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Details

Stereochemistry ABSOLUTE
Molecular Formula C37H70N2O12
Molecular Weight 734.9579
Optical Activity UNSPECIFIED
Defined Stereocenters 18 / 18
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AZAERYTHROMYCIN A

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@@H](C)CN[C@H](C)[C@@H](O)[C@](C)(O)[C@@H](CC)OC(=O)[C@@H]2C

InChI

InChIKey=HRKNNHYKWGYTEN-HOQMJRDDSA-N
InChI=1S/C37H70N2O12/c1-14-26-37(10,45)30(41)23(6)38-18-19(2)16-35(8,44)32(51-34-28(40)25(39(11)12)15-20(3)47-34)21(4)29(22(5)33(43)49-26)50-27-17-36(9,46-13)31(42)24(7)48-27/h19-32,34,38,40-42,44-45H,14-18H2,1-13H3/t19-,20-,21+,22-,23-,24+,25+,26-,27+,28-,29+,30-,31+,32-,34+,35-,36-,37-/m1/s1

HIDE SMILES / InChI
Azaerythromycin A is a novel intermediate of Azithromycin which acts as an antibiotic. Azithromycin binds to the 50S subunit of the bacterial ribosome, and thus inhibits translation of mRNA.

Approval Year

Targets

Targets

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Quantitative thin-layer chromatographic method of analysis of azithromycin in pure and capsule forms.
2003 Jan
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
Azaerythromycin A inhibited Toxoplasma gondii with IC50 65 uM.
Name Type Language
AZAERYTHROMYCIN A
USP-RS  
Common Name English
AZATHRAMYCIN
Common Name English
AZAERYTHROMYCIN A [USP-RS]
Common Name English
9-DEOXO-9A-AZA-9A-HOMOERYTHROMYCIN A
Common Name English
6-DEMETHYLAZITHROMYCIN
Common Name English
AZITHROMYCIN IMPURITY A [EP IMPURITY]
Common Name English
Code System Code Type Description
PUBCHEM
9810601
Created by admin on Sat Dec 16 05:50:08 GMT 2023 , Edited by admin on Sat Dec 16 05:50:08 GMT 2023
PRIMARY
CAS
76801-85-9
Created by admin on Sat Dec 16 05:50:08 GMT 2023 , Edited by admin on Sat Dec 16 05:50:08 GMT 2023
PRIMARY
RS_ITEM_NUM
1045600
Created by admin on Sat Dec 16 05:50:08 GMT 2023 , Edited by admin on Sat Dec 16 05:50:08 GMT 2023
PRIMARY
EPA CompTox
DTXSID30998123
Created by admin on Sat Dec 16 05:50:08 GMT 2023 , Edited by admin on Sat Dec 16 05:50:08 GMT 2023
PRIMARY
FDA UNII
4LSP9FJT5B
Created by admin on Sat Dec 16 05:50:08 GMT 2023 , Edited by admin on Sat Dec 16 05:50:08 GMT 2023
PRIMARY