PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
32770567-0	2021	Epigallocatechin gallate and theaflavin gallate interaction in SARS-CoV-2 spike-protein central channel with reference to the hydroxychloroquine interaction: Bioinformatics and molecular docking study.	epigallocatechin gallate	0-24	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	74-79	
32770567-7	2021	Moreover, out of three distinct binding sites (I, II and III) of spike core when HCQ binds only with site III (farthest from the nCoV-RBD of ACE2 contact), epigallocatechin gallate and theaflavin gallate bind all three sites.	epigallocatechin gallate	156-180	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	65-70	
32770567-6	2021	In the current study we demonstrated by bioinformatics (CASTp: computed atlas of surface topography of protein, PyMol: molecular visualization) and molecular docking (PatchDock and Autodock) experiments that tea flavonoids catechin products mainly epigallocatechin gallate or other like theaflavin gallate demonstrated higher atomic contact energy (ACE) value, binding energy, Ki value, ligand efficiency, surface area and more amino acid interactions than hydroxychloroquine (HCQ) during binding in the central channel of the spike protein.	epigallocatechin gallate	248-272	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	527-532	
34461999-0	2021	Epigallocatechin gallate from green tea effectively blocks infection of SARS-CoV-2 and new variants by inhibiting spike binding to ACE2 receptor.	epigallocatechin gallate	0-24	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	114-119	
33425427-7	2020	The results showed that hesperidin, nabiximols, pectolinarin, epigallocatechin gallate, and rhoifolin had better poses than nelfinavir, chloroquine, and hydroxychloroquine sulfate as spike glycoprotein inhibitors.	epigallocatechin gallate	62-86	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	183-188	
33149560-8	2020	However, 4 polyphenols such as epigallocatechin gallate (EGCG), homoeriodictyol, isorhamnetin, and curcumin interact, in addition to the Spike protein and its binding sites in GRP78, with the ATPase domain of GRP78.	epigallocatechin gallate	31-55	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	137-142	
33149560-8	2020	However, 4 polyphenols such as epigallocatechin gallate (EGCG), homoeriodictyol, isorhamnetin, and curcumin interact, in addition to the Spike protein and its binding sites in GRP78, with the ATPase domain of GRP78.	epigallocatechin gallate	57-61	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	137-142	
34243689-8	2021	Affinity of phytoconstituents towards SARS-CoV-2 spike protein-human ACE2 complex decreased as isomeldenin > tinosporaside > EGCG whereas in case of unbound ACE2, the strength of binding followed the order isomeldenin > tinosporaside > ellagic acid.	epigallocatechin gallate	125-129	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	49-54	
34243689-11	2021	SAR analysis revealed that isomeldenin, tinosporaside, EGCG and ellagic acid bind to viral spike glycoproteins via H-bond, Pi-Pi, Pi-sigma and Pi-alkyl type interactions.	epigallocatechin gallate	55-59	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	91-96	
35382132-8	2022	Conclusion: EGCG can be a potential inhibitor drug which can bind with ACE-2 receptor thus inhibiting the interaction of mainly Mpro protein and spike glycoprotein of SARS-CoV-2.	epigallocatechin gallate	12-16	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	145-150	
35475273-8	2022	Conclusion: EGCG can be a potential inhibitor drug which can bind with ACE-2 receptor thus inhibiting the interaction of mainly Mpro protein and spike glycoprotein of SARS-CoV-2.	epigallocatechin gallate	12-16	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	145-150