(1S,6S,7R,8R,8aR)-1-(hydroxymethyl)-octahydroindolizine-6,7,8-triol

ID: ALA395440

Chembl Id: CHEMBL395440

PubChem CID: 23634796

Max Phase: Preclinical

Molecular Formula: C9H17NO4

Molecular Weight: 203.24

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  OC[C@H]1CCN2C[C@H](O)[C@@H](O)[C@H](O)[C@@H]12

Standard InChI:  InChI=1S/C9H17NO4/c11-4-5-1-2-10-3-6(12)8(13)9(14)7(5)10/h5-9,11-14H,1-4H2/t5-,6+,7-,8-,9-/m1/s1

Standard InChI Key:  SFCAIHRLPSMRRE-ANZWQOBJSA-N

Associated Targets(Human)

MAN1A1 Tbio Mannosyl-oligosaccharide 1,2-alpha-mannosidase IA (2 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GLA Tclin Alpha-galactosidase A (5444 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GANAB Tchem Neutral alpha-glucosidase AB (90 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: 203.24Molecular Weight (Monoisotopic): 203.1158AlogP: -2.23#Rotatable Bonds: 1
Polar Surface Area: 84.16Molecular Species: BASEHBA: 5HBD: 4
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.92CX Basic pKa: 9.32CX LogP: -2.44CX LogD: -4.35
Aromatic Rings: 0Heavy Atoms: 14QED Weighted: 0.39Np Likeness Score: 1.89

References

1. Vyavahare VP, Chakraborty C, Maity B, Chattopadhyay S, Puranik VG, Dhavale DD..  (2007)  Synthesis of 1-deoxy-1-hydroxymethyl- and 1-deoxy-1-epi-hydroxymethyl castanospermine as new potential immunomodulating agents.,  50  (22): [PMID:17918922] [10.1021/jm070660f]

Source