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T16677Psicofuranine；化合物 T16677Psicofuranine
Psicofuranine also specifically inhibits GMP synthase and interrupts parasite growth. Psicofuramine is a nucleoside antibiotic. It has the inhibition of xanthosine 5´-phosphate aminase. Psicofuranine shows dose-dependent inhibition of P. falciparum growth(IC50: 0.3 mM).
价 格：￥电议型 号：T16677产 地：中国大陆
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T16577PRMT5-IN-2；化合物 T16577PRMT5-IN-2
PRMT5-IN-2 is an inhibitor of protein arginine methyltransferase 5.
价 格：￥电议型 号：T16577产 地：中国大陆
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T16515PF 750；化合物PF 750PF-750|||UNII-7756CPP14K|||ZINC27647189；PF-750|||UNII-7756CPP14K|||ZINC27647189
PF 750 (ZINC27647189) is a selective and covalent inhibitor of FAAH. PF 750 shows IC50s varying from 16.2 to 595 nM in different incubation times.
价 格：￥电议型 号：T16515产 地：中国大陆
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T16505PF-4778574；化合物 T16505PF-4778574
PF-4778574 is a positive AMPA receptor allosteric modulation (EC50: 45 to 919 nM in different cells).
价 格：￥电议型 号：T16505产 地：中国大陆
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T16495PF-06747711；化合物 T16495PF-06747711
PF-06747711 is an effective and selective retinoic acid receptor-related orphan C2 inverse agonist (IC50: 4.1 nM). PF-06747711 also has anti-skin inflammatory activity.
价 格：￥电议型 号：T16495产 地：中国大陆
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T16477PF-03715455；化合物 T16477PF-03715455
PF-03715455 potently inhibits LPS-induced TNFα production in human whole blood (IC50=1.7 nM). PF-03715455 is an effective inhibitor of inhaled p38 MAPK. PF-03715455 displays some selectivity for p38α over p38β (respective IC50: 0.88 and 23 nM). PF-03715455 has the potential for the treatment of COPD.
价 格：￥电议型 号：T16477产 地：中国大陆
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T16451PEAQX tetrasodium hydrate；PEAQX四钠水合物NVP-AAM077 tetrasodium hydrate|||PEAQX tetrasodium hydrate (4598
PEAQX tetrasodium hydrate (PEAQX tetrasodium hydrate (459836-30-7 free base)) is an orally available NMDA antagonist that is potent and selective. The IC50 value of PEAQX tetrasodium hydrate (459836-30-7 free base) against hNMDAR 1A/2A was 270 nM and 29600 nM against hNMDAR 1A/2B, respectively.
价 格：￥电议型 号：T16451产 地：中国大陆
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T16387Ombrabulin；化合物 T16387AVE8062|||AC7700；AVE8062|||AC7700
Ombrabulin is a derivative of CA-4 phosphate. It is known to show antivascular effects through selective disruption of the tubulin cytoskeleton of endothelial cells.
价 格：￥电议型 号：T16387产 地：中国大陆
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T16386Ombrabulin hydrochloride化合物 T16386AVE8062 (hydrochloride)|||AC7700 (hydrochloride)
Ombrabulin hydrochloride is a synthetic, selective CA-4 phosphate ester or derivative of Ombrabulin to disrupt the tubulin cytoskeleton of endothelial cells and has antivascular effects. Ombrabulin is a tubulin polymerizing inhibitor, a member of the combretastatin A-4 compound class, which is a water-soluble tubulin depolymerizing tumor vascularizing compound.
价 格：￥电议型 号：T16386产 地：中国大陆
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T16377Odiparcil；化合物 T16377SB-424323；SB-424323
Odiparcil is an orally active beta-d-thioxyloside analog. Odiparcil is an indirect thrombin inhibitor that exerts its anticoagulant effect through activation of antithrombin II (heparin cofactor II). It also has an antithrombotic activity associated with a reduced risk of adverse bleeding events.
价 格：￥电议型 号：T16377产 地：中国大陆
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T16366NVR 3-778；化合物NVR 3-778NVR 3-778
NVR 3-778 is a first-in-Class and oral bioavailable HBV CAM belonging to the SBA class It has anti-HBV activity.
价 格：￥电议型 号：T16366产 地：中国大陆
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T16356Glyoxalic acid化合物 T16356Oxalaldehydic acid|||NSC 27785|||Formylformic acid
Glyoxalic acid is an organic compound. It is both an aldehyde and a carboxylic acid.
价 格：￥电议型 号：T16356产 地：中国大陆
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T16350NSC-87877；化合物NSC-87877NSC-87877
NSC-87877 is an effective inhibitor of Shp2 and Shp1 protein tyrosine phosphatases (IC50=0.318 μM, 0.355 μM of shp2 and shp1, respectively).It also inhibits dual-specificity phosphatase 26 (DUSP26).
价 格：￥电议型 号：T16350产 地：中国大陆
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T16332NKH477；化合物 T16332Colforsin dapropate hydrochloride；Colforsin dapropate hydrochloride
NKH477 is a novel water-soluble forskolin derivative that improves cardiac failure mainly through its beneficial effects on diastolic cardiac function. NKH477 shows an antiproliferative effect in vivo with an altered cytokine profile to inhibit the acute rejection of rat orthotopic lung allografts. NKH477 directly activates the catalytic unit of adenylate cyclase and enhances intracellular cAMP .
价 格：￥电议型 号：T16332产 地：中国大陆
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T16277NCT-502；化合物NCT-502N-(4,6-dimethylpyridin-2-yl)-4-[5-(trifluoromethyl)pyridin-2-yl]piperazine-1-carbo
NCT-502 (N-(4,6-dimethylpyridin-2-yl)-4-[5-(trifluoromethyl)pyridin-2-yl]piperazine-1-carbothioamide) is a human phosphoglycerate dehydrogenase inhibitor, cytotoxic to PHGDH-dependent cancer cells. It decreases glucose-derived serine production and it has an IC50 of 3.7 μM against PHGDH.
价 格：￥电议型 号：T16277产 地：中国大陆
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T1618Dipyridamole；双嘧达莫Persantin|||Dypyridamole|||Dipyridamol|||NSC-515776|||Dipyudamine；Persantin|||Dypyr
Dipyridamole (Persantin) is a Platelet Aggregation Inhibitor. The physiologic effect of dipyridamole is by means of Decreased Platelet Aggregation.
价 格：￥电议型 号：T1618产 地：中国大陆
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T16177N-(Azido-PEG2)-N-Boc-PEG3-acid；化合物 T16177N-(Azido-PEG2)-N-Boc-PEG3-acid
N-(Azido-PEG2)-N-Boc-PEG3-acid is a polyethylene glycol (PEG) derived linker compound, specifically designed for PROTAC synthesis[1].
价 格：￥电议型 号：T16177产 地：中国大陆
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T16145MS-444化合物 T16145BE-34776
MS-444 suppresses the activity of purified smooth muscle myosin light chain kinase (MLCK) (IC50: 10 μM).
价 格：￥电议型 号：T16145产 地：中国大陆
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T16137MRS1177；化合物 T16137MRS1177
MRS1177 is an effective and selective antagonist of the human Adenosine A3 receptor (hA3AR) (Ki: 0.3 nM).
价 格：￥电议型 号：T16137产 地：中国大陆
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T16118MLS0315771；化合物MLS0315771MLS0315771
MLS0315771 is an effective and biologically active competitive phosphomannose isomerase (MPI) inhibitor (IC50: ~1 μM and a Ki: 1.4 μM).
价 格：￥电议型 号：T16118产 地：中国大陆
