NP-MRD: Showing NP-Card for 3,4,4'-trihydroxy-6-methyl-12',16'-dioxaspiro[oxane-2,17'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1'(10'),3',5',7'-tetraene-2',9',13'-trione (NP0243467)

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Record Information

Version

2.0

Created at

2022-09-07 04:01:09 UTC

Updated at

2022-09-07 04:01:09 UTC

NP-MRD ID

NP0243467

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,4,4'-trihydroxy-6-methyl-12',16'-dioxaspiro[oxane-2,17'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1'(10'),3',5',7'-tetraene-2',9',13'-trione

Description

3,4,4'-Trihydroxy-6-methyl-12',16'-dioxaspiro[oxane-2,17'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]Heptadecane]-1'(10'),3'(8'),4',6'-tetraene-2',9',13'-trione belongs to the class of organic compounds known as benzoisochromanequinones. These are benzo derivatives of isochromanequinones. Isochromanequinones are structurally characterized by a quinone fused to an isochromane, and forming a naphtho[2,3-c]pyran-6,9-dione skeleton. 3,4,4'-Trihydroxy-6-methyl-12',16'-dioxaspiro[oxane-2,17'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]Heptadecane]-1'(10'),3'(8'),4',6'-tetraene-2',9',13'-trione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241501422D          

 29 33  0  0  0  0            999 V2000
    4.0518   -3.2433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4956   -2.6340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6898   -2.8110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1336   -2.2017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3278   -2.3788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3831   -1.4154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5750   -1.2494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1889   -1.2383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7451   -1.8476    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9947   -1.0613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2442   -0.2749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9956    0.0658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9037    0.8856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5130    1.4419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0956    1.0516    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6880    0.3344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8822    0.1573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6327   -0.6290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8269   -0.8061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1628   -1.2956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2707   -0.1968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4649   -0.3739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2154   -1.1602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0913    0.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1582    1.0218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9640    1.1989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5202    0.5896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3260    0.7666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5756    1.5530    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  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  2  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
  8 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 21 27  1  0  0  0  0
 27 28  1  0  0  0  0
 17 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END

     RDKit          3D

 47 51  0  0  0  0  0  0  0  0999 V2000
   -3.2510   -1.9184   -1.3101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8054   -0.4766   -1.3263 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4829    0.2669   -0.2401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8835    0.1159    1.1344 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6206   -0.7370    1.9529 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4304   -0.3457    1.0026 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4543   -1.7245    0.9821 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8794    0.2435   -0.2824 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4224   -0.4396   -1.3325 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2544    1.5887   -0.3554 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5329    2.2738    0.5891 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8788    3.7450    0.7157 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4606    4.2535    1.2019 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6600    5.3886    1.7192 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4351    3.2530    0.9802 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8622    2.4227    0.0223 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4335    1.0744   -0.1157 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5867    0.0660   -0.2943 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1098   -1.2992   -0.4957 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3264   -2.2628   -0.6742 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5438   -1.5556   -0.4951 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1078   -2.8050   -0.6751 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3426   -3.8972   -0.8693 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5071   -2.9097   -0.6506 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3559   -1.8602   -0.4606 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7846   -0.6247   -0.2830 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4018   -0.4807   -0.3009 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8663    0.8432   -0.1096 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5962    1.8549    0.0703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3707   -2.5731   -1.4626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9687   -2.1320   -2.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8041   -2.1446   -0.3678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1691   -0.0363   -2.2993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6461    1.3522   -0.4866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5318   -0.1461   -0.1610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8843    1.1138    1.6158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5742   -0.5559    1.7548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8783   -0.0521    1.9063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3762   -2.0897    1.8992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4926    1.8490    1.5888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5682    3.8602    1.5493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1737    4.2087   -0.2258 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8012    2.9458   -0.9671 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3956   -4.0180   -0.9159 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9134   -3.9020   -0.7947 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4354   -1.9795   -0.4477 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4082    0.2462   -0.1278 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  6  8  1  0
  8 10  1  6
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
  8  9  1  0
  9  2  1  0
 18  8  1  0
 27 21  1  0
 16 11  1  0
 28 17  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  6
  3 34  1  0
  3 35  1  0
  4 36  1  1
  5 37  1  0
  6 38  1  1
  7 39  1  0
 11 40  1  1
 12 41  1  0
 12 42  1  0
 16 43  1  6
 23 44  1  0
 24 45  1  0
 25 46  1  0
 26 47  1  0
M  END


  Mrv1533004241501422D          

 29 33  0  0  0  0            999 V2000
    4.0518   -3.2433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4956   -2.6340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6898   -2.8110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1336   -2.2017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3278   -2.3788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3831   -1.4154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5750   -1.2494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1889   -1.2383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7451   -1.8476    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9947   -1.0613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2442   -0.2749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9956    0.0658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9037    0.8856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5130    1.4419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0956    1.0516    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6880    0.3344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8822    0.1573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6327   -0.6290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8269   -0.8061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1628   -1.2956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2707   -0.1968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4649   -0.3739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2154   -1.1602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0913    0.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1582    1.0218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9640    1.1989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5202    0.5896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3260    0.7666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5756    1.5530    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  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  2  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
  8 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 21 27  1  0  0  0  0
 27 28  1  0  0  0  0
 17 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0243467

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC(O)C(O)C2(OC3CC(=O)OC3C3=C2C(=O)C2=C(O)C=CC=C2C3=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C20H18O9/c1-7-5-10(22)19(26)20(28-7)15-14(18-11(29-20)6-12(23)27-18)16(24)8-3-2-4-9(21)13(8)17(15)25/h2-4,7,10-11,18-19,21-22,26H,5-6H2,1H3

> <INCHI_KEY>
GCPUYRAAAXESMB-UHFFFAOYSA-N

> <FORMULA>
C20H18O9

> <MOLECULAR_WEIGHT>
402.355

> <EXACT_MASS>
402.09508216

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
38.554107691683384

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3,4,4'-trihydroxy-6-methyl-12',16'-dioxaspiro[oxane-2,17'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1'(10'),3',5',7'-tetraene-2',9',13'-trione

> <ALOGPS_LOGP>
0.94

> <JCHEM_LOGP>
0.5984636323333329

> <ALOGPS_LOGS>
-0.95

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.222728600575795

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.175854939720466

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2624406836476414

> <JCHEM_POLAR_SURFACE_AREA>
139.59000000000003

> <JCHEM_REFRACTIVITY>
94.97099999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.56e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,4,4'-trihydroxy-6-methyl-12',16'-dioxaspiro[oxane-2,17'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1'(10'),3',5',7'-tetraene-2',9',13'-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       7.563  -6.054   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.525  -4.917   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.021  -5.247   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.983  -4.110   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       2.479  -4.440   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.449  -2.642   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.940  -2.332   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.953  -2.312   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.991  -3.449   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       7.457  -1.981   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       7.923  -0.513   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.325   0.123   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.154   1.653   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      10.291   2.691   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       7.645   1.963   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.884   0.624   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.380   0.294   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.914  -1.174   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.410  -1.505   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.171  -2.418   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.372  -0.367   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.868  -0.698   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.402  -2.166   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -0.170   0.440   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.295   1.907   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.800   2.238   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.838   1.100   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.342   1.431   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.808   2.899   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    9                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10   18                                             
CONECT    9    8    2                                                       
CONECT   10    8   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   11   17                                                  
CONECT   17   16   18   28                                                  
CONECT   18   17    8   19                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   27                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   21   28                                                  
CONECT   28   27   17   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₁₈O₉

Average Mass

402.3550 Da

Monoisotopic Mass

402.09508 Da

IUPAC Name

3,4,4'-trihydroxy-6-methyl-12',16'-dioxaspiro[oxane-2,17'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1'(10'),3',5',7'-tetraene-2',9',13'-trione

Traditional Name

3,4,4'-trihydroxy-6-methyl-12',16'-dioxaspiro[oxane-2,17'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1'(10'),3',5',7'-tetraene-2',9',13'-trione

CAS Registry Number

Not Available

SMILES

CC1CC(O)C(O)C2(OC3CC(=O)OC3C3=C2C(=O)C2=C(O)C=CC=C2C3=O)O1

InChI Identifier

InChI=1S/C20H18O9/c1-7-5-10(22)19(26)20(28-7)15-14(18-11(29-20)6-12(23)27-18)16(24)8-3-2-4-9(21)13(8)17(15)25/h2-4,7,10-11,18-19,21-22,26H,5-6H2,1H3

InChI Key

GCPUYRAAAXESMB-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzoisochromanequinones. These are benzo derivatives of isochromanequinones. Isochromanequinones are structurally characterized by a quinone fused to an isochromane, and forming a naphtho[2,3-c]pyran-6,9-dione skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isochromanequinones

Sub Class

Benzoisochromanequinones

Direct Parent

Benzoisochromanequinones

Alternative Parents

Substituents

Benzoisochromanequinone
Naphthopyranone
Naphthopyran
Naphthoquinone
Naphthalene
Furopyran
Aryl ketone
Quinone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Ketal
Pyranone
Gamma butyrolactone
Benzenoid
Pyran
Oxane
Furan
Vinylogous acid
Oxolane
Carboxylic acid ester
1,2-diol
Ketone
Lactone
Secondary alcohol
Polyol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Acetal
Aldehyde
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organic oxygen compound
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	0.94	ALOGPS
logP	0.6	ChemAxon
logS	-0.95	ALOGPS
pKa (Strongest Acidic)	8.18	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	139.59 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	94.97 m³·mol⁻¹	ChemAxon
Polarizability	38.55 Å³	ChemAxon
Number of Rings	5	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

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

74072921

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3,4,4'-trihydroxy-6-methyl-12',16'-dioxaspiro[oxane-2,17'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1'(10'),3',5',7'-tetraene-2',9',13'-trione (NP0243467)

MOL for NP0243467 (3,4,4'-trihydroxy-6-methyl-12',16'-dioxaspiro[oxane-2,17'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1'(10'),3',5',7'-tetraene-2',9',13'-trione)

3D MOL for NP0243467 (3,4,4'-trihydroxy-6-methyl-12',16'-dioxaspiro[oxane-2,17'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1'(10'),3',5',7'-tetraene-2',9',13'-trione)

3D SDF for NP0243467 (3,4,4'-trihydroxy-6-methyl-12',16'-dioxaspiro[oxane-2,17'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1'(10'),3',5',7'-tetraene-2',9',13'-trione)

3D-SDF for NP0243467 (3,4,4'-trihydroxy-6-methyl-12',16'-dioxaspiro[oxane-2,17'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1'(10'),3',5',7'-tetraene-2',9',13'-trione)

PDB for NP0243467 (3,4,4'-trihydroxy-6-methyl-12',16'-dioxaspiro[oxane-2,17'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1'(10'),3',5',7'-tetraene-2',9',13'-trione)

3D PDB for NP0243467 (3,4,4'-trihydroxy-6-methyl-12',16'-dioxaspiro[oxane-2,17'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1'(10'),3',5',7'-tetraene-2',9',13'-trione)

SMILES for NP0243467 (3,4,4'-trihydroxy-6-methyl-12',16'-dioxaspiro[oxane-2,17'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1'(10'),3',5',7'-tetraene-2',9',13'-trione)

INCHI for NP0243467 (3,4,4'-trihydroxy-6-methyl-12',16'-dioxaspiro[oxane-2,17'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1'(10'),3',5',7'-tetraene-2',9',13'-trione)

Structure for NP0243467 (3,4,4'-trihydroxy-6-methyl-12',16'-dioxaspiro[oxane-2,17'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1'(10'),3',5',7'-tetraene-2',9',13'-trione)

3D Structure for NP0243467 (3,4,4'-trihydroxy-6-methyl-12',16'-dioxaspiro[oxane-2,17'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1'(10'),3',5',7'-tetraene-2',9',13'-trione)