U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C37H66FNO13
Molecular Weight 751.9172
Optical Activity UNSPECIFIED
Defined Stereocenters 18 / 18
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FLURITHROMYCIN

SMILES

[H][C@@]1(C[C@@](C)(OC)[C@@H](O)[C@H](C)O1)O[C@H]2[C@H](C)[C@@H](O[C@]3([H])O[C@H](C)C[C@@H]([C@H]3O)N(C)C)[C@](C)(O)C[C@](C)(F)C(=O)[C@H](C)[C@@H](O)[C@](C)(O)[C@@H](CC)OC(=O)[C@@H]2C

InChI

InChIKey=XOEUHCONYHZURQ-HNUBZJOYSA-N
InChI=1S/C37H66FNO13/c1-14-24-37(10,46)29(42)21(5)28(41)34(7,38)17-35(8,45)31(52-33-26(40)23(39(11)12)15-18(2)48-33)19(3)27(20(4)32(44)50-24)51-25-16-36(9,47-13)30(43)22(6)49-25/h18-27,29-31,33,40,42-43,45-46H,14-17H2,1-13H3/t18-,19+,20-,21+,22+,23+,24-,25+,26-,27+,29-,30+,31-,33+,34+,35-,36-,37-/m1/s1

HIDE SMILES / InChI
FLURITHROMYCIN, an erythromycin fluorine derivative, was isolated from the fermentation broth of Streptomyces erythraeus ATCC 31772. It is used as an antibacterial drug. The spectrum of activity of FLURITHROMYCIN is almost identical to that of erythromycin but it is more stable to acid.

Approval Year

PubMed

PubMed

TitleDatePubMed
Inhibition of human neutrophil elastase by erythromycin and flurythromycin, two macrolide antibiotics.
2001 Oct
Comparison of systemic flurithromycin therapy and clinical procedures in the treatment of periodontal diseases.
2004 Apr
Fluroquinolone resistance in typhoidal Salmonella and its detection by nalidixic acid disc diffusion.
2004 Jun
Structure-activity relationships for three macrolide antibiotics in Haemophilus influenzae.
2004 Oct
Patents

Sample Use Guides

In Vitro Use Guide
Flurithromycin in vitro antibacterial activity was determined on recent clinical isolates of respiratory pathogens. The range of MIC for Streptococcus pneumoniae and Streptococcus beta-haemolyticus group A is from 0.0015 to 0.006 microgram/ml, for Haemophilus influenzae from 0.012 to 0.4 microgram/ml, for Staphylococcus aureus from 0.1 to 3.1 micrograms/ml.
Name Type Language
FLURITHROMYCIN
INN   WHO-DD  
INN  
Official Name English
FLURITHROMYCIN [MI]
Common Name English
flurithromycin [INN]
Common Name English
Flurithromycin [WHO-DD]
Common Name English
(8S)-8-FLUOROERYTHROMYCIN
Common Name English
Classification Tree Code System Code
WHO-ATC J01FA14
Created by admin on Fri Dec 15 15:46:59 UTC 2023 , Edited by admin on Fri Dec 15 15:46:59 UTC 2023
WHO-VATC QJ01FA14
Created by admin on Fri Dec 15 15:46:59 UTC 2023 , Edited by admin on Fri Dec 15 15:46:59 UTC 2023
NCI_THESAURUS C261
Created by admin on Fri Dec 15 15:46:59 UTC 2023 , Edited by admin on Fri Dec 15 15:46:59 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C65735
Created by admin on Fri Dec 15 15:46:59 UTC 2023 , Edited by admin on Fri Dec 15 15:46:59 UTC 2023
PRIMARY
INN
5534
Created by admin on Fri Dec 15 15:46:59 UTC 2023 , Edited by admin on Fri Dec 15 15:46:59 UTC 2023
PRIMARY
DRUG CENTRAL
1221
Created by admin on Fri Dec 15 15:46:59 UTC 2023 , Edited by admin on Fri Dec 15 15:46:59 UTC 2023
PRIMARY
FDA UNII
56C9DTE69V
Created by admin on Fri Dec 15 15:46:59 UTC 2023 , Edited by admin on Fri Dec 15 15:46:59 UTC 2023
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EPA CompTox
DTXSID40905085
Created by admin on Fri Dec 15 15:46:59 UTC 2023 , Edited by admin on Fri Dec 15 15:46:59 UTC 2023
PRIMARY
CAS
82664-20-8
Created by admin on Fri Dec 15 15:46:59 UTC 2023 , Edited by admin on Fri Dec 15 15:46:59 UTC 2023
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ChEMBL
CHEMBL2106403
Created by admin on Fri Dec 15 15:46:59 UTC 2023 , Edited by admin on Fri Dec 15 15:46:59 UTC 2023
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SMS_ID
100000080949
Created by admin on Fri Dec 15 15:46:59 UTC 2023 , Edited by admin on Fri Dec 15 15:46:59 UTC 2023
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WIKIPEDIA
Flurithromycin
Created by admin on Fri Dec 15 15:46:59 UTC 2023 , Edited by admin on Fri Dec 15 15:46:59 UTC 2023
PRIMARY
MESH
C045925
Created by admin on Fri Dec 15 15:46:59 UTC 2023 , Edited by admin on Fri Dec 15 15:46:59 UTC 2023
PRIMARY
MERCK INDEX
m12191
Created by admin on Fri Dec 15 15:46:59 UTC 2023 , Edited by admin on Fri Dec 15 15:46:59 UTC 2023
PRIMARY
DRUG BANK
DB13338
Created by admin on Fri Dec 15 15:46:59 UTC 2023 , Edited by admin on Fri Dec 15 15:46:59 UTC 2023
PRIMARY
PUBCHEM
71260
Created by admin on Fri Dec 15 15:46:59 UTC 2023 , Edited by admin on Fri Dec 15 15:46:59 UTC 2023
PRIMARY
EVMPD
SUB07747MIG
Created by admin on Fri Dec 15 15:46:59 UTC 2023 , Edited by admin on Fri Dec 15 15:46:59 UTC 2023
PRIMARY