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T6188Desvenlafaxine succinate hydrate琥珀酸去甲文拉法辛；O-Desmethylvenlafaxine succinate hydrate；WY 45233 Succinat
Desvenlafaxine succinate hydrate is an antidepressant of the serotonin-norepinephrine reuptake inhibitor (SNRI).
价 格：￥电议型 号：T6188产 地：中国大陆
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T6187TDZD-8TDZD8；GSK-3β Inhibitor I；TDZD 8；NP 01139
TDZD-8 is an inhibitor of GSK-3β, with an IC50 of 2 μM; minimal inhibitory effect observed on CDK1, casein kinase II, PKA and PKC.
价 格：￥电议型 号：T6187产 地：中国大陆
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T6186TRAM-34TRAM 34；Triarylmethane-34；TRAM34
TRAM-34(Kd=20 nM), an effective and specific inhibitor of the intermediate-conductance Ca2+-activated K+ channel (IKCa1, KCa3.1), does not block cytochrome P450. The selective activity of TRAM-34 is 200 to 1500-fold than other ion channels.
价 格：￥电议型 号：T6186产 地：中国大陆
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T6185Gambogic Acid藤黄酸；藤黄酸 A；Beta-Guttiferrin；Guttic Acid；Guttatic Acid
Gambogic Acid ( EC50=0.78-1.64 uM) activates caspases. Gambogic Acid competitively suppresses Bcl-XL, Bcl-2, Bcl-W, Bcl-B, Bfl-1 and Mcl-1. The IC50s of Gambogic Acid for Bcl-XL, Bcl-2, Bcl-W, Bcl-B, Bfl-1 and Mcl-1 are 1.47, 1.21, 2.02, 0.66, 1.06 and 0.
价 格：￥电议型 号：T6185产 地：中国大陆
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T6184OrantinibNSC 702827；SU6668；TSU-68
TSU-68, a excellent effective against PDGFR autophosphorylation with Ki of 8 nM, also highly inhibits Flk-1 and FGFR1 trans-phosphorylation. It shows little effect against IGF-1R, Met, Src, Lck, Zap70, Abl and CDK2 and does not suppresses EGFR.
价 格：￥电议型 号：T6184产 地：中国大陆
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T6183ISRIB (trans-isomer)trans-isomer；ISRIB；ISRIB trans-isomer；trans-ISRIB
ISRIB (trans-isomer), the trans-isomer of ISRIB, is a effective and specific PERK inhibitor (IC50: 5 nM).
价 格：￥电议型 号：T6183产 地：中国大陆
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T6181UPF 1069
UPF 1069 is a specific PARP2 inhibitor ( IC50: 0.3 μM). It is ~27-fold selective against PARP1.
价 格：￥电议型 号：T6181产 地：中国大陆
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T6180INH6
INH6, an effective Hec1 inhibitor, selectively disrupts the Hec1/Nek2 interaction and induces chromosome mis-alignment.
价 格：￥电议型 号：T6180产 地：中国大陆
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T6179Moxalactam sodium salt拉氧头孢钠；FestamoxinLy；Shiomarin；Antibiotic 6059S；Latamoxef sodium；6059 S；Moxalact
Moxalactam sodium salt is an antibiotic compound more effective against Escherichia coli and Pseudomonas aeruginosathan cephalosporins.
价 格：￥电议型 号：T6179产 地：中国大陆
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T6177PF-562271 besylatePF-00562271 Besylate
PF-562271 (besylate) is a potent, ATP-competitive, reversible inhibitor of FAK with IC50 of 1.5 nM, ~10-fold less potent for Pyk2 than FAK and >100-fold selectivity against other protein kinases, except for some CDKs.
价 格：￥电议型 号：T6177产 地：中国大陆
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T6176IKK 16IKK Inhibitor VII；IKK16；IKK-16
IKK-16 (IKK Inhibitor VII) is a selective IκB kinase (IKK) inhibitor for IKK-2, IKK complex and IKK-1 with IC50 of 40 nM, 70 nM and 200 nM, respectively.
价 格：￥电议型 号：T6176产 地：中国大陆
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T6175ADL-5859ADL5859 HCl；ADL5859 Hydrochloride
ADL5859 HCl is a selective δ-opioid receptor agonist ( Ki: 0.8 nM), selectivity against opioid receptor κ, μ, and little inhibition for the hERG channel.
价 格：￥电议型 号：T6175产 地：中国大陆
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T6174R406R-406 besylate
R406 is an effective Syk inhibitor (IC50: 41 nM) and shows no effects on Lyn.
价 格：￥电议型 号：T6174产 地：中国大陆
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T6173BI 25364-[[(7R)-8-环戊基-7-乙基-5,6,7,8-四氢-5-甲基-6-氧代-2-喋啶基]氨基]-3-甲氧基-N-(1-甲基-4-哌啶基)苯甲酰胺
BI2536 is an effective Plk1 inhibitor (IC50: 0.83 nM). It has 4- and 11-fold greater selectivity than Plk2 and Plk3.
价 格：￥电议型 号：T6173产 地：中国大陆
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T6172MRS 2578
MRS2578, an effective P2Y6 receptor antagonist with IC50 of 37 nM, shows insignificant inhibition at P2Y1, P2Y2, P2Y4, and P2Y11 receptors.
价 格：￥电议型 号：T6172产 地：中国大陆
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T6171BI-D1870
BI-D1870 is a cell-permeable, ATP-competitive inhibitor of ribosomal S6 kinases (RSKs; IC50s: 31/24/18/15 nM for RSK1/2/3/4).
价 格：￥电议型 号：T6171产 地：中国大陆
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T6170ElesclomolSTA-4783；伊利司莫
Elesclomol (STA-4783) is an effective oxidative stress inducer that elicits pro-apoptosis of tumor cells.
价 格：￥电议型 号：T6170产 地：中国大陆
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T6169Indirubin靛玉红；Indigopurpurin；NSC 105327；Couroupitine B；Indigo red
Indirubin is a potent cyclin-dependent kinases and GSK-3β inhibitor with IC50 of about 5 uM and 0.6 uM.
价 格：￥电议型 号：T6169产 地：中国大陆
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T6168ZSTK474
PI3K Inhibitor ZSTK474 is an orally available, s-triazine derivative, ATP-competitive phosphatidylinositol 3-kinase (PI3K) inhibitor with potential antineoplastic activity.
价 格：￥电议型 号：T6168产 地：中国大陆
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T6167SU9516
SU9516 is a potent CDK2 inhibitor, with an IC50 of 22 nM, and also has inhibitory effects on CDK1 and CDK4, with IC50s of 40 nM and 200 nM, respectively.
价 格：￥电议型 号：T6167产 地：中国大陆
