8 Results for "

3744

" in MedChemExpress (MCE) Product Catalog:
Products (8)

8 Results for "3744" in MCE Product Catalog:

Cat. No.: HY-P3744
CAS No.: 81493-98-3
Target:  

EGFR

Domaines de recherche:  

Others

pp60v-src Autophosphorylation site is a synthetic peptide. pp60v-src Autophosphorylation site can be used for various biochemical studies .
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Cat. No.: HY-N3744
CAS No.: 70897-14-2
Dihydrocitflavanone is a natural flavonoid.
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Cat. No.: HY-157322
CAS No.: 423748-49-6
Target:  

Fluorescent Dye

Domaines de recherche:  

Infection

SAV13 is an inhibitor of SaeR. SAV13 is an analogue of HR3744. SAV13 inhibits SaeR-DNA probe binding and has antivirulence properties .
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Cat. No.: HY-181629
CAS No.: 3106975-38-3
Domaines de recherche:  

Cancer

ZSTK3744 is an aryl hydrocarbon receptor (AhR) agonist. ZSTK3744 directly binds to AhR, upregulates the expression of AhR target genes including CYP1A1, CYP1B1 and TIPARP, and mediates cell growth inhibitory activity in triple-negative breast cancer cells. ZSTK3744 induces apoptosis in triple-negative breast cancer cells. ZSTK3744 exhibits anti-tumor activity and can be used in the research of chemoresistant triple-negative breast cancer .
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Cat. No.: HY-181629A
Domaines de recherche:  

Cancer

ZSTK3744 hydrochloride is an aryl hydrocarbon receptor (AhR) agonist. ZSTK3744 hydrochloride directly binds to AhR, upregulates the expression of AhR target genes including CYP1A1, CYP1B1 and TIPARP, and mediates cell growth inhibitory activity in triple-negative breast cancer cells. ZSTK3744 hydrochloride induces apoptosis in triple-negative breast cancer cells. ZSTK3744 hydrochloride exhibits anti-tumor activity and can be used in the research of chemoresistant triple-negative breast cancer .
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Cat. No.: HY-P84047
Synonyms: LAR; BNAH2

Host:  

Mouse

Application:  

FC, ELISA

Reactivity:  

Human

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Cat. No.: HY-P84047A
Synonyms: LAR; BNAH2

Host:  

Mouse

Application:  

FC, ELISA

Reactivity:  

Human

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Cat. No.: HY-185310
CAS No.: 438204-56-9
Domaines de recherche:  

Cancer

MKI-2 is a selective MASTL inhibitor with an IC50 of 37.44 nM. MKI-2 induces mitotic catastrophe resulting from the modulation of the MASTL-PP2A axis in breast cancer cells. MKI-2 reduces phospho-ENSA, total, phospho-c-Myc levels. MKI-2 inhibts cancer cells proliferation, migration and induces DNA damage. MKI-2 inhibits germinal vesicle breakdown in mouse oocytes. MKI-2 can be used for the research of cancer, such as breast cancer .
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