GB1471902A - Styrylsulphonylamidines - Google Patents

Info

Publication number

GB1471902A

GB1471902A GB4860175A GB4860175A GB1471902A GB 1471902 A GB1471902 A GB 1471902A GB 4860175 A GB4860175 A GB 4860175A GB 4860175 A GB4860175 A GB 4860175A GB 1471902 A GB1471902 A GB 1471902A

Authority

GB

United Kingdom

Prior art keywords

carbon atoms

formula

prepared

compound

alkyl

Prior art date

1973-06-11

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Expired

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• 125000004432 carbon atom Chemical group C* 0.000 abstract 6
• -1 nitro, amino Chemical group 0.000 abstract 5
• 125000000217 alkyl group Chemical group 0.000 abstract 4
• 150000001875 compounds Chemical class 0.000 abstract 4
• 229910052736 halogen Inorganic materials 0.000 abstract 3
• 150000002367 halogens Chemical class 0.000 abstract 3
• 229910052739 hydrogen Inorganic materials 0.000 abstract 3
• 239000001257 hydrogen Substances 0.000 abstract 3
• 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 3
• 239000000543 intermediate Substances 0.000 abstract 3
• 125000002905 alkanoylamido group Chemical group 0.000 abstract 2
• 125000005504 styryl group Chemical group 0.000 abstract 2
• PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 1
• 125000003545 alkoxy group Chemical group 0.000 abstract 1
• 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
• 150000001408 amides Chemical class 0.000 abstract 1
• 230000000202 analgesic effect Effects 0.000 abstract 1
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
• 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 1
• 239000008194 pharmaceutical composition Substances 0.000 abstract 1
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
• 239000007858 starting material Substances 0.000 abstract 1
• 125000003011 styrenyl group Chemical class [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
• BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 1
• 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 abstract 1