(S)-5-(4-chlorophenyl)-3-(2-hydroxyphenyl)-N-phenyl-4,5-dihydropyrazole-1-carbothioamide

ID: ALA255894

Chembl Id: CHEMBL255894

PubChem CID: 136036631

Max Phase: Preclinical

Molecular Formula: C22H18ClN3OS

Molecular Weight: 407.93

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Oc1ccccc1C1=NN(C(=S)Nc2ccccc2)[C@H](c2ccc(Cl)cc2)C1

Standard InChI:  InChI=1S/C22H18ClN3OS/c23-16-12-10-15(11-13-16)20-14-19(18-8-4-5-9-21(18)27)25-26(20)22(28)24-17-6-2-1-3-7-17/h1-13,20,27H,14H2,(H,24,28)/t20-/m0/s1

Standard InChI Key:  ZSALNCBCUVGPNE-FQEVSTJZSA-N

Alternative Forms

  1. Parent:

    ALA255894

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Associated Targets(Human)

HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Mycobacterium tuberculosis (203094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Yersinia pestis (750 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ybtE AMP-binding enzyme family protein (69 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: 407.93Molecular Weight (Monoisotopic): 407.0859AlogP: 5.59#Rotatable Bonds: 3
Polar Surface Area: 47.86Molecular Species: NEUTRALHBA: 3HBD: 2
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 8.68CX Basic pKa: 0.82CX LogP: 6.00CX LogD: 5.98
Aromatic Rings: 3Heavy Atoms: 28QED Weighted: 0.56Np Likeness Score: -1.16

References

1. Stirrett KL, Ferreras JA, Jayaprakash V, Sinha BN, Ren T, Quadri LE..  (2008)  Small molecules with structural similarities to siderophores as novel antimicrobials against Mycobacterium tuberculosis and Yersinia pestis.,  18  (8): [PMID:18394884] [10.1016/j.bmcl.2008.03.025]

Source