Home - Products - Others - Other Targets - Ethanolamine

Ethanolamine

CAS No. 141-43-5

Ethanolamine( 2-Aminoethanol | monoethanolamine | 2-Hydroxyethylamine )

Catalog No. M19560 CAS No. 141-43-5

2-Aminoethanol (ethanolamine) can inhibit the GABA degrading enzyme GABA aminotransferase (GABA-T).

Purity : >98% (HPLC)

COA

Datasheet

HNMR

HPLC

MSDS

Handing Instructions

Size	Price / USD	Stock	Quantity
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

Ethanolamine
Note

Research use only, not for human use.
Brief Description

2-Aminoethanol (ethanolamine) can inhibit the GABA degrading enzyme GABA aminotransferase (GABA-T).
Description

2-Aminoethanol (ethanolamine) can inhibit the GABA degrading enzyme GABA aminotransferase (GABA-T). Strengthening of the antioxidant mechanisms by plant pretreatment with 2-aminoethanol could be helpful in the development of a broad tolerance to adverse stress conditions.
In Vitro

——
In Vivo

——
Synonyms

2-Aminoethanol | monoethanolamine | 2-Hydroxyethylamine
Pathway

Others
Target

Other Targets
Recptor

GABA transaminase
Research Area

——
Indication

——

Chemical Information

CAS Number

141-43-5
Formula Weight

61.08
Molecular Formula

C2H7NO
Purity

>98% (HPLC)
Solubility

DMSO:10 mM
SMILES

NCCO
Chemical Name

——

Shipping & Storage Information

Storage

(-20℃)
Shipping

With Ice Pack
Stability

≥ 2 years

Reference

1.L?scher W. Effect of 2-aminoethanol on the synthesis binding uptake and metabolism of GABA. Neurosci Lett. 1983 Dec 11;42(3):293-7.

Calculator

Molecular Weight Calculator

Dilution Calculator

Molarity Calculator

molnova catalog

related products

Gastrin I (1-14), hu...

Gastrin I (1-14), human is 1-14 fragment of human gastrin I peptide. Gastrin I is an endogenous, gastrointestinal peptide hormone. Gastrin is the major hormonal regulator of gastric acid secretion.
Moschamine

Moschamine is a very potent compound that is able to inhibit COX-I by 58% and COX-II by 54%, at the concentration of 0.1 μmol L⁻1, it may suppress cAMP formation via binding to 5-HT1 receptors in the cells. Moschamine exerts antitumour effects on HeLa, MCF7 and A431 cells.
PRDX1-IN-1

PRDX1-IN-1 is a selective inhibtor of PRDX1 with an IC50 value of 0.164 μM. PRDX1-IN-1 can be used in researches related to cancer.PRDX1-IN-1 promots intracellular ROS accumulation, and inhibits the proliferation, invasion and migration of cancer cells besides inducing apoptosis. PRDX1-IN-1 could be used in cancer research.

Sign In Join Free