Page last updated: 2024-12-06
5-bromo-4-chloroindoxyl acetate
Description
5-bromo-4-chloroindoxyl acetate: improved substrate for esterases [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
5-bromo-4-chloro-3-indolyl acetate : An acetate ester obtained by formal condensation of the carboxy group of acetic acid with the hydroxy group of 5-bromo-4-chloroindoxyl. [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]
Cross-References
ID Source | ID |
PubMed CID | 65116 |
CHEBI ID | 90149 |
SCHEMBL ID | 154466 |
MeSH ID | M0125731 |
Synonyms (35)
Synonym |
bcda |
5-bromo-4-chloro-3-indolyl acetate, esterase substrate |
3252-36-6 |
B-6244 |
5-bromo-4-chloro-3-indoxyl-3-acetate |
(5-bromo-4-chloro-1h-indol-3-yl) acetate |
5-bromo-4-chloro-indolyl acetate |
FT-0660580 |
5-bromo-4-chloro-3-indolyl acetate |
AKOS016003752 |
5-bromo-4-chloroindoxyl acetate |
1h-indol-3-ol, 5-bromo-4-chloro-, acetate (ester) |
5-bromo-4-chloro-1h-indol-3-yl acetate |
TD8107 |
CS-B0598 |
SCHEMBL154466 |
HY-52112 |
CHEBI:90149 |
acetic acid-(5-bromo-4-chloro-indol-3-yl ester) |
B4830 |
3-acetoxy-4-chloro-5-bromoindole |
1h-indol-3-ol, 5-bromo-4-chloro-, 3-acetate |
mfcd00037932 |
DTXSID60186238 |
AS-61767 |
x-acetate;x-3-acetate;5-bromo-4-chloro-3-indolyl acetate;acetic acid-(5-bromo-4-chloro-1h-indol-3-yl) ester |
5-bromo-4-chloro-3-indolyl-ace-tate |
Q27162356 |
SY021723 |
1h-indol-3-ol,5-bromo-4-chloro-,3-acetate |
esterase chromogenic substrate-1 |
AMY27037 |
A853808 |
AC-37013 |
PD078627 |
Roles (1)
Role | Description |
chromogenic compound | Colourless, endogenous or exogenous pigment precursors that may be transformed by biological mechanisms into coloured compounds. They are used in biochemical assays and in diagnosis as indicators, particularly in the form of enzyme substrates. |
[role 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] |
Drug Classes (3)
Class | Description |
bromoindole | An organobromine compound that is a compound based on an indole skeleton, containing one or more bromine atoms. |
chloroindole | A compound based on an indole skeleton, containing one or more chlorine atoms |
acetate ester | Any carboxylic ester where the carboxylic acid component is acetic acid. |
[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 (11)
Timeframe | Studies, This Drug (%) | All Drugs % |
pre-1990 | 10 (90.91) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (9.09) | 24.3611 |
2020's | 0 (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: 11.84
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.
Metric | This Compound (vs All) |
---|
Research Demand Index | 11.84 (24.57) | Research Supply Index | 2.48 (2.92) | Research Growth Index | 4.32 (4.65) | Search Engine Demand Index | 0.00 (26.88) | Search Engine Supply Index | 0.00 (0.95) |
| |
Study Types
Publication Type | This drug (%) | All Drugs (%) |
Trials | 0 (0.00%) | 5.53% |
Reviews | 2 (18.18%) | 6.00% |
Case Studies | 1 (9.09%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 8 (72.73%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |