JPS55160783A - Cephalosporin derivative - Google Patents

Info

Publication number

JPS55160783A

JPS55160783A JP6857079A JP6857079A JPS55160783A JP S55160783 A JPS55160783 A JP S55160783A JP 6857079 A JP6857079 A JP 6857079A JP 6857079 A JP6857079 A JP 6857079A JP S55160783 A JPS55160783 A JP S55160783A

Authority

JP

Japan

Prior art keywords

compound

formula

substituted

acid

cephem

Prior art date

1979-06-01

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
• Discuss

• 229930186147 Cephalosporin Natural products 0.000 title 1
• 229940124587 cephalosporin Drugs 0.000 title 1
• 150000001780 cephalosporins Chemical class 0.000 title 1
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
• 150000001875 compounds Chemical class 0.000 abstract 3
• XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 abstract 2
• NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 abstract 1
• 125000002373 5 membered heterocyclic group Chemical group 0.000 abstract 1
• 241000894006 Bacteria Species 0.000 abstract 1
• 239000002253 acid Substances 0.000 abstract 1
• 125000000217 alkyl group Chemical group 0.000 abstract 1
• 125000002947 alkylene group Chemical group 0.000 abstract 1
• -1 amidino, guanidino Chemical group 0.000 abstract 1
• 239000003242 anti bacterial agent Substances 0.000 abstract 1
• 230000000844 anti-bacterial effect Effects 0.000 abstract 1
• 239000000463 material Substances 0.000 abstract 1
• 238000000034 method Methods 0.000 abstract 1
• 235000019260 propionic acid Nutrition 0.000 abstract 1
• IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical group O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 abstract 1
• 150000003839 salts Chemical class 0.000 abstract 1
• 238000001228 spectrum Methods 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