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            首頁 > 技術(shù)文章 > ApexBio 4-HQN PARP inhibitor說明書

            ApexBio 4-HQN PARP inhibitor說明書

             更新時(shí)間:2018-08-16 點(diǎn)擊量:1717

            ApexBio是生物研究用肽和實(shí)驗(yàn)室試劑的主要供應(yīng)商。我們?cè)诩?xì)胞凋亡,表觀遺傳學(xué),癌癥生物學(xué)等研究領(lǐng)域擁有廣泛的產(chǎn)品線。Apexbio還提供定制服務(wù),包括肽合成,抗體生產(chǎn)和分析開發(fā)。

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            4-HQN PARP inhibitor

            窗體頂端

            Catalog No.A4524

            窗體底端

            Size

            Price

            10mM (in 1mL DMSO)

            $60.00

            50mg

            $85.00

             

            化學(xué)性質(zhì)

            卡號(hào) 491-36-1

            化學(xué)名稱 1H - 喹唑啉-4-酮

            Canonical SMILES C1 = CC = C2C(= C1)C(= O)N = CN2

            C 8 H 6 N 2 O. M.Wt 146.15

            可溶性 > DMSO中> 55.6mg / mL 存儲(chǔ) 在室溫下干燥

            運(yùn)輸條件 評(píng)估樣品解決方案:裝有藍(lán)色冰。所有其他可用尺寸:根據(jù)要求提供RT或藍(lán)冰

            一般提示 為了獲得更高的溶解度,請(qǐng)?jiān)?7℃下加熱管并在超聲波浴中搖動(dòng)一段時(shí)間。庫存溶液可在-20℃以下儲(chǔ)存數(shù)月。

            背景

            聚(ADP-核糖)聚合酶抑制劑(PARP)(IC50 =9.5μM); 顯示對(duì)NAD +的混合抑制。保護(hù)免受缺血再灌注誘導(dǎo)的ROS產(chǎn)生,以及隨后的大鼠心臟線粒體和細(xì)胞損傷。體內(nèi)LPS誘導(dǎo)的內(nèi)毒素小鼠的抗炎作用; 減少NF-κB和AP-1活化。

            1. Cat.No                 .Product                                      NameInformation
            2. A8181                   (-)-JQ1BET                               bromodomain inhibitor
            3. B7679                 (R)-(+)-Etomoxir sodium salt            carnitine palmitoyltransferase I (CPT1) inhibitor
            4. B7718               (R)-PFI 2 hydrochloride                     SETD7 histone lysine methyltransferase inhibitor
            5. C4834                   (S)-PFI-2 (hydrochloride)             Negative control of (R)-PFI 2 hydrochloride
            6. A4510               1,2,3,4,5,6-HexabromocyclohexaneJ          AK2 tyrosine kinase inhibitor
            7. C4119              2',3',5'-triacetyl-5-Azacytidine   prodrug form of 5-azacytidine, a DNA methyltransferase inhibitor
            8. B5972               2,4-Pyridinedicarboxylic Acid                 Histone LSD inhibitor
            9. C4445                      2-D08                               Sumoylation inhibitor
            10. B5969                2-hexyl-4-Pentynoic Acid                 Potent and robust HDACs inhibitor
            11. A4188                  2-Methoxyestradiol (2-MeOE2)        Apoptotic, antiproliferative and antiangiogenic agen
            1. A8182         3-Deazaneplanocin A (DZNep) hydrochloride      SAHH and ENZ2 inhibitor
            2. A1905        3-Deazaneplanocin,DZNep             S-adenosylhomocysteine and EZH2 inhibitor
            3. C3552        4'-bromo-Resveratrol                        Sirt1 and Sirt3 inhibitor
            4. A4524         4-HQN                                       PARP inhibitor
            5. C4018         4-iodo-SAHA         class I and class II histone deacetylase (HDAC) inhibitor
            6. B4106       4SC-202                                  Class I HDAC inhibitor
            7. C3505       5-(N,N-dimethyl)-Amiloride (hydrochloride)      NHE1, NHE2, and NHE3 inhibitor
            8. A1907         5-Azacytidine                           DNA methyltransferase inhibitor.
            9. B4947        A 366                      G9a/GLP histone lysine methyltransferase inhibitor
            10. A4160        A-966492                                PARP-1/-2 inhibitor, highly potent
            1. B1182           ABC294640                           Sphingosine kinase 2 inhibitor,selective and competitive
            2. A3002         ABT-888 (Veliparib)                                      Potent PARP inhibitor
            3. B5936           ACY-241                                Selective and orally active HDAC6 inhibitor
            4. B6120          Adox                                          indirect methyltransferase inhibitor
            5. A4158         AG-14361                                     Potent PARP1 inhibitor
            6. B7323            AGK 2                                        SIRT2 inhibitor, potent and selective
            7. C5709               AGK7                                     cell-permeable, selective inhibitor of SIRT2
            8. B4713              AK-7                                   selective and brain-permeable SIRT2 inhibitor
            9. A4542            Alexidine dihydrochloride                                PTPMT1 inhibitor
            10. A4119               AMG-900                                           Aurora kinase inhibitor

             

             

             

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