Table of Contents
12 relations: Energy, Glucuronic acid, Glucuronidase, Glucuronidation, Glycoside, Glycosidic bond, Kidney, Miquelianin, Morphine-6-glucuronide, Quercetin, Scutellarin, Solubility.
- Glucuronides
- Toxicology stubs
Energy
Energy is the quantitative property that is transferred to a body or to a physical system, recognizable in the performance of work and in the form of heat and light.
Glucuronic acid
Glucuronic acid (from Greek γλεῦκος "sweet wine, must" and οὖρον "urine") is a uronic acid that was first isolated from urine (hence the name "uronic acid").
See Glucuronide and Glucuronic acid
Glucuronidase
Glucuronidase may refer to several enzymes.
See Glucuronide and Glucuronidase
Glucuronidation
Glucuronidation is often involved in drug metabolism of substances such as drugs, pollutants, bilirubin, androgens, estrogens, mineralocorticoids, glucocorticoids, fatty acid derivatives, retinoids, and bile acids.
See Glucuronide and Glucuronidation
Glycoside
In chemistry, a glycoside is a molecule in which a sugar is bound to another functional group via a glycosidic bond.
Glycosidic bond
A glycosidic bond or glycosidic linkage is a type of ether bond that joins a carbohydrate (sugar) molecule to another group, which may or may not be another carbohydrate.
See Glucuronide and Glycosidic bond
Kidney
In humans, the kidneys are two reddish-brown bean-shaped blood-filtering organs that are a multilobar, multipapillary form of mammalian kidneys, usually without signs of external lobulation.
Miquelianin
Miquelianin (quercetin 3-O-glucuronide) is a flavonol glucuronide, a type of phenolic compound present in wine, in species of St John's wort, like Hypericum hirsutum, in Nelumbo nucifera (Indian lotus) or in green beans.
See Glucuronide and Miquelianin
Morphine-6-glucuronide
Morphine-6-glucuronide (M6G) is a major active metabolite of morphine.
See Glucuronide and Morphine-6-glucuronide
Quercetin
Quercetin is a plant flavonol from the flavonoid group of polyphenols.
Scutellarin
Scutellarin is a flavone, a type of phenolic chemical compound.
See Glucuronide and Scutellarin
Solubility
In chemistry, solubility is the ability of a substance, the solute, to form a solution with another substance, the solvent.
See Glucuronide and Solubility
See also
Glucuronides
- Ethyl glucuronide
- Glucuronide
Toxicology stubs
- Agada
- Amurca
- Antagonism (chemistry)
- Antireticular cytotoxic serum
- Automatism (toxicology)
- Benthiocarb
- Burton's line
- Cardiotoxicity
- Cholinesterase reactivator
- Committee on Toxicity
- Dermatotoxin
- Ethel Browning (toxicologist)
- European Union System for the Evaluation of Substances
- Fish sting
- Fixed-dose procedure
- Genitotoxin
- Gerontogens
- Glucuronide
- Hepatotoxin
- Hydrocarbon poisoning
- Jamaican vomiting sickness
- Kalium Database
- LT50
- Lowest published toxic dose
- Lowest-observed-adverse-effect level
- MKOFTEN
- MafB toxins
- Margin of exposure
- Marinobufagenin
- Maurice Zeeman
- Measured environmental concentration
- Median toxic dose
- Mouse ear swelling test
- Mouse unit
- No-observed-adverse-effect level
- Predicted environmental concentration
- Reed–Muench method
- Romen Sova
- Scillitoxin
- Superwarfarin
- Threshold of toxilogical concern
- Total gaseous mercury
- Toxicophore
- Up-and-down procedure
- Virtually safe dose
References
Also known as Alpha-D-glucuronoside, Glucuronide conjugation, Glucuronides, Glucuronopyranoside, Glucuronopyranosides, Glucuronoside.