calcium

Calcium Carbonate is the carbonic salt of calcium (CaCO3).

Calcium Channel antagonist 4 is a voltage-gated calcium channel inhibitor (IC50 : 5-20 μM).

Calcium Channel antagonist 3 is a voltage-gated calcium channel inhibitor (IC50 : 5-20 μM).

(3S,5R)-Pitavastatin calcium is the enantiomer of Pitavastatin which is a potent HMG-CoA reductase inhibitor.

(3S,5S)-Pitavastatin calcium is the 3-epimer of Pitavastatin which is a potent HMG-CoA reductase inhibitor.

Calcium 2-oxoglutarate, an intermediate in the production of GTP or ATP in the Krebs cycle, is a reversible inhibitor of tyrosinase (IC50: 15 mM).

Gemcabene calcium , a first-in-class lipid-lowering agent, lowers low-density lipoprotein cholesterol (LDL-C), decreases triglycerides, and raises high-density lipoprotein cholesterol (HDL-C) andexerting anti-inflammatory activity, lowers pro-inflammatory acute-phase protein, C-reactive protein (CRP).

N-type calcium channel blocker-1 is an orally active analgesic agent with a high affinity for functionally blocking N-type calcium channels.

(Z)-Pitavastatin calcium is the Z-isomer of Pitavastatin hemicacium and a potent inhibitor of hydroxymethylglutaryl-CoA (HMG-CoA) reductase.

Rosuvastatin-D6 Calcium is deuterium labeled Rosuvastatin Calcium (TMSM-3411), which is a competitive HMG-CoA reductase inhibitor (IC50 of 11 nM).

Calcium Stearate is a potent Alternative to Poly(vinyl alcohol) in Poly-Lactic-co-Glycolic Acid Nanoparticles Synthesis.

Calcium 4-Oxopentanoate (calcium levulinate) is an orally effective calcium supplement commonly used as a food additive. In the liver, it is reduced to form 4-hydroxypentanoate, a process enhanced by ethanol. Calcium 4-Oxopentanoate is also employed in studies related to calcium deficiency.

Bumadizone Calcium, a non-steroidal anti-inflammatory drug, is used to treat pain and arthritis.

Lonazolac Calcium, a nonsteroidal anti-inflammatory drug (NSAID), is used to treat inflammation and pain.

Calcium decanoate is a biochemical.

Calcium lignosulfonate is a granulating agent for limestone and ores, compaction aid for coal and metal wastes and also dispersing agent for gypsum and clay slurries.

Dicalcium phosphate is the calcium phosphate with the formula CaHPO4 and its dihydrate. The "di" prefix in the common name arises because the formation of the HPO42– anion involves the removal of two protons from phosphoric acid, H3PO4. It is al

Levomefolate calcium pentahydrate is the calcium salt of 5-methyltetrahydrofolic acid, a biologically active form of folic acid that functions, in conjunction with Vitamin B12. Levomefolate is included in formulations of certain oral contraceptives to ens

Calcium gluconate monohydrate is a useful organic compound for research related to life sciences. The catalog number is T35350 and the CAS number is 66905-23-5.

Ciprostene is the 9β-methyl analog of carbaprostacyclin and a stable analog of PGI2. Ciprostene exhibits biological activity similar to PGI2, but is 30-fold less potent. In patas monkeys, ciprostene induces hypotension and causes tachycardia when administered at a dose of 0.16 μg/kg/min. In addition, ciprostene inhibits ADP-induced platelet aggregation ex vivo and in vitro with ID50 values of 9.1 μg/kg/min and 60 ng/ml, respectively.

DMNPE-4 AM-caged-calcium, a photolabile analogue of EGTA, is a highly efficient Ca2+-selective cage. At pH 7.2 and pH 7.4, its Kd for Ca2+ is measured at 48 nM and 19 nM, respectively. Upon photolysis, DMNPE-4 AM-caged-calcium exhibits a decreased affinity for Ca2+ (~2 nM Kd).

Aspirin calcium is the prototypical analgesic used in the treatment of mild to moderate pain. It has anti-inflammatory and antipyretic properties and acts as an inhibitor of cyclooxygenase which results in the inhibition of the biosynthesis of prostaglandins. Aspirin also inhibits platelet aggregation and is used in the prevention of arterial and venous thrombosis. (From Martindale, The Extra Pharmacopoeia, 30th ed, p5)

IS-741 calcium is a phospholipase A2 inhibitor.

Calcium Channel antagonist 2 is a calcium channel antagonist (IC50=5-20 μM) that can be used to study diseases due to Ca2+ channels like pain and diabetes.