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词条 ZM-241,385
释义

  1. References

  2. External links

{{chembox
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 360578336
| ImageFile = ZM241385.png
| ImageSize =
| IUPACName = 4-(2-(7-amino-2-(furan-2-yl)-[1,2,4]triazolo[1,5-a][1,3,5]triazin-5-ylamino)ethyl)phenol
| OtherNames =
| Section1 = {{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo = 139180-30-6
| PubChem = 176407
| IUPHAR_ligand = 405
| ChEMBL_Ref = {{ebicite|changed|EBI}}
| ChEMBL = 113142
| SMILES = Oc1ccc(CCNc2nc3nc(c4ccco4)nn3c(N)n2)cc1
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 153646
| InChI = 1/C16H15N7O2/c17-14-20-15(18-8-7-10-3-5-11(24)6-4-10)21-16-19-13(22-23(14)16)12-2-1-9-25-12/h1-6,9,24H,7-8H2,(H3,17,18,19,20,21,22)
| InChIKey = PWTBZOIUWZOPFT-UHFFFAOYAJ
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/C16H15N7O2/c17-14-20-15(18-8-7-10-3-5-11(24)6-4-10)21-16-19-13(22-23(14)16)12-2-1-9-25-12/h1-6,9,24H,7-8H2,(H3,17,18,19,20,21,22)
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = PWTBZOIUWZOPFT-UHFFFAOYSA-N
| Section2 = {{Chembox Properties
| C=16|H=15|N=7|O=2
| Appearance =
| Density =
| MeltingPt =
| BoilingPt =
| Solubility =
| Section3 = {{Chembox Hazards
| MainHazards =
| FlashPt =
| AutoignitionPt =
}}ZM-241,385 is a high affinity antagonist ligand selective for the adenosine A2A receptor.[1]

In animal models, ZM-241,385 has been shown to protect against beta amyloid neurotoxicity and therefore may be useful as a treatment for Alzheimer's disease.[2] ZM-241,385 has also been shown to enhance L-DOPA derived dopamine release and therefore may be useful in the treatment of Parkinson's disease.[3]

References

1. ^{{cite journal | vauthors = Palmer TM, Poucher SM, Jacobson KA, Stiles GL | title = 125I-4-(2-(7-amino-2-(2-furyl)(1,2,4)triazolo(2,3-a)(1,3,5) triazin-5-yl-amino)ethyl)phenol, a high affinity antagonist radioligand selective for the A2a adenosine receptor | journal = Molecular Pharmacology | volume = 48 | issue = 6 | pages = 970–4 |date=December 1995 | pmid = 8848012 | doi = | url = http://molpharm.aspetjournals.org/cgi/content/abstract/48/6/970 | issn = | pmc=3479638}}
2. ^{{cite journal | vauthors = Dall'Igna OP, Porciúncula LO, Souza DO, Cunha RA, Lara DR, Dall'lgna OP | title = Neuroprotection by caffeine and adenosine A2A receptor blockade of beta-amyloid neurotoxicity | journal = British Journal of Pharmacology | volume = 138 | issue = 7 | pages = 1207–9 |date=April 2003 | pmid = 12711619 | pmc = 1573785 | doi = 10.1038/sj.bjp.0705185 | url = | issn = }}
3. ^{{cite journal | vauthors = Gołembiowska K, Dziubina A | title = Striatal adenosine A(2A) receptor blockade increases extracellular dopamine release following l-DOPA administration in intact and dopamine-denervated rats | journal = Neuropharmacology | volume = 47 | issue = 3 | pages = 414–26 |date=September 2004 | pmid = 15275831 | doi = 10.1016/j.neuropharm.2004.04.018 | url = | issn = }}

External links

{{MeshName|ZM+241385}}{{Adenosinergics}}{{nervous-system-drug-stub}}

3 : Phenols|Furans|Adenosine receptor antagonists

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