NP-MRD: Showing NP-Card for (2s,3r,4r,5r,6s)-2-{[(2r,3r,4s,5r,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[18-(2-hydroxypropan-2-yl)-2,6,6,10,16-pentamethyl-17,21,23-trioxaheptacyclo[20.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁶,²⁰]pentacosan-7-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol (NP0268782)

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Record Information

Version

2.0

Created at

2022-09-08 14:01:10 UTC

Updated at

2022-09-08 14:01:11 UTC

NP-MRD ID

NP0268782

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3r,4r,5r,6s)-2-{[(2r,3r,4s,5r,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[18-(2-hydroxypropan-2-yl)-2,6,6,10,16-pentamethyl-17,21,23-trioxaheptacyclo[20.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁶,²⁰]pentacosan-7-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol

Description

(2S,3R,4R,5R,6S)-2-{[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[18-(2-hydroxypropan-2-yl)-2,6,6,10,16-pentamethyl-17,21,23-trioxaheptacyclo[20.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁶,²⁰]Pentacosan-7-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (2s,3r,4r,5r,6s)-2-{[(2r,3r,4s,5r,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[18-(2-hydroxypropan-2-yl)-2,6,6,10,16-pentamethyl-17,21,23-trioxaheptacyclo[20.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁶,²⁰]pentacosan-7-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol is found in Ziziphus jujuba. Based on a literature review very few articles have been published on (2S,3R,4R,5R,6S)-2-{[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[18-(2-hydroxypropan-2-yl)-2,6,6,10,16-pentamethyl-17,21,23-trioxaheptacyclo[20.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁶,²⁰]Pentacosan-7-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082216012D          

 56 64  0  0  1  0            999 V2000
    9.6504   -2.3178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3059   -1.5681    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.4845   -1.4916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1400   -0.7420    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3186   -0.6655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8416   -1.3386    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1861   -2.0883    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.0075   -2.1648    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7091   -2.7614    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0535   -3.5111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8876   -2.6849    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4107   -3.3580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5892   -3.2815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5432   -1.9353    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0202   -1.2621    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6757   -0.5125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5558   -1.0326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2114   -0.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7344   -0.9561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6883    0.3902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3439    1.1398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5224    1.2163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0454    0.5432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7317    1.3062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3899   -0.2064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9247   -0.9020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1031   -0.8551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0153    0.0715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0112    0.9139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9611    1.1784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2343    0.6858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9704    1.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0903    1.7329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8719    1.0227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3371    0.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0929   -0.0048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.1765   -0.7574    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2059   -1.0023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7890   -0.2905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2331   -0.9001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5098    0.3137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6149    1.1320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2469    0.6841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6170   -0.0689    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    9.4384   -0.1454    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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   10.6044   -0.9715    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 20 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 30 34  1  0  0  0  0
 25 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 32 36  1  0  0  0  0
 32 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 41 44  1  0  0  0  0
 40 45  1  0  0  0  0
 45 46  1  0  0  0  0
 38 46  1  0  0  0  0
 31 46  1  0  0  0  0
 46 47  1  0  0  0  0
 22 48  1  0  0  0  0
 17 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
  4 51  1  0  0  0  0
 51 52  1  6  0  0  0
 51 53  1  0  0  0  0
 53 54  1  6  0  0  0
 53 55  1  0  0  0  0
  2 55  1  0  0  0  0
 55 56  1  1  0  0  0
M  END

     RDKit          3D

124132  0  0  0  0  0  0  0  0999 V2000
   -4.5238    2.2210   -2.4598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5633    2.8291   -1.5429 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -7.3627   -4.1182    1.9523 O   0  0  0  0  0  0  0  0  0  0  0  0
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   10.2283   -0.4844   -1.4242 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309082216012D          

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M  END
> <DATABASE_ID>
NP0268782

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]2OC2CCC3(C)C(CCC4(C)C3CCC3C5C6(C)OC(CC6OC55CC43CO5)C(C)(C)O)C2(C)C)[C@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C42H68O14/c1-19-27(44)29(46)31(48)34(51-19)54-32-30(47)28(45)21(16-43)52-35(32)53-24-12-13-38(6)22(36(24,2)3)11-14-39(7)23(38)10-9-20-33-40(8)26(15-25(55-40)37(4,5)49)56-42(33)17-41(20,39)18-50-42/h19-35,43-49H,9-18H2,1-8H3/t19-,20?,21+,22?,23?,24?,25?,26?,27-,28-,29+,30-,31+,32+,33?,34-,35-,38?,39?,40?,41?,42?/m0/s1

> <INCHI_KEY>
UVECFACYEYHBAX-GRNQANPSSA-N

> <FORMULA>
C42H68O14

> <MOLECULAR_WEIGHT>
796.992

> <EXACT_MASS>
796.46090687

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
124

> <JCHEM_AVERAGE_POLARIZABILITY>
87.64664827869588

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,4R,5R,6S)-2-{[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[18-(2-hydroxypropan-2-yl)-2,6,6,10,16-pentamethyl-17,21,23-trioxaheptacyclo[20.2.1.0^{1,14}.0^{2,11}.0^{5,10}.0^{15,22}.0^{16,20}]pentacosan-7-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol

> <JCHEM_LOGP>
1.6037687973333319

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
9

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.711991264344295

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.097656809671786

> <JCHEM_PKA_STRONGEST_BASIC>
-2.98108376939566

> <JCHEM_POLAR_SURFACE_AREA>
206.21999999999997

> <JCHEM_REFRACTIVITY>
196.77780000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4R,5R,6S)-2-{[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[18-(2-hydroxypropan-2-yl)-2,6,6,10,16-pentamethyl-17,21,23-trioxaheptacyclo[20.2.1.0^{1,14}.0^{2,11}.0^{5,10}.0^{15,22}.0^{16,20}]pentacosan-7-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      18.014  -4.327   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      17.371  -2.927   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      15.838  -2.784   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      15.195  -1.385   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      13.661  -1.242   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      12.771  -2.499   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.414  -3.898   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      14.947  -4.041   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      12.524  -5.155   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      13.167  -6.554   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      10.990  -5.012   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.100  -6.268   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       8.567  -6.126   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      10.347  -3.612   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      11.238  -2.356   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      10.595  -0.957   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       9.061  -0.814   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.171  -2.070   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.638  -1.928   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.995  -0.528   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.104  -1.785   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.885   0.728   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.242   2.128   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.709   2.271   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.818   1.014   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.232   2.438   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.461  -0.385   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.593  -1.684   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.059  -1.596   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.471  -0.164   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -0.029   0.133   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.021   1.706   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.794   2.200   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.304   1.280   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       1.811   3.231   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       0.169   3.235   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      -1.628   1.909   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -2.496   0.609   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -3.907  -0.009   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -3.755  -1.541   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -4.906  -2.565   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -6.057  -3.588   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -3.883  -3.716   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      -5.930  -1.414   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0      -2.251  -1.871   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      -1.473  -0.542   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -0.435  -1.680   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       8.418   0.586   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       8.614   2.113   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       9.794   1.277   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      16.085  -0.129   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      15.442   1.271   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0      17.618  -0.271   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0      18.509   0.985   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0      18.261  -1.671   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0      19.795  -1.813   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   55                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   51                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   15                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11   15                                                       
CONECT   15   14    6   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   48                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22   27                                             
CONECT   21   20                                                            
CONECT   22   20   23   48                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27   34                                             
CONECT   26   25                                                            
CONECT   27   25   20   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   34                                                  
CONECT   31   30   32   46                                                  
CONECT   32   31   33   36   37                                             
CONECT   33   32   34                                                       
CONECT   34   33   30   25   35                                             
CONECT   35   34   36                                                       
CONECT   36   35   32                                                       
CONECT   37   32   38                                                       
CONECT   38   37   39   46                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41   45                                                  
CONECT   41   40   42   43   44                                             
CONECT   42   41                                                            
CONECT   43   41                                                            
CONECT   44   41                                                            
CONECT   45   40   46                                                       
CONECT   46   45   38   31   47                                             
CONECT   47   46                                                            
CONECT   48   22   17   49   50                                             
CONECT   49   48                                                            
CONECT   50   48                                                            
CONECT   51    4   52   53                                                  
CONECT   52   51                                                            
CONECT   53   51   54   55                                                  
CONECT   54   53                                                            
CONECT   55   53    2   56                                                  
CONECT   56   55                                                            
MASTER        0    0    0    0    0    0    0    0   56    0  128    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₂H₆₈O₁₄

Average Mass

796.9920 Da

Monoisotopic Mass

796.46091 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]2OC2CCC3(C)C(CCC4(C)C3CCC3C5C6(C)OC(CC6OC55CC43CO5)C(C)(C)O)C2(C)C)[C@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C42H68O14/c1-19-27(44)29(46)31(48)34(51-19)54-32-30(47)28(45)21(16-43)52-35(32)53-24-12-13-38(6)22(36(24,2)3)11-14-39(7)23(38)10-9-20-33-40(8)26(15-25(55-40)37(4,5)49)56-42(33)17-41(20,39)18-50-42/h19-35,43-49H,9-18H2,1-8H3/t19-,20?,21+,22?,23?,24?,25?,26?,27-,28-,29+,30-,31+,32+,33?,34-,35-,38?,39?,40?,41?,42?/m0/s1

InChI Key

UVECFACYEYHBAX-GRNQANPSSA-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
Ziziphus jujuba	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Steroid
17-oxasteroid
Naphthopyran
O-glycosyl compound
Glycosyl compound
Disaccharide
Naphthalene
Furopyran
Furofuran
Ketal
Pyran
Oxane
Tetrahydrofuran
Tertiary alcohol
Furan
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Polyol
Ether
Dialkyl ether
Acetal
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source

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

5318720

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

MOL for NP0268782 ((2s,3r,4r,5r,6s)-2-{[(2r,3r,4s,5r,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[18-(2-hydroxypropan-2-yl)-2,6,6,10,16-pentamethyl-17,21,23-trioxaheptacyclo[20.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁶,²⁰]pentacosan-7-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol)

3D MOL for NP0268782 ((2s,3r,4r,5r,6s)-2-{[(2r,3r,4s,5r,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[18-(2-hydroxypropan-2-yl)-2,6,6,10,16-pentamethyl-17,21,23-trioxaheptacyclo[20.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁶,²⁰]pentacosan-7-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol)

3D SDF for NP0268782 ((2s,3r,4r,5r,6s)-2-{[(2r,3r,4s,5r,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[18-(2-hydroxypropan-2-yl)-2,6,6,10,16-pentamethyl-17,21,23-trioxaheptacyclo[20.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁶,²⁰]pentacosan-7-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol)

3D-SDF for NP0268782 ((2s,3r,4r,5r,6s)-2-{[(2r,3r,4s,5r,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[18-(2-hydroxypropan-2-yl)-2,6,6,10,16-pentamethyl-17,21,23-trioxaheptacyclo[20.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁶,²⁰]pentacosan-7-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol)

PDB for NP0268782 ((2s,3r,4r,5r,6s)-2-{[(2r,3r,4s,5r,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[18-(2-hydroxypropan-2-yl)-2,6,6,10,16-pentamethyl-17,21,23-trioxaheptacyclo[20.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁶,²⁰]pentacosan-7-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol)

3D PDB for NP0268782 ((2s,3r,4r,5r,6s)-2-{[(2r,3r,4s,5r,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[18-(2-hydroxypropan-2-yl)-2,6,6,10,16-pentamethyl-17,21,23-trioxaheptacyclo[20.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁶,²⁰]pentacosan-7-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol)

SMILES for NP0268782 ((2s,3r,4r,5r,6s)-2-{[(2r,3r,4s,5r,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[18-(2-hydroxypropan-2-yl)-2,6,6,10,16-pentamethyl-17,21,23-trioxaheptacyclo[20.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁶,²⁰]pentacosan-7-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol)

INCHI for NP0268782 ((2s,3r,4r,5r,6s)-2-{[(2r,3r,4s,5r,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[18-(2-hydroxypropan-2-yl)-2,6,6,10,16-pentamethyl-17,21,23-trioxaheptacyclo[20.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁶,²⁰]pentacosan-7-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol)

Structure for NP0268782 ((2s,3r,4r,5r,6s)-2-{[(2r,3r,4s,5r,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[18-(2-hydroxypropan-2-yl)-2,6,6,10,16-pentamethyl-17,21,23-trioxaheptacyclo[20.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁶,²⁰]pentacosan-7-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol)