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Details

Stereochemistry ABSOLUTE
Molecular Formula C30H46O8
Molecular Weight 534.6814
Optical Activity UNSPECIFIED
Defined Stereocenters 12 / 12
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PERIPLOCYMARIN

SMILES

CO[C@H]1C[C@H](O[C@H]2CC[C@]3(C)[C@H]4CC[C@]5(C)[C@H](CC[C@]5(O)[C@@H]4CC[C@]3(O)C2)C6=CC(=O)OC6)O[C@H](C)[C@H]1O

InChI

InChIKey=XRWQBDJPMXRDOQ-YUUDFPFBSA-N
InChI=1S/C30H46O8/c1-17-26(32)23(35-4)14-25(37-17)38-19-5-9-27(2)21-6-10-28(3)20(18-13-24(31)36-16-18)8-12-30(28,34)22(21)7-11-29(27,33)15-19/h13,17,19-23,25-26,32-34H,5-12,14-16H2,1-4H3/t17-,19+,20-,21+,22-,23+,25+,26-,27-,28-,29+,30+/m1/s1

HIDE SMILES / InChI

Molecular Formula C30H46O8
Molecular Weight 534.6814
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 12 / 12
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Aurintricarboxylic acid inhibits influenza virus neuraminidase.
2009-02
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:25:39 GMT 2025
Edited
by admin
on Mon Mar 31 22:25:39 GMT 2025
Record UNII
9M3584249U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PERIPLOCYMARIN [MI]
Preferred Name English
PERIPLOCYMARIN
MI  
Common Name English
PERIPLOCYMARIN, (+)-
Systematic Name English
CARD-20(22)-ENOLIDE, 3-((2,6-DIDEOXY-3-O-METHYL-.BETA.-D-RIBO-HEXOPYRANOSYL)OXY)-5,14-DIHYDROXY-, (3.BETA.,5.BETA.)-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID301317267
Created by admin on Mon Mar 31 22:25:39 GMT 2025 , Edited by admin on Mon Mar 31 22:25:39 GMT 2025
PRIMARY
MERCK INDEX
m8560
Created by admin on Mon Mar 31 22:25:39 GMT 2025 , Edited by admin on Mon Mar 31 22:25:39 GMT 2025
PRIMARY Merck Index
PUBCHEM
12305974
Created by admin on Mon Mar 31 22:25:39 GMT 2025 , Edited by admin on Mon Mar 31 22:25:39 GMT 2025
PRIMARY
FDA UNII
9M3584249U
Created by admin on Mon Mar 31 22:25:39 GMT 2025 , Edited by admin on Mon Mar 31 22:25:39 GMT 2025
PRIMARY
CAS
32476-67-8
Created by admin on Mon Mar 31 22:25:39 GMT 2025 , Edited by admin on Mon Mar 31 22:25:39 GMT 2025
PRIMARY