ID: ALA407337

Max Phase: Preclinical

Molecular Formula: C7H15NO4

Molecular Weight: 177.20

Molecule Type: Small molecule

Associated Items:

Representations

Synonyms (1): 6-deoxyhomoDMDP
Synonyms from Alternative Forms(1):

    Canonical SMILES:  OCC[C@H]1N[C@H](CO)[C@@H](O)[C@@H]1O

    Standard InChI:  InChI=1S/C7H15NO4/c9-2-1-4-6(11)7(12)5(3-10)8-4/h4-12H,1-3H2/t4-,5-,6-,7-/m1/s1

    Standard InChI Key:  AGFACLQFIYFFOI-DBRKOABJSA-N

    Associated Targets(Human)

    Glycogen debranching enzyme 27 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Associated Targets(non-human)

    Oligo-1,6-glucosidase 218 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

    Acidic alpha-glucosidase 551 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Alpha-L-fucosidase 1 358 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Sucrase-isomaltase 908 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Lactase-glycosylceramidase 87 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Uncharacterized protein 99 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: 177.20Molecular Weight (Monoisotopic): 177.1001AlogP: -2.58#Rotatable Bonds: 3
    Polar Surface Area: 92.95Molecular Species: BASEHBA: 5HBD: 5
    #RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 5#RO5 Violations (Lipinski): 0
    CX Acidic pKa: 13.22CX Basic pKa: 9.14CX LogP: -2.83CX LogD: -4.56
    Aromatic Rings: 0Heavy Atoms: 12QED Weighted: 0.33Np Likeness Score: 2.34

    References

    1. Minami Y, Kuriyama C, Ikeda K, Kato A, Takebayashi K, Adachi I, Fleet GW, Kettawan A, Okamoto T, Asano N..  (2008)  Effect of five-membered sugar mimics on mammalian glycogen-degrading enzymes and various glucosidases.,  16  (6): [PMID:18258441] [10.1016/j.bmc.2008.01.032]
    2. Asano N, Kato A, Miyauchi M, Kizu H, Kameda Y, Watson AA, Nash RJ, Fleet GW..  (1998)  Nitrogen-containing furanose and pyranose analogues from Hyacinthus orientalis.,  61  (5): [PMID:9599261] [10.1021/np9705726]
    3. 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