JP5844358B2

JP5844358B2 - ベンゾトリアゾロジアゼピン化合物を含むブロモドメイン阻害剤

ベンゾトリアゾロジアゼピン化合物を含むブロモドメイン阻害剤 Download PDF

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Publication number: JP5844358B2
Authority: JP; Japan
Prior art keywords: alkyl; methyl; chlorophenyl; triazolo; ethylacetamide
Prior art date: 2010-06-22
Legal status : Expired - Fee Related

Application number

JP2013515827A

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English (en)

Japanese (ja)

Other versions

JP2013529611A (ja

JP2013529611A5 (enExample

Inventor

バイリー，ジェームズ，マシュー

Original Assignee

グラクソスミスクラインエルエルシー

Priority date

2010-06-22

Filing date

2011-06-20

Publication date

2016-01-13

2010-06-22 Priority claimed from GBGB1010514.6A external-priority patent/GB201010514D0/en

2011-04-21 Priority claimed from GBGB1106801.2A external-priority patent/GB201106801D0/en

2011-06-20 Application filed by グラクソスミスクラインエルエルシー, グラクソスミスクラインエルエルシー filed Critical グラクソスミスクラインエルエルシー

2013-07-22 Publication of JP2013529611A publication Critical patent/JP2013529611A/ja

2014-06-05 Publication of JP2013529611A5 publication Critical patent/JP2013529611A5/ja

2016-01-13 Application granted granted Critical

2016-01-13 Publication of JP5844358B2 publication Critical patent/JP5844358B2/ja

Status Expired - Fee Related legal-status Critical Current

2031-06-20 Anticipated expiration legal-status Critical

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102000001805 Bromodomains Human genes 0.000 title description 49
108050009021 Bromodomains Proteins 0.000 title description 48
239000003112 inhibitor Substances 0.000 title description 18
WTJDTOLWJBAXRX-UHFFFAOYSA-N triazolo[4,5-g][1,2]benzodiazepine Chemical class C1=CC2=NN=CC=CC2=C2C1=NN=N2 WTJDTOLWJBAXRX-UHFFFAOYSA-N 0.000 title 1
150000001875 compounds Chemical class 0.000 claims description 151
125000000217 alkyl group Chemical group 0.000 claims description 91
150000003839 salts Chemical class 0.000 claims description 89
-1 —CO-carbocyclyl Chemical group 0.000 claims description 53
125000000623 heterocyclic group Chemical group 0.000 claims description 32
239000001257 hydrogen Substances 0.000 claims description 28
229910052739 hydrogen Inorganic materials 0.000 claims description 28
125000005843 halogen group Chemical group 0.000 claims description 27
239000008194 pharmaceutical composition Substances 0.000 claims description 26
125000003545 alkoxy group Chemical group 0.000 claims description 25
125000004452 carbocyclyl group Chemical group 0.000 claims description 19
239000003814 drug Substances 0.000 claims description 17
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 16
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 15
150000002431 hydrogen Chemical class 0.000 claims description 14
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
206010028980 Neoplasm Diseases 0.000 claims description 11
125000005842 heteroatom Chemical group 0.000 claims description 10
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
229910052757 nitrogen Inorganic materials 0.000 claims description 10
229910052760 oxygen Inorganic materials 0.000 claims description 10
229910052717 sulfur Inorganic materials 0.000 claims description 10
125000004433 nitrogen atom Chemical group N* 0.000 claims description 9
201000011510 cancer Diseases 0.000 claims description 8
125000004093 cyano group Chemical group *C#N 0.000 claims description 7
239000003085 diluting agent Substances 0.000 claims description 7
230000004968 inflammatory condition Effects 0.000 claims description 7
239000000546 pharmaceutical excipient Substances 0.000 claims description 7
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 7
125000003118 aryl group Chemical group 0.000 claims description 6
230000001684 chronic effect Effects 0.000 claims description 6
229910052736 halogen Inorganic materials 0.000 claims description 6
150000002367 halogens Chemical class 0.000 claims description 6
238000004519 manufacturing process Methods 0.000 claims description 6
125000000719 pyrrolidinyl group Chemical group 0.000 claims description 6
QKKNSYUKNJSTRL-NDEPHWFRSA-N 2-[(4s)-6-(4-chlorophenyl)-1-methyl-8-[3-(pyrrolidin-1-ylmethyl)phenyl]-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=C(CN3CCCC3)C=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 QKKNSYUKNJSTRL-NDEPHWFRSA-N 0.000 claims description 5
UCHHERPHYGYXQM-NDEPHWFRSA-N 2-[(4s)-6-(4-chlorophenyl)-1-methyl-8-[4-(pyrrolidin-1-ylmethyl)phenyl]-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=CC(CN3CCCC3)=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 UCHHERPHYGYXQM-NDEPHWFRSA-N 0.000 claims description 5
230000001363 autoimmune Effects 0.000 claims description 5
239000003937 drug carrier Substances 0.000 claims description 5
125000004193 piperazinyl group Chemical group 0.000 claims description 5
125000003386 piperidinyl group Chemical group 0.000 claims description 5
238000002560 therapeutic procedure Methods 0.000 claims description 5
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 4
PJPRMRNFJZOFLA-FQEVSTJZSA-N 2-[(4s)-6-(4-chlorophenyl)-1-methyl-8-(1h-pyrazol-4-yl)-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C2=CNN=C2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 PJPRMRNFJZOFLA-FQEVSTJZSA-N 0.000 claims description 4
WMKQEPQCESYBNS-FQEVSTJZSA-N 2-[(4s)-6-(4-chlorophenyl)-1-methyl-8-(1h-pyrazol-5-yl)-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2NN=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 WMKQEPQCESYBNS-FQEVSTJZSA-N 0.000 claims description 4
HFCOQWDWESZNEW-DEOSSOPVSA-N 2-[(4s)-6-(4-chlorophenyl)-1-methyl-8-(2-methylphenyl)-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C(=CC=CC=2)C)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 HFCOQWDWESZNEW-DEOSSOPVSA-N 0.000 claims description 4
PILKZSVRGDSFDN-LJAQVGFWSA-N 2-[(4s)-6-(4-chlorophenyl)-1-methyl-8-[3-[(4-methylpiperazin-1-yl)methyl]phenyl]-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=C(CN3CCN(C)CC3)C=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 PILKZSVRGDSFDN-LJAQVGFWSA-N 0.000 claims description 4
DODSTUSXECRXBY-LJAQVGFWSA-N 2-[(4s)-6-(4-chlorophenyl)-1-methyl-8-[4-[(4-methylpiperazin-1-yl)methyl]phenyl]-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=CC(CN3CCN(C)CC3)=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 DODSTUSXECRXBY-LJAQVGFWSA-N 0.000 claims description 4
LBNZQYJSQFKTMP-QHCPKHFHSA-N 2-[(4s)-6-(4-chlorophenyl)-1-methyl-8-phenyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=CC=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 LBNZQYJSQFKTMP-QHCPKHFHSA-N 0.000 claims description 4
MXNRKTOXHIEBKM-QFIPXVFZSA-N 2-[(4s)-6-(4-chlorophenyl)-1-methyl-8-pyridin-4-yl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=CN=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 MXNRKTOXHIEBKM-QFIPXVFZSA-N 0.000 claims description 4
SPAMVIHCDISFJZ-DEOSSOPVSA-N 2-[(4s)-6-(4-chlorophenyl)-8-(3-methoxyphenyl)-1-methyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=C(OC)C=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 SPAMVIHCDISFJZ-DEOSSOPVSA-N 0.000 claims description 4
DBNRUVQIPZTZFK-DEOSSOPVSA-N 2-[(4s)-6-(4-chlorophenyl)-8-(4-methoxyphenyl)-1-methyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=CC(OC)=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 DBNRUVQIPZTZFK-DEOSSOPVSA-N 0.000 claims description 4
JZVFVHUUEWVBPO-SANMLTNESA-N 2-[(4s)-6-(4-chlorophenyl)-8-[3-(ethylaminomethyl)phenyl]-1-methyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound CCNCC1=CC=CC(C=2C=C3C(N4C(C)=NN=C4[C@H](CC(=O)NCC)N=C3C=3C=CC(Cl)=CC=3)=CC=2)=C1 JZVFVHUUEWVBPO-SANMLTNESA-N 0.000 claims description 4
PHVGVVDKYSSPKA-SANMLTNESA-N 2-[(4s)-6-(4-chlorophenyl)-8-[4-(ethylaminomethyl)phenyl]-1-methyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound C1=CC(CNCC)=CC=C1C1=CC=C2N3C(C)=NN=C3[C@H](CC(=O)NCC)N=C(C=3C=CC(Cl)=CC=3)C2=C1 PHVGVVDKYSSPKA-SANMLTNESA-N 0.000 claims description 4
USCJQEZHNLJYPQ-SANMLTNESA-N 2-[(4s)-6-(4-chlorophenyl)-8-[4-[(dimethylamino)methyl]phenyl]-1-methyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=CC(CN(C)C)=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 USCJQEZHNLJYPQ-SANMLTNESA-N 0.000 claims description 4
125000004429 atom Chemical group 0.000 claims description 4
KPCZJLGGXRGYIE-UHFFFAOYSA-N [C]1=CC=CN=C1 Chemical group [C]1=CC=CN=C1 KPCZJLGGXRGYIE-UHFFFAOYSA-N 0.000 claims description 3
230000005784 autoimmunity Effects 0.000 claims description 3
229940049706 benzodiazepine Drugs 0.000 claims description 3
125000003226 pyrazolyl group Chemical group 0.000 claims description 3
125000002757 morpholinyl group Chemical group 0.000 claims description 2
125000004076 pyridyl group Chemical group 0.000 claims description 2
150000001557 benzodiazepines Chemical class 0.000 claims 1
KYTREVLPRJOBEM-UHFFFAOYSA-N triazolo[4,5-i][1,2]benzodiazepine Chemical group C1=CC2=CC=CN=NC2=C2C1=NN=N2 KYTREVLPRJOBEM-UHFFFAOYSA-N 0.000 claims 1
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 132
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 105
235000002639 sodium chloride Nutrition 0.000 description 85
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 69
239000011541 reaction mixture Substances 0.000 description 62
239000000203 mixture Substances 0.000 description 59
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 53
239000000243 solution Substances 0.000 description 49
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 48
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 44
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 43
239000002904 solvent Substances 0.000 description 42
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 34
235000019253 formic acid Nutrition 0.000 description 34
239000007787 solid Substances 0.000 description 34
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 34
239000000543 intermediate Substances 0.000 description 33
238000002360 preparation method Methods 0.000 description 32
238000000034 method Methods 0.000 description 30
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 27
238000004895 liquid chromatography mass spectrometry Methods 0.000 description 27
239000012044 organic layer Substances 0.000 description 27
DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 22
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 21
210000004027 cell Anatomy 0.000 description 21
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 21
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 19
201000010099 disease Diseases 0.000 description 19
235000019439 ethyl acetate Nutrition 0.000 description 19
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
108090000623 proteins and genes Proteins 0.000 description 17
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 16
238000001819 mass spectrum Methods 0.000 description 16
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 15
229910052796 boron Inorganic materials 0.000 description 15
239000000843 powder Substances 0.000 description 15
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 14
108010033040 Histones Proteins 0.000 description 13
229960000583 acetic acid Drugs 0.000 description 13
239000010410 layer Substances 0.000 description 13
229940125763 bromodomain inhibitor Drugs 0.000 description 12
JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 11
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 11
235000011054 acetic acid Nutrition 0.000 description 11
239000012267 brine Substances 0.000 description 11
238000006243 chemical reaction Methods 0.000 description 11
239000002158 endotoxin Substances 0.000 description 11
239000003921 oil Substances 0.000 description 11
235000018102 proteins Nutrition 0.000 description 11
102000004169 proteins and genes Human genes 0.000 description 11
230000002829 reductive effect Effects 0.000 description 11
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 11
239000000725 suspension Substances 0.000 description 11
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 10
YNHIGQDRGKUECZ-UHFFFAOYSA-L bis(triphenylphosphine)palladium(ii) dichloride Chemical compound [Cl-].[Cl-].[Pd+2].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 YNHIGQDRGKUECZ-UHFFFAOYSA-L 0.000 description 10
239000012530 fluid Substances 0.000 description 10
229920006008 lipopolysaccharide Polymers 0.000 description 10
235000019198 oils Nutrition 0.000 description 10
238000012360 testing method Methods 0.000 description 10
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
238000003556 assay Methods 0.000 description 9
238000009472 formulation Methods 0.000 description 9
239000012299 nitrogen atmosphere Substances 0.000 description 9
239000011734 sodium Substances 0.000 description 9
239000011780 sodium chloride Substances 0.000 description 9
239000003826 tablet Substances 0.000 description 9
UXRDAJMOOGEIAQ-CKOZHMEPSA-N [(8r,9s,10r,13s,14s,17r)-17-acetyl-10,13-dimethyl-16-methylidene-3-oxo-1,2,8,9,11,12,14,15-octahydrocyclopenta[a]phenanthren-17-yl] acetate Chemical compound C1=CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC(=C)[C@](OC(=O)C)(C(C)=O)[C@@]1(C)CC2 UXRDAJMOOGEIAQ-CKOZHMEPSA-N 0.000 description 8
239000004480 active ingredient Substances 0.000 description 8
239000002585 base Substances 0.000 description 8
238000004128 high performance liquid chromatography Methods 0.000 description 8
230000004048 modification Effects 0.000 description 8
238000012986 modification Methods 0.000 description 8
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 8
108090000765 processed proteins & peptides Proteins 0.000 description 8
238000000746 purification Methods 0.000 description 8
229910000029 sodium carbonate Inorganic materials 0.000 description 8
USGDSUYKHJTOBN-KRWDZBQOSA-N [(4s)-6-(4-chlorophenyl)-4-[2-(ethylamino)-2-oxoethyl]-1-methyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-8-yl] trifluoromethanesulfonate Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(OS(=O)(=O)C(F)(F)F)C=C11)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 USGDSUYKHJTOBN-KRWDZBQOSA-N 0.000 description 7
239000002253 acid Substances 0.000 description 7
230000001154 acute effect Effects 0.000 description 7
239000007864 aqueous solution Substances 0.000 description 7
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 7
239000002027 dichloromethane extract Substances 0.000 description 7
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 7
239000000047 product Substances 0.000 description 7
239000012321 sodium triacetoxyborohydride Substances 0.000 description 7
239000012453 solvate Substances 0.000 description 7
239000000126 substance Substances 0.000 description 7
239000003981 vehicle Substances 0.000 description 7
UXTPELVEOZWSPO-DEOSSOPVSA-N 2-[(4s)-6-(4-chlorophenyl)-8-(4-formylphenyl)-1-methyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=CC(C=O)=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 UXTPELVEOZWSPO-DEOSSOPVSA-N 0.000 description 6
JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 6
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
239000007995 HEPES buffer Substances 0.000 description 6
102000006947 Histones Human genes 0.000 description 6
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 6
206010051379 Systemic Inflammatory Response Syndrome Diseases 0.000 description 6
239000000443 aerosol Substances 0.000 description 6
125000003310 benzodiazepinyl group Chemical class N1N=C(C=CC2=C1C=CC=C2)* 0.000 description 6
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RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 6
208000015181 infectious disease Diseases 0.000 description 6
239000003446 ligand Substances 0.000 description 6
239000000314 lubricant Substances 0.000 description 6
125000003588 lysine group Chemical group [H]N([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 description 6
RYZOXPQDWCYWSH-DEOSSOPVSA-N 2-[(4s)-6-(4-chlorophenyl)-8-(3-formylphenyl)-1-methyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=C(C=O)C=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 RYZOXPQDWCYWSH-DEOSSOPVSA-N 0.000 description 5
102100033641 Bromodomain-containing protein 2 Human genes 0.000 description 5
108010077544 Chromatin Proteins 0.000 description 5
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241001465754 Metazoa Species 0.000 description 5
GXPYEYLUXCAMOH-UHFFFAOYSA-N O=S(C(F)(F)F)(OC(C=C1)=CC2=C1C=NC=CN2)=O Chemical compound O=S(C(F)(F)F)(OC(C=C1)=CC2=C1C=NC=CN2)=O GXPYEYLUXCAMOH-UHFFFAOYSA-N 0.000 description 5
206010040047 Sepsis Diseases 0.000 description 5
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QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
239000011230 binding agent Substances 0.000 description 5
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