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产品数:86101
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T16940STAT5-IN-2STAT-5-IN-2,STAT5IN2,STAT5 IN 2
STAT5-IN-2 is an inhibitor of STAT5 with antileukemic effects (EC50s: 9 μM and 5 μM in K562 and KU812 cells, respectively).
价 格:¥电议型 号:T16940产 地:中国大陆
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TP1881L1Pep 2-8 ammonium salt(1541011-97-5 free base)Pep 2 8 ammonium salt(1541011 97 5 free base),Pep 28 am
Pep 2-8 ammonium salt is Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor. Potent inhibitor of PCSK9 binding to LDL receptor (IC50 = 0.8 μM). Restores LDL uptake in HepG2 cells treated with PCSK9.
价 格:¥电议型 号:TP1881L1产 地:中国大陆
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T9884EN523inhibit,EN-523,Inhibitor,non-catalytic,EN523,OTUB1 recruiter,EN 523,deubiquitinase,allosteric c
EN523 targets non-catalytic allosteric cysteine C23 in K48 ubiquitin-specific deuquitinase OTUB1.
价 格:¥电议型 号:T9884产 地:中国大陆
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T38605NCT-504NCT 504,NCT504
NCT-504 is a selective allosteric inhibitor of PIP4Kγ , with an IC 50 of 15.8 μM. NCT-504 is potential for the research of Huntington´s disease.
价 格:¥电议型 号:T38605产 地:中国大陆
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T8836CY5-SE triethylamine saltoligonucleotides,reactive,dye,amino-groups,inhibit,CY-5-SE triethylamine sa
Fluorolink Cy5 triethanolamine salt is a hydrophilic amine-reactive fluorescent probe. It displays excitation/emission maxima of 646/662 nm, respectively. Cy5-SE-conjugated ligands have been used in the characterization of hematopoietic tumor microenvironments.
价 格:¥电议型 号:T8836产 地:中国大陆
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T16704LQuilseconazole Formic acid(1340593-70-5 Free base)
Quilseconazole Formic acid is a selective inhibitor of fungal Cyp51 with potent activities against Cryptococcus neoformans and Cryptococcus gattii.
价 格:¥电议型 号:T16704L产 地:中国大陆
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T7103idalopirdine5-HT Receptor,Serotonin Receptor,Lu AE-58054,idalopirdine,Inhibitor,inhibit,5-hydroxytry
Idalopirdine, a selective 5-HT6 receptor antagonist( Ki : 0.83 nM),as a treatment for Alzheimer´s disease.
价 格:¥电议型 号:T7103产 地:中国大陆
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T64351GI-560192
GI-560192 is a potent smo cilial modulator with an EC50 value of 0.02 ?M. GI-560192 modulates the translocation and/or accumulation of smoothened to the primary cilia by hedgehog signaling pathway.
价 格:¥电议型 号:T64351产 地:中国大陆
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T11155Eg5 Inhibitor V, trans-24Eg5 Inhibitor V, trans 24,Eg-5 Inhibitor V, trans-24,Eg5 Inhibitor V, trans
Eg5 Inhibitor V, trans-24 is a specific and potent Eg5 inhibitor that can be used in cancer research with an IC50 value of 0.65 uM.
价 格:¥电议型 号:T11155产 地:中国大陆
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T6965RG7112E1 activating enzyme,Inhibitor,RO-5045337,E1/E2/E3 Enzyme,RG7112,Ubiquitin conjugating enzyme,
RG7112 (RO5045337) is an orally bioavailable and selective p53-MDM2 inhibitor.
价 格:¥电议型 号:T6965产 地:中国大陆
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T12204NecroX-5NecroX 5,NecroX5
NecroX-5, a derivative of NecroX, exhibits anti-inflammatory and anti-cancer activities. NecroX-5 reduces intracellular calcium concentration.
价 格:¥电议型 号:T12204产 地:中国大陆
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T72345-Amino-2-chloropyridine5 Amino 2 chloropyridine,5Amino2chloropyridine
5-Amino-2-chloropyridine is Pyridine intermediates
价 格:¥电议型 号:T7234产 地:中国大陆
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T9609GRK5-IN-2metabolic,bicyclic,insulin,kinase,inhibit,Inhibitor,disease,pyridine-based,GRK5 IN 2,GRK-5-
GRK5-IN-2, a pyridine-based bicyclic compound, is a potent G-protein-coupled receptor kinase 5 (GRK5) inhibitor. It regulates the expression and/or release of insulin and is useful for the metabolic disease research.
价 格:¥电议型 号:T9609产 地:中国大陆
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TP2212La-MSH, amide Acetate(581-05-5 free base)a MSH, amide Acetate(581 05 5 free base),aMSH, amide Acetate
a-MSH, amide Acetate as an endogenous neuropeptide. It is an endogenous melanocortin receptor 4 (MC4R) agonist with anti-inflammatory and antipyretic activities. α-MSH is a post-translational derivative of pro-opiomelanocortin (POMC)
价 格:¥电议型 号:TP2212L产 地:中国大陆
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TD0087LSulfo-Cy5.5 TrifluoroacetateSulfo-Cy-5.5 Trifluoroacetate,SulfoCy5.5 Trifluoroacetate,Sulfo Cy5.5 Tr
Sulfo-Cy5.5 Trifluoroacetate is a kind of cyano dye, which is very suitable for non-invasive in vivo near-infrared imaging, and is suitable for applications that require a low fluorescence background.
价 格:¥电议型 号:TD0087L产 地:中国大陆
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T9759MAO-B-IN-5MAO B IN 5,MAOBIN5
MAO-B-IN-5 is a potent, selective and orally active MAO-B inhibitor with an IC 50 of 0.204 μM. MAO-B-IN-5 has the research potential in Parkinson´s disease (PD) [1].
价 格:¥电议型 号:T9759产 地:中国大陆
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T86112,3-dihydro-1H-indene-5-sulfonamide2,3 dihydro 1H indene 5 sulfonamide,2,3dihydro1Hindene5sulfonamid
2,3-dihydro-1H-indene-5-sulfonamide is Carbonic anhydrase 12 (human) inhibitor.
价 格:¥电议型 号:T8611产 地:中国大陆
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TQ00186-Amino-5-azacytidineInhibitor,Bacterial,inhibit,6Amino5azacytidine,6 Amino 5 azacytidine
6-Amino-5-azacytidine has an inhibitory of the growth of E. coli.
价 格:¥电议型 号:TQ0018产 地:中国大陆
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T6068MK-5108MK 5108,VX689,Aurora Kinase,VX 689,inhibit,Autophagy,MK-5108,Inhibitor
MK-5108 is a highly potent and specific Aurora-A kinase inhibitor with an IC50 value of 0.064 nM.
价 格:¥电议型 号:T6068产 地:中国大陆
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TP1012CH 5450CH5450,inhibit,MAB elastase 2,CH 5450,Inhibitor,Ang I,chymase,CH-5450
CH 5450 (Z-Ile-Glu-Pro-Phe-Ome) is a short peptide inhibitor of chymase in the human heart
价 格:¥电议型 号:TP1012产 地:中国大陆