ID: ALA4176488

Max Phase: Preclinical

Molecular Formula: C25H25Cl2N3O5

Molecular Weight: 518.40

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1[nH]c(C(=O)Nc2ccc(C(=O)N[C@@H](Cc3ccccc3)C(=O)O)cc2OC(C)C)c(Cl)c1Cl

Standard InChI:  InChI=1S/C25H25Cl2N3O5/c1-13(2)35-19-12-16(23(31)30-18(25(33)34)11-15-7-5-4-6-8-15)9-10-17(19)29-24(32)22-21(27)20(26)14(3)28-22/h4-10,12-13,18,28H,11H2,1-3H3,(H,29,32)(H,30,31)(H,33,34)/t18-/m0/s1

Standard InChI Key:  IOENDXXUMVWGKE-SFHVURJKSA-N

Associated Targets(non-human)

DNA gyrase subunit B 290 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

Properties

Molecular Weight: 518.40Molecular Weight (Monoisotopic): 517.1171AlogP: 5.10#Rotatable Bonds: 9
Polar Surface Area: 120.52Molecular Species: ACIDHBA: 4HBD: 4
#RO5 Violations: 2HBA (Lipinski): 8HBD (Lipinski): 4#RO5 Violations (Lipinski): 2
CX Acidic pKa: 3.37CX Basic pKa: CX LogP: 4.87CX LogD: 1.46
Aromatic Rings: 3Heavy Atoms: 35QED Weighted: 0.31Np Likeness Score: -0.94

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