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Key Documents

SML2480

Sigma-Aldrich

米拉贝隆

≥98% (HPLC)

同義詞:

2-氨基-N-[4-[2-[[(2R)-2-羟基-2-苯乙基]氨基]乙基]苯基]-4-噻唑乙酰胺, 2-(2-氨基-1,3-噻唑-4-基)-N-[4-[2-[((2R)-2-羟基-2-苯乙基)氨基]乙基]苯基]乙酰胺, YM 178, YM178(R)-米拉贝隆

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About This Item

經驗公式(希爾表示法):
C21H24N4O2S
CAS號碼:
分子量::
396.51
MDL號碼:
分類程式碼代碼:
12352200
NACRES:
NA.77

化驗

≥98% (HPLC)

形狀

powder

光學活性

[α]/D -16 to -22°, c = 0.5 in methanol

顏色

white to beige

溶解度

DMSO: 2 mg/mL, clear

儲存溫度

2-8°C

SMILES 字串

O[C@@H](CNCCC1=CC=C(NC(CC2=CSC(N)=N2)=O)C=C1)C3=CC=CC=C3

InChI

1S/C21H24N4O2S/c22-21-25-18(14-28-21)12-20(27)24-17-8-6-15(7-9-17)10-11-23-13-19(26)16-4-2-1-3-5-16/h1-9,14,19,23,26H,10-13H2,(H2,22,25)(H,24,27)/t19-/m0/s1

InChI 密鑰

PBAPPPCECJKMCM-IBGZPJMESA-N

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應用

米拉贝隆(Mirabegron)已被用作体外实验中的β3-肾上腺素能受体(β3-AR) 激动剂,用于确定β3-AR 刺激是否特异性地激活人棕色脂肪组织(BAT)生热。

生化/生理作用

米拉贝隆是一种强效、选择性β3-肾上腺素能受体激动剂,可激活膀胱逼尿肌中的β3-肾上腺素能受体,导致肌肉松弛和膀胱容量增加。
米拉贝隆是一种非抗毒蕈碱口服活性药,有望用于治疗具有膀胱过度活动症(OAB)症状的患者。它以β3-AR为靶点对尿频储存期的神经控制起作用,从而有助于膀胱的放松。 米拉贝隆也用于治疗儿科患者的神经源性逼尿肌过度活动(NDO)。

象形圖

Health hazard

訊號詞

Warning

危險聲明

危險分類

Repr. 2

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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存取文件庫

Kentaro Konishi et al.
European journal of drug metabolism and pharmacokinetics, 43(3), 301-309 (2017-11-23)
Mirabegron is cleared by multiple mechanisms, including drug-metabolizing enzymes. One of the most important clearance pathways is direct glucuronidation. In humans, M11 (O-glucuronide), M13 (carbamoyl-glucuronide), and M14 (N-glucuronide) have been identified, of which M11 is one of the major metabolites
Toshiyuki Takasu et al.
The Journal of pharmacology and experimental therapeutics, 321(2), 642-647 (2007-02-13)
We evaluated the pharmacological characteristics of (R)-2-(2-aminothiazol-4-yl)-4'-{2-[(2-hydroxy-2-phenylethyl)amino]-ethyl} acetanilide (YM178). YM178 increased cyclic AMP accumulation in Chinese hamster ovary (CHO) cells expressing human beta3-adrenoceptor (AR). The half-maximal effective concentration (EC50) value was 22.4 nM. EC50 values of YM178 for human beta1-
Rebecca Bragg et al.
The Consultant pharmacist : the journal of the American Society of Consultant Pharmacists, 29(12), 823-837 (2014-12-19)
To review the literature regarding the efficacy and safety of mirabegron for the treatment of overactive bladder (OAB). A literature search was performed using MEDLINE (PubMed) prior to December 31, 2013, using the terms "mirabegron" and "randomized-controlled trial." All published
Camila Bitencourt Mendes-Silvério et al.
European journal of pharmacology, 829, 79-84 (2018-04-15)
Mirabegron is a β3-adrenoceptor agonist and released on the marked for the treatment of overactive bladder. Because mirabegron is the only β3-adrenoceptor agonist available and substances that increase the levels of cyclic adenosine monophosphate (cAMP) inhibit platelet activity, we tested

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