5-(3,4-Dihydroxy-pyrrolidin-2-yl)-2-methyl-furan-3-carboxylic acid isopropyl ester

ID: ALA87642

PubChem CID: 44319797

Max Phase: Preclinical

Molecular Formula: C13H19NO5

Molecular Weight: 269.30

Molecule Type: Small molecule

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  Cc1oc(C2NCC(O)C2O)cc1C(=O)OC(C)C

Standard InChI:  InChI=1S/C13H19NO5/c1-6(2)18-13(17)8-4-10(19-7(8)3)11-12(16)9(15)5-14-11/h4,6,9,11-12,14-16H,5H2,1-3H3

Standard InChI Key:  WUHCEDIWTMBUQC-UHFFFAOYSA-N

Molfile:  

     RDKit          2D

 19 20  0  0  0  0  0  0  0  0999 V2000
    7.3000   -1.1167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4167   -2.1167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4917   -1.2917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7042   -2.5292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7167   -1.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6292   -0.3542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1750   -2.4417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0792   -2.0417    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4125   -3.3292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5917   -3.3250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4500   -0.2625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3750   -2.5292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1375    0.3083    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8917   -4.0042    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0917   -3.9875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5417   -1.9042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9417   -0.9250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6125   -1.6792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7542   -0.8292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  3  2  0
  3  1  1  0
  4  2  1  0
  5  1  2  0
  6  1  1  0
  7  5  1  0
  8  4  1  0
  9  4  1  0
 10  9  1  0
 11  6  1  0
 12  8  1  0
 13  6  2  0
 14  9  1  0
 15 10  1  0
 16  5  1  0
 17 11  1  0
 18 17  1  0
 19 17  1  0
  2  7  1  0
 12 10  1  0
M  END

Associated Targets(Human)

FUCA1 Tchem Alpha-L-fucosidase I (304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GLA Tclin Alpha-galactosidase A (5444 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GLB1 Tchem Beta-galactosidase (339 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GBA1 Tclin Beta-glucocerebrosidase (14647 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MANBA Tchem Beta-mannosidase (62 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NAGA Tbio Alpha-galactosidase B (11 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

GLB1 Beta-galactosidase (500 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lacA Beta-galactosidase (64 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GLAA Glucoamylase (78 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lacZ Beta-galactosidase (1278 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Si Sucrase-isomaltase (908 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: 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

Calculated Properties

Molecular Weight: 269.30Molecular Weight (Monoisotopic): 269.1263AlogP: 0.52#Rotatable Bonds: 3
Polar Surface Area: 91.93Molecular Species: NEUTRALHBA: 6HBD: 3
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski):
CX Acidic pKa: 13.16CX Basic pKa: 7.93CX LogP: 0.20CX LogD: -0.45
Aromatic Rings: 1Heavy Atoms: 19QED Weighted: 0.69Np Likeness Score: 0.28

References

1. Robina I, Moreno-Vargas AJ, Fernández-Bolaños JG, Fuentes J, Demange R, Vogel P..  (2001)  New leads for selective inhibitors of alpha-L-fucosidases. Synthesis and glycosidase inhibitory activities of [(2R,3S,4R)-3,4-dihydroxypyrrolidin-2-yl]furan derivatives.,  11  (18): [PMID:11549468] [10.1016/s0960-894x(01)00497-8]

Source