6 Results for "

ST3GAL1

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "ST3GAL1" in MCE Product Catalog:

Cat. No.: HY-RS13846
Research Areas:  

Others

ST3GAL1 Human Pre-designed siRNA Set A contains three designed siRNAs for ST3GAL1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS20651
Research Areas:  

Others

St3gal1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for St3gal1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-172888
Research Areas:  

Cancer

SPP-037 is an orally active and selective inhibitor of ST6GAL1 (IC50 = 3.59 μM). SPP-037 inhibits integrin α2,6-sialylation and integrin-FAK-paxillin pathway. SPP-037 inhibits cancer cell proliferation, migration and exhibits antiangiogenic activity. SPP-037 has anti-tumor activity in MDA-MB-231 xenograft mouse model. SPP-037 can be used for the research of triple-negative breast cancer .
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Cat. No.: HY-RS27162
Research Areas:  

Others

St3gal1 Rat Pre-designed siRNA Set A contains three designed siRNAs for St3gal1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-E70298
Synonyms: ST3GAL1
Target:  

Endogenous Metabolite

Research Areas:  

Cancer

ST3 β-Gal α-2,3-Sialyltransferase 1 (ST3GAL1) is a sialyltransferase whose overexpression in ovarian cancer cell lines enhances cell growth, migration, and invasion capabilities, as well as increases tumorigenicity and resistance to paclitaxel in vivo. ST3 β-Gal α-2,3-Sialyltransferase 1 catalyzes the transfer of sialic acid from cytidine monophosphate-sialic acid to galactose-containing substrates and can be utilized in studies of cancer progression and chemotherapy resistance .
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Cat. No.: HY-163548
CAS No.: 3067911-81-0
Target:  

Sialyltransferase

Research Areas:  

Cancer

SPP-002 is a ST6GAL1 inhibitor with a human IC50 of 16.7 μM. SPP-002 selectively inhibits N-glycan sialylation over O-glycan sialylation and binds strongly to the enzyme active site. SPP-002 suppresses expression of signaling proteins in the integrin/FAK/paxillin pathway. SPP-002 can be used for the research of triple negative breast cancer metastasis .
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