レラバクタム

レラバクタム 化学構造式
1174018-99-5
CAS番号.
1174018-99-5
化学名:
レラバクタム
别名:
[(2S,5R)-7-オキソ-2-[(ピペリジン-4-イル)カルバモイル]-1,6-ジアザビシクロ[3.2.1]オクタン-6-イル]オキシダンスルホン酸;硫酸[(2S,5R)-7-オキソ-2-[(ピペリジン-4-イル)カルバモイル]-1,6-ジアザビシクロ[3.2.1]オクタン-6-イル];レラバクタム;レレバクタム;硫酸(2S,5R)-2-(ピペリジン-4-イルカルバモイル)-7-オキソ-1,6-ジアザビシクロ[3.2.1]オクタン-6-イル;(4S,7R)-4-[(4-ピペリジニル)アミノカルボニル]ヘキサヒドロ-2-オキソ-3,7-メタノ-1H-1,3-ジアゼピン-1-イルスルファート
英語名:
Relebactam
英語别名:
MK7655;CS-2637;RELEBACTAM;Relibactam;2H4]-Relebactam;Cefadroxil Monomer;MK-7655(Relebactam);Relebactam(MK-7655);MK-7655;MK 7655;MK7655;(2S,5R)-7-oxo-2-(piperidin-1-ium-4-ylcarbamoyl)-1,6-diazabicyclo[3.2.1]octan-6-yl sulfate
CBNumber:
CB82546782
化学式:
C12H20N4O6S
分子量:
348.38
MOL File:
1174018-99-5.mol

レラバクタム 物理性質

融点 :
>252°C (dec.)
比重(密度) :
1.59
貯蔵温度 :
Hygroscopic, -20°C Freezer, Under inert atmosphere
溶解性:
DMSO(微量)、水(微量)
酸解離定数(Pka):
-4.59±0.18(Predicted)
外見 :
個体
色:
オフホワイトからライトイエロー
安定性::
吸湿性
InChI:
InChI=1S/C12H20N4O6S/c17-11(14-8-3-5-13-6-4-8)10-2-1-9-7-15(10)12(18)16(9)22-23(19,20)21/h8-10,13H,1-7H2,(H,14,17)(H,19,20,21)/t9-,10+/m1/s1
InChIKey:
SMOBCLHAZXOKDQ-ZJUUUORDSA-N
SMILES:
S(O)(ON1C(=O)[N@@]2C[C@@]1([H])CC[C@H]2C(NC1CCNCC1)=O)(=O)=O

安全性情報

レラバクタム 価格

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入

レラバクタム 化学特性,用途語,生産方法

説明

Relebactam (formerly known as MK-7655) is a novel,intravenous,class A and class C B-lactamase inhibitor and is currently under evaluation in combination with imipenem/cilastatin for the treatment of resistant Gram-negative infections.In vitro studies demonstrated that relebactam restored imipenem's activity against KPC-producing Enterobacteriacae,lowering imipenem MICs from 16-64 to 0.12-1mg/L at a concentration of 4 mg/L. Moreover, relebactam is able to lower imipenem MICs for P. aeruginosa,particularly in strains with depressed OprD expression and increased AmpC expression.Conversely, the addition of relebactam to imipenem does not seem to provide any adjunctive benefit against A.baumanii or S.maltophilia or against MBL-producing Enterobacteriacae.A non-inferiority, Phase 3 trial evaluating the efficacy and safety of imipenem/relebactam compared to piperacillin/tazobactam for the treatment of HAP and VAP(ClinicalTrials.gov Identifier: NCT02493764) is currently recruiting. A Phase 3 study evaluating the efficacy and safety of imipenem/relebactam (200/100-500/250 mg depending on renal function) compared to colistimethate sodium plus imipenem/cilastatin for the treatment of imipenem-resistant bacterial infections,including HAP, VAP, cIAIs and cUTIs, has recently been completed and results are pending(ClinicalTrials.gov Identifier: NCTO2452047).In Phase 2 trials, imipenem/relebactam was well tolerated, with diarrhea, nausea, vomiting and headache being the most commonly reported adverse events.

使用

Relebactam is a novel β-lactamase inhibitor in combination with Primaxin. It has also demonstrated the potential to enhance the activity of imipenem against P.aeruginosa, including those strains with depressed OprD expression and increased AmpC expression.

作用機序

Relebactam is a beta-lactamase inhibitor known to inhibit many types of beta-lactamases including Ambler class A and Ambler class C enzymes, helping to prevent imipenem from degrading in the body.Label,Similar to the structurally-related avibactam, first, relebactam binds non-covalently to a beta-lactamase binding site, then, it covalently acylates the serine residue in the active site of the enzyme.In contrast to some other beta-lactamase inhibitors, once relebactam de-acylates from the active site, it can reform it's 5 membered ring and is capable of rebinding to target enzymes.
https://go.drugbank.com/drugs/DB12377

臨床応用

Recently, another carbapenem-β-lactamase inhibitor, imipenem/cilastatin-relebactam (RecarbrioTM), was approved by the FDA. Relebactam, a bicyclic diazabicyclooctane, is structurally related to avibactam but differs by the addition of a piperidine ring to the 2-position carbonyl group. Like meropenem- vaborbactam (VabomereTM), imipenem-relebactam(RecarbrioTM) is active against class A and class C carbapenemases and is approved for the treatment of multidrug-resistant intraabdominal infections secondary to Bacteroides caccae, Bacteroides fragilis, Bacteroides ovatus, Bacteroides thetaiotaomicron, Bacteroides uniformis, Bacteroides vulgatus, Bifidobacterium stercoris, Citrobacter freundii, Enterobacter cloacae, Escherichia coli, Fusobacterium nucleatum, Klebsiella aerogenes, Klebsiella oxytoca, Klebsiella pneumoniae, Parabacteroides distasonis, and Pseudomonas aeruginosa and multidrug-resistant complicated urinary tract infections secondary to E. cloacae, E. coli, K. aerogenes, K. pneumoniae and P. aeruginosa.

合成

Relebactam is a β-lactamase inhibitor in clinical trials as a combination therapy for the treatment of bacterial infection resistant to β-lactam antibiotics. Its unusual structural challenges have inspired a rapid synthesis featuring an iridium-catalyzed N–H insertion and a series of late stage transformations designed around the reactivity of the labile bicyclo[3.2.1]urea at the core of the target.
説明図
In 2014, Qualified Infectious Disease Product (QIDP) and Fast Track designations were assigned by the FDA for the treatment of complicated urinary tract infections, complicated intra-abdominal infections and hospital-acquired bacterial pneumonia/ventilator-associated bacterial pneumonia.
A Concise Synthesis of a β-Lactamase Inhibitor

レラバクタム 上流と下流の製品情報

原材料

準備製品


レラバクタム 生産企業

Global( 119)Suppliers
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1174018-99-5(レラバクタム)キーワード:


  • 1174018-99-5
  • Sulfuric acid Mono-[7-oxo-2-(piperidin-4-ylcarbaMoyl)-1,6-diaza-bicyclo[3.2.1]oct-6-yl] ester
  • Sulfuric acid mono[(1R,2S,5R)-7-oxo-2-[(4-piperidinylamino)carbonyl]-1,6-diazabicyclo[3.2.1]oct-6-yl] ester
  • MK-7655(Relebactam)
  • RELEBACTAM
  • MK7655
  • (2S,5R)-sulfuric acid mono{[(4-aminopiperidin-4-yl)carbonyl]-7-oxo-1,6-diazabicyclo[3.2.1]oct-6-yl}ester
  • (2S,5R)-7-oxo-2-(piperidin-1-ium-4-ylcarbamoyl)-1,6-diazabicyclo[3.2.1]octan-6-yl sulfate
  • Relebactam(MK-7655)
  • MK-7655;MK 7655;MK7655
  • CS-2637
  • (1R,2S,5R)-7-Oxo-2-(piperidin-4-ylcarbamoyl)-1,6-diazabicyclo[3.2.1]octan-6-yl hydrogen sulfate
  • 2H4]-Relebactam
  • Relibactam
  • (2S,5R)-7-oxo-2-(piperidin-4-ylcarbamoyl)-1,6-diazabicyclo[3.2.1]octan-6-yl hydrogen sulfate (Relebactam)
  • Cefadroxil Monomer
  • [(2S,5R)-7-オキソ-2-[(ピペリジン-4-イル)カルバモイル]-1,6-ジアザビシクロ[3.2.1]オクタン-6-イル]オキシダンスルホン酸
  • 硫酸[(2S,5R)-7-オキソ-2-[(ピペリジン-4-イル)カルバモイル]-1,6-ジアザビシクロ[3.2.1]オクタン-6-イル]
  • レラバクタム
  • レレバクタム
  • 硫酸(2S,5R)-2-(ピペリジン-4-イルカルバモイル)-7-オキソ-1,6-ジアザビシクロ[3.2.1]オクタン-6-イル
  • (4S,7R)-4-[(4-ピペリジニル)アミノカルボニル]ヘキサヒドロ-2-オキソ-3,7-メタノ-1H-1,3-ジアゼピン-1-イルスルファート
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