NP-MRD: Showing NP-Card for Laurencenone C (NP0064604)

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Record Information

Version

2.0

Created at

2022-04-28 08:48:09 UTC

Updated at

2022-04-28 08:48:09 UTC

NP-MRD ID

NP0064604

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Laurencenone C

Description

(?)-Laurencenone C belongs to the class of organic compounds known as chamigranes. These are sesquiterpenoids characterized by a 1,1,5,9-tetramethylspiro[5,5]undecane skeleton, formally obtained by linking the C1-C6 and C6-C11 of farnesane together. They are predominantly isolated from algae. Laurencenone C is found in Laurencia dendroidea and Marchantia polymorpha. Laurencenone C was first documented in 2010 (PMID: 20798895). Based on a literature review a small amount of articles have been published on (?)-Laurencenone C (PMID: 35389217).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 39  0  0  0  0  0  0  0  0999 V2000
    4.0653   -0.0598   -0.0057 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6542    0.2032   -0.2819 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9045   -0.4908   -1.1569 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4868   -0.1144   -1.3370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2587    0.1944   -0.0789 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6802    0.5409    1.0206 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8586    1.3011    0.3955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2204    1.3165   -0.2347 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9868    2.6935    0.2079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3938    1.0732   -0.8213 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7790   -0.2417   -1.3177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6619   -0.4341   -2.1749 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0686   -1.4158   -0.7600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0685   -1.0548    0.2859 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1994   -2.2453    0.5333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8544   -0.7890    1.5785 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1803   -0.9150    0.6808 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4815    0.8416    0.5122 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6679   -0.2590   -0.9297 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3917   -1.2999   -1.6884 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0136   -0.9698   -1.9049 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4360    0.7385   -2.0773 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1353   -0.3821    1.4895 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2368    1.0918    1.8641 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4469    1.8394    1.1337 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5140    1.9279   -0.4642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7297    3.2932   -0.7138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2032    2.8481    0.9347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9127    3.1837    0.6074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1406    1.8700   -0.9609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8634   -2.0345   -0.2482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6997   -2.0250   -1.5821 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8667   -2.0876    0.4050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3307   -2.6667    1.5734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4684   -3.1179   -0.1331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6528   -0.0526    1.4111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1836   -0.5442    2.4171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3441   -1.7572    1.8206 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  5  4  1  6
  5  6  1  0
  6  7  1  0
  5  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  1
 14 16  1  0
  7  2  1  0
 14  5  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  6 23  1  0
  6 24  1  0
  7 25  1  0
  7 26  1  0
  9 27  1  0
  9 28  1  0
  9 29  1  0
 10 30  1  0
 13 31  1  0
 13 32  1  0
 15 33  1  0
 15 34  1  0
 15 35  1  0
 16 36  1  0
 16 37  1  0
 16 38  1  0
M  END


  Mrv1652304282210482D          

 16 17  0  0  1  0            999 V2000
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8266   -0.7392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1558   -1.1265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  6 14  1  0  0  0  0
 12 15  1  0  0  0  0
  5 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0064604

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC[C@@]2(CC1)C(C)=CC(=O)CC2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O/c1-11-5-7-15(8-6-11)12(2)9-13(16)10-14(15,3)4/h5,9H,6-8,10H2,1-4H3/t15-/m1/s1

> <INCHI_KEY>
SNJATGMAHZJTNR-OAHLLOKOSA-N

> <FORMULA>
C15H22O

> <MOLECULAR_WEIGHT>
218.34

> <EXACT_MASS>
218.167065328

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
25.991296622507694

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(6R)-1,5,5,9-tetramethylspiro[5.5]undeca-1,8-dien-3-one

> <ALOGPS_LOGP>
4.65

> <JCHEM_LOGP>
3.654931166

> <ALOGPS_LOGS>
-3.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.7815436826187865

> <JCHEM_POLAR_SURFACE_AREA>
17.07

> <JCHEM_REFRACTIVITY>
69.06949999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.44e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(6R)-1,5,5,9-tetramethylspiro[5.5]undeca-1,8-dien-3-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -1.746   0.770   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.410  -1.380   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.157  -2.103   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.954   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.644  -0.564   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
CONECT    1    2    7                                                       
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   16                                                  
CONECT    6    5    7   10   14                                             
CONECT    7    6    1    8    9                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    6   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13    6                                                       
CONECT   15   12                                                            
CONECT   16    5                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   34    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₂O

Average Mass

218.3400 Da

Monoisotopic Mass

218.16707 Da

IUPAC Name

(6R)-1,5,5,9-tetramethylspiro[5.5]undeca-1,8-dien-3-one

Traditional Name

(6R)-1,5,5,9-tetramethylspiro[5.5]undeca-1,8-dien-3-one

CAS Registry Number

Not Available

SMILES

CC1=CC[C@@]2(CC1)C(C)=CC(=O)CC2(C)C

InChI Identifier

InChI=1S/C15H22O/c1-11-5-7-15(8-6-11)12(2)9-13(16)10-14(15,3)4/h5,9H,6-8,10H2,1-4H3/t15-/m1/s1

InChI Key

SNJATGMAHZJTNR-OAHLLOKOSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Laurencia dendroidea	LOTUS Database	35616633
Marchantia polymorpha	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as chamigranes. These are sesquiterpenoids characterized by a 1,1,5,9-tetramethylspiro[5,5]undecane skeleton, formally obtained by linking the C1-C6 and C6-C11 of farnesane together. They are predominantly isolated from algae.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Chamigranes

Alternative Parents

Substituents

Chamigrane sesquiterpenoid
Cyclohexenone
Cyclic ketone
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	4.65	ALOGPS
logP	3.65	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	17.07 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	69.07 m³·mol⁻¹	ChemAxon
Polarizability	25.99 Å³	ChemAxon
Number of Rings	2	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

10472242

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Bracket

METLIN ID

Not Available

PubChem Compound

14108777

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Ghosh S, Erchinger JE, Maji R, List B: Catalytic Asymmetric Spirocyclizing Diels-Alder Reactions of Enones: Stereoselective Total and Formal Syntheses of alpha-Chamigrene, beta-Chamigrene, Laurencenone C, Colletoic Acid, and Omphalic Acid. J Am Chem Soc. 2022 Apr 20;144(15):6703-6708. doi: 10.1021/jacs.2c01971. Epub 2022 Apr 7. [PubMed:35389217 ]
White DE, Stewart IC, Seashore-Ludlow BA, Grubbs RH, Stoltz BM: A general enantioselective route to the chamigrene natural product family. Tetrahedron. 2010 Mar 26;66(26):4668-4686. doi: 10.1016/j.tet.2010.04.128. [PubMed:20798895 ]

Showing NP-Card for Laurencenone C (NP0064604)

MOL for NP0064604 (Laurencenone C)

3D MOL for NP0064604 (Laurencenone C)

3D SDF for NP0064604 (Laurencenone C)

3D-SDF for NP0064604 (Laurencenone C)

PDB for NP0064604 (Laurencenone C)

3D PDB for NP0064604 (Laurencenone C)

SMILES for NP0064604 (Laurencenone C)

INCHI for NP0064604 (Laurencenone C)

Structure for NP0064604 (Laurencenone C)

3D Structure for NP0064604 (Laurencenone C)