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About This Item
经验公式（希尔记法）:
C13H14N2O3
CAS号:
分子量:
246.26
MDL编号:
UNSPSC代码:
12352209
eCl@ss:
32160406
PubChem化学物质编号:
NACRES:
NA.22
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质量水平
方案
98%
表单
solid
旋光性
[α]24/D −21°, c = 1 in methanol
反应适用性
reaction type: solution phase peptide synthesis
mp
138-140 °C (lit.)
应用
peptide synthesis
SMILES字符串
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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储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
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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