NP-MRD: Showing NP-Card for 4-{2-[4-(acetyloxy)-3,5-dimethoxyphenyl]ethyl}-2-methoxyphenyl acetate (NP0165313)

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Record Information

Version

2.0

Created at

2022-09-03 00:24:45 UTC

Updated at

2022-09-03 00:24:46 UTC

NP-MRD ID

NP0165313

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-{2-[4-(acetyloxy)-3,5-dimethoxyphenyl]ethyl}-2-methoxyphenyl acetate

Description

Moscatilin diacetate belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids. 4-{2-[4-(acetyloxy)-3,5-dimethoxyphenyl]ethyl}-2-methoxyphenyl acetate is found in Dendrobium loddigesii. 4-{2-[4-(acetyloxy)-3,5-dimethoxyphenyl]ethyl}-2-methoxyphenyl acetate was first documented in 1994 (PMID: 7798962). Based on a literature review very few articles have been published on moscatilin diacetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032202242D          

 28 29  0  0  0  0            999 V2000
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   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
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 O   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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  2  0  0  0  0
  8 21  1  0  0  0  0
  5 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
  3 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
M  END

     RDKit          3D

 52 53  0  0  0  0  0  0  0  0999 V2000
    4.6311   -2.8151   -0.3325 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8300   -2.0596    0.8436 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9862   -1.0166    1.2104 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8979   -0.6586    0.4414 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0528    0.3710    0.7893 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8755    0.7492   -0.0446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3188   -0.0580    0.4626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5525    0.2347   -0.3036 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8940   -0.5108   -1.4330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0340   -0.2569   -2.1590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3370   -1.0294   -3.2849 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4697   -2.0833   -3.6885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8978    0.7549   -1.7993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0600    1.0312   -2.5185 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2578    0.4478   -2.1309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5422    0.7000   -2.8558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2260   -0.3147   -1.1302 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5718    1.4995   -0.6846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4203    2.5127   -0.3101 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2555    3.3659    0.7834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4193    1.2456    0.0522 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2890    1.0709    1.9339 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3884    0.7141    2.7172 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2395   -0.3204    2.3700 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3223   -0.6331    3.1909 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5630   -0.0556    3.0714 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7256   -0.3802    3.9393 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7404    0.8142    2.1630 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3575   -2.1093   -1.1678 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5686   -3.3594   -0.5999 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7830   -3.5236   -0.2489 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6708   -1.1934   -0.4855 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0859    0.4853   -1.0987 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6144    1.8180    0.0908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4647    0.1273    1.5334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0278   -1.1278    0.3392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1942   -1.2963   -1.6850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6338   -2.9158   -2.9984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6586   -2.3720   -4.7400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4252   -1.6803   -3.6706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2192    1.2424   -2.1701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3027    1.2631   -3.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9856   -0.2713   -3.1531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7877    2.8562    1.6713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5200    4.1655    0.4942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2106    3.8317    1.0938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1822    1.8478    0.9292 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6345    1.8804    2.2172 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5909    1.2574    3.6271 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4574   -1.2889    4.5209 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6339   -0.5642    3.3106 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9305    0.4311    4.6723 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 10 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 13 18  1  0
 18 19  1  0
 19 20  1  0
 18 21  2  0
  5 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  2  0
 24  3  1  0
 21  8  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  4 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
  9 37  1  0
 12 38  1  0
 12 39  1  0
 12 40  1  0
 16 41  1  0
 16 42  1  0
 16 43  1  0
 20 44  1  0
 20 45  1  0
 20 46  1  0
 21 47  1  0
 22 48  1  0
 23 49  1  0
 27 50  1  0
 27 51  1  0
 27 52  1  0
M  END


  Mrv1652309032202242D          

 28 29  0  0  0  0            999 V2000
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   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
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 O   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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  2  0  0  0  0
  8 21  1  0  0  0  0
  5 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
  3 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0165313

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(CCC2=CC(OC)=C(OC(C)=O)C(OC)=C2)=CC=C1OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H24O7/c1-13(22)27-17-9-8-15(10-18(17)24-3)6-7-16-11-19(25-4)21(28-14(2)23)20(12-16)26-5/h8-12H,6-7H2,1-5H3

> <INCHI_KEY>
MADYYOXZBZYPPY-UHFFFAOYSA-N

> <FORMULA>
C21H24O7

> <MOLECULAR_WEIGHT>
388.416

> <EXACT_MASS>
388.152203113

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
41.67059968380381

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-{2-[4-(acetyloxy)-3,5-dimethoxyphenyl]ethyl}-2-methoxyphenyl acetate

> <ALOGPS_LOGP>
3.76

> <JCHEM_LOGP>
3.2511166596666663

> <ALOGPS_LOGS>
-4.97

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.431746993930892

> <JCHEM_POLAR_SURFACE_AREA>
80.29000000000002

> <JCHEM_REFRACTIVITY>
102.0506

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.16e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-{2-[4-(acetyloxy)-3,5-dimethoxyphenyl]ethyl}-2-methoxyphenyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.002  -9.240   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       9.336 -10.010   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       8.002 -12.320   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       8.002 -13.860   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.336 -14.630   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.668 -14.630   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.335 -12.320   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.335 -13.860   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.001 -14.630   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   24                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   22                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   21                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   13   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18    8                                                       
CONECT   22    5   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23    3   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   58    0
END

View in JSmol

Synonyms

Value	Source
Moscatilin diacetic acid	Generator

Chemical Formula

C₂₁H₂₄O₇

Average Mass

388.4160 Da

Monoisotopic Mass

388.15220 Da

IUPAC Name

4-{2-[4-(acetyloxy)-3,5-dimethoxyphenyl]ethyl}-2-methoxyphenyl acetate

Traditional Name

4-{2-[4-(acetyloxy)-3,5-dimethoxyphenyl]ethyl}-2-methoxyphenyl acetate

CAS Registry Number

Not Available

SMILES

COC1=CC(CCC2=CC(OC)=C(OC(C)=O)C(OC)=C2)=CC=C1OC(C)=O

InChI Identifier

InChI=1S/C21H24O7/c1-13(22)27-17-9-8-15(10-18(17)24-3)6-7-16-11-19(25-4)21(28-14(2)23)20(12-16)26-5/h8-12H,6-7H2,1-5H3

InChI Key

MADYYOXZBZYPPY-UHFFFAOYSA-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
Dendrobium loddigesii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Stilbenes

Sub Class

Not Available

Direct Parent

Stilbenes

Alternative Parents

Substituents

Stilbene
Phenol ester
Dimethoxybenzene
M-dimethoxybenzene
Methoxybenzene
Anisole
Phenoxy compound
Phenol ether
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Dicarboxylic acid or derivatives
Carboxylic acid ester
Carboxylic acid derivative
Ether
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Organooxygen compound
Organic oxide
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	3.76	ALOGPS
logP	3.25	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	80.29 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	102.05 m³·mol⁻¹	ChemAxon
Polarizability	41.67 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

9915673

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11740968

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Chen CC, Wu LG, Ko FN, Teng CM: Antiplatelet aggregation principles of Dendrobium loddigesii. J Nat Prod. 1994 Sep;57(9):1271-4. doi: 10.1021/np50111a014. [PubMed:7798962 ]
LOTUS database [Link]

Showing NP-Card for 4-{2-[4-(acetyloxy)-3,5-dimethoxyphenyl]ethyl}-2-methoxyphenyl acetate (NP0165313)

MOL for NP0165313 (4-{2-[4-(acetyloxy)-3,5-dimethoxyphenyl]ethyl}-2-methoxyphenyl acetate)

3D MOL for NP0165313 (4-{2-[4-(acetyloxy)-3,5-dimethoxyphenyl]ethyl}-2-methoxyphenyl acetate)

3D SDF for NP0165313 (4-{2-[4-(acetyloxy)-3,5-dimethoxyphenyl]ethyl}-2-methoxyphenyl acetate)

3D-SDF for NP0165313 (4-{2-[4-(acetyloxy)-3,5-dimethoxyphenyl]ethyl}-2-methoxyphenyl acetate)

PDB for NP0165313 (4-{2-[4-(acetyloxy)-3,5-dimethoxyphenyl]ethyl}-2-methoxyphenyl acetate)

3D PDB for NP0165313 (4-{2-[4-(acetyloxy)-3,5-dimethoxyphenyl]ethyl}-2-methoxyphenyl acetate)

SMILES for NP0165313 (4-{2-[4-(acetyloxy)-3,5-dimethoxyphenyl]ethyl}-2-methoxyphenyl acetate)

INCHI for NP0165313 (4-{2-[4-(acetyloxy)-3,5-dimethoxyphenyl]ethyl}-2-methoxyphenyl acetate)

Structure for NP0165313 (4-{2-[4-(acetyloxy)-3,5-dimethoxyphenyl]ethyl}-2-methoxyphenyl acetate)

3D Structure for NP0165313 (4-{2-[4-(acetyloxy)-3,5-dimethoxyphenyl]ethyl}-2-methoxyphenyl acetate)