Norcrohalane A, an Unusual C <sub>15</sub> <i>nor</i> ‐Halimane‐Type Diterpenoid from <i>Croton crassifolius</i>

An unusual C<sub>15</sub> nor-halimane-type diterpenoid, norcrohalane A (1), a new nor-lasserane-type sesquiterpenoid, norcrolasane A (2), along with four known compounds (3-6) were isolated from the roots of Croton crassifolius. Compound 1 represents the first example of a C<sub>15</sub> nor-halimane-type diterpenoid, which features a rare 6/6/6 tricyclic ring system, and the A ring is aromatic. Compound 2 is a rare nor-lasserane-type sesquiterpenoid. Their structures and absolute configurations were established by a combination of mass spectrometry, nuclear magnetic resonance, electronic circular dichroism calculation, and single-crystal X-ray diffraction analyses. The anti-neuroinflammatory activities of 1-6 were evaluated for their inhibitory effects on nitric oxide (NO) production in lipopolysaccharide-induced BV2 cells, and compounds 1 and 2 showed moderate inhibition on NO production with IC<sub>50</sub> values of 26.82 ± 0.61 and 17.35 ± 0.78 µM, respectively.

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Publication Details

Journal
Chemistry & Biodiversity
Published
2024-12-23
DOI
https://doi.org/10.1002/cbdv.202403123
Citations
1
Primary Topic
Bioactive Natural Diterpenoids Research
Type
article
Field-Weighted Citation Impact
0.23
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article

Norcrohalane A, an Unusual C 15 nor ‐Halimane‐Type Diterpenoid from Croton crassifolius

Huilin Ou, Yu-Bo Zhang, Qing Tang, Can‐Jie Li et al.
1 citations
Chemistry & Biodiversity
Bioactive Natural Diterpenoids Research
0.23
article

Norcrohalane A, an Unusual C 15 nor ‐Halimane‐Type Diterpenoid from Croton crassifolius

Huilin Ou, Yu-Bo Zhang, Qing Tang, Can‐Jie Li, Yujun Tang, Wei Zheng, Tian-Yuan Wu, Huihui Zhu, Qian-Yi Situ
article en
1 citations

Abstract

An unusual C<sub>15</sub> nor-halimane-type diterpenoid, norcrohalane A (1), a new nor-lasserane-type sesquiterpenoid, norcrolasane A (2), along with four known compounds (3-6) were isolated from the roots of Croton crassifolius. Compound 1 represents the first example of a C<sub>15</sub> nor-halimane-type diterpenoid, which features a rare 6/6/6 tricyclic ring system, and the A ring is aromatic. Compound 2 is a rare nor-lasserane-type sesquiterpenoid. Their structures and absolute configurations were established by a combination of mass spectrometry, nuclear magnetic resonance, electronic circular dichroism calculation, and single-crystal X-ray diffraction analyses. The anti-neuroinflammatory activities of 1-6 were evaluated for their inhibitory effects on nitric oxide (NO) production in lipopolysaccharide-induced BV2 cells, and compounds 1 and 2 showed moderate inhibition on NO production with IC<sub>50</sub> values of 26.82 ± 0.61 and 17.35 ± 0.78 µM, respectively.

Chemistry & BiodiversityVol. 22(5)
Jinan University (CN), Jinan University (LB)
Clean water and sanitation
Openalex Percentile: Top 40%
Bioactive Natural Diterpenoids Research
0.23
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