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1. ¹ú¼Ò×ÔÈ»¿ÆÑ§»ù½ðÃæÉÏ»ù½ðÏîÄ¿(81973213) ¡°»ùÓÚÉú¶¯ÖÐÐÄÌåÇý¶¯Õ½ÂÔµÄ̦ɫËá¶þ¾ÛÌå¶àÑù¿â¹¹½¨¼°ÆäÉñ¾­±£»£»¤µÄ¹¹Ð§ºÍ»úÖÆÑо¿¡± (2020-2023£¬£¬£¬56ÍòÔª£¬£¬£¬ÔÚÑÐ)¡£

2. ¹ú¼Ò×ÔÈ»¿ÆÑ§»ù½ðÃæÉÏ»ù½ðÏîÄ¿(81673315) ¡°»ùÓÚ¶à°Ðµã¿¹°¢¶û´Äº£Ä¬Ö¢µÄ¶à½ÚæßÂ̽ºÃ¹ËØÀ໯ºÏÎïµÄÓÅÑ¡Óë×÷ÓûúÖÆÑо¿¡± (2017-2020£¬£¬£¬52ÍòÔª£¬£¬£¬ÔÚÑÐ)¡£

3. ¹ú¼ÒÖØµãÑз¢ÍýÏëÏîÄ¿(2018YFC0311003) ¡°º£Ñó΢ÉúÎïºòѡҩÎïµÄ¸ßЧ·¢Ã÷Óë´´Ô족ÏîÄ¿×Ó¿ÎÌâ (2018-2021£¬£¬£¬27.8ÍòÔª£¬£¬£¬ÔÚÑÐ)¡£

4. ¹ã¶«Ê¡×ÔÈ»¿ÆÑ§ÓÅÒìÇàÄê»ù½ðÏîÄ¿(2017A03036027) ¡°µØÒÂÄÚÉúÕæ¾úÖп¹ÍíÄê³Õ´ô»îÐÔÒòËØµÄ·¢Ã÷¼°Æä×÷ÓûúÖÆÑо¿¡± (2017-2021, 100ÍòÔª£¬£¬£¬ÔÚÑÐ)¡£

¹ãÖÝÊÐÖé½­¿Æ¼¼ÐÂÐÇÏîÄ¿(201610010021) ¡°µØÒÂÄÚÉúÕæ¾úÖп¹AD»îÐÔÒòËØÑо¿¡± (2016-2019, 30ÍòÔª£¬£¬£¬½áÌâ)¡£

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[1] Huang Hui-Yun, Huang Jia-Hua, Wang Yong-Heng, Hu Dan, Lu Yong-Jun, She Zhi-Gang, Chen Guo-Dong*, Yao Xin-Sheng, Gao Hao*. The oxidation cascade of a rare multifunctional P450 enzyme involved in asperterpenoid A biosynthesis. Frontiers in Chemistry, 2021, 9, 785431.

[2] Zhao Huan, ¡ì Zou Jian, ¡ì Xu Wei, Hu Dan, Guo Liang-Dong, Chen Jia-Xu, Chen Guo-Dong,* So Kwok-Fai, Yao Xin-Sheng, Gao Hao.* Diisoprenyl-cyclohexene/ane-type meroterpenoids from Biscogniauxia sp. and their anti-inflammatory activities. Journal of Organic Chemistry, 2021, 86, 11177-11188.

[3] Chen Guo-Dong,¡ì Zhao Bing-Xin,¡ì Huang Mei-Juan, Tang Jia, Li Yan-Bing, Guo Liang-Dong, He Rong-Rong, Hu Dan,* Yao Xin-Sheng, Gao Hao.* Tripodalsporormielones A¨CC, unprecedented cage-like polyketides with complex polyvdent bridged and fused ring systems. Acta Pharmaceutica Sinica B, 2021, 11, 3648-3654.

[4] Tian Dan-Mei, Cao Ling-Yun, Li Qing-Wen, Huang Hui-Yun, Xu Wei, Chen Guo-Dong*, Song Zhao-Hui, He Yi, Yao Xin-Sheng, Tang Jin-Shan*. Benzannulated 5,5-spiroketal sesquiterpenes from the roots of Angelica pubescens. Bioorganic Chemistry, 2021, 107, 104604.

[5] Chen Guo-Dong, Hu Dan, Gao Hao, Yao Xin-Sheng*. The importance of researches on the fungal bioactive secondary metabolites in developing the comprehensive health industry. Chinese Journal of Natural Medicines, 2020, 18, 241-242.

[6] Chen Guo-Dong¡ì, Hu Dan¡ì, Huang Mei-Juan¡ì, Tang Jia, Wang Xiao-Xia, Zou Jian, Xie Jun, Zhang Wei-Guang, Guo Liang-Dong, Yao Xin-Sheng*, Abe Ikuro*, Gao Hao*. Sporormielones A¨CE, bioactive novel C-C coupled orsellinic acid derivative dimers, and their biosynthetic origin. Chemical Communications, 2020, 56, 4607-4610. (¡ìco-first author)

[7] Chen Guo-Dong, Wang Chuan-Xi, Hu Dan, Gao Hao, Yao Xin-Sheng*. Discovery of new metabolites from fungi in special habits and their biological function evaluations. Toxicon, 2019, 158, S29-S29.

[8] Zou Jian¡ì, Chen Guo-Dong¡ì, Zhao Huan, Wang Xiao-Xia, Zhang Zai-Jun, Qu Yi-Bo, He Rong-Rong, So Kwok-Fai, Yao Xin-Sheng, Gao Hao*. Triangeliphthalides A-D: bioactive phthalide trimers with new skeletons from Angelica sinensis and their production mechanism. Chemical Communications, 2019, 55, 6221-6224. (¡ìco-first author)

[9] Zhao Huan¡ì, Wang Mei-Zhi¡ì, Chen Guo-Dong*, Hu Dan, Li En-Qing, Qu Yi-Bo, Zhou Li-Bing, Guo Liang-Dong, Yao Xin-Sheng, Gao Hao*. Dimericbiscognienynes B and C: new diisoprenyl-cyclohexene-type meroterpenoid dimers from Biscogniauxia sp. Chinese Chemical Letters, 2019, 30, 51-54.

[10] Wang Gao-Qian¡ì, Chen Guo-Dong¡ì, Qin Sheng-Ying¡ì, Hu Dan*, Awakawa Takayoshi, Li Shao-Yang, Lv Jian-Ming, Wang Chuan-Xi, Abe Ikuro*, Gao Hao*. Biosynthetic pathway for furanosteroid demethoxyviridin and identification of an unusual pregnane side-chain cleavage. Nature Communications, 2018, 9, 1838 (¡ìco-first author)

[11] Zou Jian¡ì, Chen Guo-Dong¡ì, Zhao Huan, Huang Ying, Luo Xiang, Xu Wei, He Rong-Rong, Hu Dan, Yao Xin-Sheng, Gao Hao*. Triligustilides A and B: Two pairs of phthalide trimers from Angelica sinensis with a complex polycyclic skeleton and their activities. Organic Letters, 2018, 20, 884-887 (¡ìco-first author)

[12] Li Jiao-Jiao¡ì, Chen Guo-Dong¡ì, Fan Hong-Xia, Hu Dan, Zhou Zheng-Qun, Lan Kang-Hua, Zhang Hui-Ping, Maeda Hideaki, Yao Xing-Sheng, Gao Hao*. Houttuynoid M, an anti-HSV active houttuynoid from Houttuynia cordata featuring a bis-houttuynin chain tethered to a flavonoid core. Journal of Natural Products, 2017, 80, 3010-3013 (¡ìco-first author)

[13] Zhao Huan¡ì, Chen Guo-Dong¡ì, Zou Jian, He Rong-Rong, Qin Sheng-Ying, Hu Dan, Li Guo-Qiang, Guo Liang-Dong, Yao Xin-Sheng*, Gao Hao*. Dimericbiscognienyne A: A meroterpenoid dimer from Biscogniauxia sp. with new skeleton and its activity. Organic Letters, 2017, 19, 38-41 (¡ìco-first author)

[14] Sun Tian-Yu, Zou Jian, Chen Guo-Dong*, Hu Dan, Wu Bin, Liu Xing-Zhong, Yao Xin-Sheng, Gao Hao*. A set of interesting sequoiatone stereoisomers from a wetland soil-derived fungus Talaromyces flavus. Acta Pharmaceutica Sinica B, 2017, 7, 167-172.

[15] Wang Chuan-Xi¡ì, Chen Guo-Dong¡ì, Feng Chun-Chi, He Rong-Rong, Qin Sheng-Ying, Hu Dan, Chen He-Ru, Liu Xing-Zhong, Yao Xin-Sheng*, Gao, Hao*. Same data, different structures: diastereoisomers with substantially identical NMR data from nature. Chemical Communications, 2016, 52, 1250-1253 (¡ìco-first author)

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