1-(5-Chloro-2-formylamino-benzenesulfonyl)-1H-pyrrole-2-carboxylic acid ethyl ester

ID: ALA357327

Chembl Id: CHEMBL357327

Cas Number: 173908-56-0

PubChem CID: 464862

Max Phase: Preclinical

Molecular Formula: C14H13ClN2O5S

Molecular Weight: 356.79

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCOC(=O)c1cccn1S(=O)(=O)c1cc(Cl)ccc1NC=O

Standard InChI:  InChI=1S/C14H13ClN2O5S/c1-2-22-14(19)12-4-3-7-17(12)23(20,21)13-8-10(15)5-6-11(13)16-9-18/h3-9H,2H2,1H3,(H,16,18)

Standard InChI Key:  UAAYCFMPECWIOA-UHFFFAOYSA-N

Associated Targets(Human)

MT4 (17854 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

pol Human immunodeficiency virus type 1 reverse transcriptase (18245 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
pol Human immunodeficiency virus type 2 pol protein (31 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: 356.79Molecular Weight (Monoisotopic): 356.0234AlogP: 2.12#Rotatable Bonds: 6
Polar Surface Area: 94.47Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.40CX Basic pKa: CX LogP: 2.06CX LogD: 2.06
Aromatic Rings: 2Heavy Atoms: 23QED Weighted: 0.63Np Likeness Score: -1.32

References

1. Artico M, Silvestri R, Massa S, Loi AG, Corrias S, Piras G, La Colla P..  (1996)  2-Sulfonyl-4-chloroanilino moiety: a potent pharmacophore for the anti-human immunodeficiency virus type 1 activity of pyrrolyl aryl sulfones.,  39  (2): [PMID:8558522] [10.1021/jm950568w]

Source