ID: ALA216361

Max Phase: Preclinical

Molecular Formula: C23H30N4O3S2

Molecular Weight: 474.65

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCCNC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(Cn2ccnc2)cc1

Standard InChI:  InChI=1S/C23H30N4O3S2/c1-4-5-10-25-23(28)26-32(29,30)22-21(14-20(31-22)13-17(2)3)19-8-6-18(7-9-19)15-27-12-11-24-16-27/h6-9,11-12,14,16-17H,4-5,10,13,15H2,1-3H3,(H2,25,26,28)

Standard InChI Key:  QMKDXFGVHANNCT-UHFFFAOYSA-N

Associated Targets(Human)

Angiotensin II type 2 (AT-2) receptor 2549 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Angiotensin II type 2 (AT-2) receptor 803 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: 474.65Molecular Weight (Monoisotopic): 474.1759AlogP: 4.65#Rotatable Bonds: 10
Polar Surface Area: 93.09Molecular Species: ACIDHBA: 6HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 5.73CX Basic pKa: 6.55CX LogP: 4.35CX LogD: 4.13
Aromatic Rings: 3Heavy Atoms: 32QED Weighted: 0.42Np Likeness Score: -1.16

References

1. Wu X, Wan Y, Mahalingam AK, Murugaiah AM, Plouffe B, Botros M, Karlén A, Hallberg M, Gallo-Payet N, Alterman M..  (2006)  Selective angiotensin II AT2 receptor agonists: arylbenzylimidazole structure-activity relationships.,  49  (24): [PMID:17125268] [10.1021/jm0606185]

Source