Mona Diri , Moses K. Langat , Eduard Mas-Claret , Thomas A.K. Prescott , Cristina D. Cruz , Päivi Tammela , Sianne Schwikkard
{"title":"Crotoscheffleriolides, ent-clerodane diterpenoids from Kenyan Croton scheffleri","authors":"Mona Diri , Moses K. Langat , Eduard Mas-Claret , Thomas A.K. Prescott , Cristina D. Cruz , Päivi Tammela , Sianne Schwikkard","doi":"10.1016/j.phytochem.2025.114460","DOIUrl":null,"url":null,"abstract":"<div><div>Kenyan <em>Croton scheffleri</em> has yielded nineteen compounds. The stem bark gave six undescribed <em>ent-</em>clerodane diterpenoids (<strong>1</strong>–<strong>4</strong>, <strong>6</strong> and <strong>7</strong>), three undescribed sesquiterpene lactones (<strong>9</strong>, <strong>11</strong> and <strong>12</strong>) and four known compounds (<strong>5</strong>, <strong>8</strong>, <strong>10</strong> and <strong>13</strong>). From the leaves six known compounds were identified, ayanin (<strong>14</strong>), pheophytin a (<strong>15</strong>), ferulic acid (<strong>16</strong>), 1,3,4-trihydroxybenzene (<strong>17</strong>), sitosterol (<strong>18</strong>), and podosterol (<strong>19</strong>). The structures of the compounds were determined using spectroscopic and spectrometric methods, NMR, IR, UV, polarimetry, ECD, HRESIMS, and GC-MS. The undescribed compounds were assessed against HIV-1 Reverse Transcriptase and both gram-positive bacteria <em>Staphylococcus aureus</em> 29213 and <em>Enterococcus faecalis</em> 29212, as well as gram-negative bacteria <em>Escherichia coli</em> 25922 and <em>Pseudomonas aeruginosa</em> 27853. Compounds <strong>1</strong>, <strong>4</strong>, <strong>5</strong>, <strong>6</strong>, <strong>7</strong>, <strong>10</strong>, <strong>12</strong> and <strong>19</strong> increased the proliferation of serum starved dermal fibroblast cells at a concentration of 100 nM. All compounds inhibited human dermal fibroblast cell proliferation at 100 μM, while compounds <strong>1</strong>, <strong>4</strong> and <strong>19</strong> inhibited fibroblast proliferation at 10 μM.</div></div>","PeriodicalId":20170,"journal":{"name":"Phytochemistry","volume":"235 ","pages":"Article 114460"},"PeriodicalIF":3.2000,"publicationDate":"2025-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0031942225000834","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Kenyan Croton scheffleri has yielded nineteen compounds. The stem bark gave six undescribed ent-clerodane diterpenoids (1–4, 6 and 7), three undescribed sesquiterpene lactones (9, 11 and 12) and four known compounds (5, 8, 10 and 13). From the leaves six known compounds were identified, ayanin (14), pheophytin a (15), ferulic acid (16), 1,3,4-trihydroxybenzene (17), sitosterol (18), and podosterol (19). The structures of the compounds were determined using spectroscopic and spectrometric methods, NMR, IR, UV, polarimetry, ECD, HRESIMS, and GC-MS. The undescribed compounds were assessed against HIV-1 Reverse Transcriptase and both gram-positive bacteria Staphylococcus aureus 29213 and Enterococcus faecalis 29212, as well as gram-negative bacteria Escherichia coli 25922 and Pseudomonas aeruginosa 27853. Compounds 1, 4, 5, 6, 7, 10, 12 and 19 increased the proliferation of serum starved dermal fibroblast cells at a concentration of 100 nM. All compounds inhibited human dermal fibroblast cell proliferation at 100 μM, while compounds 1, 4 and 19 inhibited fibroblast proliferation at 10 μM.
期刊介绍:
Phytochemistry is a leading international journal publishing studies of plant chemistry, biochemistry, molecular biology and genetics, structure and bioactivities of phytochemicals, including ''-omics'' and bioinformatics/computational biology approaches. Phytochemistry is a primary source for papers dealing with phytochemicals, especially reports concerning their biosynthesis, regulation, and biological properties both in planta and as bioactive principles. Articles are published online as soon as possible as Articles-in-Press and in 12 volumes per year. Occasional topic-focussed special issues are published composed of papers from invited authors.