L-Ornithine - Moligand™, 10mM in Water , Agonist of GPRC6 receptor, CAS No.70-26-8, Agonist of GPRC6 receptor

CAS: 70-26-8 Cat. No.: L425600 Peso molecular: 132.16 Número EC: 200-731-7
Disponible para pedir
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. 10mM in Water
Synonyms
L-ornithine|ornithine|70-26-8|(S)-2,5-Diaminopentanoic acid|(S)-Ornithine|(S)-2,5-diaminovaleric acid|Ornithine [INN]|(2S)-2,5-diaminopentanoic acid|L-Norvaline, 5-amino-|(S)-alpha,delta-Diaminovaleric acid|Ornithinum [Latin]|Ornitina [Spanish]|Ornithine
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
L425600-1ml
1
69,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™, 10mM in Water Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 23 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Information

L-ornithine ((S)-2,5-Diaminopentanoic acid) has an antifatigue effect by increasing the efficiency of energy consumption and promoting the excretion of ammonia. It is one of the key reactants in the urea cycle.

Specifications

Sinónimos
L-ornithine | ornithine | 70-26-8 | (S)-2, 5-Diaminopentanoic acid | (S)-Ornithine | (S)-2, 5-diaminovaleric acid | Ornithine [INN] | (2S)-2, 5-diaminopentanoic acid | L-Norvaline, 5-amino- | (S)-alpha, delta-Diaminovaleric acid | Ornithinum [Latin] | Ornitina [Spanish] | Ornithine
Especificaciones y pureza
Moligand™, 10mM in Water
Mecanismos bioquímicos y fisiológicos
L-ornithine ((S)-2, 5-Diaminopentanoic acid) has an antifatigue effect by increasing the efficiency of energy consumption and promoting the excretion of ammonia. It is one of the key reactants in the urea cycle.
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Grado
Moligand™
Tipo de acción
AGONIST
Mecanismo de acción
Agonist of GPRC6 receptor
Propiedades del producto
ALogP-3.697
hba_count1
Recuento HBD2
Enlace rotable4
Nombres e identificadores
Sonrisas canónicasC(CC(C(=O)O)N)CN
IUPAC Name(2S)-2,5-diaminopentanoic acid
InChIKeyAHLPHDHHMVZTML-BYPYZUCNSA-N
INCHI1S/C5H12N2O2/c6-3-1-2-4(7)5(8)9/h4H,1-3,6-7H2,(H,8,9)/t4-/m0/s1
Isómeros SMILES C(C[C@@H](C(=O)O)N)CN
Peso molecular 132.16
Reaxy-Rn 1722296
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1722296&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClaseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids
Direct ParentL-alpha-amino acids
Alternative Parents Fatty acids and conjugates  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents L-alpha-amino acid - Fatty acid - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Primary aliphatic amine - Organic nitrogen compound - Carbonyl group - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom.
External Descriptors Other amino acids
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
GPRC6A Tchem G-protein coupled receptor family C group 6 member A (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
F2 Tclin Thrombin (11687 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PGR Tclin Progesterone receptor (8562 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A4 Tclin Serotonin transporter (12625 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRM1 Tclin Mu opioid receptor (19785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD3 Tclin Dopamine D3 receptor (14368 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE3A Tclin Phosphodiesterase 3A (3309 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2B Tclin Serotonin 2b (5-HT2b) receptor (10323 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ODC1 Tclin Ornithine decarboxylase (70 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE4A Tclin Phosphodiesterase 4A (1943 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA3 Tchem Adenosine A3 receptor (15931 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH3 Tclin Histamine H3 receptor (10389 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDR Tclin Vascular endothelial growth factor receptor 2 (20924 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
DMSO (mg/ml) Solubilidad máxima<1
Agua (mg/ml) Solubilidad máxima26
Agua (mM) Solubilidad máxima196.731234866828
Peso molecular132.160 g/mol
XLogP3-4.400
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count4
Rotatable Bond Count4
Exact Mass132.09 Da
Monoisotopic Mass132.09 Da
Topological Polar Surface Area89.300 Ų
Heavy Atom Count9
Formal Charge0
Complexity95.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Anqi Peng, Keke Yu, Shuwei Yu, Yingying Li, Hao Zuo, Ping Li, Juan Li, Jianan Huang, Zhonghua Liu, Jian Zhao.  (2023)  Aluminum and Fluoride Stresses Altered Organic Acid and Secondary Metabolism in Tea (Camellia sinensis) Plants: Influences on Plant Tolerance, Tea Quality and Safety.  INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES,  24  (5): (4640).  [PMID:36902071] [10.3390/ijms24054640]
2. Jia Xu, Xinzhou Yao, Yingying Lin, Shuyan Chi, Shuang Zhang, Junming Cao, Beiping Tan, Shiwei Xie.  (2022)  Schizochytrium limacinum altered antioxidant capacity and transcriptome profiles in Pacific white shrimp fed a low-fishmeal diet.  Aquaculture Reports,      [PMID:] [10.1016/j.aqrep.2022.101399]
3. Wang Ying, Li ZhiRong, Chen RongXiang.  (2022)  Simultaneous Determination of Metabolites Related to Arginine Metabolism in Rat plasma by Hydrophilic Interaction Chromatography–Tandem Mass Spectrometry.  JOURNAL OF CHROMATOGRAPHIC SCIENCE,  61  (3): (203-210).  [PMID:35704851] [10.1093/chromsci/bmac047]
4. Xiaoxiao Chen, Pu Li, Gaojun Wu, Zhe Wang, Chaobiao Huang.  (2022)  Turn-on signal fluorescence sensor based on DNA derived bio-dots/polydopamine nanoparticles for the detection of glutathione.  RSC Advances,  12  (3): (1807-1812).  [PMID:35425189] [10.1039/D1RA08107A]
5. Penghui Li, Yujie Xu, Yanrui Zhang, Jiamin Fu, Shuwei Yu, Huimin Guo, Zhihui Chen, Changsong Chen, Xiaogen Yang, Shucai Wang, Jian Zhao.  (2020)  Metabolite Profiling and Transcriptome Analysis Revealed the Chemical Contributions of Tea Trichomes to Tea Flavors and Tea Plant Defenses.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:32852206] [10.1021/acs.jafc.0c04075]
6. Mingjie Deng, Feiyan Lin, Caiping Zhou, Yuyan Chen, Leijie Xuan, Hongzhe Wang, Tiantian Feng, Lufeng Hu.  (2020)  Determination of 27 amino acids’ levels in seminal plasma of asthenospermia and oligospermia patients and diagnostic value analysis.  JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS,      [PMID:32126460] [10.1016/j.jpba.2020.113211]
7. Hao-Hua Deng, Xiao-Qiong Shi, Hua-Ping Peng, Quan-Quan Zhuang, Yu Yang, Ai-Lin Liu, Xing-Hua Xia, Wei Chen.  (2018)  Gold Nanoparticle-Based Photoluminescent Nanoswitch Controlled by Host–Guest Recognition and Enzymatic Hydrolysis for Arginase Activity Assay.  ACS Applied Materials & Interfaces,      [PMID:29373021] [10.1021/acsami.7b19513]
8. Zhang Qian, Wang Junsong, Liao Shanting, Li Pei, Xu Dingqiao, Lv Yan, Yang Minghua, Kong Lingyi.  (2017)  Optimization of Huang-Lian-Jie-Du-Decoction for Ischemic Stroke Treatment and Mechanistic Study by Metabolomic Profiling and Network Analysis.  Frontiers in Pharmacology,      [PMID:28400733] [10.3389/fphar.2017.00165]
9. Yinan Zhao, Shubiao Zhang, Yuan Zhang, Shaohui Cui, Huiying Chen, Defu Zhi, Yuhong Zhen, Shufen Zhang, Leaf Huang.  (2014)  Tri-peptide cationic lipids for gene delivery.  Journal of Materials Chemistry B,  (1): (119-126).  [PMID:25580248] [10.1039/C4TB01312C]
10. Qiao Tong, Weijie Shen, Lu Zhang, Yu Cao, Xi Zou, Tingting Shi, Rang Xiao Zhuang, Shourong Liu, Jianjun Xi.  (2025)  A “turn-on” fluorescence polyethyleneimine-based nanosensor chemosensor for sensing of l-lysine.  TALANTA,      [PMID:40184936] [10.1016/j.talanta.2025.128045]
11. Xinying Ma, Zhanghua Sun, Meifeng Chen, Fenghai Li, Huiping Lv, Qi Zhu.  (2025)  A novel voltammetric sensor based on a polyornithine film-incorporated gold nanoparticle modified electrode for the determination of ractopamine.  International Journal of Electrochemical Science,      [PMID:] [10.1016/j.ijoes.2025.101010]
12. Yun Chen, Xia Hua, Siyu Li, Jiamei Zhao, Huan Yu, Dongyao Wang, Jiqiang Yang, Lijun Liu.  (2024)  Aromatic compound 2-acetyl-1-pyrroline coordinates nitrogen assimilation and methane mitigation in fragrant rice.  CURRENT BIOLOGY,      [PMID:39047736] [10.1016/j.cub.2024.06.063]
13. Lu Wang, Limei Xiao, Shoujing Zheng, Jie Pang, Jiebo Chen.  (2024)  Characterization and assessment of free amino acids in different varieties of sugarcane.  INDUSTRIAL CROPS AND PRODUCTS,      [PMID:] [10.1016/j.indcrop.2024.118306]
14. Yamin Liu, Xunjiang Wang, Jiaojiao Wei, Kangning Fu, Yilin Chen, Linnan Li, Zhengtao Wang, Li Yang.  (2024)  Comprehensive Profiling of Amino Acids and Derivatives in Biological Samples: A Robust UHPLC-MS/MS Method for Investigating Acute Lung Injury.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:38537486] [10.1016/j.chroma.2024.464816]
15. Qian Tan, Linbo Gou, Tai-Ping Fan, Yujie Cai.  (2024)  Enzymatic properties of ornithine decarboxylase from Clostridium aceticum DSM1496.  BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY,      [PMID:38225812] [10.1002/bab.2556]
16. Jing Wang, Min Du, Xin Wang, Junchen He, Alei Zhang, Kequan Chen.  (2024)  Highly efficient bio-production of putrescine from L-arginine with arginase and L-ornithine decarboxylase in engineered Escherichia coli.  BIORESOURCE TECHNOLOGY,      [PMID:39260727] [10.1016/j.biortech.2024.131471]
17. Wenjun Zhang, Chuntao Dong, Zhaosheng Li, Huina Shi, Yijun Xu, Mingchen Zhu.  (2024)  Serum targeted metabolomics uncovering specific amino acid signature for diagnosis of intrahepatic cholangiocarcinoma.  JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS,      [PMID:39241676] [10.1016/j.jpba.2024.116457]
18. Piaopiao Chen, Iqra Ilyas, Su He, Yichen Xing, Zhigang Jin, Chaobiao Huang.  (2019)  Ratiometric pH Sensing and Imaging in Living Cells with Dual-Emission Semiconductor Polymer Dots.  MOLECULES,  24  (16): (2923).  [PMID:31409040] [10.3390/molecules24162923]
19. Xiao Xina, Hu Meng, Gao Li, Yuan Huan, Chong Baochen, Liu Yu, Zhang Rou, Gong Yanqiu, Du Dan, Zhang Yong, Yang Hao, Liu Xiaohui, Zhang Yan, Zhang Huiyuan, Xu Heng, Zhao Yi, Meng Wenbo, Xie Dan, Lei Peng, Qi Shiqian, Peng Yong, Tan Tao, Yu Yang, Hu Hongbo, Dong Biao, Dai Lunzhi.  (2025)  Low-input redoxomics facilitates global identification of metabolic regulators of oxidative stress in the gut.  Signal Transduction and Targeted Therapy,  10  (1): (1-18).  [PMID:39774148] [10.1038/s41392-024-02094-7]
20. Zengbo Wang, Junwu Cai, Bailiang Li, Huizi Tan.  (2025)  Exploring the genetic information of Lactobacillus helveticus strains hydrolyzing soy protein using genome-wide association analysis.  INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY,      [PMID:40267622] [10.1016/j.ijfoodmicro.2025.111214]
21. Tianping Chen, Yanru Tao, Xi Cao, Shiyi He, Hua Zhao, Jiangling Hu, Hongmei Wang, Xinhui Jiang.  (2025)  Development of an HPLC method for the determination of amines in a leukemia mouse model.  Analytical Methods,      [PMID:41160401] [10.1039/D5AY01549A]
22. Biqing Chen, Zengkun Wang, Jiayin Gao, Haizhu Sun, Yinghan Zhao, Yan Liu, Jianyu Liu, Xiaohong Qiu.  (2025)  Label-free gold nanostar-based SERS with machine learning: A platform for detecting endometrial cancer-associated polyamine metabolites.  CLINICA CHIMICA ACTA,      [PMID:41475445] [10.1016/j.cca.2025.120811]
23. Chi Yan, Xingyu Chen, Wenqing Gao, Chunlan Tang, Liwen Du, Chengyi Xie, Feng Xu, Keqi Tang, Jiancheng Yu.  (2025)  Chiral Derivatization Enables High-Resolution Ion Mobility Spectrometry of 30 Amino Acid Enantiomers.  ANALYTICAL CHEMISTRY,      [PMID:41451537] [10.1021/acs.analchem.5c06382]
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