PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
11578225-8	2001	Anthracene 5 adopts in the crystal a conformation of approximate C(2)(h) symmetry with pairs of peri groups on the same edge of the molecule oriented syn.	anthracene	0-10	synemin	Homo sapiens	150-153	
11674564-4	1999	All the cycloadditions occurred exclusively on the pi-face syn to the etheno bridge of 2, thereby in cases of the cycloadditions with anthracene, cyclopentadiene, 1,3-cyclohexadiene, and 6,6-dimethylfulvene producing the corresponding adducts 11a, 18b, 22b, and 23b that contain three double bonds aligned in parallel.	anthracene	134-144	synemin	Homo sapiens	59-62	
7093935-1	1982	The relative stabilities of conformers of the syn and anti-diastereomers of the fjord and bay-region diol-epoxides of benzo(c)phenanthrene (BCP) and benzo(a)anthracene (BA) have been calculated.	anthracene	157-167	synemin	Homo sapiens	46-49	
21337526-2	2011	The coordination cage accelerated the Diels-Alder reaction of anthracene at the electronically unfavorable, terminal benzene ring to give a compact, cavity-restrained syn-adduct.	anthracene	62-72	synemin	Homo sapiens	167-170	
16323842-1	2005	[reaction: see text] A double Diels-Alder reaction of the formal syn-bis(dehydro)octafluoroparacyclophane with anthracene leads to formation of a novel cage compound that contains a highly pyramidal double bond.	anthracene	111-121	synemin	Homo sapiens	65-68	
16052272-1	2005	Structurally controlled zinc porphyrin-anthracene dyads, syn-arranged 1 and anti-arranged 2, were newly synthesized employing a diarylurea linkage, and the excitation energy transfer (EET) from the anthracene to the zinc porphyrin chromophore was investigated by steady-state fluorescence emission spectroscopy as well as fluorescence lifetime measurement, especially focusing on the effect of the chromophoric orientation on the EET.	anthracene	39-49	synemin	Homo sapiens	57-60	
16052272-7	2005	These results showed that the syn-arrangement of the zinc porphyrin and anthracene chromophores was more preferred for intramolecular EET to the anti-arrangement.	anthracene	72-82	synemin	Homo sapiens	30-33	
34546251-3	2021	This precursor has been used for the synthesis of a versatile class of syn-thienoacenes comprising up to 13 fused rings, helical acenes and donor-acceptor acenes.	anthracene	129-135	synemin	Homo sapiens	71-74	
34546251-3	2021	This precursor has been used for the synthesis of a versatile class of syn-thienoacenes comprising up to 13 fused rings, helical acenes and donor-acceptor acenes.	anthracene	155-161	synemin	Homo sapiens	71-74	
33393192-4	2021	This strategy has been also used to the synthesis of doubly naphthalene-fused porphyrins and syn - and anti -fused-anthracene-bridged porphyrin dimers.	anthracene	115-125	synemin	Homo sapiens	40-43	
21710966-8	2011	The biradical mechanism for dimerization of anthracene and pentacene proceeds via syn or anti transition states and biradical minima through stepwise biradical pathways, while dimerization of heptacene proceeds via asynchronous ring closure of the complex formed by two heptacene molecules.	anthracene	44-54	synemin	Homo sapiens	82-85	
20936665-4	2011	Upon introducing a substituent at the 10-position of anthracene, we obtained a U-shaped isomer with syn geometry that yielded an excimer upon excitation and can decompose without steric protection.	anthracene	53-63	synemin	Homo sapiens	100-103	
20329777-4	2010	In the cases of anthracene and anthraquinone derivatives, the presence of syn and anti conformers was detected, and their interconversion barriers, due to the Ar-N rotation, were measured.	anthracene	16-26	synemin	Homo sapiens	74-77