FLAP
5-lipoxygenase-activating protein; 5-LO activating protein
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FLAP 관련 제품 (41)
관련 제품 (41)
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Antibodies (2)
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MK-886
0 ImagesSynonyms: L 663536 -
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FEN1-IN-1
0 ImagesFEN1-IN-1 (compound 1) is a small molecule flap endonuclease 1 (FEN1) inhibitor with antitumor activity. FEN1-IN-1 binds to the active site of FEN1 and partly achieves inhibition by the co-ordination of Mg2+ ions. FEN1-IN-1 initiaties a DNA damage response and activates the ATM checkpoint signalling pathway, the phosphorylation of histone H2AX and the ubiquitination of FANCD2 in mammalian cells. FEN1-IN-1 is promising for research of cancers. -
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Quiflapon
0 ImagesSynonyms: MK-591Quiflapon (MK-591) is a selective and specific 5-lipoxygenase-activating protein (FLAP) inhibitor with an IC50 of 1.6 nM in a FLAP binding assay. Quiflapon is also a potent and orally active Leukotriene biosynthesis (LT) inhibitor, shows IC50 values of 3.1 and 6.1 nM in intact human and elicited rat PMNLs, respectively. Quiflapon induces cell apoptosis. -
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- FEN1-IN-4
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Fiboflapon
0 ImagesSynonyms: GSK2190915; AM-803 -
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AM-643
0 ImagesCat. No.: HY-125089CAS No.: 1233114-22-1 -
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FEN1-IN-9
0 ImagesCat. No.: HY-185455CAS No.: 758720-87-5FEN1-IN-9 is a selective flap endonuclease 1 (FEN1) inhibitor with an IC50 of 37.9 μM. FEN1-IN-9 can be used for the research of DNA damage repair. -
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L 689037
0 ImagesCat. No.: HY-120580CAS No.: 136668-50-3L 689037 is a leukotriene biosynthesis (LT) inhibitor and a 5-lipoxygenase-activating protein (FLAP) binder. [125I]-L 691,831 serves as a standard probe to precisely locate the key structural domains that determine the binding of inhibitors to FLAP. L 689037 can be used in the research of asthma and inflammatory bowel disease. -
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Quiflapon sodium
0 ImagesSynonyms: MK-591 sodium -
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FEN1-IN-2
0 ImagesFEN1-IN-2 (compound 20) is a flap endonuclease 1 (FEN1) inhibitor, with IC50 values of 3 nM and 226 nM for FEN1 and XPG, respectively. -
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- Atuliflapon
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Diflapolin
0 ImagesDiflapolin is a highly active dual 5-lipoxygenase-activating protein (FLAP)/soluble epoxide hydrolase (sEH) inhibitor with marked anti-inflammatory efficacy and high target selectivity. Diflapolin inhibits 5-LOX product formation in intact human monocytes and neutrophils with IC50s?of? 30 and 170?nM, respectively, and suppressed the activity of isolated sEH (IC50=20?nM). -
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MSC778
0 ImagesCat. No.: HY-177512CAS No.: 3098173-17-9MSC778 is an effective and orally active flap endonuclease 1 (FEN1) inhibitor with an IC50 of 3 nM and a KD of 2.9 nM. MSC778 exhibits 145-fold, 516-fold, and 65-fold selectivity over EXO1, GEN1, and XPG, respectively. MSC778 selectively kills BRCA2-deficient cells and potentiates the activity of Niraparib (HY-10619) to induce tumor stasis in a BRCA2 KO DLD-1 mouse xenograft. MSC778 can be used in the research of colorectal cancer. -
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- AM679
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Fiboflapon sodium
0 ImagesSynonyms: GSK2190915 sodium salt; AM-803 sodium -
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FEN1-IN-7
0 ImagesFEN1-IN-7 (compound 16) is a selective inhibitor of Flap endonuclease-1 (FEN1, IC50=18 nM), involving in mammalian cells to repair DNA damage. FEN1-IN-7 also targets to related endonuclease, xeroderma pigmentosum G (XPG) with an IC50 value of 3.04 μM. FEN1-IN-7 increases the cellular sensitivity of cancer cells to potent DNA alkylating agents or methylating agents. -
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- Veliflapon
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- FEN1-IN-5
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(S)-Veliflapon
0 ImagesSynonyms: (S)-BAY X 1005; (S)-DG-031(S)-Veliflapon ((S)-BAY X 1005) is an orally active inhibitor of leukotriene biosynthesis and 5-lipoxygenase activating protein (FLAP). (S)-Veliflapon inhibits the formation of leukotriene B4 (LTB4) in rat, mouse and human leukocytes with IC50 values of 0.026 µM, 0.039 µM and 0.22 µM respectively. (S)-Veliflapon showes enantioselectivity in human whole blood. -
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FEN1-IN-6
0 ImagesCat. No.: HY-153791CAS No.: 824983-84-8FEN1-IN-6 (compound 9) is a potent inhibitor of Flap endonuclease-1 (FEN1, IC50=10 nM), involving in mammalian cells to repair DNA damage. FEN1-IN-6 also targets to related endonuclease, xeroderma pigmentosum G (XPG) with an IC50 value of 23 nM. -
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