NP-MRD: Showing NP-Card for (2s,3r,4z)-6-[(z)-benzoyloxy]-2-{[(z)-benzoyloxy]methyl}-2,3-dihydroxyhex-4-en-1-yl acetate (NP0211073)

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Record Information

Version

2.0

Created at

2022-09-05 09:10:52 UTC

Updated at

2022-09-05 09:10:52 UTC

NP-MRD ID

NP0211073

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3r,4z)-6-[(z)-benzoyloxy]-2-{[(z)-benzoyloxy]methyl}-2,3-dihydroxyhex-4-en-1-yl acetate

Description

Grandiuvarins B belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid. (2s,3r,4z)-6-[(z)-benzoyloxy]-2-{[(z)-benzoyloxy]methyl}-2,3-dihydroxyhex-4-en-1-yl acetate is found in Uvaria grandiflora. Based on a literature review very few articles have been published on Grandiuvarins B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052211102D          

 31 32  0  0  1  0            999 V2000
   -4.6184   -5.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7934   -5.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3809   -6.6809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3809   -5.2520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5559   -5.2520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -4.5375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7309   -3.8230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -2.0625    0.0000 C   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
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
  6 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 26 31  1  0  0  0  0
M  END

     RDKit          3D

 55 56  0  0  0  0  0  0  0  0999 V2000
   -3.3440   -5.5226   -0.1364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9711   -4.0668    0.0169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6525   -3.4426    0.8440 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0131   -3.4492   -0.6419 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5191   -2.2054   -0.6794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0091   -1.4899    0.4939 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0391   -2.2742    1.1848 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9110   -0.7836    1.4364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8113    0.1107    0.9772 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8998    0.1851    0.2057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3328   -0.8641   -0.3211 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6352    1.4223   -0.0736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7324    1.3885   -0.8733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4087    2.5638   -1.1225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9867    3.7499   -0.5757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8732    3.7608    0.2312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1895    2.5843    0.4854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1143   -0.3255   -0.0420 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0435    0.4720   -0.7526 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9411   -0.7757   -0.9300 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1902   -0.9591   -0.5263 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6709   -0.7346    0.8510 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6992    0.2668    0.8206 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8548    0.0797    0.1050 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0531   -0.9753   -0.5478 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9003    1.1041    0.0760 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7114    2.2824    0.7876 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6680    3.2636    0.7838 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8244    3.0856    0.0726 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0205    1.9054   -0.6438 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0597    0.9152   -0.6425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1190   -5.8949   -1.1376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4335   -5.6647    0.0381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8179   -6.1430    0.6131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0455   -1.4490   -1.3493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5557   -2.3422   -1.3621 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5216   -2.6501    0.4578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1935   -0.1976    2.1537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4570   -1.4878    2.1324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1135    0.4764   -1.3347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2787    2.5828   -1.7473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5151    4.6891   -0.7662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5320    4.6913    0.6674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3061    2.6311    1.1333 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1942    0.2511    0.8463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2161    1.2966   -0.2512 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7022   -0.9633   -1.9939 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8845   -1.3067   -1.3147 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9163   -0.4440    1.5725 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1971   -1.6475    1.2595 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8023    2.4386    1.3551 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4933    4.1599    1.3417 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5743    3.8729    0.0791 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9602    1.8197   -1.1912 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2306    0.0095   -1.2032 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  1
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
  6 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  2  0
 17 12  1  0
 31 26  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  5 35  1  0
  5 36  1  0
  7 37  1  0
  8 38  1  0
  8 39  1  0
 13 40  1  0
 14 41  1  0
 15 42  1  0
 16 43  1  0
 17 44  1  0
 18 45  1  1
 19 46  1  0
 20 47  1  0
 21 48  1  0
 22 49  1  0
 22 50  1  0
 27 51  1  0
 28 52  1  0
 29 53  1  0
 30 54  1  0
 31 55  1  0
M  END


  Mrv1652309052211102D          

 31 32  0  0  1  0            999 V2000
   -4.6184   -5.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7934   -5.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3809   -6.6809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3809   -5.2520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5559   -5.2520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -4.5375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7309   -3.8230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -2.0625    0.0000 C   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
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
  6 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 26 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0211073

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC[C@](O)(COC(=O)C1=CC=CC=C1)[C@H](O)\C=C/COC(=O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H24O8/c1-17(24)30-15-23(28,16-31-22(27)19-11-6-3-7-12-19)20(25)13-8-14-29-21(26)18-9-4-2-5-10-18/h2-13,20,25,28H,14-16H2,1H3/b13-8-/t20-,23+/m1/s1

> <INCHI_KEY>
OCQFOVJTJRPGIU-FFSPDELUSA-N

> <FORMULA>
C23H24O8

> <MOLECULAR_WEIGHT>
428.437

> <EXACT_MASS>
428.147117733

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
42.87322710838977

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3R,4Z)-6-[(Z)-benzoyloxy]-2-{[(Z)-benzoyloxy]methyl}-2,3-dihydroxyhex-4-en-1-yl acetate

> <JCHEM_LOGP>
2.7232585179999997

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.284747583004016

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.192310351447519

> <JCHEM_PKA_STRONGEST_BASIC>
-3.46593492090087

> <JCHEM_POLAR_SURFACE_AREA>
119.36000000000001

> <JCHEM_REFRACTIVITY>
111.77460000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4Z)-6-[(Z)-benzoyloxy]-2-{[(Z)-benzoyloxy]methyl}-2,3-dihydroxyhex-4-en-1-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -8.621 -11.137   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -7.081 -11.137   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -6.311 -12.471   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -6.311  -9.804   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -4.771  -9.804   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.001  -8.470   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -3.231  -7.136   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -2.667 -10.780   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.000 -10.780   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.334 -13.090   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000 -13.860   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000 -15.400   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.334 -16.170   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.667 -15.400   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -6.668  -8.470   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -5.335  -6.160   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -8.002  -6.160   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -9.336  -5.390   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0     -10.669  -6.160   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0     -10.669  -7.700   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0     -12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0     -13.337  -6.160   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0     -14.670  -5.390   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0     -14.670  -3.850   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0     -13.337  -3.080   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0     -12.003  -3.850   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   18                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18    6   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   31                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   26                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₄O₈

Average Mass

428.4370 Da

Monoisotopic Mass

428.14712 Da

IUPAC Name

(2S,3R,4Z)-6-[(Z)-benzoyloxy]-2-{[(Z)-benzoyloxy]methyl}-2,3-dihydroxyhex-4-en-1-yl acetate

Traditional Name

(2S,3R,4Z)-6-[(Z)-benzoyloxy]-2-{[(Z)-benzoyloxy]methyl}-2,3-dihydroxyhex-4-en-1-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC[C@](O)(COC(=O)C1=CC=CC=C1)[C@H](O)\C=C/COC(=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C23H24O8/c1-17(24)30-15-23(28,16-31-22(27)19-11-6-3-7-12-19)20(25)13-8-14-29-21(26)18-9-4-2-5-10-18/h2-13,20,25,28H,14-16H2,1H3/b13-8-/t20-,23+/m1/s1

InChI Key

OCQFOVJTJRPGIU-FFSPDELUSA-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
Uvaria grandiflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Benzoic acid esters

Alternative Parents

Substituents

Benzoate ester
Tricarboxylic acid or derivatives
Benzoyl
Glycerolipid
Tertiary alcohol
Secondary alcohol
Carboxylic acid ester
1,2-diol
Carboxylic acid derivative
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Organic oxide
Organic oxygen compound
Alcohol
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	2.72	ChemAxon
pKa (Strongest Acidic)	12.19	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	119.36 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	111.77 m³·mol⁻¹	ChemAxon
Polarizability	42.87 Å³	ChemAxon
Number of Rings	2	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

Not Available

Chemspider ID

17621647

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16717100

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3r,4z)-6-[(z)-benzoyloxy]-2-{[(z)-benzoyloxy]methyl}-2,3-dihydroxyhex-4-en-1-yl acetate (NP0211073)

MOL for NP0211073 ((2s,3r,4z)-6-[(z)-benzoyloxy]-2-{[(z)-benzoyloxy]methyl}-2,3-dihydroxyhex-4-en-1-yl acetate)

3D MOL for NP0211073 ((2s,3r,4z)-6-[(z)-benzoyloxy]-2-{[(z)-benzoyloxy]methyl}-2,3-dihydroxyhex-4-en-1-yl acetate)

3D SDF for NP0211073 ((2s,3r,4z)-6-[(z)-benzoyloxy]-2-{[(z)-benzoyloxy]methyl}-2,3-dihydroxyhex-4-en-1-yl acetate)

3D-SDF for NP0211073 ((2s,3r,4z)-6-[(z)-benzoyloxy]-2-{[(z)-benzoyloxy]methyl}-2,3-dihydroxyhex-4-en-1-yl acetate)

PDB for NP0211073 ((2s,3r,4z)-6-[(z)-benzoyloxy]-2-{[(z)-benzoyloxy]methyl}-2,3-dihydroxyhex-4-en-1-yl acetate)

3D PDB for NP0211073 ((2s,3r,4z)-6-[(z)-benzoyloxy]-2-{[(z)-benzoyloxy]methyl}-2,3-dihydroxyhex-4-en-1-yl acetate)

SMILES for NP0211073 ((2s,3r,4z)-6-[(z)-benzoyloxy]-2-{[(z)-benzoyloxy]methyl}-2,3-dihydroxyhex-4-en-1-yl acetate)

INCHI for NP0211073 ((2s,3r,4z)-6-[(z)-benzoyloxy]-2-{[(z)-benzoyloxy]methyl}-2,3-dihydroxyhex-4-en-1-yl acetate)

Structure for NP0211073 ((2s,3r,4z)-6-[(z)-benzoyloxy]-2-{[(z)-benzoyloxy]methyl}-2,3-dihydroxyhex-4-en-1-yl acetate)

3D Structure for NP0211073 ((2s,3r,4z)-6-[(z)-benzoyloxy]-2-{[(z)-benzoyloxy]methyl}-2,3-dihydroxyhex-4-en-1-yl acetate)