NP-MRD: Showing NP-Card for (2z,8e,10e)-heptadeca-2,8,10-trien-4,6-diyn-1-ol (NP0325188)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-12 05:44:48 UTC

Updated at

2022-09-12 05:44:49 UTC

NP-MRD ID

NP0325188

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2z,8e,10e)-heptadeca-2,8,10-trien-4,6-diyn-1-ol

Description

(2Z,8E,10E)-heptadeca-2,8,10-trien-4,6-diyn-1-ol belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms. (2z,8e,10e)-heptadeca-2,8,10-trien-4,6-diyn-1-ol is found in Leptinella plumosa. Based on a literature review very few articles have been published on (2Z,8E,10E)-heptadeca-2,8,10-trien-4,6-diyn-1-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 40 39  0  0  0  0  0  0  0  0999 V2000
   -7.4149   -0.3260    0.3476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6824   -0.1979    1.6506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1833   -0.3811    1.4710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7170    0.6788    0.5302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2390    0.6384    0.2604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875   -0.6931   -0.3524 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4451   -0.8242   -0.6764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6354    0.1790   -0.4212 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8031    0.0728   -0.7340 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6367    1.0548   -0.4920 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0265    0.8985   -0.8160 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1990    0.7814   -1.0771 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5780    0.6569   -1.3670 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7638    0.5569   -1.5960 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1707    0.4409   -1.8540 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0765    0.5568   -0.8973 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5899    0.8175    0.4918 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0212   -0.2355    1.2932 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4739   -0.5961    0.5933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3648    0.6057   -0.2548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9958   -1.1654   -0.2222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0605   -0.9939    2.3231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8813    0.7633    2.1647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0749   -1.4081    1.0315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6691   -0.3785    2.4302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2202    0.4856   -0.4542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0400    1.6778    0.8866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6523    0.8353    1.1901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9798    1.4841   -0.4202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4959   -0.8236   -1.2635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2098   -1.5232    0.3403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1060   -1.7530   -1.1169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0332    1.0736    0.0143 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2023   -0.8288   -1.1746 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2591    1.9648   -0.0520 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5306    0.2526   -2.8551 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1345    0.4689   -1.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0782    1.7741    0.8124 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5153    0.9906    0.5167 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8766   -1.1006    0.8441 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  3  0
 12 13  1  0
 13 14  3  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  0
  2 23  1  0
  3 24  1  0
  3 25  1  0
  4 26  1  0
  4 27  1  0
  5 28  1  0
  5 29  1  0
  6 30  1  0
  6 31  1  0
  7 32  1  0
  8 33  1  0
  9 34  1  0
 10 35  1  0
 15 36  1  0
 16 37  1  0
 17 38  1  0
 17 39  1  0
 18 40  1  0
M  END


  Mrv1652309122207442D          

 18 17  0  0  0  0            999 V2000
    1.7605   -1.8414    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
    3.1895   -1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9039   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6184   -1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474   -1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7618   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4763   -1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1908   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9052   -1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6197   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3342   -2.6664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0487   -3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7631   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4776   -3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4776   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7631   -1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  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  3  0  0  0  0
 12 13  1  0  0  0  0
 13 14  3  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0325188

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC\C=C\C=C\C#CC#C\C=C/CO

> <INCHI_IDENTIFIER>
InChI=1S/C17H22O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18/h7-10,15-16,18H,2-6,17H2,1H3/b8-7+,10-9+,16-15-

> <INCHI_KEY>
MNRSGFGJPZSJIX-ZVHWMEOJSA-N

> <FORMULA>
C17H22O

> <MOLECULAR_WEIGHT>
242.362

> <EXACT_MASS>
242.167065328

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
31.58728104557442

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2Z,8E,10E)-heptadeca-2,8,10-trien-4,6-diyn-1-ol

> <JCHEM_LOGP>
4.824270410333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.565614055972503

> <JCHEM_PKA_STRONGEST_BASIC>
-2.5514004119176272

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
83.8665

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2Z,8E,10E)-heptadeca-2,8,10-trien-4,6-diyn-1-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       3.286  -3.437   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.620  -2.667   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.954  -3.437   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.287  -2.667   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.621  -3.437   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.955  -2.667   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.288  -3.437   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.622  -2.667   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.956  -3.437   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      15.289  -2.667   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      16.623  -3.437   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      17.957  -4.207   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      19.290  -4.977   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      20.624  -5.747   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      21.958  -6.517   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      23.292  -5.747   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      23.292  -4.207   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      21.958  -3.437   0.000  0.00  0.00           O+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                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   34    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₂₂O

Average Mass

242.3620 Da

Monoisotopic Mass

242.16707 Da

IUPAC Name

(2Z,8E,10E)-heptadeca-2,8,10-trien-4,6-diyn-1-ol

Traditional Name

(2Z,8E,10E)-heptadeca-2,8,10-trien-4,6-diyn-1-ol

CAS Registry Number

Not Available

SMILES

CCCCCC\C=C\C=C\C#CC#C\C=C/CO

InChI Identifier

InChI=1S/C17H22O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18/h7-10,15-16,18H,2-6,17H2,1H3/b8-7+,10-9+,16-15-

InChI Key

MNRSGFGJPZSJIX-ZVHWMEOJSA-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
Leptinella plumosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Long-chain fatty alcohols

Alternative Parents

Substituents

Long chain fatty alcohol
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
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	4.82	ChemAxon
pKa (Strongest Acidic)	15.57	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	83.87 m³·mol⁻¹	ChemAxon
Polarizability	31.59 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

8737543

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10562155

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2z,8e,10e)-heptadeca-2,8,10-trien-4,6-diyn-1-ol (NP0325188)

MOL for NP0325188 ((2z,8e,10e)-heptadeca-2,8,10-trien-4,6-diyn-1-ol)

3D MOL for NP0325188 ((2z,8e,10e)-heptadeca-2,8,10-trien-4,6-diyn-1-ol)

3D SDF for NP0325188 ((2z,8e,10e)-heptadeca-2,8,10-trien-4,6-diyn-1-ol)

3D-SDF for NP0325188 ((2z,8e,10e)-heptadeca-2,8,10-trien-4,6-diyn-1-ol)

PDB for NP0325188 ((2z,8e,10e)-heptadeca-2,8,10-trien-4,6-diyn-1-ol)

3D PDB for NP0325188 ((2z,8e,10e)-heptadeca-2,8,10-trien-4,6-diyn-1-ol)

SMILES for NP0325188 ((2z,8e,10e)-heptadeca-2,8,10-trien-4,6-diyn-1-ol)

INCHI for NP0325188 ((2z,8e,10e)-heptadeca-2,8,10-trien-4,6-diyn-1-ol)

Structure for NP0325188 ((2z,8e,10e)-heptadeca-2,8,10-trien-4,6-diyn-1-ol)

3D Structure for NP0325188 ((2z,8e,10e)-heptadeca-2,8,10-trien-4,6-diyn-1-ol)