Home | Screening data | Screen comparisons | Search for compounds | Structure search

Compound InformationSONAR Target prediction
Name:

METRONIDAZOLE

Unique Identifier:SPE01500412
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:
Molecular Weight:162.083 g/mol
X log p:2.247  (online calculus)
Lipinksi Failures0
TPSA58.74
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:3
Rotatable Bond Count:3
Canonical Smiles:[O-][N+](=O)c1cnc(C)n1CCO
Source:synthetic
Therapeutics:antiprotozoal
Generic_name:Metronidazole
Chemical_iupac_name:2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethanol
Drug_type:Approved Drug
Kegg_compound_id:C07203
Drugbank_id:APRD00631
Melting_point:160 oC
H2o_solubility:<0.1g/100mL
Logp:-0.262
Cas_registry_number:443-48-1
Mass_spectrum:http://webbook.nist.gov/cgi/cbook.cgi?Spec=C443481&Index=0&Type=Mass&Large=on
Drug_category:Radiation-Sensitizing Agents; Anti-Infectives; Antiprotozoals; ATC:A01AB17;
ATC:D06BX01; ATC:G01AF01; ATC:J01XD01; ATC:P01AB01
Indication:Treatment of acute acne rosacea
Pharmacology:Metronidazole, a synthetic antibacterial and antiprotozoal agent of the
nitroimidazole class, is used against protozoa such as Trichomonas vaginalis,
amebiasis, and giardiasis. Metronidazole is extremely effective against anaerobic
bacterial infections and is also used to treat Crohn-s disease,
antibiotic-associated diarrhea, and rosacea.
Mechanism_of_action:Unionized metronidazole is selective for anaerobic bacteria due to their ability to
intracellularly reduce metronidazole to its active form. This reduced metronidazole
then disrupts DNA-s helical structure, inhibiting bacterial nucleic acid synthesis
and resulting in bacterial cell death.
Organisms_affected:Bacteria and protozoa

Found: 205 nonactive as graph: single | with analogs [1] << Back 201 202 203 204 205
Species: 4932
Condition: YPT6
Replicates: 2
Raw OD Value: r im 0.4772±0.00876812
Normalized OD Score: sc h 0.9356±0.0254951
Z-Score: -0.9682±0.392496
p-Value: 0.351326
Z-Factor: -2.07479
Fitness Defect: 1.046
Bioactivity Statement: Nonactive
Experimental Conditions
Library:SPECMTS3
Plate Number and Position:18|H8
Drug Concentration:50.00 nM
OD Absorbance:600 nm
Robot Temperature:25.70 Celcius
Date:2008-06-05 YYYY-MM-DD
Plate CH Control (+):0.040999999999999995±0.00056
Plate DMSO Control (-):0.486±0.02470
Plate Z-Factor:0.8167
png
ps
pdf

DBLink | Rows returned: 3
4173 2-(2-methyl-5-nitro-imidazol-1-yl)ethanol
68592 2-(2-methyl-5-nitro-imidazol-1-yl)ethanol hydrochloride
184191 azane; 2-(2-methyl-5-nitro-imidazol-1-yl)ethanol; platinum(+2) cation; dichloride

internal high similarity DBLink | Rows returned: 1
BTB 09707 1.0000

active | Cluster 6826 | Additional Members: 11 | Rows returned: 1
Prest334 0

Service provided by the Mike Tyers Laboratory