4-[(4-Chloro-2-nitrophenyl)thio]-pyridine

ID: ALA3359635

Chembl Id: CHEMBL3359635

PubChem CID: 101886683

Max Phase: Preclinical

Molecular Formula: C11H7ClN2O2S

Molecular Weight: 266.71

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  O=[N+]([O-])c1cc(Cl)ccc1Sc1ccncc1

Standard InChI:  InChI=1S/C11H7ClN2O2S/c12-8-1-2-11(10(7-8)14(15)16)17-9-3-5-13-6-4-9/h1-7H

Standard InChI Key:  VGQCOWWMSJJMKU-UHFFFAOYSA-N

Alternative Forms

Associated Targets(Human)

PDE7A Tclin Phosphodiesterase 7A (1104 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE7B Tclin Phosphodiesterase 7B (96 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE3A Tclin Phosphodiesterase 3A (3309 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE4D Tclin Phosphodiesterase 4D (3546 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE4B Tclin Phosphodiesterase 4B (2748 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: 266.71Molecular Weight (Monoisotopic): 265.9917AlogP: 3.79#Rotatable Bonds: 3
Polar Surface Area: 56.03Molecular Species: NEUTRALHBA: 4HBD:
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 4.54CX LogP: 3.49CX LogD: 3.49
Aromatic Rings: 2Heavy Atoms: 17QED Weighted: 0.63Np Likeness Score: -2.05

References

1. García AM, Brea J, Morales-García JA, Perez DI, González A, Alonso-Gil S, Gracia-Rubio I, Ros-Simó C, Conde S, Cadavid MI, Loza MI, Perez-Castillo A, Valverde O, Martinez A, Gil C..  (2014)  Modulation of cAMP-specific PDE without emetogenic activity: new sulfide-like PDE7 inhibitors.,  57  (20): [PMID:25264825] [10.1021/jm501090m]

Source