Page last updated: 2024-11-08

lgc 40863

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

Description

LGC 40863: one of the pyrimidinyl-oxy-benzoate herbicides; structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID178117
SCHEMBL ID118872
MeSH IDM0290458

Synonyms (34)

Synonym
pyribenzoxim
(benzhydrylideneamino) 2,6-bis[(4,6-dimethoxypyrimidin-2-yl)oxy]benzoate
pyribenzoxim [iso:bsi]
unii-vbd478968p
vbd478968p ,
o-(2,6-bis((4,6-dimethoxy-2-pyrimidinyl)oxy)benzoyl)oxime
benzophenone o-(2,6-bis(4,6-dimethoxypyrimidin-2-yloxy)benzoyl)oxime
lgc 40863
lgc-40863
pyanchor
168088-61-7
benzophenone o-(2,6-bis((4,6-dimethoxypyrimidin-2-yl)oxy)benzoyl) oxime
AKOS015913761
pyribenzoxim [iso]
kiljabi gold
methanone, diphenyl-, o-(2,6-bis((4,6-dimethoxy-2-pyrimidinyl)oxy)benzoyl)oxime
diphenylmethanone o-(2,6-bis((4,6-dimethoxy-2-pyrimidinyl)oxy)benzoyl)oxime
SCHEMBL118872
DTXSID2057996
A1-01910
pyribenzoxim, pestanal(r), analytical standard
AS-73635
(diphenylmethylidene)amino 2,6-bis[(4,6-dimethoxypyrimidin-2-yl)oxy]benzoate
benzophenone o-(2,6-bis((4,6-dimethoxypyrimidin-2-yl)oxy)benzoyl)oxime
pyribenzoxim 100 microg/ml in acetonitrile
diphenylmethanone o-(2,6-bis((4,6-dimethoxypyrimidin-2-yl)oxy)benzoyl) oxime
mfcd09751192
OVXMBIVWNJDDSM-UHFFFAOYSA-N
methanone, diphenyl-, o-[2,6-bis[(4,6-dimethoxy-2-pyrimidinyl)oxy]benzoyl]oxime
Q27291746
pyanchor; o-(2,6-bis(4,6-dimethoxypyrimidin-2-yloxy)benzoyl)oxime benzophenone
A882195
CS-0065630
HY-116489

Research Excerpts

Pharmacokinetics

ExcerptReferenceRelevance
" The elimination half-lives of radioactivity from tissues was in the range of 7 to 77 h and Tmax values of 12, 24 and 12 h were observed for blood, liver and kidney, respectively."( In vivo pharmacokinetics of pyribenzoxim in rats.
Kang, SH; Kim, JH; Koo, SJ; Lee, HS; Liu, KH; Moon, JK; Sung, HJ, 2001
)
0.31

Bioavailability

ExcerptReferenceRelevance
" These results demonstrate that the bioavailability of LGC-40863 is negligible."( Pharmacokinetic analysis for assessing developmental toxicity of a new synthetic acetolactate synthase inhibitor, LGC-40863, in rats.
Ahn, SC; Cho, JH; Chung, MK; Han, SS; Roh, JK; Shim, HO; Shin, HC, 1998
)
0.3

Dosage Studied

ExcerptRelevanceReference
"2% at the lowest dosage level but not at higher dosages."( Pharmacokinetic analysis for assessing developmental toxicity of a new synthetic acetolactate synthase inhibitor, LGC-40863, in rats.
Ahn, SC; Cho, JH; Chung, MK; Han, SS; Roh, JK; Shim, HO; Shin, HC, 1998
)
0.3
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (8)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's1 (12.50)18.2507
2000's4 (50.00)29.6817
2010's2 (25.00)24.3611
2020's1 (12.50)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%
Other8 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]