Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN370765 10Z-Nonadecenoic acid 73033-09-7
10Z-Nonadecenoic acid is a kind of long-chain fatty acid with anti-tumor activity.
YN373037 Praeruptorin B 73069-28-0
Praeruptorin B is an inhibitor of sterol regulatory element-binding proteins(SREBPs).
YN250606 1-Deoxynojirimycin hydrochlor... 73285-50-4
1-Deoxynojirimycin hydrochloride (Duvoglustat hydrochloride) is a potent and orally activeα-glucosidaseinhibitor. 1-Deoxynojirimycin hydrochloride suppresses postpr and ial blood glucose and is widely used for diabetes mellitus. 1-D...
COH-SR4 is anAMPKactivator. COH-SR4 shows potent anti-proliferative activities against leukemia, melanoma, breast and lung cancers. COH-SR4 inhibits adipocyte differentiation via AMPK activation, and is promising ...
YN250710 Mevastatin 73573-88-3
Mevastatin is a competitive inhibitor of HMG-Coenzyme A (HMG-CoA) reductase with a binding affinity 10,000 times greater than the HMG-CoA substrate itself.
YN250911 Omeprazole 73590-58-6
Omeprazole is a proton pump inhibitor, used to treat dyspepsia, peptic ulcer disease, gastroesophageal reflux disease, laryngopharyngeal reflux, and Zollinger–Ellison syndrome.
YN483890 Adrenocorticotropic Hormone ... 73724-75-1
Adrenocorticotropic Hormone (ACTH) (18-39), human TFA is a corticotropinlike intermediate lobe peptide, which is is produced in the melanotrophs of the intermediate lobe of the pituitary.
YN470036 Calcitriol Impurities A 73837-24-8
Calcitriol Impurities A is the impurity of Calcitriol, Calcitriol is the hormonally active form of vitamin D, Calcitriol is the active metabolite of vitamin D3 that activates the vitamin D receptor (VDR).
YN440419 Metadoxine 74536-44-0
Metadoxine, also known as pyridoxine-pyrrolidone carboxylate, is a drug used to treat chronic and acute alcohol intoxication.
YN370768 CE(20:5(5Z,8Z,11Z,14Z,17... 74892-97-0
CE(20:5(5Z,8Z,11Z,14Z,17Z) is an endogenous metabolite.
YN370983 Lovastatin hydroxy acid sodiu... 75225-50-2
Lovastatin hydroxy acid sodium (Mevinolinic acid sodium) is a highly potent inhibitor of HMG-CoA reductase with a Ki of 0.6nM.
AZ-1355 is an effctive lipid-lowering compound, which also inhibits platelet aggregation in vivo and elevates the prostagl and in I2/thromboxane A2ratio in vitro.
YN320241 (Rac)-WAY-161503 75704-24-4
(Rac)-WAY-161503 is a potent, selective, highly affinity5-HT2Creceptoragonist with a Ki of 4nM and an EC50of 12nM. (Rac)-WAY-161503 displays higher affinity for 5-HT2Cthan 5-HT2A and 5-HT2Breceptors. (Rac)-WAY...
YN373249 Momordicoside A 75801-95-5
Momordicoside A is isolated fromMomordica charantia L. Momordicoside A has the inhibitory effect onprotein tyrosine phosphatase (PTP1B).
YN321804 Pancreatic Polypeptide, huma... 75976-10-2
Pancreatic Polypeptide, human is a C-terminally amidated 36 amino acid peptide, which acts as aneuropeptide Y(NPY)Y4/Y5receptor agonist.
YN373379 6-Methoxytricin 76015-42-4
6-Methoxytricin (Compound 6) is an flavonoid isolated fromArtemisia iwayomogi. 6-Methoxytricin (Compound 6) is an inhibitor on aldose reductase (AR) and advanced glycation endproduct (AGE) formation activities with IC50 values...
YN482073 Mildronate 76144-81-5
Mildronate (Meldonium) functions as a cardioprotective drug by cpmpetetively inhibitingBBOX1 and OCTN2. Mildronate (Meldonium) exhibitsIC50 values of 34-62μM for human recombinant BBOX and an EC50 of 21μM for human...
YN374325 1-Myristoyl-2-stearoyl-sn-gly... 76343-22-1
1-Myristoyl-2-stearoyl-sn-glycero-3-phosphocholine is an endogenous metabolite.
YN373231 Dihydrocurcumin 76474-56-1
Dihydrocurcumin, a major metabolites of curcumin, reduces lipid accumulation and oxidative stress. Dihydrocurcumin regulates mRNA and protein expression levels of SREBP-1C, PNPLA3 and PPARα, increases protein expr...
Mifobate (SR-202) is a potent and specific PPARγ with Kdapp of. Mifobate (SR-202) selectively inhibits Thiazolidinedione (TZD)-induced PPARγ transcriptional activity (IC50=140μM). Mifobate (SR-202) does not aff...
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