NP-MRD: Showing NP-Card for 5-(2-{2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-3,6-dioxo-7h,8h,9h,10h-cyclohexa[f]azulen-5-yl}ethyl)-2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-7h,8h,9h,10h-cyclohexa[f]azulene-3,6-dione (NP0154035)

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Record Information

Version

2.0

Created at

2022-09-02 10:47:16 UTC

Updated at

2022-09-02 10:47:16 UTC

NP-MRD ID

NP0154035

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-(2-{2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-3,6-dioxo-7h,8h,9h,10h-cyclohexa[f]azulen-5-yl}ethyl)-2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-7h,8h,9h,10h-cyclohexa[f]azulene-3,6-dione

Description

5-{2-[2,7-Dihydroxy-8a,10a-dimethyl-3,6-dioxo-1-(propan-2-yl)-3H,6H,7H,8H,8aH,9H,10H,10aH-cyclohexa[f]azulen-5-yl]ethyl}-2,7-dihydroxy-8a,10a-dimethyl-1-(propan-2-yl)-3H,6H,7H,8H,8aH,9H,10H,10aH-cyclohexa[f]azulene-3,6-dione belongs to the class of organic compounds known as sesquaterpenoids. These are terpenoids with at least 7 consecutive isoprene units. Based on a literature review very few articles have been published on 5-{2-[2,7-dihydroxy-8a,10a-dimethyl-3,6-dioxo-1-(propan-2-yl)-3H,6H,7H,8H,8aH,9H,10H,10aH-cyclohexa[f]azulen-5-yl]ethyl}-2,7-dihydroxy-8a,10a-dimethyl-1-(propan-2-yl)-3H,6H,7H,8H,8aH,9H,10H,10aH-cyclohexa[f]azulene-3,6-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022212472D          

 48 53  0  0  0  0            999 V2000
   -3.9093   -1.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0846   -1.0234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.9693    0.4422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7715    0.6348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3420    0.9781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4068    1.8005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6386    0.5470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8913    0.8967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1521    0.5304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 15 36  1  0  0  0  0
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  9 47  1  0  0  0  0
  4 47  1  0  0  0  0
 47 48  1  0  0  0  0
M  END

     RDKit          3D

 98103  0  0  0  0  0  0  0  0999 V2000
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 47 48  1  6
 47  4  1  0
 47  9  1  0
 43 11  1  0
 36 15  1  0
 31 16  1  0
 27 18  1  0
  1 49  1  0
  1 50  1  0
  1 51  1  0
  2 52  1  0
  3 53  1  0
  3 54  1  0
  3 55  1  0
  6 56  1  0
 10 57  1  0
 13 58  1  0
 13 59  1  0
 14 60  1  0
 14 61  1  0
 17 62  1  0
 22 63  1  0
 24 64  1  0
 25 65  1  0
 25 66  1  0
 25 67  1  0
 26 68  1  0
 26 69  1  0
 26 70  1  0
 28 71  1  0
 28 72  1  0
 28 73  1  0
 29 74  1  0
 29 75  1  0
 30 76  1  0
 30 77  1  0
 32 78  1  0
 32 79  1  0
 32 80  1  0
 33 81  1  0
 33 82  1  0
 34 83  1  1
 35 84  1  0
 40 85  1  6
 41 86  1  0
 42 87  1  0
 42 88  1  0
 44 89  1  0
 44 90  1  0
 44 91  1  0
 45 92  1  0
 45 93  1  0
 46 94  1  0
 46 95  1  0
 48 96  1  0
 48 97  1  0
 48 98  1  0
M  END


  Mrv1652309022212472D          

 48 53  0  0  0  0            999 V2000
   -3.9093   -1.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0846   -1.0234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6909   -1.7484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6536   -0.3199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9693    0.4422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7715    0.6348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3420    0.9781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4068    1.8005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6386    0.5470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8913    0.8967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1521    0.5304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4589    1.0848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2844    1.8911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5012    2.1431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6758    2.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4614    3.2013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9829    2.5621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8079    2.5713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2700    1.8879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9888    1.1124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0628    2.1163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7135    1.6092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0906    2.9408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7740    3.4030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5159    3.0422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7155    4.2259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3150    3.2221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9302    3.7718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1225    4.0243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3752    4.3739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6360    4.0077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7498    4.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0250    4.5620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2394    4.3100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3716    4.8644    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0648    3.5037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7208    3.2517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2445    0.8328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8555    1.3871    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4191    0.0265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2047   -0.2255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8081   -0.5279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0225   -0.2759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2569   -1.0669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4990   -0.9151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3240   -0.9059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8311   -0.2552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1638   -1.0101    0.0000 C   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  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 23 27  1  0  0  0  0
 18 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 16 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 15 36  1  0  0  0  0
 36 37  2  0  0  0  0
 12 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 11 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
  9 47  1  0  0  0  0
  4 47  1  0  0  0  0
 47 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0154035

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1=C(O)C(=O)C2=CC3=C(CCC4=C5C=C6C(=O)C(O)=C(C(C)C)C6(C)CCC5(C)CC(O)C4=O)C(=O)C(O)CC3(C)CCC12C

> <INCHI_IDENTIFIER>
InChI=1S/C40H50O8/c1-19(2)29-35(47)33(45)25-15-23-21(31(43)27(41)17-37(23,5)11-13-39(25,29)7)9-10-22-24-16-26-34(46)36(48)30(20(3)4)40(26,8)14-12-38(24,6)18-28(42)32(22)44/h15-16,19-20,27-28,41-42,47-48H,9-14,17-18H2,1-8H3

> <INCHI_KEY>
NETLEACGIWNKDI-UHFFFAOYSA-N

> <FORMULA>
C40H50O8

> <MOLECULAR_WEIGHT>
658.832

> <EXACT_MASS>
658.35056857

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
98

> <JCHEM_AVERAGE_POLARIZABILITY>
73.47165805455057

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-{2-[2,7-dihydroxy-8a,10a-dimethyl-3,6-dioxo-1-(propan-2-yl)-3H,6H,7H,8H,8aH,9H,10H,10aH-cyclohexa[f]azulen-5-yl]ethyl}-2,7-dihydroxy-8a,10a-dimethyl-1-(propan-2-yl)-3H,6H,7H,8H,8aH,9H,10H,10aH-cyclohexa[f]azulene-3,6-dione

> <ALOGPS_LOGP>
4.20

> <JCHEM_LOGP>
5.430454051333333

> <ALOGPS_LOGS>
-5.45

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.876276361989833

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.274355409827914

> <JCHEM_PKA_STRONGEST_BASIC>
-3.51136515460356

> <JCHEM_POLAR_SURFACE_AREA>
149.2

> <JCHEM_REFRACTIVITY>
188.00400000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.35e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-(2-{2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-3,6-dioxo-7H,8H,9H,10H-cyclohexa[f]azulen-5-yl}ethyl)-2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-7H,8H,9H,10H-cyclohexa[f]azulene-3,6-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -7.297  -1.870   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.758  -1.910   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.023  -3.264   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.953  -0.597   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.543   0.826   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -7.040   1.185   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -4.372   1.826   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -4.493   3.361   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -3.059   1.021   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.664   1.674   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.284   0.990   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.857   2.025   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.531   3.530   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.936   4.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.261   5.505   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.728   5.976   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.701   4.783   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.241   4.800   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -6.104   3.524   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -5.579   2.076   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -7.584   3.950   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -8.799   3.004   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -7.636   5.490   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -8.911   6.352   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -10.296   5.679   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -8.802   7.888   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -6.188   6.015   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -7.336   7.041   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -5.829   7.512   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -4.434   8.165   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -3.054   7.481   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -3.266   9.006   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -1.913   8.516   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.447   8.045   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       0.694   9.080   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -0.121   6.540   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       1.345   6.070   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       2.323   1.555   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       3.464   2.589   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       2.649   0.049   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       4.115  -0.421   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       1.508  -0.985   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       0.042  -0.515   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       0.479  -1.992   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -0.932  -1.708   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -2.471  -1.691   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -3.418  -0.476   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -4.039  -1.886   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   47                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   47                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   43                                                  
CONECT   12   11   13   38                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   36                                                  
CONECT   16   15   17   31                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   27                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   27                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   23   18   28   29                                             
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   16   32   33                                             
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   15   37                                                  
CONECT   37   36                                                            
CONECT   38   12   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43                                                       
CONECT   43   42   11   44   45                                             
CONECT   44   43                                                            
CONECT   45   43   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46    9    4   48                                             
CONECT   48   47                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  106    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₀H₅₀O₈

Average Mass

658.8320 Da

Monoisotopic Mass

658.35057 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)C1=C(O)C(=O)C2=CC3=C(CCC4=C5C=C6C(=O)C(O)=C(C(C)C)C6(C)CCC5(C)CC(O)C4=O)C(=O)C(O)CC3(C)CCC12C

InChI Identifier

InChI=1S/C40H50O8/c1-19(2)29-35(47)33(45)25-15-23-21(31(43)27(41)17-37(23,5)11-13-39(25,29)7)9-10-22-24-16-26-34(46)36(48)30(20(3)4)40(26,8)14-12-38(24,6)18-28(42)32(22)44/h15-16,19-20,27-28,41-42,47-48H,9-14,17-18H2,1-8H3

InChI Key

NETLEACGIWNKDI-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquaterpenoids. These are terpenoids with at least 7 consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquaterpenoids

Direct Parent

Sesquaterpenoids

Alternative Parents

Substituents

Sesquaterpenoid
Cyclohexenone
Cyclic ketone
Secondary alcohol
Ketone
Enol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source

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

162853559

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-(2-{2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-3,6-dioxo-7h,8h,9h,10h-cyclohexa[f]azulen-5-yl}ethyl)-2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-7h,8h,9h,10h-cyclohexa[f]azulene-3,6-dione (NP0154035)

MOL for NP0154035 (5-(2-{2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-3,6-dioxo-7h,8h,9h,10h-cyclohexa[f]azulen-5-yl}ethyl)-2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-7h,8h,9h,10h-cyclohexa[f]azulene-3,6-dione)

3D MOL for NP0154035 (5-(2-{2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-3,6-dioxo-7h,8h,9h,10h-cyclohexa[f]azulen-5-yl}ethyl)-2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-7h,8h,9h,10h-cyclohexa[f]azulene-3,6-dione)

3D SDF for NP0154035 (5-(2-{2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-3,6-dioxo-7h,8h,9h,10h-cyclohexa[f]azulen-5-yl}ethyl)-2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-7h,8h,9h,10h-cyclohexa[f]azulene-3,6-dione)

3D-SDF for NP0154035 (5-(2-{2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-3,6-dioxo-7h,8h,9h,10h-cyclohexa[f]azulen-5-yl}ethyl)-2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-7h,8h,9h,10h-cyclohexa[f]azulene-3,6-dione)

PDB for NP0154035 (5-(2-{2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-3,6-dioxo-7h,8h,9h,10h-cyclohexa[f]azulen-5-yl}ethyl)-2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-7h,8h,9h,10h-cyclohexa[f]azulene-3,6-dione)

3D PDB for NP0154035 (5-(2-{2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-3,6-dioxo-7h,8h,9h,10h-cyclohexa[f]azulen-5-yl}ethyl)-2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-7h,8h,9h,10h-cyclohexa[f]azulene-3,6-dione)

SMILES for NP0154035 (5-(2-{2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-3,6-dioxo-7h,8h,9h,10h-cyclohexa[f]azulen-5-yl}ethyl)-2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-7h,8h,9h,10h-cyclohexa[f]azulene-3,6-dione)

INCHI for NP0154035 (5-(2-{2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-3,6-dioxo-7h,8h,9h,10h-cyclohexa[f]azulen-5-yl}ethyl)-2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-7h,8h,9h,10h-cyclohexa[f]azulene-3,6-dione)

Structure for NP0154035 (5-(2-{2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-3,6-dioxo-7h,8h,9h,10h-cyclohexa[f]azulen-5-yl}ethyl)-2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-7h,8h,9h,10h-cyclohexa[f]azulene-3,6-dione)

3D Structure for NP0154035 (5-(2-{2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-3,6-dioxo-7h,8h,9h,10h-cyclohexa[f]azulen-5-yl}ethyl)-2,7-dihydroxy-1-isopropyl-8a,10a-dimethyl-7h,8h,9h,10h-cyclohexa[f]azulene-3,6-dione)