N1018
3-Nitro-L-tyrosine ethyl ester hydrochloride
≥99% (titration)
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About This Item
Empirical Formula (Hill Notation):
C11H14N2O5 · HCl
CAS Number:
Molecular Weight:
290.70
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
Assay
≥99% (titration)
form
powder
color
yellow
mp
185 °C
application(s)
peptide synthesis
storage temp.
2-8°C
SMILES string
Cl.CCOC(=O)[C@@H](N)Cc1ccc(O)c(c1)[N+]([O-])=O
InChI
1S/C11H14N2O5.ClH/c1-2-18-11(15)8(12)5-7-3-4-10(14)9(6-7)13(16)17;/h3-4,6,8,14H,2,5,12H2,1H3;1H/t8-;/m0./s1
InChI key
GITKQXFBNJTMRP-QRPNPIFTSA-N
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Biochem/physiol Actions
3-Nitro-L-tyrosine ethyl ester hydrochloride or NTEE is used measure enzyme activity following carboxylate modification.
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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S K Niture et al.
European journal of biochemistry, 268(3), 832-840 (2001-02-13)
Fusarium moniliforme NCIM 1276 isolated from a tropical mangrove ecosystem produces a single extracellular endo-polygalacturonase with an M(r) of 38 kDa and a carbohydrate content of 4%. It has an alkaline pI of 8.1. The K(m) is 0.12 mg.mL(-1), V(max)
Guinevere Strack et al.
The journal of physical chemistry. B, 113(35), 12154-12159 (2009-08-12)
The biochemical system logically processing biochemical signals using immune-specific and biocatalytic reactions was designed, and the generated output signals were analyzed by AFM and optical means. Different patterns of immune signals resulted in the formation of various interfacial structures followed
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