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カタログ番号 | 製品名 | 別名 | ターゲット |
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T0218 | Biperiden | Bipariden,Akineton,KL 373,Biperidine | AChR |
Biperiden (Bipariden) is a muscarinic antagonist that has effects in both the central and peripheral nervous systems. It has been used in the treatment of arteriosclerotic, idiopathic, and postencephalitic parkinsonism. ... | |||
T9771 | Velufenacin | AChR | |
Velufenacin is an antagonist of muscarinic receptor[1]. | |||
T23297 | (S)-(+)-Dimethindene maleate | AChR , Histamine Receptor | |
(S)-(+)-Dimethindene maleate is an orally available, selective muscarinic M2 receptor and histamine H1 receptor antagonist that inhibits muscarinic M1, M3, and M4 receptors. | |||
T16989 | Tarafenacin D-tartrate | SVT-40776 D-tartrate | Others |
Tarafenacin D-tartrate is a highly selective M3 muscarinic receptor antagonist (Ki= 0.19 nM), ~200 fold selectivity over the M2 receptor. | |||
T13992 | CHF5407 | SVT-47060 | AChR |
CHF5407(SVT-47060) is a potent and selective muscarinic M3 receptor antagonist with prolonged action at muscarinic receptors.CHF5407 has an effect on bronchospasm and may be used in the study of respiratory disorders.CHF... | |||
T13385 | Zamifenacin fumarate | UK-76654 fumarate | AChR |
Zamifenacin fumarate (UK-76654 fumarate) is a potent and gut-selective antagonist of muscarinic M3 receptor. | |||
T6364 | Desfesoterodine | 5-HMT,(R)-5-Hydroxymethyl Tolterodine,PNU-200577,5-HM,5-hydroxymethyl Tolterodine | AChR |
Desfesoterodine (5-HMT) is a new muscarinic receptor antagonist with Kb of 0.84 nM. | |||
T7895 | Syn-Ake acetate | Dipeptide diaminobutyroyl benzylamide | AChR |
Syn-Ake acetate (Dipeptide diaminobutyroyl benzylamide) is a muscarinic acetylcholine receptor antagonist. | |||
T10914L | Cyclodrine | Cyclopent | AChR |
Cyclodrine (Cyclopent) is a cholinergic (muscarinic, nicotinic) (mAChR and nAChR) receptor antagonist. | |||
T10914 | Cyclodrine hydrochloride | AChR | |
Cyclodrine hydrochloride is a dual cholinergic muscarinic receptor (mAChR) and nicotinic receptor (nAChR) antagonist that can be used in the study of neurologically related diseases. | |||
T31207 | GSK233705 | Darotropium bromide,GSK 233705,GSK-233705B,GSK233705,GSK233705B,GSK-233705,GSK 233705B | AChR |
GSK233705 (Darotropium bromide) is a muscarinic receptor antagonist used in conjunction with the prevention and treatment of chronic obstructive pulmonary disease (COPD) and asthma in humans. | |||
T5655 | MAChR-IN-1 hydrochloride | AChR | |
mAChR-IN-1 hydrochloride is a potent muscarinic cholinergic receptor (mAChR) antagonist, with an IC50 of 17 Nm. | |||
T1542 | Pirenzepine dihydrochloride | Pirenzepine HCl,Bisvanil,Tabe,LS519 | AChR |
Pirenzepine dihydrochloride (LS519) is a selective M1 muscarinic receptor antagonist, inhibiting gastric secretion. | |||
T23508 | VU 0255035 | AChR | |
muscarinic M1 antagonist | |||
T1534 | Darifenacin hydrobromide | Darifenacin HBr,UK-88525 | AChR |
Darifenacin hydrobromide (UK-88525) is a selective muscarinic receptor antagonist used to treat urinary incontinence and overactive bladder syndrome. | |||
T29687 | Afacifenacin | Afacifenacin fumarate,SMP-986,NS 986,NS-986,SMP 986,NS986,SMP986 | AChR |
Afacifenacin (SMP-986) fumarate is an M3 muscarinic receptor-selective antagonist used in the study of ischemic heart disease, urinary incontinence and cystitis and other disorders. | |||
T8147 | Solifenacin | YM905 free base | AChR |
Solifenacin (YM905 free base) (YM905 free base) is a novel muscarinic receptor antagonist, its pKis for M1, M2 and M3 receptors is of 7.6, 6.9 and 8.0, respectively. | |||
T28722 | SCH 57790 | SCH57790,SCH-57790 | AChR |
SCH 57790 is a novel and selective muscarinic M(2) receptor antagonist that releases acetylcholine and enhances cognition in experimental animals for the treatment of Alzheimer's disease. | |||
T0099 | Tolterodine tartrate | Detrol LA,PNU-200583E,Kabi-2234 | AChR |
Tolterodine tartrate (PNU-200583E) is a potent antagonist for muscarinic receptor. It show selectivity for the urinary bladder and salivary glands in vivo. | |||
T7079 | Batefenterol | GSK961081,TD-5959 | Adrenergic Receptor , AChR |
Batefenterol (TD-5959) (GSK961081, TD-5959) is a muscarinic receptor antagonist and β2-adrenoceptor agonist. It displays high affinity for hM2, hM3 muscarinic and hβ2-adrenoceptor (Ki:1.4/1.3/3.7 nM). | |||
TP1902L1 | G-Protein antagonist peptide acetate | Adrenergic Receptor | |
G-Protein antagonist peptide acetate is a truncated substance P-related peptide, competes with receptor for G protein binding. G-Protein antagonist peptide acetate inhibits the activation of Gi or Go by M2 muscarinic cho... | |||
T10000 | (±)-Tazifylline | Histamine Receptor | |
(±)-Tazifylline is a selective and long-acting antagonist of histamine H1 receptor. Tazifylline shows much lower affinity for H2 receptors, α- and β-adrenoceptors, 5-hydroxytryptamine and muscarinic receptor subtypes. | |||
T60536 | Terodiline | Calcium Channel , AChR | |
Terodiline is an orally available selective muscarinic M1 receptor and calcium channel antagonist for the study of diseases caused by abnormal bladder function. | |||
T13370 | YM-46303 | AChR | |
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... | |||
T1179 | Tiotropium bromide | Tiopropium,BA679 BR | AChR |
Tiotropium bromide (BA679 BR) is a long-acting, 24 hour, anticholinergic bronchodilator used in the management of chronic obstructive pulmonary disease (COPD). Tiotropium is a muscarinic receptor antagonist, on topical a... | |||
T14345 | Atropine methyl bromide | Methylatropine bromide | AChR |
Atropine methyl bromide (Methylatropine bromide) is a quaternary ammonium salt of atropine, characterized as a muscarinic receptor (mAChR) antagonist. It functions as a mydriatic to dilate the pupil during ophthalmic exa... | |||
T5051 | Isopropamide Iodide | AChR | |
Isopropamide iodide is a long-acting anticholinergic drug. It is used in the treatment of peptic ulcers and other gastrointestinal disorders. It also acts as a muscarinic receptor antagonist which can be applied to the t... | |||
T12489L | Pimethixene maleate | Pimetixene maleate | Dopamine Receptor , 5-HT Receptor , AChR , Histamine Receptor |
Pimethixene maleate (Pimetixene maleate) is a potent 5-HT2B receptor antagonist with sedative and antitussive activity.Pimethixene maleate inhibits 5-HT1A, 5-HT2A, 5-HT2B, 5-HT2C, histamine H1, dopamine D2 and D4.4 as we... | |||
T4494 | CLOZAPINE N-OXIDE | Dopamine Receptor , 5-HT Receptor , AChR , Drug Metabolite | |
Clozapine N-oxide is the major metabolite of Clozapine and is blood-brain barrier permeable. Clozapine N-oxide is an agonist of DREADDs and activates the DREADD receptors hM3Dq and hM4Di. Clozapine N-oxide is also a dopa... | |||
T1006 | Propantheline bromide | Neopepulsan,Pro-Banthine,Neometantyl | AChR |
Propantheline bromide (Pro-Banthine) competitively antagonizes acetylcholine activity mediated by muscarinic receptors at neuroeffector sites on smooth muscle and exocrine gland cells. Propantheline Bromide is the bromid... | |||
T6426 | Buclizine dihydrochloride | Longifene,Buclina,Buclizine HCl,UCB-4445 | 5-HT Receptor , AChR , Histamine Receptor |
Buclizine dihydrochloride (Buclina) is the hydrochloride salt form of buclizine, a piperazine histamine H1 receptor antagonist with primarily antiemetic and antivertigo activities. Buclizine dihydrochloride binds to and ... | |||
T6707 | Tiotropium Bromide hydrate | BA-679 BR hydrate,BA 679BR | AChR |
Tiotropium Bromide hydrate (BA-679 BR hydrate) is a potent anticholinergic and bronchodilator, serving as a muscarinic receptor antagonist, specifically targeting mAChR. It is developed for treating chronic obstructive a... | |||
T68599 | Orphenadrine | Orphenadrine (free base) | Sodium Channel , NMDAR , AChR |
Orphenadrine is a noncompetitive N-methyl-D-aspartate (NMDA) receptor antagonist that inhibits clonal HERG channels in a concentration-dependent manner, producing an IC of 0.85 μM in HEK cells.Orphenadrine is an antagoni... | |||
T38192 | Unifiram | Others | |
Unifiram is a nootropic agent.1It increases acetylcholine (ACh) release in the rat cerebral cortexin vivoand induces a long-lasting increase in the amplitude of field excitatory postsynaptic potentials (fEPSPs) in the ra... | |||
T23124 | PD 102807 | Others | |
M4 muscarinic receptor antagonist | |||
T22876 | J 104129 fumarate | Others | |
M3 muscarinic receptor antagonist | |||
T29047 | UH-AH 37 | UH-AH-37,UH-AH37 | |
UH-AH 37 is a antagonist of human muscarinic acetylcholine receptor. | |||
T2278L | Piboserod hydrochloride | SB 207266 hydrochloride,Piboserod HCl,SB 207266A | |
Piboserod HCl is a selective antagonist of 5-HT4 and muscarinic receptor. | |||
T23379 | Solifenacin hydrochloride | Others | |
Solifenacin Hcl is a muscarinic receptor antagonist. | |||
T25697L | Levophencynonate HCl | Levophencynonate hydrochloride,R-(-)-Phencynonate hydrochloride | |
Levophencynonate HCl is a muscarinic receptor antagonist. | |||
T2138L | Oxyphencyclimine | Oxiphencycliminum,Antulcus,Zamanil,Manir,Caridan,Naridan | |
Oxyphencyclimine is a muscarinic receptor antagonist (MRA) anticholinergic drug used to treat peptic ulcers. | |||
T22709 | DAU 5884 hydrochloride | Others | |
muscarinic M3 receptor antagonist | |||
T23452 | Telenzepine dihydrochloride | Others | |
muscarinic M1 receptor antagonist | |||
T12680 | (±)-Darifenacin | (±)-UK-88525 | Others |
(±)-Darifenacin is the racemate of Darifenacin. Darifenacin is a selective antagonist of M3 muscarinic receptor. | |||
T27199 | Doxacurium Chloride | BW A 938U,BWA938U,Nuromax,BW-A-938U | |
Doxacurium Chloride is a muscarinic acetylcholine receptor M2 antagonist. | |||
T25697 | Levophencynonate | Levo-phencynonate | |
Levophencynonate is a muscarinic receptor antagonist. | |||
T71014 | Aprophit | ||
Aprophit is a muscarinic antagonist that has been shown to selectively acylate muscarinic receptor proteins. | |||
T69234 | Piperilate HCl | ||
Piperilate HCl is an antispasmodic, antimuscarinic agent. It is a muscarinic cholinergic receptor antagonist. | |||
T15211 | Elucaine | Others | |
Elucaine is an antagonist of the muscarinic acetylcholine receptor. It has anti-ulcerative activity. |
カタログ番号 | 製品名 | 別名 | ターゲット |
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T21532 | Anisodamine | 6-Hydroxyhyoscyamine,6-beta-Hydroxyhyoscyamine | AChR |
Anisodamine (6-beta-Hydroxyhyoscyamine) is an antagonist of muscarinic and nicotinic cholinoceptor with similar affinities at the muscarinic receptor as scopolamine and atropine. Anisodamine improve the microcirculation ... |
カタログ番号 | 製品名 | ||
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L9830 | Anti-Parkinson's Disease Compound Library | 857 compounds | |
A unique collection of 857 compounds with anti-PD activities or acting on main drug targets of PD can be used for HTS and HCS. |