NP-MRD: Showing NP-Card for (4s,8e,10e,12e,14e,16e,18e,20e,22z,24e)-25-[(1s,4s,6r)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-6,6,10,14,19,23-hexamethyl-2,7-dioxopentacosa-8,10,12,14,16,18,20,22,24-nonaen-4-yl dodecanoate (NP0186402)

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Record Information

Version

2.0

Created at

2022-09-04 02:14:41 UTC

Updated at

2022-09-04 02:14:41 UTC

NP-MRD ID

NP0186402

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4s,8e,10e,12e,14e,16e,18e,20e,22z,24e)-25-[(1s,4s,6r)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-6,6,10,14,19,23-hexamethyl-2,7-dioxopentacosa-8,10,12,14,16,18,20,22,24-nonaen-4-yl dodecanoate

Description

Tobiraxanthin B belongs to the class of organic compounds known as sesquaterpenoids. These are terpenoids with at least 7 consecutive isoprene units. (4s,8e,10e,12e,14e,16e,18e,20e,22z,24e)-25-[(1s,4s,6r)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-6,6,10,14,19,23-hexamethyl-2,7-dioxopentacosa-8,10,12,14,16,18,20,22,24-nonaen-4-yl dodecanoate is found in Pittosporum tobira. Based on a literature review very few articles have been published on Tobiraxanthin B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042204142D          

 58 59  0  0  1  0            999 V2000
   -6.0770   -2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3625   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6480   -2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9336   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2191   -2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5046   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7901   -2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0757   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3612   -2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3533   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0677   -2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7822   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7822   -3.7934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4967   -2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4967   -1.7309    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2112   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9256   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6401   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9256   -2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.4967    0.7441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.2191    0.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.6480    0.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3625    0.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0770    0.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7914    0.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7914   -0.4934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5059    0.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2204    0.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9349    0.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -9.6493   -0.4934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3638   -0.9059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3638   -1.7309    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.5388   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9513   -2.4454    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.2368   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3638   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  -11.6013   -3.8743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6013   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1888   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.8884   -1.2937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2176   -0.9064    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
  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  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 15 20  1  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  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 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  1  0  0  0  0
 33 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
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 53 55  1  0  0  0  0
 55 56  1  0  0  0  0
 48 56  1  0  0  0  0
 56 57  1  0  0  0  0
 56 58  1  0  0  0  0
M  END

     RDKit          3D

136137  0  0  0  0  0  0  0  0999 V2000
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   15.1580   -0.9286    1.5240 C   0  0  0  0  0  0  0  0  0  0  0  0
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   13.8734    2.2741   -0.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5737    2.2889   -1.0757 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2913    3.4902   -1.8913 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9489    3.2416   -2.5628 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8335    3.1983   -1.5889 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.8101    2.3369   -1.5063 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7237    2.3009   -0.6519 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.6806    1.2876    0.4141 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.1570    2.5337    1.7628 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4597    2.4925   -1.4402 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.5223    0.5282    0.6599 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6693    0.1187    1.1148 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.9379   -0.4329    1.6624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7514   -1.7511    2.2439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9575   -1.2059    2.2127 C   0  0  0  0  0  0  0  0  0  0  0  0
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  -11.1975   -2.0600    2.4161 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4444   -2.1680    2.1389 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


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M  END
> <DATABASE_ID>
NP0186402

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCC(=O)O[C@H](CC(C)=O)CC(C)(C)C(=O)\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(\C)/C=C/[C@@]12O[C@]1(C)C[C@@H](O)CC2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C52H78O6/c1-12-13-14-15-16-17-18-19-20-31-48(56)57-46(36-44(6)53)39-49(7,8)47(55)33-32-42(4)29-23-27-40(2)25-21-22-26-41(3)28-24-30-43(5)34-35-52-50(9,10)37-45(54)38-51(52,11)58-52/h21-30,32-35,45-46,54H,12-20,31,36-39H2,1-11H3/b22-21+,27-23+,28-24+,33-32+,35-34+,40-25+,41-26+,42-29+,43-30-/t45-,46+,51+,52-/m0/s1

> <INCHI_KEY>
MGPHPUSGWQQMIO-LPPNNJRWSA-N

> <FORMULA>
C52H78O6

> <MOLECULAR_WEIGHT>
799.19

> <EXACT_MASS>
798.579840232

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
136

> <JCHEM_AVERAGE_POLARIZABILITY>
98.66658101925944

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4S,8E,10E,12E,14E,16E,18E,20E,22Z,24E)-25-[(1S,4S,6R)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-6,6,10,14,19,23-hexamethyl-2,7-dioxopentacosa-8,10,12,14,16,18,20,22,24-nonaen-4-yl dodecanoate

> <JCHEM_LOGP>
12.588078504333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.68568086710973

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.139560482256122

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7377022034819802

> <JCHEM_POLAR_SURFACE_AREA>
93.2

> <JCHEM_REFRACTIVITY>
251.28130000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
27

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(4S,8E,10E,12E,14E,16E,18E,20E,22Z,24E)-25-[(1S,4S,6R)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-6,6,10,14,19,23-hexamethyl-2,7-dioxopentacosa-8,10,12,14,16,18,20,22,24-nonaen-4-yl dodecanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0     -11.344  -4.771   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -10.010  -5.541   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -8.676  -4.771   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.343  -5.541   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.009  -4.771   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.675  -5.541   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.342  -4.771   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.008  -5.541   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.674  -4.771   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.659  -5.541   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.993  -4.771   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.327  -5.541   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.327  -7.081   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       4.660  -4.771   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.660  -3.231   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.994  -2.461   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.328  -3.231   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.662  -2.461   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       7.328  -4.771   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.327  -2.461   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.327  -0.921   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.867  -0.921   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.787  -0.921   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.327   0.619   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.660   1.389   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.993   1.389   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.659   0.619   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.674   1.389   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.674   2.929   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -2.008   0.619   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -3.342   1.389   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -4.675   0.619   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -6.009   1.389   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -6.009   2.929   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -7.343   0.619   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -8.676   1.389   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0     -10.010   0.619   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0     -11.344   1.389   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0     -12.677   0.619   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0     -12.677  -0.921   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0     -14.011   1.389   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0     -15.345   0.619   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0     -16.678   1.389   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0     -18.012   0.619   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0     -19.346   1.389   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0     -18.012  -0.921   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0     -19.346  -1.691   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0     -19.346  -3.231   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0     -17.806  -3.231   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0     -18.576  -4.565   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0     -17.242  -5.335   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0     -19.346  -5.898   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0     -20.886  -5.898   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0     -21.656  -7.232   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0     -21.656  -4.565   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0     -20.886  -3.231   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0     -22.192  -2.415   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0     -20.939  -1.692   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   15   21                                                       
CONECT   21   20   22   23   24                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   21   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49   50   56                                             
CONECT   49   48   50                                                       
CONECT   50   49   48   51   52                                             
CONECT   51   50                                                            
CONECT   52   50   53                                                       
CONECT   53   52   54   55                                                  
CONECT   54   53                                                            
CONECT   55   53   56                                                       
CONECT   56   55   48   57   58                                             
CONECT   57   56                                                            
CONECT   58   56                                                            
MASTER        0    0    0    0    0    0    0    0   58    0  118    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₅₂H₇₈O₆

Average Mass

799.1900 Da

Monoisotopic Mass

798.57984 Da

IUPAC Name

(4S,8E,10E,12E,14E,16E,18E,20E,22Z,24E)-25-[(1S,4S,6R)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-6,6,10,14,19,23-hexamethyl-2,7-dioxopentacosa-8,10,12,14,16,18,20,22,24-nonaen-4-yl dodecanoate

Traditional Name

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCC(=O)O[C@H](CC(C)=O)CC(C)(C)C(=O)\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(\C)/C=C/[C@@]12O[C@]1(C)C[C@@H](O)CC2(C)C

InChI Identifier

InChI=1S/C52H78O6/c1-12-13-14-15-16-17-18-19-20-31-48(56)57-46(36-44(6)53)39-49(7,8)47(55)33-32-42(4)29-23-27-40(2)25-21-22-26-41(3)28-24-30-43(5)34-35-52-50(9,10)37-45(54)38-51(52,11)58-52/h21-30,32-35,45-46,54H,12-20,31,36-39H2,1-11H3/b22-21+,27-23+,28-24+,33-32+,35-34+,40-25+,41-26+,42-29+,43-30-/t45-,46+,51+,52-/m0/s1

InChI Key

MGPHPUSGWQQMIO-LPPNNJRWSA-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
Pittosporum tobira	LOTUS Database	35616633

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
Fatty alcohol ester
Oxepane
Fatty acid ester
Fatty acyl
Alpha,beta-unsaturated ketone
Enone
Cyclic alcohol
Acryloyl-group
Secondary alcohol
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	12.59	ChemAxon
pKa (Strongest Acidic)	15.14	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	93.2 Å²	ChemAxon
Rotatable Bond Count	27	ChemAxon
Refractivity	251.28 m³·mol⁻¹	ChemAxon
Polarizability	98.67 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101183206

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4s,8e,10e,12e,14e,16e,18e,20e,22z,24e)-25-[(1s,4s,6r)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-6,6,10,14,19,23-hexamethyl-2,7-dioxopentacosa-8,10,12,14,16,18,20,22,24-nonaen-4-yl dodecanoate (NP0186402)

MOL for NP0186402 ((4s,8e,10e,12e,14e,16e,18e,20e,22z,24e)-25-[(1s,4s,6r)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-6,6,10,14,19,23-hexamethyl-2,7-dioxopentacosa-8,10,12,14,16,18,20,22,24-nonaen-4-yl dodecanoate)

3D MOL for NP0186402 ((4s,8e,10e,12e,14e,16e,18e,20e,22z,24e)-25-[(1s,4s,6r)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-6,6,10,14,19,23-hexamethyl-2,7-dioxopentacosa-8,10,12,14,16,18,20,22,24-nonaen-4-yl dodecanoate)

3D SDF for NP0186402 ((4s,8e,10e,12e,14e,16e,18e,20e,22z,24e)-25-[(1s,4s,6r)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-6,6,10,14,19,23-hexamethyl-2,7-dioxopentacosa-8,10,12,14,16,18,20,22,24-nonaen-4-yl dodecanoate)

3D-SDF for NP0186402 ((4s,8e,10e,12e,14e,16e,18e,20e,22z,24e)-25-[(1s,4s,6r)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-6,6,10,14,19,23-hexamethyl-2,7-dioxopentacosa-8,10,12,14,16,18,20,22,24-nonaen-4-yl dodecanoate)

PDB for NP0186402 ((4s,8e,10e,12e,14e,16e,18e,20e,22z,24e)-25-[(1s,4s,6r)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-6,6,10,14,19,23-hexamethyl-2,7-dioxopentacosa-8,10,12,14,16,18,20,22,24-nonaen-4-yl dodecanoate)

3D PDB for NP0186402 ((4s,8e,10e,12e,14e,16e,18e,20e,22z,24e)-25-[(1s,4s,6r)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-6,6,10,14,19,23-hexamethyl-2,7-dioxopentacosa-8,10,12,14,16,18,20,22,24-nonaen-4-yl dodecanoate)

SMILES for NP0186402 ((4s,8e,10e,12e,14e,16e,18e,20e,22z,24e)-25-[(1s,4s,6r)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-6,6,10,14,19,23-hexamethyl-2,7-dioxopentacosa-8,10,12,14,16,18,20,22,24-nonaen-4-yl dodecanoate)

INCHI for NP0186402 ((4s,8e,10e,12e,14e,16e,18e,20e,22z,24e)-25-[(1s,4s,6r)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-6,6,10,14,19,23-hexamethyl-2,7-dioxopentacosa-8,10,12,14,16,18,20,22,24-nonaen-4-yl dodecanoate)

Structure for NP0186402 ((4s,8e,10e,12e,14e,16e,18e,20e,22z,24e)-25-[(1s,4s,6r)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-6,6,10,14,19,23-hexamethyl-2,7-dioxopentacosa-8,10,12,14,16,18,20,22,24-nonaen-4-yl dodecanoate)

3D Structure for NP0186402 ((4s,8e,10e,12e,14e,16e,18e,20e,22z,24e)-25-[(1s,4s,6r)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-6,6,10,14,19,23-hexamethyl-2,7-dioxopentacosa-8,10,12,14,16,18,20,22,24-nonaen-4-yl dodecanoate)