LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 10 of total 23

Search options

  1. Article ; Online: Immune Checkpoint Inhibitors: Recent Clinical Advances and Future Prospects.

    Banday, Abid H / Abdalla, Mohnad

    Current medicinal chemistry

    2022  Volume 30, Issue 28, Page(s) 3215–3237

    Abstract: Immune checkpoints are vital molecules and pathways of the immune system with defined roles of controlling immune responses from being destructive to the healthy cells in the body. They include inhibitory receptors and ligands, which check the ... ...

    Abstract Immune checkpoints are vital molecules and pathways of the immune system with defined roles of controlling immune responses from being destructive to the healthy cells in the body. They include inhibitory receptors and ligands, which check the recognition of most cancers by the immune system. This happens when proteins on the surface of T cells called immune checkpoint proteins identify partner proteins on the cancer cells and bind to them, sending brake signals to the T cells to evade immune attack. However, drugs called immune checkpoint inhibitors block checkpoint proteins from binding to their partner proteins, thereby inhibiting the brake signals from being sent to T cells. This eventually allows the T cells to destroy cancer cells and arbitrate robust tumor regression. Many such inhibitors have already been approved and are in various developmental stages. The well-illustrated inhibitory checkpoints include the cytotoxic T lymphocyte-associated molecule-4 (CTLA-4), programmed cell death receptor-1 (PD-1), and programmed cell death ligand-1 (PD-L1). Though many molecules blocking these checkpoints have shown promise in treating many malignancies, such treatment options have limited success in terms of the immune response in most patients. Against this backdrop, exploring new pathways and next-generation inhibitors becomes imperative for developing more responsive and effective immune checkpoint therapy. Owing to the complex biology and unexplored ambiguities in the mechanistic aspects of immune checkpoint pathways, analysis of the activity profile of new drugs is the subject of strenuous investigation. We herein report the recent progress in developing new inhibitory pathways and potential therapeutics and delineate the developments based on their merit. Further, the ensuing challenges towards developing efficacious checkpoint therapies and the impending opportunities are also discussed.
    MeSH term(s) Humans ; Immune Checkpoint Inhibitors/metabolism ; Immune Checkpoint Inhibitors/pharmacology ; Immune Checkpoint Inhibitors/therapeutic use ; Immunotherapy ; Neoplasms/drug therapy ; Neoplasms/metabolism ; T-Lymphocytes
    Chemical Substances Immune Checkpoint Inhibitors
    Language English
    Publishing date 2022-08-19
    Publishing country United Arab Emirates
    Document type Journal Article
    ZDB-ID 1319315-6
    ISSN 1875-533X ; 0929-8673
    ISSN (online) 1875-533X
    ISSN 0929-8673
    DOI 10.2174/0929867329666220819115849
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: Potential Repurposed Therapeutics and New Vaccines against COVID-19 and Their Clinical Status.

    Banday, Abid H / Shameem, Shameem A / Ajaz, Sheikh J

    SLAS discovery : advancing life sciences R & D

    2020  Volume 25, Issue 10, Page(s) 1097–1107

    Abstract: SARS-CoV-2, the virus that causes coronavirus disease 2019 (COVID-19), was first reported in Wuhan, China, in December 2019. Since then, the virus has stretched its grip to almost all the countries in the world, affecting millions of people and causing ... ...

    Abstract SARS-CoV-2, the virus that causes coronavirus disease 2019 (COVID-19), was first reported in Wuhan, China, in December 2019. Since then, the virus has stretched its grip to almost all the countries in the world, affecting millions of people and causing enormous casualties. The World Health Organization (WHO) declared COVID-19 a pandemic on March 11, 2019. As of June 12, 2020, almost 7.30 million people have already been infected globally, with 413,000 reported casualties. In the United States alone, 2.06 million people have been infected and 115,000 have succumbed to this pandemic. A multipronged approach has been launched toward combating this pandemic, with the main focus on exhaustive screening, developing efficacious therapies, and vaccines for long-term immunity. Several pharmaceutical companies in collaboration with various academic institutions and governmental organizations have started investigating new therapeutics and repurposing approved drugs so as to find fast and affordable treatments against this disease. The present communication is aimed at highlighting the efforts that are currently underway to treat or prevent SARS-CoV-2 infection, with details on the science, clinical status, and timeline for selected investigational drugs and vaccines. This article is going to be of immense help to the scientific community and researchers as it brings forth all the necessary clinical information of the most-talked-about therapeutics against SARS-CoV-2. All the details pertaining to the clinical status of each therapeutic candidate have been updated as of June 12, 2020.
    MeSH term(s) Adenosine Monophosphate/analogs & derivatives ; Adenosine Monophosphate/pharmacology ; Alanine/analogs & derivatives ; Alanine/pharmacology ; Amides/pharmacology ; Animals ; Antibodies, Monoclonal/pharmacology ; Antibodies, Monoclonal, Humanized/pharmacology ; Antiviral Agents/pharmacology ; COVID-19/drug therapy ; COVID-19/prevention & control ; COVID-19 Vaccines/pharmacology ; Chloroquine/pharmacology ; Clinical Trials as Topic ; Cyclopropanes ; Drug Evaluation, Preclinical ; Drug Repositioning ; Humans ; Isoindoles ; Lactams/pharmacology ; Lactams, Macrocyclic ; Mice, Transgenic ; Proline/analogs & derivatives ; Pyrazines/pharmacology ; SARS-CoV-2/drug effects ; Small Molecule Libraries/pharmacology ; Sulfonamides/pharmacology ; Vaccines, Synthetic/pharmacology
    Chemical Substances Amides ; Antibodies, Monoclonal ; Antibodies, Monoclonal, Humanized ; Antiviral Agents ; COVID-19 Vaccines ; Cyclopropanes ; Isoindoles ; Lactams ; Lactams, Macrocyclic ; Pyrazines ; Small Molecule Libraries ; Sulfonamides ; Vaccines, Synthetic ; remdesivir (3QKI37EEHE) ; Adenosine Monophosphate (415SHH325A) ; Chloroquine (886U3H6UFF) ; danoprevir (911Z9PCQ5F) ; Proline (9DLQ4CIU6V) ; favipiravir (EW5GL2X7E0) ; sarilumab (NU90V55F8I) ; Alanine (OF5P57N2ZX)
    Keywords covid19
    Language English
    Publishing date 2020-07-21
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2885123-7
    ISSN 2472-5560 ; 2472-5552
    ISSN (online) 2472-5560
    ISSN 2472-5552
    DOI 10.1177/2472555220945281
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: Synthesis, Aromatase Inhibitory, Antiproliferative and Molecular Modeling Studies of Functionally Diverse D-Ring Pregnenolone Pyrazoles.

    Banday, Abid H / Saeed, Bahjat A / Al-Masoudi, Najim A

    Anti-cancer agents in medicinal chemistry

    2020  Volume 21, Issue 13, Page(s) 1671–1679

    Abstract: Background: Aromatase, a cytochrome P450 hemoprotein that is responsible for estrogen biosynthesis by conversion of androgens into estrogens, has been an attractive target in the treatment of hormonedependent breast cancer. Design of new steroidal ... ...

    Abstract Background: Aromatase, a cytochrome P450 hemoprotein that is responsible for estrogen biosynthesis by conversion of androgens into estrogens, has been an attractive target in the treatment of hormonedependent breast cancer. Design of new steroidal aromatase inhibitors becomes imperative.
    Objective: Synthesis and biological evaluation of two classes of structurally and functionally diverse D-ring pregnenolone pyrazoles as type I aromatase inhibitors and antiproliferative agents.
    Methods: Pregnenolone (1) was converted to 3β-hydroxy-21-hydroxymethylidenepregn-5-en-20-one (2), which upon cyclization with phenylhydrazine generated regioisomeric pairs of pyrazoles 4 and 5. Further, Knoevenagel condensation of pregnenolone (1) with 3-oxo-3-phenylpropanenitrile (6) produced 2-benzoyl-3-(3b-hydroxyandrostan- 5-ene-20-ylidene)-but-2-enenitrile (7), which upon cyclization with hydrazine or phenylhydrazine generated the pyrazoles 8 and 9. All new steroidal derivatives were tested for their aromatase inhibition activity using Dibenzylfluorescein (DBF) based fluorescence assay developed by Stresser et al. Antiproliferative activities were measured using Sulforhodamine B assay. The activities were promising and there was a coherence between aromatase inhibitory and antiproliferative activities.
    Results: The study reveals the immense potential of pregnenolone pyrazoles as aromatase inhibitors for the treatment of breast cancer. Molecular docking studies proved efficient binding of the new steroidal analogs on human placental aromatase.
    Conclusion: In the overall study, most of the compounds exhibited potential activity for the treatment of hormone dependent breast cancer. Compounds 4c and 4d were found to be the most promising pharmacons. Furthermore, compounds 4c and 4d were applied for their molecular docking study on human placental aromatase to predict their possible binding modes with the enzyme. These studies revealed that such molecules have high scope and potential for further investigation towards the treatment of estrogen dependent breast cancer.
    MeSH term(s) Antineoplastic Agents/chemical synthesis ; Antineoplastic Agents/chemistry ; Antineoplastic Agents/pharmacology ; Aromatase/metabolism ; Aromatase Inhibitors/chemical synthesis ; Aromatase Inhibitors/chemistry ; Aromatase Inhibitors/pharmacology ; Cell Proliferation/drug effects ; Drug Screening Assays, Antitumor ; Humans ; Models, Molecular ; Molecular Structure ; Pregnenolone/chemical synthesis ; Pregnenolone/chemistry ; Pregnenolone/pharmacology ; Pyrazoles/chemical synthesis ; Pyrazoles/chemistry ; Pyrazoles/pharmacology ; Tumor Cells, Cultured
    Chemical Substances Antineoplastic Agents ; Aromatase Inhibitors ; Pyrazoles ; Pregnenolone (73R90F7MQ8) ; Aromatase (EC 1.14.14.1)
    Language English
    Publishing date 2020-11-25
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 2217610-X
    ISSN 1875-5992 ; 1871-5206
    ISSN (online) 1875-5992
    ISSN 1871-5206
    DOI 10.2174/1871520620999201124213655
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  4. Article ; Online: Synthesis, 17α-hydroxylase-C

    Banday, Abid H / Shameem, Shameem A / Banday, Javid A / Ganaie, Bashir A

    Anti-cancer agents in medicinal chemistry

    2018  Volume 18, Issue 13, Page(s) 1919–1926

    Abstract: Background: The potential of steroids for development into lead pharmacological molecules lies in the regulation of a variety of biological processes by these molecules and also because of these being a fundamental class of signaling molecules. Steroid ... ...

    Abstract Background: The potential of steroids for development into lead pharmacological molecules lies in the regulation of a variety of biological processes by these molecules and also because of these being a fundamental class of signaling molecules. Steroid based scaffolds have been extensively used as active pharmaceutical agents for the treatment of various diseases including the deadly disease of cancer which despite the recent advances in the early diagnosis, prevention and therapy, remains a clinical challenge affecting millions of people world over and is one of the leading causes of death. It thus warrants the development of new drugs against this dreadful disease through exploitation of emerging molecularly defined targets.
    Methods: The present study explores the effect of novel steroidal pyrazolines as presumed inhibitors of 5α- reductase (5AR) and 17α-hydroxylase-C
    Results: All the synthesised D-ring 1,5-disubstituted pyrazolinyl pregnenolone derivatives (5a-l) were screened for prostate cancer cell inhibitory, 5α-reductase and 17α-hydroxylase-C
    Conclusion: A series of D-ring 1,5-disubstituted pyrazolinyl pregnenolone derivatives (5a-l) were synthesized and screened for their prostate cancer cell inhibitory, 5a-reductase and 17α-hydroxylase-C17,20-lyase inhibitory activity. Amongst all the compounds screened for their 5α-reductase inhibitory activities, compound 5c, 5e, 5g and 5l were found to be the most active whereas compounds 5g and 5h were found to have moderate 17α- hydroxylase-C
    MeSH term(s) Antineoplastic Agents/chemical synthesis ; Antineoplastic Agents/chemistry ; Antineoplastic Agents/pharmacology ; Cell Proliferation/drug effects ; Cell Survival/drug effects ; Dose-Response Relationship, Drug ; Drug Screening Assays, Antitumor ; Enzyme Inhibitors/chemical synthesis ; Enzyme Inhibitors/chemistry ; Enzyme Inhibitors/pharmacology ; Humans ; Molecular Conformation ; Pregnenolone/chemical synthesis ; Pregnenolone/chemistry ; Pregnenolone/pharmacology ; Steroid 17-alpha-Hydroxylase/antagonists & inhibitors ; Steroid 17-alpha-Hydroxylase/metabolism ; Structure-Activity Relationship ; Tumor Cells, Cultured
    Chemical Substances Antineoplastic Agents ; Enzyme Inhibitors ; Pregnenolone (73R90F7MQ8) ; Steroid 17-alpha-Hydroxylase (EC 1.14.14.19)
    Language English
    Publishing date 2018-04-25
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2217610-X
    ISSN 1875-5992 ; 1871-5206
    ISSN (online) 1875-5992
    ISSN 1871-5206
    DOI 10.2174/1871520618666180426100942
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  5. Article ; Online: Development of

    Zhou, Yang / Banday, Abid H / Hruby, Victor J / Cai, Minying

    Molecules (Basel, Switzerland)

    2019  Volume 24, Issue 19

    Abstract: Cancer vaccine is a promising immunotherapeutic approach to train the immune system with vaccines to recognize and eliminate tumors. Adjuvants are compounds that are necessary in cancer vaccines to mimic an infection process and amplify immune responses. ...

    Abstract Cancer vaccine is a promising immunotherapeutic approach to train the immune system with vaccines to recognize and eliminate tumors. Adjuvants are compounds that are necessary in cancer vaccines to mimic an infection process and amplify immune responses. The Toll-like receptor 2 and 6 (TLR2/TLR6) agonist dipalmitoyl-
    MeSH term(s) Humans ; Lipopeptides/chemical synthesis ; Lipopeptides/chemistry ; Lipopeptides/pharmacology ; Molecular Conformation ; Molecular Docking Simulation ; Molecular Dynamics Simulation ; Molecular Structure ; Toll-Like Receptor 2/agonists ; Toll-Like Receptor 2/chemistry ; Toll-Like Receptor 6/agonists ; Toll-Like Receptor 6/chemistry
    Chemical Substances Lipopeptides ; S-(2,3-bis(palmitoyloxy)propyl)cysteine ; Toll-Like Receptor 2 ; Toll-Like Receptor 6
    Language English
    Publishing date 2019-09-27
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 1413402-0
    ISSN 1420-3049 ; 1431-5165 ; 1420-3049
    ISSN (online) 1420-3049
    ISSN 1431-5165 ; 1420-3049
    DOI 10.3390/molecules24193512
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  6. Article: A New Cycloartane Glycoside from the Aerial Part of Astragalus grahamianus

    Shameem, Shameem A. / Banday, Abid H. / Khan, Khaliquz Zaman / Tantry, Mudasir A. / Ganai, Bashir A.

    Chemistry of natural compounds. 2022 Jan., v. 58, no. 1

    2022  

    Abstract: A new 9,19-cyclolanostane type arabinoside, 16,23;22,25-diepoxy-3β,22,23,24-tetrahydroxy-9,19-cyclolanostane-3-O-α-L-arabinopyranoside (1), together with two known compounds (2 and 3), was isolated from the aerial part of Astragalus grahamianus. The ... ...

    Abstract A new 9,19-cyclolanostane type arabinoside, 16,23;22,25-diepoxy-3β,22,23,24-tetrahydroxy-9,19-cyclolanostane-3-O-α-L-arabinopyranoside (1), together with two known compounds (2 and 3), was isolated from the aerial part of Astragalus grahamianus. The structures of these compounds were characterized and identified by 1D and 2D NMR spectroscopic techniques and HR-ESI-MS and by comparison of their spectral data with those reported in the literature. All these compounds are reported from this plant for the first time.
    Keywords Astragalus ; aerial parts ; chemistry ; glycosides ; spectral analysis
    Language English
    Dates of publication 2022-01
    Size p. 71-74.
    Publishing place Springer US
    Document type Article
    ZDB-ID 213866-9
    ISSN 0009-3130
    ISSN 0009-3130
    DOI 10.1007/s10600-022-03598-w
    Database NAL-Catalogue (AGRICOLA)

    More links

    Kategorien

  7. Article: Potential Repurposed Therapeutics and New Vaccines against COVID-19 and Their Clinical Status

    Banday, Abid H / Shameem, Shameem A / Ajaz, Sheikh J

    SLAS Discov

    Abstract: SARS-CoV-2, the virus that causes coronavirus disease 2019 (COVID-19), was first reported in Wuhan, China, in December 2019. Since then, the virus has stretched its grip to almost all the countries in the world, affecting millions of people and causing ... ...

    Abstract SARS-CoV-2, the virus that causes coronavirus disease 2019 (COVID-19), was first reported in Wuhan, China, in December 2019. Since then, the virus has stretched its grip to almost all the countries in the world, affecting millions of people and causing enormous casualties. The World Health Organization (WHO) declared COVID-19 a pandemic on March 11, 2019. As of June 12, 2020, almost 7.30 million people have already been infected globally, with 413,000 reported casualties. In the United States alone, 2.06 million people have been infected and 115,000 have succumbed to this pandemic. A multipronged approach has been launched toward combating this pandemic, with the main focus on exhaustive screening, developing efficacious therapies, and vaccines for long-term immunity. Several pharmaceutical companies in collaboration with various academic institutions and governmental organizations have started investigating new therapeutics and repurposing approved drugs so as to find fast and affordable treatments against this disease. The present communication is aimed at highlighting the efforts that are currently underway to treat or prevent SARS-CoV-2 infection, with details on the science, clinical status, and timeline for selected investigational drugs and vaccines. This article is going to be of immense help to the scientific community and researchers as it brings forth all the necessary clinical information of the most-talked-about therapeutics against SARS-CoV-2. All the details pertaining to the clinical status of each therapeutic candidate have been updated as of June 12, 2020.
    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #658373
    Database COVID19

    Kategorien

  8. Article ; Online: Potential Immunotherapy against SARS-CoV-2

    Banday, Abid H. / Shah, Shameem A. / Ajaz, Sheikh J.

    Coronaviruses

    Strategy and Status

    2020  Volume 1, Issue 1, Page(s) 23–31

    Abstract: SARS-CoV-2, the novel coronavirus that was first reported in Wuhan, China in December 2019, has engrossed the world with immense distress. It has shattered the global healthcare system and has inflicted so much pain on humanity. COVID-19, the disease ... ...

    Abstract SARS-CoV-2, the novel coronavirus that was first reported in Wuhan, China in December 2019, has engrossed the world with immense distress. It has shattered the global healthcare system and has inflicted so much pain on humanity. COVID-19, the disease caused by a microscopic enemy, has now spread to almost all the countries in the world affecting millions of people and causing enormous casualties. World Health Organization (WHO) declared COVID-19 a pandemic on March 11, 2019. As of June 15, 2020, almost 7.70 million people have already been infected globally with 428,000 reported casualties. In the United States alone, 2.14 million people have been infected and 117,000 people have succumbed to this pandemic. A multipronged approach has been launched towards combating this pandemic with the main focus on exhaustive screening, developing efficacious therapies, and vaccines for long-term immunity. Several pharmaceutical companies in collaboration with various academic institutions and governmental organizations have started investigating new therapeutics and repurposing approved drugs so as to find fast and affordable treatments against this disease. The present communication aims at highlighting the efforts that are currently underway to treat or prevent SARS-CoV-2 infection through immunotherapy. Emphasis has been laid on discussing the approaches and platforms that are being utilized for the speedy development of therapeutic antibodies and preventive vaccines against SARS-CoV-2. The manuscript also presents a detailed discussion regarding strategy, clinical status, and timeline for the development of safe and enduring immunotherapy against SARS-CoV-2. All the details pertaining to the clinical status of each candidate have been last updated on June 15, 2020.
    Keywords covid19
    Language English
    Publisher Bentham Science Publishers Ltd.
    Publishing country nl
    Document type Article ; Online
    ISSN 2666-7967
    DOI 10.2174/2666796701999200625212040
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  9. Article ; Online: Potential Repurposed Therapeutics and New Vaccines against COVID-19 and Their Clinical Status

    Banday, Abid H. / Shameem, Shameem A. / Ajaz, Sheikh J.

    SLAS DISCOVERY: Advancing the Science of Drug Discovery

    2020  , Page(s) 247255522094528

    Abstract: SARS-CoV-2, the virus that causes coronavirus disease 2019 (COVID-19), was first reported in Wuhan, China, in December 2019. Since then, the virus has stretched its grip to almost all the countries in the world, affecting millions of people and causing ... ...

    Abstract SARS-CoV-2, the virus that causes coronavirus disease 2019 (COVID-19), was first reported in Wuhan, China, in December 2019. Since then, the virus has stretched its grip to almost all the countries in the world, affecting millions of people and causing enormous casualties. The World Health Organization (WHO) declared COVID-19 a pandemic on March 11, 2019. As of June 12, 2020, almost 7.30 million people have already been infected globally, with 413,000 reported casualties. In the United States alone, 2.06 million people have been infected and 115,000 have succumbed to this pandemic. A multipronged approach has been launched toward combating this pandemic, with the main focus on exhaustive screening, developing efficacious therapies, and vaccines for long-term immunity. Several pharmaceutical companies in collaboration with various academic institutions and governmental organizations have started investigating new therapeutics and repurposing approved drugs so as to find fast and affordable treatments against this disease. The present communication is aimed at highlighting the efforts that are currently underway to treat or prevent SARS-CoV-2 infection, with details on the science, clinical status, and timeline for selected investigational drugs and vaccines. This article is going to be of immense help to the scientific community and researchers as it brings forth all the necessary clinical information of the most-talked-about therapeutics against SARS-CoV-2. All the details pertaining to the clinical status of each therapeutic candidate have been updated as of June 12, 2020.
    Keywords covid19
    Language English
    Publisher SAGE Publications
    Publishing country us
    Document type Article ; Online
    ZDB-ID 2885123-7
    ISSN 2472-5560 ; 2472-5552
    ISSN (online) 2472-5560
    ISSN 2472-5552
    DOI 10.1177/2472555220945281
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  10. Article ; Online: Development of N -Acetylated Dipalmitoyl- S -Glyceryl Cysteine Analogs as Efficient TLR2/TLR6 Agonists

    Yang Zhou / Abid H. Banday / Victor J. Hruby / Minying Cai

    Molecules, Vol 24, Iss 19, p

    2019  Volume 3512

    Abstract: Cancer vaccine is a promising immunotherapeutic approach to train the immune system with vaccines to recognize and eliminate tumors. Adjuvants are compounds that are necessary in cancer vaccines to mimic an infection process and amplify immune responses. ...

    Abstract Cancer vaccine is a promising immunotherapeutic approach to train the immune system with vaccines to recognize and eliminate tumors. Adjuvants are compounds that are necessary in cancer vaccines to mimic an infection process and amplify immune responses. The Toll-like receptor 2 and 6 (TLR2/TLR6) agonist dipalmitoyl- S -glyceryl cysteine (Pam 2 Cys) was demonstrated as an ideal candidate for synthetic vaccine adjuvants. However, the synthesis of Pam 2 Cys requires expensive N -protected cysteine as a key reactant, which greatly limits its application as a synthetic vaccine adjuvant in large-scaled studies. Here, we report the development of N-acetylated Pam 2 Cys analogs as TLR2/TLR6 agonists. Instead of N -protected cysteine, the synthesis utilizes N -acetylcysteine to bring down the synthetic costs. The N -acetylated Pam 2 Cys analogs were demonstrated to activate TLR2/TLR6 in vitro. Moreover, molecular docking studies were performed to provide insights into the molecular mechanism of how N-acetylated Pam 2 Cys analogs bind to TLR2/TLR6. Together, these results suggest N -acetylated Pam 2 Cys analogs as inexpensive and promising synthetic vaccine adjuvants to accelerate the development of cancer vaccines in the future.
    Keywords cancer vaccine ; synthetic vaccine ; adjuvant ; toll-like receptor ; pam 2 cys ; n -acetylated pam 2 cys ; Organic chemistry ; QD241-441
    Subject code 540 ; 290
    Language English
    Publishing date 2019-09-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

To top