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

Details

Stereochemistry ABSOLUTE
Molecular Formula C37H67NO13.C12H22O12
Molecular Weight 1092.2227
Optical Activity UNSPECIFIED
Defined Stereocenters 27 / 27
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ERYTHROMYCIN LACTOBIONATE

SMILES

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

InChI

InChIKey=NNRXCKZMQLFUPL-WBMZRJHASA-N
InChI=1S/C37H67NO13.C12H22O12/c1-14-25-37(10,45)30(41)20(4)27(39)18(2)16-35(8,44)32(51-34-28(40)24(38(11)12)15-19(3)47-34)21(5)29(22(6)33(43)49-25)50-26-17-36(9,46-13)31(42)23(7)48-26;13-1-3(15)10(7(18)8(19)11(21)22)24-12-9(20)6(17)5(16)4(2-14)23-12/h18-26,28-32,34,40-42,44-45H,14-17H2,1-13H3;3-10,12-20H,1-2H2,(H,21,22)/t18-,19-,20+,21+,22-,23+,24+,25-,26+,28-,29+,30-,31+,32-,34+,35-,36-,37-;3-,4-,5+,6+,7-,8-,9-,10-,12+/m11/s1

HIDE SMILES / InChI

Molecular Formula C12H22O12
Molecular Weight 358.2959
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 9 / 9
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula C37H67NO13
Molecular Weight 733.9268
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 18 / 18
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:01:01 UTC 2023
Edited
by admin
on Fri Dec 15 15:01:01 UTC 2023
Record UNII
33H58I7GLQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ERYTHROMYCIN LACTOBIONATE
EP   MART.   MI   ORANGE BOOK   USP   USP-RS   VANDF   WHO-DD   WHO-IP  
Common Name English
D-GLUCONIC ACID, 4-O-.BETA.-D-GALACTOPYRANOSYL-, COMPD. WITH ERYTHROMYCIN (1:1)
Common Name English
ERYTHROMYCIN LACTOBIONATE [VANDF]
Common Name English
STERILE ERYTHROMYCIN LACTOBIONATE [USP MONOGRAPH]
Common Name English
ERYTHROMYCIN LACTOBIONATE [USP IMPURITY]
Common Name English
Erythromycin lactobionate [WHO-DD]
Common Name English
ERYTHROMYCIN LACTOBIONATE [EP MONOGRAPH]
Common Name English
ERYTHROMYCINI LACTOBIONAS [WHO-IP LATIN]
Common Name English
ERYTHROMYCIN LACTOBIONATE [JAN]
Common Name English
ERYTHROMYCIN MONO(4-O-.BETA.-D-GALACTOPYRANOSYL-D-GLUCONATE) (SALT)
Common Name English
ERYTHROMYCIN LACTOBIONATE [MART.]
Common Name English
ERYTHROMYCIN LACTOBIONATE [ORANGE BOOK]
Common Name English
ERYTHROMYCIN LACTOBIONATE [USP-RS]
Common Name English
ERYTHROMYCIN LACTOBIONATE [WHO-IP]
Common Name English
ERYTHROMYCIN LACTOBIONATE [MI]
Common Name English
ERYTHROMYCIN, LACTOBIONATE (1:1) (SALT)
Common Name English
ERYTHROCIN
Code English
Classification Tree Code System Code
NCI_THESAURUS C261
Created by admin on Fri Dec 15 15:01:01 UTC 2023 , Edited by admin on Fri Dec 15 15:01:01 UTC 2023
Code System Code Type Description
CAS
3847-29-8
Created by admin on Fri Dec 15 15:01:01 UTC 2023 , Edited by admin on Fri Dec 15 15:01:01 UTC 2023
PRIMARY
EPA CompTox
DTXSID801009322
Created by admin on Fri Dec 15 15:01:01 UTC 2023 , Edited by admin on Fri Dec 15 15:01:01 UTC 2023
PRIMARY
RS_ITEM_NUM
1247003
Created by admin on Fri Dec 15 15:01:01 UTC 2023 , Edited by admin on Fri Dec 15 15:01:01 UTC 2023
PRIMARY
DRUG BANK
DBSALT001219
Created by admin on Fri Dec 15 15:01:01 UTC 2023 , Edited by admin on Fri Dec 15 15:01:01 UTC 2023
PRIMARY
NCI_THESAURUS
C47988
Created by admin on Fri Dec 15 15:01:01 UTC 2023 , Edited by admin on Fri Dec 15 15:01:01 UTC 2023
PRIMARY
RXCUI
24347
Created by admin on Fri Dec 15 15:01:01 UTC 2023 , Edited by admin on Fri Dec 15 15:01:01 UTC 2023
PRIMARY RxNorm
FDA UNII
33H58I7GLQ
Created by admin on Fri Dec 15 15:01:01 UTC 2023 , Edited by admin on Fri Dec 15 15:01:01 UTC 2023
PRIMARY
MESH
C010948
Created by admin on Fri Dec 15 15:01:01 UTC 2023 , Edited by admin on Fri Dec 15 15:01:01 UTC 2023
PRIMARY
PUBCHEM
71469
Created by admin on Fri Dec 15 15:01:01 UTC 2023 , Edited by admin on Fri Dec 15 15:01:01 UTC 2023
PRIMARY
DAILYMED
33H58I7GLQ
Created by admin on Fri Dec 15 15:01:01 UTC 2023 , Edited by admin on Fri Dec 15 15:01:01 UTC 2023
PRIMARY
WHO INTERNATIONAL PHARMACOPEIA
ERYTHROMYCIN LACTOBIONATE
Created by admin on Fri Dec 15 15:01:01 UTC 2023 , Edited by admin on Fri Dec 15 15:01:01 UTC 2023
PRIMARY Description: White or slightly yellow crystals or a white, crystalline powder; odour, faint.Solubility: Freely soluble in water, ethanol (~750 g/l) TS and methanol R; slightly soluble in acetone R; practically insoluble in ether R.Category: Antibacterial drug.Storage: Erythromycin lactobionate should be kept in a tightly closed container, protected from light.Additional information: Each mg of erythromycin lactobionate is equivalent to 0.6722 mg of erythromycin.Definition: Erythromycin lactobionate contains not less than 600 IU of erythromycin per mg, calculated with reference to the anhydrous substance.
ChEMBL
CHEMBL532
Created by admin on Fri Dec 15 15:01:01 UTC 2023 , Edited by admin on Fri Dec 15 15:01:01 UTC 2023
PRIMARY
ECHA (EC/EINECS)
223-348-7
Created by admin on Fri Dec 15 15:01:01 UTC 2023 , Edited by admin on Fri Dec 15 15:01:01 UTC 2023
PRIMARY
MERCK INDEX
m5011
Created by admin on Fri Dec 15 15:01:01 UTC 2023 , Edited by admin on Fri Dec 15 15:01:01 UTC 2023
PRIMARY Merck Index
EVMPD
SUB124999
Created by admin on Fri Dec 15 15:01:01 UTC 2023 , Edited by admin on Fri Dec 15 15:01:01 UTC 2023
PRIMARY
EVMPD
SUB01944MIG
Created by admin on Fri Dec 15 15:01:01 UTC 2023 , Edited by admin on Fri Dec 15 15:01:01 UTC 2023
PRIMARY
SMS_ID
100000088884
Created by admin on Fri Dec 15 15:01:01 UTC 2023 , Edited by admin on Fri Dec 15 15:01:01 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
IMPURITY -> PARENT
IMPURITY -> PARENT
IMPURITY -> PARENT
IMPURITY -> PARENT
IMPURITY -> PARENT
IMPURITY -> PARENT
Related Record Type Details
ACTIVE MOIETY