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T1562RebamipideOPC12759;Proamipide;瑞巴派特
Rebamipide is a quinolinone derivative with anti-ulcer and anti-inflammatory activities. Rebamipide induces cyclooxygenase 2 (COX2) synthesis which results in an increase in endogenous prostaglandin synthesis in the gastric mucosa. This agent also inhibit
价 格:¥电议型 号:T1562产 地:中国大陆
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T15617JNJ-38877618OMO-1
JNJ-38877618 is an effective and highly selective inhibitor of Met kinase (IC50s: 2 and 3 nM for wild type and mutant Met, respectively).
价 格:¥电议型 号:T15617产 地:中国大陆
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T15616JNJ-10198409JNJ-?10198409;3-氟-N-(6,7-二甲氧基-2,4-二氢茚并[1,2-C〕吡唑-3-基苯基胺
JNJ- 10198409 is a relatively selective and ATP competitive PDGF-RTK inhibitor (IC50=2 nM). JNJ-10198409 has good activity against PDGFR-β kinase (IC50=4.2 nM) and PDGFR-α kinase (IC50=45 nM). It is a dual-mechanism, antiangiogenic, and tumor cell antipro
价 格:¥电议型 号:T15616产 地:中国大陆
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T15611JH-RE-06
JH-RE-06 disrupts mutagenic translesion synthesis (TLS) by preventing the recruitment of mutagenic POLζ. JH-RE-06 is an effective REV1-REV7 interface inhibitor (IC50=0.78 μM; Kd=0.42 μM), which targets REV1 that interacts with the REV7 subunit of POLζ. JH
价 格:¥电议型 号:T15611产 地:中国大陆
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T1561Clobetasol propionate丙酸氯倍他索;Temovate;Dermovate;CCl 4725;Clobetasol 17-propionate;CGP9555
Clobetasol propionate exerts its effect by binding to cytoplasmic glucocorticoid receptors and subsequently activates glucocorticoid receptor-mediated gene expression. This results in the synthesis of certain anti-inflammatory proteins while inhibiting th
价 格:¥电议型 号:T1561产 地:中国大陆
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T15609JC-1CBIC2
JC-1 is a fluorescent lipophilic carbocyanine dye. It has been used to measure mitochondrial membrane potential. JC 1 can be used in a probe for measuring mitochondrial membrane potential by flow cytometry.
价 格:¥电议型 号:T15609产 地:中国大陆
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T15595LIRL-1620 acetateIRL-1620 acetate(142569-99-1 free base)
IRL-1620 acetate is an effective and selective agonist of Endothelin B receptor (ETB) with a Ki of 16 pM which is more selective than ETA with a Ki of 19 μM.
价 格:¥电议型 号:T15595L产 地:中国大陆
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T15568Imirestat咪瑞司他;Alcon 1576;AL 1576;HOE 843
Imirestat is an aldose reductase inhibitor that can be used in diabetes research.
价 格:¥电议型 号:T15568产 地:中国大陆
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T15562ImazamoxCL29926;(±)-Imazamox;甲氧咪草烟
Imazamox is a systemic herbicide with high selectivity, high activity, safety and broadspectrum activity. Imazamox inhibits the production of acetolactate synthase (ALS) in plants, which would then inhibit plant growth and ultimately lead to plant death.
价 格:¥电议型 号:T15562产 地:中国大陆
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T1556OrnidazoleTiberal;NSC 95075;Ornidazolum;Ro 7-0207;奥硝唑
Ornidazole is a nitroimidazole antiprotozoal agent used in ameba and trichomonas infections. It is partially plasma-bound and also has radiation-sensitizing action.
价 格:¥电议型 号:T1556产 地:中国大陆
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T1549Raloxifene hydrochloride盐酸雷洛昔芬;Keoxifene hydrochloride;Raloxifene HCl;LY139481 hydrochloride;LY15675
Raloxifene hydrochloride is a second generation selective estrogen receptor modulator (SERM) used to prevent osteoporosis in postmenopausal women. It has estrogen agonist effects on bone and cholesterol metabolism but behaves as a complete estrogen antago
价 格:¥电议型 号:T1549产 地:中国大陆
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T15432GSK256073
GSK256073 is an orally active GPR109A agonist. GSK256073 also is a long-lasting and non-flushing HCA2 (hydroxy-carboxylic acid receptor 2) full agonist (pEC50: 7.5). GSK256073 acutely improves glucose homeostasis via inhibition of lipolysis.
价 格:¥电议型 号:T15432产 地:中国大陆
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T15430GSK2256294AGSK 2256294
GSK2256294A is potent, selective inhibitor of recombinant human, rat and mouse sEH with IC50 of 27 pM, 61 pM and 189 pM, respectively.
价 格:¥电议型 号:T15430产 地:中国大陆
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T14878CAY10566
CAY10566 shows excellent cellular activity in blocking the conversion of saturated long-chain fatty acid-CoAs (LCFA-CoAs) to monounsaturated LCFA-CoAs in HepG2 cells (IC50=7.9 nM or 6.8 nM). CAY10566 is a potent, orally bioavailable and selective stearoyl
价 格:¥电议型 号:T14878产 地:中国大陆
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T14856CalcipotriolCalcipotriene;MC 903;卡泊三醇
Calcipotriol is a synthetic VitD3 analogue. Which has a high affinity for the vitamin D receptor.
价 格:¥电议型 号:T14856产 地:中国大陆
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T14565BI-671800Cmpd A;AP-761
BI-671800 is a highly specific and potent antagonist of chemoattractant receptor-homologous molecule on Th2 cells (DP2/CRTH2). With IC50 values of 4.5 nM and 3.7 nM for PGD2 binding to CRTH2 in hCRTH2 and mCRTH2 transfected cells, respectively. BI-671800
价 格:¥电议型 号:T14565产 地:中国大陆
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T14561BI-3812
BI-3812 is an inhibitor of BCL6. Which inhibiting the BTB domain of BCL6 (IC50: 3 nM). BI-3812 also has antitumor activity.
价 格:¥电议型 号:T14561产 地:中国大陆
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T14385AZD9056 hydrochloride
AZD9056 hydrochloride is a P2X7 inhibitor,Which plays a significant role in pain-causing diseases and inflammation.
价 格:¥电议型 号:T14385产 地:中国大陆