NP-MRD: Showing NP-Card for (1s,2r,3r,4r,5r,6s,7s,9r,12r)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate (NP0221067)

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Record Information

Version

2.0

Created at

2022-09-05 22:32:57 UTC

Updated at

2022-09-05 22:32:57 UTC

NP-MRD ID

NP0221067

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,3r,4r,5r,6s,7s,9r,12r)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate

Description

(1S,2R,3R,4R,5R,6S,7S,9R,12R)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-7-yl benzoate belongs to the class of organic compounds known as agarofurans. These are organic compounds containing an agarofuran moiety( a three-ring system, with core fragment oxatricyclo[7.2.1.0^{1,6}]Dodec-2-ene). (1s,2r,3r,4r,5r,6s,7s,9r,12r)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate is found in Maytenus boaria. Based on a literature review very few articles have been published on (1S,2R,3R,4R,5R,6S,7S,9R,12R)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-7-yl benzoate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309062200322D          

 43 47  0  0  1  0            999 V2000
    5.5386    1.6276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5382    0.7927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3856    1.0239    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7906    0.2794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0331   -0.2371    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6599    0.5054    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9349    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8351    0.5561    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7254    1.4139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3349   -0.1234    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6531    0.4578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8934    0.0350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0405   -0.1577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4033    0.7610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0588   -0.8122    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4269   -1.5948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2845   -1.6626    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2306   -2.5885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6944   -3.4367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8874   -3.7558    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2830   -4.0853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1067   -4.1308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4791   -4.8670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0278   -5.5576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2041   -5.5120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8317   -4.7759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7420   -0.9114    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4408   -1.5482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5838   -0.9369    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1848   -1.6064    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8524   -2.2043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0430   -3.0572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6277   -2.0048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8268   -1.2042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6197   -0.9763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2135   -1.5490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0144   -2.3496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2215   -2.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7368   -0.5133    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8592   -1.3122    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1399   -1.9639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4806   -2.7445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2423   -1.7104    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
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  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  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 21 26  1  0  0  0  0
 17 27  1  0  0  0  0
 10 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
  5 29  1  0  0  0  0
 29 30  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 33 38  1  0  0  0  0
 15 39  1  0  0  0  0
 10 39  1  0  0  0  0
 39 40  1  6  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  2  0  0  0  0
M  END


  Mrv1652309062200322D          

 43 47  0  0  1  0            999 V2000
    5.5386    1.6276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5382    0.7927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3856    1.0239    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7906    0.2794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0331   -0.2371    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6599    0.5054    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9349    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8351    0.5561    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7254    1.4139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3349   -0.1234    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6531    0.4578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8934    0.0350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0405   -0.1577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4033    0.7610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0588   -0.8122    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4269   -1.5948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2845   -1.6626    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2306   -2.5885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6944   -3.4367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8874   -3.7558    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2830   -4.0853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1067   -4.1308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4791   -4.8670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0278   -5.5576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2041   -5.5120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8317   -4.7759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7420   -0.9114    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4408   -1.5482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5838   -0.9369    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1848   -1.6064    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8524   -2.2043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0430   -3.0572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6277   -2.0048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8268   -1.2042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6197   -0.9763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2135   -1.5490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0144   -2.3496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2215   -2.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7368   -0.5133    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8592   -1.3122    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1399   -1.9639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4806   -2.7445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2423   -1.7104    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
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  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  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 21 26  1  0  0  0  0
 17 27  1  0  0  0  0
 10 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
  5 29  1  0  0  0  0
 29 30  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 33 38  1  0  0  0  0
 15 39  1  0  0  0  0
 10 39  1  0  0  0  0
 39 40  1  6  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0221067

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1[C@@H](O)[C@@H](OC(C)=O)[C@H](OC(=O)C2=CC=CC=C2)[C@]2(C)[C@H](C[C@@H]3[C@@H](OC(C)=O)[C@]12OC3(C)C)OC(=O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C33H38O10/c1-18-25(36)26(39-19(2)34)28(42-30(38)22-15-11-8-12-16-22)32(6)24(41-29(37)21-13-9-7-10-14-21)17-23-27(40-20(3)35)33(18,32)43-31(23,4)5/h7-16,18,23-28,36H,17H2,1-6H3/t18-,23-,24+,25-,26-,27-,28+,32+,33-/m1/s1

> <INCHI_KEY>
SOTGPCCKMHIJCT-IGPYCKTMSA-N

> <FORMULA>
C33H38O10

> <MOLECULAR_WEIGHT>
594.657

> <EXACT_MASS>
594.246497424

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
62.2532697003267

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,3R,4R,5R,6S,7S,9R,12R)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-7-yl benzoate

> <JCHEM_LOGP>
4.229362283333334

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.757675378758105

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3421927893312047

> <JCHEM_POLAR_SURFACE_AREA>
134.66000000000003

> <JCHEM_REFRACTIVITY>
151.3899

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,3R,4R,5R,6S,7S,9R,12R)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-7-yl benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      10.339   3.038   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.338   1.480   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      11.920   1.911   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       8.942   0.522   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.528  -0.443   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.832   0.943   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       7.345   2.461   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.292   1.038   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.087   2.639   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.358  -0.230   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.086   0.855   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.668   0.065   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.076  -0.294   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.753   1.420   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.976  -1.516   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.664  -2.977   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.264  -3.104   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.164  -4.832   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.163  -6.415   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.656  -7.011   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.262  -7.626   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.799  -7.711   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.494  -9.085   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.652 -10.374   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.114 -10.289   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.419  -8.915   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.118  -1.701   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.423  -2.890   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.690  -1.749   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       7.812  -2.999   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       9.058  -4.115   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       9.414  -5.707   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      10.505  -3.742   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      10.877  -2.248   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      12.357  -1.822   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      13.465  -2.891   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      13.094  -4.386   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      11.614  -4.811   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       3.242  -0.958   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       3.470  -2.450   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       2.128  -3.666   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       2.764  -5.123   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       0.452  -3.193   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   29                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   27   39                                             
CONECT   11   10   12                                                       
CONECT   12   11   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12   16   39                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   27                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   21                                                       
CONECT   27   17   10   28   29                                             
CONECT   28   27                                                            
CONECT   29   27    5   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   38                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   33                                                       
CONECT   39   15   10   40                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   94    0
END

View in JSmol

Synonyms

Value	Source
(1S,2R,3R,4R,5R,6S,7S,9R,12R)-4,12-Bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0,]dodecan-7-yl benzoic acid	Generator

Chemical Formula

C₃₃H₃₈O₁₀

Average Mass

594.6570 Da

Monoisotopic Mass

594.24650 Da

IUPAC Name

(1S,2R,3R,4R,5R,6S,7S,9R,12R)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-7-yl benzoate

Traditional Name

(1S,2R,3R,4R,5R,6S,7S,9R,12R)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-7-yl benzoate

CAS Registry Number

Not Available

SMILES

C[C@@H]1[C@@H](O)[C@@H](OC(C)=O)[C@H](OC(=O)C2=CC=CC=C2)[C@]2(C)[C@H](C[C@@H]3[C@@H](OC(C)=O)[C@]12OC3(C)C)OC(=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C33H38O10/c1-18-25(36)26(39-19(2)34)28(42-30(38)22-15-11-8-12-16-22)32(6)24(41-29(37)21-13-9-7-10-14-21)17-23-27(40-20(3)35)33(18,32)43-31(23,4)5/h7-16,18,23-28,36H,17H2,1-6H3/t18-,23-,24+,25-,26-,27-,28+,32+,33-/m1/s1

InChI Key

SOTGPCCKMHIJCT-IGPYCKTMSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Maytenus boaria	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as agarofurans. These are organic compounds containing an agarofuran moiety( a three-ring system, with core fragment oxatricyclo[7.2.1.0^{1,6}]Dodec-2-ene).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Agarofurans

Alternative Parents

Substituents

Agarofuran
Tetracarboxylic acid or derivatives
Benzoate ester
Benzoic acid or derivatives
Benzoyl
Oxepane
Cyclitol or derivatives
Monocyclic benzene moiety
Benzenoid
Tetrahydrofuran
Cyclic alcohol
Carboxylic acid ester
Secondary alcohol
Ether
Dialkyl ether
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Alcohol
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organooxygen 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	4.23	ChemAxon
pKa (Strongest Acidic)	13.76	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	134.66 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	151.39 m³·mol⁻¹	ChemAxon
Polarizability	62.25 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	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

162902643

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2r,3r,4r,5r,6s,7s,9r,12r)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate (NP0221067)

MOL for NP0221067 ((1s,2r,3r,4r,5r,6s,7s,9r,12r)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D MOL for NP0221067 ((1s,2r,3r,4r,5r,6s,7s,9r,12r)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D SDF for NP0221067 ((1s,2r,3r,4r,5r,6s,7s,9r,12r)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D-SDF for NP0221067 ((1s,2r,3r,4r,5r,6s,7s,9r,12r)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

PDB for NP0221067 ((1s,2r,3r,4r,5r,6s,7s,9r,12r)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D PDB for NP0221067 ((1s,2r,3r,4r,5r,6s,7s,9r,12r)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

SMILES for NP0221067 ((1s,2r,3r,4r,5r,6s,7s,9r,12r)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

INCHI for NP0221067 ((1s,2r,3r,4r,5r,6s,7s,9r,12r)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

Structure for NP0221067 ((1s,2r,3r,4r,5r,6s,7s,9r,12r)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D Structure for NP0221067 ((1s,2r,3r,4r,5r,6s,7s,9r,12r)-4,12-bis(acetyloxy)-5-(benzoyloxy)-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)