NP-MRD: Showing NP-Card for 7-benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]trideca-2,6-diene-8,13-dione (NP0222034)

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Record Information

Version

2.0

Created at

2022-09-05 23:45:41 UTC

Updated at

2022-09-05 23:45:41 UTC

NP-MRD ID

NP0222034

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]trideca-2,6-diene-8,13-dione

Description

7-Benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]Trideca-2,6-diene-8,13-dione belongs to the class of organic compounds known as aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring. 7-benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]trideca-2,6-diene-8,13-dione is found in Garcinia multiflora. 7-Benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]Trideca-2,6-diene-8,13-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004191513412D          

 42 45  0  0  0  0            999 V2000
   -0.6187   -1.7667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2711   -1.2617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1600   -0.4442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3965   -0.1317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2854    0.6858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4781    0.9983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1305    0.4933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5704   -0.1741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8615   -0.9689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3477   -1.6144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6497   -2.3821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1359   -3.0276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6800   -2.9053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4380   -3.7953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7205   -1.0768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4515   -1.8568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4285   -1.5004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3356   -0.4114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8753   -1.0756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7115   -1.0420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0948   -0.3050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7484   -0.8084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7052    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6575    0.3908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8138    0.3455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4821    1.1426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9596    1.8154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6157    2.5653    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7810    1.7383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2585    2.4111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0798    2.3340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4238    1.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9463    0.9113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1249    0.9884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6284    1.1920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2718    1.9360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7402    0.0402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2355    0.6999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9378    1.1907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8267    2.0082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7013    0.8782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0346   -1.5742    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  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  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
 12 14  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 18 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 29 34  1  0  0  0  0
 26 35  1  0  0  0  0
  7 35  1  0  0  0  0
 35 36  2  0  0  0  0
 18 37  1  0  0  0  0
  7 37  1  0  0  0  0
 37 38  2  0  0  0  0
  5 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
  2 42  1  0  0  0  0
M  END


  Mrv1533004191513412D          

 42 45  0  0  0  0            999 V2000
   -0.6187   -1.7667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2711   -1.2617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1600   -0.4442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3965   -0.1317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2854    0.6858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4781    0.9983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1305    0.4933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5704   -0.1741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8615   -0.9689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3477   -1.6144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6497   -2.3821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1359   -3.0276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6800   -2.9053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4380   -3.7953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7205   -1.0768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4515   -1.8568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4285   -1.5004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3356   -0.4114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8753   -1.0756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7115   -1.0420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0948   -0.3050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7484   -0.8084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7052    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6575    0.3908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8138    0.3455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4821    1.1426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9596    1.8154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6157    2.5653    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7810    1.7383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2585    2.4111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0798    2.3340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4238    1.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9463    0.9113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1249    0.9884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6284    1.1920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2718    1.9360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7402    0.0402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2355    0.6999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9378    1.1907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8267    2.0082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7013    0.8782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0346   -1.5742    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  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  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
 12 14  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 18 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 29 34  1  0  0  0  0
 26 35  1  0  0  0  0
  7 35  1  0  0  0  0
 35 36  2  0  0  0  0
 18 37  1  0  0  0  0
  7 37  1  0  0  0  0
 37 38  2  0  0  0  0
  5 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
  2 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0222034

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC(CC12CC(CC=C(C)C)C(C)(C)C3(C=CC(C)(C)OC3=C(C(=O)C3=CC=CC=C3)C1=O)C2=O)C(C)=C

> <INCHI_IDENTIFIER>
InChI=1S/C38H48O4/c1-24(2)16-18-28(26(5)6)22-37-23-29(19-17-25(3)4)36(9,10)38(34(37)41)21-20-35(7,8)42-33(38)30(32(37)40)31(39)27-14-12-11-13-15-27/h11-17,20-21,28-29H,5,18-19,22-23H2,1-4,6-10H3

> <INCHI_KEY>
MBFYFWIEWICZQJ-UHFFFAOYSA-N

> <FORMULA>
C38H48O4

> <MOLECULAR_WEIGHT>
568.798

> <EXACT_MASS>
568.355260026

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
90

> <JCHEM_AVERAGE_POLARIZABILITY>
65.58333953224374

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7-benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]trideca-2,6-diene-8,13-dione

> <ALOGPS_LOGP>
6.94

> <JCHEM_LOGP>
9.107689131333334

> <ALOGPS_LOGS>
-6.38

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.914799999877492

> <JCHEM_POLAR_SURFACE_AREA>
60.440000000000005

> <JCHEM_REFRACTIVITY>
175.0608

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.35e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]trideca-2,6-diene-8,13-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0      -1.155  -3.298   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.373  -2.355   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.165  -0.829   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.740  -0.246   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.533   1.280   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.892   1.864   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.110   0.921   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.065  -0.325   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.608  -1.809   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.649  -3.014   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.213  -4.447   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.254  -5.651   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.269  -5.423   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.818  -7.085   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.212  -2.010   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.710  -3.466   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.533  -2.801   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.360  -0.768   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.367  -2.008   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.928  -1.945   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.644  -0.569   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.864  -1.509   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.783   0.467   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.827   0.730   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.252   0.645   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.633   2.133   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.525   3.389   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       4.883   4.789   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       7.058   3.245   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.949   4.501   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.482   4.357   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.124   2.957   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       9.233   1.701   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       7.700   1.845   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       3.040   2.225   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       2.374   3.614   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       3.248   0.075   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       4.173   1.307   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -1.751   2.223   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -1.543   3.749   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -3.176   1.639   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -3.798  -2.939   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   42                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   39                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   35   37                                             
CONECT    8    7    9                                                       
CONECT    9    8   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    9   16   17   18                                             
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   15   19   25   37                                             
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23   24                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   21   25                                                       
CONECT   25   24   18   26                                                  
CONECT   26   25   27   35                                                  
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   29                                                       
CONECT   35   26    7   36                                                  
CONECT   36   35                                                            
CONECT   37   18    7   38                                                  
CONECT   38   37                                                            
CONECT   39    5   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42    2                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   90    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₈H₄₈O₄

Average Mass

568.7980 Da

Monoisotopic Mass

568.35526 Da

IUPAC Name

7-benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]trideca-2,6-diene-8,13-dione

Traditional Name

7-benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]trideca-2,6-diene-8,13-dione

CAS Registry Number

Not Available

SMILES

CC(C)=CCC(CC12CC(CC=C(C)C)C(C)(C)C3(C=CC(C)(C)OC3=C(C(=O)C3=CC=CC=C3)C1=O)C2=O)C(C)=C

InChI Identifier

InChI=1S/C38H48O4/c1-24(2)16-18-28(26(5)6)22-37-23-29(19-17-25(3)4)36(9,10)38(34(37)41)21-20-35(7,8)42-33(38)30(32(37)40)31(39)27-14-12-11-13-15-27/h11-17,20-21,28-29H,5,18-19,22-23H2,1-4,6-10H3

InChI Key

MBFYFWIEWICZQJ-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
Garcinia multiflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Aromatic monoterpenoids

Alternative Parents

Substituents

Aromatic monoterpenoid
Benzoyl
Aryl ketone
Cyclohexenone
Monocyclic benzene moiety
Pyran
Benzenoid
Vinylogous ester
Ketone
Oxacycle
Organoheterocyclic compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	6.94	ALOGPS
logP	9.11	ChemAxon
logS	-6.4	ALOGPS
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	60.44 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	175.06 m³·mol⁻¹	ChemAxon
Polarizability	65.58 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

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

56667952

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]trideca-2,6-diene-8,13-dione (NP0222034)

MOL for NP0222034 (7-benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]trideca-2,6-diene-8,13-dione)

3D MOL for NP0222034 (7-benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]trideca-2,6-diene-8,13-dione)

3D SDF for NP0222034 (7-benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]trideca-2,6-diene-8,13-dione)

3D-SDF for NP0222034 (7-benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]trideca-2,6-diene-8,13-dione)

PDB for NP0222034 (7-benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]trideca-2,6-diene-8,13-dione)

3D PDB for NP0222034 (7-benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]trideca-2,6-diene-8,13-dione)

SMILES for NP0222034 (7-benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]trideca-2,6-diene-8,13-dione)

INCHI for NP0222034 (7-benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]trideca-2,6-diene-8,13-dione)

Structure for NP0222034 (7-benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]trideca-2,6-diene-8,13-dione)

3D Structure for NP0222034 (7-benzoyl-4,4,12,12-tetramethyl-9-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-11-(3-methylbut-2-en-1-yl)-5-oxatricyclo[7.3.1.0¹,⁶]trideca-2,6-diene-8,13-dione)