Ornithine

别名: 2,5-二氨基戊酸;L-鸟氨酸;L-鸟氨酸 标准品;L-鸟氨酸,BR;L-鸟氨酸,L-Ornithine;L-鸟氨酸盐酸盐;鸟氨酸;2,5-二氨基戊酸 L-鸟氨酸 L-2,5-二氨基戊酸 L-氨基戊氨酸 L-鸟粪氨基酸 二氨戊酸
目录号: V8762 纯度: ≥98%
L-鸟氨酸((S)-2,5-二氨基戊酸)是一种非蛋白质衍生氨基酸 (AA),主要用于尿素循环,以清除体内多余的氮。
Ornithine CAS号: 70-26-8
产品类别: New1
产品仅用于科学研究,不针对患者销售
规格 价格 库存 数量
100mg
250mg
500mg
Other Sizes

Other Forms of Ornithine:

  • L-Ornithine-d7 hydrochloride (L-ornithine hydrochloride-d7)
  • L-Ornithine-1,2,3,4,5-13C5 hydrochloride (L-Ornithine hydrochloride-13C5)
  • DL-Ornithine hydrochloride
  • Poly-L-ornithine hydrochloride (MW 15000-30000)
  • L-鸟氨酸盐酸盐
点击了解更多
InvivoChem产品被CNS等顶刊论文引用
产品描述
L-鸟氨酸((S)-2,5-二氨基戊酸)是一种非蛋白质衍生氨基酸 (AA),主要用于尿素循环,以清除体内多余的氮。 L-鸟氨酸具有肾脏保护作用。
生物活性&实验参考方法
体外研究 (In Vitro)
L-鸟氨酸 (0–10 mM) 影响 HK-2 细胞中的 Ca2+ 信号传导,并以浓度依赖性方式激活 CaSR [2]。在 HK-2 细胞中,L-鸟氨酸 (10 mM) 刺激 TRPC 通道介导的 Ca2+ 进入途径 [2]。通过 ROCE 途径,L-鸟氨酸(100 或 300 μM;24 小时)表现出对 HK-2 细胞中 ROS 生成的保护作用 [2]。当 H2O2 暴露于 HK-2 细胞时,L-鸟氨酸 (10 μM) 可防止 ROS 和氧化损伤 [2]。
药代性质 (ADME/PK)
Absorption, Distribution and Excretion
Absorbed from the small intestine via a sodium-dependent active transport process
Metabolism / Metabolites
Ornithine undergoes extensive metabolism in the liver to L-arginine, polyamines, and proline, and several other metabolites.
Ornithine undergoes extensive metabolism in the liver to L-arginine, polyamines, and proline, and several other metabolites.
毒性/毒理 (Toxicokinetics/TK)
Toxicity Summary
L-Ornithine is metabolised to L-arginine. L-arginine stimulates the pituitary release of growth hormone. Burns or other injuries affect the state of L-arginine in tissues throughout the body. As De novo synthesis of L-arginine during these conditions is usually not sufficient for normal immune function, nor for normal protein synthesis, L-ornithine may have immunomodulatory and wound-healing activities under these conditions (by virtue of its metabolism to L-arginine).
Toxicity Data
Oral, rat LD50 = 10000 mg/kg
参考文献

[1]. Effect of L-ornithine hydrochloride ingestion on intermittent maximal anaerobic cycle ergometer performance and fatigue recovery after exercise. Eur J Appl Physiol. 2011 Nov;111(11):2837-43.

[2]. l-ornithine activates Ca2+ signaling to exert its protective function on human proximal tubular cells. Cell Signal. 2020 Mar;67:109484.

其他信息
L-ornithine is an optically active form of ornithine having L-configuration. It has a role as a hepatoprotective agent, an algal metabolite and a mouse metabolite. It is an ornithine and a non-proteinogenic L-alpha-amino acid. It is a conjugate base of a L-ornithinium(1+). It is a conjugate acid of a L-ornithinate. It is an enantiomer of a D-ornithine.
Produced during the urea cycle, ornithine is an amino acid produced from the splitting off of urea from arginine. L-Ornithine allows for the disposal of excess nitrogen and acts as a precursor of citrulline and arginine.
Ornithine is a metabolite found in or produced by Escherichia coli (strain K12, MG1655).
L-Ornithine is a metabolite found in or produced by Escherichia coli (strain K12, MG1655).
L-ornithine has been reported in Euphorbia prostrata, Glycine max, and other organisms with data available.
Ornithine is a naturally occurring amino acid found in meat, fish, dairy and eggs. Ornithine is one of the key reactants in the urea cycle that is responsible for 80% of the nitrogen excretion in the body. Ornithine enhances liver function and helps detoxify harmful substances.
Ornithine is an amino acid produced in the urea cycle by the splitting off of urea from arginine. It is a central part of the urea cycle, which allows for the disposal of excess nitrogen. L-Ornithine is also a precursor of citrulline and arginine. In order for ornithine produced in the cytosol to be converted to citrulline, it must first cross the inner mitochondrial membrane into the mitochondrial matrix where it is carbamylated by ornithine transcarbamylase. This transfer is mediated by the mitochondrial ornithine transporter (SLC25A15; AF112968; ORNT1). Mutations in the mitochondrial ornithine transporter result in hyperammonemia, hyperornithinemia, homocitrullinuria (HHH) syndrome, a disorder of the urea cycle. The pathophysiology of thef the disease may involve diminished ornithine transport into mitochondria, resulting in ornithine accumulation in the cytoplasm and reduced ability to clear carbamoyl phosphate and ammonia loads. (OMIM 838970). (A3420).
An amino acid produced in the urea cycle by the splitting off of urea from arginine.
See also: Lysine (annotation moved to).
Drug Indication
Used for nutritional supplementation, also for treating dietary shortage or imbalance. It has been claimed that ornithine improves athletic performance, has anabolic effects, has wound-healing effects, and is immuno-enhancing.
Mechanism of Action
L-Ornithine is metabolised to L-arginine. L-arginine stimulates the pituitary release of growth hormone. Burns or other injuries affect the state of L-arginine in tissues throughout the body. As De novo synthesis of L-arginine during these conditions is usually not sufficient for normal immune function, nor for normal protein synthesis, L-ornithine may have immunomodulatory and wound-healing activities under these conditions (by virtue of its metabolism to L-arginine).
Pharmacodynamics
A non-essential and nonprotein amino acid, ornithine is critical for the production of the body's proteins, enzymes and muscle tissue. Ornithine plays a central role in the urea cycle and is important for the disposal of excess nitrogen (ammonia). Ornithine is the starting point for the synthesis of many polyamines such as putrescine and spermine. Ornithine supplements are claimed to enhance the release of growth hormone and to burn excess body fat. Ornithine is necessary for proper immune function and good liver function.
*注: 文献方法仅供参考, InvivoChem并未独立验证这些方法的准确性
化学信息 & 存储运输条件
分子式
C5H12N2O2
分子量
132.16098
精确质量
132.089
CAS号
70-26-8
相关CAS号
L-Ornithine hydrochloride;3184-13-2
PubChem CID
6262
外观&性状
White to off-white solid powder
密度
1.2±0.1 g/cm3
沸点
308.7±32.0 °C at 760 mmHg
熔点
140ºC
闪点
140.5±25.1 °C
蒸汽压
0.0±1.4 mmHg at 25°C
折射率
1.508
LogP
-0.96
tPSA
89.34
氢键供体(HBD)数目
3
氢键受体(HBA)数目
4
可旋转键数目(RBC)
4
重原子数目
9
分子复杂度/Complexity
95
定义原子立体中心数目
1
SMILES
N[C@@H](CCCN)C(O)=O
InChi Key
AHLPHDHHMVZTML-BYPYZUCNSA-N
InChi Code
InChI=1S/C5H12N2O2/c6-3-1-2-4(7)5(8)9/h4H,1-3,6-7H2,(H,8,9)/t4-/m0/s1
化学名
(2S)-2,5-diaminopentanoic acid
HS Tariff Code
2934.99.9001
存储方式

Powder      -20°C    3 years

                     4°C     2 years

In solvent   -80°C    6 months

                  -20°C    1 month

注意: 请将本产品存放在密封且受保护的环境中(例如氮气保护),避免吸湿/受潮和光照。
运输条件
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
溶解度数据
溶解度 (体外实验)
H2O : ~50 mg/mL (~378.33 mM)
DMSO : ~1.3 mg/mL (~9.84 mM)
溶解度 (体内实验)
注意: 如下所列的是一些常用的体内动物实验溶解配方,主要用于溶解难溶或不溶于水的产品(水溶度<1 mg/mL)。 建议您先取少量样品进行尝试,如该配方可行,再根据实验需求增加样品量。

注射用配方
(IP/IV/IM/SC等)
注射用配方1: DMSO : Tween 80: Saline = 10 : 5 : 85 (如: 100 μL DMSO 50 μL Tween 80 850 μL Saline)
*生理盐水/Saline的制备:将0.9g氯化钠/NaCl溶解在100 mL ddH ₂ O中,得到澄清溶液。
注射用配方 2: DMSO : PEG300Tween 80 : Saline = 10 : 40 : 5 : 45 (如: 100 μL DMSO 400 μL PEG300 50 μL Tween 80 450 μL Saline)
注射用配方 3: DMSO : Corn oil = 10 : 90 (如: 100 μL DMSO 900 μL Corn oil)
示例: 注射用配方 3 (DMSO : Corn oil = 10 : 90) 为例说明, 如果要配制 1 mL 2.5 mg/mL的工作液, 您可以取 100 μL 25 mg/mL 澄清的 DMSO 储备液,加到 900 μL Corn oil/玉米油中, 混合均匀。
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注射用配方 4: DMSO : 20% SBE-β-CD in Saline = 10 : 90 [如:100 μL DMSO 900 μL (20% SBE-β-CD in Saline)]
*20% SBE-β-CD in Saline的制备(4°C,储存1周):将2g SBE-β-CD (磺丁基-β-环糊精) 溶解于10mL生理盐水中,得到澄清溶液。
注射用配方 5: 2-Hydroxypropyl-β-cyclodextrin : Saline = 50 : 50 (如: 500 μL 2-Hydroxypropyl-β-cyclodextrin (羟丙基环胡精) 500 μL Saline)
注射用配方 6: DMSO : PEG300 : Castor oil : Saline = 5 : 10 : 20 : 65 (如: 50 μL DMSO 100 μL PEG300 200 μL Castor oil 650 μL Saline)
注射用配方 7: Ethanol : Cremophor : Saline = 10: 10 : 80 (如: 100 μL Ethanol 100 μL Cremophor 800 μL Saline)
注射用配方 8: 溶解于Cremophor/Ethanol (50 : 50), 然后用生理盐水稀释。
注射用配方 9: EtOH : Corn oil = 10 : 90 (如: 100 μL EtOH 900 μL Corn oil)
注射用配方 10: EtOH : PEG300Tween 80 : Saline = 10 : 40 : 5 : 45 (如: 100 μL EtOH 400 μL PEG300 50 μL Tween 80 450 μL Saline)


口服配方
口服配方 1: 悬浮于0.5% CMC Na (羧甲基纤维素钠)
口服配方 2: 悬浮于0.5% Carboxymethyl cellulose (羧甲基纤维素)
示例: 口服配方 1 (悬浮于 0.5% CMC Na)为例说明, 如果要配制 100 mL 2.5 mg/mL 的工作液, 您可以先取0.5g CMC Na并将其溶解于100mL ddH2O中,得到0.5%CMC-Na澄清溶液;然后将250 mg待测化合物加到100 mL前述 0.5%CMC Na溶液中,得到悬浮液。
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口服配方 3: 溶解于 PEG400 (聚乙二醇400)
口服配方 4: 悬浮于0.2% Carboxymethyl cellulose (羧甲基纤维素)
口服配方 5: 溶解于0.25% Tween 80 and 0.5% Carboxymethyl cellulose (羧甲基纤维素)
口服配方 6: 做成粉末与食物混合


注意: 以上为较为常见方法,仅供参考, InvivoChem并未独立验证这些配方的准确性。具体溶剂的选择首先应参照文献已报道溶解方法、配方或剂型,对于某些尚未有文献报道溶解方法的化合物,需通过前期实验来确定(建议先取少量样品进行尝试),包括产品的溶解情况、梯度设置、动物的耐受性等。

请根据您的实验动物和给药方式选择适当的溶解配方/方案:
1、请先配制澄清的储备液(如:用DMSO配置50 或 100 mg/mL母液(储备液));
2、取适量母液,按从左到右的顺序依次添加助溶剂,澄清后再加入下一助溶剂。以 下列配方为例说明 (注意此配方只用于说明,并不一定代表此产品 的实际溶解配方):
10% DMSO → 40% PEG300 → 5% Tween-80 → 45% ddH2O (或 saline);
假设最终工作液的体积为 1 mL, 浓度为5 mg/mL: 取 100 μL 50 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀/澄清;向上述体系中加入50 μL Tween-80,混合均匀/澄清;然后继续加入450 μL ddH2O (或 saline)定容至 1 mL;

3、溶剂前显示的百分比是指该溶剂在最终溶液/工作液中的体积所占比例;
4、 如产品在配制过程中出现沉淀/析出,可通过加热(≤50℃)或超声的方式助溶;
5、为保证最佳实验结果,工作液请现配现用!
6、如不确定怎么将母液配置成体内动物实验的工作液,请查看说明书或联系我们;
7、 以上所有助溶剂都可在 Invivochem.cn网站购买。
制备储备液 1 mg 5 mg 10 mg
1 mM 7.5666 mL 37.8329 mL 75.6659 mL
5 mM 1.5133 mL 7.5666 mL 15.1332 mL
10 mM 0.7567 mL 3.7833 mL 7.5666 mL

1、根据实验需要选择合适的溶剂配制储备液 (母液):对于大多数产品,InvivoChem推荐用DMSO配置母液 (比如:5、10、20mM或者10、20、50 mg/mL浓度),个别水溶性高的产品可直接溶于水。产品在DMSO 、水或其他溶剂中的具体溶解度详见上”溶解度 (体外)”部分;

2、如果您找不到您想要的溶解度信息,或者很难将产品溶解在溶液中,请联系我们;

3、建议使用下列计算器进行相关计算(摩尔浓度计算器、稀释计算器、分子量计算器、重组计算器等);

4、母液配好之后,将其分装到常规用量,并储存在-20°C或-80°C,尽量减少反复冻融循环。

计算器

摩尔浓度计算器可计算特定溶液所需的质量、体积/浓度,具体如下:

  • 计算制备已知体积和浓度的溶液所需的化合物的质量
  • 计算将已知质量的化合物溶解到所需浓度所需的溶液体积
  • 计算特定体积中已知质量的化合物产生的溶液的浓度
使用摩尔浓度计算器计算摩尔浓度的示例如下所示:
假如化合物的分子量为350.26 g/mol,在5mL DMSO中制备10mM储备液所需的化合物的质量是多少?
  • 在分子量(MW)框中输入350.26
  • 在“浓度”框中输入10,然后选择正确的单位(mM)
  • 在“体积”框中输入5,然后选择正确的单位(mL)
  • 单击“计算”按钮
  • 答案17.513 mg出现在“质量”框中。以类似的方式,您可以计算体积和浓度。

稀释计算器可计算如何稀释已知浓度的储备液。例如,可以输入C1、C2和V2来计算V1,具体如下:

制备25毫升25μM溶液需要多少体积的10 mM储备溶液?
使用方程式C1V1=C2V2,其中C1=10mM,C2=25μM,V2=25 ml,V1未知:
  • 在C1框中输入10,然后选择正确的单位(mM)
  • 在C2框中输入25,然后选择正确的单位(μM)
  • 在V2框中输入25,然后选择正确的单位(mL)
  • 单击“计算”按钮
  • 答案62.5μL(0.1 ml)出现在V1框中
g/mol

分子量计算器可计算化合物的分子量 (摩尔质量)和元素组成,具体如下:

注:化学分子式大小写敏感:C12H18N3O4  c12h18n3o4
计算化合物摩尔质量(分子量)的说明:
  • 要计算化合物的分子量 (摩尔质量),请输入化学/分子式,然后单击“计算”按钮。
分子质量、分子量、摩尔质量和摩尔量的定义:
  • 分子质量(或分子量)是一种物质的一个分子的质量,用统一的原子质量单位(u)表示。(1u等于碳-12中一个原子质量的1/12)
  • 摩尔质量(摩尔重量)是一摩尔物质的质量,以g/mol表示。
/

配液计算器可计算将特定质量的产品配成特定浓度所需的溶剂体积 (配液体积)

  • 输入试剂的质量、所需的配液浓度以及正确的单位
  • 单击“计算”按钮
  • 答案显示在体积框中
动物体内实验配方计算器(澄清溶液)
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量)
第二步:请输入动物体内配方组成(配方适用于不溶/难溶于水的化合物),不同的产品和批次配方组成不同,如对配方有疑问,可先联系我们提供正确的体内实验配方。此外,请注意这只是一个配方计算器,而不是特定产品的确切配方。
+
+
+

计算结果:

工作液浓度 mg/mL;

DMSO母液配制方法 mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL)。如该浓度超过该批次药物DMSO溶解度,请首先与我们联系。

体内配方配制方法μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL ddH2O,混匀澄清。

(1) 请确保溶液澄清之后,再加入下一种溶剂 (助溶剂) 。可利用涡旋、超声或水浴加热等方法助溶;
            (2) 一定要按顺序加入溶剂 (助溶剂) 。

临床试验信息
NCT Number Recruitment interventions Conditions Sponsor/Collaborators Start Date Phases
NCT06455267 RECRUITING Dietary Supplement: Now Foods L-Ornithine Capsules Mild to Severe Crohns Disease The Third Xiangya Hospital of Central South University 2024-04-01 Not Applicable
NCT03159390 UNKNOWN STATUS Other: phenylacetate salt of ornithine Healthy Texas A&M University 2015-02 Not Applicable
NCT01722578 COMPLETED Drug: L-ornithine L-aspartate
Drug: Placebo
Cirrhosis of Liver
Hepatic Encephalopathy
Dayanand Medical College and Hospital 2013-12 Phase 4
NCT00896831 UNKNOWN STATUS Drug: L-ornithine-L-aspartate
Drug: placebo
Hepatic Encephalopathy Hospital de Clinicas de Porto Alegre 2008-11 Phase 4
NCT03846843 COMPLETED Drug: OCR-002 IR Oral Tablet
Drug: OCR-002 Oral Solution
Drug: OCR-002 IV Solution
Cirrhosis Ocera Therapeutics, Inc. 2016-08-15 Phase 1
生物数据图片
  • A. Mean Fura-2 Fluorescent traces of HK-2 cells in 1.2 mM [Ca2+]o solution upon application of L-ornithine (L-Orn) to elicit concentration-dependent response (0 mM, 1.0 mM, 3.0 mM, and 10 mM). Bar diagram depicts peak ratiometric [Ca2+]i after L-Orn application. B. Whole-cell patch clamp current of HK-2 cell upon concentration dependent application of L-Orn (100, 500, and 1000 uM) with voltage sweep from −100 to +100 mV. Bar diagram depicts peak current at +100 mV. Fura-2 fluorescent traces of transfected HK-2 cells with C. 0 nM, D. 10 nM, or E. 20 nM CaSR siRNA bathed in 0.5 mM [Ca2+]o solution with application of 10 mM L-Orn followed by 2.0 mM [Ca2+]o. F. Bar diagram depicts peak [Ca2+]i entry for C-D. Two-tailed t-test statistical analysis performed for A, B, and F. *, p<0.05; **, p<0.01.[2]. Shin S, et al. l-ornithine activates Ca2+ signaling to exert its protective function on human proximal tubular cells. Cell Signal. 2020 Mar;67:109484.
  • Mean Fura-2 fluorescent traces of HK-2 cells bathed in 0.5 mM [Ca2+]o solution incubated in A. 1 μM NPS-2143 (NPS), B. 1 μM SKF-96163 (SKF), or C. 12 μM 2-APB, with application of 10 mM L-ornithine (L-Orn) followed by 2.0 mM [Ca2+]o solution. D. Bar diagram depicts peak Ca2+ entry for A, B, and C. Average whole-cell patch clamp current of HK-2 cell upon application of L-Orn followed by inhibition with E. NPS, F. SKF, or G. 2-APB, with voltage sweep from −100 to +100 mV. Bar diagram for each current graph depicts peak current at +100 mV. Two-tailed t-test statistical analysis performed for D, E, F, and G. +, added activator/inhibitor. *, p<0.05; **, p<0.01.[2]. Shin S, et al. l-ornithine activates Ca2+ signaling to exert its protective function on human proximal tubular cells. Cell Signal. 2020 Mar;67:109484.
  • A. Mean Fura-2 fluorescent traces of HK-2 cells bathed in 0.5 mM [Ca2+]o solution incubated in 3 μM Pyr6 or 3 μM Pyr10, with application of 10 mM L-ornithine (L-Orn) followed by 2.0 mM [Ca2+]o solution. Bar diagram depicts peak Ca2+ entry for A. Average whole-cell patch clamp current of HK-2 cell upon application of L-Orn followed by inhibition with B. Pyr6, or C. Pyr10, with voltage sweep from −100 to +100 mV. Bar diagram for each current graph depicts peak current at +100 mV. +, added activator/inhibitor. Two-tailed t-test statistical analysis performed for A, B, and C. *, p<0.05; **, p<0.01.[2]. Shin S, et al. l-ornithine activates Ca2+ signaling to exert its protective function on human proximal tubular cells. Cell Signal. 2020 Mar;67:109484.
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