NP-MRD: Showing NP-Card for 3-[(1s,4as,7s,7ar)-3-[(2r)-2-hydroxy-3-methylbutanoyl]-4,7-dimethyl-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-1-yl]-4-hydroxy-5-methylchromen-2-one (NP0239128)

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Record Information

Version

2.0

Created at

2022-09-06 22:38:59 UTC

Updated at

2022-09-06 22:38:59 UTC

NP-MRD ID

NP0239128

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[(1s,4as,7s,7ar)-3-[(2r)-2-hydroxy-3-methylbutanoyl]-4,7-dimethyl-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-1-yl]-4-hydroxy-5-methylchromen-2-one

Description

3-[(1S,4aS,7S,7aR)-3-[(2R)-2-hydroxy-3-methylbutanoyl]-4,7-dimethyl-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-1-yl]-4-hydroxy-5-methyl-2H-chromen-2-one belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. Based on a literature review very few articles have been published on 3-[(1S,4aS,7S,7aR)-3-[(2R)-2-hydroxy-3-methylbutanoyl]-4,7-dimethyl-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-1-yl]-4-hydroxy-5-methyl-2H-chromen-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072200392D          

 31 34  0  0  1  0            999 V2000
    3.9934   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7079   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8513   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9934   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4943   -3.9674    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2394   -4.7521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0094   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4943   -2.6326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  3 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  2  0  0  0  0
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 16 17  2  0  0  0  0
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 16 22  1  0  0  0  0
 22 23  1  0  0  0  0
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 26 27  1  6  0  0  0
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 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 31 30  1  6  0  0  0
  2 31  1  0  0  0  0
 26 31  1  0  0  0  0
M  END

     RDKit          3D

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    2.8880   -3.4333   -0.4315 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7779   -2.4781   -0.5625 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8768   -1.1492   -0.3161 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1645   -0.6566    0.1087 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1465   -1.5302    0.1545 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5558    0.6676    0.5052 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9460    1.0835    1.6982 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6076    1.7405   -0.5187 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3079    2.3863   -0.8805 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.6768    0.5854   -1.9818 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9819    2.0696   -0.2035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9767    2.7033   -0.9530 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3788    2.2609   -2.3044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6185    3.7941   -0.3669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2630    4.2051    0.8978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2908    3.5732    1.6084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6293    2.4747    1.0517 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7050    1.8459    1.7079 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0563    0.7845    1.2075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1943    0.3297    1.9825 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5949   -2.1489   -0.1062 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3089   -2.5098    1.2610 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5637   -2.4417    2.1594 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0987   -4.0146    1.1748 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.6846    2.0998   -0.4225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6508   -0.8469   -1.7696 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.6328    2.4512   -3.0985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8178    1.2326   -2.3293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2579    2.9087   -2.6152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4052    4.2748   -0.9381 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.9637    3.8399    2.6038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5562   -2.7258   -0.4049 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5092   -2.0482    1.7976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3980   -1.7148    2.9309 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.2095   -2.9105   -2.0028 H   0  0  0  0  0  0  0  0  0  0  0  0
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 20 50  1  0
 21 51  1  0
M  END


  Mrv1652309072200392D          

 31 34  0  0  1  0            999 V2000
    3.9934   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7079   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8513   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9934   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.9934   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.2394   -4.7521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0094   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4943   -2.6326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0239128

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@@H](O)C(=O)C1=C(C)[C@H]2CC[C@H](C)[C@H]2[C@H](O1)C1=C(O)C2=C(C)C=CC=C2OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H30O6/c1-11(2)20(26)22(28)23-14(5)15-10-9-13(4)17(15)24(31-23)19-21(27)18-12(3)7-6-8-16(18)30-25(19)29/h6-8,11,13,15,17,20,24,26-27H,9-10H2,1-5H3/t13-,15+,17+,20+,24-/m0/s1

> <INCHI_KEY>
DGKDRSQFWYQETD-QWLDHPCISA-N

> <FORMULA>
C25H30O6

> <MOLECULAR_WEIGHT>
426.509

> <EXACT_MASS>
426.204238686

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
45.77956578616454

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-[(1S,4aS,7S,7aR)-3-[(2R)-2-hydroxy-3-methylbutanoyl]-4,7-dimethyl-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-1-yl]-4-hydroxy-5-methyl-2H-chromen-2-one

> <JCHEM_LOGP>
3.8529973476666672

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.089591026995251

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.6654732683726206

> <JCHEM_PKA_STRONGEST_BASIC>
-3.634542439302276

> <JCHEM_POLAR_SURFACE_AREA>
93.06

> <JCHEM_REFRACTIVITY>
117.96809999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
3-[(1S,4aS,7S,7aR)-3-[(2R)-2-hydroxy-3-methylbutanoyl]-4,7-dimethyl-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-1-yl]-4-hydroxy-5-methylchromen-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       7.454  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.454  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.788  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.122  -4.620   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      11.455  -5.390   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      10.122  -3.080   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.788  -2.310   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      11.455  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.455  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.789  -3.080   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.788  -6.930   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.454  -7.700   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.454  -9.240   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.788 -10.010   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      10.122  -9.240   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.788 -11.550   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.122 -12.320   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.455 -11.550   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.122 -13.860   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.788 -14.630   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.454 -13.860   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.454 -12.320   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.121 -11.550   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.121 -10.010   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.787  -9.240   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       6.121  -6.930   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.656  -7.406   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.180  -8.871   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.751  -6.160   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.656  -4.914   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.121  -5.390   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   31                                                  
CONECT    3    2    4   11                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    3   12                                                       
CONECT   12   11   13   26                                                  
CONECT   13   12   14   24                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   22                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   16   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   13   25                                                  
CONECT   25   24                                                            
CONECT   26   12   27   31                                                  
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30    2   26                                                  
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₀O₆

Average Mass

426.5090 Da

Monoisotopic Mass

426.20424 Da

IUPAC Name

3-[(1S,4aS,7S,7aR)-3-[(2R)-2-hydroxy-3-methylbutanoyl]-4,7-dimethyl-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-1-yl]-4-hydroxy-5-methyl-2H-chromen-2-one

Traditional Name

3-[(1S,4aS,7S,7aR)-3-[(2R)-2-hydroxy-3-methylbutanoyl]-4,7-dimethyl-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-1-yl]-4-hydroxy-5-methylchromen-2-one

CAS Registry Number

Not Available

SMILES

CC(C)[C@@H](O)C(=O)C1=C(C)[C@H]2CC[C@H](C)[C@H]2[C@H](O1)C1=C(O)C2=C(C)C=CC=C2OC1=O

InChI Identifier

InChI=1S/C25H30O6/c1-11(2)20(26)22(28)23-14(5)15-10-9-13(4)17(15)24(31-23)19-21(27)18-12(3)7-6-8-16(18)30-25(19)29/h6-8,11,13,15,17,20,24,26-27H,9-10H2,1-5H3/t13-,15+,17+,20+,24-/m0/s1

InChI Key

DGKDRSQFWYQETD-QWLDHPCISA-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 terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Sesquiterpenoid
Hydroxycoumarin
4-hydroxycoumarin
Iridoid-skeleton
Coumarin
1-benzopyran
Benzopyran
Pyranone
Benzenoid
Pyran
Acyloin
Heteroaromatic compound
Vinylogous acid
Alpha-hydroxy ketone
Secondary alcohol
Lactone
Ketone
Oxacycle
Organoheterocyclic compound
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	3.85	ChemAxon
pKa (Strongest Acidic)	5.67	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	93.06 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	117.97 m³·mol⁻¹	ChemAxon
Polarizability	45.78 Å³	ChemAxon
Number of Rings	4	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

163193661

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-[(1s,4as,7s,7ar)-3-[(2r)-2-hydroxy-3-methylbutanoyl]-4,7-dimethyl-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-1-yl]-4-hydroxy-5-methylchromen-2-one (NP0239128)

MOL for NP0239128 (3-[(1s,4as,7s,7ar)-3-[(2r)-2-hydroxy-3-methylbutanoyl]-4,7-dimethyl-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-1-yl]-4-hydroxy-5-methylchromen-2-one)

3D MOL for NP0239128 (3-[(1s,4as,7s,7ar)-3-[(2r)-2-hydroxy-3-methylbutanoyl]-4,7-dimethyl-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-1-yl]-4-hydroxy-5-methylchromen-2-one)

3D SDF for NP0239128 (3-[(1s,4as,7s,7ar)-3-[(2r)-2-hydroxy-3-methylbutanoyl]-4,7-dimethyl-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-1-yl]-4-hydroxy-5-methylchromen-2-one)

3D-SDF for NP0239128 (3-[(1s,4as,7s,7ar)-3-[(2r)-2-hydroxy-3-methylbutanoyl]-4,7-dimethyl-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-1-yl]-4-hydroxy-5-methylchromen-2-one)

PDB for NP0239128 (3-[(1s,4as,7s,7ar)-3-[(2r)-2-hydroxy-3-methylbutanoyl]-4,7-dimethyl-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-1-yl]-4-hydroxy-5-methylchromen-2-one)

3D PDB for NP0239128 (3-[(1s,4as,7s,7ar)-3-[(2r)-2-hydroxy-3-methylbutanoyl]-4,7-dimethyl-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-1-yl]-4-hydroxy-5-methylchromen-2-one)

SMILES for NP0239128 (3-[(1s,4as,7s,7ar)-3-[(2r)-2-hydroxy-3-methylbutanoyl]-4,7-dimethyl-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-1-yl]-4-hydroxy-5-methylchromen-2-one)

INCHI for NP0239128 (3-[(1s,4as,7s,7ar)-3-[(2r)-2-hydroxy-3-methylbutanoyl]-4,7-dimethyl-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-1-yl]-4-hydroxy-5-methylchromen-2-one)

Structure for NP0239128 (3-[(1s,4as,7s,7ar)-3-[(2r)-2-hydroxy-3-methylbutanoyl]-4,7-dimethyl-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-1-yl]-4-hydroxy-5-methylchromen-2-one)

3D Structure for NP0239128 (3-[(1s,4as,7s,7ar)-3-[(2r)-2-hydroxy-3-methylbutanoyl]-4,7-dimethyl-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-1-yl]-4-hydroxy-5-methylchromen-2-one)