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street name for lysergic acid diethylamide (同)back breaker, battery-acid, dose, dot, Elvis, loony toons, Lucy in the sky with diamonds, pane, superman, window pane, Zen
any of various water-soluble compounds having a sour taste and capable of turning litmus red and reacting with a base to form a salt
having the characteristics of an acid; "an acid reaction"

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2017/08/15 05:36:15」(JST)

Carbamoyl aspartic acid (or ureidosuccinic acid) is a carbamate derivative which serves as an intermediate in pyrimidine biosynthesis.

^ "ureidosuccinic acid - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 26 March 2005. Identification. Retrieved 27 June 2012.

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5. 腫瘍随伴性および自己免疫性脳炎 paraneoplastic and autoimmune encephalitis

Regulation of Cell Wall Plasticity by Nucleotide Metabolism in Lactococcus lactis.

Solopova A1, Formosa-Dague C2, Courtin P3, Furlan S3, Veiga P3, Péchoux C4, Armalyte J3, Sadauskas M3, Kok J1, Hols P2, Dufrêne YF2, Kuipers OP1, Chapot-Chartier MP3, Kulakauskas S5.
The Journal of biological chemistry.J Biol Chem.2016 May 20;291(21):11323-36. doi: 10.1074/jbc.M116.714303. Epub 2016 Mar 28.
To ensure optimal cell growth and separation and to adapt to environmental parameters, bacteria have to maintain a balance between cell wall (CW) rigidity and flexibility. This can be achieved by a concerted action of peptidoglycan (PG) hydrolases and PG-synthesizing/modifying enzymes. In a search f
PMID 27022026

[Study on Serum Metabolite Profiling in Pi-deficiency Rats Based on LC-MS Technique].

Jia LQ, Zhen BX, Xu Ying, Yang GL.
Zhongguo Zhong xi yi jie he za zhi Zhongguo Zhongxiyi jiehe zazhi = Chinese journal of integrated traditional and Western medicine / Zhongguo Zhong xi yi jie he xue hui, Zhongguo Zhong yi yan jiu yuan zhu ban.Zhongguo Zhong Xi Yi Jie He Za Zhi.2016 Mar;36(3):359-65.
OBJECTIVE: To explore metabolite profiling changes in serum of rats with pi-qi deficiency syndrome (PQDS) and pi-yang deficiency syndrome (PYDS) based on liquid chromatograph-mass spectrometer (LC-MS) technique, and to explore the essence of Pi-deficiency syndrome (PDS) from small molecule metabolit
PMID 27236897

Diversion of aspartate in ASS1-deficient tumours fosters de novo pyrimidine synthesis.

Rabinovich S1, Adler L1, Yizhak K2, Sarver A1, Silberman A1, Agron S1, Stettner N1, Sun Q3, Brandis A4, Helbling D5, Korman S6, Itzkovitz S7, Dimmock D5, Ulitsky I1, Nagamani SC3,8, Ruppin E2,9,10, Erez A1.
Nature.Nature.2015 Nov 19;527(7578):379-83. doi: 10.1038/nature15529. Epub 2015 Nov 11.
Cancer cells hijack and remodel existing metabolic pathways for their benefit. Argininosuccinate synthase (ASS1) is a urea cycle enzyme that is essential in the conversion of nitrogen from ammonia and aspartate to urea. A decrease in nitrogen flux through ASS1 in the liver causes the urea cycle diso
PMID 26560030

Chromium(III) complexes with amino acids. III. Chromium(III) complexes with acidic, basic and carbamoyl amino acids.

,
Bulletin of the Chemical Society of Japan 50(9), 2288-2291, 1977
… Syntheses by both the isothermal matrix in a solid state and by the usual solution method have been tried for chromium (III) complexes with L- and DL-asparagine, L- and DL-aspartic acid, L- and DL-glutamine, L- and DL-glutamic acid, L- and DL-lysine, and L-ornithine. …
NAID 130001970235

INTERACTION BETWEEN HELIANGINE AND PYRIMIDINES IN ADVENTITIOUS ROOT FORMATION OF PHASEOLUS CUTTINGS

SHIBAOKA HIROH,ANZAI TADASHI,MITSUHASHI MIEKO,SHIMOKORIYAMA MASAMI
Plant and cell physiology 8(4), 647-656, 1967-12
… The promotion was almost completely reversed by 3×10^<-4>M uracil, uridine, cytidine, orotic acid or 6×10^<-4>M carbamoyl DL-aspartic acid, and partly by 3×10^<-4>M thymine or thymidine. … M carbamoyl phosphate and 3×10^<-4>M L-aspartic acid reduced the promotion by heliangine. …
NAID 110003721827

リンク元	「カルバモイルアスパラギン酸」
関連記事	「aspartic」

Carbamoyl aspartic acid
Names
	IUPAC name 2-(Carbamoylamino)butanedioic acid
Identifiers
CAS Number	923-37-5 ; 13184-27-5 S ;
3D model (JSmol)	Interactive image; Interactive image;
3DMet	B00115
Beilstein Reference	1726861, 1726860 S
ChEBI	CHEBI:15859 ;
ChemSpider	273 ; 1267120 R ; 84022 S ;
DrugBank	DB04252 ;
ECHA InfoCard	100.011.906
EC Number	213-096-6
KEGG	C00438 ;
MeSH	ureidosuccinic+acid
PubChem CID	279; 1550569 R; 93072 S;
	InChI InChI=1S/C5H8N2O5/c6-5(12)7-2(4(10)11)1-3(8)9/h2H,1H2,(H,8,9)(H,10,11)(H3,6,7,12) Key: HLKXYZVTANABHZ-UHFFFAOYSA-N ;
	SMILES [nH2]:c(:[o]):[nH]C(Cc(:[o]):[oH])c(:[o]):[oH] ; NC(=O)NC(CC(O)=O)C(O)=O ;
Properties
Chemical formula	C5H8N2O5
Molar mass	176.13 g·mol−1
log P	−0.663
Acidity (pKa)	3.649
Basicity (pKb)	10.348
Related compounds
Related alkanoic acids	3-Ureidopropionic acid; beta-Ureidoisobutyric acid; N-Acetylaspartic acid;
Related compounds	Biuret; Bromisoval; Carbromal;
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references