全国服务咨询热线:

18438616290

Products产品中心
首页 > 产品中心 > 生化试剂 > 小分子化合物 > abs47028131Tranilast 53902-12-8

Tranilast 53902-12-8

简要描述:Tranilast 53902-12-8
Tranilast is an antiallergic drug by inhibiting lipid mediator and cytokine release from inflammatory cells, used for the treatment of allergic disorders such as asthma,

  • 产品型号:abs47028131
  • 厂商性质:生产厂家
  • 更新时间:2026-01-19
  • 访  问  量:618

详细介绍

品牌absinCAS53902-12-8
分子式C18H17NO5纯度99%
分子量327.33货号abs47028131
规格10mg供货周期现货
主要用途used for the treatment of allergic diso应用领域化工,生物产业,农林牧渔,制药/生物制药,综合

Tranilast  53902-12-8

产品描述
描述

Tranilast is an antiallergic drug by inhibiting lipid mediator and cytokine release from inflammatory cells, used for the treatment of allergic disorders such as asthma, allergic rhinitis and atopic dermatitis.

纯度
99%
储存/保存方法
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
基本信息
别名
曲尼si特;MK 341;SB 252218
外观
淡黄色或淡黄绿色结晶性粉末
可溶性/溶解性
DMSO : 32.7 mg/mL (100 mM)
生物活性
靶点
Angiotensin Receptor
In vitro(体外研究)
Tranilast is an anti-allergic drug inhibiting the release of substances such as histamine and prostaglandins from mast cells, which suppresses collagen synthesis of fibroblasts derived from keloid tissues. Tranilast (3-300 mM) suppresses the collagen synthesis of fibroblasts from keloid and hypertrophic scar tissue but not healthy skin fibroblasts. Tranilast (30-300 mM) inhibits the release of transforming growth factor (TGF)-beta 1 from keloid fibroblasts, which enhances the collagen synthesis of keloid fibroblasts. Tranilast improves keloids and hypertrophic scars which originate from the abnormal proliferation and excessive collagen accumulation of fibroblasts. Tranilast inhibits the release of TGF-beta 1, IL-1 beta and PGE2 from the human monocytes-macrophages. Tranilast inhibits the proliferation stimulated with fetal bovine serum (FBS), TGF-beta 1 and platelet-derived growth factor-BB (PDGF-BB) as well as PDGF-BB-induced migration. Tranilast exhibits inhibitory effects on spontaneous collagen synthesis and TGF-beta 1-induced collagen and glycosaminoglycan synthesis.
In vivo(体内研究)
Tranilast results in a 58% reduction in TGF-beta1-induced 3-hydroxyproline incorporation in the diabetic heart of rats. Tranilast attenuates cardiac fibrosis by 37% in association with reduction in phospho-Smad2 in the diabetic heart of rats. Tranilast treatment completely prevents the increase in chymaselike activity, reduces the chymase mRNA levels by 43%, and decreases the carotid intima/media ratio by 63% in the carotid artery of dogs.
参考文献
参考文献
研究领域
研究领域
CancerCancer MetabolismCellular metabolic process
CancerCancer MetabolismMetabolic signaling pathwayMetabolism of lipids and lipoproteins
CardiovascularBloodBlood Pressure regulation
CardiovascularBloodSerum Proteins
CardiovascularVasculatureVasoconstrictionOther
MetabolismPathways and ProcessesMetabolic signaling pathwaysLipid and lipoprotein metabolismLipid metabolism
Drug DiscoverySmall Molecule DrugLead Compound Discovery
Tranilast  53902-12-8温馨提示:本产品仅作科研实验使用,不支持临床等研究

产品咨询

留言框

  • 产品:

  • 您的单位:

  • 您的姓名:

  • 联系电话:

  • 常用邮箱:

  • 省份:

  • 详细地址:

  • 补充说明:

  • 验证码:

    请输入计算结果(填写阿拉伯数字),如:三加四=7
爱必信(上海)生物科技有限公司
地址:上海市浦东新区新浩路58号申江科创园18栋
邮箱:lanwu@univ-bio.com
传真:
关注我们
欢迎您关注我们的微信公众号了解更多信息:
欢迎您关注我们的微信公众号
了解更多信息