NP-MRD: Showing NP-Card for (1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15r)-2,4-bis(acetyloxy)-8,16-dihydroxy-5,9,12,12-tetramethyl-7-{[(2e)-2-methylbut-2-enoyl]oxy}-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-15-yl (2e)-2-methylbut-2-enoate (NP0259052)

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Record Information

Version

2.0

Created at

2022-09-08 00:47:20 UTC

Updated at

2022-09-08 00:47:20 UTC

NP-MRD ID

NP0259052

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15r)-2,4-bis(acetyloxy)-8,16-dihydroxy-5,9,12,12-tetramethyl-7-{[(2e)-2-methylbut-2-enoyl]oxy}-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-15-yl (2e)-2-methylbut-2-enoate

Description

Euphoppin B belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups. (1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15r)-2,4-bis(acetyloxy)-8,16-dihydroxy-5,9,12,12-tetramethyl-7-{[(2e)-2-methylbut-2-enoyl]oxy}-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-15-yl (2e)-2-methylbut-2-enoate is found in Euphorbia aleppica. Based on a literature review very few articles have been published on Euphoppin B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082202472D          

 45 49  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309082202472D          

 45 49  0  0  1  0            999 V2000
    1.3217   -6.5261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0961   -5.7325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4450   -4.3468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6449   -4.1454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0194   -3.7547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7938   -2.9611    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9938   -2.7597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7682   -1.9661    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3426   -1.3740    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1427   -1.5754    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3597   -0.5721    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0197    0.1796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7953   -1.1738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8217   -1.9984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0990   -2.3965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3683   -2.3690    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2480   -2.5364    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5033   -3.3209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9515   -3.9343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2069   -4.7188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1311   -4.0209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8124   -1.9347    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6047   -2.1644    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8846   -2.9405    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6967   -3.0861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2288   -2.4557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9766   -3.8622    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0681   -1.4818    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8926   -1.4554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5620   -0.8302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7860   -1.1101    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9528   -0.3022    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7359   -0.0427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3522   -0.5911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9028    0.7653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2865    1.3138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6859    1.0248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8527    1.8327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1842   -0.5457    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4754    0.2262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5426   -1.1726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3870   -0.3624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2719   -1.0417    0.0000 C   0  0  0  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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
 10  9  1  6  0  0  0
 11 10  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 18 16  1  1  0  0  0
 18  8  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 25 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  0  0  0  0
 33 32  1  0  0  0  0
 33 24  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  2  0  0  0  0
 39 40  1  0  0  0  0
 41 33  1  0  0  0  0
 13 41  1  0  0  0  0
 41 42  1  1  0  0  0
 11 43  1  6  0  0  0
 10 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0259052

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(/C)C(=O)O[C@@H]1C[C@H]2[C@@H]([C@H]3[C@@]4(C)OC(O)[C@@]13[C@H](OC(C)=O)[C@H]1[C@@H](OC(C)=O)[C@@H](C)C[C@]1(OC(=O)C(\C)=C\C)[C@@H]4O)C2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C34H48O11/c1-11-15(3)27(37)43-21-13-20-22(31(20,8)9)25-32(10)29(39)33(44-28(38)16(4)12-2)14-17(5)24(41-18(6)35)23(33)26(42-19(7)36)34(21,25)30(40)45-32/h11-12,17,20-26,29-30,39-40H,13-14H2,1-10H3/b15-11+,16-12+/t17-,20-,21+,22-,23+,24-,25-,26+,29+,30?,32+,33+,34-/m0/s1

> <INCHI_KEY>
RCPSEGYLRQOTBU-MDCFLRISSA-N

> <FORMULA>
C34H48O11

> <MOLECULAR_WEIGHT>
632.747

> <EXACT_MASS>
632.319662366

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
93

> <JCHEM_AVERAGE_POLARIZABILITY>
66.7477119766325

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,3R,4S,5S,7R,8R,9R,10R,11S,13S,15R)-2,4-bis(acetyloxy)-8,16-dihydroxy-5,9,12,12-tetramethyl-7-{[(2E)-2-methylbut-2-enoyl]oxy}-17-oxapentacyclo[7.6.2.0^{1,10}.0^{3,7}.0^{11,13}]heptadecan-15-yl (2E)-2-methylbut-2-enoate

> <JCHEM_LOGP>
3.8347396879999995

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.914882312509683

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.736680874147028

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7287486951264563

> <JCHEM_POLAR_SURFACE_AREA>
154.89000000000001

> <JCHEM_REFRACTIVITY>
159.65170000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,3R,4S,5S,7R,8R,9R,10R,11S,13S,15R)-2,4-bis(acetyloxy)-8,16-dihydroxy-5,9,12,12-tetramethyl-7-{[(2E)-2-methylbut-2-enoyl]oxy}-17-oxapentacyclo[7.6.2.0^{1,10}.0^{3,7}.0^{11,13}]heptadecan-15-yl (2E)-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       2.467 -12.182   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.046 -10.701   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.118  -9.595   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.612  -9.971   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.697  -8.114   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.204  -7.738   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       3.770  -7.009   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       3.348  -5.527   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.855  -5.151   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.434  -3.670   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.506  -2.565   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.000  -2.941   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.405  -1.068   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.770   0.335   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.351  -2.191   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       3.400  -3.730   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.052  -4.473   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.421  -4.422   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.063  -4.735   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.539  -6.199   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.510  -7.344   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.986  -8.808   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       3.978  -7.506   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       7.116  -3.611   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.596  -4.040   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       9.118  -5.489   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      10.634  -5.761   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.627  -4.584   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      11.156  -7.209   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       9.460  -2.766   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      11.000  -2.717   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.516  -1.550   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.067  -2.072   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       7.379  -0.564   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       8.840  -0.080   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       9.991  -1.103   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       9.152   1.429   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       8.001   2.452   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      10.614   1.913   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      10.925   3.421   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       5.944  -1.019   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       6.487   0.422   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       1.013  -2.189   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       0.722  -0.676   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -0.508  -1.944   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    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   18                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   43                                                  
CONECT   11   10   12   43                                                  
CONECT   12   11   13   18                                                  
CONECT   13   12   14   15   41                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16    8   12   19                                             
CONECT   19   18   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   19   25   33                                                  
CONECT   25   24   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   25   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   24   34   41                                             
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40                                                       
CONECT   40   39                                                            
CONECT   41   33   13   42                                                  
CONECT   42   41                                                            
CONECT   43   11   10   44   45                                             
CONECT   44   43                                                            
CONECT   45   43                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   98    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₄₈O₁₁

Average Mass

632.7470 Da

Monoisotopic Mass

632.31966 Da

IUPAC Name

(1R,2R,3R,4S,5S,7R,8R,9R,10R,11S,13S,15R)-2,4-bis(acetyloxy)-8,16-dihydroxy-5,9,12,12-tetramethyl-7-{[(2E)-2-methylbut-2-enoyl]oxy}-17-oxapentacyclo[7.6.2.0^{1,10}.0^{3,7}.0^{11,13}]heptadecan-15-yl (2E)-2-methylbut-2-enoate

Traditional Name

CAS Registry Number

Not Available

SMILES

C\C=C(/C)C(=O)O[C@@H]1C[C@H]2[C@@H]([C@H]3[C@@]4(C)OC(O)[C@@]13[C@H](OC(C)=O)[C@H]1[C@@H](OC(C)=O)[C@@H](C)C[C@]1(OC(=O)C(\C)=C\C)[C@@H]4O)C2(C)C

InChI Identifier

InChI=1S/C34H48O11/c1-11-15(3)27(37)43-21-13-20-22(31(20,8)9)25-32(10)29(39)33(44-28(38)16(4)12-2)14-17(5)24(41-18(6)35)23(33)26(42-19(7)36)34(21,25)30(40)45-32/h11-12,17,20-26,29-30,39-40H,13-14H2,1-10H3/b15-11+,16-12+/t17-,20-,21+,22-,23+,24-,25-,26+,29+,30?,32+,33+,34-/m0/s1

InChI Key

RCPSEGYLRQOTBU-MDCFLRISSA-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
Euphorbia aleppica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tetracarboxylic acids and derivatives

Direct Parent

Tetracarboxylic acids and derivatives

Alternative Parents

Substituents

Tetracarboxylic acid or derivatives
Monoterpenoid
Carane monoterpenoid
Fatty acid ester
Fatty acyl
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Cyclic alcohol
Secondary alcohol
Hemiacetal
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	3.83	ChemAxon
pKa (Strongest Acidic)	11.74	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	154.89 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	159.65 m³·mol⁻¹	ChemAxon
Polarizability	66.75 Å³	ChemAxon
Number of Rings	5	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

101691209

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15r)-2,4-bis(acetyloxy)-8,16-dihydroxy-5,9,12,12-tetramethyl-7-{[(2e)-2-methylbut-2-enoyl]oxy}-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-15-yl (2e)-2-methylbut-2-enoate (NP0259052)

MOL for NP0259052 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15r)-2,4-bis(acetyloxy)-8,16-dihydroxy-5,9,12,12-tetramethyl-7-{[(2e)-2-methylbut-2-enoyl]oxy}-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-15-yl (2e)-2-methylbut-2-enoate)

3D MOL for NP0259052 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15r)-2,4-bis(acetyloxy)-8,16-dihydroxy-5,9,12,12-tetramethyl-7-{[(2e)-2-methylbut-2-enoyl]oxy}-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-15-yl (2e)-2-methylbut-2-enoate)

3D SDF for NP0259052 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15r)-2,4-bis(acetyloxy)-8,16-dihydroxy-5,9,12,12-tetramethyl-7-{[(2e)-2-methylbut-2-enoyl]oxy}-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-15-yl (2e)-2-methylbut-2-enoate)

3D-SDF for NP0259052 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15r)-2,4-bis(acetyloxy)-8,16-dihydroxy-5,9,12,12-tetramethyl-7-{[(2e)-2-methylbut-2-enoyl]oxy}-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-15-yl (2e)-2-methylbut-2-enoate)

PDB for NP0259052 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15r)-2,4-bis(acetyloxy)-8,16-dihydroxy-5,9,12,12-tetramethyl-7-{[(2e)-2-methylbut-2-enoyl]oxy}-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-15-yl (2e)-2-methylbut-2-enoate)

3D PDB for NP0259052 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15r)-2,4-bis(acetyloxy)-8,16-dihydroxy-5,9,12,12-tetramethyl-7-{[(2e)-2-methylbut-2-enoyl]oxy}-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-15-yl (2e)-2-methylbut-2-enoate)

SMILES for NP0259052 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15r)-2,4-bis(acetyloxy)-8,16-dihydroxy-5,9,12,12-tetramethyl-7-{[(2e)-2-methylbut-2-enoyl]oxy}-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-15-yl (2e)-2-methylbut-2-enoate)

INCHI for NP0259052 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15r)-2,4-bis(acetyloxy)-8,16-dihydroxy-5,9,12,12-tetramethyl-7-{[(2e)-2-methylbut-2-enoyl]oxy}-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-15-yl (2e)-2-methylbut-2-enoate)

Structure for NP0259052 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15r)-2,4-bis(acetyloxy)-8,16-dihydroxy-5,9,12,12-tetramethyl-7-{[(2e)-2-methylbut-2-enoyl]oxy}-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-15-yl (2e)-2-methylbut-2-enoate)

3D Structure for NP0259052 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15r)-2,4-bis(acetyloxy)-8,16-dihydroxy-5,9,12,12-tetramethyl-7-{[(2e)-2-methylbut-2-enoyl]oxy}-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-15-yl (2e)-2-methylbut-2-enoate)