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经验公式(希尔记法):
C13H14N2O3
化学文摘社编号:
分子量:
246.26
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22
MDL number:
产品名称
N-(3-吲哚乙酰基)-L-丙氨酸, 98%
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
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
Quality Level
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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