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

Details

Stereochemistry ABSOLUTE
Molecular Formula C40H65NO15
Molecular Weight 799.9418
Optical Activity UNSPECIFIED
Defined Stereocenters 16 / 16
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEUCOMYCIN A6

SMILES

[H][C@@]2(O[C@H]1[C@@H](CC=O)C[C@@H](C)[C@@H](O)\C=C\C=C\C[C@@H](C)OC(=O)C[C@@H](OC(C)=O)[C@@H]1OC)O[C@H](C)[C@@]([H])(O[C@H]3C[C@@](C)(O)[C@@H](OC(=O)CC)[C@H](C)O3)[C@@H]([C@H]2O)N(C)C

InChI

InChIKey=ABTSKZKCMFRYNP-HUFPKKMTSA-N
InChI=1S/C40H65NO15/c1-11-30(45)54-38-25(5)51-32(21-40(38,7)48)55-35-24(4)52-39(34(47)33(35)41(8)9)56-36-27(17-18-42)19-22(2)28(44)16-14-12-13-15-23(3)50-31(46)20-29(37(36)49-10)53-26(6)43/h12-14,16,18,22-25,27-29,32-39,44,47-48H,11,15,17,19-21H2,1-10H3/b13-12+,16-14+/t22-,23-,24-,25+,27+,28+,29-,32+,33-,34-,35-,36+,37+,38+,39+,40-/m1/s1

HIDE SMILES / InChI

Molecular Formula C40H65NO15
Molecular Weight 799.9418
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 16 / 16
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 07:09:45 GMT 2023
Edited
by admin
on Sat Dec 16 07:09:45 GMT 2023
Record UNII
5FN79UZP05
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEUCOMYCIN A6
Common Name English
LEUCOMYCIN V, 3-ACETATE 4B-PROPANOATE
Common Name English
ANTIBIOTIC YL 704B3
Common Name English
TURIMYCIN A3
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID20860188
Created by admin on Sat Dec 16 07:09:45 GMT 2023 , Edited by admin on Sat Dec 16 07:09:45 GMT 2023
PRIMARY
FDA UNII
5FN79UZP05
Created by admin on Sat Dec 16 07:09:45 GMT 2023 , Edited by admin on Sat Dec 16 07:09:45 GMT 2023
PRIMARY
PUBCHEM
11954019
Created by admin on Sat Dec 16 07:09:45 GMT 2023 , Edited by admin on Sat Dec 16 07:09:45 GMT 2023
PRIMARY
CAS
18361-48-3
Created by admin on Sat Dec 16 07:09:45 GMT 2023 , Edited by admin on Sat Dec 16 07:09:45 GMT 2023
PRIMARY