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：3845865
自主品牌
已选条件
-
T21700NOS-IN-1?
2-Imino-4-methylpiperidine is a potent, general NOS inhibitor.
价 格：￥电议型 号：T21700产 地：中国大陆
-
T20513IDO1-IN-1IDO1IN1；2-HzBTZ；IDO1 inhibitor 1；2 HzBTZ；IDO1-inhibitor-1；IDO1 IN 1；2-肼基苯并噻唑
IDO1-IN-1 is an indoleamine 2,3-dioxygenase 1 (IDO1) inhibitor.
价 格：￥电议型 号：T20513产 地：中国大陆
-
T2051SKLB4771FLT3-?IN-?1；FLT3-IN-1
FLT3-IN-1 is a novel potent and selective Flt3 inhibitor.
价 格：￥电议型 号：T2051产 地：中国大陆
-
T1842XMD17-109XMD17 109；XMD17109；ERK5-IN-1
XMD17-109 is a new selective ERK-5 inhibitor (EC50: 4.2 uM, HEK293 cells).
价 格：￥电议型 号：T1842产 地：中国大陆
-
T1826PI3K-IN-1XL765；SAR245409；Voxtalisib (SAR245409, XL765) Analogue；Voxtalisib Analogue
Voxtalisib (SAR245409, XL765)Analogue is a dual inhibitor of mTOR/PI3K, mostly for p110γ , also inhibits DNA-PK and mTOR.
价 格：￥电议型 号：T1826产 地：中国大陆
-
T17697BRD7-IN-1
BRD7-IN-1, a modified derivative of BI7273 (BRD7/9 inhibitor), binds to a VHL ligand via a linker to form a PROTAC VZ185 (VZ185 against BRD7/9 with DC50s of 4.5 and 1.8 nM, respectively).
价 格：￥电议型 号：T17697产 地：中国大陆
-
T16944STK16-IN-1
STK16-IN-1 is an inhibitor of STK16 kinase (IC50: 295 nM).
价 格：￥电议型 号：T16944产 地：中国大陆
-
T16432Pan-RAS-IN-1
Pan-RAS-IN-1 is an inhibitor of pan-Ras. It disrupts the interaction of Ras proteins and their effectors.
价 格：￥电议型 号：T16432产 地：中国大陆
-
T16162Mutated EGFR-IN-1Osimertinib analog；AZD9291中间体1
Mutated EGFR-IN-1 is a useful intermediate for the inhibitors design for mutated EGFR, such as L858R EGFR, Exonl9 deletion activating mutant, and T790M resistance mutant.
价 格：￥电议型 号：T16162产 地：中国大陆
-
T16007MALAT1-IN-1
MALAT1-IN-1 modulated Malat1 downstream genes in a dose-dependent manner without affecting the expression of nuclear enriched abundant transcript 1 (Neat1). MALAT1-IN-1 is an effective and specific Malat1 inhibitor.
价 格：￥电议型 号：T16007产 地：中国大陆
-
T15782Lp-PLA2-IN-1Lp-PLA2 inhibitor 1；Lp-PLA2 -IN-1
Lp-PLA2 -IN-1 suppresses Lp-PLA2 activity processes for their preparation. Lp-PLA2 -IN-1also inhibits to compositions containing them and to their use in the treatment of diseases associated with the activity of Lp-PLA2, for example, atherosclerosis, Alzh
价 格：￥电议型 号：T15782产 地：中国大陆
-
T15660KHK-IN-1KHK-IN-8；Ketohexokinase inhibitor 8
KHK-IN-1 is a reversible and ATP-competitive inhibitor of ketohexokinase (KHK) with IC50 of 12 nM. In the ATP-binding region of KHK, KHK-IN-1 interacts with Asp-27B.
价 格：￥电议型 号：T15660产 地：中国大陆
-
T15649KDM5-IN-1
KDM5-IN-1 is an effective and selective inhibitor of KDM5 with an IC50 of 15.1 nM.
价 格：￥电议型 号：T15649产 地：中国大陆
-
T15413GPR120 Agonist 3GPR120-IN-1
GPR120-IN-1 is a selective agonist of Gpr120 ( logEC50: -7.62).
价 格：￥电议型 号：T15413产 地：中国大陆
-
T15274FEN1-IN-1LNT-1
FEN1-IN-1 is an inhibitor of flap endonuclease 1 (FEN1). FEN1-IN-1 binds to the active site of FEN1. It partly achieves inhibition by the co-ordination of Mg2+ ions.
价 格：￥电议型 号：T15274产 地：中国大陆
-
T15109DGAT1-IN-1
DGAT1-IN-1 is a potent inhibitor of diacylglycerol O- acyltransferase type 1(DGAT1, IC50 of < 10 nM).
价 格：￥电议型 号：T15109产 地：中国大陆
-
T14860CaMKII-IN-1
CaMKII-IN-1 is a potent and highly selective inhibitor of CaMKII (IC50 = 63 nM). CaMKII-IN-1 exhibited more than 100-fold higher selectivity for CaMKII over CaMKIV, MLCK, p38a, Akt1, and PKC.
价 格：￥电议型 号：T14860产 地：中国大陆
-
T14692BMX-IN-1BMX kinase inhibitor
BMX-IN-1 is a selective inhibitor of bone marrow tyrosine kinase on chromosome X (BMX, IC50 = 8 nM) and the related Bruton’s tyrosine kinase (BTK, IC50 = 10.4 nM), but BMX-IN-1 is more than 47-656 fold less potent against Blk, JAK3, EGFR, Itk, or Tec acti
价 格：￥电议型 号：T14692产 地：中国大陆
-
T14175Aldose reductase-IN-1
Aldose reductase-IN-1 is a aldose reductase inhibitor (IC50: 28.9 pM).
价 格：￥电议型 号：T14175产 地：中国大陆
-
T14151AKR1C1-IN-1
AKR1C1-IN-1 is a human 20α-hydroxysteroid dehydrogenase (AKR1C1) inhibitor (Ki: 4 nM for AKR1C1).
价 格：￥电议型 号：T14151产 地：中国大陆
