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About:
Potential therapeutic targets for combating SARS-CoV-2: Drug repurposing, clinical trials and recent advancements
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An Entity of Type :
schema:ScholarlyArticle
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wasabi.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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Attributes
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Potential therapeutic targets for combating SARS-CoV-2: Drug repurposing, clinical trials and recent advancements
Creator
Kulkarni, Sanjay
Mutalik, Srinivas
Nikam, Ajinkya
Fernandes, Gasper
Gopalan, Divya
Mutalik, Sadhana
Pandey, Abhjieet
Prassl, Ruth
Shreya, Ajjappla
Biophysics, Ruth
Nikam, Nitin
Singh Padya, Bharath
Source
Elsevier; Medline; PMC
abstract
The present pandemic of SARS-CoV-2 has been a tough task for the whole world to deal with. With the absence of specific drugs or vaccines against SARS-CoV-2, the situation is very difficult to control. Apart from the absence of specific therapies, the lack of knowledge about potential therapeutic targets and individual perception is adding to the complications. The present review describes the novel SARS-CoV-2 structure, surface proteins, asymptomatic and symptomatic transmission in addition to the genotype and phenotype of SARS-CoV-2 along with genetic strains and similarity between SARS, MERS and SARS-CoV-2. Therapeutic strategies such as inhibition of the endocytic pathway and suppressing RNA polymerase activity by metal ions, which could be quite beneficial for controlling COVID-19, are outlined. The drug repurposing for SARS-CoV-2 is discussed in detail along with therapeutic classes such as antivirals, antibiotics, and amino quinolones and their probable role in suppressing SARS-CoV-2 with reference to case studies. The ongoing clinical trials both with respect to drug repurposing and vaccines are summarized along with a brief description. The recent advancements and future perspective of ongoing research for therapy and detection of SARS-CoV-2 are provided. The review, in brief, summarizes epidemiology, therapy and the current scenario for combating SARS-CoV-2.
has issue date
2020-06-01
(
xsd:dateTime
)
bibo:doi
10.1016/j.lfs.2020.117883
bibo:pmid
32497632
has license
no-cc
sha1sum (hex)
04617a86a87b436dd59ee5be9f396e48304e5200
schema:url
https://doi.org/10.1016/j.lfs.2020.117883
resource representing a document's title
Potential therapeutic targets for combating SARS-CoV-2: Drug repurposing, clinical trials and recent advancements
has PubMed Central identifier
PMC7263255
has PubMed identifier
32497632
schema:publication
Life Sci
resource representing a document's body
covid:04617a86a87b436dd59ee5be9f396e48304e5200#body_text
is
schema:about
of
named entity 'Therapeutic Targets'
named entity 'C-reactive protein'
named entity 'bat'
named entity 'enzyme'
named entity 'SARS-CoV-2'
named entity 'Baricitinib'
named entity 'transmembrane domain'
named entity 'proteases'
named entity 'influenza'
named entity 'prodrug'
named entity 'liver'
named entity 'clinical study'
named entity 'actinomycete'
named entity 'genetic material'
named entity 'Hubei'
named entity 'China'
named entity 'flavivirus'
named entity 'pathogenicity'
named entity 'host cell'
named entity 'JAK1'
named entity 'double-blind'
named entity 'anti-bacterial'
named entity 'respiratory viral infections'
named entity 'plasma'
named entity 'SARS-CoV'
named entity 'immunosuppressant'
named entity 'fever'
named entity 'parasite'
named entity 'spike protein'
named entity 'Staphylococcal'
named entity 'oral mucosa'
named entity 'oral administration'
named entity 'protein'
named entity 'methylprednisolone'
named entity 'COVID-19'
named entity 'bronchial epithelial cells'
named entity 'coronavirus'
named entity 'cathepsin'
named entity 'secretion'
named entity 'peptidoglycan'
named entity 'transcription'
named entity 'chloroquine'
named entity 'virus'
named entity 'COVID-19'
named entity 'recombination hotspots'
named entity 'viral life cycle'
named entity 'viral replication'
named entity 'SARS-CoV-2'
named entity 'ARDS'
named entity 'catalytic site'
named entity 'TMPRSS2'
named entity 'purine'
named entity 'leukopenia'
named entity 'non-human primate'
named entity 'janus kinase'
named entity 'intravenous'
named entity 'clinical trials'
named entity 'ferritin'
named entity 'upper respiratory'
named entity 'vaccines'
named entity 'RT-PCR'
named entity 'vaccines'
named entity 'immune reaction'
named entity 'RBD'
named entity 'virucidal'
named entity 'Phase-1'
named entity 'receptor'
named entity 'immune cell'
named entity 'HIV protease inhibitors'
named entity 'endocytosis'
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