エルクサドリン

エルクサドリン 化学構造式
864821-90-9
CAS番号.
864821-90-9
化学名:
エルクサドリン
别名:
エルクサドリン;5-{[(2S)-2-アミノ-3-(4-カルバモイル-2,6-ジメチルフェニル)-N-[(1S)-1-(5-フェニル-1H-イミダゾール-2-イル)エチル]プロパンアミド]メチル}-2-メトキシ安息香酸;5-[[[(2S)-2-アミノ-3-(4-カルバモイル-2,6-ジメチルフェニル)プロパノイル]-[(1S)-1-(5-フェニル-1H-イミダゾール-2-イル)エチル]アミノ]メチル]-2-メトキシ安息香酸
英語名:
Eluxadoline
英語别名:
CS-2329;EOS-61916;Eluxadolin;Eluxadoline;API-Diarrhea;JNJ 27018966;The yi lu Lin;Eluxadoline 13CD4;Eluxadoline (Viberzi);Eluxadoline(JNJ 27018966)
CBNumber:
CB12723517
化学式:
C32H35N5O5
分子量:
569.65
MOL File:
864821-90-9.mol

エルクサドリン 物理性質

融点 :
>180°C (dec.)
沸点 :
834.2±65.0 °C(Predicted)
比重(密度) :
1.284±0.06 g/cm3(Predicted)
貯蔵温度 :
Refrigerator
溶解性:
DMSO(微量)、メタノール(微量)
外見 :
個体
酸解離定数(Pka):
4.01±0.10(Predicted)
色:
ホワイトからオフホワイト
InChIKey:
QFNHIDANIVGXPE-FNZWTVRRSA-N
SMILES:
C(O)(=O)C1=CC(CN(C(=O)[C@@H](N)CC2=C(C)C=C(C(N)=O)C=C2C)[C@H](C2NC(C3=CC=CC=C3)=CN=2)C)=CC=C1OC
CAS データベース:
864821-90-9
安全性情報
  • リスクと安全性に関する声明
  • 危険有害性情報のコード(GHS)
DEA Controlled Substances CSCN: 9725
CAS SCH: IV
NARC: N
絵表示(GHS) GHS hazard pictograms
注意喚起語
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
H361 生殖能または胎児への悪影響のおそれの疑い 生殖毒性 2 警告 P201, P202, P281, P308+P313, P405,P501
注意書き
P201 使用前に取扱説明書を入手すること。
P202 全ての安全注意を読み理解するまで取り扱わないこ と。
P281 指定された個人用保護具を使用すること。
P308+P313 暴露または暴露の懸念がある場合:医師の診断/手当てを 受けること。
P405 施錠して保管すること。
P501 内容物/容器を...に廃棄すること。

エルクサドリン 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

エルクサドリン 化学特性,用途語,生産方法

効能

止瀉薬, オピオイド受容体作動/拮抗薬

説明

Eluxadoline, originally developed by Janssen and currently marketed by Allergan (formerly Actavis), was approved in May 2015 by the FDA for the treatment of diarrhea-predominant irritable bowel syndrome (IBS-D). Eluxadoline, an orally dosed agent, employs a unique mechanism for IBS-D treatment, as it functions simultaneously as a μ- and κ-opioid receptor agonist and a δ- opioid receptor antagonist, leading to a first-in-class therapy for treatment of IBS-D. Specifically, in animal studies, eluxadoline was found to interact with opioid receptors in the gut, inhibiting neurogenically mediated secretion and reducing intestinal contractility. Additionally, the treatment led to a decrease in stress-induced acceleration of upper GI transit without causing rebound constipation, earning its mark as a first-line therapeutic treatment for IBS-D. In two phase III clinical trials of over 2400 patients with IBS-D, patients taking eluxadoline showed a greater improvement toward the end point (≥30% improvement from their baseline IBS-D score on at least 50% of days treated with eluxadoline) compared to patients treated with placebo.

使用

Eluxadoline is an orally-active drug used to reduce symptoms of irritable bowel syndrome such as diarrhea and abdominal pain.

定義

ChEBI: An amino acid amide obtained by the formal condensation of the carboxy group of 4-carbamoyl-2,6-dimethyl-L-phenylalanine with the secondary amino group of 2-methoxy-5-({[(1S)-1-(4-phenylimidazol-2-yl)ethyl]amino}methyl)ben oic acid. It has mixed opioid receptor activity and is used for treatment of irritable bowel syndrome with diarrhoea.

薬物動態学

Following oral administration of 100 mg VIBERZI in healthy subjects, the Cmax of eluxadoline was approximately 2 to 4 ng/mL, and AUC was 12 to 22 ng. h/mL. Eluxadoline has approximately linear pharmacokinetics with no accumulation upon repeated twice-daily dosing. The variability of eluxadoline pharmacokinetic parameters ranges from 51% to 98%.
Absorption: The absolute bioavailability of eluxadoline has not been determined. The median Tmax value was 1.5 hours (1 to 8 hours) under fed conditions and 2 hours (range: 0.5 to 6 hours) under fasting conditions.
The administration of VIBERZI with a high-fat meal that contained approximately 800 to 1000 total calories, with 50% of calories derived from fat content, decreased the Cmax of eluxadoline by 50% and AUC by 60%.
Distribution: Plasma protein binding of eluxadoline was 81%.
Elimination: The mean plasma elimination half-life of eluxadoline ranged from 3.7 hours to 6 hours.
Metabolism: The metabolism of eluxadoline is not established. There is evidence that glucuronidation can occur to form an acyl glucuronide metabolite.
Excretion: Following a single oral dose of 300 mg [14C] eluxadoline in healthy male subjects, 82.2% of the total radioactivity was recovered in feces within 336 hours and less than 1% was recovered in urine within 192 hours.

エルクサドリン 上流と下流の製品情報

原材料

準備製品


エルクサドリン 生産企業

Global( 176)Suppliers
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Protheragen-ING
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ATK CHEMICAL COMPANY LIMITED
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Beijing Yibai Biotechnology Co., Ltd
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sales04@yibaibiotech.com CHINA 419 58

864821-90-9(エルクサドリン)キーワード:


  • 864821-90-9
  • JNJ 27018966
  • Eluxadoline
  • 5-(((S)-2-amino-3-(4-carbamoyl-2,6-dimethylphenyl)-N-((S)-1-(4-phenyl-1H-imidazol-2-yl)ethyl)propanamido)methyl)-2-methoxybenzoic acid
  • Eluxadolin
  • API-Diarrhea
  • Benzoic acid, 5-[[[(2S)-2-amino-3-[4-(aminocarbonyl)-2,6-dimethylphenyl]-1-oxopropyl][(1S)-1-(5-phenyl-1H-imidazol-2-yl)ethyl]amino]methyl]-2-methoxy-
  • CS-2329
  • Eluxadoline (Viberzi)
  • EOS-61916
  • 5-(((S)-2-amino-3-(4-carbamoyl-2,6-dimethylphenyl)-N-((S)-1-(5-phenyl-1H-imidazol-2-yl)ethyl)propanamido)methyl)-2-methoxybenzoic acid
  • Eluxadoline(JNJ 27018966)
  • Eluxadoline 13CD4
  • The yi lu Lin
  • 5-{[(2S)-2-amino-3-(4-carbamoyl-2,6-dimethylphenyl)-N-[(1S)-1-(5-phenyl-1H-imidazol-2-yl)ethyl]propanamido]methyl}-2-methoxybenzoic acid
  • エルクサドリン
  • 5-{[(2S)-2-アミノ-3-(4-カルバモイル-2,6-ジメチルフェニル)-N-[(1S)-1-(5-フェニル-1H-イミダゾール-2-イル)エチル]プロパンアミド]メチル}-2-メトキシ安息香酸
  • 5-[[[(2S)-2-アミノ-3-(4-カルバモイル-2,6-ジメチルフェニル)プロパノイル]-[(1S)-1-(5-フェニル-1H-イミダゾール-2-イル)エチル]アミノ]メチル]-2-メトキシ安息香酸
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