20 Results for "

proliferative disorders

" in MedChemExpress (MCE) Product Catalog:
Products (20)

20 Results for "proliferative disorders" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-124822
CAS No.: 73439-19-7
Purity:  99.73%
Target:  

AMPK

Research Areas:  

Metabolic Disease Cancer

COH-SR4 is an AMPK activator. COH-SR4 shows potent anti-proliferative activities against leukemia, melanoma, breast and lung cancers. COH-SR4 inhibits adipocyte differentiation via AMPK activation. COH-SR4 can be used for the research of obesity and related metabolic disorders .
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1
1 Cited Publications
Cat. No.: HY-108359
CAS No.: 237430-03-4
Purity:  99.85%
Synonyms: 9-Nitropaullone; NSC 705701
Target:  

CDK GSK-3 Apoptosis

Research Areas:  

Cancer

Alsterpaullone (9-Nitropaullone) is a potent CDK inhibitor, with IC50s of 35 nM, 15 nM, 200 nM and 40 nM for CDK1/cyclin B, CDK2/cyclin A, CDK2/cyclin E and CDK5/p35, respectively. Alsterpaullone also competes with ATP for binding to GSK-3alpha/GSK-3beta with IC50s of both 4 nM. Alsterpaullone has antitumor activity, and possesses potential for the study in neurodegenerative and proliferative disorders . Alsterpaullone induces apoptosis in leukemia cell line .
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1 Cited Publications
Cat. No.: HY-148489
CAS No.: 2468784-55-4
Purity:  99.23%
Target:  

Casein Kinase

Research Areas:  

Cancer

CSNK1-IN-1 is a CSNK1A1 inhibitor. CSNK1-IN-1 has inhibitory activity for CSNK1A1 kinase with IC50 values of 21 μM. CSNK1-IN-1 can be used for the research of proliferative disorders .
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Cat. No.: HY-148491
CAS No.: 2468783-76-6
Purity:  99.22%
Target:  

Casein Kinase

Research Areas:  

Cancer

CSNK1-IN-2 is a CSNK1A1 inhibitor. CSNK1-IN-1 has inhibitory activity for CSNK1A1 kinase with IC50 values of 44 nM. CSNK1-IN-2 can be used for the research of proliferative disorders .
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Cat. No.: HY-159647A
CAS No.: 2892065-49-3
Research Areas:  

Cancer

(S,S)-PLX-4545 (Compound I) is an orally active and cereblon-based molecular glue degrader of IKZF2 (zinc finger transcription factor Helios). (S,S)-PLX-4545 can be used for the study of IKZF2-mediated diseases or disorders, such as proliferative diseases or disorders and/or cancer .
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Cat. No.: HY-133095
CAS No.: 101439-76-3
Purity:  99.65%
Target:  

STAT PPAR

Research Areas:  

Inflammation/Immunology

BML-260 is a potent inhibitor of dual-specific phosphatases JSP-1 and DUSP22. BML-260 can activate UCP1 and thermogenesis in adipocytes in a JSP-1-independent manner. The effect of BML-260 on adipocytes is partially achieved through the activation of CREB, STAT3, and PPAR signaling pathways. BML-260 can be used in the research of inflammatory and proliferative disorders associated with JNK signaling dysfunction as well as obesity .
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Cat. No.: HY-118858
CAS No.: 1229591-56-3
Purity:  99.20%
Target:  

EAAT

Research Areas:  

Neurological Disease Cancer

UCPH-102 is a highly selective EAAT1 inhibitor with an IC50 of 0.43 µM. UCPH-102 exhibits a specific anti-proliferative effect on T-ALL cells. UCPH-102 also shows good blood-brain permeability, which can be used in studies of amyotrophic lateral sclerosis, Alzheimer’s disease, chronic pain and obsessive compulsive disorder .
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Cat. No.: HY-12812
CAS No.: 1548743-69-6
Purity:  99.40%
Research Areas:  

Neurological Disease Cancer

Autotaxin modulator 1 is an autotaxin (ATX) enzyme inhibitor, extracted from patent WO 2014018881 A1, Compound Example 12b. Autotaxin modulator 1 is expected to be useful for researching demyelination due to injury or disease, as well as for researching proliferative disorders such as cancer .
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Cat. No.: HY-153759
CAS No.: 686769-92-6
Purity:  ≥95.0%
Target:  

PPAR

Research Areas:  

Metabolic Disease

CRX000227 is a PPAR modulator. CRX000227 can be used for research of metabolic or cell proliferative disorders .
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Cat. No.: HY-137122
CAS No.: 32502-20-8
Target:  

PIN1

Research Areas:  

Inflammation/Immunology

3-Pyridine toxoflavin (compound 49) is a PIN1 inhibitor. 3-Pyridine toxoflavin can be used for the research of immune disease proliferative disorder .
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Cat. No.: HY-401475
CAS No.: 262433-52-3
Target:  

PKC

Protein kinase inhibitor 9 (Compound example 175) is an inhibitor of serine/threonine and tyrosine kinase activity. Protein kinase inhibitor 9 can be used for the research of cancer, hyper proliferative disorders, rheumatoid arthritis, disorders of the immune system, transplant rejections and imflammatory disorders .
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Cat. No.: HY-114700
CAS No.: 443872-20-6
Target:  

PPAR

ZINC08438472 is a potent and selective peroxisome proliferator activated receptors-α (PPAR-α) agonist with an EC50 value of 12.1 nM. ZINC08438472 is promising for research of diabetes, hyperlipidaemia and inflammatory disorders .
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Cat. No.: HY-135816
CAS No.: 292640-28-9
Target:  

Casein Kinase Pim

Research Areas:  

Inflammation/Immunology Cancer

CK2/PIM1-IN-1 is an inhibitor of CK2 and PIM1, with IC50s of 3.787 μM and 4.327 μM for CK2 and PIM1, respectively. CK2/PIM1-IN-1 is developed for the research of proliferative disorders such as cancer, as well as other kinase-associated conditions including inflammation, pain, vascular disorders, pathogenic infections and certain immunological disorders .
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Cat. No.: HY-153057
CAS No.: 380192-76-7
Research Areas:  

Metabolic Disease Cancer

PRMT5-IN-46 (compound 278) inhibits PRMT5 with IC50s of 1-10 μM. PRMT5 is a methyltransferase which is associated with specific genetic alterations. PRMT5-IN-46 can be used for research of proliferative diseases, metabolic disorders, and blood diseases .
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Cat. No.: HY-N11507
CAS No.: 2319668-87-4
Synonyms: TKV
Tibesaikosaponin V (TKV) is a triterpene diglycoside, which can be isolated from the methanol extract of the roots of Bupleurum chinense DC.. Tibesaikosaponin V inhibits lipid accumulation and triacylglycerol content occurred without cytotoxicity to adipocytes. Tibesaikosaponin V suppresses the mRNA expression of nuclear transcription factors, such as peroxisome proliferator-activated receptor γ (PPARγ) and CCAAT/enhancer binding protein α (C/EBPα). Tibesaikosaponin V inhibits 3T3-L1 preadipocyte differentiation. Tibesaikosaponin V can be used fro research of obesity and its associated metabolic disorders .
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Cat. No.: HY-184833
CAS No.: 2417137-50-7
Target:  

JAK STAT

Tyk2-IN-25 is a TYK2 inhibitor that binds to the JH2 domain of TYK2. Tyk2-IN-25 inhibits p-STAT4 and p-STAT3 in human peripheral blood mononuclear cells. Tyk2-IN-25 is applicable to research related to multiple diseases such as immune and inflammatory diseases, and neurological diseases .
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Cat. No.: HY-183856
CAS No.: 2570386-33-1
Target:  

MEK

Research Areas:  

Cancer

MEK4 IN-4 is a MEK4 inhibitor (IC50 = 0.041 μM) that inhibits the kinase catalytic activity of MEK4 via competitive blockade of ATP binding. MEK4 IN-4 can be used to investigate cell proliferative diseases and disorders associated with MEK4 activity, including cancer .
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Cat. No.: HY-150872
BRD9 ligand-3 is a BRD9 ligand. BRD9 ligand-3 serves as a PROTAC target protein ligand for the synthesis of PROTACs, such as PROTAC BRD9 Degrader-4 (HY-145403). BRD9 ligand-3 is applicable to cancer-related research .
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Cat. No.: HY-179687
CAS No.: 3108318-77-7
Target:  

JAK STAT

Research Areas:  

Cardiovascular Disease

JAK2-IN-18 (Compound example1) is a selective JAK2 inhibitor. JAK2-IN-18 can inhibit JAK-STAT signaling and shows an IC50 of <100 nM for pSTAT5 in HEL9217 cells. JAK2-IN-18 can inhibit the proliferation of abnormally proliferating myeloid cells and can be used for the research of myeloproliferative disorders, such as essential thrombocythemia .
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Cat. No.: HY-188017
CAS No.: 3060895-25-9
Target:  

ROCK

ROCK-IN-18 is a blood-brain barrier-permeable selective inhibitor of the ROCK2 protein kinase. ROCK-IN-18 is applicable to research related to cardiovascular diseases, neurological diseases, breast cancer, colon cancer, pancreatic cancer and other disorders .
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