1. GPCR/G Protein Neuronal Signaling
  2. Opioid Receptor
  3. CR 665 acetate

CR 665 acetate  (Synonyms: JNJ 38488502 acetate; FE 200665 acetate)

目录号: HY-111011
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CR 665 (JNJ 38488502) acetate 是一种 κ-阿片类激动剂,可通过激活肠道传入神经上的受体有效抑制内脏疼痛。CR 665 acetate 表现出外周选择性,其药代动力学特征与羟可酮等非选择性阿片类药物不同。CR 665 acetate 已证明对内脏疼痛耐受阈值具有有益作用,且不会出现阿片类药物穿透大脑后出现的延迟镇痛反应。CR 665 acetate 因其止痛特性而被建议用于术后疼痛的研究。

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CR 665 acetate Chemical Structure

CR 665 acetate Chemical Structure

CAS No. : 958873-83-1

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生物活性

CR 665 (JNJ 38488502) acetate is a kappa-opioid agonist that may effectively treat visceral pain by activating receptors on afferent nerves within the gut. CR 665 acetate exhibits peripheral selectivity, differentiating its pharmacokinetic profile from that of non-selective opioids like oxycodone. CR 665 acetate has demonstrated a beneficial effect on visceral pain tolerance thresholds without the delayed analgesic response characteristic of opioids that penetrate the brain. CR 665 acetate is proposed for use in managing postoperative pain due to its pain-relieving properties.

分子量

731.88

Formula

C38H53N9O6

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
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Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
CR 665 acetate
目录号:
HY-111011
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