Ecdysteroids of the root bark of Vitex canescens
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CAL is a minor phytoecdysteroid and oxidized derivative of 20E, naturally occurring and isolated from kaladana seeds (Ipomoea hederacea), Vitex canescens, and Cyanotis arachnoidea.
“Calonysterone (CAL), a minor phytoecdysteroid and oxidized derivative of 20E, is regarded as a naturally occurring compound, having been isolated from kaladana seeds (Ipomoea hederacea) [16], Vitex canescens [17] and Cyanotis arachnoidea [18].”
Cites
Ecdysteroids from Pfaffia iresinoides and reassignment of some 13CNMR chemical shifts☆
Nishimoto, N., Shiobara, Y., Fujino, M., Inoue, S.-S., Takemoto, T., de Oliveira, F., Akisue, G., Akisue, M. K., Hashimoto, G., & Tanaka, O. (1987) · Phytochemistry · doi:10.1016/s0031-9422(00)83865-0 · Cited by 53 · see citing works
Ecdysteroids from Vitex glabrata
Werawattanametin, K., Podimuang, V., & Suksamrarn, A. (1986) · Journal of Natural Products · doi:10.1021/np50044a041 · Cited by 53 · see citing works
Isolation of ecdysteroids fromVitex strickeri using RLCC and recycling HPLC
Minli, Z., Stout, M. J., & Kubo, I. (1992) · Phytochemistry · doi:10.1016/0031-9422(91)83046-n · Cited by 43 · see citing works
Ecdysteroids from Vitex pinnata
Suksamrarn, A., & Sommechai, C. (1993) · Phytochemistry · doi:10.1016/s0031-9422(00)94985-9 · Cited by 43 · see citing works
New ecdysteroids from Polypodium vulgare
Coll, J., Reixach, N., Sánchez-Baeza, F. J., Casas, J., & Camps, F. (1994) · Tetrahedron · doi:10.1016/s0040-4020(01)85247-9 · Cited by 40 · see citing works
Shidasterone, an insect metamorphosing substance from Blechnum niponicum: Structure.
Hikino, H., Okuyama, T., Arihara, S., Hikino, Y., Takemoto, T., Mori, H., & Shibata, K. (1975) · Chemical and Pharmaceutical Bulletin · doi:10.1248/cpb.23.1458 · Cited by 38 · see citing works
Phytoecdysteroids of<i>Diploclisia glaucescens</i>Seed
Miller, R., Clardy, J., Kozlowski, J., Mikolajczak, K., Plattner, R., Powell, R., Smith, C., Weisleder, D., & Qi-Tai, Z. (1985) · Planta Medica · doi:10.1055/s-2007-969388 · Cited by 37 · see citing works
Suksamrarn, A., Ganpinyo, P., & Sommechai, C. (1994) · Tetrahedron Letters · doi:10.1016/s0040-4039(00)73380-6 · Cited by 35 · see citing works
Ecdysteroids from Vitex canescens
Suksamrarn, A., Sommechai, C., Charulpong, P., & Chitkul, B. (1995) · Phytochemistry · doi:10.1016/0031-9422(94)00712-3 · Cited by 30 · see citing works
Maurer, P., Girault, J., LARCHEVÊQUE, M., & Lafont, R. (1993) · Archives of Insect Biochemistry and Physiology · doi:10.1002/arch.940230105 · Cited by 29 · see citing works
24-Epi-pterosterone: A novel phytoecdysone from the roots of Athyrium yokoscense
Ohta, S., Guo, J.-R., Hiraga, Y., & Suga, T. (1996) · Phytochemistry · doi:10.1016/0031-9422(95)00688-5 · Cited by 22 · see citing works
Structure of calonysterone, an unusually modified phytoecdysone
Canonica, L., Danieli, B., Ferrari, G., Krepinsky, J., & Rainoldi, G. (1973) · Journal of the Chemical Society, Chemical Communications · doi:10.1039/c39730000737 · Cited by 19 · see citing works
Synthesis of shidasterone and the unambiguous determination of its configuration at C-22
Roussel, P. G., Turner, N. J., & Dinan, L. N. (1995) · Journal of the Chemical Society Chemical Communications · doi:10.1039/c39950000933 · Cited by 18 · see citing works
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Additional minor ecdysteroid components of Leuzea carthamoides
Buděšínský, M., Vokáč, K., Harmatha, J., & Cvačka, J. (2008) · Steroids · doi:10.1016/j.steroids.2007.12.021 · Cited by 89 · see citing works
Ecdysteroids from Vitex Species: Distribution and Compilation of Their 13C‐NMR Spectral Data
Filho, J. G. D. S., Duringer, J. M., Maia, G. L. D. A., Tavares, J. F., Xavier, H. S., da Silva, M. S., da Cunha, E. V. L., & Barbosa‐Filho, J. M. (2008) · Chemistry & Biodiversity · doi:10.1002/cbdv.200890067 · Cited by 48 · see citing works
Csábi, J., Hsieh, T.-J., Hasanpour, F., Martins, A., Kele, Z., Gáti, T., Simon, A., Tóth, G., & Hunyadi, A. (2015) · Journal of Natural Products · doi:10.1021/acs.jnatprod.5b00249 · Cited by 27 · see citing works
Asymmetric dihydroxylation of stachysterone C: stereoselective synthesis of 24-epi-abutasterone
Yingyongnarongkul, B., & Suksamrarn, A. (1998) · Tetrahedron · doi:10.1016/s0040-4020(98)83015-9 · Cited by 27 · see citing works
Regioselective synthesis of 24-epi-pterosterone
Suksamrarn, A., Yingyongnarongkul, B., & Charoensuk, S. (1999) · Tetrahedron · doi:10.1016/s0040-4020(98)01030-8 · Cited by 25 · see citing works
Highly oxygenated ecdysteroids from Vitex canescens root bark
Suksamrarn, A., Promrangsan, N., & Jintasirikul, A. (2000) · Phytochemistry · doi:10.1016/s0031-9422(99)00458-6 · Cited by 24 · see citing works
Suksamrarn, A., Yingyongnarongkul, B., & Promrangsan, N. (1998) · Tetrahedron · doi:10.1016/s0040-4020(98)00915-6 · Cited by 24 · see citing works
Terpenoids from Vitex trifolia and their anti-inflammatory activities
Bao, F., Tang, R., Cheng, L. P., Zhang, C., Qiu, C.-Y., Yuan, T., Zhu, L., Li, H., & Chen, L. (2018) · Journal of Natural Medicines · doi:10.1007/s11418-018-1178-x · Cited by 19 · see citing works
Vitex negundo: - A Chinese Chaste Tree
Vimal, A., Vikram, L., Singhal, S. K., & Bhandari, A. (2011) · Cited by 14 · see citing works
Iridoids from Vitex negundo var. heterophylla and their antioxidant activities
Niu, Y., Wang, D., Chu, X.-Y., Gao, S., Yang, D.-X., Chen, L.-X., & Li, H. (2019) · Phytochemistry Letters · doi:10.1016/j.phytol.2019.11.018 · Cited by 12 · see citing works
Caffeoylquinic acid derivatives from two Brazilian Vitex species
Leitão, S. G., da Fonseca, E. N., dos Santos, T. C., França, F., & Monachè, F. D. (2007) · Biochemical Systematics and Ecology · doi:10.1016/j.bse.2007.09.004 · Cited by 10 · see citing works
New ecdysteroid and ecdysteroid glycosides from the roots of Serratula chinensis
Zhang, Z.-Y., Yang, W.-Q., Fan, C., Zhao, H.-N., Huang, X.-J., Wang, Y., & Ye, W. (2016) · Journal of Asian Natural Products Research · doi:10.1080/10286020.2016.1209492 · Cited by 8 · see citing works
One-step synthesis of shidasterone from 20-hydroxyecdysone
Одиноков, В. Н., Галяутдинов, И. В., Nedopekin, D. V., Khalilov, L. M., & Lafont, R. (2002) · Mendeleev Communications · doi:10.1070/mc2002v012n04abeh001627 · Cited by 5 · see citing works
Tsubuki, M., Iwabuchi, K., & Honda, T. (2005) · Tetrahedron Asymmetry · doi:10.1016/j.tetasy.2005.11.001 · Cited by 2 · see citing works
Shidasterone (Stachysterone D)
(2012) · Springer eBooks · doi:10.1007/978-1-4614-0543-6_371 · Cited by 1 · see citing works
Osman, A. A., Laczkó, D., Vágvölgyi, M., Tóth, N., Kemény, K. K., Szatmári, P., Seres-Bokor, A., Hunyadi, A., & Ducza, E. (2026) · Nutrients · doi:10.3390/nu18122023
“Calonysterone (CAL), a minor phytoecdysteroid and oxidized derivative of 20E, is regarded as a naturally occurring compound, having been isolated from kaladana seeds ( Ipomoea hederacea ) [16], Vitex canescens [17] and Cyanotis arachnoidea [18].”
Phytoecdysteroids from the stem bark of Vitex doniana with anti-inflammatory activities
Ochieng, C. O., Ishiola, I. O., Opiyo, S. A., Manguro, I., & Owuor, P. O. (2014)
(2012) · Springer eBooks · doi:10.1007/978-1-4614-0543-6_404
(2012) · Springer eBooks · doi:10.1007/978-1-4614-0543-6_200
(2012) · Springer eBooks · doi:10.1007/978-1-4614-0543-6_40
Azimova, S. S. (2012) · Springer eBooks · doi:10.1007/978-1-4614-0543-6_79
Azimova, S. S. (2012) · Springer eBooks · doi:10.1007/978-1-4614-0543-6_187
Spectroscopic Techniques for the Characterization of Ecdysteroids
Pogam, P. L., & Beniddir, M. A. (2026) · Springer eBooks · doi:10.1007/978-981-95-8423-9_2
- Authors
- Suksamrarn, A., Promrangsan, N., Chitkul, B., Homvisasevongsa, S., & Sirikate, A.
- Affiliations
- Ramkhamhaeng University (TH)
- Corresponding author
- Suksamrarn, Apichart
- ORCID
- Suksamrarn, Apichart
- Venue
- Phytochemistry
- Publisher
- Elsevier BV
- Published
- 1997-07
- Volume
- 45
- Issue
- 6
- Pages
- 1149-1152
- ISSN
- 0031-9422 (ISSN-L)
- OpenAlex
- W2022001881
- Cited by
- 24
- References
- 13
- Citations by year
- 2026: 2 · 2022: 1 · 2019: 1 · 2018: 1 · 2016: 1 · 2015: 1 · 2014: 1 · 2012: 6
- FWCI
- 0.47
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Phytochemistry (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Phytochemical Studies and Bioactivities
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Phytochemistry and Biological Activities
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioactive Natural Diterpenoids Research
- Keywords
- ecdysteroids, root bark, 20-hydroxyecdysone, turkesterone, natural product isolation
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