| 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 | ¥ ƼǡȀdždž | > 0 | > 0 | -- | -- | 2 | ¥ ƼǡȀdždž | - + | |
| g | ¥ ƼƆȀdždž | 2 | > 0 | 6 | ¥ ƼƆȀdždž | - + | |||
| 0g | ¥ ŞȋȀdždž | > 0 | -- | 2 | ¥ ŞȋȀdždž | - + | |||
| 2g | ¥ ȋƆȀdždž | -- | > 0 | 3 | > 0 | 6 | ¥ ȋƆȀdždž | - + | |
| 00g | ¥ ŞǡŞȀdždž | -- | 8 | 2 | 8 | ¥ ŞǡŞȀdždž | - + | ||
| 00g | ¥ ĸƆIJĠȀdždž | -- | -- | 2 | 2 | ¥ ĸƆIJĠȀdždž | - + | ||
| kg | ¥ ŞĸIJdžȀdždž | -- | -- | -- | -- | 2 | ¥ ŞĸIJdžȀdždž | - + | |
| 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
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