| 词条 | Adafenoxate |
| 释义 |
| Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 477241824 | ImageFile = Adafenoxate.svg | ImageSize = 250 | IUPACName = 2-(4-chlorophenoxy)acetic acid 2-(1-adamantylamino)ethyl ester | OtherNames = | Section1 = {{Chembox Identifiers | UNII_Ref = {{fdacite|correct|FDA}} | UNII = B8VQU4C05J | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 58080 | InChI = 1/C20H26ClNO3/c21-17-1-3-18(4-2-17)25-13-19(23)24-6-5-22-20-10-14-7-15(11-20)9-16(8-14)12-20/h1-4,14-16,22H,5-13H2 | InChIKey = PLSMXIQMWYSHIV-UHFFFAOYAK | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 1S/C20H26ClNO3/c21-17-1-3-18(4-2-17)25-13-19(23)24-6-5-22-20-10-14-7-15(11-20)9-16(8-14)12-20/h1-4,14-16,22H,5-13H2 | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = PLSMXIQMWYSHIV-UHFFFAOYSA-N | CASNo_Ref = {{cascite|changed|??}} | CASNo=82168-26-1 | PubChem=64517 | ChEMBL_Ref = {{ebicite|changed|EBI}} | ChEMBL = 2104053 | SMILES = Clc4ccc(cc4)OCC(=O)OCCNC12CC3CC(C1)CC(C2)C3 }} | Section2 = {{Chembox Properties | C=20 | H=26 | Cl=1 | N=1 | O=3 | MolarMass = 363.87834 g/mol | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = | Section3 = {{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }}Adafenoxate is a compound related to centrophenoxine, that has been found to act as a nootropic in rats.[1] References1. ^{{cite journal |vauthors =Petkov VD, Getova D, Mosharrof AH |title=A study of nootropic drugs for anti-anxiety action |journal=Acta Physiol Pharmacol Bulg |volume=13 |issue=4 |pages=25–30 |year=1987 |pmid=2896427 |doi= |url=}} {{Nootropics}}{{Acetylcholine receptor modulators}}{{nervous-system-drug-stub}}{{amine-stub}} 6 : Adamantanes|Amines|Chloroarenes|Cholinergics|Nootropics|Phenol ethers |
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