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产品数:86101
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T11025hDHODH-IN-3
hDHODH-IN-3 is an inhibitor of human dihydroorotate dehydrogenase with a pMIC50 value of 8.6. hDHODH-IN-3 can inhibit measles virus replication.
价 格:¥电议型 号:T11025产 地:中国大陆
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T60122AldometanibCompoundIA47
Aldometanib (LXY-05-029) is an orally active aldolase inhibitor. Aldometanib prevents FBP from binding to v-ATPase-associated aldolase and activates lysosomal AMPK. Aldometanib can be used for the research of metabolic homeostasis [1].
价 格:¥电议型 号:T60122产 地:中国大陆
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TP2105LUFP-101 acetateUFP 101 acetate,UFP101 acetate
UFP-101 acetate is a selective and competitive antagonist of the NOP receptor (pKi = 10.24) with >3000-fold selectivity over δ, μ, and κ opioid receptors.
价 格:¥电议型 号:TP2105L产 地:中国大陆
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T9384Pomalidomide-PEG3-OHPomalidomide-PEG-3-OH,Pomalidomide PEG3 OH,PomalidomidePEG3OH
Pomalidomide-PEG3-OH enables the synthesis of molecules for targeted protein degradation and PROTAC (proteolysis-targeting chimeras) technology.
价 格:¥电议型 号:T9384产 地:中国大陆
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T20719Oxadiargyl
Oxadiargyl, a protoporphyrinogen oxidase inhibitor, is used as a herbicide in China.
价 格:¥电议型 号:T20719产 地:中国大陆
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T7426ALSTERPAULLONECDK5,GSK-3,p35,NSC-705701,9-Nitropaullone,NSC705701,ALSTERPAULLONE,Glycogen synthase k
Alsterpaullone is a Cyclin-Dependent Kinase Inhibitor, Mediated Toxicity in HeLa Cells Through Apoptosis-Inducing Effec
价 格:¥电议型 号:T7426产 地:中国大陆
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T8593RU 249695-HT1B,Serotonin Receptor,fluid,RU 24969,5-HT1A,RU24969,locomotion,Inhibitor,5-HT Receptor,5
RU 24969 is a selective agonist of 5-HT1A and 5-HT1B receptors.
价 格:¥电议型 号:T8593产 地:中国大陆
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TN27032,3-Dihydroxy-4-methoxyacetophenoneinhibit,2,3Dihydroxy4methoxyacetophenone,Inhibitor,2,3 Dihydroxy
2,3-Dihydroxy-4-methoxyacetophenone is a natural product,it improves cognitive function and may be helpful for the treatment of Alzheimer´s disease.
价 格:¥电议型 号:TN2703产 地:中国大陆
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T64354Cystathionine-γ-lyase-IN-1
Cystathionine-γ-lyase-IN-1 is a selective inhibitor of cystathionine γ-lyase (CSE) enzyme (IC50= 6.3 μM).
价 格:¥电议型 号:T64354产 地:中国大陆
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T38622Bcl-xL antagonist 2Bcl xL antagonist 2,BclxL antagonist 2
Bcl-xL antagonist 2 is an effective and selective antagonist of Bcl-xL with an IC50 of 91 nM and a Ki of 65 nM. Bcl-xL antagonist 2 induces apoptosis in cancer cells and can be used in studies about chronic lymphocytic leukemia and non-Hodgkin’s lymphoma.
价 格:¥电议型 号:T38622产 地:中国大陆
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T61318BRD4 Inhibitor-20
BRD4 Inhibitor-20 is a potent bromodomain protein 4 (BRD4) inhibitor with oral activity. BRD4 Inhibitor-20 has antiproliferative activity in cancer cell lines and is used in studies of various cancers, such as colon cancer.
价 格:¥电议型 号:T61318产 地:中国大陆
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TQ0025E7046Inhibitor,E-7046,Prostaglandin Receptor,E7046,E 7046,inhibit
E7046 is a specific, orally bioavailable EP4 antagonist (IC50: 13.5 nM, Ki: 23.14 nM), exhibiting anti-tumor activities.
价 格:¥电议型 号:TQ0025产 地:中国大陆
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T6879LLY-507protein,inhibit,methyltransferase,methylation,breast,cancer,SMYD2,LLY-507,p53,Inhibitor,Histo
LLY-507 is an effective, cell-active, and specific inhibitor of protein-lysine Methyltransferase SMYD2.
价 格:¥电议型 号:T6879产 地:中国大陆
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T9699TAK-615LPA1,fibrosis,LPL Receptor,Lysophospholipid Receptor,TAK615,modulator,TAK-615,NAM,inhibit,pul
TAK-615 is commonly used to study pulmonary fibrosis and is a negative allosteric modulator of LPA1 receptors.
价 格:¥电议型 号:T9699产 地:中国大陆
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TP1865LRhodopsin Epitope Tag acetateRhodopsin Epitope Tag acetate
Rhodopsin Epitope Tag acetate is a 9-amino acid peptide representing C terminus of bovine rhodopsin widely used as an epitope tag. A number of anti-rhodopsin antibodies can recognize this epitope.
价 格:¥电议型 号:TP1865L产 地:中国大陆
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T6530HC-030031HC-030031,HC 030031,TRP Channel,Transient receptor potential channels,Inhibitor,inhibit
HC-030031 is a potent TRPA1 inhibitor, which antagonizes AITC- and formalin-evoked calcium influx with IC50s of 6.2±0.2 and 5.3±0.2 μM, respectively.
价 格:¥电议型 号:T6530产 地:中国大陆
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TN71857-Cyano-7-deazaguanine
3H-Pyrrolo[2,3-d]pyrimidine-5-carbonitrile, 2-amino-4,7-dihydro-4-oxo- is a marine derived natural products found in Streptomyces qinglanensis.
价 格:¥电议型 号:TN7185产 地:中国大陆
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TQ0263EPZ031686
EPZ031686 is an effective inhibitor of SMYD3 inhibitor with an IC50 of 3 nM and can be used in studies about cancer.
价 格:¥电议型 号:TQ0263产 地:中国大陆
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T7309TAS-103 dihydrochlorideBMS247615,Topoisomerase,TAS-103,TAS103,inhibit,TAS 103 dihydrochloride,BMS-24
TAS-103 (dihydrochloride) is a novel anticancer agent targeting both topoisomerase (Topo) I and Topo II.
价 格:¥电议型 号:T7309产 地:中国大陆
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T6775BAY 41-2272Inhibitor,inhibit,Guanylate Cyclase,BAY 41 2272,BAY 412272,BAY 41-2272
BAY 41-2272 is a direct and NO-independent soluble guanylate cyclase (sGC) stimulator.
价 格:¥电议型 号:T6775产 地:中国大陆