NP-MRD: Showing NP-Card for 3-{5,7-dimethoxy-2,2-dimethyl-6-[(1e)-3-methylbuta-1,3-dien-1-yl]chromen-8-yl}propanoic acid (NP0317147)

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Record Information

Version

2.0

Created at

2022-09-11 16:49:45 UTC

Updated at

2022-09-11 16:49:45 UTC

NP-MRD ID

NP0317147

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-{5,7-dimethoxy-2,2-dimethyl-6-[(1e)-3-methylbuta-1,3-dien-1-yl]chromen-8-yl}propanoic acid

Description

3-{5,7-dimethoxy-2,2-dimethyl-6-[(1e)-3-methylbuta-1,3-dien-1-yl]chromen-8-yl}propanoic acid is found in Drummondita hassellii.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112218492D          

 26 27  0  0  0  0            999 V2000
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    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
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    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   -0.4125    0.0000 C   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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 O   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
   -1.4289    0.0000    0.0000 O   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 O   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
    2.4256    0.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -0.5558    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   -1.6500    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
  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  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  2  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  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 12 18  2  0  0  0  0
  6 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 11 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  2  0  0  0  0
 10 26  1  0  0  0  0
M  END

     RDKit          3D

 52 53  0  0  0  0  0  0  0  0999 V2000
    5.9977   -1.3925   -0.5928 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0661   -0.4919   -0.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4242    0.8856    0.0065 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6630   -0.8720   -0.4718 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7164    0.0158   -0.2432 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3013   -0.1272   -0.2869 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6737   -1.3314   -0.3667 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3393   -2.5313   -0.4106 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6289   -3.2872    0.7664 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7358   -1.3690   -0.4019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5041   -0.2460   -0.3558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8376    0.9882   -0.2700 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7132    2.1793   -0.2056 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9217    2.6721    1.1908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8195    3.8759    1.1510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0946    4.4045    2.2591 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3273    4.3933   -0.0227 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5309    1.0621   -0.2359 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2099    2.2491   -0.1555 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6633    2.9439    0.9438 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8683   -0.3267   -0.3921 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5533   -1.5308   -0.4898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4682   -1.6987    0.7334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4092   -1.4971   -1.7596 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6962   -2.7321   -0.5380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3911   -2.6607   -0.4975 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0559   -1.1905   -0.5317 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7349   -2.4156   -0.8660 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0464    1.1118    1.0457 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9726    1.6217   -0.6889 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5280    1.0195    0.0595 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3686   -1.8579   -0.7689 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1061    1.0304    0.0373 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7197   -3.6365    1.2773 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2051   -4.1714    0.4321 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2774   -2.7060    1.4599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7146    1.9907   -0.6432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2513    2.9885   -0.8129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0225    2.9803    1.6977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4218    1.8926    1.8219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9922    5.2229   -0.4812 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7316    3.2625    0.8342 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0853    3.9061    1.0209 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5178    2.4315    1.9140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2702   -2.3896    0.4087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8980   -2.1422    1.5754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8576   -0.7064    1.0586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4198   -1.8541   -1.4803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9606   -2.1726   -2.5431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4295   -0.4804   -2.2034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1634   -3.7293   -0.6105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8227   -3.5816   -0.5394 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 19  1  0
 19 18  1  0
 18 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 17  1  0
 15 16  2  0
 12 11  1  0
 11 10  2  0
 10 26  1  0
 26 25  2  0
 25 22  1  0
 22 23  1  0
 22 24  1  0
 22 21  1  0
 10  7  1  0
  7  8  1  0
  8  9  1  0
  7  6  2  0
  6  5  1  0
  5  4  2  0
  4  2  1  0
  2  3  1  0
  2  1  2  0
  6 18  1  0
 21 11  1  0
 20 42  1  0
 20 43  1  0
 20 44  1  0
 13 37  1  0
 13 38  1  0
 14 39  1  0
 14 40  1  0
 17 41  1  0
 26 52  1  0
 25 51  1  0
 23 45  1  0
 23 46  1  0
 23 47  1  0
 24 48  1  0
 24 49  1  0
 24 50  1  0
  9 34  1  0
  9 35  1  0
  9 36  1  0
  5 33  1  0
  4 32  1  0
  3 29  1  0
  3 30  1  0
  3 31  1  0
  1 27  1  0
  1 28  1  0
M  END


  Mrv1652309112218492D          

 26 27  0  0  0  0            999 V2000
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    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
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    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   -0.4125    0.0000 C   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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 O   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
   -1.4289    0.0000    0.0000 O   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 O   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
    2.4256    0.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -0.5558    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   -1.6500    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
  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  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  2  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  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 12 18  2  0  0  0  0
  6 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 11 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  2  0  0  0  0
 10 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0317147

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(CCC(O)=O)C2=C(C=CC(C)(C)O2)C(OC)=C1\C=C\C(C)=C

> <INCHI_IDENTIFIER>
InChI=1S/C21H26O5/c1-13(2)7-8-14-18(24-5)15(9-10-17(22)23)20-16(19(14)25-6)11-12-21(3,4)26-20/h7-8,11-12H,1,9-10H2,2-6H3,(H,22,23)/b8-7+

> <INCHI_KEY>
DSIKSJZZYCHEKA-BQYQJAHWSA-N

> <FORMULA>
C21H26O5

> <MOLECULAR_WEIGHT>
358.434

> <EXACT_MASS>
358.178023937

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
39.68962517132617

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-{5,7-dimethoxy-2,2-dimethyl-6-[(1E)-3-methylbuta-1,3-dien-1-yl]-2H-chromen-8-yl}propanoic acid

> <JCHEM_LOGP>
4.148122654

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.9987487775906545

> <JCHEM_PKA_STRONGEST_BASIC>
-4.412034807896106

> <JCHEM_POLAR_SURFACE_AREA>
64.99000000000001

> <JCHEM_REFRACTIVITY>
103.57330000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
3-{5,7-dimethoxy-2,2-dimethyl-6-[(1E)-3-methylbuta-1,3-dien-1-yl]chromen-8-yl}propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.334  -5.390   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  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -2.667   4.620   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       0.000   4.620   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.667  -0.000   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.528   0.677   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.518  -1.037   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   18                                                  
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7   11   26                                                  
CONECT   11   10   12   21                                                  
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   12    6   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   11   22                                                       
CONECT   22   21   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22   26                                                       
CONECT   26   25   10                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₆O₅

Average Mass

358.4340 Da

Monoisotopic Mass

358.17802 Da

IUPAC Name

3-{5,7-dimethoxy-2,2-dimethyl-6-[(1E)-3-methylbuta-1,3-dien-1-yl]-2H-chromen-8-yl}propanoic acid

Traditional Name

3-{5,7-dimethoxy-2,2-dimethyl-6-[(1E)-3-methylbuta-1,3-dien-1-yl]chromen-8-yl}propanoic acid

CAS Registry Number

Not Available

SMILES

COC1=C(CCC(O)=O)C2=C(C=CC(C)(C)O2)C(OC)=C1\C=C\C(C)=C

InChI Identifier

InChI=1S/C21H26O5/c1-13(2)7-8-14-18(24-5)15(9-10-17(22)23)20-16(19(14)25-6)11-12-21(3,4)26-20/h7-8,11-12H,1,9-10H2,2-6H3,(H,22,23)/b8-7+

InChI Key

DSIKSJZZYCHEKA-BQYQJAHWSA-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
Drummondita hassellii	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	4.15	ChemAxon
pKa (Strongest Acidic)	4	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	64.99 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	103.57 m³·mol⁻¹	ChemAxon
Polarizability	39.69 Å³	ChemAxon
Number of Rings	2	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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-{5,7-dimethoxy-2,2-dimethyl-6-[(1e)-3-methylbuta-1,3-dien-1-yl]chromen-8-yl}propanoic acid (NP0317147)

MOL for NP0317147 (3-{5,7-dimethoxy-2,2-dimethyl-6-[(1e)-3-methylbuta-1,3-dien-1-yl]chromen-8-yl}propanoic acid)

3D MOL for NP0317147 (3-{5,7-dimethoxy-2,2-dimethyl-6-[(1e)-3-methylbuta-1,3-dien-1-yl]chromen-8-yl}propanoic acid)

3D SDF for NP0317147 (3-{5,7-dimethoxy-2,2-dimethyl-6-[(1e)-3-methylbuta-1,3-dien-1-yl]chromen-8-yl}propanoic acid)

3D-SDF for NP0317147 (3-{5,7-dimethoxy-2,2-dimethyl-6-[(1e)-3-methylbuta-1,3-dien-1-yl]chromen-8-yl}propanoic acid)

PDB for NP0317147 (3-{5,7-dimethoxy-2,2-dimethyl-6-[(1e)-3-methylbuta-1,3-dien-1-yl]chromen-8-yl}propanoic acid)

3D PDB for NP0317147 (3-{5,7-dimethoxy-2,2-dimethyl-6-[(1e)-3-methylbuta-1,3-dien-1-yl]chromen-8-yl}propanoic acid)

SMILES for NP0317147 (3-{5,7-dimethoxy-2,2-dimethyl-6-[(1e)-3-methylbuta-1,3-dien-1-yl]chromen-8-yl}propanoic acid)

INCHI for NP0317147 (3-{5,7-dimethoxy-2,2-dimethyl-6-[(1e)-3-methylbuta-1,3-dien-1-yl]chromen-8-yl}propanoic acid)

Structure for NP0317147 (3-{5,7-dimethoxy-2,2-dimethyl-6-[(1e)-3-methylbuta-1,3-dien-1-yl]chromen-8-yl}propanoic acid)

3D Structure for NP0317147 (3-{5,7-dimethoxy-2,2-dimethyl-6-[(1e)-3-methylbuta-1,3-dien-1-yl]chromen-8-yl}propanoic acid)