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 > abs810399IPI-145 1201438-56-3

IPI-145 1201438-56-3

简要描述:IPI-145 1201438-56-3
Duvelisib is an orally bioavailable, highly selective and potent small molecule inhibitor of the delta and gamma isoforms of phosphoinositide-3 kinase (PI3K) with potential immuno

  • 产品型号:abs810399
  • 厂商性质:生产厂家
  • 更新时间:2026-02-04
  • 访  问  量:1165

详细介绍

品牌absinCAS1201438-56-3
分子式C22H17ClN6O纯度>98%
分子量416.86货号abs810399
规格5mg供货周期现货
主要用途is an orally bioavailable应用领域化工,生物产业,农林牧渔,制药/生物制药,综合

IPI-145 1201438-56-3

产品描述
描述

Duvelisib is an orally bioavailable, highly selective and potent small molecule inhibitor of the delta and gamma isoforms of phosphoinositide-3 kinase (PI3K) with potential immunomodulating and antineoplastic activities.

纯度
>98%
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
IPI-145; INK1197
外观
白色至类白色粉末
可溶性/溶解性
DMSO : 77 mg/mL (184.7 mM)
生物活性
靶点
PI3Kα,PI3Kβ,PI3Kγ, PI3Kδ
In vitro(体外研究)
IPI-145 suppresses murine/human B-cell proliferation with EC50 of 0.5 nM/0.5 nM and also inhibits human T-cell proliferation with EC50 of 9.5 nM.
In vivo(体内研究)
IPI-145 (10 mg/kg, p.o.) shows well pharmacokinetics with Cmax and AUC of 390 ng/mL and 137 ng•h/mL in mouse and rat. IPI-145 (10 mg/kg) is active in murine DTH model with ~50% ear swelling. IPI-145 (10 mg/kg) demonstrates dose-dependent effect in rat collagen induced arthritis (CIA) model. IPI-145 prevents inflammation and protects joint bone and cartilage in the rat CIA model. IPI-145 (10 mg/kg,QD) demonstrates activity in rat adjuvant induced polyarthritis model.
研究领域
研究领域
CancerCancer Metabolism
CancerTumor biomarkers
Drug DiscoverySmall Molecule DrugLead Compound Discovery
IPI-145 1201438-56-3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