Cart
sales@molnova.com
BR-1
CAS No. 893449-38-2
BR-1( PRL-3 Inhibitor )
Catalog No. M24917 CAS No. 893449-38-2
BR-1 is a phosphatase of regenerating liver 3 (PRL-3) inhibitor which blocks the migration and invasion of metastatic cancer cells.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 33 | In Stock |
|
| 5MG | 28 | In Stock |
|
| 10MG | 47 | In Stock |
|
| 25MG | 93 | In Stock |
|
| 50MG | 138 | In Stock |
|
| 100MG | 206 | In Stock |
|
| 200MG | 309 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameBR-1
-
NoteResearch use only, not for human use.
-
Brief DescriptionBR-1 is a phosphatase of regenerating liver 3 (PRL-3) inhibitor which blocks the migration and invasion of metastatic cancer cells.
-
DescriptionBR-1 is a phosphatase of regenerating liver 3 (PRL-3) inhibitor which blocks the migration and invasion of metastatic cancer cells.
-
In Vitro——
-
In Vivo——
-
SynonymsPRL-3 Inhibitor
-
PathwayOthers
-
TargetOther Targets
-
RecptorPRL-3
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number893449-38-2
-
Formula Weight485.21
-
Molecular FormulaC17H11Br2NO2S2
-
Purity>98% (HPLC)
-
SolubilityDMSO:10 mM
-
SMILESC1=CC=C(C(=C1)COC2=C(C=C(C=C2)Br)/C=C/3\C(=O)NC(=S)S3)Br
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Min G , Lee S K , Kim H N , et al. Rhodanine-based PRL-3 inhibitors blocked the migration and invasion of metastatic cancer cells[J]. Bioorganic & Medicinal Chemistry Letters, 2013, 23(13):3769-3774.
molnova catalog
related products
-
26-Dihydroxypyridine...
26-Dihydroxypyridine hydrochloride is used as a reagent to synthesize uridine phosphorylase inhibitors that increase Uridine (Urd) (U829910) levels.
-
Proinsulin C-Peptide...
Human proinsulin, the single-chain peptide precursor of insulin, consists of the insulin A and B chains connected by the 31 amino acid C-peptide. Cleavage of proinsulin by proteolytic enzymes produces insulin and free C-peptide.
-
α-Conotoxin MI
α-Conotoxin M I is a potent and selective inhibitor of mAChR and α1β1γδ nAChR, but has no effect on nicotine-stimulated dopamine release. α-Conotoxins are small, disulfide-rich peptides that competitively inhibit muscle and neuronal nicotinic AChRs.
