| 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 | ¥ ƈǫǠǕǕ | > | > | -- | -- | -- | -- | ¥ ƈǫǠǕǕ | - + |
| 5g | ¥ ĕŹǠǕǕ | 4 | > | -- | 2 | ¥ ĕŹǠǕǕ | - + | ||
| g | ¥ ȖƭȰǠǕǕ | 2 | 6 | -- | ¥ ȖƭȰǠǕǕ | - + | |||
| 25g | ¥ ŹĞǶǠǕǕ | -- | 2 | -- | -- | ¥ ŹĞǶǠǕǕ | - + | ||
| g | ¥ ȖƭƈǶǠǕǕ | -- | -- | -- | -- | -- | -- | ¥ ȖƭƈǶǠǕǕ | - + |
| 5g | ¥ ĕȖŹǫǠǕǕ | -- | -- | -- | -- | -- | -- | ¥ ĕȖŹǫǠǕǕ | - + |
| g | 请询价 | -- | -- | -- | -- | -- | -- | -- | - + |
| 大货 | 请询价 | -- | -- | -- | -- | -- | -- | -- | - + |
2.89
[]. E C Riesgo, et al. Crowded Cu(I) complexes involving benzo[h]quinoline: pi-stacking effects and long-lives excited states. Inorg Chem. 2 Jul 2;4(4):343-22.
[2]. E J LaVoie, et al. Identification of the metabolites of benzo[f]quinoline and benzo[h]quinoline formed by rat liver homogenate. Carcinogenesis. 983 Sep;4(9):33-8.
[3]. E J LaVoie, et al. The carcinogenicity of quinoline and benzoquinolines in newborn CD- mice. Jpn J Cancer Res. 987 Feb;78(2):39-43.
[4]. Halehatty R Prakash Naik, et al. Synthesis of novel benzo[h]quinolines: wound healing, antibacterial, DNA binding and in vitro antioxidant activity. Eur J Med Chem. 29 Mar;44(3):98-9.
[5]. John B Sutherland, et al. Fungal biotransformation of benzo[f]quinoline, benzo[h]quinoline, and phenanthridine. Appl Microbiol Biotechnol. 25 May;67(3):45-.
H32-H35-H39-H335
P26-P264-P27-P27-P28-P32+P352-P34+P34-P35+P35+P338-P33-P362+P364-P43+P233-P45-P5
GHS7
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