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：3711574
自主品牌
已选条件
-
T0794Mepenzolate BromideHCAR2,PUMA-G,inhibit,Muscarinic acetylcholine receptor,Inhibitor,hM3R,gastrointes
Mepenzolate Bromide is a muscarinic antagonist used to treat gastrointestinal conditions.
价 格：￥电议型 号：T0794产 地：中国大陆
-
T8725A 582941 HCl (848591-90-2(free base))A 582941 HCl (848591902(free base)),A 582941 HCl (848591 90 2(f
A-582941 is a alpha7 neuronal nicotinic receptor agonist with broad spectrum cognition-enhancing properties
价 格：￥电议型 号：T8725产 地：中国大陆
-
T8808LLYN-1604 dihydrochlorideanti-tumor,Unc-51 like kinase,negative,LYN-1604,LYN 1604,cancer,Autophagy,br
LYN-1604 is a novel ULK1 activator.It inducing cell death involved in ATF3, RAD21, and caspase3, accompanied by autophagy and apoptosis.
价 格：￥电议型 号：T8808L产 地：中国大陆
-
T6583MG-101RKO,MG-101,colon cancer,Bax,HepG2,Proteasome,MG 101,Inhibitor,mitochondria,HCT116,inhibit,Apop
MG-101 (ALLN) is a cell-permeable and potent inhibitor of cysteine proteases including calpains and lysosomal cathepsins.
价 格：￥电议型 号：T6583产 地：中国大陆
-
T6572Lorcaserin HClLorcaserin HCl
Lorcaserin is a selective serotonin agonist that has been recently approved as a weight loss agent.
价 格：￥电议型 号：T6572产 地：中国大陆
-
T15465HC-070
HC-070 is a TRPC5 and TRPC4 antagonist (IC50 = 9.3 nM and 46 nM).
价 格：￥电议型 号：T15465产 地：中国大陆
-
T6503Fluorometholone AcetateInhibitor,Carbonate dehydratase,Fluorometholone,Fluorometholone Acetate,hCA-I
Fluorometholone Acetate is a synthetic corticosteroid, used in the treatment of steroid responsive inflammatory conditions of the eye.
价 格：￥电议型 号：T6503产 地：中国大陆
-
T8800NSAHDNA/RNA Synthesis,HCT116,MDA-231,Panc1,Inhibitor,NSAH,inhibit,S-phase
NSAH is a nonnucleoside inhibitor of human ribonucleotide reductase (hRR).with cell-free IC50 of 32 μM and cell-based IC50 of ~250 nM, respectively.
价 格：￥电议型 号：T8800产 地：中国大陆
-
T8313HCH6-1inhibit,inflammatory,FPR1,HCH6-1,cell infiltration,HCH6 1,antagonist,pulmonary,acute lung inju
HCH6-1 is a competitive Formyl peptide receptor 1 (FPR1) antagonist.
价 格：￥电议型 号：T8313产 地：中国大陆
-
T8500VLX600iron,HCT116,Autophagy,glycolytic,VLX 600,colon,chelator,cancer,OXPHOS,VLX600,Mitochondrial Met
VLX600 is an iron-chelating oxidative phosphorylation (OXPHOS) inhibitor, is a cell-permeable anticancer agent. It acts by reducing mitochondrial oxidative phosphorylation in tumor cells.
价 格：￥电议型 号：T8500产 地：中国大陆
-
T6148CX-6258 hydrochlorideCX6258 hydrochloride,Pim,CX6258,CX-6258,Pim kinases,4E-BP1,CX 6258 hydrochlorid
CX-6258 HCl is an effective, orally efficacious Pim1/2/3 kinase inhibitor (IC50: 5/25/16 nM).
价 格：￥电议型 号：T6148产 地：中国大陆
-
T8931LICCB-19 hydrochlorideICCB19,ubiquitination,cIAP2,TRADD,cIAP1,RDA,ICCB 19 hydrochloride,Receptor-inte
ICCB-19 HCl is an inhibitor of TRADD (TNFRSF1A Associated Via Death Domain). It binds to a pocket on the N-terminal TRAF2-binding domain of TRADD (TRADD-N), which interacts with the C-terminal domain (TRADD-C) and TRAF2 to modulate the ubiquitination of RIPK1 and beclin 1.
价 格：￥电议型 号：T8931L产 地：中国大陆
-
T8416Capmatinib xHClApoptosis,c-Met/HGFR,ATP competitive,inhibit,INC-280,Inhibitor,Capmatinib,SNU-5,INCB-
Capmatinib xHCl is a potent, orally active, selective, and ATP competitive c-Met kinase inhibitor, potently blocking in vitro kinase activity (IC50 = 0.13 nM) as well as constitutive or HGF-stimulated activity in cells (IC50 values range from 0.3 to 1.1 nM).
价 格：￥电议型 号：T8416产 地：中国大陆
-
T8827EMAC10101dEMAC-10101d,Carbonic Anhydrase,hCA II,EMAC10101d,Inhibitor,inhibit,Carbonate dehydratase
compound EMAC10101d, bearing a 2,4-dichorophenyl substituent in position 4 of the dihydrothiazole ring, was the most potent and selective toward hCA II with an inhibitory activity in the low nanomolar range.
价 格：￥电议型 号：T8827产 地：中国大陆
-
T11227L1Eravacycline HCl
Eravacycline HCl is potent antibiotic with broad-spectrum antibacterial activity.
价 格：￥电议型 号：T11227L1产 地：中国大陆
-
T6729LomibuvirRdRp,Lomibuvir,cis-Lomibuvir,cis-isomer,DNA/RNA Synthesis,HCV,inhibit,Inhibitor,non-nucleos
Lomibuvir (VX-222) is a selective, non-nucleoside allosteric inhibitor of HCV NS5B polymerase (RdRp) with a Kd of 17 nM. Lomibuvir inhibits the 1b/Con1 HCV subgenomic replicon with an EC 50 of 5.2 nM. Lomibuvir preferentially inhibits elongative RNA synthesis rather than de novo -initiated RNA synthesis [1].
价 格：￥电议型 号：T6729产 地：中国大陆
-
T34374RO5203648 HClRO5203648 HCl,RO-5203648 HCl
RO5203648 HCl is a partial agonist of trace amine-related receptor 1 (TAAR1) with antipsychotic and antidepressant-like activities. RO5203648 HCl can be used in studies about neuropsychiatric therapeutics.
价 格：￥电议型 号：T34374产 地：中国大陆
-
T7401(S)-3-AMino-2-Methylpropanoic acid-HCl(S) 3 AMino 2 Methylpropanoic acid HCl,(S)3AMino2Methylpropano
(S)-3-AMino-2-Methylpropanoic acid-HCl is a chemical compound.
价 格：￥电议型 号：T7401产 地：中国大陆
-
T7811Pilsicainide HClatrial tachyarrhythmias,SUN-1165,Pilsicainide HCl,antiarrhythmic,inhibit,orally acti
Pilsicainide HCl is a pure sodium channel blocker
价 格：￥电议型 号：T7811产 地：中国大陆
-
T28145ND-322 HClND 322 HCl
ND-322 HCl is a selective inhibitor of MT1-MMP and MMP2 and reduces in vitro melanoma cell growth, migration and invasion.
价 格：￥电议型 号：T28145产 地：中国大陆
