Page last updated: 2024-12-06

mebhydroline

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

Description

Mebhydroline is a synthetic phenylpiperazine derivative. It was initially synthesized and patented in 1959 as a potential antihistamine and anti-emetic agent. However, its pharmacological profile revealed a significant affinity for serotonin receptors, particularly 5-HT2A receptors. This has led to research exploring its potential therapeutic effects in various conditions, including anxiety, depression, and addiction. Mebhydroline is also recognized for its unique pharmacodynamic properties, including the ability to enhance dopamine release in the brain. The compound is known to exhibit both agonist and antagonist activity at different serotonin receptor subtypes, making it a complex and intriguing target for further research. Its potential therapeutic applications are currently being investigated in preclinical models, with ongoing efforts to understand its precise mechanisms of action and potential side effects.'

mebhydroline: see also rcored for mebhydrolin 1,5-naphthalenedisulfonate, RN: 6153-33-9 [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID22530
CHEMBL ID1625607
CHEBI ID135144
SCHEMBL ID29802
MeSH IDM0046467

Synonyms (60)

Synonym
mebhydroline
mebhydroline [inn-french]
mebhidrolina [inn-spanish]
mebhydrolin [inn:ban]
mebhydrolinum [inn-latin]
5-benzyl-1,3,4,5-tetrahydro-2-methyl-2h-pyrido(4,3-b)indole
einecs 208-364-4
BRD-K29713308-077-02-5
3-benzyl-6-methyl-1,2,3,4-tetrahydro-.gamma.-carboline
mebhydrolin
ENAMINE_003214
OPREA1_493964
5-benzyl-2-methyl-2,3,4,5-tetrahydro-1h-pyrido[4,3-b]indole
BAS 07119675
AB00053596
CHEBI:135144
AKOS000115947
HMS1403C02
5-benzyl-2-methyl-3,4-dihydro-1h-pyrido[4,3-b]indole
bexidal (tn)
D08161
mebhydrolin (inn)
524-81-2
1h-pyrido[4,3-b]indole, 2,3,4,5-tetrahydro-2-methyl-5-(phenylmethyl)-
9suk9b7xvy ,
nsc 757830
mebhydrolinum
mebhidrolina
unii-9suk9b7xvy
ST077696
5-benzyl-2-methyl-1h,2h,3h,4h,5h-pyrido[4,3-b]indole
EN300-02843
nsc-757830
CCG-25295
bexidal
CHEMBL1625607
mebhydrolin [inn]
mebhydrolin [who-dd]
mebhydrolin [mart.]
mebhydroline [mi]
MLS006011579
smr000097302
SCHEMBL29802
DTXSID5048558
5-benzyl-1,3,4,5-tetrahydro-2-methyl-2h-pyrido[4,3-b]indole
FQQIIPAOSKSOJM-UHFFFAOYSA-N
5-benzyl-2-methyl-2,3,4,5-tetrahydro-1h-pyrido[4,3-b]indole #
AB00053596_15
SBI-0051644.P002
CS-0013654
HY-B1303A
Z56841337
STL554133
FT-0737366
DB13808
Q1994982
BRD-K29713308-077-04-1
BRD-K29713308-077-03-3
NCGC00085849-02
MS-23933

Research Excerpts

Treatment

ExcerptReferenceRelevance
"The mebhydroline treatment's superiority over placebo was shown statistically at the 95% confidence level for the symptoms itchy nose in study A and for nasal congestion in study B."( Three explorative studies on the efficacy of the antihistamine mebhydroline (Omeril).
Lenders, H; Pabst, G; Reh, C; Ulbrich, E; Waitzinger, J, 1995
)
1.01
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
indolesAny compound containing an indole skeleton.
[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]

Pathways (1)

PathwayProteinsCompounds
Mebhydrolin H1-Antihistamine Action87

Protein Targets (1)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Spike glycoproteinSevere acute respiratory syndrome-related coronavirusPotency35.48130.009610.525035.4813AID1479145
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Ceullar Components (1)

Processvia Protein(s)Taxonomy
virion membraneSpike glycoproteinSevere acute respiratory syndrome-related coronavirus
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (2)

Assay IDTitleYearJournalArticle
AID588519A screen for compounds that inhibit viral RNA polymerase binding and polymerization activities2011Antiviral research, Sep, Volume: 91, Issue:3
High-throughput screening identification of poliovirus RNA-dependent RNA polymerase inhibitors.
AID1159607Screen for inhibitors of RMI FANCM (MM2) intereaction2016Journal 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.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (14)

TimeframeStudies, This Drug (%)All Drugs %
pre-19906 (42.86)18.7374
1990's3 (21.43)18.2507
2000's2 (14.29)29.6817
2010's2 (14.29)24.3611
2020's1 (7.14)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 66.99

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 very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index66.99 (24.57)
Research Supply Index3.00 (2.92)
Research Growth Index4.54 (4.65)
Search Engine Demand Index107.57 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (66.99)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials4 (26.67%)5.53%
Reviews0 (0.00%)6.00%
Case Studies4 (26.67%)4.05%
Observational0 (0.00%)0.25%
Other7 (46.67%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]