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DNA/RNA Synthesis

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DNA/RNA Synthesis

Chemical Structure Cat. No. Product Name CAS No.
Ancitabine hydrochloride Chemical Structure
BCP12373 Ancitabine hydrochloride 10212-25-6
Ancitabine hydrochloride is a hydrochloride salt resulting from the reaction of equimolar amounts of ancitabine and hydrogen chloride. It has a role as an antimetabolite and an antineoplastic agent. It contains an ancitabine(1+).
DATP-N3 Chemical Structure
BCP46395 DATP-N3 1048021-78-8
DATP is a purine nucleoside triphosphate used in the synthesis of DNA by being incorporated into DNA.
DCTP-N3 Chemical Structure
BCP49643 DCTP-N3 1048021-94-8
DCTP is a nucleoside triphosphate that can be used for DNA synthesis. Deoxycytidine triphosphate has many applications, such as real-time PCR, cDNA synthesis, and DNA sequencing.
6-Thio-2'-Deoxyguanosine Chemical Structure
BCP16135 6-Thio-2'-Deoxyguanosine 789-61-7
6-Thio-2'-Deoxyguanosine is a nucleoside analog and telomerase substrate.
Bersiporocin dihydrochloride Chemical Structure
BCP49201 Bersiporocin dihydrochloride 2241808-53-5
Bersiporocin is a prolyl-tRNA synthetase inhibitor.
DDD85646 Chemical Structure
BCP28646 DDD85646 1215010-55-1
DDD85646 is a potent inhibitor of trypanosoma brucei N-myristoyltransferase (TbNMT IC50=2 nm; hNMTIC50=4 nm). The enzyme N-myristoyltransferase (NMT) is a potential drug target for human African trypanosomiasis.
AVN-944 Chemical Structure
BCP23877 AVN-944 297730-17-7
AVN944 is a biotech drug that demonstrated a statistically meaningful impact on IMPDH and other proteins that are critical to activities in cancer cells, including nucleotide biosynthesis, energy and metabolism, DNA replication, apoptosis and cell cycle control. AVN944 has been associated with cancer cell death in clinical trials. It is being investigated for the treatment of patients with advanced hematologic malignancies.
Zinostatin Chemical Structure
BCP48970 Zinostatin 9014-02-2
Zinostatin is a cytotoxic enediyne that alkylates DNA and RNA like mitomycin does. It has antineoplastic and antibiotic properties. It is isolated from the bacterium Streptomyces carzinostaticus. It may be active against hepatocellular carcinoma.
Bractoppin Chemical Structure
BCP48934 Bractoppin 2290527-07-8
Bractoppin is a potent and selective drug-like inhibitor of phosphopeptide recognition by the human BRCA1 tandem(t) BRCT domain (binding IC50: 74 nM). Bractoppin diminishes BRCA1 recruitment to DNA breaks, in turn suppressing damage-induced G2 arrest and assembly of the recombinase, RAD51. Bractoppin preferentially inhibits BRCA1 tBRCT-dependent steps in the DNA damage response.
DDTT Chemical Structure
BCP25080 DDTT 1192027-04-5
DDTT as a novel efficient sulfur transfer reagents suitable for DNA and RNA synthesis.
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