Page last updated: 2024-12-08

topsentin a

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

Description

topsentin A: number of carbony group = 1 for topsentin A and no carbonyl group for nortopsentin B and D; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID183527
CHEMBL ID372191
SCHEMBL ID17243841
SCHEMBL ID17537642
MeSH IDM0369566

Synonyms (19)

Synonym
nsc623150
nsc-623150
deoxytopsentin
topsentin a
1h-indol-3-yl-[5-(1h-indol-3-yl)-1h-imidazol-2-yl]methanone
CHEMBL372191
112515-42-1
nsc 623150
deoxytopsentine
methanone, 1h-indol-3-yl(5-(1h-indol-3-yl)-1h-imidazol-2-yl)-
DTXSID70150086
SCHEMBL17243841
SCHEMBL17537642
bdbm50475485
methanone, 1h-indol-3-yl[5-(1h-indol-3-yl)-1h-imidazol-2-yl]-
3-[2-(1h-indole-3-carbonyl)-1h-imidazol-4-yl]-1h-indole
topsentine a
1h-indol-3-yl[5-(1h-indol-3-yl)-1h-imidazol-2-yl]methanone
V3E7XP2A9Q
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (13)

Assay IDTitleYearJournalArticle
AID419045Inhibition of 6-His tagged Staphylococcus aureus recombinant sortase delta N24 expressed in Escherichia coli BL21 (DE3)2009Bioorganic & medicinal chemistry, Apr-01, Volume: 17, Issue:7
Probing of the cis-5-phenyl proline scaffold as a platform for the synthesis of mechanism-based inhibitors of the Staphylococcus aureus sortase SrtA isoform.
AID1225229Inhibition of recombinant his-tagged human pyruvate kinase M1 expressed in Escherichia coli BL-21(DE3) using PEP as substrate at 10 uM after 5 mins by L-LDH coupled assay relative to control2015Journal of natural products, Mar-27, Volume: 78, Issue:3
Synthetic analogues of the marine bisindole deoxytopsentin: potent selective inhibitors of MRSA pyruvate kinase.
AID254837Inhibitory activity against Sortase A from Staphylococcus aureus2005Bioorganic & medicinal chemistry letters, Nov-15, Volume: 15, Issue:22
Bis(indole) alkaloids as sortase A inhibitors from the sponge Spongosorites sp.
AID401678Cytotoxicity against human A549 cells after 48 hrs by SRB assay2005Journal of natural products, May, Volume: 68, Issue:5
Cytotoxic bisindole alkaloids from a marine sponge Spongosorites sp.
AID255501Minimum inhibitory concentration against Staphylococcus aureus Newman strain2005Bioorganic & medicinal chemistry letters, Nov-15, Volume: 15, Issue:22
Bis(indole) alkaloids as sortase A inhibitors from the sponge Spongosorites sp.
AID401681Cytotoxicity against human XF498 cells after 48 hrs by SRB assay2005Journal of natural products, May, Volume: 68, Issue:5
Cytotoxic bisindole alkaloids from a marine sponge Spongosorites sp.
AID1225230Inhibition of recombinant his-tagged human pyruvate kinase M2 expressed in Escherichia coli BL-21(DE3) using PEP as substrate at 10 uM after 5 mins by L-LDH coupled assay relative to control2015Journal of natural products, Mar-27, Volume: 78, Issue:3
Synthetic analogues of the marine bisindole deoxytopsentin: potent selective inhibitors of MRSA pyruvate kinase.
AID401682Cytotoxicity against human HCT15 cells after 48 hrs by SRB assay2005Journal of natural products, May, Volume: 68, Issue:5
Cytotoxic bisindole alkaloids from a marine sponge Spongosorites sp.
AID401680Cytotoxicity against human SK-MEL-2 cells after 48 hrs by SRB assay2005Journal of natural products, May, Volume: 68, Issue:5
Cytotoxic bisindole alkaloids from a marine sponge Spongosorites sp.
AID1225232Inhibition of recombinant his-tagged human pyruvate kinase L expressed in Escherichia coli BL-21(DE3) using PEP as substrate at 10 uM after 5 mins by L-LDH coupled assay relative to control2015Journal of natural products, Mar-27, Volume: 78, Issue:3
Synthetic analogues of the marine bisindole deoxytopsentin: potent selective inhibitors of MRSA pyruvate kinase.
AID1225231Inhibition of recombinant his-tagged human pyruvate kinase R expressed in Escherichia coli BL-21(DE3) using PEP as substrate at 10 uM after 5 mins by L-LDH coupled assay relative to control2015Journal of natural products, Mar-27, Volume: 78, Issue:3
Synthetic analogues of the marine bisindole deoxytopsentin: potent selective inhibitors of MRSA pyruvate kinase.
AID1225224Inhibition of recombinant his-tagged methicillin-resistant Staphylococcus aureus pyruvate kinase expressed in Escherichia coli BL-21(DE3) using PEP as substrate after 5 mins by L-LDH coupled assay2015Journal of natural products, Mar-27, Volume: 78, Issue:3
Synthetic analogues of the marine bisindole deoxytopsentin: potent selective inhibitors of MRSA pyruvate kinase.
AID401679Cytotoxicity against human SKOV3 cells after 48 hrs by SRB assay2005Journal of natural products, May, Volume: 68, Issue:5
Cytotoxic bisindole alkaloids from a marine sponge Spongosorites sp.
[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-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's6 (42.86)29.6817
2010's6 (42.86)24.3611
2020's2 (14.29)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%
Other14 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]