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Compound InformationSONAR Target prediction
Name:

AMPICILLIN SODIUM

Unique Identifier:SPE01500123
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:
Molecular Weight:353.245 g/mol
X log p:8.457  (online calculus)
Lipinksi Failures1
TPSA102.81
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:7
Rotatable Bond Count:5
Canonical Smiles:[Na+].[O-]C(=O)C1N2C(SC1(C)C)C(NC(=O)C(N)c1ccccc1)C2=O
Source:semisynthetic
Therapeutics:antibacterial
Generic_name:Ampicillin
Chemical_iupac_name:7-(2-amino-2-phenyl-acetyl)amino-3,3-dimethyl-6-oxo-2-thia-5-azabicyclo[3.2.0]heptan
e-4-carboxylicacid
Drug_type:Approved Drug
Pharmgkb_id:PA448419
Kegg_compound_id:C06574
Drugbank_id:APRD00320
Melting_point:208 oC
H2o_solubility:1.01E+004 mg/L
Logp:1.35
Cas_registry_number:69-53-4
Drug_category:Anti-bacterial Agents; Penicillins; ATC:J01CA01; ATC:J01CA02; ATC:J01CA06;
ATC:J01CA14; ATC:J01CA15; ATC:S01AA19
Indication:For treatment of infection (Respiratory, GI, UTI and meningitis) due to E. coli, P.
mirabilis, enterococci, Shigella, S. typhosa and other Salmonella,
nonpenicillinase-producing N. gononhoeae, H. influenzae, staphylococci, streptococci
including streptoc
Pharmacology:Ampicillin is a penicillin beta-lactam antibiotic used in the treatment of bacterial
infections caused by susceptible, usually gram-positive, organisms. The name
"penicillin" can either refer to several variants of penicillin available, or to the
group of antibiotics derived from the penicillins. Ampicillin has in vitro
activity against gram-positive and gram-negative aerobic and anaerobic bacteria. The
bactericidal activity of Ampicillin results from the inhibition of cell wall
synthesis and is mediated through Ampicillin binding to penicillin binding proteins
(PBPs). Ampicillin is stable against hydrolysis by a variety of beta-lactamases,
including penicillinases, and cephalosporinases and extended spectrum
beta-lactamases.
Mechanism_of_action:By binding to specific penicillin-binding proteins (PBPs) located inside the
bacterial cell wall, Ampicillin inhibits 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 Ampicillin interferes with an autolysin
inhibitor.
Organisms_affected:Enteric bacteria and other eubacteria

Found: 205 nonactive as graph: single | with analogs [1] << Back 171 172 173 174 175 176 177 178 179 180  Next >> [205]
Species: 4932
Condition: SET2
Replicates: 2
Raw OD Value: r im 0.7173±0.00403051
Normalized OD Score: sc h 1.0018±0.0101382
Z-Score: 0.1070±0.59439
p-Value: 0.67602
Z-Factor: -16.7386
Fitness Defect: 0.3915
Bioactivity Statement: Nonactive
Experimental Conditions
Library:Spectrum
Plate Number and Position:10|E8
Drug Concentration:50.00 nM
OD Absorbance:600 nm
Robot Temperature:24.00 Celcius
Date:2007-11-15 YYYY-MM-DD
Plate CH Control (+):0.041475±0.00082
Plate DMSO Control (-):0.7089749999999999±0.12749
Plate Z-Factor:0.4040
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DBLink | Rows returned: 27<< Back 1 2 3 4 5 Next >> 
6560160 (2S,5S,6R)-6-[[(2R)-2-amino-2-phenyl-acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-
2-carboxylic acid
6604512 (2S,5R,6R)-6-[[(2S)-2-amino-2-phenyl-acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-
2-carboxylic acid trihydrate
6604648 (2S,5R,6S)-6-[[(2S)-2-amino-2-phenyl-acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-
2-carboxylic acid
6993156 (2R,5S,6R)-6-[[(2R)-2-azaniumyl-2-phenyl-acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]hept
ane-2-carboxylate
6993157 (2R,5S,6R)-6-[[(2R)-2-amino-2-phenyl-acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-
2-carboxylic acid
7048611 (2S,5R,6R)-6-[[(2R)-2-azaniumyl-2-phenyl-acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]hept
ane-2-carboxylate

internal high similarity DBLink | Rows returned: 4
SPE01500160 0.9136
SPE01502034 0.9333
SPE01500120 0.9565
SPE01500465 0.9610

active | Cluster 15024 | Additional Members: 10 | Rows returned: 3
Prest1097 0.426470588235294
Prest1304 0.407407407407407
Prest1280 0.323943661971831

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