Page last updated: 2024-09-24

phenylglycine nitrile

Description

phenylglycine nitrile: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID76372
CHEMBL ID1229843
SCHEMBL ID197012
MeSH IDM0444749

Synonyms (45)

Synonym
einecs 221-129-0
n-phenylglycinenitrile
ai3-02755
acetonitrile, phenylamino-
brn 2206191
nsc 7611
CHEMBL1229843
xbn69be6x2 ,
unii-xbn69be6x2
ec 221-129-0
3009-97-0
acetonitrile, anilino-
1-anilinoacetonitrile
nsc7611
wln: nc1mr
glycinonitrile, n-phenyl-
acetonitrile, (phenylamino)-
phenylglycine nitrile
anilinoacetonitrile
(phenylamino)acetonitrile
nsc-7611
n-(cyanomethyl)aniline
2-anilinoacetonitrile
AKOS000253573
HMS1719B17
A820195
2-(phenylamino)acetonitrile
n-phenylglycinonitrile
FT-0634598
SCHEMBL197012
n-cyanomethylaniline
KAXCEFLQAYFJKV-UHFFFAOYSA-N
mfcd00044430
W-106957
n-phenylglycinonitrile, aldrichcpr
acetonitrile, anilino- (8ci)
DTXSID80184175
Z56347332
phenylaminoacetonitril
EN300-16652
STR05177
H12014
Q27452740
acetonitrile, 2-(phenylamino)-
CS-W021451

Bioassays (4)

Assay IDTitleYearJournalArticle
AID588519A screen for compounds that inhibit viral RNA polymerase binding and polymerization activities2011Antiviral research, Sep, Volume: 91, Issue:3
High-throughput screening identification of poliovirus RNA-dependent RNA polymerase inhibitors.
AID540299A screen for compounds that inhibit the MenB enzyme of Mycobacterium tuberculosis2010Bioorganic & medicinal chemistry letters, Nov-01, Volume: 20, Issue:21
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.
AID1640019Luciferase/luciferin-expressing antifolate-resistant parasites were used to infect a culture of HepG2 cells that were pre-incubated with compounds. Infected hepatocytes emit light due to the luciferase reaction. Assay results are presented as the percent 2018Science (New York, N.Y.), 12-07, Volume: 362, Issue:6419
Open-source discovery of chemical leads for next-generation chemoprotective antimalarials.
AID1640018Luciferase/luciferin-expressing antifolate-resistant parasites were used to infect a culture of HepG2 cells that were pre-incubated with compounds. Infected hepatocytes emit light due to the luciferase reaction. Assay results are presented as the percent 2018Science (New York, N.Y.), 12-07, Volume: 362, Issue:6419
Open-source discovery of chemical leads for next-generation chemoprotective antimalarials.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (6)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (16.67)29.6817
2010's5 (83.33)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

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%
Other6 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]