Page last updated: 2024-10-14

nimbidiol

Description

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

Cross-References

ID SourceID
PubMed CID11334829
CHEMBL ID202413
MeSH IDM0480469

Synonyms (3)

Synonym
CHEMBL202413
nimbidiol
(4as,10as)-6,7-dihydroxy-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2h-phenanthren-9-one
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (12)

Assay IDTitleYearJournalArticle
AID1872893Inhibition of rat intestinal lactase preincubated for 10 mins followed by substrate addition2022European journal of medicinal chemistry, May-05, Volume: 235Recent results from non-basic glycosidase inhibitors: How structural diversity can inform general strategies for improving inhibition potency.
AID1872891Inhibition of rat intestinal sucrase preincubated for 10 mins followed by substrate addition2022European journal of medicinal chemistry, May-05, Volume: 235Recent results from non-basic glycosidase inhibitors: How structural diversity can inform general strategies for improving inhibition potency.
AID1872890Inhibition of rat intestinal maltase preincubated for 10 mins followed by substrate addition2022European journal of medicinal chemistry, May-05, Volume: 235Recent results from non-basic glycosidase inhibitors: How structural diversity can inform general strategies for improving inhibition potency.
AID260365Antitumor activity against human cervical carcinoma HeLa cell line2006Bioorganic & medicinal chemistry letters, Feb-15, Volume: 16, Issue:4
Isolation, synthesis, and anti-tumor activities of a novel class of podocarpic diterpenes.
AID1872897Inhibition of baker's yeast sucrase preincubated for 10 mins followed by substrate addition2022European journal of medicinal chemistry, May-05, Volume: 235Recent results from non-basic glycosidase inhibitors: How structural diversity can inform general strategies for improving inhibition potency.
AID260367Antitumor activity against human nasopharyngeal carcinoma CNE cell line2006Bioorganic & medicinal chemistry letters, Feb-15, Volume: 16, Issue:4
Isolation, synthesis, and anti-tumor activities of a novel class of podocarpic diterpenes.
AID1872896Inhibition of Aspergillus niger maltase preincubated for 10 mins followed by substrate addition2022European journal of medicinal chemistry, May-05, Volume: 235Recent results from non-basic glycosidase inhibitors: How structural diversity can inform general strategies for improving inhibition potency.
AID260368Antitumor activity against human breast adenocarcinoma MCF7 cell line2006Bioorganic & medicinal chemistry letters, Feb-15, Volume: 16, Issue:4
Isolation, synthesis, and anti-tumor activities of a novel class of podocarpic diterpenes.
AID260366Antitumor activity against human lung adenocarcinoma A549 cell line2006Bioorganic & medicinal chemistry letters, Feb-15, Volume: 16, Issue:4
Isolation, synthesis, and anti-tumor activities of a novel class of podocarpic diterpenes.
AID1872895Inhibition of rat intestinal gluco-amylase preincubated for 10 mins followed by substrate addition2022European journal of medicinal chemistry, May-05, Volume: 235Recent results from non-basic glycosidase inhibitors: How structural diversity can inform general strategies for improving inhibition potency.
AID1872892Inhibition of rat intestinal isomaltase preincubated for 10 mins followed by substrate addition2022European journal of medicinal chemistry, May-05, Volume: 235Recent results from non-basic glycosidase inhibitors: How structural diversity can inform general strategies for improving inhibition potency.
AID1872894Inhibition of rat intestinal trehalase preincubated for 10 mins followed by substrate addition2022European journal of medicinal chemistry, May-05, Volume: 235Recent results from non-basic glycosidase inhibitors: How structural diversity can inform general strategies for improving inhibition potency.
[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's2 (40.00)29.6817
2010's2 (40.00)24.3611
2020's1 (20.00)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%
Reviews1 (20.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other4 (80.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]