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DNA/RNA Synthesis

Chemical Structure Cat. No. Product Name CAS No.
beta-Boswellic Acid Chemical Structure
BCP35037 beta-Boswellic Acid 631-69-6
beta-Boswellic Acid is a triterpenoid with anti-hyperlipidemic, anti-carcinogenic and anti-tumor activities.
(S)-Crizotinib Chemical Structure
BCP34894 (S)-Crizotinib 1374356-45-2
(S)-Crizotinib is an MTH1 inhibitor. By inhibiting MTH1, (S)-Crizotinib disrupts nucleotide pool homeostasis, induces an increase in DNA single-strand breaks, activates DNA repair in human colon carcinoma cells, and effectively suppresses tumor growth in animal models.
DTP3 TFA Chemical Structure
BCP34038 DTP3 TFA DTP3
DTP3 TFA is a potent and selective GADD45β/MKK7 (growth arrest and DNA-damage-inducible β/mitogen-activated protein kinase kinase 7) inhibitor.
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.
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