JPS5470294A - Cephalosporin derivative and its preparation - Google Patents

Info

Publication number

JPS5470294A

JPS5470294A JP13493977A JP13493977A JPS5470294A JP S5470294 A JPS5470294 A JP S5470294A JP 13493977 A JP13493977 A JP 13493977A JP 13493977 A JP13493977 A JP 13493977A JP S5470294 A JPS5470294 A JP S5470294A

Authority

JP

Japan

Prior art keywords

formula

compound

cephalosporin

derivative

antibiotic

Prior art date

1977-11-09

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 abstract 4
• 229940124587 cephalosporin Drugs 0.000 title abstract 4
• 150000001780 cephalosporins Chemical class 0.000 title abstract 4
• 150000001875 compounds Chemical class 0.000 abstract 5
• 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 3
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
• OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 abstract 2
• 239000003242 anti bacterial agent Substances 0.000 abstract 2
• 230000003115 biocidal effect Effects 0.000 abstract 2
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
• RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 1
• 241000894006 Bacteria Species 0.000 abstract 1
• WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
• KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 abstract 1
• 229930182555 Penicillin Natural products 0.000 abstract 1
• JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 abstract 1
• 125000004442 acylamino group Chemical group 0.000 abstract 1
• 125000003545 alkoxy group Chemical group 0.000 abstract 1
• GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
• 229910052794 bromium Inorganic materials 0.000 abstract 1
• 229910052736 halogen Inorganic materials 0.000 abstract 1
• 230000026030 halogenation Effects 0.000 abstract 1
• 238000005658 halogenation reaction Methods 0.000 abstract 1
• 150000002367 halogens Chemical class 0.000 abstract 1
• 125000001183 hydrocarbyl group Chemical group 0.000 abstract 1
• 230000007062 hydrolysis Effects 0.000 abstract 1
• 238000006460 hydrolysis reaction Methods 0.000 abstract 1
• 150000003949 imides Chemical group 0.000 abstract 1
• 125000001841 imino group Chemical group [H]N=* 0.000 abstract 1
• 125000001181 organosilyl group Chemical group [SiH3]* 0.000 abstract 1
• 229940049954 penicillin Drugs 0.000 abstract 1
• 238000006884 silylation reaction Methods 0.000 abstract 1
• 239000002904 solvent Substances 0.000 abstract 1
• 230000002194 synthesizing effect Effects 0.000 abstract 1

Cited By (1)