Page last updated: 2024-11-06

adafenoxate

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

Description

adafenoxate: structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID64517
CHEMBL ID2104053
CHEMBL ID1592191
SCHEMBL ID194591
MeSH IDM0152872

Synonyms (27)

Synonym
adafenoxate
STK083943
2-[(3s,5s,7s)-tricyclo[3.3.1.1~3,7~]dec-1-ylamino]ethyl (4-chlorophenoxy)acetate
NCGC00160658-01
2-(1-adamantylamino)ethyl 2-(4-chlorophenoxy)acetate
82168-26-1
cas-82168-26-1
dtxcid2026280
dtxsid4046280 ,
tox21_111965
CHEMBL2104053
adafenoxatum [latin]
2-(1-adamantylamino)ethyl (p-chlorophenoxy)acetate
2-(1-tricyclo(3.3.1.1(3,7))decylamino)ethyl (4-chlorphenoxy)acetat
adafenoxato [spanish]
adafenoxatum
adafenoxato
b8vqu4c05j ,
unii-b8vqu4c05j
adafenoxate [inn]
acetic acid, 2-(4-chlorophenoxy)-, 2-(tricyclo(3.3.1.13,7)dec-1-ylamino)ethyl ester
SCHEMBL194591
adafenoxat
CHEMBL1592191
FT-0764210
Q4678359
AKOS040750126

Research Excerpts

Overview

Adafenoxate proved to be a more potent monoamine uptake inhibitor than the other three drugs. It inhibited the uptake in the frontal cortex and striatum without selectivity for either monoaminergic system.

ExcerptReferenceRelevance
"4. Adafenoxate proved to be a more potent monoamine uptake inhibitor than the other three drugs; it inhibited the uptake in the frontal cortex and striatum without selectivity for either monoaminergic system."( Biogenic monoamine uptake by rat brain synaptosomes during aging. Effects of nootropic drugs.
Alova, LG; Stancheva, SL, 1994
)
0.8

Actions

ExcerptReferenceRelevance
"Adafenoxate was found to increase also the number of entries into and escapes from the dark compartment without punishment responding."( A study of nootropic drugs for anti-anxiety action.
Getova, D; Mosharrof, AH; Petkov, VD, 1987
)
0.99

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]

Protein Targets (3)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
phosphopantetheinyl transferaseBacillus subtilisPotency56.23410.141337.9142100.0000AID1490
potassium voltage-gated channel subfamily H member 2 isoform dHomo sapiens (human)Potency12.58930.01789.637444.6684AID588834
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency30.04740.000323.4451159.6830AID743065; AID743067
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (4)

Assay IDTitleYearJournalArticle
AID504749qHTS profiling for inhibitors of Plasmodium falciparum proliferation2011Science (New York, N.Y.), Aug-05, Volume: 333, Issue:6043
Chemical genomic profiling for antimalarial therapies, response signatures, and molecular targets.
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.
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.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (18)

TimeframeStudies, This Drug (%)All Drugs %
pre-19908 (44.44)18.7374
1990's7 (38.89)18.2507
2000's0 (0.00)29.6817
2010's2 (11.11)24.3611
2020's1 (5.56)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

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%
Other18 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]