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About This Item
Empirical Formula (Hill Notation):
C11H14N2O
CAS Number:
Molecular Weight:
190.24
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
optical activity
[α]20/D +18.5°, c = 1 in methanol
reaction suitability
reaction type: solution phase peptide synthesis
mp
86-89 °C (lit.)
application(s)
peptide synthesis
SMILES string
N[C@@H](CO)Cc1c[nH]c2ccccc12
InChI
1S/C11H14N2O/c12-9(7-14)5-8-6-13-11-4-2-1-3-10(8)11/h1-4,6,9,13-14H,5,7,12H2/t9-/m1/s1
InChI key
UDQCRUSSQAXPJY-SECBINFHSA-N
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Liliana Raimundo et al.
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Impairment of the tumour suppressor p53 pathway is a major event in human cancers, making p53 activation one of the most attractive therapeutic strategies to halt cancer. Here, we have identified a new selective p53 activator and investigated its potential
Griet Van Zeebroeck et al.
Nature chemical biology, 5(1), 45-52 (2008-12-09)
Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting transceptors is unknown. We have screened 319 amino acid analogs to identify compounds that act on Gap1
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