NP-MRD: Showing NP-Card for flavaspidic acid pb (NP0271382)

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Record Information

Version

2.0

Created at

2022-09-08 17:39:23 UTC

Updated at

2022-09-08 17:39:24 UTC

NP-MRD ID

NP0271382

Secondary Accession Numbers

None

Natural Product Identification

Common Name

flavaspidic acid pb

Description

Flavaspidic acid PB, also known as flavaspidate PB, belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. Flavaspidic acid PB is an extremely weak basic (essentially neutral) compound (based on its pKa). flavaspidic acid pb is found in Dryopteris crassirhizoma. A polyphenol that is a phloroglucinol derivative isolated from the rhizomes of Dryopteris crassirhizoma and has been shown to exhibit radical scavenging and antibacterial activity.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231521492D          

 31 32  0  0  0  0            999 V2000
    0.7145    1.2375    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
    0.0000   -0.0000    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
   -1.4289    0.0000    0.0000 O   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
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   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   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 O   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
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6085   -4.2112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6165   -4.8067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1468   -5.7252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    0.0000 O   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 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 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
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 22 27  1  0  0  0  0
 15 27  1  0  0  0  0
 27 28  2  0  0  0  0
 21 29  1  0  0  0  0
 13 30  2  0  0  0  0
  6 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END

     RDKit          3D

 59 60  0  0  0  0  0  0  0  0999 V2000
    4.1776    4.3025    0.1502 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9836    2.9388    0.7768 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6706    1.9305   -0.0992 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5750    0.5450    0.3590 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5374    0.1823    1.1313 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5358   -0.4236    0.0366 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5682   -1.7126    0.5288 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5505   -2.1825    1.3271 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5486   -2.6458    0.2197 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6365   -4.0300    0.7826 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5244   -2.2552   -0.5767 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5133   -3.1716   -0.8865 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4407   -0.9691   -1.1007 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3102   -0.6496   -1.9537 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9738   -0.4549   -1.2776 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0027   -1.2201   -1.6177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8515   -2.2044   -2.6185 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3379   -1.1374   -1.0287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6932   -2.5344   -0.5107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4050   -0.8518   -2.1000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5290   -0.1256    0.0203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8120   -0.0068    0.6297 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5483    0.6585    0.3978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7537    1.6565    1.4386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7796    2.4068    1.7865 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0443    1.8411    2.1136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9626    2.9477    3.1516 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2227    0.5307   -0.2344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2890    1.2884    0.1354 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4358   -0.0906   -0.7869 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4230    1.1988   -1.2655 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0052    4.2059   -0.9288 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4491    4.9884    0.6268 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2201    4.6361    0.3387 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9365    2.6870    0.9260 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5251    2.8944    1.7660 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7969    2.2009   -0.1347 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3961    2.0173   -1.1576 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3370   -1.8101    1.6910 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4778   -4.7258   -0.0602 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6441   -4.1948    1.1769 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8295   -4.2293    1.5177 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5879   -4.0975   -0.4994 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5138    0.2053   -2.6175 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1840   -1.5242   -2.6819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8681   -1.8688   -3.5773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7382   -2.9978   -0.1951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3373   -2.4469    0.4066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1868   -3.1474   -1.2791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9074   -0.1543   -2.8146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2635   -0.3014   -1.6706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7048   -1.7638   -2.6217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5651   -0.5897    0.3357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8733    2.1562    1.4389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3794    0.9344    2.6949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0002    3.1190    3.5064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3679    2.6424    4.0338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6198    3.8821    2.6933 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6829    1.5205   -1.8433 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 18 21  1  0
 21 22  1  0
 21 23  2  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  1  0
 23 28  1  0
 28 29  2  0
 13 30  2  0
 30 31  1  0
 30  6  1  0
 28 15  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  2 36  1  0
  3 37  1  0
  3 38  1  0
  8 39  1  0
 10 40  1  0
 10 41  1  0
 10 42  1  0
 12 43  1  0
 14 44  1  0
 14 45  1  0
 17 46  1  0
 19 47  1  0
 19 48  1  0
 19 49  1  0
 20 50  1  0
 20 51  1  0
 20 52  1  0
 22 53  1  0
 26 54  1  0
 26 55  1  0
 27 56  1  0
 27 57  1  0
 27 58  1  0
 31 59  1  0
M  END


  Mrv1533004231521492D          

 31 32  0  0  0  0            999 V2000
    0.7145    1.2375    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
    0.0000   -0.0000    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
   -1.4289    0.0000    0.0000 O   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
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   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   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 O   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
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6085   -4.2112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6165   -4.8067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1468   -5.7252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    0.0000 O   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 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 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
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 22 27  1  0  0  0  0
 15 27  1  0  0  0  0
 27 28  2  0  0  0  0
 21 29  1  0  0  0  0
 13 30  2  0  0  0  0
  6 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0271382

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC(=O)C1=C(O)C(C)=C(O)C(CC2=C(O)C(C)(C)C(O)=C(C(=O)CC)C2=O)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C23H28O8/c1-6-8-14(25)15-18(27)10(3)17(26)11(19(15)28)9-12-20(29)16(13(24)7-2)22(31)23(4,5)21(12)30/h26-28,30-31H,6-9H2,1-5H3

> <INCHI_KEY>
NGODKUCEKYYIFN-UHFFFAOYSA-N

> <FORMULA>
C23H28O8

> <MOLECULAR_WEIGHT>
432.469

> <EXACT_MASS>
432.178417862

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
44.48860106325759

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(3-butanoyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-3,5-dihydroxy-4,4-dimethyl-6-propanoylcyclohexa-2,5-dien-1-one

> <ALOGPS_LOGP>
2.86

> <JCHEM_LOGP>
4.926018702333334

> <ALOGPS_LOGS>
-3.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
5.60453069383707

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.176068728597467

> <JCHEM_PKA_STRONGEST_BASIC>
-4.592119989389842

> <JCHEM_POLAR_SURFACE_AREA>
152.35999999999999

> <JCHEM_REFRACTIVITY>
117.16229999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.16e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(3-butanoyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-3,5-dihydroxy-4,4-dimethyl-6-propanoylcyclohexa-2,5-dien-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+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       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.334  -6.930   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.136  -7.861   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.151  -8.973   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.141 -10.687   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -6.668 -11.550   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -9.336 -10.010   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -6.668  -6.930   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -4.001 -11.550   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   30                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   30                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   27                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18   22   29                                                  
CONECT   22   21   23   27                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25                                                            
CONECT   27   22   15   28                                                  
CONECT   28   27                                                            
CONECT   29   21                                                            
CONECT   30   13    6   31                                                  
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   64    0
END

View in JSmol

Synonyms

Value	Source
Flavaspidate PB	Generator

Chemical Formula

C₂₃H₂₈O₈

Average Mass

432.4690 Da

Monoisotopic Mass

432.17842 Da

IUPAC Name

2-[(3-butanoyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-3,5-dihydroxy-4,4-dimethyl-6-propanoylcyclohexa-2,5-dien-1-one

Traditional Name

2-[(3-butanoyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-3,5-dihydroxy-4,4-dimethyl-6-propanoylcyclohexa-2,5-dien-1-one

CAS Registry Number

Not Available

SMILES

CCCC(=O)C1=C(O)C(C)=C(O)C(CC2=C(O)C(C)(C)C(O)=C(C(=O)CC)C2=O)=C1O

InChI Identifier

InChI=1S/C23H28O8/c1-6-8-14(25)15-18(27)10(3)17(26)11(19(15)28)9-12-20(29)16(13(24)7-2)22(31)23(4,5)21(12)30/h26-28,30-31H,6-9H2,1-5H3

InChI Key

NGODKUCEKYYIFN-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
Dryopteris crassirhizoma	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Alkyl-phenylketones

Alternative Parents

Substituents

Alkyl-phenylketone
Acylphloroglucinol derivative
Butyrophenone
Benzenetriol
Phloroglucinol derivative
P-cresol
O-cresol
Benzoyl
Aryl alkyl ketone
Toluene
Phenol
Benzenoid
Monocyclic benzene moiety
Vinylogous acid
Cyclic ketone
Polyol
Enol
Hydrocarbon derivative
Organic oxide
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

polyphenol (CHEBI:65898 )
aromatic ketone (CHEBI:65898 )
beta-hydroxy ketone (CHEBI:65898 )

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	2.86	ALOGPS
logP	4.93	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	3.18	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	152.36 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	117.16 m³·mol⁻¹	ChemAxon
Polarizability	44.49 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

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

Not Available

PDB ID

Not Available

ChEBI ID

65898

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for flavaspidic acid pb (NP0271382)

MOL for NP0271382 (flavaspidic acid pb)

3D MOL for NP0271382 (flavaspidic acid pb)

3D SDF for NP0271382 (flavaspidic acid pb)

3D-SDF for NP0271382 (flavaspidic acid pb)

PDB for NP0271382 (flavaspidic acid pb)

3D PDB for NP0271382 (flavaspidic acid pb)

SMILES for NP0271382 (flavaspidic acid pb)

INCHI for NP0271382 (flavaspidic acid pb)

Structure for NP0271382 (flavaspidic acid pb)

3D Structure for NP0271382 (flavaspidic acid pb)