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Details

Stereochemistry ACHIRAL
Molecular Formula C14H12O3
Molecular Weight 228.2433
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SESELIN

SMILES

CC1(C)OC2=CC=C3C=CC(=O)OC3=C2C=C1

InChI

InChIKey=QUVCQYQEIOLHFZ-UHFFFAOYSA-N
InChI=1S/C14H12O3/c1-14(2)8-7-10-11(17-14)5-3-9-4-6-12(15)16-13(9)10/h3-8H,1-2H3

HIDE SMILES / InChI

Molecular Formula C14H12O3
Molecular Weight 228.2433
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Structure and in vitro antiparasitic activity of constituents of Citropsis articulata root bark.
2011-10-28
Anti-human immunodeficiency virus-1 constituents of the bark of Poncirus trifoliata.
2010-07
A prenyloxycoumarin from Psiadia dentata.
2001-05
Anti-AIDS agents. 15. Synthesis and anti-HIV activity of dihydroseselins and related analogs.
1994-11-11
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:04:02 GMT 2025
Edited
by admin
on Mon Mar 31 21:04:02 GMT 2025
Record UNII
5634E8957P
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SESELIN
Common Name English
2H-1-BENZOPYRAN-6-ACRYLIC ACID, 5-HYDROXY-2,2-DIMETHYL-, .DELTA.-LACTONE
Preferred Name English
AMYROLIN
Common Name English
SESELINE
Common Name English
2H,8H-BENZO(1,2-B:3,4-B')DIPYRAN-2-ONE, 8,8-DIMETHYL-
Systematic Name English
8,8-DIMETHYL-2H,8H-BENZO(1,2-B:3,4-B')DIPYRAN-2-ONE
Systematic Name English
Code System Code Type Description
FDA UNII
5634E8957P
Created by admin on Mon Mar 31 21:04:02 GMT 2025 , Edited by admin on Mon Mar 31 21:04:02 GMT 2025
PRIMARY
CAS
523-59-1
Created by admin on Mon Mar 31 21:04:02 GMT 2025 , Edited by admin on Mon Mar 31 21:04:02 GMT 2025
PRIMARY
EPA CompTox
DTXSID60200322
Created by admin on Mon Mar 31 21:04:02 GMT 2025 , Edited by admin on Mon Mar 31 21:04:02 GMT 2025
PRIMARY
PUBCHEM
68229
Created by admin on Mon Mar 31 21:04:02 GMT 2025 , Edited by admin on Mon Mar 31 21:04:02 GMT 2025
PRIMARY