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T9041AES-350Histone deacetylases,AES 350,MV4-11,AES-350,Apoptosis,acute myeloid leukemia,AML,Inhibitor,in
AES-350 is a potent and orally active HDAC6 inhibitor(IC50 and a Ki of 0.0244 μM and 0.035 μM, respectively). It is also against HDAC-3, -8, and -11 in an enzymatic activity assay with IC50 values of 0.187 μM, 0.245 μM, and >1μM, respectively. AES-350 triggers apoptosis in AML cells through HDAC inhibition and can be used for acute myeloid leukemia (AML) research.
价 格:¥电议型 号:T9041产 地:中国大陆
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T61518TAK-653
TAK-653, an AMPA receptor potentiator with minimal agonistic activity, produces an antidepressant-like effect with a favorable safety profile in rats.
价 格:¥电议型 号:T61518产 地:中国大陆
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T6924Riviciclib hydrochlorideinhibit,Inhibitor,Riviciclib,CDK,Riviciclib hydrochloride,Cyclin dependent k
P276-00 is a novel CDK1, CDK4 and CDK9 inhibitor with IC50 of 79 nM, 63 nM and 20 nM, respectively. Phase 2/3.
价 格:¥电议型 号:T6924产 地:中国大陆
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T39389KDM2B-IN-2KDM2B IN 2,KDM-2B-IN-2,KDM2BIN2
KDM2B-IN-2 is a potent histone demethylase (kdm2b) inhibitor.
价 格:¥电议型 号:T39389产 地:中国大陆
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T8084Dimethyl 4-hydroxyisophthalateDimethyl 4-hydroxyisophthalate,inhibit,Dimethyl 4 hydroxyisophthalate,
Dimetghyl 4-Hydroxyisophthalate is a methyl salicylate analogue, used as a building block in the chemical synthesis.
价 格:¥电议型 号:T8084产 地:中国大陆
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T6767TCS7010Aurora Kinase,inhibit,TCS 7010,Apoptosis,TCS-7010,TCS7010,Inhibitor
Aurora A Inhibitor I is a novel, potent, and selective inhibitor of Aurora A with IC50 of 3.4 nM in a cell-free assay. It is 1000-fold more selective for Aurora A than Aurora B.
价 格:¥电议型 号:T6767产 地:中国大陆
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T7815LAOD9604 acetate(221231-10-3 free base)AOD9604 acetate(221231103 free base),AOD-9604 acetate(221231-1
AOD9604 acetate is a potential anti-obesity peptide based on the human growth hormone.
价 格:¥电议型 号:T7815L产 地:中国大陆
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T13246UCT943UCT-943,UCT943
UCT943 is an inhibitor of Plasmodium falciparum PI4K (IC50 = 23 nM).
价 格:¥电议型 号:T13246产 地:中国大陆
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T75283,7-dimethylocta-2,6-dienyl 5,9,13-trimethyltetradeca-4,8,12-enoate3,7dimethylocta2,6dienyl 5,9,13tr
3,7-dimethylocta-2,6-dienyl 5,9,13-trimethyltetradeca-4,8,12-enoate is a chemical compound
价 格:¥电议型 号:T7528产 地:中国大陆
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T6443Chloroprocaine hydrochlorideinhibit,Na,K-ATPase,Sodium potassium pump,Chloroprocaine,anesthetic,2-Ch
Chloroprocaine HCl is a local anesthetic during surgical procedures.
价 格:¥电议型 号:T6443产 地:中国大陆
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T7596FirocoxibLPS,COX-2,fever,ML1785713,Cyclooxygenase,COX,inhibit,Firocoxib,Inhibitor,anti-inflammatory,
Firocoxib is a selective non-steroidal inhibitor of cycooxygenase-2 (COX-2) (IC50 of 0.13 μM), with anti-inflammatory for use in dogs and horses.
价 格:¥电议型 号:T7596产 地:中国大陆
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T60057WAY-388657WAY 388657,WAY388657
WAY-388657 is a Notum Pectinacetylesterase inhibitor with IC50 < 0.025 μM.
价 格:¥电议型 号:T60057产 地:中国大陆
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T7083GLPG1837GLPG-1837,ABBV 974,Cystic fibrosis transmembrane conductance regulator,Inhibitor,CFTR,Autoph
GLPG1837 is an effective CFTR potentiator, with EC50s of 3 nM and 339 nM for F508del and G551D CFTR, respectively.
价 格:¥电议型 号:T7083产 地:中国大陆
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T38163ML-148ML-148,ML 148,selective,Inhibitor,prostaglandin-signaling,15-PGDH,15-Hydroxyprostaglandin dehy
ML-148 is a selective inhibitor of 15-hydroxy prostaglandin dehydrogenase (15-PGDH, IC50 = 56 nM). ML-148 can be used to profile across a panel of related dehydrogenase or reductase enzymes and in studies about prostaglandin-signaling pathways.
价 格:¥电议型 号:T38163产 地:中国大陆
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T6648Rotundine5-hydroxytryptamine Receptor,Inhibitor,Dopamine Receptor,Rotundine,5-HT Receptor,inhibit,Se
Rotundine (L-tetrahydropalmatine, L-THP) is a selective dopamine D1 receptor antagonist with IC50 of 166 nM.
价 格:¥电议型 号:T6648产 地:中国大陆
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T60199NCRW0005-F05NCRW0005F05
NCRW0005-F05 is a potent agonist of orphan G-protein coupled receptor GPR139 with an IC 50 value of 0.21 μM. NCRW0005-F05 can be used to research diabetes, obesity and Parkinson´s disease [1].
价 格:¥电议型 号:T60199产 地:中国大陆
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T7712LDisomotide TFA 181477-43-0(free base)Disomotide TFA 181477430(free base),Disomotide TFA 181477 43 0(
Disomotide is an oligopeptide for the treatment of melanoma.
价 格:¥电议型 号:T7712L产 地:中国大陆
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T6683STF-62247renal,STF-62247,VHL,carcinoma,inhibit,cytotoxic,cell,RCC,Inhibitor,STF62247,intracytoplasmi
STF-62247 is TGN inhibitor with IC50 of 0.625 μM and 16 μM in RCC4 and RCC4/VHL cells, respectively.
价 格:¥电议型 号:T6683产 地:中国大陆
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T12163N6-(2-Phenylethyl)adenosineP1 receptor,A1AR,derivative,N-6-(2-Phenylethyl)adenosine,Adenosine Recept
N6-(2-Phenylethyl)adenosine is an adenosine derivative and an agonist of adenosine receptors with Ki values of 11.8 nM and 30.1 nM for rat and human A1.
价 格:¥电议型 号:T12163产 地:中国大陆
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T60072ZL0590non-KAc binding site,ZL0590,ZL-0590,BRD4 BD1,Inhibitor,acute airway inflammation,inhibit,Epige
ZL0590 is an effective and selective inhibitor of BD1-BRD4 (IC50 = 90 nM) with anti-inflammatory activities.
价 格:¥电议型 号:T60072产 地:中国大陆