NP-MRD: Showing NP-Card for 7-{[(1r,2s,4ar,5s,6s,8as)-6-hydroxy-1,2,4a,5-tetramethyl-octahydronaphthalen-1-yl]methoxy}chromen-2-one (NP0325235)

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Record Information

Version

2.0

Created at

2022-09-12 05:50:00 UTC

Updated at

2022-09-12 05:50:00 UTC

NP-MRD ID

NP0325235

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-{[(1r,2s,4ar,5s,6s,8as)-6-hydroxy-1,2,4a,5-tetramethyl-octahydronaphthalen-1-yl]methoxy}chromen-2-one

Description

Kamolol belongs to the class of organic compounds known as coumarins and derivatives. These are polycyclic aromatic compounds containing a 1-benzopyran moiety with a ketone group at the C2 carbon atom (1-benzopyran-2-one). 7-{[(1r,2s,4ar,5s,6s,8as)-6-hydroxy-1,2,4a,5-tetramethyl-octahydronaphthalen-1-yl]methoxy}chromen-2-one is found in Ferula iliensis and Ferula microcarpa. Based on a literature review very few articles have been published on Kamolol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122207502D          

 28 31  0  0  1  0            999 V2000
    0.4973   -3.6447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3272   -3.6159    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7643   -4.3156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5888   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9762   -3.5583    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4133   -4.2580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8006   -3.5296    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2378   -4.2292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1880   -2.8011    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0125   -2.7723    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7508   -2.1015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9263   -2.1303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5390   -2.8587    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6569   -2.0645    0.0000 C   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
    0.0000   -1.6500    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
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  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  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  6  0  0  0
  5 13  1  0  0  0  0
 13 14  1  0  0  0  0
  2 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 21 27  1  0  0  0  0
 27 28  2  0  0  0  0
 18 28  1  0  0  0  0
M  END

     RDKit          3D

 60 63  0  0  0  0  0  0  0  0999 V2000
    0.5166   -2.4880    0.0006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6917   -1.5980   -0.2261 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8683   -2.3656    0.3032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0265   -1.5140    0.7306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9981   -0.1852    0.0390 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1713   -0.3593   -1.4287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1558    0.6424    0.5569 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.4677   -0.0959    0.4473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1706    1.9830   -0.0679 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5488    2.9135    0.9308 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9457    2.4234   -0.7665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6714    1.7946   -0.4133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7537    0.5612    0.4360 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5326   -0.2668    0.4950 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2073   -0.6530    1.9500 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7147    0.4325   -0.0027 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8682   -0.3581    0.2429 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1386   -0.0033   -0.0885 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4367    1.1933   -0.7130 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7241    1.5403   -1.0426 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7430    0.6443   -0.7286 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0317    0.9723   -1.0491 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0412    0.0829   -0.7371 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7304   -1.0909   -0.1222 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5939   -1.9584    0.1970 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4775   -1.3601    0.1649 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4797   -0.5650   -0.1021 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1633   -0.8760    0.2134 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2793   -2.3660   -0.7887 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1846   -3.5638   -0.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9205   -2.4075    1.0293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425   -1.4498   -1.3290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5615   -3.0240    1.1413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1657   -3.0775   -0.5164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9599   -2.0392    0.3717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1489   -1.4392    1.8283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1699    0.0226   -1.7940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4199    0.1019   -2.0597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1901   -1.4497   -1.6825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9606    0.7592    1.6560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5131   -0.8329    1.2840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2711    0.6570    0.6269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5990   -0.6343   -0.4945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0534    2.0016   -0.7773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9863    3.7362    0.7922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1352    2.3850   -1.8826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8497    3.5392   -0.5859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1254    1.5274   -1.3597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9787    2.5008    0.1126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9564    0.9409    1.4840 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8637   -0.6958    2.1344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7919   -1.5174    2.2703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5920    0.2175    2.5581 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8828    1.4027    0.4553 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6567    0.5846   -1.1136 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5928    1.8396   -0.9260 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9483    2.4707   -1.5273 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2951    1.8939   -1.5342 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0852    0.3015   -0.9736 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0123   -1.8316    0.7014 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  1  0
  5  6  1  6
  5  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  1
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  1  0
 27 28  2  0
 14  2  1  0
 28 18  1  0
 13  5  1  0
 27 21  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  6
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  6 37  1  0
  6 38  1  0
  6 39  1  0
  7 40  1  1
  8 41  1  0
  8 42  1  0
  8 43  1  0
  9 44  1  6
 10 45  1  0
 11 46  1  0
 11 47  1  0
 12 48  1  0
 12 49  1  0
 13 50  1  1
 15 51  1  0
 15 52  1  0
 15 53  1  0
 16 54  1  0
 16 55  1  0
 19 56  1  0
 20 57  1  0
 22 58  1  0
 23 59  1  0
 28 60  1  0
M  END


  Mrv1652309122207502D          

 28 31  0  0  1  0            999 V2000
    0.4973   -3.6447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3272   -3.6159    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7643   -4.3156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5888   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9762   -3.5583    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4133   -4.2580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8006   -3.5296    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2378   -4.2292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1880   -2.8011    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0125   -2.7723    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7508   -2.1015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9263   -2.1303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5390   -2.8587    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6569   -2.0645    0.0000 C   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
    0.0000   -1.6500    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
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  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  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  6  0  0  0
  5 13  1  0  0  0  0
 13 14  1  0  0  0  0
  2 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 21 27  1  0  0  0  0
 27 28  2  0  0  0  0
 18 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0325235

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CC[C@@]2(C)[C@H](C)[C@@H](O)CC[C@@H]2[C@]1(C)COC1=CC=C2C=CC(=O)OC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H32O4/c1-15-11-12-23(3)16(2)19(25)8-9-21(23)24(15,4)14-27-18-7-5-17-6-10-22(26)28-20(17)13-18/h5-7,10,13,15-16,19,21,25H,8-9,11-12,14H2,1-4H3/t15-,16+,19-,21-,23-,24+/m0/s1

> <INCHI_KEY>
VZHMLYJMPGDZPE-OFIDYMHDSA-N

> <FORMULA>
C24H32O4

> <MOLECULAR_WEIGHT>
384.516

> <EXACT_MASS>
384.23005951

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
43.05993463417423

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-{[(1R,2S,4aR,5S,6S,8aS)-6-hydroxy-1,2,4a,5-tetramethyl-decahydronaphthalen-1-yl]methoxy}-2H-chromen-2-one

> <JCHEM_LOGP>
4.682742603666668

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.21533303261725

> <JCHEM_PKA_STRONGEST_BASIC>
-0.9549578850506196

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
109.81669999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
7-{[(1R,2S,4aR,5S,6S,8aS)-6-hydroxy-1,2,4a,5-tetramethyl-octahydronaphthalen-1-yl]methoxy}chromen-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       0.928  -6.803   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.611  -6.750   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.427  -8.056   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.966  -8.002   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.689  -6.642   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.505  -7.948   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.228  -6.589   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -6.044  -7.894   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.951  -5.229   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -7.490  -5.175   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -5.135  -3.923   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.596  -3.977   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.873  -5.336   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.226  -3.854   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   14                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7   13                                             
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    5   14                                                  
CONECT   14   13    2   15   16                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   28                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   27                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   21   28                                                  
CONECT   28   27   18                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₂O₄

Average Mass

384.5160 Da

Monoisotopic Mass

384.23006 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H]1CC[C@@]2(C)[C@H](C)[C@@H](O)CC[C@@H]2[C@]1(C)COC1=CC=C2C=CC(=O)OC2=C1

InChI Identifier

InChI=1S/C24H32O4/c1-15-11-12-23(3)16(2)19(25)8-9-21(23)24(15,4)14-27-18-7-5-17-6-10-22(26)28-20(17)13-18/h5-7,10,13,15-16,19,21,25H,8-9,11-12,14H2,1-4H3/t15-,16+,19-,21-,23-,24+/m0/s1

InChI Key

VZHMLYJMPGDZPE-OFIDYMHDSA-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
Ferula iliensis	LOTUS Database	35616633
Ferula microcarpa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumarins and derivatives. These are polycyclic aromatic compounds containing a 1-benzopyran moiety with a ketone group at the C2 carbon atom (1-benzopyran-2-one).

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Not Available

Direct Parent

Coumarins and derivatives

Alternative Parents

Substituents

Coumarin
Benzopyran
1-benzopyran
Alkyl aryl ether
Pyranone
Pyran
Benzenoid
Cyclic alcohol
Heteroaromatic compound
Lactone
Secondary alcohol
Oxacycle
Ether
Organoheterocyclic compound
Organic oxygen compound
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
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

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

166295

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

191499

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-{[(1r,2s,4ar,5s,6s,8as)-6-hydroxy-1,2,4a,5-tetramethyl-octahydronaphthalen-1-yl]methoxy}chromen-2-one (NP0325235)

MOL for NP0325235 (7-{[(1r,2s,4ar,5s,6s,8as)-6-hydroxy-1,2,4a,5-tetramethyl-octahydronaphthalen-1-yl]methoxy}chromen-2-one)

3D MOL for NP0325235 (7-{[(1r,2s,4ar,5s,6s,8as)-6-hydroxy-1,2,4a,5-tetramethyl-octahydronaphthalen-1-yl]methoxy}chromen-2-one)

3D SDF for NP0325235 (7-{[(1r,2s,4ar,5s,6s,8as)-6-hydroxy-1,2,4a,5-tetramethyl-octahydronaphthalen-1-yl]methoxy}chromen-2-one)

3D-SDF for NP0325235 (7-{[(1r,2s,4ar,5s,6s,8as)-6-hydroxy-1,2,4a,5-tetramethyl-octahydronaphthalen-1-yl]methoxy}chromen-2-one)

PDB for NP0325235 (7-{[(1r,2s,4ar,5s,6s,8as)-6-hydroxy-1,2,4a,5-tetramethyl-octahydronaphthalen-1-yl]methoxy}chromen-2-one)

3D PDB for NP0325235 (7-{[(1r,2s,4ar,5s,6s,8as)-6-hydroxy-1,2,4a,5-tetramethyl-octahydronaphthalen-1-yl]methoxy}chromen-2-one)

SMILES for NP0325235 (7-{[(1r,2s,4ar,5s,6s,8as)-6-hydroxy-1,2,4a,5-tetramethyl-octahydronaphthalen-1-yl]methoxy}chromen-2-one)

INCHI for NP0325235 (7-{[(1r,2s,4ar,5s,6s,8as)-6-hydroxy-1,2,4a,5-tetramethyl-octahydronaphthalen-1-yl]methoxy}chromen-2-one)

Structure for NP0325235 (7-{[(1r,2s,4ar,5s,6s,8as)-6-hydroxy-1,2,4a,5-tetramethyl-octahydronaphthalen-1-yl]methoxy}chromen-2-one)

3D Structure for NP0325235 (7-{[(1r,2s,4ar,5s,6s,8as)-6-hydroxy-1,2,4a,5-tetramethyl-octahydronaphthalen-1-yl]methoxy}chromen-2-one)