跳轉至內容
Merck
全部照片(3)

Key Documents

R6520

Sigma-Aldrich

咯利普兰

solid, ≥98% (HPLC)

同義詞:

4- [3-(环戊基氧基)-4-甲氧基苯基]-2-吡咯烷酮, ZK 62711

登入查看組織和合約定價


About This Item

經驗公式(希爾表示法):
C16H21NO3
CAS號碼:
分子量::
275.34
EC號碼:
MDL號碼:
分類程式碼代碼:
41106305
PubChem物質ID:
NACRES:
NA.77

生物源

synthetic (organic)

品質等級

化驗

≥98% (HPLC)

形狀

solid

顏色

white to off-white

溶解度

H2O: 0.2 mg/mL
ethanol: 7 mg/mL
DMSO: 7.3 mg/mL

SMILES 字串

COc1ccc(cc1OC2CCCC2)C3CNC(=O)C3

InChI

1S/C16H21NO3/c1-19-14-7-6-11(12-9-16(18)17-10-12)8-15(14)20-13-4-2-3-5-13/h6-8,12-13H,2-5,9-10H2,1H3,(H,17,18)

InChI 密鑰

HJORMJIFDVBMOB-UHFFFAOYSA-N

尋找類似的產品? 前往 產品比較指南

一般說明

咯利普兰增强组织保护、解剖修复和功能恢复。用于治疗哮喘、关节炎、亨廷顿氏(Huntington′s)病和多发性硬化症。 咯利普兰抑制损伤引起的环AMP减少,这种减少与急性中枢神经系统损伤有关。它起抗抑郁的作用,在髓磷脂抑制剂存在的情况下,刺激神经突生长和轴突再生。

應用

咯利普兰可用于:
  • 研究其对睾丸扭转-复位损伤的影响(36)
  • 阻断磷酸二酯酶-4(PDE4)的作用(37)
  • 作为化学性诱导长期增强(cLTP)诱导培养基的成分(38)

生化/生理作用

选择性 cAMP 特异性磷酸二酯酶 (PDE4) 抑制剂。

特點和優勢

该化合物是受体分类及信号转导手册上磷酸二酯酶页面上的特色化合物。想要浏览手册的其他页面, 请单击此处
这种化合物是环核苷酸研究的特色产品。点击此处发现更多特色环核苷酸产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。

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

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


分析證明 (COA)

輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。

已經擁有該產品?

您可以在文件庫中找到最近購買的產品相關文件。

存取文件庫

CNS Regeneration: Basic Science and Clinical Advances (2011)
Luís M Costa et al.
Behavioural brain research, 243, 66-73 (2013-01-09)
Numerous animal model studies in the past decade have demonstrated that pharmacological elevation of cyclic AMP (cAMP) alone, or in combination with other treatments, can promote axonal regeneration after spinal cord injury. Elevation of cAMP via the phosphodiesterase 4 (PDE4)
Raehannah J Jamshidi et al.
The Journal of pharmacology and experimental therapeutics, 359(2), 319-328 (2016-10-21)
A single administration of the κ opioid receptor (KOR) antagonist, norbinaltorphimine (norBNI), produces long-term reduction in KOR function in heterologous expression systems and brain that is mediated by activation of c-Jun N-terminal kinase (JNK). In this study, we examined the
Dong Yan et al.
The Journal of pharmacology and experimental therapeutics, 366(1), 220-236 (2018-04-15)
The contribution of gene expression changes to the adverse and therapeutic effects of β2-adrenoceptor agonists in asthma was investigated using human airway epithelial cells as a therapeutically relevant target. Operational model-fitting established that the long-acting β2-adrenoceptor agonists (LABA) indacaterol, salmeterol
Hao Huang et al.
Acta pharmacologica Sinica, 37(12), 1543-1554 (2016-09-27)
Phosphodiesterase 4 (PDE4) isozymes are involved in different functions, depending on their patterns of distribution in the brain. The PDE4 subtypes are distributed in different inflammatory cells, and appear to be important regulators of inflammatory processes. In this study we

我們的科學家團隊在所有研究領域都有豐富的經驗,包括生命科學、材料科學、化學合成、色譜、分析等.

聯絡技術服務