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レラバクタム

Relebactam

HCID 44129647
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基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
部分構造検索類似構造を探す

基本情報

CAS
1174018-99-5
標準SMILES
O=C(NC1CCNCC1)[C@@H]1CC[C@@H]2CN1C(=O)N2OS(=O)(=O)O
InChIKey
SMOBCLHAZXOKDQ-ZJUUUORDSA-N
分子式
C12H20N4O6S
平均分子量
348.38 g/mol
単同位体質量
348.11035554

概要

Relebactam is a diazabicyclooctane beta-lactamase inhibitor, similar in structure to [avibactam]. It includes a piperidine ring which reduces export from bacterial cells by producing a positive charge. It is currently available in a combination product which includes [imipenem] and [cilastatin] to treat complicated urinary tract infections (UTIs), pyelonephritis, and complicated intra-abdominal infections in adults. It is considered to be a last-line treatment option and gained FDA approval as part of the combination product RecarbrioⓇ in July 2019.

名称と識別子

優先名称
Relebactam
IUPAC
[(2S,5R)-7-oxo-2-(piperidin-4-ylcarbamoyl)-1,6-diazabicyclo[3.2.1]octan-6-yl] hydrogen sulfate
現地名
レラバクタム
英語名
Relebactam
分子式
C12H20N4O6S
分子量
348.38

名称と別名

Relebactam1174018-99-5Relebactam anhydrousMK-7655(-)-Relebactam anhydrous1OQF7TT3PFrelebactamum[(2S,5R)-7-oxo-2-(piperidin-4-ylcarbamoyl)-1,6-diazabicyclo[3.2.1]octan-6-yl] hydrogen sulfateMK7655(-)-relebactam monohydrateRECARBRIO COMPONENT RELEBACTAMMK-7655 MONOHYDRATE
名称をさらに表示
[(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(1R,2S,5R)-7-Oxo-2-(piperidin-4-ylcarbamoyl)-1,6-diazabicyclo[3.2.1]octan-6-yl hydrogen sulfateCS-2637RelibactamRuilai Batan2H4]-RelebactamCefadroxil MonomerMK-7655(Relebactam)Relebactam(MK-7655)
MK-7655A COMPONENT RELEBACTAMSulfuric acid mono-((2S,5R)-7-oxo-2-(piperidin-4-ylcarbamoyl)-1,6-diaza-bicyclo(3.2.1)oct-6-yl) esterRECARBRIO COMPONENT RELEBACTAM MONOHYDRATE1174020-13-3((2S,5R)-7-oxo-2-(piperidin-4-ylcarbamoyl)-1,6-diazabicyclo(3.2.1)octan-6-yl) hydrogen sulfateRefChem:879223DTXCID501513269((1R,2S,5R)-7-oxo-2-((piperidin-4-yl)carbamoyl)-1,6-diazabicyclo(3.2.1)octan-6-yl)oxidanesulfonic acid

物性

構造計算による物性

XLogP
-3.6
極性表面積
137 Ų
水素結合供与体数
3
水素結合受容体数
7
回転可能結合数
4
重原子数
23
形式電荷
0
複雑度
585

実験および物理化学的性質

DrugsPharmaceuticals -> Listed in ZINC15
Human Drugs · 2 件

FDA approved drugs -> Active ingredient

FDA approved drugs -> Active ingredient

物理化学的性質

融点
252 °C · >252°C (dec.)
比重(密度)
1.59 · 1.59
貯蔵温度
-20 °C · Hygroscopic, -20°C Freezer, Under inert atmosphere
溶解性
DMSO(微量)、水(微量)
酸解離定数(Pka)
-4.59 · -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

安全と法規制

安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。

GHS分類

GHS Classification · 6 件

Warning

H373 (100%): May causes damage to organs through prolonged or repeated exposure [Warning Specific target organ toxicity, repeated exposure]

P260, P319, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 36 reports by companies from 2 notifications to the ECHA C&L Inventory.

Warning

H361d (100%): Suspected of damaging the unborn child [Warning Reproductive toxicity]

危険有害性情報

Hazard Classes and Categories · 2 件

STOT RE 2 (100%)

Repr. 2 (100%)

安全データ

危険有害性情報
コード 危険有害性情報 危険有害性クラス 区分 注意喚起語 シンボル P コード H303

化学と産業

薬理情報

Protein BindingRelebactam is approximately 22% plasma protein bound.
PharmacodynamicsRelebactam prevents the hydrolysis of [imipenem], allowing it to exert its bactericidal effect.
Mechanism of Action · 1 件

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. 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.

Biological Half-LifeRelebactam has a half-life of 1.2 hours as per official FDA labeling. Values reported in pharmacokinetic studies vary from 1.35-1.8 hours.
Metabolism/MetabolitesRelebactam does not undergo significant metabolism and can be found mostly unchanged in human plasma.
FDA Pharmacological Classification · 5 件

1OQF7TT3PF

RELEBACTAM ANHYDROUS

Established Pharmacologic Class [EPC] - beta Lactamase Inhibitor

Mechanisms of Action [MoA] - beta Lactamase Inhibitors

Relebactam anhydrous is a beta Lactamase Inhibitor. The mechanism of action of relebactam anhydrous is as a beta Lactamase Inhibitor.

MeSH Pharmacological ClassificationEndogenous substances and drugs that inhibit or block the activity of BETA-LACTAMASES.
Absorption, Distribution and Excretion · 4 件

Currently, relebactam is only available as an intravenous product; therefore, there is no relevant absorption data in the literature.

関連反応

1 件
反応記録を作成
HRID 451295 の反応式
HRID 451295生成物としてuspto-grants-2013_07

化合物ノート

読み込み中…

このページの内容基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
その他の操作
ノートを作成反応を作成見積依頼を出す

データベース識別子

CAS
1174018-99-5、1174020-13-3
PubChem CID
44129647
ChEMBL
CHEMBL3112741、CHEMBL3301605
UNII
1OQF7TT3PF
EC Number
112-516-4、813-387-3
Nikkaji
J3.628.086G、J3.809.098D

Approximately 90-100% of relebactam is renally eliminated.

Relebactam has a volume of distribution of approximately 19 L with both single and steady state dosing.

Relebactam has a reported total clearance of approximately 130-150 mL/min (8 L/h). About 30% of the total drug clearance can be attributed to active tubular secretion.

応用分野 · 2 件

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.

上流・下流製品情報

上流原料

tert-butyl 4-((1R,2S,5R)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxamido)piperidine-1-carboxylateN,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