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
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：3767990
自主品牌
已选条件
-
T62178TLR7/8 antagonist 1；化合物 TLR7/8 antagonist 1TLR7/8 antagonist 1
TLR7/8 Antagonist 1 (Compound 16c), an imidazoquinoline derivative, is a potent TLR7/8 agonist with IC50 values of 3.91 and 2.19 μM for TLR7 and TLR8, respectively. rel-O-2050 (TLR-2050) is a key target for drug development in infectious diseases, cancer and autoimmune diseases.
价 格：￥电议型 号：T62178产 地：中国大陆
-
T62177TLR7/8 agonist 6；化合物 TLR7/8 agonist 6TLR7/8 agonist 6
TLR7/8 agonist 6 (Compound 4), an imidazoquinoline derivative, is a potent TLR7/8 agonist with IC50 values of 0.18 and 5.34 μM for TLR7 and TLR8, respectively. TLR7/8 Antagonist
价 格：￥电议型 号：T62177产 地：中国大陆
-
T61826NLRP3-IN-4；化合物 NLRP3-IN-4NLRP3-IN-4
NLRP3-IN-4 is a highly efficient and orally bioavailable inhibitor of NLRP3 inflammasome, which exhibits strong anti-inflammatory properties specifically targeted towards colitis.
价 格：￥电议型 号：T61826产 地：中国大陆
-
T61601TLR7/8 antagonist 2；化合物 TLR7/8 antagonist 2TLR7/8 antagonist 2
TLR7/8 antagonist 2 (Compound 15) is a highly potent and orally active agonist of TLR7/8, exhibiting IC50 values of 4.9 and 0.6 nM for TLR7 and TLR8, respectively. Its strong affinity for these receptors makes it a promising candidate for the treatment and investigation of autoimmune diseases, including lupus erythematosus, which is associated with inappropriate activation of TLR7 and TLR8. Consequently, TLR7/8 antagonist 2 represents a valuable tool for research in the field of autoimmune disea
价 格：￥电议型 号：T61601产 地：中国大陆
-
T61392NLRP3-IN-10；化合物NLRP3-IN-10ZVN26391；ZVN26391
NLRP3-IN-10 (ZVN26391) is a potent NLRP3 inhibitor. NLRP3-IN-10 inhibits IL-1β release with an IC50 value of 251.1 nM. NLRP3-IN-10 attenuates ASC speck formation, leading to suppress activation of NLRP3 inflammasome.
价 格：￥电议型 号：T61392产 地：中国大陆
-
T61132NLRP3-IN-11；NLRP3抑制剂11NLRP3-IN-11
NLRP3-IN-11 is an NLRP3 protein inhibitor with potential anti-inflammatory activity.NLRP3-IN-11 can be used in the study of atherosclerosis and parkinsonism.
价 格：￥电议型 号：T61132产 地：中国大陆
-
T60894TLR7/8 agonist 4；化合物 TLR7/8 agonist 4TLR7/8 agonist 4
TLR7/8 agonist 4 (compound 41) is a potent agonist of TLR7/8 with anti-cancer activity [1].
价 格：￥电议型 号：T60894产 地：中国大陆
-
T608595-Pentadecylresorcinol；化合物 5-Pentadecylresorcinol5-Pentadecylresorcinol
5-Pentadecylresorcinol (Adipostatin A) has good larvicidal activity against Aedes aegypti that is an inhibitor of glycerol-3-phosphate dehydrogenase (GPDH) with an IC 50 of 4.1 μM [1] [2].
价 格：￥电议型 号：T60859产 地：中国大陆
-
T60756NLRP3 antagonist 1；化合物 NLRP3 antagonist 1NLRP3 antagonist 1
NLRP3 antagonist 1 shows potential for the cancer research that is a potent NLRP3 antagonist. NLRP3 is involved in the body´s intrinsic immunity against stress injury and pathogenic infections that is mainly expressed in macrophages and neutrophils [1].
价 格：￥电议型 号：T60756产 地：中国大陆
-
T60563NLRP3/AIM2-IN-1；化合物 NLRP3/AIM2-IN-1NLRP3/AIM2-IN-1
NLRP3/AIM2-IN-1 is an inhibitor of thermal sepsis (IC50 = 3.136 ± 0.7667 μM).
价 格：￥电议型 号：T60563产 地：中国大陆
-
T60442NLRP3/AIM2-IN-3；化合物NLRP3/AIM2-IN-3NLRP3/AIM2-IN-3
NLRP3/AIM2-IN-3 is a unique molecule that inhibits NLRP3 and AIM2 inflammasome activation in a species-specific manner. It has an IC50 value for cell lysis of 0.077 ± 0.008 μ M. NLRP3/AIM2-IN-3 is a potent inhibitor of NLRP3 and AIM2 inflammasome-dependent cell lysis with an IC50 value for cell lysis of 0.077 ± 0.008 μ M. NLRP3/AIM2-IN-3 inhibits LPS/nigericin NLRP3/AIM2-IN-3 inhibits LPS/nigericin-stimulated cell lysis in THP-1 macrophages with an IC50 value of 0.077 ± 0.008 μM. NLRP3/AIM2-IN-3
价 格：￥电议型 号：T60442产 地：中国大陆
-
T60404NLRP3/AIM2-IN-2；化合物NLRP3/AIM2-IN-2NLRP3/AIM2-IN-2
NLRP3/AIM2-IN-2 is a novel potent inhibitor with different species-specific effects on NLRP3 and AIM2 inflammasome dependent pyroptosis with IC50 of 0.2392 ± 0.0233 μ M.
价 格：￥电议型 号：T60404产 地：中国大陆
-
T60249RhlR antagonist 1；化合物 RhlR antagonist 1RhlR antagonist 1
RhlR antagonist 1 is a highly effective antagonist of the RhlR protein, showing an IC50 value of 26 μM. It exhibits selective antagonistic activity against RhlR, with minimal effect on LasR and PqsR. RhlR antagonist 1 strongly inhibits biofilm formation in both static and dynamic environments and reduces the production of virulence factors, such as rhamnolipid and pyocyanin, in P. aeruginosa. These characteristics make RhlR antagonist 1 a valuable tool for the development of molecules that modul
价 格：￥电议型 号：T60249产 地：中国大陆
-
T5843TarenflurbilR-氟比洛芬MPC7869|||(R)-Flurbiprofen|||R-flurbiprofen|||氟比洛芬|||R-氟比洛芬
Tarenflurbil ((R)-Flurbiprofen) is the non-cyclooxygenase inhibiting R-enantiomer of the non-steroidal anti-inflammatory drug flurbiprofen, which was assessed as a remedy for Alzheimer´s disease.
价 格：￥电议型 号：T5843产 地：中国大陆
-
T5668Triacetylresveratrol三乙酰基白藜芦醇乙酰化白藜芦醇|||三乙酰基白藜芦醇|||Acetyl-trans-resveratrol
Triacetylresveratrol (Acetyl-trans-resveratrol) has anti-cancer activity,it inhibits the phosphorylation of STAT3 and NFκB, down-regulates Mcl-1, and up-regulates Bim and Puma in pancreatic cancer cells.
价 格：￥电议型 号：T5668产 地：中国大陆
-
T5561TLR7/8 agonist 1 dihydrochloride；二盐酸TLR7/8 agonist 1TLR7/8 agonist-5d；TLR7/8 agonist-5d|||二盐酸TLR7/8
TLR7/8 agonist 1 dihydrochloride (TLR7/8 agonist-5d) is a TLR7/8 agonist which shows prominent immunostimulatory activities.
价 格：￥电议型 号：T5561产 地：中国大陆
-
T5385Radiprodil；化合物RadiprodilRGH-896；RGH-896
Radiprodil (RGH-896) (RGH-896) is an orally active and selective NMDA NR2B receptors antagonist. It was a potential treatment of neuropathic pain associated with diabetic peripheral neuropathy (DPNP).
价 格：￥电议型 号：T5385产 地：中国大陆
-
T5336LZacopride；化合物 T5336LRacemic zacopride；Racemic zacopride
Zacopride is a selective agonist of inward rectifier potassium current (I K1) channel, inhibiting ventricular arrhythmias without affecting atrial arrhythmias.
价 格：￥电议型 号：T5336L产 地：中国大陆
-
T5195LAlrestatin Sodium；化合物 T5195LAY 22284A|||AY-22284A|||Alrestatine sodium|||AY22284A；AY 22284A|||AY-222
Alrestatin is a specific inhibitor of the aldose reductase enzyme.
价 格：￥电议型 号：T5195L产 地：中国大陆
-
T5195Alrestatin；阿瑞司他丁AY-22284|||阿瑞司他丁|||AY22284|||AY22284|||Aldose Reductase|||AY-22284|||inhibit|||Inhib
Alrestatin (AY-22284) is a specific inhibitor of aldose reductase and attenuates glucose-induced angiotensin II production in rat vascular smooth muscle in vitro.
价 格：￥电议型 号：T5195产 地：中国大陆
