Jiang-Hai Ye
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Jiang-Hai Ye has a total of 20 co-authors. Here are the top co-authors by number of shared publications:
Ren-Song Chen
Guizhou University of Traditional Chinese Medicine , Guiyang 550025 , P.R. China
2 shared publicationsChen-Liang Zhao
Guizhou University of Traditional Chinese Medicine , Guiyang 550025 , P.R. China
1 shared publication- Chen-Liang Zhao
College of Pharmacy, Guizhou University of Traditional Chinese Medicine, Dongqing South Road, Guiyang 550025, China
1 shared publication - Cheng-Hong Jian
Guizhou University of Traditional Chinese Medicine , Guiyang 550025 , P.R. China
1 shared publication Chuan-Yan Xu
Guizhou University of Traditional Chinese Medicine , Guiyang 550025 , P. R. China
1 shared publication- Hong-Jie Zhang
School of Chinese Medicine, Hong Kong Baptist University, Hong Kong SAR, China
1 shared publication
Latest Publications
- Open Access
- 4 February 2026
- Published by Walter de Gruyter GmbH in Zeitschrift für Kristallographie - New Crystal Structures
- Vol. 241 (2) , 219-220
Crystal structure of 1 α ,5 α -dihydroxy-1-deoxo-13-deoxyenmein, C 20 H 28 O 6
C 20 H 28 O 6 , monoclinic, C 2 (no. 5), a = 21.874(7) Å, b = 6.708(2) Å, c = 14.092(5) Å, β = 113.441(9)°, V = 1897.1(10) Å 3 , Z = 4, R gt ( F ) = 0.0557, wR ref ( F 2 ) = 0.1325, T = 296.15 K.
- 4 February 2026
- Published by Walter de Gruyter GmbH in Zeitschrift für Kristallographie - New Crystal Structures
- Vol. 241 (2) , 219-220
Open AccessCrystal structure of 1 α ,5 α -dihydroxy-1-deoxo-13-deoxyenmein, C 20 H 28 O 6
C 20 H 28 O 6 , monoclinic, C 2 (no. 5), a = 21.874(7) Å, b = 6.708(2) Å, c = 14.092(5) Å, β = 113.441(9)°, V = 1897.1(10) Å 3 , Z = 4, R gt ( F ) = 0.0557, wR ref ( F 2 ) = 0.1325, T = 296.15 K.
- Open Access
- 1 December 2023
- Published by Walter de Gruyter GmbH in Zeitschrift für Kristallographie - New Crystal Structures
- Vol. 239 (1) , 117-120
Crystal structure of (5aS,6aS,8aR,9R,11aS, 11bS,13R,13aS)-1,1,8a,11a-tetramethyl-9-((S)-1-((S)-5-methyl-6-oxo-3,6-dihydro-2H-pyran-2-yl)ethyl)-3-oxo-1,7,8,8a,9,10,11,11a,11b,12,13,13a-dodecahydro-3H,6H-cyclopenta[5,6]cyclopropa[1,8a]naphtho[2,1-c]oxepin-13-yl acetate, C32H44O6
C32H44O6, monoclinic, P21 (no. 4), a = 12.2561 Å, b = 10.3674(4) Å, c = 23.3835(8) Å, β = 98.463°, V = 2938.85(19) Å3, Z = 2, R gt (F) = 0.0602, wRref (F 2) = 0.1537, T = 273(2) K.
- 1 December 2023
- Published by Walter de Gruyter GmbH in Zeitschrift für Kristallographie - New Crystal Structures
- Vol. 239 (1) , 117-120
Open AccessCrystal structure of (5aS,6aS,8aR,9R,11aS, 11bS,13R,13aS)-1,1,8a,11a-tetramethyl-9-((S)-1-((S)-5-methyl-6-oxo-3,6-dihydro-2H-pyran-2-yl)ethyl)-3-oxo-1,7,8,8a,9,10,11,11a,11b,12,13,13a-dodecahydro-3H,6H-cyclopenta[5,6]cyclopropa[1,8a]naphtho[2,1-c]oxepin-13-yl acetate, C32H44O6
C32H44O6, monoclinic, P21 (no. 4), a = 12.2561 Å, b = 10.3674(4) Å, c = 23.3835(8) Å, β = 98.463°, V = 2938.85(19) Å3, Z = 2, R gt (F) = 0.0602, wRref (F 2) = 0.1537, T = 273(2) K.
- Open Access
- 24 February 2023
- Published by Walter de Gruyter GmbH in Zeitschrift für Kristallographie - New Crystal Structures
- Vol. 238 (3) , 417-419
Synthesis and crystal structure of (4aR,7S)-7-hydroxy-7-isopropyl-1,1-dimethyldecahydro-2H,6H-8a,4a-(epoxymethano)phenanthren-12-one, C20H32O3
C20H32O3, monoclinic, P21 (no. 4), a = 7.8981(17) Å, b = 10.302(2) Å, c = 11.028(3) Å, β = 90.020(2)°, V = 897.3(3) Å3, Z = 2, R gt (F) = 0.0603, wR ref (F 2) = 0.1342, T = 273(2) K.
- 24 February 2023
- Published by Walter de Gruyter GmbH in Zeitschrift für Kristallographie - New Crystal Structures
- Vol. 238 (3) , 417-419
Open AccessSynthesis and crystal structure of (4aR,7S)-7-hydroxy-7-isopropyl-1,1-dimethyldecahydro-2H,6H-8a,4a-(epoxymethano)phenanthren-12-one, C20H32O3
C20H32O3, monoclinic, P21 (no. 4), a = 7.8981(17) Å, b = 10.302(2) Å, c = 11.028(3) Å, β = 90.020(2)°, V = 897.3(3) Å3, Z = 2, R gt (F) = 0.0603, wR ref (F 2) = 0.1342, T = 273(2) K.
- Open Access
Rubesanolides F and G: Two Novel Lactone-Type Norditerpenoids from Isodon rubescens
A phytochemical investigation of the leaves of the medicinal plant Isodon rubescens led to the isolation of the two new degraded abietane lactone diterpenoids rubesanolides F (1) and G (2). Their structures were elucidated based on the analyses of the HRESIMS and 1D/2D NMR spectral data, and their absolute configurations were determined by ECD spectrum calculations and X-ray single crystal diffraction methods. Compounds 1 and 2, with a unique γ-lactone subgroup between C-8 and C-20, were found to form a carbonyl carbon at C-13 by removal of the isopropyl group in an abietane diterpene skeleton. Rubesanolide G (2) is a rare case of abietane that possesses a cis-fused configuration between rings B and C. The two isolates were evaluated for their biological activities against two cancer cell lines (A549 and HL60), three fungal strains (Candida alba, Aspergillus niger and Rhizopus nigricans) and three bacterial strains (Escherichia coli, Staphylococcus aureus and Bacillus subtilis).
Open AccessRubesanolides F and G: Two Novel Lactone-Type Norditerpenoids from Isodon rubescens
A phytochemical investigation of the leaves of the medicinal plant Isodon rubescens led to the isolation of the two new degraded abietane lactone diterpenoids rubesanolides F (1) and G (2). Their structures were elucidated based on the analyses of the HRESIMS and 1D/2D NMR spectral data, and their absolute configurations were determined by ECD spectrum calculations and X-ray single crystal diffraction methods. Compounds 1 and 2, with a unique γ-lactone subgroup between C-8 and C-20, were found to form a carbonyl carbon at C-13 by removal of the isopropyl group in an abietane diterpene skeleton. Rubesanolide G (2) is a rare case of abietane that possesses a cis-fused configuration between rings B and C. The two isolates were evaluated for their biological activities against two cancer cell lines (A549 and HL60), three fungal strains (Candida alba, Aspergillus niger and Rhizopus nigricans) and three bacterial strains (Escherichia coli, Staphylococcus aureus and Bacillus subtilis).