| 词条 | R-30490 |
| 释义 |
| Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 439017639 | IUPAC_name = N-[4-(methoxymethyl)-1-(2-phenylethyl)piperidin-4-yl]-N-phenylpropanamide | image = R-30490.svg | tradename = | pregnancy_category = | legal_CA = Schedule I | legal_UK = Class A | routes_of_administration = | bioavailability = | protein_bound = | metabolism = | elimination_half-life = | excretion = | CAS_number_Ref = {{cascite|correct|cas}} | CAS_number = 60618-49-7 | ATC_prefix = | ATC_suffix = | ChEMBL_Ref = {{ebicite|changed|EBI}} | ChEMBL = 609147 | PubChem = 124716 | ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} | ChemSpiderID = 111042 | UNII_Ref = {{fdacite|changed|FDA}} | UNII = 03DNV05OD4 | DrugBank_Ref = {{drugbankcite|changed|drugbank}} | DrugBank = DB09179 | C=24 | H=32 | N=2 | O=2 | molecular_weight = 380.522 g/mol | smiles = CCC(=O)N(c1ccccc1)C2(COC)CCN(CC2)CCc3ccccc3 | StdInChI_Ref = {{stdinchicite|changed|chemspider}} | StdInChI = 1S/C24H32N2O2/c1-3-23(27)26(22-12-8-5-9-13-22)24(20-28-2)15-18-25(19-16-24)17-14-21-10-6-4-7-11-21/h4-13H,3,14-20H2,1-2H3 | StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} | StdInChIKey = GARXJOUQUSNOGK-UHFFFAOYSA-N }}R-30490 (also known as 4-Methoxymethylfentanyl) is an opioid analgesic related to the highly potent animal tranquilizer carfentanil, and with only slightly lower potency. It was first synthesised by a team of chemists at Janssen Pharmaceutica led by Paul Janssen, who were investigating the structure-activity relationships of the fentanyl family of drugs. R-30490 was found to be the most selective agonist for the μ-opioid receptor out of all the fentanyl analogues tested, but it has never been introduced for medical use in humans, although the closely related drug sufentanil is widely used for analgesia and anesthesia during major surgery.[1][2][3][4] Side effects of fentanyl analogs are similar to those of fentanyl itself, which include itching, nausea and potentially serious respiratory depression, which can be life-threatening. Fentanyl analogs have killed hundreds of people throughout Europe and the former Soviet republics since the most recent resurgence in use began in Estonia in the early 2000s, and novel derivatives continue to appear.[5] References1. ^{{cite journal |author1=Cometta-Morini, C. |author2=Maguire, P. A. |author3=Loew, G. H. | title = Molecular determinants of mu receptor recognition for the fentanyl class of compounds. | journal = Molecular Pharmacology | year = 1992 | volume = 41 | issue = 1 | pages = 185–196 | pmid = 1310142 }} {{Opioid receptor modulators}}2. ^{{Cite journal | last1 = Maguire | first1 = P. | last2 = Tsai | first2 = N. | last3 = Kamal | first3 = J. | last4 = Cometta-Morini | first4 = C. | last5 = Upton | first5 = C. | last6 = Loew | first6 = G. | doi = 10.1016/0014-2999(92)90685-W | title = Pharmacological profiles of fentanyl analogs at μ, δ and κ opiate receptors | journal = European Journal of Pharmacology | volume = 213 | issue = 2 | pages = 219–225 | year = 1992 | pmid = 1355735| pmc = }} 3. ^{{Cite journal | last1 = Meert | first1 = T. F. | doi = 10.1007/BF00449683 | title = Pharmacotherapy of opioids: Present and future developments | journal = Pharmacy World & Science | volume = 18 | issue = 1| pages = 1–15 | year = 1996 | pmid = 8861825 | pmc = }} 4. ^{{Cite journal | last1 = Subramanian | first1 = G. | last2 = Paterlini | first2 = M. G. | last3 = Portoghese | first3 = P. S. | last4 = Ferguson | first4 = D. M. | title = Molecular Docking Reveals a Novel Binding Site Model for Fentanyl at the μ-Opioid Receptor | doi = 10.1021/jm9903702 | journal = Journal of Medicinal Chemistry | volume = 43 | issue = 3 | pages = 381–391 | year = 2000 | pmid = 10669565| pmc = }} 5. ^{{cite journal | url=http://www.ijdp.org/article/S0955-3959%2815%2900097-3/abstract | title=Fentanyls: Are we missing the signs? Highly potent and on the rise in Europe. | author=Jane Mounteney | author2=Isabelle Giraudon | author3=Gleb Denissov | author4=Paul Griffiths | journal=International Journal of Drug Policy | date=July 2015 | volume=26 | issue=7 | pages=626–631 | doi=10.1016/j.drugpo.2015.04.003 | pmid=25976511}} 6 : Synthetic opioids|Piperidines|Propionamides|Anilides|Mu-opioid agonists|Fentanyl |
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