CAS 69-52-3
:Ampicilina sódica
Descrição:
Ampicilina sódica é um antibiótico penicilínico semissintético que é utilizado principalmente para tratar uma variedade de infecções bacterianas. É um pó cristalino branco a off-white que é solúvel em água, o que facilita sua administração por injeção ou formulações orais. O composto é um sal de sódio da ampicilina, melhorando sua estabilidade e solubilidade. A ampicilina atua inibindo a síntese da parede celular bacteriana, tornando-a eficaz contra um amplo espectro de bactérias Gram-positivas e algumas Gram-negativas. Seu mecanismo de ação envolve a ligação a proteínas ligadoras de penicilina, levando à lise celular e morte das bactérias. Ampicilina sódica é frequentemente utilizado em ambientes clínicos para infecções como infecções do trato respiratório, infecções do trato urinário e meningite. No entanto, é importante notar que algumas bactérias podem apresentar resistência à ampicilina, necessitando de testes de suscetibilidade antes do uso. Assim como com qualquer antibiótico, os efeitos colaterais potenciais podem incluir reações alérgicas, distúrbios gastrointestinais e alterações na flora normal. A dosagem e administração adequadas são cruciais para minimizar o risco de desenvolvimento de resistência e garantir a eficácia terapêutica.
Fórmula:C16H19N3O4S·Na
InChI:InChI=1S/C16H19N3O4S.Na/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);/t9-,10-,11+,14-;/m1./s1
Chave InChI:InChIKey=CFOQSNKFOROIKY-YWUHCJSESA-N
SMILES:C(O)(=O)[C@@H]1N2[C@@]([C@H](NC([C@H](N)C3=CC=CC=C3)=O)C2=O)(SC1(C)C)[H].[Na]
Sinónimos:- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-(2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-, monosodium salt, <span class="text-smallcaps">D</span>-(-)-
- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[(aminophenylacetyl)amino]-3,3-dimethyl-7-oxo-, monosodium salt, [2S-[2α,5α,6β(S*)]]-
- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-, sodium salt (1:1), (2S,5R,6R)-
- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2R)-aminophenylacetyl]amino]-3,3-dimethyl-7-oxo-, monosodium salt, (2S,5R,6R)-
- 4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-, sodium salt, (2S,5R,6R)- (1:1)
- 6-(2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-,sodiumsalt,d-(-)-4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid
- <span class="text-smallcaps">D</span>-α-Aminobenzylpenicillin sodium salt
- Alpen-n
- Amcill-s
- Ampi-Dry 5000
- Ampicillin Sodium
- Ampicillin Sodium oral
- Ampicillin Sodium, Sterile Usp
- Ampicillin, Sodium Salt
- Ampicin
- Anhypen
- Binotal sodium
- Binotalsodium
- Britapen injection
- Cilleral
- Citteral
- D-(-)-Alpha-Aminobenzylpenicillin Sodium Salt
- D-6-(-Amino-phenylacetamido)penicillanicacidsodiumsalt
- Domicillin
- Monosodium ampicillin
- Omnipen-N
- Pamecil
- Pen A/N
- Penbritin S
- Pentrex
- Polycillin N
- Principen N
- Sodium 6-(2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
- Sodium 6-[<span class="text-smallcaps">D</span>-α-aminophenylacetamido]penicillanoate
- Sodium 6-{[Amino(Phenyl)Acetyl]Amino}-3,3-Dimethyl-7-Oxo-4-Thia-1-Azabicyclo[3.2.0]Heptane-2-Carboxylate
- Sodium <span class="text-smallcaps">D</span>-α-aminobenzylpenicillanate
- Sodium P-50
- Sodium [2S-[2Alpha,5Alpha,6Beta(S*)]]-6-(Aminophenylacetamido)-3,3-Dimethyl-7-Oxo-4-Thia-1-Azabicyclo[3.2.0]Heptane-2-Carboxylate
- Sodium ampicillin
- Sodium ampicillinate
- Sodium binotal
- Solampi
- Totacillin N
- sodium (2S,5R,6R)-6-{[(2R)-2-amino-2-phenylacetyl]amino}-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
- sodium (2S,5R,6R)-6-{[amino(phenyl)acetyl]amino}-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
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18 produtos.
Ampicillin sodium salt
CAS:<p>Ampicillin sodium salt, 69-52-3, is the salt of ampicillin, a broad-spectrum, semi-synthetic, -lactam antibiotic commonly used for selection of transformed cells. Learn more.</p>Fórmula:C16H18N3NaO4SCor e Forma:White to pale cream, Powder or crystals or crystalline powderPeso molecular:371.39Ampicillin Sodium
CAS:Ampicillin and its saltsFórmula:C16H19N3O4S·NaCor e Forma:White Off-White Crystalline PowderPeso molecular:372.0994Ampicillin Sodium
CAS:<p>Ampicillin Sodium</p>Fórmula:C16H18N3O4S·NaPureza:Specific optical rotation (Typical Value in Batch COA)Cor e Forma: white or almost white. hygroscopic powderPeso molecular:371.38659g/molAmpicillin Sodium Salt
CAS:Fórmula:C16H19N3O4S·NaCor e Forma:White To Off-White SolidPeso molecular:348.40 22.99Ampicillin sodium salt, cell culture grade
CAS:Fórmula:C16H18N3NaO4SPureza:≥ 91.0% (anhydrous basis)Cor e Forma:White to light-yellow powderPeso molecular:371.39Ampicillin sodium salt
CAS:Fórmula:C16H18N3NaO4SPureza:≥ 845μg/mg (anhydrous basis)Cor e Forma:White to off-white or pale yellow powderPeso molecular:371.39Ampicillin sodium salt, EP grade
CAS:Fórmula:C16H18N3NaO4SPureza:≤ 2.0%Cor e Forma:White or almost white crystalline powderPeso molecular:371.39Ampicillin sodium salt
CAS:Fórmula:C16H18N3NaO4SPureza:845~988 mg/mg (Potency, anhydrous basis)Cor e Forma:SolidPeso molecular:371.39Ampicillin sodium
CAS:<p>Ampicillin sodium (Domicillin) is a broad-spectrum β -lactam antibiotic,combates a variety of Gram-positive and Gram-negative bacteria. High-Quality, Low-Cost!</p>Fórmula:C16H18N3NaO4SPureza:97.98% - 99.26%Cor e Forma:White To Off-White SolidPeso molecular:371.39Ampicillin Sodium Salt
CAS:<p>Applications Sodium Salt of Ampicillin, an orally active, semi-synthetic antibiotic; structurally related to penicillin. Antibacterial.<br>References Ivashkiv, E., et al.: Anal. Profiles Drug Subs., 2, 1 (1973), Campoli-Richards, D.M., et al.: Drugs, 33, 577 (1987), Sill, M. L., et al.: Antimicrob. Agents Chemother., 52, 1551 (2008),<br></p>Fórmula:C16H18N3O4S·NaCor e Forma:Off-WhitePeso molecular:371.39Ampicillin sodium salt - Bio-X ™
CAS:<p>Ampicillin is a β-lactam antibiotic with a broad spectrum of activity against Gram-positive and Gram-negative bacteria. It is used in the treatment of bacterial infections, including those caused by methicillin-resistant Staphylococcus aureus (MRSA), Streptococcus pneumoniae, and Listeria monocytogenes. Ampicillin binds to penicillin-binding proteins in the bacterial cell wall by competitive inhibition. It prevents the formation of an antibiotic-inhibitor complex with the enzyme cell wall synthesis that is required for cell wall biosynthesis, inhibiting protein synthesis and cell division.</p>Fórmula:C16H19N3O4S·NaPureza:Min. 85 Area-%Cor e Forma:PowderPeso molecular:372.4 g/molAmpicillin sodium
CAS:<p>Ampicillin sodium is a broad-spectrum antibiotic, which is a semisynthetic derivative of penicillin. It is sourced from the natural fermentation products of Penicillium fungi, followed by chemical modification. Ampicillin functions by inhibiting bacterial cell wall synthesis. This is achieved through the irreversible binding to penicillin-binding proteins (PBPs), which play a crucial role in constructing the peptidoglycan layer of bacterial cell walls. This interruption of cell wall synthesis leads to cell lysis and ultimately the death of the bacteria.</p>Fórmula:C16H18N3O4S·NaPureza:Min. 95%Cor e Forma:White PowderPeso molecular:371.4 g/molAmpicillin Sodium Salt (AMP-Na)
CAS:Fórmula:C16H18N3O4SNaCor e Forma:White to off-white, Crystalline powder, ClearPeso molecular:371.4Ampicillin Sodium Salt (AMP-Na) for tissue culture
CAS:Fórmula:C16H18N3O4SNaCor e Forma:White to off-white, Crystalline powder, ClearPeso molecular:371.4
