Page last updated: 2024-11-12

2,5-dimethylcelecoxib

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

Description

2,5-dimethylcelecoxib: non-COX-2 inhibitory structural analog of celecoxib [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID11545682
CHEMBL ID2163630
SCHEMBL ID2228663
MeSH IDM0493627

Synonyms (26)

Synonym
2,5-dimethylcelecoxib
2,5-dimethyl-celecoxib
4-[5-(2,5-dimethylphenyl)-3-(trifluoromethyl)pyrazol-1-yl]benzenesulfonamide
457639-26-8
4-(5-(2,5-dimethylphenyl)-3-(trifluoromethyl)-1h-pyrazol-1-yl)benzenesulfonamide
dimethyl celecoxib
CHEMBL2163630
4-[5-(2,5-dimethylphenyl)-3-(trifluoromethyl)-1h-pyrazol-1-yl]-benzenesulfonamide
SCHEMBL2228663
HB3717
c18h16f3n3o2s
2,5-dimethyl celecoxib
DTXSID00196614
2,5-dimethyl-celecoxib, vetranal(tm), analytical standard
2,5-dimethyl-celecoxib, >=98% (hplc)
AKOS027475480
4-[5-(2,5-dimethylphenyl)-3-(trifluoromethyl)-1h-pyrazol-1-yl]benzenesulfonamide
NCGC00485044-01
BCP08101
FT-0667393
2,5-dimethyl celecoxib, dmc
CCG-357033
benzenesulfonamide, 4-[5-(2,5-dimethylphenyl)-3-(trifluoromethyl)-1h-pyrazol-1-yl]-; 4-[5-(2,5-dimethylphenyl)-3-(trifluoromethyl)-1h-pyrazol-1-yl]benzenesulfonamide
2,5-dimethylcelecoxib 100 microg/ml in acetonitrile
ntfosuuwgcdxef-uhfffaoysa-n
2,5-dimethylcelecoxib-d4

Research Excerpts

Compound-Compound Interactions

ExcerptReferenceRelevance
" We propose that this novel drug combination should receive further evaluation as a potentially effective anticancer therapy."( Aggravated endoplasmic reticulum stress as a basis for enhanced glioblastoma cell killing by bortezomib in combination with celecoxib or its non-coxib analogue, 2,5-dimethyl-celecoxib.
Chen, TC; Golden, EB; Hofman, FM; Kardosh, A; Louie, SG; Petasis, NA; Pyrko, P; Schönthal, AH; Uddin, J, 2008
)
0.35

Bioavailability

ExcerptReferenceRelevance
"The ATP-binding cassette transporter P-glycoprotein (P-gp) is known to limit both brain penetration and oral bioavailability of many chemotherapy drugs."( A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
Ambudkar, SV; Brimacombe, KR; Chen, L; Gottesman, MM; Guha, R; Hall, MD; Klumpp-Thomas, C; Lee, OW; Lee, TD; Lusvarghi, S; Robey, RW; Shen, M; Tebase, BG, 2019
)
0.51
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (7)

Assay IDTitleYearJournalArticle
AID1296008Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screening2020SLAS discovery : advancing life sciences R & D, 01, Volume: 25, Issue:1
Cytotoxic Profiling of Annotated and Diverse Chemical Libraries Using Quantitative High-Throughput Screening.
AID1347160Primary screen NINDS Rhodamine qHTS for Zika virus inhibitors2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1347159Primary screen GU Rhodamine qHTS for Zika virus inhibitors: Unlinked NS2B-NS3 protease assay2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1346986P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1346987P-glycoprotein substrates identified in KB-8-5-11 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID697540Binding affinity to mouse recombinant CDH11 extracellular domain 1-2 by surface plasmon resonance2012Journal of medicinal chemistry, Aug-09, Volume: 55, Issue:15
Predicting new indications for approved drugs using a proteochemometric method.
AID697539Cytotoxicity against human MDA-MB-231 cells after 48 hrs by MTS assay2012Journal of medicinal chemistry, Aug-09, Volume: 55, Issue:15
Predicting new indications for approved drugs using a proteochemometric method.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (41)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's11 (26.83)29.6817
2010's19 (46.34)24.3611
2020's11 (26.83)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 10.99

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 Index10.99 (24.57)
Research Supply Index3.76 (2.92)
Research Growth Index4.75 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (10.99)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews3 (7.14%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other39 (92.86%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]