NP-MRD: Showing NP-Card for 5-hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2e)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxofuran-2-ylidene]-2-oxo-1-benzofuran-4-carbaldehyde (NP0205071)

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Record Information

Version

2.0

Created at

2022-09-05 00:54:03 UTC

Updated at

2022-09-05 00:54:04 UTC

NP-MRD ID

NP0205071

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2e)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxofuran-2-ylidene]-2-oxo-1-benzofuran-4-carbaldehyde

Description

5-Hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2E)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxo-2,5-dihydrofuran-2-ylidene]-2-oxo-2,3-dihydro-1-benzofuran-4-carbaldehyde belongs to the class of organic compounds known as benzofurans. These are organic compounds containing a benzene ring fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. 5-hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2e)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxofuran-2-ylidene]-2-oxo-1-benzofuran-4-carbaldehyde is found in Russula ochroleuca. Based on a literature review very few articles have been published on 5-hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2E)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxo-2,5-dihydrofuran-2-ylidene]-2-oxo-2,3-dihydro-1-benzofuran-4-carbaldehyde.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052202542D          

 29 31  0  0  0  0            999 V2000
   -1.8169   -5.5052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9032   -4.6847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6568   -4.3492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2357   -4.1998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5683   -3.7149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0992   -3.2299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0992   -2.4049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    1.7771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    3.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    3.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -2.7604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3687   -2.8174    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -3.4849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -4.2695    0.0000 O   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  3  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  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  3  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 23 26  2  0  0  0  0
 13 26  1  0  0  0  0
  9 26  1  0  0  0  0
  8 27  1  0  0  0  0
 27 28  1  0  0  0  0
  6 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END

     RDKit          3D

 43 45  0  0  0  0  0  0  0  0999 V2000
   -8.4188    0.6334   -0.6075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3602    1.3532   -0.3148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5420    2.7457    0.1749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0567    0.7818   -0.4734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9503    0.3116   -0.5953 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6307   -0.2285   -0.7523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5026    0.2724   -0.2369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3333   -0.5551   -0.6115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1191   -0.2691   -0.2276 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2860    0.8776    0.6100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4995    1.7345    1.0648 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6495    0.7782    0.7573 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1288   -0.3328    0.0828 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4479   -0.7570    0.0039 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5101   -0.0416    0.6538 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3969    0.5715    1.1980 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4467    1.3170    1.8323 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4592    1.5727    3.1235 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5730    1.8278    1.0101 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6911   -1.8826   -0.7174 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6615   -2.6023   -1.3650 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9878   -3.6846   -2.0441 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3346   -2.1513   -1.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3627   -2.9464   -1.9587 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7836   -3.9964   -2.6011 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0785   -1.0146   -0.5425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8418   -1.5536   -1.3654 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2025   -1.4233   -1.4913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0019   -2.1676   -2.1193 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2914   -0.3730   -0.9615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4180    1.0245   -0.5025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5659    3.2752    0.0264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2850    3.3138   -0.4124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7612    2.7955    1.2559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4740    1.1577    0.3651 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6485    1.2074    3.7274 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2444    2.1301    3.5967 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7476    1.1887    0.1111 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4846    1.8093    1.6410 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3698    2.8519    0.6209 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7001   -2.2435   -0.8023 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9303   -4.4382   -2.5617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6682   -2.8702   -2.0693 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2  1  2  3
  2  4  1  0
  4  5  3  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8 27  1  0
 27 28  1  0
 28 29  2  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 14 20  1  0
 20 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  2  0
 23 26  2  0
 14 15  1  0
 15 16  3  0
 16 17  1  0
 17 19  1  0
 17 18  2  3
 28  6  1  0
 26  9  1  0
 26 13  1  0
  3 32  1  0
  3 33  1  0
  3 34  1  0
  1 30  1  0
  1 31  1  0
  7 35  1  0
 20 41  1  0
 22 42  1  0
 24 43  1  0
 19 38  1  0
 19 39  1  0
 19 40  1  0
 18 36  1  0
 18 37  1  0
M  END


  Mrv1652309052202542D          

 29 31  0  0  0  0            999 V2000
   -1.8169   -5.5052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9032   -4.6847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6568   -4.3492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2357   -4.1998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5683   -3.7149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0992   -3.2299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0992   -2.4049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    1.7771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    3.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    3.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -2.7604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3687   -2.8174    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -3.4849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -4.2695    0.0000 O   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  3  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  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  3  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 23 26  2  0  0  0  0
 13 26  1  0  0  0  0
  9 26  1  0  0  0  0
  8 27  1  0  0  0  0
 27 28  1  0  0  0  0
  6 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0205071

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=C)C#CC1=C\C(OC1=O)=C1/C(=O)OC2=C(C=C(O)C(C=O)=C12)C#CC(C)=C

> <INCHI_IDENTIFIER>
InChI=1S/C23H14O6/c1-12(2)5-7-14-9-17(25)16(11-24)19-20(23(27)29-21(14)19)18-10-15(22(26)28-18)8-6-13(3)4/h9-11,25H,1,3H2,2,4H3/b20-18+

> <INCHI_KEY>
FZNSNRDGUCILLQ-CZIZESTLSA-N

> <FORMULA>
C23H14O6

> <MOLECULAR_WEIGHT>
386.359

> <EXACT_MASS>
386.079038171

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
41.107217728784185

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2E)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxo-2,5-dihydrofuran-2-ylidene]-2-oxo-2,3-dihydro-1-benzofuran-4-carbaldehyde

> <JCHEM_LOGP>
4.598468395666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.9191529188046985

> <JCHEM_PKA_STRONGEST_BASIC>
-5.998872358794627

> <JCHEM_POLAR_SURFACE_AREA>
89.9

> <JCHEM_REFRACTIVITY>
106.27919999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
5-hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2E)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxofuran-2-ylidene]-2-oxo-1-benzofuran-4-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.392 -10.276   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.553  -8.745   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.959  -8.118   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.307  -7.840   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.061  -6.934   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.185  -6.029   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.185  -4.489   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.650  -4.013   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.320  -1.303   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       2.126  -0.057   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.924   1.777   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.924   3.317   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.924   4.857   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.590   5.627   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.258   5.627   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       7.591  -2.843   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.924  -4.383   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       3.590  -5.153   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.555  -5.259   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       1.650  -6.505   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       2.126  -7.970   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   28                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   27                                                  
CONECT    9    8   10   26                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   26                                                  
CONECT   14   13   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   14   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   13    9                                                  
CONECT   27    8   28                                                       
CONECT   28   27    6   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₁₄O₆

Average Mass

386.3590 Da

Monoisotopic Mass

386.07904 Da

IUPAC Name

5-hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2E)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxo-2,5-dihydrofuran-2-ylidene]-2-oxo-2,3-dihydro-1-benzofuran-4-carbaldehyde

Traditional Name

5-hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2E)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxofuran-2-ylidene]-2-oxo-1-benzofuran-4-carbaldehyde

CAS Registry Number

Not Available

SMILES

CC(=C)C#CC1=C\C(OC1=O)=C1/C(=O)OC2=C(C=C(O)C(C=O)=C12)C#CC(C)=C

InChI Identifier

InChI=1S/C23H14O6/c1-12(2)5-7-14-9-17(25)16(11-24)19-20(23(27)29-21(14)19)18-10-15(22(26)28-18)8-6-13(3)4/h9-11,25H,1,3H2,2,4H3/b20-18+

InChI Key

FZNSNRDGUCILLQ-CZIZESTLSA-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
Russula ochroleuca	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzofurans. These are organic compounds containing a benzene ring fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzofurans

Sub Class

Not Available

Direct Parent

Benzofurans

Alternative Parents

Substituents

Benzofuran
Coumaran
1-hydroxy-2-unsubstituted benzenoid
Aryl-aldehyde
2-furanone
Dicarboxylic acid or derivatives
Benzenoid
Vinylogous acid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Dihydrofuran
Enol ester
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Oxacycle
Hydrocarbon derivative
Aldehyde
Carbonyl group
Organic oxide
Organic oxygen compound
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	4.6	ChemAxon
pKa (Strongest Acidic)	7.92	ChemAxon
pKa (Strongest Basic)	-6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	89.9 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	106.28 m³·mol⁻¹	ChemAxon
Polarizability	41.11 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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9713038

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11538257

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2e)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxofuran-2-ylidene]-2-oxo-1-benzofuran-4-carbaldehyde (NP0205071)

MOL for NP0205071 (5-hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2e)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxofuran-2-ylidene]-2-oxo-1-benzofuran-4-carbaldehyde)

3D MOL for NP0205071 (5-hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2e)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxofuran-2-ylidene]-2-oxo-1-benzofuran-4-carbaldehyde)

3D SDF for NP0205071 (5-hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2e)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxofuran-2-ylidene]-2-oxo-1-benzofuran-4-carbaldehyde)

3D-SDF for NP0205071 (5-hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2e)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxofuran-2-ylidene]-2-oxo-1-benzofuran-4-carbaldehyde)

PDB for NP0205071 (5-hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2e)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxofuran-2-ylidene]-2-oxo-1-benzofuran-4-carbaldehyde)

3D PDB for NP0205071 (5-hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2e)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxofuran-2-ylidene]-2-oxo-1-benzofuran-4-carbaldehyde)

SMILES for NP0205071 (5-hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2e)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxofuran-2-ylidene]-2-oxo-1-benzofuran-4-carbaldehyde)

INCHI for NP0205071 (5-hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2e)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxofuran-2-ylidene]-2-oxo-1-benzofuran-4-carbaldehyde)

Structure for NP0205071 (5-hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2e)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxofuran-2-ylidene]-2-oxo-1-benzofuran-4-carbaldehyde)

3D Structure for NP0205071 (5-hydroxy-7-(3-methylbut-3-en-1-yn-1-yl)-3-[(2e)-4-(3-methylbut-3-en-1-yn-1-yl)-5-oxofuran-2-ylidene]-2-oxo-1-benzofuran-4-carbaldehyde)