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731746-84-2

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731746-84-2 Usage

Explanation

This is the chemical name of the compound, also known as histidine.

Explanation

Histidine cannot be synthesized by the human body and must be obtained through diet or supplements.

Explanation

Histidine is one of the 20 standard amino acids that make up proteins in living organisms.

Explanation

Histidine is a precursor to histamine, a compound involved in various physiological processes such as immune response and digestion.

Explanation

Histidine is involved in the synthesis of metalloproteins, which are proteins containing metal ions.

Explanation

Histidine plays a role in the transmission of nerve signals in the nervous system.

Explanation

Histidine helps to maintain the pH balance in the body, ensuring proper functioning of enzymes and other biological processes.

Explanation

Histidine is found in high concentrations in hemoglobin, the protein responsible for transporting oxygen in the blood.

Explanation

Histidine is essential for the transport and utilization of iron in the body, which is necessary for various biological processes such as oxygen transport and enzyme function.

Explanation

Histidine is a key component of carnosine, a dipeptide that acts as a buffer against the build-up of lactic acid during high-intensity exercise.

Classification

Essential amino acid

Proteinogenic

One of the 23 proteinogenic amino acids

Biological processes

Precursor for histamine

Involvement

Synthesis of metalloproteins

Role

Neurotransmission

Function

Immune response

pH balance

Maintaining the body's pH balance

Growth and repair

Tissue growth and repair

Hemoglobin concentration

High concentrations in hemoglobin

Iron transport and utilization

Crucial for iron transport and utilization

Carnosine component

Key component of carnosine

Check Digit Verification of cas no

The CAS Registry Mumber 731746-84-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,1,7,4 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 731746-84:
(8*7)+(7*3)+(6*1)+(5*7)+(4*4)+(3*6)+(2*8)+(1*4)=172
172 % 10 = 2
So 731746-84-2 is a valid CAS Registry Number.

731746-84-2Downstream Products

731746-84-2Relevant articles and documents

Discovery of α-Substituted Imidazole-4-acetic Acid Analogues as a Novel Class of ρ1γ-Aminobutyric Acid Type A Receptor Antagonists with Effect on Retinal Vascular Tone

Krall, Jacob,Brygger, Benjamin M.,Sigureardóttir, Sara B.,Ng, Clarissa K. L.,Bundgaard, Christoffer,Kehler, Jan,Nielsen, Birgitte,Bek, Toke,Jensen, Anders A.,Fr?lund, Bente

, p. 2299 - 2310 (2016/10/25)

The ρ-containing γ-aminobutyric acid type A receptors (GABAARs) play an important role in controlling visual signaling. Therefore, ligands that selectively target these GABAARs are of interest. In this study, we demonstrate that the partial GABAAR agonist imidazole-4-acetic acid (IAA) is able to penetrate the blood–brain barrier in vivo; we prepared a series of α- and N-alkylated, as well as bicyclic analogues of IAA to explore the structure–activity relationship of this scaffold focusing on the acetic acid side chain of IAA. The compounds were prepared via IAA from l-histidine by an efficient minimal-step synthesis, and their pharmacological properties were characterized at native rat GABAARs in a [3H]muscimol binding assay and at recombinant human α1β2γ2Sand ρ1GABAARs using the FLIPR membrane potential assay. The (+)-α-methyl- and α-cyclopropyl-substituted IAA analogues ((+)-6 a and 6 c, respectively) were identified as fairly potent antagonists of the ρ1GABAAR that also displayed significant selectivity for this receptor over the α1β2γ2SGABAAR. Both 6 a and 6 c were shown to inhibit GABA-induced relaxation of retinal arterioles from porcine eyes.

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