Collect. Czech. Chem. Commun.
1972, 37, 603-609
https://doi.org/10.1135/cccc19720603
Triterpenes. XXI. 3,4-Seco derivatives of betulinic acid
J. Klinot, V. Šumanová and A. Vystrčil
Crossref Cited-by Linking
- Kazakova Oxana, Smirnova Irina, Nguyen Ha Thi Thu, Heise Niels V., Hoenke Sophie, Serbian Immo, Csuk René: α-Glucosidase and cholinesterase inhibiting potential of a series of semisynthetic nitrogen triterpenic derivatives. Med Chem Res 2023, 32, 485. <https://doi.org/10.1007/s00044-023-03014-0>
- Tolmacheva Irina, Beloglazova Yulia, Nazarov Mikhail, Gagarskikh Olga, Grishko Victoria: Synthesis and Anticancer Activity of A-Ring-Modified Derivatives of Dihydrobetulin. IJMS 2023, 24, 9863. <https://doi.org/10.3390/ijms24129863>
- Giniyatullina G. V., Kazakova O. B.: Synthesis and Cytotoxicity of Lupane Mono- and Bis-Piperazinylamides. Chem Nat Compd 2021, 57, 698. <https://doi.org/10.1007/s10600-021-03453-4>
- Tolmacheva Irina A., Nazarov Alexey V., Eroshenko Daria V., Grishko Victoria V.: Synthesis, cytotoxic evaluation, and molecular docking studies of the semi-synthetic “triterpenoid-steroid” hybrids. Steroids 2018, 140, 131. <https://doi.org/10.1016/j.steroids.2018.10.005>
- Smirnova Irina E., Kazakova Oxana B.: Structure – Anti-influenza Type a Activity Relationship among a Series of Nitrogen Lupane Triterpenoids. Natural Product Communications 2018, 13. <https://doi.org/10.1177/1934578X1801301008>
- Salimova Elena V., Tretyakova Elena V., Parfenova Lyudmila V., Odinokov Victor N.: Synthesis of 5,19-(2,6-Dimethylpyridin-4-yl)-trisnorlupane and Oleanane. Natural Product Communications 2016, 11. <https://doi.org/10.1177/1934578X1601100315>
- Goswami Animesh, Guo Zhiwei, Tully Thomas P., Rinaldi Frank A., Huang Xiaohua Stella, Swidorski Jacob J., Regueiro-Ren Alicia: Microbial transformations of betulinic and betulonic acids. Journal of Molecular Catalysis B: Enzymatic 2015, 117, 45. <https://doi.org/10.1016/j.molcatb.2015.04.012>
- Khusnutdinova E. F., Lopatina T. V., Kazakova O. B., Akhmatshina G. F., Kukovinets O. S.: Synthesis and Cytotoxicity of Triterpene A-seco-Acid Propargylamides. Chem Nat Compd 2014, 50, 853. <https://doi.org/10.1007/s10600-014-1099-1>
- Shenvi Suvarna, Rijesh K., Diwakar Latha, Reddy G. Chandrasekara: Beckmann rearrangement products of methyl 3-oxo-tirucall-8, 24-dien-21-oate from Boswellia serrata gum and their anti-tumor activity. Phytochemistry Letters 2014, 7, 114. <https://doi.org/10.1016/j.phytol.2013.11.006>
- Kennedy María L., Llanos Gabriel G., Castanys Santiago, Gamarro Francisco, Bazzocchi Isabel L., Jiménez Ignacio A.: Terpenoids from Maytenus Species and Assessment of Their Reversal Activity against a Multidrug‐Resistant Leishmania tropica Line. Chemistry & Biodiversity 2011, 8, 2291. <https://doi.org/10.1002/cbdv.201000356>
- Kazakova O. B., Giniyatullina G. V., Tolstikov G. A.: Synthesis of a-secomethylenamino- and substituted amidoximotriterpenoids. Russ J Bioorg Chem 2011, 37. <https://doi.org/10.1134/S1068162011050086>
- Cichewicz Robert H., Kouzi Samir A.: Chemistry, biological activity, and chemotherapeutic potential of betulinic acid for the prevention and treatment of cancer and HIV infection. Medicinal Research Reviews 2004, 24, 90. <https://doi.org/10.1002/med.10053>
- Sejbal Jan, Homolová Martina, Tišlerová Iva, Křeček Václav: Preparation and Conformational Analysis of 1,2-Seco Derivatives of 19β,28-Epoxy-18α-oleanane. Collect. Czech. Chem. Commun. 2000, 65, 1339. <https://doi.org/10.1135/cccc20001339>
- Aalbersberg William, Singh Yogendra: Dammarane triterpenoids from Dysoxylum richii. Phytochemistry 1991, 30, 921. <https://doi.org/10.1016/0031-9422(91)85280-D>
- Baas Wim J.: Naturally occurring seco-ring-A-triterpenoids and their possible biological significance. Phytochemistry 1985, 24, 1875. <https://doi.org/10.1016/S0031-9422(00)83085-X>
- Baas Wim J.: Dihydronyctanthic acid methyl ester and other 3,4-seco-pentacyclic triterpenoids from Hoya lacunosa. Phytochemistry 1983, 22, 2809. <https://doi.org/10.1016/S0031-9422(00)97702-1>
- Baas Wim J., Figdor Carl G.: Triterpene Composition of Hoya australis Cuticular Wax in Relation to Leaf Age. Zeitschrift für Pflanzenphysiologie 1978, 87, 243. <https://doi.org/10.1016/S0044-328X(78)80125-1>
- Aplin R. T., Cox I. R.: Application of mass spectrometry to the structural investigation of triterpenes. II—3,4‐A‐seco‐triterpenoids. Org. Mass Spectrom. 1975, 10, 981. <https://doi.org/10.1002/oms.1210101108>
- KLINOT J., SUMANOVA V., VYSTRCIL A.: ChemInform Abstract: TRITERPENE 21. MITT. 3,4‐SECO‐DERIVATE VON BETULINSAEURE. Chemischer Informationsdienst 1972, 3. <https://doi.org/10.1002/chin.197221261>