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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
Isolation and culture of biliary epithelial cells from bile duct remnants of patients with biliary atresia.
2004 Sep
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
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SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY