L-Kynurenine-¹³C₁₀ sulfate hemihydrate

Cat. No.: HY-104026CS Purity: 99.90%: Data Sheet
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L-Kynurenine-¹³C10 (sulfate hemihydrate) is the ¹³C labeled L-Kynurenine sulfate. L-Kynurenine sulfate hemihydrate, an aryl hydrocarbon receptor (AHR) agonist that activates AHR-directed, naive T cell polarization to the anti-inflammatory Treg phenotype.

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L-Kynurenine-<sup>13</sup>C<sub>10</sub> sulfate hemihydrate

L-Kynurenine-¹³C₁₀ sulfate hemihydrate 화학구조

사이즈	가격	재고	수량
100 μg		해외재고보유	Estimated Time of Arrival: December 31

or 대량구매 문의

* 장바구니에 담기 전 물품의 수량을 선택해 주십시오.

This product is a controlled substance and not for sale in your territory.

고객리뷰

Based on 1 Customer Validation

Other Forms of L-Kynurenine-¹³C₁₀ sulfate hemihydrate:

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Biological Activity
순도&문서
References
고객리뷰

제품 설명	L-Kynurenine-¹³C10 (sulfate hemihydrate) is the ¹³C labeled L-Kynurenine sulfate. L-Kynurenine sulfate hemihydrate, an aryl hydrocarbon receptor (AHR) agonist that activates AHR-directed, naive T cell polarization to the anti-inflammatory Treg phenotype^[1]^[2].
Application	1. This compound can be used as a tracer. 2. This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
분자량	318.17
화학식	¹³C₁₀H₇N₂O₇S.1/2H₂O
Unlabeled CAS	2922-83-0
Appearance	Solid
Color	White to off-white
SMILES	O[13C]([13C@@](N)[13C][13C]([13C]1=[13C]([13C]=[13C][13C]=[13C]1)N)=O)=O.O=S(O)(O)=O.[1/2].O
선적	Room temperature in continental US; may vary elsewhere.
보관	4°C, sealed storage, away from moisture *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
순도&문서	Purity: 99.90% Select Batch: Data Sheet (273 KB) SDS (251 KB) COA (256 KB) Handling Instructions (2659 KB)
References	[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. [Content Brief] [2]. Benjamin J Moyer, et al. Inhibition of the aryl hydrocarbon receptor prevents Western diet-induced obesity. Model for AHR activation by kynurenine via oxidized-LDL, TLR2/4, TGFβ, and IDO1. Toxicol Appl Pharmacol. 2016 Jun 1;300:13-24. [Content Brief]