Hong Liang
Research Subjects
Hong Liang has a total of 127 co-authors. Here are the top co-authors by number of shared publications:
- Qingying Zhang
State Key Laboratory of Natural and Biomimetic Drugs and Department of Natural Medicines, School of Pharmaceutical Sciences, Peking University Health Science Center, Beijing 100191, China
10 shared publications - Pengfei Tu
Peking University
9 shared publications Qing-Ying Zhang
State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, 100191, People's Republic of China
9 shared publicationsPeng-Fei Tu
Department of Natural Medicines, School of Pharmaceutical Sciences, Peking University Health Science Center, Beijing 100191, People's Republic of China
7 shared publications- Jun Zhang
College of Life Sciences, Institute of Life Science and Green Development, Hebei University, Baoding, P. R. China
6 shared publications Yi Qian
Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China
6 shared publications
Latest Publications
- 26 December 2024
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 90 (1) , 648-652
Structure Revision of Heptacyclic Naphthoquinone Dimer Arnebidin Based on NMR Spectroscopic Analysis and X-ray Crystallography
Arnebidin, a heptacyclic naphthoquinone dimer with a tricyclo[3.3.0.01,3]octane core, which was first isolated from Arnebia hispidissima and later found from A. euchroma. Its structure was identified by the analysis of NMR and EI-MS data. In the present work, a heptacyclic naphthoquinone dimer ((±)-1) was obtained from the petroleum ether portion of the ethanol extract of Arnebia euchroma. By comparing the NMR data of 1 with the literatures, compound 1 should be identified as arnebidin. However, the single-crystal X-ray diffraction analysis followed by reinterpretation of the NMR data revealed that the structure of 1 was a heptacyclic naphthoquinone dimer with a tricyclo[3.2.1.02,7]octane core. Thus, we proposed that arnebidin should be revised to 1.
- 26 December 2024
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 90 (1) , 648-652
Structure Revision of Heptacyclic Naphthoquinone Dimer Arnebidin Based on NMR Spectroscopic Analysis and X-ray Crystallography
Arnebidin, a heptacyclic naphthoquinone dimer with a tricyclo[3.3.0.01,3]octane core, which was first isolated from Arnebia hispidissima and later found from A. euchroma. Its structure was identified by the analysis of NMR and EI-MS data. In the present work, a heptacyclic naphthoquinone dimer ((±)-1) was obtained from the petroleum ether portion of the ethanol extract of Arnebia euchroma. By comparing the NMR data of 1 with the literatures, compound 1 should be identified as arnebidin. However, the single-crystal X-ray diffraction analysis followed by reinterpretation of the NMR data revealed that the structure of 1 was a heptacyclic naphthoquinone dimer with a tricyclo[3.2.1.02,7]octane core. Thus, we proposed that arnebidin should be revised to 1.
- 16 December 2024
- Published by Elsevier in Phytochemistry
- Vol. 232, 114368
Anthraquinones from the root of Arnebia euchroma (Royle) I. M. Johnst. and their cytotoxic activities
- 16 December 2024
- Published by Elsevier in Phytochemistry
- Vol. 232, 114368
Anthraquinones from the root of Arnebia euchroma (Royle) I. M. Johnst. and their cytotoxic activities
- 13 May 2024
- Published by Elsevier in Phytochemistry
- Vol. 224, 114140
Cevanine-type steroidal alkaloids from the bulbs of Fritillaria cirrhosa D. Don
- 13 May 2024
- Published by Elsevier in Phytochemistry
- Vol. 224, 114140
Cevanine-type steroidal alkaloids from the bulbs of Fritillaria cirrhosa D. Don
- 21 February 2024
- Published by Elsevier in Acta Pharmaceutica Sinica B
- Vol. 14 (5) , 2358
Author correction to ‘Pharmacologically targeting molecular motor promotes mitochondrial fission for anti-cancer’ [Acta Pharm Sin B 11 (2021) 1853–1866]
- 21 February 2024
- Published by Elsevier in Acta Pharmaceutica Sinica B
- Vol. 14 (5) , 2358
Author correction to ‘Pharmacologically targeting molecular motor promotes mitochondrial fission for anti-cancer’ [Acta Pharm Sin B 11 (2021) 1853–1866]
- 14 February 2022
- Published by Elsevier in Phytochemistry
- Vol. 197, 113129
Cirrhosinones A-H, 24-hydroxy cevanine-type alkaloids from Fritillaria cirrhosa
- 14 February 2022
- Published by Elsevier in Phytochemistry
- Vol. 197, 113129
Cirrhosinones A-H, 24-hydroxy cevanine-type alkaloids from Fritillaria cirrhosa
- Open Access
- 1 July 2021
- Published by Elsevier in Acta Pharmaceutica Sinica B
- Vol. 11 (7) , 1853-1866
Pharmacologically targeting molecular motor promotes mitochondrial fission for anti-cancer
- 1 July 2021
- Published by Elsevier in Acta Pharmaceutica Sinica B
- Vol. 11 (7) , 1853-1866
Open AccessPharmacologically targeting molecular motor promotes mitochondrial fission for anti-cancer
- 1 May 2021
- Published by Elsevier in Phytochemistry
- Vol. 185, 112674
Oleanane-type saponins and prosapogenins from Albizia julibrissin and their cytotoxic activities
- 1 May 2021
- Published by Elsevier in Phytochemistry
- Vol. 185, 112674
Oleanane-type saponins and prosapogenins from Albizia julibrissin and their cytotoxic activities
- 1 November 2020
- Published by Elsevier in Fitoterapia
- Vol. 147, 104776
Discovery of novel potential plant growth regulators from Corydalis mucronifera
- 1 November 2020
- Published by Elsevier in Fitoterapia
- Vol. 147, 104776
Discovery of novel potential plant growth regulators from Corydalis mucronifera
- 30 September 2020
- Published by Taylor & Francis in Natural Product Research
- Vol. 36 (9) , 2239-2245
Three new p -coumaroylated sesquiterpenoids from Pilea cavaleriei
Four p-coumaroylated sesquiterpenoids (1–4), including three new ones (1, 2, and 4), were isolated from the whole plants of Pilea cavaleriei. Their structures were established on the basis of comprehensive spectroscopic analysis and comparison with data reported in the literature. Compounds 1–4 were evaluated for their antimycobacterial activities, and 2 and 4 were active against Mycobacterium tuberculosis H37Rv with the MIC values of 19.6 ± 0.19 and 17.4 ± 0.12 μg/mL, respectively.
- 30 September 2020
- Published by Taylor & Francis in Natural Product Research
- Vol. 36 (9) , 2239-2245
Three new p -coumaroylated sesquiterpenoids from Pilea cavaleriei
Four p-coumaroylated sesquiterpenoids (1–4), including three new ones (1, 2, and 4), were isolated from the whole plants of Pilea cavaleriei. Their structures were established on the basis of comprehensive spectroscopic analysis and comparison with data reported in the literature. Compounds 1–4 were evaluated for their antimycobacterial activities, and 2 and 4 were active against Mycobacterium tuberculosis H37Rv with the MIC values of 19.6 ± 0.19 and 17.4 ± 0.12 μg/mL, respectively.
- 1 March 2020
- Published by Elsevier in Fitoterapia
- Vol. 141, 104464
AChE inhibitory alkaloids from Coptis chinensis
- 1 March 2020
- Published by Elsevier in Fitoterapia
- Vol. 141, 104464
AChE inhibitory alkaloids from Coptis chinensis