NP-MRD: Showing NP-Card for 2-[(2e,6e,10r)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dien-1-yl]-5-methylbenzene-1,3-diol (NP0286733)

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Record Information

Version

2.0

Created at

2022-09-09 15:26:36 UTC

Updated at

2022-09-09 15:26:36 UTC

NP-MRD ID

NP0286733

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(2e,6e,10r)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dien-1-yl]-5-methylbenzene-1,3-diol

Description

Cosmosporin A belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Based on a literature review very few articles have been published on Cosmosporin A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092217262D          

 26 26  0  0  1  0            999 V2000
    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 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
    2.1434    1.2375    0.0000 O   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
    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
    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
   -0.7145    3.7125    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
   -1.4289    4.9500    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
   -0.7145    6.1875    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
   -2.8579    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    6.1875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5724    7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6993    6.4895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8743    5.0605    0.0000 O   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  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  0  0  0  0
  2 14  1  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
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 23 26  1  0  0  0  0
M  END

     RDKit          3D

 60 60  0  0  0  0  0  0  0  0999 V2000
    2.1596   -2.0818   -0.9363 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2352   -0.8256   -0.2045 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2150   -0.4604    0.5660 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4148   -1.2429    0.8321 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6842   -0.5108    0.6130 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2361   -0.2577   -0.6132 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6018   -0.7112   -1.7546 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4255    0.4454   -0.7689 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0904    0.9124    0.3176 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3771    1.6730    0.1318 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5701    0.6792    1.5608 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3997   -0.0129    1.7078 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8544   -0.2601    2.9639 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0672    0.1254   -0.3756 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1580   -0.6036    0.1165 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3678    0.2631   -0.0062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4363   -0.0252   -0.7209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4659   -1.3151   -1.4773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5897    0.9104   -0.7773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8417    0.2366   -0.2533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0180    1.1869   -0.3076 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.2263    1.5765   -1.6221 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2694    0.4853    0.1706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5933   -0.6449   -0.7881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4263    1.4703    0.1008 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1773    0.0500    1.4710 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0343   -2.7132   -0.9853 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7320   -1.9419   -1.9756 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3696   -2.7234   -0.4364 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1404    0.5244    1.0651 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3778   -1.4969    1.9351 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4282   -2.2450    0.3578 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7496   -1.2228   -1.6766 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8154    0.6152   -1.7729 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5032    2.4246    0.9318 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2013    0.9450    0.2062 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3674    2.0955   -0.8785 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0856    1.0428    2.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3312    0.0761    3.7735 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2451    1.0704    0.1468 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0168    0.3243   -1.4641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0721   -0.8960    1.1824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2693   -1.5410   -0.4597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3767    1.2098    0.5344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3490   -1.3549   -2.1451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5271   -1.4173   -2.0583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4942   -2.1838   -0.7794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3823    1.7632   -0.1102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7480    1.3329   -1.7886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0583   -0.6112   -0.9232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6521   -0.1596    0.7595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8414    2.1044    0.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7261    1.0276   -2.2735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9783   -1.5592   -0.5564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3994   -0.3820   -1.8293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6528   -0.9734   -0.7094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2885    2.3131    0.8145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5777    1.8482   -0.9449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3554    0.9172    0.3570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4104    0.7246    2.1459 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  1  0
 23 26  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 12  5  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
 14 40  1  0
 14 41  1  0
 15 42  1  0
 15 43  1  0
 16 44  1  0
 18 45  1  0
 18 46  1  0
 18 47  1  0
 19 48  1  0
 19 49  1  0
 20 50  1  0
 20 51  1  0
 21 52  1  1
 22 53  1  0
 24 54  1  0
 24 55  1  0
 24 56  1  0
 25 57  1  0
 25 58  1  0
 25 59  1  0
 26 60  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  7 33  1  0
  8 34  1  0
 10 35  1  0
 10 36  1  0
 10 37  1  0
 11 38  1  0
 13 39  1  0
M  END


  Mrv1652309092217262D          

 26 26  0  0  1  0            999 V2000
    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 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
    2.1434    1.2375    0.0000 O   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
    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
    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
   -0.7145    3.7125    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
   -1.4289    4.9500    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
   -0.7145    6.1875    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
   -2.8579    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    6.1875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5724    7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6993    6.4895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8743    5.0605    0.0000 O   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  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  0  0  0  0
  2 14  1  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
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 23 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0286733

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C22H34O4/c1-15(9-11-18-19(23)13-17(3)14-20(18)24)7-6-8-16(2)10-12-21(25)22(4,5)26/h8-9,13-14,21,23-26H,6-7,10-12H2,1-5H3/b15-9+,16-8+/t21-/m1/s1

> <INCHI_KEY>
UTVRMYTWZUFVGI-SDJVXUTESA-N

> <FORMULA>
C22H34O4

> <MOLECULAR_WEIGHT>
362.51

> <EXACT_MASS>
362.245709575

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
42.515594490231564

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(2E,6E,10R)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dien-1-yl]-5-methylbenzene-1,3-diol

> <JCHEM_LOGP>
4.787093300666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.647010709032333

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.193001081003347

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0892666139021854

> <JCHEM_POLAR_SURFACE_AREA>
80.92

> <JCHEM_REFRACTIVITY>
109.25659999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2-[(2E,6E,10R)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dien-1-yl]-5-methylbenzene-1,3-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.334   8.470   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.667   9.240   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.667  10.780   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.334  11.550   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.001  11.550   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -5.335  10.780   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -6.668  11.550   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -6.668  13.090   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -8.002  10.780   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -9.336  10.010   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -8.772  12.114   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -7.232   9.446   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   14                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   12                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11    5   13                                                  
CONECT   13   12                                                            
CONECT   14    2   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25   26                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   23                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₄O₄

Average Mass

362.5100 Da

Monoisotopic Mass

362.24571 Da

IUPAC Name

2-[(2E,6E,10R)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dien-1-yl]-5-methylbenzene-1,3-diol

Traditional Name

2-[(2E,6E,10R)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dien-1-yl]-5-methylbenzene-1,3-diol

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C22H34O4/c1-15(9-11-18-19(23)13-17(3)14-20(18)24)7-6-8-16(2)10-12-21(25)22(4,5)26/h8-9,13-14,21,23-26H,6-7,10-12H2,1-5H3/b15-9+,16-8+/t21-/m1/s1

InChI Key

UTVRMYTWZUFVGI-SDJVXUTESA-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 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

Farsesane sesquiterpenoid
Sesquiterpenoid
Fatty alcohol
Resorcinol
M-cresol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Toluene
Phenol
Fatty acyl
Benzenoid
Monocyclic benzene moiety
Tertiary alcohol
Secondary alcohol
1,2-diol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
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	4.79	ChemAxon
pKa (Strongest Acidic)	9.19	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	80.92 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	109.26 m³·mol⁻¹	ChemAxon
Polarizability	42.52 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

146682493

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[(2e,6e,10r)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dien-1-yl]-5-methylbenzene-1,3-diol (NP0286733)

MOL for NP0286733 (2-[(2e,6e,10r)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dien-1-yl]-5-methylbenzene-1,3-diol)

3D MOL for NP0286733 (2-[(2e,6e,10r)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dien-1-yl]-5-methylbenzene-1,3-diol)

3D SDF for NP0286733 (2-[(2e,6e,10r)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dien-1-yl]-5-methylbenzene-1,3-diol)

3D-SDF for NP0286733 (2-[(2e,6e,10r)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dien-1-yl]-5-methylbenzene-1,3-diol)

PDB for NP0286733 (2-[(2e,6e,10r)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dien-1-yl]-5-methylbenzene-1,3-diol)

3D PDB for NP0286733 (2-[(2e,6e,10r)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dien-1-yl]-5-methylbenzene-1,3-diol)

SMILES for NP0286733 (2-[(2e,6e,10r)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dien-1-yl]-5-methylbenzene-1,3-diol)

INCHI for NP0286733 (2-[(2e,6e,10r)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dien-1-yl]-5-methylbenzene-1,3-diol)

Structure for NP0286733 (2-[(2e,6e,10r)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dien-1-yl]-5-methylbenzene-1,3-diol)

3D Structure for NP0286733 (2-[(2e,6e,10r)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dien-1-yl]-5-methylbenzene-1,3-diol)