ID Source | ID |
---|---|
PubMed CID | 1302 |
CHEMBL ID | 12952 |
CHEBI ID | 91939 |
SCHEMBL ID | 145769 |
SCHEMBL ID | 10029028 |
Synonym |
---|
smr001233475 |
MLS002154184 |
BRD-A87719232-001-02-4 |
dl-naproxen |
BPBIO1_000187 |
OPREA1_018821 |
BSPBIO_000169 |
PRESTWICK3_000045 |
AB00513799 |
STK301546 |
2-(6-methoxynaphthalen-2-yl)propanoic acid |
NCGC00094733-02 |
NCGC00094733-01 |
NCGC00094733-03 |
2-(6-methoxy-2-naphthyl)propanoic acid |
23981-80-8 |
(+/-)-6-methoxy-alpha-methyl-2-naphthaleneacetic acid |
M1220 |
(+/-)-2-(6-methoxy-2-naphthyl)propionic acid |
naproxen2-(6-methoxy-naphthalen-2-yl)-propionic acid |
bdbm50009860 |
2-(6-methoxy-naphthalen-2-yl)-propionic acid(naproxen) |
2-(6-methoxy-naphthalen-2-yl)-propionic acid |
26159-31-9 |
AKOS000121315 |
NCGC00021127-02 |
NCGC00021127-04 |
NCGC00021127-03 |
NCGC00021127-05 |
HMS2095I11 |
HMS2230K21 |
2-(6-methoxy-2-naphthyl)propionic acid |
CHEMBL12952 |
(+-)-2-(6-methoxy-2-naphthyl)propionic acid |
racemic naproxen |
(rs)-naproxen |
alpha-(6-methoxy-2-naphthyl)propionic acid |
einecs 245-969-2 |
ec 247-485-7 |
2-naphthaleneacetic acid, 6-methoxy-alpha-methyl- |
FT-0638374 |
FT-0605171 |
FT-0602835 |
HMS3374N03 |
CCG-220045 |
SCHEMBL145769 |
AKOS016038194 |
(+)2-(6-methoxy-2-naphthyl) propionic acid |
(+/-)-2-(6-methoxy-2-naphthyl) propionic acid |
(rs)-2-(6-methoxynaphthalen-2-yl)propanoic acid |
(+)-alpha-(6-methoxy-2-naphthyl)propionic acid |
6-methoxy-alpha-methyl-2-naphthalenacetic acid |
6-methoxy-2naphthyl-alpha-methylacetic acid |
racemic 2-(6-methoxy-2-naphthyl)propionic acid |
6-methoxy-2-naphthyl-alpha-methylacetic acid |
6-methoxy-alpha-methyl-2-naphthaleneacetic acid |
6-methoxy-alpha-methyl-2-naphthylacetic acid |
2-(6-methoxynaphth-2-yl)-propionic acid |
2-(6-methoxy-2-naphthyl)-propionic acid |
2-(6-methoxy-2-naphtyl)propionic acid |
SCHEMBL10029028 |
MLS006011863 |
Q-201030 |
6-methoxy-alpha-methyl-2-naphthaleneessigsaure |
AC-25684 |
rac-naproxen |
2-(6-methoxy-2-naphthyl)propanoic acid, aldrichcpr |
( inverted exclamation marka)-naproxen |
CS-W009085 |
CHEBI:91939 |
naproxen (racemic) |
HMS3712I11 |
DTXSID70860274 |
Q27163737 |
2-(6-methoxy-2-naphthalenyl)propanoic acid |
F14583 |
AS-47598 |
mfcd00439456 |
BBL038237 |
(+)-alpha-methyl-6-methoxy-2-naphthylacetic acid |
msnt?1-(mesitylene-2-sulfonyl)-3-nitro-1,2,4-triazole |
2-(6-methoxynaphthalen-2-yl)propanoicacid |
rac naproxen |
EN300-21613 |
HY-15029 |
rac naproxen-13c,d3 |
Z104505002 |
SY051309 |
Class | Description |
---|---|
naphthalenes | Any benzenoid aromatic compound having a skeleton composed of two ortho-fused benzene rings. |
[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] |
Protein | Taxonomy | Measurement | Average (µ) | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
Chain A, Beta-lactamase | Escherichia coli K-12 | Potency | 11.0792 | 0.0447 | 17.8581 | 100.0000 | AID485294; AID485341 |
TDP1 protein | Homo sapiens (human) | Potency | 25.9290 | 0.0008 | 11.3822 | 44.6684 | AID686978 |
bromodomain adjacent to zinc finger domain 2B | Homo sapiens (human) | Potency | 1.4125 | 0.7079 | 36.9043 | 89.1251 | AID504333 |
geminin | Homo sapiens (human) | Potency | 1.1220 | 0.0046 | 11.3741 | 33.4983 | AID624297 |
TAR DNA-binding protein 43 | Homo sapiens (human) | Potency | 14.1254 | 1.7783 | 16.2081 | 35.4813 | AID652104 |
[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) |
---|---|---|---|---|---|---|---|
Epidermal growth factor receptor | Homo sapiens (human) | IC50 (µMol) | 10.0000 | 0.0000 | 0.5369 | 10.0000 | AID1264567 |
Prostaglandin G/H synthase 1 | Ovis aries (sheep) | IC50 (µMol) | 0.1800 | 0.0003 | 2.1774 | 10.0000 | AID1264568 |
Prostaglandin G/H synthase 2 | Homo sapiens (human) | IC50 (µMol) | 0.2800 | 0.0001 | 0.9950 | 10.0000 | AID1264569 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID1508630 | Primary qHTS for small molecule stabilizers of the endoplasmic reticulum resident proteome: Secreted ER Calcium Modulated Protein (SERCaMP) assay | 2021 | Cell reports, 04-27, Volume: 35, Issue:4 | A target-agnostic screen identifies approved drugs to stabilize the endoplasmic reticulum-resident proteome. |
AID1794808 | Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL). | 2014 | Journal of biomolecular screening, Jul, Volume: 19, Issue:6 | A High-Throughput Assay to Identify Inhibitors of the Apicoplast DNA Polymerase from Plasmodium falciparum. |
AID1794808 | Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL). | |||
AID651635 | Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression | |||
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. |
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. |
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. |
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. |
AID1745845 | Primary qHTS for Inhibitors of ATXN expression | |||
AID1159607 | Screen for inhibitors of RMI FANCM (MM2) intereaction | 2016 | Journal of biomolecular screening, Jul, Volume: 21, Issue:6 | A High-Throughput Screening Strategy to Identify Protein-Protein Interaction Inhibitors That Block the Fanconi Anemia DNA Repair Pathway. |
AID1264567 | Inhibition of EGFR (unknown origin) using tyrosine 4 as substrate by fluorescence analysis | 2015 | ACS medicinal chemistry letters, Oct-08, Volume: 6, Issue:10 | Synthesis and Evaluation of Novel Erlotinib-NSAID Conjugates as More Comprehensive Anticancer Agents. |
AID178383 | Effective dose for Anti-inflammatory activity was determined by carrageenan induced rat hind paw edema model | 2004 | Bioorganic & medicinal chemistry letters, Feb-23, Volume: 14, Issue:4 | Synthesis and evaluation of S-4-(3-thienyl)phenyl-alpha-methylacetic acid. |
AID1264569 | Inhibition of recombinant human COX-2 preincubated for 15 mins by fluorescence analysis | 2015 | ACS medicinal chemistry letters, Oct-08, Volume: 6, Issue:10 | Synthesis and Evaluation of Novel Erlotinib-NSAID Conjugates as More Comprehensive Anticancer Agents. |
AID1264592 | Drug level in human HCC827 cells treated with 2-(4-(3-ethynylphenylamino)-6-(2-methoxyethoxy)quinazolin-7-yloxy)ethyl 2-(6-methoxynaphthalen-2-yl)propanoate by LC-MS/MS analysis | 2015 | ACS medicinal chemistry letters, Oct-08, Volume: 6, Issue:10 | Synthesis and Evaluation of Novel Erlotinib-NSAID Conjugates as More Comprehensive Anticancer Agents. |
AID1264568 | Inhibition of Ovine COX-1 preincubated for 15 mins by fluorescence analysis | 2015 | ACS medicinal chemistry letters, Oct-08, Volume: 6, Issue:10 | Synthesis and Evaluation of Novel Erlotinib-NSAID Conjugates as More Comprehensive Anticancer Agents. |
[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 | 0 (0.00) | 18.2507 |
2000's | 2 (18.18) | 29.6817 |
2010's | 6 (54.55) | 24.3611 |
2020's | 3 (27.27) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
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.
| This Compound (12.03) All Compounds (24.57) |
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 | 11 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |