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Compound InformationSONAR Target prediction
Name:

Piperacillin sodium salt

Unique Identifier:Prest1028
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:C23H26N5NaO7S
Molecular Weight:515.347 g/mol
X log p:7.558  (online calculus)
Lipinksi Failures2
TPSA160.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:12
Rotatable Bond Count:9
Canonical Smiles:[Na+].[O-]C(=O)C1N2C(SC1(C)C)C(NC(=O)C(NC(=O)N1CCN(CC)C(=O)C1=O)c1cccc
c1)C2=O
Generic_name:Piperacillin
Chemical_iupac_name:7-[2-(4-ethyl-2,3-dioxo-piperazin-1-yl)carbonylamino-2-phenyl-acetyl]amino-3,3-dimet
hyl-6-oxo-2-thia-5-azabicyclo[3.2.0]heptane-4-carboxylate
Drug_type:Approved Drug
Pharmgkb_id:PA450975
Kegg_compound_id:C07361
Drugbank_id:APRD00325
Cas_registry_number:66258-76-2
Drug_category:Anti-bacterial Agents; Penicillins; ATC:J01CA12
Indication:For the treatment of polymicrobial infections.
Pharmacology:Piperacillin 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. Piperacillin has in
vitro
activity against gram-positive and gram-negative aerobic and anaerobic
bacteria. The bactericidal activity of Piperacillin results from the inhibition of
cell wall synthesis and is mediated through Piperacillin binding to penicillin
binding proteins (PBPs). Piperacillin 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, Piperacillin 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 Piperacillin 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 1122.0000±0
Normalized OD Score: sc h 0.9674±0
Z-Score: -0.7351±0
p-Value: 0.462268
Z-Factor: -25.0424
Fitness Defect: 0.7716
Bioactivity Statement: Nonactive
Experimental Conditions
Library:Prestwick
Plate Number and Position:10|D6
Drug Concentration:50.00 nM
OD Absorbance:0 nm
Robot Temperature:23.30 Celcius
Date:2006-10-10 YYYY-MM-DD
Plate CH Control (+):870.5±769.75857
Plate DMSO Control (-):982.5±305.13061
Plate Z-Factor:-45.8313
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DBLink | Rows returned: 182 3 Next >> 
4834 6-[[2-[(4-ethyl-2,3-dioxo-piperazine-1-carbonyl)amino]-2-phenyl-acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-
1-azabicyclo[3.2.0]heptane-2-carboxylate
4835 6-[[2-[(4-ethyl-2,3-dioxo-piperazine-1-carbonyl)amino]-2-phenyl-acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-
1-azabicyclo[3.2.0]heptane-2-carboxylic acid
43066 sodium
(2R,5S,6S)-6-[[(2R)-2-[(4-ethyl-2,3-dioxo-piperazine-1-carbonyl)amino]-2-phenyl-acetyl]amino]-3,3-dimeth
yl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
43067 (2R,5S,6S)-6-[[(2R)-2-[(4-ethyl-2,3-dioxo-piperazine-1-carbonyl)amino]-2-phenyl-acetyl]amino]-3,3-dimeth
yl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
43672 (2S,5R,6R)-6-[[(2R)-2-[(4-ethyl-2,3-dioxo-piperazine-1-carbonyl)amino]-2-phenyl-acetyl]amino]-3,3-dimeth
yl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
73246 (2S,5R,6R)-6-[[(2R)-2-[(4-ethyl-2,3-dioxo-piperazine-1-carbonyl)amino]-2-phenyl-acetyl]amino]-3,3-dimeth
yl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid hydrate

internal high similarity DBLink | Rows returned: 0

active | Cluster 3276 | Additional Members: 16 | Rows returned: 1
SPE01500448 0.459459459459459

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