Name | Antagonist G |
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Synonyms |
arginyl-tryptophyl-n-methylphenylalanyl-tryptophyl-leucyl-methioninamide
AntagonistG,Arg-D-Trp-N-Methyl-Phe-D-Trp-Leu-Met-NH2 ARG-D-TRP-N-ME-PHE-D-TRP-LEU-MET-NH2 H-ARG-D-TRP-N-ME-PHE-D-TRP-LEU-MET-NH2 |
Description | Antagonist G is a potent vasopressin antagonist. Antagonist G is also a weak antagonist of GRP and Bradykinin. Antagonist G induces AP-1 transcription and sensitizes cells to chemotherapy[1][2]. |
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Related Catalog | |
In Vitro | Antagonist G (0-100 μM) induces apoptosis is redox-sensitive and caspase-dependently in SCLC cells[2]. Antagonist G activates JNK1 in SCLC cells[2]. Antagonist G is not intrinsically a free radical oxygen donor but stimulates free radical generation specifically within SCLC cells (6.2-fold) and increases the activity of the redox-sensitive transcription factor AP-1 by 61%[2]. Cell Viability Assay[2] Cell Line: SCLC cell lines NCI-H69, NCI-H510 and CHO-K1 cells. Concentration: 0-100 μM. Incubation Time: 24 h. Result: Inhibited cell growh. |
References |
Density | 1.35g/cm3 |
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Molecular Formula | C49H66N12O6S |
Molecular Weight | 951.19000 |
Exact Mass | 950.49500 |
PSA | 324.60000 |
LogP | 6.47350 |
Index of Refraction | 1.666 |