ursolic acid has been researched along with betulinic acid in 116 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (0.86) | 18.7374 |
1990's | 4 (3.45) | 18.2507 |
2000's | 28 (24.14) | 29.6817 |
2010's | 73 (62.93) | 24.3611 |
2020's | 10 (8.62) | 2.80 |
Authors | Studies |
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Cosentino, LM; Hashimoto, A; Ikeshiro, Y; Kashiwada, Y; Lee, KH; Nagao, T; Okabe, H | 1 |
Hata, K; Hori, K; Takahashi, S | 1 |
Broedel, SE; Cihlar, RL; ElSohly, HN; Ferreira, D; Jacob, MR; Joshi, AS; Khan, IA; Khan, SI; Li, XC; Raulli, RE; Walker, LA; Zhang, Z | 1 |
Cuong, NM; Fong, HH; Hoang, VD; Hung, NV; Pezzuto, JM; Soejarto, DD; Tan, GT; Zhang, HJ | 1 |
Johnson, RK; Kingston, DG; Prakash Chaturvedula, VS; Schilling, JK | 1 |
Fong, HH; Mesecar, AD; Nguyen, MC; Nguyen, QC; Nguyen, VH; Pezzuto, JM; Santarsiero, BD; Soejarto, DD; Tan, GT | 1 |
Franzblau, SG; Gu, JQ; Montenegro, G; Timmermann, BN; Wang, Y | 1 |
Ando, M; Fu, L; Hasegawa, T; Hirose, K; Kataoka, T; Kiuchi, M; Li, N; Mitsui, T; Oka, S; Sakai, J; Wang, J; Zhang, S; Zhao, M | 1 |
Habib-Jiwan, JL; Hoet, S; Muccioli, GG; Opperdoes, FR; Pieters, L; Quetin-Leclercq, J | 1 |
Alexacou, KM; Cheng, K; Gimisis, T; Hao, J; Hayes, JM; Leonidas, DD; Liu, J; Ni, P; Oikonomakos, NG; Sun, H; Wen, X; Zhang, L; Zhang, P; Zographos, SE | 1 |
Chadwick, LR; Franzblau, SG; Jaki, BU; Lankin, DC; Pauli, GF; Wang, Y; Zhang, F | 1 |
Abdel Bar, FM; Ahmad, KF; Bachawal, SV; El Sayed, KA; Sylvester, PW; Zaghloul, AM | 1 |
Bae, K; Ha, do T; Ngoc, TM; Nhiem, NX; Thu, NB; Tuan, DT; Yim, N | 1 |
Auwerx, J; Boudjelal, G; Genet, C; Lobstein, A; Saladin, R; Schmidt, C; Schoonjans, K; Souchet, M; Strehle, A; Wagner, A | 1 |
Carcache de Blanco, EJ; Chai, H; Farnsworth, NR; Kardono, LB; Kinghorn, AD; Ren, Y; Riswan, S; Soejarto, DD | 1 |
Chen, J; Chen, L; Cheng, K; Gong, Y; Hao, J; Jiang, H; Li, H; Li, L; Liang, Z; Liu, H; Liu, J; Luo, C; Sun, H; Wen, X; Zhang, L; Zhang, P; Zhang, X; Zheng, M; Zhu, X | 1 |
El-Kabbani, O; Endo, S; Hara, A; Iinuma, M; Matsunaga, T; Soda, M; Tajima, K; Takemura, M; Zhao, HT | 1 |
Gatbonton-Schwager, TN; Letterio, JJ; Tochtrop, GP | 1 |
Chin, YW; Jee, JG; Jeong, YJ; Keum, YS; Kim, Y; Lee, J; Lee, JM; Yu, MS | 1 |
Batista-Gonzalez, A; Brunhofer, G; Fallarero, A; Gopi Mohan, C; Karlsson, D; Shinde, P; Vuorela, P | 1 |
Chen, K; Huang, X; Peng, Y; Qiu, Y; Shi, Y; Sun, D; Wang, H; Wang, Q; Xiao, S; Yu, F; Yu, M; Zhang, C; Zhang, L; Zhang, Z; Zhao, C; Zheng, Y; Zhou, D; Zhu, L | 1 |
Cuong, NX; Jo, SH; Kim, YH; Kwon, YI; Luyen, BT; Minh, CV; Nam, NH; Tai, BH; Thao, NP; Yang, SY | 1 |
Feng, Y; Mei, Z; Wang, C; Yang, G; Yang, J; Yang, X; Zhao, P; Zhou, Q | 1 |
Cai, L; Jiang, S; Jiang, X; Li, J; Li, X; Liang, G; Liu, K; Lu, L; Na, H; Wang, C; Wang, Q; Xu, X; Yu, F; Zhang, T; Zhang, Z; Zheng, B | 1 |
Ba Thi, C; D'hooghe, M; Dang Thi, TA; Doan Duy, T; Kim Tuyet, NT; Pham The, C; Thanh Nguyen, H; Van Nguyen, T | 1 |
Fan, Z; Han, X; Jiao, P; Peng, Y; Wan, C; Wang, H; Wang, Q; Xiao, S; Xu, R; Yu, F; Zhang, L; Zhang, Y; Zhou, D; Zhou, X | 1 |
Ahn, HC; Cho, SC; Choi, BY; Fei, X; Keum, YS; Kim, HJ; Lee, K; Seo, SY | 1 |
Csuk, R; Heller, L; Wiemann, J | 1 |
Cassera, MB; Dalal, S; Goetz, M; Kingston, DG; Su, Q | 1 |
Csuk, R; Heller, L; Kuhfs, J; Sommerwerk, S | 1 |
Li, X; Liu, K; Na, H; Wang, C; Zou, C | 1 |
Csuk, R; Heller, L; Kerzig, C; Kramell, AE; Sommerwerk, S | 1 |
Bailon-Moscoso, N; Castillo-Veintimilla, P; Romero-Benavides, JC; Ruano, AL; Silva-Rivas, R; Vivanco-Jaramillo, S | 1 |
Alcaro, S; Corona, A; Cottiglia, F; Distinto, S; Floris, C; Fois, B; Maccioni, E; Malpure, NV; Meleddu, R; Sonar, VP; Tramontano, E | 1 |
Alho, DPS; Figueiredo, SAC; Gonçalves, BMF; Leal, AS; Mendes, VIS; Salvador, JAR; Silvestre, SM; Valdeira, AS | 1 |
Cao, G; Chang, Y; Chen, D; He, X; Huang, X; Liu, J; Luo, H; Ni, S; Shen, Q; Sun, H; Wang, P; Wen, X; Zhou, H | 1 |
Dong, YS; Sun, WL; Wen, C; Xing, Y; Xiu, ZL; Yu, XX; Zhang, BW | 1 |
Baikova, IP; Giniyatullina, GV; Kataev, VE; Kazakova, OB; Lopatina, TV; Medvedeva, NI; Smirnova, IE | 1 |
Anaya-Eugenio, GD; Burdette, JE; Chai, HB; Czarnecki, AA; de Blanco, EJC; Kinghorn, AD; Ninh, TN; Ren, Y; Soejarto, DD; Yuan, C | 1 |
Efdi, M; Itoh, T; Katsurayama, K; Koketsu, M; Ninomiya, M | 1 |
Appendino, G; Bellido, ML; Calzado, MA; Caprioglio, D; Cruz, C; Galera, N; Jinénez, C; Minassi, A; Muñoz, E; Prados, ME; Rogati, F | 1 |
Borkova, L; Hodon, J; Kazakova, A; Pokorny, J; Urban, M | 1 |
Brandes, B; Csuk, R; Fischer, L; Hoenke, S | 1 |
Buckle, R; Eldridge, GR; Ellis, M; Garo, E; Hu, JF; Huang, Z; Lawrence, JA; Norman, VL; Rathinavelu, S; Starks, CM; Williams, RB | 1 |
Awale, S; Dibwe, DF; Kim, MJ; Omar, AM; Sun, S; Tawila, AM; Toyooka, N; Ueda, JY | 1 |
Chen, C; Cheng, K; Dai, L; Hu, K; Li, H; Liu, L; Sun, H; Wen, X; Xu, Q; Yuan, H | 1 |
Bianchi, E; Cole, JR; Eckert, DJ; Trumbull, ER; Wiedhopf, RM | 1 |
Fang, Z; Yang, Y; Zhou, G | 1 |
Giner, RM; Gueho, J; Hostettmann, K; Julien, HR; Máñez, S; Recio, MC; Ríos, JL | 1 |
Giner, RM; Máñez, S; Recio, MC; Ríos, JL | 1 |
Kirby, GC; Simmonds, MS; Steele, JC; Warhurst, DC | 1 |
Kim, YK; Ryu, SY; Yoon, SK | 1 |
Biabani, MA; Kulshreshtha, DK; Kundu, B; Pathak, A; Puri, SK; Singh, SK; Srivastava, S | 1 |
Chandramu, C; Dashavantha, RV; Krupadanam, DG; Manohar, RD | 1 |
Baglin, I; Cavé, C; Lacaille-Dubois, MA; Mitaine-Offer, AC; Nour, M; Tan, K | 1 |
Baglin, I; Cavé, C; Chauffert, B; Lacaille-Dubois, MA; Mitaine-Offer, AC; Nour, M; Poumaroux, A; Tan, K | 1 |
Bérangère, C; Caussarieu, N; Lafosse, M; Morin, P; Morin-Allory, L | 1 |
Becker, H; Hostanska, K; Scher, JM; Urech, K | 1 |
Li, N; Li, X; Li, ZL; Wang, JH; Wang, Y; Xu, J; Zhang, P | 1 |
Im, KR; Jeong, TS; Lee, WS; Park, YD; Sung, ND | 1 |
Chang, CS; Chang, YS; Chao, DC; Chen, JC; Ho, TY; Hsiang, CY; Li, CC; Wu, SL | 1 |
Bremner, JB; Chokchaisiri, R; Suksamrarn, A; Tanachatchairatana, T | 1 |
Hao, J; Sun, H; Wen, X; Zhang, P | 1 |
Duval, RE; Finance, C; Fontanay, S; Grare, M; Mayer, J | 1 |
Jäger, S; Kopp, T; Laszczyk, MN; Scheffler, A; Trojan, H | 1 |
Ahmad, AS; Mansour, AI; Nafady, AM; Ramadan, MA | 1 |
Christensen, SB; Hansen, EW; Jäger, AK; Moesby, L; Saaby, L | 1 |
Chen, YS; Lin, XY; Xie, JM; Yao, H; Zhang, YH | 1 |
Li, GL; Song, CH; Suo, YR; Xia, L; You, JM; Zheng, J | 1 |
Fukushima, EO; Mizutani, M; Muranaka, T; Ohyama, K; Ono, E; Saito, K; Seki, H; Umemoto, N | 1 |
Nielsen, CH; Saaby, L | 1 |
Chen, YJ; Cheng, SX; Kou, X; Long, Y; Wang, C; Wang, GH; Wang, WP | 1 |
Gao, L; Lin, CZ; Zhao, ZX; Zhu, CC | 1 |
He, C; Ma, G; Peng, Y; Wei, H; Xiao, P | 1 |
David, JM; David, JP; e Silva, Mde L; Fontana, R; Lima, LS; Reis, PS; Santos, RA; Silva, LC | 1 |
Cruz, LN; Garcia, CR; Gnoatto, SC; Gosmann, G; Innocente, AM; Moraes, MS; Nakabashi, M; Silva, GN; Sonnet, P | 1 |
Bruni, R; Caligiani, A; Malavasi, G; Marseglia, A; Palla, G; Tognolini, M | 1 |
Cruz, LN; da Silva, GN; de Moraes, MS; Garcia, CR; Gnoatto, SC; Gosmann, G; Graebin, C; Maria, NR; Nakabashi, M; Schuck, DC | 1 |
Casanova, BB; Fuentefria, AM; Gnoatto, SC; Gosmann, G; Innocente, A; Klein, F; Lana, AD; Muniz, MN; Pereira, D; Sonnet, P | 1 |
Casanova, BB; Frasson, AP; Gnoatto, SC; Gosmann, G; Innocente, AM; Tasca, T; Vieira, Pde B | 1 |
Inn, KS; Jang, DS; Jo, SJ; Kim, HI; Kim, HJ; Kim, JE; Lee, CM; Lee, NR; Quan, FS | 1 |
Bhadra, S; Chanda, J; Chaudhary, SK; Choudhury, S; Harwansh, R; Mukherjee, PK | 1 |
He, QQ; Ma, CM; Ma, JN; Yang, L; Zhang, JY | 1 |
Broniatowski, M; Flasiński, M; Hąc-Wydro, K | 1 |
Bai, LY; Chiu, CF; Lin, WY; Weng, JR | 1 |
Chen, G; Hu, N; Li, G; Liu, D; Liu, S; Suo, Y; Wu, H; You, J | 1 |
Gaikwad, NB; Kshirsagar, PR; Nimbalkar, MS; Pai, SR | 1 |
Andujar, S; Arena, ME; Bardón, A; Gilabert, M; Marcinkevicius, K; Schiavone, M | 1 |
Bye, R; Flores-Bocanegra, L; Linares, E; Mata, R; Pérez-Vásquez, A; Torres-Piedra, M | 1 |
Huang, GQ; Li, B; Lu, RM; Wei, JH; Zhong, ZG | 1 |
Hegde, HV; Joshi, RK; Kholkute, SD; Pai, SR; Upadhya, V | 1 |
Gray, CA; Johnson, JA; Li, H; Morrison, SA; Webster, D | 1 |
Fu, HZ; Yan, QW; Zhang, TX; Zhong, RJ; Zhou, GP | 1 |
da Silva, GN; Dos Santos, F; E Silva, AA; Gnoatto, SC; Gosmann, G; Trindade, FT | 1 |
Bhattacharjee, D; Jagadeesh, B; Jain, N; Kavitha, R; Lakshmi, JK; Mallavadhani, UV; Pattnaik, B | 1 |
Günther, G; Morales, J; Rodríguez, L; Valdés, K | 1 |
Adamczyk-Grochala, J; Deregowska, A; Kwasniewicz, E; Lewinska, A; Wnuk, M | 1 |
Adamczyk-Grochala, J; Bednarz, D; Lewinska, A; Wnuk, M | 1 |
Irie, K; Kaido, Y; Kawabata, K; Kawakami, B; Kitamura, K; Matsuura, T; Murakami, S; Naruse, S; Ohigashi, H; Taira, S; Takahashi, M; Uemae, T | 1 |
Ajiboye, HO; Ajiboye, TO; Oloyede, HOB; Salawu, MO | 1 |
Ahn, SJ; Bang, IS; Cho, E; Choi, MH; Kim, JM; Kook, JK; Lim, YK; Park, SN | 1 |
Chou, CH; Jhan, YL; Tsai, SJ; Wang, CM; Yeh, KL | 1 |
Henao, IC; Pereañez, JA; Preciado, LM; Rey-Suárez, P | 1 |
Ren, T; Xu, Z | 1 |
Cui, CL; Liang, YN; Liao, ZX; Liu, HB; Liu, SJ; Tang, ZS; Zhang, Y | 1 |
Al-Harrasi, A; Csuk, R; Fischer Née Heller, L; Kahnt, M | 1 |
Arnason, JT; Dobson, CC; Durst, T; Foster, BC; Harris, CS; Liu, R; Sanchez, P | 1 |
Kai, H; Matsuno, K; Mutoh, J; Nakamura, S; Nakashima, K; Tojoh, Y; Wada, M | 1 |
Gnoatto, SCB; Macedo, AJ; Primon-Barros, M; Silva, GNSD | 1 |
Cui, H; Jin, C; Jin, M; Li, G; Wang, J; Wang, R; Ye, C; Zhou, W; Zhou, Y | 1 |
Gubaidullin, RR; Khalitova, RR; Nedopekina, DA; Spivak, AY | 1 |
Garcia, AWA; Gnoatto, SCB; Kawano, DF; Krummenauer, ME; Lopes, W; Schrank, A; Vainstein, MH | 1 |
Castro, MM; Duarte, IF; Duarte, MF; Guerra, ÂR; Oliveira, H; Paulino, AF | 1 |
Croft, SL; Loiseau, PM; Pomel, S | 1 |
Azevedo Dos Santos, AP; Baggio Gnoatto, SC; Berton Zanchi, F; Bioni Garcia Teles, C; de Almeida E Silva, A; de Souza Rodrigues, M; Soares de Maria de Medeiros, P; Sol Sol de Medeiros, D; Tasca Cargnin, S | 1 |
Alhadrami, HA; Azhar, EI; Rateb, ME; Sayed, AM; Sharif, AM | 1 |
6 review(s) available for ursolic acid and betulinic acid
Article | Year |
---|---|
Medicinal plants used as anthelmintics: Ethnomedical, pharmacological, and phytochemical studies.
Topics: Anthelmintics; Humans; Medicine, Traditional; Phytotherapy; Plants, Medicinal | 2017 |
Oleanane-, ursane-, and quinone methide friedelane-type triterpenoid derivatives: Recent advances in cancer treatment.
Topics: Animals; Antineoplastic Agents; Chemistry Techniques, Synthetic; Humans; Indolequinones; Neoplasms; Oleanolic Acid; Structure-Activity Relationship; Triterpenes | 2017 |
Design and synthesis of pentacyclic triterpene conjugates and their use in medicinal research.
Topics: Animals; Antineoplastic Agents, Phytogenic; Antiviral Agents; Biomedical Research; Cell Proliferation; Drug Design; Humans; Neoplasms; Triterpenes; Viruses | 2019 |
A review of natural and modified betulinic, ursolic and echinocystic acid derivatives as potential antitumor and anti-HIV agents.
Topics: Anti-HIV Agents; Antineoplastic Agents; Betulinic Acid; HIV-1; HT29 Cells; Humans; Molecular Structure; Oleanolic Acid; Pentacyclic Triterpenes; Structure-Activity Relationship; Triterpenes; Tumor Cells, Cultured; Ursolic Acid | 2003 |
Potential use of nanocarriers with pentacyclic triterpenes in cancer treatments.
Topics: Animals; Antineoplastic Agents; Betulinic Acid; Biological Availability; Drug Delivery Systems; Drug Liberation; Humans; Nanocapsules; Neoplasms; Oleanolic Acid; Pentacyclic Triterpenes; Solubility; Triterpenes; Unilamellar Liposomes; Ursolic Acid; Water | 2016 |
Chitosan Contribution to Therapeutic and Vaccinal Approaches for the Control of Leishmaniasis.
Topics: Amphotericin B; Animals; Antimony; Antiprotozoal Agents; Betulinic Acid; Biocompatible Materials; Chitosan; Curcumin; Drug Carriers; Drug Compounding; Humans; Hydrogen-Ion Concentration; Leishmaniasis; Leishmaniasis Vaccines; Macrophages; Nanoparticles; Paromomycin; Pentacyclic Triterpenes; Polymers; Rifampin; Selenium; Thiomalates; Titanium; Triterpenes; Ursolic Acid | 2020 |
110 other study(ies) available for ursolic acid and betulinic acid
Article | Year |
---|---|
Anti-AIDS agents 38. Anti-HIV activity of 3-O-acyl ursolic acid derivatives.
Topics: Anti-HIV Agents; Cell Line; HIV-1; Humans; Magnetic Resonance Spectroscopy; Microbial Sensitivity Tests; Molecular Structure; Spectrometry, Mass, Fast Atom Bombardment; Triterpenes; Ursolic Acid | 2000 |
Differentiation- and apoptosis-inducing activities by pentacyclic triterpenes on a mouse melanoma cell line.
Topics: Animals; Apoptosis; Betulinic Acid; Cell Differentiation; Inhibitory Concentration 50; Magnetic Resonance Spectroscopy; Melanoma, Experimental; Mice; Molecular Structure; Oxidation-Reduction; Pentacyclic Triterpenes; Pyridinium Compounds; Spectroscopy, Fourier Transform Infrared; Structure-Activity Relationship; Triterpenes; Tumor Cells, Cultured | 2002 |
Fatty acid synthase inhibitors from plants: isolation, structure elucidation, and SAR studies.
Topics: Antifungal Agents; Candida albicans; Combretaceae; Cryptococcus neoformans; Enzyme Inhibitors; Fatty Acid Synthases; Inhibitory Concentration 50; Isoflavones; Melastomataceae; Molecular Structure; Moraceae; Paspalum; Plants, Medicinal; Saccharomyces cerevisiae; Structure-Activity Relationship; Tannins; Triterpenes | 2002 |
Natural anti-HIV agents. Part IV. Anti-HIV constituents from Vatica cinerea.
Topics: Anti-HIV Agents; Chlorophyll; Ericales; Humans; Inhibitory Concentration 50; Molecular Conformation; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Osteosarcoma; Plant Leaves; Plant Stems; Plants, Medicinal; Sesquiterpenes; Stereoisomerism; Triterpenes; Tumor Cells, Cultured; Vietnam | 2003 |
New cytotoxic lupane triterpenoids from the twigs of Coussarea paniculata.
Topics: Antineoplastic Agents, Phytogenic; Drug Screening Assays, Antitumor; Female; Guyana; Humans; Inhibitory Concentration 50; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Ovarian Neoplasms; Plant Stems; Plants, Medicinal; Rubiaceae; Stereoisomerism; Triterpenes; Tumor Cells, Cultured | 2003 |
New 3-O-acyl betulinic acids from Strychnos vanprukii Craib.
Topics: Anti-HIV Agents; Antineoplastic Agents, Phytogenic; Betulinic Acid; Crystallography, X-Ray; Drug Screening Assays, Antitumor; Humans; Inhibitory Concentration 50; Molecular Structure; Pentacyclic Triterpenes; Plant Leaves; Plants, Medicinal; Stereoisomerism; Strychnos; Triterpenes; Tumor Cells, Cultured | 2004 |
Constituents of Senecio chionophilus with potential antitubercular activity.
Topics: Antitubercular Agents; Chile; Microbial Sensitivity Tests; Molecular Structure; Mycobacterium tuberculosis; Nuclear Magnetic Resonance, Biomolecular; Plant Roots; Plants, Toxic; Senecio; Sesquiterpenes; Stereoisomerism | 2004 |
Three new triterpenes from Nerium oleander and biological activity of the isolated compounds.
Topics: Anti-Inflammatory Agents, Non-Steroidal; Drug Screening Assays, Antitumor; Humans; Intercellular Adhesion Molecule-1; Japan; Models, Biological; Molecular Structure; Nerium; Oleanolic Acid; Plant Leaves; Plants, Medicinal; Triterpenes; Tumor Cells, Cultured | 2005 |
Antitrypanosomal activity of triterpenoids and sterols from the leaves of Strychnos spinosa and related compounds.
Topics: Animals; Benin; Cell Line, Tumor; Molecular Structure; Plant Leaves; Plants, Medicinal; Sterols; Stigmasterol; Structure-Activity Relationship; Strychnos; Triterpenes; Trypanocidal Agents; Trypanosoma brucei brucei | 2007 |
Naturally occurring pentacyclic triterpenes as inhibitors of glycogen phosphorylase: synthesis, structure-activity relationships, and X-ray crystallographic studies.
Topics: Adenosine Monophosphate; Allosteric Site; Animals; Binding Sites; Crystallography, X-Ray; Glycogen Phosphorylase; Hypoglycemic Agents; Kinetics; Models, Molecular; Muscles; Oleanolic Acid; Pentacyclic Triterpenes; Protein Binding; Protein Conformation; Rabbits; Stereoisomerism; Structure-Activity Relationship; Triterpenes | 2008 |
Purity-activity relationships of natural products: the case of anti-TB active ursolic acid.
Topics: Animals; Antitubercular Agents; Biological Products; Chlorocebus aethiops; Inhibitory Concentration 50; Molecular Structure; Mycobacterium tuberculosis; Structure-Activity Relationship; Triterpenes; Ursolic Acid; Vero Cells | 2008 |
Antiproliferative triterpenes from Melaleuca ericifolia.
Topics: Animals; Drug Screening Assays, Antitumor; Egypt; Melaleuca; Mice; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Plant Leaves; Plants, Medicinal; Triterpenes | 2008 |
Palbinone and triterpenes from Moutan Cortex (Paeonia suffruticosa, Paeoniaceae) stimulate glucose uptake and glycogen synthesis via activation of AMPK in insulin-resistant human HepG2 Cells.
Topics: AMP-Activated Protein Kinases; Cell Line, Tumor; Diabetes Mellitus, Type 2; Drugs, Chinese Herbal; Glucose; Glycogen; Glycogen Synthase Kinase 3; Glycogen Synthase Kinase 3 beta; Humans; Hypoglycemic Agents; Insulin Resistance; Paeonia; Phosphorylation; Terpenes; Triterpenes | 2009 |
Structure-activity relationship study of betulinic acid, a novel and selective TGR5 agonist, and its synthetic derivatives: potential impact in diabetes.
Topics: 3T3-L1 Cells; Animals; Betulinic Acid; CHO Cells; Cricetinae; Cricetulus; Male; Mice; Mice, Inbred C57BL; Molecular Conformation; Pentacyclic Triterpenes; Receptors, G-Protein-Coupled; Stereoisomerism; Structure-Activity Relationship; Triterpenes | 2010 |
Cytotoxic and NF-kappaB inhibitory constituents of Artocarpus rigida.
Topics: Antineoplastic Agents, Phytogenic; Artocarpus; Drug Screening Assays, Antitumor; Flavonoids; HT29 Cells; Humans; Indonesia; Molecular Structure; NF-kappa B; NF-kappa B p50 Subunit; Plant Stems; Stilbenes; Transcription Factor RelA | 2010 |
Identification of pentacyclic triterpenes derivatives as potent inhibitors against glycogen phosphorylase based on 3D-QSAR studies.
Topics: Animals; Enzyme Inhibitors; Glycogen Phosphorylase, Muscle Form; Models, Molecular; Molecular Conformation; Muscle, Skeletal; Pentacyclic Triterpenes; Quantitative Structure-Activity Relationship; Rabbits; Stereoisomerism | 2011 |
Selective inhibition of the tumor marker aldo-keto reductase family member 1B10 by oleanolic acid.
Topics: Aldehyde Reductase; Aldo-Keto Reductases; Antineoplastic Agents, Phytogenic; Drug Resistance, Neoplasm; HeLa Cells; HT29 Cells; Humans; Mitomycin; Models, Molecular; Molecular Structure; Mutation; Oleanolic Acid; Pentacyclic Triterpenes | 2011 |
Bryonolic acid transcriptional control of anti-inflammatory and antioxidant genes in macrophages in vitro and in vivo.
Topics: Animals; Anti-Inflammatory Agents; Antioxidants; Dose-Response Relationship, Drug; Heme Oxygenase-1; Lipopolysaccharides; Macrophages; Mice; Mice, Inbred C57BL; NF-E2-Related Factor 1; Nitric Oxide; Nitric Oxide Synthase Type II; Oleanolic Acid; Triterpenes | 2012 |
Identification of myricetin and scutellarein as novel chemical inhibitors of the SARS coronavirus helicase, nsP13.
Topics: Adenosine Triphosphate; Antiviral Agents; Apigenin; Breast; Cell Line; Cell Proliferation; Colorimetry; DNA; DNA Helicases; Epithelial Cells; Female; Flavonoids; Fluorescence Resonance Energy Transfer; Hepacivirus; Humans; Hydrolysis; Inhibitory Concentration 50; Kinetics; Methyltransferases; RNA Helicases; Severe acute respiratory syndrome-related coronavirus; Species Specificity; Viral Nonstructural Proteins; Viral Proteins | 2012 |
Exploration of natural compounds as sources of new bifunctional scaffolds targeting cholinesterases and beta amyloid aggregation: the case of chelerythrine.
Topics: Acetylcholinesterase; Amyloid beta-Peptides; Benzophenanthridines; Binding Sites; Butyrylcholinesterase; Catalytic Domain; Cholinesterase Inhibitors; Humans; Isoquinolines; Kinetics; Molecular Docking Simulation; Structure-Activity Relationship | 2012 |
Development of oleanane-type triterpenes as a new class of HCV entry inhibitors.
Topics: Animals; Antiviral Agents; Cell Line, Tumor; Cytotoxins; HEK293 Cells; Hemolytic Agents; Hepacivirus; Humans; Oleanolic Acid; Rabbits; Structure-Activity Relationship; Virus Internalization | 2013 |
Rat intestinal sucrase inhibition of constituents from the roots of Rosa rugosa Thunb.
Topics: Animals; Dose-Response Relationship, Drug; Enzyme Inhibitors; Intestine, Small; Molecular Conformation; Plant Roots; Rats; Rosa; Structure-Activity Relationship; Sucrase; Triterpenes | 2014 |
Chemical constituents from Eucalyptus citriodora Hook leaves and their glucose transporter 4 translocation activities.
Topics: Animals; Cell Line; Chalcones; Crystallography, X-Ray; Eucalyptus; Glucose Transporter Type 4; Models, Molecular; Molecular Structure; Plant Leaves; Rats; Xanthenes | 2014 |
Conjugation of a nonspecific antiviral sapogenin with a specific HIV fusion inhibitor: a promising strategy for discovering new antiviral therapeutics.
Topics: Amino Acid Sequence; Antiviral Agents; Cell Line; Cell Line, Tumor; Cell Survival; Enfuvirtide; HIV Envelope Protein gp41; HIV Fusion Inhibitors; HIV-1; Humans; Models, Chemical; Models, Molecular; Molecular Sequence Data; Molecular Structure; Peptide Fragments; Protein Structure, Secondary; Sapogenins; Structure-Activity Relationship | 2014 |
Synthesis and cytotoxic evaluation of novel ester-triazole-linked triterpenoid-AZT conjugates.
Topics: Araliaceae; Cytotoxins; Drug Evaluation, Preclinical; Eleutherococcus; Esters; Hep G2 Cells; Humans; Plant Extracts; Triazoles; Triterpenes; Zidovudine | 2014 |
Synthesis and biological evaluation of ring A and/or C expansion and opening echinocystic acid derivatives for anti-HCV entry inhibitors.
Topics: Antiviral Agents; Dose-Response Relationship, Drug; Hepacivirus; Microbial Sensitivity Tests; Molecular Structure; Oleanolic Acid; Structure-Activity Relationship | 2015 |
Discovery of α-mangostin as a novel competitive inhibitor against mutant isocitrate dehydrogenase-1.
Topics: Binding, Competitive; Drug Discovery; Humans; Isocitrate Dehydrogenase; MCF-7 Cells; Molecular Structure; Mutation; Recombinant Proteins; Structure-Activity Relationship; Xanthones | 2015 |
Targeting cancer cells with oleanolic and ursolic acid derived hydroxamates.
Topics: Antineoplastic Agents; Cell Line, Tumor; Cell Proliferation; Drug Screening Assays, Antitumor; HT29 Cells; Humans; Oleanolic Acid; Structure-Activity Relationship; Triterpenes; Ursolic Acid | 2016 |
Antiplasmodial phloroglucinol derivatives from Syncarpia glomulifera.
Topics: Antimalarials; Cell Survival; Dose-Response Relationship, Drug; HEK293 Cells; Humans; Malaria; Molecular Structure; Myrtaceae; Parasitic Sensitivity Tests; Phloroglucinol; Plant Bark; Plasmodium falciparum; Structure-Activity Relationship | 2016 |
Urea derivates of ursolic, oleanolic and maslinic acid induce apoptosis and are selective cytotoxic for several human tumor cell lines.
Topics: Animals; Apoptosis; Cell Line, Tumor; Cell Proliferation; Humans; Mice; NIH 3T3 Cells; Oleanolic Acid; Structure-Activity Relationship; Triterpenes; Ursolic Acid | 2016 |
Triterpene sapogenin-polyarginine conjugates exhibit promising antibacterial activity against Gram-positive strains.
Topics: Animals; Anti-Bacterial Agents; Gram-Positive Bacteria; Humans; Microbial Sensitivity Tests; Microscopy, Electron, Transmission; Molecular Structure; Peptides; Plasma; Sapogenins; Triterpenes | 2016 |
Rhodamine B conjugates of triterpenoic acids are cytotoxic mitocans even at nanomolar concentrations.
Topics: Animals; Apoptosis; Cell Line, Tumor; Dose-Response Relationship, Drug; Humans; Hydrophobic and Hydrophilic Interactions; Mice; Mitochondria; NIH 3T3 Cells; Rhodamines; Structure-Activity Relationship; Triterpenes | 2017 |
Natural product-inspired esters and amides of ferulic and caffeic acid as dual inhibitors of HIV-1 reverse transcriptase.
Topics: Amides; Anti-HIV Agents; Binding Sites; Caffeic Acids; Coumaric Acids; DNA-Directed DNA Polymerase; Esters; HIV Reverse Transcriptase; Plant Extracts; Ribonuclease H, Human Immunodeficiency Virus; Structure-Activity Relationship; Triterpenes | 2017 |
Discovery of pentacyclic triterpene 3β-ester derivatives as a new class of cholesterol ester transfer protein inhibitors.
Topics: Animals; Cholesterol Ester Transfer Proteins; Dose-Response Relationship, Drug; Drug Discovery; Esters; Guinea Pigs; Humans; Mice; Mice, Transgenic; Molecular Structure; Structure-Activity Relationship; Triterpenes | 2017 |
Pentacyclic triterpenes as α-glucosidase and α-amylase inhibitors: Structure-activity relationships and the synergism with acarbose.
Topics: Acarbose; alpha-Amylases; alpha-Glucosidases; Drug Synergism; Inhibitory Concentration 50; Kinetics; Oleanolic Acid; Pentacyclic Triterpenes; Structure-Activity Relationship; Triterpenes | 2017 |
Synthesis and antimycobacterial activity of triterpeni≿ A-ring azepanes.
Topics: Antitubercular Agents; Azepines; Dose-Response Relationship, Drug; Microbial Sensitivity Tests; Molecular Structure; Mycobacterium tuberculosis; Structure-Activity Relationship; Triterpenes | 2018 |
Cytotoxic and NF-κB and mitochondrial transmembrane potential inhibitory pentacyclic triterpenoids from Syzygium corticosum and their semi-synthetic derivatives.
Topics: Antineoplastic Agents, Phytogenic; Cell Line, Tumor; Cell Proliferation; HT29 Cells; Humans; Membrane Potential, Mitochondrial; Molecular Conformation; NF-kappa B; Plant Extracts; Plant Leaves; Structure-Activity Relationship; Syzygium; Triterpenes; Ursolic Acid | 2018 |
Sentulic acid isolated from Sandoricum koetjape Merr attenuates lipopolysaccharide and interferon gamma co-stimulated nitric oxide production in murine macrophage RAW264 cells.
Topics: Animals; Cyclooxygenase 2; Down-Regulation; Interferon-gamma; Interleukin-6; Lipopolysaccharides; Macrophages; Meliaceae; Mice; Nitric Oxide; Nitric Oxide Synthase Type II; RAW 264.7 Cells; Signal Transduction; Toll-Like Receptors; Triterpenes; Tumor Necrosis Factor-alpha | 2018 |
Triterpenoid Hydroxamates as HIF Prolyl Hydrolase Inhibitors.
Topics: Enzyme Inhibitors; HEK293 Cells; Humans; Hypoxia-Inducible Factor-Proline Dioxygenases; NF-kappa B; Triterpenes | 2018 |
Design, synthesis and cytotoxicity of BODIPY FL labelled triterpenoids.
Topics: Antineoplastic Agents; Boron Compounds; Cell Proliferation; Dose-Response Relationship, Drug; Drug Design; Drug Screening Assays, Antitumor; Fluorescent Dyes; Humans; MCF-7 Cells; Molecular Structure; Structure-Activity Relationship; Triterpenes | 2020 |
Optimized plant compound with potent anti-biofilm activity across gram-negative species.
Topics: Amines; Anti-Bacterial Agents; Biofilms; Dose-Response Relationship, Drug; Gram-Negative Bacteria; Microbial Sensitivity Tests; Molecular Structure; Structure-Activity Relationship | 2020 |
Chemical constituents of Callistemon citrinus from Egypt and their antiausterity activity against PANC-1 human pancreatic cancer cell line.
Topics: Antineoplastic Agents, Phytogenic; Cell Death; Cell Line, Tumor; Cell Proliferation; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; Egypt; Humans; Molecular Structure; Myrtaceae; Pancreatic Neoplasms; Structure-Activity Relationship; Terpenes; Tumor Microenvironment | 2020 |
Synthesis and anti-inflammatory activity of saponin derivatives of δ-oleanolic acid.
Topics: Acetyl-CoA Carboxylase; AMP-Activated Protein Kinases; Animals; Anti-Inflammatory Agents; Dose-Response Relationship, Drug; Glycyrrhizic Acid; Humans; Interleukin-6; Liver; Macrophages; Male; Medicine, Chinese Traditional; Mice; Mice, Inbred BALB C; Oleanolic Acid; Pentacyclic Triterpenes; Phosphorylation; Sapogenins; Saponins; Tumor Necrosis Factor-alpha | 2021 |
Tumor inhibitory agents from Vauquelinia corymbosa (Rosaceae).
Topics: Antineoplastic Agents, Phytogenic; Betulinic Acid; Pentacyclic Triterpenes; Plants, Medicinal; Triterpenes; Ursolic Acid | 1976 |
[Isolation and identification of chemical constituents from Hedyotis chrysotricha (Palib.) Merr].
Topics: Anti-Infective Agents; Antineoplastic Agents, Phytogenic; Betulinic Acid; Cyclopentane Monoterpenes; Drugs, Chinese Herbal; Glucosides; Pentacyclic Triterpenes; Pyrans; Triterpenes; Ursolic Acid | 1992 |
Investigations on the steroidal anti-inflammatory activity of triterpenoids from Diospyros leucomelas.
Topics: Animals; Anti-Inflammatory Agents; Betulinic Acid; Female; Mice; Pentacyclic Triterpenes; Plants, Medicinal; Steroids; Triterpenes; Ursolic Acid | 1995 |
Effect of selected triterpenoids on chronic dermal inflammation.
Topics: Animals; Anti-Inflammatory Agents; Betulinic Acid; Dermatitis, Contact; Dexamethasone; Drug Evaluation, Preclinical; Female; Mice; Oleanolic Acid; Pentacyclic Triterpenes; Tetradecanoylphorbol Acetate; Triterpenes; Ursolic Acid | 1997 |
In vitro and in vivo evaluation of betulinic acid as an antimalarial.
Topics: Animals; Antimalarials; Betulinic Acid; Disease Models, Animal; Euphorbiaceae; Malaria; Mice; Microbial Sensitivity Tests; Oleanolic Acid; Pentacyclic Triterpenes; Phytotherapy; Plant Extracts; Plant Roots; Plasmodium berghei; Plasmodium falciparum; Random Allocation; Structure-Activity Relationship; Triterpenes; Ursolic Acid | 1999 |
Cytotoxic triterpenes from stem bark of Physocarpus intermedius.
Topics: Antineoplastic Agents, Phytogenic; Betulinic Acid; Humans; Magnetic Resonance Spectroscopy; Oleanolic Acid; Pentacyclic Triterpenes; Plant Stems; Rosales; Triterpenes; Tumor Cells, Cultured; Ursolic Acid | 2000 |
Synthesis of combinatorial libraries based on terpenoid scaffolds.
Topics: Animals; Antimalarials; Betulinic Acid; Combinatorial Chemistry Techniques; Drug Evaluation, Preclinical; Indicators and Reagents; Oxidation-Reduction; Oximes; Pentacyclic Triterpenes; Plasmodium falciparum; Resins, Plant; Terpenes; Triterpenes; Ursolic Acid | 2002 |
Isolation, characterization and biological activity of betulinic acid and ursolic acid from Vitex negundo L.
Topics: Animals; Anti-Bacterial Agents; Bacillus subtilis; Betulinic Acid; Dose-Response Relationship, Drug; Escherichia coli; Feeding Behavior; Humans; Insecticides; Larva; Microbial Sensitivity Tests; Moths; Pentacyclic Triterpenes; Phytotherapy; Plant Extracts; Plant Leaves; Triterpenes; Ursolic Acid; Vitex | 2003 |
New ursolic and betulinic derivatives as potential cytotoxic agents.
Topics: Antineoplastic Agents; Betulinic Acid; Cell Survival; Drug Screening Assays, Antitumor; HT29 Cells; Humans; Inhibitory Concentration 50; Molecular Structure; Pentacyclic Triterpenes; Structure-Activity Relationship; Triterpenes; Ursolic Acid | 2003 |
Rapid analysis of triterpenic acids by liquid chromatography using porous graphitic carbon and evaporative light scattering detection.
Topics: Betulinic Acid; Carbon; Chromatography, Liquid; Glycyrrhetinic Acid; Light; Models, Chemical; Models, Molecular; Oleanolic Acid; Pentacyclic Triterpenes; Scattering, Radiation; Time Factors; Triterpenes; Ultraviolet Rays; Ursolic Acid | 2004 |
Apoptosis inducing activity of viscin, a lipophilic extract from Viscum album L.
Topics: Antineoplastic Agents, Phytogenic; Apoptosis; Betulinic Acid; Cell Line, Tumor; Cell Proliferation; Chromatography, High Pressure Liquid; Erythroblasts; Gas Chromatography-Mass Spectrometry; Humans; Indicators and Reagents; Leukemia, Lymphoid; Leukemia, Monocytic, Acute; Oleanolic Acid; Pentacyclic Triterpenes; Plant Extracts; Triterpenes; Ursolic Acid; Viscum | 2005 |
Antibacterial constituents from fruit bodies of ascomyce Bulgaria inquinans.
Topics: Anti-Bacterial Agents; Ascomycota; Betulinic Acid; China; Magnetic Resonance Spectroscopy; Pentacyclic Triterpenes; Phytosterols; Spectrometry, Mass, Electrospray Ionization; Triterpenes; Ursolic Acid | 2005 |
Human ACAT-1 and ACAT-2 inhibitory activities of pentacyclic triterpenes from the leaves of Lycopus lucidus TURCZ.
Topics: Animals; Betulinic Acid; Cell Line; Enzyme Inhibitors; Humans; Lycopus; Molecular Structure; Oleanolic Acid; Pentacyclic Triterpenes; Plant Leaves; Sterol O-Acyltransferase; Sterol O-Acyltransferase 2; Triterpenes; Ursolic Acid | 2006 |
Inhibition of Escherichia coli heat-labile enterotoxin-induced diarrhea by Chaenomeles speciosa.
Topics: 1-Butanol; Acetates; Animals; Antidiarrheals; Bacterial Toxins; Betulinic Acid; Diarrhea; Dose-Response Relationship, Drug; Enterotoxins; Enzyme-Linked Immunosorbent Assay; Escherichia coli Proteins; Female; Fruit; Immunoglobulin M; Mice; Mice, Inbred BALB C; Models, Molecular; Molecular Structure; Oleanolic Acid; Pentacyclic Triterpenes; Plant Extracts; Protein Binding; Protein Subunits; Rosaceae; Triterpenes; Ursolic Acid | 2007 |
Antimycobacterial activity of cinnamate-based esters of the triterpenes betulinic, oleanolic and ursolic acids.
Topics: Acetylation; Antitubercular Agents; Betulinic Acid; Cinnamates; Indicators and Reagents; Magnetic Resonance Spectroscopy; Methylation; Microbial Sensitivity Tests; Mycobacterium tuberculosis; Oleanolic Acid; Pentacyclic Triterpenes; Spectrometry, Mass, Fast Atom Bombardment; Spectroscopy, Fourier Transform Infrared; Triterpenes; Ursolic Acid | 2008 |
Efficient access to 2-isobetulinic acid, 2-isooleanolic acid, and 2-isoursolic acid.
Topics: Betulinic Acid; Molecular Conformation; Oleanolic Acid; Pentacyclic Triterpenes; Stereoisomerism; Triterpenes; Ursolic Acid | 2008 |
Ursolic, oleanolic and betulinic acids: antibacterial spectra and selectivity indexes.
Topics: Anti-Bacterial Agents; Betulinic Acid; Cell Line; Cell Survival; Drug Resistance, Bacterial; Eukaryotic Cells; Gram-Negative Bacteria; Gram-Positive Bacteria; Humans; Microbial Sensitivity Tests; Oleanolic Acid; Pentacyclic Triterpenes; Toxicity Tests; Triterpenes; Ursolic Acid | 2008 |
Pentacyclic triterpene distribution in various plants - rich sources for a new group of multi-potent plant extracts.
Topics: Betulinic Acid; Chromatography, Gas; Chromatography, High Pressure Liquid; Molecular Structure; Oleanolic Acid; Pentacyclic Triterpenes; Plant Extracts; Triterpenes; Ursolic Acid | 2009 |
Chemical composition of the stem bark and leaves of Ficus pandurata Hance.
Topics: Betulinic Acid; Ficus; Magnetic Resonance Spectroscopy; Molecular Structure; Oleanolic Acid; Pentacyclic Triterpenes; Plant Bark; Plant Leaves; Sitosterols; Spectrophotometry, Infrared; Spectrophotometry, Ultraviolet; Stigmasterol; Triterpenes; Ursolic Acid | 2009 |
Isolation of immunomodulatory triterpene acids from a standardized rose hip powder (Rosa canina L.).
Topics: Betulinic Acid; Cell Line; Cell Survival; Humans; Immunologic Factors; Interleukin-6; Oleanolic Acid; Pentacyclic Triterpenes; Plant Extracts; Rosa; Triterpenes; Ursolic Acid | 2011 |
[Studies on the triterpenoids of Vitex trifolia].
Topics: Betulinic Acid; Ethanol; Molecular Structure; Oleanolic Acid; Pentacyclic Triterpenes; Plants, Medicinal; Spectrophotometry, Infrared; Spectrophotometry, Ultraviolet; Triterpenes; Ursolic Acid; Vitex | 2010 |
Development of a new HPLC method with precolumn fluorescent derivatization for rapid, selective and sensitive detection of triterpenic acids in fruits.
Topics: Betulinic Acid; Chromatography, High Pressure Liquid; Fluorescent Dyes; Food Analysis; Fruit; Oleanolic Acid; Pentacyclic Triterpenes; Triterpenes; Ursolic Acid | 2011 |
CYP716A subfamily members are multifunctional oxidases in triterpenoid biosynthesis.
Topics: Amino Acid Sequence; Betulinic Acid; Biosynthetic Pathways; Cloning, Molecular; Cytochrome P-450 Enzyme System; Intramolecular Transferases; Medicago truncatula; Multienzyme Complexes; Oleanolic Acid; Pentacyclic Triterpenes; Phylogeny; Saccharomyces cerevisiae; Triterpenes; Ursolic Acid; Vitis | 2011 |
Triterpene acids from rose hip powder inhibit self-antigen- and LPS-induced cytokine production and CD4⁺ T-cell proliferation in human mononuclear cell cultures.
Topics: Acids; Autoantigens; B-Lymphocytes; Betulinic Acid; CD4-Positive T-Lymphocytes; Cell Proliferation; Cell Survival; Cells, Cultured; Dose-Response Relationship, Immunologic; Flow Cytometry; Humans; Immunologic Factors; Inhibitory Concentration 50; Interleukin-10; Lipopolysaccharides; Oleanolic Acid; Pentacyclic Triterpenes; Plant Preparations; Rosa; Thyroglobulin; Triterpenes; Tumor Necrosis Factor-alpha; Ursolic Acid | 2012 |
[Study on the chemical constituents of Leptopus chineseis].
Topics: Betulinic Acid; Euphorbiaceae; Magnetic Resonance Spectroscopy; Molecular Structure; Pentacyclic Triterpenes; Plants, Medicinal; Triterpenes; Ursolic Acid | 2011 |
Triterpenes from Callicarpa integerrima Champ.
Topics: Betulinic Acid; Callicarpa; Molecular Conformation; Molecular Structure; Oleanolic Acid; Pentacyclic Triterpenes; Plant Leaves; Plant Stems; Plants, Medicinal; Saponins; Triterpenes; Ursolic Acid | 2012 |
[Chemical constituents of Dolomiaea souliei].
Topics: 4-Butyrolactone; Asteraceae; Betulinic Acid; Emodin; Lactones; Pentacyclic Triterpenes; Sesquiterpenes; Triterpenes; Ursolic Acid | 2012 |
Bioactive oleanane, lupane and ursane triterpene acid derivatives.
Topics: Animals; Artemia; Betulinic Acid; Esters; Free Radical Scavengers; Lamiaceae; Nuclear Magnetic Resonance, Biomolecular; Oleanolic Acid; Pentacyclic Triterpenes; Plant Extracts; Triterpenes; Ursolic Acid | 2012 |
Synthesis and antiplasmodial activity of betulinic acid and ursolic acid analogues.
Topics: Antimalarials; Betulinic Acid; Erythrocytes; HEK293 Cells; Humans; Inhibitory Concentration 50; Parasitic Sensitivity Tests; Pentacyclic Triterpenes; Plasmodium falciparum; Triterpenes; Ursolic Acid | 2012 |
A simple GC-MS method for the screening of betulinic, corosolic, maslinic, oleanolic and ursolic acid contents in commercial botanicals used as food supplement ingredients.
Topics: Betulinic Acid; Dietary Supplements; Gas Chromatography-Mass Spectrometry; Oleanolic Acid; Pentacyclic Triterpenes; Plant Extracts; Plants; Triterpenes; Ursolic Acid | 2013 |
Two series of new semisynthetic triterpene derivatives: differences in anti-malarial activity, cytotoxicity and mechanism of action.
Topics: Antimalarials; Betulinic Acid; Cell Line; Cell Survival; Epithelial Cells; Humans; Pentacyclic Triterpenes; Plasmodium falciparum; Triterpenes; Ursolic Acid | 2013 |
Synthesis of isosteric triterpenoid derivatives and antifungal activity.
Topics: Antifungal Agents; Arthrodermataceae; Betulinic Acid; Microbial Sensitivity Tests; Pentacyclic Triterpenes; Triterpenes; Ursolic Acid; Yeasts | 2014 |
Anti-Trichomonas vaginalis activity from triterpenoid derivatives.
Topics: Antitrichomonal Agents; Betulinic Acid; Drug Resistance; Erythrocytes; Female; HeLa Cells; Hemolysis; Humans; Male; Metronidazole; Microbial Sensitivity Tests; Pentacyclic Triterpenes; Piperazine; Piperazines; Trichomonas vaginalis; Triterpenes; Ursolic Acid | 2014 |
Inhibition of estrogen signaling through depletion of estrogen receptor alpha by ursolic acid and betulinic acid from Prunella vulgaris var. lilacina.
Topics: Betulinic Acid; Breast Neoplasms; Cell Line, Tumor; Drug Evaluation, Preclinical; Estrogen Receptor alpha; Estrogen Receptor Modulators; Estrogens; Female; Humans; Male; MCF-7 Cells; Neoplasm Proteins; Pentacyclic Triterpenes; Phytotherapy; Plants, Medicinal; Promoter Regions, Genetic; Prostate-Specific Antigen; Prostatic Neoplasms; Prunella; RNA, Messenger; RNA, Neoplasm; Signal Transduction; Triterpenes; Ursolic Acid | 2014 |
RP-HPLC simultaneous estimation of betulinic acid and ursolic acid in Carissa spinarum.
Topics: Apocynaceae; Betulinic Acid; Chromatography, High Pressure Liquid; Molecular Structure; Pentacyclic Triterpenes; Plant Roots; Plants, Medicinal; Triterpenes; Ursolic Acid | 2014 |
Chemical constituents of gold-red apple and their α-glucosidase inhibitory activities.
Topics: alpha-Glucosidases; alpha-Linolenic Acid; Betulinic Acid; Fruit; Glycoside Hydrolase Inhibitors; Magnetic Resonance Spectroscopy; Malus; Oleanolic Acid; Pentacyclic Triterpenes; Spectrometry, Mass, Electrospray Ionization; Triterpenes; Ursolic Acid | 2014 |
Incorporation of pentacyclic triterpenes into mitochondrial membrane--studies on the interactions in model 2D lipid systems.
Topics: Betulinic Acid; Cardiolipins; Hydrogen Bonding; Mitochondrial Membranes; Models, Molecular; Pentacyclic Triterpenes; Phosphatidylcholines; Phosphatidylethanolamines; Thermodynamics; Triterpenes; Ursolic Acid | 2014 |
Anti-tumor activities of triterpenes from Syzygium kusukusense.
Topics: Antineoplastic Agents; Antineoplastic Agents, Phytogenic; Betulinic Acid; Cell Line, Tumor; Cell Survival; Humans; Pentacyclic Triterpenes; Plant Stems; Syzygium; Triterpenes; Ursolic Acid | 2014 |
Simultaneous determination of six triterpenic acids in some Chinese medicinal herbs using ultrasound-assisted dispersive liquid-liquid microextraction and high-performance liquid chromatography with fluorescence detection.
Topics: Betulinic Acid; Chromatography, High Pressure Liquid; Fluorescence; Limit of Detection; Liquid Phase Microextraction; Medicine, Chinese Traditional; Oleanolic Acid; Pentacyclic Triterpenes; Plants, Medicinal; Solvents; Triterpenes; Ultrasonics; Ursolic Acid | 2015 |
Quantitative determination of three pentacyclic triterpenes from five Swertia L. species endemic to Western Ghats, India, using RP-HPLC analysis.
Topics: Betulinic Acid; Chromatography, High Pressure Liquid; India; Molecular Structure; Oleanolic Acid; Pentacyclic Triterpenes; Plants, Medicinal; Species Specificity; Swertia; Triterpenes; Ursolic Acid | 2015 |
Sesqui- and triterpenoids from the liverwort Lepidozia chordulifera inhibitors of bacterial biofilm and elastase activity of human pathogenic bacteria.
Topics: Betulinic Acid; Biofilms; Enzyme Inhibitors; Hepatophyta; Molecular Structure; Pancreatic Elastase; Pentacyclic Triterpenes; Pseudomonas aeruginosa; Quorum Sensing; Sesquiterpenes; Staphylococcus aureus; Structure-Activity Relationship; Terpenes; Triterpenes; Ursolic Acid | 2015 |
α-Glucosidase Inhibitors from Vauquelinia corymbosa.
Topics: Betulinic Acid; Glycoside Hydrolase Inhibitors; Inhibitory Concentration 50; Molecular Docking Simulation; Pentacyclic Triterpenes; Plant Extracts; Rosaceae; Triterpenes; Ursolic Acid | 2015 |
[Study on Chemical Composition of Phyllanthus emblica].
Topics: Betulinic Acid; Gallic Acid; Oleanolic Acid; Pentacyclic Triterpenes; Phyllanthus emblica; Phytochemicals; Plants, Medicinal; Quercetin; Rutin; Triterpenes; Ursolic Acid | 2015 |
Determination of betulinic acid, oleanolic acid and ursolic acid from Achyranthes aspera L. using RP-UFLC-DAD analysis and evaluation of various parameters for their optimum yield.
Topics: Achyranthes; Betulinic Acid; Chromatography, Reverse-Phase; Oleanolic Acid; Pentacyclic Triterpenes; Triterpenes; Ursolic Acid | 2016 |
Antimycobacterial triterpenes from the Canadian medicinal plant Sarracenia purpurea.
Topics: Anti-Bacterial Agents; Betulinic Acid; Carbon-13 Magnetic Resonance Spectroscopy; Mass Spectrometry; Methanol; Microbial Sensitivity Tests; Mycobacterium tuberculosis; Pentacyclic Triterpenes; Phytotherapy; Plant Extracts; Plants, Medicinal; Proton Magnetic Resonance Spectroscopy; Sarraceniaceae; Solvents; Triterpenes; Ursolic Acid | 2016 |
[Chemical Constituents from Camellia oleifera Stem].
Topics: Betulinic Acid; Camellia; Drugs, Chinese Herbal; Flavonoids; Furans; Lignans; Oleanolic Acid; Pentacyclic Triterpenes; Phytochemicals; Plant Stems; Plants, Medicinal; Triterpenes; Ursolic Acid | 2015 |
Larvicidal activity of natural and modified triterpenoids against Aedes aegypti (Diptera: Culicidae).
Topics: Aedes; Animals; Betulinic Acid; Dengue; Diflubenzuron; Insect Vectors; Insecticides; Larva; Pentacyclic Triterpenes; Triterpenes; Ursolic Acid | 2016 |
Synthesis, structural studies, and cytotoxic evaluation of novel ursolic acid hybrids with capabilities to arrest breast cancer cells in mitosis.
Topics: Betulinic Acid; Cell Cycle; Click Chemistry; Drug Screening Assays, Antitumor; Female; Humans; Mitosis; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Pentacyclic Triterpenes; Triazoles; Triterpenes; Ursolic Acid | 2017 |
Ursolic acid-mediated changes in glycolytic pathway promote cytotoxic autophagy and apoptosis in phenotypically different breast cancer cells.
Topics: Apoptosis; Autophagy; Betulinic Acid; Breast Neoplasms; Cell Line, Tumor; DNA Damage; Extracellular Signal-Regulated MAP Kinases; Female; G1 Phase Cell Cycle Checkpoints; Glycolysis; Humans; Models, Biological; Nitrosation; Oxidative Stress; Pentacyclic Triterpenes; Phenotype; Signal Transduction; Triterpenes; Ursolic Acid | 2017 |
Phytochemical-induced nucleolar stress results in the inhibition of breast cancer cell proliferation.
Topics: Antineoplastic Agents, Phytogenic; Betulinic Acid; Breast Neoplasms; Cell Line, Tumor; Cell Nucleolus; Cell Proliferation; Cell Survival; Female; Gene Expression Regulation, Neoplastic; Humans; Isothiocyanates; MCF-7 Cells; Pentacyclic Triterpenes; Protein Carbonylation; Sulfoxides; Superoxides; Triterpenes; Ursolic Acid | 2017 |
Triterpenoids Isolated from Ziziphus jujuba Enhance Glucose Uptake Activity in Skeletal Muscle Cells.
Topics: Animals; Betulinic Acid; Carbohydrate Metabolism; Cell Survival; Cells, Cultured; Glucose; Muscle Fibers, Skeletal; Pentacyclic Triterpenes; Plant Extracts; Rats; Triterpenes; Ursolic Acid; Ziziphus | 2017 |
Influence of oxidative stress on the antibacterial activity of betulin, betulinic acid and ursolic acid.
Topics: Anti-Bacterial Agents; Betulinic Acid; DNA Fragmentation; Escherichia coli; Glutathione; Malondialdehyde; Microbial Sensitivity Tests; Oxidative Stress; Pentacyclic Triterpenes; Pseudomonas aeruginosa; Reactive Oxygen Species; Staphylococcus aureus; Triterpenes; Ursolic Acid | 2017 |
Antimicrobial Mechanism of Oleanolic and Ursolic Acids on Streptococcus mutans UA159.
Topics: Anti-Bacterial Agents; Bacterial Proteins; Betulinic Acid; Gene Expression Regulation, Bacterial; Oleanolic Acid; Pentacyclic Triterpenes; Streptococcus mutans; Triterpenes; Ursolic Acid | 2018 |
Anti-Proliferative Activity of Triterpenoids and Sterols Isolated from Alstonia scholaris against Non-Small-Cell Lung Carcinoma Cells.
Topics: A549 Cells; Alstonia; Antineoplastic Agents; Betulinic Acid; Carcinoma, Non-Small-Cell Lung; Cell Proliferation; Humans; Lung Neoplasms; Pentacyclic Triterpenes; Phytosterols; Plant Extracts; Plant Leaves; Sterols; Tetrazolium Salts; Thiazoles; Triterpenes; Ursolic Acid | 2017 |
Betulinic, oleanolic and ursolic acids inhibit the enzymatic and biological effects induced by a P-I snake venom metalloproteinase.
Topics: Animals; Betulinic Acid; Bothrops; Crotalid Venoms; Edema; Hemorrhage; Metalloproteases; Mice; Molecular Structure; Muscular Diseases; Oleanolic Acid; Pentacyclic Triterpenes; Triterpenes; Ursolic Acid | 2018 |
Study of isomeric pentacyclic triterpene acids in traditional Chinese medicine of Forsythiae Fructus and their binding constants with β-cyclodextrin by capillary electrophoresis.
Topics: beta-Cyclodextrins; Betulinic Acid; Drugs, Chinese Herbal; Electrophoresis, Capillary; Forsythia; Fruit; Isomerism; Molecular Structure; Oleanolic Acid; Pentacyclic Triterpenes; Structure-Activity Relationship; Thermodynamics; Triterpenes; Ursolic Acid | 2018 |
[Chemical Constituents from Rubus stans].
Topics: Betulinic Acid; Kaempferols; Pentacyclic Triterpenes; Rubus; Sitosterols; Triterpenes; Ursolic Acid | 2016 |
Ethylenediamine Derived Carboxamides of Betulinic and Ursolic Acid as Potential Cytotoxic Agents.
Topics: Betulinic Acid; Cell Proliferation; Cytotoxins; Drug Screening Assays, Antitumor; Ethylenediamines; HT29 Cells; Humans; Molecular Structure; Pentacyclic Triterpenes; Structure-Activity Relationship; Triterpenes; Ursolic Acid | 2018 |
Effect of an anxiolytic botanical containing Souroubea sympetala and Platanus occidentalis on in-vitro diazepam human cytochrome P450-mediated metabolism.
Topics: Anti-Anxiety Agents; Betulinic Acid; Chromatography, High Pressure Liquid; Cytochrome P-450 Enzyme System; Diazepam; Humans; Microsomes, Liver; Pentacyclic Triterpenes; Plant Extracts; Plant Leaves; Triterpenes; Ursolic Acid | 2019 |
Quantification of three triterpenic acids in dried rosemary using HPLC-fluorescence detection and 4-(4,5-diphenyl-1H-imidazole-2-yl)benzoyl chloride derivatization.
Topics: Benzoates; Betulinic Acid; Calibration; Chromatography, High Pressure Liquid; Fluorescence; Food Analysis; Imidazoles; Limit of Detection; Oleanolic Acid; Pentacyclic Triterpenes; Reproducibility of Results; Rosmarinus; Temperature; Triterpenes; Ursolic Acid | 2019 |
Triterpene Derivatives as Relevant Scaffold for New Antibiofilm Drugs.
Topics: Animals; Anti-Bacterial Agents; Betulinic Acid; Biofilms; Chlorocebus aethiops; Dose-Response Relationship, Drug; Enterococcus faecalis; Microbial Sensitivity Tests; Molecular Conformation; Pentacyclic Triterpenes; Staphylococcus aureus; Staphylococcus epidermidis; Structure-Activity Relationship; Triterpenes; Ursolic Acid; Vero Cells | 2019 |
A new pentacyclic triterpenoid from the leaves of
Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Betulinic Acid; Drug Evaluation, Preclinical; Lipopolysaccharides; Mice; Molecular Structure; Nitric Oxide; Oleanolic Acid; Pentacyclic Triterpenes; Plant Extracts; Plant Leaves; RAW 264.7 Cells; Rhododendron; Triterpenes; Ursolic Acid | 2020 |
Antimicrobial properties of amine- and guanidine-functionalized derivatives of betulinic, ursolic and oleanolic acids: Synthesis and structure/activity evaluation.
Topics: Acinetobacter baumannii; Anti-Bacterial Agents; Antifungal Agents; Betulinic Acid; Candida albicans; Cell Survival; Cryptococcus neoformans; Dose-Response Relationship, Drug; Escherichia coli; HEK293 Cells; Humans; Methicillin-Resistant Staphylococcus aureus; Microbial Sensitivity Tests; Molecular Structure; Oleanolic Acid; Pentacyclic Triterpenes; Pseudomonas aeruginosa; Structure-Activity Relationship; Triterpenes; Ursolic Acid | 2020 |
A Highly Active Triterpene Derivative Capable |of Biofilm Damage to Control
Topics: Betulinic Acid; Biofilms; Cell Line; Cryptococcosis; Cryptococcus neoformans; Drug Resistance, Fungal; Humans; Microbial Sensitivity Tests; Molecular Structure; Pentacyclic Triterpenes; Triterpenes; Ursolic Acid | 2019 |
Triple Negative Breast Cancer and Breast Epithelial Cells Differentially Reprogram Glucose and Lipid Metabolism upon Treatment with Triterpenic Acids.
Topics: Betulinic Acid; Breast; Cell Cycle; Cell Line, Tumor; Cell Survival; Citric Acid Cycle; Epithelial Cells; Female; Glucose; Glycolysis; Hexosamines; Humans; Lipid Metabolism; Magnetic Resonance Spectroscopy; Metabolome; Metabolomics; Pentacyclic Triterpenes; Triple Negative Breast Neoplasms; Triterpenes; Ursolic Acid | 2020 |
Ursolic and betulinic semisynthetic derivatives show activity against CQ-resistant Plasmodium falciparum isolated from Amazonia.
Topics: Antimalarials; Betulinic Acid; Binding Sites; Brazil; Chloroquine; DNA Topoisomerases, Type II; Drug Resistance; Life Cycle Stages; Molecular Docking Simulation; Pentacyclic Triterpenes; Plasmodium falciparum; Protozoan Proteins; Structure-Activity Relationship; Triterpenes; Ursolic Acid | 2021 |
Olive-Derived Triterpenes Suppress SARS COV-2 Main Protease: A Promising Scaffold for Future Therapeutics.
Topics: Antiviral Agents; Betulinic Acid; Coronavirus 3C Proteases; COVID-19; COVID-19 Drug Treatment; Humans; Molecular Docking Simulation; Molecular Dynamics Simulation; Olea; Pentacyclic Triterpenes; Protease Inhibitors; SARS-CoV-2; Triterpenes; Ursolic Acid | 2021 |