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For: Olajide OA, Ajayi AM, Wright CW. Anti-inflammatory properties of cryptolepine: ANTI-INFLAMMATORY PROPERTIES OF CRYPTOLEPINE. Phytother Res 2009;23:1421-5. [DOI: 10.1002/ptr.2794] [Cited by in Crossref: 41] [Cited by in F6Publishing: 45] [Article Influence: 2.9] [Reference Citation Analysis]
Number Citing Articles
1 Tudu CK, Bandyopadhyay A, Kumar M, Radha, Das T, Nandy S, Ghorai M, Gopalakrishnan AV, Proćków J, Dey A. Unravelling the pharmacological properties of cryptolepine and its derivatives: a mini-review insight. Naunyn Schmiedebergs Arch Pharmacol 2023;396:229-38. [PMID: 36251044 DOI: 10.1007/s00210-022-02302-7] [Reference Citation Analysis]
2 Falanga AP, Terracciano M, Oliviero G, Roviello GN, Borbone N. Exploring the Relationship between G-Quadruplex Nucleic Acids and Plants: From Plant G-Quadruplex Function to Phytochemical G4 Ligands with Pharmaceutic Potential. Pharmaceutics 2022;14:2377. [DOI: 10.3390/pharmaceutics14112377] [Reference Citation Analysis]
3 He Y, Chu Q, Zhang S, Guo L, Ma Y, Zhang B, Zhang Z, Zhao W, Hu Y, Yang C, Du S, Wu T, Liu Y. Discovery of cryptolepine derivatives as novel promising agents against phytopathogenic bacteria. Front Chem Sci Eng . [DOI: 10.1007/s11705-022-2196-5] [Reference Citation Analysis]
4 Chu QR, He YH, Tang C, Zhang ZJ, Luo XF, Zhang BQ, Zhou Y, Wu TL, Du SS, Yang CJ, Liu YQ. Design, Synthesis, and Antimicrobial Activity of Quindoline Derivatives Inspired by the Cryptolepine Alkaloid. J Agric Food Chem 2022. [PMID: 35226498 DOI: 10.1021/acs.jafc.1c07536] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
5 Nyerges M, Biró K, Tatai J, Pollák B, Molnár M. Microwave-Induced One Step Synthesis of Structurally Diverse Linear Indoloquinolines: Concise Synthesis of Norneocryptolepine. HETEROCYCLES 2022;104:1745. [DOI: 10.3987/com-22-14718] [Reference Citation Analysis]
6 Mante PK, Adomako NO, Antwi P, Kusi-Boadum NK. Chronic administration of cryptolepine nanoparticle formulation alleviates seizures in a neurocysticercosis model. Curr Res Pharmacol Drug Discov 2021;2:100040. [PMID: 34909669 DOI: 10.1016/j.crphar.2021.100040] [Reference Citation Analysis]
7 Ahmed RH, Galaly SR, Moustafa N, Ahmed RR, Ali TM, Elesawy BH, Ahmed OM, Abdul-Hamid M. Curcumin and Mesenchymal Stem Cells Ameliorate Ankle, Testis, and Ovary Deleterious Histological Changes in Arthritic Rats via Suppression of Oxidative Stress and Inflammation. Stem Cells Int 2021;2021:3516834. [PMID: 34795765 DOI: 10.1155/2021/3516834] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
8 Rodphon W, Laohapaisan P, Supantanapong N, Reamtong O, Ngiwsara L, Lirdprapamongkol K, Thongsornkleeb C, Khunnawutmanotham N, Tummatorn J, Svasti J, Ruchirawat S. Synthesis of Isocryptolepine-Triazole Adducts and Evaluation of Their Cytotoxic Activity. ChemMedChem 2021. [PMID: 34610210 DOI: 10.1002/cmdc.202100554] [Reference Citation Analysis]
9 Domfeh S, Narkwa P, Quaye O, Kusi K, Rivera O, Danaah M, Musah B, Awandare G, Mensah K, Mutocheluh M. Cryptolepine and Nibima inhibit hepatitis B virus replication. Scientific African 2021;13:e00942. [DOI: 10.1016/j.sciaf.2021.e00942] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
10 Chowdhury S, Bhuiya S, Das S. Comparative binding studies on the interaction of the indoloquinoline alkaloid cryptolepine with the B and the non-canonical protonated form of DNA: A spectroscopic insight. Biochim Biophys Acta Gen Subj 2021;1865:129993. [PMID: 34453987 DOI: 10.1016/j.bbagen.2021.129993] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
11 Domfeh SA, Narkwa PW, Quaye O, Kusi KA, Awandare GA, Ansah C, Salam A, Mutocheluh M. Cryptolepine inhibits hepatocellular carcinoma growth through inhibiting interleukin-6/STAT3 signalling. BMC Complement Med Ther 2021;21:161. [PMID: 34078370 DOI: 10.1186/s12906-021-03326-x] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
12 Chen YJ, Liu H, Zhang SY, Li H, Ma KY, Liu YQ, Yin XD, Zhou R, Yan YF, Wang RX, He YH, Chu QR, Tang C. Design, Synthesis, and Antifungal Evaluation of Cryptolepine Derivatives against Phytopathogenic Fungi. J Agric Food Chem 2021;69:1259-71. [PMID: 33496176 DOI: 10.1021/acs.jafc.0c06480] [Cited by in Crossref: 19] [Cited by in F6Publishing: 22] [Article Influence: 9.5] [Reference Citation Analysis]
13 Bai R, Yao C, Zhong Z, Ge J, Bai Z, Ye X, Xie T, Xie Y. Discovery of natural anti-inflammatory alkaloids: Potential leads for the drug discovery for the treatment of inflammation. Eur J Med Chem 2021;213:113165. [PMID: 33454546 DOI: 10.1016/j.ejmech.2021.113165] [Cited by in Crossref: 25] [Cited by in F6Publishing: 26] [Article Influence: 12.5] [Reference Citation Analysis]
14 Shnyder SD, Wright CW. Recent Advances in the Chemistry and Pharmacology of Cryptolepine. Prog Chem Org Nat Prod 2021;115:177-203. [PMID: 33797643 DOI: 10.1007/978-3-030-64853-4_4] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
15 Olajide OA, Sarker SD. Alzheimer's disease: natural products as inhibitors of neuroinflammation. Inflammopharmacology 2020;28:1439-55. [PMID: 32930914 DOI: 10.1007/s10787-020-00751-1] [Cited by in Crossref: 20] [Cited by in F6Publishing: 24] [Article Influence: 6.7] [Reference Citation Analysis]
16 Mensah-kane P, Mensah KB, Antwi AO, Forkuo AD, Ansah C. Cryptolepine, the major alkaloid of Cryptolepis sanguinolenta (Lindl.) Schlechter (Apocynaceae), attenuates early and late-phase symptoms of asthma. Scientific African 2020;9:e00540. [DOI: 10.1016/j.sciaf.2020.e00540] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
17 Batiha GE, Beshbishy AM, Alkazmi LM, Nadwa EH, Rashwan EK, Yokoyama N, Igarashi I. In vitro and in vivo growth inhibitory activities of cryptolepine hydrate against several Babesia species and Theileria equi. PLoS Negl Trop Dis 2020;14:e0008489. [PMID: 32853247 DOI: 10.1371/journal.pntd.0008489] [Cited by in Crossref: 6] [Cited by in F6Publishing: 9] [Article Influence: 2.0] [Reference Citation Analysis]
18 Allijn IE, Brinkhuis RP, Storm G, Schiffelers RM. Anti-Inflammatory Properties of Plant Derived Natural Products - A Systematic Review. Curr Med Chem 2019;26:4506-36. [PMID: 31119997 DOI: 10.2174/0929867325666190523123357] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 2.0] [Reference Citation Analysis]
19 Mensah KB, Benneh C, Forkuo AD, Ansah C. Cryptolepine, the Main Alkaloid of the Antimalarial Cryptolepis sanguinolenta (Lindl.) Schlechter, Induces Malformations in Zebrafish Embryos. Biochem Res Int 2019;2019:7076986. [PMID: 31360547 DOI: 10.1155/2019/7076986] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 0.8] [Reference Citation Analysis]
20 Ameyaw EO, Asmah KB, Biney RP, Henneh IT, Owusu-Agyei P, Prah J, Forkuo AD. Isobolographic analysis of co-administration of two plant-derived antiplasmodial drug candidates, cryptolepine and xylopic acid, in Plasmodium berghei. Malar J 2018;17:153. [PMID: 29618354 DOI: 10.1186/s12936-018-2283-8] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 1.4] [Reference Citation Analysis]
21 Osafo N, Mensah KB, Yeboah OK. Phytochemical and Pharmacological Review of Cryptolepis sanguinolenta (Lindl.) Schlechter. Adv Pharmacol Sci 2017;2017:3026370. [PMID: 29750083 DOI: 10.1155/2017/3026370] [Cited by in Crossref: 22] [Cited by in F6Publishing: 25] [Article Influence: 3.7] [Reference Citation Analysis]
22 Wang W, Yin R, Zhang M, Yu R, Hao C, Zhang L, Jiang T. Boronic Acid Modifications Enhance the Anti-Influenza A Virus Activities of Novel Quindoline Derivatives. J Med Chem 2017;60:2840-52. [PMID: 28267329 DOI: 10.1021/acs.jmedchem.6b00326] [Cited by in Crossref: 24] [Cited by in F6Publishing: 24] [Article Influence: 4.0] [Reference Citation Analysis]
23 Dey A, Mukherjee A, Chaudhury M. Alkaloids From Apocynaceae. Studies in Natural Products Chemistry 2017. [DOI: 10.1016/b978-0-444-63931-8.00010-2] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 2.0] [Reference Citation Analysis]
24 Pal HC, Katiyar SK. Cryptolepine, a Plant Alkaloid, Inhibits the Growth of Non-Melanoma Skin Cancer Cells through Inhibition of Topoisomerase and Induction of DNA Damage. Molecules 2016;21:E1758. [PMID: 28009843 DOI: 10.3390/molecules21121758] [Cited by in Crossref: 29] [Cited by in F6Publishing: 31] [Article Influence: 4.1] [Reference Citation Analysis]
25 References. Anti-Diabetes Mellitus Plants 2016. [DOI: 10.1201/9781315368115-8] [Reference Citation Analysis]
26 He YH, Li Z, Ni MM, Zhang XY, Li MF, Meng XM, Huang C, Li J. Cryptolepine derivative-6h inhibits liver fibrosis in TGF-β1-induced HSC-T6 cells by targeting the Shh pathway. Can J Physiol Pharmacol 2016;94:987-95. [PMID: 27295431 DOI: 10.1139/cjpp-2016-0157] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 1.0] [Reference Citation Analysis]
27 Forkuo AD, Ansah C, Boadu KM, Boampong JN, Ameyaw EO, Gyan BA, Arku AT, Ofori MF. Synergistic anti-malarial action of cryptolepine and artemisinins. Malar J 2016;15:89. [PMID: 26879905 DOI: 10.1186/s12936-016-1137-5] [Cited by in Crossref: 21] [Cited by in F6Publishing: 23] [Article Influence: 3.0] [Reference Citation Analysis]
28 Koninti RK, Sappati S, Satpathi S, Gavvala K, Hazra P. Spectroscopy and Dynamics of Cryptolepine in the Nanocavity of Cucurbit[7]uril and DNA. ChemPhysChem 2016;17:506-15. [DOI: 10.1002/cphc.201501011] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 1.6] [Reference Citation Analysis]
29 Sidoryk K, Jaromin A, Edward JA, Świtalska M, Stefańska J, Cmoch P, Zagrodzka J, Szczepek W, Peczyńska-Czoch W, Wietrzyk J, Kozubek A, Zarnowski R, Andes DR, Kaczmarek Ł. Searching for new derivatives of neocryptolepine: synthesis, antiproliferative, antimicrobial and antifungal activities. Eur J Med Chem 2014;78:304-13. [PMID: 24686017 DOI: 10.1016/j.ejmech.2014.03.060] [Cited by in Crossref: 19] [Cited by in F6Publishing: 20] [Article Influence: 2.1] [Reference Citation Analysis]
30 Suyenaga ES, Klein-júnior LC, Passos CDS, Marin R, Santin JR, Machado ID, Farsky SHP, Henriques AT. Beyond Organoleptic Characteristics: The Pharmacological Potential of Flavonoids and their Role in Leukocyte Migration and in L -Selectin and β2-Integrin Expression During Inflammation: EFFECT OF FLAVONOIDS ON LEUKOCYTE MIGRATION. Phytother Res 2014;28:1406-11. [DOI: 10.1002/ptr.5144] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 1.1] [Reference Citation Analysis]
31 Pozzatti P, dos Reis GO, Pereira DF, Horst H, Espindola L, Heller M, Micke GA, Pizzolatti MG, Fröde TS. Relationship of chemical structure and anti-inflammatory activity of dihydrocorynantheol and its analogues. Pharmacological Reports 2013;65:1263-71. [DOI: 10.1016/s1734-1140(13)71484-1] [Reference Citation Analysis]
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33 Olajide OA, Bhatia HS, de Oliveira AC, Wright CW, Fiebich BL. Inhibition of Neuroinflammation in LPS-Activated Microglia by Cryptolepine. Evid Based Complement Alternat Med 2013;2013:459723. [PMID: 23737832 DOI: 10.1155/2013/459723] [Cited by in Crossref: 35] [Cited by in F6Publishing: 40] [Article Influence: 3.5] [Reference Citation Analysis]
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36 Kuntworbe N, Al-Kassas R. Design and in vitro haemolytic evaluation of cryptolepine hydrochloride-loaded gelatine nanoparticles as a novel approach for the treatment of malaria. AAPS PharmSciTech 2012;13:568-81. [PMID: 22477022 DOI: 10.1208/s12249-012-9775-6] [Cited by in Crossref: 22] [Cited by in F6Publishing: 25] [Article Influence: 2.0] [Reference Citation Analysis]
37 Meng J, Yu S, Wan S, Ren S, Jiang T. Synthesis, Saccharide-Binding and Anti-cancer Cell Proliferation Properties of Arylboronic Acid Derivatives of Indoquinolines: Bioactivity of Arylboronic Acid Derivatives of Indoquinolines. Chemical Biology & Drug Design 2011;78:816-25. [DOI: 10.1111/j.1747-0285.2011.01196.x] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.4] [Reference Citation Analysis]
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41 Ansah C, Boadu Mens K, Woode E, Duwiejua M. Reproductive and Developmental Toxicity of Cryptolepis sanguinolenta in Mice. Research J of Pharmacology 2010;4:9-14. [DOI: 10.3923/rjpharm.2010.9.14] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.3] [Reference Citation Analysis]