US8530490, 22

ID: ALA3664406

Chembl Id: CHEMBL3664406

PubChem CID: 44544549

Max Phase: Preclinical

Molecular Formula: C21H28FN3O6S

Molecular Weight: 469.54

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CC[C@@H](NS(=O)(=O)CCCOCn1ccc(=O)[nH]c1=O)c1ccc(F)c(OCC2CC2)c1

Standard InChI:  InChI=1S/C21H28FN3O6S/c1-2-18(16-6-7-17(22)19(12-16)31-13-15-4-5-15)24-32(28,29)11-3-10-30-14-25-9-8-20(26)23-21(25)27/h6-9,12,15,18,24H,2-5,10-11,13-14H2,1H3,(H,23,26,27)/t18-/m1/s1

Standard InChI Key:  ZFYCJIJRMPSSBM-GOSISDBHSA-N

Associated Targets(Human)

DUT Tchem dUTP pyrophosphatase (446 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: 469.54Molecular Weight (Monoisotopic): 469.1683AlogP: 1.90#Rotatable Bonds: 13
Polar Surface Area: 119.49Molecular Species: NEUTRALHBA: 7HBD: 2
#RO5 Violations: HBA (Lipinski): 9HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: 9.67CX Basic pKa: CX LogP: 1.59CX LogD: 1.59
Aromatic Rings: 2Heavy Atoms: 32QED Weighted: 0.43Np Likeness Score: -1.18

References

1.  (2013)  Uracil compound or salt thereof having human deoxyuridine triphosphatase inhibitory activity, 
2.  (2014)  Anti-tumor effect potentiator, 

Source

Source(1):