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：3732880
自主品牌
已选条件
-
T9878CroconazoleCROCONAZOLE
Croconazole exhibited dose-dependent inhibitory activity on the 5-lipoxygenase (5-LOX) of neutrophils. Croconazole is an antimycotic agent. The IC50s for the synthesis of leukotriene B4 (LTB4) and 5-hydroxyeicosatetraenoic acid (5-HETE) is 7.8 +/- 1.7 and
价 格：￥电议型 号：T9878产 地：中国大陆
-
T7085MebhydrolinMebhydrolin,inhibit,Histamine Receptor,Inhibitor
Mebhydrolin is a specific histamine H1 receptor antagonist.
价 格：￥电议型 号：T7085产 地：中国大陆
-
TQ0209Ailanthoneinhibit,Inhibitor,Ailanthone,Androgen Receptor
Ailanthone is an effective inhibitor of both full-length androgen receptor (AR) (IC50: 69 nM) and constitutively active truncated AR splice variants (IC50: 309 nM).
价 格：￥电议型 号：TQ0209产 地：中国大陆
-
TN2108ProtohypericinProtohypericin,naphthodianthrone,Inhibitor,NSCLC,inhibit
Protohypericin is a naturally occurring naphthodianthrone derived from plant Hypericum perforatum.Radioiodinated protohypericin is used in Tumor necrosis targeted radiotherapy. Protohypericin exhibits photocytotoxicity.
价 格：￥电议型 号：TN2108产 地：中国大陆
-
T6S1369Vitexinneurodegeneration,Vitexin,anti-cancer,anti-nociceptive,inhibit,Medicinal,anti-hypertensive,an
1. Vitexin has antinociceptive and antispasmodic activities. 2. Vitexin exhibits a prominent first-pass effect. 3. Vitexin has antioxidant, antimyeloperoxidase, and α-glucosidase inhibitory activities. 4. Vitexin can either inhibit or induce activities of CYP2C11 and CYP3A1. 5. Vitexin induces the novel p53-dependent metastatic and apoptotic pathway. 6. Vitexin protects brain against cerebral I/R injury, and this effect may be regulated by mitogen-activated protein kinase (MAPK) and apoptosis si
价 格：￥电议型 号：T6S1369产 地：中国大陆
-
T8849PF-9601Nexcitotoxicity,neurodegenerative diseases,MAO,PF9601N,Monoamine Oxidase,MAO-B inhibitor,neur
PF-9601N showed high potency and selectivity as a MAO-BI (monoamine oxidase type B inhibitor) and also demonstrated remarkable neuroprotective properties in several in vivo and cellular models of PD.
价 格：￥电议型 号：T8849产 地：中国大陆
-
T9030SU4984inhibit,growth,Fibroblast growth factor receptor,Insulin Receptor,fibroblast,insulin,SU4984,SU
SU4984 is a cell-permeable, ATP-competitive and reversible inhibitor of the fibroblast growth factor receptor 1 (FGFR1).
价 格：￥电议型 号：T9030产 地：中国大陆
-
T19343sn-Glycerol 3-phosphateinhibit,Endogenous Metabolite,sn Glycerol 3 phosphate,snGlycerol 3phosphate,I
Glycerol 3-phosphate is produced by the reduction of dihydroxyacetone phosphate by NADH formed during glycolysis of the cytoplasmic glycerol 3-phosphate dehydrogenase pathway.
价 格：￥电议型 号：T19343产 地：中国大陆
-
T6923Ozanimodneurosurgery,sphingosine 1-phosphate (S1P),LPL Receptor,inhibit,RPC1063,Lysophospholipid Rec
Ozanimod (RPC1063) is a specific oral S1P Receptor 1 modulator. Ozanimod has been used in trials studying the treatment of Crohn´s Disease, Ulcerative Colitis, Multiple Sclerosis, and Relapsing Multiple Sclerosis.
价 格：￥电议型 号：T6923产 地：中国大陆
-
T23470Tracazolate hydrochloride
Tracazolate hydrochloride is a modulator of the GABAA receptor with anxiolytic and anticonvulsant activity. Tracazolate hydrochloride potentiates α1β1γ2s and α1β3γ2 with EC50s of 13.2 μM and 1.5 μM.
价 格：￥电议型 号：T23470产 地：中国大陆
-
T99683-Piperidinyl(1-pyrrolidinyl)methanone hydrochloride3Piperidinyl(1pyrrolidinyl)methanone hydrochlori
3-Piperidinyl(1-pyrrolidinyl)methanone hydrochloride can be used in the synthesis of piperidin-4-yl-urea derivatives which are MCH-R1 antagonists.
价 格：￥电议型 号：T9968产 地：中国大陆
-
T8202Kaempferol 3-O-gentiobiosideKaempferol 3Ogentiobioside,inhibit,Kaempferol 3 O gentiobioside,Inhibito
Kaempferol 3-O-gentiobioside is a flavonoid isolated from C. alata leaves with antidiabetic activity. It possesses activity against α-glucosidase and displays a carbohydrate enzyme inhibitory effect (IC50: 50 μM).
价 格：￥电议型 号：T8202产 地：中国大陆
-
TN7058DihydrolapachenoleInhibitor,Dihydrolapachenole,inhibit
dihydrolapachenol is a natural isolated from the heartwood of T. chrysantha.
价 格：￥电议型 号：TN7058产 地：中国大陆
-
T6951Pramipexole dihydrochloride hydratetransient,Pramipexole dihydrochloride,Pramipexole dihydrochloride
Pramipexole Dihydrochloride is the hydrochloride salt of pramipexole, a benzothiazole derivative. As a nonergot dopamine agonist, pramipexole binds to D2 and D3 dopamine receptors in the striatum and substantia nigra of the brain.
价 格：￥电议型 号：T6951产 地：中国大陆
-
T11013L1Dextrorotation nimorazole phosphate ester TFADextrorotationnimorazolephosphateesterTFA
Dextrorotation nimorazole phosphate ester TFA is an anti-anaerobic and anti-parasitic agent.
价 格：￥电议型 号：T11013L1产 地：中国大陆
-
TN1576Diallyl disulfidecholesterol biosynthesis,squalene monooxygenase,Inhibitor,inhibit,Diallyl disulfide
Diallyl disulfide has antitumor effect, the effect can be enhanced by miR-200b and miR-22.
价 格：￥电议型 号：TN1576产 地：中国大陆
-
T35341NVP-BSK805 dihydrochloride
NVP-BSK805 dihydrochloride is an effective and selective inhibitor of JAK2 with IC50s of 0.5 nM, 10.76 nM, 18.68 nM, and 31.63 nM for JAK2, TYK2, JAK3, and JAK1.
价 格：￥电议型 号：T35341产 地：中国大陆
-
T28036MI-2-2cell proliferation,inhibit,menin-MLL interaction,Epigenetic Reader Domain,Inhibitor,Hoxa9 expr
MI-2-2 is an inhibitor of bivalent protein-protein interaction between menin and MLL with an IC50 of 46 nM. MI-2-2 binds to menin with Kd of 22 nM.
价 格：￥电议型 号：T28036产 地：中国大陆
-
T8606n-acetylciprofloxacinnacetylciprofloxacin,n acetylciprofloxacin
n-acetylciprofloxacin is inhibitor of H37Rv.
价 格：￥电议型 号：T8606产 地：中国大陆
-
T94371-methoxycyclopropanecarboxylic acid1methoxycyclopropanecarboxylic acid,1 methoxycyclopropanecarboxy
1-methoxycyclopropanecarboxylic acid is an agonist of free fatty acid receptor 3 (FFAR3, human).
价 格：￥电议型 号：T9437产 地：中国大陆
