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
(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年
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:3847384
已选条件
-
T11997MELK-IN-1;尼达尼布杂质LNintedanib Impurity L|||MELK inhibitor 17;Nintedanib Impurity L|||MELK inhibitor 17
MELK-IN-1 (MELK inhibitor 17) is a potent inhibitor of maternal embryonic leucine zipper kinase (MELK),(IC50:3nm;Ki:0.39 nM).
价 格:¥电议型 号:T11997产 地:中国大陆
-
T11983MDRTB-IN-1;化合物 T11983MDRTB-IN-1
MDRTB-IN-1 (5aα) is an antibiotic which is against Mycobacterium tuberculosis H37Rv(MIC90 :10.5 μM).
价 格:¥电议型 号:T11983产 地:中国大陆
-
T11982MDM2-IN-1;化合物 T11982MDM2-IN-1
MDM2-IN-1 is a synthetic MDM2-p53 interaction (MDM2) inhibitor and contains the trans (D-)configuration.
价 格:¥电议型 号:T11982产 地:中国大陆
-
T11974Mcl1-IN-12;化合物 T11974Mcl1-IN-12
Mcl1-IN-12 has anti-tumor activity.It is a selective Mcl-1 inhibitor, less potent at Bcl-2, with Kis of 0.29 and 3.1 μM, respectively.
价 格:¥电议型 号:T11974产 地:中国大陆
-
T11973Mcl1-IN-11;化合物 T11973Mcl1-IN-11
Mcl1-IN-11 (Compound G) is a selective Mcl-1 inhibitor, less potent at Bcl-2, with Kis of 0.06 and 4.2 μM, respectively.
价 格:¥电议型 号:T11973产 地:中国大陆
-
T11968MCL-1/BCL-2-IN-1化合物 T11968MCL1/BCL2IN1|||MCL 1/BCL 2 IN 1
MCL-1/BCL-2-IN-2 (Compound Nap-1) is a potent and selective dual inhibitor of Mcl-1 and Bcl-2 with IC 50 s of 4.45 and 3.18 μM, respectively [1].
价 格:¥电议型 号:T11968产 地:中国大陆
-
T11945MARK-IN-1;化合物 T11945MARK-IN-1
MARK-IN-1 is a potent microtubule affinity regulating kinase (MARK) inhibitor, (IC50<0.25 nM).
价 格:¥电议型 号:T11945产 地:中国大陆
-
T11943MAPK13-IN-1;MAPK13抑制剂1MAPK13-IN-1
MAPK13-IN-1 is a potent MAPK13 (p38δ) inhibitor (IC50: 620 nM).
价 格:¥电议型 号:T11943产 地:中国大陆
-
T11939MAGL-IN-1;化合物 T11939MAGL-IN-1
MAGL-IN-1 is a selective and potent monoacylglycerol lipase (MAGL) inhibitor with an IC50 of 80 nM.
价 格:¥电议型 号:T11939产 地:中国大陆
-
T11924M3258;化合物 T11924LMP7-IN-1;LMP7-IN-1
LMP7-IN-1 may used in the research of inflammatory and autoimmune diseases, neurodegenerative diseases, proliferative diseases and cancer, is an inhibitor of immunoproteasome (LMP7).
价 格:¥电议型 号:T11924产 地:中国大陆
-
T11919LysRs-IN-1;化合物LysRs-IN-19-carboxymethylguanine;9-carboxymethylguanine
LysRs-IN-1 is an inhibitor of Lysyl-tRNA synthetase (LysRs).
价 格:¥电议型 号:T11919产 地:中国大陆
-
T11916Lyn-IN-1;巴非替尼Bafetinib analog;巴非替尼|||Bafetinib analog
Lyn-IN-1 (Bafetinib analog) is a selective and potent dual inhibitor of Bcr-Abl and Lyn
价 格:¥电议型 号:T11916产 地:中国大陆
-
T11888LtaS-IN-1;化合物LtaS-IN-1LtaS-IN-1
LtaS-IN-1 is an effective inhibitor of Lipoteichoic acid synthesis in multidrug-resistant (MDR) E. faecium and by altering the cell wall morphology. LtaS-IN-1 is against Enterococcus spp 28 strains with varying MIC values ranging from 0.5 μg/mL to 64 μg/mL. LtaS-IN-1 inhibits strain E1630 and E1590 with MIC values of 0.5 μg/mL.
价 格:¥电议型 号:T11888产 地:中国大陆
-
T11829LDH-IN-1;化合物LDH-IN-1LDH-IN-1
LDH-IN-1 is a pyrazole-based human lactate dehydrogenase (LDH) inhibitor(IC50s of 32 and 27 nM for LDHA and LDHB, respectively).
价 格:¥电议型 号:T11829产 地:中国大陆
-
T11820LAT1-IN-12-氨基-2-去甲菠烷羧酸2-氨基-2-去甲菠烷羧酸|||BCH
LAT1-IN-1 (BCH) (BCH) significantly inhibit cellular uptake of amino acids and mTOR phosphorylation, which induces the suppression of cancer growth and apoptosis. is a selective and competitive inhibitor of large neutral amino acid transporter 1 (LAT1).
价 格:¥电议型 号:T11820产 地:中国大陆
-
T11756Kgp-IN-1;化合物 T11756Kgp-IN-1
Kgp-IN-1 is an arginine-specific gingipain (Rgp) inhibitor.
价 格:¥电议型 号:T11756产 地:中国大陆
-
T11748KDM2A/7A-IN-1;KDM2A/7A 抑制剂1KDM2A/7A-IN-1
KDM2A/7A-IN-1 is a cell-permeable and selective inhibitor of the histone lysine demethylase KDM2A/7A with potential antitumor activity for the study of duodenal adenomas and ossifying fibromucoid tumors.
价 格:¥电议型 号:T11748产 地:中国大陆
-
T11735K-Ras G12C-IN-1;化合物 T11735K-Ras G12C-IN-1
K-Ras G12C-IN-1 is a novel and irreversible inhibitor of mutant K-ras G12C.
价 格:¥电议型 号:T11735产 地:中国大陆
-
T11707JAK2/FLT3-IN-1;化合物 T11707JAK2/FLT3-IN-1
JAK2/FLT3-IN-1 has anti-cancer activity. JAK2/FLT3-IN-1 is a potent and orally effective dual JAK2/FLT3 (Janus kinase 2/ FMS-like tyrosine kinase 3) inhibitor with IC50 values of 0.7 nM, 4 nM, 26 nM and 39 nM for JAK2, FLT3, JAK1 and JAK3, respectively.
价 格:¥电议型 号:T11707产 地:中国大陆
-
T11703JAK-IN-1;化合物 T11703JAK-IN-1
JAK-IN-1 shows improved selectivity for JAK3 over JAK1. JAK-IN-1 is a JAK1/2/3 inhibitor with IC50s of 0.26, 0.8 and 3.2 nM, respectively.
价 格:¥电议型 号:T11703产 地:中国大陆