| 词条 | HOCPCA |
| 释义 |
| ImageFile =3-hydroxycyclopent-1-enecarboxylic acid.svg | ImageSize =180px | ImageAlt = | IUPACName =3-Hydroxycyclopent-1-enecarboxylic acid | OtherNames = |Section1={{Chembox Identifiers | CASNo = 867178-11-8 | CASNo_Ref = {{cascite|correct|}} | PubChem = 21750168 | ChEMBL = 2431324 | ChemSpiderID = 26333262 | SMILES = C1CC(=CC1O)C(=O)O | InChI = 1/C6H8O3/c7-5-2-1-4(3-5)6(8)9/h3,5,7H,1-2H2,(H,8,9) | InChIKey = VKJGQKRRULDFCI-UHFFFAOYAO | StdInChI = 1S/C6H8O3/c7-5-2-1-4(3-5)6(8)9/h3,5,7H,1-2H2,(H,8,9) | StdInChIKey = VKJGQKRRULDFCI-UHFFFAOYSA-N}} |Section2={{Chembox Properties | C=6 | H=8 | O=3 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = }} |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }}HOCPCA (3-hydroxycyclopent-1-enecarboxylic acid) is a compound with an affinity for the GHB receptor 39 times greater than that of GHB itself.[1] See also
References1. ^{{ cite journal |vauthors=Wellendorph P, Høg S, Greenwood JR, de Lichtenberg A, Nielsen B, Frølund B, Brehm L, Clausen RP, Bräuner-Osborne H | title = Novel Cyclic γ-Hydroxybutyrate (GHB) Analogs with High Affinity and Stereoselectivity of Binding to GHB Sites in Rat Brain | journal = The Journal of Pharmacology and Experimental Therapeutics | year = 2005 | volume = 315 | issue = 1 | pages = 346–351 | doi = 10.1124/jpet.105.090472 | pmid = 16014570 | url = http://jpet.aspetjournals.org/content/315/1/346.full.pdf | format = pdf }} {{GHBergics}}{{nervous-system-drug-stub}} 3 : Neurochemistry|Carboxylic acids|GHB receptor agonists |
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