169 Results for "

Pyrazole

" in MedChemExpress (MCE) Product Catalog:
Products (169)

169 Results for "Pyrazole" in MCE Product Catalog:

Cat. No.: HY-W002461
CAS No.: 2458-26-6
3-Phenyl-1H-pyrazole is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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Cat. No.: HY-182458
CAS No.: 949560-05-8
Target:  

c-Met/HGFR

Domaines de recherche:  

Cancer

GNE-203 is a heterobicyclic pyrazole compound and receptor tyrosine kinase inhibitor targeting c-Met.GNE-203 can be used for the research of cancer .
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Cat. No.: HY-10179R
CAS No.: 827318-97-8
Synonyms: PHA-739358 (Standard)
Domaines de recherche:  

Cancer

Danusertib (Standard) is the analytical standard of Danusertib. This product is intended for research and analytical applications. Danusertib is a pyrrolo-pyrazole and aurora kinase inhibitor with IC50 of 13, 79, and 61 nM for Aurora A, B, and C, respectively.
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Cat. No.: HY-143296
Target:  

SphK

Domaines de recherche:  

Cancer

SphK1-IN-1 (compound 48) is a SphK1 inhibitor with effective antitumor activity. SphK1-IN-1 inhibits SphK1 ATPase with an IC50 value of 4.02 μM. SphK1-IN-1 can be used for the research of cancer .
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Cat. No.: HY-149530
CAS No.: 3055550-22-3
Pureté:  99.92%
Target:  

EGFR Apoptosis

Domaines de recherche:  

Cancer

EGFR-IN-86 (compound 4i) is an EGFR inhibitor (IC50: 1.5 nM) with high activity against glioblastoma. EGFR-IN-86 induces apoptosis and arrests the U87 cell cycle in the G2/M phase .
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Cat. No.: HY-11087
CAS No.: 271576-80-8
Pureté:  98.73%
Synonyms: SD-06
Target:  

p38 MAPK Autophagy

Domaines de recherche:  

Inflammation/Immunology

SD 0006 (SD-06) is an orally active, selective, ATP-competitive and potent diaryl pyrazole inhibitor of p38α MAP kinase, with an IC50 of 110 nM for p38α .
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Cat. No.: HY-120122
CAS No.: 1446352-67-5
Pureté:  99.11%
Target:  

MDM-2/p53

Domaines de recherche:  

Cancer

PK7088 is a pyrazole and a specific peptide. PK7088 supports the reactivation of mutant p53 by converting it to a form exhibiting wild-type properties. PK7088 exhibit anticancer activity in cancer research .
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Cat. No.: HY-133726R
CAS No.: 581809-46-3
Domaines de recherche:  

Infection

Bixafen (Standard) is the analytical standard of Bixafen. This product is intended for research and analytical applications. Bixafen, a member of the pyrazole class of fungicides, serves as a broad-spectrum agent for controlling pathogens in cereal crops by functioning as a succinate dehydrogenase inhibitor.
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Cat. No.: HY-148481
CAS No.: 2755995-01-6
Target:  

Deubiquitinase

Domaines de recherche:  

Cancer

USP7-IN-10 (compound 1) is a potent ubiquitin-specific protease 7 (USP7) inhibitor, with an IC50 of 13.39 nM .
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Cat. No.: HY-151618
CAS No.: 2750233-50-0
Target:  

Apoptosis

Domaines de recherche:  

Cancer

Antitumor agent-79 shows good antiproliferative activities against hepatocellular carcinoma and breast cancer cells with IC50 values of 0.7-7.9 μM. Antitumor agent-79 induces cancer cells apoptosis and shows in vivo antitumor effects. Antitumor agent-79 can be used for the research of cancer .
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Cat. No.: HY-145568A
CAS No.: 2340299-00-3
Target:  

Kallikrein

Domaines de recherche:  

Cardiovascular Disease Metabolic Disease

Feniralstat (compound 30) hydrochloride, a pyrazole derivative, is a potent kallikrein inhibitor with an IC50 of 6.7 nM for Human plasma kallikrein (pKal). Feniralstat has no inhibition on Human KLKl, Human FXIa, Human Factor Xlla (all IC50>40 μM) .
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Cat. No.: HY-136633
CAS No.: 447399-55-5
Pureté:  99.80%
Domaines de recherche:  

Others

Pyroxasulfone is a broad-spectrum pyrazole Herbicide. Pyroxasulfone is effective against a variety of annual grass weeds and some broadleaf weeds. Pyroxasulfone causes reduced plant height, decreased above-ground dry weight and yield loss in pinto beans and red Mexican beans .
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Cat. No.: HY-111108R
CAS No.: 1964515-43-2
Domaines de recherche:  

Cancer

LDH-IN-1 (Standard) is the analytical standard of LDH-IN-1 (HY-111108). This product is intended for research and analytical applications. LDH-IN-1 is a novel pyrazole-based inhibitor of human lactate dehydrogenase (LDH) with IC50s of 32 and 27 nM for LDHA and LDHB, respectively.
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Cat. No.: HY-W654191
Fipronil detrifluoromethylsulfinyl- 13C2, 15N2 is 13C and 15N labeled 5-Amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrile .
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Cat. No.: HY-B1557A
CAS No.: 138-92-1
Synonyms: Ametazole dihydrochloride
Target:  

Histamine Receptor

Domaines de recherche:  

Metabolic Disease

Betazole (Ametazole) dihydrochloride, a pyrazole analogue of histamine, is an orally active H2 receptor agonist. Betazole dihydrochloride induces gastric acid secretion, and causes an immediate and significant increase in common bile duct pressure. Betazole dihydrochloride has been used as a diagnostic agent known as histalog, for investigating gastric acid secretory capacity .
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Cat. No.: HY-147751
CAS No.: 1965244-85-2
Domaines de recherche:  

Cardiovascular Disease

APJ receptor agonist 6 (compound 9) is a potent APJ (apelin receptor) agonist, with Ki of 1.3 μM. APJ receptor agonist 6 has EC50 values of 0.070 , 0.097, and 0.063 μM for calcium, cAMP, and β-arrestin, respectively .
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Cat. No.: HY-170358
CAS No.: 861382-34-5
Target:  

Parasite

Domaines de recherche:  

Infection

Antileishmanial agent-31 (Compound p1) is a pyrazole derivative. Antileishmanial agent-31 has anti-leishmania activity with an IC50 of 35.53 μg/mL. In addition, Antileishmanial agent-31 has high stability. Antileishmanial agent-31 can be used for anti-leishmaniasis research .
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Cat. No.: HY-189228
Target:  

HPPD Drug Derivative

Domaines de recherche:  

Others

HPPD-IN-15 is a potent HPPD inhibitor with an IC50 of 52 nM (Arabidopsis thaliana). HPPD-IN-15 inhibits HPPD through chelation of Fe 2+ by the pyrazole group, π-π stacking, and insertion of the benzyl group into a hydrophobic pocket. HPPD-IN-15 can be used for herbicide development research .
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Cat. No.: HY-11087R
CAS No.: 271576-80-8
Synonyms: SD-06 (Standard)
Domaines de recherche:  

Inflammation/Immunology

SD 0006 (Standard) is the analytical standard of SD 0006 (HY-11087). This product is intended for research and analytical applications. SD 0006 (SD-06) is an orally active, selective, ATP-competitive and potent diaryl pyrazole inhibitor of p38α MAP Kinase, with an IC50 of 110 nM for p38α .
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Cat. No.: HY-158985
CAS No.: 2267315-06-8
Target:  

AUTACs Autophagy

Domaines de recherche:  

Cancer

Amino-PEG3-2G degrader-1 (compound ) is a conjugate of a PEG Linker and a pyrazole-linked FBnG tag for ubiquitin-proteasome system (UPS) induction. Amino-PEG3-2G degrader-1 can be used to synthesize autophagy-targeting chimeras (AUTACs) .
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