(Arg6,D-Trp7.9,N-Me-Phe8)-Substance P (6-11) structure
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Common Name | (Arg6,D-Trp7.9,N-Me-Phe8)-Substance P (6-11) | ||
|---|---|---|---|---|
| CAS Number | 115150-59-9 | Molecular Weight | 951.19000 | |
| Density | 1.35g/cm3 | Boiling Point | N/A | |
| Molecular Formula | C49H66N12O6S | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of (Arg6,D-Trp7.9,N-Me-Phe8)-Substance P (6-11)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]. |
| Name | Antagonist G |
|---|---|
| Synonym | More Synonyms |
| 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 |
|---|---|
| Molecular Formula | C49H66N12O6S |
| Molecular Weight | 951.19000 |
| Exact Mass | 950.49500 |
| PSA | 324.60000 |
| LogP | 6.47350 |
| Index of Refraction | 1.666 |
| 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 |