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Details

Stereochemistry ACHIRAL
Molecular Formula C16H24N4O3
Molecular Weight 320.3868
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DENBUFYLLINE

SMILES

CCCCN1C2=C(N(CC(C)=O)C=N2)C(=O)N(CCCC)C1=O

InChI

InChIKey=HJPRDDKCXVCFOH-UHFFFAOYSA-N
InChI=1S/C16H24N4O3/c1-4-6-8-19-14-13(18(11-17-14)10-12(3)21)15(22)20(16(19)23)9-7-5-2/h11H,4-10H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C16H24N4O3
Molecular Weight 320.3868
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Denbufylline is a selective xanthine derivative that inhibits PDE IV and has bronchodilatory properties. Shown to exhibit negative inotropic effects by acting on verapamil-sensitive sites of Ca2+ channels in guinea pig ventricle papillary muscle independently of its PDE inhibitory activity. Denbufylline, a selective type 4 phosphodiesterase (PDE-4) inhibitor, is a potent activator of the hypothalamo-pituitary-adrenal (HPA) axis when given orally or intraperitoneally (i.p.) to adult male rats. Denbufylline was being developed as an agent for the therapy of dementia.

CNS Activity

Curator's Comment: Patients who received denbufylline tended to improve in terms of cognitive scores, but the effects were not statistically significant. MMSE scores were found to be higher among patients who received denbufylline when these latter were combined as a single group, regardless of their diagnosis or dosage regimen. Denbufylline induced a statistically significant and clinically relevant improvement in both SDAT and MID patients

Approval Year

Doses

Doses

DosePopulationAdverse events​
100 mg 2 times / day multiple, oral
Highest studied dose
Dose: 100 mg, 2 times / day
Route: oral
Route: multiple
Dose: 100 mg, 2 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
PubMed

PubMed

TitleDatePubMed
The effect of selective phosphodiesterase 3 and 4 isoenzyme inhibitors and established anti-asthma drugs on inflammatory cell activation.
1996-11
Patents

Sample Use Guides

The patients with dementia of the Alzheimer type (DAT) were randomly allocated to denbufylline 25, 50 or 100 mg or to placebo given twice daily for 16 weeks.
Route of Administration: Oral
In Vitro Use Guide
Cyclic AMP PDE activity of human eosinophil homogenates was inhibited by denbufylline (IC50 = 360 nM).
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:30:08 GMT 2025
Edited
by admin
on Mon Mar 31 18:30:08 GMT 2025
Record UNII
04B949KO6F
Record Status Validated (UNII)
Record Version
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Name Type Language
DENBUFYLLINE
INN   MART.  
INN  
Official Name English
BRL 30892
Preferred Name English
denbufylline [INN]
Common Name English
BRL-30892
Code English
DENBUFYLLINE [MART.]
Common Name English
7-ACETONYL-1,3-DIBUTYLXANTHINE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C744
Created by admin on Mon Mar 31 18:30:08 GMT 2025 , Edited by admin on Mon Mar 31 18:30:08 GMT 2025
Code System Code Type Description
PUBCHEM
2984
Created by admin on Mon Mar 31 18:30:08 GMT 2025 , Edited by admin on Mon Mar 31 18:30:08 GMT 2025
PRIMARY
EVMPD
SUB06974MIG
Created by admin on Mon Mar 31 18:30:08 GMT 2025 , Edited by admin on Mon Mar 31 18:30:08 GMT 2025
PRIMARY
NCI_THESAURUS
C76316
Created by admin on Mon Mar 31 18:30:08 GMT 2025 , Edited by admin on Mon Mar 31 18:30:08 GMT 2025
PRIMARY
SMS_ID
100000083159
Created by admin on Mon Mar 31 18:30:08 GMT 2025 , Edited by admin on Mon Mar 31 18:30:08 GMT 2025
PRIMARY
MESH
C043898
Created by admin on Mon Mar 31 18:30:08 GMT 2025 , Edited by admin on Mon Mar 31 18:30:08 GMT 2025
PRIMARY
CAS
57076-71-8
Created by admin on Mon Mar 31 18:30:08 GMT 2025 , Edited by admin on Mon Mar 31 18:30:08 GMT 2025
PRIMARY
FDA UNII
04B949KO6F
Created by admin on Mon Mar 31 18:30:08 GMT 2025 , Edited by admin on Mon Mar 31 18:30:08 GMT 2025
PRIMARY
INN
5921
Created by admin on Mon Mar 31 18:30:08 GMT 2025 , Edited by admin on Mon Mar 31 18:30:08 GMT 2025
PRIMARY
EPA CompTox
DTXSID30205687
Created by admin on Mon Mar 31 18:30:08 GMT 2025 , Edited by admin on Mon Mar 31 18:30:08 GMT 2025
PRIMARY
ChEMBL
CHEMBL277465
Created by admin on Mon Mar 31 18:30:08 GMT 2025 , Edited by admin on Mon Mar 31 18:30:08 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY