2-methyl-5,6-cyclopentapyrimidine profile

2-methyl-5,6-cyclopentapyrimidine: structure given in first source; RN given is CAS no. reported in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID Source	ID
PubMed CID	160264
SCHEMBL ID	11561562
MeSH ID	M0209993

Synonyms (11)

Synonym
2-methyl-5,6-trimethylenepyrimidine
5h-cyclopentapyrimidine, 6,7-dihydro-2-methyl-
2-methyl-5,6-cyclopentapyrimidine
2-methyl-6,7-dihydro-5h-cyclopentapyrimidine
ccris 6513
6,7-dihydro-2-methyl-5h-cyclopentapyrimidine
2-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidine
36274-29-0
AKOS006277956
SCHEMBL11561562
DTXSID90189818

Research Excerpts

Toxicity

Excerpt	Reference	Relevance
" The material was highly toxic by inhalation, with the approximate lethal concentration in rats following single 4-h exposures being 9 ppm."	( Toxicity of 2-methyl-5,6-cyclopentapyrimidine (MCPP). Kennedy, GL, 1992)	0.66

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

Research

Studies (5)

Timeframe	Studies, This Drug (%)	All Drugs %
pre-1990	0 (0.00)	18.7374
1990's	1 (20.00)	18.2507
2000's	2 (40.00)	29.6817
2010's	1 (20.00)	24.3611
2020's	1 (20.00)	2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 13.04

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.

Metric	This Compound (vs All)
Research Demand Index	13.04 (24.57)
Research Supply Index	1.79 (2.92)
Research Growth Index	4.83 (4.65)
Search Engine Demand Index	0.00 (26.88)
Search Engine Supply Index	0.00 (0.95)

This Compound (13.04)

All Compounds (24.57)

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	5 (100.00%)	84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Substance	Relationship Strength	Studies	Classes	Roles
3,3-dimethylallyl pyrophosphate 3,3-dimethylallyl pyrophosphate: isomeric with isopentenyl pyrophosphate. prenyl diphosphate : A prenol phosphate that is a phosphoantigen comprising the O-pyrophosphate of prenol.	2.02	1	prenol phosphate	epitope; Escherichia coli metabolite; mouse metabolite; phosphoantigen
di-(2-ethylhexyl) terephthalate [no description available]	2.21	1
xylose xylopyranose: structure in first source	2.02	1	D-xylose
mono(2-ethyl-5-hydroxyhexyl) phthalate mono(2-ethyl-5-hydroxyhexyl) phthalate: a metabolite of bis(2-ethylhexyl) phthalate. mono(2-ethyl-5-hydroxyhexyl) phthalate : A phthalic acid monoester obtained by formal condensation of one of the carboxy groups of phthalic acid with the primary hydroxy group of 2-ethylhexane-1,5-diol	2.21	1	phthalic acid monoester	human urinary metabolite; human xenobiotic metabolite
erythritol [no description available]	2.41	1	butane-1,2,3,4-tetrol	antioxidant; human metabolite; plant metabolite
1-deoxy-d-xylulose 5-phosphate deoxyxylulose phosphate: structure in first source. 1-deoxy-D-xylulose 5-phosphate : The 5-phospho derivative of 1-deoxy-D-xylulose.	2.02	1	xylulose phosphate	Escherichia coli metabolite
pyrophosphate Diphosphates: Inorganic salts of phosphoric acid that contain two phosphate groups.	2.49	2	diphosphate ion

2-methyl-5,6-cyclopentapyrimidine

Description