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：3871730
自主品牌
已选条件
-
T27310Fengabine；酚加宾SL79229|||SL 79.229-00|||SL-79229|||SL 79229|||SL 79-229|||SL 79,229-00；SL79229|||SL 79
Fengabine (SL-79229) is a GABA receptor agonist with antidepressant activity and is used to treat depression.
价 格：￥电议型 号：T27310产 地：中国大陆
-
T2731Usnic Acid；松萝酸Usniacin；Usniacin|||松萝酸|||地衣酸
Usnic Acid (Usniacin) is an antimicrobial, antitumor and enzyme inhibiting agent shown to uncouple oxidative phosphorylation in mouse-liver mitochondria. Usnic acid induces necrosis in certain cells.
价 格：￥电议型 号：T2731产 地：中国大陆
-
T27309Fenazinel Dihydrochloride；化合物 T27309SIPI5052|||SIPI 5052|||SIPI-5052；SIPI5052|||SIPI 5052|||SIPI-505
Fenazinel Dihydrochloride, a N-methyl-D-aspartate (NMDA) receptor antagonist, is used potentially for the treatment of ischemic stroke.
价 格：￥电议型 号：T27309产 地：中国大陆
-
T27308FEMA-4809；化合物FEMA-4809FEMA4809|||FEMA 4809；FEMA4809|||FEMA 4809
FEMA-4809, a highly potent TRPM8 receptor activator, TRPM8 is the ion channel responsible for the cool perception, which is triggered either by temperatures below 25 °C or by ligands such as (-)-menthol. FEMA-4809 is used as a cooling agent.
价 格：￥电议型 号：T27308产 地：中国大陆
-
T27307LFasnall HCl；Fasnall盐酸盐Fasnall HCl（929978-58-5 Free base）；Fasnall HCl（929978-58-5 Free base）
Fasnall HCl is a selective FASN inhibitor that acts through its co-factor binding sites. Fasnall HCl also shows potent anti-tumor activity in the MMTV-Neu model of HER2(+) breast cancer, particularly when combined with carboplatin.
价 格：￥电议型 号：T27307L产 地：中国大陆
-
T27307Fasnall；化合物FasnallFasnall
Fasnall is a selective FASN inhibitor that acts through its co-factor binding sites. Fasnall shows potent anti-tumor activity in the MMTV-Neu model of HER2(+) breast cancer, particularly in combination with carboplatin.
价 格：￥电议型 号：T27307产 地：中国大陆
-
T27306Fasidotril；化合物 T27306BP 1137|||BP1137|||BP-1.137|||BP1.137|||BP-1137|||BP 1.137；BP 1137|||BP1137|||B
Fasidotril is a NEP/ACE inhibitor. Fasidotril was an effective oral antihypertensive agent during chronic treatment in high-renin renovascular rats, normal-renin SHR, and low-renin DOCA-salt hypertensive rats and in patients with essential hypertension.
价 格：￥电议型 号：T27306产 地：中国大陆
-
T27305Fascaplysin chloride；化合物 T27305NSC622398|||NSC 622398|||Fascaplysin|||NSC-622398；NSC622398|||NSC 622
Fascaplysin is a cyclin D kinase 4/ cyclin D1 inhibitor (IC50 = 0.35 μM). Fascaplysin induces caspase mediated crosstalk between autophagy and apoptosis through the inhibition of PI3K/AKT/mTOR signaling cascade in human leukemia HL-60 cells.
价 格：￥电议型 号：T27305产 地：中国大陆
-
T27304Farnesiferol C；化合物 T27304Farnesiferol-C；Farnesiferol-C
Farnesiferol C induces apoptosis via regulation of L11 and c-Myc.
价 格：￥电议型 号：T27304产 地：中国大陆
-
T27303Farglitazar；法格列扎GI-262570|||GI-2570|||GW 262570X|||GI 262570|||GI262570；GI-262570|||GI-2570|||GW 262
Farglitazar (GI-262570) is a PPAR-γ agonist and insulin sensitizer that inhibits stellate cell activation by activating receptor γ via oxidative enzymes proliferators and is used in the study of diabetes.
价 格：￥电议型 号：T27303产 地：中国大陆
-
T27302Falipamil；化合物 T27302AQ-A 39|||AQ-A-39|||AQ-A39；AQ-A 39|||AQ-A-39|||AQ-A39
Falipamil is a verapamil derivative and a calcium channel antagonist. Falipamil exerts antitachycardic effects by a direct action on the sinus node. Falipamil decreases HR at exercise in normal subjects and may exert antianginal effects in patients with myocardial ischemia. Falipamil exhibits effects on the electrical activity of the heart, reflecting the predominant direct vagolytic effect of this drug.
价 格：￥电议型 号：T27302产 地：中国大陆
-
T27301Fagaronine chloride；化合物 T27301NSC157995|||NSC 157995|||NSC-157995；NSC157995|||NSC 157995|||NSC-15799
Fagaronine chloride is a potent inhibitor of Topoisomerases I.
价 格：￥电议型 号：T27301产 地：中国大陆
-
T27300Olorofim化合物OlorofimOlorofim|||F901318|||F-901318
Olorofim is a novel selective antifungal compound with inhibitory effect on Aspergillus fumigatus DHODH (IC50: 44 nM) and almost no inhibitory effect on human DHODH (>100 uM).Olorofim has good efficacy against various pathogenic filamentous and dimorphic fungi such as Penicillium spp, Dermatophilus spp and Fusarium spp.
价 格：￥电议型 号：T27300产 地：中国大陆
-
T2730Gossypol (acetic acid)；醋酸棉酚(±)-Gossypol-acetic acid|||Pogosin|||AT101|||Gossypol acetic acid；(±)-Gos
Gossypol acetic acid (AT101), a polyphenolic compound isolated from cottonseeds, binds with Bcl-2, Bcl-xL, Mcl-1, and does not inhibit BIR3 domain and BID.
价 格：￥电议型 号：T2730产 地：中国大陆
-
T27273EP 171；化合物 T27273EP171|||EP-171；EP171|||EP-171
EP 171 is a potent agonist of TP-receptors.
价 格：￥电议型 号：T27273产 地：中国大陆
-
T27173Diflumidone sodium；化合物 T27173BA 41648|||BA 4164 8|||BA41648|||BA-4164-8|||BA 4164-8；BA 41648|||BA 41
Diflumidone sodium is a non-steroidal agent with anti-inflammatory activity.
价 格：￥电议型 号：T27173产 地：中国大陆
-
T27073CPI-7c；化合物 T27073CPI 7c；CPI 7c
CPI-7c inhibits MDM2-p53 interaction and promotes MDM2 degradation.
价 格：￥电议型 号：T27073产 地：中国大陆
-
T26990CGI-17341；化合物 T26990CGI17341；CGI17341
CGI-17341 is an orally active representative of the 5-nitroimidazole series of antimicrobial agents. CGI 17341 inhibits the drug-susceptible and multi-drug-resistant strains of Mycobacterium tuberculosis at concentrations ranging from 0.1 to 0.3 micrograms/ml.
价 格：￥电议型 号：T26990产 地：中国大陆
-
T2699BMS 777607；化合物BMS-777607BMS777607|||BMS-777607|||BMS 817378；BMS777607|||BMS-777607|||BMS 817378
BMS 777607 (BMS 817378) is a Met-related inhibitor for c-Met/Axl/Ron/Tyro3 (IC50: 3.9/1.1/1.8/4.3 nM). BMS-777607 has been investigated for the basic science of Malignant Solid Tumour.
价 格：￥电议型 号：T2699产 地：中国大陆
-
T26981Ceralasertib formate；化合物 T26981Ceralasertib|||AZD-6738|||AZD 6738|||AZD6738；Ceralasertib|||AZD-6738|
Ceralasertib is an orally available inhibitor of ataxia telangiectasia and rad3 related (ATR) kinase. Ceralasertib selectively inhibits ATR activity by blocking the downstream phosphorylation of the serine/threonine protein kinase CHK1. This prevents ATR-mediated signaling, and results in the inhibition of DNA damage checkpoint activation, disruption of DNA damage repair, and the induction of tumor cell apoptosis.
价 格：￥电议型 号：T26981产 地：中国大陆
