NP-MRD: Showing NP-Card for RP-2 (NP0027788)

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Record Information

Version

2.0

Created at

2021-06-19 19:51:06 UTC

Updated at

2021-06-29 23:54:07 UTC

NP-MRD ID

NP0027788

Secondary Accession Numbers

None

Natural Product Identification

Common Name

RP-2

Provided By

JEOL Database JEOL Logo

Description

RP-2 is found in Agaricus blazei. RP-2 was first documented in 2005 (Hirotani, M., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192121513D          

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M  END

     RDKit          3D

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M  END


  Mrv1652306192121513D          

 60 63  0  0  0  0            999 V2000
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    2.2269   -5.8092   -0.4652 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1962   -6.7053   -1.9876 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7322   -6.6757   -0.9988 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2904   -4.9755    0.5471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0918   -3.2699    1.5647 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1536   -3.5280   -3.9072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9918   -1.7914   -3.7371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4051   -2.7852   -4.2538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0572   -0.6336   -3.3669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9847    1.2859   -2.2571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3187    3.0366   -0.7761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7406    3.6701    2.1795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0158    3.2393    1.0234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0724    4.7156    0.7935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6644    4.6265    0.3028 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1157    4.5868    1.4909 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7474    5.0577    2.5254 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6298    5.2491    0.7869 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0960    2.1730    2.4993 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    1.3504    2.6747 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8388    2.8104    3.5793 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5394    3.0325   -0.4205 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7434    0.7406   -1.0776 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6848    0.6986    0.4176 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9193    0.5733    0.4712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4824    1.4420    2.6915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1720    0.9915    2.3623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6192   -0.6115    2.0170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1713   -1.1753    2.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8636   -1.7033   -0.6389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2534   -0.7311    0.7834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6666   -2.3856    0.9777 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 27  1  0  0  0  0
  8  3  2  0  0  0  0
 16 17  1  0  0  0  0
  3  4  1  0  0  0  0
 27 26  1  0  0  0  0
 26 25  1  0  0  0  0
 25 13  1  0  0  0  0
 12 13  2  0  0  0  0
 17 18  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
 13 14  1  0  0  0  0
  7  8  1  0  0  0  0
 27 28  1  1  0  0  0
  7  6  2  0  0  0  0
  8  9  1  0  0  0  0
 18 21  1  0  0  0  0
  3  2  1  0  0  0  0
 21 23  1  0  0  0  0
  2  1  1  0  0  0  0
 14 16  1  0  0  0  0
 23 16  1  0  0  0  0
 14 15  1  0  0  0  0
 18 19  1  6  0  0  0
  7 10  1  0  0  0  0
 21 22  1  0  0  0  0
  6 27  1  0  0  0  0
 18 20  1  0  0  0  0
 12 11  1  0  0  0  0
 23 24  2  0  0  0  0
 11 10  2  0  0  0  0
 16 43  1  6  0  0  0
 21 50  1  6  0  0  0
  4 32  1  0  0  0  0
  5 33  1  0  0  0  0
 11 38  1  0  0  0  0
 10 37  1  0  0  0  0
 26 56  1  0  0  0  0
 26 57  1  0  0  0  0
 25 54  1  0  0  0  0
 25 55  1  0  0  0  0
 14 39  1  6  0  0  0
 28 58  1  0  0  0  0
 28 59  1  0  0  0  0
 28 60  1  0  0  0  0
  9 34  1  0  0  0  0
  9 35  1  0  0  0  0
  9 36  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
  1 31  1  0  0  0  0
 15 40  1  0  0  0  0
 15 41  1  0  0  0  0
 15 42  1  0  0  0  0
 19 44  1  0  0  0  0
 19 45  1  0  0  0  0
 19 46  1  0  0  0  0
 22 51  1  0  0  0  0
 22 52  1  0  0  0  0
 22 53  1  0  0  0  0
 20 47  1  0  0  0  0
 20 48  1  0  0  0  0
 20 49  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0027788

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C1=C([H])C2=C(C([H])=C([H])C(OC([H])([H])[H])=C2C([H])([H])[H])[C@@]2(C1=C(C([H])([H])C2([H])[H])[C@@]([H])(C([H])([H])[H])[C@@]1([H])OC(C([H])([H])[H])(C([H])([H])[H])[C@]([H])(C1=O)C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C25H32O3/c1-14-17-8-9-19-18(15(2)23-22(26)16(3)24(4,5)28-23)12-13-25(19,6)20(17)10-11-21(14)27-7/h8-11,15-16,23H,12-13H2,1-7H3/t15-,16+,23-,25+/m1/s1

> <INCHI_KEY>
OFFDOAVXTQWJAC-CJVUMSGVSA-N

> <FORMULA>
C25H32O3

> <MOLECULAR_WEIGHT>
380.528

> <EXACT_MASS>
380.23514489

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
43.73731555897521

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,4R)-2-[(1R)-1-[(9bS)-7-methoxy-6,9b-dimethyl-1H,2H,9bH-cyclopenta[a]naphthalen-3-yl]ethyl]-4,5,5-trimethyloxolan-3-one

> <ALOGPS_LOGP>
5.44

> <JCHEM_LOGP>
5.408772581666668

> <ALOGPS_LOGS>
-5.59

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.099546550666677

> <JCHEM_PKA_STRONGEST_BASIC>
-4.1439788984928505

> <JCHEM_POLAR_SURFACE_AREA>
35.53

> <JCHEM_REFRACTIVITY>
114.5696

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.67e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,4R)-2-[(1R)-1-[(9bS)-7-methoxy-6,9b-dimethyl-1H,2H-cyclopenta[a]naphthalen-3-yl]ethyl]-4,5,5-trimethyloxolan-3-one

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 60 63  0  0  0  0  0  0  0  0999 V2000
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    2.0236    4.5939    1.5715 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7560    1.0648   -0.0311 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4100    3.0500   -0.6075 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2489    3.0683   -1.8231 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1419    0.9143    1.9980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7060   -0.5483    1.8656 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0918   -0.9630    0.4310 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5485   -1.4704    0.3856 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.1157    4.5868    1.4909 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7474    5.0577    2.5254 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6298    5.2491    0.7869 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0960    2.1730    2.4993 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    1.3504    2.6747 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8388    2.8104    3.5793 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5394    3.0325   -0.4205 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7434    0.7406   -1.0776 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6848    0.6986    0.4176 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9193    0.5733    0.4712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4824    1.4420    2.6915 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.8636   -1.7033   -0.6389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2534   -0.7311    0.7834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6666   -2.3856    0.9777 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 27  1  0
  8  3  2  0
 16 17  1  0
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 25 13  1  0
 12 13  2  0
 17 18  1  0
  4  5  2  0
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 27 28  1  1
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 18 21  1  0
  3  2  1  0
 21 23  1  0
  2  1  1  0
 14 16  1  0
 23 16  1  0
 14 15  1  0
 18 19  1  6
  7 10  1  0
 21 22  1  0
  6 27  1  0
 18 20  1  0
 12 11  1  0
 23 24  2  0
 11 10  2  0
 16 43  1  6
 21 50  1  6
  4 32  1  0
  5 33  1  0
 11 38  1  0
 10 37  1  0
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 25 54  1  0
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 14 39  1  6
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 28 59  1  0
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  1 29  1  0
  1 30  1  0
  1 31  1  0
 15 40  1  0
 15 41  1  0
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 19 44  1  0
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 22 51  1  0
 22 52  1  0
 22 53  1  0
 20 47  1  0
 20 48  1  0
 20 49  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0       1.596  -6.083  -1.317  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.188  -4.932  -2.044  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.415  -4.003  -1.394  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.011  -4.122  -0.062  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.780  -3.140   0.531  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.180  -2.012  -0.196  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.785  -1.878  -1.550  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.024  -2.875  -2.151  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.465  -2.740  -3.590  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.228  -0.677  -2.297  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.764   0.390  -1.685  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.983   0.381  -0.266  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.044   1.421   0.583  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.997   2.900   0.265  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.013   3.671   1.119  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.603   3.536   0.402  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.019   3.246   1.668  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.448   3.171   1.472  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.024   4.594   1.571  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.018   2.326   2.612  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.668   2.581   0.065  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.756   1.065  -0.031  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.410   3.050  -0.608  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.249   3.068  -1.823  0.00  0.00           O+0
HETATM   25  C   UNK     0      -2.142   0.914   1.998  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.706  -0.548   1.866  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.092  -0.963   0.431  0.00  0.00           C+0
HETATM   28  C   UNK     0      -3.549  -1.470   0.386  0.00  0.00           C+0
HETATM   29  H   UNK     0       2.227  -5.809  -0.465  0.00  0.00           H+0
HETATM   30  H   UNK     0       2.196  -6.705  -1.988  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.732  -6.676  -0.999  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.290  -4.976   0.547  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.092  -3.270   1.565  0.00  0.00           H+0
HETATM   34  H   UNK     0       1.154  -3.528  -3.907  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.992  -1.791  -3.737  0.00  0.00           H+0
HETATM   36  H   UNK     0      -0.405  -2.785  -4.254  0.00  0.00           H+0
HETATM   37  H   UNK     0      -1.057  -0.634  -3.367  0.00  0.00           H+0
HETATM   38  H   UNK     0      -1.985   1.286  -2.257  0.00  0.00           H+0
HETATM   39  H   UNK     0      -2.319   3.037  -0.776  0.00  0.00           H+0
HETATM   40  H   UNK     0      -2.741   3.670   2.180  0.00  0.00           H+0
HETATM   41  H   UNK     0      -4.016   3.239   1.023  0.00  0.00           H+0
HETATM   42  H   UNK     0      -3.072   4.716   0.794  0.00  0.00           H+0
HETATM   43  H   UNK     0      -0.664   4.627   0.303  0.00  0.00           H+0
HETATM   44  H   UNK     0       3.116   4.587   1.491  0.00  0.00           H+0
HETATM   45  H   UNK     0       1.747   5.058   2.525  0.00  0.00           H+0
HETATM   46  H   UNK     0       1.630   5.249   0.787  0.00  0.00           H+0
HETATM   47  H   UNK     0       3.096   2.173   2.499  0.00  0.00           H+0
HETATM   48  H   UNK     0       1.525   1.350   2.675  0.00  0.00           H+0
HETATM   49  H   UNK     0       1.839   2.810   3.579  0.00  0.00           H+0
HETATM   50  H   UNK     0       2.539   3.033  -0.421  0.00  0.00           H+0
HETATM   51  H   UNK     0       1.743   0.741  -1.078  0.00  0.00           H+0
HETATM   52  H   UNK     0       2.685   0.699   0.418  0.00  0.00           H+0
HETATM   53  H   UNK     0       0.919   0.573   0.471  0.00  0.00           H+0
HETATM   54  H   UNK     0      -1.482   1.442   2.692  0.00  0.00           H+0
HETATM   55  H   UNK     0      -3.172   0.992   2.362  0.00  0.00           H+0
HETATM   56  H   UNK     0      -0.619  -0.612   2.017  0.00  0.00           H+0
HETATM   57  H   UNK     0      -2.171  -1.175   2.635  0.00  0.00           H+0
HETATM   58  H   UNK     0      -3.864  -1.703  -0.639  0.00  0.00           H+0
HETATM   59  H   UNK     0      -4.253  -0.731   0.783  0.00  0.00           H+0
HETATM   60  H   UNK     0      -3.667  -2.386   0.978  0.00  0.00           H+0
CONECT    1    2   29   30   31                                             
CONECT    2    3    1                                                       
CONECT    3    8    4    2                                                  
CONECT    4    3    5   32                                                  
CONECT    5    4    6   33                                                  
CONECT    6    5    7   27                                                  
CONECT    7    8    6   10                                                  
CONECT    8    3    7    9                                                  
CONECT    9    8   34   35   36                                             
CONECT   10    7   11   37                                                  
CONECT   11   12   10   38                                                  
CONECT   12   27   13   11                                                  
CONECT   13   25   12   14                                                  
CONECT   14   13   16   15   39                                             
CONECT   15   14   40   41   42                                             
CONECT   16   17   14   23   43                                             
CONECT   17   16   18                                                       
CONECT   18   17   21   19   20                                             
CONECT   19   18   44   45   46                                             
CONECT   20   18   47   48   49                                             
CONECT   21   18   23   22   50                                             
CONECT   22   21   51   52   53                                             
CONECT   23   21   16   24                                                  
CONECT   24   23                                                            
CONECT   25   26   13   54   55                                             
CONECT   26   27   25   56   57                                             
CONECT   27   12   26   28    6                                             
CONECT   28   27   58   59   60                                             
CONECT   29    1                                                            
CONECT   30    1                                                            
CONECT   31    1                                                            
CONECT   32    4                                                            
CONECT   33    5                                                            
CONECT   34    9                                                            
CONECT   35    9                                                            
CONECT   36    9                                                            
CONECT   37   10                                                            
CONECT   38   11                                                            
CONECT   39   14                                                            
CONECT   40   15                                                            
CONECT   41   15                                                            
CONECT   42   15                                                            
CONECT   43   16                                                            
CONECT   44   19                                                            
CONECT   45   19                                                            
CONECT   46   19                                                            
CONECT   47   20                                                            
CONECT   48   20                                                            
CONECT   49   20                                                            
CONECT   50   21                                                            
CONECT   51   22                                                            
CONECT   52   22                                                            
CONECT   53   22                                                            
CONECT   54   25                                                            
CONECT   55   25                                                            
CONECT   56   26                                                            
CONECT   57   26                                                            
CONECT   58   28                                                            
CONECT   59   28                                                            
CONECT   60   28                                                            
MASTER        0    0    0    0    0    0    0    0   60    0  126    0
END

RDKit          3D

60 63  0  0  0  0  0  0  0  0999 V2000
    1.5959   -6.0828   -1.3171 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1881   -4.9316   -2.0440 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4150   -4.0027   -1.3939 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0111   -4.1223   -0.0617 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7800   -3.1399    0.5312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1804   -2.0122   -0.1959 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7849   -1.8777   -1.5503 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0242   -2.8753   -2.1511 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4646   -2.7401   -3.5901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2278   -0.6765   -2.2973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7644    0.3902   -1.6852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9827    0.3814   -0.2663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0436    1.4208    0.5834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9968    2.8999    0.2645 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0131    3.6709    1.1185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6030    3.5360    0.4019 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0191    3.2459    1.6682 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4476    3.1706    1.4715 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0236    4.5939    1.5715 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0181    2.3263    2.6120 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6677    2.5807    0.0649 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7560    1.0648   -0.0311 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4100    3.0500   -0.6075 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2489    3.0683   -1.8231 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1419    0.9143    1.9980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7060   -0.5483    1.8656 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0918   -0.9630    0.4310 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5485   -1.4704    0.3856 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2269   -5.8092   -0.4652 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1962   -6.7053   -1.9876 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7322   -6.6757   -0.9988 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2904   -4.9755    0.5471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0918   -3.2699    1.5647 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1536   -3.5280   -3.9072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9918   -1.7914   -3.7371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4051   -2.7852   -4.2538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0572   -0.6336   -3.3669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9847    1.2859   -2.2571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3187    3.0366   -0.7761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7406    3.6701    2.1795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0158    3.2393    1.0234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0724    4.7156    0.7935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6644    4.6265    0.3028 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1157    4.5868    1.4909 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7474    5.0577    2.5254 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6298    5.2491    0.7869 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0960    2.1730    2.4993 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    1.3504    2.6747 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8388    2.8104    3.5793 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5394    3.0325   -0.4205 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7434    0.7406   -1.0776 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6848    0.6986    0.4176 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9193    0.5733    0.4712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4824    1.4420    2.6915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1720    0.9915    2.3623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6192   -0.6115    2.0170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1713   -1.1753    2.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8636   -1.7033   -0.6389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2534   -0.7311    0.7834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6666   -2.3856    0.9777 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 27  1  0
  8  3  2  0
 16 17  1  0
  3  4  1  0
 27 26  1  0
 26 25  1  0
 25 13  1  0
 12 13  2  0
 17 18  1  0
  4  5  2  0
  5  6  1  0
 13 14  1  0
  7  8  1  0
 27 28  1  1
  7  6  2  0
  8  9  1  0
 18 21  1  0
  3  2  1  0
 21 23  1  0
  2  1  1  0
 14 16  1  0
 23 16  1  0
 14 15  1  0
 18 19  1  6
  7 10  1  0
 21 22  1  0
  6 27  1  0
 18 20  1  0
 12 11  1  0
 23 24  2  0
 11 10  2  0
 16 43  1  6
 21 50  1  6
  4 32  1  0
  5 33  1  0
 11 38  1  0
 10 37  1  0
 26 56  1  0
 26 57  1  0
 25 54  1  0
 25 55  1  0
 14 39  1  6
 28 58  1  0
 28 59  1  0
 28 60  1  0
  9 34  1  0
  9 35  1  0
  9 36  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 15 40  1  0
 15 41  1  0
 15 42  1  0
 19 44  1  0
 19 45  1  0
 19 46  1  0
 22 51  1  0
 22 52  1  0
 22 53  1  0
 20 47  1  0
 20 48  1  0
 20 49  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₂₅H₃₂O₃

Average Mass

380.5280 Da

Monoisotopic Mass

380.23514 Da

IUPAC Name

(2R,4R)-2-[(1R)-1-[(9bS)-7-methoxy-6,9b-dimethyl-1H,2H,9bH-cyclopenta[a]naphthalen-3-yl]ethyl]-4,5,5-trimethyloxolan-3-one

Traditional Name

(2R,4R)-2-[(1R)-1-[(9bS)-7-methoxy-6,9b-dimethyl-1H,2H-cyclopenta[a]naphthalen-3-yl]ethyl]-4,5,5-trimethyloxolan-3-one

CAS Registry Number

Not Available

SMILES

[H]C1=C([H])C2=C(C([H])=C([H])C(OC([H])([H])[H])=C2C([H])([H])[H])[C@@]2(C1=C(C([H])([H])C2([H])[H])[C@@]([H])(C([H])([H])[H])[C@@]1([H])OC(C([H])([H])[H])(C([H])([H])[H])[C@]([H])(C1=O)C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C25H32O3/c1-14-17-8-9-19-18(15(2)23-22(26)16(3)24(4,5)28-23)12-13-25(19,6)20(17)10-11-21(14)27-7/h8-11,15-16,23H,12-13H2,1-7H3/t15-,16+,23-,25+/m1/s1

InChI Key

OFFDOAVXTQWJAC-CJVUMSGVSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Agaricus blazei	JEOL database	Hirotani, M., et al, Tetrahedron 61, 189 (2005)

Chemical Taxonomy

Classification

Not classified

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	5.44	ALOGPS
logP	5.41	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	18.1	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	35.53 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	114.57 m³·mol⁻¹	ChemAxon
Polarizability	43.74 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

Hirotani, M., et al. (2005). Hirotani, M., et al, Tetrahedron 61, 189 (2005). Tetrahedron.

Showing NP-Card for RP-2 (NP0027788)

MOL for NP0027788 (RP-2)

3D MOL for NP0027788 (RP-2)

3D SDF for NP0027788 (RP-2)

3D-SDF for NP0027788 (RP-2)

PDB for NP0027788 (RP-2)

3D PDB for NP0027788 (RP-2)

SMILES for NP0027788 (RP-2)

INCHI for NP0027788 (RP-2)

Structure for NP0027788 (RP-2)

3D Structure for NP0027788 (RP-2)