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T12243Norverapamil-d7;化合物 T12243D591 D7|||(±)-Norverapamil D7;D591 D7|||(±)-Norverapamil D7
Norverapamil D7 is a deuterium labeled Norverapamil . Norverapamil is a blocker of L-type calcium channel and an inhibitor of P-glycoprotein (P-gp) function .
价 格:¥电议型 号:T12243产 地:中国大陆
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T12236NMS-859;化合物NMS-859ZINC169324353;ZINC169324353
NMS-859 is an effective and covalent inhibitor of valosin-containing protein (VCP)/p97 with IC50s of 0.37 μM and 0.36 μM for wild-type VCP in the presence of 60 μM and 1 mM ATP in cells, respectively.
价 格:¥电议型 号:T12236产 地:中国大陆
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T12199LNB-598 hydrochloride;化合物 T12199LNB-598 hydrochloride
NB-598 hydrochloride is a competitive squalene epoxidase (SE) inhibitor.
价 格:¥电议型 号:T12199L产 地:中国大陆
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T12199NB-598 Maleate;化合物 T12199NB-598 Maleate
NB-598 Maleate is a competitive squalene epoxidase (SE) inhibitor.
价 格:¥电议型 号:T12199产 地:中国大陆
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T12166Nacubactam;那库巴坦OP0595 free acid;OP0595 free acid|||那库巴坦
Nacubactam (OP0595 free acid) is a potent inhibitor of non-β-lactam-β-lactamase with activity against class A and class C β-lactamases.
价 格:¥电议型 号:T12166产 地:中国大陆
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T12159APNEA;N6-[2-(4-氨基苯基)乙基]腺嘌呤(2R,3R,4S,5R)-2-[6-[2-(4-aminophenyl)ethylamino]purin-9-yl]-5-(hydroxymeth
APNEA ((2R,3R,4S,5R)-2-[6-[2-(4-aminophenyl)ethylamino]purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol) is a non-selective agonist of adenosine A3 receptor.
价 格:¥电议型 号:T12159产 地:中国大陆
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T12032Mibefradil dihydrochloride;盐酸米贝地尔Ro 40-5967 (dihydrochloride);盐酸米贝地尔|||Ro 40-5967 (dihydrochloride)|
Mibefradil dihydrochloride (Ro 40-5967 (dihydrochloride)) is an blocker of calcium channel with moderate selectivity for T-type Ca2+ channels (T-type and L-type currents with IC50s of 2.7 μM and 18.6 μM, respectively).
价 格:¥电议型 号:T12032产 地:中国大陆
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T11978McN3716;帕莫酸甲酯NSC359682|||Methyl palmoxirate;NSC359682|||Methyl palmoxirate
McN3716 is a carnitine palmitoyltransferase I (CPT-1) inhibitor for the study of metabolic diseases.
价 格:¥电议型 号:T11978产 地:中国大陆
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T11959MBM-17S;化合物 T11959MBM-17S
MBM-17S, a potent NIMA-related kinase 2 (Nek2) inhibitor with an IC50 of 3 nM, effectively inhibits cancer cell proliferation by inducing cell cycle arrest and apoptosis. It demonstrates antitumor activities without evident toxicity to mice.
价 格:¥电议型 号:T11959产 地:中国大陆
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T11859LLitronesib;化合物 T11859LKF-89617|||LY-2523355;KF-89617|||LY-2523355
Litronesib is a selective inhibitor of mitosis-specific kinesin Eg5. It also has antitumor activity.
价 格:¥电议型 号:T11859L产 地:中国大陆
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T11859Litronesib Racemate化合物 T11859LY-2523355 Racemate|||KF-89617 Racemate
Litronesib is a selective, allosteric inhibitor of kinesin Eg5.Litronesib (Racemate) is the racemate of litronesib.
价 格:¥电议型 号:T11859产 地:中国大陆
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T1184Rivaroxaban;利伐沙班BAY 59-7939;BAY 59-7939|||利伐沙班
Rivaroxaban (BAY 59-7939) is an orally bioavailable oxazolidinone derivative and direct inhibitor of the coagulation factor Xa with anticoagulant activity. Upon oral administration, rivaroxaban selectively binds to both free factor Xa and factor Xa bound in the prothrombinase complex. This interferes with the conversion of prothrombin (factor II) to thrombin and eventually prevents the formation of cross-linked fibrin clots. Rivaroxaban does not affect existing thrombin levels.
价 格:¥电议型 号:T1184产 地:中国大陆
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T11828LDC7559;化合物LDC7559LDC7559
LDC7559 inhibits gasdermin D (GSDMD) by blocking neutrophil extracellular trap (NET) at late stage.
价 格:¥电议型 号:T11828产 地:中国大陆
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T11822LAU159;化合物LAU159LAU159
LAU159 is a functionally selective positive α1β3 GABA(A) receptor modulator(EC50 : 2.2 μM).
价 格:¥电议型 号:T11822产 地:中国大陆
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T11759Kif15-IN-2;化合物 T11759Kif15-IN-2
Kif15-IN-2 is used for the research of cellular proliferative diseases. Kif15-IN-2 is an inhibitor of the mitotic kinesin Kif15.
价 格:¥电议型 号:T11759产 地:中国大陆
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T11740Delcasertib;化合物DelcasertibKAI-9803|||BMS-875944;KAI-9803|||BMS-875944
Delcasertib (KAI-9803) is a potent and selective inhibitor of δ-protein kinase C (δPKC).
价 格:¥电议型 号:T11740产 地:中国大陆
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T11731LJTV-519 Formate;化合物JTV-519 FormateJTV-519 Formate (145903-06-6 Free base);JTV-519 Formate (145903-06
JTV-519 Formate is a Ca2+-dependent blocker of sarcoplasmic reticulum Ca2+-stimulated ATPase (SERCA). JTV-519 Formate is also a partial agonist of ryanodine receptors in striated muscle. JTV-519 Formate exhibits antiarrhythmic and cardioprotective properties.
价 格:¥电议型 号:T11731L产 地:中国大陆
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T11719LJMV 2959;化合物 T11719LJMV 2959
JMV 2959 is an antagonist of growth hormone secretagogue receptor type 1a (GHS-R1a) (IC50: 32 nM).
价 格:¥电议型 号:T11719L产 地:中国大陆
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T11719JMV 2959 hydrochloride (925238-89-7 free base);化合物JMV 2959 hydrochlorideJMV 2959 hydrochloride;JMV 2
JMV 2959 hydrochloride (925238-89-7 free base) is a growth hormone secretagogue receptor type 1a (GHS-R1a) antagonist with an IC50 of 32±3 nM in LLC-PK1 cells.
价 格:¥电议型 号:T11719产 地:中国大陆
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T11659Inogatran;伊诺加群H-314-27;伊诺加群|||H-314-27
Inogatran is a synthetic thrombin inhibitor, developed for the possible treatment and prophylaxis of venous and arterial thrombotic diseases.
价 格:¥电议型 号:T11659产 地:中国大陆