RX 67668

Names

[ CAS No. ]:
40709-76-0

[ Name ]:
RX 67668

Biological Activity

[Description]:

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].

[Related Catalog]:

Research Areas >> Neurological Disease
Signaling Pathways >> Neuronal Signaling >> AChE

[Target]

IC50: 5 μM (acetylcholinesterase) and 5 μM (butyrylcholinesterase)[1]


[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.

[2]. Metcalf G, wt al. Evaluation of RX 72601 as an anti-curare agent. Br J Anaesth. 1975 Apr;47(4):451-6.

Chemical & Physical Properties

[ Molecular Formula ]:
C16H24ClN

[ Molecular Weight ]:
265.82100

[ Exact Mass ]:
265.16000

[ PSA ]:
3.24000

[ LogP ]:
4.54850


Related Compounds