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：3494310
自主品牌
已选条件
-
TP1309Gastric mucinAntibiotic,inhibit,Inhibitor,Gastric mucin,Bacterial
Gastric mucin is a large glycoprotein which is thought to play a major role in the protection of the gastrointestinal tract from acid, proteases, pathogenic microorganisms, and mechanical trauma.
价 格：￥电议型 号：TP1309产 地：中国大陆
-
T7101Tyrphostin AG30HER1,ErbB-1,Inhibitor,EGFR,Tyrphostin AG30,Epidermal growth factor receptor,Tyrphosti
Tyrphostin AG30 (AG30) is a potent protein tyrosine kinases (PTK) inhibitor.
价 格：￥电议型 号：T7101产 地：中国大陆
-
T9179CLP-3094LNCaP,Inhibitor,Androgen Receptor,CLP3094,inhibit,prostate,CLP 3094,resistance,CLP-3094,anti
CLP-3094 is a potent androgen receptor BF3 (binding function 3) inhibitor. BF3-IN-1 inhibits AR transcriptional activity with IC50 of 4 μM. CLP-3094 is a selective and potent GPR142 antagonist.
价 格：￥电议型 号：T9179产 地：中国大陆
-
T9230KM 91104V-ATPase human HSC,a3-b2 subunits,KM-91104,KM 91104,Inhibitor,KM91104,Proton Pump,cell-perme
KM 91104 is a cell permeable inhibitor of V-ATPase. KM91104 specifically targets the interaction between V-ATPase subunit A3 and subunit B2.
价 格：￥电议型 号：T9230产 地：中国大陆
-
T9085JFD01307SCJFD-01307SC,Inhibitor,Bacterial,JFD01307SC,inhibit
JFD01307SC is a glutamine synthetase inhibitor. It is anti-tuberculosis agent and acts as a mimic of L-Glutamate and thus target enzymes involved in glutamine biosynthesis.
价 格：￥电议型 号：T9085产 地：中国大陆
-
-
T7293EC330EC-330,EC 330,EC330,inhibit,Inhibitor
EC330, a novel steroidal LIF inhibitor showed cytotoxicity in various cancer cell lines and NCI-60 cell line panel at low nano-molar range.
价 格：￥电议型 号：T7293产 地：中国大陆
-
T6530HC-030031HC-030031,HC 030031,TRP Channel,Transient receptor potential channels,Inhibitor,inhibit
HC-030031 is a potent TRPA1 inhibitor, which antagonizes AITC- and formalin-evoked calcium influx with IC50s of 6.2±0.2 and 5.3±0.2 μM, respectively.
价 格：￥电议型 号：T6530产 地：中国大陆
-
T7309TAS-103 dihydrochlorideBMS247615,Topoisomerase,TAS-103,TAS103,inhibit,TAS 103 dihydrochloride,BMS-24
TAS-103 (dihydrochloride) is a novel anticancer agent targeting both topoisomerase (Topo) I and Topo II.
价 格：￥电议型 号：T7309产 地：中国大陆
-
T36994MRT 67307 dihydrochlorideMRT 67307 dihydrochloride
MRT 67307 dihydrochloride is a dual inhibitor of the IKKε and TBK-1 with IC50s of 160 and 19 nM, respectively. MRT67307 dihydrochloride also inhibits ULK1 and ULK2 with IC50s of 45 and 38 nM, respectively. MRT67307 dihydrochloride also blocks autophagy in cells.
价 格：￥电议型 号：T36994产 地：中国大陆
-
T7152Ravuconazoleinhibit,ER30346,BMS207147,Ravuconazole,BMS 207147,Fungal,ER 30346,Inhibitor
Ravuconazole is a potent triazole antifungal that potently inhibits a wide range of fungi.
价 格：￥电议型 号：T7152产 地：中国大陆
-
TQ0082AticaprantCERC 501,inhibit,LY2456302,Opioid Receptor,Aticaprant,Inhibitor,CERC501,LY 2456302
Aticaprant (CERC-501) is a potent and centrally-penetrant antagonist of the kappa-opioid receptor (Ki: 0.807 nM).
价 格：￥电议型 号：TQ0082产 地：中国大陆
-
TN2230Soyasaponin BaInhibitor,Soyasaponin Ba,inhibit
Soyasaponin Ba may represent viable candidates for effective vaccine adjuvants due to their higher and lower or non-haemolytic effects.Soyasaponins Ab and Bb prevent scopolamine-induced memory impairment in mice without the inhibition of acetylcholinesterase.
价 格：￥电议型 号：TN2230产 地：中国大陆
-
T10730CDC801
CDC801 is an inhibitor of PDE4 and TNF-α with IC50s of 1.1 μM and 2.5 μM, respectively.
价 格：￥电议型 号：T10730产 地：中国大陆
-
T22835H2L5186303
H2L5186303 is an LPA2 antagonist and can be used in studies about asthma treatment.
价 格：￥电议型 号：T22835产 地：中国大陆
-
T8230PNU112455A hydrochlorideanticooperative,Cyclin dependent kinase,PNU112455A hydrochloride,Alzheimer’s
PNU 112455A is an ATP site competetive inhibitor of CDK2 and CDK5,binds to the ATP site of CDK2 and CDK5 with Kms of 3.6 and 3.2 μM, respectively.
价 格：￥电议型 号：T8230产 地：中国大陆
-
T8233BRD3308β-cells,glucolipotoxicity,inflammatory,BRD-3308,Human immunodeficiency virus,BRD3308,Histone
BRD3308 is a highly selective inhibitor of HDAC3(IC50 of 54 nM), attenuating PE-mediated phosphorylation of ERK but not JNK.
价 格：￥电议型 号：T8233产 地：中国大陆
-
T6422Brimonidine TartrateUK-14304,UK14304,AGN190342,Brimonidine,Adrenergic Receptor,AGN-190342,AGN 190342
Brimonidine tartrate is a quinoxaline derivative and adrenergic α-2 receptor agonist (EC50: 0.45 nM) that is used to manage intraocular pressure associated with open-angle glaucoma or ocular hypertension.
价 格：￥电议型 号：T6422产 地：中国大陆
-
T6878LJI308viability,Ribosomal S6 Kinase (RSK),LJI-308,stimulation,phosphorylation,LJI308,inhibit,mutatio
LJI308 is a potent, and pan-RSK (p90 ribosomal S6 kinase) inhibitor with IC50 of 6 nM, 4 nM, and 13 nM for RSK1, RSK2, and RSK3, respectively.
价 格：￥电议型 号：T6878产 地：中国大陆
-
T67729UCM-1306UCM1036
UCM-1306 is a potent and orally active allosteric modulator (PAM) of human dopamine D1 receptor. UCM-1306 could increase the maximal effect of endogenous dopamine (DA) both in human and mouse D1 receptors. UCM-1306 could improve motor symptoms and address the key comorbid cognitive impairment associated with long-term Parkinson’s disease (PD).
价 格：￥电议型 号：T67729产 地：中国大陆
