Page last updated: 2024-11-05

cyanophenphos

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

Description

cyanophenphos: RN given refers to cpd without isomeric designation [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID25669
CHEMBL ID2271087
CHEBI ID82112
SCHEMBL ID119236
MeSH IDM0043097

Synonyms (62)

Synonym
13067-93-1
o-ethyl o-4-cyanophenyl phenylphosphonothioate
ent 25,832-a
experimental insecticide s-4087
ai3-25832
stauffer b-10094
(+)-phenylphosphonothioic acid o-(4-cyanophenyl) o-ethyl ester
cyanofenphos [iso]
b-10094
phosphonothioic acid, phenyl-, o-ethyl ester, o-ester with p-hydroxybenzonitrile
cp 19699
(+)-cyanofenphos
(+-)-phenylphosphonothioic acid o-(4-cyanophenyl) o-ethyl ester
brn 2945855
o-p-cyanophenyl o-ethyl phenyl-phosphonothioate
phosphonothioic acid, phenyl-, o-(4-cyanophenyl) o-ethyl ester, (+-)-
o-ethyl phenylphosphonothioate, o-ester with p-hydroxybenzonitrile
upjohn u-32714
(-)-phenylphosphonothioic acid o-(4-cyanophenyl) o-ethyl ester
s 4087
surecide
phosphonothioic acid, phenyl-, o-(4-cyanophenyl) o-ethyl ester
(+-)-cyanofenphos
monsanto cp-19699
cyanofenphos
o-(4-cyanophenyl) o-ethyl phenylphosphonothioate
ent 25,832
(-)-cyanofenphos
phenylphosphonothioic acid, o-(4-cyanophenyl) o-ethyl ester
phenylphosphonothioic acid o-ethyl ester o-ester with p-hydroxybenzonitrile
phosphonothioic acid, phenyl-, o-(4-cyanophenyl) o-ethyl ester, (+)-
benzonitrile, p-hydroxy-, o-ester with o-ethyl phenylphosphonothioate
cyanophenphos
phosphonothioic acid, phenyl-, o-(4-cyanophenyl) o-ethyl ester, (-)-
CYP ,
s-4087 ,
4-[ethoxy(phenyl)phosphinothioyl]oxybenzonitrile
C18973
unii-1x6jv2ne2n
1x6jv2ne2n ,
62421-62-9
62421-63-0
phosphonothioic acid, phenyl-, 4-cyanophenyl ethyl ester
34460-46-3
62421-61-8
CHEMBL2271087
chebi:82112 ,
(rs)-(o-4-cyanophenyl o-ethyl phenylphosphonothioate)
o-(4-cyanophenyl) o-ethyl p-phenylphosphonothioate
cyanofenphos [mi]
SCHEMBL119236
LRNJHZNPJSPMGK-UHFFFAOYSA-N
oms 870
surazon
b 10094
o-ethyl o-(4-cyanophenyl) phenylphosphonothioate
DTXSID5041805
J-005854
cyanofenphos 10 microg/ml in isooctane
Q26841289
cyanofenphos 1000 microg/ml in acetone
cyanofenphos 1000 microg/ml in methanol

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" The oral LD50 for formulated cyanofenphos was 700 mg/kg in the control hens and 1170 mg/kg in the hens pretreated with 10 mg/kg daily for 8 days."( Protective effect of pretreatment against the acute toxicity of formulated cyanofenphos in hens.
Fukushima, M; Konno, N; Yamaguchi, Y; Yamauchi, T, 1984
)
0.27

Dosage Studied

ExcerptRelevanceReference
"The susceptibility of wild mallard ducklings to the delayed neurotoxic effect of the neurotoxic organophosphorus insecticides cyanofenphos and leptophos was evaluated following a daily dosing regimen."( Delayed neurotoxicity in the wild mallard duckling caused by the organophosphorus insecticides cyanofenphos and leptophos.
Ahmed, NS; el-Bakary, AS; el-Gendy, KS; el-Sebae, AH; Soliman, SA, 1986
)
0.27
" Surviving ducks of this group completely recovered from the cholinergic effect 2 or 3 d after finishing the dosing regimen."( Delayed neuropathy in adult Peking ducks induced by some organophosphorus esters.
Farmer, JD; Soliman, SA, 1984
)
0.27
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (2)

ClassDescription
nitrileA compound having the structure RC#N; thus a C-substituted derivative of hydrocyanic acid, HC#N. In systematic nomenclature, the suffix nitrile denotes the triply bound #N atom, not the carbon atom attached to it.
benzenesAny benzenoid aromatic compound consisting of the benzene skeleton and its substituted derivatives.
[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]

Research

Studies (10)

TimeframeStudies, This Drug (%)All Drugs %
pre-199010 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)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: 11.96

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 Index11.96 (24.57)
Research Supply Index2.48 (2.92)
Research Growth Index4.45 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.96)

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%
Other11 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]