citrate lyase

cit·rate ly·ase

citrate (pro-3S)-lyase; an enzyme that catalyzes the cleavage of citrate to oxaloacetate and acetate, in the absence of coenzyme A.
References in periodicals archive ?
They are supposed to contain 75% hydroxycitric acid, which is said to promote weight loss "because it blocks citrate lyase - the chemical responsible for storing carbohydrates in the body as fat".
HCAP(TM), after permeation through the skin, is digested into HCA by the action of an enzyme inside cells, inhibiting the activity of ATP citrate lyase.
Nerush even includes garcinia cambogia, an amazing botanical element that could potentially reduce appetites by inhibiting a fat enzyme in our bodies called citrate lyase.
Clinical studies on Citrin exhibit that HCA can help to reduce the appetite, promote satiety, help the burning of fat stored in the body, as well as inhibit new fat formation by the unique citrate lyase inhibition of HCA, which competes with citric acid to bind with the citrate lyase enzyme.
The accumulated pyruvate enters the gaba shunt pathway and is converted to citrate which is acted upon by citrate lyase and converted to acetyl CoA, used for cholesterol synthesis.
Both tissues had very low abundance for ATP citrate lyase.
2 carboxykinase 1 Glyceraldehyde-3-phosphate BTU85042 dehydrogenase ATP citrate lyase BC108138.
The Schiff's bases and their metal complexes of the present invention are useful for the modulation of metal-activated enzymes and metalloenzymes, such as Phenylalanine Hydroxylase, Tyrosine Transaminase, Phenylalanine Transaminase, Tyrosinase, various MMP (Matrix metalloproteases), Superoxide dismutase, 5-Alpha Reductase, and citrate lyase.
The key ingredient in Garcinia Cambogia is called Hydroxycitric Acid (HCA), which works in the body to inhibit the production of citrate lyase, an enzyme that the body utilizes to help turn carbohydrates into fat.
HCA blocks fat by inhibiting a key enzyme that your body needs to make fat from carbohydrates: Citrate lyase.
ETC-1002 is an investigational, once-daily, oral small molecule therapy that has been shown to be liver selective for activation of AMP kinase and inhibition of ATP citrate lyase.