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Details

Stereochemistry ABSOLUTE
Molecular Formula C27H24N2O9
Molecular Weight 520.4875
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GL-331

SMILES

COC1=CC(=CC(OC)=C1O)[C@H]2[C@@H]3[C@H](COC3=O)[C@H](NC4=CC=C(C=C4)[N+]([O-])=O)C5=CC6=C(OCO6)C=C25

InChI

InChIKey=DLROLUIVVKTFPW-LVEBQJTPSA-N
InChI=1S/C27H24N2O9/c1-34-21-7-13(8-22(35-2)26(21)30)23-16-9-19-20(38-12-37-19)10-17(16)25(18-11-36-27(31)24(18)23)28-14-3-5-15(6-4-14)29(32)33/h3-10,18,23-25,28,30H,11-12H2,1-2H3/t18-,23+,24-,25+/m0/s1

HIDE SMILES / InChI

Molecular Formula C27H24N2O9
Molecular Weight 520.4875
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Anti-AIDS agents. Part 61: Anti-HIV activity of new podophyllotoxin derivatives.
2004-08-01
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:13:11 GMT 2025
Edited
by admin
on Mon Mar 31 18:13:11 GMT 2025
Record UNII
0I81858VSZ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GL-331
Common Name English
NSC-628672
Preferred Name English
W-68
Code English
FURO(3',4':6,7)NAPHTHO(2,3-D)-1,3-DIOXOL-6(5AH)-ONE, 5,8,8A,9-TETRAHYDRO-5-(4-HYDROXY-3,5-DIMETHOXYPHENYL)-9-((4-NITROPHENYL)AMINO)-, (5R-(5.ALPHA.,5A.BETA.,8A.ALPHA.,9.BETA.))-
Common Name English
FURO(3',4':6,7)NAPHTHO(2,3-D)-1,3-DIOXOL-6(5AH)-ONE, 5,8,8A,9-TETRAHYDRO-5-(4-HYDROXY-3,5-DIMETHOXYPHENYL)-9-((4-NITROPHENYL)AMINO)-, (5R,5AR,8AS,9S)-
Common Name English
Code System Code Type Description
CAS
127882-73-9
Created by admin on Mon Mar 31 18:13:11 GMT 2025 , Edited by admin on Mon Mar 31 18:13:11 GMT 2025
PRIMARY
FDA UNII
0I81858VSZ
Created by admin on Mon Mar 31 18:13:11 GMT 2025 , Edited by admin on Mon Mar 31 18:13:11 GMT 2025
PRIMARY
PUBCHEM
148091
Created by admin on Mon Mar 31 18:13:11 GMT 2025 , Edited by admin on Mon Mar 31 18:13:11 GMT 2025
PRIMARY
NSC
628672
Created by admin on Mon Mar 31 18:13:11 GMT 2025 , Edited by admin on Mon Mar 31 18:13:11 GMT 2025
PRIMARY
EPA CompTox
DTXSID40155689
Created by admin on Mon Mar 31 18:13:11 GMT 2025 , Edited by admin on Mon Mar 31 18:13:11 GMT 2025
PRIMARY
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