This is a demo store. No orders will be fulfilled.

 
Call +1 (833) 552-7181 or Contact us
Toggle Nav
My Cart
Search
Advanced Search
Menu
Account
Settings
྾
main product photo

Oleamide - ≥70%, high purity , CAS No.301-02-0

12 Citations COA COA
    Grade & Purity:
  • ≥70%
In stock
Item Number
O105240
Grouped product items
SKU Size
Availability
 Price Qty
O105240-25g
25g
8
$26.90
O105240-100g
100g
2
$49.90
O105240-500g
500g
1
$90.90
Wish List
Bulk Order  SDS  DATASHEET  Specification Sheet

Sleep-inducing brain lipid

View related series
Cell signal transduction and Neuroscience (85) Metabolite (5307)

Basic Description

Synonyms 9-Octadecenamide, (9Z)- | (9Z)-octadec-9-enamide | Crodamide O | cis-9,10-Octadecenoamide | (Z)-9-OCTADECENAMIDE | Armoslip CP | Oleamide | Oleylamide | Adogen 73 | Crodamide OR | 9-Octadecenamide | Oleic acid amide | Slip-eze | Oleyl amide | (Z)-octadec-
Specifications & Purity ≥70%
Biochemical and Physiological Mechanisms Endogenous sleep-inducing lipid. Acts as an agonist at the CB1cannabinoid receptor (EC50= 1.64μM). Also appears to potentiate the actions of 5-HT on 5-HT2Aand2Creceptors, and act via an allosteric regulatory site on 5-HT7receptors.
Storage Temp Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Oleamide is a lipid or a brain fatty acid, that is found in the CSF (cerebrospinal fluid). It is originally obtained from the cerebrospinal fluid of cats, that are sleep-deprived.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Lipids and lipid-like molecules
Class Fatty Acyls
Subclass Fatty amides
Intermediate Tree Nodes Not available
Direct Parent Fatty amides
Alternative Parents Primary carboxylic acid amides  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aliphatic acyclic compounds
Substituents Fatty amide - Primary carboxylic acid amide - Carboxamide group - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as fatty amides. These are carboxylic acid amide derivatives of fatty acids, that are formed from a fatty acid and an amine.
External Descriptors Primary amides

Associated Targets(Human)

HTR7 Tclin 5-hydroxytryptamine receptor 7 (0 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
ABL1 Tclin Tyrosine-protein kinase ABL (18331 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AGTR1 Tclin Type-1 angiotensin II receptor (5176 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GSK3B Tclin Glycogen synthase kinase-3 beta (11785 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CSNK1D Tchem Casein kinase I delta (4546 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
S1PR1 Tclin Sphingosine 1-phosphate receptor Edg-1 (5806 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CDK2 Tchem Cyclin-dependent kinase 2 (9050 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
C5AR1 Tclin C5a anaphylatoxin chemotactic receptor (2677 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AURKA Tchem Serine/threonine-protein kinase Aurora-A (10240 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TP53 Tchem Cellular tumor antigen p53 (48468 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
U2OS (164939 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CX3CR1 Tchem C-X3-C chemokine receptor 1 (1686 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
FPR2 Tchem Lipoxin A4 receptor (3472 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
FFAR4 Tchem G-protein coupled receptor 120 (2999 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
BRD4 Tchem Bromodomain-containing protein 4 (13122 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GPR35 Tchem G-protein coupled receptor 35 (2643 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MEN1 Tchem Menin/Histone-lysine N-methyltransferase MLL (48157 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TRIM24 Tchem Transcription intermediary factor 1-alpha (2087 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
BRPF1 Tchem Peregrin (2217 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HEK-293T (167025 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Aplnr Apelin receptor (201 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Soat1 Acyl coenzyme A:cholesterol acyltransferase 1 (295 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Faah Anandamide amidohydrolase (3907 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Fgfr3 Fibroblast growth factor receptor 3 (21 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Trpv2 Transient receptor potential cation channel subfamily V member 2 (148 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
RAW264.7 (28094 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Gpr119 Glucose-dependent insulinotropic receptor (270 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Gabrp GABA-A receptor; anion channel (5731 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488195275
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488195275
IUPAC Name (Z)-octadec-9-enamide
INCHI InChI=1S/C18H35NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h9-10H,2-8,11-17H2,1H3,(H2,19,20)/b10-9-
InChIKey FATBGEAMYMYZAF-KTKRTIGZSA-N
Smiles CCCCCCCCC=CCCCCCCCC(=O)N
Isomeric SMILES CCCCCCCC/C=C\CCCCCCCC(=O)N
WGK Germany 1
RTECS RG2230000
Molecular Weight 281.48
Beilstein 2(4)1668
Reaxy-Rn 8157587
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8157587&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

23 results found

Lot Number Certificate Type Date Item
B2506383 Certificate of Analysis Jan 17, 2025 O105240
B2506391 Certificate of Analysis Jan 17, 2025 O105240
B2506402 Certificate of Analysis Jan 17, 2025 O105240
B2506856 Certificate of Analysis Jan 17, 2025 O105240
B2506408 Certificate of Analysis Jan 17, 2025 O105240
L2413569 Certificate of Analysis Dec 03, 2024 O105240
L2413570 Certificate of Analysis Dec 03, 2024 O105240
L2413584 Certificate of Analysis Dec 03, 2024 O105240
L2418039 Certificate of Analysis Dec 03, 2024 O105240
F2417403 Certificate of Analysis Jun 12, 2024 O105240
F2417404 Certificate of Analysis Jun 12, 2024 O105240
F2417406 Certificate of Analysis Jun 12, 2024 O105240
F2417405 Certificate of Analysis Jun 12, 2024 O105240
E2427146 Certificate of Analysis May 16, 2024 O105240
E2427147 Certificate of Analysis May 16, 2024 O105240
L2424577 Certificate of Analysis Apr 02, 2024 O105240
E1610033 Certificate of Analysis Jan 19, 2024 O105240
J2311639 Certificate of Analysis Sep 05, 2023 O105240
J2311685 Certificate of Analysis Sep 05, 2023 O105240
J2311648 Certificate of Analysis Sep 05, 2023 O105240
D2303565 Certificate of Analysis Mar 13, 2023 O105240
D2303566 Certificate of Analysis Mar 13, 2023 O105240
D2303564 Certificate of Analysis Mar 13, 2023 O105240

Show more⌵

Chemical and Physical Properties

Solubility Solvent:ethanol, Max Conc. mg/mL: 28.15, Max Conc. mM: 100; Solvent:DMSO, Max Conc. mg/mL: 14.07, Max Conc. mM: 50
Melt Point(°C) 65-75°C
Molecular Weight 281.500 g/mol
XLogP3 6.600
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 1
Rotatable Bond Count 15
Exact Mass 281.272 Da
Monoisotopic Mass 281.272 Da
Topological Polar Surface Area 43.100 Ų
Heavy Atom Count 20
Formal Charge 0
Complexity 236.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 1
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 1
Covalently-Bonded Unit Count 1

Citations of This Product

How to Cite Aladdin Scientific Products?
1. Jiaming Wang, Li Zou, Meili Yang, Jiajie Cheng, Yufan Jiang, Guangdong Huang, Jingjing Dong.  (2023)  Improvement of the Stability and Optical Properties of CsPbBr3 QDs.  Nanomaterials,  13  (16): (2372). 
2. Liu Kai, Yang Hao, Jiang Yilan, Liu Zhaojun, Zhang Shumeng, Zhang Zhixue, Qiao Zhun, Lu Yiming, Cheng Tao, Terasaki Osamu, Zhang Qing, Gao Chuanbo.  (2023)  Coherent hexagonal platinum skin on nickel nanocrystals for enhanced hydrogen evolution activity.  Nature Communications,  14  (1): (1-12). 
3. Zhang Shuai-nan, Li Hong-mei, Liu Qi, Li Xu-zhao, Yang Wu-de, Zhou Ying.  (2023)  Eucommiae Folium and Active Compounds Protect Against Mitochondrial Dysfunction-Calcium Overload in Epileptic Hippocampal Neurons Through the Hypertrophic Cardiomyopathy Pathway.  NEUROCHEMICAL RESEARCH,    (1-13). 
4. Xingfu Zheng, Shi Kai Song, Ziwen Zhou, Xizhou Jiang, Yongqiang Sui, Mingming Che, Qi Xu, Yan Wang, Shuai Zhao, Lin Li.  (2022)  Effect of silica dispersed by special dispersing agents with green strategy on tire rolling resistance and energy consumption.  JOURNAL OF APPLIED POLYMER SCIENCE,  139  (39): (e52933). 
5. Zhongan Zhu, Jing Liu, Yuhang Yang, Michael Adu-Frimpong, Hao Ji, Elmurat Toreniyazov, Qilong Wang, Jiangnan Yu, Ximing Xu.  (2021)  SMEDDS for improved oral bioavailability and anti-hyperuricemic activity of licochalcone A.  JOURNAL OF MICROENCAPSULATION,  38  (7-8): (459-471). 
6. Xingyu Liu, Jinwei Gao, Wanqiang Liu, Qianming Wang.  (2020)  Reinforcing effects of waterproof substrate on the photo-, thermal and pH stabilities of perovskite nanocrystals.  JOURNAL OF ALLOYS AND COMPOUNDS,  817  (152693). 
7. Chun Hui Zhou, Li Cun Jun, Will P. Gates, Ting Ting Zhu, Yu Wei Hua.  (2019)  Co-intercalation of organic cations/amide molecules into montmorillonite with tunable hydrophobicity and swellability.  APPLIED CLAY SCIENCE,  179  (105157). 
8. Yuan Ling, Lu Shuangwei, Yang Feng, Wang Yushu, Jia Yongfang, Kadhim Mayameen S., Yu Yanmei, Zhang Yong, Zhao Yong.  (2019)  A facile room-temperature synthesis of three-dimensional coral-like Ag2S nanostructure with enhanced photocatalytic activity.  JOURNAL OF MATERIALS SCIENCE,  54  (4): (3174-3186). 
9. Huanjun Wang, Weijing Yao, Qingyong Tian, Mengxiao Li, Bin Tian, Li Liu, Zhaohui Wu, Wei Wu.  (2018)  Printable Monodisperse All-Inorganic Perovskite Quantum Dots: Synthesis and Banknotes Protection Applications.  Advanced Materials Technologies,  3  (11): (1800150). 
10. Xiaolong Ma, Yaojiang Zhou, Shuang Zhang, Wenli Lei, Yuanmeng Zhao, Changsheng Shan.  (2025)  3d–5d Orbital Hybridization in Nanoflower-Like High-Entropy Alloy for Highly Efficient Overall Water Splitting at High Current Density.  Small,    (2411394). 
11. Ping Li, Siyi Wang, Mengyuan Liu, Xue Dai, Huicong Shi, Weihong Zhou, Sheng Sheng, Fuan Wu.  (2024)  Antibacterial Activity and Mechanism of Three Root Exudates from Mulberry Seedlings against Ralstonia pseudosolanacearum.  Plants-Basel,  13  (4): (482). 
12. Shulan Zhang, Renjie Chen, Mujing Qu, Biyu Long, Nannan He, Sumei Huang, Xiaohong Chen, Huili Li, Tongtong Xuan.  (2024)  Dual Strategy Based on Quantum Dot Doping and Phenylethylamine Iodide Surface Modification for High-Performance and Stable Perovskite Solar Cells.  Coatings,  14  (4): (409). 

Solution Calculators

Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.

Privacy Policy Website Terms of Use Return policy Terms and Conditions of Sale Cookie Policy Sales Policy
Products are chemical reagents for research use only and are not intended for human use. We do not sell to patients.
Copyright © 2023-present Aladdin Scientific Corp . All rights reserved.