H-p-Chloro-Phe-D-Cys-β-(3-pyridyl)-Ala-D-Trp-Lys-tBu-Gly-Cys-2-Nal-NH2 trifluoroacetate salt (Disulfide bond) structure
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Common Name | H-p-Chloro-Phe-D-Cys-β-(3-pyridyl)-Ala-D-Trp-Lys-tBu-Gly-Cys-2-Nal-NH2 trifluoroacetate salt (Disulfide bond) | ||
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| CAS Number | 209006-18-8 | Molecular Weight | 1175.85 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C59H71ClN12O8S2 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of H-p-Chloro-Phe-D-Cys-β-(3-pyridyl)-Ala-D-Trp-Lys-tBu-Gly-Cys-2-Nal-NH2 trifluoroacetate salt (Disulfide bond)PRL 2915 is a potent human somatostatin subtype 2 receptor (hsst2) antagonist with a Ki of 12 nM[1]. |
| Name | H-P-CHLORO-PHE-D-CYS-β-(3-PYRIDYL)-ALA-D-TRP-LYS-TBU-GLY-CYS-2-NAL-NH2 |
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| Synonym | More Synonyms |
| Description | PRL 2915 is a potent human somatostatin subtype 2 receptor (hsst2) antagonist with a Ki of 12 nM[1]. |
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| Related Catalog | |
| Target |
hsst2:12 nM (Ki) hsst3:100 nM (Ki) hsst5:520 nM (Ki) hsst4:895 nM (Ki) hsst1:>1000 nM (Ki) hsst2:1.8 nM (IC50, rat antagonist bioassay versus somatostatin) rat urotensin II receptor:293 nM (Ki) human urotensin II receptor:562 nM (Ki) |
| In Vitro | PRL 2915 (0.3-30 nM; 30 min) 剂量依赖性地阻断人尿紧张素 II (human urotensin II) 诱导的大鼠主动脉环的强张性收缩[2]。 |
| References |
| Molecular Formula | C59H71ClN12O8S2 |
|---|---|
| Molecular Weight | 1175.85 |
| Exact Mass | 1174.46000 |
| PSA | 378.11000 |
| LogP | 7.94310 |
| prl-2915 |