Phenylalanin

Phenylalanin
	; Skeletal formula of L-phenylalanine
	; L-Phenylalanine at physiological pH
Ball-and-stick model	Space-filling model
Hō-miâ
Pronunciation	US: /ˌfɛnəlˈæləniːn/; UK: /ˌfiːnaɪl-/
	IUPAC hō-miâ Phenylalanine
	Hē-thóng-tek IUPAC hō-miâ (S)-2-Amino-3-phenylpropanoic acid
Sek-pia̍t-hō
CAS Number	L: 63-91-2 ; D/L: 150-30-1 ; D: 673-06-3 ;
3D model (JSmol)	L: Interactive image; L Zwitterion: Interactive image;
ChEBI	L: CHEBI:17295 ; D: CHEBI:16998 ;
ChEMBL	L: ChEMBL301523 ;
ChemSpider	L: 5910 ; D/L: 969 ; D: 64639 ;
DrugBank	L: DB00120 ;
ECHA InfoCard	100.000.517
IUPHAR/BPS	L: 3313;
KEGG	L: D00021 ;
PubChem CID	L: 6140; D/L: 994; D: 71567;
UNII	L: 47E5O17Y3R ; D/L: 8P946UF12S ; D: 032K16VRCU ;
	InChI InChI=1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)/t8-/m0/s1 Key: COLNVLDHVKWLRT-QMMMGPOBSA-N ; L: Key: COLNVLDHVKWLRT-QMMMGPOBBC; D/L: Key: COLNVLDHVKWLRT-UHFFFAOYSA-N; D: Key: COLNVLDHVKWLRT-MRVPVSSYSA-N;
	SMILES L: c1ccc(cc1)C[C@@H](C(=O)O)N; L Zwitterion: [NH3+][C@@H](CC1=CC=CC=C1)C([O-])=O;
Sèng-chit
Hòa-ha̍k-sek	C9H11NO2
Mole chit-liōng	165.19 g·mol−1
Acidity (pKa)	1.83 (carboxyl), 9.13 (amino)
Gûi-hiám
NFPA 704	1 2 0
	Tû-liáu te̍k-pia̍t chí chhut, chu-liāu sī kun-kù bu̍t-chit ê piau-chún chōng-thài (tī 25 °C [77 °F], 100 kPa).
	Infobox chham-chiàu

Phenylalanine (siok-siá: Phe / F), sī chi̍t chióng an-ki-sng, R group bô ke̍k-sèng, toà tiong-sèng tiān. Jîn-thé bô-hoat-tō ka-tī ha̍p-sêng chit khoán an-ki-sng.

Tsù-kái

↑ ^1.0 ^1.1 Ihlefeldt, Franziska Stefanie; Pettersen, Fredrik Bjarte; von Bonin, Aidan; Zawadzka, Malgorzata; Görbitz, Prof. Carl Henrik (2014). "The Polymorphs of L‐Phenylalanine". Angew. Chem. Int. Ed. 53 (49): 13600–13604. doi:10.1002/anie.201406886. PMID 25336255.
↑ Dawson RM, et al. (1959). Data for Biochemical Research. Oxford: Clarendon Press.

Pún bûn-chiuⁿ sī chi̍t phiⁿ phí-á-kiáⁿ. Lí thang tàu khok-chhiong lâi pang-chō͘ Wikipedia.

[Ihlefeldt-1] 1.0 ^1.1 Ihlefeldt, Franziska Stefanie; Pettersen, Fredrik Bjarte; von Bonin, Aidan; Zawadzka, Malgorzata; Görbitz, Prof. Carl Henrik (2014). "The Polymorphs of L‐Phenylalanine". Angew. Chem. Int. Ed. 53 (49): 13600–13604. doi:10.1002/anie.201406886. PMID 25336255.

[2] Dawson RM, et al. (1959). Data for Biochemical Research. Oxford: Clarendon Press.

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