Page last updated: 2024-12-10

triiodothyronine glucuronide

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Cross-References

ID SourceID
PubMed CID3080759
CHEBI ID145228
MeSH IDM0154529

Synonyms (21)

Synonym
29919-72-0
triiodothyronine glucuronide
beta-d-glucopyranosiduronic acid, 4-(4-(2-amino-2-carboxyethyl)-2,6-diiodophenoxy)-2-iodophenyl, (s)-
T3G ,
CHEBI:145228
(2s,3s,4s,5r,6s)-6-(4-{4-[(2s)-2-amino-2-carboxyethyl]-2,6-diiodophenoxy}-2-iodophenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid
DTXSID40184035
(s)-4-(4-(2-amino-2-carboxyethyl)-2,6-diiodophenoxy)-2-iodophenyl-beta-delta-glucopyranosiduronic acid
triiodothyronine glucuronoside
(s)-4-(4-(2-amino-2-carboxyethyl)-2,6-diiodophenoxy)-2-iodophenyl-beta-d-glucopyranosiduronic acid
(2s,3s,4s,5r,6s)-6-[4-[4-[(2s)-2-amino-2-carboxyethyl]-2,6-diiodophenoxy]-2-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid
l-tyrosine, 4-[4-(beta-d-glucopyranuronosyloxy)-3-iodophenoxy]-3,5-diiodo-
(2s,3s,4s,5r,6s)-6-[4-[4-[(2s)-2-amino-2-carboxyethyl]-2,6-diiodophenoxy]-2-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylicacid
glucopyranosiduronic acid, 4-[4-(2-amino-2-carboxyethyl)-2,6-diiodophenoxy]-2-iodophenyl, l-beta-d-
4-[4-[(2s)-2-amino-2-carboxyethyl]-2,6-diiodophenoxy]-2-iodophenyl beta-d-glucopyranosiduronic acid
alanine, 3-[4-[4-(beta-d-glucopyranuronosyloxy)-3-iodophenoxy]-3,5-diiodophenyl]-, l-
C476A7CU7N
3,3',5-triiodo-l-thyronine 4'-o-beta-d-glucuronide
beta-d-glucopyranosiduronic acid, 4-[4-(2-amino-2-carboxyethyl)-2,6-diiodophenoxy]-2-iodophenyl, (s)-
beta-d-glucopyranosiduronic acid, 4-[4-[(2s)-2-amino-2-carboxyethyl]-2,6-diiodophenoxy]-2-iodophenyl
3,5,3'-triiodothyronine glucuronide
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
phenylalanine derivativeAn amino acid derivative resulting from reaction of alanine at the amino group or the carboxy group, or from the replacement of any hydrogen of phenylalanine by a heteroatom. The definition normally excludes peptides containing phenylalanine residues.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19903 (60.00)18.7374
1990's1 (20.00)18.2507
2000's1 (20.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.42

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.42 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.21 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.42)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]