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LY-341495

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Ornstein PL, Bleisch TJ, Arnold MB, Kennedy JH, Wright RA, Johnson BG, Tizzano JP, Helton DR, Kallman MJ, Schoepp DD, Hérin M (January 1998). "2-substituted (2SR)-2-amino-2-((1SR,2SR)-2-carboxycycloprop-1-yl)glycines as potent and selective antagonists of group II metabotropic glutamate receptors. 2.
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Fischer BD, Miller LL, Henry FE, Picker MJ, Dykstra LA (June 2008). "Increased efficacy of micro-opioid agonist-induced antinociception by metabotropic glutamate receptor antagonists in C57BL/6 mice: comparison with (-)-6-phosphonomethyl-deca-hydroisoquinoline-3-carboxylic acid (LY235959)".
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Matrisciano F, Panaccione I, Zusso M, Giusti P, Tatarelli R, Iacovelli L, Mathé AA, Gruber SH, Nicoletti F, Girardi P (August 2007). "Group-II metabotropic glutamate receptor ligands as adjunctive drugs in the treatment of depression: a new strategy to shorten the latency of antidepressant
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Fitzjohn SM, Bortolotto ZA, Palmer MJ, Doherty AJ, Ornstein PL, Schoepp DD, Kingston AE, Lodge D, Collingridge GL (December 1998). "The potent mGlu receptor antagonist LY341495 identifies roles for both cloned and novel mGlu receptors in hippocampal synaptic plasticity".
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Johnson BG, Wright RA, Arnold MB, Wheeler WJ, Ornstein PL, Schoepp DD (October 1999). "-LY341495 as a novel antagonist radioligand for group II metabotropic glutamate (mGlu) receptors: characterization of binding to membranes of mGlu receptor subtype expressing cells".
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Sakagami K, Yasuhara A, Chaki S, Yoshikawa R, Kawakita Y, Saito A, Taguchi T, Nakazato A (April 2008). "Synthesis, in vitro pharmacology, and pharmacokinetic profiles of 2--1-fluorocyclopropanecarboxylic acid and its 6-heptyl ester, a potent mGluR2 antagonist".
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Benneyworth MA, Xiang Z, Smith RL, Garcia EE, Conn PJ, Sanders-Bush E (August 2007). "A selective positive allosteric modulator of metabotropic glutamate receptor subtype 2 blocks a hallucinogenic drug model of psychosis".
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Kingston AE, Ornstein PL, Wright RA, Johnson BG, Mayne NG, Burnett JP, Belagaje R, Wu S, Schoepp DD (1998). "LY341495 is a nanomolar potent and selective antagonist of group II metabotropic glutamate receptors".
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Fischer BD, Zimmerman EI, Picker MJ, Dykstra LA (February 2008). "Morphine in combination with metabotropic glutamate receptor antagonists on schedule-controlled responding and thermal nociception".
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Chi H, Jang JK, Kim JH, Vezina P (October 2006). "Blockade of group II metabotropic glutamate receptors in the nucleus accumbens produces hyperlocomotion in rats previously exposed to amphetamine".
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Yoon HS, Jang JK, Kim JH (September 2008). "Blockade of group II metabotropic glutamate receptors produces hyper-locomotion in cocaine pre-exposed rats by interactions with dopamine receptors".
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O'Neill MF, Heron-Maxwell C, Conway MW, Monn JA, Ornstein P (October 2003). "Group II metabotropic glutamate receptor antagonists LY341495 and LY366457 increase locomotor activity in mice".
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Koike H, Chaki S (September 2014). "Requirement of AMPA receptor stimulation for the sustained antidepressant activity of ketamine and LY341495 during the forced swim test in rats".
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InChI=1S/C20H19NO5/c21-20(19(24)25,15-9-13(15)18(22)23)10-14-11-5-1-3-7-16(11)26-17-8-4-2-6-12(14)17/h1-8,13-15H,9-10,21H2,(H,22,23)(H,24,25)/t13-,15-,20-/m0/s1
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Moreno JL, González-Maeso J (2018). "Crosstalk Between 5-HT2A and mGlu2 Receptors: Implications in Schizophrenia and Its Treatment".
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effects in animal models, increasing the behavioural effects of hallucinogenic drugs in animal tests, and increasing the
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Pilc A, Chaki S, Nowak G, Witkin JM (March 2008). "Mood disorders: regulation by metabotropic glutamate receptors".
1364: 753:"Behavioral evidence for interactions between a hallucinogenic drug and group II metabotropic glutamate receptors" 332:, which acts as a potent and selective orthosteric antagonist for the group II metabotropic glutamate receptors ( 1738: 1590: 704:"Fast-acting antidepressants rapidly stimulate ERK signaling and BDNF release in primary neuronal cultures" 1374: 1240: 329: 175: 99: 1743: 1595: 2234: 2162: 2152: 2066: 2051: 1979: 1969: 1907: 1897: 1870: 1535: 1290: 1199: 1116: 1073: 1030: 987: 944: 818: 684: 641: 562: 518: 474: 351: 1865: 1580: 1310: 1305: 1270: 2172: 2076: 1989: 1917: 1733: 1585: 1436: 1320: 1152: 1108: 1065: 1022: 979: 936: 898: 867: 810: 774: 733: 676: 633: 597: 554: 510: 466: 430: 358: 1394: 1165: 128: 1144: 1100: 1057: 1014: 971: 928: 890: 857: 849: 802: 764: 723: 715: 668: 625: 589: 546: 502: 458: 422: 196: 108: 1275: 148: 2167: 2147: 2071: 2046: 1984: 1964: 1912: 1892: 1783: 1642: 1431: 1389: 1315: 1255: 413:
Effects of aromatic substitution, pharmacological characterization, and bioavailability".
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Carbonaro TM, Eshleman AJ, Forster MJ, Cheng K, Rice KC, Gatch MB (January 2015).
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from this with the heptyl ester increases bioavailability still further.
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It is used in scientific research in several different areas, showing
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Lepack AE, Bang E, Lee B, Dwyer JM, Duman RS (December 2016).
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is a research drug developed by the pharmaceutical company
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The Journal of Pharmacology and Experimental Therapeutics
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Vol. 32. pp. 147–189. 272:C1(1(CC2C3=CC=CC=C3OC4=CC=CC=C24)(C(=O)O)N)C(=O)O 364:The 1-fluorocyclopropane analog has a superior 107: 887:5-HT2A Receptors in the Central Nervous System 1181: 8: 30: 1819: 1512: 1212: 1188: 1174: 1166: 178: 127: 2200:Glutamate metabolism/transport modulators 2107:Tooltip Metabotropic glutamate receptor 8 2008:Tooltip Metabotropic glutamate receptor 7 1936:Tooltip Metabotropic glutamate receptor 6 1832:Tooltip Metabotropic glutamate receptor 4 1683:Tooltip Metabotropic glutamate receptor 3 1525:Tooltip Metabotropic glutamate receptor 2 1339:Tooltip Metabotropic glutamate receptor 5 1225:Tooltip Metabotropic glutamate receptor 1 861: 768: 727: 147: 60:)-2-Amino-2--3-(xanth-9-yl)propanoic acid 2220:Drugs developed by Eli Lilly and Company 2196:Ionotropic glutamate receptor modulators 404: 289: 269: 174: 79: 751:Gewirtz JC, Marek GJ (November 2000). 29: 7: 1137:Bioorganic & Medicinal Chemistry 1739:Pomaglumetad methionil (LY-2140023) 1591:Pomaglumetad methionil (LY-2140023) 25: 1105:10.1016/j.neuropharm.2008.07.012 1062:10.1016/j.neuropharm.2006.06.008 720:10.1016/j.neuropharm.2016.09.011 383:1-fluoro-LY-341,495 heptyl ester 213: 207: 38: 2135:Positive allosteric modulators: 2086:Negative allosteric modulators: 1875:Positive allosteric modulators: 1793:Negative allosteric modulators: 1657:Negative allosteric modulators: 1600:Positive allosteric modulators: 1456:Negative allosteric modulators: 1399:Positive allosteric modulators: 1197:Metabotropic glutamate receptor 297:Key:VLZBRVJVCCNPRJ-KPHUOKFYSA-N 415:Journal of Medicinal Chemistry 216: 201: 1: 2192:Receptor/signaling modulators 1019:10.1016/S0028-3908(03)00232-6 770:10.1016/S0893-133X(00)00136-6 551:10.1016/s0028-3908(99)00053-2 507:10.1016/s0028-3908(98)00145-2 463:10.1016/s0028-3908(97)00191-3 895:10.1007/978-3-319-70474-6_7 2251: 2230:MGlu3 receptor antagonists 2225:MGlu2 receptor antagonists 661:Behavioural Brain Research 191:Chemical and physical data 2185: 1724:LY-404,039 (pomaglumetad) 1571:LY-404,039 (pomaglumetad) 1149:10.1016/j.bmc.2008.02.066 933:10.1007/s00213-008-1130-y 854:10.1007/s00213-014-3658-3 673:10.1016/j.bbr.2014.05.065 594:10.1016/j.bcp.2007.09.021 368:profile and similar mGluR 305: 280: 260: 70: 37: 1603:JNJ-40411813 (ADX-71149) 582:Biochemical Pharmacology 357:, as well as modulating 976:10.1124/jpet.107.131417 757:Neuropsychopharmacology 372:affinity, and making a 807:10.1124/mol.107.035170 795:Molecular Pharmacology 384: 630:10.1038/sj.mp.4002005 382: 618:Molecular Psychiatry 34: 921:Psychopharmacology 842:Psychopharmacology 385: 2207: 2206: 2181: 2180: 2130: 2031: 1954: 1850: 1809: 1808: 1502: 1501: 1093:Neuropharmacology 1050:Neuropharmacology 1007:Neuropharmacology 904:978-3-319-70472-2 708:Neuropharmacology 539:Neuropharmacology 495:Neuropharmacology 451:Neuropharmacology 427:10.1021/jm970498o 359:dopamine receptor 323: 322: 251:Interactive image 160:CompTox Dashboard 89: 61: 27:Chemical compound 16:(Redirected from 2242: 2128: 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1428: 1425: 1423: 1420: 1418: 1415: 1413: 1410: 1407: 1406: 1403: 1400: 1396: 1393: 1391: 1388: 1386: 1385:Ibotenic acid 1383: 1381: 1378: 1376: 1373: 1371: 1368: 1366: 1363: 1361: 1358: 1356: 1353: 1351: 1348: 1345: 1344: 1342: 1337: 1328: 1322: 1319: 1317: 1314: 1312: 1309: 1307: 1304: 1302: 1301:Cyclothiazide 1299: 1297: 1294: 1292: 1289: 1286: 1285: 1282: 1279: 1277: 1274: 1272: 1269: 1267: 1264: 1262: 1259: 1257: 1254: 1252: 1251:Ibotenic acid 1249: 1247: 1244: 1242: 1239: 1237: 1234: 1231: 1230: 1228: 1223: 1214: 1211: 1209: 1205: 1201: 1198: 1191: 1186: 1184: 1179: 1177: 1172: 1171: 1168: 1158: 1154: 1150: 1146: 1142: 1138: 1130: 1127: 1122: 1118: 1114: 1110: 1106: 1102: 1098: 1094: 1087: 1084: 1079: 1075: 1071: 1067: 1063: 1059: 1056:(5): 986–92. 1055: 1051: 1044: 1041: 1036: 1032: 1028: 1024: 1020: 1016: 1013:(5): 565–74. 1012: 1008: 1001: 998: 993: 989: 985: 981: 977: 973: 969: 965: 958: 955: 950: 946: 942: 938: 934: 930: 926: 922: 914: 911: 906: 900: 896: 892: 888: 881: 878: 873: 869: 864: 859: 855: 851: 848:(1): 275–84. 847: 843: 839: 832: 829: 824: 820: 816: 812: 808: 804: 801:(2): 477–84. 800: 796: 788: 785: 780: 776: 771: 766: 763:(5): 569–76. 762: 758: 754: 747: 744: 739: 735: 730: 725: 721: 717: 713: 709: 705: 698: 695: 690: 686: 682: 678: 674: 670: 666: 662: 655: 652: 647: 643: 639: 635: 631: 627: 623: 619: 611: 608: 603: 599: 595: 591: 587: 583: 576: 573: 568: 564: 560: 556: 552: 548: 544: 540: 532: 529: 524: 520: 516: 512: 508: 504: 500: 496: 488: 485: 480: 476: 472: 468: 464: 460: 456: 452: 444: 441: 436: 432: 428: 424: 421:(3): 358–78. 420: 416: 408: 405: 399: 395: 392: 391: 387: 381: 377: 375: 367: 362: 360: 356: 353: 349: 345: 340: 338: 331: 327: 317: 310: 304: 295: 290: 286: 279: 270: 266: 259: 252: 248: 247: 245: 242: 237: 230: 228: 224: 200: 198: 194: 189: 181: 177: 173: 172: 170: 161: 157: 150: 146: 145: 143: 141: 137: 130: 126: 125: 123: 121: 117: 110: 106: 105: 103: 101: 97: 85: 80: 76: 69: 64: 59: 54: 50: 47:Clinical data 45: 41: 36: 19: 2188: 2187: 2145:Antagonists: 2144: 2134: 2114: 2085: 2044:Antagonists: 2043: 2015: 1962:Antagonists: 1961: 1943: 1890:Antagonists: 1889: 1874: 1839: 1792: 1751:Antagonists: 1750: 1744:Talaglumetad 1690: 1656: 1610:Antagonists: 1609: 1599: 1596:Talaglumetad 1532: 1469:Dipraglurant 1464:Basimglurant 1455: 1409:Antagonists: 1408: 1398: 1346: 1288:Antagonists: 1287: 1232: 1140: 1136: 1129: 1099:(4): 555–9. 1096: 1092: 1086: 1053: 1049: 1043: 1010: 1006: 1000: 970:(2): 732–9. 967: 963: 957: 927:(2): 271–8. 924: 920: 913: 886: 880: 845: 841: 831: 798: 794: 787: 760: 756: 746: 711: 707: 697: 664: 660: 654: 624:(8): 704–6. 621: 617: 610: 585: 581: 575: 542: 538: 531: 498: 494: 487: 454: 450: 443: 418: 414: 407: 363: 341: 325: 324: 313:   307:   83: 57: 1871:VU-0155,041 1796:Decoglurant 1660:Decoglurant 1494:Raseglurant 1442:Remeglurant 1427:Mavoglurant 1291:BAY 36-7620 714:: 242–252. 457:(1): 1–12. 350:effects of 234: g·mol 109:201943-63-7 66:Identifiers 52:Other names 2214:Categories 2138:AZ12216052 1878:Foliglurax 1866:VU-001,171 1779:LY-341,495 1774:LY-307,452 1729:LY-487,379 1719:LY-379,268 1638:LY-341,495 1633:LY-307,452 1581:LY-566,332 1576:LY-487,379 1566:LY-379,268 1422:LY-344,545 1402:LSN2463359 1311:LY-456,236 1306:LY-367,385 1200:modulators 400:References 361:function. 239:3D model ( 227:Molar mass 149:AQ73SP6QSF 120:ChemSpider 100:CAS Number 75:IUPAC name 18:LY-341,495 2235:Xanthenes 2189:See also: 2123:Glutamate 2115:Agonists: 2037:LSP2-9166 2024:Glutamate 2016:Agonists: 1947:Glutamate 1944:Agonists: 1856:LSP2-9166 1843:Glutamate 1840:Agonists: 1815:Group III 1801:RO4491533 1709:Glutamate 1704:Eglumegad 1691:Agonists: 1665:RO4491533 1556:Glutamate 1551:Eglumegad 1533:Agonists: 1380:Glutamate 1355:ADX-47273 1347:Agonists: 1271:Ro67-7476 1266:Ro67-4853 1261:Ro01-6128 1246:Glutamate 1233:Agonists: 667:: 111–5. 348:analgesic 330:Eli Lilly 326:LY-341495 32:LY-341495 2173:UBP-1112 2089:ADX71743 2077:UBP-1112 1990:UBP-1112 1918:UBP-1112 1789:MGS-0039 1734:MGS-0028 1648:MGS-0039 1586:MGS-0028 1508:Group II 1452:SIB-1893 1447:SIB-1757 1437:NPS-2390 1321:NPS-2390 1281:Theanine 1157:18348906 1121:12164609 1113:18675831 1078:22562384 1070:16901517 1035:22992987 1027:12941370 992:12497552 984:17982001 949:24658889 941:18392754 872:24985890 815:17526600 779:11027922 738:27634096 689:19982406 681:24909673 638:17653204 602:18164691 567:36767061 559:10530814 523:26102806 479:27186381 388:See also 355:agonists 352:μ-opioid 316:(verify) 90:-alanine 1479:GRN-529 1474:Fenobam 1459:AZD9272 1395:VU-1545 1296:CPCCOEt 1208:Group I 863:4282596 823:3097502 729:5075989 646:7906551 515:9886667 471:9680254 435:9464367 374:prodrug 232:353.374 197:Formula 129:7995676 82:2--3-(9 2082:XAP044 2019:AMN082 1699:DCG-IV 1694:CBiPES 1653:PCCG-4 1546:DCG-IV 1541:CBiPES 1155:  1119:  1111:  1076:  1068:  1033:  1025:  990:  982:  947:  939:  901:  870:  860:  821:  813:  777:  736:  726:  687:  679:  644:  636:  600:  565:  557:  521:  513:  477:  469:  433:  265:SMILES 2100:mGluR 2057:MMPIP 2001:mGluR 1929:mGluR 1861:PHCCC 1825:mGluR 1769:HYDIA 1759:CECXG 1754:APICA 1676:mGluR 1628:HYDIA 1618:CECXG 1613:APICA 1518:mGluR 1417:DMeOB 1360:CDPPB 1332:mGluR 1276:VU-71 1218:mGluR 1117:S2CID 1074:S2CID 1031:S2CID 988:S2CID 945:S2CID 819:S2CID 685:S2CID 642:S2CID 563:S2CID 519:S2CID 475:S2CID 394:CECXG 334:mGluR 285:InChI 241:JSmol 2168:MTPG 2163:MSOP 2158:MPPG 2153:MAP4 2148:CPPG 2131:-AP4 2118:DCPG 2072:MTPG 2067:MSOP 2062:MPPG 2052:MAP4 2047:CPPG 2032:-AP4 1985:MTPG 1980:MSOP 1975:MPPG 1970:MAP4 1965:CPPG 1955:-AP4 1913:MTPG 1908:MSOP 1903:MPPG 1898:MAP4 1893:CPPG 1883:MPEP 1851:-AP4 1784:MCPG 1764:EGLU 1643:MCPG 1623:EGLU 1536:BINA 1489:MTEP 1484:MPEP 1432:MCPG 1412:CTEP 1375:DHPG 1365:CHPG 1350:ACPD 1316:MCPG 1241:DHPG 1236:ACPD 1153:PMID 1109:PMID 1066:PMID 1023:PMID 980:PMID 937:PMID 899:ISBN 868:PMID 811:PMID 775:PMID 734:PMID 677:PMID 634:PMID 598:PMID 555:PMID 511:PMID 467:PMID 431:PMID 140:UNII 1370:DFB 1145:doi 1101:doi 1058:doi 1015:doi 972:doi 968:324 929:doi 925:198 891:doi 858:PMC 850:doi 846:232 803:doi 765:doi 724:PMC 716:doi 712:111 669:doi 665:271 626:doi 590:doi 547:doi 503:doi 459:doi 423:doi 370:2/3 339:). 336:2/3 165:EPA 2216:: 2198:• 2194:• 2133:; 2084:; 1873:; 1791:; 1655:; 1598:; 1454:; 1397:; 1151:. 1141:16 1139:. 1115:. 1107:. 1097:55 1095:. 1072:. 1064:. 1054:51 1052:. 1029:. 1021:. 1011:45 1009:. 986:. 978:. 966:. 943:. 935:. 923:. 897:. 866:. 856:. 844:. 840:. 817:. 809:. 799:72 797:. 773:. 761:23 759:. 755:. 732:. 722:. 710:. 706:. 683:. 675:. 663:. 640:. 632:. 622:12 620:. 596:. 586:75 584:. 561:. 553:. 543:38 541:. 517:. 509:. 499:37 497:. 473:. 465:. 455:37 453:. 429:. 419:41 417:. 211:19 205:20 56:(2 2129:L 2102:8 2030:L 2003:7 1953:L 1931:6 1849:L 1827:4 1678:3 1520:2 1334:5 1220:1 1189:e 1182:t 1175:v 1159:. 1147:: 1123:. 1103:: 1080:. 1060:: 1037:. 1017:: 994:. 974:: 951:. 931:: 907:. 893:: 874:. 852:: 825:. 805:: 781:. 767:: 740:. 718:: 691:. 671:: 648:. 628:: 604:. 592:: 569:. 549:: 525:. 505:: 481:. 461:: 437:. 425:: 243:) 220:5 217:O 214:N 208:H 202:C 167:) 163:( 88:D 84:H 58:S 20:)

Index

LY-341,495

IUPAC name
CAS Number
201943-63-7
ChemSpider
7995676
UNII
AQ73SP6QSF
CompTox Dashboard
DTXSID50942264
Edit this at Wikidata
Formula
Molar mass
JSmol
Interactive image
SMILES
InChI
(what is this?)
(verify)
Eli Lilly
mGluR2/3
antidepressant
analgesic
μ-opioid
agonists
dopamine receptor
pharmacokinetic
prodrug

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