Chemical structure
Cat.No.
Product Name
CAS no.
Target
EX229 (compound 991) is a potent AMPK activator that is 5-10-fold more potent than A769662 in activating AMPK.
YN372722 Acarbose sulfate 1221158-13-9
Acarbose (BAY g 5421) sulfate, antihyperglycemic agent, is an orally activealpha-glucosidaseinhibitor (IC50=11nM). Acarbose sulfate can potentiate the hypoglycemic effects of sulfonylureas or insulin .
GSK2033 is aLXRantagonist with pIC50s of 7 and 7.4 forLXRαorLXRβ, respectively.
YN370868 Evogliptin tartrate 1222102-51-3
Evogliptin tartrate is a potent, orally bioavailable and selectivedipeptidyl peptidase-4 (DPP-4)inhibitor, with antidiabetic activity. Evogliptin tartrate has potential for anti-atherosclerosis therapy that targets arterial inflammat...
YN372369 Omarigliptin 1226781-44-7
Omarigliptin (MK-3102) is a competitive, reversible inhibitor of DPP-4 (IC50 = 1.6 nM, Ki = 0.8 nM). It is highly selective over all proteases tested (IC50 > 67 μM), including QPP, FAP, PEP, DPP8, and DPP9 and...
YN360784 Nateglinide D5 1227666-13-8
Nateglinide D5 is a deuterium labeled Nateglinide. Nateglinide, a D-phenylalanine derivative, is an orally active and short-acting insulinotropic agent and aDPP IVinhibitor. Nateglinide inhibits ATP-sensitiveK+channels in...
YN320510 PF-04634817 1228111-63-4
PF-0463481 is a potent and orally active dualCCR2/CCR5antagonist with comparable human and rodent CCR2 potency (ratIC50=20.8nM), and displays 10-20 fold less rodent CCR5 potency (ratIC50=470nM). PF-0463481 is saf...
YN300027 Pyrintegrin 1228445-38-2
Pyrintegrin is anβ1-integrinagonist and a 2,4-disubstituted pyrimidine that promotes embryonic stem cells survival. Pyrintegrin enhances cell-extracellular matrix (ECM) adhesion-mediatedintegrinsignaling. Pyrintegrin can be used as...
YN484109 Biotin-TAT (47-57) 1231898-25-1
Biotin-TAT (47-57), a biotin tagged TAT, is a transactivator of transcription. Biotin-TAT (47-57) is one of the most widely used protein transduction domains (PTDs) into different primary cells is ATP- and temperature-dep...
YN420139 Ampkinone 1233082-79-5
Ampkinone is an indirect AMP-activated protein kinase (AMPK) activator.
YN371568 Globalagliatin 1234703-40-2
LY2608204 activates glucokinase (GK) with EC50 of 42 nM. Phase 2.
YN320433 GPR120 Agonist 2 1234844-11-1
GPR120 Agonist 2 is aGPR120agonist extracted from patent US 20110313003 A1, example 209.
YN480672 D5D-IN-326 1236767-85-3
D5D-IN-326 is a selective, orally activedelta-5 desaturase (D5D)inhibitor, with IC50s of 72 and 22nM for rat and human D5D in enzymic and cell-based assays, respectively, has no effect on D6D or D9D activity. D5D-IN...
YN374006 Soluble epoxide hydrolase inh... 1241826-88-9
Soluble epoxide hydrolase inhibitor is an inhibitor ofsoluble epoxide hydrolase, and inhibits human soluble epoxide hydrolase (h-sEH) withpIC50 of 8.4, extracted from patent WO 2010096722 A1, example 57.
YN360630 (3S,5R)-Rosuvastatin 1242184-42-4
(3S,5R)-Rosuvastatin is the (3S,5R)-enantiomer of Rosuvastatin. Rosuvastatin is a competitive HMG-CoAreductase inhibitor with an IC50 of 11nM. Rosuvastatin potently blockshuman ether-a-go-go related gene (hERG)current wit...
YN320838 Glucocorticoid receptor agoni... 1245526-82-2
Glucocorticoid receptor agonist is a potent Glucocorticoid receptor agonist.
YN370412 PF-04937319 1245603-92-2
PF-04937319 is a glucokinase activator (GKA) withEC50value of 154.4 μM, one of the most promising strategies for the treatment of type 2 diabetes mellitus. PF-04937319 is designed to maintain glucose-lowering efficacy while mit...
YN1720010 TT-OAD2 free base 1246826-07-2
TT-OAD2 free base is a non-peptideglucagon-like peptide-1 (GLP-1) receptoragonist with an EC50 of 5nM. TT-OAD2 free base has the potential for diabetes treatment.
YN410089 Curcumin D6 1246833-26-0
Curcumin D6 (Diferuloylmethane D6) is a deuterium labeled Curcumin (Turmeric yellow). Curcumin (Turmeric yellow) is a natural phenolic compound with diverse pharmacologic effects including anti-inflammatory, antioxidant, antiprolife...
TM38837 is a peripheral selectivecannabinoid receptor type 1 (CB1)receptor antagonist. TM38837 shows limited penetrance to the brain in order to minimize or prevent CNS adverse reactions, and preserves potential antiobesity effec...
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