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 | ¥ ȨɄľƔƔ | > 0 | 6 | ¥ ȨɄľƔƔ | - + | ||||
0g | ¥ ǫƔľƔƔ | 2 | > 0 | 3 | 2 | ¥ ǫƔľƔƔ | - + | ||
2g | ¥ ƵƔƔľƔƔ | > 0 | 8 | > 0 | 6 | ¥ ƵƔƔľƔƔ | - + | ||
00g | ¥ ƊůǫľƔƔ | -- | > 0 | 3 | 6 | 8 | ¥ ƊůǫľƔƔ | - + | |
00g | ¥ ƵǣȐʼnľƔƔ | -- | > 0 | -- | 2 | 2 | 2 | ¥ ƵǣȐʼnľƔƔ | - + |
kg | ¥ ƊůƊǣľƔƔ | -- | 7 | -- | 3 | 2 | ¥ ƊůƊǣľƔƔ | - + | |
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