Page last updated: 2024-08-05 15:47:59

Smad3 inhibitor

An inhibitor of the SMAD3 protein.

ChEBI ID: 87588

Members (1)

MemberDefinitionClass
SIS3 free baseAn enamide resulting from the formal condensation of the amino group of 6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline with the carboxy group of (2E)-3-(1-methyl-2-phenyl-1H-pyrrolo[2,3-b]pyridin-3-yl)acrylic acid.SIS3 free base

Research

Studies (5)

TimeframeStudies, Drugs with This Role(%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (20.00)24.3611
2020's4 (80.00)2.80

Study Types

Publication TypeStudies, Drugs with this Role (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (20.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other4 (80.00%)84.16%

Protein Targets (7)

Potency Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)Drugs
cytochrome P450 2C9, partialHomo sapiens (human)Potency0.268411
cytochrome P450 2D6Homo sapiens (human)Potency9.522111
cytochrome P450 family 3 subfamily A polypeptide 4Homo sapiens (human)Potency1.899911
GVesicular stomatitis virusPotency0.268411
HLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)Potency0.268411
Inositol hexakisphosphate kinase 1Homo sapiens (human)Potency0.268412
Interferon betaHomo sapiens (human)Potency0.268411