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：3806030
自主品牌
已选条件
-
T17276Zonampanel；唑南帕奈YM 872；YM 872|||唑南帕奈
Zonampanel is a selective glutamate receptor subtype, α-amino-3-hydroxy-5-methylisoxazole-4-propionic acid receptor antagonist.
价 格：￥电议型 号：T17276产 地：中国大陆
-
T17275YM348；化合物 T17275YM348
YM348 is an effective and orally active 5-HT2C receptor agonist. YM348 also shows a high affinity for the cloned human 5-HT2C receptor (Ki: 0.89 nM).
价 格：￥电议型 号：T17275产 地：中国大陆
-
T17274YM022化合物 T17274YM022|||YM-022
YM022 is a highly effective and selective gastrin/cholecystokinin (CCK)-B receptor antagonist. YM022 can inhibit gastrin-induced gastric acid secretion and histidine decarboxylase activation in vivo. YM022 shows the Ki values of 68 pM and 63 nM for CCK-B and CCK-A receptor, respectively.
价 格：￥电议型 号：T17274产 地：中国大陆
-
T17273YM-254890；化合物 T17273YM-254890
YM-254890 inhibits platelet aggregation induced by ADP by blocking the P2Y1 signal transduction pathway (IC50: below 0.6 μM). YM-254890 is a selective Gαq/11 protein inhibitor. YM-254890 displays no inhibition of other G protein subtypes.
价 格：￥电议型 号：T17273产 地：中国大陆
-
T17272YKL-06-062；化合物YKL-06-062YKL-06-062
YKL-06-062 is a second-generation salt-inducible kinase (SIK) inhibitor that inhibits SIK1, SIK2 and SIK3 with IC50s of 2.12 nM, 1.40 nM and 2.86 nM.
价 格：￥电议型 号：T17272产 地：中国大陆
-
T17271YKL-05-099；化合物YKL-05-099YKL-05-099
YKL-05-099 is an inhibitor of the salt-inducible kinase(SIK1 and SIK3 ; IC50s: 10 and 30 nM, respectively). It has a slightly less potent SIK2-inhibitory (IC50:40 nM).
价 格：￥电议型 号：T17271产 地：中国大陆
-
T17274-Cyclohexyl-1-phenylthiosemicarbazide；4-环己基-1-苯氨基硫脲4-Cyclohexyl-1-phenylthiosemicarbazide
4-Cyclohexyl-1-phenylthiosemicarbazide is employed as an intermediate.
价 格：￥电议型 号：T1727产 地：中国大陆
-
T17269Y-27152；化合物 T17269Y-27152
Y-27152 is a prodrug of the KATP (Kir6) channel opener Y-26763 and is a long-acting K+ channel opener.
价 格：￥电议型 号：T17269产 地：中国大陆
-
T17268Y-26763化合物 T17268Y 26763|||Y26763
Y-26763 is a K+ channel opener and active metabolite of Y-27152. This is an ATP-sensitive K+ (KATP) channel activator.
价 格：￥电议型 号：T17268产 地：中国大陆
-
T17267XL228；化合物XL228XL228
XL228 is an inhibitor of multi-targeted tyrosine kinase (IC50s: 5, 3.1, 1.6, 6.1, 2 nM for Bcr-Abl, Aurora A, IGF-1R, Src, and Lyn, respectively).
价 格：￥电议型 号：T17267产 地：中国大陆
-
T17266Xipamide；希伯胺Diurexan|||Aquaphor；希伯胺|||Diurexan|||Aquaphor
Xipamide (Diurexan) is a sulfonamide-based diuretic with antihypertensive properties. Xipamide selectively inhibits anion exchanger.
价 格：￥电议型 号：T17266产 地：中国大陆
-
T17265Ximelagatran；希美加群EXANTA|||H 376-95|||H37695|||H 376/95|||H-37695|||H 37695；EXANTA|||H 376-95|||H3769
Ximelagatran (H 376-95), a direct thrombin inhibitor, can be taken orally and acts solely by inhibiting the actions of thrombin. Ximelagatran is converted to the active agent melagatran in vivo.
价 格：￥电议型 号：T17265产 地：中国大陆
-
T17264Xenalamine；联苯酰胺苯酸Xenazoic acid|||CV58903；Xenazoic acid|||联苯酰胺苯酸|||CV58903
Xenalamine is a synthetic compound of antiviral.
价 格：￥电议型 号：T17264产 地：中国大陆
-
T17263XEN907；化合物 T17263XEN907
XEN907 is a novel spiro oxindole NaV1.7 blocker. XEN907 also inhibits hNaV1.7 (IC50: 3 nM).
价 格：￥电议型 号：T17263产 地：中国大陆
-
T17262XE 991 dihydrochloride；化合物XE 991 dihydrochlorideXE 991 dihydrochloride
XE 991 dihydrochloride is a Kv7 (KCNQ) channel blocker. XE 991 dihydrochloride potently inhibits Kv7.1 (KCNQ1), Kv7.2 (KCNQ2), Kv7.2 + Kv7.3 (KCNQ3) channel, and M-current (IC50s: 0.75 μM, 0.71 μM, 0.6 μM, and 0.98 μM, respectively).
价 格：￥电议型 号：T17262产 地：中国大陆
-
T17261Xantocillin；黄青霉素Xantocillin
Xanthocillin is a marine agent. Xanthocillin also induces autophagy through inhibition of the MEK/ERK pathway.
价 格：￥电议型 号：T17261产 地：中国大陆
-
T17260WWL70；化合物WWL70WWL70
WWL70 is a selective alpha/beta hydrolase domain 6 inhibitors (IC50: 70 nM).
价 格：￥电议型 号：T17260产 地：中国大陆
-
T1726SB-431542；化合物SB 431542SB 431542；4-[4-(1,3-苯并二唑-5-基)-5-(2-吡啶基)-1H-咪唑-2-基]-苯酰胺水合物|||SB 431542
SB-431542 is an inhibitor of ALK5/TGF-β type I Receptor (IC50=94 nM) and is selective. SB 431542 also has inhibitory activity against ALK4 and ALK7 but not other proteins. SB 431542 can be used for induced differentiation of stem cells.
价 格：￥电议型 号：T1726产 地：中国大陆
-
T17259WWL113；化合物 T17259WWL113
WWL113 is a selective and orally active Ces3 and Ces1f inhibitor (IC50: 120 nM and 100 nM for Ces3 and Ces1f, respectively). WWL113 appears to display excellent selectivity for the 60-kDa serine hydrolase.
价 格：￥电议型 号：T17259产 地：中国大陆
-
T17258WRG-28；化合物WRG-28WRG-28
WRG-28 is a potent and selective, allosteric discoidin domain receptor 2 (ddr2) inhibitor(IC50 : 230 nM)
价 格：￥电议型 号：T17258产 地：中国大陆
