Home - Products - Others - Other Targets - AU-224

AU-224

CAS No. 287399-47-7

AU-224( —— )

Catalog No. M33244 CAS No. 287399-47-7

AU-224 is an orally available benzamide derivative that is a potent gastrointestinal prokinetic.

Purity : >98% (HPLC)

COA

Datasheet

HNMR

HPLC

MSDS

Handing Instructions

Size	Price / USD	Stock	Quantity
2MG	445	Get Quote
5MG	686	Get Quote
10MG	938	Get Quote
25MG	1398	Get Quote
50MG	1822	Get Quote
100MG	2250	Get Quote
500MG	Get Quote	Get Quote
1G	Get Quote	Get Quote

Get Quotation Bulk Inquiry Add to Cart

Biological Information

Product Name

AU-224
Note

Research use only, not for human use.
Brief Description

AU-224 is an orally available benzamide derivative that is a potent gastrointestinal prokinetic.
Description

AU-224 is a benzamide derivative used as a promising gastrointestinal prokinetic agent without significant side effects.
In Vitro

——
In Vivo

AU-224 has excellent effect of promoting digestive motion while showing little side effect and can be orally administered. AU-224 shows only weak gastrointestinal prokinetic activity after oral administration due to its low lipophilicity.
Synonyms

——
Pathway

Others
Target

Other Targets
Recptor

Others
Research Area

——
Indication

——

Chemical Information

CAS Number

287399-47-7
Formula Weight

397.9
Molecular Formula

C19H28ClN3O4
Purity

>98% (HPLC)
Solubility

——
SMILES

O=C(OCCCC)CN1CCC(NC(=O)C=2C=C(Cl)C(N)=CC2OC)CC1
Chemical Name

——

Shipping & Storage Information

Storage

(-20℃)
Shipping

With Ice Pack
Stability

≥ 2 years

Reference

1. WO/2000/046201A1

Calculator

Molecular Weight Calculator

Dilution Calculator

Molarity Calculator

molnova catalog

related products

8-Hydroxyquinoline-2...

8-Hydroxyquinoline-2-carbaldehyde is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
SAR131675 (b)

SAR131675 is an effective and specific VEGFR-3 inhibitor. It inhibited VEGFR-3 tyrosine kinase activity (IC50: 20 nmol/L) and VEGFR-3 autophosphorylation (IC50: 45 nmol/L) in HEK cells, respectively.
YX-2-107

YX-2-107 is a selective and potent CDK6-degrading PROTAC with an IC50 value of 4.4 nM.YX-2-107 inhibits RB phosphorylation and FOXM1 expression in vitro, and inhibits the development of Ph+ ALL in rats.

Sign In Join Free