1993
DOI: 10.1016/s0031-9422(00)94985-9
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Ecdysteroids from Vitex pinnata

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Cited by 43 publications
(22 citation statements)
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“…This procedure was repeated with isolated 20E to obtain a completely pure compound. 20E and the two other obtained ecdysteroids were characterized by 1D and 2D NMR, mass and microanalysis data, whose were in agreement with literature [16][17][18].…”
Section: Extraction and Isolation Of 20-hydroxyecdysone (20e) Externasupporting
confidence: 81%
“…This procedure was repeated with isolated 20E to obtain a completely pure compound. 20E and the two other obtained ecdysteroids were characterized by 1D and 2D NMR, mass and microanalysis data, whose were in agreement with literature [16][17][18].…”
Section: Extraction and Isolation Of 20-hydroxyecdysone (20e) Externasupporting
confidence: 81%
“…[24] Upon hydrolysis with guanidine, canescensterone can be transformed into pinnatasterone, [12] which indicates the same stereochemistry of the steroid ring system and the side-chain at C-17. In the Musca domestica bioassay, canescensterone showed higher activity than pinnatasterone, which indicates the importance of the substituent.…”
Section: Resultsmentioning
confidence: 97%
“…Interestingly, a literature search revealed that the side-chain configuration for a number of ecdysteroids, especially with two methylene groups in the side-chain, has only been assigned tentatively. [24,27] In the past, differences in chemical shifts were used to identify the configuration at C-24. [28] However, some ecdysteroids show negligible differences in their 13 C chemical shifts even though they represent epimers (e.g., 20,26-dihydroxyecdysone).…”
Section: Configuration Of the Side-chainmentioning
confidence: 99%
“…-An extensive literature search was undertaken to identify studies on ecdysteroids in works such as periodicals, data banks such as NAPRALERT (Natural Products Alert) and that at the University of Illinois, Chicago, Chemical (24) [ 2 ] 24-Epimakisterone A (8) [ 8 ] Calonysterone (9) [8] [10] Turkesterone (2) [ 8 ] [ 9 ] 24-Epiabutasterone (11) [ 8 ] Shidasterone (5) [ 8 ] 20,26-Dihydroxyecdysone (19) [11] (24R )-11a,20,24-Trihydroxyecdysone (17) [12] 11a,20,26-Trihydroxyecdysone (15) [12] Canescensterone (4) [ (13) [24] Calonysterone (9) [24] Pterosterone (22) [24] 24-Epimakisterone A (8) [24] 20-Hydroxyecdysone (1) [24] Polypodine B (23) [24] Ajugasterone C (6) [24] Pinnatasterone (3)…”
mentioning
confidence: 99%