NP-MRD: Showing NP-Card for (7r)-9-hydroxy-5-[(3s)-3-hydroxy-2-methylbutan-2-yl]-7-methyl-4-phenyl-7h-cyclopenta[g]chromene-2,6,8-trione (NP0178455)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 16:27:03 UTC

Updated at

2022-09-03 16:27:04 UTC

NP-MRD ID

NP0178455

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(7r)-9-hydroxy-5-[(3s)-3-hydroxy-2-methylbutan-2-yl]-7-methyl-4-phenyl-7h-cyclopenta[g]chromene-2,6,8-trione

Description

(7R)-9-hydroxy-5-[(3S)-3-hydroxy-2-methylbutan-2-yl]-7-methyl-4-phenyl-2H,6H,7H,8H-cyclopenta[g]chromene-2,6,8-trione belongs to the class of organic compounds known as neoflavones. These are neoflavonoids with a structure based on the 4-phenylcoumarin skeleton. Based on a literature review very few articles have been published on (7R)-9-hydroxy-5-[(3S)-3-hydroxy-2-methylbutan-2-yl]-7-methyl-4-phenyl-2H,6H,7H,8H-cyclopenta[g]chromene-2,6,8-trione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032218272D          

 30 33  0  0  1  0            999 V2000
    3.3809    2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3809    1.3480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184    2.0625    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
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    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
   -0.7145   -0.4125    0.0000 O   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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   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
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8974   -1.0396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1274    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9524    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8974    1.8646    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  6  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  4  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
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
 17 24  1  0  0  0  0
  7 24  2  0  0  0  0
 12 24  1  0  0  0  0
  9 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
  8 29  1  0  0  0  0
 29 30  2  0  0  0  0
M  END

     RDKit          3D

 52 55  0  0  0  0  0  0  0  0999 V2000
    0.5680    2.2790    1.1369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1428    2.0367   -0.1046 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4894    2.0779    0.1267 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2322    0.7181   -0.9444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7203    1.0542   -2.0953 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4903    1.2877   -1.3949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2423   -0.2535   -0.0030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6563   -0.4970   -0.0782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4164   -0.8849    0.9963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8108   -1.0707    2.2080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5416   -1.4472    3.3124 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4573   -0.8836    2.3442 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1411   -1.0934    3.4844 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4288   -0.9818    3.6702 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9527   -1.1939    4.8185 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2647   -0.6343    2.6449 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6807   -0.3911    1.4020 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5467   -0.5151    0.2515 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2627   -1.4889   -0.6527 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1482   -1.8408   -1.6766 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3372   -1.1589   -1.7430 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6484   -0.1713   -0.8434 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7196    0.1361    0.1611 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3334   -0.4788    1.2276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8346   -0.9823    0.5574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7771   -1.4467    1.2051 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9222   -0.4142   -0.8192 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8243   -1.1877   -1.7233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4958   -0.6943   -1.2399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2187   -1.0357   -2.4011 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6706    2.2379    1.1559 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4040    3.4213    1.4370 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1769    1.8207    2.0645 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0479    2.8714   -0.8133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7102    2.1307    1.0767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3354    2.1370   -2.3964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6893    1.3486   -1.7630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6276    0.6071   -3.0254 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0549    1.9778   -0.7482 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0907    0.7509   -2.1759 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2614    2.1742   -2.2030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5537   -1.5960    3.2493 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3208   -0.5305    2.7060 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3371   -2.0477   -0.6335 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8988   -2.6193   -2.3828 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0399   -1.4352   -2.5523 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5810    0.3353   -0.9278 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0358    0.9373    0.8469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0625    0.6572   -0.8666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5595   -0.9318   -2.7749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7232   -2.2630   -1.5222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8634   -0.8274   -1.5790 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  4  7  1  0
  7 24  2  0
 24 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 12 10  2  0
 10 11  1  0
 10  9  1  0
  9  8  2  0
  8 29  1  0
 29 30  2  0
 29 27  1  0
 27 28  1  0
 27 25  1  0
 25 26  2  0
  8  7  1  0
 17 24  1  0
 23 18  1  0
 25  9  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  6
  3 35  1  0
  5 36  1  0
  5 37  1  0
  5 38  1  0
  6 39  1  0
  6 40  1  0
  6 41  1  0
 16 43  1  0
 19 44  1  0
 20 45  1  0
 21 46  1  0
 22 47  1  0
 23 48  1  0
 11 42  1  0
 27 49  1  1
 28 50  1  0
 28 51  1  0
 28 52  1  0
M  END


  Mrv1652309032218272D          

 30 33  0  0  1  0            999 V2000
    3.3809    2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3809    1.3480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184    2.0625    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
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    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
   -0.7145   -0.4125    0.0000 O   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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   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
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8974   -1.0396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1274    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9524    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8974    1.8646    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  6  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  4  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
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
 17 24  1  0  0  0  0
  7 24  2  0  0  0  0
 12 24  1  0  0  0  0
  9 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
  8 29  1  0  0  0  0
 29 30  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0178455

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](O)C(C)(C)C1=C2C(OC(=O)C=C2C2=CC=CC=C2)=C(O)C2=C1C(=O)[C@@H](C)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C24H22O6/c1-11-20(27)17-18(21(11)28)22(29)23-16(19(17)24(3,4)12(2)25)14(10-15(26)30-23)13-8-6-5-7-9-13/h5-12,25,29H,1-4H3/t11-,12+/m1/s1

> <INCHI_KEY>
HFAYPAPFNRWYPI-NEPJUHHUSA-N

> <FORMULA>
C24H22O6

> <MOLECULAR_WEIGHT>
406.434

> <EXACT_MASS>
406.141638428

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
41.55983192457942

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(7R)-9-hydroxy-5-[(3S)-3-hydroxy-2-methylbutan-2-yl]-7-methyl-4-phenyl-2H,6H,7H,8H-cyclopenta[g]chromene-2,6,8-trione

> <JCHEM_LOGP>
4.667708485999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.846998678125624

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.887935642563645

> <JCHEM_PKA_STRONGEST_BASIC>
-2.896356651244173

> <JCHEM_POLAR_SURFACE_AREA>
100.89999999999998

> <JCHEM_REFRACTIVITY>
121.02210000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(7R)-9-hydroxy-5-[(3S)-3-hydroxy-2-methylbutan-2-yl]-7-methyl-4-phenyl-7H-cyclopenta[g]chromene-2,6,8-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       6.311   5.184   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.541   3.850   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       6.311   2.516   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001   5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.461   3.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.000   4.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.799  -0.476   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       7.275  -1.941   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       7.705   0.770   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.245   0.770   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.799   2.016   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       7.275   3.481   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6    7                                             
CONECT    5    4                                                            
CONECT    6    4                                                            
CONECT    7    4    8   24                                                  
CONECT    8    7    9   29                                                  
CONECT    9    8   10   25                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   24                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   24                                                  
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   18                                                       
CONECT   24   17    7   12                                                  
CONECT   25    9   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27    8   30                                                  
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₂O₆

Average Mass

406.4340 Da

Monoisotopic Mass

406.14164 Da

IUPAC Name

(7R)-9-hydroxy-5-[(3S)-3-hydroxy-2-methylbutan-2-yl]-7-methyl-4-phenyl-2H,6H,7H,8H-cyclopenta[g]chromene-2,6,8-trione

Traditional Name

(7R)-9-hydroxy-5-[(3S)-3-hydroxy-2-methylbutan-2-yl]-7-methyl-4-phenyl-7H-cyclopenta[g]chromene-2,6,8-trione

CAS Registry Number

Not Available

SMILES

C[C@H](O)C(C)(C)C1=C2C(OC(=O)C=C2C2=CC=CC=C2)=C(O)C2=C1C(=O)[C@@H](C)C2=O

InChI Identifier

InChI=1S/C24H22O6/c1-11-20(27)17-18(21(11)28)22(29)23-16(19(17)24(3,4)12(2)25)14(10-15(26)30-23)13-8-6-5-7-9-13/h5-12,25,29H,1-4H3/t11-,12+/m1/s1

InChI Key

HFAYPAPFNRWYPI-NEPJUHHUSA-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 neoflavones. These are neoflavonoids with a structure based on the 4-phenylcoumarin skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Neoflavonoids

Sub Class

Neoflavones

Direct Parent

Neoflavones

Alternative Parents

Substituents

4-phenylcoumarin
Indanedione
Coumarin
Indanone
Benzopyran
1-benzopyran
Indane
Aryl ketone
Aryl alkyl ketone
1,3-diketone
Pyranone
Monocyclic benzene moiety
Benzenoid
1,3-dicarbonyl compound
Pyran
Heteroaromatic compound
Vinylogous acid
Secondary alcohol
Ketone
Lactone
Organoheterocyclic compound
Oxacycle
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen 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	4.67	ChemAxon
pKa (Strongest Acidic)	6.89	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	100.9 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	121.02 m³·mol⁻¹	ChemAxon
Polarizability	41.56 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

162868269

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (7r)-9-hydroxy-5-[(3s)-3-hydroxy-2-methylbutan-2-yl]-7-methyl-4-phenyl-7h-cyclopenta[g]chromene-2,6,8-trione (NP0178455)

MOL for NP0178455 ((7r)-9-hydroxy-5-[(3s)-3-hydroxy-2-methylbutan-2-yl]-7-methyl-4-phenyl-7h-cyclopenta[g]chromene-2,6,8-trione)

3D MOL for NP0178455 ((7r)-9-hydroxy-5-[(3s)-3-hydroxy-2-methylbutan-2-yl]-7-methyl-4-phenyl-7h-cyclopenta[g]chromene-2,6,8-trione)

3D SDF for NP0178455 ((7r)-9-hydroxy-5-[(3s)-3-hydroxy-2-methylbutan-2-yl]-7-methyl-4-phenyl-7h-cyclopenta[g]chromene-2,6,8-trione)

3D-SDF for NP0178455 ((7r)-9-hydroxy-5-[(3s)-3-hydroxy-2-methylbutan-2-yl]-7-methyl-4-phenyl-7h-cyclopenta[g]chromene-2,6,8-trione)

PDB for NP0178455 ((7r)-9-hydroxy-5-[(3s)-3-hydroxy-2-methylbutan-2-yl]-7-methyl-4-phenyl-7h-cyclopenta[g]chromene-2,6,8-trione)

3D PDB for NP0178455 ((7r)-9-hydroxy-5-[(3s)-3-hydroxy-2-methylbutan-2-yl]-7-methyl-4-phenyl-7h-cyclopenta[g]chromene-2,6,8-trione)

SMILES for NP0178455 ((7r)-9-hydroxy-5-[(3s)-3-hydroxy-2-methylbutan-2-yl]-7-methyl-4-phenyl-7h-cyclopenta[g]chromene-2,6,8-trione)

INCHI for NP0178455 ((7r)-9-hydroxy-5-[(3s)-3-hydroxy-2-methylbutan-2-yl]-7-methyl-4-phenyl-7h-cyclopenta[g]chromene-2,6,8-trione)

Structure for NP0178455 ((7r)-9-hydroxy-5-[(3s)-3-hydroxy-2-methylbutan-2-yl]-7-methyl-4-phenyl-7h-cyclopenta[g]chromene-2,6,8-trione)

3D Structure for NP0178455 ((7r)-9-hydroxy-5-[(3s)-3-hydroxy-2-methylbutan-2-yl]-7-methyl-4-phenyl-7h-cyclopenta[g]chromene-2,6,8-trione)