Page last updated: 2024-12-05
1-methylphenanthrene
Description
## 1-Methylphenanthrene: A Key to Understanding Biological Processes
1-Methylphenanthrene is a polycyclic aromatic hydrocarbon (PAH) with a specific chemical structure featuring a methyl group attached to the first carbon atom of the phenanthrene molecule. While it might sound complex, this compound plays a crucial role in various research fields, including:
**1. Environmental Studies:**
* **Pollution Monitoring:** 1-Methylphenanthrene is often found in environmental samples, especially in contaminated soils and sediments. It serves as a **marker for PAH pollution**, helping researchers track the presence and distribution of these harmful compounds.
* **Source Identification:** Different sources emit unique PAH profiles. By analyzing the specific ratios of 1-methylphenanthrene and other PAHs, researchers can identify the source of contamination, be it industrial waste, traffic emissions, or natural sources.
* **Bioremediation:** Understanding the fate and transformation of 1-methylphenanthrene in the environment is crucial for developing effective bioremediation strategies to clean up contaminated sites.
**2. Chemical Synthesis and Analysis:**
* **Synthesis of New Compounds:** 1-Methylphenanthrene is an important building block in organic synthesis, used to create new compounds with potential pharmaceutical or industrial applications.
* **Spectroscopic Analysis:** Its unique structure and properties make it useful in studying spectroscopic techniques like NMR and mass spectrometry, aiding in the analysis of complex organic molecules.
**3. Biological Research:**
* **Drug Development:** While not currently used in medicine, the structural similarity of 1-methylphenanthrene to certain drugs under development makes it a valuable model compound. This allows researchers to study its interactions with biomolecules and understand potential drug targets.
* **Environmental Health:** Understanding the toxicity and carcinogenic potential of 1-methylphenanthrene and other PAHs is essential for protecting human health and developing strategies to mitigate their harmful effects.
**In Summary:**
1-Methylphenanthrene is not a household name, but its importance in various research fields is undeniable. From monitoring environmental pollution to aiding drug development, this seemingly simple compound provides valuable insights into complex biological and chemical processes, shaping our understanding of the world around us.
1-methylphenanthrene: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
1-methylphenanthrene : A member of the class of phenanthrenes that is phenanthrene substituted by a methyl group at position 1. [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]
Cross-References
Synonyms (32)
Synonym |
CHEBI:35860 |
unii-44iy90klce |
44iy90klce , |
1-methyl-phenanthrene |
AB-131/40897136 |
inchi=1/c15h12/c1-11-5-4-8-15-13(11)10-9-12-6-2-3-7-14(12)15/h2-10h,1h |
nsc 146583 |
ccris 5481 |
einecs 212-622-1 |
brn 1861851 |
phenanthrene, 1-methyl- |
1-methylphenanthrene |
nsc-146583 |
832-69-9 |
nsc146583 |
1-methyl phenanthrene |
AKOS006275679 |
C19457 |
FT-0633014 |
methyl phenanthrene, 1- |
1-methylphenanthrene [iarc] |
tox21_303752 |
cas-832-69-9 |
NCGC00356988-01 |
dtxcid105648 |
dtxsid6025648 , |
DOWJXOHBNXRUOD-UHFFFAOYSA-N |
CHEMBL3561957 |
1-methylphenanthrene 10 microg/ml in acetonitrile |
1-methylphenanthrene 10 microg/ml in cyclohexane |
Q27116596 |
dl-kynureninesulfatesalt |
Roles (1)
Role | Description |
mutagen | An agent that increases the frequency of mutations above the normal background level, usually by interacting directly with DNA and causing it damage, including base substitution. |
[role 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] |
Drug Classes (1)
Class | Description |
phenanthrenes | Any benzenoid aromatic compound that consists of a phenanthrene skeleton and its substituted derivatives thereof. |
[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 (11)
Potency Measurements
Protein | Taxonomy | Measurement | Average (µ) | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
Luciferase | Photinus pyralis (common eastern firefly) | Potency | 31.7055 | 0.0072 | 15.7588 | 89.3584 | AID1224835 |
GLI family zinc finger 3 | Homo sapiens (human) | Potency | 62.9417 | 0.0007 | 14.5928 | 83.7951 | AID1259369; AID1259392 |
AR protein | Homo sapiens (human) | Potency | 12.5219 | 0.0002 | 21.2231 | 8,912.5098 | AID1259243; AID1259247 |
nuclear receptor subfamily 1, group I, member 3 | Homo sapiens (human) | Potency | 37.2573 | 0.0010 | 22.6508 | 76.6163 | AID1224838; AID1224839; AID1224893 |
progesterone receptor | Homo sapiens (human) | Potency | 54.4827 | 0.0004 | 17.9460 | 75.1148 | AID1346795 |
retinoic acid nuclear receptor alpha variant 1 | Homo sapiens (human) | Potency | 10.3079 | 0.0030 | 41.6115 | 22,387.1992 | AID1159552; AID1159555 |
estrogen-related nuclear receptor alpha | Homo sapiens (human) | Potency | 34.3316 | 0.0015 | 30.6073 | 15,848.9004 | AID1224841; AID1224848; AID1224849; AID1259403 |
estrogen nuclear receptor alpha | Homo sapiens (human) | Potency | 24.3365 | 0.0002 | 29.3054 | 16,493.5996 | AID1259244 |
thyrotropin-releasing hormone receptor | Homo sapiens (human) | Potency | 43.6486 | 0.1549 | 17.8702 | 43.6557 | AID1346891 |
Voltage-dependent calcium channel gamma-2 subunit | Mus musculus (house mouse) | Potency | 24.3365 | 0.0015 | 57.7890 | 15,848.9004 | AID1259244 |
Glutamate receptor 2 | Rattus norvegicus (Norway rat) | Potency | 24.3365 | 0.0015 | 51.7393 | 15,848.9004 | AID1259244 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Ceullar Components (1)
Research
Studies (10)
Timeframe | Studies, This Drug (%) | All Drugs % |
pre-1990 | 1 (10.00) | 18.7374 |
1990's | 1 (10.00) | 18.2507 |
2000's | 3 (30.00) | 29.6817 |
2010's | 5 (50.00) | 24.3611 |
2020's | 0 (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: 20.18
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 moderate demand-to-supply ratio for research on this compound.
Metric | This Compound (vs All) |
---|
Research Demand Index | 20.18 (24.57) | Research Supply Index | 2.40 (2.92) | Research Growth Index | 4.95 (4.65) | Search Engine Demand Index | 15.26 (26.88) | Search Engine Supply Index | 2.00 (0.95) |
| |
Study Types
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 | 10 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |