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s-pentachlorobuta-1,3-dien-yl-cysteine

Description

S-pentachlorobuta-1,3-dien-yl-cysteine: nephrotoxic; structure given in first source [MeSH]

Cross-References

ID SourceID
PubMed CID3033729
MeSH IDM0117812

Synonyms (10)

Synonym
s-pentachlorobuta-1,3-dien-yl-cysteine
ccris 2171
l-cysteine, s-(1,2,3,4,4-pentachloro-1,3-butadienyl)-
s-(1,2,3,4,4-pentachloro-1,3-butadienyl)-l-cysteine
(2r)-2-amino-3-[(1e)-1,2,3,4,4-pentachlorobuta-1,3-dienyl]sulfanylpropanoic acid
5-(1,2,3,4,4-pentachloro-1,3-butadienyl)-l-cysteine
87619-82-7
s-pentachlorobutadienyl-l-cysteine
(s-pentachlorobutadienyl)-l-cysteine
s-(1,2,3,4,4-pentachloro-1,3- butadienyl)-l-cysteine

Research

Studies (18)

TimeframeStudies, This Drug (%)All Drugs %
pre-19907 (38.89)18.7374
1990's7 (38.89)18.2507
2000's1 (5.56)29.6817
2010's0 (0.00)24.3611
2020's3 (16.67)2.80

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (4.76%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other20 (95.24%)84.16%
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
aminooxyacetic acidamino acid;
hydroxylamines;
monocarboxylic acid
anticonvulsant;
EC 2.6.1.19 (4-aminobutyrate--2-oxoglutarate transaminase) inhibitor;
EC 4.2.1.22 (cystathionine beta-synthase) inhibitor;
nootropic agent
1987200231.5low012100
pyridoxalhydroxymethylpyridine;
methylpyridines;
monohydroxypyridine;
pyridinecarbaldehyde;
vitamin B6
cofactor;
Escherichia coli metabolite;
human metabolite;
mouse metabolite;
Saccharomyces cerevisiae metabolite
1988198836.0low010000
ureaisourea;
monocarboxylic acid amide;
one-carbon compound
Daphnia magna metabolite;
Escherichia coli metabolite;
fertilizer;
flour treatment agent;
human metabolite;
mouse metabolite;
Saccharomyces cerevisiae metabolite
1986198638.0low010000
p-aminohippuric acidN-acylglycineDaphnia magna metabolite1996199628.0low001000
anethole trithionemethoxybenzenes1996199628.0low001000
egtazic aciddiether;
tertiary amino compound;
tetracarboxylic acid
chelator2002200222.0low000100
hexachlorobutadieneorganochlorine compound1986199634.8medium042000
acetylcysteineacetylcysteine;
L-cysteine derivative;
N-acetyl-L-amino acid
antidote to paracetamol poisoning;
antiinfective agent;
antioxidant;
antiviral drug;
ferroptosis inhibitor;
geroprotector;
human metabolite;
mucolytic;
radical scavenger;
vulnerary
1986199732.5low011000
manganeseelemental manganese;
manganese group element atom
Escherichia coli metabolite;
micronutrient
202320231.0low000001
fura-22002200222.0low000100
homocysteineamino acid zwitterion;
homocysteine;
serine family amino acid
fundamental metabolite;
mouse metabolite
1990200228.0low001100
s-(1,1,2,2-tetrafluoroethyl)cysteine1990199034.0low002000
fura-2-am2002200222.0low000100
s-(2-chloro-1,1,2-trifluoroethyl)cysteine1990199034.0low001000
s-(1,2,3-trichlorovinyl)cysteine1997199727.0medium001000
tretinoinretinoic acid;
vitamin A
anti-inflammatory agent;
antineoplastic agent;
antioxidant;
AP-1 antagonist;
human metabolite;
keratolytic drug;
retinoic acid receptor agonist;
retinoid X receptor agonist;
signalling molecule
202320231.0low000001
tacrolimusmacrolide lactambacterial metabolite;
immunosuppressive agent
2002200222.0low000100
s-(1,2,3,4,4-pentachloro-1,3-butadienyl)glutathione1986199036.0high011000
sulfurchalcogen;
nonmetal atom
macronutrient1988198836.0low010000
cysteinecysteiniumfundamental metabolite1986200233.3high077100
s-(1,2-dichlorovinyl)cysteineS-(1,2-dichlorovinyl)-L-cysteine1990199729.7low003000
s-(1,2-dichlorovinyl)glutathionepeptide1990199034.0low001000
s-(1,2-dichlorovinyl)homocysteine1990200228.0high001100
n-acetyl-s-pentachloro-1,3-butadienylcysteine1986198638.0medium010000
ascorbic acidascorbic acid;
vitamin C
coenzyme;
cofactor;
flour treatment agent;
food antioxidant;
food colour retention agent;
geroprotector;
plant metabolite;
skin lightening agent
202320231.0low000001
ConditionIndicatedStudiesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
Cancer of Kidney01988198836.0medium010000
Glycosuria01996199628.0medium001000
Kidney Diseases01986199035.3high012000
Kidney Neoplasms01988198836.0medium010000
Necrosis01986199732.5high011000
Proteinuria01996199628.0medium001000

Safety/Toxicity (9)

ArticleYear
Biotransformation, excretion and nephrotoxicity of haloalkene-derived cysteine S-conjugates.
Archives of toxicology, , Volume: 72, Issue:1
1997
Assessment of the role of glutathione conjugation in the protection afforded by anethol dithiolthione against hexachloro-1,3-butadiene-induced nephrotoxicity.
Toxicology and applied pharmacology, , Volume: 139, Issue:1
1996
In vivo and in vitro nephrotoxicity of the cysteine conjugate of hexachlorobutadiene.
Journal of toxicology and environmental health, , Volume: 11, Issue:4-6
Nephrotoxicity of hexachlorobutadiene and its glutathione-derived conjugates.
Toxicologic pathology, , Volume: 14, Issue:2
1986
Toxicity of S-pentachlorobutadienyl-L-cysteine studied with isolated rat renal cortical mitochondria.
Archives of biochemistry and biophysics, , Nov-01, Volume: 258, Issue:2
1987
A mechanism of S-(1,2,3,4,4-pentachloro-1,3-butadienyl)-L-cysteine toxicity to rabbit renal proximal tubules.
Toxicology and applied pharmacology, , Sep-30, Volume: 90, Issue:3
1987
Cytotoxicity of S-(1,2,3,4,4-pentachlorobutadienyl)-L cysteine after apical and basolateral exposure of LLC-PK monolayers. Involvement of an amino acid transport system.
Chemico-biological interactions, , Volume: 75, Issue:1
1990
Renal cysteine conjugate beta-lyase-mediated toxicity studied with primary cultures of human proximal tubular cells.
Toxicology and applied pharmacology, , Volume: 103, Issue:3
1990
Pentachlorobutadienyl-L-cysteine (PCBC) toxicity: the importance of mitochondrial dysfunction.
Journal of biochemical toxicology, ,Winter, Volume: 6, Issue:4
1991