NP-MRD: Showing NP-Card for (2e)-3-{2-methyl-3-[(1e)-1-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-5,6,8,8a-tetrahydro-1h-naphthalen-1-yl]prop-1-en-2-yl]oxiran-2-yl}prop-2-enoic acid (NP0165798)

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Record Information

Version

2.0

Created at

2022-09-03 01:02:03 UTC

Updated at

2022-09-03 01:02:03 UTC

NP-MRD ID

NP0165798

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e)-3-{2-methyl-3-[(1e)-1-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-5,6,8,8a-tetrahydro-1h-naphthalen-1-yl]prop-1-en-2-yl]oxiran-2-yl}prop-2-enoic acid

Description

Hamigerone belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. (2e)-3-{2-methyl-3-[(1e)-1-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-5,6,8,8a-tetrahydro-1h-naphthalen-1-yl]prop-1-en-2-yl]oxiran-2-yl}prop-2-enoic acid is found in Hamigera avellanea. (2e)-3-{2-methyl-3-[(1e)-1-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-5,6,8,8a-tetrahydro-1h-naphthalen-1-yl]prop-1-en-2-yl]oxiran-2-yl}prop-2-enoic acid was first documented in 2014 (PMID: 25184147). Based on a literature review very few articles have been published on Hamigerone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032203022D          

 30 32  0  0  0  0            999 V2000
   -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 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    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
    0.7145   -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
    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
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -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
    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
    0.7145   -2.8875    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   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -4.4270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -4.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0467   -5.1747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5199   -4.3551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8685   -3.6074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6904   -3.5355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1636   -4.2113    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0391   -2.7878    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
  2  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
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
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 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
  9 17  1  0  0  0  0
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 26 27  2  0  0  0  0
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 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
M  END

     RDKit          3D

 62 64  0  0  0  0  0  0  0  0999 V2000
    1.1254    3.7547    1.3653 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1736    2.6897    0.9588 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5242    2.1837    1.8135 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0437    2.2241   -0.4409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9542    1.1206   -0.5904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9975    1.3821   -1.3292 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.3033   -1.6704    1.2497 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6703   -0.5566    2.1733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8064   -1.1572   -0.1047 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6933   -0.1898    0.0496 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5292   -0.7689   -0.6365 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6583   -1.0337   -0.0129 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7244   -0.7444    1.4458 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8550   -1.6111   -0.7336 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2183   -1.0316   -1.9480 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1223   -0.9320   -0.7898 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3869   -1.7821   -0.9379 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3504    0.4794   -0.4789 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5162    0.8813    0.0032 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7983    2.2733    0.3303 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9170    2.6173    0.7861 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8032    3.2204    0.1285 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0512    3.3723    1.8176 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4266    4.3649    0.4641 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6202    4.4856    2.0439 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0403    1.8847   -0.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1875    3.5426   -1.2495 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.4587   -2.6902   -1.6464 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.6086   -2.5859   -0.0575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6695   -3.8730    0.8651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5004   -3.6657   -0.9521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4528   -2.2352    1.6850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0453    0.3543    1.6609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8500   -0.3571    2.8694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5335   -0.9177    2.7964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3815   -2.1085   -0.5673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4657   -0.0057    1.1233 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4318   -0.9619   -1.6938 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7370    0.3438    1.5804 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6588   -1.1827    1.8997 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9010   -1.2121    2.0204 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8743   -2.7216   -0.7773 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2088   -1.2340   -1.3985 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6034   -2.1757    0.0691 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1212   -2.6811   -1.5643 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5984    1.2425   -0.6238 H   0  0  0  0  0  0  0  0  0  0  0  0
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 12 11  1  0
 11 10  1  0
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 17  9  1  0
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  4 34  1  0
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  1 31  1  0
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 30 62  1  0
 17 50  1  6
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 16 48  1  0
 16 49  1  0
M  END


  Mrv1652309032203022D          

 30 32  0  0  0  0            999 V2000
   -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 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    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
    0.7145   -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
    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
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.0391   -2.7878    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  2  4  1  0  0  0  0
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  5  6  2  0  0  0  0
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M  END
> <DATABASE_ID>
NP0165798

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC2=CC(C)=C(CC(C)=O)C(\C=C(/C)C3OC3(C)\C=C\C(O)=O)C2C(C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H32O5/c1-13-9-18-10-14(2)23(29)17(5)22(18)20(19(13)12-16(4)26)11-15(3)24-25(6,30-24)8-7-21(27)28/h7-9,11,14,17,20,22,24H,10,12H2,1-6H3,(H,27,28)/b8-7+,15-11+

> <INCHI_KEY>
JXLMEPREHWJPBB-XHBXSBNISA-N

> <FORMULA>
C25H32O5

> <MOLECULAR_WEIGHT>
412.526

> <EXACT_MASS>
412.22497413

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
45.98881216979643

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-3-{2-methyl-3-[(1E)-1-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-1,5,6,7,8,8a-hexahydronaphthalen-1-yl]prop-1-en-2-yl]oxiran-2-yl}prop-2-enoic acid

> <ALOGPS_LOGP>
3.71

> <JCHEM_LOGP>
3.5527157220000007

> <ALOGPS_LOGS>
-5.03

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
15.766881920095045

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.412108855745752

> <JCHEM_PKA_STRONGEST_BASIC>
-4.285649648408325

> <JCHEM_POLAR_SURFACE_AREA>
83.97

> <JCHEM_REFRACTIVITY>
118.40449999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.83e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-3-{2-methyl-3-[(1E)-1-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-5,6,8,8a-tetrahydro-1H-naphthalen-1-yl]prop-1-en-2-yl]oxiran-2-yl}prop-2-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -2.667  -3.080   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       0.000  -3.080   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       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.104  -8.264   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       0.564  -8.264   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.087  -9.659   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.970  -8.129   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.621  -6.734   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -3.155  -6.600   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -4.039  -7.861   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -3.806  -5.204   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   18                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   17                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15    9   18                                                  
CONECT   18   17    5   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22   24                                                       
CONECT   24   23   22   25   26                                             
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₂O₅

Average Mass

412.5260 Da

Monoisotopic Mass

412.22497 Da

IUPAC Name

(2E)-3-{2-methyl-3-[(1E)-1-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-1,5,6,7,8,8a-hexahydronaphthalen-1-yl]prop-1-en-2-yl]oxiran-2-yl}prop-2-enoic acid

Traditional Name

(2E)-3-{2-methyl-3-[(1E)-1-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-5,6,8,8a-tetrahydro-1H-naphthalen-1-yl]prop-1-en-2-yl]oxiran-2-yl}prop-2-enoic acid

CAS Registry Number

Not Available

SMILES

CC1CC2=CC(C)=C(CC(C)=O)C(\C=C(/C)C3OC3(C)\C=C\C(O)=O)C2C(C)C1=O

InChI Identifier

InChI=1S/C25H32O5/c1-13-9-18-10-14(2)23(29)17(5)22(18)20(19(13)12-16(4)26)11-15(3)24-25(6,30-24)8-7-21(27)28/h7-9,11,14,17,20,22,24H,10,12H2,1-6H3,(H,27,28)/b8-7+,15-11+

InChI Key

JXLMEPREHWJPBB-XHBXSBNISA-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
Hamigera avellanea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Bicyclic monoterpenoids

Alternative Parents

Substituents

Bicyclic monoterpenoid
Epoxy fatty acid
Fatty acyl
Ketone
Cyclic ketone
Carboxylic acid derivative
Carboxylic acid
Dialkyl ether
Oxirane
Ether
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Oxacycle
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Organic oxide
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	3.71	ALOGPS
logP	3.55	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	4.41	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	83.97 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	118.4 m³·mol⁻¹	ChemAxon
Polarizability	45.99 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

78444967

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139587826

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Giridharan P, Verekar SA, Gohil AR, Mishra PD, Khanna A, Deshmukh SK: Antiproliferative activity of hamigerone and radicinol isolated from Bipolaris papendorfii. Biomed Res Int. 2014;2014:890904. doi: 10.1155/2014/890904. Epub 2014 Aug 12. [PubMed:25184147 ]
LOTUS database [Link]

Showing NP-Card for (2e)-3-{2-methyl-3-[(1e)-1-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-5,6,8,8a-tetrahydro-1h-naphthalen-1-yl]prop-1-en-2-yl]oxiran-2-yl}prop-2-enoic acid (NP0165798)

MOL for NP0165798 ((2e)-3-{2-methyl-3-[(1e)-1-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-5,6,8,8a-tetrahydro-1h-naphthalen-1-yl]prop-1-en-2-yl]oxiran-2-yl}prop-2-enoic acid)

3D MOL for NP0165798 ((2e)-3-{2-methyl-3-[(1e)-1-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-5,6,8,8a-tetrahydro-1h-naphthalen-1-yl]prop-1-en-2-yl]oxiran-2-yl}prop-2-enoic acid)

3D SDF for NP0165798 ((2e)-3-{2-methyl-3-[(1e)-1-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-5,6,8,8a-tetrahydro-1h-naphthalen-1-yl]prop-1-en-2-yl]oxiran-2-yl}prop-2-enoic acid)

3D-SDF for NP0165798 ((2e)-3-{2-methyl-3-[(1e)-1-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-5,6,8,8a-tetrahydro-1h-naphthalen-1-yl]prop-1-en-2-yl]oxiran-2-yl}prop-2-enoic acid)

PDB for NP0165798 ((2e)-3-{2-methyl-3-[(1e)-1-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-5,6,8,8a-tetrahydro-1h-naphthalen-1-yl]prop-1-en-2-yl]oxiran-2-yl}prop-2-enoic acid)

3D PDB for NP0165798 ((2e)-3-{2-methyl-3-[(1e)-1-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-5,6,8,8a-tetrahydro-1h-naphthalen-1-yl]prop-1-en-2-yl]oxiran-2-yl}prop-2-enoic acid)

SMILES for NP0165798 ((2e)-3-{2-methyl-3-[(1e)-1-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-5,6,8,8a-tetrahydro-1h-naphthalen-1-yl]prop-1-en-2-yl]oxiran-2-yl}prop-2-enoic acid)

INCHI for NP0165798 ((2e)-3-{2-methyl-3-[(1e)-1-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-5,6,8,8a-tetrahydro-1h-naphthalen-1-yl]prop-1-en-2-yl]oxiran-2-yl}prop-2-enoic acid)

Structure for NP0165798 ((2e)-3-{2-methyl-3-[(1e)-1-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-5,6,8,8a-tetrahydro-1h-naphthalen-1-yl]prop-1-en-2-yl]oxiran-2-yl}prop-2-enoic acid)

3D Structure for NP0165798 ((2e)-3-{2-methyl-3-[(1e)-1-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-5,6,8,8a-tetrahydro-1h-naphthalen-1-yl]prop-1-en-2-yl]oxiran-2-yl}prop-2-enoic acid)