Table 1.
Yields and purities of [azasulfuryl4]-GHRP 6 analogs.
Azasulfurylpeptides | Crude Purity (%) a | Isolated Purity (%) b | Isolated Yields (%) c | HRMS | |
---|---|---|---|---|---|
m/z (cal) | m/z (obs) | ||||
His-D-Trp-Ala-AsF-D-Phe-Lys-NH2 (3a) | 73% | >99% | 12% | 893.3851 | 893.3832 |
His-D-Trp-Ala-AsY-D-Phe-Lys-NH2 (3b) | 70% | >99% | 9% | 909.3801 | 909.3805 |
His-D-Trp-Ala-(4-F)AsF-D-Phe-Lys-NH2 (3c) | 65% | >99% | 3% | 911.3757 | 911.3769 |
His-D-Trp-Ala-(4-MeO)AsF-D-Phe-Lys-NH2 (3d) | 75% | >99% | 10% | 923.3957 | 923.3936 |
His-D-Trp-Ala-2-AsNal-D-Phe-Lys-NH2 (3e) | 61% | >99% | 10% | 943.4008 | 943.4007 |
Ala-D-Trp-Ala-(4-F)AsF-D-Phe-Lys-NH2 (3f) | 79% | >99% | 23% | 845.3647 | 845.3539 |
a Crude purities of peptide obtained after an aliquot cleavage of resin using TFA:H2O:TES (95:2.5:2.5), followed by LC-MS analysis using 5–80% MeOH (0.1% FA) in H2O (0.1% FA) as eluant. b Isolated purities of peptide obtained by a LC-MS analysis using two separate gradients of MeOH (0.1% FA) in H2O (0.1% FA) or MeCN (0.1% FA) in H2O (0.1% FA). c Isolated yields calculated from resin loading.