ERYTHROMYCIN ACISTRATE

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Synonyms
Status
Molecule Category Free-form
UNII 6383U5A1KE
EPA CompTox DTXSID9022992

Structure

InChI Key CVBHEIRZLPKMSH-SNWVVRALSA-N
Smiles 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]2O[C@H](C)C[C@H](N(C)C)[C@H]2OC(C)=O)[C@](C)(O)C[C@@H](C)C(=O)[C@H](C)[C@@H](O)[C@]1(C)O
InChI
InChI=1S/C39H69NO14/c1-15-27-39(11,47)32(43)21(4)29(42)19(2)17-37(9,46)34(54-36-31(51-25(8)41)26(40(12)13)16-20(3)49-36)22(5)30(23(6)35(45)52-27)53-28-18-38(10,48-14)33(44)24(7)50-28/h19-24,26-28,30-34,36,43-44,46-47H,15-18H2,1-14H3/t19-,20-,21+,22+,23-,24+,26+,27-,28+,30+,31-,32-,33+,34-,36+,37-,38-,39-/m1/s1

Physicochemical Descriptors

Property Name Value
Molecular Formula C39H69NO14
Molecular Weight 775.97
AlogP 2.36
Hydrogen Bond Acceptor 15.0
Hydrogen Bond Donor 4.0
Number of Rotational Bond 8.0
Polar Surface Area 199.98
Molecular species NEUTRAL
Aromatic Rings 0.0
Heavy Atoms 54.0

Pharmacology

Mechanism of Action Action Reference
Bacterial 70S ribosome inhibitor INHIBITOR PubMed

Related Entries

Cross References

Resources Reference
CAS NUMBER 96128-89-1
ChEBI 135882
ChEMBL CHEMBL2110577
DrugCentral 1049
FDA SRS 6383U5A1KE
PubChem 5284554
ZINC ZINC000085540310
CONTENTS