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Compound Detail

CHEMBL81721

TRIIODOPHENOL
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Oc1c(I)cc(I)cc1I

Basic Information

ChEMBL ID CHEMBL81721
Name TRIIODOPHENOL
Phase Preclinical
Structure Type MOL
InChI Key VAPDZNUFNKUROY-UHFFFAOYSA-N

Known Names

2,4,6-Triiodo-Phenol(Tip)
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
13
Publications
1
Known Names

Molecular Properties

471.8
MW (Da)
3.21
ALogP
1
HBA
1
HBD
20.2
PSA (Ų)
0.58
QED
0
Ro5 Violations
0
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C6H3I3O
MW 471.80
Aromatic Rings 1
Heavy Atoms 10
NP-Likeness -0.32

Activity Summary

IC50 1 meas. best 5.5

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Transthyretin
CHEMBL3194
IC50 5.5 5.5 3200.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Transthyretin IC50 = 3200.0 nM 5.5 Inhibition of TTR mediated fibrillogenesis assessed as acid-induced protein aggr... 19651509

Literature References

PubMed DOI Target Context # Activities
18160525 10.1128/aac.01019-07 Cryptosporidium parvum 13
19651509 10.1016/j.bmcl.2009.03.004 Transthyretin 3
3097319 10.1021/jm00162a006 Transthyretin 2
- 10.6019/CHEMBL4495565 SARS-CoV-2 2
- 10.6019/CHEMBL4808148 Histone deacetylase 6 2
3919186 10.1021/jm00381a018 Transthyretin 1
3100800 10.1021/jm00384a014 Transthyretin 1
3100800 10.1021/jm00384a014 Thyroid hormone receptor 1
3097319 10.1021/jm00162a006 Unchecked 1
18160525 10.1128/aac.01019-07 HCT-8 1
- 10.21203/rs.3.rs-23951/v1 SARS-CoV-2 1
- 10.6019/CHEMBL4495564 Replicase polyprotein 1ab 1
34555615 10.1016/j.ejmech.2021.113847 Transthyretin 1

Data from ChEMBL 36 via Core Engine