Page last updated: 2024-11-05

propionitrile

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

Description

propionitrile: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

propionitrile : A nitrile that is acrylonitrile in which the carbon-carbon double bond has been reduced to a single bond. [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 CID7854
CHEMBL ID15871
CHEBI ID26307
MeSH IDM0047183

Synonyms (69)

Synonym
EN300-21609
10419-75-7
ether cyanatus
nsc7966
propylnitrile
ethyl cyanide
cyanoethane
propionic nitrile
propionitrile
107-12-0
propanenitrile
wln: nc2
propiononitrile
nsc-7966
hydrocyanic ether
ch3chcn
inchi=1/c3h5n/c1-2-3-4/h2h2,1h
NCGC00091259-01
hsdb 117
ethylkyanid [czech]
rcra waste no. p101
un2404
brn 0773680
ai3-08777
ccris 4706
propannitril [czech]
einecs 203-464-4
nsc 7966
rcra waste number p101
propionitrile, 99%
AKOS000200375
chebi:26307 ,
CHEMBL15871
P0514
A801585
NCGC00091259-02
propionitril
ethylkyanid
unii-e16n05fx3s
e16n05fx3s ,
propionitrile [un2404] [flammable liquid]
4-02-00-00728 (beilstein handbook reference)
propannitril
cas-107-12-0
dtxcid401879
dtxsid1021879 ,
NCGC00258687-01
tox21_201135
STL168048
68130-67-6
einecs 268-599-3
propionitrile [hsdb]
propionitrile [mi]
proprionitrile
etcn
c2h5cn
propionitrile-3,3,3-d3
24300-21-8
Q-201630
n-propanenitrile
un 2404
ch3ch2cn
propionitrile, purum, >=99.0% (gc)
propionitrile, analytical standard
F0001-0138
mfcd00001948
Q414458
propionitrile 1000 microg/ml in methanol
ethylcyanide

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" The test relies on a gene dosage selection system in which hyperploidy is detected by the simultaneous increase in copy number of two alleles residing on the right arm of chromosome VIII: arg4-8 and cup1S (Rockmill and Fogel."( The detection of mitotic and meiotic chromosome gain in the yeast Saccharomyces cerevisiae: effects of methyl benzimidazol-2-yl carbamate, methyl methanesulfonate, ethyl methanesulfonate, dimethyl sulfoxide, propionitrile and cyclophosphamide monohydrate.
Fogel, S; Maloney, DH; Moser, SF; Piegorsch, WW; Resnick, MA; Whittaker, SG, 1990
)
0.47
" Daily dosage levels (mg/kg body wt) were: ACN at 0, 125, 190, and 275; ADN at 0, 20, 40, and 80; PN at 0, 20, 40, and 80."( Evaluation of the teratogenic potential of three aliphatic nitriles in the rat.
Berteau, PE; Johannsen, FR; Levinskas, GJ; Rodwell, DE, 1986
)
0.27
" The hepatic microsomal metabolizing activity for nitriles was at a maximum 13 h after ethanol dosing (4."( Influence of ethanol on the in vivo and in vitro metabolism of nitriles in mice.
Hashimoto, K; Tanii, H, 1986
)
0.27
" Although the data demonstrate stimulation of gastric output of acid and pepsin by certain doses of cysteamine or propionitrile, cysteamine produced dose-response increases in acid secretion only during the 1st hour following administration."( Secretory changes associated with chemically-induced duodenal ulceration: simultaneous measurements of acid, pepsin, base and pancreatic enzymes in rats with chronic gastric fistula.
Gallagher, GT; Szabo, S, 1984
)
0.48
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
polar aprotic solventA solvent with a comparatively high relative permittivity (or dielectric constant), greater than ca. 15, and a sizable permanent dipole moment, that cannot donate suitably labile hydrogen atoms to form strong hydrogen bonds.
[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 (2)

ClassDescription
volatile organic compoundAny organic compound having an initial boiling point less than or equal to 250 degreeC (482 degreeF) measured at a standard atmospheric pressure of 101.3 kPa.
aliphatic nitrileAny nitrile derived from an aliphatic compound.
[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 (5)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
AR proteinHomo sapiens (human)Potency27.05850.000221.22318,912.5098AID1259243
aldehyde dehydrogenase 1 family, member A1Homo sapiens (human)Potency35.48130.011212.4002100.0000AID1030
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency60.57640.003041.611522,387.1992AID1159555
retinoid X nuclear receptor alphaHomo sapiens (human)Potency24.33510.000817.505159.3239AID1159527
lethal factor (plasmid)Bacillus anthracis str. A2012Potency31.62280.020010.786931.6228AID912
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (2)

Assay IDTitleYearJournalArticle
AID19262Aqueous solubility2000Bioorganic & medicinal chemistry letters, Jun-05, Volume: 10, Issue:11
Prediction of drug solubility from Monte Carlo simulations.
AID1145366Octanol-water partition coefficient, log P of the compound1976Journal of medicinal chemistry, May, Volume: 19, Issue:5
Application of SCAP to drug design. 1. Prediction of octanol-water partition coefficients using solvent-dependent conformational analyses.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (77)

TimeframeStudies, This Drug (%)All Drugs %
pre-199031 (40.26)18.7374
1990's11 (14.29)18.2507
2000's23 (29.87)29.6817
2010's10 (12.99)24.3611
2020's2 (2.60)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 53.43

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 very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index53.43 (24.57)
Research Supply Index4.41 (2.92)
Research Growth Index4.42 (4.65)
Search Engine Demand Index85.14 (26.88)
Search Engine Supply Index2.01 (0.95)

This Compound (53.43)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews2 (2.47%)6.00%
Case Studies3 (3.70%)4.05%
Observational0 (0.00%)0.25%
Other76 (93.83%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]