NP-MRD: Showing NP-Card for Euphylonane B (NP0332080)

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Record Information

Version

2.0

Created at

2023-11-02 00:01:32 UTC

Updated at

2024-09-03 04:17:53 UTC

NP-MRD ID

NP0332080

Natural Product DOI

https://doi.org/10.57994/1208

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Euphylonane B

Description

Euphylonane B belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. Based on a literature review very few articles have been published on Euphylonane B.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 11022300012D          

 44 48  0  0  1  0            999 V2000
    4.4526    0.0664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7752    0.5373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1214    1.2862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9776    0.7482    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2475    1.5278    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2204    1.0755    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5790    1.5945    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4923    0.6876    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1577    0.1999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3416   -0.1235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8818   -0.7470    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5545   -1.5043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7062   -0.7134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1938   -0.0480    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8210   -0.5840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6703   -1.3952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2974   -1.9312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0752   -1.6561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7023   -2.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5517   -3.0033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7739   -3.2784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1468   -2.7423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8925   -1.6703    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5638   -0.3986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0633    0.1374    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4823   -0.5733    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3073   -0.5658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8360    0.4266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0873    0.9485    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5398    1.4846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8651    1.2236    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2380    1.7597    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0158    2.0348    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3886    2.5708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5393    3.3819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0878    3.9180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8656    3.6429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0628    4.7291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5643    5.2651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8406    5.0042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3171    3.6570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7936    2.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9442    3.1210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4207    1.7738    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
  4  2  1  0  0  0  0
  4  5  1  1  0  0  0
  6  4  1  0  0  0  0
  6  7  1  6  0  0  0
  8  6  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 11 10  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 14 13  1  0  0  0  0
  4 14  1  0  0  0  0
 14  2  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
 16 23  2  0  0  0  0
 10 24  2  0  0  0  0
 25 24  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 25 28  1  1  0  0  0
 29 25  1  0  0  0  0
 29 30  1  6  0  0  0
 31 29  1  0  0  0  0
 31  8  1  0  0  0  0
 31 32  1  6  0  0  0
 31 33  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 35 41  2  0  0  0  0
 33 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  2  0  0  0  0
  6 44  1  0  0  0  0
M  END


  Mrv2104 11022300012D          

 44 48  0  0  1  0            999 V2000
    4.4526    0.0664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7752    0.5373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1214    1.2862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9776    0.7482    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2475    1.5278    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2204    1.0755    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5790    1.5945    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4923    0.6876    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1577    0.1999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3416   -0.1235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8818   -0.7470    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5545   -1.5043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7062   -0.7134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1938   -0.0480    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8210   -0.5840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6703   -1.3952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2974   -1.9312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0752   -1.6561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7023   -2.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5517   -3.0033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7739   -3.2784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1468   -2.7423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8925   -1.6703    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5638   -0.3986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0633    0.1374    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4823   -0.5733    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3073   -0.5658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8360    0.4266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0873    0.9485    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5398    1.4846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8651    1.2236    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2380    1.7597    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0158    2.0348    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3886    2.5708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5393    3.3819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0878    3.9180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8656    3.6429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0628    4.7291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5643    5.2651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8406    5.0042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3171    3.6570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7936    2.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9442    3.1210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4207    1.7738    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
  4  2  1  0  0  0  0
  4  5  1  1  0  0  0
  6  4  1  0  0  0  0
  6  7  1  6  0  0  0
  8  6  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 11 10  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 14 13  1  0  0  0  0
  4 14  1  0  0  0  0
 14  2  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
 16 23  2  0  0  0  0
 10 24  2  0  0  0  0
 25 24  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 25 28  1  1  0  0  0
 29 25  1  0  0  0  0
 29 30  1  6  0  0  0
 31 29  1  0  0  0  0
 31  8  1  0  0  0  0
 31 32  1  6  0  0  0
 31 33  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 35 41  2  0  0  0  0
 33 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  2  0  0  0  0
  6 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0332080

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@]12[C@]3([H])C=C(C)[C@@H](OC(=O)C(C)C(C)C)[C@]4(O)[C@@H](O)[C@@](C)(OC)C=C([C@H](C)C[C@@]1(OC(=O)C1=CC=CC=C1)C2(C)C)[C@@]34O

> <INCHI_IDENTIFIER>
InChI=1S/C34H46O8/c1-18(2)21(5)27(35)41-26-19(3)15-23-25-30(6,7)32(25,42-28(36)22-13-11-10-12-14-22)16-20(4)24-17-31(8,40-9)29(37)34(26,39)33(23,24)38/h10-15,17-18,20-21,23,25-26,29,37-39H,16H2,1-9H3/t20-,21?,23+,25-,26-,29+,31+,32+,33+,34+/m1/s1

> <INCHI_KEY>
MAIXOIWOLCRTHW-ZNZBANLESA-N

> <FORMULA>
C34H46O8

> <MOLECULAR_WEIGHT>
582.734

> <EXACT_MASS>
582.319268441

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
88

> <JCHEM_AVERAGE_POLARIZABILITY>
64.94204775386305

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,4R,5R,6R,9S,10R,12S,14R,15S)-6-[(2,3-dimethylbutanoyl)oxy]-4,5,15-trihydroxy-3-methoxy-3,7,11,11,14-pentamethyltetracyclo[7.5.1.0^{5,15}.0^{10,12}]pentadeca-1,7-dien-12-yl benzoate

> <JCHEM_LOGP>
4.438258343

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.145240607078877

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.577129790816524

> <JCHEM_PKA_STRONGEST_BASIC>
-3.794942636095008

> <JCHEM_POLAR_SURFACE_AREA>
122.52000000000001

> <JCHEM_REFRACTIVITY>
157.88160000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4R,5R,6R,9S,10R,12S,14R,15S)-6-[(2,3-dimethylbutanoyl)oxy]-4,5,15-trihydroxy-3-methoxy-3,7,11,11,14-pentamethyltetracyclo[7.5.1.0^{5,15}.0^{10,12}]pentadeca-1,7-dien-12-yl benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-NOV-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-NOV-23         0                                  
HETATM    1  C   UNK     0       8.312   0.124   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.047   1.003   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.693   2.401   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.558   1.397   0.000  0.00  0.00           C+0
HETATM    5  H   UNK     0       6.062   2.852   0.000  0.00  0.00           H+0
HETATM    6  C   UNK     0       4.145   2.008   0.000  0.00  0.00           C+0
HETATM    7  H   UNK     0       2.948   2.976   0.000  0.00  0.00           H+0
HETATM    8  C   UNK     0       2.786   1.284   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.028   0.373   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.504  -0.231   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.513  -1.394   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.902  -2.808   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.051  -1.332   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.962  -0.090   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       7.132  -1.090   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.851  -2.604   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.022  -3.605   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.474  -3.091   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.644  -4.092   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.363  -5.606   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.911  -6.120   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.741  -5.119   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.399  -3.118   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.052  -0.744   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.118   0.256   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -0.900  -1.070   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -2.440  -1.056   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.560   0.796   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.163   1.771   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -1.008   2.771   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       1.615   2.284   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       0.444   3.285   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       1.896   3.798   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       0.725   4.799   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       1.007   6.313   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -0.164   7.314   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -1.616   6.800   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       0.117   8.828   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -1.053   9.828   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       1.569   9.341   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       2.459   6.826   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       3.348   4.312   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       3.629   5.826   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       4.519   3.311   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4   14                                             
CONECT    3    2                                                            
CONECT    4    2    5    6   14                                             
CONECT    5    4                                                            
CONECT    6    4    7    8   44                                             
CONECT    7    6                                                            
CONECT    8    6    9   10   31                                             
CONECT    9    8                                                            
CONECT   10    8   11   24                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13    4    2   15                                             
CONECT   15   14   16                                                       
CONECT   16   15   17   23                                                  
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17                                                       
CONECT   23   16                                                            
CONECT   24   10   25                                                       
CONECT   25   24   26   28   29                                             
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   25                                                            
CONECT   29   25   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29    8   32   33                                             
CONECT   32   31                                                            
CONECT   33   31   34   42                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   41                                                  
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41   35                                                            
CONECT   42   33   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42    6                                                       
MASTER        0    0    0    0    0    0    0    0   44    0   96    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₄₆O₈

Average Mass

582.7340 Da

Monoisotopic Mass

582.31927 Da

IUPAC Name

(3S,4R,5R,6R,9S,10R,12S,14R,15S)-6-[(2,3-dimethylbutanoyl)oxy]-4,5,15-trihydroxy-3-methoxy-3,7,11,11,14-pentamethyltetracyclo[7.5.1.0^{5,15}.0^{10,12}]pentadeca-1,7-dien-12-yl benzoate

Traditional Name

(3S,4R,5R,6R,9S,10R,12S,14R,15S)-6-[(2,3-dimethylbutanoyl)oxy]-4,5,15-trihydroxy-3-methoxy-3,7,11,11,14-pentamethyltetracyclo[7.5.1.0^{5,15}.0^{10,12}]pentadeca-1,7-dien-12-yl benzoate

CAS Registry Number

Not Available

SMILES

[H][C@]12[C@]3([H])C=C(C)[C@@H](OC(=O)C(C)C(C)C)[C@]4(O)[C@@H](O)[C@@](C)(OC)C=C([C@H](C)C[C@@]1(OC(=O)C1=CC=CC=C1)C2(C)C)[C@@]34O

InChI Identifier

InChI=1S/C34H46O8/c1-18(2)21(5)27(35)41-26-19(3)15-23-25-30(6,7)32(25,42-28(36)22-13-11-10-12-14-22)16-20(4)24-17-31(8,40-9)29(37)34(26,39)33(23,24)38/h10-15,17-18,20-21,23,25-26,29,37-39H,16H2,1-9H3/t20-,21?,23+,25-,26-,29+,31+,32+,33+,34+/m1/s1

InChI Key

MAIXOIWOLCRTHW-ZNZBANLESA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Fatty alcohol ester
Benzoate ester
Benzoic acid or derivatives
Benzoyl
Fatty acid ester
Fatty acyl
Benzenoid
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Ether
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aromatic homopolycyclic compound

Molecular Framework

Aromatic 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	4.44	ChemAxon
pKa (Strongest Acidic)	11.58	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	122.52 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	157.88 m³·mol⁻¹	ChemAxon
Polarizability	64.94 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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Euphylonane B (NP0332080)

MOL for NP0332080 (Euphylonane B)

3D MOL for NP0332080 (Euphylonane B)

3D SDF for NP0332080 (Euphylonane B)

3D-SDF for NP0332080 (Euphylonane B)

PDB for NP0332080 (Euphylonane B)

3D PDB for NP0332080 (Euphylonane B)

SMILES for NP0332080 (Euphylonane B)

INCHI for NP0332080 (Euphylonane B)

Structure for NP0332080 (Euphylonane B)

3D Structure for NP0332080 (Euphylonane B)