PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
34161119-3	2021	METHODS: The effect of quercetin (75microM) and vitamin C (100 microM) on CXCR4, CXCR7 chemokine receptors, alpha4, alpha5 and beta1 integrins, ki-67 proliferation marker and Vascular endothelial growth factor, VEGF was evaluated using Quantitative Reverse Transcription PCR (RT-qPCR).	Quercetin	23-32	atypical chemokine receptor 3	Homo sapiens	81-86	
34161119-4	2021	RESULTS: The effect of quercetin and vitamin C alone was different on PC3 and DU145 prostate cancer cell lines, but sequential combination reduced significantly the expression of CXCR and CXCR7 chemokine receptors, alpha4, alpha5 and beta1 integrin subunits, VEGF and Ki-67 proliferation markers in PC3 and DU145 cell lines.	Quercetin	23-32	atypical chemokine receptor 3	Homo sapiens	188-193	
35120520-11	2022	The docking scores toward proteins 3ODU of CXCR4 and 6K3F of CXCR7 were - 7.71 and - 7.17 for curcumin, - 5.97 and - 6.03 for quercetin, - 5.68 and - 5.49 for trans-resveratrol, and - 4.88 and - 4.70 for (1 s,4 s)-eucalyptol respectively indicating that all compounds, except quercetin, have more interactions with CXCR4 than with CXCR7.	Quercetin	126-135	atypical chemokine receptor 3	Homo sapiens	61-66	
35120520-11	2022	The docking scores toward proteins 3ODU of CXCR4 and 6K3F of CXCR7 were - 7.71 and - 7.17 for curcumin, - 5.97 and - 6.03 for quercetin, - 5.68 and - 5.49 for trans-resveratrol, and - 4.88 and - 4.70 for (1 s,4 s)-eucalyptol respectively indicating that all compounds, except quercetin, have more interactions with CXCR4 than with CXCR7.	Quercetin	276-285	atypical chemokine receptor 3	Homo sapiens	61-66	
35120520-16	2022	CONCLUSIONS: Curcumin showed the top binding interaction against active sites of CXCR4 and CXCR7 receptors, with the best safety profile, followed by quercetin, resveratrol, and eucalyptol.	Quercetin	150-159	atypical chemokine receptor 3	Homo sapiens	91-96