NP-MRD: Showing NP-Card for (1r,2r,7r,8r)-2,6,6,9-tetramethyltricyclo[5.4.0.0²,⁸]undec-9-ene (NP0324009)

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Record Information

Version

2.0

Created at

2022-09-12 03:48:36 UTC

Updated at

2022-09-12 03:48:36 UTC

NP-MRD ID

NP0324009

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,7r,8r)-2,6,6,9-tetramethyltricyclo[5.4.0.0²,⁸]undec-9-ene

Description

Alpha-Longipinene, also known as α-longipinene, belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. (1r,2r,7r,8r)-2,6,6,9-tetramethyltricyclo[5.4.0.0²,⁸]undec-9-ene is found in Abies sibirica, Bazzania trilobata, Bellis perennis, Cryptomeria japonica, Dacrydium cupressinum, Halocarpus bidwillii, Halocarpus biformis, Hypericum rumeliacum, Larix gmelinii, Larix gmelinii, Larix kaempferi, Larix sibirica, Metacalypogeia alternifolia, Microbiota decussata, Picea koraiensis, Pinus brutia, Pinus densiflora, Pinus pumila and Scapania undulata. (1r,2r,7r,8r)-2,6,6,9-tetramethyltricyclo[5.4.0.0²,⁸]undec-9-ene was first documented in 2008 (PMID: 18493792). Based on a literature review a significant number of articles have been published on alpha-Longipinene (PMID: 31164939) (PMID: 19967999) (PMID: 35430531) (PMID: 33616837) (PMID: 33202940) (PMID: 32251305).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          2D

 39 41  0  0  0  0  0  0  0  0999 V2000
   -2.3597    2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0607    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2384    2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5374    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0607    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.0607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0607    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.0607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.5607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4624    1.3944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6351    0.4592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6351   -1.0408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4624   -1.9760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6351   -2.9113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8116   -3.3275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6587    3.0000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6097    3.5490    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5255    1.3061    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4212    3.7388    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2184    2.8365    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0146    1.2395    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5607    0.0000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1828   -2.5495    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5161   -0.3630    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1828    4.0495    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4888    2.7435    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4888    2.7435    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9812    2.8152    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7404    2.1797    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5936    1.6130    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1273    0.3062    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1273   -0.8878    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4458   -2.3028    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8079   -3.8465    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8498   -4.1893    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7064   -1.8613    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1607   -4.6789    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0736   -4.1382    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6091   -2.8462    0.0000 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
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  1
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
  7  2  1  0
  8  5  1  0
 13  6  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  3 19  1  0
  4 20  1  0
  4 21  1  0
  5 22  1  1
  6 23  1  6
  7 24  1  1
  9 25  1  0
  9 26  1  0
  9 27  1  0
 10 28  1  0
 10 29  1  0
 11 30  1  0
 11 31  1  0
 12 32  1  0
 12 33  1  0
 14 34  1  0
 14 35  1  0
 14 36  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
M  END


  Mrv1652309122205482D          

 15 17  0  0  1  0            999 V2000
    1.5823    1.3164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0057    0.7264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1483    0.9753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3470    0.2918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1540   -0.3961    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8947   -0.7175    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2353   -0.0019    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4319    0.4030    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3385    0.6982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9566    1.2052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7810    0.9482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1398    0.1794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7634   -0.5979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5022   -0.9650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8844   -1.4139    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
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  2  1  1  0  0  0
  7  8  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0324009

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC[C@@H]2[C@@H]3[C@H]1[C@]2(C)CCCC3(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C15H24/c1-10-6-7-11-13-12(10)15(11,4)9-5-8-14(13,2)3/h6,11-13H,5,7-9H2,1-4H3/t11-,12+,13-,15-/m1/s1

> <INCHI_KEY>
HICYDYJTCDBHMZ-QVHKTLOISA-N

> <FORMULA>
C15H24

> <MOLECULAR_WEIGHT>
204.357

> <EXACT_MASS>
204.187800773

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
71.4629329045141

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,7R,8R)-2,6,6,9-tetramethyltricyclo[5.4.0.0^{2,8}]undec-9-ene

> <JCHEM_LOGP>
4.101158186333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
65.6944

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,7R,8R)-2,6,6,9-tetramethyltricyclo[5.4.0.0^{2,8}]undec-9-ene

> <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       2.954   2.457   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.877   1.356   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.277   1.821   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.648   0.545   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.287  -0.739   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.670  -1.339   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.306  -0.003   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.806   0.752   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.632   1.303   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.786   2.250   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.325   1.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.994   0.335   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.292  -1.116   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.671  -1.801   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.517  -2.639   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    8                                                  
CONECT    6    5    7   13                                                  
CONECT    7    6    2    8                                                  
CONECT    8    7    5    9   10                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    6   14   15                                             
CONECT   14   13                                                            
CONECT   15   13                                                            
MASTER        0    0    0    0    0    0    0    0   15    0   34    0
END

View in JSmol

Synonyms

Value	Source
a-Longipinene	Generator
Α-longipinene	Generator

Chemical Formula

C₁₅H₂₄

Average Mass

204.3570 Da

Monoisotopic Mass

204.18780 Da

IUPAC Name

(1R,2R,7R,8R)-2,6,6,9-tetramethyltricyclo[5.4.0.0^{2,8}]undec-9-ene

Traditional Name

(1R,2R,7R,8R)-2,6,6,9-tetramethyltricyclo[5.4.0.0^{2,8}]undec-9-ene

CAS Registry Number

Not Available

SMILES

CC1=CC[C@@H]2[C@@H]3[C@H]1[C@]2(C)CCCC3(C)C

InChI Identifier

InChI=1S/C15H24/c1-10-6-7-11-13-12(10)15(11,4)9-5-8-14(13,2)3/h6,11-13H,5,7-9H2,1-4H3/t11-,12+,13-,15-/m1/s1

InChI Key

HICYDYJTCDBHMZ-QVHKTLOISA-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
Abies sibirica	LOTUS Database	35616633
Bazzania trilobata	LOTUS Database	35616633
Bellis perennis	LOTUS Database	35616633
Cryptomeria japonica	LOTUS Database	35616633
Dacrydium cupressinum	LOTUS Database	35616633
Halocarpus bidwillii	LOTUS Database	35616633
Halocarpus biformis	LOTUS Database	35616633
Hypericum rumeliacum	LOTUS Database	35616633
Larix gmelini	LOTUS Database	35616633
Larix gmelinii var. olgensis	LOTUS Database	35616633
Larix kaempferi	LOTUS Database	35616633
Larix sibirica	LOTUS Database	35616633
Metacalypogeia alternifolia	LOTUS Database	35616633
Microbiota decussata	LOTUS Database	35616633
Picea koraiensis	LOTUS Database	35616633
Pinus brutia	LOTUS Database	35616633
Pinus densiflora	LOTUS Database	35616633
Pinus pumila	LOTUS Database	35616633
Scapania undulata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Longipinane sesquiterpenoid
Sesquiterpenoid
Branched unsaturated hydrocarbon
Polycyclic hydrocarbon
Cyclic olefin
Unsaturated aliphatic hydrocarbon
Unsaturated hydrocarbon
Olefin
Hydrocarbon
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	4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	65.69 m³·mol⁻¹	ChemAxon
Polarizability	71.46 Å³	ChemAxon
Number of Rings	3	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

C00036714

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

92042758

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Rinkel J, Dickschat JS: Mechanistic investigations on multiproduct beta-himachalene synthase from Cryptosporangium arvum. Beilstein J Org Chem. 2019 May 2;15:1008-1019. doi: 10.3762/bjoc.15.99. eCollection 2019. [PubMed:31164939 ]
Kopke D, Schroder R, Fischer HM, Gershenzon J, Hilker M, Schmidt A: Does egg deposition by herbivorous pine sawflies affect transcription of sesquiterpene synthases in pine? Planta. 2008 Aug;228(3):427-38. doi: 10.1007/s00425-008-0747-8. Epub 2008 May 21. [PubMed:18493792 ]
Baldovino S, Rojas J, Rojas LB, Lucena M, Buitrago A, Morales A: Chemical composition and antibacterial activity of the essential oil of Monticalia andicola (Asteraceae) collected in Venezuela. Nat Prod Commun. 2009 Nov;4(11):1601-4. [PubMed:19967999 ]
Kim S, Bae S, Lee DS: Characterization of scents from Juniperus chinensis by headspace in-needle microextraction using graphene oxide-polyaniline nanocomposite coated wire followed by gas chromatography-mass spectrometry. Talanta. 2022 Aug 1;245:123463. doi: 10.1016/j.talanta.2022.123463. Epub 2022 Apr 8. [PubMed:35430531 ]
Ethington MW, Hughes GP, VanDerLaan NR, Ginzel MD: Chemically-mediated colonization of black cherry by the peach bark beetle, Phloeotribus liminaris. J Chem Ecol. 2021 Mar;47(3):303-312. doi: 10.1007/s10886-021-01256-z. Epub 2021 Feb 22. [PubMed:33616837 ]
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Makarow R, Schafer S, Kaul P: Identification of Anoplophora glabripennis (Moschulsky) by its emitted specific volatile organic compounds. Sci Rep. 2020 Mar 23;10(1):5194. doi: 10.1038/s41598-020-61897-0. [PubMed:32251305 ]
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LOTUS database [Link]

Showing NP-Card for (1r,2r,7r,8r)-2,6,6,9-tetramethyltricyclo[5.4.0.0²,⁸]undec-9-ene (NP0324009)

MOL for NP0324009 ((1r,2r,7r,8r)-2,6,6,9-tetramethyltricyclo[5.4.0.0²,⁸]undec-9-ene)

3D MOL for NP0324009 ((1r,2r,7r,8r)-2,6,6,9-tetramethyltricyclo[5.4.0.0²,⁸]undec-9-ene)

3D SDF for NP0324009 ((1r,2r,7r,8r)-2,6,6,9-tetramethyltricyclo[5.4.0.0²,⁸]undec-9-ene)

3D-SDF for NP0324009 ((1r,2r,7r,8r)-2,6,6,9-tetramethyltricyclo[5.4.0.0²,⁸]undec-9-ene)

PDB for NP0324009 ((1r,2r,7r,8r)-2,6,6,9-tetramethyltricyclo[5.4.0.0²,⁸]undec-9-ene)

3D PDB for NP0324009 ((1r,2r,7r,8r)-2,6,6,9-tetramethyltricyclo[5.4.0.0²,⁸]undec-9-ene)

SMILES for NP0324009 ((1r,2r,7r,8r)-2,6,6,9-tetramethyltricyclo[5.4.0.0²,⁸]undec-9-ene)

INCHI for NP0324009 ((1r,2r,7r,8r)-2,6,6,9-tetramethyltricyclo[5.4.0.0²,⁸]undec-9-ene)

Structure for NP0324009 ((1r,2r,7r,8r)-2,6,6,9-tetramethyltricyclo[5.4.0.0²,⁸]undec-9-ene)

3D Structure for NP0324009 ((1r,2r,7r,8r)-2,6,6,9-tetramethyltricyclo[5.4.0.0²,⁸]undec-9-ene)