Fig. 5. ORTEP diagram of 8. Letters A and B indicate the doubly disordered carbonyl oxygen sites A and B with respective occupancy factors 0.77 and 0.23.Published as part of Raksat, Achara, Choodej, Siwattra, Aree, Thammarat, Ebrahimi, Samad Nejad & Pudhom, Khanitha, 2022, Cassane-type diterpenes from roots of Pterolobium macropterum and their anti-inflammatory activity, pp. 1-8 in Phytochemistry (113074) 196 on page 6, DOI: 10.1016/j.phytochem.2021.113074, http://zenodo.org/record/823670
Chen, Xiu-Mei, Lu, Wang, Zhang, Zi-Han, Zhang, Jia-Yao, Tuong, Thi Mai Luong, Liu, Ling-Li, Kim, You...
Fig. 2. Key COSY (black bond line) and key HMBC correlations of compounds 1, 4 and 6.Published as pa...
Fig. 2. Structures of compounds 1–5.Published as part of Kakumu, Yuya, Nguyen, Minh Tu Thi & Mitsuna...
Fig. 3. Key NOESY correlations of 1 3 and 7–8.Published as part of Raksat, Achara, Choodej, Siwattra...
Fig. 4. Experimental and calculated CD spectra for 4–5 and 7.Published as part of Raksat, Achara, Ch...
Fig. 2. COSY and selected HMBC (1H → 13C) correlations of 1–8.Published as part of Raksat, Achara, C...
Raksat, Achara, Choodej, Siwattra, Aree, Thammarat, Ebrahimi, Samad Nejad, Pudhom, Khanitha (2022): ...
Fig. 1. Isolated compounds (1–10) from the roots extract of P. macropterum.Published as part of Raks...
Fig. 6. Effect of 3 and 10 on the expression of iNOS and COX-2 protein. The purity of 3 and 10 is 99...
Fig. 3. Key NOESY correlations of compounds 1, 2, 4, 5, 7, and 8.Published as part of Chen, Xiu-Mei,...
Fig. 2. Key HMBC correlations of compounds 1–5 and 7.Published as part of Chen, Xiu-Mei, Lu, Wang, Z...
Fig. 5. Plausible biosynthetic pathway of compounds 1–16.Published as part of Chen, Xiu-Mei, Lu, Wan...
Fig. 4. X-ray crystallographic structure of Pulcherritam A (1).Published as part of Chen, Xiu-Mei, L...
Fig. 1. Structures of compounds 1–16 from C. pulcherrima.Published as part of Chen, Xiu-Mei, Lu, Wan...
Fig. 2. Key COSY (bold bonds) and HMBC (black arrows) correlations of 1, 2, 3, 14, and 15.Published ...
Chen, Xiu-Mei, Lu, Wang, Zhang, Zi-Han, Zhang, Jia-Yao, Tuong, Thi Mai Luong, Liu, Ling-Li, Kim, You...
Fig. 2. Key COSY (black bond line) and key HMBC correlations of compounds 1, 4 and 6.Published as pa...
Fig. 2. Structures of compounds 1–5.Published as part of Kakumu, Yuya, Nguyen, Minh Tu Thi & Mitsuna...
Fig. 3. Key NOESY correlations of 1 3 and 7–8.Published as part of Raksat, Achara, Choodej, Siwattra...
Fig. 4. Experimental and calculated CD spectra for 4–5 and 7.Published as part of Raksat, Achara, Ch...
Fig. 2. COSY and selected HMBC (1H → 13C) correlations of 1–8.Published as part of Raksat, Achara, C...
Raksat, Achara, Choodej, Siwattra, Aree, Thammarat, Ebrahimi, Samad Nejad, Pudhom, Khanitha (2022): ...
Fig. 1. Isolated compounds (1–10) from the roots extract of P. macropterum.Published as part of Raks...
Fig. 6. Effect of 3 and 10 on the expression of iNOS and COX-2 protein. The purity of 3 and 10 is 99...
Fig. 3. Key NOESY correlations of compounds 1, 2, 4, 5, 7, and 8.Published as part of Chen, Xiu-Mei,...
Fig. 2. Key HMBC correlations of compounds 1–5 and 7.Published as part of Chen, Xiu-Mei, Lu, Wang, Z...
Fig. 5. Plausible biosynthetic pathway of compounds 1–16.Published as part of Chen, Xiu-Mei, Lu, Wan...
Fig. 4. X-ray crystallographic structure of Pulcherritam A (1).Published as part of Chen, Xiu-Mei, L...
Fig. 1. Structures of compounds 1–16 from C. pulcherrima.Published as part of Chen, Xiu-Mei, Lu, Wan...
Fig. 2. Key COSY (bold bonds) and HMBC (black arrows) correlations of 1, 2, 3, 14, and 15.Published ...
Chen, Xiu-Mei, Lu, Wang, Zhang, Zi-Han, Zhang, Jia-Yao, Tuong, Thi Mai Luong, Liu, Ling-Li, Kim, You...
Fig. 2. Key COSY (black bond line) and key HMBC correlations of compounds 1, 4 and 6.Published as pa...
Fig. 2. Structures of compounds 1–5.Published as part of Kakumu, Yuya, Nguyen, Minh Tu Thi & Mitsuna...