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Ampicillin Trihydrate

CAT: 0013-GTR19161672-02Size: 1 gDry Ice: NoHazardous: No
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CAT#:0013-GTR19161672-02Size:1 g
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Description
Ampicillin Trihydrate is a β-lactam antibiotic, which inhibits bacterial cell-wall synthesis (peptidoglycan cross-linking) by inactivating transpeptidases on the inner surface of the bacterial cell membrane. (In Vitro) :Ampicillin trihydrate (D- (-) -α-Aminobenzylpenicillin trihydrate) inhibits the growth of E. coli of swine origin in a dose-dependent manner. The effective inhibitory concentration of Ampicillin trihydrate is 2.5 uG/mL. (In Vivo) :Ampicillin trihydrate (D- (-) -α-Aminobenzylpenicillin trihydrate) is very effective in alleviating the symptoms of hemorrhagic enteritis in a 11-week old pig.Ampicillin trihydrate produces maximum concentrations in bile twice as high as in serum. The peak concentration of ampicillin after an oral dose is as twice as high in portal blood as in peripheral blood.Ampicillin trihydrate provides neuroprotection against ischemia-reperfusion brain injury. Ampicillin trihydrate reduces the activities of MMPs and increases the expression level of GLT-1. Pretreatment with Ampicillin trihydrate significantly reduces medial hippocampal cell death following global forebrain ischemia.
CAS Number
7177-48-2
Product Name Alternative
Amcill | Aminobenzyl Penicillin | KS-R1 | KS R1 | KSR1 | Omnipen | Pentrexyl | Polycillin | Ukapen
Field of Research
Pharmacology & Drug Discovery
Purity
>98% (HPLC)
Solubility
Water: 2 mg/mL (4.95 mM) ; DMSO: 81 mg/mL (200.76 mM)
Smiles
O=C ([C@@H] (C (C) (C) S[C@]1 ([H]) [C@@H]2NC ([C@H] (N) C3=CC=CC=C3) =O) N1C2=O) O.[H]O[H].[H]O[H].[H]O[H]
Molecular Formula
C16H19N3O4S·3H2O
Molecular Weight
403.45
Storage Conditions
Storage temperature: -20°C. Stability: ≥ 2 years
Notes
For research use only.
Other Product Names
(2S,5R,6R) -6- ((R) -2-amino-2-phenylacetamido) -3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid trihydrate

Chemical Information

Ampicillin Trihydrate

Ampicillin trihydrate is a hydrate. It contains an ampicillin.

CAS Number7177-48-2
PubChem CID23565
IUPAC Name(2S,5R,6R)-6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid;trihydrate
Molecular FormulaC16H25N3O7S
Molecular Weight403.5
Topological Polar Surface Area141
Hydrogen Bond Donor Count6
Hydrogen Bond Acceptor Count9
Rotatable Bond Count4
Heavy Atom Count27
Formal Charge0
Complexity562
SMILES
CC1([C@@H](N2[C@H](S1)[C@@H](C2=O)NC(=O)[C@@H](C3=CC=CC=C3)N)C(=O)O)C.O.O.O
InChI
InChI=1S/C16H19N3O4S.3H2O/c1-16(2)11(15(22)23)19-13(21)10(14(19)24-16)18-12(20)9(17)8-6-4-3-5-7-8;;;/h3-7,9-11,14H,17H2,1-2H3,(H,18,20)(H,22,23);3*1H2/t9-,10-,11+,14-;;;/m1.../s1
InChIKey
RXDALBZNGVATNY-CWLIKTDRSA-N
Chemical Structure
2D Structure
2D structure of Ampicillin Trihydrate
CAS: 7177-48-2
CID: 23565
Formula: C16H25N3O7S
MW: 403.5
Interactive 3D Structure
Loading 3D structure...
View on PubChemRaw 3D data
Computed Properties
PropertyValue
Molecular Weight403.5
Hydrogen Bond Donor Count6
Hydrogen Bond Acceptor Count9
Rotatable Bond Count4
Exact Mass403.14132132
Monoisotopic Mass403.14132132
Topological Polar Surface Area141 Ų
Heavy Atom Count27
Formal Charge0
Complexity562
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count4
Compound Is CanonicalizedYes

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