NP-MRD: Showing NP-Card for ethyl (8e,17e,19e)-18-bromotricosa-8,17,19-trien-4,6-diynoate (NP0307297)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-11 00:19:43 UTC

Updated at

2022-09-11 00:19:44 UTC

NP-MRD ID

NP0307297

Secondary Accession Numbers

None

Natural Product Identification

Common Name

ethyl (8e,17e,19e)-18-bromotricosa-8,17,19-trien-4,6-diynoate

Description

ethyl (8e,17e,19e)-18-bromotricosa-8,17,19-trien-4,6-diynoate is found in Phakellia carduus.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112202192D          

 28 27  0  0  0  0            999 V2000
    5.1414    6.2684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    5.8559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    5.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    4.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9980    3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2836    3.7934    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.9980    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1414    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8559    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5704    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9993    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7138    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4283    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1427    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8572    2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5717    3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2862    3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0006    4.2059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0006    5.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7151    5.4434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4296    5.0309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7151    6.2684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.4296    6.6809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4296    7.5059    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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  3  0  0  0  0
 19 20  1  0  0  0  0
 20 21  3  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

     RDKit          3D

 63 62  0  0  0  0  0  0  0  0999 V2000
   -8.9253    0.5139   -2.1750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8550    0.5401   -1.0986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5469    1.9760   -0.7473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5128    2.0640    0.3043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9781    0.9371    0.8228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9721    1.1233    1.8477 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4545    2.8971    2.4113 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -4.3708    0.1224    2.4359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6562   -1.2734    2.1155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4337   -2.0429    1.7460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6600   -1.6174    0.5769 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9905   -0.2882    0.5825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9578   -0.1907    1.7267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3659    1.1807    1.6723 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3274    1.4830    0.4196 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5223    0.7530    0.0437 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1815   -0.1658    0.7001 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3507   -0.7499    0.1050 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3354   -1.2598   -0.4106 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4660   -1.8434   -1.0262 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4269   -2.3304   -1.5682 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5955   -2.9003   -2.2402 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8203   -2.3978   -1.5094 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8248   -0.9188   -1.5856 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9099   -0.3054   -2.1838 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8245   -0.1502   -1.0086 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8294    1.2698   -1.0812 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5852    1.8648   -0.4391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7859    1.1261   -1.8227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2054   -0.5444   -2.3340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4942    0.9730   -3.0806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9347    0.0305   -1.4890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2710    0.0397   -0.2037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2150    2.5540   -1.6263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4926    2.4202   -0.3694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1849    3.0326    0.6580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3411    0.0146    0.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6214    0.3734    3.2165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3983   -1.4035    1.2913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1293   -1.7990    3.0005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7517   -2.1046    2.6622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7006   -3.1306    1.5901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8616   -2.3916    0.3856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3691   -1.6372   -0.3147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6416    0.5696    0.5155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3998   -0.2670   -0.4021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2762   -1.0331    1.5805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4698   -0.3912    2.6967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2531    1.8912    1.7335 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2090    1.4336    2.5958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3807    1.4344   -0.4566 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6299    2.5902    0.3891 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9189    1.0401   -0.9655 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8627   -0.4545    1.6782 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5968   -2.4814   -3.2745 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5569   -4.0103   -2.2705 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7585   -2.6986   -0.4357 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7594   -2.8448   -1.9022 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7515    1.6148   -0.5747 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8932    1.6175   -2.1347 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7480    1.8414   -1.1691 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3415    1.3686    0.5095 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8316    2.9353   -0.1974 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  6  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  3  0
 19 20  1  0
 20 21  3  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  1  0
 27 28  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  2 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  5 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  0
 11 44  1  0
 12 45  1  0
 12 46  1  0
 13 47  1  0
 13 48  1  0
 14 49  1  0
 14 50  1  0
 15 51  1  0
 15 52  1  0
 16 53  1  0
 17 54  1  0
 22 55  1  0
 22 56  1  0
 23 57  1  0
 23 58  1  0
 27 59  1  0
 27 60  1  0
 28 61  1  0
 28 62  1  0
 28 63  1  0
M  END


  Mrv1652309112202192D          

 28 27  0  0  0  0            999 V2000
    5.1414    6.2684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    5.8559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    5.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    4.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9980    3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2836    3.7934    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.9980    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1414    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8559    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5704    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9993    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7138    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4283    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1427    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8572    2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5717    3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2862    3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0006    4.2059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0006    5.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7151    5.4434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4296    5.0309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7151    6.2684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.4296    6.6809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4296    7.5059    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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  3  0  0  0  0
 19 20  1  0  0  0  0
 20 21  3  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0307297

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC\C=C\C(\Br)=C/CCCCCCC\C=C\C#CC#CCCC(=O)OCC

> <INCHI_IDENTIFIER>
InChI=1S/C25H35BrO2/c1-3-5-18-21-24(26)22-19-16-14-12-10-8-6-7-9-11-13-15-17-20-23-25(27)28-4-2/h7,9,18,21-22H,3-6,8,10,12,14,16,19-20,23H2,1-2H3/b9-7+,21-18+,24-22+

> <INCHI_KEY>
GHVRQXGOEFTAJV-YCLUIVRGSA-N

> <FORMULA>
C25H35BrO2

> <MOLECULAR_WEIGHT>
447.457

> <EXACT_MASS>
446.182043

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
52.13187247968753

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
ethyl (8E,17E,19E)-18-bromotricosa-8,17,19-trien-4,6-diynoate

> <JCHEM_LOGP>
8.356384850666668

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.042608851335702

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
128.4151

> <JCHEM_ROTATABLE_BOND_COUNT>
18

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
ethyl (8E,17E,19E)-18-bromotricosa-8,17,19-trien-4,6-diynoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       9.597  11.701   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.264  10.931   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.264   9.391   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.930   8.621   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.930   7.081   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.596   6.311   0.000  0.00  0.00           C+0
HETATM    7 Br   UNK     0       4.263   7.081   0.000  0.00  0.00          Br+0
HETATM    8  C   UNK     0       5.596   4.771   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.264   4.771   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.597   4.001   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.931   4.771   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.265   4.001   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.598   4.771   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.932   4.001   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      16.266   4.771   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      17.599   4.001   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      18.933   4.771   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      20.267   5.541   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      21.600   6.311   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      22.934   7.081   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      24.268   7.851   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      24.268   9.391   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      25.602  10.161   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      26.935   9.391   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      25.602  11.701   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      26.935  12.471   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      26.935  14.011   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₅BrO₂

Average Mass

447.4570 Da

Monoisotopic Mass

446.18204 Da

IUPAC Name

ethyl (8E,17E,19E)-18-bromotricosa-8,17,19-trien-4,6-diynoate

Traditional Name

ethyl (8E,17E,19E)-18-bromotricosa-8,17,19-trien-4,6-diynoate

CAS Registry Number

Not Available

SMILES

CCC\C=C\C(\Br)=C/CCCCCCC\C=C\C#CC#CCCC(=O)OCC

InChI Identifier

InChI=1S/C25H35BrO2/c1-3-5-18-21-24(26)22-19-16-14-12-10-8-6-7-9-11-13-15-17-20-23-25(27)28-4-2/h7,9,18,21-22H,3-6,8,10,12,14,16,19-20,23H2,1-2H3/b9-7+,21-18+,24-22+

InChI Key

GHVRQXGOEFTAJV-YCLUIVRGSA-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
Phakellia carduus	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	8.36	ChemAxon
pKa (Strongest Basic)	-7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	18	ChemAxon
Refractivity	128.42 m³·mol⁻¹	ChemAxon
Polarizability	52.13 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for ethyl (8e,17e,19e)-18-bromotricosa-8,17,19-trien-4,6-diynoate (NP0307297)

MOL for NP0307297 (ethyl (8e,17e,19e)-18-bromotricosa-8,17,19-trien-4,6-diynoate)

3D MOL for NP0307297 (ethyl (8e,17e,19e)-18-bromotricosa-8,17,19-trien-4,6-diynoate)

3D SDF for NP0307297 (ethyl (8e,17e,19e)-18-bromotricosa-8,17,19-trien-4,6-diynoate)

3D-SDF for NP0307297 (ethyl (8e,17e,19e)-18-bromotricosa-8,17,19-trien-4,6-diynoate)

PDB for NP0307297 (ethyl (8e,17e,19e)-18-bromotricosa-8,17,19-trien-4,6-diynoate)

3D PDB for NP0307297 (ethyl (8e,17e,19e)-18-bromotricosa-8,17,19-trien-4,6-diynoate)

SMILES for NP0307297 (ethyl (8e,17e,19e)-18-bromotricosa-8,17,19-trien-4,6-diynoate)

INCHI for NP0307297 (ethyl (8e,17e,19e)-18-bromotricosa-8,17,19-trien-4,6-diynoate)

Structure for NP0307297 (ethyl (8e,17e,19e)-18-bromotricosa-8,17,19-trien-4,6-diynoate)

3D Structure for NP0307297 (ethyl (8e,17e,19e)-18-bromotricosa-8,17,19-trien-4,6-diynoate)