CR 665 – High Purity 99.36% – GMP Manufacturer

CR 665 – High Purity 99.36% – GMP Manufacturer

$2.00

CR 665 is a GMP-grade peptide agonist of the peripheral ?-opioid receptor (purity 99.36%), offering potent peripheral analgesic activity without typical opioid CNS or gastrointestinal side effects. Ideal for models of visceral or peripheral pain. For laboratory research use only.?For wholesale prices, other specifications and uses, please consult our staff?

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描述

CR 665 (CAS No. 228546-92-7), also known as FE-200665 or JNJ 38488502, is an all-D-amino-acid peptide with high selectivity for peripheral ?-opioid receptors (over ? and ? receptors). Unlike conventional opioids, CR 665 offers potent analgesic effects with minimal central nervous system penetration and reduced gastrointestinal inhibition. Preclinical and early-phase human studies suggest strong efficacy in pain relief, particularly visceral pain, with minimal side effects such as respiratory depression or euphoria. Produced under GMP standards at 99.36% purity, CR 665 is designed for reliable and reproducible research performance. Intended strictly for laboratory research use only.


Product Specifications

Parameter Details
Product Name CR 665
Synonyms FE-200665; JNJ 38488502
CAS No. 228546-92-7
Purity ? 99.36% (GMP-grade)
Chemical Formula C??H??N?O?
Molecular Weight Approx. 671.8 g/mol
Mechanism Peripheral ?-opioid receptor (KOR) agonist
Selectivity Highly selective for KOR over ?/? receptors
Appearance White to off-white solid
Solubility Soluble in DMSO; aqueous solubility may require buffers or sonication
Storage Conditions Store at –20 °C; protect from light and moisture
Manufacturing Standard GMP-compliant
Applications Peripheral pain models, visceral pain research, inflammation studies
Regulatory Status For laboratory research use only

Mechanism of Action & Research Applications

Mechanism of Action
CR 665 selectively activates peripheral ?-opioid receptors (KOR), which are primarily located outside the central nervous system. This selective activation provides potent analgesia while avoiding common opioid-related central side effects such as respiratory depression, addiction, or gastrointestinal transit inhibition.

Research Applications

  • Visceral Pain Models: Effective in preclinical and early human studies focusing on visceral nociception.

  • Peripheral Pain Studies: Ideal for exploring analgesic mechanisms with limited CNS involvement.

  • Selective Receptor Engagement: Minimizes off-target effects, making it valuable for pain pharmacology assays.

  • Anti-inflammatory Research: May be used to study peripheral receptor modulation in inflammatory settings.

    images-cr-665-oxidized-formula


Side Effects (Research Context Only)

CR 665 is intended for in vitro and preclinical model research. In animal and early human studies, it demonstrated potent analgesic effects with minimal side effects—no significant CNS depression or gastrointestinal inhibition. No long-term safety data is available; standard laboratory safety protocols must be followed.


Disclaimer

CR 665 is strictly for laboratory research use only. It is not approved for clinical, therapeutic, or diagnostic use. Handle according to institutional safety guidelines.

其他信息

重量 0.6 公斤
尺寸 61 × 34 × 61 厘米

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