N-Ethyl-3-Hydroxy-2-Phenyl-N-(Pyridin-4-Ylmethyl)Propanamide N-乙基-3-羟基-2-苯基-N-(吡啶-4-基甲基)丙酰胺
CAS 1508-75-4 MFCD00058580
信息真实价格透明
资金保障
专业采购外包团队在线服务
信息真实价格透明
资金保障
专业采购外包团队在线服务
品牌质保精细包装
现货库存
一流品牌服务
分类
- {SNA} Antagonists, Bioactive Small Molecules, Cell Signaling and Neuroscience, Cholinergics, Neuroscience, Neurotransmission, Neurotransmitters, T, 细胞生物学
- {SNA} Antagonists, Bioactive Small Molecules, Cell Biology, Cell Signaling and Neuroscience, Cholinergics,
- Heterocycles
- Pharmaceuticals
- {uni_hamburg} no charge; nitrogen heterocycle; carbocycle; aromatic; 6RingOnly; 6ring; amide; alcohol; racemate; 1fragment
- {SNA} Antagonists, Bioactive Small Molecule Alphabetical Index, Cholinergics, Neuroscience, Neurotransmission, Neurotransmitters, T, 生物活性小分子, 细胞信号转导和神经科学, 细胞生物学
- Intermediates & Fine Chemicals,
产品应用
- M4毒蕈碱型乙酰胆碱受体拮抗剂。
相关文献及参考
- [2]. Hernandez, M., et al., Different muscarinic receptor subtypes mediating the phasic activity and basal tone of pig isolated intravesical ureter. Br J Pharmacol, 1993. 110(4): p. 1413-20.
- ########
- Short: EINECS Title: EINECS (European Inventory of Existing Commercial Chemical Substances) Source: Official Journal of the European Communities Volume: C 146 A (15.06.1990) Page: 1 Year: 1990 Internet Resource: http://ecb.jrc.ec.europa.eu/esis/index.php?PGM=ein Publish_Date: 1990/06/15
- Short: IV/8A Title: Enthalpies of Fusion and Transition of Organic Compounds Author: Zhang, Z.-Y.; Frenkel, M.; March, K.N.; Wilhoit, R.C. Editor: Marsh, K.N. Source: Landolt-Börnstein, New Series Volume: IV/8A Year: 1995 Keyword: organic compounds; enthaly of fusion; melting point; phase transition ISBN: 3-540-58854-X ISBN: 978-3-540-58854-2 Internet Resource: DOI:10.1007/b55145 RefComment: VIII, 588 pages.
- [1]. Lazareno, S., N.J. Buckley, and F.F. Rober
安全信息
GHS Symbol
- P264 Wash hands thoroughly after handling. 处理后要彻底洗净双手。
- P501 Dispose of contents/container to..… 处理内容物/容器.....
- P261 Avoid breathing dust/fume/gas/mist/vapours/spray. 避免吸入粉尘/烟/气体/烟雾/蒸汽/喷雾。
- P280 Wear protective gloves/protective clothing/eye protection/face protection. 戴防护手套/防护服/眼睛的保护物/面部保护物。
- P305+P351+P338
- P301+P312+P330
- P270 Do not eat, drink or smoke when using this product. 使用本产品时不要吃东西,喝水或吸烟。
- H332 Harmful if inhaled 吸入有害
- H315 Causes skin irritation 会刺激皮肤
- H317 May cause an allergic skin reaction 可能导致皮肤过敏
- H302 Harmful if swallowed 吞食有害
- H312 Harmful in contact with skin 皮肤接触有害
- H335 May cause respiratory irritation 可能导致呼吸道刺激
- H319 Causes serious eye irritation 严重刺激眼睛
- S22 Do not breathe dust 不要吸入粉尘;
- S36 Wear suitable protective clothing 穿戴适当的防护服;
- S26 In case of contact with eyes, rinse immediately with plenty of water and seek medical advice 眼睛接触后,立即用大量水冲洗并征求医生意见;
- R36/37/38 Irritating to eyes, respiratory system and skin 对眼睛、呼吸系统和皮肤有刺激性
- R20/21/22 Harmful by inhalation, in contact with skin and if swallowed 吸入、皮肤接触和不慎吞咽有害
- R42/43
TYPE OF TEST : LD50 - Lethal dose, 50 percent kill ROUTE OF EXPOSURE : Oral SPECIES OBSERVED : Rodent - rat DOSE/DURATION : 865 mg/kg TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value REFERENCE : NIIRDN Drugs in Japan (Ethical Drugs). (Yakugyo Jiho Co., Ltd., Tokyo, Japan) Volume(issue)/page/year: -,760,1990
TYPE OF TEST : LD50 - Lethal dose, 50 percent kill ROUTE OF EXPOSURE : Intraperitoneal SPECIES OBSERVED : Rodent - mouse DOSE/DURATION : 695 mg/kg TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value REFERENCE : NIIRDN Drugs in Japan (Ethical Drugs). (Yakugyo Jiho Co., Ltd., Tokyo, Japan) Volume(issue)/page/year: -,760,1990
TYPE OF TEST : LD50 - Lethal dose, 50 percent kill ROUTE OF EXPOSURE : Subcutaneous SPECIES OBSERVED : Rodent - rat DOSE/DURATION : 872 mg/kg TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value REFERENCE : NIIRDN Drugs in Japan (Ethical Drugs). (Yakugyo Jiho Co., Ltd., Tokyo, Japan) Volume(issue)/page/year: -,760,1990
TYPE OF TEST : LD50 - Lethal dose, 50 percent kill ROUTE OF EXPOSURE : Oral SPECIES OBSERVED : Rodent - mouse DOSE/DURATION : 565 mg/kg TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value REFERENCE : NIIRDN Drugs in Japan (Ethical Drugs
TYPE OF TEST : LD50 - Lethal dose, 50 percent kill ROUTE OF EXPOSURE : Intraperitoneal SPECIES OBSERVED : Rodent - rat DOSE/DURATION : 1210 mg/kg TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value REFERENCE : NIIRDN Drugs in Japan (Ethical Drugs). (Yakugyo Jiho Co., Ltd., Tokyo, Japan) Volume(issue)/page/year: -,760,1990
其他信息
- 眼科用药:托吡卡胺是一种抗胆碱药,常温下为白色结晶性粉末,无臭,在水中微溶,在乙醇、稀盐酸、稀硫酸和氯仿中易溶,能阻滞乙酰胆碱引起的虹膜括约肌及睫状肌兴奋作用。其0.5%溶液可引起瞳孔散大;1%溶液可引起睫状肌麻痹及瞳孔散大。临床上主要用于治疗滴眼散瞳和调节麻痹。 托吡卡胺是托品酸的合成衍生物。具有较低的解离常数,眼内通透性良好,组织扩散力强,可能是其起始迅速,维持时间短的原因。本品0.5%、1%溶液滴眼后20-30分钟内散瞳及调节麻痹作用达高峰。随后作用逐渐降低,调节麻痹(残余的)2~6小时。散瞳(残余的)约7小时。托吡卡胺是类似阿托品的药物,故可使闭角型青光眼眼压急剧升高,也可能激发未被诊断的闭角型青光眼。 托吡卡胺滴眼液的睫状肌调节麻痹作用强度与剂量密切相关,其0.25%、0.5%、0.75%和1%四种浓度均有调节麻痹作用。滴眼后,最大残余调节度数分别为0.25%3.17屈光度、1%1.30屈光度。残余调节度数能保持在2.0屈光度或以下者,0.75%和1%溶液可维持40分钟,0.5%约为15分钟。1%溶液一滴滴眼后隔5~25分钟再滴第二次,能获得更满意的睫状肌麻痹作用约20~30分钟。经2~6小时能阅读书报,调节功能于6小时内恢复至滴药前水平。
- TCI Shanghai:托品酰胺 Tropicamide,>;99.0%(LC)(T)(1508-75-4)
- 托吡卡胺价格(试剂级):更新日期 产品编号 产品名称 包装 价格 2014/06/02 T1470 托品酰胺 Tropicamide 10G 2010元
- 用途一:抗胆碱药,散瞳药。
- MSDS 信息:N-Ethyl-3-hydroxy-2-phenyl-N-(pyridin-4-ylmethyl)propanamide(1508-75-4).msds
- color:white
- MOL 文件:1508-75-4.mol
- Sigma Aldrich:1508-75-4(sigmaaldrich)