Carebastine-d5

Carebastine-d5 Suppliers list
Company Name: Chemsky(shanghai)International Co.,Ltd.  
Tel: 021-50135380
Email: shchemsky@sina.com
Company Name: Cato Research Chemicals Inc.  
Tel: 020-81960175
Email: min.he@cato-chem.com
Company Name: Energy Chemical  
Tel: 400-0056266
Email: marketing1@energy-chemical.com
Company Name: Foshan Treasure Biotechnology Co., Ltd  
Tel: 0757-85921206 18520245316
Email: 2329783215@qq.com
Company Name: ChemeGen  
Tel: 18818260767
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Carebastine-d5 Basic information
Product Name:Carebastine-d5
Synonyms:4-[4-[4-(Diphenylmethoxy-d5)-1-piperidinyl]-1-oxobutyl]-α,a-dimethylbenzeneacetic Acid;Carebastine-d5;4-[4-[4-(Diphenylmethoxy-d5)-1-piperidinyl]-1-oxobutyl]-a,a-dimethylbenzeneacetic Acid;4-[4-[4-(DiphenylMethoxy-d5)-1-piperidinyl]-1-oxobutyl]-α,α-diMethylbenzeneacetic Acid;Valine Impurity 136
CAS:1189661-02-6
MF:C32H37NO4
MW:499.64048
EINECS:
Product Categories:Intermediates & Fine Chemicals;Isotope Labeled Compounds;Metabolites & Impurities;Pharmaceuticals;Isotope Labelled Compounds
Mol File:1189661-02-6.mol
Carebastine-d5 Structure
Carebastine-d5 Chemical Properties
Melting point 72-74°C
storage temp. -20°C Freezer
solubility Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form Solid
color Off-White to Light Yellow
Safety Information
MSDS Information
Carebastine-d5 Usage And Synthesis
DescriptionCarebastine-d5 is intended for use as an internal standard for the quantification of carebastine by GC- or LC-MS. Carebastine is an active metabolite of ebastine and a histamine H1 receptor antagonist (Ki = 75.86 nM). It inhibits histamine-induced contraction of isolated guinea pig trachea (IC50 = 120 nM). It also inhibits histamine release from isolated rat peritoneal mast cells and human basophils when used at concentrations ranging from 30 to 100 μM. Carebastine decreases production of chemokine (C-C motif) ligand 5 (CCL5) and CCL2 in human nasal epithelial cells isolated from patients with nasal allergies.
Chemical PropertiesOff-White Solid
UsesThe active labelled carboxylic acid metabolite of Ebastine.
IC 50H1 Receptor
References[1] J. VINCENT. The pharmacokinetics, antihistamine and concentration-effect relationship of ebastine in healthy subjects.[J]. British journal of clinical pharmacology, 1988, 26 5: 497-502. DOI: 10.1111/j.1365-2125.1988.tb05288.x
[2] KWANG-HYEON LIU. Characterization of ebastine, hydroxyebastine, and carebastine metabolism by human liver microsomes and expressed cytochrome P450 enzymes: major roles for CYP2J2 and CYP3A.[J]. Drug Metabolism and Disposition, 2006, 34 11: 1793-1797. DOI: 10.1124/dmd.106.010488
[3] SHIGERU HISHINUMA . Asp73-dependent and -independent regulation of the affinity of ligands for human histamine H1 receptors by Na+[J]. Biochemical pharmacology, 2017, 128: Pages 46-54. DOI: 10.1016/j.bcp.2016.12.021
[4] I YAKUO. [Pharmacological study of ebastine, a novel histamine H1-receptor antagonist].[J]. Folia Pharmacologica Japonica, 1994, 103 3: 121-135. DOI: 10.1254/fpj.103.121
[5] YOKO YAMAUCHI  Tatsuo S  Terumichi Fujikura. The Effect of H1 Antagonists Carebastine and Olopatadine on Histamine Induced Expression of CC Chemokines in Cultured Human Nasal Epithelial Cells[J]. Allergology International, 2007, 56 2: Pages 171-177. DOI: 10.2332/allergolint.o-06-446
Carebastine-d5 Preparation Products And Raw materials
Tag:Carebastine-d5(1189661-02-6) Related Product Information
Pranlukast-d4 Carebastine 1-(4-tert-butylphenyl)-4-[4-[(2,3,4,5,6-pentadeuteriophenyl)-phenylmethoxy]piperidin-1-yl]butan-1-one Hydroxy Ebastine Ebastine Mecamylamine hydrochloride