NP-MRD: Showing NP-Card for (2s)-7-[(3s)-5-hydroxy-3-methylpentyl]-1,1,5,6-tetramethyl-3,4-dihydro-2h-naphthalen-2-ol (NP0193482)

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Record Information

Version

2.0

Created at

2022-09-04 10:55:55 UTC

Updated at

2022-09-04 10:55:55 UTC

NP-MRD ID

NP0193482

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-7-[(3s)-5-hydroxy-3-methylpentyl]-1,1,5,6-tetramethyl-3,4-dihydro-2h-naphthalen-2-ol

Description

Chinnar, also known as isofregenedadiol, belongs to the class of organic compounds known as tetralins. These are polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane. (2s)-7-[(3s)-5-hydroxy-3-methylpentyl]-1,1,5,6-tetramethyl-3,4-dihydro-2h-naphthalen-2-ol was first documented in 2017 (PMID: 28551884). Based on a literature review very few articles have been published on Chinnar (PMID: 32968836).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 54 55  0  0  0  0  0  0  0  0999 V2000
    0.6241    0.6290   -2.6613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3028    0.4627   -1.4856 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1352    0.6876   -0.1972 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5492    1.0967    0.0933 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4370   -0.0960    0.0002 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8987    0.1901    0.2759 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4854    1.1732   -0.6774 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6235   -1.1111    0.2667 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0789   -1.0067    0.6440 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6972   -0.1639   -0.2779 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7810    0.5152    0.8245 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1045    0.1294    0.5975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5138   -0.0885   -0.6993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6110    0.0807   -1.7170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0854   -0.1609   -3.1222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9154   -0.5089   -1.0432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6243   -0.9612    0.2178 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4022   -0.0120    1.3562 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7137    1.2768    0.9091 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9767   -0.0192    1.7877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5858   -1.3241    2.4717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7491    1.1100    2.7794 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5707    1.1054   -2.3732 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7977   -0.3358   -3.1378 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1409    1.2971   -3.4241 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8563    1.9415   -0.5388 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5642    1.4272    1.1665 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3569   -0.6513   -0.9600 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0569   -0.8349    0.7667 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9169    0.6193    1.3127 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3248    1.7130   -0.1858 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8041    1.9406   -1.0373 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9195    0.6434   -1.5521 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4756   -1.6166   -0.7031 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1553   -1.7878    1.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2235   -0.6619    1.6818 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5934   -1.9857    0.5752 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9373   -0.7162   -1.0886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4637    0.6858    1.8592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7447    0.6367   -3.8118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8461   -1.1738   -3.4707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2112   -0.0832   -3.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9197   -1.3735   -1.7399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4814    0.3059   -1.5358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3185   -1.9815    0.5170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7080   -0.9904   -0.0055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1094   -0.2946    2.1686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5713    1.2707    0.4082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5548   -1.1394    2.8916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4653   -2.0905    1.7024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3019   -1.5685    3.2664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0426    1.8742    2.3441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4085    0.7238    3.7429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7104    1.6670    2.9366 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2 14  1  0
 14 15  1  0
 14 13  2  0
 13 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 20 12  1  0
 12 11  2  0
 11  3  1  0
 12 13  1  0
  7 31  1  0
  7 32  1  0
  7 33  1  0
  6 30  1  1
  8 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  0
  5 28  1  0
  5 29  1  0
  4 26  1  0
  4 27  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
 15 40  1  0
 15 41  1  0
 15 42  1  0
 16 43  1  0
 16 44  1  0
 17 45  1  0
 17 46  1  0
 18 47  1  1
 19 48  1  0
 21 49  1  0
 21 50  1  0
 21 51  1  0
 22 52  1  0
 22 53  1  0
 22 54  1  0
 11 39  1  0
M  END


  Mrv1652309042212552D          

 22 23  0  0  1  0            999 V2000
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2452   -1.7466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4706   -1.7466    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  3 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  2 14  1  0  0  0  0
 14 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 12 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0193482

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](CCO)CCC1=C(C)C(C)=C2CC[C@H](O)C(C)(C)C2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O2/c1-13(10-11-21)6-7-16-12-18-17(15(3)14(16)2)8-9-19(22)20(18,4)5/h12-13,19,21-22H,6-11H2,1-5H3/t13-,19-/m0/s1

> <INCHI_KEY>
PQDATHUEVFNPAK-DJJJIMSYSA-N

> <FORMULA>
C20H32O2

> <MOLECULAR_WEIGHT>
304.474

> <EXACT_MASS>
304.24023027

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
37.51269675733883

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-7-[(3S)-5-hydroxy-3-methylpentyl]-1,1,5,6-tetramethyl-1,2,3,4-tetrahydronaphthalen-2-ol

> <JCHEM_LOGP>
4.950634478999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.10979172295286

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.625941220412948

> <JCHEM_PKA_STRONGEST_BASIC>
-1.8759771003804184

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
94.08430000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-7-[(3S)-5-hydroxy-3-methylpentyl]-1,1,5,6-tetramethyl-3,4-dihydro-2H-naphthalen-2-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -8.002  -4.620   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -6.058  -3.260   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -4.612  -3.260   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   14                                                  
CONECT    3    2    4   11                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    3   12                                                       
CONECT   12   11   13   20                                                  
CONECT   13   12   14   16                                                  
CONECT   14   13    2   15                                                  
CONECT   15   14                                                            
CONECT   16   13   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   12   21   22                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Value	Source
Isofregenedadiol	MeSH

Chemical Formula

C₂₀H₃₂O₂

Average Mass

304.4740 Da

Monoisotopic Mass

304.24023 Da

IUPAC Name

(2S)-7-[(3S)-5-hydroxy-3-methylpentyl]-1,1,5,6-tetramethyl-1,2,3,4-tetrahydronaphthalen-2-ol

Traditional Name

(2S)-7-[(3S)-5-hydroxy-3-methylpentyl]-1,1,5,6-tetramethyl-3,4-dihydro-2H-naphthalen-2-ol

CAS Registry Number

Not Available

SMILES

C[C@H](CCO)CCC1=C(C)C(C)=C2CC[C@H](O)C(C)(C)C2=C1

InChI Identifier

InChI=1S/C20H32O2/c1-13(10-11-21)6-7-16-12-18-17(15(3)14(16)2)8-9-19(22)20(18,4)5/h12-13,19,21-22H,6-11H2,1-5H3/t13-,19-/m0/s1

InChI Key

PQDATHUEVFNPAK-DJJJIMSYSA-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 tetralins. These are polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Tetralins

Sub Class

Not Available

Direct Parent

Tetralins

Alternative Parents

Substituents

Tetralin
Fatty alcohol
Fatty acyl
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aromatic homopolycyclic compound

Molecular Framework

Aromatic 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	4.95	ChemAxon
pKa (Strongest Acidic)	14.63	ChemAxon
pKa (Strongest Basic)	-1.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.46 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	94.08 m³·mol⁻¹	ChemAxon
Polarizability	37.51 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	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

28289100

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15819259

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Gayathri V, Muralisankar T, Rajaram R, Muniasamy M, Santhanam P: Assessment of Heavy Metals Pollution in Noyyal and Chinnar Rivers, Western Ghats of Tamil Nadu, India with Reference to Crabs (Gecarcinucidae)-A Baseline Study. Bull Environ Contam Toxicol. 2020 Oct;105(4):538-545. doi: 10.1007/s00128-020-02986-8. Epub 2020 Sep 24. [PubMed:32968836 ]
Athira K, Reddy CS, Saranya KRL, Joseph S, Jaishanker R: Habitat monitoring and conservation prioritisation of protected areas in Western Ghats, Kerala, India. Environ Monit Assess. 2017 Jun;189(6):295. doi: 10.1007/s10661-017-5998-z. Epub 2017 May 27. [PubMed:28551884 ]
LOTUS database [Link]

Showing NP-Card for (2s)-7-[(3s)-5-hydroxy-3-methylpentyl]-1,1,5,6-tetramethyl-3,4-dihydro-2h-naphthalen-2-ol (NP0193482)

MOL for NP0193482 ((2s)-7-[(3s)-5-hydroxy-3-methylpentyl]-1,1,5,6-tetramethyl-3,4-dihydro-2h-naphthalen-2-ol)

3D MOL for NP0193482 ((2s)-7-[(3s)-5-hydroxy-3-methylpentyl]-1,1,5,6-tetramethyl-3,4-dihydro-2h-naphthalen-2-ol)

3D SDF for NP0193482 ((2s)-7-[(3s)-5-hydroxy-3-methylpentyl]-1,1,5,6-tetramethyl-3,4-dihydro-2h-naphthalen-2-ol)

3D-SDF for NP0193482 ((2s)-7-[(3s)-5-hydroxy-3-methylpentyl]-1,1,5,6-tetramethyl-3,4-dihydro-2h-naphthalen-2-ol)

PDB for NP0193482 ((2s)-7-[(3s)-5-hydroxy-3-methylpentyl]-1,1,5,6-tetramethyl-3,4-dihydro-2h-naphthalen-2-ol)

3D PDB for NP0193482 ((2s)-7-[(3s)-5-hydroxy-3-methylpentyl]-1,1,5,6-tetramethyl-3,4-dihydro-2h-naphthalen-2-ol)

SMILES for NP0193482 ((2s)-7-[(3s)-5-hydroxy-3-methylpentyl]-1,1,5,6-tetramethyl-3,4-dihydro-2h-naphthalen-2-ol)

INCHI for NP0193482 ((2s)-7-[(3s)-5-hydroxy-3-methylpentyl]-1,1,5,6-tetramethyl-3,4-dihydro-2h-naphthalen-2-ol)

Structure for NP0193482 ((2s)-7-[(3s)-5-hydroxy-3-methylpentyl]-1,1,5,6-tetramethyl-3,4-dihydro-2h-naphthalen-2-ol)

3D Structure for NP0193482 ((2s)-7-[(3s)-5-hydroxy-3-methylpentyl]-1,1,5,6-tetramethyl-3,4-dihydro-2h-naphthalen-2-ol)