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：3706169
自主品牌
已选条件
-
T6659SB 415286inhibit,GSK-3,Inhibitor,Glycogen synthase kinase 3,Glycogen synthase kinase-3,Apoptosis,SB-
SB415286 is a potent GSK3α inhibitor with IC50/Ki of 78 nM/31 nM with equally effective inhibition of GSK-3β.
价 格：￥电议型 号：T6659产 地：中国大陆
-
T6623OxibendazoleInhibitor,Apoptosis,inhibit,Parasite,Oxibendazole
Oxibendazole is a benzimidazole drug that interferes with metabolic pathways, used to protect against roundworms, strongyles, threadworms, pinworms and lungworm infestations in horses and some domestic pets.
价 格：￥电议型 号：T6623产 地：中国大陆
-
T8609CHEMBRDG-BB 7118966CHEMBRDGBB 7118966,CHEMBRDG BB 7118966
CHEMBRDG-BB 7118966 is an inhibitor of Bromodomain-containing protein 4 (human).
价 格：￥电议型 号：T8609产 地：中国大陆
-
T6766AtipamezoleAdrenergic Receptor,Beta Receptor,Atipamezole,MPV-1248,Inhibitor,MPV1248,inhibit
Atipamezole is a synthetic α2 adrenergic receptor antagonist. It has also been researched in humans as a potential anti-Parkinsonian drug.
价 格：￥电议型 号：T6766产 地：中国大陆
-
T8410ASP7663pain,ASP-7663,inhibit,TRP Channel,ASP7663,Transient receptor potential channels,Inhibitor,ASP
ASP7663 is a TRPA1 Receptor Agonist and exhibiting an abdominal analgesic effect in vivo.
价 格：￥电议型 号：T8410产 地：中国大陆
-
T22947LY266097 hydrochlorideLY-266097 hydrochloride,LY266097 hydrochloride
LY266097 hydrochloride is an antagonist of 5-HT2 with pKis of 7.7, 9.8, and 7.6 for human 5-HT2A, 5-HT2B, and 5-HT2C and can be used in studies about depression.
价 格：￥电议型 号：T22947产 地：中国大陆
-
T6671SirtinolSirtuin,Autophagy,Sirtinol,Apoptosis,Inhibitor,inhibit
Sirtinol is a selective SIRT1/2 inhibitor (IC50: 131/38 μM).
价 格：￥电议型 号：T6671产 地：中国大陆
-
T9104TJ191cancer,TJ 191,Apoptosis,PMBC,MOLT-3,CEM,inhibit,C8166,Inhibitor,MOLT-4,MT-2,TJ191,HSB-2,TJ-191,
TJ191 is a selective anti-cancer agent, targeting low TβRIII-expressing malignant T-cell leukemia/lymphoma cells.
价 格：￥电议型 号：T9104产 地：中国大陆
-
T6649(S)-(+)-RolipramTNFα,tumor,inhibit,(S)(+)Rolipram,mononuclear,Apoptosis,phosphodiesterase,(S) (+) Ro
S-(+)-Rolipram inhibits human monocyte cyclic AMP-specific PDE4 with IC50 of 0.75 μM, has anti-inflammatory and anti-depressant activity in the central nervous system, less potent than its R enantiomer.
价 格：￥电议型 号：T6649产 地：中国大陆
-
T60663LOseltamivir acid methyl ester hydrochlorideOseltamiviracidmethylesterhydrochloride
Oseltamivir acid methyl ester hydrochloride is a precursor form of oseltamivir acid. Oseltamivir acid methyl ester is converted to oseltamivir acid converted by carboxylesterase 1 (CES1).
价 格：￥电议型 号：T60663L产 地：中国大陆
-
T6853GSK591GSK 591,EPZ-015866,GSK591,Inhibitor,GSK 3203591,EPZ 015866,inhibit,GSK-3203591,GSK-591,Histone
GSK591, Alternative Names are EPZ015866, GSK3203591, is a potent selective inhibitor of the arginine methyltransferase PRMT5 (IC50=11 nM).
价 格：￥电议型 号：T6853产 地：中国大陆
-
TN3669Cis-N-FeruloyltyramineCis N Feruloyltyramine,CisNFeruloyltyramine
Cis-N-Feruloyltyramine shows cytotoxicity against the P-388 cancer cell line. N-cis-Feruloyltyramine and N-trans-Feruloyltyramine are the inhibitors of in vitro prostaglandin (PG) synthesis.
价 格：￥电议型 号：TN3669产 地：中国大陆
-
T17247VU0661013
VU0661013 is an effective and selective inhibitor of MCL-1.
价 格：￥电议型 号：T17247产 地：中国大陆
-
T6893MK-886leukotriene,FLAP,5-LOX,5-LO activating protein,non-competitive,L-663536,L663536,keratin-1,Leuk
MK-886 is an inhibitor of leukotriene biosynthesis, inhibiting 5-lipoxygenase-activating protein (FLAP). It is also a moderately potent PPARα antagonist.
价 格：￥电议型 号：T6893产 地：中国大陆
-
T6697TCIDhydrolase,C-terminal,Neuronal,Deubiquitinase,transporter,ubiquitination,DUBs,inhibit,TCID,glycin
TCID(IC50=0.6 μM) is a DUB inhibitor of ubiquitin C-terminal hydrolase L3. It has the 125-fold selectivity to L1.
价 格：￥电议型 号：T6697产 地：中国大陆
-
T36683VedaprofenVedaprofen,Inhibitor,nonsteroidal,PM150,PM-150,Escherichia coli,inhibit,CERM-10202,CERM102
Vedaprofen inhibits COX-1 and reduces prostaglandin H2 synthesis with anti-inflammatory activities. Vedaprofen is an inhibitor of Escherichia coli sliding clamp with the IC50 of 222 μM and Ki of 131 μM.
价 格：￥电议型 号：T36683产 地：中国大陆
-
T11665Ionomycin calciumCa2+ channels,PKC,ionophore,Calcium Channel,Ionomycin,SQ 23377,Ionomycin calcium,An
lonomycin calcium is a potent, selective calcium ionophore and an antibiotic produced by Streptomyces conglobatus. also induces the activation of protein kinase C (PKC). Ionomycin calcium is highly specific for divalent cations (Ca>Mg>Sr=Ba). Ionomycin promotes apoptosis.
价 格：￥电议型 号：T11665产 地：中国大陆
-
T6629PYR-41E3 ligating enzyme,E1 activating enzyme,E1/E2/E3 Enzyme,Inhibitor,PYR-41,Ubiquitin conjugating
PYR-41 is the first cell-permeable inhibitor of ubiquitin-activating enzyme E1, with no activity at E2.
价 格：￥电议型 号：T6629产 地：中国大陆
-
T64366WAY-606956WAY606956
WAY-606956 is a GSK-3 inhibitor with IC50 of 0.101-1 μM of GSK-3α and GSK-3β in Calipe Assay.
价 格：￥电议型 号：T64366产 地：中国大陆
-
T6609NMS-E973NMS-E973,Leukemia,NMS E973,inhibit,HSP,Heat shock proteins,Adenocarcinoma,Hsp90α,ovary,colon
NMS-E973 is a potent and selective Hsp90 inhibitor with DC50 of <10 nM for Hsp90 binding, no activiy against a panel of 52 diverse protein kinases.
价 格：￥电议型 号：T6609产 地：中国大陆
