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T14218Amicarbazone；胺唑草酮BAY314666|||BAY-MKH 3586；BAY314666|||胺唑草酮|||BAY-MKH 3586
Amicarbazone (BAY-MKH3586; BAY314666) is a potent PSII inhibitor, disrupting photosynthetic electron transport by binding to the Qb domain of photosystem II. This broad-spectrum herbicide is effective through foliar and root application, showcasing rapid absorption and translocation. However, its effectiveness can be compromised by common PSII inhibitor resistance. With an IC50 value indicating high potency, amicarbazone leads to chlorosis, stunted growth, tissue necrosis, and death in sensitive
价 格：￥电议型 号：T14218产 地：中国大陆
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T1403Climbazole；甘宝素BAY-e 6975；甘宝素|||BAY-e 6975
Climbazole (BAY-e 6975) is a broad-spectrum imidazole antifungal agent with anti-dandruff benefits.
价 格：￥电议型 号：T1403产 地：中国大陆
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T13936Triptotriterpenic acid A；化合物 T13936Maytenfolic acid|||Abrusgenic acid；Maytenfolic acid|||Abrusgenic
Triptotriterpenic acid A is a natural product isolate from Tripterygium wilfordii.
价 格：￥电议型 号：T13936产 地：中国大陆
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T13766Maytansinoid DM4；化合物 T13766Maytansinoid DM4
Maytansinoid DM4, a thiol-containing maytansine derivative, is a highly potent cytotoxic moiety utilized in ADC applications.
价 格：￥电议型 号：T13766产 地：中国大陆
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T13467(±)-Enitociclib；化合物(±)-BAY-1251152(±)-BAY-1251152；(±)-BAY-1251152
(±)-Enitociclib ((±)-BAY-1251152) is a racemic mixture of BAY-1251152. BAY-1251152 is highly selective inhibitor of PTEF/CDK9.
价 格：￥电议型 号：T13467产 地：中国大陆
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T13442(R)-BAY1238097；化合物 T13442(R)-BAY1238097
(R)-BAY1238097 is the R-isomer with lower activity of BAY1238097. BAY1238097 is a selective BET inhibitor.
价 格：￥电议型 号：T13442产 地：中国大陆
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T13345Wnt pathway activator 2；化合物Wnt pathway activator 2Wnt pathway activator 2
Wnt pathway activator 2 is a potent Wnt activator with an IC50 of 13 nM.
价 格：￥电议型 号：T13345产 地：中国大陆
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T13332(Rac)-WAY-161503；化合物(Rac)-WAY-161503(Rac)-WAY-161503
(Rac)-WAY-161503 is a selective and high-affinity agonist of the 5-HT2C receptor (Ki: 4 nM; EC50: 12 nM), with anti-obesity and antidepressant effects.
价 格：￥电议型 号：T13332产 地：中国大陆
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T13331WAY127093B racemate；化合物WAY127093B外消旋体WAY127093B racemate
WAY127093B racemate is the racemate of WAY127093B. WAY127093B is a phosphodiesterase IV inhibitor with oral activity in rats and guinea pigs.
价 格：￥电议型 号：T13331产 地：中国大陆
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T13330LWAY-213613；化合物WAY-213613WAY-213613
WAY-213613 is a potent and selective nonsubstrate reuptake inhibitor of GLT-1/EAAT2 (IC50: 85 nM EAAT2). It displays 59- and 44-fold selectivity over EAAT1 and EAAT3 (IC50s: 5 and 3.8 μM, respectively). WAY-213613 shows no activity at ionotropic and metabotropic glutamate receptors.
价 格：￥电议型 号：T13330L产 地：中国大陆
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T13330WAY-213613 hydrochloride；化合物WAY-213613 hydrochlorideWAY-213613 hydrochloride (868359-05-1 free base)
WAY-213613 hydrochloride is a potent, selective nonsubstrate reuptake inhibitor of GLT-1/EAAT2 with IC 50 of 85 nM. WAY-213613 hydrochloride inhibits EAAT1 and EAAT3 with IC50 values of 5 and 3.8 microM, respectively. WAY-213613 hydrochloride shows no activity at ionotropic and metabotropic glutamate receptors. It is a potential tool for the elucidation of EAAT2 function and can be used for the research of central nervous system [1] [2].
价 格：￥电议型 号：T13330产 地：中国大陆
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T13295Veliflapon化合物 T13295DG-031|||BAY X 1005
Veliflapon is an orally active and selective inhibitor of 5-lipoxygenase activating protein (FLAP). Veliflapon inhibits the synthesis of the leukotrienes B4 and C4.
价 格：￥电议型 号：T13295产 地：中国大陆
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T12976Sorafenib-d4；化合物 T12976Sorafenib (D4)|||Bay 43-9006 (D4)；Sorafenib (D4)|||Bay 43-9006 (D4)
Sorafenib D4 is the deuterium labeled Sorafenib. Sorafenib is an inhibitor of multikinase (Raf-1, B-Raf, and VEGFR-3 IC50s of 6 nM, 20 nM, and 22 nM, respectively).
价 格：￥电议型 号：T12976产 地：中国大陆
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T12736Rivaroxaban-d4；化合物 T12736BAY 59-7939 D4；BAY 59-7939 D4
Rivaroxaban D4 is a deuterium labeled Rivaroxaban. Rivaroxaban is a highly potent,selective and direct inhibitor of Factor Xa (FXa)(IC50:0.7 nM; Ki:0.4 nM).
价 格：￥电议型 号：T12736产 地：中国大陆
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T12698Regorafenib-d3；化合物 T12698Regorafenib D3|||BAY 73-4506 D3；Regorafenib D3|||BAY 73-4506 D3
Regorafenib D3 is a deuterium labeled Regorafenib. Regorafenib is a multi-targeted receptor inhibitor of tyrosine kinase.
价 格：￥电议型 号：T12698产 地：中国大陆
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T12697Refametinib R enantiomer；Refametinib （R对映体）RDEA119 R enantiomer|||Refametinib R enantiomer|||BAY 869
Refametinib R enantiomer (RDEA119 R enantiomer) is an MEK inhibitor with an EC50 of 2.0-15 nM.Refametinib (R enantiomer) has anticancer activity and can be used in cancer research.
价 格：￥电议型 号：T12697产 地：中国大陆
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T12691Rapamycin-d3；化合物 T12691AY-22989-d3|||Sirolimus-d3；AY-22989-d3|||Sirolimus-d3
Rapamycin-d3 is the deuterium labeled Rapamycin. Rapamycin is a potent and specific inhibitor of mTOR(IC50 of 0.1 nM in HEK293 cells).
价 格：￥电议型 号：T12691产 地：中国大陆
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T12660LBAY1238097；化合物BAY1238097BAY1238097
BAY1238097 is a potent and selective bromodomain and extra-terminal motif (BET) inhibitor with anticancer activity that exhibits strong antiproliferative activity in AML (Acute Myeloid Leukemia) and MM (Multiple Myeloma) models.BAY1238097 can be used for the study of advanced refractory malignancies.
价 格：￥电议型 号：T12660L产 地：中国大陆
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T12660(Rac)-BAY1238097；化合物 T12660(Rac)-BAY1238097
(Rac)-BAY1238097 is a inhibitor of BET(IC50 of 1.02 μM for BRD4),used in cancer research.
价 格：￥电议型 号：T12660产 地：中国大陆
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T12659(Rac)-BAY-985；化合物 T12659(Rac)-BAY-985
(Rac)-BAY-985 is a potent, ATP-competitive and selective inhibitor of TBK1(IC50 of 1.5 nM),with antitumor efficacy.
价 格：￥电议型 号：T12659产 地：中国大陆
