NP-MRD: Showing NP-Card for 15-butanoyl-8,9-dihydroxy-7-methoxy-6,18-dimethyl-3,5,19-trioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁹.0¹⁶,²⁰]icosa-1(20),2(10),12,15,17-pentaene-11,14-dione (NP0200663)

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Record Information

Version

2.0

Created at

2022-09-04 19:33:04 UTC

Updated at

2022-09-04 19:33:05 UTC

NP-MRD ID

NP0200663

Secondary Accession Numbers

None

Natural Product Identification

Common Name

15-butanoyl-8,9-dihydroxy-7-methoxy-6,18-dimethyl-3,5,19-trioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁹.0¹⁶,²⁰]icosa-1(20),2(10),12,15,17-pentaene-11,14-dione

Description

15-Butanoyl-8,9-dihydroxy-7-methoxy-6,18-dimethyl-3,5,19-trioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁹.0¹⁶,²⁰]Icosa-1(20),2(10),12,15,17-pentaene-11,14-dione belongs to the class of organic compounds known as cycloheptapyrans. These are organic heterocyclic compounds containing a cycloheptane derivative fused to a pyran. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds. Based on a literature review very few articles have been published on 15-butanoyl-8,9-dihydroxy-7-methoxy-6,18-dimethyl-3,5,19-trioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁹.0¹⁶,²⁰]Icosa-1(20),2(10),12,15,17-pentaene-11,14-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042221332D          

 33 37  0  0  0  0            999 V2000
   -2.7333   -0.6997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2530   -0.0289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4320   -0.1094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9517    0.5614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2926    1.3127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1307    0.4810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4170    1.0979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3250    1.9178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9891    2.4074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8971    3.2272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7451    2.0771    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8652    1.2167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6477    0.9555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9315    0.1808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5027   -0.5240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9517   -1.2161    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6843   -0.6283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0926   -0.0534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1730    0.7676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2868   -0.2306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0434   -0.9866    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7559    0.2113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4484   -0.5543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9817    1.0048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2968    1.4647    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7818    1.2060    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3561    0.6137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1562    0.8149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1303   -0.1798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7046   -0.7721    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5047   -0.5709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3302   -0.3810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1044   -1.1745    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  2  0  0  0  0
  4  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
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
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 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 12 19  2  0  0  0  0
  7 19  1  0  0  0  0
 18 20  1  0  0  0  0
  6 20  1  0  0  0  0
 20 21  2  0  0  0  0
 14 22  1  0  0  0  0
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 30 31  1  0  0  0  0
 29 32  1  0  0  0  0
 22 32  1  0  0  0  0
 32 33  1  0  0  0  0
M  END

     RDKit          3D

 57 61  0  0  0  0  0  0  0  0999 V2000
   -8.0053    2.5216    0.3387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1813    1.2982    0.0961 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7018    1.5491    0.2582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9326    0.3028    0.0063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5727   -0.7355   -0.2907 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4785    0.2561    0.0940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7343   -0.8091   -0.1154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0040   -2.2087   -0.4754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0338   -3.0958   -0.6260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4516   -4.4927   -0.9955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7008   -2.7593   -0.4532 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3583   -1.4371   -0.1071 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0201   -1.2834    0.0242 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7515   -0.1833    0.4924 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2396    1.0842    0.5853 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1125    1.9705    0.6209 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0519    1.5663    0.6468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2200    0.8829    0.4006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3202   -0.4647    0.0649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5771    1.3687    0.4269 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9042    2.5566    0.6945 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0424   -0.7157    0.8072 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9008   -1.5653    1.9329 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2071   -1.6919   -0.3730 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9099   -2.3082   -0.3309 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3243   -0.8716   -1.4888 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5485   -0.2758   -1.5063 C   0  0  1  0  0  0  0  0  0  0  0  0
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    4.8842    0.5694   -0.3173 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2768    0.5784   -0.2147 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.1826    1.0693    1.9350 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.3636    2.2882   -0.5183 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.1456   -4.9182   -0.2411 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2070    2.5896    0.9144 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4848   -2.4105    1.7070 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0184   -2.3920   -0.2263 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3211   -1.0706   -1.6668 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8663    0.3161   -3.5018 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6560    0.6484   -3.1608 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3717    1.6786   -2.4874 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5824    1.6184   -0.5158 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4457    2.5812    0.3511 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.0321   -0.6345    1.3880 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
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 31 54  1  0
 31 55  1  0
 32 56  1  1
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 23 46  1  0
M  END


  Mrv1652309042221332D          

 33 37  0  0  0  0            999 V2000
   -2.7333   -0.6997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2530   -0.0289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4320   -0.1094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9517    0.5614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2926    1.3127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1307    0.4810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4170    1.0979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3250    1.9178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9891    2.4074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8971    3.2272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7451    2.0771    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8652    1.2167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6477    0.9555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.2968    1.4647    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.3561    0.6137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.1303   -0.1798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7046   -0.7721    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.3302   -0.3810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1044   -1.1745    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
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  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
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M  END
> <DATABASE_ID>
NP0200663

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC(=O)C1=C2C=C(C)OC3=C2C(=CC(=O)C2=C3OC3OC(C)C(OC)C(O)C23O)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C24H24O9/c1-5-6-13(25)16-11-7-9(2)31-20-15(11)12(18(16)27)8-14(26)17-21(20)33-23-24(17,29)22(28)19(30-4)10(3)32-23/h7-8,10,19,22-23,28-29H,5-6H2,1-4H3

> <INCHI_KEY>
GPTONKSPQNETHU-UHFFFAOYSA-N

> <FORMULA>
C24H24O9

> <MOLECULAR_WEIGHT>
456.447

> <EXACT_MASS>
456.142032353

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
47.155971736463556

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
15-butanoyl-8,9-dihydroxy-7-methoxy-6,18-dimethyl-3,5,19-trioxapentacyclo[11.6.1.0^{2,10}.0^{4,9}.0^{16,20}]icosa-1(20),2(10),12,15,17-pentaene-11,14-dione

> <JCHEM_LOGP>
0.3093740363333329

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.525123481605242

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.208144006570253

> <JCHEM_PKA_STRONGEST_BASIC>
2.5669059772556944

> <JCHEM_POLAR_SURFACE_AREA>
128.59

> <JCHEM_REFRACTIVITY>
118.53349999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
15-butanoyl-8,9-dihydroxy-7-methoxy-6,18-dimethyl-3,5,19-trioxapentacyclo[11.6.1.0^{2,10}.0^{4,9}.0^{16,20}]icosa-1(20),2(10),12,15,17-pentaene-11,14-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -5.102  -1.306   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.206  -0.054   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.673  -0.204   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.777   1.048   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -2.413   2.450   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -0.244   0.898   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.778   2.049   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.607   3.580   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.846   4.494   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.675   6.024   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.257   3.877   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.482   2.271   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.942   1.784   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.472   0.338   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.672  -0.978   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.510  -2.270   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.144  -1.173   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.039  -0.100   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.190   1.433   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.535  -0.430   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.081  -1.842   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       7.011   0.394   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.437  -1.035   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       7.432   1.876   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       6.154   2.734   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       8.926   2.251   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       9.998   1.146   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.492   1.521   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.577  -0.336   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      10.649  -1.441   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      12.142  -1.066   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.083  -0.711   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       7.662  -2.192   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   20                                                  
CONECT    7    6    8   19                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   19                                                  
CONECT   13   12   14   25                                                  
CONECT   14   13   15   22                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18   12    7                                                  
CONECT   20   18    6   21                                                  
CONECT   21   20                                                            
CONECT   22   14   23   24   32                                             
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24   13                                                       
CONECT   26   24   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   32                                                  
CONECT   30   29   31                                                       
CONECT   31   30                                                            
CONECT   32   29   22   33                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₄O₉

Average Mass

456.4470 Da

Monoisotopic Mass

456.14203 Da

IUPAC Name

15-butanoyl-8,9-dihydroxy-7-methoxy-6,18-dimethyl-3,5,19-trioxapentacyclo[11.6.1.0^{2,10}.0^{4,9}.0^{16,20}]icosa-1(20),2(10),12,15,17-pentaene-11,14-dione

Traditional Name

15-butanoyl-8,9-dihydroxy-7-methoxy-6,18-dimethyl-3,5,19-trioxapentacyclo[11.6.1.0^{2,10}.0^{4,9}.0^{16,20}]icosa-1(20),2(10),12,15,17-pentaene-11,14-dione

CAS Registry Number

Not Available

SMILES

CCCC(=O)C1=C2C=C(C)OC3=C2C(=CC(=O)C2=C3OC3OC(C)C(OC)C(O)C23O)C1=O

InChI Identifier

InChI=1S/C24H24O9/c1-5-6-13(25)16-11-7-9(2)31-20-15(11)12(18(16)27)8-14(26)17-21(20)33-23-24(17,29)22(28)19(30-4)10(3)32-23/h7-8,10,19,22-23,28-29H,5-6H2,1-4H3

InChI Key

GPTONKSPQNETHU-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 cycloheptapyrans. These are organic heterocyclic compounds containing a cycloheptane derivative fused to a pyran. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Cycloheptapyrans

Sub Class

Not Available

Direct Parent

Cycloheptapyrans

Alternative Parents

Substituents

Cycloheptapyran
Azulene
Furopyran
Aryl ketone
Tropone
Pyran
Oxane
Monosaccharide
Vinylogous ester
Tertiary alcohol
Furan
Secondary alcohol
Ketone
1,2-diol
Oxacycle
Ether
Dialkyl ether
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	0.31	ChemAxon
pKa (Strongest Acidic)	11.21	ChemAxon
pKa (Strongest Basic)	2.57	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	128.59 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	118.53 m³·mol⁻¹	ChemAxon
Polarizability	47.16 Å³	ChemAxon
Number of Rings	5	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

162814663

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 15-butanoyl-8,9-dihydroxy-7-methoxy-6,18-dimethyl-3,5,19-trioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁹.0¹⁶,²⁰]icosa-1(20),2(10),12,15,17-pentaene-11,14-dione (NP0200663)

MOL for NP0200663 (15-butanoyl-8,9-dihydroxy-7-methoxy-6,18-dimethyl-3,5,19-trioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁹.0¹⁶,²⁰]icosa-1(20),2(10),12,15,17-pentaene-11,14-dione)

3D MOL for NP0200663 (15-butanoyl-8,9-dihydroxy-7-methoxy-6,18-dimethyl-3,5,19-trioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁹.0¹⁶,²⁰]icosa-1(20),2(10),12,15,17-pentaene-11,14-dione)

3D SDF for NP0200663 (15-butanoyl-8,9-dihydroxy-7-methoxy-6,18-dimethyl-3,5,19-trioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁹.0¹⁶,²⁰]icosa-1(20),2(10),12,15,17-pentaene-11,14-dione)

3D-SDF for NP0200663 (15-butanoyl-8,9-dihydroxy-7-methoxy-6,18-dimethyl-3,5,19-trioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁹.0¹⁶,²⁰]icosa-1(20),2(10),12,15,17-pentaene-11,14-dione)

PDB for NP0200663 (15-butanoyl-8,9-dihydroxy-7-methoxy-6,18-dimethyl-3,5,19-trioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁹.0¹⁶,²⁰]icosa-1(20),2(10),12,15,17-pentaene-11,14-dione)

3D PDB for NP0200663 (15-butanoyl-8,9-dihydroxy-7-methoxy-6,18-dimethyl-3,5,19-trioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁹.0¹⁶,²⁰]icosa-1(20),2(10),12,15,17-pentaene-11,14-dione)

SMILES for NP0200663 (15-butanoyl-8,9-dihydroxy-7-methoxy-6,18-dimethyl-3,5,19-trioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁹.0¹⁶,²⁰]icosa-1(20),2(10),12,15,17-pentaene-11,14-dione)

INCHI for NP0200663 (15-butanoyl-8,9-dihydroxy-7-methoxy-6,18-dimethyl-3,5,19-trioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁹.0¹⁶,²⁰]icosa-1(20),2(10),12,15,17-pentaene-11,14-dione)

Structure for NP0200663 (15-butanoyl-8,9-dihydroxy-7-methoxy-6,18-dimethyl-3,5,19-trioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁹.0¹⁶,²⁰]icosa-1(20),2(10),12,15,17-pentaene-11,14-dione)

3D Structure for NP0200663 (15-butanoyl-8,9-dihydroxy-7-methoxy-6,18-dimethyl-3,5,19-trioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁹.0¹⁶,²⁰]icosa-1(20),2(10),12,15,17-pentaene-11,14-dione)