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D4065

Dirithromycin

analytical standard, for drug analysis

Synonym(e):

[9S(R)]-9-Deoxo-11-deoxy-9,11-[imino-[2-(2-methoxy)-ethyliden]-oxy]-erthromycin; LY-237216

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Über diesen Artikel

Empirische Formel (Hill-System):
C42H78N2O14
CAS-Nummer:
Molekulargewicht:
835.07
UNSPSC Code:
41116107
PubChem Substance ID:
MDL number:


Quality Level

assay

≥95% (TLC)

form

solid

mol wt

apparent mol wt 835.1

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

format

neat

SMILES string

CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]3O[C@H](C)C[C@@H]([C@H]3O)N(C)C)[C@](C)(O)C[C@@H](C)C4N[C@@H](COCCOC)OC([C@H]4C)[C@]1(C)O

InChI

1S/C42H78N2O14/c1-15-29-42(10,49)37-24(4)32(43-30(56-37)21-52-17-16-50-13)22(2)19-40(8,48)36(58-39-33(45)28(44(11)12)18-23(3)53-39)25(5)34(26(6)38(47)55-29)57-31-20-41(9,51-14)35(46)27(7)54-31/h22-37,39,43,45-46,48-49H,15-21H2,1-14H3/t22-,23-,24+,25+,26-,27+,28+,29-,30-,31+,32+,33-,34+,35+,36-,37-,39+,40-,41+,42-/m1/s1

InChI key

WLOHNSSYAXHWNR-KZYCBHIHSA-N

General description

Chemical structure: macrolide

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.


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pictograms

Exclamation mark

signalword

Warning

hcodes

pcodes

Hazard Classifications

Skin Sens. 1

Lagerklasse

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves



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P A Moore
Journal of the American Dental Association (1939), 130(9), 1341-1343 (1999-09-24)
When treating oral infections, clinicians have used the macrolide antibiotic erythromycin as an alternative antibiotic for patients who have documented allergic reactions to penicillins. In this article, the author reports on his assessment of the pharmacology of erythromycin and the
G G Zhanel et al.
Drugs, 61(4), 443-498 (2001-04-28)
The first macrolide, erythromycin A, demonstrated broad-spectrum antimicrobial activity and was used primarily for respiratory and skin and soft tissue infections. Newer 14-, 15- and 16-membered ring macrolides such as clarithromycin and the azalide, azithromycin, have been developed to address
In vitro activity of azithromycin and dirithromycin against axenic Entamoeba histolytica.
S Ranque et al.
European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 23(12), 932-933 (2004-12-16)



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