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Details

Stereochemistry ABSOLUTE
Molecular Formula C41H67NO15
Molecular Weight 813.9684
Optical Activity UNSPECIFIED
Defined Stereocenters 18 / 18
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TROLEANDOMYCIN

SMILES

[H][C@]2(O[C@@H]1O[C@H](C)C[C@@H]([C@H]1OC(C)=O)N(C)C)[C@@H](C)C[C@@]3(CO3)C(=O)[C@H](C)[C@@H](OC(C)=O)[C@@H](C)[C@@H](C)OC(=O)[C@H](C)[C@@]([H])(O[C@H]4C[C@H](OC)[C@@H](OC(C)=O)[C@H](C)O4)[C@@H]2C

InChI

InChIKey=LQCLVBQBTUVCEQ-QTFUVMRISA-N
InChI=1S/C41H67NO15/c1-19-17-41(18-49-41)38(46)23(5)34(53-27(9)43)21(3)25(7)52-39(47)24(6)35(56-32-16-31(48-14)36(26(8)51-32)54-28(10)44)22(4)33(19)57-40-37(55-29(11)45)30(42(12)13)15-20(2)50-40/h19-26,30-37,40H,15-18H2,1-14H3/t19-,20+,21-,22+,23+,24+,25+,26-,30-,31-,32-,33-,34-,35-,36-,37+,40-,41+/m0/s1

HIDE SMILES / InChI
Molecular Formula C41H67NO15
Molecular Weight 813.9684
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 18 / 18
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:08:19 UTC 2023
Edited
by admin
on Fri Dec 15 16:08:19 UTC 2023
Record UNII
C4DZ64560D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TROLEANDOMYCIN
INN   MART.   MI   ORANGE BOOK   USAN   USP   VANDF   WHO-DD  
USAN   INN  
Official Name English
OLEANDOMYCIN (AS TROLEANDOMYCIN)
VANDF  
Common Name English
OLEANDOMYCIN (AS TROLEANDOMYCIN) [VANDF]
Common Name English
NSC-108166
Code English
OLEANDOMYCIN TRIACETATE ESTER
Common Name English
TROLEANDOMYCIN [USP IMPURITY]
Common Name English
TROLEANDOMYCIN [MI]
Common Name English
TRIACETYLOLEANDOMYCIN [JAN]
Common Name English
TROLEANDOMYCIN [ORANGE BOOK]
Common Name English
TROLEANDOMYCIN [MART.]
Common Name English
TROLEANDOMYCIN [VANDF]
Common Name English
Triacetyloleandomycin
JAN  
Common Name English
Troleandomycin [WHO-DD]
Common Name English
troleandomycin [INN]
Common Name English
TROLEANDOMYCIN [USAN]
Common Name English
Classification Tree Code System Code
WHO-ATC J01FA08
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
WHO-VATC QJ01FA08
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
NCI_THESAURUS C261
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
FDA ORPHAN DRUG 39089
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
Code System Code Type Description
FDA UNII
C4DZ64560D
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
PRIMARY
RXCUI
10864
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
PRIMARY RxNorm
EVMPD
SUB11333MIG
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
PRIMARY
ECHA (EC/EINECS)
220-392-9
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
PRIMARY
CAS
2751-09-9
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
PRIMARY
MERCK INDEX
m11219
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
PRIMARY Merck Index
INN
805
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
PRIMARY
NCI_THESAURUS
C66643
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
PRIMARY
NSC
108166
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
PRIMARY
MESH
D014217
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
PRIMARY
DRUG CENTRAL
2769
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
PRIMARY
WIKIPEDIA
TROLEANDOMYCIN
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
PRIMARY
CHEBI
45735
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
PRIMARY
PUBCHEM
202225
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
PRIMARY
SMS_ID
100000076956
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
PRIMARY
EPA CompTox
DTXSID2023721
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
PRIMARY
DRUG BANK
DB01361
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
PRIMARY
ChEMBL
CHEMBL564085
Created by admin on Fri Dec 15 16:08:19 UTC 2023 , Edited by admin on Fri Dec 15 16:08:19 UTC 2023
PRIMARY
Related Record Type Details
CYTOCHROME P450 3A4
METABOLIC ENZYME -> INDUCER
CYTOCHROME P450 3A5
METABOLIC ENZYME -> INDUCER
Related Record Type Details
Structure of TROLEANDOMYCIN
ACTIVE MOIETY
NIH
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