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Compound InformationSONAR Target prediction
Name:

Cefixime

Unique Identifier:Prest1090
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:C16H15N5O7S2
Molecular Weight:440.349 g/mol
X log p:1.403  (online calculus)
Lipinksi Failures0
TPSA156.07
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:10
Rotatable Bond Count:9
Canonical Smiles:Nc1scc(n1)C(=NOCC(O)=O)C(=O)NC1C2SCC(C=C)=C(N2C1=O)C(O)=O
Generic_name:Cefixime
Chemical_iupac_name:8-[[2-(2-amino-1,3-thiazol-4-yl)-2-(carboxymethoxyimino)acetyl]amino]-4-ethenyl-7-ox
o-2-thia-6-azabicyclo[4.2.0]oct-4-ene-5-carboxylic acid
Drug_type:Approved Drug
Pharmgkb_id:PA448844
Kegg_compound_id:C06881
Drugbank_id:APRD00583
Melting_point:218-225 oC
H2o_solubility:55.11 mg/L
Logp:-0.559
Cas_registry_number:79350-37-1
Drug_category:Anti-bacterial Agents; Cephalosporins; ATC:J01DD08
Indication:For use in the treatment of the following infections when caused by susceptible
strains of the designated microorganisms:(1) uncomplicated urinary tract infections
caused by Escherichia coli and Proteus mirabilis, (2) otitis media
caused by Haemophilus influenzae (beta-lactamase positive and negative
strains), Moraxella catarrhalis (most of which are beta-lactamase positive),
and S. pyogenes, (3) pharyngitis and tonsillitis caused by S.
pyogenes
, (4) acute bronchitis and acute exacerbations of chronic bronchitis
caused by Streptococcus pneumoniae and Haemophilus influenzae
(beta-lactamase positive and negative strains), and (5) uncomplicated gonorrhea
(cervical/urethral) caused by Neisseria gonorrhoeae (penicillinase- and
non-penicillinase-producing strains).
Pharmacology:Cefixime, an antibiotic, is a third-generation cephalosporin like ceftriaxone and
cefotaxime. Cefixime is highly stable in the presence of beta-lactamase enzymes. As
a result, many organisms resistant to penicillins and some cephalosporins due to the
presence of beta-lactamases, may be susceptible to cefixime. The antibacterial
effect of cefixime results from inhibition of mucopeptide synthesis in the bacterial
cell wall.
Mechanism_of_action:Like all beta-lactam antibiotics, cefixime binds to specific penicillin-binding
proteins (PBPs) located inside the bacterial cell wall, causing the inhibition of
the third and last stage of bacterial cell wall synthesis. Cell lysis is then
mediated by bacterial cell wall autolytic enzymes such as autolysins; it is possible
that cefixime interferes with an autolysin inhibitor.
Organisms_affected:Enteric bacteria and other eubacteria

Found: 3 nonactive as graph: single | with analogs 2 3 Next >> 
Species: 9606
Condition: TMPPre001
Replicates: 2
Raw OD Value: r im 1998.0000±0
Normalized OD Score: sc h 0.9399±0
Z-Score: -1.3537±0
p-Value: 0.175818
Z-Factor: -32.5467
Fitness Defect: 1.7383
Bioactivity Statement: Nonactive
Experimental Conditions
Library:Prestwick
Plate Number and Position:6|G3
Drug Concentration:50.00 nM
OD Absorbance:0 nm
Robot Temperature:24.00 Celcius
Date:2006-10-10 YYYY-MM-DD
Plate CH Control (+):1009.5±953.84240
Plate DMSO Control (-):2021±558.06298
Plate Z-Factor:-4.4864
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DBLink | Rows returned: 82 Next >> 
2675 7-[[2-(2-amino-1,3-thiazol-4-yl)-2-(carboxymethoxyimino)acetyl]amino]-3-ethenyl-8-oxo-5-thia-1-azabicycl
o[4.2.0]oct-2-ene-2-carboxylic acid
54362 (6R,7R)-7-[[2-(2-amino-1,3-thiazol-4-yl)-2-(carboxymethoxyimino)acetyl]amino]-3-ethenyl-8-oxo-5-thia-1-a
zabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
5353520 7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(carboxymethoxyimino)acetyl]amino]-3-ethenyl-8-oxo-5-thia-1-azab
icyclo[4.2.0]oct-2-ene-2-carboxylic acid
5362065 (6R,7R)-7-[[(2E)-2-(2-amino-1,3-thiazol-4-yl)-2-(carboxymethoxyimino)acetyl]amino]-3-ethenyl-8-oxo-5-thi
a-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
5491577 (6R,7R)-7-[[(2E)-2-(2-amino-1,3-thiazol-4-yl)-2-(carboxymethoxyimino)acetyl]amino]-3-ethenyl-8-oxo-5-thi
a-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid trihydrate
5943039 7-[[(2E)-2-(2-amino-1,3-thiazol-4-yl)-2-(carboxymethoxyimino)acetyl]amino]-3-ethenyl-8-oxo-5-thia-1-azab
icyclo[4.2.0]oct-2-ene-2-carboxylic acid

internal high similarity DBLink | Rows returned: 0

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

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