NP-MRD: Showing NP-Card for 5,7-dihydroxy-8-(3-methylbut-2-enyl)4-phenylchromen-2-one (NP0028019)

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Record Information

Version

2.0

Created at

2021-06-19 20:01:19 UTC

Updated at

2021-06-29 23:54:32 UTC

NP-MRD ID

NP0028019

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,7-dihydroxy-8-(3-methylbut-2-enyl)4-phenylchromen-2-one

Provided By

JEOL Database JEOL Logo

Description

5,7-dihydroxy-8-(3-methylbut-2-enyl)4-phenylchromen-2-one is found in Marila pluricostata. 5,7-dihydroxy-8-(3-methylbut-2-enyl)4-phenylchromen-2-one was first documented in 2005 (Lopez-Perez, J. L., et al.). Based on a literature review very few articles have been published on 5,7-dihydroxy-8-(3-methylbut-2-en-1-yl)-4-phenyl-2H-chromen-2-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192122013D          

 42 44  0  0  0  0            999 V2000
   -4.8763    0.0013    4.8490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6049    0.6598    4.3799 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5010    0.6602    5.4017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5214    1.1777    3.1380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3531    1.8705    2.4862 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7980    1.0779    1.3225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2616    1.2813    0.0232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2163    2.2313   -0.2057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7712    0.5230   -1.0343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8064   -0.4651   -0.8078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4515   -1.1432   -1.9428 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2910   -0.7060    0.4775 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7584   -1.6959    0.8225 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5268   -2.5503   -0.1031 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2076   -3.9077   -0.2479 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9264   -4.7061   -1.1386 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9664   -4.1553   -1.8863 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2918   -2.8068   -1.7444 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5760   -2.0050   -0.8544 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1174   -1.8381    2.1094 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5341   -1.0656    3.2073 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8769   -1.2590    4.3673 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3933   -0.1112    2.8543 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8218    0.0783    1.5182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2694    0.5202    5.7294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6855   -1.0433    5.1163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6578    0.0101    4.0819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8371    1.1602    6.3163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5957    1.1712    5.0698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2237   -0.3687    5.6541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3981    1.1147    2.4925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5485    2.0979    3.1917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6875    2.8576    2.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4286    2.2457   -1.1539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1353    0.6750   -2.0466 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0165   -1.9607   -1.7140 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3975   -4.3507    0.3283 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6774   -5.7589   -1.2485 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5269   -4.7787   -2.5791 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1043   -2.3796   -2.3274 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8379   -0.9532   -0.7561 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8867   -2.5361    2.4260 H   0  0  0  0  0  0  0  0  0  0  0  0
  6 24  2  0  0  0  0
 16 17  2  0  0  0  0
 12 10  2  0  0  0  0
 17 18  1  0  0  0  0
 12 24  1  0  0  0  0
 18 19  2  0  0  0  0
 19 14  1  0  0  0  0
 13 14  1  0  0  0  0
  6  7  1  0  0  0  0
 12 13  1  0  0  0  0
 24 23  1  0  0  0  0
 23 21  1  0  0  0  0
  6  5  1  0  0  0  0
 21 20  1  0  0  0  0
 21 22  2  0  0  0  0
 20 13  2  0  0  0  0
 10 11  1  0  0  0  0
  5  4  1  0  0  0  0
  9  7  2  0  0  0  0
  4  2  2  3  0  0  0
 14 15  2  0  0  0  0
  2  1  1  0  0  0  0
  9 10  1  0  0  0  0
  2  3  1  0  0  0  0
 15 16  1  0  0  0  0
  7  8  1  0  0  0  0
  9 35  1  0  0  0  0
 20 42  1  0  0  0  0
 15 37  1  0  0  0  0
 16 38  1  0  0  0  0
 17 39  1  0  0  0  0
 18 40  1  0  0  0  0
 19 41  1  0  0  0  0
  5 32  1  0  0  0  0
  5 33  1  0  0  0  0
 11 36  1  0  0  0  0
  4 31  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  3 28  1  0  0  0  0
  3 29  1  0  0  0  0
  3 30  1  0  0  0  0
  8 34  1  0  0  0  0
M  END

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
   -4.8763    0.0013    4.8490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6049    0.6598    4.3799 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5010    0.6602    5.4017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5214    1.1777    3.1380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3531    1.8705    2.4862 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7980    1.0779    1.3225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2616    1.2813    0.0232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2163    2.2313   -0.2057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7712    0.5230   -1.0343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8064   -0.4651   -0.8078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4515   -1.1432   -1.9428 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2910   -0.7060    0.4775 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7584   -1.6959    0.8225 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5268   -2.5503   -0.1031 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2076   -3.9077   -0.2479 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9264   -4.7061   -1.1386 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9664   -4.1553   -1.8863 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2918   -2.8068   -1.7444 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5760   -2.0050   -0.8544 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1174   -1.8381    2.1094 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5341   -1.0656    3.2073 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8769   -1.2590    4.3673 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3933   -0.1112    2.8543 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8218    0.0783    1.5182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2694    0.5202    5.7294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6855   -1.0433    5.1163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6578    0.0101    4.0819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8371    1.1602    6.3163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5957    1.1712    5.0698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2237   -0.3687    5.6541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3981    1.1147    2.4925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5485    2.0979    3.1917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6875    2.8576    2.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4286    2.2457   -1.1539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1353    0.6750   -2.0466 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0165   -1.9607   -1.7140 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3975   -4.3507    0.3283 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6774   -5.7589   -1.2485 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5269   -4.7787   -2.5791 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1043   -2.3796   -2.3274 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8379   -0.9532   -0.7561 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8867   -2.5361    2.4260 H   0  0  0  0  0  0  0  0  0  0  0  0
  6 24  2  0
 16 17  2  0
 12 10  2  0
 17 18  1  0
 12 24  1  0
 18 19  2  0
 19 14  1  0
 13 14  1  0
  6  7  1  0
 12 13  1  0
 24 23  1  0
 23 21  1  0
  6  5  1  0
 21 20  1  0
 21 22  2  0
 20 13  2  0
 10 11  1  0
  5  4  1  0
  9  7  2  0
  4  2  2  3
 14 15  2  0
  2  1  1  0
  9 10  1  0
  2  3  1  0
 15 16  1  0
  7  8  1  0
  9 35  1  0
 20 42  1  0
 15 37  1  0
 16 38  1  0
 17 39  1  0
 18 40  1  0
 19 41  1  0
  5 32  1  0
  5 33  1  0
 11 36  1  0
  4 31  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  8 34  1  0
M  END


  Mrv1652306192122013D          

 42 44  0  0  0  0            999 V2000
   -4.8763    0.0013    4.8490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6049    0.6598    4.3799 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5010    0.6602    5.4017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5214    1.1777    3.1380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3531    1.8705    2.4862 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7980    1.0779    1.3225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2616    1.2813    0.0232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2163    2.2313   -0.2057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7712    0.5230   -1.0343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8064   -0.4651   -0.8078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4515   -1.1432   -1.9428 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2910   -0.7060    0.4775 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7584   -1.6959    0.8225 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5268   -2.5503   -0.1031 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2076   -3.9077   -0.2479 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9264   -4.7061   -1.1386 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9664   -4.1553   -1.8863 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2918   -2.8068   -1.7444 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5760   -2.0050   -0.8544 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1174   -1.8381    2.1094 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5341   -1.0656    3.2073 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8769   -1.2590    4.3673 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3933   -0.1112    2.8543 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8218    0.0783    1.5182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2694    0.5202    5.7294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6855   -1.0433    5.1163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6578    0.0101    4.0819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8371    1.1602    6.3163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5957    1.1712    5.0698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2237   -0.3687    5.6541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3981    1.1147    2.4925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5485    2.0979    3.1917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6875    2.8576    2.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4286    2.2457   -1.1539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1353    0.6750   -2.0466 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0165   -1.9607   -1.7140 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3975   -4.3507    0.3283 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6774   -5.7589   -1.2485 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5269   -4.7787   -2.5791 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1043   -2.3796   -2.3274 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8379   -0.9532   -0.7561 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8867   -2.5361    2.4260 H   0  0  0  0  0  0  0  0  0  0  0  0
  6 24  2  0  0  0  0
 16 17  2  0  0  0  0
 12 10  2  0  0  0  0
 17 18  1  0  0  0  0
 12 24  1  0  0  0  0
 18 19  2  0  0  0  0
 19 14  1  0  0  0  0
 13 14  1  0  0  0  0
  6  7  1  0  0  0  0
 12 13  1  0  0  0  0
 24 23  1  0  0  0  0
 23 21  1  0  0  0  0
  6  5  1  0  0  0  0
 21 20  1  0  0  0  0
 21 22  2  0  0  0  0
 20 13  2  0  0  0  0
 10 11  1  0  0  0  0
  5  4  1  0  0  0  0
  9  7  2  0  0  0  0
  4  2  2  3  0  0  0
 14 15  2  0  0  0  0
  2  1  1  0  0  0  0
  9 10  1  0  0  0  0
  2  3  1  0  0  0  0
 15 16  1  0  0  0  0
  7  8  1  0  0  0  0
  9 35  1  0  0  0  0
 20 42  1  0  0  0  0
 15 37  1  0  0  0  0
 16 38  1  0  0  0  0
 17 39  1  0  0  0  0
 18 40  1  0  0  0  0
 19 41  1  0  0  0  0
  5 32  1  0  0  0  0
  5 33  1  0  0  0  0
 11 36  1  0  0  0  0
  4 31  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  3 28  1  0  0  0  0
  3 29  1  0  0  0  0
  3 30  1  0  0  0  0
  8 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0028019

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C(O[H])=C2C(OC(=O)C([H])=C2C2=C([H])C([H])=C([H])C([H])=C2[H])=C1C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H18O4/c1-12(2)8-9-14-16(21)11-17(22)19-15(10-18(23)24-20(14)19)13-6-4-3-5-7-13/h3-8,10-11,21-22H,9H2,1-2H3

> <INCHI_KEY>
SRGRDIADLLPPQM-UHFFFAOYSA-N

> <FORMULA>
C20H18O4

> <MOLECULAR_WEIGHT>
322.36

> <EXACT_MASS>
322.12050906

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
34.7986499410549

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,7-dihydroxy-8-(3-methylbut-2-en-1-yl)-4-phenyl-2H-chromen-2-one

> <ALOGPS_LOGP>
4.40

> <JCHEM_LOGP>
4.337994549

> <ALOGPS_LOGS>
-4.55

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.564585603063948

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.250403985776072

> <JCHEM_PKA_STRONGEST_BASIC>
-6.967064292547591

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
103.30590000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.12e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,7-dihydroxy-8-(3-methylbut-2-en-1-yl)-4-phenylchromen-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
   -4.8763    0.0013    4.8490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6049    0.6598    4.3799 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5010    0.6602    5.4017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5214    1.1777    3.1380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3531    1.8705    2.4862 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7980    1.0779    1.3225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2616    1.2813    0.0232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2163    2.2313   -0.2057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7712    0.5230   -1.0343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8064   -0.4651   -0.8078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4515   -1.1432   -1.9428 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2910   -0.7060    0.4775 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7584   -1.6959    0.8225 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5268   -2.5503   -0.1031 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2076   -3.9077   -0.2479 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9264   -4.7061   -1.1386 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9664   -4.1553   -1.8863 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2918   -2.8068   -1.7444 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5760   -2.0050   -0.8544 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1174   -1.8381    2.1094 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5341   -1.0656    3.2073 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8769   -1.2590    4.3673 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3933   -0.1112    2.8543 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8218    0.0783    1.5182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2694    0.5202    5.7294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6855   -1.0433    5.1163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6578    0.0101    4.0819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8371    1.1602    6.3163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5957    1.1712    5.0698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2237   -0.3687    5.6541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3981    1.1147    2.4925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5485    2.0979    3.1917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6875    2.8576    2.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4286    2.2457   -1.1539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1353    0.6750   -2.0466 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0165   -1.9607   -1.7140 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3975   -4.3507    0.3283 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6774   -5.7589   -1.2485 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5269   -4.7787   -2.5791 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1043   -2.3796   -2.3274 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8379   -0.9532   -0.7561 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8867   -2.5361    2.4260 H   0  0  0  0  0  0  0  0  0  0  0  0
  6 24  2  0
 16 17  2  0
 12 10  2  0
 17 18  1  0
 12 24  1  0
 18 19  2  0
 19 14  1  0
 13 14  1  0
  6  7  1  0
 12 13  1  0
 24 23  1  0
 23 21  1  0
  6  5  1  0
 21 20  1  0
 21 22  2  0
 20 13  2  0
 10 11  1  0
  5  4  1  0
  9  7  2  0
  4  2  2  3
 14 15  2  0
  2  1  1  0
  9 10  1  0
  2  3  1  0
 15 16  1  0
  7  8  1  0
  9 35  1  0
 20 42  1  0
 15 37  1  0
 16 38  1  0
 17 39  1  0
 18 40  1  0
 19 41  1  0
  5 32  1  0
  5 33  1  0
 11 36  1  0
  4 31  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  8 34  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0      -4.876   0.001   4.849  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.605   0.660   4.380  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.501   0.660   5.402  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.521   1.178   3.138  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.353   1.871   2.486  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.798   1.078   1.323  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.262   1.281   0.023  0.00  0.00           C+0
HETATM    8  O   UNK     0      -3.216   2.231  -0.206  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.771   0.523  -1.034  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.806  -0.465  -0.808  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.452  -1.143  -1.943  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.291  -0.706   0.478  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.758  -1.696   0.823  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.527  -2.550  -0.103  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.208  -3.908  -0.248  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.926  -4.706  -1.139  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.966  -4.155  -1.886  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.292  -2.807  -1.744  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.576  -2.005  -0.854  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.117  -1.838   2.109  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.534  -1.066   3.207  0.00  0.00           C+0
HETATM   22  O   UNK     0       0.877  -1.259   4.367  0.00  0.00           O+0
HETATM   23  O   UNK     0      -0.393  -0.111   2.854  0.00  0.00           O+0
HETATM   24  C   UNK     0      -0.822   0.078   1.518  0.00  0.00           C+0
HETATM   25  H   UNK     0      -5.269   0.520   5.729  0.00  0.00           H+0
HETATM   26  H   UNK     0      -4.686  -1.043   5.116  0.00  0.00           H+0
HETATM   27  H   UNK     0      -5.658   0.010   4.082  0.00  0.00           H+0
HETATM   28  H   UNK     0      -2.837   1.160   6.316  0.00  0.00           H+0
HETATM   29  H   UNK     0      -1.596   1.171   5.070  0.00  0.00           H+0
HETATM   30  H   UNK     0      -2.224  -0.369   5.654  0.00  0.00           H+0
HETATM   31  H   UNK     0      -4.398   1.115   2.493  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.549   2.098   3.192  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.688   2.858   2.142  0.00  0.00           H+0
HETATM   34  H   UNK     0      -3.429   2.246  -1.154  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.135   0.675  -2.047  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.017  -1.961  -1.714  0.00  0.00           H+0
HETATM   37  H   UNK     0       0.398  -4.351   0.328  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.677  -5.759  -1.248  0.00  0.00           H+0
HETATM   39  H   UNK     0       3.527  -4.779  -2.579  0.00  0.00           H+0
HETATM   40  H   UNK     0       4.104  -2.380  -2.327  0.00  0.00           H+0
HETATM   41  H   UNK     0       2.838  -0.953  -0.756  0.00  0.00           H+0
HETATM   42  H   UNK     0       1.887  -2.536   2.426  0.00  0.00           H+0
CONECT    1    2   25   26   27                                             
CONECT    2    4    1    3                                                  
CONECT    3    2   28   29   30                                             
CONECT    4    5    2   31                                                  
CONECT    5    6    4   32   33                                             
CONECT    6   24    7    5                                                  
CONECT    7    6    9    8                                                  
CONECT    8    7   34                                                       
CONECT    9    7   10   35                                                  
CONECT   10   12   11    9                                                  
CONECT   11   10   36                                                       
CONECT   12   10   24   13                                                  
CONECT   13   14   12   20                                                  
CONECT   14   19   13   15                                                  
CONECT   15   14   16   37                                                  
CONECT   16   17   15   38                                                  
CONECT   17   16   18   39                                                  
CONECT   18   17   19   40                                                  
CONECT   19   18   14   41                                                  
CONECT   20   21   13   42                                                  
CONECT   21   23   20   22                                                  
CONECT   22   21                                                            
CONECT   23   24   21                                                       
CONECT   24    6   12   23                                                  
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    3                                                            
CONECT   29    3                                                            
CONECT   30    3                                                            
CONECT   31    4                                                            
CONECT   32    5                                                            
CONECT   33    5                                                            
CONECT   34    8                                                            
CONECT   35    9                                                            
CONECT   36   11                                                            
CONECT   37   15                                                            
CONECT   38   16                                                            
CONECT   39   17                                                            
CONECT   40   18                                                            
CONECT   41   19                                                            
CONECT   42   20                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   88    0
END

RDKit          3D

42 44  0  0  0  0  0  0  0  0999 V2000
   -4.8763    0.0013    4.8490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6049    0.6598    4.3799 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5010    0.6602    5.4017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5214    1.1777    3.1380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3531    1.8705    2.4862 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7980    1.0779    1.3225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2616    1.2813    0.0232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2163    2.2313   -0.2057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7712    0.5230   -1.0343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8064   -0.4651   -0.8078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4515   -1.1432   -1.9428 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2910   -0.7060    0.4775 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7584   -1.6959    0.8225 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5268   -2.5503   -0.1031 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2076   -3.9077   -0.2479 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9264   -4.7061   -1.1386 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9664   -4.1553   -1.8863 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2918   -2.8068   -1.7444 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5760   -2.0050   -0.8544 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1174   -1.8381    2.1094 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5341   -1.0656    3.2073 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8769   -1.2590    4.3673 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3933   -0.1112    2.8543 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8218    0.0783    1.5182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2694    0.5202    5.7294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6855   -1.0433    5.1163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6578    0.0101    4.0819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8371    1.1602    6.3163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5957    1.1712    5.0698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2237   -0.3687    5.6541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3981    1.1147    2.4925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5485    2.0979    3.1917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6875    2.8576    2.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4286    2.2457   -1.1539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1353    0.6750   -2.0466 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0165   -1.9607   -1.7140 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3975   -4.3507    0.3283 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6774   -5.7589   -1.2485 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5269   -4.7787   -2.5791 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1043   -2.3796   -2.3274 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8379   -0.9532   -0.7561 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8867   -2.5361    2.4260 H   0  0  0  0  0  0  0  0  0  0  0  0
  6 24  2  0
 16 17  2  0
 12 10  2  0
 17 18  1  0
 12 24  1  0
 18 19  2  0
 19 14  1  0
 13 14  1  0
  6  7  1  0
 12 13  1  0
 24 23  1  0
 23 21  1  0
  6  5  1  0
 21 20  1  0
 21 22  2  0
 20 13  2  0
 10 11  1  0
  5  4  1  0
  9  7  2  0
  4  2  2  3
 14 15  2  0
  2  1  1  0
  9 10  1  0
  2  3  1  0
 15 16  1  0
  7  8  1  0
  9 35  1  0
 20 42  1  0
 15 37  1  0
 16 38  1  0
 17 39  1  0
 18 40  1  0
 19 41  1  0
  5 32  1  0
  5 33  1  0
 11 36  1  0
  4 31  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  8 34  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₂₀H₁₈O₄

Average Mass

322.3600 Da

Monoisotopic Mass

322.12051 Da

IUPAC Name

5,7-dihydroxy-8-(3-methylbut-2-en-1-yl)-4-phenyl-2H-chromen-2-one

Traditional Name

5,7-dihydroxy-8-(3-methylbut-2-en-1-yl)-4-phenylchromen-2-one

CAS Registry Number

Not Available

SMILES

[H]OC1=C([H])C(O[H])=C2C(OC(=O)C([H])=C2C2=C([H])C([H])=C([H])C([H])=C2[H])=C1C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C20H18O4/c1-12(2)8-9-14-16(21)11-17(22)19-15(10-18(23)24-20(14)19)13-6-4-3-5-7-13/h3-8,10-11,21-22H,9H2,1-2H3

InChI Key

SRGRDIADLLPPQM-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Marila pluricostata	JEOL database	Lopez-Perez, J. L., et al, J. Nat. Prod. 68, 369 (2005)

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as prenylated neoflavonoids. These are neoflavonoids that features a C5-isoprenoid substituent at any position of the A, B, or C ring. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Neoflavonoids

Sub Class

Prenylated neoflavonoids

Direct Parent

Prenylated neoflavonoids

Alternative Parents

Substituents

Prenylated neoflavonoid
4-phenylcoumarin
7-hydroxycoumarin
Hydroxycoumarin
Coumarin
Benzopyran
1-benzopyran
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Monocyclic benzene moiety
Pyran
Benzenoid
Heteroaromatic compound
Lactone
Oxacycle
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen 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	4.4	ALOGPS
logP	4.34	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	7.25	ChemAxon
pKa (Strongest Basic)	-7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	103.31 m³·mol⁻¹	ChemAxon
Polarizability	34.8 Å³	ChemAxon
Number of Rings	3	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

HMDB0131486

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB089582

KNApSAcK ID

Not Available

Chemspider ID

4983772

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6483315

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Lopez-Perez, J. L., et al. (2005). Lopez-Perez, J. L., et al, J. Nat. Prod. 68, 369 (2005). J. Nat. Prod..

Showing NP-Card for 5,7-dihydroxy-8-(3-methylbut-2-enyl)4-phenylchromen-2-one (NP0028019)

MOL for NP0028019 (5,7-dihydroxy-8-(3-methylbut-2-enyl)4-phenylchromen-2-one)

3D MOL for NP0028019 (5,7-dihydroxy-8-(3-methylbut-2-enyl)4-phenylchromen-2-one)

3D SDF for NP0028019 (5,7-dihydroxy-8-(3-methylbut-2-enyl)4-phenylchromen-2-one)

3D-SDF for NP0028019 (5,7-dihydroxy-8-(3-methylbut-2-enyl)4-phenylchromen-2-one)

PDB for NP0028019 (5,7-dihydroxy-8-(3-methylbut-2-enyl)4-phenylchromen-2-one)

3D PDB for NP0028019 (5,7-dihydroxy-8-(3-methylbut-2-enyl)4-phenylchromen-2-one)

SMILES for NP0028019 (5,7-dihydroxy-8-(3-methylbut-2-enyl)4-phenylchromen-2-one)

INCHI for NP0028019 (5,7-dihydroxy-8-(3-methylbut-2-enyl)4-phenylchromen-2-one)

Structure for NP0028019 (5,7-dihydroxy-8-(3-methylbut-2-enyl)4-phenylchromen-2-one)

3D Structure for NP0028019 (5,7-dihydroxy-8-(3-methylbut-2-enyl)4-phenylchromen-2-one)