NP-MRD: Showing NP-Card for (1s,2r,5s,6s,7s,9r)-5-(acetyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate (NP0170989)

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Record Information

Version

2.0

Created at

2022-09-03 07:19:18 UTC

Updated at

2022-09-03 07:19:18 UTC

NP-MRD ID

NP0170989

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,5s,6s,7s,9r)-5-(acetyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate

Description

Triptogelin G-2 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,5s,6s,7s,9r)-5-(acetyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate is found in Celastrus flagellaris, Microtropis fokienensis and Tripterygium wilfordii. Based on a literature review very few articles have been published on triptogelin G-2.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032209192D          

 29 32  0  0  1  0            999 V2000
    3.5355    2.0462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1509    1.3163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5908    0.6183    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3266    1.2844    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9420    0.5545    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3913   -0.1453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0182   -0.8878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1934   -0.9383    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8439   -1.6856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6930   -0.2588    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0948    0.1310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5832    0.4298    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2150    1.2124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6426    1.2803    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0180    2.0150    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5694    2.7074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2545    2.6651    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9448    3.4420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4962    4.1344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8716    4.8691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6955    4.9113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1441    4.2189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7687    3.4843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1003    0.5291    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4934    1.2544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7485   -0.4174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5372   -0.1755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0718   -1.1765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0114   -0.8402    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  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  1  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
 14 24  1  0  0  0  0
  5 24  1  0  0  0  0
 10 24  1  0  0  0  0
 24 25  1  1  0  0  0
 12 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 26 29  1  0  0  0  0
 10 29  1  0  0  0  0
M  END

     RDKit          3D

 61 64  0  0  0  0  0  0  0  0999 V2000
    4.0427   -0.4544    2.4808 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1504   -0.0309    1.3821 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9112    1.2070    1.2671 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5625   -0.8797    0.4783 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7140   -0.4204   -0.5573 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5437   -0.6728   -1.8420 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8036   -0.3015   -3.0677 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4211    0.2375   -2.8256 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2146    0.3711   -4.1931 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3756   -0.4636   -1.8098 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3228   -1.5174   -2.3014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3713   -1.3807   -1.1807 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7942   -1.8461    0.1040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4227   -1.3413    0.4430 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4173   -0.1838    1.2185 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0019   -0.0566    2.5129 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4383   -1.0905    3.0945 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0215    1.1905    3.2639 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4164    1.2519    4.5692 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4179    2.3957    5.3246 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0432    3.5590    4.7565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4979    3.5498    3.4370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4810    2.3751    2.7144 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4658   -1.1873   -0.7483 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8340   -2.5982   -1.1671 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4714    0.1236   -1.1679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1555    0.6911   -2.3849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3153    0.5302   -0.0001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1417    0.4778   -1.0800 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7880    0.0712    3.4341 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0737   -0.0974    2.2099 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0955   -1.5417    2.5916 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5504    0.6584   -0.5496 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4745   -0.0673   -1.6768 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8762   -1.7206   -1.9083 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7589   -1.1012   -3.8492 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3826    0.5304   -3.5714 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5731    1.3028   -2.4742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9910    1.1571   -4.2387 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6097    0.7821   -4.8558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4839   -0.5794   -4.6615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7398   -1.3767   -3.2891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9317   -2.5511   -2.2704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2888   -1.9017   -1.4057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7941   -2.9773    0.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4558   -1.6045    0.9579 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0200   -2.1453    1.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7836    0.3364    5.0290 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7839    2.3457    6.3488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0431    4.4623    5.3498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8577    4.4813    3.0092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8343    2.3543    1.6804 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0862   -2.7177   -2.2121 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7870   -2.8287   -0.5963 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1268   -3.3538   -0.7575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9813    0.1986   -3.3242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2646    0.6384   -2.1973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9110    1.7758   -2.4158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1388    1.2613   -0.2845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9239   -0.3569    0.3491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8077    1.0301    0.8228 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5 24  1  0
 24 25  1  6
 24 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10 29  1  1
 29 26  1  0
 26 27  1  0
 26 28  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 10  8  1  0
 23 18  1  0
 10 24  1  0
 26 12  1  0
  9 39  1  0
  9 40  1  0
  9 41  1  0
  8 38  1  1
  7 36  1  0
  7 37  1  0
  6 34  1  0
  6 35  1  0
  5 33  1  1
  1 30  1  0
  1 31  1  0
  1 32  1  0
 25 53  1  0
 25 54  1  0
 25 55  1  0
 14 47  1  1
 13 45  1  0
 13 46  1  0
 12 44  1  6
 11 42  1  0
 11 43  1  0
 27 56  1  0
 27 57  1  0
 27 58  1  0
 28 59  1  0
 28 60  1  0
 28 61  1  0
 19 48  1  0
 20 49  1  0
 21 50  1  0
 22 51  1  0
 23 52  1  0
M  END


  Mrv1652309032209192D          

 29 32  0  0  1  0            999 V2000
    3.5355    2.0462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1509    1.3163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5908    0.6183    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3266    1.2844    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9420    0.5545    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3913   -0.1453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0182   -0.8878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1934   -0.9383    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8439   -1.6856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6930   -0.2588    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0948    0.1310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5832    0.4298    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2150    1.2124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6426    1.2803    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0180    2.0150    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5694    2.7074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2545    2.6651    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9448    3.4420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4962    4.1344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8716    4.8691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6955    4.9113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1441    4.2189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7687    3.4843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1003    0.5291    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4934    1.2544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7485   -0.4174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5372   -0.1755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0718   -1.1765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0114   -0.8402    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  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  1  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
 14 24  1  0  0  0  0
  5 24  1  0  0  0  0
 10 24  1  0  0  0  0
 24 25  1  1  0  0  0
 12 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 26 29  1  0  0  0  0
 10 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0170989

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C24H32O5/c1-15-11-12-19(27-16(2)25)23(5)20(28-21(26)17-9-7-6-8-10-17)13-18-14-24(15,23)29-22(18,3)4/h6-10,15,18-20H,11-14H2,1-5H3/t15-,18-,19+,20+,23+,24+/m1/s1

> <INCHI_KEY>
MDUQZKJGFROTKT-JSJPKNAYSA-N

> <FORMULA>
C24H32O5

> <MOLECULAR_WEIGHT>
400.515

> <EXACT_MASS>
400.22497413

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
43.76340905883089

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

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

> <ALOGPS_LOGP>
4.57

> <JCHEM_LOGP>
4.434534391333333

> <ALOGPS_LOGS>
-5.56

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.213432151411397

> <JCHEM_POLAR_SURFACE_AREA>
61.83

> <JCHEM_REFRACTIVITY>
108.52950000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.10e-03 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       6.600   3.820   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.882   2.457   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       6.703   1.154   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       4.343   2.398   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.625   1.035   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.464  -0.271   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.767  -1.657   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.228  -1.751   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.575  -3.146   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.294  -0.483   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.177   0.245   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.089   0.802   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.401   2.263   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.200   2.390   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.900   3.761   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.063   5.054   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -0.475   4.975   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.764   6.425   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.926   7.718   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.627   9.089   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.165   9.168   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.002   7.875   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.302   6.504   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.054   0.988   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.788   2.341   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.397  -0.779   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.869  -0.328   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.001  -2.196   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       0.021  -1.568   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   24                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   24   29                                             
CONECT   11   10   12                                                       
CONECT   12   11   13   26                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   24                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   18                                                       
CONECT   24   14    5   10   25                                             
CONECT   25   24                                                            
CONECT   26   12   27   28   29                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   26   10                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₂O₅

Average Mass

400.5150 Da

Monoisotopic Mass

400.22497 Da

IUPAC Name

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

Traditional Name

(1S,2R,5S,6S,7S,9R)-5-(acetyloxy)-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]1CC[C@H](OC(C)=O)[C@@]2(C)[C@H](C[C@@H]3C[C@]12OC3(C)C)OC(=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C24H32O5/c1-15-11-12-19(27-16(2)25)23(5)20(28-21(26)17-9-7-6-8-10-17)13-18-14-24(15,23)29-22(18,3)4/h6-10,15,18-20H,11-14H2,1-5H3/t15-,18-,19+,20+,23+,24+/m1/s1

InChI Key

MDUQZKJGFROTKT-JSJPKNAYSA-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 flagellaris	LOTUS Database	35616633
Microtropis fokienensis	LOTUS Database	35616633
Tripterygium wilfordii	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
Benzoate ester
Benzoic acid or derivatives
Benzoyl
Oxepane
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Benzenoid
Tetrahydrofuran
Carboxylic acid ester
Ether
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Organooxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
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	4.57	ALOGPS
logP	4.43	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	61.83 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	108.53 m³·mol⁻¹	ChemAxon
Polarizability	43.76 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

C00040565

Chemspider ID

23279414

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44419629

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,5s,6s,7s,9r)-5-(acetyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate (NP0170989)

MOL for NP0170989 ((1s,2r,5s,6s,7s,9r)-5-(acetyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D MOL for NP0170989 ((1s,2r,5s,6s,7s,9r)-5-(acetyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D SDF for NP0170989 ((1s,2r,5s,6s,7s,9r)-5-(acetyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D-SDF for NP0170989 ((1s,2r,5s,6s,7s,9r)-5-(acetyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

PDB for NP0170989 ((1s,2r,5s,6s,7s,9r)-5-(acetyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D PDB for NP0170989 ((1s,2r,5s,6s,7s,9r)-5-(acetyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

SMILES for NP0170989 ((1s,2r,5s,6s,7s,9r)-5-(acetyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

INCHI for NP0170989 ((1s,2r,5s,6s,7s,9r)-5-(acetyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

Structure for NP0170989 ((1s,2r,5s,6s,7s,9r)-5-(acetyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D Structure for NP0170989 ((1s,2r,5s,6s,7s,9r)-5-(acetyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)