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:3243175
已选条件
-
T30494BMS 214428;化合物 T30494BMS214428|||BMS-214428|||UNII-6774Z74TWN;BMS214428|||BMS-214428|||UNII-6774Z74T
BMS 214428 is a bio-active chemical.
价 格:¥电议型 号:T30494产 地:中国大陆
-
T30238Axitirome;化合物 T30238CGS-26214|||CGS 26214|||CGS26214;CGS-26214|||CGS 26214|||CGS26214
Axitirome, also known as CGS 26214, is a hypolipidemic agent.
价 格:¥电议型 号:T30238产 地:中国大陆
-
T29970AMG-222;化合物 T29970AMG 222|||ALS-2-0426 free base|||ALS-2-0426|||ALS-20426;AMG 222|||ALS-2-0426 free
AMG-222 (ALS-2-0426, ALS-20426) is a DPP-4 inhibitor and may be used in the treatment of type 2 diabetes.
价 格:¥电议型 号:T29970产 地:中国大陆
-
T29944Amadinone acetate;化合物 T29944RS 2208|||RS-2208;RS 2208|||RS-2208
Amadinone acetate is a biochemical.
价 格:¥电议型 号:T29944产 地:中国大陆
-
T29161STOCK2S-26016;化合物 T29161WNK IN B|||WNK-IN-B|||Compound B;WNK IN B|||WNK-IN-B|||Compound B
WNK-IN-B is an inhibitor of Wnk signalling. WNK-IN-B is a cell-permeable diaminoacridine derivative that targets the CCT domain of SPAK and OSR1 via reversible binding. WNK-IN-B selectively suppress hypotonic shock-induced WNK signaling pathway activation in mpkDCT and MOVAS (100 ?M) cultures without affecting p38 MAPK phosphorylation.
价 格:¥电议型 号:T29161产 地:中国大陆
-
T29067Upacicalcet;乌帕卡塞PLS-240|||SK-1403|||AJT-240;PLS-240|||SK-1403|||AJT-240
Upacicalcet (AJT-240) is an intraventricular calcium mimetic, a SHPT available for human hemodialysis, that inhibits excessive parathyroid hormone (PTH) secretion by directly acting on parathyroid cell membrane calcium-sensitive receptors, thereby lowering blood levels of PTH.Upacicalcet is an orthosteric modulator of calcium-sensitive receptors and prevents adenine-induced secondary vascular calcification and bone disease in a rat model of adenine-induced secondary hyperparathyroidism.
价 格:¥电议型 号:T29067产 地:中国大陆
-
T28951Tesofensine;化合物 T28951NS 2330|||NS2330|||NS-2330;NS 2330|||NS2330|||NS-2330
Tesofensine, a serotonin–noradrenaline–dopamine reuptake inhibitor, is used potentially for the treatment of obesity.
价 格:¥电议型 号:T28951产 地:中国大陆
-
T28645S-22153;化合物 T28645S-22153
S22153 is an antagonist of melatonin receptor.
价 格:¥电议型 号:T28645产 地:中国大陆
-
T28644S20928;化合物 T28644S 20928|||S-20928;S 20928|||S-20928
S20928 is an antagonist of melatonin receptor.
价 格:¥电议型 号:T28644产 地:中国大陆
-
T28197NS-2710;化合物 NS-2710NS 2710|||NS2710;NS 2710|||NS2710
NS-2710 is a non-selective GABA(A) receptor partial agonist for the study of anxiety disorders.
价 格:¥电议型 号:T28197产 地:中国大陆
-
T28196NS-220;化合物 T28196LS-191458|||NS 220;LS-191458|||NS 220
NS-220, a selective agonist of peroxisome proliferator-activated receptor alpha, potently decreases plasma triglyceride and glucose levels and modifies lipoprotein profiles in KK-Ay mice.
价 格:¥电议型 号:T28196产 地:中国大陆
-
T28114MS2177;化合物 T28114MS 2177|||MS-2177;MS 2177|||MS-2177
MS2177 is a potent and selective inhibitor of SETD8, the only methyltransferase known to catalyze monomethylation of histone H4 lysine 20 (H4K20). MS2177 has an in vitro IC50 of 1.9 μM (σ = 1.05 μM, n = 4) in ascintillation proximity assay. Binding of MS2177 to SETD8 was confirmed by isothermal titration calorimetry (ITC), having a KD of 1.3 μM.
价 格:¥电议型 号:T28114产 地:中国大陆
-
T28103MRS2603;化合物 T28103MRS-2603|||MRS 2603;MRS-2603|||MRS 2603
MRS2603 is an antagonist of P2Y1 and P2Y13 receptors in 1321N1 human astrocytoma cells.
价 格:¥电议型 号:T28103产 地:中国大陆
-
T28102MRS2567;化合物 T28102MRS-2567|||MRS 2567;MRS-2567|||MRS 2567
MRS2567 is a potent P2Y6 nucleotide receptors antagonists.
价 格:¥电议型 号:T28102产 地:中国大陆
-
T28100MRS2298;化合物 T28100MRS-2298|||MRS 2298;MRS-2298|||MRS 2298
MRS2298, a potent antagonists of the P2Y 1 receptor, has antiaggregatory activity in human platelets.
价 格:¥电议型 号:T28100产 地:中国大陆
-
T28099MRS2179;化合物 T28099MRS 2179|||MRS-2179;MRS 2179|||MRS-2179
MRS2179 is a competitive P2Y1 receptor antagonist (Kb = 100 nM) with no appreciable activity at P2Y2, P2Y4, or P2Y6 at concentrations up to 30 ?M, or at P2Y12 and P2Y13. It inhibits ADP-induced platelet shape change and aggregation (pA2 = 6.55) in vitro and prolongs bleeding time in rats and mice compared to controls.
价 格:¥电议型 号:T28099产 地:中国大陆
-
T28074MLS-2064;化合物 T28074MLS-2064
MLS-2064 is a STAT3 and Akt signaling inhibitor.
价 格:¥电议型 号:T28074产 地:中国大陆
-
T27962Ancremonam;化合物 T27962LYS228|||LYS-228|||LYS 228;LYS228|||LYS-228|||LYS 228
LYS228 is a potent antibiotics against Carbapenem-Resistant Enterobacteriaceae (MIC90 = 2 uM/mL). LYS228 is potent in the presence of all classes of beta-lactamases.
价 格:¥电议型 号:T27962产 地:中国大陆
-
T27599Imiloxan;咪洛克生RS-21361|||RS 21361|||RS21361;RS-21361|||RS 21361|||RS21361
Imiloxan (RS-21361) is an α2 adrenergic receptor antagonist used in the treatment of major depressive disorder.
价 格:¥电议型 号:T27599产 地:中国大陆
-
T27565Hyzetimibe;化合物 T27565HS25|||HS 25|||HS-25;HS25|||HS 25|||HS-25
Hyzetimibe, a cholesterol absorption blocker, is used potentially for the treatment of hypercholesterolemia.
价 格:¥电议型 号:T27565产 地:中国大陆