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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC28942 | T-705RTP sodium |
T-705RTP sodium, a nucleotide analog, selectively inhibits RNA-dependent RNA polymerase (RdRp) of the influenza virus. T-705RTP sodium competitively incorporates ATP/GTP and a single molecule of T-705RTP sodium is incorporated into a nascent RNA strand, which then inhibits subsequent virus RNA extension.
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| DC28439 | Sorivudine |
Sorivudine (BV-araU) is an orally active synthetic pyrimidine nucleoside antimetabolite drug. Sorivudine derives its antiviral activity from selective conversion by a specific thymidine kinase present in certain DNA viruses to nucleotides, which can in turn interfere with viral DNA synthesis.
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| DC28404 | Caracemide |
Caracemide (NSC-253272) inhibits the enzyme ribonucleotide reductase of Escherichia coli. Caracemide is a novel anticancer agent derived from a hydroxamic acid and has demonstrated to produce severe central nervous system (CNS) toxicity.
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| DC28171 | Rifalazil |
Rifalazil (KRM-1648; ABI-1648), a rifamycin derivative, inhibits the bacterial DNA-dependent RNA polymerase and kills bacterial cells by blocking off the β-subunit in RNA polymerase. Rifalazil (KRM-1648; ABI-1648) is an antibiotic, exhibits high potency against mycobacteria, gram-positive bacteria, Helicobacter pylori, C. pneumoniae and C. trachomatis with MIC values from 0.00025 to 0.0025 μg/ml. Rifalazil (KRM-1648; ABI-1648) has the potential for the treatment of Chlamydia infection, Clostridium difficile associated diarrhea (CDAD), and tuberculosis (TB).
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| DC10430 | COH29 |
COH29 is a potent ribonucleotide reductase (RNR) inhibitor with anticancer activity with an IC50 of 8 μM in KB cell.
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