NP-MRD: Showing NP-Card for Pongapinone A (NP0054713)

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Record Information

Version

2.0

Created at

2022-04-28 00:58:50 UTC

Updated at

2022-04-28 00:58:50 UTC

NP-MRD ID

NP0054713

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Pongapinone A

Description

Pongapinone a belongs to the class of organic compounds known as 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position. Thus, pongapinone a is considered to be a flavonoid. Pongapinone A is found in Millettia pinnata. Based on a literature review very few articles have been published on Pongapinone a.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282202582D          

 30 33  0  0  0  0            999 V2000
    1.9233  -10.1854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -9.7729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -8.9479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -8.5354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089   -8.9479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089   -9.7729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4944   -8.5354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2201   -8.9479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -7.7104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -7.2979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089   -7.2979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089   -6.4729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4944   -6.0604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2201   -6.4729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9345   -6.0604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9345   -5.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2201   -4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4944   -5.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7192   -4.9805    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2041   -5.6479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7192   -6.3154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -6.0604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -8.5354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -7.7104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523  -10.1854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523  -11.0104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378  -11.4229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233  -11.0104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0251  -12.1514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2505  -12.1514    0.0000 C   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
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 15 21  1  0  0  0  0
 12 22  1  0  0  0  0
  3 23  1  0  0  0  0
 23 24  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
  1 28  1  0  0  0  0
 27 29  1  0  0  0  0
 27 30  1  0  0  0  0
M  END

     RDKit          3D

 52 55  0  0  0  0  0  0  0  0999 V2000
   -2.4592   -4.1910   -1.4091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4432   -3.2942   -1.0149 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7547   -1.9694   -0.8148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0128   -1.4629   -0.9821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3350   -0.1348   -0.7820 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3416    0.7170   -0.3952 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0422    0.2369   -0.2134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1245    1.1832    0.1836 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0639    1.4216    1.6030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7332   -1.0719   -0.4149 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5938   -1.6423   -0.2634 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7231   -2.9149   -0.4321 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8007   -0.9460    0.0514 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9557   -1.6052    0.1852 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9215   -2.9830    0.0036 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2189   -0.9428    0.5056 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3327   -1.7757    0.6309 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5577   -1.2425    0.9326 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7055    0.1079    1.1135 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6044    0.9168    0.9874 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3372    0.4152    0.6815 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0373    2.2000    1.2157 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3491    2.1802    1.7504 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7997    0.8767    1.4144 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7093    2.1105   -0.1780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9363    2.5535   -0.3395 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0434    1.6767   -0.7541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6359    2.1664   -2.0645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1184    1.6728    0.3282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6038    0.3694   -0.9526 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6350   -4.2279   -2.4820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1583   -5.2444   -1.1128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4103   -4.0321   -0.8374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8402   -2.1185   -1.2950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2659    2.4958    1.8153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7953    0.8327    2.1651 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9373    1.2269    2.0224 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8422    0.1090    0.1624 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7120   -3.5922    0.8103 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2497   -2.8465    0.4963 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4420   -1.8613    1.0347 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4999    1.0620    0.5894 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3216    2.2460    2.8632 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9588    2.9722    1.2910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9338    2.7993    0.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1614    3.6066   -0.1651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8346    2.7674   -2.5500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4829    2.8507   -1.9073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8383    1.3131   -2.7150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0686    1.2793   -0.0882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8320    1.0203    1.1668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2869    2.7129    0.6375 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  1  0
 27 29  1  0
 27 30  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  7 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 21  2  0
 21 20  1  0
 20 19  2  0
 19 24  1  0
 24 23  1  0
 23 22  1  0
 19 18  1  0
 18 17  2  0
 10  3  1  0
 17 16  1  0
 30  5  1  0
 22 20  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  4 34  1  0
 25 45  1  0
 26 46  1  0
 28 47  1  0
 28 48  1  0
 28 49  1  0
 29 50  1  0
 29 51  1  0
 29 52  1  0
  9 35  1  0
  9 36  1  0
  9 37  1  0
 13 38  1  0
 15 39  1  0
 21 42  1  0
 23 43  1  0
 23 44  1  0
 18 41  1  0
 17 40  1  0
M  END


  Mrv1652304282202582D          

 30 33  0  0  0  0            999 V2000
    1.9233  -10.1854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -9.7729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -8.9479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -8.5354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089   -8.9479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089   -9.7729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4944   -8.5354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2201   -8.9479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -7.7104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -7.2979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089   -7.2979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089   -6.4729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4944   -6.0604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2201   -6.4729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9345   -6.0604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9345   -5.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2201   -4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4944   -5.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7192   -4.9805    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2041   -5.6479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7192   -6.3154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -6.0604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -8.5354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -7.7104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523  -10.1854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523  -11.0104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378  -11.4229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233  -11.0104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0251  -12.1514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2505  -12.1514    0.0000 C   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
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 15 21  1  0  0  0  0
 12 22  1  0  0  0  0
  3 23  1  0  0  0  0
 23 24  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
  1 28  1  0  0  0  0
 27 29  1  0  0  0  0
 27 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0054713

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(C=CC(C)(C)O2)C(OC)=C1C(=O)\C=C(/O)C1=CC2=C(OCO2)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H22O7/c1-23(2)8-7-14-18(30-23)11-20(26-3)21(22(14)27-4)16(25)10-15(24)13-5-6-17-19(9-13)29-12-28-17/h5-11,24H,12H2,1-4H3/b15-10-

> <INCHI_KEY>
CHMQLCYFVBURMW-GDNBJRDFSA-N

> <FORMULA>
C23H22O7

> <MOLECULAR_WEIGHT>
410.422

> <EXACT_MASS>
410.136553048

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
43.27831076461465

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2Z)-3-(2H-1,3-benzodioxol-5-yl)-1-(5,7-dimethoxy-2,2-dimethyl-2H-chromen-6-yl)-3-hydroxyprop-2-en-1-one

> <ALOGPS_LOGP>
3.22

> <JCHEM_LOGP>
3.345292748333332

> <ALOGPS_LOGS>
-4.75

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
18.95189219729381

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.663947004102813

> <JCHEM_PKA_STRONGEST_BASIC>
-4.262879885702986

> <JCHEM_POLAR_SURFACE_AREA>
83.45000000000002

> <JCHEM_REFRACTIVITY>
111.85600000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.33e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
pongapinone A

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       3.590 -19.013   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.924 -18.243   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.924 -16.703   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.590 -15.933   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.257 -16.703   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.257 -18.243   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.923 -15.933   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -0.411 -16.703   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.590 -14.393   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.924 -13.623   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.257 -13.623   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.257 -12.083   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.923 -11.313   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.411 -12.083   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.744 -11.313   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.744  -9.773   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.411  -9.003   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.923  -9.773   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -3.209  -9.297   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -4.114 -10.543   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -3.209 -11.789   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       3.590 -11.313   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       6.258 -15.933   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.258 -14.393   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.258 -19.013   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.258 -20.553   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.924 -21.323   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       3.590 -20.553   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       5.647 -22.683   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.201 -22.683   0.000  0.00  0.00           C+0
CONECT    1    2    6   28                                                  
CONECT    2    1    3   25                                                  
CONECT    3    2    4   23                                                  
CONECT    4    3    5    9                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7                                                            
CONECT    9    4   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   22                                                  
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   21                                                  
CONECT   16   15   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17   13                                                       
CONECT   19   16   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   15                                                       
CONECT   22   12                                                            
CONECT   23    3   24                                                       
CONECT   24   23                                                            
CONECT   25    2   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29   30                                             
CONECT   28   27    1                                                       
CONECT   29   27                                                            
CONECT   30   27                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₂O₇

Average Mass

410.4220 Da

Monoisotopic Mass

410.13655 Da

IUPAC Name

(2Z)-3-(2H-1,3-benzodioxol-5-yl)-1-(5,7-dimethoxy-2,2-dimethyl-2H-chromen-6-yl)-3-hydroxyprop-2-en-1-one

Traditional Name

pongapinone A

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C=CC(C)(C)O2)C(OC)=C1C(=O)\C=C(/O)C1=CC2=C(OCO2)C=C1

InChI Identifier

InChI=1S/C23H22O7/c1-23(2)8-7-14-18(30-23)11-20(26-3)21(22(14)27-4)16(25)10-15(24)13-5-6-17-19(9-13)29-12-28-17/h5-11,24H,12H2,1-4H3/b15-10-

InChI Key

CHMQLCYFVBURMW-GDNBJRDFSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Pongamia pinnata	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

2,2-dimethyl-1-benzopyrans

Alternative Parents

Substituents

2,2-dimethyl-1-benzopyran
Cinnamic acid or derivatives
Benzodioxole
Anisole
Aryl ketone
Styrene
Alkyl aryl ether
Benzenoid
Acryloyl-group
Vinylogous acid
Alpha,beta-unsaturated ketone
Enone
Ketone
Acetal
Enol
Oxacycle
Ether
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Aldehyde
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Chalcones and dihydrochalcones (LMPK12120391 )

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	3.22	ALOGPS
logP	3.35	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	5.66	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	83.45 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	111.86 m³·mol⁻¹	ChemAxon
Polarizability	43.28 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

C00007014

Chemspider ID

4943244

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6438794

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Pongapinone A (NP0054713)

MOL for NP0054713 (Pongapinone A)

3D MOL for NP0054713 (Pongapinone A)

3D SDF for NP0054713 (Pongapinone A)

3D-SDF for NP0054713 (Pongapinone A)

PDB for NP0054713 (Pongapinone A)

3D PDB for NP0054713 (Pongapinone A)

SMILES for NP0054713 (Pongapinone A)

INCHI for NP0054713 (Pongapinone A)

Structure for NP0054713 (Pongapinone A)

3D Structure for NP0054713 (Pongapinone A)