ALIH Citakan:Disambig info

Prolin

modél bal-jeung-tongkat

modél ngeusi-rohang

Wasta

Wasta IUPAC

Prolin

Wasta IUPAC sistematik

Asam pirolidin-2-karboksilat^[1]

Pananda

Nomer CAS

L: 147-85-3^Y
D/L: 609-36-9^Y
D: 344-25-2^Y

Modél 3D (JSmol)

L: Gambar interaktif
L Zwitterion: Gambar interaktif

Rujukan Beilstein

80812

ChEBI

ChEMBL

L: ChEMBL72275^Y

ChemSpider

L: 128566^Y
D/L: 594^Y
D: 8640^Y

DrugBank

L: DB00172^Y

ECHA InfoCard

100.009.264

Nomer EC

210-189-3

Rujukan Gmelin

26927

KEGG

L: C00148^Y

MeSH

Proline

PubChem CID

L: 145742
D/L: 614
D: 8988

UNII

CompTox Dashboard (EPA)

L: DTXSID9041104

InChI

InChI=1S/C5H9NO2/c7-5(8)4-2-1-3-6-4/h4,6H,1-3H2,(H,7,8)/t4-/m0/s1^Y
Key: ONIBWKKTOPOVIA-BYPYZUCNSA-N^Y
D/L: Key: ONIBWKKTOPOVIA-UHFFFAOYSA-N
D: Key: ONIBWKKTOPOVIA-SCSAIBSYSA-N

SMILES

L: C1C[C@H](NC1)C(=O)O
L Zwitterion: [O-]C(=O)[C@H](CCC2)[NH2+]2

Sipat

Rumus kimia

C₅H₉NO₂

Massa molar

115132 g·mol⁻¹

Panampilan

Kristal transparan

Titik lebur

^{[convert: precision too large]} (dékomposa)

Solubilitas

1.5g/100g ethanol 19 degC^[2]

log P

-0.06

Kaasaman (pK_a)

1.99 (karboksil), 10.96 (amino)^[3]

Iwal disebutkeun séjén, data nu dipidangkeun keur matéri dina kaayaan baku (dina 25 °C, 100 kPa).

Rujukan kotak info

Prolin (lambang Pro atawa P)^[4] nyaéta asam organik anu jumplukan asam amino protéinogenik (dipaké dina biosintésis protéin), najan teu ngandung gugus amino -NH₂, ngan boga amina sekundér. Nitrogén amina sekundérna dina wangun NH₂⁺ dina kaayaan biologis, anapon gugus karboksil dina wangun −COO⁻. "Ranté gigir" ti karbon α nyambung ka nitrogén ngabentuk buleudan pirolidin, diklasipikasikeun jadi asam amino alipatik. Di manusa teu kaasup ésénsial, sabab ku awak bisa disintésis tina asam amino non-ésénsial L-glutamat. Ieu asam amino dikode ku sakabéh kodon anu dimimitian ku CC (CCU, CCC, CCA, jeung CCG).

Baca ogé

[édit | édit sumber]

Hiperprolinemia
Depisiénsi prolidase
Prolinol

Rujukan

[édit | édit sumber]

↑ Pubchem. "Proline". pubchem.ncbi.nlm.nih.gov. Diarsipkan dari versi asli tanggal 16 January 2014. Diakses tanggal 8 May 2018.
↑ H.-D. Belitz; W. Grosch; P. Schieberle (2009-01-15). Food Chemistry. p. 15. ISBN 978-3-540-69933-0. Diarsipkan dari versi asli tanggal 2016-05-15.
↑ Nelson, D.L., Cox, M.M., Principles of Biochemistry. NY: W.H. Freeman and Company.
↑ "Nomenclature and Symbolism for Amino Acids and Peptides". IUPAC-IUB Joint Commission on Biochemical Nomenclature. 1983. Diarsipkan dari versi asli tanggal 9 October 2008. Diakses tanggal 5 March 2018. Archived 9 Oktober 2008 di Wayback Machine

Bacaan salajengna

[édit | édit sumber]

Balbach, J.; Schmid, F. X. (2000), "Proline isomerization and its catalysis in protein folding", di Pain, R. H., Mechanisms of Protein Folding (2nd ed.), Oxford University Press, pp. 212–49, ISBN 978-0-19-963788-1 .
For a thorough scientific overview of disorders of proline and hydroxyproline metabolism, one can consult chapter 81 of OMMBID Charles Scriver, Beaudet, A.L., Valle, D., Sly, W.S., Vogelstein, B., Childs, B., Kinzler, K.W. (Accessed 2007). The Online Metabolic and Molecular Bases of Inherited Disease. New York: McGraw-Hill. - Summaries of 255 chapters, full text through many universities. There is also the OMMBID blog.

Tutumbu kaluar

[édit | édit sumber]

Citakan:Modulator reséptor glutamat ionotropik Citakan:Modulator reséptor glisin