PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
17317686-7	2007	Further fractionation of decasaccharides by anion-exchange chromatography revealed that most of the decasaccharides had HGF-inducing activity and the extent of sulfation was roughly related to the activity.	decasaccharides	25-40	hepatocyte growth factor	Homo sapiens	120-123
17317686-7	2007	Further fractionation of decasaccharides by anion-exchange chromatography revealed that most of the decasaccharides had HGF-inducing activity and the extent of sulfation was roughly related to the activity.	decasaccharides	100-115	hepatocyte growth factor	Homo sapiens	120-123
16624894-10	2006	Decasaccharides and dodecasaccharides containing one or two GalNAc4,6SO3 residues stimulated thrombin inhibition by HCII and prolonged the clotting time of normal but not HCII-depleted human plasma.	decasaccharides	0-15	coagulation factor II, thrombin	Homo sapiens	93-101
16624894-10	2006	Decasaccharides and dodecasaccharides containing one or two GalNAc4,6SO3 residues stimulated thrombin inhibition by HCII and prolonged the clotting time of normal but not HCII-depleted human plasma.	decasaccharides	0-15	serpin family D member 1	Homo sapiens	116-120
11799124-8	2002	At restricted concentrations of oligosaccharides (4 ng/ml), HGF/SF required decasaccharides, whereas at higher concentrations (100 ng/ml) even tetrasaccharides were able to partly restore DNA synthesis.	decasaccharides	76-91	hepatocyte growth factor	Homo sapiens	60-66
12000311-4	2002	From decasaccharides and longer, the k(ass) and affinity for FGF-2 was reduced substantially (tetradecasaccharide k(ass) 470000 M(-1) x s(-1), K(d) 30 nM).	decasaccharides	5-20	fibroblast growth factor 2	Rattus norvegicus	61-66
16120610-7	2005	In contrast, high affinity interactions with PTN required decasaccharides with E units (GlcUAbeta1-3GalNAc(4, 6-O-disulfate)), B units (GlcUA(2-O-sulfate)beta1-3GalNAc(4-O-sulfate)), and/or their IdoUA-containing counterparts (iE and iB) in addition to D/iD units, although the biological significance of such strong interactions remains to be investigated.	decasaccharides	58-73	pleiotrophin	Sus scrofa	45-48
7585697-7	1995	For oligosaccharides larger than decasaccharides, a small basic protein, angiogenin (M(r) = 14,120), was used to form the complex (an inhomogeneous hexadecasaccharide fraction was the largest available for this study).	decasaccharides	33-48	angiogenin	Homo sapiens	73-83
8973550-1	1996	On intravenous injection to rats, decasaccharides gave rise to a short-lived peak of lipoprotein lipase (LPL) activity, whereas octa- and hexasaccharides caused only marginal increases.	decasaccharides	34-49	lipoprotein lipase	Rattus norvegicus	85-103
8973550-1	1996	On intravenous injection to rats, decasaccharides gave rise to a short-lived peak of lipoprotein lipase (LPL) activity, whereas octa- and hexasaccharides caused only marginal increases.	decasaccharides	34-49	lipoprotein lipase	Rattus norvegicus	105-108
8973550-2	1996	In isolated hearts perfused by a single pass, decasaccharides released LPL more efficiently than conventional heparin on a mass basis.	decasaccharides	46-61	lipoprotein lipase	Rattus norvegicus	71-74
8973550-12	1996	Thus injection of decasaccharides leads to accelerated turnover of LPL with loss of functional LPL from extrahepatic tissues.	decasaccharides	18-33	lipoprotein lipase	Rattus norvegicus	67-70
8973550-12	1996	Thus injection of decasaccharides leads to accelerated turnover of LPL with loss of functional LPL from extrahepatic tissues.	decasaccharides	18-33	lipoprotein lipase	Rattus norvegicus	95-98
8810923-2	1996	The results show that heparin decasaccharides form a 1:1 complex with dimeric LPL and that decasaccharides are the shortest heparin fragments which can completely satisfy the heparin binding regions in dimeric LPL.	decasaccharides	30-45	lipoprotein lipase	Homo sapiens	78-81
8810923-2	1996	The results show that heparin decasaccharides form a 1:1 complex with dimeric LPL and that decasaccharides are the shortest heparin fragments which can completely satisfy the heparin binding regions in dimeric LPL.	decasaccharides	30-45	lipoprotein lipase	Homo sapiens	210-213
8810923-7	1996	The number of ionic interactions between LPL and high-affinity decasaccharides was estimated to be 10.	decasaccharides	63-78	lipoprotein lipase	Homo sapiens	41-44
30205243-4	2018	BMP-2 could bind to heparin hexasaccharides (dp6) and octasaccharides (dp8), but decasaccharides (dp10) were the minimum chain length required for both efficient binding of BMP-2 and consequent heparin-dependent cell responses.	decasaccharides	81-96	bone morphogenetic protein 2	Homo sapiens	173-178
6940150-2	1981	Direct measurements of the kinetic behavior of the hexasaccharides, octasaccharides, and decasaccharides showed that these fractions greatly enhanced the rate of Factor Xa inactivation by antithrombin.	decasaccharides	89-104	coagulation factor X	Homo sapiens	162-171
6940150-2	1981	Direct measurements of the kinetic behavior of the hexasaccharides, octasaccharides, and decasaccharides showed that these fractions greatly enhanced the rate of Factor Xa inactivation by antithrombin.	decasaccharides	89-104	serpin family C member 1	Homo sapiens	188-200
6940150-5	1981	The avidity of the hexasaccharides, octasaccharides, and decasaccharides for the protease inhibitor increased as a function of size with the respective dissociation constants ranging from 5.5 X 10(-6) M to 2.9 X 10(-7) M. These data suggest that the region of the heparin molecule needed for catalyzing Factor Xa-antithrombin interaction is intimately related to the antithrombin binding domain.	decasaccharides	57-72	coagulation factor X	Homo sapiens	303-312
6940150-5	1981	The avidity of the hexasaccharides, octasaccharides, and decasaccharides for the protease inhibitor increased as a function of size with the respective dissociation constants ranging from 5.5 X 10(-6) M to 2.9 X 10(-7) M. These data suggest that the region of the heparin molecule needed for catalyzing Factor Xa-antithrombin interaction is intimately related to the antithrombin binding domain.	decasaccharides	57-72	serpin family C member 1	Homo sapiens	313-325
6940150-5	1981	The avidity of the hexasaccharides, octasaccharides, and decasaccharides for the protease inhibitor increased as a function of size with the respective dissociation constants ranging from 5.5 X 10(-6) M to 2.9 X 10(-7) M. These data suggest that the region of the heparin molecule needed for catalyzing Factor Xa-antithrombin interaction is intimately related to the antithrombin binding domain.	decasaccharides	57-72	serpin family C member 1	Homo sapiens	367-379
32348723-3	2020	This work uses native mass spectrometry to investigate PF4 interactions with relatively short heparin chains (up to decasaccharides).	decasaccharides	116-131	platelet factor 4	Homo sapiens	55-58
21913222-6	2012	HAS2 mRNA expression was altered after the treatment with both tetrasaccharides and decasaccharides.	decasaccharides	84-99	hyaluronan synthase 2	Homo sapiens	0-4
21913222-7	2012	Phosphorylation of Akt was suppressed after 1 h treatment with HA decasaccharides, and the effect was partially reversed by anti-CD44 monoclonal antibody.	decasaccharides	66-81	AKT serine/threonine kinase 1	Homo sapiens	19-22
21913222-7	2012	Phosphorylation of Akt was suppressed after 1 h treatment with HA decasaccharides, and the effect was partially reversed by anti-CD44 monoclonal antibody.	decasaccharides	66-81	CD44 molecule (Indian blood group)	Homo sapiens	129-133