From Surf Wiki (app.surf) — the open knowledge base
8-Cyclopentyl-1,3-dimethylxanthine
| Column 1 |
|---|
| .mw-parser-output .plainlist ol,.mw-parser-output .plainlist ul{line-height:inherit;list-style:none;margin:0;padding:0}.mw-parser-output .plainlist ol li,.mw-parser-output .plainlist ul li{margin-bottom:0}None |
| In general: uncontrolled |
| IUPAC name |
| 8-Cyclopentyl-1,3-dimethyl-7H-purine-2,6-dione |
| 35873-49-5 Y |
| 1917 |
| 385 |
| 1843 Y |
| U7PWT4CPL5 |
| CHEBI:109538 |
| ChEMBL106265 Y |
| DTXSID70189432 |
| C12H16N4O2 |
| 248.286 g·mol−1 |
| Interactive image |
| SMILES |
| Cn3c(=O)c2nc(C1CCCC1)[nH]c2n(C)c3=O |
| InChI |
| InChI=1S/C12H16N4O2/c1-15-10-8(11(17)16(2)12(15)18)13-9(14-10)7-5-3-4-6-7/h7H,3-6H2,1-2H3,(H,13,14) YKey:SCVHFRLUNIOSGI-UHFFFAOYSA-N Y |
| .mw-parser-output .nobold{font-weight:normal} (verify) |
8-Cyclopentyl-1,3-dimethylxanthine (8-Cyclopentyltheophylline, 8-CPT, CPX) is a drug which acts as a potent and selective antagonist for the adenosine receptors, with some selectivity for the A1 receptor subtype, as well as a non-selective phosphodiesterase inhibitor. It has stimulant effects in animals with slightly higher potency than caffeine.
- 8-Chlorotheophylline
- 8-Phenyltheophylline
- DMPX
- DPCPX
- Xanthine
Ask Mako anything about 8-Cyclopentyl-1,3-dimethylxanthine — get instant answers, deeper analysis, and related topics.
Research with MakoFree with your Surf account
Create a free account to save articles, ask Mako questions, and organize your research.
Sign up freeThis content may have been generated or modified by AI. CloudSurf Software LLC is not responsible for the accuracy, completeness, or reliability of AI-generated content. Always verify important information from primary sources.
Report