NP-MRD: Showing NP-Card for 4,6-dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde (NP0270778)

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Record Information

Version

2.0

Created at

2022-09-08 16:50:32 UTC

Updated at

2022-09-08 16:50:32 UTC

NP-MRD ID

NP0270778

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,6-dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde

Description

4,6-Dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. 4,6-dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde is found in Aspergillus rugulosus. 4,6-Dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241504482D          

 27 27  0  0  0  0            999 V2000
    3.5724    9.4875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    5.7750    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
    0.7145    4.5375    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
    0.0000    3.3000    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    2.0625    0.0000 O   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
    2.1434    1.2375    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
    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 O   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
    0.0000    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
    1.4289    3.3000    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
    4.2868    8.2500    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  2  0  0  0  0
  7  8  1  4  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  4  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 17 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 14 23  1  0  0  0  0
 23 24  1  0  0  0  0
 10 25  1  0  0  0  0
  6 26  1  0  0  0  0
  2 27  1  0  0  0  0
M  END

     RDKit          3D

 59 59  0  0  0  0  0  0  0  0999 V2000
    6.5689    2.8573    0.4610 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5395    1.3889    0.4384 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4764    0.6256    1.2927 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6486    0.7066   -0.3334 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6935    1.4135   -1.1639 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2623    1.0915   -0.8419 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8005   -0.2643   -1.0534 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3842   -1.3853   -0.2235 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8509   -0.6295   -1.8927 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1051    0.3042   -2.7481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3930    0.0552   -2.6516 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8221    0.2035   -1.2063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6710    1.5347   -0.6144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3104   -0.8329   -0.6451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7935   -0.8955    0.7922 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0303   -1.1999    0.8543 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2825   -1.5093    1.0604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7462   -2.8268    1.2002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8169   -3.8423    1.1068 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0796   -3.0511    1.4201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0359   -2.0281    1.5171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3463   -2.4055    1.7429 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5918   -0.7398    1.3797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5144    0.3829    1.4582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7331    0.3104    1.6425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2421   -0.5059    1.1557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7957    0.9058    0.9657 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5659    3.3161    0.6302 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1900    3.1917    1.3211 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0374    3.2878   -0.4590 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9840   -0.3517    1.5132 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6266    1.2178    2.2410 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4574    0.5023    0.8191 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6845   -0.3675   -0.3310 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9109    1.1892   -2.2579 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8016    2.5293   -1.1116 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6486    1.8987   -1.3085 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1801    1.3317    0.2804 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7584   -1.0307    0.7435 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1146   -1.9729   -0.7761 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5528   -2.1049    0.0322 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5763   -1.7186   -1.9784 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4030    0.2117   -3.8256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2994    1.3438   -2.4800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9299    0.8365   -3.2321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6423   -0.9657   -2.9655 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3662    1.9443   -0.7921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8383    1.6396    0.4543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3854    2.2651   -1.1074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4089   -1.7757   -1.2027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1461   -1.7353    1.2742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4548    0.0434    1.3168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8538   -3.6248    0.9374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4358   -4.0741    1.5232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1193   -1.8108    1.8401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1026    1.3828    1.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6982    0.8970    0.8476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1937    1.2998   -0.0076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0740    1.5403    1.8178 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  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 26  2  0
 26 27  1  0
 26 23  1  0
 23 24  1  0
 24 25  2  0
 23 21  2  0
 21 22  1  0
 21 20  1  0
 20 18  2  0
 18 19  1  0
 18 17  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  0
 10 44  1  0
 11 45  1  0
 11 46  1  0
 13 47  1  0
 13 48  1  0
 13 49  1  0
 14 50  1  0
 15 51  1  0
 15 52  1  0
 27 57  1  0
 27 58  1  0
 27 59  1  0
 24 56  1  0
 22 55  1  0
 20 54  1  0
 19 53  1  0
M  END


  Mrv1533004241504482D          

 27 27  0  0  0  0            999 V2000
    3.5724    9.4875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    5.7750    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
    0.7145    4.5375    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
    0.0000    3.3000    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    2.0625    0.0000 O   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
    2.1434    1.2375    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
    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 O   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
    0.0000    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
    1.4289    3.3000    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
    4.2868    8.2500    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  2  0  0  0  0
  7  8  1  4  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  4  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 17 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 14 23  1  0  0  0  0
 23 24  1  0  0  0  0
 10 25  1  0  0  0  0
  6 26  1  0  0  0  0
  2 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0270778

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCCC(C)=CCCC(C)=CCOC1=C(C)C(C=O)=C(O)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C23H32O4/c1-16(2)8-6-9-17(3)10-7-11-18(4)12-13-27-23-19(5)20(15-24)21(25)14-22(23)26/h8,10,12,14-15,25-26H,6-7,9,11,13H2,1-5H3

> <INCHI_KEY>
GBEALZXDMSUKNN-UHFFFAOYSA-N

> <FORMULA>
C23H32O4

> <MOLECULAR_WEIGHT>
372.505

> <EXACT_MASS>
372.23005951

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
42.26581982888849

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,6-dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde

> <ALOGPS_LOGP>
5.76

> <JCHEM_LOGP>
6.765042280666666

> <ALOGPS_LOGS>
-5.03

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.694886100243819

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.952692348156829

> <JCHEM_PKA_STRONGEST_BASIC>
-4.912266382384008

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
114.83159999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.51e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,6-dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       6.668  17.710   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668  16.170   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335  15.400   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335  13.860   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  13.090   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  11.550   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  10.780   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667   9.240   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334   8.470   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.335  10.780   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.002  15.400   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   27                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   26                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   25                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   23                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   14   24                                                  
CONECT   24   23                                                            
CONECT   25   10                                                            
CONECT   26    6                                                            
CONECT   27    2                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₂O₄

Average Mass

372.5050 Da

Monoisotopic Mass

372.23006 Da

IUPAC Name

4,6-dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde

Traditional Name

4,6-dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde

CAS Registry Number

Not Available

SMILES

CC(C)=CCCC(C)=CCCC(C)=CCOC1=C(C)C(C=O)=C(O)C=C1O

InChI Identifier

InChI=1S/C23H32O4/c1-16(2)8-6-9-17(3)10-7-11-18(4)12-13-27-23-19(5)20(15-24)21(25)14-22(23)26/h8,10,12,14-15,25-26H,6-7,9,11,13H2,1-5H3

InChI Key

GBEALZXDMSUKNN-UHFFFAOYSA-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
Aspergillus rugulosus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Farsesane sesquiterpenoid
Hydroxybenzaldehyde
4-alkoxyphenol
Benzaldehyde
Benzoyl
M-cresol
Phenol ether
Resorcinol
Phenoxy compound
Alkyl aryl ether
Phenol
Aryl-aldehyde
1-hydroxy-2-unsubstituted benzenoid
Toluene
Benzenoid
Monocyclic benzene moiety
Vinylogous acid
Ether
Organooxygen compound
Aldehyde
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
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	5.76	ALOGPS
logP	6.77	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	7.95	ChemAxon
pKa (Strongest Basic)	-4.9	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	10	ChemAxon
Refractivity	114.83 m³·mol⁻¹	ChemAxon
Polarizability	42.27 Å³	ChemAxon
Number of Rings	1	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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,6-dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde (NP0270778)

MOL for NP0270778 (4,6-dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde)

3D MOL for NP0270778 (4,6-dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde)

3D SDF for NP0270778 (4,6-dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde)

3D-SDF for NP0270778 (4,6-dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde)

PDB for NP0270778 (4,6-dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde)

3D PDB for NP0270778 (4,6-dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde)

SMILES for NP0270778 (4,6-dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde)

INCHI for NP0270778 (4,6-dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde)

Structure for NP0270778 (4,6-dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde)

3D Structure for NP0270778 (4,6-dihydroxy-2-methyl-3-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]benzaldehyde)