您好,欢迎来到易推广 请登录 免费注册

上海陶术生物科技有限公司 主营产品:生物试剂,实验服务等

当前位置:易推广 > 上海陶术生物科技有限公司 > 产品展示

企业档案

会员类型:会员

已获得易推广信誉   等级评定
139成长值

(0 -40)基础信誉积累,可浏览访问

(41-90)良好信誉积累,可接洽商谈

(91+  )优质信誉积累,可持续信赖

易推广会员:5

工商认证 【已认证】

最后认证时间:

注册号: 【已认证】

法人代表: 【已认证】

企业类型:生产商 【已认证】

注册资金:人民币万 【已认证】

产品数:86101

参观次数:3775805

手机网站:http://m.yituig.com/c135739/

旗舰版地址:http://tsbiochem.app17.com

自主品牌

已选条件

  • T15946MA-2029;化合物 T15946MA-2029

    MA-2029 is selective for the motilin receptor over various other receptors and ion channels. MA-2029 is a selective and competitive motilin receptor antagonist (IC50=4.9 nM). MA-2029 may be useful for gastrointestinal disorders associated with disturbed gastrointestinal motility.

    价 格:¥电议型 号:T15946产 地:中国大陆

  • T15945MA-0204;化合物MA-0204MA-0204

    MA-0204 is a highly selective and orally available peroxisome proliferator-activated receptor δ (PPARδ) modulator (EC50s: 0.4 nM, 7.9 nM and 10 nM for human, mouse and rat PPARδ, respectively). It is a potential treatment for Duchene Muscular Dystrophy (DMD).

    价 格:¥电议型 号:T15945产 地:中国大陆

  • T15944M77976;化合物M77976M77976

    M77976 is a selective ATP-competitive inhibitor of pyruvate dehydrogenase kinase 4 (PDK4) with an inhibitory effect on PDK4, having an IC50 value of 648 μM. It is used for research related to obesity and diabetes.

    价 格:¥电议型 号:T15944产 地:中国大陆

  • T15943M443;化合物 M443M443

    M443 is a potent small molecule inhibitor of MRK that inhibits radiation-induced activation of p38 and Chk2 and can be used in cancer research.

    价 格:¥电议型 号:T15943产 地:中国大陆

  • T15942MK-7622;化合物MK-7622M1 receptor modulator;M1 receptor modulator

    MK-7622 (M1 receptor modulator) is a modulator of muscarinic M1 receptor positive allosteric.

    价 格:¥电议型 号:T15942产 地:中国大陆

  • T15940m-PEG9-Amine;化合物 T15940m-PEG9-Amine

    m-PEG9-Amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

    价 格:¥电议型 号:T15940产 地:中国大陆

  • T1594Vecuronium bromide;维库溴铵ORG NC 45;ORG NC 45|||维库溴铵

    Vecuronium bromide (ORG NC 45) is a synthetic, intermediate-acting mono-quaternary steroid and non-depolarizing neuromuscular blocking agent, with muscle relaxant activity.

    价 格:¥电议型 号:T1594产 地:中国大陆

  • T15939m-PEG8-Tos;化合物 T15939m-PEG8-Tos

    Tos-PEG8-m, a PEG-based PROTAC linker, is a derivative of silybin ethers. It is utilized in the synthesis of Silymarin[1].

    价 格:¥电议型 号:T15939产 地:中国大陆

  • T15938m-PEG8-thiol;化合物 T15938m-PEG8-thiol

    m-PEG8-thiol is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

    价 格:¥电议型 号:T15938产 地:中国大陆

  • T15937m-PEG8-succinimidyl carbonate;化合物 T15937m-PEG8-succinimidyl carbonate

    m-PEG8-succinimidyl carbonate is a polyethylene glycol (PEG)-derived linker, specifically designed for the synthesis of PROteolysis TArgeting Chimeras (PROTACs)[1].

    价 格:¥电议型 号:T15937产 地:中国大陆

  • T15936m-PEG8-NHS ester;化合物 T15936m-PEG8-NHS ester

    m-PEG8-NHS ester is a non-cleavable 8 unit polyethylene glycol (PEG) linker compound, employed in the synthesis of antibody-drug conjugates (ADCs).

    价 格:¥电议型 号:T15936产 地:中国大陆

  • T15935m-PEG8-Ms;化合物 T15935m-PEG8-Ms

    m-PEG8-Ms is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

    价 格:¥电议型 号:T15935产 地:中国大陆

  • T15934m-PEG8-Mal;化合物 T15934m-PEG8-Mal

    m-PEG8-Mal is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

    价 格:¥电议型 号:T15934产 地:中国大陆

  • T15933m-PEG8-CH2COOH;化合物 T15933m-PEG8-CH2COOH

    m-PEG8-CH2COOH is a PEG--based PROTAC linker can be used in the synthesis of PROTACs.

    价 格:¥电议型 号:T15933产 地:中国大陆

  • T15932m-PEG9-NHS ester;化合物 T15932m-PEG8-CH2CH2-NHS ester;m-PEG8-CH2CH2-NHS ester

    m-PEG8-CH2CH2-NHS ester is a PEG--based PROTAC linker can be used in the synthesis of PROTACs.

    价 格:¥电议型 号:T15932产 地:中国大陆

  • T1593Ezetimibe;依泽替米贝SCH 58235;依泽替米贝|||SCH 58235

    Ezetimibe (SCH 58235) is a Dietary Cholesterol Absorption Inhibitor. The physiologic effect of ezetimibe is by means of Decreased Cholesterol Absorption.

    价 格:¥电议型 号:T1593产 地:中国大陆

  • T15929m-PEG8-Br;化合物 T15929m-PEG8-Br

    m-PEG8-Br is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

    价 格:¥电议型 号:T15929产 地:中国大陆

  • T15928m-PEG8-azide;化合物 T15928m-PEG8-azide

    m-PEG8-azide is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

    价 格:¥电议型 号:T15928产 地:中国大陆

  • T15927m-PEG8-Amine;化合物 T15927m-PEG8-Amine

    m-PEG8-Amine is a cleavable linker vital in ADC synthesis. m-PEG8-Amine joins cytotoxic drugs to antibodies, enabling precise delivery to cells or proteins. The cleavable nature ensures controlled drug release, optimizing ADC effectiveness.

    价 格:¥电议型 号:T15927产 地:中国大陆

  • T15926m-PEG7-Tos;化合物 T15926m-PEG7-Tos

    m-PEG7-Tos is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

    价 格:¥电议型 号:T15926产 地:中国大陆

快速导航

在线咨询

提交