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T16863SCH 546738;化合物 T16863SCH 546738
SCH 546738 is an effective and non-competitive CXCR3 antagonist. SCH 546738 bindings to the human CXCR3 receptor is determined (Ki: 0.4 nM) in multiple experiments.
价 格:¥电议型 号:T16863产 地:中国大陆
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T16860SBI-553;化合物SBI-553SBI-553
SBI-553 is an effective and brain penetrant NTR1 allosteric modulator (EC50: 0.34 μM).
价 格:¥电议型 号:T16860产 地:中国大陆
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T16853SB-633825;化合物 T16853SB-633825
SB-633825 can inhibit cancer cell growth and angiogenesis. SB-633825 is an effective and ATP-competitive inhibitor of TIE2, LOK, and BRK (IC50s: 3.5 nM, 66 nM, 150 nM, respectively).
价 格:¥电议型 号:T16853产 地:中国大陆
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T16833S1P1 Agonist III;化合物 T16833S1P1 Agonist III
S1P1 Agonist III is an effective and orally active S1P1 agonist (EC50: 18 nM).
价 格:¥电议型 号:T16833产 地:中国大陆
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T16832S18-000003;化合物S18-000003S18-000003
S18-000003 is an effective orally bioavailable retinoic acid receptor-related orphan receptor-gamma-t inhibitor (IC50: 29 nM). S18-000003 inhibits IL-17 production.
价 格:¥电议型 号:T16832产 地:中国大陆
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T16823S-acetyl-PEG4-alcohol;化合物 T16823S-acetyl-PEG4-alcohol
S-acetyl-PEG4-alcohol is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格:¥电议型 号:T16823产 地:中国大陆
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T15803LY223982化合物 T15803SKF107324|||CGS23131
LY223982 is an effective and specific inhibitor of the leukotriene B4 receptor (IC50: 13.2 nM). It also can against [3H]LTB4 binding to LTB4 receptor.
价 格:¥电议型 号:T15803产 地:中国大陆
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T14390L(2R,3S)-Azelaprag;化合物T14390L(2R,3S)-Azelaprag
(2R,3S)-N-(4-(2,6-dimethoxyphenyl)-5-(5-methylpyridin-3-yl)-4H-1,2,4-triazol-3-yl)-3-(5-methylpyrimidin-2-yl)butane-2-sulfonamide is an Apelin receptor agonist with an EC50 for Apelin receptors of 0.012 ?M.(2R,3S)-N-(4-(2,6-dimethoxyphenyl)-5-(5-methylpyridin-3-yl)-4H-1,2,4-triazol-3-yl)-3-(5- methylpyrimidin-2-yl)butane-2-sulfonamide is used in the treatment of heart failure, atherosclerosis, obesity, diabetes mellitus, amyotrophic lateral sclerosis, coronary artery disease, hypertension, strok
价 格:¥电议型 号:T14390L产 地:中国大陆
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T13883Secaubryenol;化合物 T13883Secaubryenol
Secaubryenol is a 3,4-secocycloartane triterpenes isolated from Coussarea macrophylla.
价 格:¥电议型 号:T13883产 地:中国大陆
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T13427(3S,4R)-Tofacitinib;(3S,4R)-托法替尼(3S,4R)-Tofacitinib
(3S,4R)-Tofacitinib is an less active enantiomer of Tofacitinib. Tofacitinib is a JAK3 inhibitor(IC50 : 1 nM).
价 格:¥电议型 号:T13427产 地:中国大陆
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T13426L(3S,4S)-Tofacitinib(3S,4S)-托法替尼(3S,4S)-托法替尼
(3S,4S)-Tofacitinib, a less active enantiomer of tofacitinib, is a Janus kinases inhibitor.
价 格:¥电议型 号:T13426L产 地:中国大陆
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T13238Tyrphostin AG1433;化合物Tyrphostin AG1433SU1433|||AG1433;SU1433|||AG1433
Tyrphostin AG1433 (AG1433) is an inhibitor of tyrosine kinases and also a dual inhibitor of PDGFRβ(IC50s = 5.0 μM) and VEGFR-2 (Flk-1/KDR)(IC50s = 9.3 μM).
价 格:¥电议型 号:T13238产 地:中国大陆
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T131624(3S,5S,6R,10R,13S,17S) androstane-3,6,17-triol;化合物 (3S,5S,6R,10R,13S,17S) androstane-3,6,17-triol(3S
androstane-3,6,17-triol is a useful organic compound for research related to life sciences and the catalog number is T131624.
价 格:¥电议型 号:T131624产 地:中国大陆
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T13045Syk-IN-3;Syk 抑制剂 3Syk-IN-3
Syk-IN-3 is a Syk inhibitor with potential anti-inflammatory and anticancer activity and can be used to study immune dysregulation.
价 格:¥电议型 号:T13045产 地:中国大陆
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T13043SX-3228;化合物 T13043SX-3228
SX-3228 is a selective agonist of benzodiazepine1 (BZ1) receptor(IC50 of 17 nM).
价 格:¥电议型 号:T13043产 地:中国大陆
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T13023Sulfadiazine-d4;化合物 T13023Sulfadiazine D4;Sulfadiazine D4
Sulfadiazine D4 is a deuterium labeled Sulfadiazine. Sulfadiazine used for the treatment of toxoplasmosis.
价 格:¥电议型 号:T13023产 地:中国大陆
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T13011Statine;化合物 T13011(S,S)-Statine|||(3S,4S)-Statine;(S,S)-Statine|||(3S,4S)-Statine
Statine is a protease inhibitor that is active against pepsin and other acid proteases.
价 格:¥电议型 号:T13011产 地:中国大陆
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T13004SSTC3;化合物 SSTC3SSTC3
SSTC3 is a casein kinase 1α (CK1α) activator with a Kd of 32 nM.SSTC3 has potential antitumor activity, inhibits WNT signaling, and suppresses SHH medulloblastoma tumor growth.SSTC3 is a potent HIF1α inhibitor with a Kd of 32 nM.
价 格:¥电议型 号:T13004产 地:中国大陆
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T13003SSR128129E free acid;化合物 T13003SSR free acid;SSR free acid
SSR128129E free acid is an orally available and allosteric inhibitor of FGFR(IC50 of 1.9 μM for FGFR1).
价 格:¥电议型 号:T13003产 地:中国大陆
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T12993SQ-31765;化合物 T12993SQ-31765
SQ-31765 is a blocker of benzazepine calcium channel.
价 格:¥电议型 号:T12993产 地:中国大陆