首页工具

登录

搜索结果

Search Results for " muscarinic acetylcholine receptor m1 "

Targets Recommended: AChR

17

抑制剂 & 化合物

1

天然产物

2

重组蛋白

如果没找到您满意的产品或者您对产品有其他要求，可以联系我们专业顾问为您提供针对性的合理建议。 QQ咨询网站留言咨询

Cat. No.	Product Name	Target	Signaling Pathways
T15942	MK-7622 M1 receptor modulator	AChR	Neuroscience
	MK-7622 (M1 receptor modulator) 是毒蕈碱 M1 受体阳性变构的调节剂。
T7002	Trihexyphenidyl hydrochloride Triesifenidile,Benzhexol hydrochloride,Tremin,Artane hydrochloride,盐酸苯海索	AChR	Neuroscience
	Trihexyphenidyl hydrochloride (Benzhexol hydrochloride) 是一种抗毒蕈碱类的抗帕金森病药物，结合至M1毒蕈碱受体。
T1049	Oxybutynin chloride Oxybutynin hydrochloride,盐酸奥昔布宁,Oxybutynin HCl	Potassium Channel; AChR	Membrane transporter/Ion channel; Neuroscience
	Oxybutynin chloride (Oxybutynin HCl) 是一种抗胆碱能药物，用于缓解泌尿和膀胱困难。它抑制血管 Kv 通道，IC50为 11.51 μM。
T8219	VU0238441	AChR	Neuroscience
	VU0238441是一种泛毒蕈碱型乙酰胆碱受体阳性变构调节剂，对 M1、M2、M3、M5 和 M4 的EC50分别为 3.2、2.8、2.2、2.1 和大于 10 μM。
T1475	Fesoterodine fumarate Toviaz,SPM 907,富马酸非索罗定	AChR	Neuroscience
	Fesoterodine fumarate (Toviaz) 是可口服的，非亚型选择性的竞争性毒蕈碱受体拮抗剂，用于膀胱过度活动症，对 M1、M2、M3、M4 和 M5 受体的pKi 值分别为 8.0、7.7、7.4、7.3 和 7.5。
T24469	MIPS1455 MIPS-1455,MIPS 1455
	MIPS1455 is a photoactivatable allosteric M1 muscarinic acetylcholine receptor ligand.
T27961	LY593093 LY 593093,LY-593093
	LY593093 is a selective partial orthosteric agonist of M1 muscarinic acetylcholine receptor.
T16758	Rispenzepine	Others	Others
	Rispenzepine 是一种新型的毒蕈碱型乙酰胆碱受体（mAChRs)的拮抗剂，选择性地靶向M1 和 M3 受体亚型，可用于治疗免疫系统疾病、感染、呼吸系统疾病。
T60728	M1 ligand 1
	M1 ligand 1 (compound 3b-b) 是槟榔碱衍生物的 N- 去甲基同源物，是毒蕈碱乙酰胆碱受体 M1 的配体。M1 ligand 1 用作正电子发射断层扫描(PET)的放射性示踪剂。
T17245	VU0467485 AZ13713945	Others	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, respectively). VU0467485 displays selecti
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 pesticide poisonings as well as som
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 investigating peptic ulcers. Additionally, Pirenzepine exhibits anti-proliferative activity against cancer cells [1] [2].
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, respectively). In vitro, methoctramine inhibits acetylcholine-induced reductions in isolated guinea pig tracheal tube contractions when used at a concentration of 1 μM.[2] In vivo, methoctramine inhibits bradycardia and bronchoconstriction induced by acetylcholinein guinea pigs wit...
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 surgery. Atropine is a competitive antagonist of the muscarinic acetylcholine receptor types M1, M2, M3, M4 and M5. It is classified as an anticholinergic drug (parasympatholytic).
T60577	Cycrimine
	Cycrimine 是毒蕈碱胆碱能受体(mAChR)M1的口服活性拮抗剂，可降低帕金森模型中乙酰胆碱的水平。Cycrimine 具有解痉活性，可用于研究行为和精神障碍。
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). Furthermore, Zanapezil exhibits moderate inhibition of muscarinic M1 and M2 receptor binding with Ki values of 234 and 340 nM, respectively. This compound holds promise for the investigation of the initial stages of Alzheimer's disease (AD).
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, 0.977, and 0.933 μM, respectively). Arecaidine propargyl ester induces contractions in isolated guinea pig atrium (pD2= 8.67). It induces apoptosis and the production of reactive oxygen species (ROS) in U87 and U251 glioblastoma cells when used at a concentration of 100 μM.2Arecai...

化合物

Cat.No: T15942

Synonym: M1 receptor modulator

Target: AChR

Trihexyphenidyl hydrochloride

Cat.No: T7002

Synonym: Triesifenidile,Benzhexol hydrochloride,Tremin,Artane hydrochloride,盐酸苯海索

Target: AChR

Oxybutynin chloride

Cat.No: T1049

Synonym: Oxybutynin hydrochloride,盐酸奥昔布宁,Oxybutynin HCl

Target: Potassium Channel, AChR

Cat.No: T8219

Target: AChR

Fesoterodine fumarate

Cat.No: T1475

Synonym: Toviaz,SPM 907,富马酸非索罗定

Target: AChR

Cat.No: T24469

Synonym: MIPS-1455,MIPS 1455

Cat.No: T27961

Synonym: LY 593093,LY-593093

Cat.No: T16758

Target: Others

Cat.No: T60728

Cat.No: T17245

Synonym: AZ13713945

Target: Others

Cat.No: T23763

Synonym: NSC 72861,NSC72861,NSC-72861

Cat.No: T61228

Methoctramine (hydrate)

Cat.No: T37728

Atropine Oxide Hydrochloride

Cat.No: T69232

Cat.No: T60577

Zanapezil free base

Cat.No: T38895

Synonym: TAK-147 free base,Zanapezil free base

Arecaidine propargyl ester (hydrobromide)

Cat.No: T36241

Cat. No.	Product Name	Target	Signaling Pathways
TN1653	Fustin	ERK; Beta Amyloid; AChR	MAPK; Neuroscience
	Fustin 是植物漆树 (Rhus verniciflua Stokes) 的植物性黄烷醇成分。 Fustin 对 6-羟基多巴胺诱导的神经元细胞死亡具有保护作用。

天然产物

Cat.No: TN1653

Target: ERK, Beta Amyloid, AChR

Species：

Expression System：

Tag：

Cat. No.	Product Name	Species	Expression System
TMPH-03338	CHRM1 Protein, Rat, Recombinant (His) Muscarinic acetylcholine receptor...	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. Primary transducing effect is Pi turnover. CHRM1 Protein, Rat, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 21.1 kDa and the accession number is P08482.
TMPH-01714	CHRM1 Protein, Human, Recombinant (His) Muscarinic acetylcholine receptor...	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. Primary transducing effect is Pi turnover. CHRM1 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 20.8 kDa and the accession number is P11229.

重组蛋白

CHRM1 Protein, Rat, Recombinant (His)

Cat.No: TMPH-03338

Species: Rat

Expression System: E. coli

CHRM1 Protein, Human, Recombinant (His)

Cat.No: TMPH-01714

Species: Human

Expression System: E. coli

我们的所有产品和服务仅用于科学研究，不能被用于人体，我们也不向个人提供产品和服务。

Copyright © 2015-2024 TargetMol Chemicals Inc. All rights reserved. 沪ICP备20019793号-4

沪公网安备 31010602006700号

沪公网安备 31010602006700号

TargetMol Loading

联系我们

电话：

400-820-0310

邮箱：

service@tsbiochem.com

QQ：

2881945090（终端用户）

2885109491（经销商）

经销：

终端：

地址：

上海市静安区江场三路238号8楼