ID Source | ID |
---|---|
PubMed CID | 701 |
CHEMBL ID | 31596 |
SCHEMBL ID | 41804 |
MeSH ID | M0305422 |
Synonym |
---|
MLS002177803 , |
smr001261797 |
ethyl alpha-methylacetylacetate |
nsc 1102 |
unii-ne9woz20je |
ethyl alpha-acetylpropionate |
alpha-methylacetoacetic ester |
ai3-05606 |
ne9woz20je , |
einecs 210-179-9 |
acetoacetic acid, 2-methyl-, ethyl ester |
butanoic acid, 2-methyl-3-oxo-, ethyl ester |
ethyl-2-methyl acetoacetate |
NCGC00090968-01 |
ethyl methylacetoacetate |
.alpha.-methylacetoacetic ester |
ethyl .alpha.-methylacetoacetate |
ethyl .alpha.-methylacetylacetate |
nsc1102 |
ETHYL-2-METHYLACETOACETATE , |
ethyl 2-methylacetoacetate |
ethyl 2-methyl-3-oxobutanoate , |
ethyl 2-acetylpropionate |
ethyl .alpha.-acetylpropionate |
nsc-1102 |
609-14-3 |
ethyl 2-methyl-3-oxobutyrate |
ethyl 2-methylacetoacetate, 90% |
E-8300 |
CHEMBL31596 |
AKOS005138021 |
M0698 |
2-acetylpropionic acid ethyl ester |
2-methylacetoacetic acid ethyl ester |
A832951 |
NCGC00090968-02 |
ethyl-2-methyl-acetoacetate |
NCGC00258690-01 |
dtxsid2033493 , |
dtxcid0013493 |
cas-609-14-3 |
tox21_201138 |
FT-0613000 |
AM20100481 |
ethyl2-methylacetoacetate |
SCHEMBL41804 |
ethyl 2-methyl-3-oxidanylidene-butanoate |
cid_701 |
bdbm74254 |
3-keto-2-methyl-butyric acid ethyl ester |
ethyl 2-methyl-acetoacetate |
ethyl-alpha-methylacetoacetate |
2-methyl-3-oxobutanoic acid ethyl ester |
2-methyl acetoacetic acid ethyl ester |
2-methyl-3-oxo-butanoic acid ethyl ester |
ethyl 2-methylaceto-acetate |
alpha-methylacetoacetic acid ethyl ester |
2-methyl-3-oxo-butyric acid ethyl ester |
ethyl 2-methyl-3-oxo-butyrate |
ethyl 2-methylacetoaceate |
2-methyl acetoacetic ethyl ester |
alpha-methyl-acetoacetic acid ethyl ester |
2-methyl-3-oxobutyric acid ethyl ester |
ethyl ester of 2-methyl-3-oxobutanoic acid |
ethyl 3-oxo-2-methylbutanoate |
ethyl (+/-)-2-methylacetoacetate |
acetoacetic acid, .alpha.-methyl-, ethyl ester |
ethyl 2-acetylpropanoate |
1522-45-8 |
F0001-1597 |
CS-W004822 |
mfcd00009164 |
GS-3290 |
SY005677 |
F11259 |
STL196835 |
Q27284827 |
BP-31062 |
ethyl2-methyl-3-oxobutanoate |
EN300-49163 |
Z586248936 |
Protein | Taxonomy | Measurement | Average (µ) | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
WRN | Homo sapiens (human) | Potency | 15.8489 | 0.1683 | 31.2583 | 100.0000 | AID651768 |
USP1 protein, partial | Homo sapiens (human) | Potency | 354.8130 | 0.0316 | 37.5844 | 354.8130 | AID743255 |
TDP1 protein | Homo sapiens (human) | Potency | 6.5131 | 0.0008 | 11.3822 | 44.6684 | AID686978; AID686979 |
GLI family zinc finger 3 | Homo sapiens (human) | Potency | 48.9036 | 0.0007 | 14.5928 | 83.7951 | AID1259369 |
67.9K protein | Vaccinia virus | Potency | 1.5673 | 0.0001 | 8.4406 | 100.0000 | AID720579; AID720580 |
IDH1 | Homo sapiens (human) | Potency | 0.9200 | 0.0052 | 10.8652 | 35.4813 | AID686970 |
nuclear factor erythroid 2-related factor 2 isoform 1 | Homo sapiens (human) | Potency | 74.9780 | 0.0006 | 27.2152 | 1,122.0200 | AID651741 |
DNA polymerase eta isoform 1 | Homo sapiens (human) | Potency | 89.1251 | 0.1000 | 28.9256 | 213.3130 | AID588591 |
DNA polymerase kappa isoform 1 | Homo sapiens (human) | Potency | 100.0000 | 0.0316 | 22.3146 | 100.0000 | AID588579 |
Nuclear receptor ROR-gamma | Homo sapiens (human) | Potency | 0.0047 | 0.0266 | 22.4482 | 66.8242 | AID651802 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Protein | Taxonomy | Measurement | Average | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
ORF73 | Human gammaherpesvirus 8 | EC50 (µMol) | 75.0000 | 0.0600 | 8.1346 | 32.1400 | AID435023 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Process | via Protein(s) | Taxonomy |
---|---|---|
nucleus | Nuclear receptor ROR-gamma | Homo sapiens (human) |
nucleoplasm | Nuclear receptor ROR-gamma | Homo sapiens (human) |
nuclear body | Nuclear receptor ROR-gamma | Homo sapiens (human) |
chromatin | Nuclear receptor ROR-gamma | Homo sapiens (human) |
nucleus | Nuclear receptor ROR-gamma | Homo sapiens (human) |
[Information is prepared from geneontology information from the June-17-2024 release] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2006 | Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5 | Microsphere-based protease assays and screening application for lethal factor and factor Xa. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1 | High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2006 | Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5 | Microsphere-based protease assays and screening application for lethal factor and factor Xa. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1 | High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID504812 | Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | 2010 | Endocrinology, Jul, Volume: 151, Issue:7 | A small molecule inverse agonist for the human thyroid-stimulating hormone receptor. |
AID504810 | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | 2010 | Endocrinology, Jul, Volume: 151, Issue:7 | A small molecule inverse agonist for the human thyroid-stimulating hormone receptor. |
AID651635 | Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression | |||
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2006 | Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5 | Microsphere-based protease assays and screening application for lethal factor and factor Xa. |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1 | High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID1745845 | Primary qHTS for Inhibitors of ATXN expression | |||
AID167125 | Eye irritation potential accessed using Draize in vivo rabbit eye irritation test | 2003 | Journal of medicinal chemistry, Apr-10, Volume: 46, Issue:8 | Mapping property distributions of molecular surfaces: algorithm and evaluation of a novel 3D quantitative structure-activity relationship technique. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (12.50) | 18.2507 |
2000's | 3 (37.50) | 29.6817 |
2010's | 3 (37.50) | 24.3611 |
2020's | 1 (12.50) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 8 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |