NP-MRD: Showing NP-Card for (+)-dalmanol B (NP0009858)

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Record Information

Version

2.0

Created at

2021-01-05 19:34:36 UTC

Updated at

2021-07-15 17:04:27 UTC

NP-MRD ID

NP0009858

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-dalmanol B

Provided By

NPAtlas

Description

(17R,18R)-18-[(2R)-4-(2,6-dihydroxyphenyl)-4-oxobutan-2-yl]-3,11,15-trihydroxy-17-methyl-8-oxapentacyclo[10.6.2.0²,⁷.0⁹,¹⁹.0¹⁶,²⁰]Icosa-1(19),2,4,6,9,11,14,16(20)-octaen-13-one belongs to the class of organic compounds known as isoflavonoids. These are natural products derived from 3-phenylchromen-4-one. (+)-dalmanol B is found in Daldinia and Daldinia eschscholtzii. Based on a literature review very few articles have been published on (17R,18R)-18-[(2R)-4-(2,6-dihydroxyphenyl)-4-oxobutan-2-yl]-3,11,15-trihydroxy-17-methyl-8-oxapentacyclo[10.6.2.0²,⁷.0⁹,¹⁹.0¹⁶,²⁰]Icosa-1(19),2,4,6,9,11,14,16(20)-octaen-13-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106533D          

 62 67  0  0  0  0            999 V2000
    1.5110   -1.2725    2.2723 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7371   -0.6152    1.1762 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5882    0.1470    0.2007 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5562   -0.8213   -0.4359 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5087   -2.0000   -0.0908 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5164   -0.3381   -1.4369 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5472    0.9921   -1.8044 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7017    1.9269   -1.2686 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4491    1.4603   -2.7497 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3339    0.5976   -3.3398 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.4999   -2.5382   -1.7762 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5026    0.1420    1.6771 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2132    0.7863    0.5916 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0811    2.8913    0.8923 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4978    2.4293    2.0806 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2172    4.1956    0.4734 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.1803   -0.7904    3.2386 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9830    0.6496   -0.5647 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6873    2.9030   -1.5044 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4721    2.5085   -3.0381 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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  3  4  1  0  0  0  0
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  7  9  1  0  0  0  0
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  2 14  1  0  0  0  0
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M  END

     RDKit          3D

 62 67  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652306242106533D          

 62 67  0  0  0  0            999 V2000
    1.5110   -1.2725    2.2723 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7371   -0.6152    1.1762 C   0  0  2  0  0  0  0  0  0  0  0  0
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    4.4721    2.5085   -3.0381 H   0  0  0  0  0  0  0  0  0  0  0  0
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  3  4  1  0  0  0  0
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 17 18  1  0  0  0  0
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 12  6  1  0  0  0  0
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 38 62  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0009858

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C([H])=C([H])C(O[H])=C1C(=O)C([H])([H])[C@@]([H])(C([H])([H])[H])[C@@]1([H])C2=C3C(OC4=C([H])C([H])=C([H])C(O[H])=C24)=C([H])C(O[H])=C2C(=O)C([H])=C(O[H])C(=C32)[C@]1([H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C30H24O8/c1-12(9-17(34)25-14(31)5-3-6-15(25)32)23-13(2)24-18(35)10-19(36)26-20(37)11-22-28(30(24)26)29(23)27-16(33)7-4-8-21(27)38-22/h3-8,10-13,23,31-33,35,37H,9H2,1-2H3/t12-,13-,23-/m1/s1

> <INCHI_KEY>
DXVDILBJEQUZBA-NSCUQIJASA-N

> <FORMULA>
C30H24O8

> <MOLECULAR_WEIGHT>
512.514

> <EXACT_MASS>
512.147117733

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
52.21808588706276

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(17R,18R)-18-[(2R)-4-(2,6-dihydroxyphenyl)-4-oxobutan-2-yl]-3,11,15-trihydroxy-17-methyl-8-oxapentacyclo[10.6.2.0^{2,7}.0^{9,19}.0^{16,20}]icosa-1(19),2,4,6,9,11,14,16(20)-octaen-13-one

> <ALOGPS_LOGP>
3.82

> <JCHEM_LOGP>
4.4207586086666675

> <ALOGPS_LOGS>
-5.14

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.707154595752697

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.266968410068263

> <JCHEM_PKA_STRONGEST_BASIC>
2.5271922726266056

> <JCHEM_POLAR_SURFACE_AREA>
144.52

> <JCHEM_REFRACTIVITY>
143.7143

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.75e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(17R,18R)-18-[(2R)-4-(2,6-dihydroxyphenyl)-4-oxobutan-2-yl]-3,11,15-trihydroxy-17-methyl-8-oxapentacyclo[10.6.2.0^{2,7}.0^{9,19}.0^{16,20}]icosa-1(19),2,4,6,9,11,14,16(20)-octaen-13-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

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 38 61  1  0
 38 62  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       1.511  -1.272   2.272  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.737  -0.615   1.176  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.588   0.147   0.201  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.556  -0.821  -0.436  0.00  0.00           C+0
HETATM    5  O   UNK     0       2.509  -2.000  -0.091  0.00  0.00           O+0
HETATM    6  C   UNK     0       3.516  -0.338  -1.437  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.547   0.992  -1.804  0.00  0.00           C+0
HETATM    8  O   UNK     0       2.702   1.927  -1.269  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.449   1.460  -2.750  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.334   0.598  -3.340  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.321  -0.713  -2.993  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.414  -1.190  -2.042  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.500  -2.538  -1.776  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.503   0.142   1.677  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.213   0.786   0.592  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.913   2.073   0.182  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.081   2.891   0.892  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.498   2.429   2.081  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.217   4.196   0.473  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.337   4.675  -0.682  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.184   3.869  -1.422  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.464   2.591  -0.992  0.00  0.00           C+0
HETATM   23  O   UNK     0      -2.280   1.906  -1.759  0.00  0.00           O+0
HETATM   24  C   UNK     0      -2.589   0.687  -1.397  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.457   0.017  -2.269  0.00  0.00           C+0
HETATM   26  C   UNK     0      -3.864  -1.269  -2.020  0.00  0.00           C+0
HETATM   27  O   UNK     0      -4.715  -1.982  -2.848  0.00  0.00           O+0
HETATM   28  C   UNK     0      -3.373  -1.850  -0.864  0.00  0.00           C+0
HETATM   29  C   UNK     0      -3.783  -3.116  -0.529  0.00  0.00           C+0
HETATM   30  O   UNK     0      -4.563  -3.720  -1.330  0.00  0.00           O+0
HETATM   31  C   UNK     0      -3.367  -3.714   0.632  0.00  0.00           C+0
HETATM   32  C   UNK     0      -2.521  -3.060   1.509  0.00  0.00           C+0
HETATM   33  O   UNK     0      -2.099  -3.636   2.672  0.00  0.00           O+0
HETATM   34  C   UNK     0      -2.095  -1.774   1.182  0.00  0.00           C+0
HETATM   35  C   UNK     0      -2.506  -1.182   0.012  0.00  0.00           C+0
HETATM   36  C   UNK     0      -2.093   0.102  -0.250  0.00  0.00           C+0
HETATM   37  C   UNK     0      -1.360  -0.998   2.186  0.00  0.00           C+0
HETATM   38  C   UNK     0      -2.335  -0.389   3.208  0.00  0.00           C+0
HETATM   39  H   UNK     0       1.180  -0.790   3.239  0.00  0.00           H+0
HETATM   40  H   UNK     0       1.365  -2.347   2.371  0.00  0.00           H+0
HETATM   41  H   UNK     0       2.595  -1.063   2.148  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.372  -1.495   0.535  0.00  0.00           H+0
HETATM   43  H   UNK     0       2.237   0.889   0.687  0.00  0.00           H+0
HETATM   44  H   UNK     0       0.983   0.650  -0.565  0.00  0.00           H+0
HETATM   45  H   UNK     0       2.687   2.903  -1.504  0.00  0.00           H+0
HETATM   46  H   UNK     0       4.472   2.509  -3.038  0.00  0.00           H+0
HETATM   47  H   UNK     0       6.056   0.957  -4.093  0.00  0.00           H+0
HETATM   48  H   UNK     0       6.030  -1.407  -3.466  0.00  0.00           H+0
HETATM   49  H   UNK     0       3.971  -3.044  -1.163  0.00  0.00           H+0
HETATM   50  H   UNK     0      -0.324   0.664   2.609  0.00  0.00           H+0
HETATM   51  H   UNK     0       1.113   3.001   2.630  0.00  0.00           H+0
HETATM   52  H   UNK     0       0.872   4.807   1.054  0.00  0.00           H+0
HETATM   53  H   UNK     0      -0.144   5.672  -1.056  0.00  0.00           H+0
HETATM   54  H   UNK     0      -1.619   4.271  -2.345  0.00  0.00           H+0
HETATM   55  H   UNK     0      -3.825   0.499  -3.160  0.00  0.00           H+0
HETATM   56  H   UNK     0      -5.077  -1.573  -3.687  0.00  0.00           H+0
HETATM   57  H   UNK     0      -3.698  -4.725   0.887  0.00  0.00           H+0
HETATM   58  H   UNK     0      -1.524  -3.336   3.395  0.00  0.00           H+0
HETATM   59  H   UNK     0      -0.698  -1.672   2.802  0.00  0.00           H+0
HETATM   60  H   UNK     0      -2.393  -0.987   4.122  0.00  0.00           H+0
HETATM   61  H   UNK     0      -2.023   0.634   3.496  0.00  0.00           H+0
HETATM   62  H   UNK     0      -3.313  -0.326   2.690  0.00  0.00           H+0
CONECT    1    2   39   40   41                                             
CONECT    2    1    3   14   42                                             
CONECT    3    2    4   43   44                                             
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   12                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7   45                                                       
CONECT    9    7   10   46                                                  
CONECT   10    9   11   47                                                  
CONECT   11   10   12   48                                                  
CONECT   12   11   13    6                                                  
CONECT   13   12   49                                                       
CONECT   14    2   15   37   50                                             
CONECT   15   14   16   36                                                  
CONECT   16   15   17   22                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17   51                                                       
CONECT   19   17   20   52                                                  
CONECT   20   19   21   53                                                  
CONECT   21   20   22   54                                                  
CONECT   22   21   23   16                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   36                                                  
CONECT   25   24   26   55                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26   56                                                       
CONECT   28   26   29   35                                                  
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   57                                                  
CONECT   32   31   33   34                                                  
CONECT   33   32   58                                                       
CONECT   34   32   35   37                                                  
CONECT   35   34   36   28                                                  
CONECT   36   35   15   24                                                  
CONECT   37   34   38   14   59                                             
CONECT   38   37   60   61   62                                             
CONECT   39    1                                                            
CONECT   40    1                                                            
CONECT   41    1                                                            
CONECT   42    2                                                            
CONECT   43    3                                                            
CONECT   44    3                                                            
CONECT   45    8                                                            
CONECT   46    9                                                            
CONECT   47   10                                                            
CONECT   48   11                                                            
CONECT   49   13                                                            
CONECT   50   14                                                            
CONECT   51   18                                                            
CONECT   52   19                                                            
CONECT   53   20                                                            
CONECT   54   21                                                            
CONECT   55   25                                                            
CONECT   56   27                                                            
CONECT   57   31                                                            
CONECT   58   33                                                            
CONECT   59   37                                                            
CONECT   60   38                                                            
CONECT   61   38                                                            
CONECT   62   38                                                            
MASTER        0    0    0    0    0    0    0    0   62    0  134    0
END

RDKit          3D

62 67  0  0  0  0  0  0  0  0999 V2000
    1.5110   -1.2725    2.2723 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7371   -0.6152    1.1762 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5882    0.1470    0.2007 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5562   -0.8213   -0.4359 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5087   -2.0000   -0.0908 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5164   -0.3381   -1.4369 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5472    0.9921   -1.8044 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7017    1.9269   -1.2686 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4491    1.4603   -2.7497 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3339    0.5976   -3.3398 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3205   -0.7128   -2.9932 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4142   -1.1904   -2.0416 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4999   -2.5382   -1.7762 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5026    0.1420    1.6771 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2132    0.7863    0.5916 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.3372    4.6749   -0.6821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1839    3.8692   -1.4217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4638    2.5909   -0.9923 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2796    1.9061   -1.7586 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5888    0.6867   -1.3974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4567    0.0166   -2.2692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8643   -1.2692   -2.0200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7153   -1.9819   -2.8475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3730   -1.8499   -0.8637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7829   -3.1159   -0.5289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5628   -3.7204   -1.3300 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3669   -3.7140    0.6321 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5209   -3.0600    1.5094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0995   -3.6357    2.6721 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0953   -1.7736    1.1816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5063   -1.1817    0.0118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0930    0.1022   -0.2504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3600   -0.9975    2.1864 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3350   -0.3893    3.2085 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1803   -0.7904    3.2386 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3648   -2.3470    2.3707 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5948   -1.0635    2.1478 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3717   -1.4950    0.5349 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2372    0.8890    0.6872 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9830    0.6496   -0.5647 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6873    2.9030   -1.5044 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4721    2.5085   -3.0381 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0565    0.9568   -4.0930 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0300   -1.4065   -3.4659 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9713   -3.0440   -1.1631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3241    0.6638    2.6086 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1130    3.0005    2.6295 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8717    4.8066    1.0535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1441    5.6718   -1.0556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6191    4.2714   -2.3453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8254    0.4989   -3.1598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0771   -1.5726   -3.6865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6982   -4.7247    0.8874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5237   -3.3360    3.3948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6983   -1.6718    2.8020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3926   -0.9866    4.1225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0235    0.6341    3.4959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3125   -0.3262    2.6903 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  2  0
  4  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
  2 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  1  0
 26 28  2  0
 28 29  1  0
 29 30  2  0
 29 31  1  0
 31 32  2  0
 32 33  1  0
 32 34  1  0
 34 35  2  0
 35 36  1  0
 34 37  1  0
 37 38  1  0
 12  6  1  0
 37 14  1  0
 36 15  2  0
 22 16  1  0
 36 24  1  0
 35 28  1  0
  1 39  1  0
  1 40  1  0
  1 41  1  0
  2 42  1  6
  3 43  1  0
  3 44  1  0
  8 45  1  0
  9 46  1  0
 10 47  1  0
 11 48  1  0
 13 49  1  0
 14 50  1  1
 18 51  1  0
 19 52  1  0
 20 53  1  0
 21 54  1  0
 25 55  1  0
 27 56  1  0
 31 57  1  0
 33 58  1  0
 37 59  1  1
 38 60  1  0
 38 61  1  0
 38 62  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₃₀H₂₄O₈

Average Mass

512.5140 Da

Monoisotopic Mass

512.14712 Da

IUPAC Name

(17R,18R)-18-[(2R)-4-(2,6-dihydroxyphenyl)-4-oxobutan-2-yl]-3,11,15-trihydroxy-17-methyl-8-oxapentacyclo[10.6.2.0^{2,7}.0^{9,19}.0^{16,20}]icosa-1(19),2,4,6,9,11,14,16(20)-octaen-13-one

Traditional Name

(17R,18R)-18-[(2R)-4-(2,6-dihydroxyphenyl)-4-oxobutan-2-yl]-3,11,15-trihydroxy-17-methyl-8-oxapentacyclo[10.6.2.0^{2,7}.0^{9,19}.0^{16,20}]icosa-1(19),2,4,6,9,11,14,16(20)-octaen-13-one

CAS Registry Number

Not Available

SMILES

C[C@H](CC(=O)C1=C(O)C=CC=C1O)[C@@H]1[C@@H](C)C2=C3C(=C(O)C=C4OC5=C(C(O)=CC=C5)C1=C34)C(=O)C=C2O

InChI Identifier

InChI=1S/C30H24O8/c1-12(9-17(34)25-14(31)5-3-6-15(25)32)23-13(2)24-18(35)10-19(36)26-20(37)11-22-28(30(24)26)29(23)27-16(33)7-4-8-21(27)38-22/h3-8,10-13,23,31-33,35,37H,9H2,1-2H3/t12-,13-,23-/m1/s1

InChI Key

DXVDILBJEQUZBA-NSCUQIJASA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Daldinia	NPAtlas	21434637
Daldinia eschscholtzii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoflavonoids. These are natural products derived from 3-phenylchromen-4-one.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Not Available

Direct Parent

Isoflavonoids

Alternative Parents

Substituents

Isoflavonoid
Dibenzopyran
Naphthopyran
Xanthene
Alkyl-phenylketone
Butyrophenone
2-naphthol
1-naphthol
Benzopyran
Naphthalene
1-benzopyran
Phenylketone
Benzoyl
Resorcinol
Aryl alkyl ketone
Aryl ketone
Phenol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Monocyclic benzene moiety
Pyran
Benzenoid
Heteroaromatic compound
Vinylogous acid
Ketone
Polyol
Organoheterocyclic compound
Oxacycle
Organooxygen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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	3.82	ALOGPS
logP	4.42	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	6.27	ChemAxon
pKa (Strongest Basic)	2.53	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	144.52 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	143.71 m³·mol⁻¹	ChemAxon
Polarizability	52.22 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA002498

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78440054

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53260055

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for (+)-dalmanol B (NP0009858)

MOL for NP0009858 ((+)-dalmanol B)

3D MOL for NP0009858 ((+)-dalmanol B)

3D SDF for NP0009858 ((+)-dalmanol B)

3D-SDF for NP0009858 ((+)-dalmanol B)

PDB for NP0009858 ((+)-dalmanol B)

3D PDB for NP0009858 ((+)-dalmanol B)

SMILES for NP0009858 ((+)-dalmanol B)

INCHI for NP0009858 ((+)-dalmanol B)

Structure for NP0009858 ((+)-dalmanol B)

3D Structure for NP0009858 ((+)-dalmanol B)