NP-MRD: Showing NP-Card for methyl (2s,3s,4s,5s,6r)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate (NP0319573)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-11 20:40:43 UTC

Updated at

2022-09-11 20:40:44 UTC

NP-MRD ID

NP0319573

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2s,3s,4s,5s,6r)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate

Description

Methyl (2S,3S,4S,5S,6R)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]Dodeca-1(12),8,10-triene-4-carboxylate belongs to the class of organic compounds known as flavaglines. These are heterocyclic compounds with a structure characterized by a cyclopenta[b]benzofuran skeleton. methyl (2s,3s,4s,5s,6r)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate is found in Aglaia odorata. Based on a literature review very few articles have been published on methyl (2S,3S,4S,5S,6R)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]Dodeca-1(12),8,10-triene-4-carboxylate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309112222402D          

 39 43  0  0  1  0            999 V2000
   -1.1406   -0.2463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3612   -0.5167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2056   -1.3269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8294   -1.8667    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5739   -1.5973    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2507   -1.1256    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2670   -0.3007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5608    0.1258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1617   -0.2726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5771    0.9506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9085   -1.6236    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1788   -0.8441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7333   -1.6398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2973   -1.0377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0579   -0.2482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6219    0.3538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1008   -1.2251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3402   -2.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1436   -2.2020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7076   -1.5999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7762   -2.6167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9727   -2.4293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2959   -2.9010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6381   -2.4030    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6219   -3.2279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3281   -3.6544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3118   -4.4792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5893   -4.8775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5731   -5.7024    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2793   -6.1289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8831   -4.4510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8994   -3.6262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8133   -2.3868    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3153   -3.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6359   -3.8046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1379   -4.4624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6807   -4.3600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0013   -3.5999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5033   -2.9421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  6  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  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  2  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 11 24  1  0  0  0  0
 24 25  1  6  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  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  2  0  0  0  0
 25 32  1  0  0  0  0
 24 33  1  0  0  0  0
  5 33  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 34 39  1  0  0  0  0
M  END


  Mrv1652309112222402D          

 39 43  0  0  1  0            999 V2000
   -1.1406   -0.2463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3612   -0.5167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2056   -1.3269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8294   -1.8667    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5739   -1.5973    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2507   -1.1256    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2670   -0.3007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5608    0.1258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1617   -0.2726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5771    0.9506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9085   -1.6236    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1788   -0.8441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7333   -1.6398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2973   -1.0377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0579   -0.2482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6219    0.3538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1008   -1.2251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3402   -2.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1436   -2.2020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7076   -1.5999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7762   -2.6167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9727   -2.4293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2959   -2.9010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6381   -2.4030    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6219   -3.2279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3281   -3.6544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3118   -4.4792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5893   -4.8775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5731   -5.7024    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2793   -6.1289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8831   -4.4510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8994   -3.6262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8133   -2.3868    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3153   -3.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6359   -3.8046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1379   -4.4624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6807   -4.3600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0013   -3.5999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5033   -2.9421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  6  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  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  2  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 11 24  1  0  0  0  0
 24 25  1  6  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  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  2  0  0  0  0
 25 32  1  0  0  0  0
 24 33  1  0  0  0  0
  5 33  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 34 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0319573

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@H]1[C@H](OC(C)=O)[C@@]2(O)C3=C(OC)C=C(OC)C=C3O[C@]2([C@@H]1C1=CC=CC=C1)C1=CC=C(OC)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C30H30O9/c1-17(31)38-27-24(28(32)37-5)25(18-9-7-6-8-10-18)30(19-11-13-20(34-2)14-12-19)29(27,33)26-22(36-4)15-21(35-3)16-23(26)39-30/h6-16,24-25,27,33H,1-5H3/t24-,25+,27-,29-,30-/m0/s1

> <INCHI_KEY>
NJDCYEFLQWDCCN-GKUJDVGKSA-N

> <FORMULA>
C30H30O9

> <MOLECULAR_WEIGHT>
534.561

> <EXACT_MASS>
534.188982546

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
54.938225718246954

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (2S,3S,4S,5S,6R)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0^{2,6}]dodeca-1(12),8,10-triene-4-carboxylate

> <JCHEM_LOGP>
3.3351414906666674

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.976643515189824

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.601055012442547

> <JCHEM_PKA_STRONGEST_BASIC>
-4.2695675150146775

> <JCHEM_POLAR_SURFACE_AREA>
109.75000000000001

> <JCHEM_REFRACTIVITY>
138.5665

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2S,3S,4S,5S,6R)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0^{2,6}]dodeca-1(12),8,10-triene-4-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.129  -0.460   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -0.674  -0.965   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.384  -2.477   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -1.548  -3.485   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.071  -2.982   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.335  -2.101   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.365  -0.561   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.047   0.235   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.302  -0.509   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.077   1.774   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.562  -3.031   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.067  -1.576   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.102  -3.061   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.155  -1.937   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.708  -0.463   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.761   0.661   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.655  -2.287   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.102  -3.761   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.601  -4.110   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      10.654  -2.987   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.049  -4.885   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.549  -4.535   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.286  -5.415   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.058  -4.486   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.027  -6.025   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.346  -6.821   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.315  -8.361   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.967  -9.105   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       2.936 -10.644   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       4.255 -11.441   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.649  -8.309   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.679  -6.769   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.518  -4.455   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       0.589  -5.683   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       1.187  -7.102   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       0.257  -8.330   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -1.271  -8.139   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -1.869  -6.720   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -0.940  -5.492   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   33                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    6   12   13   24                                             
CONECT   12   11                                                            
CONECT   13   11   14   22                                                  
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18                                                       
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22                                                       
CONECT   22   21   13   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   11   25   33                                             
CONECT   25   24   26   32                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   31                                                  
CONECT   29   28   30                                                       
CONECT   30   29                                                            
CONECT   31   28   32                                                       
CONECT   32   31   25                                                       
CONECT   33   24    5   34                                                  
CONECT   34   33   35   39                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   34                                                       
MASTER        0    0    0    0    0    0    0    0   39    0   86    0
END

View in JSmol

Synonyms

Value	Source
Methyl (2S,3S,4S,5S,6R)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0,]dodeca-1(12),8,10-triene-4-carboxylic acid	Generator

Chemical Formula

C₃₀H₃₀O₉

Average Mass

534.5610 Da

Monoisotopic Mass

534.18898 Da

IUPAC Name

methyl (2S,3S,4S,5S,6R)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0^{2,6}]dodeca-1(12),8,10-triene-4-carboxylate

Traditional Name

methyl (2S,3S,4S,5S,6R)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0^{2,6}]dodeca-1(12),8,10-triene-4-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@H]1[C@H](OC(C)=O)[C@@]2(O)C3=C(OC)C=C(OC)C=C3O[C@]2([C@@H]1C1=CC=CC=C1)C1=CC=C(OC)C=C1

InChI Identifier

InChI=1S/C30H30O9/c1-17(31)38-27-24(28(32)37-5)25(18-9-7-6-8-10-18)30(19-11-13-20(34-2)14-12-19)29(27,33)26-22(36-4)15-21(35-3)16-23(26)39-30/h6-16,24-25,27,33H,1-5H3/t24-,25+,27-,29-,30-/m0/s1

InChI Key

NJDCYEFLQWDCCN-GKUJDVGKSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Aglaia odorata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavaglines. These are heterocyclic compounds with a structure characterized by a cyclopenta[b]benzofuran skeleton.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzofurans

Sub Class

Flavaglines

Direct Parent

Flavaglines

Alternative Parents

Substituents

Flavagline skeleton
Stilbene
Coumaran
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Dicarboxylic acid or derivatives
Methyl ester
Tertiary alcohol
Cyclic alcohol
Carboxylic acid ester
Carboxylic acid derivative
Oxacycle
Ether
Alcohol
Carbonyl group
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	3.34	ChemAxon
pKa (Strongest Acidic)	11.6	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	109.75 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	138.57 m³·mol⁻¹	ChemAxon
Polarizability	54.94 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163194112

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (2s,3s,4s,5s,6r)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate (NP0319573)

MOL for NP0319573 (methyl (2s,3s,4s,5s,6r)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)

3D MOL for NP0319573 (methyl (2s,3s,4s,5s,6r)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)

3D SDF for NP0319573 (methyl (2s,3s,4s,5s,6r)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)

3D-SDF for NP0319573 (methyl (2s,3s,4s,5s,6r)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)

PDB for NP0319573 (methyl (2s,3s,4s,5s,6r)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)

3D PDB for NP0319573 (methyl (2s,3s,4s,5s,6r)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)

SMILES for NP0319573 (methyl (2s,3s,4s,5s,6r)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)

INCHI for NP0319573 (methyl (2s,3s,4s,5s,6r)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)

Structure for NP0319573 (methyl (2s,3s,4s,5s,6r)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)

3D Structure for NP0319573 (methyl (2s,3s,4s,5s,6r)-3-(acetyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)