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Trimebutine

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    Trimebutine
  • Trimebutine
Cat No: 31574
Biochemicals - Ion Channel Modulation
Cayman

Trimebutine is an opioid receptor agonist.{61029,61030,61031} It binds to μ-, δ-, and κ-opioid receptors with Ki values of 0.34, 0.5, and 0.58 μM, respectively, in canine myenteric plexus synaptosomes.{61030} Trimebutine inhibits twitch contraction an...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 3,4,5-trimethoxy-benzoic acid, 2-(dimethylamino)-2-phenylbutyl ester
Correlated keywords:
  • 58997-88-9 ?opioid ?opioid ?opiod A Ch LMMP MR 2266 Ltype Triton
Product Overview:
Trimebutine is an opioid receptor agonist.{61029,61030,61031} It binds to μ-, δ-, and κ-opioid receptors with Ki values of 0.34, 0.5, and 0.58 μM, respectively, in canine myenteric plexus synaptosomes.{61030} Trimebutine inhibits twitch contraction and acetylcholine (ACh) release induced by low-frequency electrical stimulation in isolated guinea pig longitudinal muscle with myenteric plexus (LM-MP; EC50s = 0.274 and 0.215 μM, respectively), effects that are inhibited by the opioid receptor antagonists naloxone and MR2266.{61031} It increases twitch contraction and ACh release induced by high-frequency electrical stimulation in isolated guinea pig LM-MP when used at concentrations of 1 μM or less, but inhibits these effects at 10 μM or more. Trimebutine (30, 100, and 300 μM) decreases the amplitude and frequency of spontaneous contractions in isolated guinea pig colonic smooth muscle strips.{61032} It also inhibits large conductance calcium-activated potassium (BKCa) and L-type calcium currents in colonic smooth muscle cells in a concentration-dependent manner.
Size 5 g
Shipping dry ice
CAS Number 39133-31-8
Molecular Formula C22H29NO5
SMILES O=C(C1=CC(OC)=C(C(OC)=C1)OC)OCC(C2=CC=CC=C2)(N(C)C)CC
Molecular Weight 387,5
Formulation A crystalline solid
Purity ≥98%
Custom Code 2922.19
UNSPSC code 12352100

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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ISO Guide 34:2009

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