Lisina

Lisina
	; Formula rerangka L-lisina
Model bola-batang	Model isi ruang
Nama
	Nama IUPAC (2S)-2,6-Diaminohexanoic acid (L-lysine) (2R)-2,6-Diaminohexanoic acid (D-lysine)
	Nama lain Lysine, D-lysine, L-lysine, LYS, h-Lys-OH
Pengecam
No. Pendaftaran CAS	70-54-2 DL ; 56-87-1 L ; 923-27-3 D ;
Imej model 3D Jmol	Imej berinteraktif; Zwitterion: Imej berinteraktif; Protonated zwitterion: Imej berinteraktif;
ChEBI	CHEBI:25094 ;
ChEMBL	ChEMBL28328 ;
ChemSpider	843 ; 5747 L ;
ECHA InfoCard	100.000.673
IUPHAR/BPS	724;
KEGG	C16440 ;
PubChem CID	866;
UNII	AI4RT59273 DL ; K3Z4F929H6 L ; 3HQ6U6424Q D ;
CompTox Dashboard (EPA)	DTXSID90859004 ;
	InChI InChI=1S/C6H14N2O2/c7-4-2-1-3-5(8)6(9)10/h5H,1-4,7-8H2,(H,9,10) Key: KDXKERNSBIXSRK-UHFFFAOYSA-N ; InChI=1/C6H14N2O2/c7-4-2-1-3-5(8)6(9)10/h5H,1-4,7-8H2,(H,9,10) Key: KDXKERNSBIXSRK-UHFFFAOYAY;
	SMILES NCCCCC(N)C(=O)O; Zwitterion: NCCCCC([NH3+])C(=O)[O-]; Protonated zwitterion: [NH3+]CCCCC([NH3+])C(=O)[O-];
Sifat
Formula kimia	C6H14N2O2
Jisim molar	146.19 g·mol−1
Keterlarutan dalam air	1.5 kg/L
Farmakologi
Kod ATC	B05XB03
	Kecuali jika dinyatakan sebaliknya, data diberikan untuk bahan-bahan dalam keadaan piawainya (pada 25 °C [77 °F], 100 kPa).
	pengesahan (apa yang perlu: /?)
	Rujukan kotak info

Lisina (bahasa Inggeris: Lysinecode: en is deprecated , disingkatkan kepada Lys or K)^[2] ialah sejenis asid amino alfa yang penting dalam biosintesis protein.

Rujukan

^ ^a ^b Williams, P. A.; Hughes, C. E.; Harris, K. D. M (2015). "L‐Lysine: Exploiting Powder X‐ray Diffraction to Complete the Set of Crystal Structures of the 20 Directly Encoded Proteinogenic Amino Acids". Angew. Chem. Int. Ed. 54 (13): 3973–3977. doi:10.1002/anie.201411520. PMID 25651303.
^ "IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN). Nomenclature and symbolism for amino acids and peptides. Recommendations 1983". Biochemical Journal. 219 (2): 345–373. 15 April 1984. doi:10.1042/bj2190345. PMC 1153490. PMID 6743224.

[Williams-1] Williams, P. A.; Hughes, C. E.; Harris, K. D. M (2015). "L‐Lysine: Exploiting Powder X‐ray Diffraction to Complete the Set of Crystal Structures of the 20 Directly Encoded Proteinogenic Amino Acids". Angew. Chem. Int. Ed. 54 (13): 3973–3977. doi:10.1002/anie.201411520. PMID 25651303.

[2] "IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN). Nomenclature and symbolism for amino acids and peptides. Recommendations 1983". Biochemical Journal. 219 (2): 345–373. 15 April 1984. doi:10.1042/bj2190345. PMC 1153490. PMID 6743224.

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