NP-MRD: Showing NP-Card for 5-[(3r)-8,8-dimethyl-2h,3h,4h-pyrano[2,3-f]chromen-3-yl]-2,4-dihydroxybenzaldehyde (NP0145784)

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Record Information

Version

2.0

Created at

2022-09-02 01:03:15 UTC

Updated at

2022-09-02 01:03:15 UTC

NP-MRD ID

NP0145784

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-[(3r)-8,8-dimethyl-2h,3h,4h-pyrano[2,3-f]chromen-3-yl]-2,4-dihydroxybenzaldehyde

Description

5'-Formylglabridin belongs to the class of organic compounds known as pyranoisoflavonoids. These are isoflavonoids that contain a pyran ring fused to either of the A, B, or C ring of the isoflavonoid skeleton. 5-[(3r)-8,8-dimethyl-2h,3h,4h-pyrano[2,3-f]chromen-3-yl]-2,4-dihydroxybenzaldehyde is found in Glycyrrhiza glabra. 5-[(3r)-8,8-dimethyl-2h,3h,4h-pyrano[2,3-f]chromen-3-yl]-2,4-dihydroxybenzaldehyde was first documented in 2010 (PMID: 20022509). Based on a literature review very few articles have been published on 5'-formylglabridin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022203032D          

 26 29  0  0  1  0            999 V2000
    4.6465   -0.1178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465    0.9428    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
    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
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    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
    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 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5855   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5855    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4105    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    1.8414    0.0000 O   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
    3.6020    1.1270    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
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  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  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 17 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 15 23  1  0  0  0  0
 23 24  1  0  0  0  0
 14 25  1  0  0  0  0
 10 25  1  0  0  0  0
  7 26  1  0  0  0  0
  2 26  1  0  0  0  0
M  END

     RDKit          3D

 46 49  0  0  0  0  0  0  0  0999 V2000
   -5.8885   -0.9183    0.9338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0959   -0.0456   -0.0290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0929    0.8383   -0.7943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3467   -0.9111   -0.9657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0377   -0.8898   -1.1141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2999    0.0687   -0.2787 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9518    0.8962    0.6093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1934    1.7924    1.3806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8244    1.8664    1.2744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2145    1.0357    0.3885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9428    0.1467   -0.3796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211   -0.6790   -1.2751 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0518   -1.2231   -0.8840 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6310   -0.4726    0.2986 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0967   -0.4824    0.3427 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8712    0.5947   -0.0291 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2536    0.6065   -0.0320 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9905    1.7855   -0.4382 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3363    2.8198   -0.7966 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9114   -0.5318    0.3619 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2968   -0.5624    0.3725 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1766   -1.6491    0.7484 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7750   -1.6101    0.7346 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1541   -2.7765    1.1447 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2354    1.0204    0.1836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3101    0.8305    0.7219 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7145   -0.3369    1.4235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2291   -1.2559    1.7473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3352   -1.7274    0.3370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9488    0.2707   -1.1630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4374    1.6337   -0.1009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5181    1.3371   -1.5855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9207   -1.6057   -1.5655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4932   -1.5198   -1.7951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6977    2.4362    2.0702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2277    2.5597    1.8698 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7535   -1.2718   -1.7378 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8122   -2.2523   -0.5626 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1250   -0.8374    1.2085 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3787    1.4908   -0.3395 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0579    1.8816   -0.4695 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9057    0.1685    0.1189 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7037   -2.5391    1.0550 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1592   -2.8436    1.1992 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8019    1.5704    0.9300 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4638    1.2915   -0.8818 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2 26  1  0
 26  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  2  0
  6 11  1  0
 11 10  2  0
 10 25  1  0
 25 14  1  0
 14 13  1  0
 13 12  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 17 20  2  0
 20 21  1  0
 20 22  1  0
 22 23  2  0
 23 24  1  0
 10  9  1  0
  9  8  2  0
  4  2  1  0
 12 11  1  0
 23 15  1  0
  8  7  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  3 31  1  0
  3 32  1  0
  5 34  1  0
  4 33  1  0
 25 45  1  0
 25 46  1  0
 14 39  1  1
 13 37  1  0
 13 38  1  0
 16 40  1  0
 18 41  1  0
 21 42  1  0
 22 43  1  0
 24 44  1  0
  9 36  1  0
  8 35  1  0
M  END


  Mrv1652309022203032D          

 26 29  0  0  1  0            999 V2000
    4.6465   -0.1178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465    0.9428    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
    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
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    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
    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 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5855   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5855    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4105    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    1.8414    0.0000 O   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
    3.6020    1.1270    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
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  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  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 17 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 15 23  1  0  0  0  0
 23 24  1  0  0  0  0
 14 25  1  0  0  0  0
 10 25  1  0  0  0  0
  7 26  1  0  0  0  0
  2 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0145784

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)OC2=C(C=C1)C1=C(C[C@@H](CO1)C1=CC(C=O)=C(O)C=C1O)C=C2

> <INCHI_IDENTIFIER>
InChI=1S/C21H20O5/c1-21(2)6-5-15-19(26-21)4-3-12-7-14(11-25-20(12)15)16-8-13(10-22)17(23)9-18(16)24/h3-6,8-10,14,23-24H,7,11H2,1-2H3/t14-/m0/s1

> <INCHI_KEY>
XIEKVEQDEUJPTD-AWEZNQCLSA-N

> <FORMULA>
C21H20O5

> <MOLECULAR_WEIGHT>
352.386

> <EXACT_MASS>
352.131073744

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
37.35735388276953

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-[(3R)-8,8-dimethyl-2H,3H,4H,8H-pyrano[2,3-f]chromen-3-yl]-2,4-dihydroxybenzaldehyde

> <ALOGPS_LOGP>
4.10

> <JCHEM_LOGP>
4.454803624

> <ALOGPS_LOGS>
-4.70

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.3270708101321

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.686655015454276

> <JCHEM_PKA_STRONGEST_BASIC>
-4.585078035989654

> <JCHEM_POLAR_SURFACE_AREA>
75.99000000000001

> <JCHEM_REFRACTIVITY>
99.93759999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.04e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-[(3R)-8,8-dimethyl-2H,3H,4H-pyrano[2,3-f]chromen-3-yl]-2,4-dihydroxybenzaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       8.673  -0.220   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.673   1.760   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.414   3.437   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.104  -0.564   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.746   0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.516  -0.564   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.056  -0.564   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.826  -1.897   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -4.056  -3.231   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -4.826   0.770   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -6.366   0.770   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -4.056   2.104   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.516   2.104   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -1.746   3.437   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       6.724   2.104   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   26                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    8   26                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   25                                                  
CONECT   11   10    6   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   25                                                  
CONECT   15   14   16   23                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   15   24                                                  
CONECT   24   23                                                            
CONECT   25   14   10                                                       
CONECT   26    7    2                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₀O₅

Average Mass

352.3860 Da

Monoisotopic Mass

352.13107 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1(C)OC2=C(C=C1)C1=C(C[C@@H](CO1)C1=CC(C=O)=C(O)C=C1O)C=C2

InChI Identifier

InChI=1S/C21H20O5/c1-21(2)6-5-15-19(26-21)4-3-12-7-14(11-25-20(12)15)16-8-13(10-22)17(23)9-18(16)24/h3-6,8-10,14,23-24H,7,11H2,1-2H3/t14-/m0/s1

InChI Key

XIEKVEQDEUJPTD-AWEZNQCLSA-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
Glycyrrhiza glabra	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranoisoflavonoids. These are isoflavonoids that contain a pyran ring fused to either of the A, B, or C ring of the isoflavonoid skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Pyranoisoflavonoids

Direct Parent

Pyranoisoflavonoids

Alternative Parents

Substituents

Pyranoisoflavonoid
Hydroxyisoflavonoid
Isoflavanol
Isoflavan
Pyranochromene
2,2-dimethyl-1-benzopyran
Chromane
Benzopyran
1-benzopyran
Hydroxybenzaldehyde
Benzaldehyde
Benzoyl
Resorcinol
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Phenol
Aryl-aldehyde
Monocyclic benzene moiety
Benzenoid
Vinylogous acid
Organoheterocyclic compound
Oxacycle
Ether
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aldehyde
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	4.1	ALOGPS
logS	-4.7	ALOGPS

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

24649960

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

46230506

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Kuroda M, Mimaki Y, Honda S, Tanaka H, Yokota S, Mae T: Phenolics from Glycyrrhiza glabra roots and their PPAR-gamma ligand-binding activity. Bioorg Med Chem. 2010 Jan 15;18(2):962-70. doi: 10.1016/j.bmc.2009.11.027. Epub 2009 Nov 26. [PubMed:20022509 ]
LOTUS database [Link]

Showing NP-Card for 5-[(3r)-8,8-dimethyl-2h,3h,4h-pyrano[2,3-f]chromen-3-yl]-2,4-dihydroxybenzaldehyde (NP0145784)

MOL for NP0145784 (5-[(3r)-8,8-dimethyl-2h,3h,4h-pyrano[2,3-f]chromen-3-yl]-2,4-dihydroxybenzaldehyde)

3D MOL for NP0145784 (5-[(3r)-8,8-dimethyl-2h,3h,4h-pyrano[2,3-f]chromen-3-yl]-2,4-dihydroxybenzaldehyde)

3D SDF for NP0145784 (5-[(3r)-8,8-dimethyl-2h,3h,4h-pyrano[2,3-f]chromen-3-yl]-2,4-dihydroxybenzaldehyde)

3D-SDF for NP0145784 (5-[(3r)-8,8-dimethyl-2h,3h,4h-pyrano[2,3-f]chromen-3-yl]-2,4-dihydroxybenzaldehyde)

PDB for NP0145784 (5-[(3r)-8,8-dimethyl-2h,3h,4h-pyrano[2,3-f]chromen-3-yl]-2,4-dihydroxybenzaldehyde)

3D PDB for NP0145784 (5-[(3r)-8,8-dimethyl-2h,3h,4h-pyrano[2,3-f]chromen-3-yl]-2,4-dihydroxybenzaldehyde)

SMILES for NP0145784 (5-[(3r)-8,8-dimethyl-2h,3h,4h-pyrano[2,3-f]chromen-3-yl]-2,4-dihydroxybenzaldehyde)

INCHI for NP0145784 (5-[(3r)-8,8-dimethyl-2h,3h,4h-pyrano[2,3-f]chromen-3-yl]-2,4-dihydroxybenzaldehyde)

Structure for NP0145784 (5-[(3r)-8,8-dimethyl-2h,3h,4h-pyrano[2,3-f]chromen-3-yl]-2,4-dihydroxybenzaldehyde)

3D Structure for NP0145784 (5-[(3r)-8,8-dimethyl-2h,3h,4h-pyrano[2,3-f]chromen-3-yl]-2,4-dihydroxybenzaldehyde)