ID: ALA5172913

Max Phase: Preclinical

Molecular Formula: C18H19FN2O4S

Molecular Weight: 378.43

Associated Items:

Representations

Canonical SMILES:  CCOc1ccc(F)cc1NC(=O)c1ccccc1NS(=O)(=O)C1CC1

Standard InChI:  InChI=1S/C18H19FN2O4S/c1-2-25-17-10-7-12(19)11-16(17)20-18(22)14-5-3-4-6-15(14)21-26(23,24)13-8-9-13/h3-7,10-11,13,21H,2,8-9H2,1H3,(H,20,22)

Standard InChI Key:  TXZPRVKJSAUJSV-UHFFFAOYSA-N

Associated Targets(Human)

TSPO Tchem Translocator protein (484 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MRGPRX1 Tchem Mas-related G-protein coupled receptor member X1 (365 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD5 Tchem Dopamine D5 receptor (1597 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH1 Tclin Histamine H1 receptor (7573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 378.43Molecular Weight (Monoisotopic): 378.1050AlogP: 3.38#Rotatable Bonds: 7
Polar Surface Area: 84.50Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.60CX Basic pKa: CX LogP: 2.55CX LogD: 2.37
Aromatic Rings: 2Heavy Atoms: 26QED Weighted: 0.77Np Likeness Score: -2.01

References

1. Sharma S, Peng Q, Vadukoot AK, Aretz CD, Jensen AA, Wallick AI, Dong X, Hopkins CR..  (2022)  Synthesis and Biological Characterization of a Series of 2-Sulfonamidebenzamides as Allosteric Modulators of MrgX1.,  13  (5.0): [PMID:35586421] [10.1021/acsmedchemlett.2c00100]

Source