• RADICICOL CHEMBL414883

    Alternate Names:

    Monorden
    Radicicol
    C1462
    DB03758
    8-CHLORO-9,11-DIHYDROXY-14-METHYL-1A,14,15,15A-TETRAHYDRO-6H-OXIRENO[2,3-E][2]BENZOXACYCLOTETRADECINE-6,12(7H)-DIONE #
    8-CHLORO-1A,14,15,15A-TETRAHYDRO-9,11-DIHYDROXY-14-METHYL-6H-OXIRENO[E][2]BENZOXACYCLOTETRADECIN-6,12(7H)-DIONE
    NCGC00162457-01
    SMP2_000231
    6H-OXIRENO[E][2]BENZOXACYCLOTETRADECIN-6,12(7H)-DIONE, 8-CHLORO-1A,14,15,15A-TETRAHYDRO-9,11-DIHYDROXY-14-METHYL-
    WYZWZEOGROVVHK-JVLMNHKTSA-N
    CHEMBL1596863
    MONORDEN (B117339F008)
    RHI-12648
    MONORDENE
    MONORDERNE
    5353918
    ZINC13515668
    BDBM50347503
    WYZWZEOGROVVHK-HBUVGVEXSA-N
    SCHEMBL4514365
    11268547
    957231-40-2
    6H-OXIRENO[E][2]BENZOXACYCLOTETRADECIN-6,12(7H)-DIONE, 8-CHLORO-1A,14,15,15A-TETRAHYDRO-9,11-DIHYDROXY-14-METHYL-, (1AR,2Z,4E,14R,15AR)-
    5137-90-6
    11021-61-7
    (4R,6R,8R,9Z,11E)-16-CHLORO-17,19-DIHYDROXY-4-METHYL-3,7-DIOXATRICYCLO[13.4.0.0;{6,8}]NONADECA-1(19),9,11,15,17-PENTAENE-2,13-DIONE
    (1AR,2Z,4E,14R,15AR)-8-CHLORO-1A,14,15,15A-TETRAHYDRO-9,11-DIHYDROXY-14-METHYL-6H-OXIRENO[E][2]BENZOXACYCLOTETRADECIN-6,12(7H)-DIONE
    CCG-208260
    AKOS024456686
    ZINC13521629
    DPR000073
    DNC001195
    2024AH
    HMS3648C16
    MOLPORT-003-959-447
    BDBM15361
    SCHEMBL868832
    R2146_SIGMA
    [1AS-(1AR
    I60EH8GECX
    UNII-I60EH8GECX
    2Q8I
    4EGK
    3CGY
    2ZBK
    MONORDEN A
    MELANOTETAN II
    RADISICO
    RDC
    (1AR,2Z,4E,14R,15AR)-8-CHLORO-9,11-DIHYDROXY-14-METHYL-1A,14,15,15A-TETRAHYDRO-6H-OXIRENO[E][2]BENZOXACYCLOTETRADECINE-6,12(7H)-DIONE
    CHEBI:556075
    12772-57-5
    6323491
    1BGQ
    2WER
    MICROLACTONE, 1
    (2Z,4E)-8-CHLORO-9,11-DIHYDROXY-14-METHYL-1A,14,15,15A-TETRAHYDRO-6H-OXIRENO[E][2]BENZOXACYCLOTETRADECINE-6,12(7H)-DIONE
    NSC294404
    SCHEMBL110205
    AMBOTZLS-1055
    NSC-294404
    RADICICOL, DIHETEROSPORA CHLAMYDOSPORIA
    5359013
    (9E,11E)-16-CHLORO-17,19-DIHYDROXY-4-METHYL-3,7-DIOXATRICYCLO[13.4.0.0?,?]NONADECA-1(15),9,11,16,18-PENTAENE-2,13-DIONE
    BRD-A39996500-001-01-4
    LS-101110
    PL023964
    HE064766
    5-CHLORO-6-(7,8-EPOXY-10-HYDROXY-2-OXO-3,5-UNDECADIENYL)-BETA-RESORCYLIC ACID MU-LACTONE
    6H-OXIRENO(E)(2)BENZOXACYCLOTETRADECIN-6,12(7H)-DIONE, 8-CHLORO-1A,14,15,15A-TETRAHYDRO-9,11-DIHYDROXY-14-METHYL-
    SCHEMBL4354191
    AMBOTZ12772-57-5
    KF9-A
    C18H17CLO6
    5311380
    CTK6B6269
    AC1L1JGN
    RADICICOL FROM DIHETEROSPORA CHLAMYDOSPORIA
    8-CHLORO-9,11-DIHYDROXY-14-METHYL-1A,14,15,15A-TETRAHYDRO-6H-OXIRENO[E][2]BENZOXACYCLOTETRADECINE-6,12(7H)-DIONE
    5033
    KF58332
    NSC 294404
    16-CHLORO-17,19-DIHYDROXY-4-METHYL-3,7-DIOXA-TRICYCLO[13.4.0.0*6,8*]NONADECA-1(19),9,11,15,17-PENTAENE-2,13-DIONE
    (Z)-(R)-16-CHLORO-17,19-DIHYDROXY-4-(R)-METHYL-3,7-DIOXA-TRICYCLO[13.4.0.0*6,8*]NONADECA-1(19),9,11,15,17-PENTAENE-2,13-DIONE
    (9Z,11E)-(4S,6R,8S)-16-CHLORO-17,19-DIHYDROXY-4-METHYL-3,7-DIOXA-TRICYCLO[13.4.0.0*6,8*]NONADECA-1(19),9,11,15,17-PENTAENE-2,13-DIONE
    (9Z,11E)-(4R,6R,8R)-17,19-DIHYDROXY-4-METHYL-3,7-DIOXA-TRICYCLO[13.4.0.0*6,8*]NONADECA-1(15),9,11,16,18-PENTAENE-2,13-DIONE
    (9Z,11E)-(4R,6R,8R)-16-CHLORO-17,19-DIHYDROXY-4-METHYL-3,7-DIOXA-TRICYCLO[13.4.0.0*6,8*]NONADECA-1(19),9,11,15,17-PENTAENE-2,13-DIONE
    (9E,11E)-(4R,6S,8S)-16-CHLORO-17,19-DIHYDROXY-4-METHYL-3,7-DIOXA-TRICYCLO[13.4.0.0*6,8*]NONADECA-1(19),9,11,15,17-PENTAENE-2,13-DIONE
    (9E,11E)-(4R,6R,8R)-16-CHLORO-17,19-DIHYDROXY-4-METHYL-3,7-DIOXA-TRICYCLO[13.4.0.0*6,8*]NONADECA-1(15),9,11,16,18-PENTAENE-2,13-DIONE
    (RA)/17-(ALLYLAMINO)-17-DEMETHOXYGELDANAMYCIN
    ZINC100031525
    BDBM50073099
    CID_16196977
    CHEMBL453386
    44323216
    178101729
    NEUROTROPHIN-3
    NTF3
    (1S,4R,6R,8R,15R,16S)-16-CHLORO-4-METHYL-3,7-DIOXATRICYCLO[13.4.0.0^{6,8}]NONADECANE-2,13,17,19-TETRONE
    46936786

    Drug Info:

    Drug Categories therapeutic uses
    Drug Categories protein-tyrosine kinases, antagonists & inhibitors
    Drug Categories polyketides
    Drug Categories polycyclic compounds
    Drug Categories pharmacologic actions
    Drug Categories organic chemicals
    Drug Categories molecular mechanisms of pharmacological action
    Drug Categories macrocyclic compounds
    Drug Categories lactones
    Drug Categories enzyme inhibitors
    Drug Categories chemical actions and uses
    Drug Categories antiprotozoals
    Drug Categories antiparasitic agents
    Drug Categories antimalarials
    Drug Categories antifungal agents
    Drug Categories anti-infective agents
    Drug Groups experimental
    Drug Type small molecule
    Name of the Ligand Species (if a Peptide) Human
    (2 More Sources)