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：3811254
自主品牌
已选条件
-
TP1996MCH(human, mouse, rat)MCH(human, mouse, rat),inhibit,MCHR1 (GPR24),Inhibitor,Melanin concentrating h
Potent endogenous agonist at melanin-concentration hormone (MCH) receptors (IC50 values are 0.3 and 1.5 nM and EC50 values are 3.9 and 0.1 nM at MCH1 and MCH2 receptors respectively). Increases food intake in vivo.
价 格：￥电议型 号：TP1996产 地：中国大陆
-
T24159IHR-1IHR 1；IHR1
IHR-1 is a Potent Smo antagonist (IC50 = 7.6 nM). Selectively inhibits Hedgehog signaling over Wnt and Notch signaling pathways. Blocks Smo accumulation in primary cilium in vitro.
价 格：￥电议型 号：T24159产 地：中国大陆
-
T11966MCHR1 antagonist 2
MCHR1 antagonist 2 is an antagonist of melanin-concentratin hormone receptor 1(MCH1-R, IC50 = 65 nM) and also inhibits hERG.
价 格：￥电议型 号：T11966产 地：中国大陆
-
T82176HR1；化合物 HR1HR1
HR1, a mastoid protease, enhances the permeability of human erythrocyte membranes and can induce cytoplasmic membrane permeation in bacteria and mast cells [1].
价 格：￥电议型 号：T82176产 地：中国大陆
-
T72146Loxoprofenol-SRS tromethamine；化合物 Loxoprofenol-SRS tromethamineHR1405–01；HR1405–01
Loxoprofenol-SRS tromethamine (HR1405-01), the active metabolite of Loxoprofen, represents a non-steroidal anti-inflammatory drug (NSAID) designed for intravenous administration. It is recognized for its enhanced anti-inflammatory and analgesic properties, positioning it as a safe option within its class.
价 格：￥电议型 号：T72146产 地：中国大陆
-
T71111Famitinib malate；化合物 Famitinib malateSHR1020 malate；SHR1020 malate
Famitinib malate (SHR1020) is an orally active multi-targeted kinase inhibitor that effectively inhibits the activity of c-kit, VEGFR-2, and PDGFRβ with IC50 values of 2.3 nM, 4.7 nM, and 6.6 nM, respectively. It induces cell apoptosis and demonstrates potent antitumor activity in human gastric cancer cells and xenografts, making it a valuable compound for cancer research.
价 格：￥电议型 号：T71111产 地：中国大陆
-
T68796Thr101；化合物 Thr101Thr101
Thr101, also known as NOX Inhibitor VII, is a dose-dependent inhibitor of HDAC1, HDAC3, HDAC4, HDAC5, HDAC6, HDAC7, HDAC8, and HDAC9. Thr101 is also a NOX inhibitor.
价 格：￥电议型 号：T68796产 地：中国大陆
-
T39960SHR168442SHR168442SHR168442
SHR168442 is a potent RORγ modulator, exhibiting an IC50 value of 0.035 μM.
价 格：￥电议型 号：T39960产 地：中国大陆
-
T29749AHR-16329；化合物 T29749AHR16329；AHR16329
AHR-16329 can be used in ocular pharmacology.
价 格：￥电议型 号：T29749产 地：中国大陆
-
T27829Lidamidine Hydrochloride；化合物 T27829WHR1142A|||WHR-1142A|||Lidaral|||WHR 1142A；WHR1142A|||WHR-1142A||
Lidamidine Hydrochloride is an alpha2-adrenergic receptor agonist. Lidamidine Hydrochloride inhibits intestinal secretion, reduces intestinal transit, and inhibits smooth muscle contraction.
价 格：￥电议型 号：T27829产 地：中国大陆
-
T26777Besigliptin Tosylate；化合物 T26777SHR 117887|||SHR-117887|||SHR117887；SHR 117887|||SHR-117887|||SHR1178
Besigliptin Tosylate, a DPP-4 inhibitor, is used potentially for the treatment of type 2 diabetes.
价 格：￥电议型 号：T26777产 地：中国大陆
-
T23679AHR-13268D；化合物 T23679AHR 13268D|||AHR13268D；AHR 13268D|||AHR13268D
AHR-13268D is a new agent of antiallergic/antihistaminic.
价 格：￥电议型 号：T23679产 地：中国大陆
-
T23677AHR-10718；化合物 T23677AHR10718|||AHR 10718；AHR10718|||AHR 10718
AHR-10718 has an antiarrhythmic effect.
价 格：￥电议型 号：T23677产 地：中国大陆
-
T12904SHR1653；化合物 T12904SHR1653
SHR1653 is a highly potent, selective and brain penetrated antagonist of oxytocin receptor (OTR)(IC50 of 15 nM for hOTR).
价 格：￥电议型 号：T12904产 地：中国大陆
-
T11966MCHR1 antagonist 2；化合物MCHR1 antagonist 2MCHR1 antagonist 2
MCHR1 antagonist 2 is an antagonist of melanin-concentratin hormone receptor 1(MCH1-R, IC50 = 65 nM) and also inhibits hERG.
价 格：￥电议型 号：T11966产 地：中国大陆
-
T10173MCHR1 antagonist 1；化合物 T10173MCHR1 antagonist 1
MCHR1 antagonist 1 is a selective antagonist of melanin-concentrating hormone-1 (MCH1) receptor (Kb: 1 nM, Ki: 4 nM at human MCH1).
价 格：￥电议型 号：T10173产 地：中国大陆
