NP-MRD: Showing NP-Card for Ceanothetric acid (NP0077553)

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Record Information

Version

2.0

Created at

2022-04-28 22:41:04 UTC

Updated at

2022-04-28 22:41:04 UTC

NP-MRD ID

NP0077553

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Ceanothetric acid

Description

(1S,2R,5R,7S,8R,9R,10R,13R,14S,15R,18S)-7-hydroxy-2,6,6,9-tetramethyl-15-(prop-1-en-2-yl)pentacyclo[11.7.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁸]Icosane-1,8,18-tricarboxylic acid belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Ceanothetric acid is found in Hovenia trichocarea and Hovenia trichocarpa. Based on a literature review very few articles have been published on (1S,2R,5R,7S,8R,9R,10R,13R,14S,15R,18S)-7-hydroxy-2,6,6,9-tetramethyl-15-(prop-1-en-2-yl)pentacyclo[11.7.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁸]Icosane-1,8,18-tricarboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292200412D          

 37 41  0  0  1  0            999 V2000
    2.0088   -2.3851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5963   -3.0996    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0088   -3.8141    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8338   -3.8141    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2463   -3.0996    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8338   -2.3851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0713   -3.0996    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4838   -3.8141    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0713   -4.5285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2463   -4.5285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2908   -3.6425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3770   -2.8220    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6233   -2.4865    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4518   -1.6795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0649   -1.1275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6672   -1.4246    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.5539   -4.4244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0959   -3.8225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7357   -2.3459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3588   -3.8141    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7713   -3.0996    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -0.4482   -3.6425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3908   -1.6795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1754   -1.4246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2223   -1.1275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1261   -4.4815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2094   -5.2352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9466   -4.3953    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.0887   -5.0135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  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  6  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 12 17  1  6  0  0  0
 11 18  1  0  0  0  0
 11 19  1  0  0  0  0
  7 20  1  6  0  0  0
  4 21  1  6  0  0  0
  3 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 25 24  1  1  0  0  0
  2 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
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 26 29  1  1  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 24 32  1  6  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
  3 35  1  1  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
M  END

     RDKit          3D

 81 85  0  0  0  0  0  0  0  0999 V2000
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   -2.4980    2.2190    1.5928 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.3431    2.1252    0.0059 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0072    3.1392    0.7186 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.2438   -1.2046    1.6949 C   0  0  0  0  0  0  0  0  0  0  0  0
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 16 53  1  0
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M  END


  Mrv1652304292200412D          

 37 41  0  0  1  0            999 V2000
    2.0088   -2.3851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5963   -3.0996    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    3.2463   -3.0996    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -0.4482   -3.6425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3908   -1.6795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1754   -1.4246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2223   -1.1275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1261   -4.4815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2094   -5.2352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9466   -4.3953    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4213   -4.5285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0088   -5.2430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0887   -5.0135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  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  6  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 12 17  1  6  0  0  0
 11 18  1  0  0  0  0
 11 19  1  0  0  0  0
  7 20  1  6  0  0  0
  4 21  1  6  0  0  0
  3 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 25 24  1  1  0  0  0
  2 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 24 28  1  0  0  0  0
 26 29  1  1  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 24 32  1  6  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
  3 35  1  1  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0077553

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=C)[C@@H]1CC[C@@]2(CC[C@@]3([C@H](CC[C@@H]4[C@@]5(C)[C@H]([C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)C(O)=O)[C@H]12)C(O)=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H44O7/c1-15(2)16-9-12-29(24(34)35)13-14-30(25(36)37)17(20(16)29)7-8-19-27(30,5)11-10-18-26(3,4)22(31)21(23(32)33)28(18,19)6/h16-22,31H,1,7-14H2,2-6H3,(H,32,33)(H,34,35)(H,36,37)/t16-,17+,18-,19-,20-,21+,22-,27+,28-,29-,30+/m0/s1

> <INCHI_KEY>
BAXRQVCGTADURA-SGXUKMBQSA-N

> <FORMULA>
C30H44O7

> <MOLECULAR_WEIGHT>
516.675

> <EXACT_MASS>
516.308703757

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
55.65544677483054

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,5R,7S,8R,9R,10R,13R,14S,15R,18S)-7-hydroxy-2,6,6,9-tetramethyl-15-(prop-1-en-2-yl)pentacyclo[11.7.0.0^{2,10}.0^{5,9}.0^{14,18}]icosane-1,8,18-tricarboxylic acid

> <ALOGPS_LOGP>
2.66

> <JCHEM_LOGP>
4.765514987333334

> <ALOGPS_LOGS>
-4.44

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-3

> <JCHEM_PKA>
4.425151907125129

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.9119886995464306

> <JCHEM_PKA_STRONGEST_BASIC>
-3.14193522434065

> <JCHEM_POLAR_SURFACE_AREA>
132.13

> <JCHEM_REFRACTIVITY>
135.8276

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.89e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,5R,7S,8R,9R,10R,13R,14S,15R,18S)-7-hydroxy-2,6,6,9-tetramethyl-15-(prop-1-en-2-yl)pentacyclo[11.7.0.0^{2,10}.0^{5,9}.0^{14,18}]icosane-1,8,18-tricarboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       3.750  -4.452   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.980  -5.786   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.750  -7.120   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.290  -7.120   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.060  -5.786   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.290  -4.452   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.600  -5.786   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.370  -7.120   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.600  -8.453   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.060  -8.453   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.876  -6.799   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.037  -5.268   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.630  -4.641   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.310  -3.135   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       9.454  -2.105   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       6.845  -2.659   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      11.371  -4.498   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      10.367  -8.259   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.379  -7.135   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.973  -4.379   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.451  -8.651   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.980  -8.453   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.440  -8.453   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.670  -7.120   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.440  -5.786   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.409  -4.641   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.998  -5.268   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.837  -6.799   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.729  -3.135   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.194  -2.659   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -0.415  -2.105   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -0.235  -8.365   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       0.391  -9.772   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      -1.767  -8.204   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       4.520  -8.453   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       3.750  -9.787   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       5.766  -9.358   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   25                                                  
CONECT    3    2    4   22   35                                             
CONECT    4    3    5   10   21                                             
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8   13   20                                             
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9    4                                                       
CONECT   11    8   12   18   19                                             
CONECT   12   11   13   17                                                  
CONECT   13   12    7   14                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   12                                                            
CONECT   18   11                                                            
CONECT   19   11                                                            
CONECT   20    7                                                            
CONECT   21    4                                                            
CONECT   22    3   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   28   32                                             
CONECT   25   24    2   26                                                  
CONECT   26   25   27   29                                                  
CONECT   27   26   28                                                       
CONECT   28   27   24                                                       
CONECT   29   26   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   24   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35    3   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   82    0
END

View in JSmol

Synonyms

Value	Source
(1S,2R,5R,7S,8R,9R,10R,13R,14S,15R,18S)-7-Hydroxy-2,6,6,9-tetramethyl-15-(prop-1-en-2-yl)pentacyclo[11.7.0.0,.0,.0,]icosane-1,8,18-tricarboxylate	Generator

Chemical Formula

C₃₀H₄₄O₇

Average Mass

516.6750 Da

Monoisotopic Mass

516.30870 Da

IUPAC Name

(1S,2R,5R,7S,8R,9R,10R,13R,14S,15R,18S)-7-hydroxy-2,6,6,9-tetramethyl-15-(prop-1-en-2-yl)pentacyclo[11.7.0.0^{2,10}.0^{5,9}.0^{14,18}]icosane-1,8,18-tricarboxylic acid

Traditional Name

(1S,2R,5R,7S,8R,9R,10R,13R,14S,15R,18S)-7-hydroxy-2,6,6,9-tetramethyl-15-(prop-1-en-2-yl)pentacyclo[11.7.0.0^{2,10}.0^{5,9}.0^{14,18}]icosane-1,8,18-tricarboxylic acid

CAS Registry Number

Not Available

SMILES

CC(=C)[C@@H]1CC[C@@]2(CC[C@@]3([C@H](CC[C@@H]4[C@@]5(C)[C@H]([C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)C(O)=O)[C@H]12)C(O)=O)C(O)=O

InChI Identifier

InChI=1S/C30H44O7/c1-15(2)16-9-12-29(24(34)35)13-14-30(25(36)37)17(20(16)29)7-8-19-27(30,5)11-10-18-26(3,4)22(31)21(23(32)33)28(18,19)6/h16-22,31H,1,7-14H2,2-6H3,(H,32,33)(H,34,35)(H,36,37)/t16-,17+,18-,19-,20-,21+,22-,27+,28-,29-,30+/m0/s1

InChI Key

BAXRQVCGTADURA-SGXUKMBQSA-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
Hovenia trichocarea	Plant	KNApSAcK
Hovenia trichocarpa	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
19-oxosteroid
3-carboxy steroid
Steroid acid
19-hydroxysteroid
18-hydroxysteroid
18-oxosteroid
16-hydroxysteroid
16-beta-hydroxysteroid
Oxosteroid
Hydroxysteroid
Steroid
Tricarboxylic acid or derivatives
Beta-hydroxy acid
Hydroxy acid
Cyclic alcohol
Secondary alcohol
Carboxylic acid
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	2.66	ALOGPS
logP	4.77	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	3.91	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	-3	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	132.13 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	135.83 m³·mol⁻¹	ChemAxon
Polarizability	55.66 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	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

163072265

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Ceanothetric acid (NP0077553)

MOL for NP0077553 (Ceanothetric acid)

3D MOL for NP0077553 (Ceanothetric acid)

3D SDF for NP0077553 (Ceanothetric acid)

3D-SDF for NP0077553 (Ceanothetric acid)

PDB for NP0077553 (Ceanothetric acid)

3D PDB for NP0077553 (Ceanothetric acid)

SMILES for NP0077553 (Ceanothetric acid)

INCHI for NP0077553 (Ceanothetric acid)

Structure for NP0077553 (Ceanothetric acid)

3D Structure for NP0077553 (Ceanothetric acid)