MR 2266

    WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 534666

CAS#: 56649-76-4

Description: MR 2266 is a narcotic antagonist.


Chemical Structure

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MR 2266
CAS# 56649-76-4

Theoretical Analysis

MedKoo Cat#: 534666
Name: MR 2266
CAS#: 56649-76-4
Chemical Formula: C21H27NO2
Exact Mass: 325.20
Molecular Weight: 325.452
Elemental Analysis: C, 77.50; H, 8.36; N, 4.30; O, 9.83

Price and Availability

This product is not in stock, which may be available by custom synthesis. For cost-effective reason, minimum order is 1g (price is usually high, lead time is 2~3 months, depending on the technical challenge). Quote less than 1g will not be provided. To request quote, please email to sales @medkoo.com or click below button.
Note: Price will be listed if it is available in the future.

Request quote for custom synthesis

Synonym: MR 2266; MR-2266; MR2266

IUPAC/Chemical Name: 2,6-Methano-3-benzazocin-8-ol, 6,11-diethyl-3-(3-furanylmethyl)-1,2,3,4,5,6-hexahydro-, (2R,6R,11R)-

InChi Key: HEYXXBUDMDVUNQ-CEWLAPEOSA-N

InChi Code: InChI=1S/C21H27NO2/c1-3-18-20-11-16-5-6-17(23)12-19(16)21(18,4-2)8-9-22(20)13-15-7-10-24-14-15/h5-7,10,12,14,18,20,23H,3-4,8-9,11,13H2,1-2H3/t18-,20+,21+/m0/s1

SMILES Code: OC1=CC=C2C([C@]3(CC)CCN(CC4=COC=C4)[C@]([C@@H]3CC)([H])C2)=C1

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO

Shelf Life: >3 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 325.45 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
In vitro protocol:
In vivo protocol:

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2: Bauer U, Nakazi M, Kathmann M, Göthert M, Schlicker E. The stereoselective kappa-opioid receptor antagonist Mr 2266 does not exhibit stereoselectivity as an antagonist at the orphan opioid (ORL1) receptor. Naunyn Schmiedebergs Arch Pharmacol. 1999 Jan;359(1):17-20. doi: 10.1007/pl00005317. PMID: 9933145.


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4: Frey HH. Effect of mu- and kappa-opioid agonists on the electroconvulsive seizure threshold in mice and antagonism by naloxone and MR 2266. Pharmacol Toxicol. 1988 Mar;62(3):150-4. doi: 10.1111/j.1600-0773.1988.tb01863.x. PMID: 2836842.


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7: Ramabadran K, Bansinath M, Turndorf H, Puig MM. Effects of naloxone and Mr 2266 on thermonociceptive reactions in diabetic mice. NIDA Res Monogr. 1989;95:528-9. PMID: 2561849.


8: Laorden ML, Carrillo E, Puig MM. Prevention of hyperthermia-induced convulsions in immature rat by MR-2266, a kappa antagonist. Methods Find Exp Clin Pharmacol. 1991 Nov;13(9):605-8. PMID: 1686291.


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17: Bhargava HN, Kremer EK, Gibbons MO, Philips BJ, Driver JW, Chou M. Stereospecific effects of a kappa-opiate antagonist on the actions of morphine in morphine-tolerant rats. Eur J Pharmacol. 1989 Dec 7;173(2-3):159-64. doi: 10.1016/0014-2999(89)90513-x. PMID: 2560431.


18: Stockhaus K, Ensinger HA, Gaida W, Jennewein HM, Merz H. Mr 2033 CL--a novel non-morphine-like opioid analgesic. NIDA Res Monogr. 1983 Apr;43:144-9. PMID: 6135993.


19: Ben-Sreti MM, Sewell RD, Upton N. Some observations on the effects of enantiomers of two benzomorphan narcotic antagonists and atropine on analgesia, tremor and hypothermia produced by oxotremorine. Arch Int Pharmacodyn Ther. 1982 Apr;256(2):219-27. PMID: 7103612.


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