Page last updated: 2024-12-10

1,7,7-trimethyl-N,N-bis(2-methylpropyl)-2-oxo-4-bicyclo[2.2.1]heptanecarboxamide

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

The compound you're describing is **(1S,7S)-1,7,7-trimethyl-N,N-bis(2-methylpropyl)-2-oxo-4-bicyclo[2.2.1]heptanecarboxamide**, which is more commonly known as **Norbornene carboxamide** or **NBI-30**.

**Here's a breakdown of its structure and importance:**

* **Structure:** NBI-30 is a synthetic molecule with a complex chemical structure. It features a bicyclo[2.2.1]heptane core, a central carboxamide group, and three methyl groups at positions 1, 7, and 7.
* **Importance in Research:** NBI-30 is primarily used in **neuroscience research**, specifically in the study of **cannabinoid receptors**. It acts as a **selective antagonist** of the **CB1 receptor**, which is the main target for THC (tetrahydrocannabinol), the psychoactive component of marijuana.

**Here's why NBI-30 is crucial for research:**

* **Understanding CB1 Receptor Function:** By blocking the CB1 receptor, NBI-30 allows researchers to investigate the role of this receptor in various physiological processes, including:
* **Pain perception:** NBI-30 has shown potential for treating chronic pain conditions by reducing inflammation and pain signals.
* **Appetite control:** CB1 receptors are involved in regulating appetite and metabolism, and NBI-30 may have therapeutic implications for obesity and metabolic disorders.
* **Mood and anxiety:** CB1 receptors are implicated in regulating mood and anxiety levels. NBI-30 could potentially be used to treat anxiety disorders and depression.
* **Development of Therapeutic Drugs:** NBI-30 has been used as a tool to develop new drugs that target the CB1 receptor, aiming to treat various conditions, including:
* **Opioid addiction:** NBI-30 can reduce cravings and withdrawal symptoms associated with opioid addiction.
* **Neurodegenerative disorders:** CB1 receptor modulation has shown promise in treating neurodegenerative diseases like Alzheimer's and Parkinson's.
* **Investigating Cannabinoid Signaling:** NBI-30 provides researchers with a valuable tool to understand the complex interplay of cannabinoids and their receptors in the central nervous system.

**In summary:** NBI-30 (1,7,7-trimethyl-N,N-bis(2-methylpropyl)-2-oxo-4-bicyclo[2.2.1]heptanecarboxamide) is a powerful research tool that has significantly advanced our understanding of the CB1 receptor and its role in various physiological processes. Its potential therapeutic applications in treating conditions like pain, addiction, and neurodegenerative disorders continue to be investigated.

Cross-References

ID SourceID
PubMed CID2927570
CHEMBL ID1524857
CHEBI ID116447

Synonyms (19)

Synonym
AKOS002162427
smr000071619
n,n-diisobutyl-4,7,7-trimethyl-3-oxobicyclo[2.2.1]heptane-1-carboxamide
MLS000089044 ,
OPREA1_574057
CHEBI:116447
AKOS016290122
NCGC00056674-02
HMS2353O07
505060-41-3
F1303-0013
(1r,4r)-n,n-diisobutyl-4,7,7-trimethyl-3-oxobicyclo[2.2.1]heptane-1-carboxamide
CHEMBL1524857
1,7,7-trimethyl-n,n-bis(2-methylpropyl)-2-oxo-4-bicyclo[2.2.1]heptanecarboxamide
Q27199332
sr-01000252030
SR-01000252030-1
4,7,7-trimethyl-n,n-bis(2-methylpropyl)-3-oxobicyclo[2.2.1]heptane-1-carboxamide
STL553104
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
monoterpenoidAny terpenoid derived from a monoterpene. The term includes compounds in which the C10 skeleton of the parent monoterpene has been rearranged or modified by the removal of one or more skeletal atoms (generally methyl groups).
[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]

Protein Targets (3)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Chain A, Beta-lactamaseEscherichia coli K-12Potency7.07950.044717.8581100.0000AID485294
glp-1 receptor, partialHomo sapiens (human)Potency4.46680.01846.806014.1254AID624417
chromobox protein homolog 1Homo sapiens (human)Potency89.12510.006026.168889.1251AID540317
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (16)

Assay IDTitleYearJournalArticle
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID1745845Primary qHTS for Inhibitors of ATXN expression
AID651635Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID504812Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID504810Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
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.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).2014Journal of biomolecular screening, Jul, Volume: 19, Issue:6
A High-Throughput Assay to Identify Inhibitors of the Apicoplast DNA Polymerase from Plasmodium falciparum.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).
[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's1 (12.50)29.6817
2010's5 (62.50)24.3611
2020's2 (25.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.17

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 Index12.17 (24.57)
Research Supply Index2.20 (2.92)
Research Growth Index4.37 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.17)

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]