NP-MRD: Showing NP-Card for (1r,3s,4r,7s,9r,12s,14s,17s,19r,22s)-14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁷,²²]tricosan-23-one (NP0211986)

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Record Information

Version

2.0

Created at

2022-09-05 10:30:04 UTC

Updated at

2022-09-05 10:30:04 UTC

NP-MRD ID

NP0211986

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3s,4r,7s,9r,12s,14s,17s,19r,22s)-14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁷,²²]tricosan-23-one

Description

Piceanonol A belongs to the class of organic compounds known as tertiary alcohols. Tertiary alcohols are compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom R3COH (R not H ). (1r,3s,4r,7s,9r,12s,14s,17s,19r,22s)-14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁷,²²]tricosan-23-one is found in Picea glehnii and Picea jezoensis. Based on a literature review very few articles have been published on Piceanonol A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052212302D          

 35 39  0  0  1  0            999 V2000
   -1.6987   -3.3050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0329   -2.8179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2781   -3.1511    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3878   -2.6640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1425   -2.9971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2314   -3.8173    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8973   -3.3303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9861   -4.1505    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6520   -3.6634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4068   -3.9965    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9926   -3.4157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7235   -2.6358    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8120   -3.5115    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4296   -2.7805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2006   -2.7838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0252   -2.7564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4611   -3.4569    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.2857   -3.4295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0725   -4.1846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8567   -4.4409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9562   -5.0014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2480   -4.2119    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9722   -4.9895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1923   -5.2586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4956   -4.8167    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5230   -5.6413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8298   -5.3038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0750   -4.9707    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1639   -5.7909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4091   -5.4577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6544   -5.1246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5655   -4.3044    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1892   -3.9713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5485   -4.7139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0058   -4.0887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  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  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  1  0  0  0
 10  9  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 19 22  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 10 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
  8 28  1  0  0  0  0
 28 29  1  1  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 32 31  1  1  0  0  0
  6 32  1  0  0  0  0
 32 33  1  0  0  0  0
  3 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
M  END

     RDKit          3D

 87 91  0  0  0  0  0  0  0  0999 V2000
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   -3.7230    2.1106   -1.5055 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.8070   -1.4435   -1.6816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0097   -1.0624   -0.8270 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.5617   -2.1584   -0.1993 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6101    0.0384    0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.9712    0.3884   -3.2003 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2313   -0.7576   -2.6197 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7407    0.7281   -1.6528 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.1743   -1.8290   -2.1779 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.9400    0.9348   -1.6341 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.2954   -2.4131    0.9595 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  6
  6 32  1  0
 32 31  1  0
 31 30  1  0
 30 28  1  0
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 23 22  1  0
 22 19  1  0
 19 20  1  0
 19 21  1  0
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 10  9  1  0
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 32 33  1  0
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  8  6  1  0
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 13 22  1  0
  1 36  1  0
  1 37  1  0
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  7 44  1  0
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 34 82  1  0
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 34 84  1  0
 35 85  1  0
 35 86  1  0
 35 87  1  0
M  END


  Mrv1652309052212302D          

 35 39  0  0  1  0            999 V2000
   -1.6987   -3.3050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.2480   -4.2119    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9722   -4.9895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1923   -5.2586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4956   -4.8167    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5230   -5.6413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8298   -5.3038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0750   -4.9707    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1639   -5.7909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4091   -5.4577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6544   -5.1246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5655   -4.3044    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1892   -3.9713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5485   -4.7139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0058   -4.0887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  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  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  1  0  0  0
 10  9  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 19 22  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 10 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
  8 28  1  0  0  0  0
 28 29  1  1  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 32 31  1  1  0  0  0
  6 32  1  0  0  0  0
 32 33  1  0  0  0  0
  3 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0211986

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@H]1CC[C@@]2(C)[C@@H](CC[C@@]3(C)C[C@@]4(O)CC[C@H]5C(C)(C)[C@H](O)CC[C@]5(C)C(=O)[C@@H]4C[C@H]23)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C31H52O4/c1-26(2)20-10-16-31(34)18-28(5)13-9-21-27(3,4)24(35-8)12-15-29(21,6)22(28)17-19(31)25(33)30(20,7)14-11-23(26)32/h19-24,32,34H,9-18H2,1-8H3/t19-,20-,21-,22-,23+,24-,28-,29-,30-,31-/m0/s1

> <INCHI_KEY>
MYTJMLDHZCUMMH-DWMBUWPLSA-N

> <FORMULA>
C31H52O4

> <MOLECULAR_WEIGHT>
488.753

> <EXACT_MASS>
488.386560154

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
87

> <JCHEM_AVERAGE_POLARIZABILITY>
58.94579849416505

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,3S,4R,7S,9R,12S,14S,17S,19R,22S)-14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0^{3,12}.0^{4,9}.0^{17,22}]tricosan-23-one

> <JCHEM_LOGP>
5.794941353

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.89227607188178

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.350671568967467

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8068229325193724

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
139.69709999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3S,4R,7S,9R,12S,14S,17S,19R,22S)-14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0^{3,12}.0^{4,9}.0^{17,22}]tricosan-23-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.171  -6.169   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.928  -5.260   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.519  -5.882   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.724  -4.973   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.133  -5.595   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.299  -7.126   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.542  -6.216   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.707  -7.748   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.950  -6.838   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.359  -7.460   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.453  -6.376   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.950  -4.920   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       8.982  -6.555   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.269  -5.190   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.708  -5.196   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.247  -5.145   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.061  -6.453   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      13.600  -6.402   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      11.335  -7.811   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.799  -8.290   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.118  -9.336   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.796  -7.862   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.281  -9.314   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.826  -9.816   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.525  -8.991   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       6.576 -10.530   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       5.282  -9.900   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.873  -9.279   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.039 -10.810   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.630 -10.188   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.222  -9.566   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.056  -8.035   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -0.353  -7.413   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -1.024  -8.799   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.878  -7.632   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   33                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   32                                             
CONECT    7    6                                                            
CONECT    8    6    9   28                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   25                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15   22                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21   22                                             
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   19   13   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   10   26   27                                             
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27    8   29   30                                             
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31    6   33                                                  
CONECT   33   32    3   34   35                                             
CONECT   34   33                                                            
CONECT   35   33                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₅₂O₄

Average Mass

488.7530 Da

Monoisotopic Mass

488.38656 Da

IUPAC Name

(1R,3S,4R,7S,9R,12S,14S,17S,19R,22S)-14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0^{3,12}.0^{4,9}.0^{17,22}]tricosan-23-one

Traditional Name

(1R,3S,4R,7S,9R,12S,14S,17S,19R,22S)-14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0^{3,12}.0^{4,9}.0^{17,22}]tricosan-23-one

CAS Registry Number

Not Available

SMILES

CO[C@H]1CC[C@@]2(C)[C@@H](CC[C@@]3(C)C[C@@]4(O)CC[C@H]5C(C)(C)[C@H](O)CC[C@]5(C)C(=O)[C@@H]4C[C@H]23)C1(C)C

InChI Identifier

InChI=1S/C31H52O4/c1-26(2)20-10-16-31(34)18-28(5)13-9-21-27(3,4)24(35-8)12-15-29(21,6)22(28)17-19(31)25(33)30(20,7)14-11-23(26)32/h19-24,32,34H,9-18H2,1-8H3/t19-,20-,21-,22-,23+,24-,28-,29-,30-,31-/m0/s1

InChI Key

MYTJMLDHZCUMMH-DWMBUWPLSA-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
Picea glehnii	LOTUS Database	35616633
Picea jezoensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tertiary alcohols. Tertiary alcohols are compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom R3COH (R not H ).

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Tertiary alcohols

Alternative Parents

Substituents

Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Ketone
Ether
Dialkyl ether
Organic oxide
Hydrocarbon derivative
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	5.79	ChemAxon
pKa (Strongest Acidic)	14.35	ChemAxon
pKa (Strongest Basic)	-0.81	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	139.7 m³·mol⁻¹	ChemAxon
Polarizability	58.95 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

8918950

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10743619

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3s,4r,7s,9r,12s,14s,17s,19r,22s)-14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁷,²²]tricosan-23-one (NP0211986)

MOL for NP0211986 ((1r,3s,4r,7s,9r,12s,14s,17s,19r,22s)-14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁷,²²]tricosan-23-one)

3D MOL for NP0211986 ((1r,3s,4r,7s,9r,12s,14s,17s,19r,22s)-14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁷,²²]tricosan-23-one)

3D SDF for NP0211986 ((1r,3s,4r,7s,9r,12s,14s,17s,19r,22s)-14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁷,²²]tricosan-23-one)

3D-SDF for NP0211986 ((1r,3s,4r,7s,9r,12s,14s,17s,19r,22s)-14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁷,²²]tricosan-23-one)

PDB for NP0211986 ((1r,3s,4r,7s,9r,12s,14s,17s,19r,22s)-14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁷,²²]tricosan-23-one)

3D PDB for NP0211986 ((1r,3s,4r,7s,9r,12s,14s,17s,19r,22s)-14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁷,²²]tricosan-23-one)

SMILES for NP0211986 ((1r,3s,4r,7s,9r,12s,14s,17s,19r,22s)-14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁷,²²]tricosan-23-one)

INCHI for NP0211986 ((1r,3s,4r,7s,9r,12s,14s,17s,19r,22s)-14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁷,²²]tricosan-23-one)

Structure for NP0211986 ((1r,3s,4r,7s,9r,12s,14s,17s,19r,22s)-14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁷,²²]tricosan-23-one)

3D Structure for NP0211986 ((1r,3s,4r,7s,9r,12s,14s,17s,19r,22s)-14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁷,²²]tricosan-23-one)