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Potent Inhibitor of Drug-Resistant HIV-1 Strains Identified from the Medicinal Plant Justicia gendarussa
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/mrc.1830openalex-snapshot
Complete assignments of 1H and 13C NMR data for seven arylnaphthalide lignans from Justicia procumbens
inferredcites →https://doi.org/10.1002/mrc.2175openalex-snapshot
Complete assignments of 1H and 13C NMR data for three new arylnaphthalene lignan from Justicia procumbens
inferredcites →https://doi.org/10.1006/viro.1995.1016openalex-snapshot
Vpr Is Required for Efficient Replication of Human Immunodeficiency Virus Type-1 in Mononuclear Phagocytes
inferredcites →https://doi.org/10.1016/0166-3542(95)00020-mopenalex-snapshot
Differential inhibition of reverse transcriptase and cellular DNA polymerase-α activities by lignans isolated from Chinese herbs, Phyllanthus myrtifolius Moon, and tannins from Lonicera japonica Thunb and Castanopsis hystrix
inferredcites →https://doi.org/10.1016/s0040-4039(01)98669-1openalex-snapshot
Structure determination of the new tetracyclic diterpene ingenol-triacetate with triple product methods
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b01055openalex-snapshot
Natural Products as Sources of New Drugs from 1981 to 2014
inferredcites →https://doi.org/10.1021/jm00093a004openalex-snapshot
HIV inhibitory natural products. Part 7. The calanolides, a novel HIV-inhibitory class of coumarin derivatives from the tropical rainforest tree, Calophyllum lanigerum
inferredcites →https://doi.org/10.1021/jm701405popenalex-snapshot
Chemical Library and Structure–Activity Relationships of 11-Demethyl-12-oxo Calanolide A Analogues as Anti-HIV-1 Agents
inferredcites →https://doi.org/10.1021/jm950922qopenalex-snapshot
Betulinic Acid and Dihydrobetulinic Acid Derivatives as Potent Anti-HIV Agents
inferredcites →https://doi.org/10.1021/np034016popenalex-snapshot
Plant Substances as Anti-HIV Agents Selected According to Their Putative Mechanism of Action
inferredcites →https://doi.org/10.1021/np050028uopenalex-snapshot
Cytotoxic Arylnaphthalene Lignans from a Vietnamese Acanthaceae, Justicia patentiflora
inferredcites →https://doi.org/10.1021/np058107topenalex-snapshot
“Studies on Biodiversity of Vietnam and Laos” 1998−2005: Examining the Impact
inferredcites →https://doi.org/10.1021/np5002785openalex-snapshot
Potent Cytotoxic Arylnaphthalene Lignan Lactones from Phyllanthus poilanei
inferredcites →https://doi.org/10.1021/np7007347openalex-snapshot
Dichapetalin-Type Triterpenoids and Lignans from the Aerial Parts of Phyllanthus acutissima
inferredcites →https://doi.org/10.1055/s-2007-993747openalex-snapshot
Antibacterial Lignans and Triterpenoids from Rostellularia procumbens
inferredcites →https://doi.org/10.1073/pnas.88.24.11241openalex-snapshot
Human immunodeficiency virus type 1 mutants resistant to nonnucleoside inhibitors of reverse transcriptase arise in tissue culture.
inferredcites →https://doi.org/10.1093/carcin/bgi133openalex-snapshot
Justicidin A decreases the level of cytosolic Ku70 leading to apoptosis in human colorectal cancer cells
inferredcites →https://doi.org/10.1126/science.6189183openalex-snapshot
Isolation of a T-Lymphotropic Retrovirus from a Patient at Risk for Acquired Immune Deficiency Syndrome (AIDS)
inferredcites →https://doi.org/10.1128/aac.00152-07openalex-snapshot
Phase I and II Study of the Safety, Virologic Effect, and Pharmacokinetics/Pharmacodynamics of Single-Dose 3-O-(3′,3′-Dimethylsuccinyl)Betulinic Acid (Bevirimat) against Human Immunodeficiency Virus Infection
inferredcites →https://doi.org/10.1128/aac.37.5.1095openalex-snapshot
Standardized peripheral blood mononuclear cell culture assay for determination of drug susceptibilities of clinical human immunodeficiency virus type 1 isolates. The RV-43 Study Group, the AIDS Clinical Trials Group Virology Committee Resistance Working Group
inferredcites →https://doi.org/10.1128/aac.39.9.2000openalex-snapshot
Anti-human immunodeficiency virus (HIV) activities of halogenated gomisin J derivatives, new nonnucleoside inhibitors of HIV type 1 reverse transcriptase
inferredcites →https://doi.org/10.1128/aac.40.1.271openalex-snapshot
Mechanism of selective inhibition of human immunodeficiency virus by ingenol triacetate
inferredcites →https://doi.org/10.1128/jvi.69.11.6705-6711.1995openalex-snapshot
Human immunodeficiency virus type 1 viral protein R (Vpr) arrests cells in the G2 phase of the cell cycle by inhibiting p34cdc2 activity
inferredcites →https://doi.org/10.1146/annurev.immunol.8.1.453openalex-snapshot
Regulation Of Hiv-1 Gene Expression
inferredcites →https://doi.org/10.1177/095632029600700502openalex-snapshot
Ingenol Derivatives are Highly Potent and Selective Inhibitors of HIV Replication in Vitro
inferredcites →https://doi.org/10.1248/cpb.50.844openalex-snapshot
Patavine, a New Arylnaphthalene Lignan Glycoside from Shoot Cultures of Haplophyllum patavinum.
inferredcites →https://doi.org/10.17615/81xb-we92openalex-snapshot
Exclusive and Persistent Use of the Entry Coreceptor CXCR4 by Human Immunodeficiency Virus Type 1 from a Subject Homozygous for CCR5 Δ32
inferredcites →https://doi.org/10.4172/jaa.1000027openalex-snapshot
Development of an Antiviral Screening Protocol: One-Stone-Two-birds
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Axial Chirality and Antiviral Activity Evaluation of Arylnaphthalene Lignan Glycosides from Justicia procumbens
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In‐silico Computational Investigations of AntiViral Lignan Derivatives as Potent Inhibitors of SARS CoV‐2
inferred← citeshttps://doi.org/10.1007/978-3-030-64853-4_3openalex-snapshot
Antileishmanial Activity of Lignans, Neolignans, and Other Plant Phenols
inferred← citeshttps://doi.org/10.1007/978-3-031-35155-6_2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-36202-6_245-1openalex-snapshot
Current Status and Future Prospects of Bioactive Phytolignans
inferred← citeshttps://doi.org/10.1007/s11101-021-09758-0openalex-snapshot
Plant-derived lignans as potential antiviral agents: a systematic review
inferred← citeshttps://doi.org/10.1007/s12013-024-01370-1openalex-snapshot
Molecular Understanding and Pharmacological Potency of Plant-Derived Compounds in Colorectal Cancer (CRC): A Critical Analysis and Future Perspectives
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Identification of Aristolactam Derivatives That Act as Inhibitors of Human Immunodeficiency Virus Type 1 Infection and Replication by Targeting Tat-Mediated Viral Transcription
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Therapeutic roles of plants for 15 hypothesised causal bases of Alzheimer’s disease
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Synthesis, Characterization, Crystal Structure, Hirshfeld surface analysis and DFT studies of novel compounds based on the methoxynaphthalene ring
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Design and synthesis of a series of 5-aryl-N-(naphthalen-1-yl)-1,3,4-oxadiazol-2-amine analogs as anticancer agents: ADMET profiling, and in-silico studies
inferred← citeshttps://doi.org/10.1016/j.phrs.2019.104284openalex-snapshot
Lignans and Neolignans: Plant secondary metabolites as a reservoir of biologically active substances
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Biological activity of plant extracts and isolated compounds from Alchornea laxiflora: Anti-HIV, antibacterial and cytotoxicity evaluation
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132214openalex-snapshot
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Indium chloride catalysed annulation of arylmethyl carbonyls & arylalkynes for the synthesis of naphthalene derivatives
inferred← citeshttps://doi.org/10.1016/s1875-5364(19)30117-7openalex-snapshot
Anti-HIV lignans from Justicia procumbens
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00068openalex-snapshot
Stable Axially Chiral Isomers of Arylnaphthalene Lignan Glycosides with Antiviral Potential Discovered from Justicia procumbens
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