NP-MRD: Showing NP-Card for (2r,3r)-5-hydroxy-2,3,8,8-tetramethyl-6-(1-phenylethenyl)-2h,3h-pyrano[2,3-f]chromen-4-one (NP0168382)

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Record Information

Version

2.0

Created at

2022-09-03 04:10:32 UTC

Updated at

2022-09-03 04:10:32 UTC

NP-MRD ID

NP0168382

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r)-5-hydroxy-2,3,8,8-tetramethyl-6-(1-phenylethenyl)-2h,3h-pyrano[2,3-f]chromen-4-one

Description

Inophynone belongs to the class of organic compounds known as pyranochromenes. These are organic heterocyclic compounds containing a pyran ring fused to a chromene (1-benzopyran) moiety. (2r,3r)-5-hydroxy-2,3,8,8-tetramethyl-6-(1-phenylethenyl)-2h,3h-pyrano[2,3-f]chromen-4-one is found in Calophyllum inophyllum. Based on a literature review very few articles have been published on Inophynone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032206102D          

 28 31  0  0  1  0            999 V2000
    1.5395   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425   -0.1178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425    0.9428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0145    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  2  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  2  0  0  0  0
 14 21  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 12 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END

     RDKit          3D

 52 55  0  0  0  0  0  0  0  0999 V2000
    3.1491    0.6203    1.0793 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3698   -0.2906    0.5531 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9604   -1.5102    0.0192 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3509   -2.2365   -0.9817 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8977   -3.4129   -1.4795 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0836   -3.9113   -0.9928 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7134   -3.2084    0.0041 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1583   -2.0297    0.4983 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9245   -0.0734    0.5039 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0332   -1.1308    0.7537 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5438   -2.3432    1.0752 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3063   -0.9084    0.6680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8201    0.3422    0.3391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9689    1.3862    0.0925 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3972    1.1547    0.1808 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2132    2.2353   -0.0768 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8353    3.5264   -0.4115 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4574    3.8559   -1.7568 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4213    4.4683    0.6353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6255    3.7146   -0.4909 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4389    2.7172   -0.2554 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1720    0.5535    0.2565 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1403   -0.4571    0.2523 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0867   -0.1775    1.4037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6076   -1.8514    0.2746 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4273   -2.3070   -1.1739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2814   -1.9554    0.9140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0106   -2.9170    1.6448 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2062    0.4649    1.1160 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7466    1.5283    1.4842 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4207   -1.8638   -1.3997 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4052   -3.9735   -2.2674 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4914   -4.8235   -1.3908 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6436   -3.5857    0.3959 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6533   -1.4846    1.2807 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1259   -3.1885    1.2737 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5636    2.9553   -2.4013 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4758    4.2905   -1.6181 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7984    4.6092   -2.2610 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7096    5.3000    0.7694 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5578    3.8993    1.5822 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3896    4.8177    0.2711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0416    4.6958   -0.7489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5326    2.8370   -0.3094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7279   -0.3303   -0.6919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9420   -0.9147    2.2398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1590   -0.2455    1.0850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9528    0.8531    1.8036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3608   -2.4920    0.7840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3646   -2.1226   -1.7526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1424   -3.3685   -1.1840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5875   -1.7119   -1.5898 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
 23 22  1  0
 22 13  1  0
 13 12  2  0
 12 10  1  0
 10 11  1  0
 10  9  2  0
  9  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  9 15  1  0
 15 14  2  0
 14 21  1  0
 21 20  2  0
 20 17  1  0
 17 18  1  0
 17 19  1  0
 17 16  1  0
 12 27  1  0
 27 28  2  0
 27 25  1  0
 25 26  1  0
 25 23  1  0
 14 13  1  0
  8  3  1  0
 16 15  1  0
 24 46  1  0
 24 47  1  0
 24 48  1  0
 23 45  1  6
 11 36  1  0
  1 29  1  0
  1 30  1  0
  4 31  1  0
  5 32  1  0
  6 33  1  0
  7 34  1  0
  8 35  1  0
 21 44  1  0
 20 43  1  0
 18 37  1  0
 18 38  1  0
 18 39  1  0
 19 40  1  0
 19 41  1  0
 19 42  1  0
 25 49  1  1
 26 50  1  0
 26 51  1  0
 26 52  1  0
M  END


  Mrv1652309032206102D          

 28 31  0  0  1  0            999 V2000
    1.5395   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425   -0.1178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425    0.9428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0145    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  2  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  2  0  0  0  0
 14 21  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 12 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0168382

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1OC2=C(C(O)=C(C(=C)C3=CC=CC=C3)C3=C2C=CC(C)(C)O3)C(=O)[C@@H]1C

> <INCHI_IDENTIFIER>
InChI=1S/C24H24O4/c1-13-15(3)27-22-17-11-12-24(4,5)28-23(17)18(21(26)19(22)20(13)25)14(2)16-9-7-6-8-10-16/h6-13,15,26H,2H2,1,3-5H3/t13-,15-/m1/s1

> <INCHI_KEY>
CLZBUZYFEDJSCK-UKRRQHHQSA-N

> <FORMULA>
C24H24O4

> <MOLECULAR_WEIGHT>
376.452

> <EXACT_MASS>
376.167459253

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
41.37412608635754

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4R,5R)-8-hydroxy-4,5,12,12-tetramethyl-9-(1-phenylethenyl)-3,11-dioxatricyclo[8.4.0.0^{2,7}]tetradeca-1(10),2(7),8,13-tetraen-6-one

> <ALOGPS_LOGP>
5.00

> <JCHEM_LOGP>
5.6880838570000005

> <ALOGPS_LOGS>
-5.04

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.676092780834697

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.701235656361984

> <JCHEM_PKA_STRONGEST_BASIC>
-4.645774128524631

> <JCHEM_POLAR_SURFACE_AREA>
55.76

> <JCHEM_REFRACTIVITY>
119.67090000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.46e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4R,5R)-8-hydroxy-4,5,12,12-tetramethyl-9-(1-phenylethenyl)-3,11-dioxatricyclo[8.4.0.0^{2,7}]tetradeca-1(10),2(7),8,13-tetraen-6-one

> <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       2.874  -4.565   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.104  -3.231   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.564  -3.231   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.206  -4.565   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.746  -4.565   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.516  -3.231   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.746  -1.897   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.206  -1.897   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.414  -1.897   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.184  -3.231   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.564  -0.564   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.386  -0.220   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.386   1.760   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       5.184   2.104   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.494   3.437   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       7.494  -1.897   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    9                                                  
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    3                                                       
CONECT    9    2   10   15                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   27                                                  
CONECT   13   12   14   22                                                  
CONECT   14   13   15   21                                                  
CONECT   15   14    9   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   17   21                                                       
CONECT   21   20   14                                                       
CONECT   22   13   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   12   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₄O₄

Average Mass

376.4520 Da

Monoisotopic Mass

376.16746 Da

IUPAC Name

(4R,5R)-8-hydroxy-4,5,12,12-tetramethyl-9-(1-phenylethenyl)-3,11-dioxatricyclo[8.4.0.0^{2,7}]tetradeca-1(10),2(7),8,13-tetraen-6-one

Traditional Name

(4R,5R)-8-hydroxy-4,5,12,12-tetramethyl-9-(1-phenylethenyl)-3,11-dioxatricyclo[8.4.0.0^{2,7}]tetradeca-1(10),2(7),8,13-tetraen-6-one

CAS Registry Number

Not Available

SMILES

C[C@H]1OC2=C(C(O)=C(C(=C)C3=CC=CC=C3)C3=C2C=CC(C)(C)O3)C(=O)[C@@H]1C

InChI Identifier

InChI=1S/C24H24O4/c1-13-15(3)27-22-17-11-12-24(4,5)28-23(17)18(21(26)19(22)20(13)25)14(2)16-9-7-6-8-10-16/h6-13,15,26H,2H2,1,3-5H3/t13-,15-/m1/s1

InChI Key

CLZBUZYFEDJSCK-UKRRQHHQSA-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

Species Name	Source	Reference
Calophyllum inophyllum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranochromenes. These are organic heterocyclic compounds containing a pyran ring fused to a chromene (1-benzopyran) moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Pyranochromenes

Alternative Parents

Substituents

Pyranochromene
2,2-dimethyl-1-benzopyran
Chromone
Aryl alkyl ketone
Aryl ketone
Styrene
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Vinylogous acid
Ketone
Oxacycle
Ether
Organic oxide
Organic oxygen compound
Organooxygen compound
Aldehyde
Hydrocarbon derivative
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	5	ALOGPS
logP	5.69	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	8.7	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	55.76 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	119.67 m³·mol⁻¹	ChemAxon
Polarizability	41.37 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

C00041013

Chemspider ID

4477018

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5318443

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3r)-5-hydroxy-2,3,8,8-tetramethyl-6-(1-phenylethenyl)-2h,3h-pyrano[2,3-f]chromen-4-one (NP0168382)

MOL for NP0168382 ((2r,3r)-5-hydroxy-2,3,8,8-tetramethyl-6-(1-phenylethenyl)-2h,3h-pyrano[2,3-f]chromen-4-one)

3D MOL for NP0168382 ((2r,3r)-5-hydroxy-2,3,8,8-tetramethyl-6-(1-phenylethenyl)-2h,3h-pyrano[2,3-f]chromen-4-one)

3D SDF for NP0168382 ((2r,3r)-5-hydroxy-2,3,8,8-tetramethyl-6-(1-phenylethenyl)-2h,3h-pyrano[2,3-f]chromen-4-one)

3D-SDF for NP0168382 ((2r,3r)-5-hydroxy-2,3,8,8-tetramethyl-6-(1-phenylethenyl)-2h,3h-pyrano[2,3-f]chromen-4-one)

PDB for NP0168382 ((2r,3r)-5-hydroxy-2,3,8,8-tetramethyl-6-(1-phenylethenyl)-2h,3h-pyrano[2,3-f]chromen-4-one)

3D PDB for NP0168382 ((2r,3r)-5-hydroxy-2,3,8,8-tetramethyl-6-(1-phenylethenyl)-2h,3h-pyrano[2,3-f]chromen-4-one)

SMILES for NP0168382 ((2r,3r)-5-hydroxy-2,3,8,8-tetramethyl-6-(1-phenylethenyl)-2h,3h-pyrano[2,3-f]chromen-4-one)

INCHI for NP0168382 ((2r,3r)-5-hydroxy-2,3,8,8-tetramethyl-6-(1-phenylethenyl)-2h,3h-pyrano[2,3-f]chromen-4-one)

Structure for NP0168382 ((2r,3r)-5-hydroxy-2,3,8,8-tetramethyl-6-(1-phenylethenyl)-2h,3h-pyrano[2,3-f]chromen-4-one)

3D Structure for NP0168382 ((2r,3r)-5-hydroxy-2,3,8,8-tetramethyl-6-(1-phenylethenyl)-2h,3h-pyrano[2,3-f]chromen-4-one)