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Merck
CN

C7000

5-Carbethoxyuracil

~90%

Synonym(s):

Isoorotic acid ethyl ester

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About This Item

Empirical Formula (Hill Notation):
C7H8N2O4
CAS Number:
Molecular Weight:
184.15
UNSPSC Code:
41106305
PubChem Substance ID:
EC Number:
249-053-3
MDL number:
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biological source

synthetic

assay

~90%

form

powder

solubility

DMSO: 25 mg/mL, clear, colorless to faintly yellow

SMILES string

CCOC(=O)C1=CNC(=O)NC1=O

InChI

1S/C7H8N2O4/c1-2-13-6(11)4-3-8-7(12)9-5(4)10/h3H,2H2,1H3,(H2,8,9,10,12)

InChI key

MKNYHTGOVKPZMU-UHFFFAOYSA-N

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Abbas Heidari-Moghadam et al.
Cell journal, 22(Suppl 1), 19-28 (2020-08-12)
Researchers have been interested in the creation of a favorable cellular model for use in vascular-muscle tissue engineering. The main objective of this study is to determine the myogenic effects of vascular endothelial growth factor (VEGF) and human umbilical vein
Amankeldi A Salybekov et al.
Frontiers in cardiovascular medicine, 8, 754254-754254 (2021-11-09)
Under vasculogenic conditioning, pro-inflammatory cell subsets of peripheral blood mononuclear cells (PBMCs) shift their phenotype to pro-regenerative cells such as vasculogenic endothelial progenitor cells, M2 macrophages, and regulatory T cells, collectively designated as regeneration-associated cells (RACs). In this study, we

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