YN481206 (3R,5S)-Atorvastatin sodium 131275-93-9

(3R,5S)-Atorvastatin sodium is an impurity of Atorvastatin. Atorvastatin is an orally active HMG-CoA reductase inhibitor, has the ability to effectively decrease blood lipids. Atorvastatin inhibits human SV-SMC proliferation...

YN470034 Paricalcitol 131918-61-1

Paricalcitol is avitamin D receptoragonist, used for the prevention and treatment of secondary hyperparathyroidism (excessive secretion of parathyroid hormone) associated with chronic renal failure.

YN360300 5-Hydroxylansoprazole 131926-98-2

5-Hydroxylansoprazole (AG1908) is an active metabolite of Lansoprazole in plasma. Lansoprazole is metabolized by CYP2C19 forming 5-Hydroxylansoprazole. Lansoprazole is a gastricproton-pumpinhibitor and is effective in the treat...

YN310251 Bisindolylmaleimide I 133052-90-1

Bisindolylmaleimide I (GF109203X) is a potent PKC inhibitor with IC50 of 20 nM, 17 nM, 16 nM, and 20 nM for PKCα, PKCβI, PKCβII, and PKCγ in cell-free assays, respectively, showing more than 3000-fold select...

YN1720034 Avexitide 133514-43-9

Avexitide (Exendin (9-39)) is a specific and competitive antagonist of glucagon-like peptide-1 (GLP-1) receptor.

YN483487 Soyasaponin Ac 133882-74-3

Soyasaponin Ac is a triterpenoid isolated from the seeds of Glycine max.

YN372824 Atorvastatin 134523-00-5

Atorvastatin is an orally activeHMG-CoAreductase inhibitor, has the ability to effectively decrease blood lipids. Atorvastatin inhibits human SV-SMC proliferation and invasion with IC50s of 0.39μM and 2.39μM, respectiv...

YN372431 Atorvastatin hemicalcium salt 134523-03-8

Atorvastatin Calcium is an inhibitor of HMG-CoA reductase used as a cholesterol-lowering medication that blocks the production of cholesterol.

YN440442 GIP (1-30) amide, porcine 134846-93-8

GIP (1-30) amide, porcine is a full glucose-dependent insulinotropic polypeptide (GIP) receptor agonist with high affinity equal to native GIP(1-42).

YN483079 6''-O-Acetylglycitin 134859-96-4

6''-O-Acetylglycitin, a acetyl glucoside, is one of the isoflavone isomer in soybeans, shows various extents of content reduction dependent on storage temperature, packaging condition, and its isoflavone isomer kind.

YN372636 Meluadrine tartrate 134865-37-5

Meluadrine tartrate is an endogenous metabolite.

YN481424 Repaglinide 135062-02-1

Repaglinide is a potassium channel blocker, which lowers blood glucose by stimulating the release of insulin from the pancreas, used the treatment of type II diabetes.

YN321129 Strontium Ranelate 135459-87-9

Strontium Ranelate (S12911) is an antiosteoporotic agent that acts by reducing bone resorption and promoting bone formation, thereby inducing a positive bone balance. Strontium Ranelate also can activate thecalcium-sensing receptor (...

YN484121 Amylin (8-37), human 135702-23-7

Amylin (8-37), human is a fragment of human Amylin. Amylin (8-37), human can direct vasodilator effects in the isolated mesenteric resistance artery of the rat. Human Amylin is a small hormone secreted by pancreatic β-cells that forms...

YN483956 IGF-I (24-41) 135861-49-3

IGF-I (24-41) is amino acids 24 to 41 fragment of Insulin-like Growth Factor I (IGF-I). IGF-I is partly responsible for systemic GH activities although it possesses a wide number of own properties (anabolic, antioxidant, a...

YN370314 Fidarestat 136087-85-9

Fidarestat (SNK 860) is an inhibitor ofaldose reductase, with IC50s of 26nM, 33μM, and 1.8μM for aldose reductase, AKR1B10 and V301L AKR1B10, respectively; Fidarestat (SNK 860) has the potential to treat diabeti...

YN320196 Lintitript 136381-85-6

Lintitript (SR 27897) is a highly potent, selective, orally active, competitive and non-peptidecholecystokinin (CCK1) receptorantagonist with an EC50 of 6nM and a Ki of 0.2nM. Lintitript displays > 33-fold selectivity more s...

YN370175 RP 70676 136609-26-2

RP 70676 is a potent inhibitor ofACAT, with IC50 of 25 and 44nM for rat and rabbit ACAT.

YN480044 RP 73163 Racemate 136609-53-5

RP 73163 Racemate is the racemate of RP 73163. RP 73163 is a potentACATinhibitor, with cholesterol lowering activity.

YN481539 NB-598 hydrochloride 136719-25-0

NB-598 hydrochloride is a potent and competitive inhibitor ofsqualene epoxidase (SE), and suppresses triglyceride biosynthesis through the farnesol pathway.