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Key Documents

SML2935

Sigma-Aldrich

SBI-425

≥98% (HPLC)

Synonym(s):

5-((5-Chloro-2-methoxyphenyl)sulfonamido)nicotinamide, 5-[[(5-Chloro-2-methoxyphenyl)sulfonyl]amino]-3-pyridinecarboxamide

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About This Item

Empirical Formula (Hill Notation):
C13H12ClN3O4S
CAS Number:
Molecular Weight:
341.77
MDL number:
UNSPSC Code:
12352200
NACRES:
NA.77

Quality Level

Assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

2-8°C

Biochem/physiol Actions

SBI-425 is an orally available, potent and selective inhibitor of TNAP (tissue-nonspecific alkaline phosphase).

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Campbell R Sheen et al.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 30(5), 824-836 (2014-11-28)
Medial vascular calcification (MVC) is a pathological phenomenon that causes vascular stiffening and can lead to heart failure; it is common to a variety of conditions, including aging, chronic kidney disease, diabetes, obesity, and a variety of rare genetic diseases.
Anthony B Pinkerton et al.
Bioorganic & medicinal chemistry letters, 28(1), 31-34 (2017-11-28)
Tissue-nonspecific alkaline phosphatase (TNAP) is an ectoenzyme crucial for bone matrix mineralization via its ability to hydrolyze extracellular inorganic pyrophosphate (ePPi), a potent mineralization inhibitor, to phosphate (Pi). By the controlled hydrolysis of ePPi, TNAP maintains the correct ratio of
Filippo Romanelli et al.
PloS one, 12(10), e0186426-e0186426 (2017-10-13)
Overexpression of tissue-nonspecific alkaline phosphatase (TNAP) in endothelium leads to arterial calcification in mice. The purpose of this study was to examine the effect of elevated endothelial TNAP on coronary atherosclerosis. In addition, we aimed to examine endogenous TNAP activity

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