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140462-76-6 分子结构
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2-[(2Z)-2-[3-(dimethylamino)propylidene]-9-oxatricyclo[9.4.0.03,8]pentadeca-1(11),3(8),4,6,12,14-hexaen-5-yl]acetic acid hydrochloride

ChemBase编号:73044
分子式:C21H24ClNO3
平均质量:373.87316
单一同位素质量:373.14447131
SMILES和InChIs

SMILES:
C\1(=C/CCN(C)C)/c2c(OCc3c1cccc3)ccc(c2)CC(=O)O.Cl
Canonical SMILES:
CN(CC/C=C/1\c2cc(ccc2OCc2c1cccc2)CC(=O)O)C.Cl
InChI:
InChI=1S/C21H23NO3.ClH/c1-22(2)11-5-8-18-17-7-4-3-6-16(17)14-25-20-10-9-15(12-19(18)20)13-21(23)24;/h3-4,6-10,12H,5,11,13-14H2,1-2H3,(H,23,24);1H/b18-8-;
InChIKey:
HVRLZEKDTUEKQH-NOILCQHBSA-N

引用这个纪录

CBID:73044 http://www.chembase.cn/molecule-73044.html

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名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
2-[(2Z)-2-[3-(dimethylamino)propylidene]-9-oxatricyclo[9.4.0.03,8]pentadeca-1(11),3(8),4,6,12,14-hexaen-5-yl]acetic acid hydrochloride
2-[(2Z)-2-[3-(dimethylamino)propylidene]-9-oxatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3(8),4,6,12,14-hexaen-5-yl]acetic acid hydrochloride
IUPAC传统名
[(2Z)-2-[3-(dimethylamino)propylidene]-9-oxatricyclo[9.4.0.03,8]pentadeca-1(11),3(8),4,6,12,14-hexaen-5-yl]acetic acid hydrochloride
[(2Z)-2-[3-(dimethylamino)propylidene]-9-oxatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3(8),4,6,12,14-hexaen-5-yl]acetic acid hydrochloride
2-[(2Z)-2-[3-(dimethylamino)propylidene]-9-oxatricyclo[9.4.0.03,8]pentadeca-1(11),3(8),4,6,12,14-hexaen-5-yl]acetic acid hydrochloride
别名
(11Z)-11-[3-(Dimethylamino)propylidene]-6,11-dihydrodibenz[b,e]oxepin-2-acetic AcidHydrochloride
ALO 4943A
KW 4679
Patanol
Opatanol
Pataday
Patanase
Allelock
Olopatadine hydrochloride
Patanol S
Olopatadine Hydrochloride
CAS号
140462-76-6
PubChem SID
162037964
PubChem CID
5282402

数据来源

数据来源

所有数据来源 商品来源 非商品来源
数据来源 数据ID
PubChem 5282402 external link

理论计算性质

理论计算性质

JChem
Acid pKa 3.7840304  质子受体
质子供体 LogD (pH = 5.5) 0.74022824 
LogD (pH = 7.4) 0.74543273  Log P 0.7462555 
摩尔折射率 109.5524 cm3 极化性 38.300964 Å3
极化表面积 49.77 Å2 可自由旋转的化学键
里宾斯基五规则 true 

分子性质

分子性质

理化性质 安全信息 药理学性质 产品相关信息 生物活性(PubChem)
溶解度
DMSO expand 查看数据来源
Methanol expand 查看数据来源
Water (Sparingly) expand 查看数据来源
外观
White Solid expand 查看数据来源
熔点
242-245°C (dec.) expand 查看数据来源
保存条件
-20°C expand 查看数据来源
Refrigerator expand 查看数据来源
MSDS下载
下载链接 expand 查看数据来源
生物活性机理
Histamine H1-receptor antagonist, expand 查看数据来源
Mediator release inhibitor expand 查看数据来源
成盐信息
HCl expand 查看数据来源
hydrochloride expand 查看数据来源
质检报告
下载链接 expand 查看数据来源
应用领域
Antiallergic agent expand 查看数据来源
Used in the treatment of allergic rhinitis, urticaria, allergic conjunctivitis and asthma expand 查看数据来源

详细说明

详细说明

Selleck Chemicals Selleck Chemicals TRC TRC
Selleck Chemicals -  S2494 external link
Research Area: Immunology
Biological Activity:
Olopatadine hydrochloride(Opatanol) is a histamine blocker and mast cell stabilizer with an IC50 of 559 µM for the release of histamine. Evaluation of the interaction of olopatadine with histamine receptors revealed a relatively high affinity for the H1 receptor (Ki = 31.6 nM, pKi = 7.5 ± 0.1) but lower affinities for H2 receptors (Ki = 100 µM, pKi = 4.0 ± 0.19) and H3 receptors (Ki = 79.4 µM, pKi = 4.1 ± 0.16,). The H1 selectivity of olopatadine was superior to that of other ocularly used anti-histamines studied, such as ketotifen, levocabastine, antazoline and pheniramine. [1][2]
Toronto Research Chemicals -  O575000 external link
Dual acting histamine H1-receptor antagonist and mast cell stabilizer. Antiallergic; antihistaminic.

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Sharif NA et al. J Pharmacol Exp Ther. 1996 Sep
  • Kamei, C., et al.: Arzneim.-Forsch., 45, 1005 (1995)
  • Sharif, N.A., et al.: J. Pharmacol. Exp. Ther., 278, 1252 (1995)
  • Abelson, M.B., et al.: Am. J. Ophthalmol., 125, 797 (1995)
  • Eur. Pat., 1987, Kyowa Hakko Kogyo, 235 796; CA, 108, 167330, (synth, pharmacol)
  • Oshima, E. et al., J. Med. Chem., 1992, 35, 2074, (synth, cryst struct, pharmacol)
  • Ikeda, K. et al., Int. Arch. Allergy Appl. Immunol., 1995, 106, 157, (pharmacol)
  • Ikemura, T. et al., Int. Arch. Allergy Appl. Immunol., 1996, 110, 57; 64, (pharmacol)
  • Sharif, N.A. et al., J. Pharmacol. Exp. Ther., 1996, 278, 1252, (pharmacol)
  • Berdy, G.J. et al., Clin. Ther., 2000, 22, 826-833; 2001, 23, 1272-1280, (pharmacol)
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专利

专利

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