Pharmaceutical

NXL 104

  • CAS: 1192491-61-4
  • Purity: 99%
  • Manufacturers supply cost-effective and customizable NXL 104 1192491-61-4
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Quality products?make an important contribution to long-term revenue and profitability. Manufacturers supply cost-effective and customizable NXL 104 1192491-61-4

1.What is the NXL 104 ?

Avibactam (NXL104) is a novel β-lactamase inhibitor with a non-lactam structural scaffold. NXL104 irreversibly inhibits lactamase from Mycobacterium tuberculosis.

(2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxamide
1383814-64-9

(2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxamide

(2S,5R)-1,6-diazabicyclo[3.2.1]octane-2-carboxamide 7-oxo-6-(sulfoxy)monosodium salt
1192491-61-4

(2S,5R)-1,6-diazabicyclo[3.2.1]octane-2-carboxamide 7-oxo-6-(sulfoxy)monosodium salt

Conditions
Conditions Yield
(2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxamide; With pyridine; sulfur trioxide pyridine complex; at 20 ℃; for 20h;
With sodium dihydrogenphosphate; In water;
80%
Multi-step reaction with 2 steps
1.1: α-picoline; thiocyanate trioxide / tetrahydrofuran / 24 h / 20 °C / Inert atmosphere
2.1: 2,2,2-trifluoroethanol; tetrafluoroboric acid
2.2: 1 h / 0 °C
With α-picoline; tetrafluoroboric acid; thiocyanate trioxide; 2,2,2-trifluoroethanol; In tetrahydrofuran;
Multi-step reaction with 2 steps
1: triethylamine; sulfur trioxide trimethylamine complex / ethanol; water
2: sodium 2-ethylhexanoic acid / ethanol
With sulfur trioxide trimethylamine complex; triethylamine; sodium 2-ethylhexanoic acid; In ethanol; water;
Multi-step reaction with 2 steps
1: triethylamine; sulfur trioxide trimethylamine complex / ethanol; water
2: sodium 2-ethylhexanoic acid / ethanol
With sulfur trioxide trimethylamine complex; triethylamine; sodium 2-ethylhexanoic acid; In ethanol; water;
Multi-step reaction with 3 steps
1.1: sodium hexamethyldisilazane; 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone / tetrahydrofuran / 0.17 h / -78 °C / Inert atmosphere
1.2: -78 - 20 °C / Inert atmosphere
2.1: palladium 10% on activated carbon; hydrogen / acetonitrile / 1.33 h / 20 °C / Inert atmosphere
3.1: sodium hydrogencarbonate / dimethylsulfoxide-d6; water-d2
With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; palladium 10% on activated carbon; hydrogen; sodium hexamethyldisilazane; sodium hydrogencarbonate; In tetrahydrofuran; dimethylsulfoxide-d6; water-d2; acetonitrile;
(1R,2S,5R)-7-oxo-6-sulfonyloxy-1,6-diazabicyclo[3,2,1]octane-2-carboxamide tributylbenzylammonium

(1R,2S,5R)-7-oxo-6-sulfonyloxy-1,6-diazabicyclo[3,2,1]octane-2-carboxamide tributylbenzylammonium

(2S,5R)-1,6-diazabicyclo[3.2.1]octane-2-carboxamide 7-oxo-6-(sulfoxy)monosodium salt
1192491-61-4

(2S,5R)-1,6-diazabicyclo[3.2.1]octane-2-carboxamide 7-oxo-6-(sulfoxy)monosodium salt

Conditions
Conditions Yield
With sodium 2-ethylhexanoic acid; In ethanol; water; at 15 - 40 ℃; for 4h;
80%
With sodium 2-ethylhexanoic acid; In ethanol;
4.6 g
With sodium isooctanoate; In ethanol; water; at 35 - 40 ℃; for 4h;

2.What is the CAS number for NXL 104 ?

The CAS number of NXL 104 is 1192491-61-4.

More information of NXL 104 1192491-61-4 are:

CAS?Number

1192491-61-4

PSA

142.44000

LogP

0.45350

3.What are another words for NXL 104 ?

Synonyms?for?NXL 104 1192491-61-4:AvibactaM SodiuM Salt;NXL 104;Sulfuric Acid Mono[(1R,2S,5R)-2-(aMinocarbonyl)-7-oxo-1,6-diazabicyclo[3.2.1]oct-6-yl] Ester SodiuM Salt;Avibactam (sodium);AvibactaM SodiuM NXL 104;sodium (1R,2S,5R)-2-carbamoyl-7-oxo-1,6-diazabicyclo[3.2.1]octan-6-yl sulfate;(2S,5R)-7-Oxo-6-(sulfooxy)-1,6-diazabicyclo[3.2.1]octane-2-carboxamide monosodium salt

4.What is the molecular formula of NXL 104?

The chemical formula of ?NXL 104 is?C7H10N3NaO6S which containing 7 Carbon atoms,10 Hydrogen atoms,3 Nitrogen atoms,1 Sodium atoms,6 Oxygen atoms and 1 Sulfur atoms,and the molecular weight of??NXL 104?is 287.229.

5.What is NXL 104 (1192491-61-4) used for?

Avibactam is a β-lactamase inhibitor (IC50s = 8, 80, and 38 nM for TEM-1, P99, and KPC-2 β-lactamases, respectively). It restores the antimicrobial activity of ceftazidime , ceftriaxone , imipenem , and piperacillin against antibiotic-resistant Enterobacteriaceae in vitro (MIC90 reduction 4-1,024-fold across 190 E. coli and K. pneumoniae clinical isolates). Formulations containing avibactam have been used to treat carbapenem-resistant Enterobacteriaceae infections.

Relevant articles related to NXL 104:

Article

Source

Understanding the Role of Water in Different Solid Forms of Avibactam Sodium and Its Affecting Mechanism

Cheng, Xiaowei,Ding, Zhiyong,Hao, Hongxun,Huang, Xin,Li, Guiping,Liu, Han,Mao, Yafei,Su, Wei,Tian, Beiqian

, p. 1150 - 1161 (2020)

Stable crystal form of avibactam sodium and preparation method thereof

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Paragraph 0021-0023, (2020/10/04)

6.Buy NXL 104 with the best price .

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