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：3876325
自主品牌
已选条件
-
T17005FPR Agonist 43FPR Agonist 43
FPR Agonist 43 is a dual agonist of formyl peptide receptor 1 and formyl peptide receptor 2 (FPR2)/ALX.
价 格：￥电议型 号：T17005产 地：中国大陆
-
T17008TC-S 7005TC S 7005,TCS 7005
TC-S 7005 is an effective inhibitor of Polo-like kinases (IC50s: 214 nM, 4 nM and 24 nM for Plk1, Plk2, and Plk3).
价 格：￥电议型 号：T17008产 地：中国大陆
-
T7005UlixertinibERK,VRT 752271,Ulixertinib,inhibit,VRT-752271,BVD 523,BVD523,Inhibitor,Extracellular sign
Ulixertinib (BVD-523, VRT752271) is an effective and reversible ERK1/ERK2 inhibitor. The IC50 of Ulixertinib is less than 0.3 nM for ERK2.
价 格：￥电议型 号：T7005产 地：中国大陆
-
T1567Olanzapine奥氮平；LY170053
Olanzapine is an atypical antipsychotic that is used currently in the treatment of schizophrenia and bipolar illness.
价 格：￥电议型 号：T1567产 地：中国大陆
-
T1567OlanzapineOlanzapine,LY170053,
Olanzapine is an atypical antipsychotic that is used currently in the treatment of schizophrenia and bipolar illness.
价 格：￥电议型 号：T1567产 地：美洲
-
T77005Felvizumab；化合物 FelvizumabFelvizumab
Felvizumab (SB 209763), a humanized IgG1κ monoclonal antibody, targets specific neutralizing epitopes on the F glycoprotein of Respiratory Syncytial Virus (RSV) [1] [2].
价 格：￥电议型 号：T77005产 地：中国大陆
-
T7005LUlixertinib hydrochloride化合物 T7005LUlixertinib HCl|||BVD-523|||VRT752271|||BVD 523|||BVD523|||VRT 75
Ulixertinib is an inhibitor of ERK protein kinase. Downmodulation of ERK protein kinase activity inhibits VEGF secretion by human myeloma cells and myeloma-induced angiogenesis. Upon oral administration, BVD-523 inhibits both ERK 1 and 2, thereby preventing the activation of ERK-mediated signal transduction pathways. This results in the inhibition of ERK-dependent tumor cell proliferation and survival.
价 格：￥电议型 号：T7005L产 地：中国大陆
-
T70059ALT-946 HCl；化合物 ALT-946 HClALT-946 HCl
ALT-946 HCl is an inhibitor of advanced glycation that has been shown to improve severe nephropathy in the diabetic transgenic (mREN-2)27 rat.
价 格：￥电议型 号：T70059产 地：中国大陆
-
T70058PQR514；化合物 PQR514PQR514
PQR514 is a potent pan-PI3K inhibitor (Ki 110alpha =2.2 nM). PQR514 is a follow-up compound for the phase-II clinical compound PQR309. PQR514 has an improved potency both in vitro and in cellular assays with respect to its predecessor compounds. It shows superiority in the suppression of cancer cellproliferation and demonstrates significant antitumor activity in an OVCAR-3 xenograft model at concentrations approximately eight times lower than PQR309
价 格：￥电议型 号：T70058产 地：中国大陆
-
T7005714-(Fmoc-amino)-tetradecanoic acid；化合物 14-(Fmoc-amino)-tetradecanoic acid14-(Fmoc-amino)-tetradecano
14-(Fmoc-amino)-tetradecanoic acid can be used as a PROTAC linker in the synthesis of PROTACs. 14-(Fmoc-amino)-tetradecanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
价 格：￥电议型 号：T70057产 地：中国大陆
-
T70056Moschamine；化合物 MoschamineMoschamine
Moschamine is an inhibitor of mitochondrial superoxide overproduction.
价 格：￥电议型 号：T70056产 地：中国大陆
-
T70055CO-101244 Free Base；化合物 CO-101244 Free BaseCO-101244 Free Base
CO-101244 Free Base is an NMDA receptor NR2B subunit blocker.
价 格：￥电议型 号：T70055产 地：中国大陆
-
T70054Novembichin；化合物 NovembichinNovembichin
Novembichin is a nitrogen mustard agent that crosslinks with DNA, causing inhibition of DNA synthesis.
价 格：￥电议型 号：T70054产 地：中国大陆
-
T70053IDP-73152 mesylate；化合物 IDP-73152 mesylateIDP-73152 mesylate
IDP-73152 mesylate is a peptide deformylase inhibitor.
价 格：￥电议型 号：T70053产 地：中国大陆
-
T70052S-3304；化合物 S-3304S-3304
S-3304 is a n orally-agent agent with potential antineoplastic activity. S-3304 inhibits matrix metalloproteinases (MMPs), thereby inducing extracellular matrix degradation, and inhibiting angiogenesis, tumor growth and invasion, and metastasis.
价 格：￥电议型 号：T70052产 地：中国大陆
-
T70051MMI-166；化合物 MMI-166MMI-166
MMI-166 is a selective matrix metalloproteinase (MMP) inhibitor that prevents tumor invasion and metastasis by downregulating the activity of MMP-2 and MMP-9.
价 格：￥电议型 号：T70051产 地：中国大陆
-
T70050Boditrectinib；化合物 BoditrectinibBoditrectinib
Boditrectinib, a potent tyrosine kinase inhibitor, functions as an antineoplastic agent and is valuable in researching cancer, inflammation, neurodegenerative diseases, and certain infectious diseases.
价 格：￥电议型 号：T70050产 地：中国大陆
-
T7005Ulixertinib；优立替尼BVD-523|||VRT752271；BVD-523|||VRT752271|||优立替尼
Ulixertinib (VRT752271) (BVD-523, VRT752271) is an effective and reversible ERK1/ERK2 inhibitor. The IC50 of Ulixertinib is less than 0.3 nM for ERK2.
价 格：￥电议型 号：T7005产 地：中国大陆
-
T670053-Thiophenemalonic Acid；化合物 3-Thiophenemalonic Acid3-Thiophenemalonic Acid
3-Thiophenemalonic Acid is a useful organic compound for research related to life sciences. The catalog number is T67005 and the CAS number is 21080-92-2.
价 格：￥电议型 号：T67005产 地：中国大陆
-
T37005Estriol 3-β-D-Glucuronide (sodium salt)；Estriol 3-β-D-Glucuronide (sodium salt)Estriol 3-β-D-Glucuro
Estriol 3-β-D-glucuronide is a metabolite of estriol . It is formed from estriol by the UDP-glucuronosyltransferase (UGT) isoform UGT1A10. Estriol 3-β-D-glucuronide binds to basolateral and canalicular liver plasma membranes with Kd values of 85 and 164 μM, respectively. It competitively inhibits the hydrolysis of 4-methylumbelliferyl-β-D-glucuronide and is a substrate for hydrolysis by Klotho-human IgG1 Fc protein (KLFc).
价 格：￥电议型 号：T37005产 地：中国大陆
