ID: ALA4741814

Max Phase: Preclinical

Molecular Formula: C21H29N5O2S

Molecular Weight: 415.56

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1ccc(S(=O)(=O)NCc2[nH]nnc2CNC23CC4CC(CC(C4)C2)C3)cc1

Standard InChI:  InChI=1S/C21H29N5O2S/c1-14-2-4-18(5-3-14)29(27,28)23-13-20-19(24-26-25-20)12-22-21-9-15-6-16(10-21)8-17(7-15)11-21/h2-5,15-17,22-23H,6-13H2,1H3,(H,24,25,26)

Standard InChI Key:  FICYXSNPMWTBRY-UHFFFAOYSA-N

Associated Targets(non-human)

Beta-lactamase VIM-2 381 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

GIM-1 protein 72 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 415.56Molecular Weight (Monoisotopic): 415.2042AlogP: 2.65#Rotatable Bonds: 7
Polar Surface Area: 99.77Molecular Species: BASEHBA: 5HBD: 3
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.58CX Basic pKa: 8.67CX LogP: 1.85CX LogD: 1.64
Aromatic Rings: 2Heavy Atoms: 29QED Weighted: 0.65Np Likeness Score: -1.24

References

1. Muhammad Z,Skagseth S,Boomgaren M,Akhter S,Fröhlich C,Ismael A,Christopeit T,Bayer A,Leiros HS.  (2020)  Structural studies of triazole inhibitors with promising inhibitor effects against antibiotic resistance metallo-β-lactamases.,  28  (15): [PMID:32631568] [10.1016/j.bmc.2020.115598]

Source