O-(D-glucopyranosylidene)amino-Z-N-phenylcarbamate

ID: ALA3787285

Chembl Id: CHEMBL3787285

PubChem CID: 127031892

Max Phase: Preclinical

Molecular Formula: C13H17N3O6

Molecular Weight: 311.29

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  O=C(Nc1ccccc1)O/N=C1\N[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

Standard InChI:  InChI=1S/C13H17N3O6/c17-6-8-9(18)10(19)11(20)12(15-8)16-22-13(21)14-7-4-2-1-3-5-7/h1-5,8-11,17-20H,6H2,(H,14,21)(H,15,16)/t8-,9-,10+,11-/m1/s1

Standard InChI Key:  FGGZIVIPIWHKIJ-CHWFTXMASA-N

Alternative Forms

1. Parent:

   

   ALA3787285

   ---

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Small molecule

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 311.29

Molecular Weight (Monoisotopic): 311.1117

AlogP: -1.40

#Rotatable Bonds: 3

Polar Surface Area: 143.64

Molecular Species: NEUTRAL

HBA: 7

HBD: 6

#RO5 Violations: 1

HBA (Lipinski): 9

HBD (Lipinski): 6

#RO5 Violations (Lipinski): 1

CX Acidic pKa: 12.11

CX Basic pKa: 1.78

CX LogP: -1.30

CX LogD: -1.30

Aromatic Rings: 1

Heavy Atoms: 22

QED Weighted: 0.30

Np Likeness Score: 0.17

References

1. Wang J, Wang X, Zhao Y, Ma X, Wan Y, Chen Z, Chen H, Gan H, Li J, Li L, Wang PG, Zhao W.  (2016)  Synthesis and biological evaluation ofd-gluconhydroximo-1,5-lactam and its oxime-substituted derivatives as pharmacological chaperones for the treatment of Gaucher disease,  7  (2): [10.1039/C5MD00501A]

2. Thanna S, Sucheck SJ..  (2016)  Targeting the trehalose utilization pathways of Mycobacterium tuberculosis.,  7  (1): [PMID:26941930] [10.1039/c5md00376h]

Source

Source(1):

• Scientific Literature