ERYTHROMYCIN ACISTRATE

/static/temp/default.svg Search structure
Synonyms
Status
Molecule Category Free-form
UNII S3Q5941GCW

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
ChEBI 135882
ChEMBL CHEMBL2110577
DrugCentral 1049
FDA SRS S3Q5941GCW
PubChem 5284554
ZINC ZINC000085540310
CONTENTS