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Cat No. | Product Name | Synonyms | Targets |
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T15942 | MK-7622 | M1 receptor modulator | AChR |
MK-7622 (M1 receptor modulator) is a modulator of muscarinic M1 receptor positive allosteric. | |||
T7002 | Trihexyphenidyl hydrochloride | Triesifenidile,Benzhexol hydrochloride,Tremin,Artane hydrochloride | AChR |
Trihexyphenidyl hydrochloride (Benzhexol hydrochloride) is an antiparkinsonian agent of the antimuscarinic class. | |||
T8219 | VU0238441 | AChR | |
VU0238441 is agonist of Muscarinic acetylcholine receptor M5 (human) with EC50 of 2.1μM. | |||
T1049 | Oxybutynin chloride | Oxybutynin hydrochloride,Oxybutynin HCl | Potassium Channel , AChR |
Oxybutynin chloride (Oxybutynin HCl) is an anticholinergic medication used to relieve urinary and bladder difficulties. It competitively antagonizes the M1, M2, and M3 subtypes of the muscarinic acetylcholine receptor. | |||
T1475 | Fesoterodine fumarate | Toviaz,SPM 907 | AChR |
Fesoterodine fumarate (Toviaz) is the fumarate salt form of fesoterodine, a competitive muscarinic receptor antagonist with muscle relaxant and urinary antispasmodic properties. Fesoterodine is rapidly hydrolyzed in vivo... | |||
T27961 | LY593093 | LY 593093,LY-593093 | |
LY593093 is a selective partial orthosteric agonist of M1 muscarinic acetylcholine receptor. | |||
T24469 | MIPS1455 | MIPS-1455,MIPS 1455 | |
MIPS1455 is a photoactivatable allosteric M1 muscarinic acetylcholine receptor ligand. | |||
T16758 | Rispenzepine | Others | |
Rispenzepine is a novel antagonist of muscarinic acetylcholine receptors (mAChRs), selectively targeting the M1 and M3 receptor subtypes, and can be used in the treatment of immune system disorders, infections, and respi... | |||
T17245 | VU0467485 | AZ13713945 | Others |
VU0467485 is a potent and selective muscarinic acetylcholine receptor 4 positive allosteric modulator. VU0467485 potentiates the activity of ACh at M4 (EC50s: 26.6 nM and 78.8 nM at the rat and human M4 receptors, respec... | |||
T60728 | M1 ligand 1 | ||
M1 ligand 1 (compound 3b-b) is a N-desmethyl congener of arecoline derivative that is a muscarinic acetylcholine receptor M1 ligand. M1 ligand 1 is able to be used as PET (positron emission tomography) radiotracer [1]. | |||
T23763 | Atropine Oxide | NSC 72861,NSC72861,NSC-72861 | |
Atropine Oxide is a derivative of Atropine. Atropine is a competitive antagonist of the muscarinic acetylcholine receptor types M1, M2, M3, M4, and M5. Atropine is a medication to treat certain types of nerve agents and ... | |||
T61228 | Pirenzepine | ||
Pirenzepine (LS 519 free base) is a selective antagonist of the M1 muscarinic acetylcholine receptor (mAChR). It effectively inhibits gastric acid secretion and reduces muscle spasm, making it a valuable compound for inv... | |||
T37728 | Methoctramine (hydrate) | ||
Methoctramine is a selective antagonist of M2 muscarinic acetylcholine receptors (IC50 = 6.1 nM in CHO-K1 cell membranes).[1] It is selective for M2 over M1, M3, M4, and M5 receptors (IC50s = 92, 770, 260, and 217 nM, re... | |||
T69232 | Atropine Oxide Hydrochloride | ||
Atropine Oxide is a derivative of Atropine. Atropine is a medication to treat certain types of nerve agent and pesticide poisonings as well as some types of slow heart rate and to decrease saliva production during surger... | |||
T60577 | Cycrimine | ||
Cycrimine is an orally active antagonist of the muscarinic cholinergic receptor (mAChR) M1 that reduces the level of acetylcholine in the Parkinson's model. Cycrimine exhibits antispasmodic activity that can be used in b... | |||
T38895 | Zanapezil free base | TAK-147 free base,Zanapezil free base | |
Zanapezil (TAK-147) is a powerful and selective inhibitor of acetylcholine esterase (AChE). It demonstrates significant and reversible inhibition of AChE activity in rat cerebral cortex homogenates (IC50 = 51.2 nM). Furt... | |||
T36241 | Arecaidine propargyl ester (hydrobromide) | ||
Arecaidine propargyl ester is an agonist of M2muscarinic acetylcholine receptors (mAChRs).1It selectively binds to M2over M1, M3, M4, and M5mAChRs in CHO cells expressing the human receptors (Kis = 0.0871, 1.23, 0.851, 0... |
Cat No. | Product Name | Synonyms | Targets |
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TN1653 | Fustin | ERK , Beta Amyloid , AChR | |
Fustin is the phytogenic flavanol component of the plant Rhus verniciflua Stokes. Fustin shows protective effects on 6-hydroxydopamine-induced neuronal cell death. |
Cat No. | Product Name | Species | Expression System |
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TMPH-03338 | CHRM1 Protein, Rat, Recombinant (His) | Rat | E. coli |
The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. ... | |||
TMPH-01714 | CHRM1 Protein, Human, Recombinant (His) | Human | E. coli |
The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. ... |