U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C20H27N5O3
Molecular Weight 385.4601
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BAMIFYLLINE

SMILES

CCN(CCO)CCN1C(CC2=CC=CC=C2)=NC3=C1C(=O)N(C)C(=O)N3C

InChI

InChIKey=VVUYEFBRTFASAH-UHFFFAOYSA-N
InChI=1S/C20H27N5O3/c1-4-24(12-13-26)10-11-25-16(14-15-8-6-5-7-9-15)21-18-17(25)19(27)23(3)20(28)22(18)2/h5-9,26H,4,10-14H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C20H27N5O3
Molecular Weight 385.4601
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Bamifylline (or bamiphylline), a selective antagonist of the A1 adenosine receptor, was studied in the therapy of asthmatic syndromes.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P30542
Gene ID: 134.0
Gene Symbol: ADORA1
Target Organism: Homo sapiens (Human)
PubMed

PubMed

TitleDatePubMed
Bamiphylline improves exercise-induced myocardial ischemia through a novel mechanism of action.
1993 Aug
Acute generalized exanthematous pustulosis induced by ingestion of bamifylline.
2002 Nov
Tumor necrosis factor-alpha in whole blood cultures of preeclamptic patients and healthy pregnant and nonpregnant women.
2004
UC blood infection with clinical strains of Mycobacterium tuberculosis: a novel model.
2007
Catecholaminergic neuron survival: getting hooked on GDNF.
2008 Jul
In human endothelial cells rapamycin causes mTORC2 inhibition and impairs cell viability and function.
2008 Jun 1
Single channel studies of the ATP-regulated potassium channel in brain mitochondria.
2009 Aug
Patents

Sample Use Guides

600 mg b.d. for 15 days
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:26:29 GMT 2023
Edited
by admin
on Fri Dec 15 15:26:29 GMT 2023
Record UNII
ZTY15D026H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BAMIFYLLINE
INN   MI   WHO-DD  
INN  
Official Name English
8-BENZYL-7-(2-(ETHYL(2-HYDROXYETHYL)AMINO)ETHYL)THEOPHYLLINE
Systematic Name English
BAMIFYLLINE [MI]
Common Name English
Bamifylline [WHO-DD]
Common Name English
BAX-2739Z FREE BASE
Code English
AC-3810 FREE BASE
Code English
bamifylline [INN]
Common Name English
1H-PURINE-2,6-DIONE, 7-(2-(ETHYL(2-HYDROXYETHYL)AMINO)ETHYL)-3,7-DIHYDRO-1,3-DIMETHYL-8-(PHENYLMETHYL)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C319
Created by admin on Fri Dec 15 15:26:29 GMT 2023 , Edited by admin on Fri Dec 15 15:26:29 GMT 2023
WHO-VATC QR03DA08
Created by admin on Fri Dec 15 15:26:29 GMT 2023 , Edited by admin on Fri Dec 15 15:26:29 GMT 2023
WHO-ATC R03DA08
Created by admin on Fri Dec 15 15:26:29 GMT 2023 , Edited by admin on Fri Dec 15 15:26:29 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID0022642
Created by admin on Fri Dec 15 15:26:29 GMT 2023 , Edited by admin on Fri Dec 15 15:26:29 GMT 2023
PRIMARY
FDA UNII
ZTY15D026H
Created by admin on Fri Dec 15 15:26:29 GMT 2023 , Edited by admin on Fri Dec 15 15:26:29 GMT 2023
PRIMARY
MERCK INDEX
m2218
Created by admin on Fri Dec 15 15:26:29 GMT 2023 , Edited by admin on Fri Dec 15 15:26:29 GMT 2023
PRIMARY Merck Index
SMS_ID
100000088426
Created by admin on Fri Dec 15 15:26:29 GMT 2023 , Edited by admin on Fri Dec 15 15:26:29 GMT 2023
PRIMARY
DRUG BANK
DB13203
Created by admin on Fri Dec 15 15:26:29 GMT 2023 , Edited by admin on Fri Dec 15 15:26:29 GMT 2023
PRIMARY
WIKIPEDIA
BAMIFYLLINE
Created by admin on Fri Dec 15 15:26:29 GMT 2023 , Edited by admin on Fri Dec 15 15:26:29 GMT 2023
PRIMARY
MESH
C006683
Created by admin on Fri Dec 15 15:26:29 GMT 2023 , Edited by admin on Fri Dec 15 15:26:29 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110760
Created by admin on Fri Dec 15 15:26:29 GMT 2023 , Edited by admin on Fri Dec 15 15:26:29 GMT 2023
PRIMARY
PUBCHEM
16229
Created by admin on Fri Dec 15 15:26:29 GMT 2023 , Edited by admin on Fri Dec 15 15:26:29 GMT 2023
PRIMARY
RXCUI
18752
Created by admin on Fri Dec 15 15:26:29 GMT 2023 , Edited by admin on Fri Dec 15 15:26:29 GMT 2023
PRIMARY RxNorm
EVMPD
SUB06097MIG
Created by admin on Fri Dec 15 15:26:29 GMT 2023 , Edited by admin on Fri Dec 15 15:26:29 GMT 2023
PRIMARY
INN
1837
Created by admin on Fri Dec 15 15:26:29 GMT 2023 , Edited by admin on Fri Dec 15 15:26:29 GMT 2023
PRIMARY
NCI_THESAURUS
C76573
Created by admin on Fri Dec 15 15:26:29 GMT 2023 , Edited by admin on Fri Dec 15 15:26:29 GMT 2023
PRIMARY
DRUG CENTRAL
287
Created by admin on Fri Dec 15 15:26:29 GMT 2023 , Edited by admin on Fri Dec 15 15:26:29 GMT 2023
PRIMARY
CAS
2016-63-9
Created by admin on Fri Dec 15 15:26:29 GMT 2023 , Edited by admin on Fri Dec 15 15:26:29 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY