丹参二醇C

丹参二醇C
别名	紫丹参甲素D
识别
CAS号	96839-30-4
PubChem	126072
SMILES	Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CC[C@@H](O)[C@]2(C)O;
性质
化学式	C18H16O5
摩尔质量	312.32 g·mol−1
熔点	213-215 °C
	若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。

丹参二醇C（英语：Tanshindiol C）是一种多环有机化合物，分子式C₁₈H₁₆O₅，属于一种丹参酮类化合物^[2]^[3]，与丹参二醇B是立体异构体，存在于丹参（Salvia miltiorrhiza）^[1]^[4]植物中。它可以环己-2-烯酮为原料，经丹参醇B（维基数据所列：Q82885063）中间体，通过多步反应制得^[5]。

参考文献

^ ^1.0 ^1.1 Luo, Hou-Wei; Wu, Bao-Jing; Wu, Mei-Yu; Yong, Zhong-Gen; Niwa, Masatake; Hirata, Yoshimasa. Pigments from Salvia miltiorrhiza. Phytochemistry. 1985-01, 24 (4): 815–817. doi:10.1016/S0031-9422(00)84900-6.
^ Yang, Y; Li, X; Peng, L; An, L; Sun, N; Hu, X; Zhou, P; Xu, Y; Li, P; Chen, J. Tanshindiol C inhibits oxidized low-density lipoprotein induced macrophage foam cell formation via a peroxiredoxin 1 dependent pathway.. Biochimica et biophysica acta. Molecular basis of disease. 2018-03, 1864 (3): 882–890. PMID 29287777. doi:10.1016/j.bbadis.2017.12.033.
^ Zhou, P; Cheng, Y; Liu, F; Wu, K; Qiu, W; Wang, S. Tanshindiol-C suppresses in vitro and in vivo hepatocellular cancer cell growth by inducing mitochondrial-mediated apoptosis, cell cycle arrest, inhibition of angiogenesis and modulation of key tumor-suppressive miRNAs.. Journal of B.U.ON. : official journal of the Balkan Union of Oncology. 2019-03, 24 (2): 622–627. PMID 31128015.
^ Yang, M; Liu, A; Guan, S; Sun, J; Xu, M; Guo, D. Characterization of tanshinones in the roots of Salvia miltiorrhiza (Dan-shen) by high-performance liquid chromatography with electrospray ionization tandem mass spectrometry.. Rapid communications in mass spectrometry : RCM. 2006, 20 (8): 1266–80. PMID 16548051. doi:10.1002/rcm.2447.
^ Wang, Fan; Yang, Hong; Yu, Shujuan; Xue, Yu; Fan, Zhoulong; Liang, Gaolin; Geng, Meiyu; Zhang, Ao; Ding, Chunyong. Total synthesis of (±)-tanshinol B, tanshinone I, and (±)-tanshindiol B and C. Organic & Biomolecular Chemistry. 2018, 16 (18): 3376–3381. doi:10.1039/C8OB00567B.

这是一篇与化学相关的小作品。您可以通过编辑或修订扩充其内容。

[Luo-1] 1.0 ^1.1 Luo, Hou-Wei; Wu, Bao-Jing; Wu, Mei-Yu; Yong, Zhong-Gen; Niwa, Masatake; Hirata, Yoshimasa. Pigments from Salvia miltiorrhiza. Phytochemistry. 1985-01, 24 (4): 815–817. doi:10.1016/S0031-9422(00)84900-6.

[2] Yang, Y; Li, X; Peng, L; An, L; Sun, N; Hu, X; Zhou, P; Xu, Y; Li, P; Chen, J. Tanshindiol C inhibits oxidized low-density lipoprotein induced macrophage foam cell formation via a peroxiredoxin 1 dependent pathway.. Biochimica et biophysica acta. Molecular basis of disease. 2018-03, 1864 (3): 882–890. PMID 29287777. doi:10.1016/j.bbadis.2017.12.033.

[3] Zhou, P; Cheng, Y; Liu, F; Wu, K; Qiu, W; Wang, S. Tanshindiol-C suppresses in vitro and in vivo hepatocellular cancer cell growth by inducing mitochondrial-mediated apoptosis, cell cycle arrest, inhibition of angiogenesis and modulation of key tumor-suppressive miRNAs.. Journal of B.U.ON. : official journal of the Balkan Union of Oncology. 2019-03, 24 (2): 622–627. PMID 31128015.

[4] Yang, M; Liu, A; Guan, S; Sun, J; Xu, M; Guo, D. Characterization of tanshinones in the roots of Salvia miltiorrhiza (Dan-shen) by high-performance liquid chromatography with electrospray ionization tandem mass spectrometry.. Rapid communications in mass spectrometry : RCM. 2006, 20 (8): 1266–80. PMID 16548051. doi:10.1002/rcm.2447.

[5] Wang, Fan; Yang, Hong; Yu, Shujuan; Xue, Yu; Fan, Zhoulong; Liang, Gaolin; Geng, Meiyu; Zhang, Ao; Ding, Chunyong. Total synthesis of (±)-tanshinol B, tanshinone I, and (±)-tanshindiol B and C. Organic & Biomolecular Chemistry. 2018, 16 (18): 3376–3381. doi:10.1039/C8OB00567B.

[2]

[3]

[1]

[4]

[5]