Home - Products - PI3K/Akt/mTOR signaling - PI3K - Palosuran hydrochloride

Palosuran hydrochloride

CAS No. ——

Palosuran hydrochloride ( —— )

Catalog No. M17710 CAS No. ——

Palosuran is a new potent and specific antagonist of the human UT receptor with an IC50 of 3.6±0.2 nM.

Purity : >98% (HPLC)

COA

Datasheet

HNMR

HPLC

MSDS

Handing Instructions

Size	Price / USD	Stock	Quantity
5MG	188	Get Quote
10MG	292	Get Quote
25MG	474	Get Quote
50MG	677	Get Quote
100MG	Get Quote	Get Quote
200MG	Get Quote	Get Quote
500MG	Get Quote	Get Quote
1G	Get Quote	Get Quote

Get Quotation Bulk Inquiry Add to Cart

Biological Information

Product Name

Palosuran hydrochloride
Note

Research use only, not for human use.
Brief Description

Palosuran is a new potent and specific antagonist of the human UT receptor with an IC50 of 3.6±0.2 nM.
Description

Palosuran is a new potent and specific antagonist of the human UT receptor with an IC50 of 3.6±0.2 nM.
In Vitro

——
In Vivo

——
Synonyms

——
Pathway

PI3K/Akt/mTOR signaling
Target

PI3K
Recptor

Urotensin Receptor (GPR14)
Research Area

——
Indication

——

Chemical Information

CAS Number

——
Formula Weight

454.99
Molecular Formula

C25H31ClN4O2
Purity

>98% (HPLC)
Solubility

——
SMILES

Cl.Cc2nc1ccccc1c(c2)NC(=O)NCCN3CCC(O)(CC3)Cc4ccccc4
Chemical Name

——

Shipping & Storage Information

Storage

(-20℃)
Shipping

With Ice Pack
Stability

≥ 2 years

Reference

1. Clozel M, et al. J Pharmacol Exp Ther, 2004, 311(1):204-212.

Calculator

Molecular Weight Calculator

Dilution Calculator

Molarity Calculator

molnova catalog

related products

Duvelisib (R enantio...

Duvelisib R enantiomer is an enantiomer of Duvelisib with lower activity. Duvelisib is a PI3K inhibitor.
ST-162

ST-162 is a potent, bifunctional MAPK/PI3K antagonist with IC50 of 191 nM and 398 nM for PI3Kα and MEK1, respectively.
3-Methyladenine

A selective PI3K inhibitor for Vps34 and PI3Kγ with IC50 of 25 uM and 60 uM in HeLa cells.

Sign In Join Free