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：3811160
自主品牌
已选条件
-
T1335Mycophenolic acidMycophenolic acid,RS-61443,Mycophenolate
Mycophenolic acid is an inosine monophosphate dehydrogenase(IMPDH) inhibitor with anti-proliferative activity.
价 格：￥电议型 号：T1335产 地：美洲
-
T13376YS-49YS-49
YS-49 is an activator of PI3K/Akt (a downstream target of RhoA).
价 格：￥电议型 号：T13376产 地：美洲
-
T13387ZatebradineZatebradine,UL-FS-49 free base,UL-FS-49CL free base
Zatebradine is a potent hyperpolarization-activated cyclic nucleotide-gated (HCN) channels inhibitor(IC50 of 1.96 ?M).
价 格：￥电议型 号：T13387产 地：美洲
-
T13440(RS)-Carbocisteine(RS)-Carbocisteine,S-(Carboxymethyl)-DL-cysteine,
(RS)-Carbocisteine is the S-carboxymethyl cysteine. (RS)-Carbocisteine is the inactive enantiomer of Carbocisteine.
价 格：￥电议型 号：T13440产 地：美洲
-
T13616cis-?9,10-?Epoxystearic acidcis-?9,10-?Epoxystearic acid,cis-9,10-Epoxyoctadecanoic acid,
cis-9,10-Epoxystearic acid is an endogenous constituent in human urine and blood. It can be produced from oleic acid by enzymic and non-enzymic epoxidation.
价 格：￥电议型 号：T13616产 地：美洲
-
T13617cis-p-Menthan-1,8-diolcis-p-Menthan-1,8-diol,4-p-Menthan-1,8-diol,
cis-?p-?Menthan-?1,?8-?diol is a natural menthane monoterpenoid.
价 格：￥电议型 号：T13617产 地：美洲
-
T13661Docosatrienoic AcidDocosatrienoic Acid,cis-13,16,19-docosatrienoic acid,(13Z,16Z,19Z)-13,16,19-Docos
Docosatrienoic acid is a rare omega-3 fatty acid; Ki value is 5×M, which inhibits the binding of LTB4 to porcine neutrophil membrane.
价 格：￥电议型 号：T13661产 地：美洲
-
T13925THS-044THS-044
THS-044 binding stabilizes the HIF2α PAS-B folded state, for regulating HIF2 activity in endogenous and clinical settings.
价 格：￥电议型 号：T13925产 地：美洲
-
T14124ADAMTS-5 InhibitorADAMTS-5 Inhibitor
ADAMTS-5 Inhibitor is a potent ADAMTS-5 (aggrecanase-2) inhibitor, with an IC50 of 1.1 ?M. ADAMTS-5 Inhibitor shows >40-fold functional selectivity over ADAMTS-4 (aggrecanase-1)[1].
价 格：￥电议型 号：T14124产 地：美洲
-
T14195ALS-8112ALS-8112
ALS-8112 is a inhibitor of respiratory syncytial virus (RSV) polymerase. The 5´-triphosphate form of ALS-8112 inhibits RSV polymerase (IC50: 0.02 μM).
价 格：￥电议型 号：T14195产 地：美洲
-
T1430BetamipronBetamipron,N-Benzoyl-β-alanine,CS-443
Betamipron is used combination with panipenem to prevent nephrotoxicity and inhibit panipenem uptake into the renal tubule.
价 格：￥电议型 号：T1430产 地：美洲
-
T1448DasatinibDasatinib,BMS-354825,
Dasatinib is a potent inhibitor of the Bcr-Abl and Src family (IC50s: 0.6, 0.8, 79 and 37 nM for Abl, Src, c-Kit, and c-KitD816V, respectively).
价 格：￥电议型 号：T1448产 地：美洲
-
T14674BMS-509744BMS-509744
BMS-509744 is an inhibitor of ATP competitive Itk (IC50: 19 nM).
价 格：￥电议型 号：T14674产 地：美洲
-
T14675BMS-564929BMS-564929
BMS-564929 is an androgen receptor (AR) agonist. Which binds to androgen receptor (AR) with a Ki of 2.11±0.16 nM.
价 格：￥电议型 号：T14675产 地：美洲
-
T14676BMS-688521BMS-688521
BMS-688521 is efficacious in a mouse allergic eosinophilic lung inflammation model and it is a highly potent, orally active inhibitor of the LFA-1/ICAM interaction. With an IC50 of 2.5 nM in the adhesion assay and an IC50 of 60 nM in the MLR assay .
价 格：￥电议型 号：T14676产 地：美洲
-
T14677BMS-690514BMS-690514
BMS-690514 is a potent and orally active inhibitor of EGFR and VEGFR. It has IC50s of 5, 20 and 60 nM for EGFR, HER 2 and HER 4, respectively.
价 格：￥电议型 号：T14677产 地：美洲
-
T14681BMS-935177BMS-935177
BMS-935177 is a potent and selective reversible inhibitor of Bruton’s tyrosine kinase (Btk), with an IC50 of 3 nM.
价 格：￥电议型 号：T14681产 地：美洲
-
T14683BMS-983970BMS-983970
BMS-983970 is an oral pan-Notch inhibitor. Which is used for treatment of multiplecancers.
价 格：￥电议型 号：T14683产 地：美洲
-
T14685BMS-986158BMS-986158
BMS-986158 is a potent BET inhibitor. With IC50s of 6.6 and 5?nM in NCI-H211 small cell lung cancer (SCLC) cells and MDA-MB231 triple negative breast cancer (TNBC) cells, respectively[1].
价 格：￥电议型 号：T14685产 地：美洲
-
T14687BMS-986165BMS-986165
BMS-986165 inhibits IL-12/23 and type I IFN pathways[1][2]. BMS-986165 is a highly selective, orally bioavailable allosteric TYK2 inhibitor for the treatment of autoimmune diseases. Which selectively binds to TYK2 pseudokinase (JH2) domain (IC50=1.0 nM)
价 格：￥电议型 号：T14687产 地：美洲
