403458
N-p-Tosylglycine
97%
Synonym(s):
N-(p-Toluenesulfonyl)glycine
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About This Item
Linear Formula:
CH3C6H4SO2NHCH2CO2H
CAS Number:
Molecular Weight:
229.25
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
97%
form
solid
reaction suitability
reaction type: solution phase peptide synthesis
mp
147-149 °C (lit.)
application(s)
peptide synthesis
SMILES string
Cc1ccc(cc1)S(=O)(=O)NCC(O)=O
InChI
1S/C9H11NO4S/c1-7-2-4-8(5-3-7)15(13,14)10-6-9(11)12/h2-5,10H,6H2,1H3,(H,11,12)
InChI key
VDKFCCZUCXYILI-UHFFFAOYSA-N
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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A Sener et al.
Biochemical pharmacology, 34(14), 2495-2499 (1985-07-15)
N-p-tosylglycine, which inhibits transglutaminase activity in islet homogenates, was found to cause a rapid and sustained facilitation of insulin release evoked by D-glucose, L-leucine or the association of Ba2+ and theophylline in intact islets. Such a facilitating action could not
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