ID: ALA2331747

Max Phase: Preclinical

Molecular Formula: C22H22ClN3O6S

Molecular Weight: 491.95

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1cn([C@H]2CCCN(S(=O)(=O)c3ccc(O)c(Oc4cccc(Cl)c4)c3)C2)c(=O)[nH]c1=O

Standard InChI:  InChI=1S/C22H22ClN3O6S/c1-14-12-26(22(29)24-21(14)28)16-5-3-9-25(13-16)33(30,31)18-7-8-19(27)20(11-18)32-17-6-2-4-15(23)10-17/h2,4,6-8,10-12,16,27H,3,5,9,13H2,1H3,(H,24,28,29)/t16-/m0/s1

Standard InChI Key:  IDMZBDJWQBWWLK-INIZCTEOSA-N

Associated Targets(Human)

HERG 29587 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cytochrome P450 2D6 33882 Activities

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Cytochrome P450 2C19 29246 Activities

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Cytochrome P450 2C9 32119 Activities

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Cytochrome P450 1A2 26471 Activities

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Cytochrome P450 3A4 53859 Activities

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Plasma 7708 Activities

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A549 127892 Activities

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Thymidylate kinase 169 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Streptococcus pneumoniae 31063 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Staphylococcus aureus 210822 Activities

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Hepatocyte 2621 Activities

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Liver microsomes 8692 Activities

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Candida albicans 78123 Activities

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Klebsiella pneumoniae 43867 Activities

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Pseudomonas aeruginosa 123386 Activities

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Haemophilus influenzae 8812 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Escherichia coli 133304 Activities

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Enterococcus faecalis 29875 Activities

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Enterococcus faecium 13803 Activities

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Staphylococcus lugdunensis 349 Activities

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Staphylococcus haemolyticus 1695 Activities

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Staphylococcus epidermidis 22802 Activities

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Streptococcus agalactiae 1777 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Streptococcus pyogenes 16140 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: 491.95Molecular Weight (Monoisotopic): 491.0918AlogP: 3.02#Rotatable Bonds: 5
Polar Surface Area: 121.70Molecular Species: NEUTRALHBA: 7HBD: 2
#RO5 Violations: 0HBA (Lipinski): 9HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.28CX Basic pKa: CX LogP: 2.89CX LogD: 2.53
Aromatic Rings: 3Heavy Atoms: 33QED Weighted: 0.57Np Likeness Score: -1.06

References

1. Martínez-Botella G, Loch JT, Green OM, Kawatkar SP, Olivier NB, Boriack-Sjodin PA, Keating TA..  (2013)  Sulfonylpiperidines as novel, antibacterial inhibitors of Gram-positive thymidylate kinase (TMK).,  23  (1): [PMID:23206863] [10.1016/j.bmcl.2012.10.128]

Source