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T1463RamelteonRamelteon,TAK-375,
Ramelteon is a Melatonin Receptor Agonist. The mechanism of action of ramelteon is as a Melatonin Receptor Agonist.
价 格:¥电议型 号:T1463产 地:美洲
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T15709Lapaquistat acetateLapaquistat acetate,TAK-475,
Lapaquistat acetate is originally intended use to Mevalonate Kinase Deficiency (MKD), it is effective at lowering low-density lipoprotein cholesterol, but it might cause liver damage. Lapaquistat acetate is a squalene synthase inhibitor. It also blocks th
价 格:¥电议型 号:T15709产 地:美洲
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T1745TAK-063TAK-063,TAK063,TAK 063
TAK-063 is a highly effective and selective PDE10A inhibitor (IC50: 0.30 nM); Its selectivity is >15000-fold over other PDEs.
价 格:¥电议型 号:T1745产 地:美洲
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T2351TAK875TAK875,Fasiglifam,
TAK875 is a potent, selective and orally bioavailable GPR40 agonist.
价 格:¥电议型 号:T2351产 地:美洲
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T2404Vonoprazan fumarateVonoprazan fumarate,TAK-438,
Vonoprazan Fumarate (TAK-438) is a novel P-CAB (potassium-competitive acid blocker) that reversibly inhibits H+/K+, ATPase.
价 格:¥电议型 号:T2404产 地:美洲
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T2709TAK901TAK901
TAK-901 has been used in trials studying the treatment of Lymphoma, Myelofibrosis, Multiple Myeloma, Myeloid Metaplasia, and Advanced Solid Tumors, among others.
价 格:¥电议型 号:T2709产 地:美洲
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T6124MubritinibMubritinib,TAK-165,
Mubritinib (TAK-165) is a potent inhibitor of HER2/ErbB2 with IC50 of 6 nM.
价 格:¥电议型 号:T6124产 地:美洲
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T6219Azilsartan MedoxomilAzilsartan Medoxomil,TAK-491,
Azilsartan medoxomil(TAK 491) is an orally administered angiotensin II receptor type 1 antagonist with IC50 of 0.62 nM, which used in the treatment of adults with essential hypertension.
价 格:¥电议型 号:T6219产 地:美洲
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T8428Subasumstat化合物TAK-981TAK-981
Subasumstat (TAK-981) is a selective the SUMOylation enzymatic cascade inhibitor, has potential immune-activating and antineoplastic activities.
价 格:¥电议型 号:T8428产 地:中国大陆
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T8388Vonoprazan;沃诺拉赞TAK-438 (free base);TAK-438 (free base)|||沃诺拉赞
Vonoprazan (TAK-438 (free base)) is an orally active potassium-competitive acid blocker.Vonoprazan can be used for the treatment of gastroduodenal ulcer and reflux esophagitis
价 格:¥电议型 号:T8388产 地:中国大陆
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T8151Mobocertinib;化合物Mobocertinibtak788;tak788
Mobocertinib (tak788) is a potent inhibitor of epidermal growth factor receptor (EGFR) and an antineoplastic agent
价 格:¥电议型 号:T8151产 地:中国大陆
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T8128Mosapride;莫沙必利TAK-370|||AS-4370;TAK-370|||AS-4370|||莫沙必利
Mosapride (AS-4370) is a selective 5HT4 agonist
价 格:¥电议型 号:T8128产 地:中国大陆
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T81153Sitakisogenin;化合物 SitakisogeninSitakisogenin
Sure, please provide the description of the chemical compound you´d like to be rewritten.
价 格:¥电议型 号:T81153产 地:中国大陆
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T80880Valziflocept;化合物 ValzifloceptBAX1810|||TAK-752;BAX1810|||TAK-752
Valziflocept (BAX1810; TAK-752) is a recombinant soluble human FcγRIIb receptor designed to act as a "decoy" or "scavenger" by targeting Fc and FcγR, binding and neutralizing pathogenic IgG. Its utility lies in mitigating the impact of autoimmune diseases, making it a focus in systemic lupus erythematosus (SLE) research [1].
价 格:¥电议型 号:T80880产 地:中国大陆
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T78636Firazorexton hydrate;化合物 Firazorexton hydrateTAK-994;TAK-994
Firazorexton hydrate (TAK-994) is a brain-penetrant and orally active agonist of the orexin type 2 receptor (OX2R) with a potent EC50 of 19 nM. It effectively reduces wakefulness fragmentation and cataplexy-like episodes in mouse models of narcolepsy [1].
价 格:¥电议型 号:T78636产 地:中国大陆
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T77171Efineptakin alfa;化合物 Efineptakin alfaEfineptakin alfa
Efineptakin alfa (NT-17), a long-acting recombinant human interleukin-7 (IL-7), promotes the proliferation and survival of CD4+ and CD8+ cells in both humans and mice. It has applications in glioblastoma research [1].
价 格:¥电议型 号:T77171产 地:中国大陆
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T77098Netakimab;化合物 NetakimabNetakimab
Netakimab, an anti-IL-17 monoclonal antibody, is utilized in the research of ankylosing spondylitis, psoriatic arthritis, and moderate-to-severe plaque psoriasis [1] [2].
价 格:¥电议型 号:T77098产 地:中国大陆
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T76048TAK-683 acetate;化合物 TAK-683 acetateTAK-683 acetate
TAK-683 acetate is a nonapeptide metastin analog and a potent full agonist of the KISS1 receptor (KISS1R), exhibiting IC 50 =170 pM and enhanced metabolic stability. This compound shows agonistic activities towards KISS1R, with EC 50 values of 0.96 nM and 1.6 nM for human and rat KISS1R, respectively. TAK-683 acetate effectively depletes GnRH in the hypothalamus and reduces plasma levels of FSH, LH, and testosterone in vivo, showcasing its potential for hormone-dependent prostate cancer research
价 格:¥电议型 号:T76048产 地:中国大陆
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T76047TAK-683 TFA;化合物 TAK-683 TFATAK-683 TFA
TAK-683 TFA, a potent full KISS1 receptor (KISS1R) agonist with a half-maximal inhibitory concentration (IC50) of 170 pM, exhibits enhanced metabolic stability. As a nonapeptide metastin analog, it demonstrates agonistic activities towards KISS1R, with effective concentration (EC50) values of 0.96 nM for humans and 1.6 nM for rats. In vivo, TAK-683 TFA reduces gonadotropin-releasing hormone (GnRH) levels in the hypothalamus and decreases plasma follicle-stimulating hormone (FSH), luteinizing hor
价 格:¥电议型 号:T76047产 地:中国大陆