NP-MRD: Showing NP-Card for (+)-Longifolene (NP0137593)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-05-30 16:57:11 UTC

Updated at

2022-05-30 16:57:11 UTC

NP-MRD ID

NP0137593

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Longifolene

Description

(+)-Longifolene is found in Abies magnifica, Bellardia trixago, Cedrela fissilis, Halocarpus biformis, Herbertus dicranus, Manoao colensoi, Larix gmelinii, Mosla chinensis, Picea abies, Pinus brutia, Pinus palustris, Pinus ponderosa and Prumnopitys andina.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
   -1.9321   -0.5338   -1.8676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2735   -0.0074   -0.8542 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4486    1.2164   -0.8860 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2580    2.2712   -0.1104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2015    1.7354    1.3190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3567    0.4512    1.2219 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6088    0.9594    0.1630 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7152    0.1061   -0.1918 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0262    0.1699   -1.6938 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9965    0.6675    0.4596 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6607   -1.3283    0.2164 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5267   -2.1093   -0.3249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7071   -1.9409    0.5309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2345   -0.5473    0.5228 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5886   -0.5529    1.1888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9346   -0.1033   -2.8685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5215   -1.4533   -1.7408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1006    1.5459   -1.8365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7169    3.2241   -0.1491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2948    2.3212   -0.4842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2116    1.5437    1.6638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6927    2.4527    1.9900 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0867    0.1504    2.1460 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9397    1.9715    0.5174 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1219   -0.0588   -1.8454 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9053    1.2101   -2.0765 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4699   -0.5615   -2.2713 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4324    1.4725   -0.1456 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7339   -0.1390    0.6246 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6840    1.0389    1.4670 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6128   -1.8077   -0.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6939   -1.4660    1.3162 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2537   -1.9218   -1.3636 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7996   -3.2007   -0.2637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5285   -2.3048    1.5635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4889   -2.6009    0.0995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4308   -0.3894    2.2751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3189    0.1104    0.7276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0276   -1.5917    1.1194 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2 14  1  0
 14 15  1  1
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11  8  1  0
  8  9  1  0
  8 10  1  0
  8  7  1  0
 14  6  1  0
  7  6  1  0
  7  3  1  0
  6 23  1  1
  5 21  1  0
  5 22  1  0
  4 19  1  0
  4 20  1  0
  3 18  1  6
  1 16  1  0
  1 17  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
 13 35  1  0
 13 36  1  0
 12 33  1  0
 12 34  1  0
 11 31  1  0
 11 32  1  0
  9 25  1  0
  9 26  1  0
  9 27  1  0
 10 28  1  0
 10 29  1  0
 10 30  1  0
  7 24  1  1
M  END


  Mrv1652309272007472D          

 17 19  0  0  0  0            999 V2000
    0.7845   -0.6674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8073    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4493   -0.7434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4494    0.7432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3289   -0.2197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0434    0.1925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6450   -0.9269    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6449   -1.7520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000    1.2375    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -1.2375    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7845    0.6674    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6451    1.7520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6451    0.9269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3596    1.3394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  8 12  1  0  0  0  0
 12 10  1  0  0  0  0
 10 16  1  0  0  0  0
 10 14  1  0  0  0  0
  1 12  1  0  0  0  0
 14  2  1  0  0  0  0
  1  2  1  0  0  0  0
  3  4  1  0  0  0  0
  5  3  1  0  0  0  0
  8  4  1  0  0  0  0
 16  5  1  0  0  0  0
  6  7  2  0  0  0  0
  8  9  1  0  0  0  0
 10 11  1  6  0  0  0
 12 13  1  6  0  0  0
 16 15  1  0  0  0  0
 16 17  1  0  0  0  0
  8  6  1  1  0  0  0
 14  6  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0137593

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@]12CC[C@@H]3C(=C)[C@@]1(C)CCCC(C)(C)[C@]23[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H24/c1-10-11-6-7-12-13(11)14(2,3)8-5-9-15(10,12)4/h11-13H,1,5-9H2,2-4H3/t11-,12-,13+,15-/m1/s1

> <INCHI_KEY>
PDSNLYSELAIEBU-GUIRCDHDSA-N

> <FORMULA>
C15H24

> <MOLECULAR_WEIGHT>
204.357

> <EXACT_MASS>
204.187800773

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
25.41899625472891

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,7S,9S)-3,3,7-trimethyl-8-methylidenetricyclo[5.4.0.0^{2,9}]undecane

> <ALOGPS_LOGP>
4.65

> <JCHEM_LOGP>
4.159091856666667

> <ALOGPS_LOGS>
-5.21

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
64.6219

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.26e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,7S,9S)-3,3,7-trimethyl-8-methylidenetricyclo[5.4.0.0^{2,9}]undecane

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 27-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-SEP-20         0                                  
HETATM    1  C   UNK     0       1.464  -1.246   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.370   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.374   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.705  -1.388   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.706   1.387   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.614  -0.410   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.948   0.359   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.204  -1.730   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.204  -3.270   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   0.770   0.000  0.00  0.00           C+0
HETATM   11  H   UNK     0       0.000   2.310   0.000  0.00  0.00           H+0
HETATM   12  C   UNK     0       0.000  -0.770   0.000  0.00  0.00           C+0
HETATM   13  H   UNK     0       0.000  -2.310   0.000  0.00  0.00           H+0
HETATM   14  C   UNK     0       1.464   1.246   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.204   3.270   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.204   1.730   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.538   2.500   0.000  0.00  0.00           C+0
CONECT    1   12    2                                                       
CONECT    2   14    1                                                       
CONECT    3    4    5                                                       
CONECT    4    3    8                                                       
CONECT    5    3   16                                                       
CONECT    6    7    8   14                                                  
CONECT    7    6                                                            
CONECT    8   12    4    9    6                                             
CONECT    9    8                                                            
CONECT   10   12   16   14   11                                             
CONECT   11   10                                                            
CONECT   12    8   10    1   13                                             
CONECT   13   12                                                            
CONECT   14   10    2    6                                                  
CONECT   15   16                                                            
CONECT   16   10    5   15   17                                             
CONECT   17   16                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   38    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₄

Average Mass

204.3570 Da

Monoisotopic Mass

204.18780 Da

IUPAC Name

(1R,2S,7S,9S)-3,3,7-trimethyl-8-methylidenetricyclo[5.4.0.0^{2,9}]undecane

Traditional Name

(1R,2S,7S,9S)-3,3,7-trimethyl-8-methylidenetricyclo[5.4.0.0^{2,9}]undecane

CAS Registry Number

Not Available

SMILES

[H][C@]12CC[C@@H]3C(=C)[C@@]1(C)CCCC(C)(C)[C@]23[H]

InChI Identifier

InChI=1S/C15H24/c1-10-11-6-7-12-13(11)14(2,3)8-5-9-15(10,12)4/h11-13H,1,5-9H2,2-4H3/t11-,12-,13+,15-/m1/s1

InChI Key

PDSNLYSELAIEBU-GUIRCDHDSA-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 magnifica	LOTUS Database	35616633
Bartsia trixago	LOTUS Database	35616633
Cedrela fissilis	LOTUS Database	35616633
Halocarpus biformis	LOTUS Database	35616633
Herbertus dicranus	LOTUS Database	35616633
Lagarostrobos colensoi	LOTUS Database	35616633
Larix gmelini	LOTUS Database	35616633
Mosla chinensis	LOTUS Database	35616633
Picea abies	LOTUS Database	35616633
Pinus brutia	LOTUS Database	35616633
Pinus palustris	LOTUS Database	35616633
Pinus ponderosa	LOTUS Database	35616633
Prumnopitys andina	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	4.16	ChemAxon
logS	-5.2	ALOGPS
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	64.62 m³·mol⁻¹	ChemAxon
Polarizability	25.42 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

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Longifolene (NP0137593)

MOL for NP0137593 ((+)-Longifolene)

3D MOL for NP0137593 ((+)-Longifolene)

3D SDF for NP0137593 ((+)-Longifolene)

3D-SDF for NP0137593 ((+)-Longifolene)

PDB for NP0137593 ((+)-Longifolene)

3D PDB for NP0137593 ((+)-Longifolene)

SMILES for NP0137593 ((+)-Longifolene)

INCHI for NP0137593 ((+)-Longifolene)

Structure for NP0137593 ((+)-Longifolene)

3D Structure for NP0137593 ((+)-Longifolene)