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Relebactam

CAS No.
1174018-99-5
Chemical Name:
Relebactam
Synonyms
MK7655;CS-2637;RELEBACTAM;Relibactam;Ruilai Batan;2H4]-Relebactam;Cefadroxil Monomer;MK-7655(Relebactam);Relebactam(MK-7655);MK-7655;MK 7655;MK7655
CBNumber:
CB82546782
Molecular Formula:
C12H20N4O6S
Molecular Weight:
348.38
MDL Number:
MFCD28502833
MOL File:
1174018-99-5.mol
Last updated:2024-11-19 23:02:33

Relebactam Properties

Melting point >252°C (dec.)
Density 1.59
storage temp. Hygroscopic, -20°C Freezer, Under inert atmosphere
solubility DMSO (Slightly), Water (Slightly)
pka -4.59±0.18(Predicted)
form Solid
color Off-White to Light Yellow
Stability Hygroscopic
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
FDA UNII 1OQF7TT3PF

Relebactam price More Price(22)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 23890 MK-7655 ≥98% 1174018-99-5 1mg $37 2024-03-01 Buy
Cayman Chemical 23890 MK-7655 ≥98% 1174018-99-5 5mg $169 2024-03-01 Buy
Cayman Chemical 23890 MK-7655 ≥98% 1174018-99-5 10mg $319 2024-03-01 Buy
Cayman Chemical 23890 MK-7655 ≥98% 1174018-99-5 25mg $704 2024-03-01 Buy
Usbiological 464603 Relebactam 1174018-99-5 1mg $305 2021-12-16 Buy
Product number Packaging Price Buy
23890 1mg $37 Buy
23890 5mg $169 Buy
23890 10mg $319 Buy
23890 25mg $704 Buy
464603 1mg $305 Buy

Relebactam Chemical Properties,Uses,Production

Description

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.

Uses

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.

Mechanism of action

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

Clinical Use

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.

Synthesis

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.
Synthesis of Relebactam
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

1174020-24-6
1174018-99-5
Synthesis of Relebactam from N,N,N-tributylbutan-1-aminium [({(2S,5R)-7-oxo-2-[(piperidin-4-ylamino)carbonyl]-1,6-diazabicyclo[3.2.1]oct-6-yl}oxy)sulfonyl]oxidanide
Global( 133)Suppliers
Supplier Tel Email Country ProdList Advantage
Heading (Nanjing)Pharmtechnologies Co., Ltd.
+86-25-58467899-832 +86-13382406280 liucheng@headingpharm.com China 46 58
Anhui Ruihan Technology Co., Ltd
+8617756083858 daisy@anhuiruihan.com China 973 58
Henan Fengda Chemical Co., Ltd
+86-371-86557731 +86-13613820652 info@fdachem.com China 20286 58
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32957 60
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29881 58
BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19553 58
Chongqing Chemdad Co., Ltd
+86-023-6139-8061 +86-86-13650506873 sales@chemdad.com China 39894 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 32165 58
HANGZHOU CLAP TECHNOLOGY CO.,LTD
86-571-88216897,88216896 13588875226 sales@hzclap.com CHINA 6312 58
Zhejiang J&C Biological Technology Co.,Limited
+1-2135480471 +1-2135480471 sales@sarms4muscle.com China 10473 58

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  • Jan 5,2024

View Lastest Price from Relebactam manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Relebactam pictures 2024-11-19 Relebactam
1174018-99-5
US $44.00-155.00 / mg 100% 10g TargetMol Chemicals Inc.
	Relebactam pictures 2024-03-29 Relebactam
1174018-99-5
US $8.00-1.00 / KG 1KG 99% g-kg-tons, free sample is available Henan Fengda Chemical Co., Ltd
Relebactam pictures 2023-09-08 Relebactam
1174018-99-5
US $30.00 / kg 1kg 99% 1000t/year Anhui Ruihan Technology Co., Ltd
  • Relebactam pictures
  • Relebactam
    1174018-99-5
  • US $44.00-155.00 / mg
  • 100%
  • TargetMol Chemicals Inc.
  • 	Relebactam pictures
  • Relebactam
    1174018-99-5
  • US $8.00-1.00 / KG
  • 99%
  • Henan Fengda Chemical Co., Ltd
  • Relebactam pictures
  • Relebactam
    1174018-99-5
  • US $30.00 / kg
  • 99%
  • Anhui Ruihan Technology Co., Ltd
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 Ruilai Batan 1174018-99-5 C12H20N4O6S