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T1501

Sigma-Aldrich

DL-Thyronine

powder

Sinônimo(s):

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

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About This Item

Fórmula empírica (Notação de Hill):
C15H15NO4
Número CAS:
1034-10-2
Peso molecular:
273.28
Número CE:
213-854-6
Número MDL:
MFCD00045864
Código UNSPSC:
12352200
ID de substância PubChem:
24899971

forma

powder

cor

off-white to gray

cadeia de caracteres SMILES

NC(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)

chave InChI

KKCIOUWDFWQUBT-UHFFFAOYSA-N

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Tissue-engineered urethra with autologous cells seeded on biodegradable scaffolds offers an alternative for lower urinary tract reconstruction. Rabbit is most commonly used as an animal model in urethra and bladder tissue repair. The goal of this study is to characterize
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Molecular and cellular endocrinology, 436, 50-58 (2016-07-28)
Thyroid-stimulating hormone (TSH) receptor is expressed in extrathyroidal tissues such as hepatocytes, adipocytes, and skeletal muscle, which suggests a possible novel role of TSH in various metabolic processes in extrathyroidal tissues independent of thyroid hormones. We investigated whether TSH has
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Cell reports, 27(13), 3887-3901 (2019-06-27)
A key feature of immune functional impairment with age is the progressive involution of thymic tissue responsible for naive T cell production. In this study, we identify two major phases of thymic epithelial cell (TEC) loss during aging: a block in
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Evidence-based complementary and alternative medicine : eCAM, 2013, 370961-370961 (2013-07-19)
The aim of this study was to examine the contribution of side population (SP) cells from kidney and bone marrow for reconstitution of kidney SP pools after ischemia-reperfusion injury (IRI). The SP and non-SP cells in kidneys following IRI were
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Biotechnology and bioengineering, 118(5), 2001-2015 (2021-02-14)
Age-related macular degeneration (AMD) associated with dysfunction of retinal pigment epithelial (RPE) cells is the most common cause of untreatable blindness. To advance gene therapy as a viable treatment for AMD there is a need for technologies that enable controlled
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