NP-MRD: Showing NP-Card for (4e,6s,8s,10s)-4,6,8,10-tetramethyltridec-4-en-3-one (NP0258574)

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Record Information

Version

2.0

Created at

2022-09-08 00:05:21 UTC

Updated at

2022-09-08 00:05:21 UTC

NP-MRD ID

NP0258574

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4e,6s,8s,10s)-4,6,8,10-tetramethyltridec-4-en-3-one

Description

Siphonarienone belongs to the class of organic compounds known as acyclic monoterpenoids. These are monoterpenes that do not contain a cycle. (4e,6s,8s,10s)-4,6,8,10-tetramethyltridec-4-en-3-one is found in Siphonaria pectinata. (4e,6s,8s,10s)-4,6,8,10-tetramethyltridec-4-en-3-one was first documented in 2004 (PMID: 15101758). Based on a literature review very few articles have been published on Siphonarienone (PMID: 18229932).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 50 49  0  0  0  0  0  0  0  0999 V2000
    5.5978    1.8775   -0.3003 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3889    0.5192   -0.8931 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8836    0.2243   -1.0971 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1839    0.2778    0.2338 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7563   -0.7469    1.2007 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7073    0.3028    0.2131 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9855   -0.8419   -0.3745 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3399   -1.0961   -1.8383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5345   -0.6546   -0.4222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1993   -0.4566    0.8712 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0397   -1.5637    1.8953 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4813    0.2235    0.9291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4016    0.2167   -0.0062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2230   -0.5142   -1.2455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6288    1.0047    0.2613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7604    1.6303    1.3600 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7533    1.1311   -0.6757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0153    0.4462   -0.2286 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5431    2.3543   -0.6727 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7351    1.7227    0.8102 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7945    2.5888   -0.4939 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8176    0.5101   -1.9103 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8391   -0.2987   -0.2986 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8829   -0.7495   -1.5941 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5425    1.0821   -1.7118 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5057    1.2730    0.6799 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0145   -1.2394    1.8231 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3246   -1.4832    0.5549 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5399   -0.3272    1.8635 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3791    1.2236   -0.3244 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3929    0.4498    1.2748 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1302   -1.8036    0.1940 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9699   -2.0002   -1.9631 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6800   -0.1928   -2.3277 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3880   -1.3755   -2.3873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6348    0.3313   -0.9825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8707   -1.4601   -1.0707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5012    0.3509    1.3687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5308   -1.2089    2.8276 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0343   -1.7157    2.1823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3991   -2.5330    1.5459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7119    0.8033    1.8665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2573   -0.5409   -1.7464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1076   -1.6352   -1.0785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6070   -0.1038   -2.0268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5499    0.8932   -1.7222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0145    2.2443   -0.6963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4647   -0.1780   -1.0344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8263    1.1762    0.0459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8439   -0.1382    0.7043 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
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 15 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  1
  5 27  1  0
  5 28  1  0
  5 29  1  0
  6 30  1  0
  6 31  1  0
  7 32  1  1
  8 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  1
 11 39  1  0
 11 40  1  0
 11 41  1  0
 12 42  1  0
 14 43  1  0
 14 44  1  0
 14 45  1  0
 17 46  1  0
 17 47  1  0
 18 48  1  0
 18 49  1  0
 18 50  1  0
M  END


  Mrv1652309082202052D          

 18 17  0  0  1  0            999 V2000
    2.9980    2.5559    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
    4.4270    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1414    2.1434    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1414    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8559    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5704    2.1434    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5704    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9993    2.1434    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.9993    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7138    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4283    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4283    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1427    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1427    3.3809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8572    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5717    2.5559    0.0000 C   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  1  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0258574

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC[C@H](C)C[C@H](C)C[C@H](C)\C=C(/C)C(=O)CC

> <INCHI_IDENTIFIER>
InChI=1S/C17H32O/c1-7-9-13(3)10-14(4)11-15(5)12-16(6)17(18)8-2/h12-15H,7-11H2,1-6H3/b16-12+/t13-,14-,15-/m0/s1

> <INCHI_KEY>
LRJDUFSHRXSRLR-IZGRLVBXSA-N

> <FORMULA>
C17H32O

> <MOLECULAR_WEIGHT>
252.442

> <EXACT_MASS>
252.24531565

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
33.35546534982225

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4E,6S,8S,10S)-4,6,8,10-tetramethyltridec-4-en-3-one

> <JCHEM_LOGP>
6.3183320903333335

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.671137680382843

> <JCHEM_POLAR_SURFACE_AREA>
17.07

> <JCHEM_REFRACTIVITY>
81.35279999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(4E,6S,8S,10S)-4,6,8,10-tetramethyltridec-4-en-3-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       5.596   4.771   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.264   4.771   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.597   4.001   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.597   2.461   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.931   4.771   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.265   4.001   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.265   2.461   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.598   4.771   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      14.932   4.001   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.932   2.461   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      16.266   4.771   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      17.599   4.001   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      17.599   2.461   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      18.933   4.771   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      18.933   6.311   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      20.267   4.001   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      21.600   4.771   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   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

C₁₇H₃₂O

Average Mass

252.4420 Da

Monoisotopic Mass

252.24532 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCC[C@H](C)C[C@H](C)C[C@H](C)\C=C(/C)C(=O)CC

InChI Identifier

InChI=1S/C17H32O/c1-7-9-13(3)10-14(4)11-15(5)12-16(6)17(18)8-2/h12-15H,7-11H2,1-6H3/b16-12+/t13-,14-,15-/m0/s1

InChI Key

LRJDUFSHRXSRLR-IZGRLVBXSA-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
Siphonaria pectinata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as acyclic monoterpenoids. These are monoterpenes that do not contain a cycle.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Acyclic monoterpenoids

Alternative Parents

Substituents

Acyclic monoterpenoid
Alpha-branched alpha,beta-unsaturated-ketone
Alpha,beta-unsaturated ketone
Enone
Acryloyl-group
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen 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

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

9251118

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11075969

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Lum TK, Wang SY, Loh TP: A highly catalytic asymmetric conjugate addition: synthesis of the C14-C20 fragment of antibiotic TMC-151A, siphonarienal and siphonarienone. Org Lett. 2008 Mar 6;10(5):761-4. doi: 10.1021/ol702715q. Epub 2008 Jan 30. [PubMed:18229932 ]
Magnin-Lachaux M, Tan Z, Liang B, Negishi E: Efficient and selective synthesis of siphonarienolone and related reduced polypropionates via Zr-catalyzed asymmetric carboalumination. Org Lett. 2004 Apr 29;6(9):1425-7. doi: 10.1021/ol0497483. [PubMed:15101758 ]
LOTUS database [Link]

Showing NP-Card for (4e,6s,8s,10s)-4,6,8,10-tetramethyltridec-4-en-3-one (NP0258574)

MOL for NP0258574 ((4e,6s,8s,10s)-4,6,8,10-tetramethyltridec-4-en-3-one)

3D MOL for NP0258574 ((4e,6s,8s,10s)-4,6,8,10-tetramethyltridec-4-en-3-one)

3D SDF for NP0258574 ((4e,6s,8s,10s)-4,6,8,10-tetramethyltridec-4-en-3-one)

3D-SDF for NP0258574 ((4e,6s,8s,10s)-4,6,8,10-tetramethyltridec-4-en-3-one)

PDB for NP0258574 ((4e,6s,8s,10s)-4,6,8,10-tetramethyltridec-4-en-3-one)

3D PDB for NP0258574 ((4e,6s,8s,10s)-4,6,8,10-tetramethyltridec-4-en-3-one)

SMILES for NP0258574 ((4e,6s,8s,10s)-4,6,8,10-tetramethyltridec-4-en-3-one)

INCHI for NP0258574 ((4e,6s,8s,10s)-4,6,8,10-tetramethyltridec-4-en-3-one)

Structure for NP0258574 ((4e,6s,8s,10s)-4,6,8,10-tetramethyltridec-4-en-3-one)

3D Structure for NP0258574 ((4e,6s,8s,10s)-4,6,8,10-tetramethyltridec-4-en-3-one)