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Details

Stereochemistry ACHIRAL
Molecular Formula C15H16N4O2
Molecular Weight 284.3131
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,3-DIETHYL-8-PHENYLXANTHINE

SMILES

CCN1C2=C(NC(=N2)C3=CC=CC=C3)C(=O)N(CC)C1=O

InChI

InChIKey=LVSWNSHUTPWCNF-UHFFFAOYSA-N
InChI=1S/C15H16N4O2/c1-3-18-13-11(14(20)19(4-2)15(18)21)16-12(17-13)10-8-6-5-7-9-10/h5-9H,3-4H2,1-2H3,(H,16,17)

HIDE SMILES / InChI

Molecular Formula C15H16N4O2
Molecular Weight 284.3131
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Melatonin alters age-related changes in transcription factors and kinase activation.
2010-12
Characterization of a stretch-activated potassium channel in chondrocytes.
2010-05
A role for fibrillar collagen deposition and the collagen internalization receptor endo180 in glioma invasion.
2010-03-22
Mesenchymal-to-epithelial transition of intercalating cells in Drosophila renal tubules depends on polarity cues from epithelial neighbours.
2010-02-10
Abeta mediated diminution of MTT reduction--an artefact of single cell culture?
2008-09-18
Characterization of human and rodent native and recombinant adenosine A(2B) receptors by radioligand binding studies.
2006-09
Characterization of adenosine receptors in the human bladder carcinoma T24 cell line.
2006-04-24
Activation of ATP-sensitive potassium channels in hypoxic cardiac failure is not mediated by adenosine-1 receptors in the isolated rat heart.
2001-04
K(ATP) channel blockers selectively interact with A(1)-adenosine receptor mediated modulation of acetylcholine release in the rat hippocampus.
2001-01-19
Characterization of human A(2B) adenosine receptors: radioligand binding, western blotting, and coupling to G(q) in human embryonic kidney 293 cells and HMC-1 mast cells.
1999-10
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:51:25 GMT 2025
Edited
by admin
on Mon Mar 31 18:51:25 GMT 2025
Record UNII
2KCV39GKGL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,3-DIETHYL-8-PHENYLXANTHINE
Systematic Name English
DEPX
Preferred Name English
DPX
Common Name English
1H-PURINE-2,6-DIONE, 1,3-DIETHYL-3,7-DIHYDRO-8-PHENYL-
Systematic Name English
1H-PURINE-2,6-DIONE, 1,3-DIETHYL-3,9-DIHYDRO-8-PHENYL-
Systematic Name English
8-PHENYL-1,3-DIETHYLXANTHINE
Systematic Name English
Code System Code Type Description
CAS
75922-48-4
Created by admin on Mon Mar 31 18:51:25 GMT 2025 , Edited by admin on Mon Mar 31 18:51:25 GMT 2025
PRIMARY
MESH
C027512
Created by admin on Mon Mar 31 18:51:25 GMT 2025 , Edited by admin on Mon Mar 31 18:51:25 GMT 2025
PRIMARY
FDA UNII
2KCV39GKGL
Created by admin on Mon Mar 31 18:51:25 GMT 2025 , Edited by admin on Mon Mar 31 18:51:25 GMT 2025
PRIMARY
EPA CompTox
DTXSID80877797
Created by admin on Mon Mar 31 18:51:25 GMT 2025 , Edited by admin on Mon Mar 31 18:51:25 GMT 2025
PRIMARY
PUBCHEM
1328
Created by admin on Mon Mar 31 18:51:25 GMT 2025 , Edited by admin on Mon Mar 31 18:51:25 GMT 2025
PRIMARY