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1982-37-2 分子结构
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10-[(1-methylpyrrolidin-3-yl)methyl]-10H-phenothiazine

ChemBase编号:778
分子式:C18H20N2S
平均质量:296.4298
单一同位素质量:296.13471965
SMILES和InChIs

SMILES:
S1c2c(N(CC3CCN(C3)C)c3c1cccc3)cccc2
Canonical SMILES:
CN1CCC(C1)CN1c2ccccc2Sc2c1cccc2
InChI:
InChI=1S/C18H20N2S/c1-19-11-10-14(12-19)13-20-15-6-2-4-8-17(15)21-18-9-5-3-7-16(18)20/h2-9,14H,10-13H2,1H3
InChIKey:
HTMIBDQKFHUPSX-UHFFFAOYSA-N

引用这个纪录

CBID:778 http://www.chembase.cn/molecule-778.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
10-[(1-methylpyrrolidin-3-yl)methyl]-10H-phenothiazine
IUPAC传统名
@methdilazine
methdilazine
商标名
Bristaline
Dilosyn
Disyncram
Disyncran
Tacaryl
Tacaryl hydrochloride
Tacazyl
Tacryl
别名
MD
Methdilazine Hcl
Methdilazine hydrochloride
Methdilazine Monohydrochloride
Methdilazinum [INN-Latin]
Methilazine hydrochloride
Methodilazine
Metodilazina [INN-Spanish]
Methdilazine
CAS号
1982-37-2
PubChem SID
160964241
46505472
PubChem CID
14677
ATC码
R06AD04
CHEMBL
1200959
Chemspider ID
14009
DrugBank ID
DB00902
KEGG ID
D04979
美国药典/FDA物质标识码
4Q13LY9Z8X
维基百科标题
Methdilazine

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 价格

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) 0.8433999  LogD (pH = 7.4) 2.5153599 
Log P 3.9367464  摩尔折射率 91.6363 cm3
极化性 35.260246 Å3 极化表面积 6.48 Å2
可自由旋转的化学键 里宾斯基五规则 true 
Log P 4.56  LOG S -4.3 
溶解度 1.47e-02 g/l 

分子性质

分子性质

理化性质 生物活性(PubChem)
溶解度
0.348 mg/L expand 查看数据来源
疏水性(logP)
4.3 expand 查看数据来源

详细说明

详细说明

DrugBank DrugBank Wikipedia Wikipedia
DrugBank -  DB00902 external link
Item Information
Drug Groups approved
Description Methdilazine is a phenothiazine compound with antihistaminic activity. It is used in the treatment of various dermatoses to relieve pruritus.
Indication Used for the symptomatic relief of hypersensitivity reactions and particularly for the control of pruritic skin disorders
Pharmacology In allergic reactions an allergen interacts with and cross-links surface IgE antibodies on mast cells and basophils. Once the mast cell-antibody-antigen complex is formed, a complex series of events occurs that eventually leads to cell-degranulation and the release of histamine (and other chemical mediators) from the mast cell or basophil. Once released, histamine can react with local or widespread tissues through histamine receptors. Histamine, acting on H1-receptors, produces pruritis, vasodilatation, hypotension, flushing, headache, tachycardia, and bronchoconstriction. Histamine also increases vascular permeability and potentiates pain. Methdilazine is a histamine H1 antagonist. It competes with histamine for the normal H1-receptor sites on effector cells of the gastrointestinal tract, blood vessels and respiratory tract. It provides effective, temporary relief of sneezing, watery and itchy eyes, and runny nose due to hay fever and other upper respiratory allergies.
Toxicity Symptoms of overdose include clumsiness or unsteadiness, convulsions, drowsiness, dryness of mouth, nose, or throat, feeling faint, flushing or redness of face, hallucinations, muscle spasms (especially of neck and back), restlessness, shortness of breath or troubled breathing, shuffling walk, tic-like movements of head and face, trembling and shaking of hands, and trouble in sleeping.
Affected Organisms
Humans and other mammals
Absorption Well absorbed in the digestive tract.
References
Rani Basu L, Mazumdar K, Dutta NK, Karak P, Dastidar SG: Antibacterial property of the antipsychotic agent prochlorperazine, and its synergism with methdilazine. Microbiol Res. 2005;160(1):95-100. [Pubmed]
Chattopadhyay D, Mukherjee T, Pal P, Saha B, Bhadra R: Altered membrane permeability as the basis of bactericidal action of methdilazine. J Antimicrob Chemother. 1998 Jul;42(1):83-6. [Pubmed]
Chattopadhyay D, Dastidar SG, Chakrabarty AN: Antimicrobial properties of methdilazine and its synergism with antibiotics and some chemotherapeutic agents. Arzneimittelforschung. 1988 Jul;38(7):869-72. [Pubmed]
External Links
Wikipedia

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Rani Basu L, Mazumdar K, Dutta NK, Karak P, Dastidar SG: Antibacterial property of the antipsychotic agent prochlorperazine, and its synergism with methdilazine. Microbiol Res. 2005;160(1):95-100. Pubmed
  • Chattopadhyay D, Mukherjee T, Pal P, Saha B, Bhadra R: Altered membrane permeability as the basis of bactericidal action of methdilazine. J Antimicrob Chemother. 1998 Jul;42(1):83-6. Pubmed
  • Chattopadhyay D, Dastidar SG, Chakrabarty AN: Antimicrobial properties of methdilazine and its synergism with antibiotics and some chemotherapeutic agents. Arzneimittelforschung. 1988 Jul;38(7):869-72. Pubmed
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专利

专利

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