A2536
L -2-氨基丁酸
BioReagent, suitable for cell culture
别名:
L-α-氨基丁酸
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关于此项目
经验公式（希尔记法）:
C4H9NO2
化学文摘社编号:
分子量:
103.12
UNSPSC Code:
12352205
NACRES:
NA.75
PubChem Substance ID:
EC Number:
216-083-3
Beilstein/REAXYS Number:
1720935
MDL number:
产品名称
L -2-氨基丁酸, BioReagent, suitable for cell culture
InChI key
QWCKQJZIFLGMSD-VKHMYHEASA-N
InChI
1S/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)/t3-/m0/s1
SMILES string
CC[C@H](N)C(O)=O
biological source
Porcine kidney
microbial
plant
product line
BioReagent
form
powder
technique(s)
cell culture | mammalian: suitable
solubility
water: 50 mg/mL, clear, colorless
shipped in
ambient
storage temp.
room temp
Quality Level
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Biochem/physiol Actions
L-α-氨基丁酸 (AABA) 是非天然氨基酸氨基丁酸的异构体，在 γ-谷氨酰循环中具有调节谷胱甘肽生物合成的活性。最近研究了 AABA 作为体外成熟培养液（NCSU 23 培养液）的补充，用于卵母细胞和胚胎的培养。本品已确认可用于细胞培养。在肽功能的研究中，AABA 也被用作丙氨酸的替代氨基酸。
General description
L-苏氨酸和 L-天冬氨酸经-转氨基反应合成 L-2-氨基丁酸。它是一种带有乙基侧链的 L-丙氨酸类似物。
signalword
Warning
hcodes
Hazard Classifications
Skin Sens. 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
l-2-Aminobutyric acid: two fully ordered polymorphs with Z?= 4
Gorbitz CH
Acta Crystallographica Section B, Structural Science, 66(2), 253-259 (2010)
A one-pot system for production of L-2-aminobutyric acid from L-threonine by L-threonine deaminase and a NADH-regeneration system based on L-leucine dehydrogenase and formate dehydrogenase
Tao R, et al.
Biotechnology Letters, 36(4), 835-841 (2014)
Izumi Kawabata et al.
Nature communications, 3, 722-722 (2012-03-08)
Synaptic remodelling coordinated with dendritic growth is essential for proper development of neural connections. After establishment of synaptic contacts, synaptic junctions are thought to become stationary and provide fixed anchoring points for further dendritic growth. However, the possibility of active
Danica P Galonić et al.
Nature chemical biology, 3(2), 113-116 (2007-01-16)
Enzymatic incorporation of a halogen atom is a common feature in the biosyntheses of more than 4,500 natural products. Halogenation of unactivated carbon centers in the biosyntheses of several compounds of nonribosomal peptide origin is carried out by a class
Cornelia Reimmann et al.
Journal of bacteriology, 186(19), 6367-6373 (2004-09-18)
In Pseudomonas aeruginosa, the antibiotic dihydroaeruginoate (Dha) and the siderophore pyochelin are produced from salicylate and cysteine by a thiotemplate mechanism involving the peptide synthetases PchE and PchF. A thioesterase encoded by the pchC gene was found to be necessary
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