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DNA/RNA Synthesis

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DNA/RNA Synthesis

Chemical Structure Cat. No. Product Name CAS No.
5'-Cytidylic acid homopolymer Chemical Structure
BCP33637 5'-Cytidylic acid homopolymer 30811-80-4
Cytidine 5'-monophosphate is a pyrimidine ribonucleoside 5'-monophosphate having cytosine as the nucleobase.
Inosine-5'-triphosphate trisodium salt Chemical Structure
BCP33636 Inosine-5'-triphosphate trisodium salt 35908-31-7
Inosine-5'-triphosphate, an inosine nucleotide, is an intermediate in the purine metabolism pathway.
Cytidine-5'-triphosphate disodium salt Chemical Structure
BCP33635 Cytidine-5'-triphosphate disodium salt 36051-68-0
Cytidine 5'-triphosphate is a pyrimidine nucleoside triphosphate that is used in the synthesis of RNA by RNA polymerases.
Guanosine-5'-triphosphate Chemical Structure
BCP33402 Guanosine-5'-triphosphate 86-01-1
GTP is a guanosine 5'-phosphate and a purine ribonucleoside 5'-triphosphate. It has a role as an Escherichia coli metabolite and a mouse metabolite. It is a conjugate acid of a GTP(3-).
Guanosine-5'-diphosphate Chemical Structure
BCP33401 Guanosine-5'-diphosphate 146-91-8
GDP is a guanosine 5'-phosphate and a purine ribonucleoside 5'-diphosphate. It has a role as an Escherichia coli metabolite and a mouse metabolite. It is a conjugate acid of a GDP(2-).
BAY-2402234 Chemical Structure
BCP33023 BAY-2402234 2225819-06-5
BAY-2402234 is a selective dihydroorotate dehydrogenase (DHODH) inhibitor for the treatment of myeloid malignancies.
PTC299 Chemical Structure
BCP32869 PTC299 1256565-36-2
PTC299 is a potent, orally bioavailable VEGFA inhibitor, targets dihydroorotate dehydrogenase (DHODH), resulting in cell growth inhibition and differentiation in leukemias, including acute myeloid leukemia, linking DHODH regulation and stress-induced VEGFA and angiogenesis.
Datelliptium chloride Chemical Structure
BCP32779 Datelliptium chloride 105118-14-7
Datelliptium chloride is a DNA-intercalating agent derived from ellipticine, with anti-tumor activities.
Pyrazofurin Chemical Structure
BCP32120 Pyrazofurin 30868-30-5
Pyrazofurin, a pyrimidine nucleoside analogue with antineoplastic activity, inhibits cell proliferation and DNA synthesis in cells by inhibiting uridine 5'-phosphate (UMP) synthase. Pyrazofurin is an active, sensitive orotate-phosphoribosyltransferase inhibitor with IC50s between 0.06-0.37 µM in the three squamous cell carcinoma (SCC) cell lines Hep-2, HNSCC-14B and HNSCC-14C.
D-I03 Chemical Structure
BCP31555 D-I03 688342-78-1
D-I03 is a small molecule that inhibits RAD52-mediated ssDNA annealing with IC50 of 5 uM, binds to RAD52 with Kd of 25.8 uM and inhibits D-loop formation with IC50 of 8 uM in vitro.
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