepatitis C virus (23859 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

Calculated Properties

Molecular Weight: 320.80Molecular Weight (Monoisotopic): 320.0386AlogP: 4.68#Rotatable Bonds: 5
Polar Surface Area: 47.29Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 2.28CX LogP: 3.20CX LogD: 3.20
Aromatic Rings: 3Heavy Atoms: 21QED Weighted: 0.74Np Likeness Score: -1.67

References

1. Zhong ZJ, Zhang DJ, Peng ZG, Li YH, Shan GZ, Zuo LM, Wu LT, Li SY, Gao RM, Li ZR..  (2013)  Synthesis and antiviral activity of a novel class of (5-oxazolyl)phenyl amines.,  69  [PMID:23999140] [10.1016/j.ejmech.2013.07.053]

Source