CAS 61-24-5

Cefalosporina C

Descrizione:

Cefalosporina C è un antibiotico beta-lattamico che appartiene alla classe di Cefalosporina C, derivato dal fungo Acremonium. È caratterizzato dalla sua struttura biciclica, che include un anello beta-lattamico e un anello diidrotiazina. Questo composto mostra un'attività antibatterica ad ampio spettro, rendendolo efficace contro una varietà di batteri Gram-positivi e Gram-negativi. Cefalosporina C è noto per la sua stabilità contro alcune beta-lattamasi, enzimi prodotti dai batteri che possono inattivare molti antibiotici. È utilizzato principalmente come precursore nella sintesi di altri antibiotici cefalosporinici, sviluppati per migliorare l'efficacia e la resistenza agli enzimi batterici. Il composto è solubile in acqua e presenta un profilo di tossicità relativamente basso, rendendolo adatto per applicazioni terapeutiche. Tuttavia, come altri antibiotici beta-lattamici, può causare reazioni allergiche in alcuni individui. La sua formula chimica è C16H17N3O7S, e viene tipicamente somministrato per iniezione o infusione in contesti clinici.

Formula: C₁₆H₂₁N₃O₈S

InChI: InChI=1S/C16H21N3O8S/c1-7(20)27-5-8-6-28-14-11(13(22)19(14)12(8)16(25)26)18-10(21)4-2-3-9(17)15(23)24/h9,11,14H,2-6,17H2,1H3,(H,18,21)(H,23,24)(H,25,26)/t9-,11-,14-/m1/s1

InChI key: InChIKey=HOKIDJSKDBPKTQ-GLXFQSAKSA-N

SMILES: C(O)(=O)C=1N2[C@@]([C@H](NC(CCC[C@H](C(O)=O)N)=O)C2=O)(SCC1COC(C)=O)[H]

Sinonimi:

• (6R,7R)-3-[(Acetyloxy)methyl]-7-[[(5R)-5-amino-5-carboxy-1-oxopentyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
• (6R,7R)-3-[(acetyloxy)methyl]-7-[(5-amino-5-carboxypentanoyl)amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
• 3-[(Acetyloxy)Methyl]-7-[(5-Amino-5-Carboxypentanoyl)Amino]-8-Oxo-5-Thia-1-Azabicyclo[4.2.0]Oct-2-Ene-2-Carboxylic Acid
• 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[(acetyloxy)methyl]-7-[(5-amino-5-carboxy-1-oxopentyl)amino]-8-oxo-, [6R-[6α,7β(R*)]]-
• 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[(acetyloxy)methyl]-7-[[(5R)-5-amino-5-carboxy-1-oxopentyl]amino]-8-oxo-, (6R,7R)-
• 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-(5-amino-5-carboxyvaleramido)-3-(hydroxymethyl)-8-oxo-, acetate (ester)
• 7-(5-Amino-5-carboxyvaleramido)cephalosporansaure
• Acide 7-(5-Amino-5-Carboxyvaleramido)Cephalosporanique
• Acido 7-(5-Amino-5-Carboxivaleramido)Cefalosporanico
• Cephalosporin C
• sodium (7R)-3-[(acetyloxy)methyl]-7-[(5-amino-5-carboxypentanoyl)amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
• Cephalosporin Impurity C
• CAPHALOSPORIN C
• (6R,7R)-3-(acetoxymethyl)-7-((R)-5-amino-5-carboxypentanamido)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
• 7-(D-5-Amino-5-carboxyvaleramido)-3-(hydrox-ymethyl)-8-oxo-5-thia-1-azabicyclo[4,2,0]oct-2-ene-2-Carboxylic acid acetate
• 7-(5-amino-5-carboxyvaleramido)cephalosporanic acid USP/EP/BP
• Cephalosporin C (7-ACA)
• C00916
• Cefazedone sodium salt Impurity 2
• 7-(5-amino-5-carboxyvaleramido)cephalosporanic acid
• HOKIDJSKDBPKTQ-GLXFQSAKSA-N
• 5-Thia-1-azabicyclo4.2.0oct-2-ene-2-carboxylic acid, 3-(acetyloxy)methyl-7-(5R)-5-amino-5-carboxy-1-oxopentylamino-8-oxo-, (6R,7R)-
• (7R)-3-[(Acetyloxy)methyl]-7-[[(R)-5-carboxy-5-amino-1-oxopentyl)amino]cepham-3-ene-4-carboxylic acid
• (7R)-3-[(Acetyloxy)methyl]-7-[[(R)-5-carboxy-5-amino-1-oxopentyl]amino]cepham-3-ene-4-carboxylic acid
• Cefodizime impurity 16
• Cephalosporins-intermediate II

(6R,7R)-3-(Acetoxymethyl)-7-((R)-5-amino-5-carboxypentanamido)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

CAS: 61-24-5

(6R,7R)-3-(Acetoxymethyl)-7-((R)-5-amino-5-carboxypentanamido)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

Purezza: 97%

Peso molecolare: 415.42g/mol

Ref: 54-OR1055040

Cefazedone Impurity 2

CAS: 61-24-5

Formula: C₁₆H₂₁N₃O₈S

Peso molecolare: 415.42

Ref: 4Z-C-108003

Cephalosporin C

CAS: 61-24-5

Formula: C₁₆H₂₁N₃O₈S

Peso molecolare: 415.42

Ref: ST-EA-CP-C265011

Cephalosporin C

CAS: 61-24-5

Cephalosporin C exhibits relatively weak resistance to Gram-positive and Gram-negative bacteria. It is stable against penicillinase, but can be decomposed by cephalosporinase. When hydrolyzed to remove its side chain, it yields 7-amino-cefenoic acid (7-ACA), which is an essential raw material for the production of semisynthetic cephalosporins.

Formula: C₁₆H₂₁N₃O₈S

Colore e forma: Solid

Peso molecolare: 415.418

Ref: TM-T206388