Cannabis Compound Database: Showing Compound Card for Acetyl-ornithine (CDB006324)

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Record Information

Version

1.0

Created at

2020-09-11 15:49:07 UTC

Updated at

2022-12-13 23:36:25 UTC

CannabisDB ID

CDB006324

Secondary Accession Numbers

Not Available

Cannabis Compound Identification

Common Name

Acetyl-ornithine

Description

N2-Acetylornithine belongs to the class of organic compounds known as n-acyl-l-alpha-amino acids. These are n-acylated alpha amino acids which have the L-configuration of the alpha-carbon atom. N2-Acetylornithine exists in all living species, ranging from bacteria to plants to humans. N2-Acetylornithine is found, on average, in the highest concentration within a few different foods, such as wheats (Triticum), nanking cherries (Prunus tomentosa), and red raspberries (Rubus idaeus) and in a lower concentration in red bell peppers (Capsicum annuum), dills (Anethum graveolens), and carrots (Daucus carota ssp. sativus). N2-Acetylornithine has also been detected, but not quantified in, several different foods, such as arabica coffees (Coffea arabica), pears (Pyrus communis), black chokeberries (Photinia melanocarpa), macadamia nuts (Macadamia), and garland chrysanthemums (Chrysanthemum coronarium). This could make N2-acetylornithine a potential biomarker for the consumption of these foods. N2-Acetylornithine is a primary metabolite. Primary metabolites are metabolically or physiologically essential metabolites. They are directly involved in an organism’s growth, development or reproduction. Based on a literature review a significant number of articles have been published on N2-Acetylornithine.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
N-Acetylornithine	ChEBI
N2-Acetyl-L-ornithine	ChEBI
(2S)-2-acetamido-5-Aminopentanoate	HMDB
(2S)-2-acetamido-5-Aminopentanoic acid	HMDB
Acetyl-ornithine	HMDB
AOR	HMDB
N(2)-Acetyl-L-ornithine	HMDB
(2S)-5-Amino-2-acetamidopentanoic acid	HMDB
N(alpha)-Acetyl-L-ornithine	HMDB
N(alpha)-Acetylornithine	HMDB
N(α)-Acetyl-L-ornithine	HMDB
N(α)-Acetylornithine	HMDB
N-Acetyl-L-ornithine	HMDB
Nalpha-Acetyl-L-ornithine	HMDB
Nalpha-Acetylornithine	HMDB
Nα-Acetyl-L-ornithine	HMDB
Nα-Acetylornithine	HMDB
N2-Acetylornithine	HMDB
N-alpha-Acetylornithine	HMDB
N-α-Acetylornithine	HMDB

Chemical Formula

C₇H₁₄N₂O₃

Average Molecular Weight

174.1977

Monoisotopic Molecular Weight

174.100442324

IUPAC Name

(2S)-5-amino-2-acetamidopentanoic acid

Traditional Name

N(2)-acetyl-L-ornithine

CAS Registry Number

Not Available

SMILES

CC(=O)N[C@@H](CCCN)C(O)=O

InChI Identifier

InChI=1S/C7H14N2O3/c1-5(10)9-6(7(11)12)3-2-4-8/h6H,2-4,8H2,1H3,(H,9,10)(H,11,12)/t6-/m0/s1

InChI Key

JRLGPAXAGHMNOL-LURJTMIESA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-acyl-l-alpha-amino acids. These are n-acylated alpha amino acids which have the L-configuration of the alpha-carbon atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

N-acyl-L-alpha-amino acids

Alternative Parents

Substituents

N-acyl-l-alpha-amino acid
Fatty acid
Acetamide
Carboxamide group
Secondary carboxylic acid amide
Amino acid
Monocarboxylic acid or derivatives
Carboxylic acid
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Amine
Primary amine
Organooxygen compound
Organonitrogen compound
Primary aliphatic amine
Hydrocarbon derivative
Carbonyl group
Organic oxide
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

N2-acyl-L-ornithine (CHEBI:16543 )
acetylornithine (CHEBI:16543 )

Ontology

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
logP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	-2.7	ALOGPS
logP	-3.6	ChemAxon
logS	-0.66	ALOGPS
pKa (Strongest Acidic)	3.82	ChemAxon
pKa (Strongest Basic)	9.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	92.42 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	42.65 m³·mol⁻¹	ChemAxon
Polarizability	17.94 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

EI-MS/GC-MS

Type	Description	Splash Key	View
GC-MS	N2-Acetylornithine, 4 TMS, GC-MS Spectrum	splash10-0fk9-1930000000-28d5f476677a51e2f8ec	Spectrum
GC-MS	N2-Acetylornithine, 3 TMS, GC-MS Spectrum	splash10-00di-2900000000-092b404eaa0526439b15	Spectrum
GC-MS	N2-Acetylornithine, non-derivatized, GC-MS Spectrum	splash10-0fk9-0930000000-6914c12040164b5148b0	Spectrum
GC-MS	N2-Acetylornithine, non-derivatized, GC-MS Spectrum	splash10-00di-0910000000-25d42f7fce94b1cb4b5c	Spectrum
GC-MS	N2-Acetylornithine, non-derivatized, GC-MS Spectrum	splash10-0fk9-1920000000-e1b66d25c11eafd0e0a9	Spectrum
GC-MS	N2-Acetylornithine, non-derivatized, GC-MS Spectrum	splash10-00di-1900000000-0f0883367079e716da18	Spectrum
GC-MS	N2-Acetylornithine, non-derivatized, GC-MS Spectrum	splash10-0fk9-1930000000-28d5f476677a51e2f8ec	Spectrum
GC-MS	N2-Acetylornithine, non-derivatized, GC-MS Spectrum	splash10-00di-2900000000-092b404eaa0526439b15	Spectrum
Predicted GC-MS	N2-Acetylornithine, non-derivatized, Predicted GC-MS Spectrum - 70eV, Positive	splash10-001l-9100000000-429f70cb44411bb90989	Spectrum
Predicted GC-MS	N2-Acetylornithine, 1 TMS, Predicted GC-MS Spectrum - 70eV, Positive	splash10-0fkc-9410000000-cee666cdbec55f97a0a0	Spectrum
Predicted GC-MS	N2-Acetylornithine, non-derivatized, Predicted GC-MS Spectrum - 70eV, Positive	Not Available	Spectrum
Predicted GC-MS	N2-Acetylornithine, non-derivatized, Predicted GC-MS Spectrum - 70eV, Positive	Not Available	Spectrum

MS/MS

Type	Description	Splash Key	View
MS/MS	LC-MS/MS Spectrum - LC-ESI-QQ , negative	splash10-00di-0900000000-52f0d0fb8a9a849e95d6	2017-09-14	View Spectrum
MS/MS	LC-MS/MS Spectrum - LC-ESI-QQ , negative	splash10-001i-0900000000-d83ff24b1fd0244f8e2e	2017-09-14	View Spectrum
MS/MS	LC-MS/MS Spectrum - LC-ESI-QQ , negative	splash10-001i-2900000000-e708e107e9183bfe0f76	2017-09-14	View Spectrum
MS/MS	LC-MS/MS Spectrum - LC-ESI-QQ , negative	splash10-053r-9400000000-afb6a5b65f59f01dc761	2017-09-14	View Spectrum
MS/MS	LC-MS/MS Spectrum - LC-ESI-QQ , negative	splash10-0a4l-9000000000-4763dc8edae338a7f336	2017-09-14	View Spectrum
MS/MS	LC-MS/MS Spectrum - LC-ESI-QTOF , negative	splash10-001i-0900000000-d157410f17955c8e0256	2017-09-14	View Spectrum
MS/MS	LC-MS/MS Spectrum - LC-ESI-QQ , positive	splash10-004i-0900000000-52b9626c047fdc01fe7b	2017-09-14	View Spectrum
MS/MS	LC-MS/MS Spectrum - LC-ESI-QQ , positive	splash10-014i-1900000000-c92081162e58f54cd2ec	2017-09-14	View Spectrum
MS/MS	LC-MS/MS Spectrum - LC-ESI-QQ , positive	splash10-00di-9200000000-476b94e0eacd5c51da0d	2017-09-14	View Spectrum
MS/MS	LC-MS/MS Spectrum - LC-ESI-QQ , positive	splash10-00di-9000000000-e57c224e36a05f66f1b9	2017-09-14	View Spectrum
MS/MS	LC-MS/MS Spectrum - LC-ESI-QQ , positive	splash10-00di-9000000000-44d1c5e14f69e175989a	2017-09-14	View Spectrum
MS/MS	LC-MS/MS Spectrum - LC-ESI-IT , positive	splash10-03fr-0900000000-5fe61be67a41d8d0facc	2017-09-14	View Spectrum
MS/MS	LC-MS/MS Spectrum - LC-ESI-QTOF , positive	splash10-01b9-4900000000-624c1afbfd5d3b3b76cb	2017-09-14	View Spectrum
MS/MS	LC-MS/MS Spectrum - LC-ESI-QTOF , positive	splash10-01b9-4900000000-624c1afbfd5d3b3b76cb	2017-09-14	View Spectrum
MS/MS	LC-MS/MS Spectrum - 10V, Negative	splash10-00di-0900000000-310a7f3b3d4c1bf3af0b	2021-09-20	View Spectrum
MS/MS	LC-MS/MS Spectrum - 40V, Positive	splash10-00di-9000000000-d0f88533afec85ff5c62	2021-09-20	View Spectrum
MS/MS	LC-MS/MS Spectrum - 10V, Positive	splash10-05r0-0900000000-f280065b578a1aa65149	2021-09-20	View Spectrum
MS/MS	LC-MS/MS Spectrum - 20V, Positive	splash10-01b9-8900000000-cf2ff97fd954fbc2ad67	2021-09-20	View Spectrum
MS/MS	LC-MS/MS Spectrum - 40V, Negative	splash10-0a59-9000000000-ff059f4dd36bc1002fbf	2021-09-20	View Spectrum
Predicted MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-056r-1900000000-28d5e48c6fc3a56a4937	2015-09-15	View Spectrum
Predicted MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-06tr-4900000000-8aa79d29a3d89249bf78	2015-09-15	View Spectrum
Predicted MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-01vx-9200000000-2f866830ef23136853fc	2015-09-15	View Spectrum
Predicted MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-00di-0900000000-9b37a30ee623b4f18e80	2015-09-15	View Spectrum
Predicted MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-0c30-4900000000-019d18f26e04ab2b397a	2015-09-15	View Spectrum
Predicted MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-052f-9100000000-b133fb2ce9e1a5eef782	2015-09-15	View Spectrum

NMR

Not Available

Pathways

Not Available

Protein Targets

Enzymes

Not Available

Transporters

Not Available

Metal Bindings

Not Available

Receptors

Not Available

Transcriptional Factors

Not Available

Concentrations Data

Cannabis Cultivar	Status	Value	Reference	Details
Alien Dawg	Detected and Quantified	0.0230 mg/g dry wt	David S. Wishart,...	details
Gabriola	Detected and Quantified	0.0148 mg/g dry wt	David S. Wishart,...	details
Island Honey	Detected and Quantified	0.0222 mg/g dry wt	David S. Wishart,...	details
Quadra	Detected and Quantified	0.0174 mg/g dry wt	David S. Wishart,...	details
Sensi Star	Detected and Quantified	0.0119 mg/g dry wt	David S. Wishart,...	details
Tangerine Dream	Detected and Quantified	0.0109 mg/g dry wt	David S. Wishart,...	details