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| 规格 | 目录价格 | 上海 | 安徽 | 武汉 | 成都 | 北方 | 深圳 | 会员价格 | 数量 |
|---|---|---|---|---|---|---|---|---|---|
| 1g | ￥ ɄůƢƵƵ | > 10 | 3 | 1 | 1 | ￥ ȐɄƢƵƵ | - + | ||
| 5g | ￥ ƊʼnǣƢƵƵ | 5 | > 10 | > 10 | 4 | ￥ ȨƭȨƢƵƵ | - + | ||
| 10g | ￥ ůȐɄƢƵƵ | > 10 | > 10 | 1 | 9 | ￥ ǫʼnȨƢƵƵ | - + | ||
| 25g | ￥ ȨƊƭƭƢƵƵ | > 10 | > 10 | -- | 2 | ￥ ʼnǣǣƢƵƵ | - + | ||
| 100g | ￥ ůȨȨƵƢƵƵ | 5 | 9 | > 10 | 2 | ￥ ƊƭǫǣƢƵƵ | - + | ||
| 500g | ￥ ȨǫȐʼnȐƢƵƵ | 1 | 7 | -- | > 10 | ￥ ȨƵůȐƵƢƵƵ | - + | ||
| 1000g | 请询价 | -- | -- | -- | -- | -- | -- | -- | - + |
| 大货 | 请询价 | -- | -- | -- | -- | -- | -- | -- | - + |
产品编号
1226768
CAS 号
520-03-6
中文名称
2-苯基-异吲哚-1,3-二酮
MDL 号
MFCD00023044
分子量
223.23
存储条件
2-8°C
网页展示纯度为入库指导纯度值，各批次间存在一定差异，实际纯度以收货为准
熔点
204-207 °C
沸点
388.8°C at 760 mmHg
闪点
旋光
描述
TPSA
37.38
LogP
2.4872
H_Acceptors
2
H_Donors
0
Rotatable_Bonds
1
[1]. Hiroko Sano, et al. N-phenylphthalimide-type cyclooxygenase (COX) inhibitors derived from thalidomide: substituent effects on subtype selectivity. Chem Pharm Bull (Tokyo). 2004 Aug;52(8):1021-2.
[2]. Kazunori Motoshima, et al. Glycogen phosphorylase a inhibitors with a phenethylphenylphthalimide skeleton derived from thalidomide-related alpha-glucosidase inhibitors and liver X receptor antagonists. Biol Pharm Bull. 2009 Sep;32(9):1618-20.
[3]. Masashi Tetsuhashi, et al. Development of tryptase inhibitors derived from thalidomide. Bioorg Med Chem. 2010 Jul 15;18(14):5323-38.
[4]. R Shimazawa, et al. Nonpeptide small-molecular inhibitors of dipeptidyl peptidase IV: N-phenylphthalimide analogs. Bioorg Med Chem Lett. 1999 Feb 22;9(4):559-62.
[5]. Stefano Mangani, et al. Identification of the binding modes of N-phenylphthalimides inhibiting bacterial thymidylate synthase through X-ray crystallography screening. J Med Chem. 2011 Aug 11;54(15):5454-67.
警示图
警示词
Warning
危险申明
H302-H315-H319-H335
警告申明
P261-P302+P352-P304+P340
GHS 编码
GHS07
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