Research graph
References from A review and in silico screening of plant-derived snake venom/toxin inhibitors: ADMET, drug-likeness, and medicinal chemistry profiling. Local targets link to admitted publications; unresolved targets remain external evidence.
Plant-Derived Toxin Inhibitors as Potential Candidates to Complement Antivenom Treatment in Snakebite Envenomations
10.3389/fimmu.2022.842576 · 2022 · External reference
Strategy for a globally coordinated response to a priority neglected tropical disease: Snakebite envenoming
10.1371/journal.pntd.0007059 · 2019 · External reference
Human-snake conflict patterns in a dense urban-forest mosaic landscape
2019 · External reference
Snakebite envenomation turns again into a neglected tropical disease!
10.1186/s40409-017-0127-6 · 2017 · External reference
Identifying the snake: First scoping review on practices of communities and healthcare providers confronted with snakebite across the world
10.1371/journal.pone.0229989 · 2020 · External reference
Snakebite envenoming
10.1038/nrdp.2017.79 · 2017 · External reference
Snakebite is Under Appreciated: Appraisal of Burden from West Africa
10.1371/journal.pntd.0004088 · 2015 · External reference
Bothrops Snakebite Envenomings in the Amazon Region
10.1007/s40475-020-00203-4 · 2020 · External reference
The Search for Natural and Synthetic Inhibitors That Would Complement Antivenoms as Therapeutics for Snakebite Envenoming
10.3390/toxins13070451 · 2021 · External reference
Unresolved reference
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Plant extracts and terpenes with antivenom properties
2024 · External reference
10.3389/fimmu.2022.842576
10.3389/fimmu.2022.842576 · External reference
DFT, molecular docking, and ADME/Tox screening investigations of market-available drugs against SARS-CoV-2
2021 · External reference
Molecular docking and ADMET study of bioactive compounds of Glycyrrhiza glabra against main protease of SARS-CoV2
10.1016/j.matpr.2020.10.055 · 2022 · External reference
Alkaloids Isolated from Vepris glandulosa with Antidiabetic Properties: An In Vitro and In Silico Analysis
External reference
Prediction of potential inhibitors of SARS-CoV-2 using 3D-QSAR, molecular docking modeling and ADMET properties
10.1016/j.heliyon.2021.e06603 · 2021 · External reference
Phytochemistry of plants in the genus Vepris: A review and in silico analysis of their ADMET properties
10.1016/j.sajb.2023.03.057 · 2023 · External reference
Plants and Phytocompounds Active Against Bothrops Venoms
10.2174/1568026619666190723153925 · 2019 · External reference
The PRISMA 2020 statement: an updated guideline for reporting systematic reviews
2021 · External reference
The application of in silico drug-likeness predictions in pharmaceutical research
10.1016/j.addr.2015.01.009 · 2015 · External reference
ADMET modeling approaches in drug discovery
10.1016/j.drudis.2019.03.015 · 2019 · External reference
Open access in silico tools to predict the ADMET profiling of drug candidates
10.1080/17460441.2020.1798926 · 2020 · External reference
Amplification of Snake Venom Toxicity by Endogenous Signaling Pathways
10.3390/toxins12020068 · 2020 · External reference
Vipers of Major clinical relevance in Europe: Taxonomy, venom composition, toxicology and clinical management of human bites
10.1016/j.tox.2021.152724 · 2021 · External reference
Present and future of snake venom proteomics profiling
10.1201/9780429054204-3 · 2021 · External reference
The Influence of the Different Disposition Characteristics of Snake Toxins on the Pharmacokinetics of Snake Venom
10.3390/toxins12030188 · 2020 · External reference
A Review and Database of Snake Venom Proteomes
10.3390/toxins9090290 · 2017 · External reference
Activation of Bothrops jararaca snake venom gland and venom production: a proteomic approach
10.1016/j.jprot.2013.10.026 · 2013 · External reference
Multifunctional toxins in snake venoms and therapeutic implications: from pain to hemorrhage and necrosis
10.3389/fevo.2019.00218 · 2019 · External reference
Computational Studies of Snake Venom Toxins
10.3390/toxins10010008 · 2017 · External reference
Activity of silver nanoparticles on prokaryotic cells and Bothrops jararacussu snake venom
10.1080/01480545.2018.1478850 · 2019 · External reference
Bothrops atrox, the most important snake involved in human envenomings in the amazon: How venomics contributes to the knowledge of snake biology and clinical toxinology
10.1016/j.toxcx.2020.100037 · 2020 · External reference
The relationship between clinics and the venom of the causative Amazon pit viper (Bothrops atrox)
2020 · External reference
Phospholipases A2: unveiling the secrets of a functionally versatile group of snake venom toxins
10.1016/j.toxicon.2012.09.006 · 2013 · External reference
Insights into and speculations about snake venom metalloproteinase (SVMP) synthesis, folding and disulfide bond formation and their contribution to venom complexity
10.1111/j.1742-4658.2008.06466.x · 2008 · External reference
Molecular mechanisms regulating matrix metalloproteinases
10.2174/1568026611208011095 · 2012 · External reference
Importance of snake venom metalloproteinases in cell biology: effects on platelets, inflammatory and endothelial cells
10.2174/138161207782023711 · 2007 · External reference
Hemorrhage Caused by Snake Venom Metalloproteinases: A Journey of Discovery and Understanding
10.3390/toxins8040093 · 2016 · External reference
Snake venom L-amino acid oxidases: an overview on their antitumor effects
10.1186/1678-9199-20-23 · 2014 · External reference
Haemotoxic snake venoms: their functional activity, impact on snakebite victims and pharmaceutical promise
10.1111/bjh.14591 · 2017 · External reference
Bleeding and Thrombosis: Insights into Pathophysiology of Bothrops Venom-Related Hemostasis Disorders
10.3390/ijms22179643 · 2021 · External reference
Enzymatic toxins from snake venom: structural characterization and mechanism of catalysis
10.1111/j.1742-4658.2011.08115.x · 2011 · External reference
Haemostatically active proteins in snake venoms
10.1016/j.toxicon.2011.01.006 · 2011 · External reference
Toxicovenomics and antivenom profiling of the Eastern green mamba snake (Dendroaspis angusticeps)
10.1016/j.jprot.2016.02.003 · 2016 · External reference
Venomic Analysis of the Poorly Studied Desert Coral Snake, Micrurus tschudii tschudii, Supports the 3FTx/PLA₂ Dichotomy across Micrurus Venoms
10.3390/toxins8060178 · 2016 · External reference
Structure, function and evolution of three-finger toxins: mini proteins with multiple targets
10.1016/j.toxicon.2010.07.010 · 2010 · External reference
The three-finger toxin fold: a multifunctional structural scaffold able to modulate cholinergic functions
10.1111/jnc.13975 · 2017 · External reference
Snake venom three-finger toxins and their potential in drug development targeting cardiovascular diseases
10.1016/j.bcp.2020.114105 · 2020 · External reference
Minor snake venom proteins: Structure, function and potential applications
10.1016/j.bbagen.2016.12.022 · 2017 · External reference
Snake venom L-amino acid oxidases: trends in pharmacology and biochemistry
2014 · External reference
Evidence for existence of venom 5’ nucleotidase in multiple forms through inhibition of concanavalin A
10.1002/cbf.1692 · 2010 · External reference
10.3724/sp.j.1141.2008.00399
10.3724/sp.j.1141.2008.00399 · External reference
Schumanniofoside, the antisnake venom principle from the stem bark of Schumanniophyton magnificum Harms
10.1016/0378-8741(86)90028-0 · 1986 · External reference
Inhibition of the lethal and myotoxic activities of Crotalus durissus terrificus venom by Tabernaemontana catharinensis: identification of one of the active components
10.1055/s-2000-8577 · 2000 · External reference
Unresolved reference
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Antiophidic solanidane steroidal alkaloids from Solanum campaniforme
10.1021/np200479a · 2011 · External reference
Solanidane and iminosolanidane alkaloids from Solanum campaniforme
10.1016/j.phytochem.2013.09.007 · 2013 · External reference
Identification of a novel and potent inhibitor of phospholipase A(2) in a medicinal plant: crystal structure at 1.93Å and Surface Plasmon Resonance analysis of phospholipase A(2) complexed with berberine
10.1016/j.bbapap.2011.03.002 · 2011 · External reference
Aristolochic acid and its derivatives as inhibitors of snake venom L-amino acid oxidase
10.1016/j.toxicon.2017.08.003 · 2017 · External reference
Antivenom activity of triterpenoid (C34H68O2) from Leucas aspera Linn. against Naja naja naja venom induced toxicity: antioxidant and histological study in mice
10.1177/0960327113494901 · 2014 · External reference
Structural Basis for the Inhibition of a Phospholipase A2-Like Toxin by Caffeic and Aristolochic Acids
2015 · External reference
Medicinal Plants with Antivenom Activities
10.1201/9780429426193-10 · 2018 · External reference
Anti-snake venom activities of ethanolic extract of fruits of Piper longum L. (Piperaceae) against Russell’s viper venom: characterization of piperine as active principle
10.1016/j.jep.2013.03.022 · 2013 · External reference
Unresolved reference
External reference
Snake venom induced local toxicities: plant secondary metabolites as an auxiliary therapy
10.2174/138955713804484730 · 2013 · External reference
An experimental study on evaluation of chemical antagonists induced snake venom neutralization
1998 · External reference
Isolation, purification and partial characterization of viper venom inhibiting factor from the root extract of the Indian medicinal plant sarsaparilla (Hemidesmus indicus R. Br.)
10.1016/0041-0101(94)90314-x · 1994 · External reference
Viper venom-induced inflammation and inhibition of free radical formation by pure compound (2-hydroxy-4-methoxy benzoic acid) isolated and purified from anantamul (Hemidesmus indicus R. BR) root extract
10.1016/s0041-0101(97)00070-6 · 1998 · External reference
In silico identification of viper phospholipaseA2 inhibitors: validation by in vitro, in vivo studies
10.1007/s00894-011-0994-7 · 2011 · External reference
Molecular modeling and snake venom phospholipase A2 inhibition by phenolic compounds: Structure-activity relationship
10.1016/j.ejmech.2016.03.008 · 2016 · External reference
Molecular mechanism of lung hemorrhage induction by VRV-PL-VIIIa from Russell’s viper (Vipera russelli) venom
10.1016/s0041-0101(99)00228-7 · 2000 · External reference
The polyphenol 3, 4, 5 - tri-hydroxy benzoic acid inhibits indian daboia russelli venom and its hemorrhagic complex induced local toxicity
10.2174/156802611797633447 · 2011 · External reference
Inhibitory effects of plant phenolic compounds on enzymatic and cytotoxic activities induced by a snake venom phospholipase A2
10.17533/udea.vitae.10653 · 2011 · External reference
Anticoagulant effect of Naja naja venom 5’nucleotidase: demonstration through the use of novel specific inhibitor, vanillic acid
10.1016/j.toxicon.2006.06.017 · 2006 · External reference
Rosmarinic acid, a new snake venom phospholipase A2 inhibitor from Cordia verbenacea (Boraginaceae): antiserum action potentiation and molecular interaction
10.1016/j.toxicon.2005.04.023 · 2005 · External reference
Biological and pathological studies of rosmarinic acid as an inhibitor of hemorrhagic Trimeresurus flavoviridis (habu) venom
10.3390/toxins2102478 · 2010 · External reference
Contribution of cinnamic acid analogues in rosmarinic acid to inhibition of snake venom induced hemorrhage
10.1016/j.bmc.2011.02.013 · 2011 · External reference
Rosmarinic acid in Argusia argentea inhibits snake venom-induced hemorrhage
10.1007/s11418-010-0428-3 · 2010 · External reference
Triacontyl p-coumarate: an inhibitor of snake venom metalloproteinases
10.1016/j.phytochem.2012.10.007 · 2013 · External reference
Structures and binding studies of the complexes of phospholipase A2 with five inhibitors
10.1016/j.bbapap.2014.12.017 · 2015 · External reference
Pharmacological Screening of Plants Recommended by Folk Medicine as Snake Venom Antidotes; IV. Protection against Jararaca Venom by Isolated Constituents1
10.1055/s-2006-959425 · 1994 · External reference
Evaluation of anti-inflammatory activity of derivatives from aerial parts of Baccharis uncinella
10.3109/13880209.2010.537828 · 2011 · External reference
Protective effects of tannic acid and related natural compounds on Crotalus adamenteus subcutaneous poisoning in mice
10.1111/j.1600-0773.1993.tb01652.x · 1993 · External reference
Isolation and characterization of ellagic acid derivatives isolated from Casearia sylvestris SW aqueous extract with anti-PLA(2) activity
10.1016/j.toxicon.2008.07.011 · 2008 · External reference
Evaluation of the inhibitory potential of casuarictin, an ellagitannin isolated from white mangrove (Laguncularia racemosa) leaves, on snake venom secretory phospholipase A2
10.3390/md17070403 · 2019 · External reference
Molecular docking studies and anti-enzymatic activities of Thai mango seed kernel extract against snake venoms
10.3390/molecules14041404 · 2009 · External reference
Flavonoids as phospholipase A2 inhibitors: importance of their structure for selective inhibition of group II phospholipase A2
10.1023/a:1027306118026 · 1997 · External reference
A structure and an absolute configuration of (+)-alternamin, a new coumarin from Murraya alternans having antidote activity against snake venom
10.1016/j.tetlet.2007.06.156 · 2007 · External reference
Citrus bioflavonoid, hesperetin, as inhibitor of two thrombin-like snake venom serine proteases isolated from Crotalus simus
10.1016/j.toxicon.2018.01.005 · 2018 · External reference
Hesperetin as an inhibitor of the snake venom serine protease from Bothrops jararaca
10.1016/j.toxicon.2021.04.016 · 2021 · External reference
Inhibitory effect of pinostrobin from Renealmia alpinia, on the enzymatic and biological activities of a PLA2
10.1016/j.ijbiomac.2016.04.042 · 2016 · External reference
Inhibitory effects of flavonoids on several venom hyaluronidases
10.1007/bf01918384 · 1991 · External reference
Phytochemical composition, antisnake venom and antibacterial activities of ethanolic extract of Aegiphila integrifolia (Jacq) Moldenke leaves
10.1016/j.toxicon.2021.05.004 · 2021 · External reference
The biflavonoid morelloflavone inhibits the enzymatic and biological activities of a snake venom phospholipase A2
10.1016/j.cbi.2014.06.015 · 2014 · External reference
Neutralization of lethal and myotoxic activities of South American rattlesnake venom by extracts and constituents of the plant Eclipta prostrata (Asteraceae)
10.1016/0041-0101(89)90151-7 · 1989 · External reference
Protective Effect of the Plant Extracts of Erythroxylum sp. against Toxic Effects Induced by the Venom of Lachesis muta Snake
10.3390/molecules21101350 · 2016 · External reference
Selective inhibition of group II phospholipase A2 by quercetin
10.1007/bf00914195 · 1993 · External reference
Quercetin as an inhibitor of snake venom secretory phospholipase A2
10.1016/j.cbi.2010.10.016 · 2011 · External reference
Umbelliferone induces changes in the structure and pharmacological activities of Bn IV, a phospholipase A2 isoform isolated from Bothrops neuwiedi
10.1016/j.toxicon.2011.02.024 · 2011 · External reference
Inhibition of Naja naja venom hyaluronidase by plant-derived bioactive components and polysaccharides
10.1007/s10541-005-0207-z · 2005 · External reference
Betulinic, oleanolic and ursolic acids inhibit the enzymatic and biological effects induced by a P-I snake venom metalloproteinase
10.1016/j.cbi.2017.12.001 · 2018 · External reference
Perspective on the Therapeutics of Anti-Snake Venom
10.3390/molecules24183276 · 2019 · External reference
Quercetin-3-O-rhamnoside from Euphorbia hirta protects against snake Venom induced toxicity
10.1016/j.bbagen.2016.03.031 · 2016 · External reference
Three new phenolic glycosides and a new triterpenoid from the stems of Scolopia chinensis
2009 · External reference
Protective effect of schizolobium parahyba flavonoids against snake venoms and isolated toxins
10.2174/156802611797633438 · 2011 · External reference
In silico and in vitro neutralization of PLA2 activity of Daboxin P by butein, mimosine and bakuchiol
10.1016/j.ijbiomac.2020.09.223 · 2020 · External reference
Anti-snake venom activity of flavonoids from the root bark extract of Parinari curatellifolia in mice
1955 · External reference
Antivenin plants used for treatment of snakebites in Uganda: ethnobotanical reports and pharmacological evidences
10.1186/s41182-019-0187-0 · 2020 · External reference
Nigerian medicinal plants with anti-snake venom activity—A review
2021 · External reference
Medicinal plants with inhibitory properties against snake venoms
10.2174/092986705774370655 · 2005 · External reference
Anti-hemorrhagic activity of four Brazilian vegetable species against Bothrops jararaca venom
10.3390/molecules14031072 · 2009 · External reference
Prospects and Challenges of Developing Plant-Derived Snake Antivenin Natural Products: A Focus on West Africa
10.1002/cmdc.202100478 · 2021 · External reference
Harpalycin 2 inhibits the enzymatic and platelet aggregation activities of PrTX-III, a D49 phospholipase A2 from Bothrops pirajai venom
10.1186/1472-6882-12-139 · 2012 · External reference
Inhibition of Neurotoxic Secretory Phospholipases A(2) Enzymatic, Edematogenic, and Myotoxic Activities by Harpalycin 2, an Isoflavone Isolated from Harpalyce brasiliana Benth
10.1155/2012/987517 · 2012 · External reference
An isoflavone from Dipteryx alata Vogel is active against the in vitro neuromuscular paralysis of Bothrops jararacussu snake venom and bothropstoxin I, and prevents venom-induced myonecrosis
10.3390/molecules19055790 · 2014 · External reference
Preliminary results on the protective effect of (-)-edunol, a pterocarpan from Brongniartia podalyrioides (Leguminosae), against Bothrops atrox venom in mice
10.1016/0378-8741(94)90086-8 · 1994 · External reference
Synthesis and pharmacological evaluation of prenylated and benzylated pterocarpans against snake venom
10.1016/j.bmcl.2003.10.044 · 2004 · External reference
Structures of cabenegrins A-I and A-II, potent anti-snake venoms
10.1016/s0040-4039(00)87726-6 · 1982 · External reference
Inhibition of the myotoxic and hemorrhagic activities of crotalid venoms by Eclipta prostrata (Asteraceae) extracts and constituents
10.1016/0041-0101(94)90207-0 · 1994 · External reference
Inhibition of snake venoms and phospholipases A(2) by extracts from native and genetically modified Eclipta alba: isolation of active coumestans
10.1111/j.1742-7843.2008.00350.x · 2009 · External reference
Cytotoxic and inflammatory potential of a phospholipase A2 from Bothrops jararaca snake venom
10.1186/s40409-018-0170-y · 2018 · External reference
10.1016/s1532-0456(00)00215-5 · 2001 · Admitted local publication
Investigation of two Flacourtiaceae plants: Bennettiodendron leprosipes and Flacourtia ramontchi
10.1055/s-0029-1185542 · 2009 · External reference
Three new phenolic glycosides and a new triterpenoid from the stems of Scolopia chinensis
10.1055/s-0029-1186157 · 2010 · External reference
Phenolic glycosides from Symplocos racemosa: natural inhibitors of phosphodiesterase I
10.1016/s0031-9422(03)00075-x · 2003 · External reference
Lapachol and synthetic derivatives: in vitro and in vivo activities against Bothrops snake venoms
10.1371/journal.pone.0211229 · 2019 · External reference
Isohemigossypolone: Antiophidic properties of a naphthoquinone isolated from Pachira aquatica Aubl
10.1016/j.cbpc.2021.109028 · 2021 · External reference
Ehretianone, a novel quinonoid xanthene from Ehretia buxifolia with antisnake venom activity
10.1021/np960355p · 1996 · External reference
Inhibitory effects on phospholipase A2 and antivenin activity of melanin extracted from Thea sinensis Linn
10.1016/j.lfs.2003.09.048 · 2004 · External reference
Identification and evaluation of agents isolated from traditionally used herbs against Ophiophagus hannah venom
2012 · External reference
Snakebite envenomation in the Brazilian Amazon: a cost-of-illness study
10.1093/trstmh/traa005 · 2020 · External reference
Antivenom and biological effects of ar-turmerone isolated from Curcuma longa (Zingiberaceae)
10.1016/0041-0101(92)90437-a · 1992 · External reference
In-vitro and in-vivo antivenin activity of 2-[2-(5,5,8a-trimethyl-2-methylene-decahydro-naphthalen-1-yl)-ethylidene]-succinaldehyde against Ophiophagus hannah venom
10.1211/jpp.62.02.0014 · 2010 · External reference
Neo-clerodane diterpenoid, a new metalloprotease snake venom inhibitor from Baccharis trimera (Asteraceae): anti-proteolytic and anti-hemorrhagic properties
10.1016/j.cbi.2004.09.016 · 2004 · External reference
Quinovic acid glycosides from Mitragyna stipulosa--first examples of natural inhibitors of snake venom phosphodiesterase I
10.1080/10575630290033169 · 2002 · External reference
Counteraction of Bothrops snake venoms by Combretum leprosum root extract and arjunolic acid
10.1016/j.jep.2014.05.056 · 2014 · External reference
Daboia russellii and Naja kaouthia venom neutralization by lupeol acetate isolated from the root extract of Indian sarsaparilla Hemidesmus indicus R.Br
10.1016/j.jep.2005.11.031 · 2006 · External reference
A new triterpenoid saponin, bredemeyeroside B. from the roots of Bredemeyera floribunda
10.1055/s-2006-957962 · 1996 · External reference
Bredemeyeroside D, a novel triterpenoid saponin from Bredemeyera floribunda: a potent snake venom antidote activity on mice
10.1002/(sici)1099-1573(199612)10:8<666::aid-ptr937>3.0.co;2-h · 1996 · External reference
Triterpenoid saponins, new metalloprotease snake venom inhibitors isolated from Pentaclethra macroloba
10.1016/j.toxicon.2007.03.024 · 2007 · External reference
Phosphodiesterase-I inhibitor quinovic acid glycosides from Bridelia ndellensis
10.1080/14786410600661658 · 2006 · External reference
Unresolved reference
External reference
Phosphodiesterase I-inhibiting Diels-Alder adducts from the leaves of Morus mesozygia
10.1055/s-0031-1280338 · 2012 · External reference
Daboia russelli venom hyaluronidase: purification, characterization and inhibition by β-3-(3-hydroxy-4-oxopyridyl) α-amino-propionic Acid
10.2174/156802611797633410 · 2011 · External reference
Snake venom neutralising factor from the root extract of Emblica officinalis Linn
10.1007/s13596-011-0008-4 · 2011 · External reference
Inhibitory effects of Piper umbellatum and Piper peltatum extracts towards myotoxic phospholipases A2 from Bothrops snake venoms: isolation of 4-nerolidylcatechol as active principle
10.1016/j.phytochem.2005.03.026 · 2005 · External reference
Inhibitory potential of important phytochemicals from Pergularia daemia (Forsk.) chiov., on snake venom (Naja naja)
10.1016/j.jgeb.2015.11.002 · 2016 · External reference
Genistein, a potent inhibitor of secretory phospholipase A 2: a new insight in down regulation of inflammation
10.1007/s10787-009-0018-8 · 2010 · External reference
In Vitro and In Vivo Evaluation of Polyherbal Formulation against Russell’s Viper and Cobra Venom and Screening of Bioactive Components by Docking Studies
10.1155/2013/781216 · 2013 · External reference
Unresolved reference
External reference
Anti-snake venom and analgesic activities of extracts and betulinic and oleanolic acids isolated from Parinari curatellifolia
10.4102/jomped.v4i1.77 · 2020 · External reference
Therapeutic application of natural inhibitors against snake venom phospholipase A(2)
10.6026/97320630008048 · 2012 · External reference
A short review on plants used as anti-snake venom
2023 · External reference
A Review on Venom Enzymes Neutralizing Ability of Secondary Metabolites from Medicinal Plants
10.3831/kpi.2017.20.020 · 2017 · External reference
The potential of phenolic acids in therapy against snakebites: A review
10.1016/j.toxicon.2021.12.019 · 2022 · External reference
Snake Venom PLA2, a Promising Target for Broad-Spectrum Antivenom Drug Development
10.1155/2017/6592820 · 2017 · External reference
Isolation and characterization of a novel dihydrostilbene from Indigofera capitata kotschy with antivenin activity against Naja nigricollis venom
10.1007/s44371-025-00118-x · 2025 · External reference
Antioxidant, cytotoxic, and anti-venom activity of Alstonia parvifolia Merr. Bark
10.4103/2221-1691.326100 · 2021 · External reference
10.3390/ph17040510
10.3390/ph17040510 · External reference
Therapeutic Potential of the Genus Zanthoxylum Phytochemicals: A Theoretical ADME/Tox Analysis
10.1016/j.sajb.2023.09.009 · 2023 · External reference
In silico investigation of saponins and tannins as potential inhibitors of SARS-CoV-2 main protease (Mpro)
10.1007/s40203-020-00071-w · 2021 · External reference
Theoretical evaluation of ADMET properties for coumarin derivatives as compounds with therapeutic potential
10.1016/j.ejps.2017.08.036 · 2017 · External reference
In Silico ADME/Tox Profiling of Natural Products: A Focus on BIOFACQUIM
10.1021/acsomega.0c01581 · 2020 · External reference
ADMET profiling of geographically diverse phytochemical using chemoinformatic tools
10.4155/fmc-2019-0206 · 2020 · External reference
Saponins of Selected Triterpenoids as Potential Therapeutic Agents: A Review
10.3390/ph16030386 · 2023 · External reference
A Computational Study on Selected Alkaloids as SARS-CoV-2 Inhibitors: PASS Prediction, Molecular Docking, ADMET Analysis, DFT, and Molecular Dynamics Simulations
10.1155/2023/9975275 · 2023 · External reference
Lipophilic Conjugates of Drugs: A Tool to Improve Drug Pharmacokinetic and Therapeutic Profiles
10.1007/s11095-021-03093-x · 2021 · External reference
Biological barriers, and the influence of protein binding on the passage of drugs across them
10.1007/s11033-020-05361-2 · 2020 · External reference
Enzyme Activity of Natural Products on Cytochrome P450
10.3390/molecules27020515 · 2022 · External reference
Relevance of Half-Life in Drug Design
10.1021/acs.jmedchem.7b00969 · 2018 · External reference
An integrated view of cisplatin-induced nephrotoxicity, hepatotoxicity, and cardiotoxicity: characteristics, common molecular mechanisms, and current clinical management
10.1007/s10157-024-02490-x · 2024 · External reference
A Synopsis of Current Theories on Drug-Induced Nephrotoxicity
2023 · External reference
Intestinal Excretion, Intestinal Recirculation, and Renal Tubule Reabsorption Are Underappreciated Mechanisms That Drive the Distribution and Pharmacokinetic Behavior of Small Molecule Drugs
10.1021/acs.jmedchem.0c01720 · 2021 · External reference
Plant toxins: alkaloids and their toxicities
10.30574/gscbps.2019.6.2.0003 · 2018 · External reference
Pharmacological activities and toxicities of alkaloids on human health
2022 · External reference
Pharmacokinetic/pharmacodynamic studies in drug product development
10.1002/jps.1167 · 2002 · External reference
Green extraction of phenolic compounds from the by-product of purple araçá (Psidium myrtoides) with natural deep eutectic solvents assisted by ultrasound: Optimization, comparison, and bioactivity
10.1016/j.foodres.2024.114731 · 2024 · External reference
