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2601-90-3,MFCD09756921
Catalog No.:AA002RB7

2601-90-3 | 2-Oleamidoacetic acid

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10mg
≥98%
in stock  
$53.00   $37.00
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50mg
≥98%
in stock  
$230.00   $161.00
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100mg
≥98%
in stock  
$405.00   $283.00
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500mg
≥98%
in stock  
$1,636.00   $1,145.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA002RB7
Chemical Name:
2-Oleamidoacetic acid
CAS Number:
2601-90-3
Molecular Formula:
C20H37NO3
Molecular Weight:
339.5127
MDL Number:
MFCD09756921
SMILES:
CCCCCCCC/C=C\CCCCCCCC(=O)NCC(=O)O
Properties
Computed Properties
 
Complexity:
340  
Covalently-Bonded Unit Count:
1  
Defined Bond Stereocenter Count:
1  
Heavy Atom Count:
24  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
17  
XLogP3:
6.6  

Downstream Synthesis Route

[1]CurrentPatentAssignee:VISKOTEEPAKBV-US2786045,1953,A

[1]Osornio,YazminM.;Uebelhart,Peter;Bosshard,Silvan;Konrad,Fabian;Siegel,JayS.;Landau,EhudM.[JournalofOrganicChemistry,2012,vol.77,#23,p.10583-10595]

[2]Ohsedo,Yutaka;Oono,Masashi;Saruhashi,Kowichiro;Watanabe,Hisayuki;Miyamoto,Nobuyoshi[RSCAdvances,2017,vol.7,#66,p.41686-41692]

[3]CurrentPatentAssignee:VISKOTEEPAKBV-US2786045,1953,A

[4]CurrentPatentAssignee:HEBREWUNIVERSITYOFJERUSALEM;UNIVERSITYOFGUELPH;VIRGINIACOMMONWEALTHUNIVERSITY;YissumResearch&Development(in:HebrewUniversity)-WO2018/216008,2018,A1Locationinpatent:Paragraph00116-00117

[1]Locationinpatent:experimentalpartDang,HungThe;Kang,GyeoungJin;Yoo,EunSook;Hong,Jongki;Choi,JaeSue;Kim,HyungSik;Chung,HaeYoung;Jung,JeeH.[BioorganicandMedicinalChemistry,2011,vol.19,#4,p.1520-1527]

[2]Rock,ErinM;Ayoub,SamanthaM;Limebeer,CherylL;Gene,Alexia;Wills,KiriL;DeVuono,MariekaV;Smoum,Reem;DiMarzo,Vincenzo;Lichtman,AronH;Mechoulam,Raphael;Parker,LindaA[Psychopharmacology,2020,vol.237,#2,p.375-384]

C21H39NO3 
  2601-90-3 

[1]Duarte,RodrigoDaCosta;Ongaratto,Renata;Piovesan,LucianaAlmeida;DeLima,VâniaRodrigues;Soldi,Valdir;Merlo,AloirAntônio;D'Oca,MarceloG.Montes[TetrahedronLetters,2012,vol.53,#19,p.2454-2460]

Literature

Title: Reversible lysine acetylation regulates activity of human glycine N-acyltransferase-like 2 (hGLYATL2): implications for production of glycine-conjugated signaling molecules.

Journal: The Journal of biological chemistry 20120511

Title: Potential anti-inflammatory actions of the elmiric (lipoamino) acids.

Journal: Bioorganic & medicinal chemistry 20070515

Title: In vivo evidence that N-oleoylglycine acts independently of its conversion to oleamide.

Journal: Prostaglandins & other lipid mediators 20061201

Title: Wang S, et al. N-Oleoyl glycine, a lipoamino acid, stimulates adipogenesis associated with activation of CB1 receptor and Akt signaling pathway in 3T3-L1 adipocyte. Biochem Biophys Res Commun. 2015 Oct 23;466(3):438-43.

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SDS
Tags:2601-90-3 Molecular Formula|2601-90-3 MDL|2601-90-3 SMILES|2601-90-3 2-Oleamidoacetic acid