| 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 | ¥ ĥƬŮŁŁ | > | > | -- | -- | -- | -- | ¥ ĥƬŮŁŁ | - + |
| 5g | ¥ ŖŢŮŁŁ | > | > | 4 | 6 | 9 | > | ¥ ŖŢŮŁŁ | - + |
| g | ¥ ƔŁŮŁŁ | > | > | ¥ ƔŁŮŁŁ | - + | ||||
| 5g | ¥ ŢĘŹŮŁŁ | > | > | 3 | 6 | 7 | ¥ ŢĘŹŮŁŁ | - + | |
| g | ¥ ƬǘǘŮŁŁ | 9 | 3 | ¥ ƬǘǘŮŁŁ | - + | ||||
| 5g | ¥ ĥƇŹĘŮŁŁ | -- | -- | ¥ ĥƇŹĘŮŁŁ | - + | ||||
| g | 请询价 | -- | -- | -- | -- | -- | -- | -- | - + |
| 大货 | 请询价 | -- | -- | -- | -- | -- | -- | -- | - + |
37.3
[]. Donald D Nolting,et al. Synthesis of bicyclo[5.3.]azulene derivatives. Nat Protoc. 9; 4(): 3–7.
[]. VardaKahn, et al.Inhibition of mushroom tyrosinase by tropolone Phytochemistry. Volume 4, Issue 5, 95, Pages 95-9
[3]. E Zachary Oblak, et al. The furan route to tropolones: probing the antiproliferative effects of β-thujaplicin analogs. Org Biomol Chem. Nov ;(43):597-64.
[4]. Jennifer A Jacobsen, et al. Identifying chelators for metalloprotein inhibitors using a fragment-based approach. J Med Chem. Jan 7;54():59-6.
[5]. Jong Yuh Cherng, et al. Preventive effects of β-thujaplicin against UVB-induced MMP- and MMP-3 mRNA expressions in skin fibroblasts. Am J Chin Med. ;4():37-9.


H34-H37-H4
P6-P6-P64-P7-P73-P-P3+P33+P33-P3+P35-P34+P34-P36+P364-P363-P39-P45-P5
GHS5,GHS7,GHS9
36
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