CALENDULADIOL

ID: ALA462795

Max Phase: Preclinical

Molecular Formula: C30H50O2

Molecular Weight: 442.73

Molecule Type: Small molecule

Associated Items:

Representations

Synonyms (1): Calenduladiol
Synonyms from Alternative Forms(1):

    Canonical SMILES:  C=C(C)[C@@H]1CC[C@@]2(C)[C@H]1[C@H]1CC[C@H]3[C@@]4(C)CC[C@H](O)C(C)(C)[C@@H]4CC[C@@]3(C)[C@]1(C)C[C@@H]2O

    Standard InChI:  InChI=1S/C30H50O2/c1-18(2)19-11-14-28(6)24(32)17-30(8)20(25(19)28)9-10-22-27(5)15-13-23(31)26(3,4)21(27)12-16-29(22,30)7/h19-25,31-32H,1,9-17H2,2-8H3/t19-,20+,21-,22+,23-,24-,25+,27-,28+,29+,30+/m0/s1

    Standard InChI Key:  AJBZENLMTKDAEK-SKESNUHASA-N

    Associated Targets(Human)

    U-251 51189 Activities

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    K562 73714 Activities

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    MDA-N 28205 Activities

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    SN12C 47755 Activities

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    ACHN 49357 Activities

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    NCI-H23 49055 Activities

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    HOP-92 41141 Activities

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    HL-60 67320 Activities

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    SK-MEL-5 47095 Activities

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    SF-539 44845 Activities

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    DU-145 51482 Activities

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    Malme-3M 44254 Activities

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    A498 42825 Activities

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    OVCAR-3 48710 Activities

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    MOLT-4 49676 Activities

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    HOP-62 47048 Activities

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    NCI/ADR-RES 33767 Activities

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    OVCAR-8 47708 Activities

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    OVCAR-5 45555 Activities

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    SNB-19 46794 Activities

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    MDA-MB-231 73002 Activities

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    SR 39847 Activities

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    TK-10 45540 Activities

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    SW-620 52400 Activities

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    KM12 47707 Activities

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    NCI-H522 44358 Activities

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    M14 47487 Activities

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    NCI-H322M 45589 Activities

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    LOX IMVI 44321 Activities

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    BT-549 31254 Activities

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    A549 127892 Activities

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    SNB-75 44215 Activities

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    HCT-116 91556 Activities

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    HCT-15 51914 Activities

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    EKVX 44102 Activities

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    SF-268 49410 Activities

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    PC-3 62116 Activities

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    MCF7 126967 Activities

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    NCI-H460 60772 Activities

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    T47D 39041 Activities

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    CAKI-1 44928 Activities

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    MDA-MB-435 38290 Activities

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    SF-295 48000 Activities

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    IGROV-1 47897 Activities

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    786-0 47912 Activities

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    UACC-257 46019 Activities

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    CCRF-CEM 65223 Activities

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    HT-29 80576 Activities

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    NCI-H226 44470 Activities

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    SK-MEL-28 48833 Activities

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    RXF 393 41971 Activities

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    Associated Targets(non-human)

    Acetylcholinesterase 657 Activities

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    Cholinesterase 8742 Activities

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    Molecule Features

    Natural Product: YesOral: NoChemical Probe: NoParenteral: No
    Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
    Chirality: NoAvailability: NoProdrug: No

    Drug Indications

    MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

    Mechanisms of Action

    Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

    Properties

    Molecular Weight: 442.73Molecular Weight (Monoisotopic): 442.3811AlogP: 7.00#Rotatable Bonds: 1
    Polar Surface Area: 40.46Molecular Species: NEUTRALHBA: 2HBD: 2
    #RO5 Violations: 1HBA (Lipinski): 2HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
    CX Acidic pKa: CX Basic pKa: CX LogP: 6.22CX LogD: 6.22
    Aromatic Rings: 0Heavy Atoms: 32QED Weighted: 0.43Np Likeness Score: 2.87

    References

    1. García A, Delgado G..  (2006)  Cytotoxic cis-fused bicyclic sesquiterpenoids from Jatropha neopauciflora.,  69  (11): [PMID:17125233] [10.1021/np060194h]
    2. PubChem BioAssay data set, 
    3. Castro MJ, Richmond V, Romero C, Maier MS, Estévez-Braun A, Ravelo AG, Faraoni MB, Murray AP..  (2014)  Preparation, anticholinesterase activity and molecular docking of new lupane derivatives.,  22  (13): [PMID:24835788] [10.1016/j.bmc.2014.04.050]