NP-MRD: Showing NP-Card for (2e,4e)-n-(2-methylpropyl)undeca-2,4-dien-8,10-diynimidic acid (NP0166779)

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Record Information

Version

2.0

Created at

2022-09-03 02:13:05 UTC

Updated at

2022-09-03 02:13:05 UTC

NP-MRD ID

NP0166779

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e,4e)-n-(2-methylpropyl)undeca-2,4-dien-8,10-diynimidic acid

Description

(2E,4E)-N-isobutylundeca-2,4-dien-8,10-diynamide belongs to the class of organic compounds known as n-acyl amines. N-acyl amines are compounds containing a fatty acid moiety linked to an amine group through an ester linkage. (2e,4e)-n-(2-methylpropyl)undeca-2,4-dien-8,10-diynimidic acid is found in Achillea aspleniifolia, Achillea macrophylla, Achillea millefolium, Artemisia dracunculus, Argyranthemum frutescens, Echinacea angustifolia and Echinacea purpurea. (2e,4e)-n-(2-methylpropyl)undeca-2,4-dien-8,10-diynimidic acid was first documented in 2020 (PMID: 32598328). Based on a literature review very few articles have been published on (2E,4E)-N-isobutylundeca-2,4-dien-8,10-diynamide.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 36 35  0  0  0  0  0  0  0  0999 V2000
    9.7445   -0.1476    0.8748 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5359   -0.2217    0.8595 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1259   -0.3321    0.8398 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9112   -0.4452    0.8338 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4554   -0.5924    0.8488 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7811    0.6996    0.3935 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3115    0.5678    0.4030 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5895    0.7209   -0.6891 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1283    0.5904   -0.6828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5814    0.7457   -1.7804 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0304    0.6194   -1.7899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7857    0.7818   -2.9435 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6913    0.3439   -0.6970 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1099    0.2102   -0.6555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5671   -0.9120    0.2547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0887   -0.6514    1.6675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0955   -0.8816    0.3131 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8155   -0.0988    0.8824 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1028   -0.9036    1.8321 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1519   -1.3694    0.0922 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0457    1.4589    1.1821 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1559    1.0153   -0.5978 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8050    0.3400    1.3245 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1332    0.9500   -1.6004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3390    0.3600    0.2695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0603    0.9729   -2.6924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6085    0.1237   -3.7000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5850    1.1677   -0.3611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4589   -0.0448   -1.6888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2895   -1.8979   -0.1151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0363   -0.9219    1.8264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7668   -1.2526    2.3403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3127    0.4154    1.9114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4604   -1.2911    1.2793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3805    0.1779    0.2689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5454   -1.4858   -0.5037 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 17  1  0
 15 14  1  0
 14 13  1  0
 13 11  2  0
 11 12  1  0
 11 10  1  0
 10  9  2  0
  9  8  1  0
  8  7  2  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  3  0
  3  2  1  0
  2  1  3  0
 16 31  1  0
 16 32  1  0
 16 33  1  0
 15 30  1  0
 17 34  1  0
 17 35  1  0
 17 36  1  0
 14 28  1  0
 14 29  1  0
 12 27  1  0
 10 26  1  0
  9 25  1  0
  8 24  1  0
  7 23  1  0
  6 21  1  0
  6 22  1  0
  5 19  1  0
  5 20  1  0
  1 18  1  0
M  END

  Mrv1652309032204132D          

 17 16  0  0  0  0            999 V2000
    6.1875    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3625    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  3  0  0  0  0
  2  3  1  0  0  0  0
  3  4  3  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  4  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0166779

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CN=C(O)\C=C\C=C\CCC#CC#C

> <INCHI_IDENTIFIER>
InChI=1S/C15H19NO/c1-4-5-6-7-8-9-10-11-12-15(17)16-13-14(2)3/h1,9-12,14H,7-8,13H2,2-3H3,(H,16,17)/b10-9+,12-11+

> <INCHI_KEY>
PSAKYIJFKFCZFO-HULFFUFUSA-N

> <FORMULA>
C15H19NO

> <MOLECULAR_WEIGHT>
229.323

> <EXACT_MASS>
229.146664236

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
28.81109434826513

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E,4E)-N-(2-methylpropyl)undeca-2,4-dien-8,10-diynimidic acid

> <ALOGPS_LOGP>
4.17

> <JCHEM_LOGP>
3.372131643102577

> <ALOGPS_LOGS>
-4.35

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.970040660984992

> <JCHEM_PKA_STRONGEST_BASIC>
6.898014834129191

> <JCHEM_POLAR_SURFACE_AREA>
32.59

> <JCHEM_REFRACTIVITY>
75.09630000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.03e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E,4E)-N-(2-methylpropyl)undeca-2,4-dien-8,10-diynimidic acid

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      11.550   9.336   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.780   8.002   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.010   6.668   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.240   5.335   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.470   4.001   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.160   2.667   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.620   2.667   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.850   1.334   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.310  -1.334   0.000  0.00  0.00           O+0
HETATM   13  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      -0.770  -1.334   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.310  -1.334   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.080  -2.667   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.080   0.000   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   32    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₉NO

Average Mass

229.3230 Da

Monoisotopic Mass

229.14666 Da

IUPAC Name

(2E,4E)-N-(2-methylpropyl)undeca-2,4-dien-8,10-diynimidic acid

Traditional Name

(2E,4E)-N-(2-methylpropyl)undeca-2,4-dien-8,10-diynimidic acid

CAS Registry Number

Not Available

SMILES

CC(C)CN=C(O)\C=C\C=C\CCC#CC#C

InChI Identifier

InChI=1S/C15H19NO/c1-4-5-6-7-8-9-10-11-12-15(17)16-13-14(2)3/h1,9-12,14H,7-8,13H2,2-3H3,(H,16,17)/b10-9+,12-11+

InChI Key

PSAKYIJFKFCZFO-HULFFUFUSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Achillea aspleniifolia	LOTUS Database	35616633
Achillea macrophylla	LOTUS Database	35616633
Achillea millefolium	LOTUS Database	35616633
Artemisia dracunculus	LOTUS Database	35616633
Chrysanthemum frutescens	LOTUS Database	35616633
Echinacea angustifolia	LOTUS Database	35616633
Echinacea purpurea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-acyl amines. N-acyl amines are compounds containing a fatty acid moiety linked to an amine group through an ester linkage.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty amides

Direct Parent

N-acyl amines

Alternative Parents

Substituents

N-acyl-amine
Secondary carboxylic acid amide
Carboxamide group
Acetylide
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

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	4.17	ALOGPS
logP	3.37	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	4.97	ChemAxon
pKa (Strongest Basic)	6.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	32.59 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	75.1 m³·mol⁻¹	ChemAxon
Polarizability	28.81 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

4523539

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5373537

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Aydin T, Akincioglu H, Gumustas M, Gulcin I, Kazaz C, Cakir A: human monoamine oxidase (hMAO) A and hMAO B inhibitors from Artemisia dracunculus L. herniarin and skimmin: human mononamine oxidase A and B inhibitors from A. dracunculus L. Z Naturforsch C J Biosci. 2020 Nov 26;75(11-12):459-466. doi: 10.1515/znc-2019-0227. [PubMed:32598328 ]
LOTUS database [Link]

Showing NP-Card for (2e,4e)-n-(2-methylpropyl)undeca-2,4-dien-8,10-diynimidic acid (NP0166779)

MOL for NP0166779 ((2e,4e)-n-(2-methylpropyl)undeca-2,4-dien-8,10-diynimidic acid)

3D MOL for NP0166779 ((2e,4e)-n-(2-methylpropyl)undeca-2,4-dien-8,10-diynimidic acid)

3D SDF for NP0166779 ((2e,4e)-n-(2-methylpropyl)undeca-2,4-dien-8,10-diynimidic acid)

3D-SDF for NP0166779 ((2e,4e)-n-(2-methylpropyl)undeca-2,4-dien-8,10-diynimidic acid)

PDB for NP0166779 ((2e,4e)-n-(2-methylpropyl)undeca-2,4-dien-8,10-diynimidic acid)

3D PDB for NP0166779 ((2e,4e)-n-(2-methylpropyl)undeca-2,4-dien-8,10-diynimidic acid)

SMILES for NP0166779 ((2e,4e)-n-(2-methylpropyl)undeca-2,4-dien-8,10-diynimidic acid)

INCHI for NP0166779 ((2e,4e)-n-(2-methylpropyl)undeca-2,4-dien-8,10-diynimidic acid)

Structure for NP0166779 ((2e,4e)-n-(2-methylpropyl)undeca-2,4-dien-8,10-diynimidic acid)

3D Structure for NP0166779 ((2e,4e)-n-(2-methylpropyl)undeca-2,4-dien-8,10-diynimidic acid)