Page last updated: 2024-12-11

dehydrocrenatidine

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

Description

dehydrocrenatidine: a janus kinase inhibitor; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID5318875
CHEMBL ID3400675
MeSH IDM000605771

Synonyms (17)

Synonym
inchi=1/c15h14n2o2/c1-4-10-15-13(12(19-3)8-16-10)9-6-5-7-11(18-2)14(9)17-15/h4-8,17h,1h2,2-3h
1-ethenyl-4,8-dimethoxy-9h-pyrido[3,4-b]indole
65236-62-6
dehydrocrenatidine
1-ethenyl-4,8-dimethoxy-9h-beta-carboline
DTXSID50415746
1-vinyl-4,8-dimethoxy-beta-carboline
CHEMBL3400675
AKOS032948581
FS-8922
4,8-dimethoxy-1-vinyl-9h-pyrido[3,4-b]indole
1-vinyl-4,8-dimethoxy-beta-carboline; 4,8-dimethoxy-1-vinyl-beta-carboline; 4,8-dimethoxy-1-vinylnorharman; 8-o-methylpicrasidine i; dehydrocrenatidine; kumujian g
o-methylpicrasidine i
B0005-146823
1-vinyl-4,8-dimethoxy--carboline; 4,8-dimethoxy-1-vinyl--carboline; 4,8-dimethoxy-1-vinylnorharman; 8-o-methylpicrasidine i; dehydrocrenatidine; kumujian g
CS-0024099
HY-N3710

Research Excerpts

Treatment

ExcerptReferenceRelevance
"Cotreatment with dehydrocrenatidine and mitogen-activated protein kinase (MAPK) inhibitors indicated that dehydrocrenatidine induced apoptosis through the activation of extracellular signal-regulated kinases (ERK) and c-Jun N-terminal kinases (JNK)."( Apoptotic effects of dehydrocrenatidine via JNK and ERK pathway regulation in oral squamous cell carcinoma.
Chen, MK; Chuang, YC; Ho, HY; Hsieh, MJ; Lin, CC; Lo, YS, 2021
)
1.27
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID1194597Inhibition of PTP1B (unknown origin) assessed as inhibition rate at 100 uM2015Bioorganic & medicinal chemistry letters, May-01, Volume: 25, Issue:9
Canthinone alkaloids are novel protein tyrosine phosphatase 1B inhibitors.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (8)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's3 (37.50)24.3611
2020's5 (62.50)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.76

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 Index12.76 (24.57)
Research Supply Index2.20 (2.92)
Research Growth Index4.96 (4.65)
Search Engine Demand Index10.37 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.76)

All Compounds (24.57)

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%
Other8 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]