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：3738273
自主品牌
已选条件
-
T11155Eg5 Inhibitor V, trans-24Eg5 Inhibitor V, trans 24,Eg-5 Inhibitor V, trans-24,Eg5 Inhibitor V, trans
Eg5 Inhibitor V, trans-24 is a specific and potent Eg5 inhibitor that can be used in cancer research with an IC50 value of 0.65 uM.
价 格：￥电议型 号：T11155产 地：中国大陆
-
T37082HS271HS271,HS-271
HS271 is a selective, highly potent and orally active IRAK4 inhibitor (IC50= 7.2 μM). HS271 shows excellent enzymatic and cellular activities, as well as excellent pharmacokinetic properties.
价 格：￥电议型 号：T37082产 地：中国大陆
-
TN7110Ginsenoside Rs2Ginsenoside Rs2,Ginsenoside Rs-2
Ginsenoside Rs2 is a natural product isolated from the leaves of Panax japonicus var..
价 格：￥电议型 号：TN7110产 地：中国大陆
-
T8326BMS-2BMS 2,BMS2
BMS-2 is a Met/Flt-3/VEGFR2 tyrosine kinase inhibitor.
价 格：￥电议型 号：T8326产 地：中国大陆
-
T8457NPS2390Inhibitor,NPS2390,Calcium-sensing receptor,NPS-2390,mGluR,inhibit,Metabotropic glutamate rece
NPS2390 is a first generation quinoxaline derivative that acts as a noncompetitive antagonist of mGluR1 and mGluR5 (IC50 of 5.2 and 82 nM, respectively)
价 格：￥电议型 号：T8457产 地：中国大陆
-
T7309TAS-103 dihydrochlorideBMS247615,Topoisomerase,TAS-103,TAS103,inhibit,TAS 103 dihydrochloride,BMS-24
TAS-103 (dihydrochloride) is a novel anticancer agent targeting both topoisomerase (Topo) I and Topo II.
价 格：￥电议型 号：T7309产 地：中国大陆
-
T7149S29434cell-permeable,inhibit,selective,S 29434,HepG2,mice,NMDPEF,S-29434,ROS,Autophagy,S29434,Inhibi
S29434 (NMDPEF) is a potent, competitiveinhibitor of quinone reductase 2 (QR2;IC50:5-16nM).
价 格：￥电议型 号：T7149产 地：中国大陆
-
T6760APS-2-79 hydrochlorideMAP2K,MAPKK,Inhibitor,Mitogen-activated protein kinase kinase,APS 2 79 hydroch
APS-2-79 is a MAPK antagonist that modulating KSR-dependent MAPK signalling by antagonizing RAF heterodimerization as well as the conformational changes required for phosphorylation and activation of KSR-bound MEK.
价 格：￥电议型 号：T6760产 地：中国大陆
-
T16936SS-208
SS-208 is a selective inhibitor of HDAC6 (IC50 = 12 nM) with anti-tumor activity. SS-208 shows selectivity over other HDAC subtypes.
价 格：￥电议型 号：T16936产 地：中国大陆
-
T18018HS-27HS27,HS 27
HS-27 is a fluorescently-tethered inhibitor of Hsp90 with SNX-5422 tethered via a PEG linker to a fluorescein isothiocyanate or FITC. HS-27 can be used in see-and-treat paradigms.
价 格：￥电议型 号：T18018产 地：中国大陆
-
T60012HS-243RA-FLSs,Inhibitor,immunology,autoimmune disease,inhibit,Interleukin-1 receptor associated kina
HS-243 is an inhibitor of IRAK-4 and IRAK-1 with IC50s of 20 and 24 nM. HS-243 shows anti-inflammatory and anticancer activity.
价 格：￥电议型 号：T60012产 地：中国大陆
-
T6964ResiquimodHepatitis C virus,R-848,S-28463,R 848,S 28463,Toll-like Receptor (TLR),Inhibitor,Resiquimo
Resiquimod is an imidazoquinoline amine and Toll-like receptor (TLR) agonist with potential immune response modifying activity. Resiquimod exerts its effect through the TLR signaling pathway by binding to and activating TLR7 and 8 mainly on dendritic cells, macrophages, and B-lymphocytes. This induces the nuclear translocation of the transcription activator NF-kB as well as activation of other transcription factors. This may lead to an increase in mRNA levels and subsequent production of cytokin
价 格：￥电议型 号：T6964产 地：中国大陆
-
T9239RS-25344RS25344,RS 25344
RS-25344 is a potent and selective phosphodiesterase (PDE) 4 inhibitor. It inhibits eosinophil chemotaxis and increases progressive motility of spermatozoa in vitro.
价 格：￥电议型 号：T9239产 地：中国大陆
-
T62209HS-276
HS-276 is an orally active, potent and highly selective TAK1 inhibitor (Ki= 2.5 nM). HS-276 exhibits significant inhibition of TAK1, CLK2, GCK, ULK2, MAP4K5, IRAK1, NUAK, CSNK1G2, CAMKKβ-1, and MLK1, with IC50 values of 8.25, 29, 33, 63, 125, 264, 270, 810, 1280, and 5585 nM, respectively. HS-276 exhibits research potential for rheumatoid arthritis (RA) research.
价 格：￥电议型 号：T62209产 地：中国大陆
-
T8378AS2863619Cyclin dependent kinase,AS2863619,STAT,AS 2863619,Inhibitor,inhibit,CDK,AS-2863619
AS2863619 is an orally active inhibitor of cyclin-dependent kinase 8 (CDK8) and CDK19 (IC50s of 0.61 nM and 4.28 nM, respectively).
价 格：￥电议型 号：T8378产 地：中国大陆
-
T6441CGS 21680 HydrochlorideCGS-21680,Inhibitor,CGS 21680,inhibit,CGS21680,CGS 21680 Hydrochloride,Adenos
CGS 21680 HCl（ IC50=22 nM）, an adenosine receptor agonist, exhibits 140-fold potency in A2 receptor over A1 receptor.
价 格：￥电议型 号：T6441产 地：中国大陆
-
T1730NPS-2143SB-262470A,Inhibitor,NPS-2143,NPS2143,inhibit,Calcium-sensing receptor,CaSR
NPS-2143 is a novel potent and selective antagonist of Ca(2+) receptor.
价 格：￥电议型 号：T1730产 地：中国大陆
-
T9033BTYNBInhibitor,inhibit,ES-2,BTYNB,c-Myc,IMP1,Myc,IGROV-1,cancer cell,SK-MEL2
MDK6620?is an inhibitor of the oncofetal mRNA-binding protein IMP1 (IC50 = 5 μM for IMP1 binding to c-Myc mRNA).?MDK6620?downregulates β-TrCP1 mRNA and reduces activation of nuclear transcriptional factors-kappa B (NF-κB).?It disrupts this enhancer function by impairing IGF2 mRNA-binding protein 1 (IGF2BP1)-RNA association
价 格：￥电议型 号：T9033产 地：中国大陆
-
T9127MYLS22OPA1,Inhibitor,MYLS22,optic,atrophy,endothelial,MYLS-22,inhibit,MYLS 22,tumor
MYLS22 is a first-in-class and selective inhibitor of optic atrophy 1 (OPA1) . MYLS22 can target endothelial OPA1 to curtail tumor growth and inhibits angiogenesis by impinging on NFkB activity and on angiogenic gene expression. It with anti-angiogenesis and anti-cancer activity.
价 格：￥电议型 号：T9127产 地：中国大陆
-
T7263SMS2-IN-2Inhibitor,SMS-2-IN-2,SMS2 IN 2,SMS2IN2,inhibit
SMS2-IN-2 is a potent, selective and orally active sphingomyelin synthase 2 (SMS2) inhibitor, (IC50s of 100 and 56 μM for SMS2 and SMS1, respectively). SMS2-IN-2 has anti-chronic inflammatory activity.
价 格：￥电议型 号：T7263产 地：中国大陆
