NP-MRD: Showing NP-Card for Royleanonic acid (NP0074295)

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Record Information

Version

2.0

Created at

2022-04-28 19:27:15 UTC

Updated at

2022-04-28 19:27:15 UTC

NP-MRD ID

NP0074295

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Royleanonic acid

Description

(4AR,10aS)-6-hydroxy-1,1-dimethyl-5,8-dioxo-7-(propan-2-yl)-1,2,3,4,4a,5,8,9,10,10a-decahydrophenanthrene-4a-carboxylic acid belongs to the class of organic compounds known as 19-oxosteroids. These are steroid derivatives carrying a C=O group at the 19-position of the steroid skeleton. Royleanonic acid is found in Rosmarinus officinalis L. and Salvia rosmarinus. Based on a literature review very few articles have been published on (4aR,10aS)-6-hydroxy-1,1-dimethyl-5,8-dioxo-7-(propan-2-yl)-1,2,3,4,4a,5,8,9,10,10a-decahydrophenanthrene-4a-carboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 53  0  0  0  0  0  0  0  0999 V2000
    5.2952   -0.0710   -0.8948 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6467    0.5274    0.3411 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8223    2.0286    0.4010 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2106    0.1411    0.3910 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7556   -0.6253    1.3630 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6648   -1.0562    2.3342 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3328   -1.0100    1.4152 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0313   -1.7402    2.3899 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4137   -0.5505    0.3979 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8220    0.2077   -0.5769 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0009    0.7611   -1.6786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4585    0.7027   -1.4193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7636    0.3068    0.0407 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2124    0.3923    0.2365 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5788    1.8647    0.4986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9948    0.0534   -1.0275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7894   -0.3988    1.3643 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9905   -1.6342    1.6888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5079   -1.3784    1.7752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0376   -0.9400    0.4353 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1598   -2.0552   -0.5187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4466   -3.1909   -0.0749 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9843   -1.9764   -1.8891 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2487    0.5786   -0.6081 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7060    1.3196   -1.5410 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5249   -0.1640   -1.6770 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7268   -1.0841   -0.6624 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1471    0.5779   -1.1785 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1622    0.1036    1.2083 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9114    2.5737    0.0707 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6767    2.3147   -0.2456 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0562    2.3933    1.4225 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9407   -0.4182    3.0914 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2883    0.3078   -2.6429 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3177    1.8421   -1.7761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9091    1.7371   -1.5019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9981    0.0977   -2.1446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2542    1.1358    0.6280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9006    2.1961    1.3201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4805    2.4680   -0.4126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6109    1.8735    0.9176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9574    0.8868   -1.7657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7334   -0.9180   -1.4440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0736    0.0072   -0.7046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8216   -0.7430    1.1428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8606    0.1845    2.3061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2946   -2.4439    1.0222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2866   -1.9978    2.7226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3717   -0.6005    2.5662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0746   -2.3587    2.0974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1488   -2.2288   -2.3764 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  5  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  1
 14 16  1  0
 14 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  6
 21 23  1  0
 21 22  2  0
 10 24  1  0
 24 25  2  0
 24  4  1  0
 20  9  1  0
 20 13  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  1
  3 30  1  0
  3 31  1  0
  3 32  1  0
  6 33  1  0
 11 34  1  0
 11 35  1  0
 12 36  1  0
 12 37  1  0
 13 38  1  1
 15 39  1  0
 15 40  1  0
 15 41  1  0
 16 42  1  0
 16 43  1  0
 16 44  1  0
 17 45  1  0
 17 46  1  0
 18 47  1  0
 18 48  1  0
 19 49  1  0
 19 50  1  0
 23 51  1  0
M  END


  Mrv1652304282221272D          

 25 27  0  0  1  0            999 V2000
    3.6730    1.1749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0972    0.4673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6965   -0.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8716   -0.2674    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4474    0.4402    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8482    1.1614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6225    0.4267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2218   -0.2944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6460   -1.0020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4708   -0.9885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3969   -0.3080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0038   -1.0291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0272    0.3997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3735    1.1208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9469    1.3777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5991    1.8555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0507    1.8284    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8521    0.3861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2529   -0.3350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2763    1.0937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0233    1.1478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1984    1.1343    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4240    1.8690    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4032   -0.6795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7388   -1.0778    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  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
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  6  0  0  0
  8 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  2  0  0  0  0
 14 17  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
  5 21  1  6  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
  3 24  1  0  0  0  0
  3 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0074295

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1=C(O)C(=O)C2=C(CC[C@H]3C(C)(C)CCC[C@]23C(O)=O)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H26O5/c1-10(2)13-15(21)11-6-7-12-19(3,4)8-5-9-20(12,18(24)25)14(11)17(23)16(13)22/h10,12,22H,5-9H2,1-4H3,(H,24,25)/t12-,20+/m0/s1

> <INCHI_KEY>
TWZMQZBMHUHORI-FKIZINRSSA-N

> <FORMULA>
C20H26O5

> <MOLECULAR_WEIGHT>
346.423

> <EXACT_MASS>
346.178023937

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
37.23078911039252

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4aR,10aS)-6-hydroxy-1,1-dimethyl-5,8-dioxo-7-(propan-2-yl)-1,2,3,4,4a,5,8,9,10,10a-decahydrophenanthrene-4a-carboxylic acid

> <ALOGPS_LOGP>
2.90

> <JCHEM_LOGP>
3.927362342

> <ALOGPS_LOGS>
-3.62

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.051239686721633

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.294608712292425

> <JCHEM_PKA_STRONGEST_BASIC>
-5.116787124118958

> <JCHEM_POLAR_SURFACE_AREA>
91.67

> <JCHEM_REFRACTIVITY>
94.32989999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.25e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4aR,10aS)-6-hydroxy-7-isopropyl-1,1-dimethyl-5,8-dioxo-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid

> <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       6.856   2.193   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.648   0.872   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.900  -0.474   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.360  -0.499   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.569   0.822   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.317   2.168   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.029   0.797   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.281  -0.550   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.072  -1.870   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.612  -1.845   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.741  -0.575   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.007  -1.921   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.051   0.746   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.697   2.092   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.767   2.572   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.985   3.464   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -0.095   3.413   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -1.591   0.721   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.339  -0.625   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.382   2.042   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.777   2.143   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.237   2.117   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       4.525   3.489   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.219  -1.268   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.979  -2.012   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   24   25                                             
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7   21                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   15                                                  
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9    4                                                       
CONECT   11    8   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   18                                                  
CONECT   14   13   15   17                                                  
CONECT   15   14    7   16                                                  
CONECT   16   15                                                            
CONECT   17   14                                                            
CONECT   18   13   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21    5   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24    3                                                            
CONECT   25    3                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   54    0
END

View in JSmol

Synonyms

Value	Source
(4AR,10as)-6-hydroxy-1,1-dimethyl-5,8-dioxo-7-(propan-2-yl)-1,2,3,4,4a,5,8,9,10,10a-decahydrophenanthrene-4a-carboxylate	Generator

Chemical Formula

C₂₀H₂₆O₅

Average Mass

346.4230 Da

Monoisotopic Mass

346.17802 Da

IUPAC Name

(4aR,10aS)-6-hydroxy-1,1-dimethyl-5,8-dioxo-7-(propan-2-yl)-1,2,3,4,4a,5,8,9,10,10a-decahydrophenanthrene-4a-carboxylic acid

Traditional Name

(4aR,10aS)-6-hydroxy-7-isopropyl-1,1-dimethyl-5,8-dioxo-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC(C)C1=C(O)C(=O)C2=C(CC[C@H]3C(C)(C)CCC[C@]23C(O)=O)C1=O

InChI Identifier

InChI=1S/C20H26O5/c1-10(2)13-15(21)11-6-7-12-19(3,4)8-5-9-20(12,18(24)25)14(11)17(23)16(13)22/h10,12,22H,5-9H2,1-4H3,(H,24,25)/t12-,20+/m0/s1

InChI Key

TWZMQZBMHUHORI-FKIZINRSSA-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
Rosmarinus officinalis L.	Plant	KNApSAcK
Salvia rosmarinus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 19-oxosteroids. These are steroid derivatives carrying a C=O group at the 19-position of the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Oxosteroids

Direct Parent

19-oxosteroids

Alternative Parents

Substituents

Abietane diterpenoid
Diterpenoid
19-oxosteroid
Phenanthrene
Hydrophenanthrene
Vinylogous acid
Ketone
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Enol
Carboxylic acid
Organooxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
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	2.9	ALOGPS
logP	3.93	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	4.29	ChemAxon
pKa (Strongest Basic)	-5.1	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	91.67 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	94.33 m³·mol⁻¹	ChemAxon
Polarizability	37.23 Å³	ChemAxon
Number of Rings	3	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

34983777

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Royleanonic acid (NP0074295)

MOL for NP0074295 (Royleanonic acid)

3D MOL for NP0074295 (Royleanonic acid)

3D SDF for NP0074295 (Royleanonic acid)

3D-SDF for NP0074295 (Royleanonic acid)

PDB for NP0074295 (Royleanonic acid)

3D PDB for NP0074295 (Royleanonic acid)

SMILES for NP0074295 (Royleanonic acid)

INCHI for NP0074295 (Royleanonic acid)

Structure for NP0074295 (Royleanonic acid)

3D Structure for NP0074295 (Royleanonic acid)