NP-MRD: Showing NP-Card for Inoscavin B (NP0006225)

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Record Information

Version

2.0

Created at

2020-12-09 03:15:17 UTC

Updated at

2021-07-15 16:54:10 UTC

NP-MRD ID

NP0006225

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Inoscavin B

Provided By

NPAtlas

Description

Inoscavin B is found in Hymenochaete xerantica, Inonotus and Inonotus xeranticus. Inoscavin B was first documented in 2006 (PMID: 16499338). Based on a literature review very few articles have been published on (3Z)-6-[(E)-2-(3,4-dihydroxyphenyl)ethenyl]-3-[(3,4-dihydroxyphenyl)methylidene]-2-methoxy-2-methyl-2H,3H,4H-furo[3,2-c]pyran-4-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI

  Mrv1652306242118263D          

 52 55  0  0  0  0            999 V2000
    1.5393   -2.1203   -1.5763 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4749   -2.1649   -0.5692 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3448   -1.2218    0.4146 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4132   -1.4649    1.4623 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0617   -1.3862    1.0430 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1219   -0.5530    0.5029 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.1712   -0.2009   -0.7785 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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M  END

     RDKit          3D

 52 55  0  0  0  0  0  0  0  0999 V2000
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M  END

  Mrv1652306242118263D          

 52 55  0  0  0  0            999 V2000
    1.5393   -2.1203   -1.5763 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4749   -2.1649   -0.5692 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.7693    2.9965   -1.6191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7043    1.8138   -0.9181 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8918    2.1097   -0.5864 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8792    2.5531    1.1865 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2592    2.1924    1.3620 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2140    0.8696    0.7635 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5660   -2.0985   -1.9127 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6293   -0.8994   -1.4097 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
  8 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 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
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 23  3  1  0  0  0  0
 32 25  1  0  0  0  0
 22  6  2  0  0  0  0
 18 11  1  0  0  0  0
  1 33  1  0  0  0  0
  1 34  1  0  0  0  0
  1 35  1  0  0  0  0
  4 36  1  0  0  0  0
  4 37  1  0  0  0  0
  4 38  1  0  0  0  0
  7 39  1  0  0  0  0
  9 40  1  0  0  0  0
 10 41  1  0  0  0  0
 12 42  1  0  0  0  0
 13 43  1  0  0  0  0
 15 44  1  0  0  0  0
 17 45  1  0  0  0  0
 18 46  1  0  0  0  0
 24 47  1  0  0  0  0
 26 48  1  0  0  0  0
 27 49  1  0  0  0  0
 29 50  1  0  0  0  0
 31 51  1  0  0  0  0
 32 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0006225

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C([H])=C(\C([H])=C(/[H])C2=C([H])C3=C(\C(=C(/[H])C4=C([H])C([H])=C(O[H])C(O[H])=C4[H])[C@](OC([H])([H])[H])(O3)C([H])([H])[H])C(=O)O2)C([H])=C1O[H]

> <INCHI_IDENTIFIER>
InChI=1S/C24H20O8/c1-24(30-2)16(9-14-5-8-18(26)20(28)11-14)22-21(32-24)12-15(31-23(22)29)6-3-13-4-7-17(25)19(27)10-13/h3-12,25-28H,1-2H3/b6-3+,16-9-/t24-/m1/s1

> <INCHI_KEY>
RNGFLTFOEGMRRY-PGODXZJGSA-N

> <FORMULA>
C24H20O8

> <MOLECULAR_WEIGHT>
436.416

> <EXACT_MASS>
436.115817604

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
45.56917597629866

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3Z)-6-[(E)-2-(3,4-dihydroxyphenyl)ethenyl]-3-[(3,4-dihydroxyphenyl)methylidene]-2-methoxy-2-methyl-2H,3H,4H-furo[3,2-c]pyran-4-one

> <ALOGPS_LOGP>
3.51

> <JCHEM_LOGP>
3.572631195

> <ALOGPS_LOGS>
-4.59

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.523637442926711

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.920839364059379

> <JCHEM_PKA_STRONGEST_BASIC>
-4.262745662976157

> <JCHEM_POLAR_SURFACE_AREA>
125.68

> <JCHEM_REFRACTIVITY>
120.03330000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.12e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3Z)-6-[(E)-2-(3,4-dihydroxyphenyl)ethenyl]-3-[(3,4-dihydroxyphenyl)methylidene]-2-methoxy-2-methylfuro[3,2-c]pyran-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 52 55  0  0  0  0  0  0  0  0999 V2000
    1.5393   -2.1203   -1.5763 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4749   -2.1649   -0.5692 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3448   -1.2218    0.4146 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4132   -1.4649    1.4623 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0617   -1.3862    1.0430 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1219   -0.5530    0.5029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2737   -0.5000    0.4918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8879    0.5345   -0.1877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3346    0.6708   -0.2531 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2024   -0.1509    0.2841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6598    0.0054    0.2063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4482   -0.9520    0.8153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8231   -0.8330    0.7661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4201    0.2253    0.1198 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7930    0.3077    0.0938 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6567    1.1942   -0.4970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2676    2.2558   -1.1475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2751    1.0507   -0.4328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1550    1.4431   -0.8075 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1496    1.4523   -0.8368 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7831    2.3662   -1.4594 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8161    0.4398   -0.1721 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2649    0.1740   -0.0189 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1703    1.0932   -0.2623 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5714    0.8391   -0.1272 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3082    1.7117    0.6496 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6726    1.5230    0.7652 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2719    0.4653    0.1023 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6268    0.2486    0.1981 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5350   -0.3926   -0.6641 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1164   -1.4696   -1.3447 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1712   -0.2009   -0.7785 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5635   -1.1314   -2.1111 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5174   -2.3918   -1.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8807   -2.8702   -2.3432 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2030   -2.1304    1.0855 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7705   -0.5163    1.9128 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9183   -2.0537    2.2903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8138   -1.2717    1.0151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7712    1.5219   -0.7861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7762   -0.9984    0.8154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9814   -1.7921    1.3295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4398   -1.5672    1.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2528    1.0737   -0.3741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7693    2.9965   -1.6191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7043    1.8138   -0.9181 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8918    2.1097   -0.5864 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8792    2.5531    1.1865 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2592    2.1924    1.3620 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2140    0.8696    0.7635 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5660   -2.0985   -1.9127 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6293   -0.8994   -1.4097 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  3  2  1  6
  3  4  1  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16 18  2  0
  8 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 30 32  2  0
 23  3  1  0
 32 25  1  0
 22  6  2  0
 18 11  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  4 36  1  0
  4 37  1  0
  4 38  1  0
  7 39  1  0
  9 40  1  0
 10 41  1  0
 12 42  1  0
 13 43  1  0
 15 44  1  0
 17 45  1  0
 18 46  1  0
 24 47  1  0
 26 48  1  0
 27 49  1  0
 29 50  1  0
 31 51  1  0
 32 52  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       1.539  -2.120  -1.576  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.475  -2.165  -0.569  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.345  -1.222   0.415  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.413  -1.465   1.462  0.00  0.00           C+0
HETATM    5  O   UNK     0       1.062  -1.386   1.043  0.00  0.00           O+0
HETATM    6  C   UNK     0       0.122  -0.553   0.503  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.274  -0.500   0.492  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.888   0.535  -0.188  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.335   0.671  -0.253  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.202  -0.151   0.284  0.00  0.00           C+0
HETATM   11  C   UNK     0      -5.660   0.005   0.206  0.00  0.00           C+0
HETATM   12  C   UNK     0      -6.448  -0.952   0.815  0.00  0.00           C+0
HETATM   13  C   UNK     0      -7.823  -0.833   0.766  0.00  0.00           C+0
HETATM   14  C   UNK     0      -8.420   0.225   0.120  0.00  0.00           C+0
HETATM   15  O   UNK     0      -9.793   0.308   0.094  0.00  0.00           O+0
HETATM   16  C   UNK     0      -7.657   1.194  -0.497  0.00  0.00           C+0
HETATM   17  O   UNK     0      -8.268   2.256  -1.147  0.00  0.00           O+0
HETATM   18  C   UNK     0      -6.275   1.051  -0.433  0.00  0.00           C+0
HETATM   19  O   UNK     0      -1.155   1.443  -0.808  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.150   1.452  -0.837  0.00  0.00           C+0
HETATM   21  O   UNK     0       0.783   2.366  -1.459  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.816   0.440  -0.172  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.265   0.174  -0.019  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.170   1.093  -0.262  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.571   0.839  -0.127  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.308   1.712   0.650  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.673   1.523   0.765  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.272   0.465   0.102  0.00  0.00           C+0
HETATM   29  O   UNK     0       8.627   0.249   0.198  0.00  0.00           O+0
HETATM   30  C   UNK     0       6.535  -0.393  -0.664  0.00  0.00           C+0
HETATM   31  O   UNK     0       7.116  -1.470  -1.345  0.00  0.00           O+0
HETATM   32  C   UNK     0       5.171  -0.201  -0.779  0.00  0.00           C+0
HETATM   33  H   UNK     0       1.563  -1.131  -2.111  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.517  -2.392  -1.279  0.00  0.00           H+0
HETATM   35  H   UNK     0       1.881  -2.870  -2.343  0.00  0.00           H+0
HETATM   36  H   UNK     0       4.203  -2.130   1.085  0.00  0.00           H+0
HETATM   37  H   UNK     0       3.771  -0.516   1.913  0.00  0.00           H+0
HETATM   38  H   UNK     0       2.918  -2.054   2.290  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.814  -1.272   1.015  0.00  0.00           H+0
HETATM   40  H   UNK     0      -3.771   1.522  -0.786  0.00  0.00           H+0
HETATM   41  H   UNK     0      -3.776  -0.998   0.815  0.00  0.00           H+0
HETATM   42  H   UNK     0      -5.981  -1.792   1.329  0.00  0.00           H+0
HETATM   43  H   UNK     0      -8.440  -1.567   1.232  0.00  0.00           H+0
HETATM   44  H   UNK     0     -10.253   1.074  -0.374  0.00  0.00           H+0
HETATM   45  H   UNK     0      -7.769   2.997  -1.619  0.00  0.00           H+0
HETATM   46  H   UNK     0      -5.704   1.814  -0.918  0.00  0.00           H+0
HETATM   47  H   UNK     0       2.892   2.110  -0.586  0.00  0.00           H+0
HETATM   48  H   UNK     0       4.879   2.553   1.187  0.00  0.00           H+0
HETATM   49  H   UNK     0       7.259   2.192   1.362  0.00  0.00           H+0
HETATM   50  H   UNK     0       9.214   0.870   0.764  0.00  0.00           H+0
HETATM   51  H   UNK     0       6.566  -2.099  -1.913  0.00  0.00           H+0
HETATM   52  H   UNK     0       4.629  -0.899  -1.410  0.00  0.00           H+0
CONECT    1    2   33   34   35                                             
CONECT    2    1    3                                                       
CONECT    3    2    4    5   23                                             
CONECT    4    3   36   37   38                                             
CONECT    5    3    6                                                       
CONECT    6    5    7   22                                                  
CONECT    7    6    8   39                                                  
CONECT    8    7    9   19                                                  
CONECT    9    8   10   40                                                  
CONECT   10    9   11   41                                                  
CONECT   11   10   12   18                                                  
CONECT   12   11   13   42                                                  
CONECT   13   12   14   43                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14   44                                                       
CONECT   16   14   17   18                                                  
CONECT   17   16   45                                                       
CONECT   18   16   11   46                                                  
CONECT   19    8   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23    6                                                  
CONECT   23   22   24    3                                                  
CONECT   24   23   25   47                                                  
CONECT   25   24   26   32                                                  
CONECT   26   25   27   48                                                  
CONECT   27   26   28   49                                                  
CONECT   28   27   29   30                                                  
CONECT   29   28   50                                                       
CONECT   30   28   31   32                                                  
CONECT   31   30   51                                                       
CONECT   32   30   25   52                                                  
CONECT   33    1                                                            
CONECT   34    1                                                            
CONECT   35    1                                                            
CONECT   36    4                                                            
CONECT   37    4                                                            
CONECT   38    4                                                            
CONECT   39    7                                                            
CONECT   40    9                                                            
CONECT   41   10                                                            
CONECT   42   12                                                            
CONECT   43   13                                                            
CONECT   44   15                                                            
CONECT   45   17                                                            
CONECT   46   18                                                            
CONECT   47   24                                                            
CONECT   48   26                                                            
CONECT   49   27                                                            
CONECT   50   29                                                            
CONECT   51   31                                                            
CONECT   52   32                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  110    0
END

RDKit          3D

52 55  0  0  0  0  0  0  0  0999 V2000
    1.5393   -2.1203   -1.5763 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4749   -2.1649   -0.5692 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3448   -1.2218    0.4146 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4132   -1.4649    1.4623 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0617   -1.3862    1.0430 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1219   -0.5530    0.5029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2737   -0.5000    0.4918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8879    0.5345   -0.1877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3346    0.6708   -0.2531 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2024   -0.1509    0.2841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6598    0.0054    0.2063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4482   -0.9520    0.8153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8231   -0.8330    0.7661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4201    0.2253    0.1198 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7930    0.3077    0.0938 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6567    1.1942   -0.4970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2676    2.2558   -1.1475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2751    1.0507   -0.4328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1550    1.4431   -0.8075 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1496    1.4523   -0.8368 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7831    2.3662   -1.4594 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8161    0.4398   -0.1721 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2649    0.1740   -0.0189 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1703    1.0932   -0.2623 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5714    0.8391   -0.1272 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3082    1.7117    0.6496 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6726    1.5230    0.7652 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2719    0.4653    0.1023 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6268    0.2486    0.1981 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5350   -0.3926   -0.6641 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1164   -1.4696   -1.3447 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1712   -0.2009   -0.7785 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5635   -1.1314   -2.1111 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5174   -2.3918   -1.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8807   -2.8702   -2.3432 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2030   -2.1304    1.0855 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7705   -0.5163    1.9128 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9183   -2.0537    2.2903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8138   -1.2717    1.0151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7712    1.5219   -0.7861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7762   -0.9984    0.8154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9814   -1.7921    1.3295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4398   -1.5672    1.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2528    1.0737   -0.3741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7693    2.9965   -1.6191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7043    1.8138   -0.9181 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8918    2.1097   -0.5864 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8792    2.5531    1.1865 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2592    2.1924    1.3620 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2140    0.8696    0.7635 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5660   -2.0985   -1.9127 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6293   -0.8994   -1.4097 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  3  2  1  6
  3  4  1  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16 18  2  0
  8 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 30 32  2  0
 23  3  1  0
 32 25  1  0
 22  6  2  0
 18 11  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  4 36  1  0
  4 37  1  0
  4 38  1  0
  7 39  1  0
  9 40  1  0
 10 41  1  0
 12 42  1  0
 13 43  1  0
 15 44  1  0
 17 45  1  0
 18 46  1  0
 24 47  1  0
 26 48  1  0
 27 49  1  0
 29 50  1  0
 31 51  1  0
 32 52  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₄H₂₀O₈

Average Mass

436.4160 Da

Monoisotopic Mass

436.11582 Da

IUPAC Name

(2R,3Z)-6-[(E)-2-(3,4-dihydroxyphenyl)ethenyl]-3-[(3,4-dihydroxyphenyl)methylidene]-2-methoxy-2-methyl-2H,3H,4H-furo[3,2-c]pyran-4-one

Traditional Name

(2R,3Z)-6-[(E)-2-(3,4-dihydroxyphenyl)ethenyl]-3-[(3,4-dihydroxyphenyl)methylidene]-2-methoxy-2-methylfuro[3,2-c]pyran-4-one

CAS Registry Number

Not Available

SMILES

COC1(C)OC2=C(\C1=C\C1=CC(O)=C(O)C=C1)C(=O)OC(\C=C\C1=CC(O)=C(O)C=C1)=C2

InChI Identifier

InChI=1S/C24H20O8/c1-24(30-2)16(9-14-5-8-18(26)20(28)11-14)22-21(32-24)12-15(31-23(22)29)6-3-13-4-7-17(25)19(27)10-13/h3-12,25-28H,1-2H3/b6-3+,16-9-

InChI Key

RNGFLTFOEGMRRY-PGODXZJGSA-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
Hymenochaete xerantica	LOTUS Database	35616633
Inonotus	NPAtlas	16499338
Phellinus xeranticus	Fungi	KNApSAcK

Species Where Detected

Species Name	Source	Reference
Inonotus xeranticus	KNApSAcK Database	22123792

Chemical Taxonomy

Classification

Not classified

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	3.51	ALOGPS
logP	3.57	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	8.92	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	125.68 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	120.03 m³·mol⁻¹	ChemAxon
Polarizability	45.57 Å³	ChemAxon
Number of Rings	4	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

NPAtlas ID

NPA016765

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9764959

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11590196

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Lee IK, Seok SJ, Kim WK, Yun BS: Hispidin derivatives from the mushroom Inonotus xeranticus and their antioxidant activity. J Nat Prod. 2006 Feb;69(2):299-301. doi: 10.1021/np050453n. [PubMed:16499338 ]

Showing NP-Card for Inoscavin B (NP0006225)

MOL for NP0006225 (Inoscavin B)

3D MOL for NP0006225 (Inoscavin B)

3D SDF for NP0006225 (Inoscavin B)

3D-SDF for NP0006225 (Inoscavin B)

PDB for NP0006225 (Inoscavin B)

3D PDB for NP0006225 (Inoscavin B)

SMILES for NP0006225 (Inoscavin B)

INCHI for NP0006225 (Inoscavin B)

Structure for NP0006225 (Inoscavin B)

3D Structure for NP0006225 (Inoscavin B)