| Substance | Relationship Strength | Studies | Trials | Classes | Roles |
|---|
ethylene chlorohydrin
Ethylene Chlorohydrin: Used as a solvent, in the manufacture of insecticides, and for treating sweet potatoes before planting. May cause nausea, vomiting, pains in head and chest, stupefaction. Irritates mucous membranes and causes kidney and liver degeneration.. chloroethanol : An organochlorine compound that is ethanol substituted by at least one chloro group. | 2.52 | 2 | 0 | chloroethanol | xenobiotic metabolite |
aminooxyacetic acid
Aminooxyacetic Acid: A compound that inhibits aminobutyrate aminotransferase activity in vivo, thereby raising the level of gamma-aminobutyric acid in tissues.. (aminooxy)acetic acid : A member of the class of hydroxylamines that is acetic acid substituted at postion 2 by an aminooxy group. It is a compound which inhibits aminobutyrate aminotransferase activity in vivo, resulting in increased levels of gamma-aminobutyric acid in tissues. | 2.88 | 4 | 0 | amino 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 |
pyruvic acid
Pyruvic Acid: An intermediate compound in the metabolism of carbohydrates, proteins, and fats. In thiamine deficiency, its oxidation is retarded and it accumulates in the tissues, especially in nervous structures. (From Stedman, 26th ed). pyruvic acid : A 2-oxo monocarboxylic acid that is the 2-keto derivative of propionic acid. It is a metabolite obtained during glycolysis. | 1.96 | 1 | 0 | 2-oxo monocarboxylic acid | cofactor;
fundamental metabolite |
1,10-phenanthroline
1,10-phenanthroline: RN given refers to parent cpd; inhibits Zn-dependent metalloproteinases | 1.96 | 1 | 0 | phenanthroline | EC 2.7.1.1 (hexokinase) inhibitor;
EC 3.4.19.3 (pyroglutamyl-peptidase I) inhibitor |
probenecid
Probenecid: The prototypical uricosuric agent. It inhibits the renal excretion of organic anions and reduces tubular reabsorption of urate. Probenecid has also been used to treat patients with renal impairment, and, because it reduces the renal tubular excretion of other drugs, has been used as an adjunct to antibacterial therapy.. probenecid : A sulfonamide in which the nitrogen of 4-sulfamoylbenzoic acid is substituted with two propyl groups. | 1.96 | 1 | 0 | benzoic acids;
sulfonamide | uricosuric drug |
acetylene
[no description available] | 6.98 | 1 | 0 | alkyne;
gas molecular entity;
terminal acetylenic compound | |
trichloroacetic acid
Trichloroacetic Acid: A strong acid used as a protein precipitant in clinical chemistry and also as a caustic for removing warts.. trichloroacetic acid : A monocarboxylic acid that is acetic acid in which all three methyl hydrogens are substituted by chlorine. | 2.99 | 4 | 0 | monocarboxylic acid;
organochlorine compound | carcinogenic agent;
metabolite;
mouse metabolite |
trichloroethylene
Trichloroethylene: A highly volatile inhalation anesthetic used mainly in short surgical procedures where light anesthesia with good analgesia is required. It is also used as an industrial solvent. Prolonged exposure to high concentrations of the vapor can lead to cardiotoxicity and neurological impairment.. triol : A chemical compound containing three hydroxy groups. | 5.22 | 11 | 1 | chloroethenes | inhalation anaesthetic;
mouse metabolite |
chlorotrifluoroethylene
[no description available] | 1.96 | 1 | 0 | | |
dichloroacetic acid
[no description available] | 2.99 | 4 | 0 | monocarboxylic acid;
organochlorine compound | astringent;
marine metabolite |
2,2,2-trichloroethanol
[no description available] | 2.52 | 2 | 0 | chloroethanol | mouse metabolite |
isoxazoles
Isoxazoles: Azoles with an OXYGEN and a NITROGEN next to each other at the 1,2 positions, in contrast to OXAZOLES that have nitrogens at the 1,3 positions.. isoxazole : A monocyclic heteroarene with a structure consisting of a 5-membered ring containing three carbon atoms and an oxygen and nitrogen atom adjacent to each other. It is the parent of the class of isoxazoles.. isoxazoles : Oxazoles in which the N and O atoms are adjacent. | 2.66 | 3 | 0 | isoxazoles;
mancude organic heteromonocyclic parent;
monocyclic heteroarene | |
glycylglycine
[no description available] | 1.96 | 1 | 0 | dipeptide zwitterion;
dipeptide | human metabolite |
acetylcysteine
N-acetyl-L-cysteine : An N-acetyl-L-amino acid that is the N-acetylated derivative of the natural amino acid L-cysteine. | 2.68 | 3 | 0 | acetylcysteine;
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 |
dichloroacetylene
[no description available] | 6.98 | 1 | 0 | organochlorine compound | |
1,7-phenanthroline
[no description available] | 1.96 | 1 | 0 | phenanthroline | |
homocysteine
Homocysteine: A thiol-containing amino acid formed by a demethylation of METHIONINE.. homocysteine : A sulfur-containing amino acid consisting of a glycine core with a 2-mercaptoethyl side-chain.. L-homocysteine : A homocysteine that has L configuration. | 1.97 | 1 | 0 | amino acid zwitterion;
homocysteine;
serine family amino acid | fundamental metabolite;
mouse metabolite |
s-(1,1,2,2-tetrafluoroethyl)cysteine
S-(1,1,2,2-tetrafluoroethyl)cysteine: toxic to human proximal tubular cells | 2.39 | 2 | 0 | | |
s-(2-chloro-1,1,2-trifluoroethyl)cysteine
S-(2-chloro-1,1,2-trifluoroethyl)cysteine: nephrotoxic cpd | 1.97 | 1 | 0 | | |
s-(1,2,3-trichlorovinyl)cysteine
S-(1,2,3-trichlorovinyl)cysteine: structure given in first source; RN given refers to (L)-isomer; RN for cpd without isomeric designation not avail 3/92 | 2.01 | 1 | 0 | | |
acivicin
[no description available] | 2.66 | 3 | 0 | isoxazoles;
non-proteinogenic L-alpha-amino acid;
organochlorine compound | antileishmanial agent;
antimetabolite;
antimicrobial agent;
antineoplastic agent;
EC 2.3.2.2 (gamma-glutamyltransferase) inhibitor;
glutamine antagonist;
metabolite |
s-pentachlorobuta-1,3-dien-yl-cysteine
S-pentachlorobuta-1,3-dien-yl-cysteine: nephrotoxic; structure given in first source | 1.97 | 1 | 0 | | |
cysteine
Cysteine: A thiol-containing non-essential amino acid that is oxidized to form CYSTINE.. L-cysteinium : The L-enantiomer of cysteinium.. cysteine : A sulfur-containing amino acid that is propanoic acid with an amino group at position 2 and a sulfanyl group at position 3. | 4.14 | 16 | 0 | cysteinium | fundamental metabolite |
s-(1,2-dichlorovinyl)cysteine
S-(1,2-dichlorovinyl)cysteine: RN given refers to (L-Cys)-isomer; structure given in first source. S-(cis-1,2-dichlorovinyl)-L-cysteine : An S-(1,2-dichlorovinyl)-L-cysteine in which the dichlorovinyl group has cis- (Z-) geometry. | 4.08 | 15 | 0 | S-(1,2-dichlorovinyl)-L-cysteine | |
s-1,2-dichlorovinyl-n-acetylcysteine
S-1,2-dichlorovinyl-N-acetylcysteine: urinary metabolite of trichloroethylene in mice | 2.42 | 2 | 0 | | |
s-(1,2-dichlorovinyl)homocysteine
S-(1,2-dichlorovinyl)homocysteine: RN given refers to (E)-isomer | 1.97 | 1 | 0 | | |
phenylalanylglycine
phenylalanylglycine: RN given refers to (DL)-isomer. Phe-Gly : A dipeptide formed from L-phenylalanine and glycine residues. | 1.96 | 1 | 0 | dipeptide | metabolite |
adenosine kinase
Adenosine Kinase: An enzyme that catalyzes the formation of ADP plus AMP from adenosine plus ATP. It can serve as a salvage mechanism for returning adenosine to nucleic acids. EC 2.7.1.20. | 2.03 | 1 | 0 | | |