PMC:7544934 / 4972-5953
Annnotations
LitCovid_Glycan-Motif-Structure
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T9 | 131-134 | https://glytoucan.org/Structures/Glycans/G00057MO | denotes | LDN |
T10 | 131-134 | https://glytoucan.org/Structures/Glycans/G31736BK | denotes | LDN |
T11 | 486-489 | https://glytoucan.org/Structures/Glycans/G00057MO | denotes | LDN |
T12 | 486-489 | https://glytoucan.org/Structures/Glycans/G31736BK | denotes | LDN |
T13 | 594-597 | https://glytoucan.org/Structures/Glycans/G00057MO | denotes | LDN |
T14 | 594-597 | https://glytoucan.org/Structures/Glycans/G31736BK | denotes | LDN |
T15 | 868-871 | https://glytoucan.org/Structures/Glycans/G00057MO | denotes | LDN |
T16 | 868-871 | https://glytoucan.org/Structures/Glycans/G31736BK | denotes | LDN |
LitCovid-PubTator
Id | Subject | Object | Predicate | Lexical cue | tao:has_database_id |
---|---|---|---|---|---|
155 | 517-523 | Gene | denotes | ERK1/2 | Gene:5595 |
156 | 629-633 | Gene | denotes | ACE2 | Gene:59272 |
157 | 814-822 | Species | denotes | patients | Tax:9606 |
158 | 107-117 | Chemical | denotes | naltrexone | MESH:D009271 |
159 | 272-282 | Chemical | denotes | naltrexone | MESH:D009271 |
160 | 384-394 | Chemical | denotes | naltrexone | MESH:D009271 |
161 | 658-666 | Disease | denotes | COVID-19 | MESH:C000657245 |
162 | 719-728 | Disease | denotes | infection | MESH:D007239 |
163 | 732-740 | Disease | denotes | COVID-19 | MESH:C000657245 |
164 | 805-813 | Disease | denotes | COVID-19 | MESH:C000657245 |
165 | 964-972 | Disease | denotes | COVID-19 | MESH:C000657245 |
LitCovid-sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T38 | 0-267 | Sentence | denotes | In this study, we report that the FDA-approved non-peptide opioid antagonist drug (Vickers & Jolly, 2006), naltrexone in low dose (LDN) suppresses high fat/LPS induced pro-inflammatory cytokine release both from macrophage cells and Adipose tissue macrophages (ATMs). |
T39 | 268-485 | Sentence | denotes | The naltrexone is already an FDA approved drug and thus the pharmacology (pharmacokinetics and pharmacodynamics) of naltrexone is well known and reported elsewhere (Gonzalez & Brogden, 1988; Toljan and Vrooman, 2018). |
T40 | 486-534 | Sentence | denotes | LDN also showed activity as an ERK1/2 inhibitor. |
T41 | 535-643 | Sentence | denotes | Moreover, virtual docking and simulation data also suggest LDN may disrupt the interaction of ACE2 with RBD. |
T42 | 644-981 | Sentence | denotes | As a reliable COVID-19 vaccine is unlikely to available before the maximal infection of COVID-19 has occurred, it is essential to establish therapeutics for the COVID-19 patients, based on our data, we proposed FDA-approved LDN can be used in combination or as an adjuvants therapy to treat mild to moderate symptomatic COVID-19 patients |
2_test
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
32930058-2836152-56195690 | 453-457 | 2836152 | denotes | 1988 |