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T7829FK962；化合物FK962FK962
FK962 is an somatostatin release enhancer , exerts cognitive-enhancing actions.
价 格：￥电议型 号：T7829产 地：中国大陆
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T76497KRFK；化合物 KRFKKRFK
KRFK, a peptide originating from TSP-1, activates TGF-β and facilitates TGF-β-mediated signaling pathways, independently of thrombospondin (TSP) receptors like CD47 and CD36. This property makes KRFK a potential research tool for chronic ocular surface inflammatory disorders [1].
价 格：￥电议型 号：T76497产 地：中国大陆
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T76398FKKSFKL-NH2；化合物 FKKSFKL-NH2FKKSFKL-NH2
FKKSFKL-NH2 is a selective peptide for protein kinase C, employed in biochemical research [1].
价 格：￥电议型 号：T76398产 地：中国大陆
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T76369CEDAEVFKDSMVPGEK；化合物 CEDAEVFKDSMVPGEKCEDAEVFKDSMVPGEK
CEDAEVFKDSMVPGEK, the peptide sequence corresponding to the rat vanilloid receptor subtype 1 (VR1), facilitates the detection and mapping of VR1 distribution [1].
价 格：￥电议型 号：T76369产 地：中国大陆
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T7207FK 3311；化合物FK 3311FK-3311|||COX-2 Inhibitor V；N-[4-乙酰基-2-(2,4-二氟苯氧基)苯基]-甲烷磺酰胺|||FK-3311|||COX-2 Inhi
FK 3311 (COX-2 Inhibitor V) is a cell permeable and orally available sulfonanilide that acts as a COX-2 inhibitor and non-steroidal anti-inflammatory drug (NSAID)
价 格：￥电议型 号：T7207产 地：中国大陆
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T71917FFK29；化合物 FFK29FFK29
FFK29 is a synthetic class II HDACi (Histone deacetylase inhibitors) which have have recently emerged as novel therapeutic options for treating various protozoan and parasitic diseases. While these HDACi demonstrated a negligible effect on the viability of mature cysts, Acanthamoeba encystation was significantly inhibited by these HDACi. In conclusion, these synthetic HDACi demonstrated potent amoebicidal effects and inhibited the growth and encystation of Acanthamoeba, thus highlighting their e
价 格：￥电议型 号：T71917产 地：中国大陆
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T71840FKBP12-IN-Q2；化合物 FKBP12-IN-Q2FKBP12-IN-Q2
FKBP12-IN-Q2 is an inhibitor of FKBP12.
价 格：￥电议型 号：T71840产 地：中国大陆
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T71046FK-1052；化合物 FK-1052FK-1052
FK-1052 is a serotonin 3 & 4 dual receptor antagonist.
价 格：￥电议型 号：T71046产 地：中国大陆
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T71045FK-1052 HCl；化合物 FK-1052 HClFK-1052 HCl
FK-1052 HCl is a serotonin 3 & 4 dual receptor antagonist.
价 格：￥电议型 号：T71045产 地：中国大陆
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T70996FK-838；化合物 FK-838FK-838
FK-838 is an adenosine subtype-1 receptor antagonist.
价 格：￥电议型 号：T70996产 地：中国大陆
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T70648FK-352；化合物 FK-352FK-352
FK-352 is a pyrazolopyridine derivative and adenosine-1 receptor antagonist.
价 格：￥电议型 号：T70648产 地：中国大陆
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T70646Deltarasin HCl；化合物 Deltarasin HClFK-352|||Deltarasin HCl|||FK352；FK-352|||Deltarasin HCl|||FK352
Deltarasin is a high affinity PDEδ-KRAS interaction inhibitor. Deltarasin can inhibit KRAS-PDEδ interactions by binding to a hydrophobic pocket on PDEδ, resulting in the impairment of cell growth, KRAS activity, and RAS/RAF signaling in human pancreatic ductal adenocarcinoma cell lines. The anti-cancer cell activity of deltarasin can be enhanced by simultaneously blocking tumor protective" autophagy
价 格：￥电议型 号：T70646产 地：中国大陆
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T70522FK-906 HCl；化合物 FK-906 HClFK-906 HCl
FK-906 HCl is a human renin inhibitor used for the long-term treatment of patients with essential hypertension.
价 格：￥电议型 号：T70522产 地：中国大陆
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T69704FK788；化合物 FK788FK788
FK788 is a diphenylcarbamate derivative that functions as a highly potent and selective IP agonist.
价 格：￥电议型 号：T69704产 地：中国大陆
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T68879FK-330 dihydrate；FK-330二水合物FR-260330 dihydrate；FR-260330 dihydrate
FK-330 dihydrate（FR-260330 dihydrate） is a novel orally active inducible nitric oxide synthase inhibitor with potential anticancer and antitumor activity to prevent ischemia and reperfusion injury in rat liver transplantation.
价 格：￥电议型 号：T68879产 地：中国大陆
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T68544FK-375 HCl；化合物 FK-375 HClFK-375 HCl
FK-375 HCl is an inhibitor of chymotrypsin.
价 格：￥电议型 号：T68544产 地：中国大陆
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T68543FK-386 HCl；化合物 FK-386 HClFK-386 HCl
FK-386 HCl is an inhibitor of chymotrypsin.
价 格：￥电议型 号：T68543产 地：中国大陆
