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Details

Stereochemistry ACHIRAL
Molecular Formula C14H22N4O2
Molecular Weight 278.3501
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-ISOAMYL-3-ISOBUTYLXANTHINE

SMILES

CC(C)CCN1C(=O)N(CC(C)C)C2=C(NC=N2)C1=O

InChI

InChIKey=HRWQHFZQHIUCCC-UHFFFAOYSA-N
InChI=1S/C14H22N4O2/c1-9(2)5-6-17-13(19)11-12(16-8-15-11)18(14(17)20)7-10(3)4/h8-10H,5-7H2,1-4H3,(H,15,16)

HIDE SMILES / InChI

Molecular Formula C14H22N4O2
Molecular Weight 278.3501
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Inhibition of cyclic nucleotide phosphodiesterases from pig coronary artery by benzo-separated analogues of 3-isobutyl-1-methylxanthine.
1986-06
Identification of the phosphodiesterase regulated by muscarinic cholinergic receptors of 1321N1 human astrocytoma cells.
1986-05
1,3-Dialkyl-8-(p-sulfophenyl)xanthines: potent water-soluble antagonists for A1- and A2-adenosine receptors.
1985-04
Stimulation by proctolin of the ouabain-insensitive sodium efflux in single barnacle muscle fibers.
1985
The modulatory action of 5-hydroxytryptamine on sodium efflux: the barnacle muscle fibre as a model system.
1985
The effects of alkylated xanthines on cyclic AMP accumulation in dog thyroid slices exposed to carbamylcholine.
1984-03
Stimulation by octopamine of the sodium efflux in barnacle muscle fibres.
1984
The role of cyclic nucleotide phosphodiesterase in the inhibition of cyclic AMP accumulation by carbachol and phosphatidate.
1982
1-Isoamyl-3-isobutylxanthine: a remarkably potent agent for the potentiation of norepinephrine, histamine, and adenosine-elicited accumulations of cyclic AMP in brain slices.
1979-11-26
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:54:30 GMT 2025
Edited
by admin
on Mon Mar 31 18:54:30 GMT 2025
Record UNII
976SW405SB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1H-PURINE-2,6-DIONE, 3,7-DIHYDRO-1-(3-METHYLBUTYL)-3-(2-METHYLPROPYL)-
Preferred Name English
1-ISOAMYL-3-ISOBUTYLXANTHINE
Systematic Name English
1H-PURINE-2,6-DIONE, 3,9-DIHYDRO-1-(3-METHYLBUTYL)-3-(2-METHYLPROPYL)-
Systematic Name English
3-ISOBUTYL-1-ISOAMYLXANTHINE
Systematic Name English
Code System Code Type Description
PUBCHEM
152034
Created by admin on Mon Mar 31 18:54:30 GMT 2025 , Edited by admin on Mon Mar 31 18:54:30 GMT 2025
PRIMARY
MESH
C024045
Created by admin on Mon Mar 31 18:54:30 GMT 2025 , Edited by admin on Mon Mar 31 18:54:30 GMT 2025
PRIMARY
CAS
63908-26-9
Created by admin on Mon Mar 31 18:54:30 GMT 2025 , Edited by admin on Mon Mar 31 18:54:30 GMT 2025
PRIMARY
FDA UNII
976SW405SB
Created by admin on Mon Mar 31 18:54:30 GMT 2025 , Edited by admin on Mon Mar 31 18:54:30 GMT 2025
PRIMARY
EPA CompTox
DTXSID30213606
Created by admin on Mon Mar 31 18:54:30 GMT 2025 , Edited by admin on Mon Mar 31 18:54:30 GMT 2025
PRIMARY