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Merck
모든 사진(1)

Key Documents

T5905

Sigma-Aldrich

L-Thyronine

≥98.0% (TLC)

동의어(들):

3-(p-[p-Hydroxyphenoxy]phenyl)-L-alanine

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About This Item

실험식(Hill 표기법):
C15H15NO4
CAS Number:
Molecular Weight:
273.28
EC Number:
MDL number:
UNSPSC 코드:
12352202
PubChem Substance ID:
NACRES:
NA.26

product name

L-Thyronine,

분석

≥98.0% (TLC)

Quality Level

형태

powder

SMILES string

N[C@@H](Cc1ccc(Oc2ccc(O)cc2)cc1)C(O)=O

InChI

1S/C15H15NO4/c16-14(15(18)19)9-10-1-5-12(6-2-10)20-13-7-3-11(17)4-8-13/h1-8,14,17H,9,16H2,(H,18,19)/t14-/m0/s1

InChI key

KKCIOUWDFWQUBT-AWEZNQCLSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


시험 성적서(COA)

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문서 라이브러리 방문

J S LoPresti et al.
The Journal of clinical endocrinology and metabolism, 70(5), 1479-1484 (1990-05-01)
A hidden pool of rT3 production represents a source of rT3 that is minimally reflected in circulating rT3 levels. To test for the existence of such a source of rT3 production in man, varying doses of the generalized deiodinase inhibitor
J Köhrle
Cellular and molecular life sciences : CMLS, 57(13-14), 1853-1863 (2001-02-24)
Thyroid hormones control growth, development, differentiation and metabolism in vertebrates. Most of the actions of the active thyroid hormone T3 (3,5,3'-triiodo-L-thyronine) are exerted via ligand-activated nuclear T3 receptors. Activation of the secretory product of the thyroid gland, L-thyroxine (3,3',5,5'-tetraiodo-L-thyronine), or
Martin A Paquette et al.
PloS one, 9(6), e101155-e101155 (2014-06-28)
Thyroid hormone (TH) exerts its effects by binding to the thyroid hormone receptor (TR), which binds to TH response elements (TREs) to regulate target gene expression. We investigated the relative ability of liganded homodimers TR and retinoid X receptor (RXR)
Lavinia Bhatt et al.
Molecular vision, 16, 283-293 (2010-02-24)
The production of reactive oxygen species (ROS) can lead to oxidative stress, which is a strong contributory factor to many ocular diseases. In this study, the removal of trophic factors is used as a model system to investigate the effects
Jana Juráňová et al.
Molecules (Basel, Switzerland), 24(1) (2019-01-02)
In this study, we compared selected silymarin components, such as quercetin (QE), 2,3-dehydrosilybin (DHS) and silybin (SB), with the anti-inflammatory drug indomethacin (IND) in terms of their wound healing potential. In view of the fact that pathological cutaneous wound healing

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