CR665 (H-D-Phe-D-Phe-D-Nle-D-Arg-NH-4-Picolyl)
CR665 (H-D-Phe-D-Phe-D-Nle-D-Arg-NH-4-Picolyl) Basic information
- Product Name:
- CR665 (H-D-Phe-D-Phe-D-Nle-D-Arg-NH-4-Picolyl)
- Synonyms:
-
- CR665 (H-D-Phe-D-Phe-D-Nle-D-Arg-NH-4-Picolyl)
- D-Argininamide, D-phenylalanyl-D-phenylalanyl-D-norleucyl-N-(4-pyridinylmethyl)-
- FE 200665|||JNJ 38488502
- CAS:
- 228546-92-7
- MF:
- C36H49N9O4
- MW:
- 671.83
- Mol File:
- 228546-92-7.mol
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CR665 (H-D-Phe-D-Phe-D-Nle-D-Arg-NH-4-Picolyl) Chemical Properties
- Density
- 1.26±0.1 g/cm3(Predicted)
- pka
- 13.36±0.46(Predicted)
- form
- Solid
- color
- White to off-white
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CR665 (H-D-Phe-D-Phe-D-Nle-D-Arg-NH-4-Picolyl) Usage And Synthesis
Uses
CR 665 (JNJ 38488502) is a peripherally selective κ-opioid agonist. CR 665 can activate the kappa opioid receptor with EC50 value of 10.9 nM. CR 665 can be used for the research of peripheral pain[1][2].
References
[1] Anne E Olesen, et al. A population pharmacokinetic and pharmacodynamic study of a peripheral κ-opioid receptor agonist CR665 and oxycodone. Clin Pharmacokinet DOI:10.1007/s40262-012-0023-8
[2] Francis M Hughes Jr, et al. Development of a Peptide-derived orally-active kappa-opioid receptor agonist targeting peripheral pain. Open Med Chem J. 2013 Nov 4;7:16-22. DOI:10.2174/1874104501307010016
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