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经验公式(希尔记法):
C6H11NO2
化学文摘社编号:
分子量:
129.16
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352106
EC Number:
221-462-1
MDL number:
Beilstein/REAXYS Number:
81093
产品名称
-吡哌酸, 99% (titration)
InChI key
HXEACLLIILLPRG-YFKPBYRVSA-N
InChI
1S/C6H11NO2/c8-6(9)5-3-1-2-4-7-5/h5,7H,1-4H2,(H,8,9)/t5-/m0/s1
SMILES string
OC(=O)[C@@H]1CCCCN1
assay
99% (titration)
form
powder
technique(s)
GC/MS: suitable
color
white
mp
272 °C (lit.)
Quality Level
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Application
L-哌啶酸已用作气相色谱-质谱分析(GC-MS)中的定量标准品。
Biochem/physiol Actions
L-哌啶酸可用于泽尔韦格氏综合征。哌啶酸也是一种植物防御代谢物。它是一种信号传导化合物,对系统获得抗性(SAR)至关重要。
L-哌啶酸是赖氨酸代谢物;其分解代谢缺陷与高磷血症、脑肝肾综合征、新生儿肾上腺脑白质营养不良和婴儿雷夫森病有关。
General description
L-哌啶酸(哌啶-2-羧酸)是含氮的杂环化合物。它属于亚氨基酸。分子量为129.2。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
S J Mihalik et al.
The Journal of biological chemistry, 264(5), 2509-2517 (1989-02-15)
L-Pipecolic acid oxidation was studied in the rabbit and cynomolgus monkey. Tissue homogenates from both species incubated with L-[2,3,4,5,6-3H]pipecolic acid produced a single radioactive product identified as alpha-aminoadipic acid. In the rabbit, L-pipecolic acid oxidation was greatest in kidney cortex
Transcriptional analysis of defense mechanisms in upland tetraploid switchgrass to greenbugs
Donze-Reiner T, et al.
BMC plant biology, 17(1), 46-46 (2017)
Pipecolic acid
Laboratory Guide to the Methods in Biochemical Genetics (2008)
Ronald J A Wanders
American journal of medical genetics. Part A, 126A(4), 355-375 (2004-04-21)
The group of peroxisomal disorders now includes 17 different disorders with Zellweger syndrome as prototype. Thanks to the explosion of new information about the functions and biogenesis of peroxisomes, the metabolic and molecular basis of most of the peroxisomal disorders
S J Mihalik et al.
Pediatric research, 25(5), 548-552 (1989-05-01)
L-Pipecolic acid, a cyclic imino acid produced during the degradation of lysine, accumulates in body fluids of infants with the generalized peroxisomal disorders, including Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease. Peroxisome-enriched fractions from normal human liver oxidized L-[3H]pipecolic
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