Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN481681 Emixustat hydrochloride 1141934-97-5
Emixustat hydrochloride strongly inhibits 11-cis-retinol production with IC50 values of 232 ± 3nM. Emixustat hydrochloride is a novel visual cycle modulator, in healthy volunteers. Oral Emixustat was safe and well t...
AM-1638 is a potent and orally bioavailableGPR40/FFA1full agonist with an EC50 of 0.16μM.
YN483676 Neopuerarin A 1150314-34-3
Neopuerarin A is an isoflavones isolated from the water extraction of the dried roots ofPueraria lobata(Willd.). Neopuerarin A shows significant hepatoprotective effect.
YN483677 Neopuerarin B 1150314-39-8
Neopuerarin B is an isoflavones isolated from the water extraction of the dried roots ofPueraria lobata(Willd.). Neopuerarin B shows significant hepatoprotective effect.
YN360529 Lesinurad sodium 1151516-14-1
Lesinurad (Selexipag, RDEA-594) sodium (Zurampic) is a selective uric acid reabsorption inhibitor (SURI) under investigation for treatment of gout. Lesinurad sodium inhibits the uric acid transporter URAT1 and ...
YN420325 AMPK activator 1 1152423-98-7
AMPK activator 1 is anAMPKactivator extracted from patent WO2013116491A1, compound No.1-75, has an EC50 of <0.1μM.
A 1120 is a high-affinity nonretinoidretinol-binding protein 4 (RBP4)antagonist with aKivalue of 8.3nM. A 1120 disrupts the interaction between RBP4 and its binding partner transthyretin.
YN483866 RETF-4NA 1160928-63-1
RETF-4NA, a chymase-specific substrate, is a sensitive and selective substrate for chymase when free or bound to α2M.
YN372584 BAY-85-8501 1161921-82-9
BAY-85-8501 is a selective, reversible and potent inhibitor ofHuman Neutrophil Elastase (HNE), with an IC50 of 65 pM.
AZD7687 is a potent, selective, reversible and orally activediacylglycerol acyltransferase 1 (DGAT1)inhibitor with an IC50 of 80nM forhuman DGAT1. AZD7687 can be used for type 2 diabetes mellitus and obesity research.
YN482906 9''-Methyl salvianolate B 1167424-31-8
9''-Methyl salvianolate B is a phenolic compound isolated from RadixSalvia miltiorrhizae.
YN320434 ALB-127158(a) 1173154-32-9
ALB-127158(a) is a potent and selective melanin concentrating hormone 1 (MCH1) receptor antagonist.
YN372266 EMD638683 1181770-72-8
EMD638683 is a highly selective inhibitor of serum- and glucocorticoid-inducible kinase 1 (SGK1) with IC50 of 3 μM. EMD638683 exhibits antihypertensive potency and anti-tumor activity.
YN372268 EMD638683 S-Form 1184940-46-2
EMD638683 S-Form is the S-form of EMD638683. EMD638683 is a highly selectiveSGK1inhibitor with IC50 of 3μM.
YN372267 EMD638683 R-Form 1184940-47-3
EMD638683 R-Form is the R-form of EMD638683. EMD638683 is a highly selectiveSGK1inhibitor with IC50 of 3μM.
YN420071 Metformin D6 hydrochloride 1185166-01-1
Metformin D6 hydrochloride is a deuterium labeled Metformin hydrochloride. Metformin hydrochloride inhibits themitochondrial respiratory chainin the liver, leading to activation ofAMPK, enhancing insulin sensitivity for type 2 diabe...
YN483442 Steviol-19-O-glucoside 1185737-16-9
Steviol-19-O-glucoside is a metabolite of steviol in the steviol glycosides biosynthesis pathway inStevia rebuadiana.
DBPR108 is a potent, selective, and orally bioavailable dipeptide-derived inhibitor of DPP4 with IC50 of 15nM; no inhibition on DDP8 and DPP9. DBPR108 is an IC50=15nM DPP IV inhibitor displays a more than 300...
ML-109 is a potent and full thyroid stimulating hormone receptor (TSHR) agonist, with an EC50of 40nM.
YN321491 Loperamide D6 hydrochloride 1189469-46-2
Loperamide D6 hydrochloride (R-18553 D6 hydrochloride) is a deuterium labeled Loperamide hydrochloride. Loperamide hydrochloride is anopioid receptoragonist for the treatment of diarrhea.
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