NP-MRD: Showing NP-Card for (1s,2r,4s,5r,6s,7r,8r,9s,12r)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2r)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl furan-3-carboxylate (NP0310990)

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Record Information

Version

2.0

Created at

2022-09-11 06:41:04 UTC

Updated at

2022-09-11 06:41:05 UTC

NP-MRD ID

NP0310990

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,4s,5r,6s,7r,8r,9s,12r)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2r)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl furan-3-carboxylate

Description

(1S,2R,4S,5R,6S,7R,8R,9S,12R)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2R)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-8-yl furan-3-carboxylate 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,4s,5r,6s,7r,8r,9s,12r)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2r)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl furan-3-carboxylate is found in Celastrus rosthornianus. Based on a literature review very few articles have been published on (1S,2R,4S,5R,6S,7R,8R,9S,12R)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2R)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-8-yl furan-3-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112208412D          

 45 49  0  0  1  0            999 V2000
    7.4036    1.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5797    1.0599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1302    0.3680    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5046   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3064    0.4114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9320    1.1465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8569   -0.2804    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0331   -0.2371    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6599    0.5054    0.0000 C   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
    2.4857    1.3034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 44 45  1  6  0  0  0
M  END

     RDKit          3D

 87 91  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309112208412D          

 45 49  0  0  1  0            999 V2000
    7.4036    1.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5797    1.0599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1302    0.3680    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5046   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3064    0.4114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9320    1.1465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8569   -0.2804    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0331   -0.2371    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6599    0.5054    0.0000 C   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
    2.4857    1.3034    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
    0.5700    0.7940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1047   -0.2071    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  1  0  0  0  0  0  0  0  0  0
    0.9576   -2.2733    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1354   -2.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2176   -1.4606    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3339   -2.8848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1587   -2.9040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3953   -3.6943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7167   -4.1636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0607   -3.6632    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
    2.6599   -2.3973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2114   -3.0897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3874   -3.0475    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5868   -3.8244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4107   -3.8666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7861   -4.6012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3375   -5.2936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5136   -5.2514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1382   -4.5168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7420   -0.9114    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1352   -1.6366    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
    3.9683   -1.6668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7927   -1.6987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2326   -1.0007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1773   -2.4286    0.0000 O   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
    2.1297   -1.2387    0.0000 O   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  1  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 17 14  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  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  1  0  0  0  0
 22 26  2  0  0  0  0
 18 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 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
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 31 36  1  0  0  0  0
 27 37  1  0  0  0  0
 12 37  1  0  0  0  0
 37 38  1  6  0  0  0
 37 39  1  0  0  0  0
  8 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
 17 44  1  0  0  0  0
 12 44  1  0  0  0  0
 44 45  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0310990

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@H](C)C(=O)O[C@H]1C[C@@H](C)[C@@]23OC(C)(C)[C@@H]([C@H]2O)[C@@H](OC(=O)C2=COC=C2)[C@H](OC(=O)C2=CC=CC=C2)[C@]3(C)[C@H]1OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C34H42O11/c1-8-18(2)29(37)42-23-16-19(3)34-26(36)24(32(5,6)45-34)25(43-31(39)22-14-15-40-17-22)28(33(34,7)27(23)41-20(4)35)44-30(38)21-12-10-9-11-13-21/h9-15,17-19,23-28,36H,8,16H2,1-7H3/t18-,19-,23+,24-,25-,26-,27+,28+,33+,34-/m1/s1

> <INCHI_KEY>
GZXHWPFETLWFJR-GAFPIEJNSA-N

> <FORMULA>
C34H42O11

> <MOLECULAR_WEIGHT>
626.699

> <EXACT_MASS>
626.272712172

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
87

> <JCHEM_AVERAGE_POLARIZABILITY>
64.69938299493634

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,4S,5R,6S,7R,8R,9S,12R)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2R)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-8-yl furan-3-carboxylate

> <JCHEM_LOGP>
5.277221018

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.5732415156603

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0513006527522477

> <JCHEM_POLAR_SURFACE_AREA>
147.8

> <JCHEM_REFRACTIVITY>
157.4437

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,4S,5R,6S,7R,8R,9S,12R)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2R)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-8-yl furan-3-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      13.820   1.897   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.282   1.978   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.443   0.687   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.142  -0.685   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.905   0.768   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       9.206   2.140   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       9.066  -0.523   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       7.528  -0.443   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.832   0.943   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.292   1.038   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.640   2.433   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.358  -0.230   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.086   0.855   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.668   0.065   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.064   1.482   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.195  -0.387   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.976  -1.516   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.664  -2.977   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.788  -4.244   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.253  -4.118   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.406  -2.726   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.623  -5.385   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.163  -5.421   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.604  -6.896   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -1.338  -7.772   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -0.113  -6.838   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.264  -3.104   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       4.965  -4.475   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       4.128  -5.767   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.590  -5.689   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       4.829  -7.139   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.367  -7.218   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.067  -8.589   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.230  -9.881   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.692  -9.803   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.991  -8.431   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       5.118  -1.701   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       5.852  -3.055   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       6.690  -1.749   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       7.408  -3.111   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       8.946  -3.171   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       9.767  -1.868   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       9.664  -4.533   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       3.242  -0.958   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       3.976  -2.312   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   39                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   37   44                                             
CONECT   13   12   14                                                       
CONECT   14   13   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   14   18   44                                                  
CONECT   18   17   19   27                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   26                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   22                                                       
CONECT   27   18   28   37                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   31                                                       
CONECT   37   27   12   38   39                                             
CONECT   38   37                                                            
CONECT   39   37    8   40                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41                                                            
CONECT   44   17   12   45                                                  
CONECT   45   44                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   98    0
END

View in JSmol

Synonyms

Value	Source
(1S,2R,4S,5R,6S,7R,8R,9S,12R)-5-(Acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2R)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0,]dodecan-8-yl furan-3-carboxylic acid	Generator

Chemical Formula

C₃₄H₄₂O₁₁

Average Mass

626.6990 Da

Monoisotopic Mass

626.27271 Da

IUPAC Name

(1S,2R,4S,5R,6S,7R,8R,9S,12R)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2R)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-8-yl furan-3-carboxylate

Traditional Name

(1S,2R,4S,5R,6S,7R,8R,9S,12R)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2R)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-8-yl furan-3-carboxylate

CAS Registry Number

Not Available

SMILES

CC[C@@H](C)C(=O)O[C@H]1C[C@@H](C)[C@@]23OC(C)(C)[C@@H]([C@H]2O)[C@@H](OC(=O)C2=COC=C2)[C@H](OC(=O)C2=CC=CC=C2)[C@]3(C)[C@H]1OC(C)=O

InChI Identifier

InChI=1S/C34H42O11/c1-8-18(2)29(37)42-23-16-19(3)34-26(36)24(32(5,6)45-34)25(43-31(39)22-14-15-40-17-22)28(33(34,7)27(23)41-20(4)35)44-30(38)21-12-10-9-11-13-21/h9-15,17-19,23-28,36H,8,16H2,1-7H3/t18-,19-,23+,24-,25-,26-,27+,28+,33+,34-/m1/s1

InChI Key

GZXHWPFETLWFJR-GAFPIEJNSA-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
Celastrus rosthornianus	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
Furoic acid ester
Benzoic acid or derivatives
Furoic acid or derivatives
Furan-3-carboxylic acid ester
Furan-3-carboxylic acid or derivatives
Benzoyl
Fatty acid ester
Oxepane
Monocyclic benzene moiety
Fatty acyl
Benzenoid
Heteroaromatic compound
Cyclic alcohol
Furan
Tetrahydrofuran
Carboxylic acid ester
Secondary alcohol
Organoheterocyclic compound
Ether
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Alcohol
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
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	5.28	ChemAxon
pKa (Strongest Acidic)	13.57	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	147.8 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	157.44 m³·mol⁻¹	ChemAxon
Polarizability	64.7 Å³	ChemAxon
Number of Rings	5	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

162867396

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,4s,5r,6s,7r,8r,9s,12r)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2r)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl furan-3-carboxylate (NP0310990)

MOL for NP0310990 ((1s,2r,4s,5r,6s,7r,8r,9s,12r)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2r)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl furan-3-carboxylate)

3D MOL for NP0310990 ((1s,2r,4s,5r,6s,7r,8r,9s,12r)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2r)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl furan-3-carboxylate)

3D SDF for NP0310990 ((1s,2r,4s,5r,6s,7r,8r,9s,12r)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2r)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl furan-3-carboxylate)

3D-SDF for NP0310990 ((1s,2r,4s,5r,6s,7r,8r,9s,12r)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2r)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl furan-3-carboxylate)

PDB for NP0310990 ((1s,2r,4s,5r,6s,7r,8r,9s,12r)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2r)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl furan-3-carboxylate)

3D PDB for NP0310990 ((1s,2r,4s,5r,6s,7r,8r,9s,12r)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2r)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl furan-3-carboxylate)

SMILES for NP0310990 ((1s,2r,4s,5r,6s,7r,8r,9s,12r)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2r)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl furan-3-carboxylate)

INCHI for NP0310990 ((1s,2r,4s,5r,6s,7r,8r,9s,12r)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2r)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl furan-3-carboxylate)

Structure for NP0310990 ((1s,2r,4s,5r,6s,7r,8r,9s,12r)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2r)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl furan-3-carboxylate)

3D Structure for NP0310990 ((1s,2r,4s,5r,6s,7r,8r,9s,12r)-5-(acetyloxy)-7-(benzoyloxy)-12-hydroxy-2,6,10,10-tetramethyl-4-{[(2r)-2-methylbutanoyl]oxy}-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl furan-3-carboxylate)