| Name | L-Glutamic acid γ-(p-nitroanilide) hydrochloride |
|---|---|
| Synonyms |
H-GLU(PNA)-OH HCL
L-GLUTAMIC ACID GAMMA-(P-NITROANILIDE) HYDROCHLORIDE (3-cbaMoyl-1-cboxy-propyl)-(4-nitrophenyl)azaniuM chloride L-GAMMA-GLUTAMYL-P-NITROANILIDE HYDROCHLORIDE (4-amino-1-cboxy-4-keto-butyl)-(4-nitrophenyl)ammonium chloride L-glutamic acid gamma-(P-nitroanilide)*hydrochlor L-GAMMA-GLUTAMYL 4-NITROANILIDE HYDROCHLORIDE L-r-Glutamyl-p-Nitroanilide Hydrochloride extrapure N-(4-nitrophenyl)-L-glutamine monohydrochloride 7-bromo-6-oxocholestan-3-yl acetate L-Glutamic acid gamma-(4-nitroanilide) monohydrochloride L-GLUTAMIC ACID GAMMA-(P-NITROANILIDE)*H YDROCHLORID GAMMA-L-GLUTAMYL-P-NITROANILIDE HYDROCHLORIDE L-y-GLUTAMYL-p-NITROANILIDE HYDROCHLORIDE extrapure (S)-2-Amino-5-((4-nitrophenyl)amino)-5-oxopentanoic acid hydrochloride Inhibitor,GGT,SNAT,GPNA,glutamine,lung,inhibit,ASCT2,Gln,Apoptosis,GPNA hydrochloride,γ-glutamyltransferase,LAT,A549,transporter (5-azanyl-1-hydroxy-1,5-dioxo-pentan-2-yl)-(4-nitrophenyl)azanium chloride L -Glutamic acid γ-(p-nitroanilide) hydrochloride l-glutamic acid γ-(p-nitroanilide) hydrochloride gamma-L-Glutamyl-4-nitroanilideHCl L-GLUTAMIC ACID γ-(P-NITROANILIDE) HYDROCHLORIDE (5-amino-1-hydroxy-1,5-dioxopentan-2-yl)-(4-nitrophenyl)azanium chloride L-Glutamic acid g-(p-nitroanilide) hydrochloride GPNA (hydrochloride) Nintedanib esylate n-(4-nitrophenyl)-l-glutaminmonohydrochloride gamma-L-Glutamyl-p-nitroanilide HCl GPNA hydrochloride, 10 mM in DMSO |
| Description | GPNA hydrochloride is a well known substrate of the enzyme γ-glutamyltransferase (GGT). GPNA hydrochloride is a specific glutamine (Gln) transporter ASCT2 inhibitor. GPNA hydrochloride also inhibit Na+-dependent carriers, such as SNAT family (SNAT1/2/4/5), and the Na+-independent leucine transporters LAT1/2. GPNA reversibly induces apoptosis in A549 cells[1]. |
|---|---|
| Related Catalog | |
| Target |
ASCT2[1] |
| In Vitro | GPNA (10-1000 μM; 48 hours) induces a dose-dependent decrease of cell viability in A549 cells[1]. Cell Viability Assay[1] Cell Line: A549 cells Concentration: 10, 100, 250, 500 , and 1000 μM Incubation Time: 48 hours Result: Induced a dose-dependent decrease of cell viability, with an IC50 roughly corresponding to ~250 μM. |
| References |
| Boiling Point | 590.6ºC at 760 mmHg |
|---|---|
| Molecular Formula | C11H14ClN3O5 |
| Molecular Weight | 303.69900 |
| Flash Point | 311ºC |
| Exact Mass | 303.06200 |
| PSA | 138.24000 |
| LogP | 2.82390 |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xi |
| RIDADR | NONH for all modes of transport |