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Details

Stereochemistry ABSOLUTE
Molecular Formula C27H58N2O6SSi3
Molecular Weight 623.081
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,3,4-TRI-O-TRIMETHYLSILYLLINCOMYCIN

SMILES

CCC[C@@H]1C[C@H](N(C)C1)C(=O)N[C@H]([C@@H](C)O)[C@H]2O[C@H](SC)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C

InChI

InChIKey=PKNYTEMTZAKTHT-ZONSCHRUSA-N
InChI=1S/C27H58N2O6SSi3/c1-14-15-19-16-20(29(3)17-19)26(31)28-21(18(2)30)22-23(33-37(5,6)7)24(34-38(8,9)10)25(27(32-22)36-4)35-39(11,12)13/h18-25,27,30H,14-17H2,1-13H3,(H,28,31)/t18-,19-,20+,21-,22-,23+,24+,25-,27-/m1/s1

HIDE SMILES / InChI

Molecular Formula C27H58N2O6SSi3
Molecular Weight 623.081
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 9 / 9
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 17:57:46 GMT 2025
Edited
by admin
on Mon Mar 31 17:57:46 GMT 2025
Record UNII
598XD7Z5W3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,3,4-TRI-O-TRIMETHYLSILYLLINCOMYCIN
Common Name English
D-ERYTHRO-.ALPHA.-D-GALACTO-OCTOPYRANOSIDE, METHYL 6,8-DIDEOXY-6-((((2S,4R)-1-METHYL-4-PROPYL-2-PYRROLIDINYL)CARBONYL)AMINO)-1-THIO-2,3,4-TRIS-O-(TRIMETHYLSILYL)-
Preferred Name English
D-ERYTHRO-D-GALACTO-OCTOPYRANOSIDE, METHYL 6,8-DIDEOXY-6-(1-METHYL-4-PROPYL-L-2-PYRROLIDINECARBOXAMIDO)-1-THIO-2,3,4-TRIS-O-(TRIMETHYLSILYL)-, TRANS- .ALPHA.-
Systematic Name English
Code System Code Type Description
FDA UNII
598XD7Z5W3
Created by admin on Mon Mar 31 17:57:46 GMT 2025 , Edited by admin on Mon Mar 31 17:57:46 GMT 2025
PRIMARY
PUBCHEM
71752839
Created by admin on Mon Mar 31 17:57:46 GMT 2025 , Edited by admin on Mon Mar 31 17:57:46 GMT 2025
PRIMARY
EPA CompTox
DTXSID00858543
Created by admin on Mon Mar 31 17:57:46 GMT 2025 , Edited by admin on Mon Mar 31 17:57:46 GMT 2025
PRIMARY
CAS
25420-97-7
Created by admin on Mon Mar 31 17:57:46 GMT 2025 , Edited by admin on Mon Mar 31 17:57:46 GMT 2025
PRIMARY