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
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:3750050
已选条件
-
T81733Myelin Oligodendrocyte Glycoprotein (40-54), Rat, Mouse;化合物 Myelin Oligodendrocyte Glycoprotein (40-
Myelin Oligodendrocyte Glycoprotein (40-54), Rat, Mouse (MOG (40-54)) is a self-antigenic epitope associated with the CD8 class of proteins within the MOG protein, presented in conjunction with H-2Db [1].
价 格:¥电议型 号:T81733产 地:中国大陆
-
T80733ZH8667;化合物 ZH8667ZH8667
ZH8667 is a TAAR1-Gs agonist that holds potential for schizophrenia research [1].
价 格:¥电议型 号:T80733产 地:中国大陆
-
T79733NLRP3-IN-20;化合物 NLRP3-IN-20NLRP3-IN-20
NLRP3-IN-20 (compound 11) is an orally administered inhibitor targeting the NLRP3 inflammasome, exhibiting potent inhibition with an IC50 of 25 nM against IL-1β secretion. It possesses excellent pharmacokinetic properties and has shown significant efficacy in models of non-alcoholic steatohepatitis, fatal septic shock, and colitis [1].
价 格:¥电议型 号:T79733产 地:中国大陆
-
T79345CDD-1733;化合物 CDD-1733CDD-1733
CDD-1733 is a potent, non-covalent, and non-peptide inhibitor of the SARS-CoV-2 main protease (Mpro) with an inhibition constant (K i) of 12 nM. It effectively inhibits Mpro variants including ΔP168, A173V, and the combined ΔP168/A173V [1].
价 格:¥电议型 号:T79345产 地:中国大陆
-
T78733ZLD115;化合物 ZLD115ZLD115
ZLD115 (compound 44), a derivative of FB23, functions as an inhibitor of the Fat Mass and Obesity-associated Protein (FTO) and demonstrates antiproliferative properties as an antileukemic agent against leukemic cell lines [1].
价 格:¥电议型 号:T78733产 地:中国大陆
-
T77733TNKS-2-IN-2;TNKS-2 抑制剂 2TNKS-2-IN-2
TNKS-2-IN-2 is a novel and potent TNKS2 selective inhibitor (IC50: 22 nM) with potential anti-tumour activity for the study of colon cancer lung cancer and breast cancer.
价 格:¥电议型 号:T77733产 地:中国大陆
-
T77695Muvalaplin;莫伐倍林LY3473329;LY3473329
Muvalaplin (LY3473329) is an orally active lipoprotein (a) Lp(a) reagent that inhibits Lp(a) formation by blocking apo(a)-apo B100 interactions.
价 格:¥电议型 号:T77695产 地:中国大陆
-
T77339BRD4-IN-4;化合物BRD4-IN-4BRD4-IN-4
BRD4-IN-4 is a selective BRD4 inhibitor with an IC50 value of 6.83 μM for BRD4.BRD4-IN-4 selectively inhibits the proliferation of the MV4-11 cell line and arrests the cells in G1 phase.BRD4-IN-4 can be used to study MLL leukemias.
价 格:¥电议型 号:T77339产 地:中国大陆
-
T77336PLH2058;化合物 PLH2058PLH2058
PLH2058 is a compound that can be used to regulate, limit or inhibit AVIL (advillin) expression. It can be used in the treatment of cancer.
价 格:¥电议型 号:T77336产 地:中国大陆
-
T77335PLH1215;化合物 PLH1215PLH1215
PLH1215 is a compound that can be used to regulate, limit, or inhibit the expression of AVIL (advillin), which can be used to treat cancer.
价 格:¥电议型 号:T77335产 地:中国大陆
-
T77334HDAC-IN-57;化合物HDAC-IN-57HDAC-IN-57
HDAC-IN-57 is an orally active pan-inhibitor of histone deacetylase (HDAC), inhibiting HDAC1, HDAC2, HDAC6, and HDAC8 with IC50 values of 2.07 nM, 4.71 nM, 2.4 nM, and 107 nM, respectively. HDAC-IN-57 inhibits LSD1 with an IC50 value of 1.34 μΜ. HDAC-IN-57 has anti-tumor activity and can induce apoptosis.
价 格:¥电议型 号:T77334产 地:中国大陆
-
T77333L(Iso)-BMT-124110 Formate;化合物 (Iso)-BMT-124110 Formate(R)-N-(8-((2-amino-2,4-dimethylpentyl)oxy)-5H-c
(Iso)-BMT-124110 Formate has an inhibitory effect on the protein serine/threonine kinase AAK, and is used in the treatment of Parkinson´s disease, schizophrenia, neuropathic pain, and Alzheimer´s disease.
价 格:¥电议型 号:T77333L产 地:中国大陆
-
T77332TV 3279;化合物TV 3279TV 3279
TV 3279 is a novel ChE-MAI inhibitor , and the neuroprotective properties depend on their ability to induce the anti-apoptotic proteins PKC, Bcl-2, Bcl-x, and SOD, and to block the nuclear translocation of the pro-apoptotic enzyme glyceraldehyde phosphate dehydrogenase in PC-12 and neuroblastoma cells.
价 格:¥电议型 号:T77332产 地:中国大陆
-
T7733Cefotaxime;头孢噻肟酸Cefotaxime
Cefotaxime is an inhibitor of penicillin binding protein.
价 格:¥电议型 号:T7733产 地:中国大陆
-
T76733Enibarcimab;化合物 EnibarcimabEnibarcimab
Enibarcimab is a humanized murine monoclonal immunoglobulin G1 (IgG1) antibody, potentially applicable in the research of acute heart failure, COVID-19 infections, and septic shock [1].
价 格:¥电议型 号:T76733产 地:中国大陆
-
T7598Calcium N5-methyltetrahydrofolate;N5-甲基四氢叶酸钙NSC173328;5-甲基四氢叶酸钙|||N5-甲基四氢叶酸钙|||NSC173328
Calcium N5-methyltetrahydrofolate (NSC-173328) is the calcium salt of levomefolic acid, which has been proposed for treatment of cardiovascular disease and advanced cancers such as breast and colorectal cancers
价 格:¥电议型 号:T7598产 地:中国大陆
-
T74733OSM-SMI-10B;化合物 OSM-SMI-10BOSM-SMI-10B
OSM-SMI-10B, a derivative of OSM-SMI-10, effectively inhibits Oncostatin M (OSM)-induced STAT3 phosphorylation in cancer cells when co-incubated with OSM [1].
价 格:¥电议型 号:T74733产 地:中国大陆
-
T73733(Rac)-1,2-Distearoyl-sn-Glycero-3-Phosphatidylglycerol sodium;化合物 (Rac)-1,2-Distearoyl-sn-Glycero-3-
(Rac)-1,2-Distearoyl-sn-Glycero-3-Phosphatidylglycerol (sodium), an anionic phospholipid, is utilized in drug delivery systems and the synthesis of liposomes [1].
价 格:¥电议型 号:T73733产 地:中国大陆
-
T73399FTX-6746;化合物 FTX-6746FTX-6746
receptor gamma (PPARG) durably eradicate tumors in urothelial cancer (UC) animal models[J]. European Journal of Cancer , 2022, 174: S33-S34. https://www.ejcancer.com/article/S0959-8049(22)00889-9/abstract FTX-6746 is an orally active PPARG inhibitor. FTX-6746 shows potent tumor inhibition in mouse xenograft models [1] .
价 格:¥电议型 号:T73399产 地:中国大陆
-
T73397ENT-C225;化合物 ENT-C225ENT-C225
ENT-C225 is a potent TrkB neurotrophin receptor (TrkBR) activator with neuroprotective activity for the study of Alzheimer´s disease and Parkinson´s disease.
价 格:¥电议型 号:T73397产 地:中国大陆