NP-MRD: Showing NP-Card for methyl (2r)-2-[(1s,2s,3as,5ar,6s,9ar,9br,11as)-2-hydroxy-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-7-oxo-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-6-methylhept-5-enoate (NP0219462)

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Record Information

Version

2.0

Created at

2022-09-05 20:27:39 UTC

Updated at

2022-09-05 20:27:39 UTC

NP-MRD ID

NP0219462

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2r)-2-[(1s,2s,3as,5ar,6s,9ar,9br,11as)-2-hydroxy-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-7-oxo-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-6-methylhept-5-enoate

Description

Methyl (2R)-2-[(1R,2R,6S,7R,11S,13S,14S,15S)-13-hydroxy-6-(hydroxymethyl)-2,6,11,15-tetramethyl-5-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-9-en-14-yl]-6-methylhept-5-enoate belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. methyl (2r)-2-[(1s,2s,3as,5ar,6s,9ar,9br,11as)-2-hydroxy-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-7-oxo-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-6-methylhept-5-enoate is found in Melia azedarach. Based on a literature review very few articles have been published on methyl (2R)-2-[(1R,2R,6S,7R,11S,13S,14S,15S)-13-hydroxy-6-(hydroxymethyl)-2,6,11,15-tetramethyl-5-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-9-en-14-yl]-6-methylhept-5-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052222272D          

 36 39  0  0  1  0            999 V2000
    4.2828    0.4942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6953   -0.2203    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5203   -0.2203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9328    0.4942    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9328   -0.9348    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.7578   -0.9348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1703   -0.2203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9953   -0.2203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4078   -0.9348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2328   -0.9348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9953   -1.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.8559   -2.4029    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    3.1306   -2.2453    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3021   -1.4384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0868   -1.1834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
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  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 12  5  1  6  0  0  0
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 13 14  1  1  0  0  0
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 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
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 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  1  0  0  0
 24 25  1  0  0  0  0
 22 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 21 30  1  0  0  0  0
 30 31  1  1  0  0  0
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 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 12 35  1  0  0  0  0
 16 35  1  0  0  0  0
 35 36  1  6  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309052222272D          

 36 39  0  0  1  0            999 V2000
    4.2828    0.4942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6953   -0.2203    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.7875   -3.8593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1745   -3.3073    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3898   -3.5622    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7771   -4.2906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7397   -4.0701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8545   -4.8871    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7767   -3.0102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0079   -3.2651    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9483   -2.2032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7329   -1.9483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3460   -2.5003    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5175   -1.6933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1306   -2.2453    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3021   -1.4384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0868   -1.1834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6998   -1.7355    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9548   -0.9508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  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
 12  5  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 21 20  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  1  0  0  0
 24 25  1  0  0  0  0
 22 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 21 30  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  0  0  0  0
 32 18  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 12 35  1  0  0  0  0
 16 35  1  0  0  0  0
 35 36  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0219462

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@H](CCC=C(C)C)[C@@H]1[C@@H](O)C[C@]2(C)C3=CC[C@H]4[C@@](C)(CO)C(=O)CC[C@]4(C)[C@H]3CC[C@@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C31H48O5/c1-19(2)9-8-10-20(27(35)36-7)26-23(33)17-31(6)22-11-12-24-28(3,21(22)13-16-30(26,31)5)15-14-25(34)29(24,4)18-32/h9,11,20-21,23-24,26,32-33H,8,10,12-18H2,1-7H3/t20-,21+,23+,24-,26-,28-,29-,30+,31-/m1/s1

> <INCHI_KEY>
FFLSZDBIGTWQDR-SLPXCYNGSA-N

> <FORMULA>
C31H48O5

> <MOLECULAR_WEIGHT>
500.72

> <EXACT_MASS>
500.350174646

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
59.140962796667694

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (2R)-2-[(1R,2R,6S,7R,11S,13S,14S,15S)-13-hydroxy-6-(hydroxymethyl)-2,6,11,15-tetramethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-14-yl]-6-methylhept-5-enoate

> <JCHEM_LOGP>
4.805941570666667

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.216793193040768

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.61098193568656

> <JCHEM_PKA_STRONGEST_BASIC>
-2.818717156650769

> <JCHEM_POLAR_SURFACE_AREA>
83.83000000000001

> <JCHEM_REFRACTIVITY>
143.81659999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2R)-2-[(1R,2R,6S,7R,11S,13S,14S,15S)-13-hydroxy-6-(hydroxymethyl)-2,6,11,15-tetramethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-14-yl]-6-methylhept-5-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       7.995   0.922   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       8.765  -0.411   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      10.305  -0.411   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      11.075   0.922   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      11.075  -1.745   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.615  -1.745   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.385  -0.411   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      14.925  -0.411   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      15.695  -1.745   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      17.235  -1.745   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.925  -3.079   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.305  -3.079   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.931  -4.485   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      12.437  -4.806   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       9.787  -5.516   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.453  -4.746   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.292  -6.277   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.988  -5.222   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.668  -6.728   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.203  -7.204   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.059  -6.174   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.594  -6.649   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.317  -8.009   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.381  -7.598   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       1.595  -9.123   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.450  -5.619   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -0.015  -6.095   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       1.770  -4.113   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.235  -3.637   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.379  -4.667   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.699  -3.161   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.844  -4.191   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.164  -2.685   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       7.629  -2.209   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.773  -3.240   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       9.249  -1.775   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   12                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    5   13   35                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   18   35                                             
CONECT   17   16                                                            
CONECT   18   16   19   32                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   30                                                  
CONECT   22   21   23   24   26                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24                                                            
CONECT   26   22   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   21   31   32                                             
CONECT   31   30                                                            
CONECT   32   30   18   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   12   16   36                                             
CONECT   36   35                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   78    0
END

View in JSmol

Synonyms

Value	Source
Methyl (2R)-2-[(1R,2R,6S,7R,11S,13S,14S,15S)-13-hydroxy-6-(hydroxymethyl)-2,6,11,15-tetramethyl-5-oxotetracyclo[8.7.0.0,.0,]heptadec-9-en-14-yl]-6-methylhept-5-enoic acid	Generator

Chemical Formula

C₃₁H₄₈O₅

Average Mass

500.7200 Da

Monoisotopic Mass

500.35017 Da

IUPAC Name

methyl (2R)-2-[(1R,2R,6S,7R,11S,13S,14S,15S)-13-hydroxy-6-(hydroxymethyl)-2,6,11,15-tetramethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-14-yl]-6-methylhept-5-enoate

Traditional Name

methyl (2R)-2-[(1R,2R,6S,7R,11S,13S,14S,15S)-13-hydroxy-6-(hydroxymethyl)-2,6,11,15-tetramethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-14-yl]-6-methylhept-5-enoate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@H](CCC=C(C)C)[C@@H]1[C@@H](O)C[C@]2(C)C3=CC[C@H]4[C@@](C)(CO)C(=O)CC[C@]4(C)[C@H]3CC[C@@]12C

InChI Identifier

InChI=1S/C31H48O5/c1-19(2)9-8-10-20(27(35)36-7)26-23(33)17-31(6)22-11-12-24-28(3,21(22)13-16-30(26,31)5)15-14-25(34)29(24,4)18-32/h9,11,20-21,23-24,26,32-33H,8,10,12-18H2,1-7H3/t20-,21+,23+,24-,26-,28-,29-,30+,31-/m1/s1

InChI Key

FFLSZDBIGTWQDR-SLPXCYNGSA-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

Species Name	Source	Reference
Melia azedarach	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Cholesterol-skeleton
Cholestane-skeleton
Hydroxy bile acid, alcohol, or derivatives
Monohydroxy bile acid, alcohol, or derivatives
Bile acid, alcohol, or derivatives
3-oxo-delta-7-steroid
3-oxosteroid
Hydroxysteroid
Oxosteroid
16-beta-hydroxysteroid
16-hydroxysteroid
3-oxo-5-alpha-steroid
Steroid
Delta-7-steroid
Methyl ester
Cyclic alcohol
Ketone
Carboxylic acid ester
Secondary alcohol
Cyclic ketone
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Alcohol
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Organic oxide
Primary alcohol
Organic oxygen compound
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	4.81	ChemAxon
pKa (Strongest Acidic)	14.61	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	143.82 m³·mol⁻¹	ChemAxon
Polarizability	59.14 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

46210319

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (2r)-2-[(1s,2s,3as,5ar,6s,9ar,9br,11as)-2-hydroxy-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-7-oxo-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-6-methylhept-5-enoate (NP0219462)

MOL for NP0219462 (methyl (2r)-2-[(1s,2s,3as,5ar,6s,9ar,9br,11as)-2-hydroxy-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-7-oxo-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-6-methylhept-5-enoate)

3D MOL for NP0219462 (methyl (2r)-2-[(1s,2s,3as,5ar,6s,9ar,9br,11as)-2-hydroxy-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-7-oxo-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-6-methylhept-5-enoate)

3D SDF for NP0219462 (methyl (2r)-2-[(1s,2s,3as,5ar,6s,9ar,9br,11as)-2-hydroxy-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-7-oxo-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-6-methylhept-5-enoate)

3D-SDF for NP0219462 (methyl (2r)-2-[(1s,2s,3as,5ar,6s,9ar,9br,11as)-2-hydroxy-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-7-oxo-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-6-methylhept-5-enoate)

PDB for NP0219462 (methyl (2r)-2-[(1s,2s,3as,5ar,6s,9ar,9br,11as)-2-hydroxy-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-7-oxo-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-6-methylhept-5-enoate)

3D PDB for NP0219462 (methyl (2r)-2-[(1s,2s,3as,5ar,6s,9ar,9br,11as)-2-hydroxy-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-7-oxo-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-6-methylhept-5-enoate)

SMILES for NP0219462 (methyl (2r)-2-[(1s,2s,3as,5ar,6s,9ar,9br,11as)-2-hydroxy-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-7-oxo-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-6-methylhept-5-enoate)

INCHI for NP0219462 (methyl (2r)-2-[(1s,2s,3as,5ar,6s,9ar,9br,11as)-2-hydroxy-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-7-oxo-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-6-methylhept-5-enoate)

Structure for NP0219462 (methyl (2r)-2-[(1s,2s,3as,5ar,6s,9ar,9br,11as)-2-hydroxy-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-7-oxo-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-6-methylhept-5-enoate)

3D Structure for NP0219462 (methyl (2r)-2-[(1s,2s,3as,5ar,6s,9ar,9br,11as)-2-hydroxy-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-7-oxo-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-6-methylhept-5-enoate)