PL91724B1 - - Google Patents

Info

Publication number

PL91724B1

PL91724B1 PL17413369A PL17413369A PL91724B1 PL 91724 B1 PL91724 B1 PL 91724B1 PL 17413369 A PL17413369 A PL 17413369A PL 17413369 A PL17413369 A PL 17413369A PL 91724 B1 PL91724 B1 PL 91724B1

Authority

PL

Poland

Prior art keywords

radical

formula

salts

phenyl

split

Prior art date

1968-10-11

Links

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• 150000003839 salts Chemical class 0.000 claims 9
• 150000001875 compounds Chemical class 0.000 claims 7
• 238000000034 method Methods 0.000 claims 7
• 239000000203 mixture Substances 0.000 claims 6
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 5
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 4
• -1 α- [p- (1-hydroxy-1-cyclohexyl) -phenyl] -propionic acid Chemical compound 0.000 claims 4
• 125000000217 alkyl group Chemical group 0.000 claims 3
• 150000001408 amides Chemical class 0.000 claims 3
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 3
• 150000002148 esters Chemical class 0.000 claims 3
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 3
• 125000002030 1,2-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([*:2])C([H])=C1[H] 0.000 claims 2
• HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims 2
• 125000003342 alkenyl group Chemical group 0.000 claims 2
• 125000000304 alkynyl group Chemical group 0.000 claims 2
• LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 2
• 239000004215 Carbon black (E152) Substances 0.000 claims 1
• SRBFZHDQGSBBOR-HWQSCIPKSA-N L-arabinopyranose Chemical compound O[C@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-HWQSCIPKSA-N 0.000 claims 1
• XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Substances CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 1
• 229940053200 antiepileptics fatty acid derivative Drugs 0.000 claims 1
• 125000003710 aryl alkyl group Chemical group 0.000 claims 1
• 125000004432 carbon atom Chemical group C* 0.000 claims 1
• 235000014113 dietary fatty acids Nutrition 0.000 claims 1
• 239000000194 fatty acid Substances 0.000 claims 1
• 229930195729 fatty acid Natural products 0.000 claims 1
• 229930195733 hydrocarbon Natural products 0.000 claims 1
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
• SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 claims 1