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产品数：86101
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TP2111LTAT-GluA2 3Y acetate(1404188-93-7 free base)TAT-GluA-2 3Y acetate(1404188-93-7 free base),TATGluA2 3
TAT-GluA2 3Y acetate is an inhibitor of AMPA receptor endocytosis. Induces increased hind paw withdrawal latencies following thermal and mechanical stimuli in rats. Also exhibits antinociceptive effects in a rat model of neuropathic pain. Rescues pentobarbital-induced memory retrieval deficits in a rat model of learning and memory.
价 格：￥电议型 号：TP2111L产 地：中国大陆
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T9568SGC-SMARCA-BRDVIIIEpigenetic Reader Domain,adipogenesis,SMARCA2/4,inhibit,PB1,SGCSMARCABRDVIII,Inhib
SGC-SMARCA-BRDVIII is a potent and selective inhibitor of SMARCA2, SMARCA4, PB1(2), PB1(3) and PB1(5) with Kds of 35 nM, 36 nM, 3.7 μM, 2.0 μM and 13 nM, respectively.
价 格：￥电议型 号：T9568产 地：中国大陆
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T93252-(2-Aminothiazole-4-yl)-2-methoxyiminoa2(2Aminothiazole4yl)2methoxyiminoa,2 (2 Aminothiazole 4 yl)
2-(2-Aminothiazole-4-yl)-2-methoxyiminoa is a compound.
价 格：￥电议型 号：T9325产 地：中国大陆
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TMA2394DL-alpha-TocopherolFerroptosis,Inhibitor,inhibit,DL alpha Tocopherol,DLalphaTocopherol
Antioxidant.
价 格：￥电议型 号：TMA2394产 地：中国大陆
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T6777Bay K 8644Bay K8644,influx,L-type,inhibit,sarcolemmal,Ca2+ channels,(±)-Bay K 8644,Bay K-8644,Bay K
Bay K 8644 is a potent, selective activator of L-type Ca2+ channel with IC50 of 17.3 nM.
价 格：￥电议型 号：T6777产 地：中国大陆
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T7775A2764 dihydrochloridenociception,A-2764 dihydrochloride,A2764,inhibit,current,A2764 dihydrochloride,
A2764 dihydrochloride is a highly selective inhibitor of TRESK.
价 格：￥电议型 号：T7775产 地：中国大陆
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T6S1500Ginsenoside RfCa channels,Calcium Channel,Ginsenoside Rf,Ca2+ channels,Endogenous Metabolite,Inhibit
Ginsenoside Rf is a trace component of ginseng root. Ginsenoside Rf inhibits N-type Ca2+ channel.
价 格：￥电议型 号：T6S1500产 地：中国大陆
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T8787Drotaverine hydrochlorideCa2+ channels,Inhibitor,Drotaverine hydrochloride,Ca channels,inhibit,Drota
Drotaverine hydrochloride is a type 4 cyclic nucleotide phosphodiesterase (PDE4) inhibitor，and is an antispasmodic drug, used to enhance cervical dilation during childbirth. Drotaverine hydrochloride is structurally related to papaverine
价 格：￥电议型 号：T8787产 地：中国大陆
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T7216MirogabalinDS 5565,DS-5565,Calcium Channel,Mirogabalin,inhibit,Inhibitor,Ca channels,Ca2+ channels
Mirogabalin is a calcium channel blocker with analgesic effects.
价 格：￥电议型 号：T7216产 地：中国大陆
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T6S2243Alisol A 24-acetateInhibitor,Alisol A 24acetate,inhibit,Alisol A 24 acetate,Alisol A 24-acetate
1. Alisol A 24-acetate has been determined for the quality control of this crude drug.
价 格：￥电议型 号：T6S2243产 地：中国大陆
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TJA2398Taurodeoxycholic acid sodium hydrateTaurodeoxycholic acid sodium,Inhibitor,Taurodeoxycholic acid sod
Taurohyodeoxycholic acid sodium salt, a hydrophilic bile salt, on bile salt and biliary lipid secretion in the rat.
价 格：￥电议型 号：TJA2398产 地：中国大陆
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T9148KA2507modulatory,KA 2507,KA-2507,colorectal,Histone deacetylases,immune,cancer,antitumor,KA2507,Inhi
KA2507 is a potent and selective HDAC6 inibitor with an IC50 of 2.5nM.
价 格：￥电议型 号：T9148产 地：中国大陆
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TN2322Yangambininhibit,Calcium Channel,Yangambin,Ca channels,Ca2+ channels,Inhibitor
Yangambin is a selective antagonist of the cardiovascular effects of platelet activating factor (PAF); it has hypotensive effect, which is probably due to a peripheral vasodilatation that involves, at least, the inhibition the Ca2+ influx through voltage-gated Ca2+ channels. Yangambin has central nervous system activity, it presents a depressant activity in the open field, forced swimming and pentobarbital sleeping time tests.
价 格：￥电议型 号：TN2322产 地：中国大陆
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T7603Pinaverium bromideInhibitor,Ca channels,Pinaverium bromide,Pinaverium,Calcium Channel,inhibit,Ca2+ c
Pinaverium bromide is an calcium channel blocker with Antispasmodic and effectively relieves pain, diarrhea and intestinal discomfort.
价 格：￥电议型 号：T7603产 地：中国大陆
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T7144BTSfibers,muscle,Myosin,subfragment,inhibit,BTS,Inhibitor,skeletal,Ca2+,actin,ATPase
BTS is a potent inhibitor of Ca2+-stimulated myosin S1 ATPase (IC50 : 5 μM) .
价 格：￥电议型 号：T7144产 地：中国大陆
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TMA2474δ-Tocotrienolinhibit,δ Tocotrienol,Inhibitor,δTocotrienol,δ-Tocotrienol
δ-Tocotrienol is a potential angiogenic inhibitor. δ-Tocotrienol is also a nontoxic activator of mir-34a which can inhibit nonsmall cell lung cancer cells (NSCLC) cell proliferation, induce apoptosis and inhibit invasion, and thus offering a potential starting point for the design of novel anticancer agents.
价 格：￥电议型 号：TMA2474产 地：中国大陆
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TQ0144(S)-(-)-Bay-K-8644Ca channels,Inhibitor,(S) ( ) Bay K 8644,inhibit,(S)()BayK8644,Calcium Channel,Ca2
(S)-(-)-Bay-K-8644 is an agonist of L-type Ca2+ channel and activates Ba2+ currents with an EC50 of 32 nM.
价 格：￥电议型 号：TQ0144产 地：中国大陆
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TQ0302ThapsigarginCa2+ channels,stress,inhibit,unfolded,Thapsigargin,Inhibitor,Apoptosis,Ca channels,Calci
Thapsigargin is a microsomal Ca2+-ATPase inhibitor and Endoplasmic Reticulum stress-inducing agent.
价 格：￥电议型 号：TQ0302产 地：中国大陆
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T6633RanolazineNa+ channels,CVT-303,Ca2+ channels,inhibit,Sodium Channel,Ranolazine,Inhibitor,Calcium Cha
Ranolazine is a calcium uptake inhibitor via the sodium/calcium channel, used to treat chronic angina. It affects the sodium-dependent calcium channels during myocardial ischemia in rabbits by altering the intracellular sodium level.
价 格：￥电议型 号：T6633产 地：中国大陆
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TN1132Procyanidin A2Procyanidin A 2,Bacterial,Procyanidin A-2,Inhibitor,Procyanidin A2,inhibit
Procyanidin A2 is a potential precursor of 5-(3´,4´-dihydroxyphenyl)-γ-valerolactone, exhibits antioxidant, anti-inflammary, anti-hyperglycemia, and anti-type 2 diabetes activities. Procyanidin A2 demonstrates liver cell regenerative activity in scratch wound healing assays and alcohol-induced liver cell injury in vitro.
价 格：￥电议型 号：TN1132产 地：中国大陆
