PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
7494868-1	1995	Single crystals of 9-methyladenine were X-irradiated at 10 K and at 65 K and were studied using K-band EPR, ENDOR and field-swept ENDOR (FSE) techniques in the temperature range 10 K to 290 K. Three major radicals are stabilized in 9-methyladenine at 10 K. These are: MA1, the adenine anion, probably protonated at N3; MA2, the species formed by net hydrogen abstraction from the 9-methyl group; and MA3, the radical formed by net hydrogen addition to C8 of the adenine moiety.	9-methyladenine	19-34	PNMA family member 1	Homo sapiens	268-271
10678351-4	2000	AdZ.F(pK7) increased the frequency of cells expressing the reporter gene, beta-galactosidase, and improved transduction by 2- to 20-fold compared with AdZ in U87, D54, and GL261 cells.	9-methyladenine	0-3	galactosidase, beta 1	Mus musculus	74-92
7494868-1	1995	Single crystals of 9-methyladenine were X-irradiated at 10 K and at 65 K and were studied using K-band EPR, ENDOR and field-swept ENDOR (FSE) techniques in the temperature range 10 K to 290 K. Three major radicals are stabilized in 9-methyladenine at 10 K. These are: MA1, the adenine anion, probably protonated at N3; MA2, the species formed by net hydrogen abstraction from the 9-methyl group; and MA3, the radical formed by net hydrogen addition to C8 of the adenine moiety.	9-methyladenine	19-34	PNMA family member 2	Homo sapiens	319-322
7494868-1	1995	Single crystals of 9-methyladenine were X-irradiated at 10 K and at 65 K and were studied using K-band EPR, ENDOR and field-swept ENDOR (FSE) techniques in the temperature range 10 K to 290 K. Three major radicals are stabilized in 9-methyladenine at 10 K. These are: MA1, the adenine anion, probably protonated at N3; MA2, the species formed by net hydrogen abstraction from the 9-methyl group; and MA3, the radical formed by net hydrogen addition to C8 of the adenine moiety.	9-methyladenine	19-34	PNMA family member 3	Homo sapiens	400-403
33256482-3	2021	Areas covered: Adrecizumab (ADZ) (HAM 8101) is a humanized targeted therapy directed against the N-terminus of adrenomedullin (ADM).	9-methyladenine	28-31	adrenomedullin	Homo sapiens	111-125
1551200-9	1992	The selective A1-adenosine receptor antagonist N-0861 (9-methyladenine derivative) antagonized the effects of adenosine on afterdepolarizations, ITi, and TA.	9-methyladenine	55-70	adenosine receptor A1	Cavia porcellus	14-35
33256482-3	2021	Areas covered: Adrecizumab (ADZ) (HAM 8101) is a humanized targeted therapy directed against the N-terminus of adrenomedullin (ADM).	9-methyladenine	28-31	adrenomedullin	Homo sapiens	127-130
33256482-4	2021	ADZ inhibits excessive circulating sepsis-induced ADM and stimulates protective effects on the endothelial barrier, and decreases interstitial vasodilatory effects.	9-methyladenine	0-3	adrenomedullin	Homo sapiens	50-53
33256482-7	2021	Expert opinion: ADZ is the first humanized antibody directed against ADM.	9-methyladenine	16-19	adrenomedullin	Homo sapiens	69-72
33256482-8	2021	The main interest of ADZ is its potential use as a "biomarker-guided therapy" in septic patients with high circulating ADM.	9-methyladenine	21-24	adrenomedullin	Homo sapiens	119-122
17263404-5	2007	The theoretical results indicate that the excess electron in both AFA(-) and MAFA(-) occupies a pi* orbital localized on adenine/9-methyladenine, and the adiabatic stability of the most stable anions amounts to 0.67 and 0.54 eV for AFA(-) and MAFA(-), respectively.	9-methyladenine	129-144	AFA	Homo sapiens	66-69
17263404-5	2007	The theoretical results indicate that the excess electron in both AFA(-) and MAFA(-) occupies a pi* orbital localized on adenine/9-methyladenine, and the adiabatic stability of the most stable anions amounts to 0.67 and 0.54 eV for AFA(-) and MAFA(-), respectively.	9-methyladenine	129-144	MAF bZIP transcription factor A	Homo sapiens	77-81
17263404-5	2007	The theoretical results indicate that the excess electron in both AFA(-) and MAFA(-) occupies a pi* orbital localized on adenine/9-methyladenine, and the adiabatic stability of the most stable anions amounts to 0.67 and 0.54 eV for AFA(-) and MAFA(-), respectively.	9-methyladenine	129-144	AFA	Homo sapiens	78-81
17263404-5	2007	The theoretical results indicate that the excess electron in both AFA(-) and MAFA(-) occupies a pi* orbital localized on adenine/9-methyladenine, and the adiabatic stability of the most stable anions amounts to 0.67 and 0.54 eV for AFA(-) and MAFA(-), respectively.	9-methyladenine	129-144	MAF bZIP transcription factor A	Homo sapiens	243-247