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Details

Stereochemistry EPIMERIC
Molecular Formula C31H32O5
Molecular Weight 484.5828
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 6
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of Hexahydro-2-hydroxy-4-[(1E,3S)-3-hydroxy-5-phenyl-1-penten-1-yl]-2H-cyclopenta[b]furan-5-yl [1,1?-biphenyl]-4-carboxylate, (3aR,4R,5R,6aS)-

SMILES

O[C@@H](CCC1=CC=CC=C1)\C=C\[C@H]2[C@@H](C[C@@H]3OC(O)C[C@H]23)OC(=O)C4=CC=C(C=C4)C5=CC=CC=C5

InChI

InChIKey=SXADHRIREHPQTN-MWBCMDMXSA-N
InChI=1S/C31H32O5/c32-25(16-11-21-7-3-1-4-8-21)17-18-26-27-19-30(33)35-29(27)20-28(26)36-31(34)24-14-12-23(13-15-24)22-9-5-2-6-10-22/h1-10,12-15,17-18,25-30,32-33H,11,16,19-20H2/b18-17+/t25-,26+,27+,28+,29-,30?/m0/s1

HIDE SMILES / InChI

Molecular Formula C31H32O5
Molecular Weight 484.5828
Charge 0
Count
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 5 / 6
E/Z Centers 1
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Wed Apr 02 19:16:27 GMT 2025
Edited
by admin
on Wed Apr 02 19:16:27 GMT 2025
Record UNII
D6KM7Q9DX5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(3aR,4R,5R,6aS)-Hexahydro-2-hydroxy-4-[(1E,3S)-3-hydroxy-5-phenyl-1-penten-1-yl]-2H-cyclopenta[b]furan-5-yl [1,1?-biphenyl]-4-carboxylate
Preferred Name English
Hexahydro-2-hydroxy-4-[(1E,3S)-3-hydroxy-5-phenyl-1-penten-1-yl]-2H-cyclopenta[b]furan-5-yl [1,1?-biphenyl]-4-carboxylate, (3aR,4R,5R,6aS)-
Systematic Name English
[1,1?-Biphenyl]-4-carboxylic acid, (3aR,4R,5R,6aS)-hexahydro-2-hydroxy-4-[(1E,3S)-3-hydroxy-5-phenyl-1-penten-1-yl]-2H-cyclopenta[b]furan-5-yl ester
Systematic Name English
Code System Code Type Description
FDA UNII
D6KM7Q9DX5
Created by admin on Wed Apr 02 19:16:27 GMT 2025 , Edited by admin on Wed Apr 02 19:16:27 GMT 2025
PRIMARY
PUBCHEM
90140950
Created by admin on Wed Apr 02 19:16:27 GMT 2025 , Edited by admin on Wed Apr 02 19:16:27 GMT 2025
PRIMARY
CAS
1415393-93-9
Created by admin on Wed Apr 02 19:16:27 GMT 2025 , Edited by admin on Wed Apr 02 19:16:27 GMT 2025
PRIMARY