PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
24513051-2	2014	All compounds are characterized by a trans double bond located in the side chain between C-22 and C-23.	Carbon	89-90	nucleolin	Homo sapiens	98-102	
24596031-2	2014	The production of biodiesel, in particular, involves the process of upgrading biomass-derived small molecules to diesel precursors containing a specific carbon range (C11 -C23).	Carbon	153-159	nucleolin	Homo sapiens	172-175	
21993223-2	2011	Single-walled carbon nanotubes were functionalized with the F3 peptide using a polyethylene glycol linker to target nucleolin, a protein found on the surface of endothelial cells in the vasculature of solid tumors.	Carbon	14-20	nucleolin	Homo sapiens	116-125	
1328482-2	1992	HCMV adsorbed to cells was neutralized by C-23 (complement-independent), but not by C-41 (complement-dependent).	Carbon	1-2	nucleolin	Homo sapiens	42-46	
15358094-3	2004	These results indicate that the orientation of the hydroxyl group at the C-3 position determines the ratio between C-23 and C-24 oxidation pathways.	Carbon	73-74	nucleolin	Homo sapiens	115-119	
12180649-6	2002	By observing the chemical structures of compounds belonging to the first group we can see that less cytotoxic activities are related to the presence of a 3beta-hydroxy group on C-3 (ring A) and a double bond between C-22 and C-23 (side chain).	Carbon	177-178	nucleolin	Homo sapiens	225-229	
12180649-6	2002	By observing the chemical structures of compounds belonging to the first group we can see that less cytotoxic activities are related to the presence of a 3beta-hydroxy group on C-3 (ring A) and a double bond between C-22 and C-23 (side chain).	Carbon	216-217	nucleolin	Homo sapiens	225-229	
11179755-3	2001	The C-23 and C-26 oxidation pathways, the minor side chain modification pathways are initiated by hydroxylations at C-23 and C-26 of the side chain and lead to the formation of the end product, calcitriol lactone.	Carbon	4-5	nucleolin	Homo sapiens	116-120	
11179755-8	2001	To prevent C-23 and C-24 hydroxylations, cis or trans double bonds, or a triple bond are incorporated in between C-23 and C-24.	Carbon	11-12	nucleolin	Homo sapiens	113-117	
11179755-8	2001	To prevent C-23 and C-24 hydroxylations, cis or trans double bonds, or a triple bond are incorporated in between C-23 and C-24.	Carbon	20-21	nucleolin	Homo sapiens	113-117	
21578527-2	2009	One- and two-dimensional (1)H and (13)C NMR spectra, as well as IR data, are in agreement with the presence of a ketoxime group at C-23.	Carbon	38-39	nucleolin	Homo sapiens	131-135	
16617161-2	2006	Although human CYP24A1 catalyzes both C-23 and C-24 oxidation pathways, rat CYP24A1 shows almost no C-23 oxidation pathway.	Carbon	15-16	nucleolin	Homo sapiens	38-42	
16235944-2	2005	Esterification with a C(1-6) acid, and selective ozonolysis to release the C(23) carbonyl, complete the assembly of all the carbons present in the lituarine macrocyclic core.	Carbon	124-131	nucleolin	Homo sapiens	75-80	
15764712-5	2005	Five metabolites were detected in the metabolism of C3O1 and O2C3 by human CYP24A1 including both C-23 and C-24 oxidation pathways.	Carbon	52-53	nucleolin	Homo sapiens	98-102	
7664636-1	1995	1 alpha, 25-Dihydroxyvitamin D3 [1 alpha, 25-(OH)2D3], the hormonal form of vitamin D3, is further metabolized in the kidney and intestine through the carbon 24 (C-24) oxidation pathway initiated by C-24 hydroxylation, and the carbon 23 (C-23) oxidation pathway initiated by C-23 hydroxylation.	Carbon	151-157	nucleolin	Homo sapiens	238-242	
7664636-1	1995	1 alpha, 25-Dihydroxyvitamin D3 [1 alpha, 25-(OH)2D3], the hormonal form of vitamin D3, is further metabolized in the kidney and intestine through the carbon 24 (C-24) oxidation pathway initiated by C-24 hydroxylation, and the carbon 23 (C-23) oxidation pathway initiated by C-23 hydroxylation.	Carbon	151-157	nucleolin	Homo sapiens	275-279	
7664636-1	1995	1 alpha, 25-Dihydroxyvitamin D3 [1 alpha, 25-(OH)2D3], the hormonal form of vitamin D3, is further metabolized in the kidney and intestine through the carbon 24 (C-24) oxidation pathway initiated by C-24 hydroxylation, and the carbon 23 (C-23) oxidation pathway initiated by C-23 hydroxylation.	Carbon	162-163	nucleolin	Homo sapiens	238-242	
7664636-1	1995	1 alpha, 25-Dihydroxyvitamin D3 [1 alpha, 25-(OH)2D3], the hormonal form of vitamin D3, is further metabolized in the kidney and intestine through the carbon 24 (C-24) oxidation pathway initiated by C-24 hydroxylation, and the carbon 23 (C-23) oxidation pathway initiated by C-23 hydroxylation.	Carbon	162-163	nucleolin	Homo sapiens	275-279	
8517874-6	1993	These data suggested that substitution of fluorines for hydrogens at C-26 and at C-27 positions may result in alteration in chemical reactivity and/or conformation of C-23, C-24 and C-25 positions of the 1,25-(OH)2D3 molecule.	Carbon	69-70	nucleolin	Homo sapiens	167-171	
8517874-6	1993	These data suggested that substitution of fluorines for hydrogens at C-26 and at C-27 positions may result in alteration in chemical reactivity and/or conformation of C-23, C-24 and C-25 positions of the 1,25-(OH)2D3 molecule.	Carbon	81-82	nucleolin	Homo sapiens	167-171	
1328482-4	1992	The cell-to-cell infection of HCMV was also blocked only by C-23, and not by C-41.	Carbon	31-32	nucleolin	Homo sapiens	60-64	
6546486-6	1984	These results indicate that when the lactonization at C-23 and C-26 positions of various vitamin D3 derivatives occurred the stereochemical configuration at their C-23 and/or C-25 positions was not changed and the difference of the stereochemical configurations determined the rate of lactonization.	Carbon	54-55	nucleolin	Homo sapiens	163-167	
34355562-4	2021	Compounds 7, 8, 10, and 11 exhibited cytotoxicity to human cancer cell lines, indicating that the presence of a lactone moiety, as well as a double bond between C-22 and C-23, might play key roles in mediating their cytotoxicity.	Carbon	161-162	nucleolin	Homo sapiens	170-174	
35119260-12	2022	Our findings show that carbon modifiers facilitated surface reconstruction and regulated CO2 diffusion to suppress HER and improve the C2-3 product selectivity.	Carbon	23-29	nucleolin	Homo sapiens	135-139	
4031656-0	1985	Synthesis of C-22, C-23-3H-labeled 3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestane.	Carbon	13-14	nucleolin	Homo sapiens	19-23	
4031656-1	1985	This report describes an efficient synthesis of C-22, C-23-(3)H-labeled 3alpha,7alpha,12alpha-trihydroxy-5beta-cholestane.	Carbon	48-49	nucleolin	Homo sapiens	54-58	
4031656-3	1985	Synthesis of C-22, C-23-(3)H-labeled 3alpha,7alpha,12alpha-trihydroxy-5beta-cholestane.	Carbon	13-14	nucleolin	Homo sapiens	19-23	
31994401-0	2020	Synthesis of Strophasterols C, E, and F. The synthesis of strophasterols C, E, and F has been accomplished from a 14,15-secoergostane derivative via a 1,3-dipolar cycloaddition of a nitrile oxide intermediate to simultaneously install an isolated cyclopentane ring and a C23 oxygen functionality in a diastereoselective manner and a regio- and diastereoselective selenohydroxylation of an olefinic intermediate under thermodynamic conditions.	Carbon	58-74	nucleolin	Homo sapiens	271-274	
33586959-0	2021	Nucleolin-Targeted Ratiometric Fluorescent Carbon Dots with a Remarkably Large Emission Wavelength Shift for Precise Imaging of Cathepsin B in Living Cancer Cells.	Carbon	43-49	nucleolin	Homo sapiens	0-9	
32931247-0	2020	Non-Innocent Role of Porous Carbon Towards Enhancing C2-3 Products in Electroreduction of Carbon Dioxide.	Carbon	28-34	nucleolin	Homo sapiens	53-57	
28874822-2	2017	AS1411, a nucleolin aptamer, is wrapped around water-soluble carbon dots and used as a probe for the detection of several types of cancer cells.	Carbon	61-67	nucleolin	Homo sapiens	10-19	
28216894-11	2017	The polar groups at C-1, C-2, C-3, C-23, and C-28 and the linkage of sugar moieties influenced the different cytotoxic activities.	Carbon	20-21	nucleolin	Homo sapiens	35-39