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:3766856

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

  • T4308F1063-0967

    F1063-0967 is a Dual-specificity phosphatase 26 (DUSP26) inhibitor with an IC50 of 11.62 μM.

    价 格:¥电议型 号:T4308产 地:中国大陆

  • T4125HSF1A

    HSF1A is a cell-permeable activator of HSF1 that protects mammalian cells against stress-induced apoptosis.

    价 格:¥电议型 号:T4125产 地:中国大陆

  • T3963VUF10460

    VUF10460 is a non-imidazole histamine H4 receptor agonist.

    价 格:¥电议型 号:T3963产 地:中国大陆

  • T3920Pseudoginsenoside F11Ginsenoside A1;拟人参皂苷 F11;拟人参皂苷F11

    Pseudoginsenoside-F11 is a component of Panax quinquefolium (American ginseng), can antagonize the learning and memory deficits induced by scopolamine, morphine, and methamphetamine in mice.

    价 格:¥电议型 号:T3920产 地:中国大陆

  • T3401Ginsenoside F1人参皂苷 F1;20(S)-Ginsenoside F1

    Ginsenoside F1 is an enzymatically modified derivative of ginsenoside Rg1, showing competitive inhibition of the activity of CYP3A4 and a weaker inhibition of the activity of CYP2D6.

    价 格:¥电议型 号:T3401产 地:中国大陆

  • T2657ElacridarGW120918;GF120918;GG918;GW0918;依克立达

    Elacridar (GF120918) is an effective BCRP and P-gp (MDR-1) inhibitor.

    价 格:¥电议型 号:T2657产 地:中国大陆

  • T22774Leukaryotic translation elongation factor 1 alpha 1 (EEF1A1) (387-394) [Multiple species](TFA)

    eukaryotic translation elongation factor 1 alpha 1 (EEF1A1) (387-394) [Multiple species](TFA) is Elongation factor 1 subunit.eukaryotic translation elongation factor 1 alpha 1 (EEF1A1) encodes an isoform of the alpha subunit of the elongation factor-1 com

    价 格:¥电议型 号:T22774L产 地:中国大陆

  • T2127OF-1OF 1;OF1

    OF-1 is a potent inhibitor of BRPF1B and BRPF2 bromodomain.

    价 格:¥电议型 号:T2127产 地:中国大陆

  • T19840GSK-F1PI4KA inhibitor-F1

    GSK-F1 is a novel potent PI4KA inhibitor.

    价 格:¥电议型 号:T19840产 地:中国大陆

  • T1967AZD-3463ALK/IGF1R inhibitor;AZD3463

    AZD3463, an orally bioavailable ALK inhibitor (Ki: 0.75 nM), can inhibit IGF1R with equivalent potency.

    价 格:¥电议型 号:T1967产 地:中国大陆

  • T16904Smurf1-IN-A01A01

    Smurf1-IN-A01 is a ubiquitin ligase Smad ubiquitination regulatory factor-1 inhibitor (kd: 3.664 nM). It increases BMP-2 responsiveness by inhibiting Smurf1-mediated Smad1/5 degradation.

    价 格:¥电议型 号:T16904产 地:中国大陆

  • T15409GNF179

    GNF179 is an optimized 8,8-dimethyl IP analog. It exhibited the potency(4.8 nM against the multidrug resistant strain W2) in vitro metabolic stability and in vivo oral bioavailability.

    价 格:¥电议型 号:T15409产 地:中国大陆

  • T13324VUF11207 fumarate

    VUF11207 fumarate is an agonist of CXCR7 and a high-potency ligand of CXCR7 (pKi: 8.1).

    价 格:¥电议型 号:T13324产 地:中国大陆

  • T13194CSF1R-IN-2

    CSF1R-IN-2 is an oral-active SRC, MET and c-FMS inhibitor (IC50s: 0.12 nM, 0.14 nM and 0.76 nM for SRC, MET and c-FMS respectively).

    价 格:¥电议型 号:T13194产 地:中国大陆

  • T12223Nifursemizone硝呋米腙;Etafurazone;NF161;5-Nitro-2-furancarbaldehyde 2-ethyl semicarbazone

    Nifursemizone is an agent with antiprotozoal.

    价 格:¥电议型 号:T12223产 地:中国大陆

  • T12125MuRF1-IN-1

    MuRF1-IN-1 is an inhibitor of muscle ring finger 1.

    价 格:¥电议型 号:T12125产 地:中国大陆

  • T10894CSF1R-IN-1

    CSF1R-IN-1 is a CSF1R inhibitor with IC50 of 0.5 nM.

    价 格:¥电议型 号:T10894产 地:中国大陆

  • T0239Lonidamine氯尼达明;Diclondazolic Acid;DICA;AF1890

    Lonidamine is an indazole carboxylic acid derivative, principally inhibiting aerobic glycolytic activity, by its effect on mitochondrially-bound hexokinase (HK).

    价 格:¥电议型 号:T0239产 地:中国大陆

  • T0239LonidamineLonidamine,AF1890,Diclondazolic Acid

    Lonidamine is an indazole carboxylic acid derivative, principally inhibiting aerobic glycolytic activity, by its effect on mitochondrially-bound hexokinase (HK).

    价 格:¥电议型 号:T0239产 地:美洲

  • T11210EP1013EP1013,F1013,

    EP1013 is a broad-spectrum selective inhibitor of Caspase used in the study of type 1 diabetes.

    价 格:¥电议型 号:T11210产 地:美洲

快速导航

在线咨询

提交