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345911

Sigma-Aldrich

N-(3-Indolylacetyl)-L-alanine

98%

Synonym(s):

IAA-L-Ala, Indole-3-acetyl-L-alanine

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About This Item

Empirical Formula (Hill Notation):
C13H14N2O3
CAS Number:
57105-39-2
Molecular Weight:
246.26
MDL number:
MFCD00050395
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
24861360
NACRES:
NA.22

Quality Level

100

assay

98%

form

solid

optical activity

[α]24/D −21°, c = 1 in methanol

reaction suitability

reaction type: solution phase peptide synthesis

mp

138-140 °C (lit.)

application(s)

peptide synthesis

SMILES string

C[C@H](NC(=O)Cc1c[nH]c2ccccc12)C(O)=O

InChI

1S/C13H14N2O3/c1-8(13(17)18)15-12(16)6-9-7-14-11-5-3-2-4-10(9)11/h2-5,7-8,14H,6H2,1H3,(H,15,16)(H,17,18)/t8-/m0/s1

InChI key

FBDCJLXTUCMFLF-QMMMGPOBSA-N

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Related Categories

wgk_germany

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flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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Miguel A Uc-Chuc et al.
International journal of molecular sciences, 21(13) (2020-07-09)
Despite the existence of considerable research on somatic embryogenesis (SE), the molecular mechanism that regulates the biosynthesis of auxins during the SE induction process remains unknown. Indole-3-acetic acid (IAA) is an auxin that is synthesized in plants through five pathways.
João Daniel Santos Fernandes et al.
PloS one, 10(7), e0132369-e0132369 (2015-07-15)
Metabolic diversity is an important factor during microbial adaptation to different environments. Among metabolic processes, amino acid biosynthesis has been demonstrated to be relevant for survival for many microbial pathogens, whereas the association between pathogenesis and amino acid uptake and

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