ID: ALA4577903

Max Phase: Preclinical

Molecular Formula: C27H25ClN6O6S3

Molecular Weight: 661.19

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CN(C)C(=O)c1ccc(-c2ccc3nc(C(c4nnc(CNS(N)(=O)=O)o4)S(=O)(=O)Cc4ccccc4)sc3c2)cc1Cl

Standard InChI:  InChI=1S/C27H25ClN6O6S3/c1-34(2)27(35)19-10-8-17(12-20(19)28)18-9-11-21-22(13-18)41-26(31-21)24(42(36,37)15-16-6-4-3-5-7-16)25-33-32-23(40-25)14-30-43(29,38)39/h3-13,24,30H,14-15H2,1-2H3,(H2,29,38,39)

Standard InChI Key:  JJHPWLJWLANJOG-UHFFFAOYSA-N

Associated Targets(Human)

Endothelial lipase 1021 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Hepatic lipase 436 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 661.19Molecular Weight (Monoisotopic): 660.0686AlogP: 3.70#Rotatable Bonds: 10
Polar Surface Area: 178.45Molecular Species: NEUTRALHBA: 10HBD: 2
#RO5 Violations: 1HBA (Lipinski): 12HBD (Lipinski): 3#RO5 Violations (Lipinski): 2
CX Acidic pKa: 8.76CX Basic pKa: 1.23CX LogP: 1.87CX LogD: 1.86
Aromatic Rings: 5Heavy Atoms: 43QED Weighted: 0.23Np Likeness Score: -1.75

References

1. Johnson JA, Tora G, Pi Z, Phillips M, Yin X, Yang R, Zhao L, Chen AY, Taylor DS, Basso M, Rose A, Behnia K, Onorato J, Chen XQ, Abell LM, Lu H, Locke G, Caporuscio C, Galella M, Adam LP, Gordon D, Wexler RR, Finlay HJ..  (2018)  Sulfonylated Benzothiazoles as Inhibitors of Endothelial Lipase.,  (12): [PMID:30613337] [10.1021/acsmedchemlett.8b00424]

Source