首页工具

登录

搜索结果

Search Results for " overactive "

24

抑制剂 & 化合物

1

天然产物

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
T5023	Propiverine hydrochloride	Others; Calcium Channel; AChR	Membrane transporter/Ion channel; Metabolism; Neuroscience; Others
	Propiverine hydrochloride 是一种痉挛剂，具有钙拮抗和抗胆碱能特性，用于研究膀胱过度活动和尿失禁。
T9419	Fesoterodine (R) Fesoterodine,弗斯特罗定	AChR	Neuroscience
	Fesoterodine ((R) Fesoterodine) 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。
T19723	AMTB hydrochloride AMTB	TRP/TRPV Channel	Membrane transporter/Ion channel
	AMTB hydrochloride (AMTB HCl) 是TRPM8通道的选择性阻滞剂。它抑制 icilin 诱导的 TRPM8 通道激活，pIC50为 6.23。它在膀胱过度活动和膀胱疼痛综合征中有研究的价值。它是电压门控钠通道的非选择性抑制剂 (NaV)。
T4612	NS309	EGFR; Potassium Channel; HER	Angiogenesis; JAK/STAT signaling; Membrane transporter/Ion channel; Tyrosine Kinase/Adaptors
	NS309 是选择性钙依赖性钾离子通道 SK/IK 的激活剂，在 BK 通道上没有激活作用。
T1472	Trospium chloride Spasmex,Sanctura,曲司氯铵,曲司氯胺	AChR	Neuroscience
	Trospium chloride (Spasmex) 是一种可口服的特异竞争性毒蕈碱胆碱能受体拮抗剂，可与毒蕈碱受体 M1、M2 和 M3 高亲和力结合，具有抗毒蕈碱活性。
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。
T0703	Flavoxate hydrochloride Flavoxate HCl,盐酸黄酮哌酯,NSC-114649,DW61,Rec-7-0040	AChR	Neuroscience
	Flavoxate hydrochloride (DW61) 是一种毒蕈碱受体 AChR 拮抗剂， IC50为 12.2 μM。
T1534	Darifenacin hydrobromide 氢溴酸达非那新,Darifenacin HBr,UK-88525	AChR	Neuroscience
	Darifenacin hydrobromide (UK-88525) 是一种选择性 M3 蕈毒碱受体拮抗剂，pKi 为 8.9。
T15273	Fedovapagon VA483,A106483	Vasopressin Receptor	GPCR/G Protein
	Fedovapagon (VA106483) 是一种具有选择性和高效性的加压素 V2 受体 (V2R) 激动剂，可抑制斑马鱼节间血管的生长。Fedovapagon 可用于研究膀胱过度活动症、夜尿症和膀胱疼痛综合征。
T1671	Mirabegron YM178,米拉贝隆	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Mirabegron (YM178) 是选择性的肾上腺素受体激动剂，EC50=22.4 nM。
T1049L	Oxybutynin Oxytrol,奥昔布宁,Ditropan,Oxibutyninum	Potassium Channel; AChR	Membrane transporter/Ion channel; Neuroscience
	Oxybutynin (Ditropan) 是一种抗胆碱能药，抑制血管 Kv 通道，IC50为 11.51 μM，可用于治疗尿失禁和膀胱过度活动症。
T12970	Solabegron GW 427353,3'-[[2-[(2R)-2-(3-氯苯基)-2-羟基乙基]氨基]乙基]氨基]-[1,1'-联苯基]-3-羧酸	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Solabegron (GW 427353) 是一种β3肾上腺素能受体 (β3-AR)的选择性激动剂, 在中国仓鼠卵巢细胞中测得 EC50=22 nM，可用于研究膀胱过度活跃和肠易激综合征。
T76690	Mavrilimumab CAM 3001	Virus Protease; CSF-1R	Microbiology/Virology; Tyrosine Kinase/Adaptors
	Mavrilimumab (CAM 3001) 是一种单克隆抗体，具有抗病毒活性，对粒细胞-巨噬细胞集落刺激因子 (GM-CSF) 受体的 α 亚基有亲和力，并阻止 GM-CSF 下游细胞内信号传导。GM-CSF 可能与呼吸衰竭和死亡相关的过度活跃炎症反应有关，可用于研究类风湿性关节炎。
T11275	Fesoterodine L-mandelate	Others	Others
	Fesoterodine L-mandelate is a efficacious antimuscarinic agent for the overactive bladder (OAB).
T68548	Tolterodine Dimer
	Tolterodine Dimer is a derivative of Tolterodine -- a muscarinic receptor antagonist that is used to treat patients with overactive bladder.
T28465	PSD-506 PSD 506,RO 3202904,RO3202904,RO-3202904
	PSD-506, a muscarinic M2/M3 antagonist, is used potentially for the treatment of overactive bladder, and urinary incontinence.
T35052	Vibegron MK4618,MK 4618,MK-4618
	Vibegron (MK-4618) is an effective and selective Beta 3 adrenergic receptor agonist, used to treat overactive bladder (OAB).
T29208	ZD-0947 AZD0947,AZD-0947,ZD 0947,AZD 0947
	ZD-0947, a K(ATP) channel activator, is used potentially for the treatment of overactive bladder (OAB).
T28125	N-5984 N5984,KRP-204,KRP 204,KRP204
	N-5984, a β3-adrenergic receptor agonist, is used potentially for the treatment of obesity, overactive bladder and type 2 diabetes.
T70338	Lu AF58786
	Lu AF58786 is a novel potent and selective inhibitor of LRRK2, inhibiting LRRK2 WT, the overactive variant G2019S, and the resistant mutant A2016T56 at 12 nM, 19 nM and 93 nM, respectively.
T61438	Propiverine
	Propiverine is a potent antimuscarinic agent that effectively inhibits cellular calcium influx, leading to the reduction of muscle spasm. It exhibits neurotropic and musculotropic effects specifically on the smooth muscles of the urinary bladder. Propiverine proves valuable in research concerning overactive bladder (OAB) [1] [2].
T61357	EP3 antagonist 3
	EP3 antagonist 3 (compound 2) is a highly effective and specific antagonist of the EP3 receptor. It displays significant oral bioavailability and exhibits a strong pKi value of 8.3. Furthermore, EP3 antagonist 3 possesses excellent pharmacokinetic characteristics, making it a suitable candidate for experimental investigations involving overactive bladder (OAB) research [1].
T40161	(Rac)-5-Hydroxymethyl Tolterodine hydrochloride (Rac)-5-Hydroxymethyl Tolterodine hydrochloride,(Rac)-PNU-200577hydrochloride,(Rac)-Desfesoterodine hydrochloride
	(Rac)-5-Hydroxymethyl Tolterodine hydrochloride, also known as (Rac)-Desfesoterodine hydrochloride, is an active metabolite of Tolterodine that functions as a mAChR antagonist. It exhibits significant affinity (K i values) for M1, M2, M3, M4, and M5 receptors, with values of 2.3 nM, 2 nM, 2.5 nM, 2.8 nM, and 2.9 nM, respectively. This compound is commonly employed in research related to overactive bladder conditions.
T72091	ADRA1D receptor antagonist 1 free base
	ADRA1D receptor antagonist 1 (free base) (化合物 (R)-9s)，是口服高效、强效及选择性的人类α1D-肾上腺素受体（α1D-AR）拮抗剂，具有Ki值为1.6 nM。该化合物能剂量依赖性降低膀胱收缩，IC30值为15 nM，适用于膀胱过度活动症（包括尿急、尿频和尿失禁）的研究。

化合物

Propiverine hydrochloride

Cat.No: T5023

Target: Others, Calcium Channel, AChR

Cat.No: T9419

Synonym: (R) Fesoterodine,弗斯特罗定

Target: AChR

AMTB hydrochloride

Cat.No: T19723

Synonym: AMTB

Target: TRP/TRPV Channel

Cat.No: T4612

Target: EGFR, Potassium Channel, HER

Trospium chloride

Cat.No: T1472

Synonym: Spasmex,Sanctura,曲司氯铵,曲司氯胺

Target: AChR

Fesoterodine fumarate

Cat.No: T1475

Synonym: Toviaz,SPM 907,富马酸非索罗定

Target: AChR

Flavoxate hydrochloride

Cat.No: T0703

Synonym: Flavoxate HCl,盐酸黄酮哌酯,NSC-114649,DW61,Rec-7-0040

Target: AChR

Darifenacin hydrobromide

Cat.No: T1534

Synonym: 氢溴酸达非那新,Darifenacin HBr,UK-88525

Target: AChR

Cat.No: T15273

Synonym: VA483,A106483

Target: Vasopressin Receptor

Cat.No: T1671

Synonym: YM178,米拉贝隆

Target: Adrenergic Receptor

Cat.No: T1049L

Synonym: Oxytrol,奥昔布宁,Ditropan,Oxibutyninum

Target: Potassium Channel, AChR

Cat.No: T12970

Synonym: GW 427353,3'-[[2-[(2R)-2-(3-氯苯基)-2-羟基乙基]氨基]乙基]氨基]-[1,1'-联苯基]-3-羧酸

Target: Adrenergic Receptor

Cat.No: T76690

Synonym: CAM 3001

Target: Virus Protease, CSF-1R

Fesoterodine L-mandelate

Cat.No: T11275

Target: Others

Tolterodine Dimer

Cat.No: T68548

Cat.No: T28465

Synonym: PSD 506,RO 3202904,RO3202904,RO-3202904

Cat.No: T35052

Synonym: MK4618,MK 4618,MK-4618

Cat.No: T29208

Synonym: AZD0947,AZD-0947,ZD 0947,AZD 0947

Cat.No: T28125

Synonym: N5984,KRP-204,KRP 204,KRP204

Cat.No: T70338

Cat.No: T61438

EP3 antagonist 3

Cat.No: T61357

(Rac)-5-Hydroxymethyl Tolterodine hydrochloride

Cat.No: T40161

Synonym: (Rac)-5-Hydroxymethyl Tolterodine hydrochloride,(Rac)-PNU-200577hydrochloride,(Rac)-Desfesoterodine hydrochloride

ADRA1D receptor antagonist 1 free base

Cat.No: T72091

Cat. No.	Product Name	Target	Signaling Pathways
TN4342	Izalpinine	Others	Others
	Izalpinin exhibits potent antioxidant activities in the 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay. Izalpinin exhibits inhibitory role of muscarinic receptor-related detrusor contractile activity, and it may be a promising lead compound to treat overactiv

天然产物

Cat.No: TN4342

Target: Others

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