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T17283Zamifenacin；化合物 T17283UK-76654；UK-76654
Zamifenacin obviously decreases colonic motility in irritable bowel syndrome. Zamifenacin is an effective gut-selective muscarinic M3 receptor antagonist.
价 格：￥电议型 号：T17283产 地：中国大陆
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T17276Zonampanel；唑南帕奈YM 872；YM 872|||唑南帕奈
Zonampanel is a selective glutamate receptor subtype, α-amino-3-hydroxy-5-methylisoxazole-4-propionic acid receptor antagonist.
价 格：￥电议型 号：T17276产 地：中国大陆
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T17268Y-26763化合物 T17268Y 26763|||Y26763
Y-26763 is a K+ channel opener and active metabolite of Y-27152. This is an ATP-sensitive K+ (KATP) channel activator.
价 格：￥电议型 号：T17268产 地：中国大陆
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T17265Ximelagatran；希美加群EXANTA|||H 376-95|||H37695|||H 376/95|||H-37695|||H 37695；EXANTA|||H 376-95|||H3769
Ximelagatran (H 376-95), a direct thrombin inhibitor, can be taken orally and acts solely by inhibiting the actions of thrombin. Ximelagatran is converted to the active agent melagatran in vivo.
价 格：￥电议型 号：T17265产 地：中国大陆
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T1725Y-27632 dihydrochloride；化合物Y-27632 dihydrochlorideY-27632 2HCl；反式-4-[(R)-1-氨基乙基]-N-(4-吡啶基)环己烷甲酰胺二盐酸盐
Y-27632 dihydrochloride (Y-27632 2HCl) is an orally potent, ATP-competitive inhibitor of ROCK-I and ROCK-II. Y-27632 dihydrochloride also inhibits isolation-induced apoptosis in mouse prostate stem or progenitor cells.
价 格：￥电议型 号：T1725产 地：中国大陆
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T17248VU6001376；化合物 T17248VU6001376
VU6001376 is an effective and selective positive allosteric modulator of the metabotropic glutamate receptor 4 (EC50: 50.1 nM).
价 格：￥电议型 号：T17248产 地：中国大陆
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T17176Salicyl-AMS；化合物Salicyl-AMSSalicyl-AMS
Salicyl-AMS is an inhibitor of mycobacterium auxin biosynthesis that inhibits the growth of mycobacterium in the presence of iron deficiency in vitro.
价 格：￥电议型 号：T17176产 地：中国大陆
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T16990Tarafenacin；化合物 T16990SVT-40776；SVT-40776
Tarafenacin is a highly selective M3 muscarinic receptor antagonist (Ki= 0.19 nM), ~200 fold selectivity over the M2 receptor.
价 格：￥电议型 号：T16990产 地：中国大陆
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T16989Tarafenacin D-tartrate；Tarafenacin D-酒石酸盐SVT-40776 D-tartrate；SVT-40776 D-tartrate
Tarafenacin D-tartrate (SVT-40776 D-tartrate) is a selective and potent muscarinic acetylcholine M3 receptor antagonist used in the study of overactive bladder and bronchial disorders.
价 格：￥电议型 号：T16989产 地：中国大陆
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T16976TAK-915；化合物 T16976TAK-915
TAK-915 is a potent, selective, and brain-penetrant phosphodiesterase 2A (PDE2A) inhibitor (IC50: 0.61 nM). TAK-915 is >4100-fold more selectivity for PDE2A than PDE1A.
价 格：￥电议型 号：T16976产 地：中国大陆
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T16906Sograzepide；化合物 T16906YM-220|||Netazepide|||YF 476；YM-220|||Netazepide|||YF 476
Sograzepide is an effective and highly selective Gastrin/CCK-B antagonist (IC50: 0.1 nM), has an inhibitory effect on Gastrin/CCK-A activity (IC50: 502 nM). Sograzepide replaces the specific binding of [125I]CCK-8 to the rat brain, cloned canine, and cloned human Gastrin/CCK-B receptors (Ki: 0.068, 0.62 and 0.19 nM, respectively).
价 格：￥电议型 号：T16906产 地：中国大陆
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T16876Guadecitabine；化合物 T16876SGI-110；SGI-110
Guadecitabine is a second-generation DNA methyltransferases inhibitor. It is used for research on acute myeloid leukemia and myelodysplastic syndromes.
价 格：￥电议型 号：T16876产 地：中国大陆
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T16814RX 67668；化合物 T16814RX 67668
RX 67668 is a muscle relaxant used to relieve skeletal muscle fatigue. RX 67668 is an effective cholinesterase inhibitor (IC50: 5 μM for both acetylcholinesterase and butyrylcholinesterase). RX 67668 can reverse the neuromuscular blockade induced by D-tubocurarine.
价 格：￥电议型 号：T16814产 地：中国大陆
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T16812RWJ-67657；化合物RWJ-67657JNJ 3026582；JNJ 3026582
RWJ-67657 (JNJ 3026582) is an orally active and selective p38α and p38β MAPK inhibitor (IC50s: 1 and 11 μM, respectively). RWJ-67657 shows no activity at p38γ and p38δ and shows a cardioprotective effect.
价 格：￥电议型 号：T16812产 地：中国大陆
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T1677LMontelukast sodium孟鲁司特钠MK0476|||孟鲁司特钠
Montelukast sodium (MK0476) is an orally available leukotriene receptor antagonist which is widely used for the prophylaxis and chronic treatment of asthma and has been linked to rare cases of clinically apparent liver injury.
价 格：￥电议型 号：T1677L产 地：中国大陆
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T16776RO9021；化合物RO9021RO9021
RO9021 is an orally bioavailable, novel ATP-competitive SYK inhibitor (average IC50: 5.6 nM).
价 格：￥电议型 号：T16776产 地：中国大陆
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T16769Ro 363；化合物 T16769Ro 363
RO 363 is an effective inotropic stimulant and is a cardiovascular modulator that decreases diastolic blood pressure and pronounces increases in myocardial contractility. Ro 363 is an effective and highly selective β1-adrenoceptor agonist.
价 格：￥电议型 号：T16769产 地：中国大陆
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T16768Ro-24-4736；化合物 T16768Ro-24-4736
Ro 24-4736 is an effective and selective platelet-activating factor antagonist.
价 格：￥电议型 号：T16768产 地：中国大陆
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T16767Ro-24-0238；化合物 T16767Ro-24-0238
Ro-24-0238 is an antagonist of platelet-activating factor and inhibitor of thromboxane synthesis. Ro-24-0238 used for lessening the inflammation and damage resulting from a local release of PAF.
价 格：￥电议型 号：T16767产 地：中国大陆
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T16766Ro 08-2750；化合物Ro 08-2750Ro 08-2750
Ro 08-2750 is a non-peptide and reversible nerve growth factor (NGF) inhibitor which binds to NGF, and with an IC50 of ~ 1 ?M. Ro 08-2750 is a selective MSI RNA-binding activity inhibitor, with an IC50 of 2.7 μM. Ro 08-2750 inhibits NGF binding to p75NTR selectively over TRKA.
价 格：￥电议型 号：T16766产 地：中国大陆
