(4-(4,5-Dibromo-1H-pyrrole-2-carboxamido)-2-isopropoxybenzoyl)glycine

ID: ALA4169932

Chembl Id: CHEMBL4169932

PubChem CID: 145953942

Max Phase: Preclinical

Molecular Formula: C17H17Br2N3O5

Molecular Weight: 503.15

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(C)Oc1cc(NC(=O)c2cc(Br)c(Br)[nH]2)ccc1C(=O)NCC(=O)O

Standard InChI:  InChI=1S/C17H17Br2N3O5/c1-8(2)27-13-5-9(3-4-10(13)16(25)20-7-14(23)24)21-17(26)12-6-11(18)15(19)22-12/h3-6,8,22H,7H2,1-2H3,(H,20,25)(H,21,26)(H,23,24)

Standard InChI Key:  WIJDXVKSDUYBTL-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA4169932

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Associated Targets(non-human)

gyrB DNA gyrase subunit B (290 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
gyrB DNA gyrase subunit B (542 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Enterococcus faecalis (29875 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 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: 503.15Molecular Weight (Monoisotopic): 500.9535AlogP: 3.39#Rotatable Bonds: 7
Polar Surface Area: 120.52Molecular Species: ACIDHBA: 4HBD: 4
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 4#RO5 Violations (Lipinski): 1
CX Acidic pKa: 3.44CX Basic pKa: CX LogP: 2.47CX LogD: -0.92
Aromatic Rings: 2Heavy Atoms: 27QED Weighted: 0.46Np Likeness Score: -0.76

References

1. Durcik M, Lovison D, Skok Ž, Durante Cruz C, Tammela P, Tomašič T, Benedetto Tiz D, Draskovits G, Nyerges Á, Pál C, Ilaš J, Peterlin Mašič L, Kikelj D, Zidar N..  (2018)  New N-phenylpyrrolamide DNA gyrase B inhibitors: Optimization of efficacy and antibacterial activity.,  154  [PMID:29778894] [10.1016/j.ejmech.2018.05.011]

Source