NP-MRD: Showing NP-Card for 5-hydroxy-8-(3',7'-dimethylocta-2',6'-dienyl)-2,2,7-trimethyl-2H-1-chrome+ (NP0030133)

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Record Information

Version

2.0

Created at

2021-06-19 21:34:18 UTC

Updated at

2021-06-29 23:57:56 UTC

NP-MRD ID

NP0030133

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-hydroxy-8-(3',7'-dimethylocta-2',6'-dienyl)-2,2,7-trimethyl-2H-1-chrome+

Provided By

JEOL Database JEOL Logo

Description

2,2,7-Trimethyl-8-(3,7-dimethyl-2,6-octadienyl)-2H-1-benzopyran-5-ol belongs to the class of organic compounds known as 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position. 5-hydroxy-8-(3',7'-dimethylocta-2',6'-dienyl)-2,2,7-trimethyl-2H-1-chrome+ is found in Peperomia serpens (Sw.) Loudon (Piperaceae). 5-hydroxy-8-(3',7'-dimethylocta-2',6'-dienyl)-2,2,7-trimethyl-2H-1-chrome+ was first documented in 2006 (Kitamura, R.O.S., et al.). Based on a literature review very few articles have been published on 2,2,7-Trimethyl-8-(3,7-dimethyl-2,6-octadienyl)-2H-1-benzopyran-5-ol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192123343D          

 54 55  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652306192123343D          

 54 55  0  0  0  0            999 V2000
    1.9979   -0.2342   -3.7825 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6836   -0.5886   -3.1455 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.7211    1.9306   -1.2693 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2789    3.3716   -0.3315 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0495    2.0107    0.4633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3817    0.4654    0.9634 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6233    0.3848    1.7142 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3284    0.4081    2.8564 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1035   -1.0416    0.5824 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7962   -2.1989   -0.7155 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8535   -0.7154   -0.6550 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7790   -4.1136    0.0708 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7319   -5.9044    0.7951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6346   -1.7081    2.1411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6450   -0.2967    3.1828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5933   -1.7301    3.6362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3450   -1.7615    5.9345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4239   -0.3322    5.4204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5680   -1.7730    5.9410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2308   -3.9368    4.5500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6602   -5.2726    3.2398 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  1  0  0  0  0
 12 11  2  0  0  0  0
 20 21  1  6  0  0  0
 11 18  1  0  0  0  0
 20 22  1  0  0  0  0
 14 12  1  0  0  0  0
 11 10  1  0  0  0  0
 17 15  1  0  0  0  0
 10  9  1  0  0  0  0
 15 14  2  0  0  0  0
  9  7  2  0  0  0  0
 17 24  1  0  0  0  0
  7  8  1  0  0  0  0
 18 19  1  0  0  0  0
  7  6  1  0  0  0  0
 19 20  1  0  0  0  0
  6  5  1  0  0  0  0
 20 23  1  0  0  0  0
  5  4  1  0  0  0  0
 23 24  2  0  0  0  0
  4  2  2  3  0  0  0
 17 18  2  0  0  0  0
  2  1  1  0  0  0  0
 12 13  1  0  0  0  0
  2  3  1  0  0  0  0
 14 45  1  0  0  0  0
 23 53  1  0  0  0  0
 24 54  1  0  0  0  0
 13 42  1  0  0  0  0
 13 43  1  0  0  0  0
 13 44  1  0  0  0  0
 16 46  1  0  0  0  0
 21 47  1  0  0  0  0
 21 48  1  0  0  0  0
 21 49  1  0  0  0  0
 22 50  1  0  0  0  0
 22 51  1  0  0  0  0
 22 52  1  0  0  0  0
 10 40  1  0  0  0  0
 10 41  1  0  0  0  0
  9 39  1  0  0  0  0
  8 36  1  0  0  0  0
  8 37  1  0  0  0  0
  8 38  1  0  0  0  0
  6 34  1  0  0  0  0
  6 35  1  0  0  0  0
  5 32  1  0  0  0  0
  5 33  1  0  0  0  0
  4 31  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  3 28  1  0  0  0  0
  3 29  1  0  0  0  0
  3 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0030133

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C(=C(C2=C1C([H])=C([H])C(O2)(C([H])([H])[H])C([H])([H])[H])C([H])([H])C(\[H])=C(/C([H])([H])[H])C([H])([H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C22H30O2/c1-15(2)8-7-9-16(3)10-11-18-17(4)14-20(23)19-12-13-22(5,6)24-21(18)19/h8,10,12-14,23H,7,9,11H2,1-6H3/b16-10+

> <INCHI_KEY>
FBTFUGPYAYRHHG-MHWRWJLKSA-N

> <FORMULA>
C22H30O2

> <MOLECULAR_WEIGHT>
326.48

> <EXACT_MASS>
326.224580206

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
38.70053524712561

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
8-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-2,2,7-trimethyl-2H-chromen-5-ol

> <ALOGPS_LOGP>
6.45

> <JCHEM_LOGP>
6.4720065600000005

> <ALOGPS_LOGS>
-5.44

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.467448858227442

> <JCHEM_PKA_STRONGEST_BASIC>
-4.923536243982119

> <JCHEM_POLAR_SURFACE_AREA>
29.46

> <JCHEM_REFRACTIVITY>
105.5189

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.18e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-2,2,7-trimethylchromen-5-ol

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 54 55  0  0  0  0  0  0  0  0999 V2000
    1.9979   -0.2342   -3.7825 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6836   -0.5886   -3.1455 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3692   -2.0626   -3.1635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1758    0.2829   -2.5817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0349    1.7763   -2.4354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1390    2.2441   -0.9735 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9563    1.7059   -0.0670 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3259    2.2775   -0.3097 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6567    0.7871    0.8743 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5791    0.0871    1.8378 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4714   -1.4270    1.7282 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2874   -2.1582    0.8331 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3171   -1.4866   -0.0350 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1459   -3.5524    0.7526 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2014   -4.2157    1.5351 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0839   -5.5784    1.4399 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3706   -3.5097    2.4107 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5059   -2.1178    2.4977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2611   -1.3567    3.3438 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4330   -1.9384    3.9468 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6506   -1.3930    3.1914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4530   -1.4279    5.3927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4678   -3.4456    3.9529 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6192   -4.1894    3.2389 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8155   -0.7549   -3.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2261    0.8326   -3.7555 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9988   -0.5408   -4.8339 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1460   -2.6217   -2.6315 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3214   -2.4273   -4.1948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5891   -2.2910   -2.6852 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0985   -0.1126   -2.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8496    2.2433   -3.0031 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8914    2.1540   -2.8752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1089    3.3410   -0.9475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1286    1.9708   -0.5831 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7211    1.9306   -1.2693 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2789    3.3716   -0.3315 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0495    2.0107    0.4633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3817    0.4654    0.9634 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6233    0.3848    1.7142 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3284    0.4081    2.8564 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1035   -1.0416    0.5824 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7962   -2.1989   -0.7155 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8535   -0.7154   -0.6550 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7790   -4.1136    0.0708 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7319   -5.9044    0.7951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6346   -1.7081    2.1411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6450   -0.2967    3.1828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5933   -1.7301    3.6362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3450   -1.7615    5.9345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4239   -0.3322    5.4204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5680   -1.7730    5.9410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2308   -3.9368    4.5500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6602   -5.2726    3.2398 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  1  0
 12 11  2  0
 20 21  1  6
 11 18  1  0
 20 22  1  0
 14 12  1  0
 11 10  1  0
 17 15  1  0
 10  9  1  0
 15 14  2  0
  9  7  2  0
 17 24  1  0
  7  8  1  0
 18 19  1  0
  7  6  1  0
 19 20  1  0
  6  5  1  0
 20 23  1  0
  5  4  1  0
 23 24  2  0
  4  2  2  3
 17 18  2  0
  2  1  1  0
 12 13  1  0
  2  3  1  0
 14 45  1  0
 23 53  1  0
 24 54  1  0
 13 42  1  0
 13 43  1  0
 13 44  1  0
 16 46  1  0
 21 47  1  0
 21 48  1  0
 21 49  1  0
 22 50  1  0
 22 51  1  0
 22 52  1  0
 10 40  1  0
 10 41  1  0
  9 39  1  0
  8 36  1  0
  8 37  1  0
  8 38  1  0
  6 34  1  0
  6 35  1  0
  5 32  1  0
  5 33  1  0
  4 31  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0       1.998  -0.234  -3.783  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.684  -0.589  -3.146  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.369  -2.063  -3.163  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.176   0.283  -2.582  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.035   1.776  -2.435  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.139   2.244  -0.974  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.956   1.706  -0.067  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.326   2.277  -0.310  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.657   0.787   0.874  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.579   0.087   1.838  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.471  -1.427   1.728  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.287  -2.158   0.833  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.317  -1.487  -0.035  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.146  -3.552   0.753  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.201  -4.216   1.535  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.084  -5.578   1.440  0.00  0.00           O+0
HETATM   17  C   UNK     0       0.371  -3.510   2.411  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.506  -2.118   2.498  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.261  -1.357   3.344  0.00  0.00           O+0
HETATM   20  C   UNK     0      -1.433  -1.938   3.947  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.651  -1.393   3.191  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.453  -1.428   5.393  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.468  -3.446   3.953  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.619  -4.189   3.239  0.00  0.00           C+0
HETATM   25  H   UNK     0       2.816  -0.755  -3.273  0.00  0.00           H+0
HETATM   26  H   UNK     0       2.226   0.833  -3.756  0.00  0.00           H+0
HETATM   27  H   UNK     0       1.999  -0.541  -4.834  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.146  -2.622  -2.632  0.00  0.00           H+0
HETATM   29  H   UNK     0       0.321  -2.427  -4.195  0.00  0.00           H+0
HETATM   30  H   UNK     0      -0.589  -2.291  -2.685  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.099  -0.113  -2.155  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.850   2.243  -3.003  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.891   2.154  -2.875  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.109   3.341  -0.948  0.00  0.00           H+0
HETATM   35  H   UNK     0      -1.129   1.971  -0.583  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.721   1.931  -1.269  0.00  0.00           H+0
HETATM   37  H   UNK     0       2.279   3.372  -0.332  0.00  0.00           H+0
HETATM   38  H   UNK     0       3.050   2.011   0.463  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.382   0.465   0.963  0.00  0.00           H+0
HETATM   40  H   UNK     0       2.623   0.385   1.714  0.00  0.00           H+0
HETATM   41  H   UNK     0       1.328   0.408   2.856  0.00  0.00           H+0
HETATM   42  H   UNK     0       4.104  -1.042   0.582  0.00  0.00           H+0
HETATM   43  H   UNK     0       3.796  -2.199  -0.716  0.00  0.00           H+0
HETATM   44  H   UNK     0       2.853  -0.715  -0.655  0.00  0.00           H+0
HETATM   45  H   UNK     0       2.779  -4.114   0.071  0.00  0.00           H+0
HETATM   46  H   UNK     0       1.732  -5.904   0.795  0.00  0.00           H+0
HETATM   47  H   UNK     0      -2.635  -1.708   2.141  0.00  0.00           H+0
HETATM   48  H   UNK     0      -2.645  -0.297   3.183  0.00  0.00           H+0
HETATM   49  H   UNK     0      -3.593  -1.730   3.636  0.00  0.00           H+0
HETATM   50  H   UNK     0      -2.345  -1.762   5.934  0.00  0.00           H+0
HETATM   51  H   UNK     0      -1.424  -0.332   5.420  0.00  0.00           H+0
HETATM   52  H   UNK     0      -0.568  -1.773   5.941  0.00  0.00           H+0
HETATM   53  H   UNK     0      -2.231  -3.937   4.550  0.00  0.00           H+0
HETATM   54  H   UNK     0      -0.660  -5.273   3.240  0.00  0.00           H+0
CONECT    1    2   25   26   27                                             
CONECT    2    4    1    3                                                  
CONECT    3    2   28   29   30                                             
CONECT    4    5    2   31                                                  
CONECT    5    6    4   32   33                                             
CONECT    6    7    5   34   35                                             
CONECT    7    9    8    6                                                  
CONECT    8    7   36   37   38                                             
CONECT    9   10    7   39                                                  
CONECT   10   11    9   40   41                                             
CONECT   11   12   18   10                                                  
CONECT   12   11   14   13                                                  
CONECT   13   12   42   43   44                                             
CONECT   14   12   15   45                                                  
CONECT   15   16   17   14                                                  
CONECT   16   15   46                                                       
CONECT   17   15   24   18                                                  
CONECT   18   11   19   17                                                  
CONECT   19   18   20                                                       
CONECT   20   21   22   19   23                                             
CONECT   21   20   47   48   49                                             
CONECT   22   20   50   51   52                                             
CONECT   23   20   24   53                                                  
CONECT   24   17   23   54                                                  
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    3                                                            
CONECT   29    3                                                            
CONECT   30    3                                                            
CONECT   31    4                                                            
CONECT   32    5                                                            
CONECT   33    5                                                            
CONECT   34    6                                                            
CONECT   35    6                                                            
CONECT   36    8                                                            
CONECT   37    8                                                            
CONECT   38    8                                                            
CONECT   39    9                                                            
CONECT   40   10                                                            
CONECT   41   10                                                            
CONECT   42   13                                                            
CONECT   43   13                                                            
CONECT   44   13                                                            
CONECT   45   14                                                            
CONECT   46   16                                                            
CONECT   47   21                                                            
CONECT   48   21                                                            
CONECT   49   21                                                            
CONECT   50   22                                                            
CONECT   51   22                                                            
CONECT   52   22                                                            
CONECT   53   23                                                            
CONECT   54   24                                                            
MASTER        0    0    0    0    0    0    0    0   54    0  110    0
END

RDKit          3D

54 55  0  0  0  0  0  0  0  0999 V2000
    1.9979   -0.2342   -3.7825 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6836   -0.5886   -3.1455 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3692   -2.0626   -3.1635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1758    0.2829   -2.5817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0349    1.7763   -2.4354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1390    2.2441   -0.9735 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9563    1.7059   -0.0670 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3259    2.2775   -0.3097 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6567    0.7871    0.8743 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5791    0.0871    1.8378 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4714   -1.4270    1.7282 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2874   -2.1582    0.8331 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3171   -1.4866   -0.0350 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1459   -3.5524    0.7526 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2014   -4.2157    1.5351 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0839   -5.5784    1.4399 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3706   -3.5097    2.4107 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5059   -2.1178    2.4977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2611   -1.3567    3.3438 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4330   -1.9384    3.9468 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6506   -1.3930    3.1914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4530   -1.4279    5.3927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4678   -3.4456    3.9529 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6192   -4.1894    3.2389 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8155   -0.7549   -3.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2261    0.8326   -3.7555 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9988   -0.5408   -4.8339 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1460   -2.6217   -2.6315 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3214   -2.4273   -4.1948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5891   -2.2910   -2.6852 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0985   -0.1126   -2.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8496    2.2433   -3.0031 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8914    2.1540   -2.8752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1089    3.3410   -0.9475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1286    1.9708   -0.5831 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7211    1.9306   -1.2693 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2789    3.3716   -0.3315 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0495    2.0107    0.4633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3817    0.4654    0.9634 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6233    0.3848    1.7142 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3284    0.4081    2.8564 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1035   -1.0416    0.5824 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7962   -2.1989   -0.7155 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8535   -0.7154   -0.6550 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7790   -4.1136    0.0708 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7319   -5.9044    0.7951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6346   -1.7081    2.1411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6450   -0.2967    3.1828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5933   -1.7301    3.6362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3450   -1.7615    5.9345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4239   -0.3322    5.4204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5680   -1.7730    5.9410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2308   -3.9368    4.5500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6602   -5.2726    3.2398 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  1  0
 12 11  2  0
 20 21  1  6
 11 18  1  0
 20 22  1  0
 14 12  1  0
 11 10  1  0
 17 15  1  0
 10  9  1  0
 15 14  2  0
  9  7  2  0
 17 24  1  0
  7  8  1  0
 18 19  1  0
  7  6  1  0
 19 20  1  0
  6  5  1  0
 20 23  1  0
  5  4  1  0
 23 24  2  0
  4  2  2  3
 17 18  2  0
  2  1  1  0
 12 13  1  0
  2  3  1  0
 14 45  1  0
 23 53  1  0
 24 54  1  0
 13 42  1  0
 13 43  1  0
 13 44  1  0
 16 46  1  0
 21 47  1  0
 21 48  1  0
 21 49  1  0
 22 50  1  0
 22 51  1  0
 22 52  1  0
 10 40  1  0
 10 41  1  0
  9 39  1  0
  8 36  1  0
  8 37  1  0
  8 38  1  0
  6 34  1  0
  6 35  1  0
  5 32  1  0
  5 33  1  0
  4 31  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₀O₂

Average Mass

326.4800 Da

Monoisotopic Mass

326.22458 Da

IUPAC Name

8-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-2,2,7-trimethyl-2H-chromen-5-ol

Traditional Name

8-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-2,2,7-trimethylchromen-5-ol

CAS Registry Number

Not Available

SMILES

[H]OC1=C([H])C(=C(C2=C1C([H])=C([H])C(O2)(C([H])([H])[H])C([H])([H])[H])C([H])([H])C(\[H])=C(/C([H])([H])[H])C([H])([H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C22H30O2/c1-15(2)8-7-9-16(3)10-11-18-17(4)14-20(23)19-12-13-22(5,6)24-21(18)19/h8,10,12-14,23H,7,9,11H2,1-6H3/b16-10+

InChI Key

FBTFUGPYAYRHHG-MHWRWJLKSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Peperomia serpens	JEOL database	Kitamura, R.O.S., et al, Phytochemistry 67, 2398 (2006)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

2,2-dimethyl-1-benzopyrans

Alternative Parents

Substituents

2,2-dimethyl-1-benzopyran
Monoterpenoid
Bicyclic monoterpenoid
Aromatic monoterpenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Oxacycle
Ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	6.45	ALOGPS
logP	6.47	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Acidic)	9.47	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	29.46 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	105.52 m³·mol⁻¹	ChemAxon
Polarizability	38.7 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

Not Available

Chemspider ID

17250526

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16091956

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Kitamura, R.O.S., et al. (2006). Kitamura, R.O.S., et al, Phytochemistry 67, 2398 (2006). Phytochem..

Showing NP-Card for 5-hydroxy-8-(3',7'-dimethylocta-2',6'-dienyl)-2,2,7-trimethyl-2H-1-chrome+ (NP0030133)

MOL for NP0030133 (5-hydroxy-8-(3',7'-dimethylocta-2',6'-dienyl)-2,2,7-trimethyl-2H-1-chrome+)

3D MOL for NP0030133 (5-hydroxy-8-(3',7'-dimethylocta-2',6'-dienyl)-2,2,7-trimethyl-2H-1-chrome+)

3D SDF for NP0030133 (5-hydroxy-8-(3',7'-dimethylocta-2',6'-dienyl)-2,2,7-trimethyl-2H-1-chrome+)

3D-SDF for NP0030133 (5-hydroxy-8-(3',7'-dimethylocta-2',6'-dienyl)-2,2,7-trimethyl-2H-1-chrome+)

PDB for NP0030133 (5-hydroxy-8-(3',7'-dimethylocta-2',6'-dienyl)-2,2,7-trimethyl-2H-1-chrome+)

3D PDB for NP0030133 (5-hydroxy-8-(3',7'-dimethylocta-2',6'-dienyl)-2,2,7-trimethyl-2H-1-chrome+)

SMILES for NP0030133 (5-hydroxy-8-(3',7'-dimethylocta-2',6'-dienyl)-2,2,7-trimethyl-2H-1-chrome+)

INCHI for NP0030133 (5-hydroxy-8-(3',7'-dimethylocta-2',6'-dienyl)-2,2,7-trimethyl-2H-1-chrome+)

Structure for NP0030133 (5-hydroxy-8-(3',7'-dimethylocta-2',6'-dienyl)-2,2,7-trimethyl-2H-1-chrome+)

3D Structure for NP0030133 (5-hydroxy-8-(3',7'-dimethylocta-2',6'-dienyl)-2,2,7-trimethyl-2H-1-chrome+)