NP-MRD: Showing NP-Card for 3',4'-Dihydroxy-5-methoxy-6,7-methylenedioxyisoflavone 3'-O-glucoside-4'-O-(2''-O-(4''''-acetyl-2''''-methoxyphenyl)glucoside) (NP0062665)

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Record Information

Version

2.0

Created at

2022-04-28 07:15:36 UTC

Updated at

2022-04-28 07:15:36 UTC

NP-MRD ID

NP0062665

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3',4'-Dihydroxy-5-methoxy-6,7-methylenedioxyisoflavone 3'-O-glucoside-4'-O-(2''-O-(4''''-acetyl-2''''-methoxyphenyl)glucoside)

Description

7-(4-{[(2S,3S,4S,5S,6R)-3-(4-acetyl-2-methoxyphenoxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-9-methoxy-2H,8H-[1,3]dioxolo[4,5-g]chromen-8-one belongs to the class of organic compounds known as isoflavonoid o-glycosides. These are o-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one. 3',4'-Dihydroxy-5-methoxy-6,7-methylenedioxyisoflavone 3'-O-glucoside-4'-O-(2''-O-(4''''-acetyl-2''''-methoxyphenyl)glucoside) is found in Iris germanica . Based on a literature review very few articles have been published on 7-(4-{[(2S,3S,4S,5S,6R)-3-(4-acetyl-2-methoxyphenoxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-9-methoxy-2H,8H-[1,3]dioxolo[4,5-g]chromen-8-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282209152D          

 57 63  0  0  1  0            999 V2000
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    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
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.8592    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.8579   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6425   -0.2549    0.0000 O   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  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
  4 10  1  0  0  0  0
 10 11  2  0  0  0  0
  9 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
 15 18  1  0  0  0  0
 19 18  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  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
 19 24  1  0  0  0  0
 23 25  1  1  0  0  0
 25 26  1  0  0  0  0
 22 27  1  6  0  0  0
 21 28  1  1  0  0  0
 20 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
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 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 33 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 14 41  1  0  0  0  0
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  2 55  1  0  0  0  0
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 56 57  1  0  0  0  0
  1 57  1  0  0  0  0
M  END

     RDKit          3D

 97103  0  0  0  0  0  0  0  0999 V2000
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   -9.0074   -4.1076    2.6825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1296   -5.1525    3.6428 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2355   -3.8700    2.1008 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2945   -3.2528    1.3509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6576   -2.3177    0.3751 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7792   -1.7282   -0.3437 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8527   -1.1624   -1.0512 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0034   -0.0900   -0.2742 C   0  0  2  0  0  0  0  0  0  0  0  0
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    0.7425   -1.3764    1.8292 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0804   -1.3100    2.0876 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.9684    0.9193    1.8041 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2598    1.0181    1.9771 O   0  0  0  0  0  0  0  0  0  0  0  0
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   10.7126   -1.0122    2.4149 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3223    0.3738    0.4867 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.6764    3.4508   -1.1355 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5605    4.4071   -1.6445 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9639    5.7545   -1.2674 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8721    5.8084    0.1393 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.7899    3.8252   -3.6436 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4925    3.3576   -3.5840 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6952    3.7256   -2.9477 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.8919   -0.4690   -2.0994 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -9.4886   -4.2991    3.6873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2012   -3.0831    2.3400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9733   -4.6067    2.8761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2333   -3.4947    1.5163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0302   -1.8802   -1.3401 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.5347    1.1418   -3.9600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3409   -0.2236   -2.8864 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
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  5  9  2  0
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 13 67  1  6
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 29 73  1  0
 29 74  1  0
 29 75  1  0
  7 62  1  0
  7 63  1  0
  7 64  1  0
M  END


  Mrv1652304282209152D          

 57 63  0  0  1  0            999 V2000
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   -5.7158    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302    3.7125    0.0000 C   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    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5724   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    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 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425    1.0799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1274    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425   -0.2549    0.0000 O   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  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
  4 10  1  0  0  0  0
 10 11  2  0  0  0  0
  9 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
 15 18  1  0  0  0  0
 19 18  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  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
 19 24  1  0  0  0  0
 23 25  1  1  0  0  0
 25 26  1  0  0  0  0
 22 27  1  6  0  0  0
 21 28  1  1  0  0  0
 20 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 30 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 33 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 14 41  1  0  0  0  0
 42 41  1  6  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 42 47  1  0  0  0  0
 46 48  1  6  0  0  0
 48 49  1  0  0  0  0
 45 50  1  1  0  0  0
 44 51  1  6  0  0  0
 43 52  1  1  0  0  0
  3 53  1  0  0  0  0
 53 54  1  0  0  0  0
  2 55  1  0  0  0  0
 55 56  1  0  0  0  0
 56 57  1  0  0  0  0
  1 57  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0062665

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC=C1O[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C=C(C=C1)C1=COC2=CC3=C(OCO3)C(OC)=C2C1=O)C(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C38H40O19/c1-15(41)16-4-6-19(21(8-16)48-2)53-36-32(46)30(44)26(12-40)57-38(36)54-20-7-5-17(9-22(20)55-37-33(47)31(45)29(43)25(11-39)56-37)18-13-50-23-10-24-34(52-14-51-24)35(49-3)27(23)28(18)42/h4-10,13,25-26,29-33,36-40,43-47H,11-12,14H2,1-3H3/t25-,26-,29-,30-,31+,32+,33-,36+,37-,38-/m1/s1

> <INCHI_KEY>
IPDCHTGYPFGNIA-WWGXNAIZSA-N

> <FORMULA>
C38H40O19

> <MOLECULAR_WEIGHT>
800.719

> <EXACT_MASS>
800.216379068

> <JCHEM_ACCEPTOR_COUNT>
19

> <JCHEM_ATOM_COUNT>
97

> <JCHEM_AVERAGE_POLARIZABILITY>
78.25039295162115

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7-(4-{[(2S,3S,4S,5S,6R)-3-(4-acetyl-2-methoxyphenoxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-9-methoxy-2H,8H-[1,3]dioxolo[4,5-g]chromen-8-one

> <ALOGPS_LOGP>
0.92

> <JCHEM_LOGP>
-0.6060084013333336

> <ALOGPS_LOGS>
-3.17

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.693054373237299

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.080219795199094

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810923549153534

> <JCHEM_POLAR_SURFACE_AREA>
268.04999999999995

> <JCHEM_REFRACTIVITY>
187.34680000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.41e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-(4-{[(2S,3S,4S,5S,6R)-3-(4-acetyl-2-methoxyphenoxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-9-methoxy-2H-[1,3]dioxolo[4,5-g]chromen-8-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -5.335   4.620   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -5.335   6.160   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -6.668   6.930   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -6.668   8.470   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -5.335   9.240   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.001   8.470   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -4.001   6.930   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -2.667   9.240   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -2.667  10.780   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -5.335  10.780   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -8.002   9.240   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -8.002   6.160   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -9.336   6.930   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -9.336   8.470   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0     -10.669   9.240   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0     -12.003   8.470   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0     -12.003   6.930   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0     -10.669   6.160   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0     -10.669   4.620   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -9.336   3.850   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0     -13.337   9.240   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0     -14.670   8.470   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0     -13.337  10.780   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -5.335   1.540   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      -5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      -4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      -1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0      -5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0      -8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   52  O   UNK     0      -8.002  -0.000   0.000  0.00  0.00           O+0
HETATM   53  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   54  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0       6.799   2.016   0.000  0.00  0.00           O+0
HETATM   56  C   UNK     0       7.705   0.770   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0       6.799  -0.476   0.000  0.00  0.00           O+0
CONECT    1    2    6   57                                                  
CONECT    2    1    3   55                                                  
CONECT    3    2    4   53                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9    4   11                                                  
CONECT   11   10                                                            
CONECT   12    9   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   41                                                  
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18   15   19                                                       
CONECT   19   18   20   24                                                  
CONECT   20   19   21   29                                                  
CONECT   21   20   22   28                                                  
CONECT   22   21   23   27                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23   19                                                       
CONECT   25   23   26                                                       
CONECT   26   25                                                            
CONECT   27   22                                                            
CONECT   28   21                                                            
CONECT   29   20   30                                                       
CONECT   30   29   31   35                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   38                                                  
CONECT   34   33   35                                                       
CONECT   35   34   30   36                                                  
CONECT   36   35   37                                                       
CONECT   37   36                                                            
CONECT   38   33   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41   14   42                                                       
CONECT   42   41   43   47                                                  
CONECT   43   42   44   52                                                  
CONECT   44   43   45   51                                                  
CONECT   45   44   46   50                                                  
CONECT   46   45   47   48                                                  
CONECT   47   46   42                                                       
CONECT   48   46   49                                                       
CONECT   49   48                                                            
CONECT   50   45                                                            
CONECT   51   44                                                            
CONECT   52   43                                                            
CONECT   53    3   54                                                       
CONECT   54   53                                                            
CONECT   55    2   56                                                       
CONECT   56   55   57                                                       
CONECT   57   56    1                                                       
MASTER        0    0    0    0    0    0    0    0   57    0  126    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₈H₄₀O₁₉

Average Mass

800.7190 Da

Monoisotopic Mass

800.21638 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC(=CC=C1O[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C=C(C=C1)C1=COC2=CC3=C(OCO3)C(OC)=C2C1=O)C(C)=O

InChI Identifier

InChI=1S/C38H40O19/c1-15(41)16-4-6-19(21(8-16)48-2)53-36-32(46)30(44)26(12-40)57-38(36)54-20-7-5-17(9-22(20)55-37-33(47)31(45)29(43)25(11-39)56-37)18-13-50-23-10-24-34(52-14-51-24)35(49-3)27(23)28(18)42/h4-10,13,25-26,29-33,36-40,43-47H,11-12,14H2,1-3H3/t25-,26-,29-,30-,31+,32+,33-,36+,37-,38-/m1/s1

InChI Key

IPDCHTGYPFGNIA-WWGXNAIZSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Iris germanica	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoflavonoid o-glycosides. These are o-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Isoflavonoid O-glycosides

Direct Parent

Isoflavonoid O-glycosides

Alternative Parents

Substituents

Isoflavonoid-4p-o-glycoside
Isoflavonoid o-glycoside
Isoflavonoid-3p-o-glycoside
Isoflavone
Phenolic glycoside
Alkyl-phenylketone
O-glycosyl compound
Glycosyl compound
Chromone
1-benzopyran
Benzopyran
Phenylketone
Benzodioxole
Acetophenone
Phenoxy compound
Methoxybenzene
Aryl alkyl ketone
Aryl ketone
Phenol ether
Benzoyl
Anisole
Pyranone
Alkyl aryl ether
Benzenoid
Pyran
Oxane
Monosaccharide
Monocyclic benzene moiety
Heteroaromatic compound
Vinylogous ester
Secondary alcohol
Ketone
Oxacycle
Organoheterocyclic compound
Polyol
Ether
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
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	0.92	ALOGPS
logP	-0.61	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	12.08	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	19	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	268.05 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	187.35 m³·mol⁻¹	ChemAxon
Polarizability	78.25 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	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

163085577

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 3',4'-Dihydroxy-5-methoxy-6,7-methylenedioxyisoflavone 3'-O-glucoside-4'-O-(2''-O-(4''''-acetyl-2''''-methoxyphenyl)glucoside) (NP0062665)

MOL for NP0062665 (3',4'-Dihydroxy-5-methoxy-6,7-methylenedioxyisoflavone 3'-O-glucoside-4'-O-(2''-O-(4''''-acetyl-2''''-methoxyphenyl)glucoside))

3D MOL for NP0062665 (3',4'-Dihydroxy-5-methoxy-6,7-methylenedioxyisoflavone 3'-O-glucoside-4'-O-(2''-O-(4''''-acetyl-2''''-methoxyphenyl)glucoside))

3D SDF for NP0062665 (3',4'-Dihydroxy-5-methoxy-6,7-methylenedioxyisoflavone 3'-O-glucoside-4'-O-(2''-O-(4''''-acetyl-2''''-methoxyphenyl)glucoside))

3D-SDF for NP0062665 (3',4'-Dihydroxy-5-methoxy-6,7-methylenedioxyisoflavone 3'-O-glucoside-4'-O-(2''-O-(4''''-acetyl-2''''-methoxyphenyl)glucoside))

PDB for NP0062665 (3',4'-Dihydroxy-5-methoxy-6,7-methylenedioxyisoflavone 3'-O-glucoside-4'-O-(2''-O-(4''''-acetyl-2''''-methoxyphenyl)glucoside))

3D PDB for NP0062665 (3',4'-Dihydroxy-5-methoxy-6,7-methylenedioxyisoflavone 3'-O-glucoside-4'-O-(2''-O-(4''''-acetyl-2''''-methoxyphenyl)glucoside))

SMILES for NP0062665 (3',4'-Dihydroxy-5-methoxy-6,7-methylenedioxyisoflavone 3'-O-glucoside-4'-O-(2''-O-(4''''-acetyl-2''''-methoxyphenyl)glucoside))

INCHI for NP0062665 (3',4'-Dihydroxy-5-methoxy-6,7-methylenedioxyisoflavone 3'-O-glucoside-4'-O-(2''-O-(4''''-acetyl-2''''-methoxyphenyl)glucoside))

Structure for NP0062665 (3',4'-Dihydroxy-5-methoxy-6,7-methylenedioxyisoflavone 3'-O-glucoside-4'-O-(2''-O-(4''''-acetyl-2''''-methoxyphenyl)glucoside))

3D Structure for NP0062665 (3',4'-Dihydroxy-5-methoxy-6,7-methylenedioxyisoflavone 3'-O-glucoside-4'-O-(2''-O-(4''''-acetyl-2''''-methoxyphenyl)glucoside))