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T15418GS-6201CVT-6883
GS-6201 is a selective antagonist of adenosine A2B receptor. GS-6201 shows high affinity and selectivity for the human adenosine A2B receptors with a Ki of 22 nM.
价 格：￥电议型 号：T15418产 地：中国大陆
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T15207Eleclazine hydrochlorideGS 6615 hydrochloride
Eleclazine hydrochloride is a novel inhibitor of late Na+ current (IC50: 0.7 uM).
价 格：￥电议型 号：T15207产 地：中国大陆
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T14944CGS 15943
CGS 15943 is an orally bioavailable non-xanthine antagonist of Adenosine Receptor. In transfected CHO cells, its Ki for human A1, A2A, A2B, and A3 Adenosine Receptors are 3.5, 4.2, 16, and 50 nM , respectively.
价 格：￥电议型 号：T14944产 地：中国大陆
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T1486Oseltamivir phosphate磷酸奥司他韦；GS 4104
Oseltamivir Phosphate is the phosphate salt of oseltamivir, a synthetic derivative prodrug of ethyl ester with antiviral activity. By blocking neuraminidases on the surfaces of influenza viruses, oseltamivir interferes with host cell release of complete v
价 格：￥电议型 号：T1486产 地：中国大陆
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T14775Bragsin26-methoxy-5-nitro-2-(trifluoromethyl)chromen-4-one；Bragsin 2
Bragsin2 is a hydration-resistant cell penetrant, selective and non-competitive inhibitor of Afr guanine nucleotide exchange factor BRAG2 that inhibits Arf GTPase activation, with an IC50 of 3 μM. Bragsin2 binds at the interface between the pleckstrin hom
价 格：￥电议型 号：T14775产 地：中国大陆
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T12519Sodium metatungstateSodium polyoxotungstate；POM-1；聚钨酸钠
Sodium metatungstate is a potent inhibitor of ecto-nucleoside triphosphate diphosphohydrolase (NTPDase)(Ki values of 2.58 μM, 3.26 μM, and 28.8 μM for NTPDase 1, NTPDase 3 and NTPDase 2 respectively).
价 格：￥电议型 号：T12519产 地：中国大陆
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T12405PentiapineCGS 10746
Pentiapine is a novel inhibitor of dopamine release.
价 格：￥电议型 号：T12405产 地：中国大陆
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T12311Tirabrutinib hydrochlorideGS-4059 (hydrochloride)；ONO-4059 (hydrochloride)
Tirabrutinib hydrochloride is a selective and novelBTK with IC50 2.2 nm inhibitor.
价 格：￥电议型 号：T12311产 地：中国大陆
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T11824LLLanraplenibGS-9876
Lanraplenib is a highly selective and orally active SYK inhibitor (IC50=9.5 nM) in development for the treatment of inflammatory diseases. Lanraplenib inhibits SYK activity in platelets via the glycoprotein VI (GPVI) receptor without prolonging bleeding t
价 格：￥电议型 号：T11824LL产 地：中国大陆
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T11616IDO-IN-13GS-4361
IDO-IN-13 is a potent indoleamine 2,3-dioxygenase 1 (IDO1) inhibitor (EC50: 17 nM).
价 格：￥电议型 号：T11616产 地：中国大陆
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T11505GSTO1-IN-1
GSTO1-IN-1 is a potent glutathione S-transferase omega 1 inhibitor (GSTO1; IC50: 31 nM).
价 格：￥电议型 号：T11505产 地：中国大陆
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T11488GSK2850163
GSK2850163 is a novel inhibitor of inositol-requiring enzyme-1 alpha (IRE1α) which can inhibit RNase activity and IRE1α kinase activity (IC50s: 200 and 20 nM).
价 格：￥电议型 号：T11488产 地：中国大陆
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T11486GSK2807 Trifluoroacetate
GSK2807 Trifluoroacetate is a selective and SAM-competitive inhibitor of SMYD3 (Ki: 14 nM; IC50: 130 nM).
价 格：￥电议型 号：T11486产 地：中国大陆
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T11485GSK2643943A
GSK2643943A is a deubiquitylating enzyme (DUB) inhibitor (IC50: 160 nM for USP20/Ub-Rho).
价 格：￥电议型 号：T11485产 地：中国大陆
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T11481GSK2239633A
GSK2239633A is an antagonist of CC-chemokine receptor 4 (CCR4).$nGSK2239633A inhibits the binding of [125I]-TARC to human CCR4 (pIC50: 7.96 ± 0.11).
价 格：￥电议型 号：T11481产 地：中国大陆
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T11469GSK-3484862
Gsk-3484862 is a non covalent inhibitor of DNA methyltransferase DNMT1 with anticancer activity. Gsk-3484862 mediates the global demethylation of mouse embryonic stem cells.
价 格：￥电议型 号：T11469产 地：中国大陆
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T11467GSK-3β inhibitor 1
GSK-3β inhibitor 1 is an inhibitor of GSK-3β( IC50 of 4.9 nM) and demonstrates high antidiabetic efficacy.
价 格：￥电议型 号：T11467产 地：中国大陆
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T11465LenacapavirGS-6207
Lenacapavir is a potent capsid-targeting inhibitor of HIV replication. Lenacapavir shows anti-HIV activity with an EC50 of 100 pM in MT-4 cells.
价 格：￥电议型 号：T11465产 地：中国大陆
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T1085LGlutathione oxidizedL-谷胱甘肽(氧化型)；氧化型谷胱甘肽；L(-)-Glutathione；GSSG；Oxidized glutathione；Glutathione disul
A GLUTATHIONE dimer formed by a disulfide bond between the cysteine sulfhydryl side chains during the course of being oxidized.
价 格：￥电议型 号：T1085L产 地：中国大陆
