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Search Results for " muscarinic acetylcholine receptor m3 "
Targets Recommended: Potassium Channel AChR

8

抑制剂 & 化合物

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天然产物

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重组蛋白

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Cat. No. Product Name Target Signaling Pathways
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。
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。
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
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).
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

Oxybutynin chloride
Cat.No: T1049
Synonym: Oxybutynin hydrochloride,盐酸奥昔布宁,Oxybutynin HCl
Target: Potassium Channel, AChR
VU0238441
Cat.No: T8219
Synonym:
Target: AChR
Fesoterodine fumarate
Cat.No: T1475
Synonym: Toviaz,SPM 907,富马酸非索罗定
Target: AChR
Rispenzepine
Cat.No: T16758
Synonym:
Target: Others
Atropine Oxide
Cat.No: T23763
Synonym: NSC 72861,NSC72861,NSC-72861
Target:
Methoctramine (hydrate)
Cat.No: T37728
Synonym:
Target:
Atropine Oxide Hydrochloride
Cat.No: T69232
Synonym:
Target:
Arecaidine propargyl ester (hydrobromide)
Cat.No: T36241
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T0804 Pilocarpine Hydrochloride

NSC 5746 HCl,盐酸毛果芸香碱,Pilocarpine HCl,(+)-Pilocarpine hydrochloride

AChR Neuroscience
Pilocarpine Hydrochloride (NSC 5746 HCl) 是一种 M3 型毒蕈碱乙酰胆碱受体激动剂,用于制作癫痫实验模型

天然产物

Pilocarpine Hydrochloride
Cat.No: T0804
Synonym: NSC 5746 HCl,盐酸毛果芸香碱,Pilocarpine HCl,(+)-Pilocarpine hydrochloride
Target: AChR
Cat. No. Product Name Species Expression System
TMPH-01716 CHRM3 Protein, Human, Recombinant (B2M & 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. CHRM3 Protein, Human, Recombinant (B2M & His) is expressed in E. coli expression system with N-6xHis-B2M tag. The predicted molecular weight is 40.7 kDa and the accession number is P20309.

重组蛋白

CHRM3 Protein, Human, Recombinant (B2M & His)
Cat.No: TMPH-01716
Species: Human
Expression System: E. coli
TargetMol Loading
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