5-(4-(4-amino-3-methylbenzylsulfonyl)piperazin-1-yl)-2-(3-chlorophenyl)-4-((1-methylcyclopropyl)methoxy)pyridazin-3(2H)-one

ID: ALA2059497

PubChem CID: 25074273

Max Phase: Preclinical

Molecular Formula: C27H32ClN5O4S

Molecular Weight: 558.10

Molecule Type: Small molecule

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  Cc1cc(CS(=O)(=O)N2CCN(c3cnn(-c4cccc(Cl)c4)c(=O)c3OCC3(C)CC3)CC2)ccc1N

Standard InChI:  InChI=1S/C27H32ClN5O4S/c1-19-14-20(6-7-23(19)29)17-38(35,36)32-12-10-31(11-13-32)24-16-30-33(22-5-3-4-21(28)15-22)26(34)25(24)37-18-27(2)8-9-27/h3-7,14-16H,8-13,17-18,29H2,1-2H3

Standard InChI Key:  UWABFAUNCKMTPQ-UHFFFAOYSA-N

Molfile:  

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M  END

Associated Targets(non-human)

CaFKS1 Beta-1,3-glucan synthase (151 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nakaseomyces glabratus (9108 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Aspergillus fumigatus (16427 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: 558.10Molecular Weight (Monoisotopic): 557.1864AlogP: 3.61#Rotatable Bonds: 8
Polar Surface Area: 110.76Molecular Species: NEUTRALHBA: 8HBD: 1
#RO5 Violations: 1HBA (Lipinski): 9HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 4.01CX LogP: 3.02CX LogD: 3.02
Aromatic Rings: 3Heavy Atoms: 38QED Weighted: 0.42Np Likeness Score: -1.33

References

1. Kuang R, Wu H, Ting PC, Aslanian RG, Cao J, Kim DW, Lee JF, Schwerdt J, Zhou G, Herr RJ, Zych AJ, Yang J, Lam SQ, Jenkins DM, Sakwa SA, Wainhaus S, Black TA, Cacciapuoti A, McNicholas PM, Xu Y, Walker SS..  (2012)  The optimization of pyridazinone series of glucan synthase inhibitors.,  22  (16): [PMID:22818082] [10.1016/j.bmcl.2012.06.091]

Source