(+/-)-N-(3-(2-hydroxy-2-(naphthalen-2-yl)ethyl)thiazol-2(3H)-ylidene)acetamide oxalate

ID: ALA3244750

Chembl Id: CHEMBL3244750

PubChem CID: 90671971

Max Phase: Preclinical

Molecular Formula: C19H18N2O6S

Molecular Weight: 312.39

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(=O)/N=c1\sccn1CC(O)c1ccc2ccccc2c1.O=C(O)C(=O)O

Standard InChI:  InChI=1S/C17H16N2O2S.C2H2O4/c1-12(20)18-17-19(8-9-22-17)11-16(21)15-7-6-13-4-2-3-5-14(13)10-15;3-1(4)2(5)6/h2-10,16,21H,11H2,1H3;(H,3,4)(H,5,6)/b18-17-;

Standard InChI Key:  HYKJXIRYAXFRQC-YBFBCAGJSA-N

Associated Targets(non-human)

Alpl Alkaline phosphatase tissue-nonspecific (94 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: 312.39Molecular Weight (Monoisotopic): 312.0932AlogP: 2.88#Rotatable Bonds: 3
Polar Surface Area: 54.59Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 0.41CX LogP: 2.37CX LogD: 2.37
Aromatic Rings: 3Heavy Atoms: 22QED Weighted: 0.81Np Likeness Score: -1.22

References

1. Bhargava KK, Lee MH, Huang Y, Cunningham LS, Agrawal KC, Sartorelli AC..  (1977)  Tetramisole analogues as inhibitors of alkaline phosphatase, an enzyme involved in the resistance of neoplastic cells to 6-thiopurines.,  20  (4): [PMID:557560] [10.1021/jm00214a021]

Source