ChemicalBook--->CAS DataBase List--->40709-76-0

40709-76-0

40709-76-0 Structure

40709-76-0 Structure
IdentificationBack Directory
[Name]

RX 67668
[CAS]

40709-76-0
[Synonyms]

RX 67668
[Molecular Formula]

C16H24ClN
[MDL Number]

MFCD34469321
[MOL File]

40709-76-0.mol
[Molecular Weight]

265.83
Hazard InformationBack Directory
[Uses]

RX 67668 is a potent cholinesterase inhibitor with an IC50 of 5 μM for both acetylcholinesterase (AChE) and butyrylcholinesterase. RX 67668 can reverse the neuromuscular blockade induced by D-tubocurarine. RX 67668 is a muscle relaxant used to relieve skeletal muscle fatigue[1][2].
[in vivo]

RX 67668 (1-4 mg/kg; i.p.) reduces by half the dose of methacholine necessary to produce red tears, whilst RX 67668 (7-2 mg/kg s.c.) is necessary to reduce the pupil diameter of the mouse to 50% of the control value[1].
Rat anterior tibialis preparation of the cat tibialis preparation demonstrates that RX 67668 (0.3-1.0 mg/kg; i.v.) is effective in reversing tubocurarine-induced muscle blockade[1].

[References]

[1] Doxey JC, et al. Some pharmacological properties of RX 67668--a new anticholinesterase. Br J Pharmacol. 1972 Nov;46(3):568P-569P. PMID:4656643
[2] Metcalf G, wt al. Evaluation of RX 72601 as an anti-curare agent. Br J Anaesth. 1975 Apr;47(4):451-6. DOI:10.1093/bja/47.4.451
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