(S)-4-(4-((4-Chlorophenyl)(Pyridin-2-Yl)Methoxy)Piperidin-1-Yl)Butanoic Acid (S)-4-(4-((4-氯苯基)(吡啶-2-基)甲氧基)哌啶-1-基)丁酸

CAS 125602-71-3 MFCD06798155

化学结构图

125602-71-3
SMILES: OC(=O)CCCN1CCC(CC1)O[C@H](C1=CC=CC=N1)C1C=CC(Cl)=CC=1

化学属性

Mol. FormulaC21H25ClN2O3
Mol. Weight388.892

别名和识别编码

Chemical Name(S)-4-(4-((4-Chlorophenyl)(Pyridin-2-Yl)Methoxy)Piperidin-1-Yl)Butanoic Acid
Chemical Name Translation(S)-4-(4-((4-氯苯基)(吡啶-2-基)甲氧基)哌啶-1-基)丁酸
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相关文献及参考

  • [2]. Tsugunobu Andoh, et al. Suppression by bepotastine besilate of substance P-induced itch-associated responses through the inhibition of the leukotriene B4 action in mice. Eur J Pharmacol. 2006 Oct 10;547(1-3):59-64.
  • [1]. Jon I Williams, et al. Non-clinical pharmacology, pharmacokinetics, and safety findings for the antihistamine bepotastine besilate. Curr Med Res Opin. 2010 Oct;26(10):2329-38.
  • [1]. Jon I Williams, et al. Non-clinical pharmacology, pharmacokinetics, and safety findings for the antihistamine bepotastine besilate. Curr Med Res Opin. 2010 Oct;26(10):2329-38.
  • [2]. Tsugunobu Andoh, et al. Suppression by bepotastine besilate of substance P-induced itch-associated responses through the inhibition of the leukotriene B4 action in mice. Eur J Pharmacol. 2006 Oct 10;547(1-3):59-64.

系列性分类

  1. Medical Research Areas
  2. GPCR & G Protein
  3. Histamine Receptor  (组胺受体)

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