首页 工具
登录
购物车

搜索结果

Search Results for " incontinence "

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

提交您的定制咨询

点击图片重新获取验证码
Cat. No. Product Name Target Signaling Pathways
T19417 Urinary Incontinence-Targeting Compound 1

Others Others
Urinary Incontinence-Targeting Compound 1, used in the research of urinary incontinence, is a sulfonanilide derivative.
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。
T10952 Dabuzalgron

达布扎琼,Ro 115-1240

Apoptosis; Adrenergic Receptor Apoptosis; GPCR/G Protein; Neuroscience
Dabuzalgron (Ro 115-1240) 是一种口服活性选择性 α-1A 肾上腺素受体激动剂,用于治疗尿失禁。它通过维持线粒体功能来预防多柔比星引起的心脏毒性。
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。
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。
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。
T3126 Bethanechol chloride

(±)-Bethanechol,Urecholine,Myocholine,氯贝胆碱,Carbamyl-β-methylcholine chloride

AChR Neuroscience
Bethanechol chloride (Carbamyl-β-methylcholine chloride) 是一种拟副交感神经剂,是毒蕈碱型受体 (mAChR) 激动剂,通过直接刺激副交感神经系统的 mAChR 发挥作用。
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。
T29687 Afacifenacin

Afacifenacin fumarate,SMP-986,NS 986,NS-986,SMP 986,NS986,SMP986

AChR Neuroscience
Afacifenacin (SMP-986) fumarate 是一种 M3 毒蕈碱受体选择性拮抗剂,可用于研究缺血性心脏病,尿失禁和膀胱炎和其他疾病。
T28257L (-)-OPC-51803

AChR Neuroscience
(-)-OPC-51803 是一种抗利尿激素 V2受体激动剂,可用于夜尿症和尿失禁的治疗。
T28257 OPC-51803

SOU-003,SOU 003,SOU003,OPC51803,OPC 51803

Vasopressin Receptor GPCR/G Protein
OPC-51803是一种可口服的非肽加压素(AVP)V(2)受体选择性激动剂,可用于治疗尿失禁和夜尿。
T0111 Solifenacin succinate

YM905,索非那新琥珀酸盐

AChR Neuroscience
Solifenacin succinate (YM905) 是毒蕈碱受体拮抗剂,对 M1、M2和M3受体的pKi 值分别为 7.6、6.9 和 8.0。
T1460 Dicyclomine hydrochloride

AChR Neuroscience
Dicyclomine hydrochloride 是口服活性毒蕈碱胆碱能受体拮抗剂。它是一种抗痉挛试剂,在体内可缓解胃肠道平滑肌痉挛。它对 M1 受体亚型和 M2 受体亚型,Ki 分别为5.1和54.6nM,在刷状缘膜和基底质膜中均表现出较高的亲和力。
T10830 CL 316243

Adrenergic Receptor GPCR/G Protein; Neuroscience
CL316243 是一种高效的 β3 肾上腺素受体选择性激动剂,EC50 为 3 nM。它是一种有效的脂肪细胞脂解刺激剂,可增加棕色脂肪组织的产热和代谢率,具有治疗肥胖症、糖尿病和急迫性尿失禁的潜力。
T60536 Terodiline

Terodiline 是一种钙通道阻滞剂和 M1 选择性毒蕈碱受体 (mAChR) 拮抗剂,在在兔输精管 (M1)、心房 (M2)、膀胱 (M3) 和回肠肌肉中的 Kb 分别为 15、160、280 和 198 nM。 Terodiline 具有治疗尿频和急迫性尿失禁的潜力 [1]。
T67956L Litoxetine HCl

litoxetine HCL(86811-09-8 Free base)

5-HT Receptor GPCR/G Protein; Neuroscience
Litoxetine HCl 是一种选择性5-羟色胺(5-HT)再摄取抑制剂(SSRI)和混合5-羟色胺拮抗剂,可用于治疗尿失禁。Litoxetine HCl 在没有抗毒蕈碱特性的浓度下(10 nM-1 microM)引起大鼠离体食道肌肉粘膜的浓度依赖性松弛,使卡巴胆碱张力降低达37%,更高浓度的Litoxetine HCl(3微摩-300微摩)与明显的松弛有关,直至取消卡巴胆碱张力。以前在离体豚鼠肠道中证明的利托西汀的抗心律失常活性,在浓度大于1 microM 时在大鼠离体食道肌肉粘膜中发挥了作用。 Litoxetine HCl 的5-HT 释放作用可以解释利托西汀对未处理的大鼠组织中的5-HT 诱导的松弛的效力,这种效力被pCPA 处理所逆转。
T10952L Dabuzalgron HCl

R1240,R-450,R450,RO-1151240,R-1240,RO1151240

Dabuzalgron, an adrenoceptor agonist, is used potentially for the treatment of urinary incontinence.
T27401 Garomefrine HCl

PNO-49B,NS-49,ABT-232,ABT232,NS49,PNO49B

Garomefrine HCl, a α1A-adrenoceptor agonist, is potential for the treatment of urinary incontinence.
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.
T26604 Alvameline Tartrate

LU-25-109T,LU 25 109T,LU-25109T,LU 25109T

Alvameline Tartrate, a muscarinic M1 receptor agonist and M2/M3 receptor antagonist, is used potentially for treatment of urinary incontinence.
T29667 Adosopine

Adosupine

Adosopine is a dibenzoazepine which affects urinary bladder hyperreflexia and may be suitable for treating urinary incontinence.
T71889 Esoxybutynin Chloride

Esoxybutynin Chloride is (S)-enantiomer of oxybutynin. Esoxybutynin Chloride exerts antimuscarinic properties. Racemic oxybutynin is used clinically to treat urinary incontinence. Sepracor was developing (S)-oxybutynin, a single-isomer version of Alza's Ditropan (racemic oxybutynin), a muscarinic acetylcholine receptor antagonist, as a potential treatment for urinary incontinence.
T71821 Norfenefrine HCl

Norfenefrine is an Adrenergic Agonist. It is used in the treatment of female stress incontinence.
T71268 Esoxybutynin Free Base

Esoxybutynin Free Base is (S)-enantiomer of oxybutynin. Esoxybutynin Free Base exerts antimuscarinic properties. Racemic oxybutynin is used clinically to treat urinary incontinence. Sepracor was developing (S)-oxybutynin, a single-isomer version of Alza's Ditropan (racemic oxybutynin), a muscarinic acetylcholine receptor antagonist, as a potential treatment for urinary incontinence.
T31404 Dextranomer

Dextranomere,Dextranomero,Debrisan,Dextranomerum

Dextranomer, for treatment of burns; consists of three-dimensional network of dextran polymers cross-linked by epichlorohydrin; dextranomer based implants usedas a bulking agent for endoscopic treatment of pediatric structural incontinence; ingredient of
T25325 Dicyclonon

LAB 145-138H,BAS 145-138

Dicyclonon is a muscarinic antagonist utilized as an antispasmodic and in urinary incontinence. It has little effect on glandular secretion or the cardiovascular system. It has some local anesthetic properties and is utilized in biliary, gastrointestinal,
T61309 (R)-Oxybutynin

(R)-Oxybutynin (Aroxybutynin) is an orally active muscarinic receptor antagonist, which exhibits antimuscarinic, antispasmodic, and anticholinergic activity. This compound, being the (R)-isomer of Oxybutynin, competitively antagonizes Carbachol-induced contractions. It is particularly useful in researching neurogenic bladder dysfunction-related incontinence [1] [2] [3].
T70379 PF-04479745 tartrate

PF-04479745, also known as PF-4479745, is a potent and selective 5-HT2C agonist (EC50 = 10 nM). PF-4479745 displayed robust pharmacology in a preclinical canine model of stress urinary incontinence (SUI) and no measurable functional agonism at the key selectivity targets 5-HT2A and 5-HT2B in relevant tissue-based assay systems.
T29742 AH-9700 free base

AH-9700 free base 用于治疗急迫性尿失禁和尿毒症。在一项放射性配体结合研究中,AH-9700 free base 对 sigma 受体表现出较高的亲和力,对膀胱功能正常的实验动物的排尿反射(即膀胱容量增加作用)有明显的抑制作用。
T73572 NS-8

NS-8,一种吡咯衍生物,能够激活Ca2+-敏感的K+通道。通过降低盆腔传入神经活动,NS-8有助于抑制排尿反射,适用于尿频与尿失禁的研究。
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

Urinary Incontinence-Targeting Compound 1
Cat.No: T19417
Synonym:
Target: Others
Propiverine hydrochloride
Cat.No: T5023
Synonym:
Target: Others, Calcium Channel, AChR
Dabuzalgron
Cat.No: T10952
Synonym: 达布扎琼,Ro 115-1240
Target: Apoptosis, Adrenergic Receptor
Oxybutynin
Cat.No: T1049L
Synonym: Oxytrol,奥昔布宁,Ditropan,Oxibutyninum
Target: Potassium Channel, AChR
Trospium chloride
Cat.No: T1472
Synonym: Spasmex,Sanctura,曲司氯铵,曲司氯胺
Target: AChR
Oxybutynin chloride
Cat.No: T1049
Synonym: Oxybutynin hydrochloride,盐酸奥昔布宁,Oxybutynin HCl
Target: Potassium Channel, AChR
Bethanechol chloride
Cat.No: T3126
Synonym: (±)-Bethanechol,Urecholine,Myocholine,氯贝胆碱,Carbamyl-β-methylcholine chloride
Target: AChR
Darifenacin hydrobromide
Cat.No: T1534
Synonym: 氢溴酸达非那新,Darifenacin HBr,UK-88525
Target: AChR
Afacifenacin
Cat.No: T29687
Synonym: Afacifenacin fumarate,SMP-986,NS 986,NS-986,SMP 986,NS986,SMP986
Target: AChR
(-)-OPC-51803
Cat.No: T28257L
Synonym:
Target: AChR
OPC-51803
Cat.No: T28257
Synonym: SOU-003,SOU 003,SOU003,OPC51803,OPC 51803
Target: Vasopressin Receptor
Solifenacin succinate
Cat.No: T0111
Synonym: YM905,索非那新琥珀酸盐
Target: AChR
Dicyclomine hydrochloride
Cat.No: T1460
Synonym:
Target: AChR
CL 316243
Cat.No: T10830
Synonym:
Target: Adrenergic Receptor
Terodiline
Cat.No: T60536
Synonym:
Target:
Litoxetine HCl
Cat.No: T67956L
Synonym: litoxetine HCL(86811-09-8 Free base)
Target: 5-HT Receptor
Dabuzalgron HCl
Cat.No: T10952L
Synonym: R1240,R-450,R450,RO-1151240,R-1240,RO1151240
Target:
Garomefrine HCl
Cat.No: T27401
Synonym: PNO-49B,NS-49,ABT-232,ABT232,NS49,PNO49B
Target:
PSD-506
Cat.No: T28465
Synonym: PSD 506,RO 3202904,RO3202904,RO-3202904
Target:
Alvameline Tartrate
Cat.No: T26604
Synonym: LU-25-109T,LU 25 109T,LU-25109T,LU 25109T
Target:
Adosopine
Cat.No: T29667
Synonym: Adosupine
Target:
Esoxybutynin Chloride
Cat.No: T71889
Synonym:
Target:
Norfenefrine HCl
Cat.No: T71821
Synonym:
Target:
Esoxybutynin Free Base
Cat.No: T71268
Synonym:
Target:
Dextranomer
Cat.No: T31404
Synonym: Dextranomere,Dextranomero,Debrisan,Dextranomerum
Target:
Dicyclonon
Cat.No: T25325
Synonym: LAB 145-138H,BAS 145-138
Target:
(R)-Oxybutynin
Cat.No: T61309
Synonym:
Target:
PF-04479745 tartrate
Cat.No: T70379
Synonym:
Target:
AH-9700 free base
Cat.No: T29742
Synonym:
Target:
NS-8
Cat.No: T73572
Synonym:
Target:
ADRA1D receptor antagonist 1 free base
Cat.No: T72091
Synonym:
Target:
TargetMol Loading
联系我们
400-820-0310

上海市静安区江场三路238号8楼