L-プロリン

proline dl-form

HCID 614CAS 147-85-3

基本情報

標準SMILES
O=C(O)C1CCCN1
InChIKey
ONIBWKKTOPOVIA-UHFFFAOYSA-N
分子式
C5H9NO2
平均分子量
115.13 g/mol
単同位体質量
115.06332853

概要

Proline is an alpha-amino acid that is pyrrolidine bearing a carboxy substituent at position 2. It has a role as a human metabolite and a Daphnia magna metabolite. It is an alpha-amino acid and a member of pyrrolidines. It is a conjugate base of a prolinium. It is a conjugate acid of a prolinate.

名称と識別子

優先名称
proline dl-form
IUPAC
pyrrolidine-2-carboxylic acid
現地名
L-プロリン
英語名
L-Proline
分子式
C5H9NO2
分子量
115.13

名称と別名

609-36-9Proline, DL-Proline DL-formUNII-DCS9E77JPQDCS9E77JPQCCRIS 8602EINECS 210-189-3NSC 97923NSC-97923PROLINE DL-FORM [MI]2-PYRROLIDINYLCARBOXYLIC ACID(+-)-proline
名称をさらに表示
L-プロリンプロリンL(-)-プロリンL-2-ピロリジンカルボン酸L(-)‐プロリンL‐プロリンL‐プロリン CRM6016‐AL-プロリン-D7プロリン, L-L-プロリン (JP17)プロリン 1プロリン 2プロリンL-プロリン CRM6016-aPROH-PRO-OHL-PROl-prolinL-Pro-OH2-pyrrolidinecarboxylic acid(S)-PYRROLIDINE-2-CARBOXYLIC ACID(2S)-pyrrolidine-2-carboxylic acidL-PolineH-L-PRO-OH
RefChem:202730210-189-3DL-Prolinepyrrolidine-2-carboxylic acidH-DL-Pro-OHD-Pyrrolidine-2-carboxylic acidMFCD000052502-Pyrrolidine carboxylic acid

データベース識別子

CAS
147-85-3、609-36-9
PubChem CID
614
DTXSID
DTXSID9041104
ChEBI
CHEBI:26271
UNII
DCS9E77JPQ
EC Number
210-189-3
Nikkaji
J1.287D

物性

構造計算による物性

XLogP
-2.5
極性表面積
49.3 Ų
水素結合供与体数
2
水素結合受容体数
3
回転可能結合数
1
重原子数
8

実験および物理化学的性質

Chemical ClassesBiological Agents -> Amino Acids and Derivatives
DrugsPharmaceuticals
Physical DescriptionBeige solid; [Sigma-Aldrich MSDS]

物理化学的性質

融点
228 °C · 228 °C (dec.) (lit.)
比旋光度
-85.5 · -85.5 º (c=4, H2O)
沸点
215.41 °C · 215.41°C (rough estimate)
比重(密度)
1.35 · 1.35
蒸気圧
0 Pa · 0Pa at 25℃
FEMA
3319 · 3319 | L-PROLINE
化学的性質 · 1 件

化学的特性L-Proline, an amino acid, is colorless to white crystal or crystalline powder that has a slight, characteristic odor with a slightly sweet taste. It is soluble in water, insoluble in ethanol, diethyl ether and n-butanol, yellow in case of hydrated ninhydrin test solution, glacial acetic acid Red after acidification; pH=6.3, decomposition point is 220-222°C; specific optical rotation [α]20D-85° (0.5-2.0mg/ml, H2O), [α]20D-60.4° (0.5-2.0mg /ml, 5mol/LHCl). It is synthesized from L-glutamine and L-glutamate via L-ornithine in intestine, and from L-ornithine in liver. It is widely used as an ingredient in infusion and infant formula.

安全と法規制

GHS分類

GHS Classification · 3 件

This chemical does not meet GHS hazard criteria for 95.5% (21 of 22) of all reports.

Not Classified

Aggregated GHS information provided per 22 reports by companies from 2 notifications to the ECHA C&L Inventory.

危険有害性情報

Regulatory InformationChemical: DL-Proline
Other Safety InformationIMAP assessments - DL-Proline: Environment tier I assessment
Hazards SummaryMay cause irritation; [Sigma-Aldrich MSDS]
Hazard Classes and CategoriesNot Classified

安全データ

F
3-10
wgk
3
tsca
TSCA listed
rtecs
TW3584000
毒性
LD50 orally in Rabbit: > 5110 mg/kg
hs_code
29339990

化学と産業

用途と製造

UsesProline is a non-essential amino acid; [Merck Index]
Household ProductsInformation on 32 consumer products that contain Proline in the following categories is provided:
Use ClassificationFlavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes
General Manufacturing InformationProline: ACTIVE
応用分野 · 4 件

解説L-プロリン,プロリン,(S)-pyrrolidine-2-carboxylic acid.C5H9NO2(115.13).略号ProまたはP.非必須アミノ酸.タンパク質構成アミノ酸として,また遊離の状態で広く分布している.タンパク質中では,ペプチド鎖の折れ曲がる位置に存在し,特殊な立体構造の保持に役立っている.ゼラチン,ツェイン,グリアジンなどの加水分解物からロダニル酸塩,ライネッケ塩を用いる沈殿法や,亜硝酸を作用させ,α-アミノ酸を分解する方法,あるいは発酵法で製造する.生体内ではグルタミン酸から合成される.L-プロリンは針状晶.分解点220~222 ℃.[α]20D-52.6°(0.5 mol L-1 塩酸).pK1 1.99,pK2 10.60,pI6.30.水,エタノールに易溶,エーテル,クロロホルムに不溶.γ-ヒドロキシ-,γ-メチル-,γ-メチル-γ-ヒドロキシプロリン類やプロリンベタインもコラーゲンや植物中に見いだされている.弱い甘味がある.

天然物の起源Reported found as a component in many proteins; also widely occurring as the free acid in natural products. A major constituent of collagen, the main fibrous protein found in bone, cartilage and other connective tissue.

使用L-Proline is an amino acid and precursor (with vitamin C) for collagen, the building block of the structure of tendons, ligaments, arteries, veins and muscles. It is important in wound healing.

一般的な説明L-Proline is a non-essential amino acid, which is a building block of proteins. Peptides bond to proline, making it a useful building block for proteins. It can be used as a cell culture media component for the commercial biomanufacturing of therapeutic recombinant proteins and monoclonal antibodies. L-Proline plays important roles in various biological processes. It is involved in the synthesis of collagen, which is one of the most abundant proteins in the human body and provides structural support to tissues such as skin, bone, cartilage, and tendons.

調製方法 · 2 件

製造方法Synthesis of L-proline: Using glutamic acid as a raw material, it is esterified with absolute ethanol under the catalysis of sulfuric acid, and triethanolamine is added to free the aminosulfate to obtain glutamic acid-δ-ethyl ester. The glutamic acid-δ-ethyl ester is then reduced with a metal reducing agent potassium borohydride to obtain crude proline, which is finally separated and purified to obtain crude L-proline.

純化方法A likely impurity is hydroxyproline. Purify L-proline via its picrate which is crystallised twice from water, then decomposed with 40% H2SO4. The picric acid is extracted with diethyl ether, the H2SO4 in solution is precipitated with Ba(OH)2, and the filtrate is evaporated. The residue is crystallised from hot absolute EtOH [Mellan & Hoover J Am Chem Soc 73 3879 1951] or EtOH/Et2O. Its solubility in H2O is >100%. It sublimes at 182-187o/0.3mm with 99.4% recovery and unracemised [Gross & Gradsky J Am Chem Soc 77 1678 1955]. It is hygroscopic and is stored in a desiccator. [Greenstein & Winitz The Chemistry of the Amino Acids J. Wiley, Vol 3 pp 2178-2199 1961, Beilstein 22 III/IV 8, 22/1 V 31.]

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補足説明 · 2 件

定義本品は、次の化学式で表されるアミノ酸である。

定義ChEBI: L-proline is pyrrolidine in which the pro-S hydrogen at position 2 is substituted by a carboxylic acid group. L-Proline is the only one of the twenty DNA-encoded amino acids which has a secondary amino group alpha to the carboxyl group. It is an essential component of collagen and is important for proper functioning of joints and tendons. It also helps maintain and strengthen heart muscles. It has a role as a micronutrient, a nutraceutical, an algal metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite, a mouse metabolite and a member of compatible osmolytes. It is a glutamine family amino acid, a proteinogenic amino acid, a proline and a L-alpha-amino acid. It is a conjugate base of a L-prolinium. It is a conjugate acid of a L-prolinate. It is an enantiomer of a D-proline. It is a tautomer of a L-proline zwitterion.

関連反応

321 件

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