Fig. 4. The chiral HPLC analyses of the hydrolysates of compounds 2 and 3.Published as part of Xu, Ce, Xu, Kuo, Yuan, Xiao-Long, Ren, Guang-Wei, Wang, Xiao-Qiang, Li, Wei, Deng, Ning, Wang, Xiu-Fang & Zhang, Peng, 2020, Characterization of diketopiperazine heterodimers as potential chemical markers for discrimination of two dominant black aspergilli, Aspergillus niger and Aspergillus tubingensis, pp. 1-8 in Phytochemistry (112399) 176 on page 4, DOI: 10.1016/j.phytochem.2020.112399, http://zenodo.org/record/829575
Fig. 1. Structures of compounds 1–5 (3 is artifact converted from 2).Published as part of Li, Feng, ...
Fig. 1. Structures of compounds 1–13.Published as part of Chen, Chun-Mei, Chen, Wei-Hao, Pang, Xiao-...
Fig. 6. A plausible biosynthetic pathway of 1–10.Published as part of Chen, Chun-Mei, Chen, Wei-Hao,...
Fig. 1. Structures of compounds 1–8.Published as part of Xu, Ce, Xu, Kuo, Yuan, Xiao-Long, Ren, Guan...
Fig. 3. Key NOESY correlations of compounds 2 and 3.Published as part of Xu, Ce, Xu, Kuo, Yuan, Xiao...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 2, 3, and 4.Published as part of Xu, Ce, X...
Fig. 7. HPLC-DAD spectra of the crude extracts of A. niger (A) and A. tubingensis (B) cultivated in ...
Xu, Ce, Xu, Kuo, Yuan, Xiao-Long, Ren, Guang-Wei, Wang, Xiao-Qiang, Li, Wei, Deng, Ning, Wang, Xiu-F...
Fig. 5. Culture and morphological characteristics of Aspergillus niger (A) and A. tubingensis (D), c...
Fig. 6. Neighbor-joining (NJ) trees based on the 18S (A), 26S (B) and ITS rDNA regions (C). HQM289 a...
Fig. 2. Key 1 H– 1 H COSY and HMBC correlations of 1 4, 10, and 11.Published as part of Chen, Chun-M...
Fig. 3. DP4+ probability analyses for candidates diastereomers of 1 and 2 (Gibbs free energies at th...
Fig. 3. Key NOESY correlations of compounds 1–3.Published as part of Al Subeh, Zeinab Y., Raja, Huze...
Fig. 4. Plausible biosynthetic pathway of 1, 2, 4 and 5, and the conversion from 2 to 3.Published as...
Fig. 1. Chemical structures of compounds 1–7.Published as part of Zang, Yi, Yu, Muyuan, Shi, Zhengyi...
Fig. 1. Structures of compounds 1–5 (3 is artifact converted from 2).Published as part of Li, Feng, ...
Fig. 1. Structures of compounds 1–13.Published as part of Chen, Chun-Mei, Chen, Wei-Hao, Pang, Xiao-...
Fig. 6. A plausible biosynthetic pathway of 1–10.Published as part of Chen, Chun-Mei, Chen, Wei-Hao,...
Fig. 1. Structures of compounds 1–8.Published as part of Xu, Ce, Xu, Kuo, Yuan, Xiao-Long, Ren, Guan...
Fig. 3. Key NOESY correlations of compounds 2 and 3.Published as part of Xu, Ce, Xu, Kuo, Yuan, Xiao...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 2, 3, and 4.Published as part of Xu, Ce, X...
Fig. 7. HPLC-DAD spectra of the crude extracts of A. niger (A) and A. tubingensis (B) cultivated in ...
Xu, Ce, Xu, Kuo, Yuan, Xiao-Long, Ren, Guang-Wei, Wang, Xiao-Qiang, Li, Wei, Deng, Ning, Wang, Xiu-F...
Fig. 5. Culture and morphological characteristics of Aspergillus niger (A) and A. tubingensis (D), c...
Fig. 6. Neighbor-joining (NJ) trees based on the 18S (A), 26S (B) and ITS rDNA regions (C). HQM289 a...
Fig. 2. Key 1 H– 1 H COSY and HMBC correlations of 1 4, 10, and 11.Published as part of Chen, Chun-M...
Fig. 3. DP4+ probability analyses for candidates diastereomers of 1 and 2 (Gibbs free energies at th...
Fig. 3. Key NOESY correlations of compounds 1–3.Published as part of Al Subeh, Zeinab Y., Raja, Huze...
Fig. 4. Plausible biosynthetic pathway of 1, 2, 4 and 5, and the conversion from 2 to 3.Published as...
Fig. 1. Chemical structures of compounds 1–7.Published as part of Zang, Yi, Yu, Muyuan, Shi, Zhengyi...
Fig. 1. Structures of compounds 1–5 (3 is artifact converted from 2).Published as part of Li, Feng, ...
Fig. 1. Structures of compounds 1–13.Published as part of Chen, Chun-Mei, Chen, Wei-Hao, Pang, Xiao-...
Fig. 6. A plausible biosynthetic pathway of 1–10.Published as part of Chen, Chun-Mei, Chen, Wei-Hao,...