469971
L-Tryptophanol
97%
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About This Item
Fórmula empírica (notación de Hill):
C11H14N2O
Número de CAS:
Peso molecular:
190.24
Número MDL:
Código UNSPSC:
12352209
ID de la sustancia en PubChem:
NACRES:
NA.22
Productos recomendados
Nivel de calidad
Ensayo
97%
actividad óptica
[α]20/D −20.5°, c = 1 in methanol
idoneidad de la reacción
reaction type: solution phase peptide synthesis
mp
73-77 °C (lit.)
aplicaciones
peptide synthesis
cadena SMILES
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-/m0/s1
Clave InChI
UDQCRUSSQAXPJY-VIFPVBQESA-N
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G M Beck et al.
Chirality, 8(7), 503-510 (1996-01-01)
Lambda-carrageenan, a linear high molecular weight sulfated polysaccharide, has been employed as a chiral selector in capillary electrophoresis for the separation of enantiomers of weakly basic pharmaceutical compounds. The racemic compounds that were enantioresolved included propranolol, pindolol, tryptophanol, laudanosine and
Mercedes Amat et al.
The Journal of organic chemistry, 74(3), 1205-1211 (2008-12-17)
The enantioselective construction of the 3-ethylindolo[2,3-a]quinolizidine moiety present in numerous indole alkaloids is reported, the key steps being a stereoselective cyclocondensation of (S)-tryptophanol with an appropriate racemic delta-oxoester and a regio- and stereoselective cyclization of the resulting oxazolopiperidones on the
Theodoros Eleftheriadis et al.
International journal of molecular medicine, 42(1), 557-568 (2018-04-26)
It is generally hypothesized in the literature that indoleamine 2,3‑dioxygenase (IDO), by degrading L‑tryptophan along the kynurenine pathway, suppresses CD4+ T‑cell function by inducing apoptosis, inhibiting proliferation and promoting differentiation towards a regulatory phenotype. These effects are either accompanied or
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Ashley A Reinke et al.
Chembiochem : a European journal of chemical biology, 11(13), 1889-1895 (2010-08-03)
In Alzheimer's disease (AD) and other neurodegenerative disorders, proteins accumulate into ordered aggregates, called amyloids. Recent evidence suggests that these structures include both large, insoluble fibrils and smaller, prefibrillar structures, such as dimers, oligomers, and protofibrils. Recently, focus has shifted
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