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产品数：86101
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T6470Diclofenac PotassiumApoptosis,Diclofenac Potassium,COX,CHO,caspase,COX-1,cascade,anti-inflammatory,n
Diclofenac potassium is a nonsteroidal anti-inflammatory drug taken to reduce inflammation and as an analgesic reducing pain in certain conditions.
价 格：￥电议型 号：T6470产 地：中国大陆
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T72345-Amino-2-chloropyridine5 Amino 2 chloropyridine,5Amino2chloropyridine
5-Amino-2-chloropyridine is Pyridine intermediates
价 格：￥电议型 号：T7234产 地：中国大陆
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T40659Lγ-Acetylenic GABA hydrochloride
γ-Acetylenic GABA hydrochloride is a GABA transaminase inhibitor.
价 格：￥电议型 号：T40659L产 地：中国大陆
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T6S0105PeiminineInhibitor,inhibit,Peiminine,Autophagy
1. Peiminine is an effective inhibitor for lung inflammation and pulmonary fibrosis in a rat model of bleomycin-induced lung injury.
价 格：￥电议型 号：T6S0105产 地：中国大陆
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T5467SAR125844Inhibitor,SAR125844,c-Met/HGFR,inhibit,SAR 125844,SAR-125844,Apoptosis
SAR125844, a potent and highly selective inhibitor of the MET receptor tyrosine kinase (RTK), for intravenous administration. (IC50 value of 4.2 nmol/L)
价 格：￥电议型 号：T5467产 地：中国大陆
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T17875Pomalidomide-C2-NH2Inhibitor,E3 Ligase Ligand-Linker Conjugates,PomalidomideC2NH2,Pomalidomide-C-2-N
Pomalidomide-C2-NH2 is a synthesized E3 ligase ligand-linker conjugate containing a Pomalidomide-based cereblon ligand and a linker.
价 格：￥电议型 号：T17875产 地：中国大陆
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T9609GRK5-IN-2metabolic,bicyclic,insulin,kinase,inhibit,Inhibitor,disease,pyridine-based,GRK5 IN 2,GRK-5-
GRK5-IN-2, a pyridine-based bicyclic compound, is a potent G-protein-coupled receptor kinase 5 (GRK5) inhibitor. It regulates the expression and/or release of insulin and is useful for the metabolic disease research.
价 格：￥电议型 号：T9609产 地：中国大陆
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TN1026Vomicineinhibit,Inhibitor,activity,Vomicine,alkaloid,antidiabetic
Vomicine is a natural product from Strychnos nux-vomica, the S. nux-vomica extracts show antihyperglycemic activity in experimental animals.
价 格：￥电议型 号：TN1026产 地：中国大陆
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TN12613-O-Caffeoylquinic acid methyl esterInhibitor,inhibit,3 O Caffeoylquinic acid methyl ester,3OCaffeoy
3-O-Caffeoylquinic acid methyl ester is a natural product from Morus alba L.
价 格：￥电议型 号：TN1261产 地：中国大陆
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T6635EMD638683inhibit,EMD-638683,EMD638683,Serum and glucocorticoid-regulated kinase,EMD 638683,Inhibitor
EMD638683,a novel SGK inhibitor with antihypertensive potency(with an IC50 of 3 μM).
价 格：￥电议型 号：T6635产 地：中国大陆
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T7622GabazineInhibitor,Gamma-aminobutyric acid Receptor,Gabazine,γ-Aminobutyric acid Receptor,inhibit,SR
Gabazine is an antagonist of GABAA receptors (Ki : 74-150 nM)
价 格：￥电议型 号：T7622产 地：中国大陆
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TP2212La-MSH, amide Acetate(581-05-5 free base)a MSH, amide Acetate(581 05 5 free base),aMSH, amide Acetate
a-MSH, amide Acetate as an endogenous neuropeptide. It is an endogenous melanocortin receptor 4 (MC4R) agonist with anti-inflammatory and antipyretic activities. α-MSH is a post-translational derivative of pro-opiomelanocortin (POMC)
价 格：￥电议型 号：TP2212L产 地：中国大陆
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T67742EX-A5386
EX-A5386 is a potent glucocorticoid receptor modulator, IC50/EC50<100nM.
价 格：￥电议型 号：T67742产 地：中国大陆
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TQ0029ASTX660Inhibitor,inhibit,ASTX-660,ASTX660,IAP,ASTX 660
ASTX660 is an orally bioavailable dual antagonist of cIAP and XIAP.
价 格：￥电议型 号：TQ0029产 地：中国大陆
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TN71672,4,5-Tribromoimidazole
2,4,5-Tribromoimidazole is a marine derived natural products found in Hexaplex trunculus.
价 格：￥电议型 号：TN7167产 地：中国大陆
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T37082HS271HS271,HS-271
HS271 is a selective, highly potent and orally active IRAK4 inhibitor (IC50= 7.2 μM). HS271 shows excellent enzymatic and cellular activities, as well as excellent pharmacokinetic properties.
价 格：￥电议型 号：T37082产 地：中国大陆
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TQ0271Falnidamol
Falnidamol is an orally active, selective EGFR tyrosine kinase inhibitor with an IC50 of 3 nM. Falnidamol displays > 1000-fold lower potency against ErbB2 (IC50=3.4 μM) and a range of other related tyrosine kinases (IC50>10 μM). Falnidamol is a pyrimido-pyrimidine compound and has anti-cancer activity.
价 格：￥电议型 号：TQ0271产 地：中国大陆
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T6917OleuropeinPPARγ,olive,PPAR,Peroxisome proliferator-activated receptors,inhibit,Apoptosis,leaves,Oleu
Oleuropein is an antioxidant polyphenol isolated from olive leaf.
价 格：￥电议型 号：T6917产 地：中国大陆
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T7295MiridesapGSK 2315698,GSK-2315698,Miridesap,Inhibitor,inhibit
Miridesap is a divalent crosslinker of SAP that causes rapid depletion of circulating SAP via hepatic clearance. It also produces significant reduction of SAP from cerebrospinal fluid and visceral amyloid deposits
价 格：￥电议型 号：T7295产 地：中国大陆
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T7604ValrubicinInhibitor,AD 32,AD32,Valrubicin,inhibit,PKC,Antibiotic,Protein kinase C
Valrubicin (AD 32) inhibits TPA- and PDBu-induced PKC activation (IC50s: 0.85 and 1.25 μM) and has antitumor and anti-inflammatory activity.
价 格：￥电议型 号：T7604产 地：中国大陆
