Page last updated: 2024-12-05

1-methylphenanthrene

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

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

ID SourceID
PubMed CID13257
CHEMBL ID3561957
CHEBI ID35860
MeSH IDM0123094

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
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
mutagenAn 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)

ClassDescription
phenanthrenesAny 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

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
LuciferasePhotinus pyralis (common eastern firefly)Potency31.70550.007215.758889.3584AID1224835
GLI family zinc finger 3Homo sapiens (human)Potency62.94170.000714.592883.7951AID1259369; AID1259392
AR proteinHomo sapiens (human)Potency12.52190.000221.22318,912.5098AID1259243; AID1259247
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency37.25730.001022.650876.6163AID1224838; AID1224839; AID1224893
progesterone receptorHomo sapiens (human)Potency54.48270.000417.946075.1148AID1346795
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency10.30790.003041.611522,387.1992AID1159552; AID1159555
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency34.33160.001530.607315,848.9004AID1224841; AID1224848; AID1224849; AID1259403
estrogen nuclear receptor alphaHomo sapiens (human)Potency24.33650.000229.305416,493.5996AID1259244
thyrotropin-releasing hormone receptorHomo sapiens (human)Potency43.64860.154917.870243.6557AID1346891
Voltage-dependent calcium channel gamma-2 subunitMus musculus (house mouse)Potency24.33650.001557.789015,848.9004AID1259244
Glutamate receptor 2Rattus norvegicus (Norway rat)Potency24.33650.001551.739315,848.9004AID1259244
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Ceullar Components (1)

Processvia Protein(s)Taxonomy
plasma membraneGlutamate receptor 2Rattus norvegicus (Norway rat)
[Information is prepared from geneontology information from the June-17-2024 release]

Research

Studies (10)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (10.00)18.7374
1990's1 (10.00)18.2507
2000's3 (30.00)29.6817
2010's5 (50.00)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: 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.

MetricThis Compound (vs All)
Research Demand Index20.18 (24.57)
Research Supply Index2.40 (2.92)
Research Growth Index4.95 (4.65)
Search Engine Demand Index15.26 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (20.18)

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%
Other10 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]