NP-MRD: Showing NP-Card for 4,6'-dihydroxy-2',5',5',6,8'a-pentamethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde (NP0321257)

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Record Information

Version

2.0

Created at

2022-09-11 23:22:36 UTC

Updated at

2022-09-11 23:22:37 UTC

NP-MRD ID

NP0321257

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,6'-dihydroxy-2',5',5',6,8'a-pentamethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde

Description

F1839-I 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. F1839-I is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171508402D          

 27 30  0  0  0  0            999 V2000
    1.8349    2.5857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5266    2.1359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2619    2.5100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9535    2.0602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9098    1.2363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6014    0.7866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4051    0.6004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9242    1.5458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5577   -0.0373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2493   -0.4871    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8223   -0.4113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1307    0.0384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1744    0.8623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5907    0.2793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4828    1.3121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3532    0.4973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5383    0.3688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0885   -0.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4626   -1.0582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2647   -0.2791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1094    0.4562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9332    0.4999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3404    1.1478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0336    1.8832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8575    1.9269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1643    1.1041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7480    1.6871    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  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  5 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
  2 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 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
 17 26  1  0  0  0  0
 26 27  1  0  0  0  0
 15 27  1  0  0  0  0
M  END

     RDKit          3D

 59 62  0  0  0  0  0  0  0  0999 V2000
    5.6025   -1.7542    0.5981 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3575   -1.2302   -0.0258 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0056   -1.7301   -1.2610 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8512   -1.2676   -1.8774 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4398   -1.7247   -3.1132 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0744   -0.3076   -1.2318 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4478    0.1624   -0.0199 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6094   -0.2812    0.6359 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9820    0.2477    1.9436 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7278    1.2793    1.9320 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5431    1.0832    0.4095 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3464    1.0724   -0.3849 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8147    0.3764   -1.6108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0741    2.4925   -0.5834 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5379    3.0744   -1.8711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5317    2.7597   -0.5313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4381    1.6174   -0.7365 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9408    0.2814   -0.3044 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0424   -0.5328    0.3599 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1321   -0.6426   -0.7242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6560    0.1182    1.5339 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5602   -1.9362    0.5851 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4403   -2.6679    1.3682 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1933   -2.0532    1.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1680   -1.1693    0.5012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6580    0.2746    0.4225 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6945    0.7373    1.8447 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4060   -2.7585    0.9971 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4292   -1.7392   -0.1474 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9244   -1.0927    1.4325 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6020   -2.4816   -1.7805 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5926   -1.3521   -3.5108 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6746   -0.1681    2.8713 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0886    1.0772   -2.4411 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1030   -0.3339   -2.0571 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3928    3.1375    0.2238 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6178    2.9681   -1.9002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0127    2.7599   -2.7595 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3409    4.1848   -1.7739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7666    3.5256   -1.3362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8382    3.3326    0.3990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8134    1.5920   -1.8047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3899    1.8058   -0.1523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7658   -0.3121   -1.2564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6902    0.3163   -0.6836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6571   -0.7194   -1.7169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8092   -1.4740   -0.4902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7753    0.2424    1.4266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5674   -0.5947    2.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2857    1.1262    1.7776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5234   -2.4257   -0.4332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0411   -3.5606    1.5325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8503   -3.1125    0.9681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1698   -1.9740    2.2832 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7279   -1.1484    1.1638 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1210   -1.5886   -0.4519 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3727    0.6669    2.2161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9876    1.7706    2.0005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2606    0.0511    2.4821 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 19 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  1
 26 12  1  0
 12 13  1  0
 13  6  1  0
  6  4  2  0
  4  5  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2  8  1  0
  8  9  1  0
  9 10  2  0
  8  7  2  0
  7 11  1  0
 12 14  1  0
 12 11  1  1
 26 18  1  0
  7  6  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
 14 36  1  1
 16 40  1  0
 16 41  1  0
 17 42  1  0
 17 43  1  0
 18 44  1  6
 20 45  1  0
 20 46  1  0
 20 47  1  0
 21 48  1  0
 21 49  1  0
 21 50  1  0
 22 51  1  6
 23 52  1  0
 24 53  1  0
 24 54  1  0
 25 55  1  0
 25 56  1  0
 27 57  1  0
 27 58  1  0
 27 59  1  0
 13 34  1  0
 13 35  1  0
  5 32  1  0
  3 31  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  9 33  1  0
M  END


  Mrv1533004171508402D          

 27 30  0  0  0  0            999 V2000
    1.8349    2.5857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5266    2.1359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2619    2.5100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9535    2.0602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9098    1.2363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6014    0.7866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4051    0.6004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9242    1.5458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5577   -0.0373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2493   -0.4871    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8223   -0.4113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1307    0.0384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1744    0.8623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5907    0.2793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4828    1.3121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3532    0.4973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5383    0.3688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0885   -0.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4626   -1.0582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2647   -0.2791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1094    0.4562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9332    0.4999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3404    1.1478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0336    1.8832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8575    1.9269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1643    1.1041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7480    1.6871    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  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  5 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
  2 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 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
 17 26  1  0  0  0  0
 26 27  1  0  0  0  0
 15 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0321257

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CCC2C(C)(C)C(O)CCC2(C)C11CC2=C(O)C=C(C)C(C=O)=C2O1

> <INCHI_IDENTIFIER>
InChI=1S/C23H32O4/c1-13-10-17(25)15-11-23(27-20(15)16(13)12-24)14(2)6-7-18-21(3,4)19(26)8-9-22(18,23)5/h10,12,14,18-19,25-26H,6-9,11H2,1-5H3

> <INCHI_KEY>
UOIBNKXNAPXQNY-UHFFFAOYSA-N

> <FORMULA>
C23H32O4

> <MOLECULAR_WEIGHT>
372.505

> <EXACT_MASS>
372.23005951

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
42.13791570791239

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4,6'-dihydroxy-2',5',5',6,8'a-pentamethyl-3',4',4'a,5',6',7',8',8'a-octahydro-2'H,3H-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde

> <ALOGPS_LOGP>
4.49

> <JCHEM_LOGP>
4.677492889999999

> <ALOGPS_LOGS>
-4.56

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.489318124923358

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.657976838899184

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8351376739541697

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
106.16959999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.04e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,6'-dihydroxy-2',5',5',6,8'a-pentamethyl-3',4',4'a,6',7',8'-hexahydro-2'H,3H-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       3.425   4.827   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.716   3.987   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.089   4.685   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.380   3.846   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.298   2.308   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.589   1.468   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.090   1.121   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.192   2.885   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.508  -0.070   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       9.799  -0.909   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       7.135  -0.768   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.844   0.072   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.926   1.610   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.836   0.521   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.635   2.449   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.393   0.928   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.872   0.688   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.032  -0.603   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.730  -1.975   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.494  -0.521   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.204   0.852   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.742   0.933   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.635   2.143   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.063   3.515   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -1.601   3.597   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       2.173   2.061   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       3.263   3.149   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   15                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   13                                                  
CONECT    6    5    7    8    9                                             
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    6   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    5   14   15                                             
CONECT   14   13                                                            
CONECT   15   13    2   16   27                                             
CONECT   16   15   17                                                       
CONECT   17   16   18   26                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   17   27                                                  
CONECT   27   26   15                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₂O₄

Average Mass

372.5050 Da

Monoisotopic Mass

372.23006 Da

IUPAC Name

4,6'-dihydroxy-2',5',5',6,8'a-pentamethyl-3',4',4'a,5',6',7',8',8'a-octahydro-2'H,3H-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde

Traditional Name

4,6'-dihydroxy-2',5',5',6,8'a-pentamethyl-3',4',4'a,6',7',8'-hexahydro-2'H,3H-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde

CAS Registry Number

Not Available

SMILES

CC1CCC2C(C)(C)C(O)CCC2(C)C11CC2=C(O)C=C(C)C(C=O)=C2O1

InChI Identifier

InChI=1S/C23H32O4/c1-13-10-17(25)15-11-23(27-20(15)16(13)12-24)14(2)6-7-18-21(3,4)19(26)8-9-22(18,23)5/h10,12,14,18-19,25-26H,6-9,11H2,1-5H3

InChI Key

UOIBNKXNAPXQNY-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

Not Available

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
Alkyl aryl ether
Aryl-aldehyde
Benzenoid
Cyclic alcohol
Secondary alcohol
Ether
Oxacycle
Alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aldehyde
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	4.49	ALOGPS
logP	4.68	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	7.66	ChemAxon
pKa (Strongest Basic)	-0.84	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	106.17 m³·mol⁻¹	ChemAxon
Polarizability	42.14 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

85087960

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,6'-dihydroxy-2',5',5',6,8'a-pentamethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde (NP0321257)

MOL for NP0321257 (4,6'-dihydroxy-2',5',5',6,8'a-pentamethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde)

3D MOL for NP0321257 (4,6'-dihydroxy-2',5',5',6,8'a-pentamethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde)

3D SDF for NP0321257 (4,6'-dihydroxy-2',5',5',6,8'a-pentamethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde)

3D-SDF for NP0321257 (4,6'-dihydroxy-2',5',5',6,8'a-pentamethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde)

PDB for NP0321257 (4,6'-dihydroxy-2',5',5',6,8'a-pentamethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde)

3D PDB for NP0321257 (4,6'-dihydroxy-2',5',5',6,8'a-pentamethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde)

SMILES for NP0321257 (4,6'-dihydroxy-2',5',5',6,8'a-pentamethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde)

INCHI for NP0321257 (4,6'-dihydroxy-2',5',5',6,8'a-pentamethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde)

Structure for NP0321257 (4,6'-dihydroxy-2',5',5',6,8'a-pentamethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde)

3D Structure for NP0321257 (4,6'-dihydroxy-2',5',5',6,8'a-pentamethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde)