NP-MRD: Showing NP-Card for 3-[(2r,3r)-2,3-dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid (NP0220605)

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Record Information

Version

2.0

Created at

2022-09-05 21:58:11 UTC

Updated at

2022-09-05 21:58:11 UTC

NP-MRD ID

NP0220605

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[(2r,3r)-2,3-dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid

Description

3-[(2R,3R)-2,3-dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid belongs to the class of organic compounds known as aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring. Based on a literature review very few articles have been published on 3-[(2R,3R)-2,3-dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052223582D          

 27 27  0  0  1  0            999 V2000
    2.8579    6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    4.5375    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    3.3000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6039    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    3.3000    0.0000 O   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
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  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
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  6  0  0  0
  7 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 15 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 20 26  2  0  0  0  0
 13 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END

     RDKit          3D

 59 59  0  0  0  0  0  0  0  0999 V2000
   -7.0508   -0.1686    0.9723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4314    0.3676   -0.2458 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2930    0.7822   -1.3786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1209    0.4936   -0.3527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2598    0.0866    0.7802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2009   -0.9001    0.4790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1223   -0.5167   -0.4776 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2064   -1.7265   -0.5776 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6955   -0.4306   -1.7754 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4805    0.7424   -0.1132 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3700    1.7997   -0.2746 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1232    1.1066   -0.5132 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9994    0.2789   -0.0050 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9578   -0.4492    1.1376 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0348   -1.1903    1.6362 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9196   -1.9568    2.8668 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9031   -2.5849    3.2977 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7297   -1.9963    3.5651 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1946   -1.1575    0.9016 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2933   -0.4392   -0.2578 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5964   -0.4300   -1.0205 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3216    0.8407   -0.8139 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5337    0.9385   -0.3075 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1267    2.3029   -0.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3392   -0.2515    0.1213 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1962    0.2927   -0.7343 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3604    0.9929   -1.9028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7018    0.4529    1.8471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8685   -1.2579    1.1276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1588    0.0240    0.9563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1434    0.1415   -2.2695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0450    1.8479   -1.6413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3671    0.7883   -1.0608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6798    0.8928   -1.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9252   -0.3449    1.5980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8775    1.0202    1.2557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7187   -1.8464    0.1330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7137   -1.1517    1.4778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1075   -2.2454    0.3936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8003   -2.4790   -1.1964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2984   -1.5816   -1.1385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0786   -0.7826   -2.4549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4082    0.7327    1.0764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0729    2.4800   -0.9204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0161    1.2163   -1.6406 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0934    2.1573   -0.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0530   -0.4706    1.7125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1246   -2.4519    3.2025 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0621   -1.7180    1.2445 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3792   -0.6724   -2.0656 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2226   -1.2735   -0.6130 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875    1.7491   -1.1110 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4450    2.7110   -1.1616 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0266    2.2962    0.4970 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3858    3.0097    0.2604 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0260   -0.6674    1.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4255    0.0422    0.2130 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3015   -1.0099   -0.6795 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7465    1.5641   -2.3990 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  6
  7 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 19  2  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  3
 23 24  1  0
 23 25  1  0
 20 26  2  0
 26 27  1  0
 15 16  1  0
 16 18  1  0
 16 17  2  0
 26 13  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  3 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
  5 35  1  0
  5 36  1  0
  6 37  1  0
  6 38  1  0
  8 39  1  0
  8 40  1  0
  8 41  1  0
  9 42  1  0
 10 43  1  1
 11 44  1  0
 12 45  1  0
 12 46  1  0
 14 47  1  0
 19 49  1  0
 21 50  1  0
 21 51  1  0
 22 52  1  0
 24 53  1  0
 24 54  1  0
 24 55  1  0
 25 56  1  0
 25 57  1  0
 25 58  1  0
 27 59  1  0
 18 48  1  0
M  END


  Mrv1652309052223582D          

 27 27  0  0  1  0            999 V2000
    2.8579    6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    4.5375    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    3.3000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6039    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    3.3000    0.0000 O   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
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  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
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  6  0  0  0
  7 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 15 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 20 26  2  0  0  0  0
 13 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0220605

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC[C@@](C)(O)[C@H](O)CC1=CC(=CC(CC=C(C)C)=C1O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H32O5/c1-14(2)7-6-10-22(5,27)19(23)13-17-12-18(21(25)26)11-16(20(17)24)9-8-15(3)4/h7-8,11-12,19,23-24,27H,6,9-10,13H2,1-5H3,(H,25,26)/t19-,22-/m1/s1

> <INCHI_KEY>
UOIWBCLMKMGORV-DENIHFKCSA-N

> <FORMULA>
C22H32O5

> <MOLECULAR_WEIGHT>
376.493

> <EXACT_MASS>
376.22497413

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
42.36015335802792

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-[(2R,3R)-2,3-dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid

> <JCHEM_LOGP>
4.381626595333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.607495886238617

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.337041713532529

> <JCHEM_PKA_STRONGEST_BASIC>
-3.216352452687034

> <JCHEM_POLAR_SURFACE_AREA>
97.99000000000001

> <JCHEM_REFRACTIVITY>
109.85389999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
3-[(2R,3R)-2,3-dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid

> <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       5.335  12.320   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335  10.780   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.668  10.010   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.001  10.010   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001   8.470   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   7.700   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.127   6.160   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.207   6.160   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       5.335  -0.000   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+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   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   26                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   19                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   15   20                                                       
CONECT   20   19   21   26                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   20   13   27                                                  
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   54    0
END

View in JSmol

Synonyms

Value	Source
3-[(2R,3R)-2,3-Dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoate	Generator

Chemical Formula

C₂₂H₃₂O₅

Average Mass

376.4930 Da

Monoisotopic Mass

376.22497 Da

IUPAC Name

3-[(2R,3R)-2,3-dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid

Traditional Name

3-[(2R,3R)-2,3-dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid

CAS Registry Number

Not Available

SMILES

CC(C)=CCC[C@@](C)(O)[C@H](O)CC1=CC(=CC(CC=C(C)C)=C1O)C(O)=O

InChI Identifier

InChI=1S/C22H32O5/c1-14(2)7-6-10-22(5,27)19(23)13-17-12-18(21(25)26)11-16(20(17)24)9-8-15(3)4/h7-8,11-12,19,23-24,27H,6,9-10,13H2,1-5H3,(H,25,26)/t19-,22-/m1/s1

InChI Key

UOIWBCLMKMGORV-DENIHFKCSA-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 aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Aromatic monoterpenoids

Alternative Parents

Substituents

Aromatic monoterpenoid
Hydroxybenzoic acid
Monocyclic monoterpenoid
Benzoic acid or derivatives
Benzoic acid
Fatty alcohol
Benzoyl
Phenol
Monocyclic benzene moiety
Benzenoid
Fatty acyl
Tertiary alcohol
Secondary alcohol
1,2-diol
Carboxylic acid
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	4.38	ChemAxon
pKa (Strongest Acidic)	4.34	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	97.99 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	109.85 m³·mol⁻¹	ChemAxon
Polarizability	42.36 Å³	ChemAxon
Number of Rings	1	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

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

26183459

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-[(2r,3r)-2,3-dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid (NP0220605)

MOL for NP0220605 (3-[(2r,3r)-2,3-dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid)

3D MOL for NP0220605 (3-[(2r,3r)-2,3-dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid)

3D SDF for NP0220605 (3-[(2r,3r)-2,3-dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid)

3D-SDF for NP0220605 (3-[(2r,3r)-2,3-dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid)

PDB for NP0220605 (3-[(2r,3r)-2,3-dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid)

3D PDB for NP0220605 (3-[(2r,3r)-2,3-dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid)

SMILES for NP0220605 (3-[(2r,3r)-2,3-dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid)

INCHI for NP0220605 (3-[(2r,3r)-2,3-dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid)

Structure for NP0220605 (3-[(2r,3r)-2,3-dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid)

3D Structure for NP0220605 (3-[(2r,3r)-2,3-dihydroxy-3,7-dimethyloct-6-en-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid)