Antibiotics

Aflatoxin M1-13C17.

A potent hepatotoxic and hepatocarcinogenic mycotoxin, found in milk of cows fed on meal contaminated with aflatoxin B2Potent liver carcinogen and DNA-damaging agent. It is also mutagenic, teratogenic, and causes immunosuppression in animals.

AFN-1252(Debio 1452) is a potent inhibitor of enoyl-acyl carrier protein reductase (FabI), inhibited all clinical isolates of Staphylococcus aureus and Staphylococcus epidermidis at concentrations of ≤0.12 μg/ml.IC50 value:Target: Antibiotic

AFN-1252(Debio 1452) is a potent inhibitor of enoyl-acyl carrier protein reductase (FabI), inhibited all clinical isolates of Staphylococcus aureus and Staphylococcus epidermidis at concentrations of ≤0.12 μg/ml.IC50 value:Target: Antibiotic

AFN-1252(Debio 1452) is a potent inhibitor of enoyl-acyl carrier protein reductase (FabI), inhibited all clinical isolates of Staphylococcus aureus and Staphylococcus epidermidis at concentrations of ≤0.12 μg/ml.IC50 value:Target: Antibiotic

AFN-1252(Debio 1452) is a potent inhibitor of enoyl-acyl carrier protein reductase (FabI), inhibited all clinical isolates of Staphylococcus aureus and Staphylococcus epidermidis at concentrations of ≤0.12 μg/ml.IC50 value:Target: Antibiotic

AFN-1252(Debio 1452) is a potent inhibitor of enoyl-acyl carrier protein reductase (FabI), inhibited all clinical isolates of Staphylococcus aureus and Staphylococcus epidermidis at concentrations of ≤0.12 μg/ml.IC50 value:Target: Antibiotic

AG 1387 is a 5-iodo analog of tyrphostin AG 555 that displays anticancer and antiviral properties. More cell-permeable and potent than AG 555 as an inhibitor of protein tyrosine kinase and DNA topoisomerase I (TOPO I). Unlike camptothecin

AG 1387 is a 5-iodo analog of tyrphostin AG 555 that displays anticancer and antiviral properties. More cell-permeable and potent than AG 555 as an inhibitor of protein tyrosine kinase and DNA topoisomerase I (TOPO I). Unlike camptothecin

Ala-Leu-Ala-Leu Daunorubicin hydrochloride.

Alamethicin (U-22324) is a polypeptide natural product antibiotic supplied as a mixture of homologs: Alamethicin and Alamethicin I. These compounds form voltage-dependent ion channels in the lipid bilayer, through the spontaneous assembly of units

Alamethicin (U-22324) is a polypeptide natural product antibiotic supplied as a mixture of homologs: Alamethicin and Alamethicin I. These compounds form voltage-dependent ion channels in the lipid bilayer, through the spontaneous assembly of units