Page last updated: 2024-11-13

Glabrescione B

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

Description

glabrescione B: a Hedgehog pathway inhibitor; isolated from Derris glabrescens; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID44257338
CHEMBL ID4291780
CHEBI ID186122
SCHEMBL ID16335460

Synonyms (15)

Synonym
LMPK12050359
5,7-dimethoxy-3',4'-diprenyloxyisoflavone
glabrescione b
CHEBI:186122
3-[3,4-bis(3-methylbut-2-enoxy)phenyl]-5,7-dimethoxychromen-4-one
SCHEMBL16335460
HY-122590
CS-0087327
65893-94-9
3-[3,4-bis-(3-methyl-but-2-enyloxy)-phenyl]-5,7-dimethoxy-chromen-4-one;glabrescine b;glabrescion b
A901959
MS-28173
CHEMBL4291780
AKOS040758261
3-[3,4-bis-(3-methyl-but-2-enyloxy)-phenyl]-5,7-dimethoxy-chromen-4-one
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
methoxyisoflavoneMembers of the class of isoflavones with at least one methoxy substituent.
[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]

Bioassays (16)

Assay IDTitleYearJournalArticle
AID1655599Inhibition of GLI1 transcriptional activity in human A375 cells assessed as downregulation of GLI2 mRNA expression at 5 uM incubated for 48 hrs by qPCR analysis2020ACS medicinal chemistry letters, May-14, Volume: 11, Issue:5
Pharmacophore-Based Virtual Screening for Identification of Negative Modulators of GLI1 as Potential Anticancer Agents.
AID1655600Inhibition of GLI1 transcriptional activity in human A375 cells assessed as downregulation of Cyclin D1 mRNA expression at 5 uM incubated for 48 hrs by qPCR analysis2020ACS medicinal chemistry letters, May-14, Volume: 11, Issue:5
Pharmacophore-Based Virtual Screening for Identification of Negative Modulators of GLI1 as Potential Anticancer Agents.
AID1655593Antiproliferative activity against human DaOY cells assessed as reduction in cell viability incubated for 72 hrs by trypan blue or crystal violet staining based assay2020ACS medicinal chemistry letters, May-14, Volume: 11, Issue:5
Pharmacophore-Based Virtual Screening for Identification of Negative Modulators of GLI1 as Potential Anticancer Agents.
AID1655598Inhibition of GLI1 transcriptional activity in human A375 cells assessed as downregulation of HIP1 mRNA expression at 5 uM incubated for 48 hrs by qPCR analysis2020ACS medicinal chemistry letters, May-14, Volume: 11, Issue:5
Pharmacophore-Based Virtual Screening for Identification of Negative Modulators of GLI1 as Potential Anticancer Agents.
AID1655595Inhibition of GLI1 transcriptional activity in HH-responsive mouse NIH3T3 cells assessed as reduction in SAG-induced luciferase activity at 5 uM incubated for 48 hrs by luciferase reporter gene assay relative to control2020ACS medicinal chemistry letters, May-14, Volume: 11, Issue:5
Pharmacophore-Based Virtual Screening for Identification of Negative Modulators of GLI1 as Potential Anticancer Agents.
AID1406172Growth inhibition of mouse Ptch+/- medulloblastoma cells at 0.5 uM after 72 hrs relative to control2018European journal of medicinal chemistry, Aug-05, Volume: 156Synergistic inhibition of the Hedgehog pathway by newly designed Smo and Gli antagonists bearing the isoflavone scaffold.
AID1655597Inhibition of GLI1 transcriptional activity in human A375 cells assessed as downregulation of PTCH1 mRNA expression at 5 uM incubated for 48 hrs by qPCR analysis2020ACS medicinal chemistry letters, May-14, Volume: 11, Issue:5
Pharmacophore-Based Virtual Screening for Identification of Negative Modulators of GLI1 as Potential Anticancer Agents.
AID1655601Antiproliferative activity against human A375 cells transfected with lentivrus-encoding shRNA against GLI1 assessed as reduction in cell viability incubated for 72 hrs by trypan blue or crystal violet staining based assay2020ACS medicinal chemistry letters, May-14, Volume: 11, Issue:5
Pharmacophore-Based Virtual Screening for Identification of Negative Modulators of GLI1 as Potential Anticancer Agents.
AID1655596Inhibition of GLI1 transcriptional activity in human A375 cells assessed as downregulation of GLI1 mRNA expression at 5 uM incubated for 48 hrs by qPCR analysis2020ACS medicinal chemistry letters, May-14, Volume: 11, Issue:5
Pharmacophore-Based Virtual Screening for Identification of Negative Modulators of GLI1 as Potential Anticancer Agents.
AID1655603Antiproliferative activity against human A375 cells transfected with lentivrus-encoding shRNA against GLI2 assessed as reduction in cell viability incubated for 72 hrs by trypan blue or crystal violet staining based assay2020ACS medicinal chemistry letters, May-14, Volume: 11, Issue:5
Pharmacophore-Based Virtual Screening for Identification of Negative Modulators of GLI1 as Potential Anticancer Agents.
AID1655594Inhibition of GLI1 transcriptional activity in HH-responsive mouse NIH3T3 cells assessed as reduction in GLI1 protein expression at 5 uM incubated for 48 hrs in presence of SAG by Western blot analysis2020ACS medicinal chemistry letters, May-14, Volume: 11, Issue:5
Pharmacophore-Based Virtual Screening for Identification of Negative Modulators of GLI1 as Potential Anticancer Agents.
AID1655592Antiproliferative activity against human A375 cells assessed as reduction in cell viability incubated for 72 hrs by trypan blue or crystal violet staining based assay2020ACS medicinal chemistry letters, May-14, Volume: 11, Issue:5
Pharmacophore-Based Virtual Screening for Identification of Negative Modulators of GLI1 as Potential Anticancer Agents.
AID1406174Growth inhibition of mouse Ptch+/- medulloblastoma cells at 2 uM after 72 hrs relative to control2018European journal of medicinal chemistry, Aug-05, Volume: 156Synergistic inhibition of the Hedgehog pathway by newly designed Smo and Gli antagonists bearing the isoflavone scaffold.
AID1406173Growth inhibition of mouse Ptch+/- medulloblastoma cells at 1 uM after 72 hrs relative to control2018European journal of medicinal chemistry, Aug-05, Volume: 156Synergistic inhibition of the Hedgehog pathway by newly designed Smo and Gli antagonists bearing the isoflavone scaffold.
AID1406171Growth inhibition of mouse Ptch+/- medulloblastoma cells at 0.25 uM after 72 hrs relative to control2018European journal of medicinal chemistry, Aug-05, Volume: 156Synergistic inhibition of the Hedgehog pathway by newly designed Smo and Gli antagonists bearing the isoflavone scaffold.
AID1406170Growth inhibition of mouse Ptch+/- medulloblastoma cells at 0.125 uM after 72 hrs relative to control2018European journal of medicinal chemistry, Aug-05, Volume: 156Synergistic inhibition of the Hedgehog pathway by newly designed Smo and Gli antagonists bearing the isoflavone scaffold.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (5)

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 (60.00)24.3611
2020's2 (40.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.80

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 Index12.80 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.59 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.80)

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%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]