NP-MRD: Showing NP-Card for Vellokaempferol 3-methyl ether (NP0053328)

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Record Information

Version

2.0

Created at

2022-04-28 00:01:03 UTC

Updated at

2022-04-28 00:01:03 UTC

NP-MRD ID

NP0053328

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Vellokaempferol 3-methyl ether

Description

(2R)-4-hydroxy-7-(4-hydroxyphenyl)-6-methoxy-2-(prop-1-en-2-yl)-2H,3H,5H-furo[3,2-g]chromen-5-one belongs to the class of organic compounds known as 6-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 6-position. Vellokaempferol 3-methyl ether is found in Vellozia stipitata. Based on a literature review very few articles have been published on (2R)-4-hydroxy-7-(4-hydroxyphenyl)-6-methoxy-2-(prop-1-en-2-yl)-2H,3H,5H-furo[3,2-g]chromen-5-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282202012D          

 27 30  0  0  1  0            999 V2000
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1274    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6425   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9524    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3649    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3649   -0.3020    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
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  2  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 17 20  1  0  0  0  0
  3 21  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
  1 24  1  0  0  0  0
 23 25  1  6  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
M  END

     RDKit          3D

 45 48  0  0  0  0  0  0  0  0999 V2000
    4.4322   -2.2720    0.0408 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0682   -1.1171    0.0805 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0857   -0.7822   -0.9316 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7338   -0.1547    1.1759 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2281    1.1346    0.5987 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7697    0.8736    0.4512 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4537   -0.1874    1.2623 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1530   -0.6461    1.3220 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1130   -0.0800    0.5872 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0967   -0.5337    0.6652 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1065    0.0014   -0.0364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4252   -0.6102    0.1452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5032   -0.3503   -0.6285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7588   -0.9430   -0.3741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9205   -1.8074    0.6735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1713   -2.3764    0.8994 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8311   -2.0929    1.4826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6287   -1.5004    1.2079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8553    1.0564   -0.8554 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8291    1.6852   -1.6118 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4626    2.8260   -0.9846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5546    1.5460   -0.9423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2787    2.5231   -1.6930 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4802    0.9857   -0.2150 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7686    1.4681   -0.2977 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0570    2.5390   -1.1240 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6178   -0.6443    1.9361 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6563   -2.9928   -0.7473 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6878   -2.5569    0.7529 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6510   -0.3685   -1.8543 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8290   -0.0561   -0.5268 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6680   -1.6963   -1.1794 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5589    0.0077    1.8747 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6316    1.3707   -0.3996 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4424    1.9810    1.2685 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9056   -1.4809    1.9605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4711    0.2830   -1.4780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5944   -0.7064   -1.0175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8541   -1.9174    1.5071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9959   -2.7704    2.2879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7798   -1.7252    1.8420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8251    3.7149   -1.1430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4569    2.9000   -1.4553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5953    2.5991    0.0843 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0033    2.8737   -1.1684 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 19  1  0
 19 11  2  0
 11 10  1  0
 10  9  1  0
  9  8  2  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  1  0
  4 27  1  0
  4  2  1  0
  2  3  1  0
  2  1  2  3
  6 25  1  0
 25 26  1  0
 25 24  2  0
 24 22  1  0
 22 23  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 22 19  1  0
 18 12  1  0
 24  9  1  0
 27  7  1  0
 21 42  1  0
 21 43  1  0
 21 44  1  0
  8 36  1  0
  5 34  1  0
  5 35  1  0
  4 33  1  1
  3 30  1  0
  3 31  1  0
  3 32  1  0
  1 28  1  0
  1 29  1  0
 26 45  1  0
 13 37  1  0
 14 38  1  0
 16 39  1  0
 17 40  1  0
 18 41  1  0
M  END


  Mrv1652304282202012D          

 27 30  0  0  1  0            999 V2000
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1274    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6425   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9524    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3649    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3649   -0.3020    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
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  2  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 17 20  1  0  0  0  0
  3 21  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
  1 24  1  0  0  0  0
 23 25  1  6  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0053328

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(OC2=CC3=C(C[C@@H](O3)C(C)=C)C(O)=C2C1=O)C1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H18O6/c1-10(2)14-8-13-15(26-14)9-16-17(18(13)23)19(24)21(25-3)20(27-16)11-4-6-12(22)7-5-11/h4-7,9,14,22-23H,1,8H2,2-3H3/t14-/m1/s1

> <INCHI_KEY>
BTWAIEWIJBTSBE-CQSZACIVSA-N

> <FORMULA>
C21H18O6

> <MOLECULAR_WEIGHT>
366.369

> <EXACT_MASS>
366.1103383

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
38.529335692907786

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R)-4-hydroxy-7-(4-hydroxyphenyl)-6-methoxy-2-(prop-1-en-2-yl)-2H,3H,5H-furo[3,2-g]chromen-5-one

> <ALOGPS_LOGP>
3.66

> <JCHEM_LOGP>
3.7928529023333324

> <ALOGPS_LOGS>
-4.00

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.57176447564135

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.292378035480131

> <JCHEM_PKA_STRONGEST_BASIC>
-4.593945927863883

> <JCHEM_POLAR_SURFACE_AREA>
85.22000000000001

> <JCHEM_REFRACTIVITY>
100.53930000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.66e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-4-hydroxy-7-(4-hydroxyphenyl)-6-methoxy-2-(prop-1-en-2-yl)-2H,3H-furo[3,2-g]chromen-5-one

> <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       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.799   2.016   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.705   0.770   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.799  -0.476   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       9.245   0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.015   2.104   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.015  -0.564   0.000  0.00  0.00           C+0
CONECT    1    2    6   24                                                  
CONECT    2    1    3   22                                                  
CONECT    3    2    4   21                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9   14                                                  
CONECT    9    8   10   12                                                  
CONECT   10    9    4   11                                                  
CONECT   11   10                                                            
CONECT   12    9   13                                                       
CONECT   13   12                                                            
CONECT   14    8   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18   14                                                       
CONECT   20   17                                                            
CONECT   21    3                                                            
CONECT   22    2   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23    1                                                       
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₁₈O₆

Average Mass

366.3690 Da

Monoisotopic Mass

366.11034 Da

IUPAC Name

(2R)-4-hydroxy-7-(4-hydroxyphenyl)-6-methoxy-2-(prop-1-en-2-yl)-2H,3H,5H-furo[3,2-g]chromen-5-one

Traditional Name

(2R)-4-hydroxy-7-(4-hydroxyphenyl)-6-methoxy-2-(prop-1-en-2-yl)-2H,3H-furo[3,2-g]chromen-5-one

CAS Registry Number

Not Available

SMILES

COC1=C(OC2=CC3=C(C[C@@H](O3)C(C)=C)C(O)=C2C1=O)C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C21H18O6/c1-10(2)14-8-13-15(26-14)9-16-17(18(13)23)19(24)21(25-3)20(27-16)11-4-6-12(22)7-5-11/h4-7,9,14,22-23H,1,8H2,2-3H3/t14-/m1/s1

InChI Key

BTWAIEWIJBTSBE-CQSZACIVSA-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
Vellozia stipitata	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 6-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 6-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavones

Direct Parent

6-prenylated flavones

Alternative Parents

Substituents

6-prenylated flavone
Furanoflavone
Furanoflavonoid or dihydroflavonoid
3-methoxyflavonoid-skeleton
Hydroxyflavonoid
5-hydroxyflavonoid
4'-hydroxyflavonoid
Furanochromone
3-methoxychromone
Chromone
1-benzopyran
Benzopyran
Coumaran
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Phenol
Alkyl aryl ether
Benzenoid
Pyran
Monocyclic benzene moiety
Heteroaromatic compound
Vinylogous acid
Oxacycle
Organoheterocyclic compound
Ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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	3.66	ALOGPS
logP	3.79	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	7.29	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	85.22 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	100.54 m³·mol⁻¹	ChemAxon
Polarizability	38.53 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163040160

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Vellokaempferol 3-methyl ether (NP0053328)

MOL for NP0053328 (Vellokaempferol 3-methyl ether)

3D MOL for NP0053328 (Vellokaempferol 3-methyl ether)

3D SDF for NP0053328 (Vellokaempferol 3-methyl ether)

3D-SDF for NP0053328 (Vellokaempferol 3-methyl ether)

PDB for NP0053328 (Vellokaempferol 3-methyl ether)

3D PDB for NP0053328 (Vellokaempferol 3-methyl ether)

SMILES for NP0053328 (Vellokaempferol 3-methyl ether)

INCHI for NP0053328 (Vellokaempferol 3-methyl ether)

Structure for NP0053328 (Vellokaempferol 3-methyl ether)

3D Structure for NP0053328 (Vellokaempferol 3-methyl ether)