NP-MRD: Showing NP-Card for (1r,4r,5s,6s)-4-(benzoyloxy)-5-[(benzoyloxy)methyl]-5,6-dihydroxycyclohex-2-en-1-yl benzoate (NP0286327)

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Record Information

Version

2.0

Created at

2022-09-09 14:51:12 UTC

Updated at

2022-09-09 14:51:12 UTC

NP-MRD ID

NP0286327

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,4r,5s,6s)-4-(benzoyloxy)-5-[(benzoyloxy)methyl]-5,6-dihydroxycyclohex-2-en-1-yl benzoate

Description

Ferrudiol belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid. (1r,4r,5s,6s)-4-(benzoyloxy)-5-[(benzoyloxy)methyl]-5,6-dihydroxycyclohex-2-en-1-yl benzoate was first documented in 2006 (PMID: 16833018). Based on a literature review very few articles have been published on Ferrudiol (PMID: 35176917).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092216512D          

 36 39  0  0  1  0            999 V2000
    4.1666    2.1327    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4488    1.3575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9185    0.7255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2007   -0.0498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6704   -0.6817    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1401   -0.0498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3848   -1.0942    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0993   -0.6817    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3848   -1.9192    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0993   -2.3317    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0993   -3.1567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3848   -3.5692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8138   -3.5692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5282   -3.1567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2427   -3.5692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2427   -4.3942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5282   -4.8067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8138   -4.3942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6704   -2.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -1.9192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -1.0942    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2414   -0.6817    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5269   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5269   -1.9192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8125   -0.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0980   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6165   -0.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6165    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0980    0.5558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8125    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2612    1.2142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7915    1.8462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6040    1.7029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8862    0.9277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3559    0.2957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5434    0.4390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
  9 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
  5 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 25 30  1  0  0  0  0
  2 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 31 36  1  0  0  0  0
M  END

     RDKit          3D

 60 63  0  0  0  0  0  0  0  0999 V2000
   -1.4035   -2.8030    0.8707 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4556   -2.2049    0.5696 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.4696    0.0510    0.0785 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5357   -0.0496   -1.0749 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -0.3467   -2.3068   -1.8332 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6007   -0.9577   -1.9697 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6969   -0.7737   -1.0845 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7774   -1.6223   -1.0392 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7814   -2.6017   -1.8232 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8933   -1.4172   -0.1235 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9388   -0.3581    0.7587 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0033   -0.1654    1.6298 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0481   -1.0542    1.6179 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0098   -2.1153    0.7390 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9501   -2.3024   -0.1243 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4697    0.1430   -2.9327 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8233    1.2649   -2.5393 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3112    1.2337   -1.1364 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3616    2.3674   -0.7297 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0329    3.1775    0.3339 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9706    2.8793    1.0162 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8034    4.3533    0.6861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4206    5.1199    1.7604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1269    6.2596    2.1406 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2548    6.6489    1.4243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6358    5.8941    0.3627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9245    4.7565   -0.0109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7125   -2.9867    0.6108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9312   -2.4222    0.2967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1088   -3.1424    0.3321 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0996   -4.4740    0.6898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8865   -5.0467    1.0054 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7142   -4.3179    0.9670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0395    1.0275   -0.0979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9070    0.2921    1.0377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2482   -0.4603   -2.0058 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6663   -1.5764   -0.1669 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1403   -3.1175   -1.5236 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8106   -1.8890   -2.5761 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1005    0.3450    0.7599 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9921    0.6826    2.3042 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8799   -0.9015    2.3003 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8282   -2.8190    0.7238 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9428   -3.1577   -0.8170 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8570    0.0938   -3.9114 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7003    2.0724   -3.1688 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1770    1.0522   -0.4768 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4683    4.8303    2.3408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8000    6.8444    2.9936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7594    7.5417    1.7687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5055    6.1728   -0.2096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2253    4.1464   -0.8619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9400   -1.3871    0.0184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0736   -2.7010    0.0850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0323   -5.0480    0.7188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8850   -6.0843    1.2834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7527   -4.7841    1.2203 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
  7  9  1  0
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 11 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
  9 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  2  0
 21  5  1  0
  5  6  1  6
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  0
  2 31  1  0
 31 32  2  0
 32 33  1  0
 33 34  2  0
 34 35  1  0
 35 36  2  0
  5  7  1  0
 36 31  1  0
 18 13  1  0
 30 25  1  0
  8 41  1  0
  7 40  1  1
  9 42  1  6
 14 43  1  0
 15 44  1  0
 16 45  1  0
 17 46  1  0
 18 47  1  0
 19 48  1  0
 20 49  1  0
 21 50  1  1
 26 51  1  0
 27 52  1  0
 28 53  1  0
 29 54  1  0
 30 55  1  0
  6 39  1  0
  4 37  1  0
  4 38  1  0
 32 56  1  0
 33 57  1  0
 34 58  1  0
 35 59  1  0
 36 60  1  0
M  END


  Mrv1652309092216512D          

 36 39  0  0  1  0            999 V2000
    4.1666    2.1327    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4488    1.3575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9185    0.7255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2007   -0.0498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6704   -0.6817    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1401   -0.0498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3848   -1.0942    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0993   -0.6817    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3848   -1.9192    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0993   -2.3317    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0993   -3.1567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3848   -3.5692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.8138   -4.3942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6704   -2.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -1.9192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -1.0942    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2414   -0.6817    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5269   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5269   -1.9192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8125   -0.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0980   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6165   -0.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6165    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0980    0.5558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8125    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2612    1.2142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7915    1.8462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6040    1.7029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8862    0.9277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3559    0.2957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5434    0.4390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
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 29 30  2  0  0  0  0
 25 30  1  0  0  0  0
  2 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 31 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0286327

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@H]1[C@H](OC(=O)C2=CC=CC=C2)C=C[C@@H](OC(=O)C2=CC=CC=C2)[C@]1(O)COC(=O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C28H24O8/c29-24-22(35-26(31)20-12-6-2-7-13-20)16-17-23(36-27(32)21-14-8-3-9-15-21)28(24,33)18-34-25(30)19-10-4-1-5-11-19/h1-17,22-24,29,33H,18H2/t22-,23-,24+,28-/m1/s1

> <INCHI_KEY>
UEYWXBQABUNMMN-QUIZSENMSA-N

> <FORMULA>
C28H24O8

> <MOLECULAR_WEIGHT>
488.492

> <EXACT_MASS>
488.147117733

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
50.12392027910565

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,4R,5S,6S)-4-(benzoyloxy)-5-[(benzoyloxy)methyl]-5,6-dihydroxycyclohex-2-en-1-yl benzoate

> <JCHEM_LOGP>
4.725442152999999

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.643992710107057

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.908854824458748

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7553891329609543

> <JCHEM_POLAR_SURFACE_AREA>
119.36000000000001

> <JCHEM_REFRACTIVITY>
129.81650000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4R,5S,6S)-4-(benzoyloxy)-5-[(benzoyloxy)methyl]-5,6-dihydroxycyclohex-2-en-1-yl benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  O   UNK     0       7.778   3.981   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       8.304   2.534   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       7.315   1.354   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       7.841  -0.093   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.851  -1.273   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.861  -0.093   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       8.185  -2.043   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       9.519  -1.273   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       8.185  -3.583   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       9.519  -4.353   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       9.519  -5.893   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.185  -6.663   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      10.852  -6.663   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.186  -5.893   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.520  -6.663   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.520  -8.203   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.186  -8.973   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.852  -8.203   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.851  -4.353   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.518  -3.583   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.518  -2.043   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.184  -1.273   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.850  -2.043   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.850  -3.583   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.517  -1.273   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.183  -2.043   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.151  -1.273   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.151   0.267   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.183   1.037   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.517   0.267   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.821   2.267   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.811   3.446   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      12.327   3.179   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      12.854   1.732   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      11.864   0.552   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      10.348   0.819   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   31                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7   21                                             
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   19                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   13                                                       
CONECT   19    9   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20    5   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   25                                                       
CONECT   31    2   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   31                                                       
MASTER        0    0    0    0    0    0    0    0   36    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₂₄O₈

Average Mass

488.4920 Da

Monoisotopic Mass

488.14712 Da

IUPAC Name

(1R,4R,5S,6S)-4-(benzoyloxy)-5-[(benzoyloxy)methyl]-5,6-dihydroxycyclohex-2-en-1-yl benzoate

Traditional Name

(1R,4R,5S,6S)-4-(benzoyloxy)-5-[(benzoyloxy)methyl]-5,6-dihydroxycyclohex-2-en-1-yl benzoate

CAS Registry Number

Not Available

SMILES

O[C@H]1[C@H](OC(=O)C2=CC=CC=C2)C=C[C@@H](OC(=O)C2=CC=CC=C2)[C@]1(O)COC(=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C28H24O8/c29-24-22(35-26(31)20-12-6-2-7-13-20)16-17-23(36-27(32)21-14-8-3-9-15-21)28(24,33)18-34-25(30)19-10-4-1-5-11-19/h1-17,22-24,29,33H,18H2/t22-,23-,24+,28-/m1/s1

InChI Key

UEYWXBQABUNMMN-QUIZSENMSA-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

Not Available

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
Cyclitol or derivatives
Tertiary alcohol
Secondary alcohol
Carboxylic acid ester
1,2-diol
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen 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	4.73	ChemAxon
pKa (Strongest Acidic)	11.91	ChemAxon
pKa (Strongest Basic)	-3.8	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	10	ChemAxon
Refractivity	129.82 m³·mol⁻¹	ChemAxon
Polarizability	50.12 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

100853802

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Teerapongpisan P, Suthiphasilp V, Maneerat T, Charoensup R, Duangyod T, Andersen RJ, Laphookhieo S: alpha-Glucosidase inhibitory and alpha-amylase inhibitory activities of compounds isolated from Uvaria rufa Blume. Nat Prod Res. 2022 Dec;36(23):6039-6043. doi: 10.1080/14786419.2022.2041010. Epub 2022 Feb 17. [PubMed:35176917 ]
Wirasathien L, Pengsuparp T, Moriyasu M, Kawanishi K, Suttisri R: Cytotoxic C-benzylated chalcone and other constituents of Ellipeiopsis cherrevensis. Arch Pharm Res. 2006 Jun;29(6):497-502. doi: 10.1007/BF02969423. [PubMed:16833018 ]
LOTUS database [Link]

Showing NP-Card for (1r,4r,5s,6s)-4-(benzoyloxy)-5-[(benzoyloxy)methyl]-5,6-dihydroxycyclohex-2-en-1-yl benzoate (NP0286327)

MOL for NP0286327 ((1r,4r,5s,6s)-4-(benzoyloxy)-5-[(benzoyloxy)methyl]-5,6-dihydroxycyclohex-2-en-1-yl benzoate)

3D MOL for NP0286327 ((1r,4r,5s,6s)-4-(benzoyloxy)-5-[(benzoyloxy)methyl]-5,6-dihydroxycyclohex-2-en-1-yl benzoate)

3D SDF for NP0286327 ((1r,4r,5s,6s)-4-(benzoyloxy)-5-[(benzoyloxy)methyl]-5,6-dihydroxycyclohex-2-en-1-yl benzoate)

3D-SDF for NP0286327 ((1r,4r,5s,6s)-4-(benzoyloxy)-5-[(benzoyloxy)methyl]-5,6-dihydroxycyclohex-2-en-1-yl benzoate)

PDB for NP0286327 ((1r,4r,5s,6s)-4-(benzoyloxy)-5-[(benzoyloxy)methyl]-5,6-dihydroxycyclohex-2-en-1-yl benzoate)

3D PDB for NP0286327 ((1r,4r,5s,6s)-4-(benzoyloxy)-5-[(benzoyloxy)methyl]-5,6-dihydroxycyclohex-2-en-1-yl benzoate)

SMILES for NP0286327 ((1r,4r,5s,6s)-4-(benzoyloxy)-5-[(benzoyloxy)methyl]-5,6-dihydroxycyclohex-2-en-1-yl benzoate)

INCHI for NP0286327 ((1r,4r,5s,6s)-4-(benzoyloxy)-5-[(benzoyloxy)methyl]-5,6-dihydroxycyclohex-2-en-1-yl benzoate)

Structure for NP0286327 ((1r,4r,5s,6s)-4-(benzoyloxy)-5-[(benzoyloxy)methyl]-5,6-dihydroxycyclohex-2-en-1-yl benzoate)

3D Structure for NP0286327 ((1r,4r,5s,6s)-4-(benzoyloxy)-5-[(benzoyloxy)methyl]-5,6-dihydroxycyclohex-2-en-1-yl benzoate)