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79794-75-5 分子结构
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ethyl 4-{13-chloro-4-azatricyclo[9.4.0.03,8]pentadeca-1(15),3(8),4,6,11,13-hexaen-2-ylidene}piperidine-1-carboxylate

ChemBase编号:338
分子式:C22H23ClN2O2
平均质量:382.88322
单一同位素质量:382.14480567
SMILES和InChIs

SMILES:
Clc1cc2c(C(=C3CCN(CC3)C(=O)OCC)c3ncccc3CC2)cc1
Canonical SMILES:
CCOC(=O)N1CCC(=C2c3ccc(cc3CCc3c2nccc3)Cl)CC1
InChI:
InChI=1S/C22H23ClN2O2/c1-2-27-22(26)25-12-9-15(10-13-25)20-19-8-7-18(23)14-17(19)6-5-16-4-3-11-24-21(16)20/h3-4,7-8,11,14H,2,5-6,9-10,12-13H2,1H3
InChIKey:
JCCNYMKQOSZNPW-UHFFFAOYSA-N

引用这个纪录

CBID:338 http://www.chembase.cn/molecule-338.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
ethyl 4-{13-chloro-4-azatricyclo[9.4.0.03,8]pentadeca-1(15),3(8),4,6,11,13-hexaen-2-ylidene}piperidine-1-carboxylate
ethyl 4-{13-chloro-4-azatricyclo[9.4.0.03,8]pentadeca-1(11),3,5,7,12,14-hexaen-2-ylidene}piperidine-1-carboxylate
ethyl 4-{13-chloro-4-azatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3,5,7,12,14-hexaen-2-ylidene}piperidine-1-carboxylate
ethyl 4-{13-chloro-4-azatricyclo[9.4.0.03,8]pentadeca-1(11),3(8),4,6,12,14-hexaen-2-ylidene}piperidine-1-carboxylate
ethyl 4-{13-chloro-4-azatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3(8),4,6,12,14-hexaen-2-ylidene}piperidine-1-carboxylate
IUPAC传统名
loratadine
ethyl 4-{13-chloro-4-azatricyclo[9.4.0.03,8]pentadeca-1(11),3,5,7,12,14-hexaen-2-ylidene}piperidine-1-carboxylate
商标名
Aerotina
Alarin
Alavert
Alerpriv
Allertidin
Bedix Loratadina
Biloina
Bonalerg
Civeran
Claratyne
Clarinase
Clarinase Reperabs
Claritin
Claritin Reditabs
Claritin-D
Claritine
Clarityn
Clarityne
Fristamin
Histaloran
Lergy
Lertamine
Lesidas
Lisino
Loracert
Loradex
Loradif
Loranox
Lorantis
Lorastine
Loratyne
Loraver
Lorfast
Loritine
Lowadina
Nularef
Optimin
Polaratyne
Pylor
Restamine
Rhinase
Rinomex
Sanelor
Sensibit
Sinhistan Dy
Sohotin
Tadine
Talorat Dy
Velodan
Versal
Zeos
Lomilan
Roletra
别名
4-(8-Chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene-1-piperidinecarboxylic acid ethyl ester
Loratidine
Loratadine
ethyl 4-(8-chloro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11(6H)-ylidene)piperidine-1-carboxylate
Loratadina [Spanish]
Loratadinum [Latin]
Loratadine
4-(8-Chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)-1-piperidinecarboxylic Acid Ethyl Ester
Claritin, Sch-29851,
Alavert
Claritin
Loratadine
Claritin-D
Claritine
Clarityn
Clarityne
Fristamin
ethyl 4-{13-chloro-4-azatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3(8),4,6,12,14-hexaen-2-ylidene}piperidine-1-carboxylate
CAS号
79794-75-5
MDL号
MFCD00672869
PubChem SID
46507853
24278525
160963801
PubChem CID
3957

理论计算性质

理论计算性质

JChem ALOGPS 2.1
质子受体 质子供体
LogD (pH = 5.5) 4.5269837  LogD (pH = 7.4) 4.5542197 
Log P 4.5545793  摩尔折射率 116.9769 cm3
极化性 41.254913 Å3 极化表面积 42.43 Å2
可自由旋转的化学键 里宾斯基五规则 true 
Log P 4.8  LOG S -4.46 
溶解度 1.34e-02 g/l 

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
0.000011 mg/ml expand 查看数据来源
Acetonitrile expand 查看数据来源
Chloroform expand 查看数据来源
DMSO: soluble50 mg/mL expand 查看数据来源
H2O: insoluble expand 查看数据来源
Methanol expand 查看数据来源
外观
white powder expand 查看数据来源
White Solid expand 查看数据来源
熔点
134-136°C expand 查看数据来源
疏水性(logP)
3.8 expand 查看数据来源
5.051 expand 查看数据来源
保存条件
-20°C expand 查看数据来源
-20°C Freezer expand 查看数据来源
MSDS下载
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
德国WGK号
2 expand 查看数据来源
个人保护装置
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand 查看数据来源
保存温度
2-8°C expand 查看数据来源
作用靶点
Histamine receptors expand 查看数据来源
相关基因信息
human ... CYP3A4(1576), HRH1(3269), KCNH1(3756), KCNH2(3757), PTAFR(5724)rat ... Hrh1(24448) expand 查看数据来源
生物活性机理
Histamine H1-receptor antagonist expand 查看数据来源
纯度
≥98% (HPLC) expand 查看数据来源
95% expand 查看数据来源
98% expand 查看数据来源
成盐信息
Free Base 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
Other pharmacol. mechanisms under investigation expand 查看数据来源
Used in the treatment of rhinitis and skin disorders expand 查看数据来源
Empirical Formula (Hill Notation)
C22H23N2O2Cl expand 查看数据来源

详细说明

详细说明

DrugBank DrugBank Selleck Chemicals Selleck Chemicals Sigma Aldrich Sigma Aldrich TRC TRC
DrugBank -  DB00455 external link
Item Information
Drug Groups approved
Description Loratadine is a derivative of azatadine and a second-generation histamine H1 receptor antagonist used in the treatment of allergic rhinitis and urticaria. Unlike most classical antihistamines (histamine H1 antagonists) it lacks central nervous system depressing effects such as drowsiness. [PubChem]
Indication A self-medication that is used alone or in combination with pseudoephedrine sulfate for the symptomatic relief of seasonal allergic rhinitis. Also used for the symptomatic relief of pruritus, erythema, and urticaria associated with chronic idiopathic urticaria in patients (not for children under 6 unless directed by a clincian).
Pharmacology Loratadine is a long acting second generation antihistamine that is similar in structure to cyproheptadine and azatadine. The pharmacology of loratadine is similar to other antihistamines, but unlike other H1-blockers, loratidine is shown to exhibit competitive, specific, and selective antagonism of H1 receptors. The exact mechanism of this interaction is unknown, but disposition of the drug suggests that loratadine's prolonged antagonism of histamine may be due to the drug's slow dissociation from the receptor or the formation of the active metabolite, desloratadine. Loratadine does not penetrate the CNS effectively and has a low affinity for CNS H1-receptors.
Toxicity somnolence, tachycardia, and headache LD50=mg/kg (orally in rat)
Affected Organisms
Humans and other mammals
Biotransformation Hepatic
Absorption Rapidly absorbed following oral administration (40% bioavailability)
Half Life 8.4 hours
Protein Binding 97-99%
References
See S: Desloratadine for allergic rhinitis. Am Fam Physician. 2003 Nov 15;68(10):2015-6. [Pubmed]
Menardo JL, Horak F, Danzig MR, Czarlewski W: A review of loratadine in the treatment of patients with allergic bronchial asthma. Clin Ther. 1997 Nov-Dec;19(6):1278-93; discussion 1523-4. [Pubmed]
Howarth PH: Histamine and asthma: an appraisal based on specific H1-receptor antagonism. Clin Exp Allergy. 1990 Aug;20 Suppl 2:31-41. [Pubmed]
Baroody FM, Naclerio RM: Antiallergic effects of H1-receptor antagonists. Allergy. 2000;55 Suppl 64:17-27. [Pubmed]
External Links
Wikipedia
RxList
Drugs.com
Selleck Chemicals -  S1358 external link
Research Area: Inflammation
Biological Activity:
Loratadine is a selective inverse peripheral histamine H1-receptor agonist with an IC50 of >32 μM. [1] Histamine is responsible for many features of allergic reactions. Loratadine (Alavert, Claritin) is a second-generation antihistamine agent closely structurally related to tricyclic antidepressants such as imipramine, and distantly related to the atypical antipsychotic quetiapine, used to treat allergies. [2]
Sigma Aldrich -  L9664 external link
Biochem/physiol Actions
Non-sedating histamine H1-receptor antagonist.
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. L9664.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.
Toronto Research Chemicals -  L469575 external link
A nonsedating-type histamine H1-receptor.

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • See S: Desloratadine for allergic rhinitis. Am Fam Physician. 2003 Nov 15;68(10):2015-6. Pubmed
  • Baroody FM, Naclerio RM: Antiallergic effects of H1-receptor antagonists. Allergy. 2000;55 Suppl 64:17-27. Pubmed
  • Menardo JL, Horak F, Danzig MR, Czarlewski W: A review of loratadine in the treatment of patients with allergic bronchial asthma. Clin Ther. 1997 Nov-Dec;19(6):1278-93; discussion 1523-4. Pubmed
  • Howarth PH: Histamine and asthma: an appraisal based on specific H1-receptor antagonism. Clin Exp Allergy. 1990 Aug;20 Suppl 2:31-41. Pubmed
  • http://www.rxlist.com/claritin-drug.htm
  • Bruttmann, G., et al.: J. Allergy Clin. Immunol., 83, 411 (1989)
  • Haria, M., et al.: Drugs, 48, 617 (1994)
  • Batenhorst, R.L. et al., Eur. J. Clin. Pharmacol., 1986, 31, 247, (pharmacol)
  • Kreutner, W. et al., Allergy (Copenhagen), 1987, 42, 57, (pharmacol)
  • Bradley, C.M. et al., Eur. J. Clin. Pharmacol., 1987, 32, 419, (pharmacol)
  • Hilbert, J. et al., J. Clin. Pharmacol., 1987, 27, 530; 694; 1988, 28, 234, (pharmacol)
  • Clissold, S.P. et al., Drugs, 1989, 37, 42, (rev)
  • Schumacher, D.P. et al., J.O.C., 1989, 54, 2242, (synth, pmr)
  • Piwinski, J.J. et al., J.O.C., 1990, 55, 3341, (metab)
  • Piwinski, J.J. et al., J. Med. Chem., 1991, 34, 457, (activity)
  • Barnett, A. et al., Chron. Drug Discovery, 1993, 3, 83, (rev)
  • Roman, I.J. et al., Clin. Rev. Allergy, 1993, 11, 89, (pharmacol, rev)
  • Haria, M. et al., Drugs, 1994, 48, 617, (rev)
  • Letari, O. et al., Eur. J. Pharmacol., 1994, 266, 219, (pharmacol)
  • Johnson, R. et al., J. Chromatogr., B: Biomed. Appl., 1994, 657, 125, (gc)
  • Negwer, M., Organic-Chemical Drugs and their Synonyms, 7th edn., Akademie-Verlag, 1994, 8869, (synonyms)
  • Caballero, R. et al., Br. J. Pharmacol., 1997, 122, 796-798, (desloratadine, pharmacol)
  • Molet, S. et al., Clin. Exp. Allergy, 1997, 27, 1167-1174, (desloratadine, pharmacol)
  • Martindale, The Extra Pharmacopoeia, 32nd edn., Pharmaceutical Press, 1999, 413
  • McClellan, K. et al., Drugs, 2001, 61, 789-796, (desloratadine, rev)
  • Barnett, A. et al., Agents Actions, 1984, 14, 590, (pharmacol)
  • Pat. Coop. Treaty (WIPO), 1985, Schering, 85 03 707; CA, 104, 116091a, (desloratadine, synth, pharmacol)
  • Villani, F.J. et al., Arzneim.-Forsch., 1986, 36, 1311, (synth)
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专利

专利

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