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Published January 31, 2022 | Version v1
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Chlomultiols A-L, sesquiterpenoids from Chloranthus multistachys and their anti-inflammatory activities

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Huang, Wei-ming, Bian, Yu-ting, Chen, Fang-you, Ning, Tian-jiao, Zhu, Zhi-ying, Chen, Zhi-chao, Luo, Yong-ming (2022): Chlomultiols A-L, sesquiterpenoids from Chloranthus multistachys and their anti-inflammatory activities. Phytochemistry (113001) 193: 1-9, DOI: 10.1016/j.phytochem.2021.113001, URL: http://dx.doi.org/10.1016/j.phytochem.2021.113001

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urn:lsid:plazi.org:pub:7175FFE6FFD8EB12FFEFFFB9FFA9FFE7

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Figure: 10.5281/zenodo.8236612 (DOI)
Figure: 10.5281/zenodo.8236614 (DOI)
Figure: 10.5281/zenodo.8236616 (DOI)
Figure: 10.5281/zenodo.8236618 (DOI)

References

  • Light yellow needle crystals (CH3OH); IR (KBr) v max: 3431, 2923, 2845, 1660, 1053 cm 1 ; UV (CH2Cl2) λ max: 195, 270 nm; HRESIMS (277.1073 [M + H]+ , calcd for C15H17O5, 277.1070); 1H and 13C NMR data, see Tables 2 and 3 8a: [α] D 20 + 29.8 (c 0.18, CH3OH); CD (CH2Cl2) λ max (Δε) 220 (+ 49.0), 271 ( 55.2); 8b: [α] D 20 35.8 (c 0.18, CH3OH); CD (CH2Cl2) λ max (Δε) 220 ( 57.0), 271 (+ 62.8).