NP-MRD: Showing NP-Card for 2-(2h-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-2,3-dihydro-1-benzopyran-4-one (NP0263517)

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Record Information

Version

2.0

Created at

2022-09-08 06:43:30 UTC

Updated at

2022-09-08 06:43:30 UTC

NP-MRD ID

NP0263517

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-(2h-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-2,3-dihydro-1-benzopyran-4-one

Description

2-(2H-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-3,4-dihydro-2H-1-benzopyran-4-one belongs to the class of organic compounds known as 8-prenylated flavanones. These are flavanones that features a C5-isoprenoid substituent at the 8-position. 2-(2h-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-2,3-dihydro-1-benzopyran-4-one is found in Pongamia pinnata. 2-(2H-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-3,4-dihydro-2H-1-benzopyran-4-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251511152D          

 30 33  0  0  0  0            999 V2000
    6.2102    8.5354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    8.1229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    7.2979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102    6.8854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102    6.0604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9246    5.6479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9246    4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    5.6479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102    4.4104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    5.6479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    6.0604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    6.8854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    7.2979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    8.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    8.5354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    8.5354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    8.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    9.3604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    3.3305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    4.6654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 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
  8 14  1  0  0  0  0
 14 15  2  0  0  0  0
  3 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
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 12 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 25 29  1  0  0  0  0
 29 30  2  0  0  0  0
 22 30  1  0  0  0  0
M  END

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
   -2.9296   -3.5866    0.6687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4057   -2.9776   -0.3925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4515   -3.6398   -1.2103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9111   -1.6434   -0.7874 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0237   -0.7881   -0.7867 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8733   -1.1888    0.2097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3676    0.1823   -0.0842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0563    1.3162    0.1920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3035    1.1759    0.7873 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0743    2.3012    1.1029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6007    2.5895   -0.0782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3616    2.6833   -0.6672 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1899    3.9021   -0.9799 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4521    5.1378   -0.7303 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3910    1.5493   -0.9733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1041    0.3053   -0.6858 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6350   -0.8187   -0.9865 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0094   -0.7689   -1.3845 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9020   -0.8528   -0.2092 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6496   -1.8617    0.7314 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4199   -2.0171    1.8615 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4817   -1.1796    2.1187 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7480   -0.1826    1.2103 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9628   -0.0250    0.0592 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8485    0.5065    1.6980 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5086   -0.2979    2.6851 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4235   -1.0879    3.1517 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2516    0.4390   -2.2564 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7007    1.6679   -1.5959 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3140    2.7475   -1.5680 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3249   -4.5763    0.9260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1555   -3.1902    1.3349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4418   -3.3079   -2.2613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4672   -3.5046   -0.7385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2516   -4.7429   -1.1669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4993   -1.6716   -1.8248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8326   -1.3028   -1.0491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0346   -1.8779    0.2716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3965   -1.1952    1.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2905    2.8581    0.1547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9762    2.0705    1.6778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4636    3.0082    1.7363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2021    3.4266    0.1692 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0980    5.9577   -1.2309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4901    5.0488   -1.1105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5424    5.3412    0.3585 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1410   -1.6644   -2.0618 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8132   -2.5331    0.5429 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2163   -2.8036    2.5868 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1977    0.7628   -0.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9791    0.3024    3.4686 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2769   -0.8899    2.1634 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7927    0.3093   -3.2639 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3329    0.5875   -2.3736 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0
  9  8  1  0
  8 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 12 15  2  0
 15 29  1  0
 29 30  2  0
 29 28  1  0
 28 18  1  0
 18 17  1  0
 17 16  1  0
 16  7  2  0
  7  6  1  0
  6  4  1  0
  4  5  1  0
  4  2  1  0
  2  3  1  0
  2  1  2  3
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 27  1  0
 27 26  1  0
 26 25  1  0
 25 23  1  0
 23 24  2  0
  7  8  1  0
 24 19  1  0
 16 15  1  0
 23 22  1  0
 10 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  0
 14 44  1  0
 14 45  1  0
 14 46  1  0
 28 53  1  0
 28 54  1  0
 18 47  1  6
  6 38  1  0
  6 39  1  0
  4 36  1  6
  5 37  1  0
  3 33  1  0
  3 34  1  0
  3 35  1  0
  1 31  1  0
  1 32  1  0
 20 48  1  0
 21 49  1  0
 26 51  1  0
 26 52  1  0
 24 50  1  0
M  END


  Mrv1533004251511152D          

 30 33  0  0  0  0            999 V2000
    6.2102    8.5354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    8.1229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    7.2979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102    6.8854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102    6.0604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9246    5.6479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9246    4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    5.6479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102    4.4104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    5.6479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    6.0604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    6.8854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    7.2979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    8.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    8.5354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    8.5354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    8.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    9.3604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    3.3305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    4.6654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 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
  8 14  1  0  0  0  0
 14 15  2  0  0  0  0
  3 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
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 12 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 25 29  1  0  0  0  0
 29 30  2  0  0  0  0
 22 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0263517

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(OC)=C2C(=O)CC(OC2=C1CC(O)C(C)=C)C1=CC=C2OCOC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H24O7/c1-12(2)15(24)8-14-19(26-3)10-21(27-4)22-16(25)9-18(30-23(14)22)13-5-6-17-20(7-13)29-11-28-17/h5-7,10,15,18,24H,1,8-9,11H2,2-4H3

> <INCHI_KEY>
HEQLSVWMTJXPGS-UHFFFAOYSA-N

> <FORMULA>
C23H24O7

> <MOLECULAR_WEIGHT>
412.438

> <EXACT_MASS>
412.152203113

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
43.45608721258829

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(2H-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-3,4-dihydro-2H-1-benzopyran-4-one

> <ALOGPS_LOGP>
2.51

> <JCHEM_LOGP>
2.9593845543333335

> <ALOGPS_LOGS>
-4.16

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.608481402913569

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.94923638528499

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0519793436982443

> <JCHEM_POLAR_SURFACE_AREA>
83.45000000000002

> <JCHEM_REFRACTIVITY>
108.7262

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.84e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(2H-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-2,3-dihydro-1-benzopyran-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      11.592  15.933   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      10.259  15.163   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      10.259  13.623   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.592  12.853   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.592  11.313   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      12.926  10.543   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      12.926   9.003   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.259  10.543   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.259   9.003   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      11.592   8.233   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       8.925   8.233   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.591   9.003   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       7.591  10.543   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       8.925  11.313   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.925  12.853   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.591  13.623   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.591  15.163   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       8.925  15.933   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.258  15.933   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.924  15.163   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.258  17.473   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.258   8.233   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.258   6.693   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.924   5.923   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.590   6.693   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.126   6.217   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       1.220   7.463   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.126   8.709   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       3.590   8.233   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.924   9.003   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   15                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    8                                                  
CONECT    6    5    7                                                       
CONECT    7    6                                                            
CONECT    8    5    9   14                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   22                                                  
CONECT   13   12   14                                                       
CONECT   14   13    8   15                                                  
CONECT   15   14    3   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   12   23   30                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   29                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   25   30                                                  
CONECT   30   29   22                                                       
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₄O₇

Average Mass

412.4380 Da

Monoisotopic Mass

412.15220 Da

IUPAC Name

2-(2H-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-3,4-dihydro-2H-1-benzopyran-4-one

Traditional Name

2-(2H-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-2,3-dihydro-1-benzopyran-4-one

CAS Registry Number

Not Available

SMILES

COC1=CC(OC)=C2C(=O)CC(OC2=C1CC(O)C(C)=C)C1=CC=C2OCOC2=C1

InChI Identifier

InChI=1S/C23H24O7/c1-12(2)15(24)8-14-19(26-3)10-21(27-4)22-16(25)9-18(30-23(14)22)13-5-6-17-20(7-13)29-11-28-17/h5-7,10,15,18,24H,1,8-9,11H2,2-4H3

InChI Key

HEQLSVWMTJXPGS-UHFFFAOYSA-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
Pongamia pinnata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 8-prenylated flavanones. These are flavanones that features a C5-isoprenoid substituent at the 8-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavans

Direct Parent

8-prenylated flavanones

Alternative Parents

Substituents

8-prenylated flavanone
5-methoxyflavonoid-skeleton
7-methoxyflavonoid-skeleton
Flavanone
Chromone
Chromane
Benzopyran
1-benzopyran
Benzodioxole
Anisole
Aryl alkyl ketone
Aryl ketone
Alkyl aryl ether
Benzenoid
Ketone
Secondary alcohol
Acetal
Ether
Organoheterocyclic compound
Oxacycle
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Aldehyde
Alcohol
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	2.51	ALOGPS
logP	2.96	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	13.95	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	83.45 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	108.73 m³·mol⁻¹	ChemAxon
Polarizability	43.46 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	Yes	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

85310187

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-(2h-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-2,3-dihydro-1-benzopyran-4-one (NP0263517)

MOL for NP0263517 (2-(2h-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-2,3-dihydro-1-benzopyran-4-one)

3D MOL for NP0263517 (2-(2h-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-2,3-dihydro-1-benzopyran-4-one)

3D SDF for NP0263517 (2-(2h-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-2,3-dihydro-1-benzopyran-4-one)

3D-SDF for NP0263517 (2-(2h-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-2,3-dihydro-1-benzopyran-4-one)

PDB for NP0263517 (2-(2h-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-2,3-dihydro-1-benzopyran-4-one)

3D PDB for NP0263517 (2-(2h-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-2,3-dihydro-1-benzopyran-4-one)

SMILES for NP0263517 (2-(2h-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-2,3-dihydro-1-benzopyran-4-one)

INCHI for NP0263517 (2-(2h-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-2,3-dihydro-1-benzopyran-4-one)

Structure for NP0263517 (2-(2h-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-2,3-dihydro-1-benzopyran-4-one)

3D Structure for NP0263517 (2-(2h-1,3-benzodioxol-5-yl)-8-(2-hydroxy-3-methylbut-3-en-1-yl)-5,7-dimethoxy-2,3-dihydro-1-benzopyran-4-one)