ID: ALA4567596

Max Phase: Preclinical

Molecular Formula: C24H20ClN5O5S3

Molecular Weight: 590.11

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  NS(=O)(=O)NCc1nnc(C(c2nc3ccc(-c4cccc(Cl)c4)cc3s2)S(=O)(=O)Cc2ccccc2)o1

Standard InChI:  InChI=1S/C24H20ClN5O5S3/c25-18-8-4-7-16(11-18)17-9-10-19-20(12-17)36-24(28-19)22(37(31,32)14-15-5-2-1-3-6-15)23-30-29-21(35-23)13-27-38(26,33)34/h1-12,22,27H,13-14H2,(H2,26,33,34)

Standard InChI Key:  QTLKEMOUBMXNFP-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: 590.11Molecular Weight (Monoisotopic): 589.0315AlogP: 4.00#Rotatable Bonds: 9
Polar Surface Area: 158.14Molecular Species: NEUTRALHBA: 9HBD: 2
#RO5 Violations: 1HBA (Lipinski): 10HBD (Lipinski): 3#RO5 Violations (Lipinski): 1
CX Acidic pKa: 8.76CX Basic pKa: 1.26CX LogP: 2.57CX LogD: 2.56
Aromatic Rings: 5Heavy Atoms: 38QED Weighted: 0.26Np Likeness Score: -1.69

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