Metabolites

Pseudothymidine is a C-nucleoside analog of thymidine.In VitroPseudothymidine is a C-nucleoside analog of thymidine. The calculated ΔΔG° 50 /mod is -0.5 kcal/mol, with a Δ T m /mod of 0.82°C. For the duplexes containing nine dA-T/ψT pairs, the Δ T m

Pseudothymidine is a C-nucleoside analog of thymidine.In VitroPseudothymidine is a C-nucleoside analog of thymidine. The calculated ΔΔG° 50 /mod is -0.5 kcal/mol, with a Δ T m /mod of 0.82°C. For the duplexes containing nine dA-T/ψT pairs, the Δ T m

Pseudothymidine is a C-nucleoside analog of thymidine.In VitroPseudothymidine is a C-nucleoside analog of thymidine. The calculated ΔΔG° 50 /mod is -0.5 kcal/mol, with a Δ T m /mod of 0.82°C. For the duplexes containing nine dA-T/ψT pairs, the Δ T m

Pseudothymidine is a C-nucleoside analog of thymidine.In VitroPseudothymidine is a C-nucleoside analog of thymidine. The calculated ΔΔG° 50 /mod is -0.5 kcal/mol, with a Δ T m /mod of 0.82°C. For the duplexes containing nine dA-T/ψT pairs, the Δ T m

Pseudothymidine is a C-nucleoside analog of thymidine.In VitroPseudothymidine is a C-nucleoside analog of thymidine. The calculated ΔΔG° 50 /mod is -0.5 kcal/mol, with a Δ T m /mod of 0.82°C. For the duplexes containing nine dA-T/ψT pairs, the Δ T m

Pyridoxal phosphate-d 5 is the deuterium labeled Pyridoxal phosphate. Pyridoxal phosphate is the active form of vitamin B6, acts as an inhibitor of reverse transcriptases, and is used for the treatment of tardive dyskinesia.In VitroStable heavy

Quetiapine sulfoxide dihydrochloride (Quetiapine S-oxide dihydrochloride) is a main metabolite of Quetiapinem. Quetiapine is a second-generation antipsychotic. Quetiapine is a 5-HT receptors agonist and a dopamine receptor antagonist .In VivoThe C

Quetiapine sulfoxide dihydrochloride (Quetiapine S-oxide dihydrochloride) is a main metabolite of Quetiapinem. Quetiapine is a second-generation antipsychotic. Quetiapine is a 5-HT receptors agonist and a dopamine receptor antagonist .In VivoThe C

Rabacfosadine (GS-9219), a novel proagent of the nucleotide analogue PMEG, is designed as a cytotoxic agent that preferentially targets lymphoid cells.In VitroIn lymphocytes, Rabacfosadine (GS-9219) is converted to its active metabolite,

Rabacfosadine (GS-9219), a novel proagent of the nucleotide analogue PMEG, is designed as a cytotoxic agent that preferentially targets lymphoid cells.In VitroIn lymphocytes, Rabacfosadine (GS-9219) is converted to its active metabolite,

Raltitrexed is a thymidylate synthase inhibitor with an IC50 of 9 nM for the inhibition of L1210 cell growth.An inhibitor of thymidylate synthase and DHFR.

Raltitrexed is a thymidylate synthase inhibitor with an IC50 of 9 nM for the inhibition of L1210 cell growth.An inhibitor of thymidylate synthase and DHFR.