Page last updated: 2024-11-05

sym-trinitrobenzene

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

Description

Trinitrobenzenes: Benzene derivatives which are substituted with three nitro groups in any position. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

1,3,5-trinitrobenzene : A trinitrobenzene in which each of the nitro groups is meta- to the other two. [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 CID7434
CHEBI ID48113
SCHEMBL ID212845
MeSH IDM0093340

Synonyms (54)

Synonym
1,3,5-trinitro-benzene
1,3,5-trinitrobenzene
benzene,1,3,5-trinitro-
nsc36931
wln: wnr cnw enw
trinitrobenzol
99-35-4
benzene, trinitro- (wet)
syn-trinitrobenzene
1,5-trinitrobenzene
trinitrobenzeen
trinitrobenzene, dry
trinitrobenzene
s-trinitrobenzene
TNB ,
trinitrobenzene, wet
nsc-36931
einecs 202-752-7
nsc 36931
rcra waste no. u234
trinitrobenzene, dry or wetted with < 30% water, by mass
un1354
ccris 3093
rcra waste number u234
ai3-08924
trinitrobenzol [german]
un0214
benzite
hsdb 6005
benzene, 1,3,5-trinitro-
symmetric trinitrobenzene
trinitrobenzeen [dutch]
2,4,6-trinitrobenzene
sym-trinitrobenzene
1,3,5-trinitrobenzol
CHEBI:48113
trinitrobenzenes
AKOS001092692
FT-0654261
T0496
2h75703r1x ,
unii-2h75703r1x
trinitrobenzene, wetted with not <30% water, by mass [un1354] [flammable solid]
trinitrobenzene, dry or wetted with <30% water, by mass
trinitrobenzene, dry or wetted with <30% water, by mass [un0214] [explosive 1.1d]
trinitrobenzene, wetted with not <30% water, by mass
sym-trinitrobenzene [mi]
SCHEMBL212845
DTXSID6021406
Z57056418
Q420320
1,3,5-trinitrobenzene (min 30wt% water)
106 - explosives in groundwater
65 - explosives in groundwater

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" No adverse effects were noted in mating or fertility indices."( Reproductive toxicity screen of 1,3,5-trinitrobenzene administered in the diet of Sprague-Dawley rats.
Caldwell, DJ; Flemming, CD; Kinkead, ER; Marit, GB; Miller, CR; Wolfe, RE,
)
0.13
" For the TK6 and V79 assays, TNB and 2, 4,6-triaminotoluene were more toxic than TNT, whereas RDX and HMX were without effect at their maximal aqueous solubility limits."( Cytotoxic and genotoxic effects of energetic compounds on bacterial and mammalian cells in vitro.
Ampleman, G; Hawari, J; Lachance, B; Robidoux, PY; Sunahara, GI; Thiboutot, S, 1999
)
0.3
" alterations in this endpoint may result in adverse effects on the organism and could be used as an early indicator of toxicity."( Toxicity of sediment-associated nitroaromatic and cyclonitramine compounds to benthic invertebrates.
Bridges, TS; Farrar, JD; Inouye, LS; Lotufo, GR; Ringelberg, DB, 2001
)
0.31
" In vitro, the toxic concentration 50% (TC50) of TNB, which induced cell death, was 16 microM following a 24-h exposure."( Effects of 1,3,5-Trinitrobenzene on cytotoxicity and metabolic activity of type I astrocytes of rats.
Quails, CW; Reddy, G; Ritchey, JW; Saliki, JT; Stair, EL,
)
0.13
" Similar to previous investigations, the high reactivity of the spiked compound hampered determination of accurate toxic concentrations of TNT and related compounds, and of the nature of toxicological interaction of compounds in a mixture in this study."( Comparative and mixture sediment toxicity of trinitrotoluene and its major transformation products to a freshwater midge.
Farrar, JD; Lotufo, GR, 2005
)
0.33
"2 mg L(-1)) was more toxic than TNT to SHM."( Toxicity of trinitrotoluene to sheepshead minnows in water exposures.
Blackburn, WM; Gibson, AB; Lotufo, GR, 2010
)
0.36

Bioavailability

ExcerptReferenceRelevance
" Tests were conducted in Sassafras sandy loam soil, which supports relatively high bioavailability of nitroaromatic EMs."( Toxicities of dinitrotoluenes and trinitrobenzene freshly amended or weathered and aged in a sandy loam soil to Enchytraeus crypticus.
Checkai, RT; Kolakowski, JE; Kuperman, RG; Kurnas, CW; Phillips, CT; Simini, M, 2006
)
0.33

Dosage Studied

ExcerptRelevanceReference
" Family studies of secondary TNP-conjugate proliferative responses demonstrated a gene dosage effect in this phenomenon."( Human immune responses to hapten-conjugated cells. II. The roles of autologous and allogeneic histocompatibility determinants in proliferative responses in vitro.
Dupont, B; Rich, RR; Seldin, MF, 1979
)
0.26
" The differentiative nature of this signal was inferred from the threshold dose-response relationship and the insensitivity of the TH-directed event to the antimitotic agent vinblastine."( Subpopulations of splenic T cells regulating an anti-hapten antibody response. II. Distinct functions of, and sequential requirement for, helper and amplifier cells.
Cudkowicz, G; Muirhead, DY, 1978
)
0.26
" Polystyrene beads with diameters of 3 to 15 mu caused target lysis, with a dose-response curve which typically went through a maximum and declined at high bead numbers."( Target cell lysis by cytotoxic T lymphocytes redirected by antibody-coated polystyrene beads.
Henkart, PA; Kolber, MA; Quinones, RR, 1989
)
0.28
" The mechanism of the effect of T3 is unknown, but the lack of effect on delayed hypersensitivity to SRBC implies that T3 (when administered at the dosage of the present protocol) acts on only some immune cells and does not exert a generalized adjuvant effect."( The effect of triiodothyronine on evanescent delayed hypersensitivity to sheep red blood cells and on the primary antibody response to trinitrophenylated Brucella abortus in severely undernourished weanling mice.
Berdusco, E; Filteau, SM; Perry, KJ; Woodward, B, 1987
)
0.27
" coli lipopolysaccharide (TNP-LPS) complexed with mouse IgG antibody to TNP specifically gave rise to a marked production of rheumatoid-like factors (RF) in the recipient mice, in contrast to the low and nonspecific RF production via polyclonal B cell activation by the same dosage of LPS or TNP-LPS alone."( Induction of rheumatoid factors in mice by immune complexes of bacterial lipopolysaccharide with mouse IgG antibody.
Hino, T; Kanoh, M; Utsumi, S, 1986
)
0.27
"Complement (C)-dependent hemolytic dose-response curves of anti-TNP IgG2b and IgM monoclonal antibodies as a function of TNP density were analyzed: sheep red cells coupled with TNP served as targets."( Mouse monoclonal antibodies at the red cell surface--II. Effect of hapten density on complement fixation and activation.
Borsos, T; Isliker, H; Kratz, HJ, 1985
)
0.27
" A carrier-specific state of tolerance, induced at a dosage which was shown not to generate significant suppressor cell activity, was associated with minimal alterations in the affinity of the primary anti-hapten PFC response."( Studies on the control of antibody synthesis. XVII. Effect of specific suppressor cells on the affinity of the antibody response by naive or primed lymphocytes.
Dekruyff, RH; Furie, RA; Siskind, GW, 1980
)
0.26
" Both gene dosage effects and Ir-gene-product interaction could influence the generation of specific immune responsiveness in F1 hybrids between high and low responders to TNP-MSA."( Two distinct high immune response phenotypes are both controlled by H-2 genes mapping K or I-A.
Hildemann, WH; Wicker, LS, 1981
)
0.26
"5 mM per 10(8) spleen cells revealed no differences in the dose-response curves of lpr splenocytes for both tolerance and suppression when compared with those of the CBA."( The induction of tolerance and suppression in autoimmune MRL mice using hapten-modified self.
Pisetsky, DS; Santoro, TJ; Scott, DW, 1981
)
0.26
" Rats dosed at 35."( Testicular effects of 1,3,5-trinitrobenzene (TNB). I. Dose response and reversibility studies.
Chandra, AM; Qualls, CW; Reddy, G, 1997
)
0.3
"Male and female Fischer-344 (F-344) and male NCI-Black-Reiter (NBR) rats were dosed with 0, 35."( 1,3,5-Trinitrobenzene-induced alpha-2u-globulin nephropathy.
Kim, S; Qualls, CW; Reddy, G; Stair, EL,
)
0.13
" This data was used to explain bell-shaped dose-response curves observed for antihapten antibody formation in response to haptenated LPS."( Absence of lipopolysaccharide high-dose paralysis in B-cell responses: implications for the one-signal theory.
Hodgkin, PD; Mamchak, AA, 2000
)
0.31
" The electrolytic experiments were carried out to elucidate the influence of various operating parameters on the performance of mineralization of total organic compounds (TOC) in spent acid, including electrode potential, reaction temperature, oxygen dosage and concentration of sulfuric acid."( Electrochemical destruction of dinitrotoluene isomers and 2,4,6-trinitrotoluene in spent acid from toluene nitration process.
Chen, WS; Liang, JS, 2009
)
0.35
" It was also found that as with DMBA, DBC produced a persistent immunosuppression, which lasted for at least 4 wk following dosing with a novel pill method for self-administration of DBC."( Dibenzo[def,p]chrysene (DBC) suppresses antibody formation in spleen cells following oral exposures of mice.
Burchiel, SW; Lauer, FT; Walker, MK, 2013
)
0.39
" Myrrh extract reduced intestinal muscle tone and acetylcholine-induced contraction of untreated and inflamed ileum/jejunum preparations based on dual calcium antagonism characterized by a right shift of the agonistic dose-response curve and a depression of the maximum effect."( Antispasmodic effects of myrrh due to calcium antagonistic effects in inflamed rat small intestinal preparations.
Goos, KH; Goos, O; Nieber, K; Vissiennon, C, 2015
)
0.42
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
explosiveA substance capable of undergoing rapid and highly exothermic decomposition.
[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 (1)

ClassDescription
trinitrobenzene
[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 (1,502)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901093 (72.77)18.7374
1990's211 (14.05)18.2507
2000's113 (7.52)29.6817
2010's72 (4.79)24.3611
2020's13 (0.87)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 6.84

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 Index6.84 (24.57)
Research Supply Index7.35 (2.92)
Research Growth Index4.19 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (6.84)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews28 (1.80%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other1,524 (98.20%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]