Benzyl-α-GalNAc
CAS No. 3554-93-6
Benzyl-α-GalNAc( —— )
Catalog No. M26345 CAS No. 3554-93-6
Benzyl-α-GalNAc is a potent inhibitor of O-glycosylation and is used to reduce mucin on cell surfaces.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 42 | In Stock |
|
| 5MG | 38 | In Stock |
|
| 10MG | 61 | In Stock |
|
| 25MG | 123 | In Stock |
|
| 50MG | 184 | In Stock |
|
| 100MG | 305 | In Stock |
|
| 200MG | 458 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameBenzyl-α-GalNAc
-
NoteResearch use only, not for human use.
-
Brief DescriptionBenzyl-α-GalNAc is a potent inhibitor of O-glycosylation and is used to reduce mucin on cell surfaces.
-
DescriptionBenzyl-α-GalNAc is a potent inhibitor of O-glycosylation and is used to reduce mucin on cell surfaces.
-
In VitroCell Viability Assay Cell Line:SUIT-2 cells Concentration:5 mM Incubation Time:72 h Result:Inhibited mucin O-glycosylation.Cell Viability Assay Cell Line:LX-2 cellsConcentration:2, 4 mM Incubation Time:48 h Result:Remarkably decreased the expression of α-SMA in a dose-dependent manner (α-SMA is the marker for the activation of HSCs, which means that quiescent cells transform into myofibroblasts).Cell Proliferation Assay Cell Line:LX-2 cells (PDGF-BB-induced)Concentration:2, 4 mM Incubation Time:48 h Result:Partly reversed PDGF-BB-induced proliferation in cells.Western Blot Analysis Cell Line:LX-2 cells Concentration:2, 4 mM Incubation Time:48 h Result:Downregulated the mRNA levels of collagens I and III in a dose-dependent manner.
-
In VivoAnimal Model:Female severe combined immunodeficient (SCID) mice (6 to 8-week-old; capan-1 tumour model).Dosage:1 mg/mice (in combination with 5-FU)Administration:Tumoural injection; single daily; days 4, 6, 8 and 10 after tumour size reaches 50-70 mm3 Result:Significantly lowered neoplastic cells compared to 5-FU alone.
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorHuman Endogenous Metabolite
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number3554-93-6
-
Formula Weight311.334
-
Molecular FormulaC15H21NO6
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 25 mg/mL (80.30 mM)
-
SMILESCC(=O)N[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1OCc1ccccc1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Su?é-Pou M, Prieto-Sánchez S, et al. Cholesteryl oleate-loaded cationic solid lipid nanoparticles as carriers for efficient gene-silencing therapy. Int J Nanomedicine. 2018 May 30;13:3223-3233.
molnova catalog
related products
-
Amyloid Bri Protein ...
Amyloid Bri Protein Precursor277 (89-106)
-
Lidocaine N-ethyl br...
Lidocaine N-ethyl bromide is a blocker of non-membrane-permeable,and Inhibits Acid-Induced Activation of Esophageal Nociceptive C Fiber Neurons.
-
Conopressin S
Conopressin S, isolated from Conus striatus, shows high affinity with vasopressin V1b receptor (AVPR1B), with a Ki of 8.3 nM.
Cart
sales@molnova.com