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Compound InformationSONAR Target prediction
Name:

CEFOTAXIME SODIUM

Unique Identifier:SPE01500165
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:
Molecular Weight:463.338 g/mol
X log p:0.164  (online calculus)
Lipinksi Failures0
TPSA188.36
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:10
Rotatable Bond Count:9
Canonical Smiles:[Na+].[O-]C(=O)C1N2C(SCC=1COC(C)=O)C(NC(=O)C(=NOC)c1csc(N)n1)C2=O
Source:semisynthetic
Therapeutics:antibacterial
Generic_name:Cefotaxime
Chemical_iupac_name:4-(acetyloxymethyl)-8-[[2-(2-amino-1,3-thiazol-4-yl)-2-methoxyimino-acetyl]amino]-7-
oxo-2-thia-6-azabicyclo[4.2.0]oct-4-ene-5-carboxylic acid
Drug_type:Approved Drug
Pharmgkb_id:PA448852
Kegg_compound_id:C06885
Drugbank_id:APRD00854
H2o_solubility:Soluble
Logp:-0.685
Cas_registry_number:63527-52-6
Drug_category:Anti-Bacterial Agents; ATC:J01DD01
Indication:Used to treat gonorrhoea, meningitis, and severe infections including infections of
the kidney (pyelonephritis) and urinary system. Also used before an operation to
prevent infection after surgery.
Pharmacology:Cefotaxime is a third generation intravenous cephalosporin antibiotic. It has broad
spectrum activity against Gram positive and Gram negative bacteria. It does not have
activity against Pseudomonas aeruginosa. Cefotaxime works by inhibiting
bacterial cell wall biosynthesis. A positive feature of cefotaxime is that it
display a resistance to penicillinases and is useful to treat infections that are
resistant to penicillin derivatives.
Mechanism_of_action:The bactericidal activity of cefotaxime results from the inhibition of cell wall
synthesis via affinity for penicillin-binding proteins (PBPs). Cefotaxime shows high
affinity for penicillin-binding proteins in the cell wall including PBP Ib and PBP
III.
Organisms_affected:Enteric bacteria and other eubacteria

Found: 205 nonactive as graph: single | with analogs 2 3 4 5 6 7 8 9 10  Next >> [205]
Species: 4932
Condition: AAT2
Replicates: 2
Raw OD Value: r im 0.7216±0.0103238
Normalized OD Score: sc h 0.9768±0.0191537
Z-Score: -1.2458±1.04484
p-Value: 0.329666
Z-Factor: -4.43547
Fitness Defect: 1.1097
Bioactivity Statement: Nonactive
Experimental Conditions
Library:SPECMTS3
Plate Number and Position:4|A11
Drug Concentration:50.00 nM
OD Absorbance:600 nm
Robot Temperature:23.60 Celcius
Date:2008-04-08 YYYY-MM-DD
Plate CH Control (+):0.03925±0.00089
Plate DMSO Control (-):0.7198±0.01536
Plate Z-Factor:0.9260
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DBLink | Rows returned: 222 3 4 Next >> 
2631 3-(acetyloxymethyl)-7-[[2-(2-amino-1,3-thiazol-4-yl)-2-methoxyimino-acetyl]amino]-8-oxo-5-thia-1-azabicy
clo[4.2.0]oct-2-ene-2-carboxylate
2632 3-(acetyloxymethyl)-7-[[2-(2-amino-1,3-thiazol-4-yl)-2-methoxyimino-acetyl]amino]-8-oxo-5-thia-1-azabicy
clo[4.2.0]oct-2-ene-2-carboxylic acid
456256 (6R,7R)-3-(acetyloxymethyl)-7-[[2-(2-amino-1,3-thiazol-4-yl)-2-methoxyimino-acetyl]amino]-8-oxo-5-thia-1
-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
657363 sodium
(6R,7R)-3-(acetyloxymethyl)-7-[[2-(2-amino-1,3-thiazol-4-yl)-2-methoxyimino-acetyl]amino]-8-oxo-5-thia-1
-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
5361298 3-(acetyloxymethyl)-7-[[(2E)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyimino-acetyl]amino]-8-oxo-5-thia-1-az
abicyclo[4.2.0]oct-2-ene-2-carboxylic acid
5361354 (6S,7S)-3-(acetyloxymethyl)-7-[[(2E)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyimino-acetyl]amino]-8-oxo-5-t
hia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

internal high similarity DBLink | Rows returned: 1
LOPAC 00795 1.0000

active | Cluster 437 | Additional Members: 14 | Rows returned: 2
SPE01503111 0.340425531914894
SPE01502033 0.289156626506024

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