NP-MRD: Showing NP-Card for Rubianol e (NP0071763)

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Record Information

Version

2.0

Created at

2022-04-28 17:06:23 UTC

Updated at

2022-04-28 17:06:23 UTC

NP-MRD ID

NP0071763

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Rubianol e

Description

[(1S,2S,5R,6S,8R,9R,10R,14S,16R,17R,19S,21S)-16-(acetyloxy)-8,17,21-trihydroxy-2,10,14,18,18-pentamethyl-6-(propan-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicos-12-en-5-yl]methyl acetate belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Rubianol e is found in Rubia yunnanensis. Based on a literature review very few articles have been published on [(1S,2S,5R,6S,8R,9R,10R,14S,16R,17R,19S,21S)-16-(acetyloxy)-8,17,21-trihydroxy-2,10,14,18,18-pentamethyl-6-(propan-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicos-12-en-5-yl]methyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282219062D          

 41 45  0  0  1  0            999 V2000
    4.8390    0.3498    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2623    1.0579    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8607    1.7785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0358    1.7911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6125    1.0830    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0141    0.3623    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5908   -0.3458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7659   -0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3643    0.3874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7876    1.0955    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    1.5394    0.4000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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  1  2  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  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
 10  9  1  1  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  1  0  0  0
 13 14  1  0  0  0  0
  9 14  1  0  0  0  0
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 14 26  1  6  0  0  0
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  6 28  1  6  0  0  0
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  2 30  1  0  0  0  0
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  2 37  1  6  0  0  0
 37 38  1  0  0  0  0
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 39 41  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652304282219062D          

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    3.5908   -0.3458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7659   -0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3643    0.3874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7876    1.0955    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3860    1.8162    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5611    1.8287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1378    1.1206    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5394    0.4000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1161   -0.3082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2912   -0.2956    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1104    0.4250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3129    1.1332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3800    1.5809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2966    1.9580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9353    0.4376    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1322   -1.0037    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9571   -0.9912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3804   -1.6993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3587   -0.2705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9410   -0.3207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8093    2.5243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4157   -0.3583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2109    1.8036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0666    0.8741    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1403    0.0524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3816   -0.2717    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1979   -1.0759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6880    1.4167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4687    1.1499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5288    2.2262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7573    1.7179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4333    2.4766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9283    3.1365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7474    3.0378    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6042    3.8952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  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
 10  9  1  1  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  1  0  0  0
 13 14  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 17 21  1  6  0  0  0
 16 22  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 14 26  1  6  0  0  0
 11 27  1  6  0  0  0
  6 28  1  6  0  0  0
  5 29  1  1  0  0  0
  2 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
  1 32  1  0  0  0  0
 32 33  1  1  0  0  0
 30 34  1  6  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
  2 37  1  6  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0071763

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@@H]1C[C@@H](O)[C@H]2[C@@]1(COC(C)=O)CC[C@@]1(C)[C@@H]3[C@@H](O)C[C@@H]4C(C)(C)[C@@H](O)[C@@H](C[C@]4(C)C3=CC[C@]21C)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C34H54O7/c1-18(2)22-14-24(38)28-33(9)11-10-21-27(32(33,8)12-13-34(22,28)17-40-19(3)35)23(37)15-26-30(5,6)29(39)25(41-20(4)36)16-31(21,26)7/h10,18,22-29,37-39H,11-17H2,1-9H3/t22-,23-,24+,25+,26+,27-,28+,29-,31+,32-,33+,34+/m0/s1

> <INCHI_KEY>
OLOLVKCRAVUVOL-ZEFPMHOGSA-N

> <FORMULA>
C34H54O7

> <MOLECULAR_WEIGHT>
574.799

> <EXACT_MASS>
574.386954079

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
95

> <JCHEM_AVERAGE_POLARIZABILITY>
65.55131322119591

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(1S,2S,5R,6S,8R,9R,10R,14S,16R,17R,19S,21S)-16-(acetyloxy)-8,17,21-trihydroxy-2,10,14,18,18-pentamethyl-6-(propan-2-yl)pentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicos-12-en-5-yl]methyl acetate

> <ALOGPS_LOGP>
4.40

> <JCHEM_LOGP>
3.2991592736666644

> <ALOGPS_LOGS>
-5.21

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.928728958114505

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.708389523936315

> <JCHEM_PKA_STRONGEST_BASIC>
-0.4473141681861844

> <JCHEM_POLAR_SURFACE_AREA>
113.29000000000002

> <JCHEM_REFRACTIVITY>
156.60500000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.53e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(1S,2S,5R,6S,8R,9R,10R,14S,16R,17R,19S,21S)-16-(acetyloxy)-8,17,21-trihydroxy-6-isopropyl-2,10,14,18,18-pentamethylpentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicos-12-en-5-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       9.033   0.653   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.823   1.975   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.073   3.320   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.534   3.343   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.743   2.022   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.493   0.676   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.703  -0.645   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.163  -0.622   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.413   0.723   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.204   2.045   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.454   3.390   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.914   3.414   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.124   2.092   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.874   0.747   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.083  -0.575   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.543  -0.552   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.206   0.793   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.584   2.115   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.709   2.951   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.554   3.655   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.746   0.817   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -0.247  -1.874   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -1.787  -1.850   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -2.577  -3.172   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -2.536  -0.505   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.623  -0.599   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.244   4.712   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       8.243  -0.669   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.994   3.367   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      11.324   1.632   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      11.462   0.098   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.046  -0.507   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       9.703  -2.008   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      12.484   2.645   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      13.941   2.146   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      12.187   4.156   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      10.747   3.207   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      10.142   4.623   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      11.066   5.855   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      12.595   5.671   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      10.461   7.271   0.000  0.00  0.00           C+0
CONECT    1    2    6   32                                                  
CONECT    2    1    3   30   37                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   10   29                                             
CONECT    6    5    1    7   28                                             
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9    5   11                                                  
CONECT   11   10   12   27                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13    9   15   26                                             
CONECT   15   14   16                                                       
CONECT   16   15   17   22                                                  
CONECT   17   16   18   21                                                  
CONECT   18   17   13   19   20                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   17                                                            
CONECT   22   16   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   14                                                            
CONECT   27   11                                                            
CONECT   28    6                                                            
CONECT   29    5                                                            
CONECT   30    2   31   34                                                  
CONECT   31   30   32                                                       
CONECT   32   31    1   33                                                  
CONECT   33   32                                                            
CONECT   34   30   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37    2   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   90    0
END

View in JSmol

Synonyms

Value	Source
[(1S,2S,5R,6S,8R,9R,10R,14S,16R,17R,19S,21S)-16-(Acetyloxy)-8,17,21-trihydroxy-2,10,14,18,18-pentamethyl-6-(propan-2-yl)pentacyclo[11.8.0.0,.0,.0,]henicos-12-en-5-yl]methyl acetic acid	Generator

Chemical Formula

C₃₄H₅₄O₇

Average Mass

574.7990 Da

Monoisotopic Mass

574.38695 Da

IUPAC Name

[(1S,2S,5R,6S,8R,9R,10R,14S,16R,17R,19S,21S)-16-(acetyloxy)-8,17,21-trihydroxy-2,10,14,18,18-pentamethyl-6-(propan-2-yl)pentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicos-12-en-5-yl]methyl acetate

Traditional Name

[(1S,2S,5R,6S,8R,9R,10R,14S,16R,17R,19S,21S)-16-(acetyloxy)-8,17,21-trihydroxy-6-isopropyl-2,10,14,18,18-pentamethylpentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicos-12-en-5-yl]methyl acetate

CAS Registry Number

Not Available

SMILES

CC(C)[C@@H]1C[C@@H](O)[C@H]2[C@@]1(COC(C)=O)CC[C@@]1(C)[C@@H]3[C@@H](O)C[C@@H]4C(C)(C)[C@@H](O)[C@@H](C[C@]4(C)C3=CC[C@]21C)OC(C)=O

InChI Identifier

InChI=1S/C34H54O7/c1-18(2)22-14-24(38)28-33(9)11-10-21-27(32(33,8)12-13-34(22,28)17-40-19(3)35)23(37)15-26-30(5,6)29(39)25(41-20(4)36)16-31(21,26)7/h10,18,22-29,37-39H,11-17H2,1-9H3/t22-,23-,24+,25+,26+,27-,28+,29-,31+,32-,33+,34+/m0/s1

InChI Key

OLOLVKCRAVUVOL-ZEFPMHOGSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Rubia yunnanensis	Plant	KNApSAcK

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
Steroid ester
1-hydroxysteroid
Hydroxysteroid
15-hydroxysteroid
Steroid
Delta-5-steroid
Dicarboxylic acid or derivatives
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Polyol
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	4.4	ALOGPS
logP	3.3	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	13.71	ChemAxon
pKa (Strongest Basic)	-0.45	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	156.6 m³·mol⁻¹	ChemAxon
Polarizability	65.55 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

163007426

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Rubianol e (NP0071763)

MOL for NP0071763 (Rubianol e)

3D MOL for NP0071763 (Rubianol e)

3D SDF for NP0071763 (Rubianol e)

3D-SDF for NP0071763 (Rubianol e)

PDB for NP0071763 (Rubianol e)

3D PDB for NP0071763 (Rubianol e)

SMILES for NP0071763 (Rubianol e)

INCHI for NP0071763 (Rubianol e)

Structure for NP0071763 (Rubianol e)

3D Structure for NP0071763 (Rubianol e)