Free shipping on all orders over $ 500

Piperlongumine

Cat. No. M5220

All AbMole products are for research use only, cannot be used for human consumption.

Piperlongumine Structure
Synonym:

PPLGM, Piplartine

Size Price Availability Quantity
5mg USD 30  USD30 In stock
10mg USD 40  USD40 In stock
50mg USD 100  USD100 In stock
100mg USD 150  USD150 In stock
Free Delivery on orders over USD 500 Bulk Inquiry?

Quality Control & Documentation
Biological Activity

Piperlongumine is a direct TrxR1 inhibitor with suppressive activity against gastric cancer and a novel inhibitor of CRM1. Piperlongumine is also an inhibitor of PI3K/Akt/mTOR in human breast cancer cells. Piperlonguminine inhibits alpha-melanocyte-stimulating hormone-induced melanogenesis by downregulation of tyrosinase expression in melanoma B16 cells. Piperlongumine also promotes autophagy via inhibition of Akt/mTOR signalling and mediates cancer cell death. Piperlongumine (50 mg/kg i.p.) causes in vivo growth inhibition of tumor cells.

Chemical Information
Molecular Weight 317.34
Formula C17H19NO5
CAS Number 20069-09-4
Solubility (25°C) DMSO 16 mg/mL warmed
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Ryu J, et al. Nat Prod Res. Piperlongumine as a potential activator of AMP-activated protein kinase in HepG2 cells.

[2] Iwashita M, et al. Eur J Pharmacol. Piperlongumine, a constituent of Piper longum L., inhibits rabbit platelet aggregation as a thromboxane A(2) receptor antagonist.

[3] Min KR, et al. Planta Med. Piperlonguminine from Piper longum with inhibitory effects on alpha-melanocyte-stimulating hormone-induced melanogenesis in melanoma B16 cells.

Related Products
2-Bromo-4-chlorophenylacetic acid

2-Bromo-4-chlorophenylacetic acid is a biochemical reagent.

CPN-351 TFA

CPN-351 TFA is a selective pentapeptide antagonist of human NMUR1 with a pA2 of 7.35. CPN-351 TFA can be used for the research of inflammation.

5-Phenyluracil

5-Phenyluracil is a pyrimidine derivative, a class of heterocyclic aromatic organic compounds crucial in biochemistry. It serves as a synthetic nucleoside analogue, meaning it mimics the structure of naturally occurring nucleosides like uridine. This structural similarity allows it to participate in biochemical reactions, often interfering with normal cellular processes, making it a valuable tool in studying nucleic acid metabolism and developing antiviral and anticancer agents.

7-Deoxyloganin

7-Deoxyloganin is a biosynthetic precursor of Loganin. 7-Deoxyloganin undergoes hydroxylation catalyzed by 7-deoxyloganin 7-hydroxylase, a cytochrome P450-dependent monooxygenase, to produce Loganin.

Mannose-BSA

Mannose-BSA is an important organic intermediate that combines the properties of mannose and bovine serum albumin, which is of unique value in the field of scientific research, and can be used as a key substance in a variety of organic synthesis reactions. Mannose is an important monosaccharide that binds specifically to mannose receptors (e.g., CD206 receptors on dendritic cells and macrophages), and therefore has a wide range of applications in immunomodulation and targeted drug delivery. BSA is a protein carrier that is commonly used for biocoupling, and its abundant surface amino groups can covalently bind to mannose to form a mannose-BSA complex.

  Catalog
Abmole Inhibitor Catalog




Keywords: Piperlongumine, PPLGM, Piplartine supplier, inhibitors, activators

All AbMole products are for research use only, cannot be used for human consumption or veterinary use. We do not provide products or services to individuals. Please comply with the intended use and do not use AbMole products for any other purpose.



Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2024 AbMole BioScience. All Rights Reserved.