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Enzyme Inhibitors
| Alternative Name | trans-4-Aminomethylcyclohexanecarbonyl-phenylalanyl-4-carboxymethylanilide |
|---|---|
| CAS | 128837-71-8 |
| Couple Type | Inhibitor |
| Purity | ≥95% (HPLC) |
| Alternative Name | N-(3-(5-chloro-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4-difluorophenyl)propane-1-sulfonamide, N-[3-[(5-Chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)carbonyl]-2,4-difluorophenyl]-1-propanesulfonamide |
|---|---|
| CAS | 918505-84-7 |
| Couple Type | Inhibitor |
| Purity | ≥99% (HPLC) |
| CAS | 518-28-5 |
|---|---|
| Couple Type | Inhibitor |
| Purity | ≥98% (HPLC) |
| CAS | 1405-20-5 |
|---|---|
| Couple Type | Activator, Inhibitor |
| Purity | ≥80% (HPLC) (sum of polymyxins B1, B2, B3, B1-I) |
| CAS | 172889-26-8 |
|---|---|
| Couple Type | Inhibitor |
| Purity | ≥98% (TLC) |
| Alternative Name | AG1879, 4-Amino-5-(4-chlorophenyl)-7-(t-butyl)pyrazolo[3,4-d]pyrimidine |
|---|---|
| CAS | 172889-27-9 |
| Couple Type | Inhibitor |
| Purity | ≥98% (TLC) |
pp242 . hydrate
ENZ-CHM132
Inhibitor of both mTORC1 and mTORC2. Induces cell death in human and murine leukemia cells.
| Alternative Name | PP-242, 2-[4-Amino-1-(1-methylethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-1H-indol-5-ol, 2-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-1H-indol-5-ol |
|---|---|
| CAS | 1092351-67-1 |
| Couple Type | Inhibitor |
| Purity | ≥99% (HPLC) |
| Purity | ≥98% |
|---|
| Alternative Name | IGF-IR Inhibitor, N-(5-Chloro-2-methoxyphenyl)-N’-(2-methyl-4-quinolinyl)urea |
|---|---|
| CAS | 196868-63-0 |
| Couple Type | Inhibitor |
| Purity | ≥98% (HPLC (UV)) |
| Alternative Name | Celastrol methyl ester |
|---|---|
| CAS | 1258-84-0 |
| Couple Type | Inhibitor |
| Purity | ≥97% (HPLC) |
| Alternative Name | Prodigiosine, 4-Methoxy-5-[(5-methyl-4-pentyl-2H-pyrrol-2-ylidene)methyl]-2,2’-bi[1H-pyrrole] |
|---|---|
| CAS | 82-89-3 |
| Couple Type | Inhibitor |
| Purity | ≥95% (HPLC) |
