JPS56123935A - Biphenyl derivative - Google Patents

Info

Publication number

JPS56123935A

JPS56123935A JP2852380A JP2852380A JPS56123935A JP S56123935 A JPS56123935 A JP S56123935A JP 2852380 A JP2852380 A JP 2852380A JP 2852380 A JP2852380 A JP 2852380A JP S56123935 A JPS56123935 A JP S56123935A

Authority

JP

Japan

Prior art keywords

agent

formula

compound

acetylamino

pref

Prior art date

1980-03-05

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.)

Granted

Links

• Espacenet
• Global Dossier
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• ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical class C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 title 1
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
• 150000001875 compounds Chemical class 0.000 abstract 2
• 229910052736 halogen Inorganic materials 0.000 abstract 2
• 150000002367 halogens Chemical class 0.000 abstract 2
• HYUJEAPUCMAAOZ-UHFFFAOYSA-N 2-(3-acetamido-5-phenylphenyl)acetic acid Chemical compound CC(=O)NC1=CC(CC(O)=O)=CC(C=2C=CC=CC=2)=C1 HYUJEAPUCMAAOZ-UHFFFAOYSA-N 0.000 abstract 1
• -1 5-(4-substituted phenyl)-3-oxocyclohexene-1-ylacetic acid methyl ester Chemical class 0.000 abstract 1
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
• 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 abstract 1
• 239000012345 acetylating agent Substances 0.000 abstract 1
• 239000003513 alkali Substances 0.000 abstract 1
• 125000003545 alkoxy group Chemical group 0.000 abstract 1
• 125000000217 alkyl group Chemical group 0.000 abstract 1
• 239000000730 antalgic agent Substances 0.000 abstract 1
• 239000002260 anti-inflammatory agent Substances 0.000 abstract 1
• 239000007864 aqueous solution Substances 0.000 abstract 1
• 210000001772 blood platelet Anatomy 0.000 abstract 1
• 239000003518 caustics Substances 0.000 abstract 1
• 239000003795 chemical substances by application Substances 0.000 abstract 1
• 230000015271 coagulation Effects 0.000 abstract 1
• 238000005345 coagulation Methods 0.000 abstract 1
• 239000000463 material Substances 0.000 abstract 1
• 238000000034 method Methods 0.000 abstract 1
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
• 239000000203 mixture Substances 0.000 abstract 1
• 150000002923 oximes Chemical class 0.000 abstract 1
• 239000000243 solution Substances 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

Cited By (2)