Drugs affecting the respiratory tract

360A iodide is a selective stabilizer of G-quadruplex , and also inhibits telomerase activity with an IC 50 of 300 nM for telomerase in TRAP-G4 assay.In Vitro360A iodide inhibits telomerase activity and stabilizes G-quadruplex, with an IC 50 of 300

360A iodide is a selective stabilizer of G-quadruplex , and also inhibits telomerase activity with an IC 50 of 300 nM for telomerase in TRAP-G4 assay.In Vitro360A iodide inhibits telomerase activity and stabilizes G-quadruplex, with an IC 50 of 300

360A iodide is a selective stabilizer of G-quadruplex , and also inhibits telomerase activity with an IC 50 of 300 nM for telomerase in TRAP-G4 assay.In Vitro360A iodide inhibits telomerase activity and stabilizes G-quadruplex, with an IC 50 of 300

3A-Amino-3A-deoxy-(2AS,3AS)-α-cyclodextrin Hydrate.

3α-Aminocholestane is a selective SH2 domain-containing inositol-5′-phosphatase 1 ( SHIP1 ) inhibitor with an IC 50 of ~2.5 μM.In VitroOPM2 cell viability is effectively reduced by 3α-Aminocholestane (3AC) treatment. RPMI8226 and U266 cells show

3α-Aminocholestane is a selective SH2 domain-containing inositol-5′-phosphatase 1 ( SHIP1 ) inhibitor with an IC 50 of ~2.5 μM.In VitroOPM2 cell viability is effectively reduced by 3α-Aminocholestane (3AC) treatment. RPMI8226 and U266 cells show

3α-Aminocholestane is a selective SH2 domain-containing inositol-5′-phosphatase 1 ( SHIP1 ) inhibitor with an IC 50 of ~2.5 μM.In VitroOPM2 cell viability is effectively reduced by 3α-Aminocholestane (3AC) treatment. RPMI8226 and U266 cells show

3α-Aminocholestane is a selective SH2 domain-containing inositol-5′-phosphatase 1 ( SHIP1 ) inhibitor with an IC 50 of ~2.5 μM.In VitroOPM2 cell viability is effectively reduced by 3α-Aminocholestane (3AC) treatment. RPMI8226 and U266 cells show

3α-Aminocholestane is a selective SH2 domain-containing inositol-5′-phosphatase 1 ( SHIP1 ) inhibitor with an IC 50 of ~2.5 μM.In VitroOPM2 cell viability is effectively reduced by 3α-Aminocholestane (3AC) treatment. RPMI8226 and U266 cells show

3α-Aminocholestane is a selective SH2 domain-containing inositol-5′-phosphatase 1 ( SHIP1 ) inhibitor with an IC 50 of ~2.5 μM.In VitroOPM2 cell viability is effectively reduced by 3α-Aminocholestane (3AC) treatment. RPMI8226 and U266 cells show

3α-Hydroxy-5α-pregnan-20-one Sulfate Pyridinium Salt.

3α-Hydroxy-5α-pregnan-20-one Sulfate Pyridinium Salt.