Sulbactam

Sulbactam Struktur
68373-14-8
CAS-Nr.
68373-14-8
Bezeichnung:
Sulbactam
Englisch Name:
Sulbactam
Synonyma:
SULBACTAM ACID;sulbactum;CP-45899;penicillanic acid 1,1-dioxide;(2S,5R)-3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide;Betamaze;SULBACTAM;Shu ba acid;Sulbactam CRS;Sulbactam >
CBNumber:
CB1419201
Summenformel:
C8H11NO5S
Molgewicht:
233.24
MOL-Datei:
68373-14-8.mol

Sulbactam Eigenschaften

Schmelzpunkt:
154-157℃
alpha 
D20 +251° (c = 0.01 in pH 5.0 buffer)
Siedepunkt:
567.7±50.0 °C(Predicted)
Dichte
1.62±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
Löslichkeit
H2O: ≥18mg/mL
Aggregatzustand
lyophilized powder
pka
2.62±0.40(Predicted)
Farbe
white to tan
Optische Aktivität
[α]/D ≥+225°, c = 1 in H2O
Wasserlöslichkeit
Soluble in water at 18mg/ml
Merck 
14,8889
Stabilität:
Hygroscopic
InChIKey
FKENQMMABCRJMK-RITPCOANSA-N
CAS Datenbank
68373-14-8
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xn
R-Sätze: 22
S-Sätze: 24/25
WGK Germany  3
HS Code  29349990
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitsschädlich bei Verschlucken. Akute Toxizität oral Kategorie 4 Warnung P264, P270, P301+P312, P330, P501
Sicherheit

Sulbactam Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

Sulbactam is prepared by partial chemical synthesis from penicillins. The oxidation of the sulfur atom to a sulfone greatly enhances the potency of sulbactam. The combination of sulbactam and ampicillin (Unasyn) is now clinically popular.

Verwenden

Sulbactam sodium is a semi-synthetic penem antibiotic formed by the oxidation of penicillanic acid to its sulfone and was invented by Barth at Pfizer in 1978. Sulbactam sodium is a weak antibiotic but its action as an irreversible inhibitor of β-lactamase is exploited to block the degradation of other penicillin derivatives. Sulbactam acts as a synergist with cephalosporins and penicillins against Gram positive bacteria and is used commercially in combination with ampicillin.

Antimicrobial activity

Sulbactam has very weak antimicrobial activity against most bacteria. Its only notable activity is against N. gonorrhoeae, N. meningitidis and Acinetobacter baumannii.

Clinical Use

Sulbactam is penicillanic acid sulfone or 1,1-dioxopenicillanicacid. This synthetic penicillin derivative is a potent inhibitorof S. aureus β-lactamase as well as many β-lactamaseselaborated by Gram-negative bacilli. Sulbactam has weak intrinsicantibacterial activity but potentiates the activity ofampicillin and carbenicillin against β-lactamase–producingS. aureus and members of the Enterobacteriaceae family. Itdoes not, however, synergize with either carbenicillin or ticarcillinagainst P. aeruginosa strains resistant to these agents.Failure of sulbactam to penetrate the cell envelope is a possibleexplanation for the lack of synergy.
Fixed-dose combinations of ampicillin sodium and sulbactamsodium, marketed under the trade name Unasyn assterile powders for injection, have been approved for use inthe United States. These combinations are recommended forthe treatment of skin, tissue, intra-abdominal, and gynecologicalinfections caused by β-lactamase–producing strainsof S. aureus, E. coli, Klebsiella spp., P. mirabilis, B. fragilis,and Enterobacter and Acinetobacter spp.

Sulbactam Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Sulbactam Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 393)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Nanjing Sinoda Biological Technology Co., Ltd
+8613401983379
sales@njmcn.cn CHINA 74 58
Hebei Yanxi Chemical Co., Ltd.
+8617531190177
peter@yan-xi.com China 5990 58
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806
sales@capotchem.com China 29797 60
Shanghai Daken Advanced Materials Co.,Ltd
+86-371-66670886
info@dakenam.com China 14936 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21700 55
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714
fandachem@gmail.com China 9354 55
Nanjing ChemLin Chemical Industry Co., Ltd.
025-83697070
product@chemlin.com.cn CHINA 3012 60
Shanghai Yingrui Biopharma Co., Ltd.
+86-21-33585366 - 03@
sales03@shyrchem.com CHINA 738 60
career henan chemical co
+86-0371-86658258
sales@coreychem.com China 29914 58
SHANDONG ZHI SHANG CHEMICAL CO.LTD
+86 18953170293
sales@sdzschem.com China 2931 58

68373-14-8(Sulbactam)Verwandte Suche:


  • (2S,5R)-3,3-DIMETHYL-4,4,7-TRIOXO-4LAMBDA6-THIA-1-AZA-BICYCLO[3.2.0]HEPTANE-2-CARBOXYLIC ACID
  • (2S-CIS)-3,3-DIMETHYL-7-OXO-4-THIA-1-AZABICYCLO[3,2,0]HEPTANE-2-CARBOXYLIC ACID 4,4-DIOXIDE
  • 3,3-DIMETHYL-4,4,7-TRIOXO-4LAMBDA6-THIA-1-AZA-BICYCLO[3.2.0]HEPTANE-2-CARBOXYLIC ACID
  • SULBACTAM
  • sulbactam acid (base)
  • PENICILLANIC ACID SULFONE
  • (2S-cis)-3,3-dimethyl-7-oxy-4-sulph-1-aza dicyclo[3,2,0]heptane-2-carboxylic acid 4,4-dioxide
  • SALBACTAM ACID
  • Sulbactam free acid
  • SULBACTAM FREE ACID((2S-CIS)-3,3-DIMETHYL-7-OXO-4-THIA-1-AZABICYCLO[3,2,0]HEPTANE-2-CARBOXYLIC ACID 4,4-DIOXIDE )
  • Sulbactam,Penicillanicacidsulfone
  • 4-Thia-1-azabicyclo3.2.0heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-, 4,4-dioxide, (2S,5R)-
  • SULBACTAM(ACIDSODIUM)
  • Sulbactam (base and/or unspecified salts)
  • (2S-cis)-3,3-Dimethyl-7-oxo-4,4-dioxide-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4-4-oxide
  • Penicillanicacid 1,1-dioxide:CP-45899:CPL45899-2:Betamaze
  • 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-, 4,4-dioxide, (2S-cis)-
  • Betamaze
  • Penicillanic acid S,S-dioxide
  • (2S,5R)-3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptan-2-carboxylic acid 4,4-dioxid
  • (2S,5β)-2β-Carboxy-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane4,4-dioxide
  • (2S,5β)-3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2β-carboxylic acid 4,4-dioxide
  • Penicillanic acid 4,4-dioxide
  • Sulbactam (250 mg) (COLD SHIPMENT REQUIRED)
  • Sulbactam (250 mg)H0C3960.976mg/mg(ai)
  • SulbactaM - See S8244
  • (2S,5R)-3,3-dimethyl-7-oxo-4,4-dioxide-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
  • Penicillanic acid dioxide
  • (2S,5R)-3,3-dimethyl-4,4,7-trioxo-4$l^{6}-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
  • Sultamicillin Impurity 1(Sultamicillin EP Impurity A)
  • Sulbactam/Sulbactam Acid
  • Sulbactam, 98%, an irreversible β-lactamase inhibitor
  • SULBACTAM(BETAMAZE)
  • Sultamicillin EP Impurity A
  • Sulbactam for peak identification CRS
  • Sulbactam CRS
  • Sulbactam >
  • Sulbactam USP/EP/BP
  • Sulbactam (CP 45899 and Betamaze)
  • (2S,5R)-3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide[Sulbactam
  • Sulbactam (COLD SHIPMENT REQUIRED) (1623670)
  • SULBACTAM ACID
  • penicillanic acid 1,1-dioxide
  • CP-45899
  • sulbactum
  • Shu ba acid
  • (2S,5R)-3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide
  • 2H5]-Sulbactam
  • methylene (2S,5R,6R)-6-[[(2R)-[[[[(2R)-aminophenylacetyl]amino][(4S)-4-[[[[[(2S,5R)-3,3-dimethyl-4,4,7-trioxo-4λ6-thia-1-azabicyclo[3.2.0]hept-2-yl]carbonyl]oxy]methoxy]carbonyl]-5,5-dimethylthiazolidin-2-yl]acetyl]amino]phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (2S,5R)-3,3-dimethyl-4,4,7-trioxo-4λ6-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (sultamicillin dimer)
  • N-[[(2RS)-1-éthylpyrrolidin-2-yl]méthyl]-2-hydroxy-5-sulfamoylbenzamide
  • Sultamicillin Impurity A
  • Sultamicillin Tosilate Dihydrate EP Impurity A
  • Sultamicillin Tosilate Dihydrate Impurity A
  • Rimsulfuron Impurity 4(Sulfosulfuron)
  • 68373-14-8
  • 6837-14-8
  • 73-14-8
  • 68373-14-6
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