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T27945LY320954；化合物 T27945LY 320954|||PDSP1_001629|||LY-320954；LY 320954|||PDSP1_001629|||LY-320954
LY320954 is an antagonist of 5-HT2A receptor.
价 格：￥电议型 号：T27945产 地：中国大陆
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T27944LY3202626；化合物 T27944LY 3202626|||LY-3202626；LY 3202626|||LY-3202626
LY3202626, an amyloid precursor protein secretase (BACE protein) inhibitor, is used for the treatment of Alzheimer´s disease.
价 格：￥电议型 号：T27944产 地：中国大陆
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T27943LY314228；化合物 T27943LY-314228|||LY 314228；LY-314228|||LY 314228
LY314228 is an antagonist of 5-HT2A receptor.
价 格：￥电议型 号：T27943产 地：中国大陆
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T27942LY307452；化合物 T27942LY 307452|||LY-307452；LY 307452|||LY-307452
LY307452 is a selective antagonist of mGluR2/3.
价 格：￥电议型 号：T27942产 地：中国大陆
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T27941LY303336；化合物 T27941LY-303336|||LY 303336；LY-303336|||LY 303336
LY303336 is an antagonist of AT1 receptor.
价 格：￥电议型 号：T27941产 地：中国大陆
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T27940LY301875；化合物 T27940LY 301875|||LY-301875；LY 301875|||LY-301875
LY301875 is an antagonist of nonpeptide angiotensin receptor.
价 格：￥电议型 号：T27940产 地：中国大陆
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T2794Astilbin；落新妇苷Neoastilbin|||Taxifolin 3-O-rhamnoside|||Isoastilbin|||Taxifolin 3-rhamnoside|||Neoisoa
Astilbin (Neoastilbin) is actions Flavonoid phytochemical found in St. John′s wort and Traditional Chinese Medicine herbal preparations.
价 格：￥电议型 号：T2794产 地：中国大陆
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T27794λ-Cyhalothrin；λ-氯氟氰菊酯lambda-Cyhalothrin|||Karate|||Icon；lambda-Cyhalothrin|||Karate|||λ-氯氟氰菊酯|||Icon
λ-Cyhalothrin (Icon) is a type II synthetic pyrethroid insecticide featuring a high-efficiency, broad-spectrum formula with an α-cyano group. It is employed across various applications for controlling a wide array of pests. As a neurotoxin, λ-Cyhalothrin acts on sodium channels in neuron membranes within the central nervous system.
价 格：￥电议型 号：T27794产 地：中国大陆
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T26794BI-135585；化合物 T26794BI-135585
BI-135585 is a potent and selective inhibitor of 11β-HSD1.
价 格：￥电议型 号：T26794产 地：中国大陆
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T26776Berteroin；化合物 T26776OR-009512|||KB-47947|||LP-088984|||KB47947|||LP088984；OR-009512|||KB-47947|||LP-
Berteroin is an erucin homolog and potential antioxidant. It is present in cruciferous vegetables, including rucola salad leaves, Chinese cabbage and mustard oil. It decreases the release of pro-inflammatory cytokines in LPS-stimulated macrophages. It also decreases expression of androgen receptors in prostate cancer cells.
价 格：￥电议型 号：T26776产 地：中国大陆
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T26486A-794282；化合物 T26486A-794282
A-794282 is a selective antagonist of mGluR1.
价 格：￥电议型 号：T26486产 地：中国大陆
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T26409A 25794；化合物 T26409A-25794|||A25794|||Abott 25794；A-25794|||A25794|||Abott 25794
A 25794 is an antibiotic with possible antidepressant properties.
价 格：￥电议型 号：T26409产 地：中国大陆
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T2600AG490；化合物AG-490Zinc02557947|||Tyrphostin AG 490|||AG 490|||AG-490|||Tyrphostin B42；Zinc02557947|||Ty
AG490 (Tyrphostin B42) is an inhibitor of EGFR (IC50: 0.1 μM). It is 135-fold more selective for EGFR than ErbB2, also inhibits JAK2 with no effect to Lyn, Lck, Syk, Btk, and Src.
价 格：￥电议型 号：T2600产 地：中国大陆
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T25794Methiomeprazine；化合物 T25794RP-10584|||Metiomeprazina|||RP 10584|||RP10584；RP-10584|||Metiomeprazina||
Methiomeprazine is an antiemetic agent.
价 格：￥电议型 号：T25794产 地：中国大陆
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T24794SJ-3366；化合物 T24794SJ 3366；SJ 3366
SJ3366 is a unique and highly potent nonnucleoside reverse transcriptase human immunodeficiency virus type 1 and HIV-2 inhibitor.
价 格：￥电议型 号：T24794产 地：中国大陆
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T2475KU-0063794；化合物KU0063794KU-0063794
KU-0063794 is a potent and highly specific dual-mTOR inhibitor of mTORC1 and mTORC2.
价 格：￥电议型 号：T2475产 地：中国大陆
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T2419BMS-794833；化合物BMS794833BMS-794833
BMS-794833 is a potent ATP competitive inhibitor of Met/VEGFR2; a prodrug of BMS-817378.
价 格：￥电议型 号：T2419产 地：中国大陆
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T23794BIO592；化合物 T23794BIO-592|||BIO 592；BIO-592|||BIO 592
BIO592 is a modulator of RORγt. BIO592 triggers inverse agonism of RORγ.
价 格：￥电议型 号：T23794产 地：中国大陆
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T23541Y-29794 oxalate；化合物 T23541Y-29794 oxalate
Inhibitor of prolyl endopeptidase
价 格：￥电议型 号：T23541产 地：中国大陆
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T22794G36；化合物G36G-36；G-36
G36 is a cell-permeable non-steroidal antagonist of GPER. G36 inhibits activation by either 17β-estradiol or the GPER-selective agonist G-1 (IC50 = 112 and 165 nM, respectively). G36 has no detectable binding activity to either ERα or ERβ. G36 blocks the activation of PI3K or calcium mobilization triggered by estrogen through GPER and it suppresses ERK activation by estrogen or G-1 but not by EGF. G-36 can be used in combination with GPER-selective agonists, like G-1, to distinguish the roles of
价 格：￥电议型 号：T22794产 地：中国大陆
