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Details

Stereochemistry ABSOLUTE
Molecular Formula C21H24FN5O6
Molecular Weight 461.4436
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RANBEZOLID

SMILES

CC(=O)NC[C@H]1CN(C(=O)O1)C2=CC(F)=C(C=C2)N3CCN(CC4=CC=C(O4)[N+]([O-])=O)CC3

InChI

InChIKey=PWHNTOQANLCTHN-KRWDZBQOSA-N
InChI=1S/C21H24FN5O6/c1-14(28)23-11-17-13-26(21(29)33-17)15-2-4-19(18(22)10-15)25-8-6-24(7-9-25)12-16-3-5-20(32-16)27(30)31/h2-5,10,17H,6-9,11-13H2,1H3,(H,23,28)/t17-/m0/s1

HIDE SMILES / InChI

Molecular Formula C21H24FN5O6
Molecular Weight 461.4436
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 11:03:29 GMT 2023
Edited
by admin
on Sat Dec 16 11:03:29 GMT 2023
Record UNII
G3NB6JBL8A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RANBEZOLID
Common Name English
ACETAMIDE, N-(((5S)-3-(3-FLUORO-4-(4-((5-NITRO-2-FURANYL)METHYL)-1-PIPERAZINYL)PHENYL)-2-OXO-5-OXAZOLIDINYL)METHYL)-
Systematic Name English
N-(((5S)-3-(3-FLUORO-4-(4-((5-NITRO-2-FURYL)METHYL)PIPERAZIN-1-YL)PHENYL)-2-OXO-OXAZOLIDIN-5-YL)METHYL)ACETAMIDE
Systematic Name English
Code System Code Type Description
PUBCHEM
496993
Created by admin on Sat Dec 16 11:03:29 GMT 2023 , Edited by admin on Sat Dec 16 11:03:29 GMT 2023
PRIMARY
EPA CompTox
DTXSID701029733
Created by admin on Sat Dec 16 11:03:29 GMT 2023 , Edited by admin on Sat Dec 16 11:03:29 GMT 2023
PRIMARY
CAS
392659-38-0
Created by admin on Sat Dec 16 11:03:29 GMT 2023 , Edited by admin on Sat Dec 16 11:03:29 GMT 2023
PRIMARY
FDA UNII
G3NB6JBL8A
Created by admin on Sat Dec 16 11:03:29 GMT 2023 , Edited by admin on Sat Dec 16 11:03:29 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY
Summary of MICs (micrograms per milliliter) of Ranbezolid for S. aureus strains. Methicillin-resistant S. aureus(n 68): MIC range = 0.25-4, MIC50 = 2, MIC90 = 4 Methicillin-susceptible S. aureus(n 65): MIC range = 0.5-4, MIC50 = 2, MIC90 = 2
ACTIVE MOIETY
For 260 pneumococcal and 266 staphylococcal strains, ranbezolid MICs ranged from 0.06 to 4 .MU.g/ml. The MICs for pneumococci were similar irrespective of the strains' .BETA.-lactam, macrolide, or quinolone susceptibilities, and ranbezolid MICs for coagulase-negative staphylococci were lower than those for Staphylococcus aureus. Ranbezolid was bacteriostatic against pneumococci. Ranbezolid MICs were similar to or lower than those of linezolid.