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T14362LAY 9944 dihydrochloride1(2chlorophenyl)N[[4[(2chlorophenyl)methylaminomethyl]cyclohexyl]methyl]metha
AY 9944 dihydrochloride is a intermediate.
价 格：￥电议型 号：T14362L产 地：中国大陆
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T99443-(9-Chloro-3-methyl-4-oxoisoxazolo[4,3-c]quinolin-5(4H)-yl)-N-(3,4,5-trimethoxyphenyl)benzeneacetam
LY402913 is a selective modulators of the multidrug resistance protein (MRP1).
价 格：￥电议型 号：T9944产 地：中国大陆
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T14362AY 9944
AY 9944 is a specific cholesterol biosynthesis inhibitor. AY 9944 inhibits the 7-dehydro cholesterol Δ7-reductase (DHCR7) enzyme (IC50=13 nM). At high doses, AY 9944 inhibits also in cultured embryos sterol Δ7-Δ8 isomerase, which causes the accumulation o
价 格：￥电议型 号：T14362产 地：中国大陆
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T11826LCH-7749944GNF-PF-2356
LCH-7749944 effectively suppresses the proliferation of human gastric cancer cells through downregulation of PAK4/c-Src/EGFR/cyclin D1 pathway and induces apoptosis. LCH-7749944 is a potent PAK4 inhibitor with an IC50 of 14.93 μM.
价 格：￥电议型 号：T11826产 地：中国大陆
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T11826LCH-7749944LCH-7749944,GNF-PF-2356,
LCH-7749944 effectively suppresses the proliferation of human gastric cancer cells through downregulation of PAK4/c-Src/EGFR/cyclin D1 pathway and induces apoptosis.?LCH-7749944 is a potent PAK4 inhibitor with an IC50 of 14.93 μM.?
价 格：￥电议型 号：T11826产 地：美洲
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T14362AY 9944AY 9944
AY 9944 is a specific cholesterol biosynthesis inhibitor. AY 9944 inhibits the 7-dehydro cholesterol Δ7-reductase (DHCR7) enzyme (IC50=13 nM). At high doses, AY 9944 inhibits also in cultured embryos sterol Δ7-Δ8 isomerase, which causes the accumulation o
价 格：￥电议型 号：T14362产 地：美洲
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T799442-O-Sinapoyl makisterone A；化合物 2-O-Sinapoyl makisterone A2-O-Sinapoyl makisterone A
Compound 2, formally known as 2-O-Sinapoyl makisterone A, is a sinapinic acid-ecdysterone hybrid that acts as a selective inhibitor of COX-2, effectively suppressing the expression of COX-2 protein [1].
价 格：￥电议型 号：T79944产 地：中国大陆
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T69944NLG802 HCl；化合物 NLG802 HClNLG802 HCl
NLG802 is an orally bioavailable prodrug of indoximod, a methylated tryptophan, with immune checkpoint inhibitory and antineoplastic activities. Upon oral administration, the indoximod prodrug NLG802 is converted to indoximod. Indoximod targets, binds to and inhibits the enzyme indoleamine 2,3-dioxygenase (IDO; IDO1), which converts the essential amino acid tryptophan into the immunosuppressive metabolite kynurenine. By increasing tryptophan levels and decreasing kynurenine levels, indoximod res
价 格：￥电议型 号：T69944产 地：中国大陆
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T39944HSD1590；HSD1590HSD1590
HSD1590 is a highly effective and potent inhibitor of ROCK1 and ROCK2, with IC50 values of 1.22 nM and 0.51 nM, respectively. It demonstrates exceptional binding affinity to ROCK, with Kd values below 2 nM. Moreover, HSD1590 showcases minimal cytotoxicity, making it an ideal compound for various applications.
价 格：￥电议型 号：T39944产 地：中国大陆
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T29944Amadinone acetate；化合物 T29944RS 2208|||RS-2208；RS 2208|||RS-2208
Amadinone acetate is a biochemical.
价 格：￥电议型 号：T29944产 地：中国大陆
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T19944DSSeb Crosslinker化合物 T19944DSSeb Cross linker|||DSSeb Cross-linker
DSSeb Crosslinker is a homobifunctional cross-linking reagent. It is useful in protein crosslinking and making antibody-drug conjugates.
价 格：￥电议型 号：T19944产 地：中国大陆
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T14362LAY 9944 dihydrochloride；化合物AY 9944 盐酸盐AY 9944 dihydrochloride
AY 9944 dihydrochloride is a intermediate.
价 格：￥电议型 号：T14362L产 地：中国大陆
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T14362AY 9944；化合物AY 9944AY 9944
AY 9944 is a specific cholesterol biosynthesis inhibitor. AY 9944 inhibits the 7-dehydro cholesterol Δ7-reductase (DHCR7) enzyme (IC50=13 nM). At high doses, AY 9944 inhibits also in cultured embryos sterol Δ7-Δ8 isomerase, which causes the accumulation of cholest-8-en-3β-ol[1][2][3]. AY 9944 causes hypocholesterolemia and accumulation of 7DHC.
价 格：￥电议型 号：T14362产 地：中国大陆
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T11826LCH-7749944；化合物LCH-7749944GNF-PF-2356；GNF-PF-2356
LCH-7749944 (GNF-PF-2356) effectively suppresses the proliferation of human gastric cancer cells through downregulation of PAK4/c-Src/EGFR/cyclin D1 pathway and induces apoptosis. LCH-7749944 is a potent PAK4 inhibitor with an IC50 of 14.93 μM.
价 格：￥电议型 号：T11826产 地：中国大陆
