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：3506711
自主品牌
已选条件
-
T11646Impurity F of Calcipotriol；化合物 T11646Impurity F of Calcipotriol
Impurity F of Calcipotriol is a impurity of Calcipotriol. Calcipotriol (MC 903; Calcipotriene) is a ligand of VDR-like receptors.
价 格：￥电议型 号：T11646产 地：中国大陆
-
T11546hDHODH-IN-1；化合物hDHODH-IN-1hDHODH-IN-1
hDHODH-IN-1 is an inhibitor of human dihydroorotate dehydrogenase (hDHODH) with an anti-inflammatory effect.
价 格：￥电议型 号：T11546产 地：中国大陆
-
T11534LHaemanthamine hydrochloride (466-75-1 free base)；化合物 T11534LHaemanthamine hydrochloride；Haemanthamin
Haemanthamine hydrochloride is an alkaloid isolated from the Amaryllidaceae plants with potent anticancer activity. It inhibits protein biosynthesis during the elongation stage of translation. It has antimalarial, pro-apoptotic, antiviral, antioxidant, and anticonvulsant activities.
价 格：￥电议型 号：T11534L产 地：中国大陆
-
T11522GYKI 52466 dihydrochloride；化合物 T11522GYKI 52466 dihydrochloride
GYKI 52466 dihydrochloride is orally active and non-competitive kainate- and AMPA-activated currents antagonist (IC50s: 7.5 μM and 11 μM). It is inactive against NMDA or γ-aminobutyric acid responses. It is a muscle relaxant and anticonvulsant agent and has good blood-brain barrier permeability.
价 格：￥电议型 号：T11522产 地：中国大陆
-
T11469GSK-3484862；化合物GSK-3484862GSK-3484862
Gsk-3484862 is a non covalent inhibitor of DNA methyltransferase DNMT1 with anticancer activity. Gsk-3484862 mediates the global demethylation of mouse embryonic stem cells.
价 格：￥电议型 号：T11469产 地：中国大陆
-
T11468GSK-3 inhibitor 1；化合物 T11468GSK-3 inhibitor 1
GSK-3 inhibitor 1 is a GSK-3 inhibitor.
价 格：￥电议型 号：T11468产 地：中国大陆
-
T11467GSK-3β inhibitor 1；化合物GSK-3β inhibitor 1GSK-3β inhibitor 1
GSK-3β inhibitor 1 is an inhibitor of GSK-3β( IC50 of 4.9 nM) and demonstrates high antidiabetic efficacy.
价 格：￥电议型 号：T11467产 地：中国大陆
-
T11466GSK-2793660；化合物 T11466GSK-2793660
GSK-2793660 is an orally active and irreversible inhibitor of Cathepsin C (CTSC). GSK-2793660 is a bioactive dipeptide that can be used for the research of bronchiectasis [1] [2].
价 格：￥电议型 号：T11466产 地：中国大陆
-
T11465Lenacapavir；化合物LenacapavirGS-6207；GS-6207
Lenacapavir (GS-6207) is a potent capsid-targeting inhibitor of HIV replication. Lenacapavir shows anti-HIV activity with an EC50 of 100 pM in MT-4 cells.
价 格：￥电议型 号：T11465产 地：中国大陆
-
T11464GRL0617；化合物GRL0617GRL0617
GRL0617 is a selective and competitive SARS-CoVPLpro and deubiquitinase noncovalent inhibitor(IC50 : 0.6 μM, Ki : 0.49 μM).
价 格：￥电议型 号：T11464产 地：中国大陆
-
T11463GR 103691；化合物GR 103691GR 103691
GR 103691 is a potent, selective dopamine D3 receptor antagonist (Ki: 0.4 nM). It shows more than 100-fold selectivity for human dopamine human (h)D3 over hD4 and hD1 sites.
价 格：￥电议型 号：T11463产 地：中国大陆
-
T11462GPR84 antagonist 8；化合物 T11462GPR84 antagonist 8
GPR84 antagonist 8 is a selective GPR84 antagonist.
价 格：￥电议型 号：T11462产 地：中国大陆
-
T11461NE 52-QQ57；化合物NE 52-QQ57NE 52-QQ57
NE 52-QQ57 is a selective, and orally available antagonist of GPR4(IC50 : 70 nM),with anti-inflammatory activity.
价 格：￥电议型 号：T11461产 地：中国大陆
-
T11460GPR4 antagonist 1；化合物 T11460GPR4 antagonist 1
GPR4 antagonist 1 is a GPR4 antagonist (IC50: 189 nM).
价 格：￥电议型 号：T11460产 地：中国大陆
-
T1146Nifedipine；硝苯地平BAY-a-1040|||Procardia XL|||Procardia|||Adalat；BAY-a-1040|||Procardia XL|||Procardia|
Nifedipine (Procardia) is a dihydropyridine calcium channel blocking agent. Nifedipine inhibits the transmembrane influx of extracellular calcium ions into myocardial and vascular smooth muscle cells, causing dilatation of the main coronary and systemic arteries and decreasing myocardial contractility. This agent also inhibits the drug efflux pump P-glycoprotein which is overexpressed in some multi-drug resistant tumors and may improve the efficacy of some antineoplastic agents.
价 格：￥电议型 号：T1146产 地：中国大陆
-
T11451GPI-1046化合物GPI-10461-(1,2-二氧代-3,3-二甲基戊基)-L脯氨酸-(3-吡啶基)-丙酯
GPI-1046 is an immunophilin ligand without antibiotic action and attenuates ethanol intake in part through the upregulation of glutamate transporter 1 (GLT1) in PFC and NAc-core.
价 格：￥电议型 号：T11451产 地：中国大陆
-
T11446GNF362；化合物 T11446GNF362
GNF362 is a selective and orally bioavailable inhibitor of inositol trisphosphate 3’ kinase B (Itpkb; IC50: 9 nM). GNF362 also inhibits Itpka and Itpkc (IC50s: 20 nM and 19 nM).
价 格：￥电议型 号：T11446产 地：中国大陆
-
T11390GENZ-882706；化合物 T11390RA03546849；RA03546849
GENZ-882706 is a potent colony stimulating factor-1 receptor (CSF-1R) Inhibitor.
价 格：￥电议型 号：T11390产 地：中国大陆
-
T11389Genz-123346；化合物 T11389Genz-123346
Genz-123346 blocks the conversion of ceramide to glucosylceramide (GL1) and inhibits GM1 with an IC50 value of 14 nM. Genz-123346 is a potent, orally available glucosylceramide synthase inhibitor.
价 格：￥电议型 号：T11389产 地：中国大陆
-
T11346LG3-C12 acetate(848301-94-0 free base)；化合物G3-C12 acetateG3-C12 acetate(848301-94-0 free base)
G3-C12 acetate shows anticancer activity.?is a galectin-3 binding peptide, with Kd of 88 nM.
价 格：￥电议型 号：T11346L产 地：中国大陆
