PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
23077784-0	2012	Molecular mapping of heterocyclic diazene derivatives for estrogen receptor modulation.	diazene	34-41	estrogen receptor 1	Homo sapiens	58-75
23077784-2	2012	The present study explored the pharmacophore features of diazene derivatives for selective estrogen receptor (ER) modulation using quantitative structure activity relationship (QSAR) and space modeling approaches.	diazene	57-64	estrogen receptor 1	Homo sapiens	91-108
23077784-2	2012	The present study explored the pharmacophore features of diazene derivatives for selective estrogen receptor (ER) modulation using quantitative structure activity relationship (QSAR) and space modeling approaches.	diazene	57-64	estrogen receptor 1	Homo sapiens	110-112
18338040-1	2008	A new type of fluorescent sensor has been developed from a perylene based molecule, N,N"-dideoxythymidine-3,4,9,10-perylene-tetracarboxylic diimide (TT-PTCDI); the strong, highly selective binding between the thymine ligand (T) and Hg2+ ion enables efficient sensing of mercury ions based on a fluorescence quenching mechanism, which is primarily caused by metal-coordination induced molecular aggregation.	diazene	140-147	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	232-235
22256971-5	2012	The dimer 4 exhibits two accessible reversible reduction couples separated by 570 mV indicating the stability of the one-electron reduced species located on the diimine-based bridge abp.	diazene	161-168	amine oxidase copper containing 1	Homo sapiens	182-185
22199407-1	2011	The C21-C34 fragment of the potent FKBP12-binding macrolide antascomicin B was prepared using Ireland-Claisen and allylic diazene rearrangements to establish the C26/C27 and the C23 stereocenters, respectively.	diazene	122-129	TBL1X/Y related 1	Homo sapiens	4-7
22199407-1	2011	The C21-C34 fragment of the potent FKBP12-binding macrolide antascomicin B was prepared using Ireland-Claisen and allylic diazene rearrangements to establish the C26/C27 and the C23 stereocenters, respectively.	diazene	122-129	FKBP prolyl isomerase 1A pseudogene 4	Homo sapiens	35-41
21761893-2	2011	The stepwise union of complex amines in the form of mixed diazenes followed by photoexpulsion of dinitrogen in a solvent cage provides completely guided assembly at challenging C(sp(3))-C(sp(3)) and C(sp(3))-C(sp(2)) connections.	diazene	58-66	regulator of calcineurin 2	Homo sapiens	208-215
21476502-6	2011	The Gibbs activation energy, DeltaG( ), for the isomerization of 5 was determined as 103.7 (102.4) kJ/mol for the conversion of the anti-(syn-) to the syn-(anti-)isomer at 45.0  C. Condensation of 5 with two chiral amino alcohols generates diimines that undergo quantitative asymmetric transformation of the first kind toward the thermodynamically favored (P,P,R,R)- or (M,M,S,S)-atropisomer, respectively.	diazene	240-248	synemin	Homo sapiens	138-141
21476502-6	2011	The Gibbs activation energy, DeltaG( ), for the isomerization of 5 was determined as 103.7 (102.4) kJ/mol for the conversion of the anti-(syn-) to the syn-(anti-)isomer at 45.0  C. Condensation of 5 with two chiral amino alcohols generates diimines that undergo quantitative asymmetric transformation of the first kind toward the thermodynamically favored (P,P,R,R)- or (M,M,S,S)-atropisomer, respectively.	diazene	240-248	synemin	Homo sapiens	151-154
21280661-3	2011	At low reductant levels, NBS oxidizes Au(I), which linearly suppresses subsequent oxidation of TMB by NBS to its blue charge-transfer complex of diamine and diimine to 2.00 mg L(-1) of Au, resulting in reduced color formation.	diazene	157-164	nibrin	Homo sapiens	25-28
21280661-3	2011	At low reductant levels, NBS oxidizes Au(I), which linearly suppresses subsequent oxidation of TMB by NBS to its blue charge-transfer complex of diamine and diimine to 2.00 mg L(-1) of Au, resulting in reduced color formation.	diazene	157-164	nibrin	Homo sapiens	102-105
20728319-1	2010	In this paper, graphene oxide nanosheets (GOS) are functionalized by bovine serum albumin (BSA) via diimide-activated amidation under ambient conditions.	diazene	100-107	albumin	Homo sapiens	76-89
20162209-4	2010	The intermolecular pi-pi stacking interactions between the enantiomeric pairs of heterochiral Cr(III)(2)Co(II) entities through the aromatic diimine terminal ligands lead to a unique two-dimensional supramolecular network.	diazene	141-148	mitochondrially encoded cytochrome c oxidase II	Homo sapiens	104-110
19294276-1	2009	Optically pure, single diastereomer fac-tris(diimine) complexes of Fe(II) are available from a remarkably facile one-pot procedure using a range of readily available (R)-2-phenylglycinol derivatives.	diazene	45-52	FA complementation group C	Homo sapiens	36-39
18973295-2	2008	A highly potent and selective GSK3 and Pim1 half-sandwich complex NP309 was successfully converted into a PAK1 inhibitor by making use of the large octahedral compounds Lambda-FL172 and Lambda-FL411 in which the cyclopentadienyl moiety of NP309 is replaced by a chloride and sterically demanding diimine ligands.	diazene	296-303	Pim-1 proto-oncogene, serine/threonine kinase	Homo sapiens	39-43
18973295-2	2008	A highly potent and selective GSK3 and Pim1 half-sandwich complex NP309 was successfully converted into a PAK1 inhibitor by making use of the large octahedral compounds Lambda-FL172 and Lambda-FL411 in which the cyclopentadienyl moiety of NP309 is replaced by a chloride and sterically demanding diimine ligands.	diazene	296-303	p21 (RAC1) activated kinase 1	Homo sapiens	106-110
18092798-1	2008	One-pot reduction/allylic diazene rearrangement of lactic acid- and mandelic acid-derived alpha,beta-unsaturated tosyl hydrazones leads to 1,4-syn- or 1,4-anti-E-2-alkenyl arrays in high yield and diastereoselectivity.	diazene	26-33	synemin	Homo sapiens	143-146
18221936-4	2008	This suggests that ROS generation could be attributed to a futile two-electron redox cycle involving oxidation of phenylenediamine to the corresponding diimine by the mitochondrial electron transfer chain and re-reduction by the DT-diaphorase.	diazene	152-159	NAD(P)H quinone dehydrogenase 1	Rattus norvegicus	229-242
18712740-1	2008	Ruthenium(II)-TPA-diimine complexes, [Ru(TPA)(diimine)]2+ (TPA=tris(2-pyridylmethyl)amine; diimine=2,2"-bipyridine (bpy), 2,2"-bipyrimidine (bpm), 1,10-phenanthroline (phen)) were synthesized and characterized by spectroscopic and crystallographic methods.	diazene	18-25	plasminogen activator, tissue type	Homo sapiens	14-17
18712740-1	2008	Ruthenium(II)-TPA-diimine complexes, [Ru(TPA)(diimine)]2+ (TPA=tris(2-pyridylmethyl)amine; diimine=2,2"-bipyridine (bpy), 2,2"-bipyrimidine (bpm), 1,10-phenanthroline (phen)) were synthesized and characterized by spectroscopic and crystallographic methods.	diazene	18-25	plasminogen activator, tissue type	Homo sapiens	41-44
18712740-1	2008	Ruthenium(II)-TPA-diimine complexes, [Ru(TPA)(diimine)]2+ (TPA=tris(2-pyridylmethyl)amine; diimine=2,2"-bipyridine (bpy), 2,2"-bipyrimidine (bpm), 1,10-phenanthroline (phen)) were synthesized and characterized by spectroscopic and crystallographic methods.	diazene	18-25	plasminogen activator, tissue type	Homo sapiens	41-44
18712740-1	2008	Ruthenium(II)-TPA-diimine complexes, [Ru(TPA)(diimine)]2+ (TPA=tris(2-pyridylmethyl)amine; diimine=2,2"-bipyridine (bpy), 2,2"-bipyrimidine (bpm), 1,10-phenanthroline (phen)) were synthesized and characterized by spectroscopic and crystallographic methods.	diazene	46-53	plasminogen activator, tissue type	Homo sapiens	14-17
17894517-2	2007	SWNTs were functionalized under ambient conditions with either the Knob protein domain from adenovirus serotype 12 (Ad 12 Knob) or its human cellular receptor, the CAR protein, via diimide-activated amidation.	diazene	181-188	CXADR pseudogene 1	Homo sapiens	164-167
16061352-5	2006	Flow cytometry analysis showed that diazene JK-279 induces G(2)/M phase arrest, mediated by the increase in p21 expression, and accompanied by an alteration in the expression of survivin.	diazene	36-43	H3 histone pseudogene 16	Homo sapiens	108-111
16626156-1	2006	Intramolecular reductive coupling of diimines in the presence of Zn/Ti(O(i)Pr)2Cl2 gives the corresponding (+/-)-2,3-diarylpiperazines in 73-83% yields with dl/meso ratio >99%:<1%.	diazene	37-45	endogenous retrovirus group W member 5	Homo sapiens	79-82
17081007-4	2006	Thus, diimine 4 leads to low selectivities, producing a 1:1 mixture of cis-syn-cis and cis-anti-cis diastereomers, while diimines 5-7 having the diimine sites more separated lead almost exclusively to the cis-anti-cis diastereomers.	diazene	6-13	synemin	Homo sapiens	75-78
12584183-2	2003	We recently reported that diamide, a diazene carbonyl derivative which oxidizes thiols to disulfides through addition/displacement reactions at the diazene bond, induces potent GSH-dependent inactivation of several PKC isozymes, including the oncogenic isozyme PKC epsilon, via S-glutathiolation.	diazene	37-44	protein kinase C, epsilon	Mus musculus	261-272
16018614-2	2005	Six perylene diimide-appended hexaazatriphenylene, HAT-PDI(6), was self-assembled in both solution and film state to form a highly stabilized dimer aggregate, in which an efficient energy transfer occurs from the hexaazatriphenylene core to the perylene-diimide moiety.	diazene	13-20	peptidyl arginine deiminase 1	Homo sapiens	55-58
15877421-6	2005	In fac-Re(phenC triple bond CH)(CO)(3)Cl, the RT excited-state decay is most consistent with a metal-to-ligand charge transfer (MLCT) assignment, whereas at 77 K, the lowest excited state is dominated by the triplet intraligand ((3)IL) state, localized within the diimine ligand.	diazene	264-271	FA complementation group C	Homo sapiens	3-6
14871110-7	2004	The planar SNx (x = 2, 3) units in the diimide 3 and the triimide 4 reveal characteristics of m-center-n-electron systems.	diazene	39-46	annexin A7	Homo sapiens	11-14
12538029-0	2003	Estrogenic diazenes: heterocyclic non-steroidal estrogens of unusual structure with selectivity for estrogen receptor subtypes.	diazene	11-19	estrogen receptor 1	Homo sapiens	100-117
11560326-5	2001	B3LYP/6-31G* calculations on an unsubstituted, uncomplexed system suggest that the initially formed P,N-ylide of the H2C=N-(CH)2-N=CH2 diimine both kinetically and thermodynamically favors an intramolecular 1,3-dipolar cycloaddition over an imine insertion into the CPN ring of an intermediate azaphosphiridine.	diazene	135-142	protein tyrosine phosphatase non-receptor type 22	Homo sapiens	2-5
34252797-0	2021	Design and In-silico study of bioimaging fluorescence Graphene quantum dot-Bovine serum albumin complex synthesized by diimide-activated amidation.	diazene	119-126	albumin	Homo sapiens	82-95
11259323-14	2001	The results demonstrate that methemoglobin can catalyze the peroxidatic formation of an ABZ sulfinamide adduct, perhaps by a diimine monocation intermediate.	diazene	125-132	hemoglobin subunit gamma 2	Homo sapiens	29-42
11666573-0	1996	Experimental and Theoretical Investigations of the Formation of the Diazene PhSN=C(H)N=NC(H)=NSPh from HCN(2)(SPh)(3) by a Thiyl-Radical-Catalyzed Mechanism: Identification of the HC(NSPh)(2)(*) Radical and X-ray Structures of HCN(2)(SPh)(3) and PhSN=C(H)N=NC(H)=NSPh.	diazene	68-75	surfactant associated 3	Homo sapiens	94-97
11666573-0	1996	Experimental and Theoretical Investigations of the Formation of the Diazene PhSN=C(H)N=NC(H)=NSPh from HCN(2)(SPh)(3) by a Thiyl-Radical-Catalyzed Mechanism: Identification of the HC(NSPh)(2)(*) Radical and X-ray Structures of HCN(2)(SPh)(3) and PhSN=C(H)N=NC(H)=NSPh.	diazene	68-75	surfactant associated 3	Homo sapiens	110-113
9202197-7	1997	Evidence suggesting this was that both diimine accumulation and the ensuing cytotoxicity were markedly increased by inactivating hepatocyte DT diaphorase but were prevented by a subtoxic concentration of the mitochondrial respiratory inhibitor cyanide.	diazene	39-46	NAD(P)H quinone dehydrogenase 1	Homo sapiens	140-153
6506753-5	1984	Synthetic diazene intermediates of phenylhydrazine and N-aminopiperidine reacted rapidly with microsomal cytochrome P-450 to form a spectral intermediate resembling the putative iron porphyrin-diazenyl complex.	diazene	10-17	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	105-121
35190135-7	2022	The synthesized diimides were fully characterized by FT-IR, multinuclear NMR, SEM, TEM, TGA, and BET analysis.	diazene	16-24	T-box transcription factor 1	Homo sapiens	88-91
35190135-7	2022	The synthesized diimides were fully characterized by FT-IR, multinuclear NMR, SEM, TEM, TGA, and BET analysis.	diazene	16-24	delta/notch like EGF repeat containing	Homo sapiens	97-100
6802831-10	1982	In addition, the diazene-bound heme of cytochrome P-450 apparently was modified irreversibly in the presence of oxygen.	diazene	17-24	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	39-55
6873062-0	1983	Reaction of monosubstituted hydrazines and diazenes with rat-liver cytochrome P450.	diazene	43-51	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	67-82
6873062-7	1983	These results, when compared to those recently described on reactions of monosubstituted hydrazines RNHNH2 and diazenes RN = NH with hemoglobin and iron-porphyrins, are consistent with a [cytochrome P450-Fe(II)(RN = NH)] structure for the 446-nm-absorbing complexes and a sigma-alkyl cytochrome P450-Fe(III)-R structure for the complexes characterized by a Soret peak around 480 nm.	diazene	111-119	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	188-203
6873062-7	1983	These results, when compared to those recently described on reactions of monosubstituted hydrazines RNHNH2 and diazenes RN = NH with hemoglobin and iron-porphyrins, are consistent with a [cytochrome P450-Fe(II)(RN = NH)] structure for the 446-nm-absorbing complexes and a sigma-alkyl cytochrome P450-Fe(III)-R structure for the complexes characterized by a Soret peak around 480 nm.	diazene	111-119	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	284-299
891549-7	1977	Sterically unhindered thiol groups in the rat hemoglobin are thought to react with the usual adduct intermediate in GSH oxidation by diazene (formed from RCON = NCOR + GSH leads to RCON(SG)NHCOR) to produce mixed disulfides, from which GSH is not easily regenerated.	diazene	133-140	nuclear receptor co-repressor 1	Rattus norvegicus	161-165
31366012-3	2019	Monoclonal antibody (mAb, Ab1) of CFB was covalently immobilized on the MCNT surface via diimide-activated conjugation between the carboxyl groups on the MCNT surface and amino groups of antibodies.	diazene	89-96	complement factor B	Homo sapiens	34-37
31525895-0	2019	Electronic Structure, Vibrational Spectra, and Spin-Crossover Properties of Vacuum-Evaporable Iron(II) Bis(dihydrobis(pyrazolyl)borate) Complexes with Diimine Coligands.	diazene	151-158	spindlin 1	Homo sapiens	47-51
32583226-1	2020	The potential chemotherapeutic properties coupled to photochemical transitions make the family of fac-[Re(CO)3(N,N)X]0/+ (N,N = a bidentate diimine such as 2,2"-bipyridine (bpy); X = halide, H2O, pyridine derivatives, PR3, etc.)	diazene	140-147	proteinase 3	Homo sapiens	218-221
30816710-2	2019	Herein, six cyclometalated Ir(III) complexes Ir1-Ir6 containing a series of extended planar diimine ligands have been designed and assessed for their efficacy as anticancer agents.	diazene	92-99	nischarin	Homo sapiens	45-48
27275644-3	2018	This part is devoted to non-aromatic molecules characterized by a lone pair located on a sp2 nitrogen atom, it embraces functional groups such as imines, amidines, guanidines, diazenes, hydrazines, oximes, and phosphazenes.	diazene	176-184	Sp2 transcription factor	Homo sapiens	89-92
30684760-0	2019	Ru(II)/N-N/PPh3 complexes as potential anticancer agents against MDA-MB-231 cancer cells (N-N = diimine or diamine).	diazene	96-103	caveolin 1	Homo sapiens	11-15
30773007-5	2019	The antidirection of the diimine linkages leads to rippled layers which pack in unique ABC mode through alternate stacking of the cage twosided faces in both AB and AC layers.	diazene	25-32	ATP binding cassette subfamily B member 6 (Langereis blood group)	Homo sapiens	87-90
29627893-4	2018	tPA monoclonal antibody was covalently attached onto single-wall carbon nanotubes (SWCNTs) using diimide-activated imidation coupling.	diazene	97-104	chromosome 20 open reading frame 181	Homo sapiens	0-3
28780158-0	2017	Corrigendum to "Easy and rapid preparation of benzoylhydrazides and their diazene derivatives as inhibitors of 15-lipoxygenase" [Bioorg.	diazene	74-81	arachidonate 15-lipoxygenase	Homo sapiens	111-126
29058431-5	2017	The synthesis of these complex diazenes was made possible through a new methodology for synthesis of aryl-alkyl diazenes using electronically attenuated hydrazine-nucleophiles for a silver-promoted addition to C3a-bromocyclotryptamines.	diazene	31-39	complement C3	Homo sapiens	210-213
29058431-6	2017	The application of Rh- and Ir-catalyzed C-H amination reactions in complex settings were used to gain rapid access to C3a- and C7-functionalized cyclotryptamine monomers, respectively, used for diazene synthesis.	diazene	194-201	complement C3	Homo sapiens	118-121
28481242-0	2017	Isotactic and Syndiotactic Alternating Ethylene/Propylene Copolymers Obtained Through Non-Catalytic Hydrogenation of Highly Stereoregular cis-1,4 Poly(1,3-diene)s. The homogeneous non-catalytic hydrogenation of cis-1,4 poly(isoprene), isotactic cis-1,4 poly(1,3-pentadiene) and syndiotactic cis-1,4 poly(1,3-pentadiene) with diimide, formed by thermal decomposition of para-toluenesulfonylhydrazide, is examined.	diazene	325-332	suppressor of cytokine signaling 1	Homo sapiens	138-143
28481242-0	2017	Isotactic and Syndiotactic Alternating Ethylene/Propylene Copolymers Obtained Through Non-Catalytic Hydrogenation of Highly Stereoregular cis-1,4 Poly(1,3-diene)s. The homogeneous non-catalytic hydrogenation of cis-1,4 poly(isoprene), isotactic cis-1,4 poly(1,3-pentadiene) and syndiotactic cis-1,4 poly(1,3-pentadiene) with diimide, formed by thermal decomposition of para-toluenesulfonylhydrazide, is examined.	diazene	325-332	suppressor of cytokine signaling 1	Homo sapiens	138-145
26938015-3	2016	Notably, release of CO from the bulkier substituted [L(tBu)Ge-P=C=O] 2 b (L(tBu)=CH[C((t)Bu)N-Dipp]2 ) furnishes, under concomitant extrusion of the diimine [Dipp-NC((t)Bu)]2, the bis-N,P-heterocyclic germylene [DippNC((t)Bu)C(H)PGe]2 5.	diazene	149-156	nudix hydrolase 4	Homo sapiens	94-100
27244250-2	2016	Our synthesis features the expedient diazene-directed assembly of two advanced fragments to secure the congested C3a-C3a" linkage in three steps, followed by a highly efficient biogenetically inspired aminal reorganization to access the heptacyclic communesin core in only two additional steps.	diazene	37-44	complement C3	Homo sapiens	113-116
27244250-2	2016	Our synthesis features the expedient diazene-directed assembly of two advanced fragments to secure the congested C3a-C3a" linkage in three steps, followed by a highly efficient biogenetically inspired aminal reorganization to access the heptacyclic communesin core in only two additional steps.	diazene	37-44	complement C3	Homo sapiens	117-120
27143882-0	2016	Conjugation of insulin onto the sidewalls of single-walled carbon nanotubes through functionalization and diimide-activated amidation.	diazene	106-113	insulin	Homo sapiens	15-22
28368589-2	2017	The nucleophilic CH2 group generated by the deprotonation attacks the 6 (bipy) or 2 (phen) positions of the diimines, dearomatizing the involved pyridine ring and generating new asymmetric, fac-capping tridentate ligands.	diazene	108-116	FA complementation group C	Homo sapiens	190-193
27112102-3	2016	Reduction of the diimines gave the saturated analogues chxn-N2S2 (1) and tmcp-N4S4 (3) the former of which could be phosphorylated with PhP(NMe2)2 to give the novel 13-membered macrocycle chxn-PS2, 2.	diazene	17-25	N-acylsphingosine amidohydrolase 1	Homo sapiens	136-139
27112102-3	2016	Reduction of the diimines gave the saturated analogues chxn-N2S2 (1) and tmcp-N4S4 (3) the former of which could be phosphorylated with PhP(NMe2)2 to give the novel 13-membered macrocycle chxn-PS2, 2.	diazene	17-25	NME/NM23 nucleoside diphosphate kinase 2	Homo sapiens	140-144
27112102-3	2016	Reduction of the diimines gave the saturated analogues chxn-N2S2 (1) and tmcp-N4S4 (3) the former of which could be phosphorylated with PhP(NMe2)2 to give the novel 13-membered macrocycle chxn-PS2, 2.	diazene	17-25	taste 2 receptor member 64 pseudogene	Homo sapiens	193-196
27165340-7	2016	It was demonstrated that the formation of the glutathione conjugate at the C-6 position of the purine ring system was due to the bioactivation of the compound to a di-imine intermediate by CYP3A4, followed by the nucleophilic addition of glutathione.	diazene	164-172	complement C6	Homo sapiens	75-78
26778243-1	2016	Functionalization of the uranyl moiety (UO2(2+)) in Cp*UO2((Mes)PDI(Me)) (1-PDI) ((Mes)PDI(Me) = 2,6-((Mes)N=CMe)2C5H3N; Mes = 2,4,6-triphenylmethyl), which bears a reduced, monoanionic pyridine(diimine) ligand, is reported.	diazene	195-202	prolyl 4-hydroxylase subunit beta	Homo sapiens	64-67
26778243-1	2016	Functionalization of the uranyl moiety (UO2(2+)) in Cp*UO2((Mes)PDI(Me)) (1-PDI) ((Mes)PDI(Me) = 2,6-((Mes)N=CMe)2C5H3N; Mes = 2,4,6-triphenylmethyl), which bears a reduced, monoanionic pyridine(diimine) ligand, is reported.	diazene	195-202	prolyl 4-hydroxylase subunit beta	Homo sapiens	76-79
26778243-1	2016	Functionalization of the uranyl moiety (UO2(2+)) in Cp*UO2((Mes)PDI(Me)) (1-PDI) ((Mes)PDI(Me) = 2,6-((Mes)N=CMe)2C5H3N; Mes = 2,4,6-triphenylmethyl), which bears a reduced, monoanionic pyridine(diimine) ligand, is reported.	diazene	195-202	prolyl 4-hydroxylase subunit beta	Homo sapiens	76-79
27165340-7	2016	It was demonstrated that the formation of the glutathione conjugate at the C-6 position of the purine ring system was due to the bioactivation of the compound to a di-imine intermediate by CYP3A4, followed by the nucleophilic addition of glutathione.	diazene	164-172	cytochrome P450 family 3 subfamily A member 4	Homo sapiens	189-195
26440694-4	2015	Treatment with RN3 provides products where RN is formally inserted into the C-C bond of the diimine or into a C-H bond of the diimine.	diazene	92-99	drosha ribonuclease III	Homo sapiens	15-18
26440694-4	2015	Treatment with RN3 provides products where RN is formally inserted into the C-C bond of the diimine or into a C-H bond of the diimine.	diazene	126-133	drosha ribonuclease III	Homo sapiens	15-18
26267011-9	2015	Finally, PDI ligands, while not being surpassed in activity, have inspired the development of related ligand families and complexes, such as pendant donor diimines (PDD), which are also highly efficient at producing linear alpha-olefins.	diazene	155-163	peptidyl arginine deiminase 1	Homo sapiens	9-12
24972167-4	2014	Thus, we analyzed the binding of chromium complex, [Cr(phen)3](3+), to transferrin for a potential delivery of this diimine complex to tumor cells for PDT.	diazene	116-123	transferrin	Homo sapiens	71-82
24512024-2	2014	The structure hosting the rhenium diimine complex is a 3D network with the formula {Mn(DMF)2[LRe(CO)3Cl]}  (ReMn; DMF = N,N-dimethylformamide), where the diimine ligand L, 2,2"-bipyridine-5,5"-dicarboxylate, acts as a strut of the MOF.	diazene	34-41	lysine acetyltransferase 8	Homo sapiens	231-234
24853468-5	2014	The regioselectivity of the pentadiene/PyrNO reaction is improved markedly (90:10 dist/prox) when catalyzed by Cu(CH3CN)4(+); (diimine)2Cu(+) catalysts increase selectivity for the proximal product (55-65%).	diazene	126-135	pyruvate dehydrogenase complex component X	Homo sapiens	87-91
23514329-1	2013	Condensation of octahydro-2,2"-bipyrimidine with P(NMe2)3 gave a 1,3,2-diazaphospholidine-4,5-diimine 4a in which the "open" (exo/exo) conformation of the diimine unit was enforced by incorporation into a tricyclic molecular backbone.	diazene	94-101	NME/NM23 nucleoside diphosphate kinase 2	Homo sapiens	51-55
31986579-1	2014	By using a rigid multicarboxylate ligand, 4,5-di(4"-carboxylphenyl)phthalic acid (H4 L), two CoII complexes formulated as [Co4 L2 (4,4"-bpy)(H2 O)6 ] 3.5 H2 O (4,4"-bpy=4,4"-bipyridine) (1) and [Co2 L(azene)(H2 O)3 ] DMF (azene=(E)-1,2-di(pyridin-4-yl)diazene, DMF=dimethylformamide) (2) have been synthesized and structurally characterized by single-crystal X-ray diffraction.	diazene	222-259	mitochondrially encoded cytochrome c oxidase II	Homo sapiens	93-97
23230571-1	2013	Reduction of Cp*2UI(THF) with KC8 in the presence of a pyridine(diimine) ligand ((Mes)PDI(Me)) results in the formation of Cp*U(PDI)(THF), which features a triply reduced PDI ligand.	diazene	64-71	prolyl 4-hydroxylase subunit beta	Homo sapiens	86-89
23230571-1	2013	Reduction of Cp*2UI(THF) with KC8 in the presence of a pyridine(diimine) ligand ((Mes)PDI(Me)) results in the formation of Cp*U(PDI)(THF), which features a triply reduced PDI ligand.	diazene	64-71	prolyl 4-hydroxylase subunit beta	Homo sapiens	128-131
23230571-1	2013	Reduction of Cp*2UI(THF) with KC8 in the presence of a pyridine(diimine) ligand ((Mes)PDI(Me)) results in the formation of Cp*U(PDI)(THF), which features a triply reduced PDI ligand.	diazene	64-71	prolyl 4-hydroxylase subunit beta	Homo sapiens	128-131
23170832-6	2012	These materials are found to be oligomers (GPC) with thermal stability (TGA) reaching 350  C. The greatest stabilities were found in the cases with X = F. Using a data bank of 8 X-ray structures of diimine derivatives, a relationship between the C N bond distance and the dihedral angle between the benzoquinone ring and the flanking phenyl planes is noted.	diazene	198-205	glycophorin C (Gerbich blood group)	Homo sapiens	43-46
23170832-6	2012	These materials are found to be oligomers (GPC) with thermal stability (TGA) reaching 350  C. The greatest stabilities were found in the cases with X = F. Using a data bank of 8 X-ray structures of diimine derivatives, a relationship between the C N bond distance and the dihedral angle between the benzoquinone ring and the flanking phenyl planes is noted.	diazene	198-205	T-box transcription factor 1	Homo sapiens	72-75