45 Results for "

Compound+39

" in MedChemExpress (MCE) Product Catalog:
Products (45)

45 Results for "Compound+39" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-151460
CAS No.: 2396465-33-9
Purity:  99.92%
Research Areas:  

Cancer

GCN2-IN-7 (compound 39) is an orally active and selective general control nonderepressible 2 (GCN2) inhibitor (IC50=5 nM). GCN2-IN-7 shows anti-tumor activity in vivo .
1
1 Cited Publications
Cat. No.: HY-141873
CAS No.: 943820-93-7
Purity:  99.70%
Target:  

Wnt β-catenin

Research Areas:  

Others

Wnt/β-catenin agonist 2 is a potent Wnt agonist. Wnt/β-catenin agonist 2 activates Wnt/β-catenin signaling and can be used in the research of diseases related to the signal transduction . (From patent WO2007078113A1, compound 39)
Cat. No.: HY-130119
CAS No.: 2378617-67-3
Target:  

Integrin

Research Areas:  

Cancer

Integrin-IN-2 (compound 39) is an orally bioavailable pan αv integrin inhibitor. Integrin-IN-2 can increases the αvβ6, αvβ3, αvβ5 and αvβ8 binding affinities with pIC50 values of 7.8, 8.4, 8.4 and 7.4, respectively .
Cat. No.: HY-162661
CAS No.: 2989271-65-8
Target:  

P2Y Receptor

Research Areas:  

Inflammation/Immunology

P2Y14R antagonist 2 (compound 39) is a potent, selective and orally active P2Y14R antagonist with an IC50 value of 0.40 nM. P2Y14R antagonist 2 shows anti-inflammatory activity. P2Y14R antagonist 2 has the potential for the research of colitis .
Cat. No.: HY-147651
CAS No.: 2353536-67-9
Purity:  99.84%
Target:  

β-catenin CDK c-Myc

Research Areas:  

Cancer

β-catenin-IN-4 (Compound 39) is a β-catenin inhibitor with a Ki of 0.64 μM. β-catenin-IN-4 reduces the protein expression levels of cyclin D1 and c-Myc .
Cat. No.: HY-177506
CAS No.: 158459-39-3
Research Areas:  

Metabolic Disease

FE100726 (Compound 39) is a Cholecystokinin 2 (CCK2) receptor agonist. FE100726 has a superior binding capacity on CCK2 receptor. FE100726 can induce gastric acid secretion in anaesthetized rat models. FE100726 can be used for diabetes research .
Cat. No.: HY-112913
CAS No.: 2169316-15-6
Purity:  99.73%
Target:  

CRAC Channel

SOCE inhibitor 1 (Compound 39) is a store-operated calcium entry (SOCE) inhibitor with an IC50 of 4.4 μM. SOCE inhibitor 1 has a good stability in plasma .
Cat. No.: HY-144809
CAS No.: 194235-21-7
Purity:  99.92%
Research Areas:  

Metabolic Disease

Pancreatic lipase/Carboxylesterase 1-IN-1 (Compound 39) is a potent dual inhibitor of pancreatic lipase (PL) and human carboxylesterase 1A (hCES1A) with IC50 values of 2.13 µM and 0.055  µM against PL and hCES1A .
Cat. No.: HY-N10158
CAS No.: 207792-17-4
Target:  

Drug Derivative

Research Areas:  

Cancer

1,7-Bis(4-hydroxyphenyl)-3-hydroxy-1,3-heptadien-5-one (compound 39), a diarylheptanoid, exhibits antiproliferative activity towards human HT-1080 fibrosarcoma and murine colon 26-L5 carcinoma cells .
Cat. No.: HY-170973
Target:  

Opioid Receptor

KOR agonist 4 (compound 39) is an agonist of Kappa Opioid Receptor. KOR agonist 4 is an activator of G-protein signaling. KOR agonist 4 binds with GTPγS with an EC50 of 14 nM and with an Emax of 83 %. KOR agonist 4 demonstrates moderate to high intrinsic clearance in human hepatocytes. KOR agonist 4 exhibits 60- and 810-fold selectivities versus the related mu (MOR) and delta (DOR) opioid receptors. KOR agonist 4 is potential for central nervous system (CNS) disorders research .
Cat. No.: HY-162124
CAS No.: 2898381-63-8
Target:  

NAMPT HDAC

Research Areas:  

Cancer

HDAC/NAMPT-IN-1 (compound 39h) is a dual inhibitor of HDAC and NAMPT with IC50 values of 0.72-37081 nM and 1618 nM .
Cat. No.: HY-144603
CAS No.: 2773476-40-5
Neuropeptide Y Y1 receptor antagonist 1 (compound 39), a fluorescent probe, is a potent antagonist of neuropeptide Y Y 1 receptor (Y 1R), with a Ki of 0.19 nM .
Cat. No.: HY-163656
CAS No.: 2957874-18-7
Research Areas:  

Cancer

MAT2A inhibitor 5(compound 39) is an orally active, selectivity and blood-brain permeability inhibitor of MAT2A with the IC50 of 11 nM. MAT2A inhibitor 5 inhibits tumor cell growth in vivo .
Cat. No.: HY-172896
Target:  

Ferroptosis

Research Areas:  

Cancer

FSP1-IN-1 (compound 39) is a potent FSP1 inhibitor with an IC50 of 35 nM. FSP1-IN-1 enhances RSL3 (HY-100218A)-induced lipid peroxide accumulation and sensitizes cancer cells to ferroptosis .
Cat. No.: HY-163282
Research Areas:  

Cancer

NB512 (compound 39a) is a dual inhibitor for BET and HDAC, which exhibits a efficient binding affinity with BRD4 bromodomains and HDAC1/2, with EC50s of 100-400 nM. NB512 exhibits an anti-proliferative activity towards cancer cells PaTu8988T and NMC .
Cat. No.: HY-178289
CAS No.: 2901788-26-7
Research Areas:  

Cancer

Fmoc-Val-Lys(Boc)-PAB-Exatecan (Compound 39-7) is a Drug-Linker Conjugates for ADC. Fmoc-Val-Lys(Boc)-PAB-Exatecan consists of the ADC Cytotoxin Exatecan (HY-13631) and a linker PAB-Val-Lys-Boc (HY-138651). Fmoc-Val-Lys(Boc)-PAB-Exatecan can be used for synthesis of ADCs .
Cat. No.: HY-P3346
CAS No.: 2891469-80-8
Target:  

Apelin Receptor (APJ)

Research Areas:  

Cardiovascular Disease

NH2-c[X-R-L-S-X]-K-G-P-(D-1Nal) (compound 39) is a potent APJ agonist, with a Ki of 0.6 nM. NH2-c[X-R-L-S-X]-K-G-P-(D-1Nal) can activate Gαi1 (EC50=0.8 nM) and recruit β-arrestin2 (EC50=31 nM). NH2-c[X-R-L-S-X]-K-G-P-(D-1Nal) exhibits prolonged cardiac effects .
Cat. No.: HY-157103
CAS No.: 1313602-85-5
Target:  

ICMT

Research Areas:  

Cancer

ICMT-IN-34 (compound 39) is an inhibitor of ICMT (IC50=0.17 μM) .
Cat. No.: HY-156370
Target:  

Tyrosinase

Research Areas:  

Cancer

Tyrosinase-IN-15 (Compound 39) is a tyrosinase inhibitor (IC50: 7.12 μM, Ki: 11.8 μM) .
Cat. No.: HY-118403
CAS No.: 300675-28-9
Target:  

Casein Kinase

CK2-IN-12 (Compound 39) is an inhibitor for protein kinase CK2 with an IC50 of 0.8 μM .