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.
ID Source | ID |
---|---|
PubMed CID | 2927570 |
CHEMBL ID | 1524857 |
CHEBI ID | 116447 |
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 |
Class | Description |
---|---|
monoterpenoid | Any 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 | Taxonomy | Measurement | Average (µ) | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
Chain A, Beta-lactamase | Escherichia coli K-12 | Potency | 7.0795 | 0.0447 | 17.8581 | 100.0000 | AID485294 |
glp-1 receptor, partial | Homo sapiens (human) | Potency | 4.4668 | 0.0184 | 6.8060 | 14.1254 | AID624417 |
chromobox protein homolog 1 | Homo sapiens (human) | Potency | 89.1251 | 0.0060 | 26.1688 | 89.1251 | AID540317 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2006 | Cytometry. 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. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1 | High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2006 | Cytometry. 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. |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1 | High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID1745845 | Primary qHTS for Inhibitors of ATXN expression | |||
AID651635 | Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression | |||
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2006 | Cytometry. 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. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1 | High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID504812 | Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | 2010 | Endocrinology, Jul, Volume: 151, Issue:7 | A small molecule inverse agonist for the human thyroid-stimulating hormone receptor. |
AID504810 | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | 2010 | Endocrinology, Jul, Volume: 151, Issue:7 | A small molecule inverse agonist for the human thyroid-stimulating hormone receptor. |
AID1159607 | Screen for inhibitors of RMI FANCM (MM2) intereaction | 2016 | Journal 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. |
AID1794808 | Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL). | 2014 | Journal of biomolecular screening, Jul, Volume: 19, Issue:6 | A High-Throughput Assay to Identify Inhibitors of the Apicoplast DNA Polymerase from Plasmodium falciparum. |
AID1794808 | Fluorescence-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] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (12.50) | 29.6817 |
2010's | 5 (62.50) | 24.3611 |
2020's | 2 (25.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
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.
| This Compound (12.17) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 8 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |