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T19600Vanilpyruvic acid;化合物 T19600Vanylpyruvic acid;Vanylpyruvic acid
Vanilpyruvic acid is a metabolite of catecholamine and precursor of vanillactic acid.
价 格:¥电议型 号:T19600产 地:中国大陆
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T1960YL-109;化合物YL-109YL-109
YL-109, a novel anticancer agent, can inhibit breast Y cell growth and invasiveness in vitro and in vivo.
价 格:¥电议型 号:T1960产 地:中国大陆
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T18960D149 Dye化合物 T18960D149|||Indoline dye D149
D149 Dye is an indoline-based dye and a high-extinction-coefficient metal-free organic sensitizer.
价 格:¥电议型 号:T18960产 地:中国大陆
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T17960Fmoc-N-PEG23-acid;化合物 T17960Fmoc-N-PEG23-acid
Fmoc-N-amido-PEG23-acid is a polyethylene glycol (PEG)-based linker utilized for the synthesis of proteolysis-targeting chimeras (PROTACs)[1].
价 格:¥电议型 号:T17960产 地:中国大陆
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T1770GNE-9605;化合物GNE9605GNE-9605
GNE-9605 is a highly effective, specifical, and brain-penetrant LRRK2 inhibitor (IC50: 19 nM).
价 格:¥电议型 号:T1770产 地:中国大陆
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T16960Sultiame;舒噻嗪Sultiame
Sultiame is an inhibitor of carbonic anhydrase. Sultiame can be used in antiepileptic research.
价 格:¥电议型 号:T16960产 地:中国大陆
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T16894SKF96067;化合物 T16894SKF96067
SKF96067 is a reversible gastric H+/K+-ATPase inhibitor.
价 格:¥电议型 号:T16894产 地:中国大陆
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T15960Mal-amido-PEG7-acid;化合物Mal-amido-PEG7-acidMaleimide-NH-PEG7-CH2CH2COOH|||Mal-NH-PEG7-COOH;Maleimide-
Mal-amido-PEG7-acid (Mal-NH-PEG7-COOH) is a PEG-based PROTAC linker that can be used to synthesize PROTACs.
价 格:¥电议型 号:T15960产 地:中国大陆
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T15630Tilmacoxib;替马考昔RWJ57504|||JTP19605|||JTE522;RWJ57504|||JTP19605|||替马考昔|||JTE522
Tilmacoxib is a highly selective, time-dependent, and irreversible inhibitor of human COX-2 ( IC50: 85 nM in an enzyme assay).
价 格:¥电议型 号:T15630产 地:中国大陆
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T14960Chroman 1;化合物Chroman 1Chroman 1
Chroman 1 is a potent inhibitor of ROCK1 (IC50?= 52 pM) and ROCK2 (IC50?= 1 pM).
价 格:¥电议型 号:T14960产 地:中国大陆
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T13960Vitamin B15;潘氨酸Pangamic Acid;潘氨酸|||Pangamic Acid
Vitamin B15 is a natural product and can used be as an agent stimulating cellular respiration, and is an immune-correcting agent.
价 格:¥电议型 号:T13960产 地:中国大陆
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T12960Sofosbuvir impurity E;化合物 T12960Sofosbuvir impurity E
Sofosbuvir impurity E is the less active impurity of Sofosbuvir. Sofosbuvir is an active HCV RNA replication inhibitor in the HCV replicon assay,with potent anti-hepatitis C virus (HCV) activity.
价 格:¥电议型 号:T12960产 地:中国大陆
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T1283Clinafloxacin;克林沙星PD 127391|||CI-960|||AM-1091;克林沙星|||PD 127391|||CI-960|||AM-1091
Clinafloxacin (CI-960)(PD-127391) is a fluoroquinolone antibiotic.
价 格:¥电议型 号:T1283产 地:中国大陆
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T12700(rel)-AR234960;化合物 T12700(rel)-AR234960
(rel)-AR234960 is an active relative configuration of AR234960. AR234960 is a non-peptide agonist of MAS.
价 格:¥电议型 号:T12700产 地:中国大陆
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T12657(Rac)-Atomoxetine D7 hydrochloride;化合物 T12657(Rac)-LY 139603 D7|||(Rac)-Tomoxetine D7 hydrochloride;
(Rac)-Atomoxetine D7 hydrochloride is a deuterium labeled (Rac)-Atomoxetine hydrochloride. (Rac)-Atomoxetine hydrochloride is a racemic form of Atomoxetine hydrochloride.
价 格:¥电议型 号:T12657产 地:中国大陆
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T124960Avenacoside B;燕麦苷BAvenacoside B
Avenacoside B can be extracted from oats and has antinematode activity, which enhances osteogenic activity.
价 格:¥电议型 号:T124960产 地:中国大陆
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T12192NCGC00229600;化合物NCGC00229600NCGC00229600
NCGC00229600 is an allosteric inverse thyrotropin receptor (TSHR) agonist. NCGC00229600 inhibits both TSH and stimulating antibody activation of TSHRs endogenously and can be used in Graves´ disease studies.
价 格:¥电议型 号:T12192产 地:中国大陆
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T11960MBM-55;化合物MBM-55MBM-55
MBM-55 is an effective inhibitor of NIMA related kinase 2 (NEK2) with an IC50 of 1 nM. MBM-55 effectively inhibits the proliferation of cancer cells by inducing cell cycle arrest and apoptosis.
价 格:¥电议型 号:T11960产 地:中国大陆
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T11830LDN-192960 hydrochloride化合物 T11830LDN192960 hydrochloride|||LDN 192960 hydrochloride
LDN-192960 hydrochloride is an inhibitor of Dual-specificity Tyrosine-regulated Kinase 2 (DYRK2) and Haspin with IC50s of 48 nM and 10 nM, respectively.
价 格:¥电议型 号:T11830产 地:中国大陆