00-82-072
| 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 | ￥ Ŋǐƭǡǡ | > 0 | > 0 | -- | -- | 2 | ￥ Ŋǐƭǡǡ | - + | |
| g | ￥ ŊƓƭǡǡ | 8 | > 0 | -- | ￥ ŊƓƭǡǡ | - + | |||
| 0g | ￥ ļƸƭǡǡ | 8 | > 0 | -- | 2 | 2 | ￥ ļƸƭǡǡ | - + | |
| 2g | ￥ ƸƓƭǡǡ | > 0 | 3 | 3 | > 0 | 6 | ￥ ƸƓƭǡǡ | - + | |
| 00g | ￥ ļǐļƭǡǡ | 9 | 8 | 8 | ￥ ļǐļƭǡǡ | - + | |||
| 00g | ￥ æƓIJŝƭǡǡ | 6 | 6 | 2 | 3 | 2 | ￥ æƓIJŝƭǡǡ | - + | |
| kg | ￥ ļæIJǡƭǡǡ | 9 | -- | -- | 2 | ￥ ļæIJǡƭǡǡ | - + | ||
| 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
20026 现货
￥ ŊƓƭǡǡ -g
020796 现货
￥ Ŋǐƭǡǡ -2g
0288 现货
￥ ļėƭǡǡ -00mg
022073 现货
￥ ŊƸƭǡǡ -0g
02736 现货
￥ Ŋėƭǡǡ -2g
02690 现货
￥ ŊIJƭǡǡ -g
088 货期咨询
￥ æŊėŝƭǡǡ -g
023 货期咨询
￥ æŊƸIJƭǡǡ -20mg
60973 货期咨询
￥ ŊæŝIJƭǡǡ -g
032896 货期咨询
￥ ƸŊƭǡǡ -g
沪ICP备7096号
