NP-MRD: Showing NP-Card for Xyloccensin O (NP0081733)

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Record Information

Version

2.0

Created at

2022-04-29 02:48:48 UTC

Updated at

2022-04-29 02:48:49 UTC

NP-MRD ID

NP0081733

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Xyloccensin O

Description

Methyl (2S)-2-(acetyloxy)-2-[(1R,3R,4R,5S,10S,12R,14S,15S,16R,18S,19R,20S,22S)-3,22-bis(acetyloxy)-5-(furan-3-yl)-16-hydroxy-4,12,18,20-tetramethyl-7-oxo-6,11,13,21-tetraoxaheptacyclo[10.8.1.1¹⁵,¹⁸.0¹,¹⁰.0⁴,⁹.0¹⁰,¹⁴.0¹⁶,²⁰]Docos-8-en-19-yl]acetate belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17. Xyloccensin O is found in Xylocarpus granatum . Based on a literature review very few articles have been published on methyl (2S)-2-(acetyloxy)-2-[(1R,3R,4R,5S,10S,12R,14S,15S,16R,18S,19R,20S,22S)-3,22-bis(acetyloxy)-5-(furan-3-yl)-16-hydroxy-4,12,18,20-tetramethyl-7-oxo-6,11,13,21-tetraoxaheptacyclo[10.8.1.1¹⁵,¹⁸.0¹,¹⁰.0⁴,⁹.0¹⁰,¹⁴.0¹⁶,²⁰]Docos-8-en-19-yl]acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292204482D          

 50 57  0  0  1  0            999 V2000
    0.7936   -1.5052    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4031   -0.8535    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3392   -0.7516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7645   -0.0311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4735    0.1174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7899    0.8793    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9752   -0.5376    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6589   -1.2995    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8408   -1.4065    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5018   -2.2860    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3765   -2.2759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9647   -2.9689    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6048   -3.7112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2181   -3.7706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.4537   -0.0586    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3691    0.1510    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8734   -0.4806    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    2.0840    0.6367    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    2.8900    1.8167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9524    2.6393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0748   -0.6879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4437   -0.0051    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8010   -0.8656    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0980   -1.7347    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4179   -1.3464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6176   -0.9833    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  1 11  1  0  0  0  0
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 12 13  1  0  0  0  0
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  9 16  1  1  0  0  0
  8 17  1  1  0  0  0
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 17 21  1  0  0  0  0
  2 22  1  0  0  0  0
 23 22  1  6  0  0  0
 23 24  1  0  0  0  0
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  1 25  1  0  0  0  0
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 30 32  1  0  0  0  0
 27 33  1  0  0  0  0
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 27 34  1  6  0  0  0
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  1 48  1  1  0  0  0
 47 49  1  0  0  0  0
  2 49  1  1  0  0  0
 47 50  1  1  0  0  0
M  END

     RDKit          3D

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 22 70  1  1
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 25 72  1  0
 25 73  1  0
 46 86  1  0
 46 87  1  0
 41 82  1  6
 44 83  1  0
 44 84  1  0
 44 85  1  0
 40 79  1  0
 40 80  1  0
 40 81  1  0
 33 75  1  6
 29 74  1  0
 38 78  1  0
 36 77  1  0
 35 76  1  0
 50 88  1  0
 50 89  1  0
 50 90  1  0
M  END


  Mrv1652304292204482D          

 50 57  0  0  1  0            999 V2000
    0.7936   -1.5052    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4031   -0.8535    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3392   -0.7516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7645   -0.0311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4735    0.1174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7899    0.8793    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9752   -0.5376    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6589   -1.2995    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8408   -1.4065    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5018   -2.2860    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3765   -2.2759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9647   -2.9689    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6048   -3.7112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2181   -3.7706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0676   -4.3941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3509   -2.0549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1605   -1.9544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9853   -1.9335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2600   -2.7114    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6051   -3.2131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9256   -2.7453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4537   -0.0586    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3691    0.1510    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8734   -0.4806    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7480   -1.2296    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6544   -1.0535    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7307    0.0365    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0840    0.6367    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1464    1.4594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8900    1.8167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9524    2.6393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5713    1.3513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8685   -0.5303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4980    0.3397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2723   -1.6002    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0547   -1.3384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6725   -1.8851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4549   -1.6234    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5080   -2.6936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1077   -2.4086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3254   -2.6703    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7256   -2.9553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5611   -3.7637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9414   -2.0316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0748   -0.6879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4437   -0.0051    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8010   -0.8656    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0980   -1.7347    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4179   -1.3464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6176   -0.9833    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  1 11  1  0  0  0  0
 10 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  9 16  1  1  0  0  0
  8 17  1  1  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 17 21  1  0  0  0  0
  2 22  1  0  0  0  0
 23 22  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  1 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 23 28  1  0  0  0  0
 28 29  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 27 33  1  0  0  0  0
 24 33  1  0  0  0  0
 27 34  1  6  0  0  0
 26 35  1  1  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 35 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 25 44  1  1  0  0  0
 24 45  1  1  0  0  0
 22 46  1  1  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
  1 48  1  1  0  0  0
 47 49  1  0  0  0  0
  2 49  1  1  0  0  0
 47 50  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0081733

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@H](OC(C)=O)[C@@H]1[C@]2(C)C[C@@]3(O)[C@@H]([C@@H]2OC(C)=O)[C@@H]2O[C@]4(C)O[C@]5(C[C@@H](OC(C)=O)[C@]6(C)[C@H](OC(=O)C=C6[C@]25O4)C2=COC=C2)[C@@]13C

> <INCHI_IDENTIFIER>
InChI=1S/C35H40O15/c1-15(36)44-20-12-34-31(6)24(23(28(40)42-8)45-16(2)37)29(4)14-33(31,41)22(26(29)46-17(3)38)27-35(34,50-32(7,48-27)49-34)19-11-21(39)47-25(30(19,20)5)18-9-10-43-13-18/h9-11,13,20,22-27,41H,12,14H2,1-8H3/t20-,22+,23+,24-,25-,26+,27+,29+,30-,31+,32-,33-,34-,35+/m1/s1

> <INCHI_KEY>
OPGFYBVPXMGZOY-XIFGAUCQSA-N

> <FORMULA>
C35H40O15

> <MOLECULAR_WEIGHT>
700.69

> <EXACT_MASS>
700.236720588

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
90

> <JCHEM_AVERAGE_POLARIZABILITY>
67.91500674009745

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (2S)-2-(acetyloxy)-2-[(1R,3R,4R,5S,10S,12R,14S,15S,16R,18S,19R,20S,22S)-3,22-bis(acetyloxy)-5-(furan-3-yl)-16-hydroxy-4,12,18,20-tetramethyl-7-oxo-6,11,13,21-tetraoxaheptacyclo[10.8.1.1^{15,18}.0^{1,10}.0^{4,9}.0^{10,14}.0^{16,20}]docos-8-en-19-yl]acetate

> <ALOGPS_LOGP>
2.54

> <JCHEM_LOGP>
1.2241909663333332

> <ALOGPS_LOGS>
-3.38

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.889190940894565

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8622293090915494

> <JCHEM_POLAR_SURFACE_AREA>
192.55999999999997

> <JCHEM_REFRACTIVITY>
161.33420000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.94e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(S)-(methyl (acetyloxy)[(1R,3R,4R,5S,10S,12R,14S,15S,16R,18S,19R,20S,22S)-3,22-bis(acetyloxy)-5-(furan-3-yl)-16-hydroxy-4,12,18,20-tetramethyl-7-oxo-6,11,13,21-tetraoxaheptacyclo[10.8.1.1^{15,18}.0^{1,10}.0^{4,9}.0^{10,14}.0^{16,20}]docos-8-en-19-yl]acetate)

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       1.481  -2.810   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.753  -1.593   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.633  -1.403   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.427  -0.058   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.751   0.219   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -3.341   1.641   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      -3.687  -1.003   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -3.097  -2.426   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.570  -2.625   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.937  -4.267   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.703  -4.248   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.801  -5.542   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -1.129  -6.928   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       0.407  -7.039   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -1.993  -8.202   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.522  -3.836   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.033  -3.648   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.573  -3.609   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -6.085  -5.061   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -4.863  -5.998   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.594  -5.124   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.847  -0.109   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.556   0.282   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.497  -0.897   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.263  -2.295   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.955  -1.966   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.097   0.068   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.890   1.189   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.007   2.724   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       5.395   3.391   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       5.511   4.927   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       6.666   2.522   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.355  -0.990   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.530   0.634   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.108  -2.987   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       7.569  -2.498   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       8.722  -3.519   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      10.182  -3.030   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       8.415  -5.028   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       5.801  -4.496   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       4.341  -4.985   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       6.954  -5.517   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       6.647  -7.026   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       3.624  -3.792   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       2.006  -1.284   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0      -0.828  -0.010   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      -1.495  -1.616   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      -0.183  -3.238   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0      -0.780  -2.513   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      -3.019  -1.836   0.000  0.00  0.00           C+0
CONECT    1    2   11   25   48                                             
CONECT    2    1    3   22   49                                             
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   17                                                  
CONECT    9    8    3   10   16                                             
CONECT   10    9   11   12                                                  
CONECT   11   10    1                                                       
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16    9                                                            
CONECT   17    8   18   21                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   17                                                       
CONECT   22    2   23   46                                                  
CONECT   23   22   24   28                                                  
CONECT   24   23   25   33   45                                             
CONECT   25   24    1   26   44                                             
CONECT   26   25   27   35                                                  
CONECT   27   26   28   33   34                                             
CONECT   28   27   23   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   27   24                                                       
CONECT   34   27                                                            
CONECT   35   26   36   40                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37                                                            
CONECT   40   35   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43                                                       
CONECT   43   42                                                            
CONECT   44   25                                                            
CONECT   45   24                                                            
CONECT   46   22   47                                                       
CONECT   47   46   48   49   50                                             
CONECT   48   47    1                                                       
CONECT   49   47    2                                                       
CONECT   50   47                                                            
MASTER        0    0    0    0    0    0    0    0   50    0  114    0
END

View in JSmol

Synonyms

Value	Source
Methyl (2S)-2-(acetyloxy)-2-[(1R,3R,4R,5S,10S,12R,14S,15S,16R,18S,19R,20S,22S)-3,22-bis(acetyloxy)-5-(furan-3-yl)-16-hydroxy-4,12,18,20-tetramethyl-7-oxo-6,11,13,21-tetraoxaheptacyclo[10.8.1.1,.0,.0,.0,.0,]docos-8-en-19-yl]acetic acid	Generator

Chemical Formula

C₃₅H₄₀O₁₅

Average Mass

700.6900 Da

Monoisotopic Mass

700.23672 Da

IUPAC Name

methyl (2S)-2-(acetyloxy)-2-[(1R,3R,4R,5S,10S,12R,14S,15S,16R,18S,19R,20S,22S)-3,22-bis(acetyloxy)-5-(furan-3-yl)-16-hydroxy-4,12,18,20-tetramethyl-7-oxo-6,11,13,21-tetraoxaheptacyclo[10.8.1.1^{15,18}.0^{1,10}.0^{4,9}.0^{10,14}.0^{16,20}]docos-8-en-19-yl]acetate

Traditional Name

(S)-(methyl (acetyloxy)[(1R,3R,4R,5S,10S,12R,14S,15S,16R,18S,19R,20S,22S)-3,22-bis(acetyloxy)-5-(furan-3-yl)-16-hydroxy-4,12,18,20-tetramethyl-7-oxo-6,11,13,21-tetraoxaheptacyclo[10.8.1.1^{15,18}.0^{1,10}.0^{4,9}.0^{10,14}.0^{16,20}]docos-8-en-19-yl]acetate)

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@H](OC(C)=O)[C@@H]1[C@]2(C)C[C@@]3(O)[C@@H]([C@@H]2OC(C)=O)[C@@H]2O[C@]4(C)O[C@]5(C[C@@H](OC(C)=O)[C@]6(C)[C@H](OC(=O)C=C6[C@]25O4)C2=COC=C2)[C@@]13C

InChI Identifier

InChI=1S/C35H40O15/c1-15(36)44-20-12-34-31(6)24(23(28(40)42-8)45-16(2)37)29(4)14-33(31,41)22(26(29)46-17(3)38)27-35(34,50-32(7,48-27)49-34)19-11-21(39)47-25(30(19,20)5)18-9-10-43-13-18/h9-11,13,20,22-27,41H,12,14H2,1-8H3/t20-,22+,23+,24-,25-,26+,27+,29+,30-,31+,32-,33-,34-,35+/m1/s1

InChI Key

OPGFYBVPXMGZOY-XIFGAUCQSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Xylocarpus granatum	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Limonoids

Alternative Parents

Substituents

Mexicanolide
Limonoid skeleton
Pentacarboxylic acid or derivatives
Naphthopyran
Naphthalene
Ortho ester
Dihydropyranone
Carboxylic acid orthoester
Pyran
Meta-dioxane
Heteroaromatic compound
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Tertiary alcohol
Furan
Cyclic alcohol
Meta-dioxolane
Orthocarboxylic acid derivative
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	2.54	ALOGPS
logP	1.22	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	13.89	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	192.56 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	161.33 m³·mol⁻¹	ChemAxon
Polarizability	67.92 Å³	ChemAxon
Number of Rings	8	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

163105411

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Xyloccensin O (NP0081733)

MOL for NP0081733 (Xyloccensin O)

3D MOL for NP0081733 (Xyloccensin O)

3D SDF for NP0081733 (Xyloccensin O)

3D-SDF for NP0081733 (Xyloccensin O)

PDB for NP0081733 (Xyloccensin O)

3D PDB for NP0081733 (Xyloccensin O)

SMILES for NP0081733 (Xyloccensin O)

INCHI for NP0081733 (Xyloccensin O)

Structure for NP0081733 (Xyloccensin O)

3D Structure for NP0081733 (Xyloccensin O)