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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T63808 | Cap-dependent endonuclease-IN-1 | Others | |
Cap-dependent endonuclease-IN-1 is a highly potent and orally active cap-dependent endonuclease inhibitor with antiviral activity for the study of influenza virus infection. | |||
T8545 | FEN1-IN-4 | FEN1 Inhibitor C2 | Others |
FEN1-IN-4 (FEN1 Inhibitor C2) is an inhibitor of human flap endonuclease-1 (hFEN1) | |||
T15507 | Hycanthone | Etrenol(mesylate),Win 249-33 | DNA/RNA Synthesis , Topoisomerase , Parasite |
Hycanthone (Etrenol(mesylate)) is a potent drug of antischistosomal. Hycanthone is a DNA intercalator that inhibits RNA synthesis and DNA topoisomerases I and II. Hycanthone inhibits nucleic acid biosynthesis and inhibit... | |||
T60379 | PUL89 Endonuclease-IN-1 | ||
pUL89 Endonuclease-IN-1 (Compound 13d), with an IC50 value of 0.88 μM, serves as a potent inhibitor of human cytomegalovirus (HCMV) pUL89 endonuclease, demonstrating antiviral activity [1]. | |||
T6823 | E3330 | HIF/HIF Prolyl-Hydroxylase , DNA/RNA Synthesis | |
E3330 is a potent and selective APE1(Ref-1) inhibitor, which suppressed NF-kappa B DNA-binding activity. | |||
T4569 | Lucanthone | Lucantona,Lucanthonum | DNA/RNA Synthesis , Autophagy |
Lucanthone (Lucanthonum) is an inhibitor of Apurinic endonuclease-1 (APE-1). | |||
T66154 | Paroxypropione | ||
It is an inhibitor of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) | |||
T9743 | FEN1-IN-SC13 | Others | |
FEN1-IN-SC13 is a potent inhibitor of DNA fragmentation endonuclease 1 (FEN1) | |||
T9147 | FEN1-IN-3 | ||
FEN1-IN-3 is a human flap endonuclease-1 ( hFEN1 ) inhibitor that stabilizes hFEN1 with an EC 50 of 6.8 μM . | |||
T15274 | FEN1-IN-1 | LNT-1 | Others |
FEN1-IN-1 (LNT-1) is an inhibitor of flap endonuclease 1 (FEN1). FEN1-IN-1 binds to the active site of FEN1. It partly achieves inhibition by the co-ordination of Mg2+ ions. | |||
T60904 | ERCC1-XPF-IN-2 | Others | |
ERCC1-XPF-IN-2 is active in nucleotide excision repair, cisplatin enhancement and γH2AX assays. ERCC1-XPF-IN-2 is a potent inhibitor of ERCC1-XPF endonuclease with an IC 50 value of 0.6 μM [1]. | |||
T61487 | APE1-IN-1 | DNA/RNA Synthesis | |
APE1-IN-1 is a potent purine/pyrimidine endonuclease 1 (APE1)-free inhibitor that crosses the blood-brain barrier with potential antitumor activity and potentiates the cytotoxicity of the alkylating agent, methyl methane... | |||
T74295 | Cap-dependent endonuclease-IN-22 | ||
Cap-dependent endonuclease-IN-22 is a powerful inhibitor of cap-dependent endonuclease (CEN) [1]. | |||
T61840 | PUL89 Endonuclease-IN-2 | ||
pUL89 Endonuclease-IN-2 (Compound 15k) is a highly effective inhibitor of the pUL89 endonuclease of human cytomegalovirus (HCMV). With an IC50 of 3.0 μM, it exhibits potent antiviral activities [1]. | |||
T69128 | NSC-13755 | ||
NSC-13755 is a human flap endonuclease 1 (FEN1) inhibitor. | |||
T61757 | Cap-dependent endonuclease-IN-26 | ||
Cap-dependent endonuclease-IN-26, a potent inhibitor of cap-dependent endonuclease (CEN) with an IC50 of 286 nM, exhibits significant antiviral activity against a broad spectrum of influenza A and B strains [1]. | |||
T74294 | Cap-dependent endonuclease-IN-12 | ||
Cap-dependent Endonuclease-IN-12 (EXP-35) is a potent inhibitor of Cap-dependent endonuclease, demonstrating low cytotoxicity. This compound exhibits inhibitory effects on H1N1 [1]. | |||
T68449 | JFD00950 | ||
JFD00950 is a human flap endonuclease 1 (FEN1) inhibitor with in vitro inhibition of flap cleavage activity as well as cytotoxic activity against a colon cancer cell line, DLD-1. | |||
T79134 | FEN1-IN-6 | FLAP | |
FEN1-IN-6 (compound 9) is a potent Flap endonuclease-1 (FEN1, IC50 = 10 nM) inhibitor, crucial for DNA damage repair in mammalian cells, and additionally targets the related endonuclease xeroderma pigmentosum G (XPG) wit... | |||
T78192 | FEN1-IN-5 | FLAP | |
FEN1-IN-5 (compound 12A) is a potent Flap endonuclease-1 (FEN1) inhibitor with an IC50 value of 12 nM, playing a role in DNA repair mechanisms [1]. |