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T68836ADS-J1;化合物 ADS-J1ADS-J1
ADS-J1 is an HIV-1 entry inhibitor that potently inhibits seminal amyloid fibrillization and block fibril-mediated enhancement of viral infection. Semen-derived amyloid fibrils, comprising SEVI (semen-derived enhancer of viral infection) fibrils and SEM1 fibrils, may remarkably enhance HIV-1 sexual transmission and are potential targets for the development of an effective microbicide.
价 格:¥电议型 号:T68836产 地:中国大陆
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T68835Mindodilol;化合物 MindodilolMindodilol
Mindodilol is a β-adrenoceptor blocker and vasodilator.
价 格:¥电议型 号:T68835产 地:中国大陆
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T68834Lortalamine;化合物 LortalamineLortalamine
Lortalamine is an antidepressant which was synthesized in the early 1980s. It acts as a potent and highly selective norepinephrine reuptake inhibitor.
价 格:¥电议型 号:T68834产 地:中国大陆
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T68833Glutathione sulfinanilide;化合物 Glutathione sulfinanilideGlutathione sulfinanilide
Glutathione sulfinanilide is a hydrophilic derivative of the protein tyrosine phosphatase inhibitor phenylarsine oxide (PAO). It inhibits angiogenesis and tumour growth.
价 格:¥电议型 号:T68833产 地:中国大陆
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T68832Itazigrel;化合物 ItazigrelItazigrel
Itazigrel is a platelet aggregation inhibitor.
价 格:¥电议型 号:T68832产 地:中国大陆
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T68831Furodysinin;化合物 FurodysininFurodysinin
Furodysinin is an agonist of human leukotriene B4 receptor.
价 格:¥电议型 号:T68831产 地:中国大陆
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T68830Etrabamine;化合物 EtrabamineEtrabamine
Etrabamine is a selective dopamine D2 receptor agonist
价 格:¥电议型 号:T68830产 地:中国大陆
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T6883Samotolisib;化合物LY3023414GTPL8918|||LY3023414;GTPL8918|||LY3023414
Samotolisib (LY3023414) is an oral ATP competitive inhibitor of the class I PI3K isoforms, DNA-PK, and mTOR. Samotolisib (LY3023414) has been used in trials studying the treatment of Neoplasm, Solid Tumor, COLON CANCER, BREAST CANCER, and Advanced Cancer, among others.
价 格:¥电议型 号:T6883产 地:中国大陆
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T68236TP0438836;化合物 TP0438836TP0438836
TP0438836 is a potent, low-absorbable sodium-dependent glucose cotransporter 1 (SGLT1) inhibitor for the treatment of type 2 diabetes. TP0438836 showed IC50 values 28nM and 7 nM for hSGLT1 and hSGLT2 resepctively.
价 格:¥电议型 号:T68236产 地:中国大陆
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T67883EZH2-IN-15;化合物 EZH2-IN-15SHR2554;SHR2554
EZH2-IN-15 is a specific inhibitor of histone modifier enhancer of zeste 2 (EZH2). EZH2 is aberrantly overexpressed in a number of human cancers that controls the adaptive response via regulation of Treg activity. Intratumoral EZH2 expression has also been shown to control the innate immunity
价 格:¥电议型 号:T67883产 地:中国大陆
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T6774AZD-8835;化合物AZD8835AZD8835;AZD8835
AZD-8835 is a mixed inhibitor of PI3Kα/δ (IC50: 6.2/5.7 nM), also with selectivity against PI3Kβ/γ (IC50: 431/90 nM).
价 格:¥电议型 号:T6774产 地:中国大陆
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T66883H-D-Ala-OtBu.HCl;化合物 H-D-Ala-OtBu.HClH-D-Ala-OtBu.HCl
H-D-Ala-OtBu.HCl is an amino acid derivative and has a wide range of applications in life science related research.
价 格:¥电议型 号:T66883产 地:中国大陆
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T658834-Fluorocinnamaldehyde;化合物 4-Fluorocinnamaldehyde4-Fluorocinnamaldehyde
4-Fluorocinnamaldehyde is a useful organic compound for research related to life sciences. The catalog number is T65883 and the CAS number is 24654-55-5.
价 格:¥电议型 号:T65883产 地:中国大陆
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T64883Z-Trp-OH;化合物 Z-Trp-OHZ-Trp-OH
Z-Trp-OH has a wide range of applications in life science related research.
价 格:¥电议型 号:T64883产 地:中国大陆
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T6409ALK kinase inhibitor-1;化合物SAR348830SAR348830;SAR348830
SAR348830 is an ALK inhibitor, targeting anaplastic lymphoma kinase.
价 格:¥电议型 号:T6409产 地:中国大陆
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T63883RAD51-IN-6;化合物 RAD51-IN-6RAD51-IN-6
RAD51-IN-6 is a potent inhibitor of RAD51, which is a eukaryotic gene. RAD51-IN-6 has shown potential for the study of mitochondrial deficiency disorders.
价 格:¥电议型 号:T63883产 地:中国大陆
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T63166L(S, R)-LSN 3318839;化合物(S,R)-LSN 3318839(S, R)-LSN 3318839(Isomer-2764704-18-7);(S, R)-LSN 3318839(Is
产品可用于生物细胞实验
价 格:¥电议型 号:T63166L产 地:中国大陆
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T63166LSN3318839;化合物LSN3318839LSN-3318839|||LSN 3318839;LSN-3318839|||LSN 3318839
LSN3318839 is a potent and orally available glucagon-like peptide-1 receptor (GLP-1R) modulator.LSN3318839 enhances GLP-1R G-protein-coupled signaling and can be used to lower blood glucose.
价 格:¥电议型 号:T63166产 地:中国大陆
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T62883BRD4 Inhibitor-23;化合物 BRD4 Inhibitor-23BRD4 Inhibitor-23
BRD4 Inhibitor-23 is a potent, orally active BRD4 inhibitor that acts on BRD4 BD-1 (IC50: 6.21 nM) and BRD4 BD-2 (IC50: 1.44 nM).
价 格:¥电议型 号:T62883产 地:中国大陆
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T6229Daclatasvir达拉他韦Daklinza|||达卡他韦|||EBP 883|||达拉他韦|||BMS-790052
Daclatasvir (EBP 883) (BMS-790052) is a highly selective inhibitor of HCV NS5A with EC50 of 9-50 pM, for a broad range of HCV replicon genotypes and the JFH-1 genotype 2a infectious virus in cell culture. Phase 3.
价 格:¥电议型 号:T6229产 地:中国大陆