Page last updated: 2024-12-11

(5alpha)-23-methyl-4-aza-21-norchol-1-ene-3,20-dione

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

Description

You're describing a **steroid** with a specific chemical structure. Here's a breakdown:

* **(5α)-:** This indicates the configuration at carbon 5 is in the alpha position. Steroids have multiple rings, and this detail affects the molecule's 3D shape.
* **23-methyl-:** A methyl group (CH3) is attached at carbon 23.
* **4-aza-:** A nitrogen atom replaces a carbon atom at position 4 in the steroid ring system.
* **21-norchol-:** This indicates a modification to the cholane backbone. Nor means a carbon atom has been removed, specifically at position 21.
* **1-ene-:** A double bond exists between carbons 1 and 2.
* **3,20-dione:** There are two ketone functional groups (C=O) at carbons 3 and 20.

**Importance in Research:**

This particular steroid is a derivative of **androstenedione**, a naturally occurring hormone. While it's not found naturally, it's synthesized and studied for several reasons:

* **Pharmacological Activity:** Modifications like the nitrogen at position 4 and the removal of carbon 21 can alter the molecule's ability to bind to hormone receptors. This could create compounds with new and interesting pharmacological effects.
* **Probing Biological Processes:** By studying how this synthetic steroid interacts with biological systems, researchers gain insights into the mechanisms of hormone action and potential targets for drug development.
* **Investigating Structure-Activity Relationships:** By systematically modifying the steroid structure and observing its effects, researchers can develop a better understanding of how molecular structure impacts biological activity.

**Specific Research Applications:**

* **Drug Discovery:** Compounds with similar structures are explored for their potential in treating conditions like cancer, inflammation, and hormone-related disorders.
* **Hormone Research:** This molecule might be used to investigate the role of androgen receptors in various biological processes.
* **Chemistry Research:** Studying the synthesis and modification of this steroid could contribute to the development of new synthetic techniques.

**Important Note:** To be truly helpful, we need more context. Is this a specific molecule being investigated in a particular study? Knowing the specific research area will help me provide more detailed and relevant information.

(5alpha)-23-methyl-4-aza-21-norchol-1-ene-3,20-dione: structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID6918127
CHEMBL ID575781
SCHEMBL ID8156652
MeSH IDM0208261

Synonyms (18)

Synonym
mk-963
mk-0963
l-654066
mk 0963
CHEMBL575781
(1s,3as,3bs,5ar,9ar,9bs,11as)-9a,11a-dimethyl-1-(3-methylbutanoyl)-1,2,3,3a,3b,4,5,5a,6,9b,10,11-dodecahydroindeno[5,4-f]quinolin-7-one
xec7u2o6sc ,
4-aza-21-norchol-1-ene-3,20-dione, 23-methyl-, (5alpha)-
l-654,066
unii-xec7u2o6sc
(5alpha)-23-methyl-4-aza-21-norchol-1-ene-3,20-dione
l 654066
103497-68-3
2h-indeno(5,4-f)quinolin-2-one, 1,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-4a,6a-dimethyl-7-(3-methyl-1-oxobutyl)-, (4ar,4bs,6as,7s,9as,9bs,11ar)-
SCHEMBL8156652
mk0963
Q27293805
AKOS040749871
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID442239Inhibition of human 5 alpha reductase assessed as -log of ratio of IC50 of drug to the IC50 of reference compound2010European journal of medicinal chemistry, Feb, Volume: 45, Issue:2
3D-QSAR studies on unsaturated 4-azasteroids as human 5alpha-reductase inhibitors: a self organizing molecular field analysis approach.
[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's4 (80.00)18.2507
2000's0 (0.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.12

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 Index12.12 (24.57)
Research Supply Index2.08 (2.92)
Research Growth Index4.20 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.12)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials2 (40.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other3 (60.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]