HYACINTHACINE A4

ID: ALA496698

Max Phase: Preclinical

Molecular Formula: C9H17NO3

Molecular Weight: 187.24

Molecule Type: Small molecule

Associated Items:

Representations

Synonyms (1): Hyacinthacine A4
Synonyms from Alternative Forms(1):

    Canonical SMILES:  C[C@H]1CC[C@@H]2[C@H](O)[C@H](O)[C@H](CO)N21

    Standard InChI:  InChI=1S/C9H17NO3/c1-5-2-3-6-8(12)9(13)7(4-11)10(5)6/h5-9,11-13H,2-4H2,1H3/t5-,6+,7-,8-,9+/m0/s1

    Standard InChI Key:  AGLLYYHKZWZSKX-QKAWAISNSA-N

    Associated Targets(non-human)

    Oligo-1,6-glucosidase 218 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Acidic alpha-glucosidase 551 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Beta-glucosidase A 127 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Beta-mannosidase 52 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Beta-galactosidase 500 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Alpha-L-fucosidase 1 358 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    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: 187.24Molecular Weight (Monoisotopic): 187.1208AlogP: -1.06#Rotatable Bonds: 1
    Polar Surface Area: 63.93Molecular Species: BASEHBA: 4HBD: 3
    #RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
    CX Acidic pKa: 13.21CX Basic pKa: 9.61CX LogP: -0.99CX LogD: -3.18
    Aromatic Rings: 0Heavy Atoms: 13QED Weighted: 0.49Np Likeness Score: 1.91

    References

    1. Yamashita T, Yasuda K, Kizu H, Kameda Y, Watson AA, Nash RJ, Fleet GW, Asano N..  (2002)  New polyhydroxylated pyrrolidine, piperidine, and pyrrolizidine alkaloids from Scilla sibirica.,  65  (12): [PMID:12502331] [10.1021/np020296h]

    Source