ID: ALA2348286

Max Phase: Preclinical

Molecular Formula: C16H17I2NO5S

Molecular Weight: 589.19

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CS(=O)(=O)N[C@H](CO)Cc1cc(I)c(Oc2ccc(O)cc2)c(I)c1

Standard InChI:  InChI=1S/C16H17I2NO5S/c1-25(22,23)19-11(9-20)6-10-7-14(17)16(15(18)8-10)24-13-4-2-12(21)3-5-13/h2-5,7-8,11,19-21H,6,9H2,1H3/t11-/m0/s1

Standard InChI Key:  BUEZCOGPQVGDGL-NSHDSACASA-N

Associated Targets(Human)

PCNA Tchem Proliferating cell nuclear antigen (81 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

Properties

Molecular Weight: 589.19Molecular Weight (Monoisotopic): 588.8917AlogP: 2.85#Rotatable Bonds: 7
Polar Surface Area: 95.86Molecular Species: NEUTRALHBA: 5HBD: 3
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski): 1
CX Acidic pKa: 9.58CX Basic pKa: CX LogP: 3.13CX LogD: 3.12
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.43Np Likeness Score: -0.04

References

1. Actis M, Inoue A, Evison B, Perry S, Punchihewa C, Fujii N..  (2013)  Small molecule inhibitors of PCNA/PIP-box interaction suppress translesion DNA synthesis.,  21  (7): [PMID:23395113] [10.1016/j.bmc.2013.01.022]

Source