规格 | 目录价格 | 上海 | 安徽 | 武汉 | 成都 | 北方 | 深圳 | 会员价格 | 数量 |
---|---|---|---|---|---|---|---|---|---|
g | ¥ ƻƅŔňň | > 0 | > 0 | -- | -- | 2 | ¥ ƻƅŔňň | - + | |
g | ¥ ƻǺŔňň | 6 | > 0 | 6 | ¥ ƻǺŔňň | - + | |||
0g | ¥ ŭşŔňň | 3 | > 0 | 2 | ¥ ŭşŔňň | - + | |||
2g | ¥ şǺŔňň | > 0 | > 0 | 6 | ¥ şǺŔňň | - + | |||
00g | ¥ ŭƅŭŔňň | -- | > 0 | 2 | 2 | 8 | ¥ ŭƅŭŔňň | - + | |
00g | ¥ șǺƩƏŔňň | -- | 6 | -- | 2 | 2 | ¥ șǺƩƏŔňň | - + | |
kg | ¥ ŭșƩňŔňň | -- | 3 | -- | 3 | 2 | ¥ ŭșƩňŔňň | - + | |
大货 | 请询价 | -- | -- | -- | -- | -- | -- | -- | - + |
78.62
[]. Manolopoulou A, et al. Synthesis of potent antagonists of substance P by modifying the methionyl and glutaminyl residues of its C-terminal hexapeptide and without using D-amino acids. Int J Pept Protein Res. 993 Apr;():-.
[2]. A Manolopoulou, et al. Synthesis of potent antagonists of substance P by modifying the methionyl and glutaminyl residues of its C-terminal hexapeptide and without using D-amino acids. Int J Pept Protein Res. 993 Apr;():-.
[3]. M Antoniou, et al. Synthesis and biological activity of analogues of the C-terminal hexapeptide of substance P with modifications at glutaminyl and methioninyl residues. Structure-activity studies. Int J Pept Protein Res. 992 Nov;0():39-00.
H302-H3-H39-H33
P26-P26-P270-P27-P280-P302+P32-P30+P30-P30+P3+P338-P330-P362+P36-P03+P233-P0-P0