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：3748673
自主品牌
已选条件
-
T13550AP5；化合物 T13550AP5
AP5 is a potent and selective agonist for the GPR40 receptor with positive allosteric modulation of endogenous ligands (AgoPAM). AP5 demonstrates a rat hIP1 EC50 of 0.49 nM against the GPR40 receptor.
价 格：￥电议型 号：T13550产 地：中国大陆
-
T13336LVTP50469 fumarate；化合物 T13336LVTP50469 fumarate
VTP50469 fumarate is a highly selective and orally active inhibitor of Menin-MLL interaction (Ki: 104 pM), and has potently anti-leukemia activity.
价 格：￥电议型 号：T13336L产 地：中国大陆
-
T13336VTP50469；化合物VTP50469VTP50469
VTP50469 is a highly selective and orally active inhibitor of Menin-MLL interaction( Ki: 104 pM) and has potently anti-leukemia activity.
价 格：￥电议型 号：T13336产 地：中国大陆
-
T13253Umibecestat；化合物UmibecestatCNP520；CNP520
Umibecestat is an inhibitor of beta-site amyloid precursor protein cleaving enzyme-1 (BACE-1), with IC50s of 11 nM and 10 nM for human BACE-1 and mouse BACE-1, respectively. Umibecestat can be used for the research of alzheimer´s disease.
价 格：￥电议型 号：T13253产 地：中国大陆
-
T13140Umbralisib R-enantiomer；厄布利塞R对映体TGR-1202 R-enantiomer|||RP5264 R-enantiomer；TGR-1202 R-enantiomer|||
Umbralisib R-enantiomer (RP5264 R-enantiomer) is a delta inhibitor of PI3K and a less active enantiomer of TGR-1202. The IC50 of Umbralisib R-enantiomers against δPI3 kinase is at least 20 times lower than that of the inhibitors against other PI3K isoforms (A, β, and γ).
价 格：￥电议型 号：T13140产 地：中国大陆
-
T12791(S)-3-Hydroxy Midostaurin；化合物 T12791(S)-CGP52421；(S)-CGP52421
(S)-3-Hydroxy Midostaurin is a potent inhibitor of kinases(IC50 of <400 nM for 13 kinases (VEGFR-2, TRK-A, FLT3, et)).
价 格：￥电议型 号：T12791产 地：中国大陆
-
T12610L3-Hydroxy Midostaurin；化合物 T12610LCGP52421；CGP52421
3-Hydroxy Midostaurin (CGP 52421), a PKC412 metabolite, inhibits FMS-like tyrosine kinase-3 (FLT3) autophosphorylation with IC50 values of roughly 132 nM in culture medium and 9.8 μM in plasma. Though less selective, it exhibits greater cytotoxicity compared to PKC412[1].
价 格：￥电议型 号：T12610L产 地：中国大陆
-
T12610(R)-3-Hydroxy Midostaurin；化合物 T12610(R)-CGP52421；(R)-CGP52421
(R)-3-Hydroxy Midostaurin is a potent inhibitor of kinases,is a major metabolite of midostaurin undergoing by the hepatic CYP3A4 enzyme,has the potential for acute myeloid leukemia (AML).
价 格：￥电议型 号：T12610产 地：中国大陆
-
T12351p53 and MDM2 proteins-interaction-inhibitor (racemic)；化合物 T12351p53-and-mdm2-proteins-interaction-in
p53 and MDM2 proteins-interaction-inhibitor (racemic) is an inhibitor of the interaction between p53 and MDM2 proteins.
价 格：￥电议型 号：T12351产 地：中国大陆
-
T12350p53 and MDM2 proteins-interaction-inhibitor dihydrochloride；化合物 T12350p53 and MDM2 proteins-interact
p53 and MDM2 proteins-interaction-inhibitor dihydrochloride is a interaction inhibitor between p53 and MDM2 proteins.
价 格：￥电议型 号：T12350产 地：中国大陆
-
T10930D-AP5；(R)-(-)-2-氨基-5-膦酰戊酸D-APV|||D-2-Amino-5-phosphonovaleric acid；(R)-(-)-2-氨基-5-膦酰戊酸|||D-APV|||D-2
D-AP5 (D-APV) is a NMDA receptor antagonist.
价 格：￥电议型 号：T10930产 地：中国大陆
-
T10875CP5V；化合物 T10875CP5V
CP5V, a PROTAC, induces mitotic inhibition, and suppresses cancer cell proliferation. It specifically degrades Cdc20 by linking Cdc20 to the VHL/VBC complex for ubiquitination followed by proteasomal degradation.
价 格：￥电议型 号：T10875产 地：中国大陆
-
T10782CGP52411；化合物CGP52411DAPH；DAPH
CGP52411 is an orally active, and ATP-competitive inhibitor of EGFR (IC50: 0.3 μM). CGP52411 blocks the toxic influx of Ca2+ ions into neuronal cells and dramatically inhibits and reverses the formation of β-amyloid Aβ42 fibril aggregates. CGP52411 can be used in studies about Alzheimer´s diseases.
价 格：￥电议型 号：T10782产 地：中国大陆
-
T10344AP521；化合物 T10344AP521
AP521 is an agonist of the human 5-HT1A receptor (IC50: 94 nM).
价 格：￥电议型 号：T10344产 地：中国大陆
-
T0186Docetaxel trihydrate；多西他赛三水合物RP-56976 (Trihydrate)|||RP56976 (NSC 628503) Trihydrate；RP-56976 (Trihy
Docetaxel trihydrate (RP-56976 Trihydrate) is an antineoplastic agent that has a unique mechanism of action as an inhibitor of cellular mitosis and that currently plays a central role in the therapy of many solid tumor including breast and lung cancer. Therapy with docetaxel has been associated with a low rate of serum enzyme elevations and rarely to instances of acute hepatic necrosis generally due to severe hypersensitivity reactions or sepsis.
价 格：￥电议型 号：T0186产 地：中国大陆
