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Details

Stereochemistry RACEMIC
Molecular Formula C15H20O2
Molecular Weight 232.3181
Optical Activity ( + / - )
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ISOALANTOLACTONE, (±)-

SMILES

[H][C@@]12C[C@@]3(C)CCCC(=C)[C@]3([H])C[C@]1([H])C(=C)C(=O)O2

InChI

InChIKey=CVUANYCQTOGILD-QVHKTLOISA-N
InChI=1S/C15H20O2/c1-9-5-4-6-15(3)8-13-11(7-12(9)15)10(2)14(16)17-13/h11-13H,1-2,4-8H2,3H3/t11-,12+,13-,15-/m1/s1

HIDE SMILES / InChI

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
Isoalantolactone inhibits constitutive NF-κB activation and induces reactive oxygen species-mediated apoptosis in osteosarcoma U2OS cells through mitochondrial dysfunction.
2014 Oct
Name Type Language
ISOALANTOLACTONE, (±)-
Common Name English
EUDESMA-4(14),11(13)-DIEN-12-OIC ACID, 8.BETA.-HYDROXY-, .GAMMA.-LACTONE, (±)-
Common Name English
REL-(3AR,4AS,8AR,9AR)-DECAHYDRO-8A-METHYL-3,5-BIS(METHYLENE)NAPHTHO(2,3-B)FURAN-2(3H)-ONE
Common Name English
(±)-ISOALANTOLACTONE
Common Name English
NAPHTHO(2,3-B)FURAN-2(3H)-ONE, DECAHYDRO-8A-METHYL-3,5-BIS(METHYLENE)-, (3AR,4AS,8AR,9AR)-REL-
Systematic Name English
Code System Code Type Description
FDA UNII
QTF89ZHT7V
Created by admin on Sat Dec 16 18:15:21 GMT 2023 , Edited by admin on Sat Dec 16 18:15:21 GMT 2023
PRIMARY
CAS
107439-69-0
Created by admin on Sat Dec 16 18:15:21 GMT 2023 , Edited by admin on Sat Dec 16 18:15:21 GMT 2023
SUPERSEDED
CAS
4677-48-9
Created by admin on Sat Dec 16 18:15:21 GMT 2023 , Edited by admin on Sat Dec 16 18:15:21 GMT 2023
PRIMARY
PUBCHEM
73285
Created by admin on Sat Dec 16 18:15:21 GMT 2023 , Edited by admin on Sat Dec 16 18:15:21 GMT 2023
PRIMARY