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：3736052
自主品牌
已选条件
-
T11606ICA-105665；化合物 T11606PF-04895162；PF-04895162
ICA-105665 (PF-04895162) is a potent and orally active neuronal Kv7.2/7.3 and Kv7.3/7.5 potassium channels opener. ICA-105665 had low cytotoxic potential in human hepatocytes but inhibited liver mitochondrial function and bile salt export protein (BSEP) transport (IC50 of 311 μM). ICA-105665 can penetrate the central nervous system (CNS) and has antiseizure effects[1][2][3][4].
价 格：￥电议型 号：T11606产 地：中国大陆
-
T1158Phenoxybenzamine hydrochloride；盐酸酚苄明NCI-c01661|||NSC 37448|||Phenoxybenzamine HCl；苯氧苯札明|||NCI-c01661
Phenoxybenzamine hydrochloride (NCI-c01661) is the hydrochloride salt form of phenoxybenzamine, a synthetic, dibenzamine alpha-adrenergic antagonist with antihypertensive and vasodilatory properties. Phenoxybenzamine non-selectively and irreversibly blocks the postsynaptic alpha-adrenergic receptor in smooth muscle, thereby preventing vasoconstriction, relieving vasospasms, and decreasing peripheral resistance. Reflex tachycardia may occur and may be enhanced by blockade of alpha-2 receptors whi
价 格：￥电议型 号：T1158产 地：中国大陆
-
T11566HIV-1 integrase inhibitor；化合物 T11566HIV-1 integrase inhibitor
Hiv-1 integrase inhibitor is an effective anti-HIV drug.
价 格：￥电议型 号：T11566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
-
T11521GW 766994；化合物 T11521GW 994；GW 994
GW 766994 is a specific and oral chemokine receptor-3 (CCR3) antagonist. It has the potential for asthma and eosinophilic bronchitis treatment.
价 格：￥电议型 号：T11521产 地：中国大陆
-
T11497Ganfeborole HCl；Ganfeborole 盐酸盐GSK3036656 HCl|||GSK656 HCl；GSK3036656 HCl|||GSK656 HCl
Ganfeborole HCl (GSK3036656 HCl) is a small molecule compound with anti-tuberculosis activity and is an inhibitor of Mycobacterium tuberculosis (Mtb) leucyl-tRNA synthetase (LeuRS; IC50: 0.2 μM).
价 格：￥电议型 号：T11497产 地：中国大陆
-
T11483GSK256066 Trifluoroacetate化合物 T11483GSK 256066 Trifluoroacetate|||GSK256066 (2,2,2-trifluoroacetic a
GSK 256066 Trifluoroacetate is a selective and high-affinity phosphodiesterase 4 (PDE) inhibitor (IC50: 3.2 pM for PDE4B). It can be used for the treatment of chronic obstructive pulmonary disease.
价 格：￥电议型 号：T11483产 地：中国大陆
-
T11470GSK 366；化合物 T11470GSK 366
GSK 366 is a potent kynurenine-3-monooxygenase (KMO) inhibitor (IC50s: 0.7 nM and 2.3 nM for P. fluorescens-KMO and human KMO).
价 格：￥电议型 号：T11470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
-
T11383GDP366；化合物GDP366GDP366
GDP366, induces cell growth inhibition, cellular senescence and mitotic catastrophe in human cancer cells. a dual inhibitor of survivin and Op18.
价 格：￥电议型 号：T11383产 地：中国大陆
-
T11366Garcinol；山竹子素Garcinol
Garcinol also inhibits histone acetyltransferases (HATs, IC50= 7 μM) and p300/CPB-associated factor (PCAF, IC50 = 5 μM). Garcinol has anti-inflammatory and anti-cancer activity. Garcinol, a polyisoprenylated benzophenone harvested from Garcinia indica, exerts anti-cholinesterase properties towards acetyl cholinesterase (AChE) and butyrylcholinesterase (BChE) with IC50s of 0.66 μM and 7.39 μM, respectively.
价 格：￥电议型 号：T11366产 地：中国大陆
-
T11266LFAS-IN-1 Tosylate；化合物 T11266LFAS-IN-1 Tosylate
FAS-IN-1 Tosylate is an effective fatty acid synthase inhibitor;Has an IC50 of 10 nM.
价 格：￥电议型 号：T11266L产 地：中国大陆
-
T11266FASN-IN-4；化合物 T11266FAS-IN-1；FAS-IN-1
FAS-IN-1 is a potent inhibitor of Fatty acid synthase (FAS) wtih IC50 of 10 nM.
价 格：￥电议型 号：T11266产 地：中国大陆
-
T11246Etoricoxib-d4；依托考昔 D4MK-0663 D4|||L-791456 D4|||Etoricoxib D4；MK-0663 D4|||依托考昔 D4|||L-791456 D4|||E
Etoricoxib D4 is a non steroidal anti-inflammatory agent, acting as a selective and orally active COX-2 inhibitor, with IC50s of 1.1 μM and 116 μM for COX-2 and COX-1 in human whole blood.Etoricoxib D4 is a deuterium labeled Etoricoxib.
价 格：￥电议型 号：T11246产 地：中国大陆
-
T11166EHMT2-IN-1；化合物 T11166EHMT2-IN-1
EHMT2-IN-1 is a potent EHMT inhibitor, . Used in the research of blood disorder or cancer.with IC50s of all <100 nM for EHMT1 peptide, EHMT2 peptide and cellular EHMT2.
价 格：￥电议型 号：T11166产 地：中国大陆
-
T1107Sarafloxacin hydrochloride；盐酸沙拉沙星Sarafloxacin HCl|||A-56620 (hydrochloride)|||A-56620 HCl；Sarafloxac
Sarafloxacin hydrochloride (A-56620 (hydrochloride)), a quinolone antibiotic drug, is a hydrochloride salt form of sarafloxacin.
价 格：￥电议型 号：T1107产 地：中国大陆
-
T10988LDegarelix acetate(214766-78-6 free base)；化合物Degarelix acetateDegarelix acetate(214766-78-6 free base
Degarelix acetate is a competitive and reversible antagonist of gonadotropin-releasing hormone receptor (GnRHR) .
价 格：￥电议型 号：T10988L产 地：中国大陆
-
T10967DC_C66；化合物 T10967DC_C66
DC_C66 DC_C66 has good selectivity for CARM1, PRMT1 (IC50 = 21μM), PRMT6 (IC50 = 47μM) and PRMT5. It is a cell-permeable, selective co-activator related arginine methyltransferase 1 (CARM1) inhibitor with IC50 of 1.8 μM.
价 格：￥电议型 号：T10967产 地：中国大陆
-
T10966DC-5163；化合物 T10966DC-5163
DC-5163 is a potent inhibitor of glyceraldehyde 3-phosphate dehydrogenase (GAPDH) with IC50 of 176.3 nM and Kd of 3.192 μM. DC-5163 selectively inhibits cancer cell proliferation and induces apoptosis, and partially inhibits the glycolysis pathway.
价 格：￥电议型 号：T10966产 地：中国大陆
