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：3769941
自主品牌
已选条件
-
T70403VUF14480；化合物 VUF14480VUF14480
VUF14480 is a covalent partial agonist that interacts with cysteine 98(3.36) of the human histamine H? receptor. VUF14480 was shown to be a partial agonist of hH4 receptor-mediated G protein signalling and β-arrestin2 recruitment. VUF14480 bound covalently to the hH? receptor with submicromolar affinity. Serine substitution of C98(3.36) prevented this covalent interaction.
价 格：￥电议型 号：T70403产 地：中国大陆
-
T69921BRF110；化合物 BRF110BRF110
BRF110 is a brain penetrant, potent and selective agonist of nuclear receptor-related 1 (Nurr1):Retinoid X receptor α (RXRα) heterodimer. BRF110 is a neuroprotective agent that prevents dopaminergic neuron demise and striatal dopaminergic denervation in vivo against PD-causing toxins. It induced dopamine biosynthesis in vivo. BRF110 chronic dosing does not induce dyskinesia in mice model.
价 格：￥电议型 号：T69921产 地：中国大陆
-
T69775VUF14862；化合物 VUF14862VUF14862
VUF14862 is a robust and fatigue-resistant photoswitchable GPCR antagonist.
价 格：￥电议型 号：T69775产 地：中国大陆
-
T69774VUF14738；化合物 VUF14738VUF14738
VUF14738 is a robust and fatigue-resistant photoswitchable GPCR antagonist.
价 格：￥电议型 号：T69774产 地：中国大陆
-
T69654VUF16839；化合物 VUF16839VUF16839
VUF16839 is a high-affinity non-imidazole histamine H3 receptor agonist.
价 格：￥电议型 号：T69654产 地：中国大陆
-
T68499F15845 HBr；化合物 F15845 HBrF15845 HBr
F 15845 is a blocker of the persistent sodium current prevents consequences of hypoxia in rat femoral artery. F15845 has been shown to selectively inhibit the persistent sodium current of Nav1.5[1] exerting cardioprotective effects following ischemia. In vitro testing showed minimal effects of F15845 on other important ion channels of the heart, including major Ca2+ and K+ channels.[1] This characteristic is thought to account for the limited effect of F15845 to change other heart parameters suc
价 格：￥电议型 号：T68499产 地：中国大陆
-
T68058Dulozafone；度氯扎封F1933；F1933
Dulozafone (F1933) has an anti- showed anticonvulsant activity in a brain amygdala ignition model and protected fully ignited rats from generalized seizures.
价 格：￥电议型 号：T68058产 地：中国大陆
-
T67837(3S)-GSK-F1；化合物 GSK-F1PI4KA inhibitor-F1；PI4KA inhibitor-F1
(3S)-GSK-F1 is a selective small molecule inhibitor of Type III Phosphatidylinositol 4?Kinase Alpha (PI4KIIIα), pIC50=8.3.
价 格：￥电议型 号：T67837产 地：中国大陆
-
T6682STF-118804；化合物STF118804STF 118804|||STF118804；STF 118804|||STF118804
STF-118804 is a highly specific NAMPT inhibitor; reduces the viability of most B-ALL cell lines with IC50 <10 nM.
价 格：￥电议型 号：T6682产 地：中国大陆
-
T6667SF1670；化合物SF1670PTP CD45 Inhibitor|||PTPase CD45 Inhibitor；PTP CD45 Inhibitor|||PTPase CD45 Inhibito
SF1670 (PTPase CD45 Inhibitor) is a specific PTEN inhibitor with IC50 of 2 μM.
价 格：￥电议型 号：T6667产 地：中国大陆
-
T66657VUF11207 trifluoroacetate salt；化合物 VUF11207 trifluoroacetate saltVUF11207 trifluoroacetate salt
VUF11207 trifluoroacetate salt is a useful organic compound for research related to life sciences. The catalog number is T66657 and the CAS number is 1378524-41-4.
价 格：￥电议型 号：T66657产 地：中国大陆
-
T6525GW 5074化合物GW5074GW5074|||3-(3,5-二溴-4-羟基苯亚甲基)-5-碘-1,3-二氢吲哚-2-酮|||Raf1 Kinase Inhibitor I
GW 5074 (Raf1 Kinase Inhibitor I)(IC50=9 nM) is an effective and specific c-Raf inhibitor. It has no effect on the activities of JNK1/2/3, MEK1, MKK6/7, CDK1/2, c-Src, p38 MAP, VEGFR2 or c-Fms.
价 格：￥电议型 号：T6525产 地：中国大陆
-
T6513Bisindolylmaleimide I；化合物Bisindolylmaleimide IGF109203X|||Go 6850；GF109203X|||Go 6850|||3-[1-[3-(二甲氨
Bisindolylmaleimide I (GF109203X) is a potent and highly selective protein kinase C (PKC) inhibitor with a Ki of 14 nM.
价 格：￥电议型 号：T6513产 地：中国大陆
-
T64068KIF18A-IN-3；化合物 KIF18A-IN-3KIF18A-IN-3
KIF18A-IN-3 is a potent inhibitor of KIF18A with an IC50 value of 61 nM. KIF18A-IN-3 significantly causes mitotic arrest and increases the number of mitotic cells in tumour tissue. kIF18A-IN-3 can be used to study tumours.
价 格：￥电议型 号：T64068产 地：中国大陆
-
T64066CSF1R-IN-3；化合物CSF1R-IN-3CSF1R-IN-3
CSF1R-IN-3 is an orally effective CSF-1R inhibitor with an IC50 value of 2.1 nM. CSF1R-IN-3 has anti-proliferative activity against colorectal cancer cells. CSF1R-IN-3 exhibits anti-tumour effects and immune enhancing effects by inhibiting the migration of macrophages and inducing the reprogramming of M2-type macrophages to M1-type macrophages, thus exhibited activity against colorectal cancer cells.
价 格：￥电议型 号：T64066产 地：中国大陆
-
T62851SLF1081851 TFA；化合物 SLF1081851 TFASLF1081851 TFA
SLF1081851 (TFA) is a Spns2 inhibitor with an IC50 value of 1.93 μM for inhibition of S1P release.SLF1081851 (TFA) plays a key role in development and the immune system.
价 格：￥电议型 号：T62851产 地：中国大陆
-
T62557CSF1R-IN-14；化合物 CSF1R-IN-14CSF1R-IN-14
CSF1R-IN-14, an isoindolinone derivative compound, is a potent inhibitor of CSF1R. CSF1R-IN-14 has potential for cancer disease research.
价 格：￥电议型 号：T62557产 地：中国大陆
-
T62390CSF1R-IN-8；化合物 CSF1R-IN-8CSF1R-IN-8
CSF1R-IN-8 (Compound 22) is a CSF-1R inhibitor (IC50: 0.012 μM).
价 格：￥电议型 号：T62390产 地：中国大陆
-
T62364CSF1R-IN-5；化合物 CSF1R-IN-5CSF1R-IN-5
CSF1R-IN-5 is a potent inhibitor of CSF1R. CSF1R-IN-5 can affect the exchange of inflammatory factors between TAM and glioma cells. CSF1R-IN-5 has the potential to be used in the study of cancer diseases.
价 格：￥电议型 号：T62364产 地：中国大陆
-
T62342CSF1R-IN-4；化合物 CSF1R-IN-4CSF1R-IN-4
CSF1R-IN-4 is a potent inhibitor of CSF-1R. CSF1R-IN-4 can affect the exchange of inflammatory factors between TAM and glioma cells. CSF1R-IN-4 has potential for the study of cancer diseases. EGFR-IN-40.
价 格：￥电议型 号：T62342产 地：中国大陆
