NP-MRD: Showing NP-Card for (3r,5ar,9as)-3-[(2s,5e)-6,10-dimethylundeca-5,9-dien-2-yl]-3,6,6,9a-tetramethyl-1h,2h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalene (NP0259640)

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Record Information

Version

2.0

Created at

2022-09-08 01:34:37 UTC

Updated at

2022-09-08 01:34:37 UTC

NP-MRD ID

NP0259640

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r,5ar,9as)-3-[(2s,5e)-6,10-dimethylundeca-5,9-dien-2-yl]-3,6,6,9a-tetramethyl-1h,2h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalene

Description

(3R,5aR,9aS)-3-[(2S,5E)-6,10-dimethylundeca-5,9-dien-2-yl]-3,6,6,9a-tetramethyl-1H,2H,3H,4H,5H,5aH,6H,7H,8H,9H,9aH-cyclopenta[a]naphthalene belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Based on a literature review very few articles have been published on (3R,5aR,9aS)-3-[(2S,5E)-6,10-dimethylundeca-5,9-dien-2-yl]-3,6,6,9a-tetramethyl-1H,2H,3H,4H,5H,5aH,6H,7H,8H,9H,9aH-cyclopenta[a]naphthalene.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082203342D          

 30 32  0  0  1  0            999 V2000
    9.6724    3.7233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2824    2.9963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309082203342D          

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 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 18 29  1  0  0  0  0
 22 29  1  0  0  0  0
 29 30  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0259640

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H](CC\C=C(/C)CCC=C(C)C)[C@@]1(C)CCC2=C1CC[C@@H]1C(C)(C)CCC[C@]21C

> <INCHI_IDENTIFIER>
InChI=1S/C30H50/c1-22(2)12-9-13-23(3)14-10-15-24(4)29(7)21-18-26-25(29)16-17-27-28(5,6)19-11-20-30(26,27)8/h12,14,24,27H,9-11,13,15-21H2,1-8H3/b23-14+/t24-,27+,29+,30+/m0/s1

> <INCHI_KEY>
JCONZYYZINSVKI-KNGMKZGOSA-N

> <FORMULA>
C30H50

> <MOLECULAR_WEIGHT>
410.73

> <EXACT_MASS>
410.39125161

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
53.30559309479717

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3R,5aR,9aS)-3-[(2S,5E)-6,10-dimethylundeca-5,9-dien-2-yl]-3,6,6,9a-tetramethyl-1H,2H,3H,4H,5H,5aH,6H,7H,8H,9H,9aH-cyclopenta[a]naphthalene

> <JCHEM_LOGP>
9.297701123

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
135.85969999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3R,5aR,9aS)-3-[(2S,5E)-6,10-dimethylundeca-5,9-dien-2-yl]-3,6,6,9a-tetramethyl-1H,2H,4H,5H,5aH,7H,8H,9H-cyclopenta[a]naphthalene

> <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      18.055   6.950   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      17.327   5.593   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      18.138   4.284   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      15.788   5.545   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      15.060   4.188   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.521   4.140   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.793   2.783   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.604   1.474   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.254   2.735   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.526   1.378   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.986   1.329   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.258  -0.028   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.070  -1.337   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.719  -0.076   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.928  -1.602   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.832   1.460   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.406   2.042   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.412   0.866   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.223  -0.443   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.495  -1.800   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.956  -1.848   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.145  -0.539   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.606  -0.587   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.920  -2.095   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.824  -1.159   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.206   0.722   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.522   2.079   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.062   2.127   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.873   0.818   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.601   2.175   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16   19                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   29                                                  
CONECT   19   18   14   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   29                                                  
CONECT   23   22   24   25   26                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   23   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   18   22   30                                             
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₅₀

Average Mass

410.7300 Da

Monoisotopic Mass

410.39125 Da

IUPAC Name

(3R,5aR,9aS)-3-[(2S,5E)-6,10-dimethylundeca-5,9-dien-2-yl]-3,6,6,9a-tetramethyl-1H,2H,3H,4H,5H,5aH,6H,7H,8H,9H,9aH-cyclopenta[a]naphthalene

Traditional Name

(3R,5aR,9aS)-3-[(2S,5E)-6,10-dimethylundeca-5,9-dien-2-yl]-3,6,6,9a-tetramethyl-1H,2H,4H,5H,5aH,7H,8H,9H-cyclopenta[a]naphthalene

CAS Registry Number

Not Available

SMILES

C[C@@H](CC\C=C(/C)CCC=C(C)C)[C@@]1(C)CCC2=C1CC[C@@H]1C(C)(C)CCC[C@]21C

InChI Identifier

InChI=1S/C30H50/c1-22(2)12-9-13-23(3)14-10-15-24(4)29(7)21-18-26-25(29)16-17-27-28(5,6)19-11-20-30(26,27)8/h12,14,24,27H,9-11,13,15-21H2,1-8H3/b23-14+/t24-,27+,29+,30+/m0/s1

InChI Key

JCONZYYZINSVKI-KNGMKZGOSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
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	9.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	135.86 m³·mol⁻¹	ChemAxon
Polarizability	53.31 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	Yes	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

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

162935002

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3r,5ar,9as)-3-[(2s,5e)-6,10-dimethylundeca-5,9-dien-2-yl]-3,6,6,9a-tetramethyl-1h,2h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalene (NP0259640)

MOL for NP0259640 ((3r,5ar,9as)-3-[(2s,5e)-6,10-dimethylundeca-5,9-dien-2-yl]-3,6,6,9a-tetramethyl-1h,2h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalene)

3D MOL for NP0259640 ((3r,5ar,9as)-3-[(2s,5e)-6,10-dimethylundeca-5,9-dien-2-yl]-3,6,6,9a-tetramethyl-1h,2h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalene)

3D SDF for NP0259640 ((3r,5ar,9as)-3-[(2s,5e)-6,10-dimethylundeca-5,9-dien-2-yl]-3,6,6,9a-tetramethyl-1h,2h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalene)

3D-SDF for NP0259640 ((3r,5ar,9as)-3-[(2s,5e)-6,10-dimethylundeca-5,9-dien-2-yl]-3,6,6,9a-tetramethyl-1h,2h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalene)

PDB for NP0259640 ((3r,5ar,9as)-3-[(2s,5e)-6,10-dimethylundeca-5,9-dien-2-yl]-3,6,6,9a-tetramethyl-1h,2h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalene)

3D PDB for NP0259640 ((3r,5ar,9as)-3-[(2s,5e)-6,10-dimethylundeca-5,9-dien-2-yl]-3,6,6,9a-tetramethyl-1h,2h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalene)

SMILES for NP0259640 ((3r,5ar,9as)-3-[(2s,5e)-6,10-dimethylundeca-5,9-dien-2-yl]-3,6,6,9a-tetramethyl-1h,2h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalene)

INCHI for NP0259640 ((3r,5ar,9as)-3-[(2s,5e)-6,10-dimethylundeca-5,9-dien-2-yl]-3,6,6,9a-tetramethyl-1h,2h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalene)

Structure for NP0259640 ((3r,5ar,9as)-3-[(2s,5e)-6,10-dimethylundeca-5,9-dien-2-yl]-3,6,6,9a-tetramethyl-1h,2h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalene)

3D Structure for NP0259640 ((3r,5ar,9as)-3-[(2s,5e)-6,10-dimethylundeca-5,9-dien-2-yl]-3,6,6,9a-tetramethyl-1h,2h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalene)