Activin and Inhibin

Doxorubicin (Adriamycin) is an antibiotic agent that inhibits DNA topoisomerase II and induces DNA damage and apoptosis.A Topo II inhibitor, DNA intercalator and powerful cytotoxic agent.

Doxorubicin (Adriamycin) is an antibiotic agent that inhibits DNA topoisomerase II and induces DNA damage and apoptosis.A Topo II inhibitor, DNA intercalator and powerful cytotoxic agent.

Doxorubicin (Adriamycin) is an antibiotic agent that inhibits DNA topoisomerase II and induces DNA damage and apoptosis.A Topo II inhibitor, DNA intercalator and powerful cytotoxic agent.

Doxorubicin (Adriamycin) is an antibiotic agent that inhibits DNA topoisomerase II and induces DNA damage and apoptosis.A Topo II inhibitor, DNA intercalator and powerful cytotoxic agent.

DP00477 is a potent IDO1 (indoleamine 2,3-dioxygenase 1) inhibitor with an IC 50 value of 7.0 µM. DP00477 has the potential for the research of cancerIn VitroDP00477 inhibits IDO1 activity with IC 50 s of 71, 6.3 µM when 5 mM GSH or 0.01% Triton-X

DP00477 is a potent IDO1 (indoleamine 2,3-dioxygenase 1) inhibitor with an IC 50 value of 7.0 µM. DP00477 has the potential for the research of cancerIn VitroDP00477 inhibits IDO1 activity with IC 50 s of 71, 6.3 µM when 5 mM GSH or 0.01% Triton-X

DP00477 is a potent IDO1 (indoleamine 2,3-dioxygenase 1) inhibitor with an IC 50 value of 7.0 µM. DP00477 has the potential for the research of cancerIn VitroDP00477 inhibits IDO1 activity with IC 50 s of 71, 6.3 µM when 5 mM GSH or 0.01% Triton-X

DP00477 is a potent IDO1 (indoleamine 2,3-dioxygenase 1) inhibitor with an IC 50 value of 7.0 µM. DP00477 has the potential for the research of cancerIn VitroDP00477 inhibits IDO1 activity with IC 50 s of 71, 6.3 µM when 5 mM GSH or 0.01% Triton-X

DP00477 is a potent IDO1 (indoleamine 2,3-dioxygenase 1) inhibitor with an IC 50 value of 7.0 µM. DP00477 has the potential for the research of cancerIn VitroDP00477 inhibits IDO1 activity with IC 50 s of 71, 6.3 µM when 5 mM GSH or 0.01% Triton-X

DPC-681 is a potent and selective inhibitor of HIV protease with IC90s for wild-type HIV-1 of 4 to 40 nM.IC50 value: 4 - 40 nM Target: HIV protease in vitro: DPC 681 is extremely potent inhibitor of wild-type HIV-1. When all of the HIV-1 strains

DPC-681 is a potent and selective inhibitor of HIV protease with IC90s for wild-type HIV-1 of 4 to 40 nM.IC50 value: 4 - 40 nM Target: HIV protease in vitro: DPC 681 is extremely potent inhibitor of wild-type HIV-1. When all of the HIV-1 strains

DPC-681 is a potent and selective inhibitor of HIV protease with IC90s for wild-type HIV-1 of 4 to 40 nM.IC50 value: 4 - 40 nM Target: HIV protease in vitro: DPC 681 is extremely potent inhibitor of wild-type HIV-1. When all of the HIV-1 strains