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产品数:86101
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已选条件
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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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TQ0230BTK IN-1Btk,SNS062,Inhibitor,SNS-062,BTK IN 1,Bruton tyrosine kinase,SNS 062,inhibit,BTK IN-1,BTK IN
BTK IN-1 (SNS062 analog) is an effective BTK inhibitor (IC50: <100 nM).
价 格:¥电议型 号:TQ0230产 地:中国大陆
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T26969CCT365623CCT365623
CCT365623 is an orally bioavailable Lysyl Oxidase inhibitor with good anti-LOX potency, selectivity, pharmacokinetic properties, as well as anti-metastatic efficacy.
价 格:¥电议型 号:T26969产 地:中国大陆
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Fr16629Compound Fr16629Compound Fr16629
价 格:¥电议型 号:Fr16629产 地:中国大陆
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T7562β-Amyloid (31-35)Abeta,β Amyloid (31 35),βAmyloid (3135),β-amyloid peptide,inhibit,Amyloid-β,Inhibit
β-Amyloid 31-35(TFA) is the shortest sequence of native Amyloid-β peptide.
价 格:¥电议型 号:T7562产 地:中国大陆
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T14362LAY 9944 dihydrochloride1(2chlorophenyl)N[[4[(2chlorophenyl)methylaminomethyl]cyclohexyl]methyl]metha
AY 9944 dihydrochloride is a intermediate.
价 格:¥电议型 号:T14362L产 地:中国大陆
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TQ0062NastorazepideZ360,CCK Receptor,Cholecystokinin Receptor,Inhibitor,Z 360,Nastorazepide,inhibit
Nastorazepide is a selective, orally available antagonist of gastrin/cholecystokinin 2 (CCK-2) receptor with potential antineoplastic activity.
价 格:¥电议型 号:TQ0062产 地:中国大陆
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Fr12622Compound Fr12622Compound Fr12622
价 格:¥电议型 号:Fr12622产 地:中国大陆
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T7622GabazineInhibitor,Gamma-aminobutyric acid Receptor,Gabazine,γ-Aminobutyric acid Receptor,inhibit,SR
Gabazine is an antagonist of GABAA receptors (Ki : 74-150 nM)
价 格:¥电议型 号:T7622产 地:中国大陆
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T8556Z-Gly-Gly-Arg-AMC TFA (66216-78-2 free base)Z Gly Gly Arg AMC TFA (66216 78 2 free base),ZGlyGlyArgA
Z-Gly-Gly-Arg-AMC is a thrombin-specific fluorogenic substrate for testing of thrombin generation in PRP and platelet-poor plasma (PPP).
价 格:¥电议型 号:T8556产 地:中国大陆
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T60202MMRi62
MMRi62, a ferroptosis inducer targeting MDM2-MDM4 (negative regulators of tumor suppressor p53). MMRi62 shows a P53-independent pro-apoptotic activity against pancreatic ductal adenocarcinoma (PDAC) cells and induce autophagy. MMRi62 inducesferroptosis, resulting in a increase of reactive oxygen and lysosomal degradation of ferritin heavy chain (FTH1). MMRi62 also leads to proteasomal degradation of mutant p53, also inhibits orthotopic xenograft PDAC mouse model in vivo with high frequency mutat
价 格:¥电议型 号:T60202产 地:中国大陆
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T10623BSH-IN-1BSH IN 1,BSHIN1
BSH-IN-1 is a potent and covalent inhibitor of gut bacterial recombinant bile salt hydrolases (BSHs; IC50s: 108 nM and 427 nM for B. longum BSH and B. theta BSH).
价 格:¥电议型 号:T10623产 地:中国大陆
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T7626Budipinemonoamine oxidase type B (MAO-B),inhibit,CNS disorders,Parkinson disease,Budipine,Inhibitor,
Budipine is a low affinity, N-methyl-D-aspartate receptor antagonist,is an antiparkinsonian agent.
价 格:¥电议型 号:T7626产 地:中国大陆
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T8620piperacillinβ-lactamase,inhibit,Gram-positive,piperacillin,semisynthetic penicillin,Inhibitor,Bacter
Piperacillin is a semisynthetic penicillin with wide spectrum of antimicrobial activity(particularly pseudomonas strains)
价 格:¥电议型 号:T8620产 地:中国大陆
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T6644RolipramHuman immunodeficiency virus,SB95952,Rolipram,ZK62711,Inhibitor,SB-95952,Bacterial,Phosphodi
Rolipram is a phosphodiesterase 4 inhibitor with antidepressant properties.
价 格:¥电议型 号:T6644产 地:中国大陆
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T9164BMS-986242glucuronidation,potent,Indoleamine 2,3-Dioxygenase (IDO),cancer,Inhibitor,BMS 986242,inhib
BMS-986242 is an orally active, potent and selective inhibitor of indoleamine-2,3-dioxygenase 1 (IDO1), and it can be used for the research of cancer.
价 格:¥电议型 号:T9164产 地:中国大陆
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T5362Y06036inhibit,Epigenetic Reader Domain,Inhibitor,Y-06036,Y 06036,Y06036
Y06036, a potent and selective BET inhibitor, can bind to the BRD4(1) bromodomain (Kd: 82 nM).
价 格:¥电议型 号:T5362产 地:中国大陆
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T6622Oxacillin sodium monohydrateInhibitor,Bacterial,Tol,Oxacillin sodium monohydrate,inhibit,mecA,Antibi
Oxacillin sodium monohydrate is an antibacterial agent and is a narrow spectrum beta-lactam antibiotic of the penicillin class.
价 格:¥电议型 号:T6622产 地:中国大陆
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T6762AS1842856AS 1842856,AS-1842856,inhibit,AS1842856,Autophagy,Inhibitor
AS1842856, a cell-permeable inhibitor, can block the transcription activity of Foxo1 (IC50: 33 nM). It can directly bind to the active Foxo1, but not the Ser256-phosphorylated form.
价 格:¥电议型 号:T6762产 地:中国大陆
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T8162Cannabidivarininhibit,Cannabidivarin,Inhibitor,GWP-42006,非拟精神病药大麻素,GWP42006,GWP 42006
Cannabidivarin is a potent inhibitor against gamma 2 subunit of GABAA receptors. it may serve as a novel drug with definite control over childhood absence epilepsy.
价 格:¥电议型 号:T8162产 地:中国大陆