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：3714950
自主品牌
已选条件
-
T1567Olanzapine奥氮平；LY170053
Olanzapine is an atypical antipsychotic that is used currently in the treatment of schizophrenia and bipolar illness.
价 格：￥电议型 号：T1567产 地：中国大陆
-
-
T15660KHK-IN-1KHK-IN-8；Ketohexokinase inhibitor 8
KHK-IN-1 is a reversible and ATP-competitive inhibitor of ketohexokinase (KHK) with IC50 of 12 nM. In the ATP-binding region of KHK, KHK-IN-1 interacts with Asp-27B.
价 格：￥电议型 号：T15660产 地：中国大陆
-
T1566Aripiprazole阿立哌唑；OPC-14597
Aripiprazole is an antipsychotic agent that is structurally related to piperazines and quinolones. It is a partial agonist of SEROTONIN RECEPTOR, 5-HT1A and DOPAMINE D2 RECEPTORS, where it also functions as a post-synaptic antagonist, and an antagonist of
价 格：￥电议型 号：T1566产 地：中国大陆
-
T15656KGA-2727
KGA-2727 is a potent and selective SGLT1 inhibitor, with Kis of 97.4 nM and 43.5 nM for human and rat SGLT1, respectively. The selectivity ratios (Ki for SGLT2/Ki for SGLT1) of KGA-2727 are 140 (human) and 390 (rat). KGA-2727 for the treatment of diabete.
价 格：￥电议型 号：T15656产 地：中国大陆
-
T15654Ketohexokinase inhibitor 1
Ketohexokinase inhibitor 1 is a ketohexokinase inhibitor (IC50s: 8.4 nM and 66 nM for KHK-C and KHK-A, respectively).
价 格：￥电议型 号：T15654产 地：中国大陆
-
T1565DeferiproneCP20；Deferidone；去铁酮
Deferiprone is an Iron Chelator. The mechanism of action of deferiprone is as an Iron Chelating Activity.
价 格：￥电议型 号：T1565产 地：中国大陆
-
T15649KDM5-IN-1
KDM5-IN-1 is an effective and selective inhibitor of KDM5 with an IC50 of 15.1 nM.
价 格：￥电议型 号：T15649产 地：中国大陆
-
T15646KBU2046
KBU2046 is an oral inhibitor of cell motility and cell invasion in vitro. KBU2046 inhibits cancer metastasis and prolongs life. KBU2046 binds chaperone heterocomplexes, selectively alters binding of client proteins that regulate motility, and lacks all of
价 格：￥电议型 号：T15646产 地：中国大陆
-
-
T1564CisplatinCDDP；cis-Diaminodichloroplatinum；顺铂
Cisplatin, a DNA-crosslinking agent, is able to suppress DNA synthesis by conforming DNA adducts in cancer cells.
价 格：￥电议型 号：T1564产 地：中国大陆
-
T15639K-756
K-756 is a direct and selective inhibitor of tankyrase (TNKS), which inhibits the ADP-ribosylation activity of TNKS1 (IC50 = 31 nM) and TNKS2 (IC50 = 36 nM).
价 格：￥电议型 号：T15639产 地：中国大陆
-
T15635JZP-430
JZP-430 is an effective, highly selective, irreversible inhibitor of α/β-hydrolase domain 6 (ABHD6) (IC50: 44 nM). It also shows ~230-fold selectivity over fatty acid amide hydrolase (FAAH) and lysosomal acid lipase (LAL).
价 格：￥电议型 号：T15635产 地：中国大陆
-
T15633JW74
JW74 antagonizes LiCl-induced activation of the canonical Wnt signaling (IC50: 420 nM).
价 格：￥电议型 号：T15633产 地：中国大陆
-
T15632JW 642
JW 642 is an effective inhibitor of monoacylglycerol lipase (MAGL) (IC50: 7.6, 14, and 3.7 nM for inhibition of MAGL in mouse, rat, and human brain membranes, respectively).
价 格：￥电议型 号：T15632产 地：中国大陆
-
T1563NifuroxazideNifuroxazid；Diarlidan；硝呋齐特；硝呋酚酰肼；Dicoferin
Nifuroxazide is an orally available and cell-permeable nitrofuran-based antidiarrheal agent. It has the inhibitory effect against the activation of cellular STAT1/3/5 transcription.
价 格：￥电议型 号：T1563产 地：中国大陆
-
T15629JTE-013
JTE-013 is an effective and specific antagonist of S1P2. JTE-013 suppresses the specific binding of radiolabeled S1P to human and rat S1P2 (IC50s: 17 nM and 22 nM, respectively).
价 格：￥电议型 号：T15629产 地：中国大陆
-
-
T15624JNJ-64619178
JNJ-64619178 is a selective, orally active, and pseudo-irreversible inhibitor of protein arginine methyltransferase 5 (IC50: 0.14 nM). It has effective activity In lung cancer.
价 格：￥电议型 号：T15624产 地：中国大陆
-
T15623JNJ-61432059
JNJ-61432059 is an oral active and selective negative modulator of TARP γ?8 Selective AMPAR(pIC50: 9.7).
价 格：￥电议型 号：T15623产 地：中国大陆
