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：3801609
自主品牌
已选条件
-
T9969EZM0414EZM0414
EZM0414 is a potent, selective, orally bioavailable inhibitor of SETD2 with IC50 of 18 nM in SETD2 biochemical assay and IC50 of 34 nM in a cellular assay. EZM0414 can be used for the research of relapsed or refractory multiple myeloma and diffuse large B-cell lymphoma [1].
价 格：￥电议型 号：T9969产 地：中国大陆
-
T6145ZM39923 hydrochlorideZM 39923 HCl；JAK3 Inhibitor IV
ZM 39923 HCl is an JAK1/3 inhibitor with pIC50 of 4.4/7.1, almost no activity to JAK2 and modestly potent to EGFR; also found to be sensitive to transglutaminase.
价 格：￥电议型 号：T6145产 地：中国大陆
-
T5605EZM 2302GSK3359088
EZM2302 is a selective, and orally available arginine methyltransferase CARM1 inhibitor (IC50: 6 nM).
价 格：￥电议型 号：T5605产 地：中国大陆
-
T1764Adezmapimod4-(4-氟苯基)-2-(4-甲基亚磺酰基苯基)-5-(4-吡啶基)-1H-咪唑；PB 203580；RWJ 64809；SB203580
SB 203580 is a p38 MAPK inhibitor (IC50: 0.3-0.5 μM). It shows more than 100-fold selectivity over PKB, LCK, and GSK-3β.
价 格：￥电议型 号：T1764产 地：中国大陆
-
T5605EZM 2302EZM 2302,GSK3359088,
EZM2302 is a selective, and orally available arginine methyltransferase CARM1 inhibitor (IC50: 6 nM).
价 格：￥电议型 号：T5605产 地：美洲
-
T63800ZM223 hydrochloride；化合物 ZM223 hydrochlorideZM223 hydrochloride
ZM223 hydrochloride is a potent, non-covalent, orally active inhibitor of NEDD8 activase (NAE).
价 格：￥电议型 号：T63800产 地：中国大陆
-
T5605EZM 2302；化合物EZM 2302GSK3359088；GSK3359088
EZM 2302 (GSK3359088) is a selective, and orally available arginine methyltransferase CARM1 inhibitor (IC50: 6 nM).
价 格：￥电议型 号：T5605产 地：中国大陆
-
T36975EZM0414 TFA；EZM0414 三氟乙酸盐IPN-60210 TFA|||SETD2-IN-1 TFA；IPN-60210 TFA|||SETD2-IN-1 TFA
EZM0414 TFA (SETD2-IN-1 TFA) is a SETD2 inhibitor with anticancer and antiproliferative effects for the study of leukemia and immune dysfunction.
价 格：￥电议型 号：T36975产 地：中国大陆
-
T1991ZM323881 hydrochloride；化合物ZM 323881 hydrochlorideZM 323881 hydrochloride|||ZM 323881 HCl；ZM 323881 h
ZM323881 hydrochloride (ZM 323881 HCl) is a potent and selective VEGFR2 inhibitor.
价 格：￥电议型 号：T1991产 地：中国大陆
-
T1764Adezmapimod；化合物SB203580PB 203580|||RWJ 64809|||SB203580；PB 203580|||4-(4-氟苯基)-2-(4-甲基亚磺酰基苯基)-5-(4-吡啶
Adezmapimod (SB 203580) is a p38 MAPK inhibitor (IC50=0.3-0.5 μM) that is selective and ATP-competitive. Adezmapimod possesses autophagy and mitochondrial autophagy activating activity. Adezmapimod displays more than 100-fold higher selectivity than PKB, LCK, and GSK-3β.
价 格：￥电议型 号：T1764产 地：中国大陆
-
T1761PD153035 hydrochloride；化合物PD153035 hydrochlorideZM 252868 HCl|||AG 1517|||Tyrphostin AG 1517|||SU 52
PD153035 hydrochloride (ZM 252868) is a effective and selective inhibitor of EGFR (Ki: 5.2 pM, IC50: 29 pM); few influence against FGFR, PGDFR, InsR, CSF-1, and Src.
价 格：￥电议型 号：T1761产 地：中国大陆
-
T11251Ezetimibe ketone；化合物 T11251EZM-K；EZM-K
Ezetimibe, a compound known as a Niemann-Pick C1-like1 (NPC1L1) inhibitor and a potent Nrf2 activator, effectively inhibits cholesterol absorption. Additionally, Ezetimibe ketone (EZM-K) represents a phase-I metabolite of Ezetimibe.
价 格：￥电议型 号：T11251产 地：中国大陆
