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:3513835
已选条件
-
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
-
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
-
T7846Aegelineαsyn,Aegeline,yeast,Inhibitor,protein,Sec22p,inhibit,toxicity,Fungal,SNARE
Aegeline is an alkaloidal-amide, isolated from the leaves of Aegle marmelos and have shown antihyperglycemic as well as antidyslipidemic activities in the validated animal models of type 2 diabetes mellitus.
价 格:¥电议型 号:T7846产 地:中国大陆
-
T8423ML417neuroprotection,dopaminergic,β-arrestin,ML417,ML-417,translocation,phosphorylation,neurons,ML 4
ML417 is a selective and brain penetrant agonist of D3 Dopamine (EC50 : 38 nM).
价 格:¥电议型 号:T8423产 地:中国大陆
-
T7117Sapropterin dihydrochloride(6R)-BH4,Sapropterin,Inhibitor,inhibit,Sapropterin dihydrochloride
Sapropterin dihydrochloride is phenylalanine hydroxylase agonist that is approved for the treatment of BH4 responsive PKU.
价 格:¥电议型 号:T7117产 地:中国大陆
-
T8478SC-43antiproliferative,Inhibitor,SC-43,SHP-1,PTPN6,Phosphatase,Apoptosis,caspase-3,SC 43,anti-fibrot
SC-43 is a potent and orally active agonist of SHP-1 (PTPN6). SC-43 inhibits the phosphorylation of STAT3 and induces cell apoptosis, and with anti-fibrotic and anticancer effects.
价 格:¥电议型 号:T8478产 地:中国大陆
-
T2573MisoprostolMisoprostol
价 格:¥电议型 号:T2573产 地:中国大陆
-
T7013VorapaxarProtease Activated Receptor (PAR),Inhibitor,SCH-530348,Vorapaxar,SCH530348,Thrombin recepto
Vorapaxar (SCH 530348) is an effective and orally active thrombin receptor (PAR-1) antagonist (Ki: 8.1 nM).
价 格:¥电议型 号:T7013产 地:中国大陆
-
T7265HSP27 inhibitor J2Heat shock proteins,inhibit,HSP-27 inhibitor J2,HSP27 inhibitor J2,Inhibitor,J 2,H
HSP27 inhibitor J2 (J2) is a HSP27 inhibitor, inhibits a production of HSP27 giant polymers, thereby having an effect of inhibiting a chaperone function of the HSP27 and reducing a cell protection function.
价 格:¥电议型 号:T7265产 地:中国大陆
-
T13890SMARCA-BD ligand 1 for Protac dihydrochlorideSMARCABD ligand 1 for Protac dihydrochloride,SMARCA BD
SMARCA-BD ligand 1 for Protac dihydrochloride binds to the BAF ATPase subunits SMARCA2, and used for degrading SMARCA2, based on PROTAC.
价 格:¥电议型 号:T13890产 地:中国大陆
-
T8818TC-G 1005TC G 1005,G protein-coupled Bile Acid Receptor 1,levels,coupled,glucose,TCG 1005,Takeda,inh
TC-G 1005 is a potent and selective GPBA agonist (EC50 :0.72 nM; hTGR5). Selective for TGR5 over FXR (farnesoid X receptor). Increases plasma GLP-1 levels and reduces blood glucose in mice. Orally available.
价 格:¥电议型 号:T8818产 地:中国大陆
-
T8861GSK199GSK 199,GSK-199,GSK199,Inhibitor,Peptidylarginine Deiminase,Protein Arginine Deiminase,inhibit
GSK199 is a selective PAD4 inhibitor(IC50 of 200 nM in the absence of calcium).
价 格:¥电议型 号:T8861产 地:中国大陆
-
TQ0022Capromorelin TartrateInhibitor,Growth hormone secretagogue receptor,GHSR,Capromorelin,inhibit,Caprom
Capromorelin Tartrate is a potent, orally active growth hormone secretagogue receptor (GHSR) agonist (Ki: 7 nM for hGHS-R1a).
价 格:¥电议型 号:TQ0022产 地:中国大陆
-
T6920ON123300Platelet-derived growth factor receptor,AMP-activated protein kinase,ON-123300,ON 123300,FGF
ON123300 is a potent and multi-targeted kinase inhibitor for CDK4/Ark5/PDGFRβ/FGFR1/RET/Fyn (IC50: 3.9/5/26/26/9.2/11 nM).
价 格:¥电议型 号:T6920产 地:中国大陆
-
TQ0292GrapiprantRQ 00000007,Inhibitor,Grapiprant,CJ 023423,RQ00000007,Prostaglandin Receptor,AAT 007,inhib
Grapiprant is a selective EP4 receptor antagonist. Grapiprant displaces [3H]-PGE2 (1 nM) binding to dog recombinant EP4 receptor (IC50: 35 nM, Ki: 24 nM).
价 格:¥电议型 号:TQ0292产 地:中国大陆
-
T8985NSC45586pleckstrin homology domain and leucine-rich repeat protein phosphatase,NSC-45586,NSC45586,in
NSC45586 is a protein phosphatase PHLPP inhibitor, which is selective for PHLPP1 and PHLPP2.
价 格:¥电议型 号:T8985产 地:中国大陆
-
T7740Protease-Activated Receptor-4 diTFAProtease Activated Receptor 4 diTFA,ProteaseActivated Receptor4 d
Protease-Activated Receptor-4 diTFA,2454 is the proteinase-activated receptor-4 (PAR4)agonist
价 格:¥电议型 号:T7740产 地:中国大陆
-
T6997SU6656PTK2 protein tyrosine kinase 2,Focal adhesion kinase,FAK,Akt,SU-6656,PTK2,Inhibitor,Protein ki
SU 6656 is a selective inhibitor of Src family kinases, with IC50 of 280 nM, 20 nM, 130 nM, and 170 nM for Src, Yes, Lyn, and Fyn, respectively.
价 格:¥电议型 号:T6997产 地:中国大陆