NP-MRD: Showing NP-Card for (9r,10s)-9,10-dihydroxy-4,6,6,9-tetramethyl-7h,8h,10h-chromeno[4,3-c]isochromen-11-one (NP0307108)

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Record Information

Version

2.0

Created at

2022-09-11 00:00:29 UTC

Updated at

2022-09-11 00:00:29 UTC

NP-MRD ID

NP0307108

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(9r,10s)-9,10-dihydroxy-4,6,6,9-tetramethyl-7h,8h,10h-chromeno[4,3-c]isochromen-11-one

Description

(12S,13R)-12,13-dihydroxy-3,13,17,17-tetramethyl-8,18-dioxatetracyclo[8.8.0.0²,⁷.0¹¹,¹⁶]Octadeca-1(10),2,4,6,11(16)-pentaen-9-one belongs to the class of organic compounds known as angular pyranocoumarins. These are organic compounds containing a pyran (or a hydrogenated derivative) angularly fused to a coumarin moiety. Based on a literature review very few articles have been published on (12S,13R)-12,13-dihydroxy-3,13,17,17-tetramethyl-8,18-dioxatetracyclo[8.8.0.0²,⁷.0¹¹,¹⁶]Octadeca-1(10),2,4,6,11(16)-pentaen-9-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112202002D          

 25 28  0  0  1  0            999 V2000
    3.9550    1.9716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149   -0.8348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0647   -1.3025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0889    2.4305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0867    2.0834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845   -0.3671    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2546   -1.1466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744   -0.2111    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1615   -1.0360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6402   -0.3417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444    1.1921    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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
  2 12  2  0  0  0  0
  6 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  2  0  0  0  0
 10 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  6  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 17 25  1  0  0  0  0
M  END

     RDKit          3D

 47 50  0  0  0  0  0  0  0  0999 V2000
    3.7168   -0.9471    0.7937 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6499    0.4961    0.4922 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7678    1.3272    0.6187 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7457    2.6609    0.3504 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5466    3.2179   -0.0705 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4155    2.4493   -0.2127 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3208    3.0373   -0.6125 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1990    2.3625   -0.7710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8455    2.9220   -1.1491 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2008    1.0252   -0.5083 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3393    0.3438   -0.0782 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4877    1.1124    0.0692 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3631   -1.0201    0.1966 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2947   -1.8058   -0.2090 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6356   -2.3589   -1.5990 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1233   -2.9556    0.7603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9681   -1.0557   -0.3580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0266    0.2719   -0.6579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3293    0.7172   -1.0727 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6419    1.6944   -1.8962 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2387    0.5137    0.1409 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5829    1.1369   -0.0657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6166    0.9940    1.3133 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3496   -0.9759    0.3860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2385   -1.7991   -0.1556 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7848   -1.1626    1.1040 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1272   -1.2581    1.6760 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5841   -1.6012   -0.0979 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6797    0.8221    0.9549 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6446    3.2374    0.4702 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5401    4.2727   -0.2799 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0170   -1.4922   -2.1782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3096   -2.7384   -2.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4106   -3.1493   -1.4905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4027   -3.7812    0.2416 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1475   -3.2716    1.0560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3921   -2.5933    1.6605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7092   -0.1658   -1.7360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5855    1.6019   -2.8523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7726    1.8333    0.7968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3825    0.3707   -0.0014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6464    1.7396   -0.9833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2602    1.3416    1.9551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2895   -1.2946   -0.1559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5707   -1.1727    1.4556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5015   -2.2411   -1.1549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0822   -2.6619    0.5238 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2 12  2  0
 12  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 14 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  1  1
 21 24  1  0
 24 25  1  0
  6  5  2  0
  5  4  1  0
  4  3  2  0
  3  2  1  0
 11 12  1  0
 25 17  1  0
 18 10  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
 15 32  1  0
 15 33  1  0
 15 34  1  0
 16 35  1  0
 16 36  1  0
 16 37  1  0
 19 38  1  6
 20 39  1  0
 22 40  1  0
 22 41  1  0
 22 42  1  0
 23 43  1  0
 24 44  1  0
 24 45  1  0
 25 46  1  0
 25 47  1  0
  5 31  1  0
  4 30  1  0
  3 29  1  0
M  END


  Mrv1652309112202002D          

 25 28  0  0  1  0            999 V2000
    3.9550    1.9716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149   -0.8348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0647   -1.3025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0889    2.4305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0867    2.0834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845   -0.3671    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2546   -1.1466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744   -0.2111    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1615   -1.0360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6402   -0.3417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444    1.1921    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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
  2 12  2  0  0  0  0
  6 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  2  0  0  0  0
 10 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  6  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 17 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0307108

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=C2C(OC(=O)C3=C2OC(C)(C)C2=C3[C@H](O)[C@](C)(O)CC2)=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H22O5/c1-10-6-5-7-12-13(10)16-15(18(22)24-12)14-11(19(2,3)25-16)8-9-20(4,23)17(14)21/h5-7,17,21,23H,8-9H2,1-4H3/t17-,20+/m0/s1

> <INCHI_KEY>
HJGHJTUHZVARGW-FXAWDEMLSA-N

> <FORMULA>
C20H22O5

> <MOLECULAR_WEIGHT>
342.391

> <EXACT_MASS>
342.146723808

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
36.339976294947014

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(12S,13R)-12,13-dihydroxy-3,13,17,17-tetramethyl-8,18-dioxatetracyclo[8.8.0.0^{2,7}.0^{11,16}]octadeca-1(10),2,4,6,11(16)-pentaen-9-one

> <JCHEM_LOGP>
1.400781227666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.863236615976902

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.221374962809833

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2498972442113274

> <JCHEM_POLAR_SURFACE_AREA>
75.99000000000001

> <JCHEM_REFRACTIVITY>
93.9584

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(12S,13R)-12,13-dihydroxy-3,13,17,17-tetramethyl-8,18-dioxatetracyclo[8.8.0.0^{2,7}.0^{11,16}]octadeca-1(10),2,4,6,11(16)-pentaen-9-one

> <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       7.383   3.680   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.887   2.225   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.399   1.934   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.903   0.479   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.895  -0.685   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.383  -0.394   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       6.375  -1.558   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.862  -1.267   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       3.854  -2.431   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       4.358   0.188   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.366   1.352   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.879   1.061   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.862   2.807   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.350   3.098   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.899   4.537   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.029   3.889   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.342   1.934   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.846   0.479   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.838  -0.685   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.342  -2.140   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.326  -0.394   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.302  -1.934   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.195  -0.638   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -0.179   1.061   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.830   2.225   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   12                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   12                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   18                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11    2    6                                                  
CONECT   13   11   14                                                       
CONECT   14   13   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   14   18   25                                                  
CONECT   18   17   10   19                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23   24                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   21   25                                                       
CONECT   25   24   17                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₂O₅

Average Mass

342.3910 Da

Monoisotopic Mass

342.14672 Da

IUPAC Name

(12S,13R)-12,13-dihydroxy-3,13,17,17-tetramethyl-8,18-dioxatetracyclo[8.8.0.0^{2,7}.0^{11,16}]octadeca-1(10),2,4,6,11(16)-pentaen-9-one

Traditional Name

(12S,13R)-12,13-dihydroxy-3,13,17,17-tetramethyl-8,18-dioxatetracyclo[8.8.0.0^{2,7}.0^{11,16}]octadeca-1(10),2,4,6,11(16)-pentaen-9-one

CAS Registry Number

Not Available

SMILES

CC1=C2C(OC(=O)C3=C2OC(C)(C)C2=C3[C@H](O)[C@](C)(O)CC2)=CC=C1

InChI Identifier

InChI=1S/C20H22O5/c1-10-6-5-7-12-13(10)16-15(18(22)24-12)14-11(19(2,3)25-16)8-9-20(4,23)17(14)21/h5-7,17,21,23H,8-9H2,1-4H3/t17-,20+/m0/s1

InChI Key

HJGHJTUHZVARGW-FXAWDEMLSA-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 angular pyranocoumarins. These are organic compounds containing a pyran (or a hydrogenated derivative) angularly fused to a coumarin moiety.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Pyranocoumarins

Direct Parent

Angular pyranocoumarins

Alternative Parents

Substituents

Angular pyranocoumarin
Benzopyran
1-benzopyran
Alkyl aryl ether
Pyranone
Benzenoid
Pyran
Heteroaromatic compound
Vinylogous ester
Tertiary alcohol
1,2-diol
Lactone
Secondary alcohol
Ether
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Hydrocarbon derivative
Alcohol
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	1.4	ChemAxon
pKa (Strongest Acidic)	13.22	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.99 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	93.96 m³·mol⁻¹	ChemAxon
Polarizability	36.34 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

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

162936541

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (9r,10s)-9,10-dihydroxy-4,6,6,9-tetramethyl-7h,8h,10h-chromeno[4,3-c]isochromen-11-one (NP0307108)

MOL for NP0307108 ((9r,10s)-9,10-dihydroxy-4,6,6,9-tetramethyl-7h,8h,10h-chromeno[4,3-c]isochromen-11-one)

3D MOL for NP0307108 ((9r,10s)-9,10-dihydroxy-4,6,6,9-tetramethyl-7h,8h,10h-chromeno[4,3-c]isochromen-11-one)

3D SDF for NP0307108 ((9r,10s)-9,10-dihydroxy-4,6,6,9-tetramethyl-7h,8h,10h-chromeno[4,3-c]isochromen-11-one)

3D-SDF for NP0307108 ((9r,10s)-9,10-dihydroxy-4,6,6,9-tetramethyl-7h,8h,10h-chromeno[4,3-c]isochromen-11-one)

PDB for NP0307108 ((9r,10s)-9,10-dihydroxy-4,6,6,9-tetramethyl-7h,8h,10h-chromeno[4,3-c]isochromen-11-one)

3D PDB for NP0307108 ((9r,10s)-9,10-dihydroxy-4,6,6,9-tetramethyl-7h,8h,10h-chromeno[4,3-c]isochromen-11-one)

SMILES for NP0307108 ((9r,10s)-9,10-dihydroxy-4,6,6,9-tetramethyl-7h,8h,10h-chromeno[4,3-c]isochromen-11-one)

INCHI for NP0307108 ((9r,10s)-9,10-dihydroxy-4,6,6,9-tetramethyl-7h,8h,10h-chromeno[4,3-c]isochromen-11-one)

Structure for NP0307108 ((9r,10s)-9,10-dihydroxy-4,6,6,9-tetramethyl-7h,8h,10h-chromeno[4,3-c]isochromen-11-one)

3D Structure for NP0307108 ((9r,10s)-9,10-dihydroxy-4,6,6,9-tetramethyl-7h,8h,10h-chromeno[4,3-c]isochromen-11-one)