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:3235387
已选条件
-
T12210Netupitant D6;化合物 T12210CID-6451149 D6;CID-6451149 D6
Netupitant D6 is the deuterium labeled Netupitant, which is a selective and orally active antagonist of neurokinin-1 receptor.
价 格:¥电议型 号:T12210产 地:中国大陆
-
T12114MSC1094308;化合物 T12114MSC1094308
MSC1094308 is a reversible and allosteric inhibitor of the type II AAA ATPase.
价 格:¥电议型 号:T12114产 地:中国大陆
-
T11499GSK726701A;化合物 T11499GSK726701A
GSK726701A is a new type of prostaglandin E2 receptor 4 (EP4) partial agonist (pEC50: 7.4).
价 格:¥电议型 号:T11499产 地:中国大陆
-
T11498GSK682753A;化合物 T11498GSK682753A
GSK682753A is a selective and highly potent inverse agonist of the epstein-barr virus-induced receptor 2 (EBI2; IC50: 53.6 nM).
价 格:¥电议型 号:T11498产 地:中国大陆
-
T11497Ganfeborole HCl;Ganfeborole 盐酸盐GSK3036656 HCl|||GSK656 HCl;GSK3036656 HCl|||GSK656 HCl
Ganfeborole HCl (GSK3036656 HCl) is a small molecule compound with anti-tuberculosis activity and is an inhibitor of Mycobacterium tuberculosis (Mtb) leucyl-tRNA synthetase (LeuRS; IC50: 0.2 μM).
价 格:¥电议型 号:T11497产 地:中国大陆
-
T11496GSK598809;化合物 T11496GSK598809
GSK598809 is a selective and potent dopamine D3 Receptor (DRD3) antagonist (pKi: 8.9).
价 格:¥电议型 号:T11496产 地:中国大陆
-
T11495LGSK 4027;化合物 T11495LGSK 4027
GSK 4027 is a PCAF/GCN5 bromodomain chemical probe. In a time-resolved fluorescence resonance energy transfer (TR-FRET) assay, it has a pIC50 of 7.4±0.11 for PCAF.
价 格:¥电议型 号:T11495L产 地:中国大陆
-
T11495GSK4028;化合物 T11495GSK4028
GSK4028 is the enantiomeric negative control of GSK4027, which is a PCAF/GCN5 bromodomain chemical probe. The pIC50 of GSK4028 is 4.9 in a TR-FRET assay.
价 格:¥电议型 号:T11495产 地:中国大陆
-
T11494GSK3532795;化合物 T11494BMS-955176;BMS-955176
GSK3532795 is a potent, orally active, second-generation HIV-1 maturation inhibitor (EC50s: 10.2, 1.9, 2.7, and 13 nM for HIV-1 WT(human serum), HIV-1 WT, HIV-1 V370A, and HIV-1 ΔV370).
价 格:¥电议型 号:T11494产 地:中国大陆
-
T11493GSK3004774;化合物 T11493GSK3004774
GSK3004774 is a nonabsorbable agonist of CaSR (pEC50: 7.3, 6.6, and 6.5 for human, mouse, and rat CaSR). GSK3004774 shows an EC50 of 50 nM for human CaSR.
价 格:¥电议型 号:T11493产 地:中国大陆
-
T11492GSK2983559 free acid;化合物GSK2983559 free acidGSK2983559 free acid
GSK2983559 free acid is an effective and selective inhibitor of receptor-interacting protein 2 (RIP2). GSK2983559 free acid shows excellent activity in blocking many proinflammatory cytokine responses in human inflammatory bowel disease explant samples an
价 格:¥电议型 号:T11492产 地:中国大陆
-
T11491GSK2973980A;化合物 T11491GSK2973980A
GSK2973980A is a selective Acyl-CoA:diacylglycerol acyltransferase 1 (DGAT1) inhibitor (IC50: 3 nM).
价 格:¥电议型 号:T11491产 地:中国大陆
-
T11490LGSK2945 hydrochloride (1438071-12-5 free base);化合物 T11490LGSK2945 hydrochloride;GSK2945 hydrochlorid
GSK2945 hydrochloride is a highly specific Rev-erbα/REV-ERBα (mouse/human reverse erythroblastosis virus α) antagonist (EC50s: 21.5 μM and 20.8 μM). It enhances cholesterol 7α-hydroxylase (CYP7A1) level and cholesterol metabolism.
价 格:¥电议型 号:T11490L产 地:中国大陆
-
T11490GSK2945;化合物 T11490GSK2945
GSK2945 is a highly specific Rev-erbα/REV-ERBα (mouse/human reverse erythroblastosis virus α) antagonist (EC50s: 21.5 μM and 20.8 μM). It enhances cholesterol 7α-hydroxylase (CYP7A1) level and cholesterol metabolism.
价 格:¥电议型 号:T11490产 地:中国大陆
-
T1149Fenofibrate;非诺贝特Procetofen|||Lipanthyl|||Lipantil;Procetofen|||非诺贝特|||Lipanthyl|||Lipantil
Fenofibrate (Lipanthyl) is a peroxisome proliferator receptor alpha agonist. Fenofibrate is a synthetic phenoxy-isobutyric acid derivate and prodrug with antihyperlipidemic activity.
价 格:¥电议型 号:T1149产 地:中国大陆
-
T11488GSK2850163;化合物GSK2850163GSK2850163
GSK2850163 is a novel inhibitor of inositol-requiring enzyme-1 alpha (IRE1α) which can inhibit RNase activity and IRE1α kinase activity (IC50s: 200 and 20 nM).
价 格:¥电议型 号:T11488产 地:中国大陆
-
T11487LFiboflapon sodium;化合物 T11487LGSK2190915 sodium salt|||AM-803 sodium;GSK2190915 sodium salt|||AM-803
Fiboflapon sodium (GSK2190915) is an orally bioavailable 5-lipoxygenase-activating protein (FLAP) inhibitor with a potency of 2.9 nM in FLAP binding, an IC50 of 76 nM for inhibition of LTB4 in human blood.
价 格:¥电议型 号:T11487L产 地:中国大陆
-
T11487Fiboflapon;化合物FiboflaponGSK2190915|||AM-803;GSK2190915|||AM-803
Fiboflapon (GSK2190915) is an orally available and effective 5-lipoxygenase-activating protein (FLAP) inhibitor that binds FLAP with a titer of 2.9 nM and inhibition of LTB4 in human blood with an IC50 of 76 nM.
价 格:¥电议型 号:T11487产 地:中国大陆
-
T11486GSK2807 Trifluoroacetate;化合物GSK2807 TrifluoroacetateGSK2807 Trifluoroacetate
GSK2807 Trifluoroacetate is a selective and SAM-competitive inhibitor of SMYD3 (Ki: 14 nM; IC50: 130 nM).
价 格:¥电议型 号:T11486产 地:中国大陆
-
T11485GSK2643943A;化合物GSK2643943AGSK2643943A
GSK2643943A is a deubiquitylating enzyme (DUB) inhibitor, with an IC 50 of 160 nM for USP20/Ub-Rho. GSK2643943A has anti-tumor efficacy.
价 格:¥电议型 号:T11485产 地:中国大陆