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:3779005
已选条件
-
T2686LEsomeprazole Sodium埃索美拉唑钠;(S)-Omeprazole sodium
Esomeprazole Sodium is the S-isomer of omeprazole with selective and irreversible proton pump inhibitor activity.Esomeprazole acts as an exosome inhibitor by blocking the exosome release via the inhibition of V-H+-ATPases
价 格:¥电议型 号:T2686L产 地:中国大陆
-
T26869BMS-986122BMS986122;BMS 986122
BMS 986122 is a positive allosteric modulator of μ-opioid receptors that increases β-arrestin recruitment stimulated by endomorphin 1 in U2OS-OPRM1 human osteosarcoma cells expressing μ-opioid receptors (EC50 = 3 μM).
价 格:¥电议型 号:T26869产 地:中国大陆
-
T2686Esomeprazole Magnesium埃索美拉唑镁;NEXIUM;(-)-Omeprazole magnesium;(S)-Omeprazole magnesium
Esomeprazole Magnesium is the S-isomer of omeprazole, can reduce gastric acid secretion with selective and irreversible proton pump inhibitor activity.Esomeprazole magnesium acts as an exosome inhibitor by blocking the exosome release via the inhibition
价 格:¥电议型 号:T2686产 地:中国大陆
-
T26859BMS-8BMS8;BMS 8
BMS-8 is a novel inhibitor of the PD-1/PD-L1 interaction (IC50: 7.2 μM) by binding directly to PD-L1 and inducing the formation of PD-L1 homodimers.
价 格:¥电议型 号:T26859产 地:中国大陆
-
T2685KU-55933ATM Kinase Inhibitor;KU55933
KU-55933 (ATM Kinase Inhibitor) is a potent and specific ATM inhibitor.
价 格:¥电议型 号:T2685产 地:中国大陆
-
T2684JNJ-1661010JNJ 1661010;Takeda-25;JNJ1661010
JNJ-1661010 is an effective and specific FAAH inhibitor (IC50: 10/ 12 nM for rat/human), shows >100-fold selectivity for FAAH-1 than FAAH-2.
价 格:¥电议型 号:T2684产 地:中国大陆
-
T2683IWP L6Porcn?Inhibitor?III;IWP-L6;Porcn Inhibitor III
IWP-L6 is an extremely effective Porcn inhibitor (EC50: 0.5 nM).
价 格:¥电议型 号:T2683产 地:中国大陆
-
T26829BitertanolSibutol;KWG0599;Biloxazol;KWG 0599;Baycor;KWG-0599
Bitertanol is a pesticide and demethylation inhibitor. Bitertanol disrupts membrane function and prevents sterol synthesis. Bitertanol also increases activity of antioxidative enzymes and alters operant behavior in animal models.
价 格:¥电议型 号:T26829产 地:中国大陆
-
T2682AcalisibCAL-120;GS-9820
Acalisib (GS-9820) is a potent and selective inhibitor of PI3Kδ.
价 格:¥电议型 号:T2682产 地:中国大陆
-
T2680NVP-BVU972
NVP-BVU972 is a selective and potent Met inhibitor with IC50 of 14 nM.
价 格:¥电议型 号:T2680产 地:中国大陆
-
T2677CrenolanibCP-868596;ARO 002
Crenolanib is an orally bioavailable type III tyrosine kinases inhibitor of PDGFRα/β and FLT3 (IC50s: 11, 3.2, and 4 nM).
价 格:¥电议型 号:T2677产 地:中国大陆
-
T2670ML167NCGC00188654;CID44968231
ML167 is a highly selective Cdc2-like kinase 4 (Clk4) inhibitor.
价 格:¥电议型 号:T2670产 地:中国大陆
-
T26689AVE-0118AVE 0118;AVE0118
AVE-0118 is a potassium channel blocker. AVE0118 effectively suppressed persistent atrial fibrillation.
价 格:¥电议型 号:T26689产 地:中国大陆
-
T26684Auten-99 HBrAuten-99;Auten-99 hydrochloride. Auten-99 HBr;Auten99;Auten 99
Auten-99 HBr is a myotubularin phosphatase Jumpy inhibitor exerting potent neuroprotective effects. AUTEN-99 activates autophagy in cell cultures and animal models. AUTEN-99 appears to effectively penetrate through the blood-brain barrier, and impedes the
价 格:¥电议型 号:T26684产 地:中国大陆
-
T2668JNK-IN-8JNK Inhibitor XVI
JNK-IN-8 is an irreversible JNK1/2/4 inhibitor (IC50: 4.7/18.7/1 nM). The selectivity is higher 10-fold than MNK2, Fms and no inhibition of Met, c-Kit, PDGFRβ in A375 cell line.
价 格:¥电议型 号:T2668产 地:中国大陆
-
T2666TaladegibLY2940680
Taladegib is an orally bioavailable small molecule antagonist of the Hedgehog (Hh)-ligand cell surface receptor smoothened (Smo) with potential antineoplastic activity.
价 格:¥电议型 号:T2666产 地:中国大陆
-
T2595Lumacaftor鲁玛卡托;VRT 826809;VX-809
VX-809 is a CFTR modulator that corrects the folding and trafficking of CFTR protein. It enhances F508del-CFTR protein maturation in FRT cells (EC50: 100 nM).
价 格:¥电议型 号:T2595产 地:中国大陆
-
T2568LFelypressin acetatePLV 2;PLV2. H-Cys-Phe-Phe-Gln-Asn-Cys-Pro-Lys-Gly-NH2 (Disulfide bond);PLV-2;2-(L
Felypressin acetate is an agonist of vasopressin 1 and acts on all arginine vasopressin receptors 1AS. Felypressin acetate can be used in dental procedures.
价 格:¥电议型 号:T2568L产 地:中国大陆
-
T2568Felypressin苯赖加压素;Felypressin Acetate;PLV-2;H-[Cys-Phe-Phe-Gln-Asn-Cys]-Pro-Lys-Gly-NH2;Octapressin
Felypressin is a synthetic analog of LYPRESSIN with a PHENYLALANINE substitution at residue 2. Felypressin is a vasoconstrictor with reduced antidiuretic activity.
价 格:¥电议型 号:T2568产 地:中国大陆