Free cookie consent management tool by TermsFeed GPCRmd
× Due to a recent server update, this page will be slow for the next 1-2 hours. We apologize for any inconvenience this may cause.

Standard Form Name: Arolac

Other Names:

  • 1,1-diethyl-3-[(8alpha)-6-methyl-9,10-didehydroergolin-8-yl]urea

  • 18016-80-3

  • 19875-60-6 (maleate (1:1))

  • 3,3-diethyl-1-[(4S,7R)-6-methyl-6,11-diazatetracyclo[7.6.1.0;{2,7}.0;{12,16}]hexadeca-1(16),2,9,12,14-pentaen-4-yl]urea

  • 3-(9,10-Didehydro-6-methylergolin-8alpha-yl)-1,1-diethylurea

  • AC1L1G87

  • Arolac

  • BPBio1_000102

  • BSPBio_000092

  • C20H26N4O

  • CHEBI:51164

  • CHEMBL157138

  • D08132

  • DB00589

  • Dopergin

  • Dopergine

  • E0QN3D755O

  • EINECS 241-925-1

  • HMS1568E14

  • Lisurid

  • Lisurida

  • Lisurida [INN-Spanish]

  • LISURIDE

  • Lisuride hydrogen maleate

  • Lisuride (INN)

  • Lisuride [INN]

  • Lisuride [INN:BAN]

  • lisuride maleate

  • Lisuride Maleate (1:1)

  • Lisuride (S)(-)

  • Lisuridum

  • Lisuridum [INN-Latin]

  • Lopac0_000751

  • LS-159312

  • Lysurid

  • Lysuride

  • Lysuride Hydrogen Maleate

  • mesorgydine

  • Methylergol Carbamide

  • N'-((8alpha)-9,10-Didehydro-6-methylergolin-8-yl)-N,N-diethylurea

  • Prestwick0_000106

  • Prestwick1_000106

  • Prestwick2_000106

  • Prestwick3_000106

  • Prestwick_525

  • Revanil

  • S-(-)-Lisuride

  • SPBio_002031

  • UNII-E0QN3D755O

  • Urea, N'-((8alpha)-9,10-didehydro-6-methylergolin-8-yl)-N,N-diethyl-


  • IUPAC name:
    3-[(6aR,9S)-7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-yl]-1,1-diethylurea



    PUBCHEM:
    28864




    InChIKey:
    BKRGVLQUQGGVSM-KBXCAEBGSA-N



    InChI:

    1S/C20H26N4O/c1-4-24(5-2)20(25)22-14-10-16-15-7-6-8-17-19(15)13(11-21-17)9-18(16)23(3)12-14/h6-8,10-11,14,18,21H,4-5,9,12H2,1-3H3,(H,22,25)/t14-,18+/m0/s1



    Image of the Standard Form:





    References in which this Standard Form is mentioned:


    National Center for Biotechnology Information. PubChem Compound Database. Data for this compound was obtained from the PubChem database. Available in: https://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=28864.

    Kossatz, Elk and Diez-Alarcia, Rebeca and Gaitonde, Supriya A. and Ramon-Duaso, Carla and Stepniewski, Tomasz Maciej and Aranda-Garcia, David and Muneta-Arrate, Itziar and Tepaz, Elodie and Saen-Oon, Suwipa and Soliva, Robert and Shahraki, Aida and Moreira, David and Brea, Jose and Loza, Maria Isabel and de la Torre, Rafael and Kolb, Peter and Bouvier, Michel and Meana, J. Javier and Robledo, Patricia and Selent, Jana. G protein-specific mechanisms in the serotonin 5-HT2A receptor regulate psychosis-related effects and memory deficits. DOI: 10.1038/s41467-024-48196-2. Available in: http://dx.doi.org/10.1038/s41467-024-48196-2.

    SUPPORTED BY

    ERNEST (COST Action CA18133)

    GLISTEN (COST Action CM1207)

    GPCRForum