NP-MRD: Showing NP-Card for (8s)-8,10-dihydroxy-7-methoxy-3-[(2e,4r)-4-methylhex-2-en-2-yl]-8-(2-oxopropyl)-1h-cyclohexa[g]isochromen-9-one (NP0207093)

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Record Information

Version

2.0

Created at

2022-09-05 03:34:21 UTC

Updated at

2022-09-05 03:34:21 UTC

NP-MRD ID

NP0207093

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(8s)-8,10-dihydroxy-7-methoxy-3-[(2e,4r)-4-methylhex-2-en-2-yl]-8-(2-oxopropyl)-1h-cyclohexa[g]isochromen-9-one

Description

(8S)-8,10-dihydroxy-7-methoxy-3-[(2E,4R)-4-methylhex-2-en-2-yl]-8-(2-oxopropyl)-1H,8H,9H-cyclohexa[g]isochromen-9-one belongs to the class of organic compounds known as naphthopyranones. Naphthopyranones are compounds containing a naphthopyran skeleton where a ring carbon bears a carboxylic acid group. Naphthtopyran is made up of the pyran ring fused to a naphthalene ring system. Based on a literature review very few articles have been published on (8S)-8,10-dihydroxy-7-methoxy-3-[(2E,4R)-4-methylhex-2-en-2-yl]-8-(2-oxopropyl)-1H,8H,9H-cyclohexa[g]isochromen-9-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052205342D          

 30 32  0  0  1  0            999 V2000
   -4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    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
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   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 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -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
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1401   -0.8748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6704   -1.7933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2007   -1.1613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9185   -0.3860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0131   -1.3045    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  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
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  8 18  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 21 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 27 30  2  0  0  0  0
 12 30  1  0  0  0  0
M  END

     RDKit          3D

 58 60  0  0  0  0  0  0  0  0999 V2000
    8.4143    0.2720    0.8344 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9229   -0.2001    0.7658 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3579    0.3890   -0.4514 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0491    0.0033   -1.7509 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9260    0.5823   -0.6135 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9508   -0.1213   -0.0772 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2994   -1.2445    0.7875 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5403    0.2522   -0.3759 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5386   -0.4160    0.1379 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1305   -0.0582   -0.1509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9010   -0.8010    0.4330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2162   -0.4624    0.1705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4652    0.6015   -0.6610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4391    1.3350   -1.2383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7073    2.3954   -2.0684 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1209    0.9960   -0.9764 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9724    1.7530   -1.5816 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2497    1.3020   -1.1949 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8491    0.9455   -0.8959 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0579    2.0087   -1.5853 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9863    0.1577   -0.3969 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5799   -0.3945   -1.5822 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0192    1.0942    0.2164 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2071    0.4030    0.7484 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1966   -0.2444   -0.1624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4411    0.3248    1.9671 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5929   -0.9441    0.4771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5934   -1.7583    1.0843 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4510   -2.1152    2.4278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3303   -1.2185    0.7279 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8509   -0.0284   -0.1232 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9170   -0.3205    1.6534 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4747    1.3331    1.0896 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0259   -1.2790    0.8448 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5097    0.3156    1.6661 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7335    1.5096   -0.3694 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2541   -1.0793   -1.8306 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3963    0.3940   -2.5757 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0127    0.5268   -1.8689 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5470    1.4166   -1.2610 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4064   -1.9089    1.0300 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9560   -2.0004    0.2502 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6609   -0.9975    1.7983 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6424   -1.2561    0.7973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7107   -1.6370    1.0869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0104    2.9546   -2.5059 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8932    2.8074   -1.2256 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8704    1.7300   -2.6976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8643   -0.7904   -2.1441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5723    1.6981    1.0324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3691    1.8303   -0.5543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9944   -0.7781    0.4043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6843    0.4548   -0.8473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6975   -1.0400   -0.7835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5364   -2.6851    2.6275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3411   -2.7132    2.7526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4388   -1.2146    3.1066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1292   -2.0794    1.3963 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  1  0
 13 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  1  6
 21 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  2  0
 21 27  1  0
 27 28  1  0
 28 29  1  0
 27 30  2  0
 18  8  1  0
 16 10  1  0
 30 12  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  0
  2 35  1  0
  3 36  1  1
  4 37  1  0
  4 38  1  0
  4 39  1  0
  5 40  1  0
  7 41  1  0
  7 42  1  0
  7 43  1  0
  9 44  1  0
 11 45  1  0
 15 46  1  0
 17 47  1  0
 17 48  1  0
 22 49  1  0
 23 50  1  0
 23 51  1  0
 25 52  1  0
 25 53  1  0
 25 54  1  0
 29 55  1  0
 29 56  1  0
 29 57  1  0
 30 58  1  0
M  END


  Mrv1652309052205342D          

 30 32  0  0  1  0            999 V2000
   -4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    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
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   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 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -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
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1401   -0.8748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6704   -1.7933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2007   -1.1613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9185   -0.3860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0131   -1.3045    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  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
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  8 18  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 21 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 27 30  2  0  0  0  0
 12 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0207093

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@H](C)\C=C(/C)C1=CC2=CC3=C(C(O)=C2CO1)C(=O)[C@](O)(CC(C)=O)C(OC)=C3

> <INCHI_IDENTIFIER>
InChI=1S/C24H28O6/c1-6-13(2)7-14(3)19-9-16-8-17-10-20(29-5)24(28,11-15(4)25)23(27)21(17)22(26)18(16)12-30-19/h7-10,13,26,28H,6,11-12H2,1-5H3/b14-7+/t13-,24+/m1/s1

> <INCHI_KEY>
AEUOEFHLXREGMT-JHASNZPQSA-N

> <FORMULA>
C24H28O6

> <MOLECULAR_WEIGHT>
412.482

> <EXACT_MASS>
412.188588622

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
45.7026821503782

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(8S)-8,10-dihydroxy-7-methoxy-3-[(2E,4R)-4-methylhex-2-en-2-yl]-8-(2-oxopropyl)-1H,8H,9H-cyclohexa[g]isochromen-9-one

> <JCHEM_LOGP>
3.4590174439999988

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.607145646497274

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.88085185454243

> <JCHEM_PKA_STRONGEST_BASIC>
-4.3135659980749965

> <JCHEM_POLAR_SURFACE_AREA>
93.06000000000002

> <JCHEM_REFRACTIVITY>
118.6148

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(8S)-8,10-dihydroxy-7-methoxy-3-[(2E,4R)-4-methylhex-2-en-2-yl]-8-(2-oxopropyl)-1H-cyclohexa[g]isochromen-9-one

> <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      -8.002  -7.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.335  -9.240   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       5.861  -1.633   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.851  -3.347   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.841  -2.168   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.315  -0.721   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       9.358  -2.435   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   18                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   30                                                  
CONECT   13   12   14   19                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   10   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17    8                                                       
CONECT   19   13   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23   27                                             
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   21   28   30                                                  
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   27   12                                                       
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₈O₆

Average Mass

412.4820 Da

Monoisotopic Mass

412.18859 Da

IUPAC Name

(8S)-8,10-dihydroxy-7-methoxy-3-[(2E,4R)-4-methylhex-2-en-2-yl]-8-(2-oxopropyl)-1H,8H,9H-cyclohexa[g]isochromen-9-one

Traditional Name

(8S)-8,10-dihydroxy-7-methoxy-3-[(2E,4R)-4-methylhex-2-en-2-yl]-8-(2-oxopropyl)-1H-cyclohexa[g]isochromen-9-one

CAS Registry Number

Not Available

SMILES

CC[C@@H](C)\C=C(/C)C1=CC2=CC3=C(C(O)=C2CO1)C(=O)[C@](O)(CC(C)=O)C(OC)=C3

InChI Identifier

InChI=1S/C24H28O6/c1-6-13(2)7-14(3)19-9-16-8-17-10-20(29-5)24(28,11-15(4)25)23(27)21(17)22(26)18(16)12-30-19/h7-10,13,26,28H,6,11-12H2,1-5H3/b14-7+/t13-,24+/m1/s1

InChI Key

AEUOEFHLXREGMT-JHASNZPQSA-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 naphthopyranones. Naphthopyranones are compounds containing a naphthopyran skeleton where a ring carbon bears a carboxylic acid group. Naphthtopyran is made up of the pyran ring fused to a naphthalene ring system.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Naphthopyranones

Direct Parent

Naphthopyranones

Alternative Parents

Substituents

Naphthopyranone
Isochromene
Benzopyran
Naphthalene
2-benzopyran
Aryl alkyl ketone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
Pyranone
Acyloin
Beta-hydroxy ketone
Benzenoid
Pyran
Vinylogous acid
Tertiary alcohol
Ketone
Oxacycle
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Alcohol
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	3.46	ChemAxon
pKa (Strongest Acidic)	7.88	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	93.06 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	118.61 m³·mol⁻¹	ChemAxon
Polarizability	45.7 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	Yes	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

163187814

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (8s)-8,10-dihydroxy-7-methoxy-3-[(2e,4r)-4-methylhex-2-en-2-yl]-8-(2-oxopropyl)-1h-cyclohexa[g]isochromen-9-one (NP0207093)

MOL for NP0207093 ((8s)-8,10-dihydroxy-7-methoxy-3-[(2e,4r)-4-methylhex-2-en-2-yl]-8-(2-oxopropyl)-1h-cyclohexa[g]isochromen-9-one)

3D MOL for NP0207093 ((8s)-8,10-dihydroxy-7-methoxy-3-[(2e,4r)-4-methylhex-2-en-2-yl]-8-(2-oxopropyl)-1h-cyclohexa[g]isochromen-9-one)

3D SDF for NP0207093 ((8s)-8,10-dihydroxy-7-methoxy-3-[(2e,4r)-4-methylhex-2-en-2-yl]-8-(2-oxopropyl)-1h-cyclohexa[g]isochromen-9-one)

3D-SDF for NP0207093 ((8s)-8,10-dihydroxy-7-methoxy-3-[(2e,4r)-4-methylhex-2-en-2-yl]-8-(2-oxopropyl)-1h-cyclohexa[g]isochromen-9-one)

PDB for NP0207093 ((8s)-8,10-dihydroxy-7-methoxy-3-[(2e,4r)-4-methylhex-2-en-2-yl]-8-(2-oxopropyl)-1h-cyclohexa[g]isochromen-9-one)

3D PDB for NP0207093 ((8s)-8,10-dihydroxy-7-methoxy-3-[(2e,4r)-4-methylhex-2-en-2-yl]-8-(2-oxopropyl)-1h-cyclohexa[g]isochromen-9-one)

SMILES for NP0207093 ((8s)-8,10-dihydroxy-7-methoxy-3-[(2e,4r)-4-methylhex-2-en-2-yl]-8-(2-oxopropyl)-1h-cyclohexa[g]isochromen-9-one)

INCHI for NP0207093 ((8s)-8,10-dihydroxy-7-methoxy-3-[(2e,4r)-4-methylhex-2-en-2-yl]-8-(2-oxopropyl)-1h-cyclohexa[g]isochromen-9-one)

Structure for NP0207093 ((8s)-8,10-dihydroxy-7-methoxy-3-[(2e,4r)-4-methylhex-2-en-2-yl]-8-(2-oxopropyl)-1h-cyclohexa[g]isochromen-9-one)

3D Structure for NP0207093 ((8s)-8,10-dihydroxy-7-methoxy-3-[(2e,4r)-4-methylhex-2-en-2-yl]-8-(2-oxopropyl)-1h-cyclohexa[g]isochromen-9-one)