NP-MRD: Showing NP-Card for methyl (5z,8z,10s)-10-hydroxy-10-[(2s,3s)-3-[(2z,5z)-octa-2,5-dien-1-yl]oxiran-2-yl]deca-5,8-dienoate (NP0244428)

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Record Information

Version

2.0

Created at

2022-09-07 05:13:36 UTC

Updated at

2022-09-07 05:13:36 UTC

NP-MRD ID

NP0244428

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (5z,8z,10s)-10-hydroxy-10-[(2s,3s)-3-[(2z,5z)-octa-2,5-dien-1-yl]oxiran-2-yl]deca-5,8-dienoate

Description

Methyl-(10r)-hydroxy-(11s,12s)-epoxy-(5z,8z,14z,17z)-eicosatetraenoate belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms. methyl (5z,8z,10s)-10-hydroxy-10-[(2s,3s)-3-[(2z,5z)-octa-2,5-dien-1-yl]oxiran-2-yl]deca-5,8-dienoate is found in Murrayella periclados. Based on a literature review very few articles have been published on Methyl-(10r)-hydroxy-(11s,12s)-epoxy-(5z,8z,14z,17z)-eicosatetraenoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072207132D          

 25 25  0  0  1  0            999 V2000
   -5.8559    5.8559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5704    5.4434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2849    5.8559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9993    5.4434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9993    4.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7138    4.2059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7138    3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9993    2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2849    3.3809    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.8724    4.0954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4599    3.3809    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7454    2.9684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0309    3.3809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7454    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0309    1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3164    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3164    2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6020    3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875    2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730    3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4586    2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7441    3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7441    4.2059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0296    2.9684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6849    3.3809    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  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  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END

     RDKit          3D

 57 57  0  0  0  0  0  0  0  0999 V2000
    9.9063    0.5999   -0.1144 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7234    1.5070   -0.5256 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9875    1.8857    0.6630 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7308    1.6344    0.9251 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8816    0.8835   -0.0398 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3780   -0.3451    0.5973 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0926   -0.5873    0.7342 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9804    0.2764    0.3009 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1009   -0.4292   -0.7174 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0074    0.1920   -1.2573 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6488   -0.7510   -0.3277 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0948   -2.0805   -0.7747 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2330   -2.8746    0.3151 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8809   -2.0280   -1.8531 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0818   -1.5059   -1.7092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5035   -0.9365   -0.4159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6957   -1.6838    0.0308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8511   -1.1296    0.2312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1268    0.2954    0.0419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5851    0.9607    1.3326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8394    0.3564    1.8883 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9845    0.4449    0.9725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1614   -0.3312   -0.0069 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9594    1.4285    1.1560 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0680    1.5407    0.2973 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5142   -0.4328   -0.0487 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3378    0.9875    0.8114 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6203    0.6225   -0.9751 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1542    1.0247   -1.3091 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1878    2.4180   -1.0442 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5197    2.4546    1.4618 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2748    1.9824    1.8846 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0630    1.6003   -0.3195 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4412    0.6899   -0.9561 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1485   -1.0514    0.9534 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8769   -1.5621    1.2380 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3239    0.4001    1.2311 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3143    1.2501   -0.0298 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645   -1.1960   -1.3596 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4501   -0.3868    0.7185 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0040   -2.6228   -1.2111 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5904   -3.0193    0.8385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6083   -2.4482   -2.8552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7364   -1.5188   -2.5869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7291   -1.1670    0.3933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6995    0.1270   -0.4394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6456   -2.7821    0.2175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7270   -1.7376    0.5716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3732    0.9065   -0.4356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0293    0.3367   -0.6704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7583    0.9290    2.0412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8148    2.0153    1.0661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0672    0.8908    2.8301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7174   -0.7118    2.1627 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9725    1.7303    0.8992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8591    2.3738   -0.4109 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2099    0.5745   -0.2449 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 11  9  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
  3 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  7 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  6
 11 40  1  1
 12 41  1  6
 13 42  1  0
 14 43  1  0
 15 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 18 48  1  0
 19 49  1  0
 19 50  1  0
 20 51  1  0
 20 52  1  0
 21 53  1  0
 21 54  1  0
 25 55  1  0
 25 56  1  0
 25 57  1  0
M  END


  Mrv1652309072207132D          

 25 25  0  0  1  0            999 V2000
   -5.8559    5.8559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5704    5.4434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2849    5.8559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9993    5.4434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9993    4.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7138    4.2059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7138    3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9993    2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2849    3.3809    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.8724    4.0954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4599    3.3809    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7454    2.9684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0309    3.3809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7454    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0309    1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3164    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3164    2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6020    3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875    2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730    3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4586    2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7441    3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7441    4.2059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0296    2.9684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6849    3.3809    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  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  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0244428

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC\C=C/C\C=C/C[C@@H]1O[C@H]1[C@@H](O)\C=C/C\C=C/CCCC(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C21H32O4/c1-3-4-5-6-10-13-16-19-21(25-19)18(22)15-12-9-7-8-11-14-17-20(23)24-2/h4-5,7-8,10,12-13,15,18-19,21-22H,3,6,9,11,14,16-17H2,1-2H3/b5-4-,8-7-,13-10-,15-12-/t18-,19-,21-/m0/s1

> <INCHI_KEY>
TZZBJXZCAVSJCY-XMRHUZDPSA-N

> <FORMULA>
C21H32O4

> <MOLECULAR_WEIGHT>
348.483

> <EXACT_MASS>
348.23005951

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
40.55451335346447

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (5Z,8Z,10S)-10-hydroxy-10-[(2S,3S)-3-[(2Z,5Z)-octa-2,5-dien-1-yl]oxiran-2-yl]deca-5,8-dienoate

> <JCHEM_LOGP>
4.514150158333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.747890202919223

> <JCHEM_PKA_STRONGEST_BASIC>
-3.346472825243132

> <JCHEM_POLAR_SURFACE_AREA>
59.06

> <JCHEM_REFRACTIVITY>
105.45150000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (5Z,8Z,10S)-10-hydroxy-10-[(2S,3S)-3-[(2Z,5Z)-octa-2,5-dien-1-yl]oxiran-2-yl]deca-5,8-dienoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0     -10.931  10.931   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -12.265  10.161   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -13.598  10.931   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -14.932  10.161   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -14.932   8.621   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -16.266   7.851   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -16.266   6.311   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -14.932   5.541   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -13.598   6.311   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0     -12.828   7.645   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0     -12.058   6.311   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -10.725   5.541   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -9.391   6.311   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0     -10.725   4.001   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -9.391   3.231   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -8.057   4.001   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -8.057   5.541   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.724   6.311   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -5.390   5.541   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.056   6.311   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.723   5.541   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.389   6.311   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.389   7.851   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -0.055   5.541   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.278   6.311   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                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9   11                                                       
CONECT   11   10    9   12                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   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   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   50    0
END

View in JSmol

Synonyms

Value	Source
Methyl-(10R)-hydroxy-(11S,12S)-epoxy-(5Z,8Z,14Z,17Z)-eicosatetraenoic acid	Generator

Chemical Formula

C₂₁H₃₂O₄

Average Mass

348.4830 Da

Monoisotopic Mass

348.23006 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC\C=C/C\C=C/C[C@@H]1O[C@H]1[C@@H](O)\C=C/C\C=C/CCCC(=O)OC

InChI Identifier

InChI=1S/C21H32O4/c1-3-4-5-6-10-13-16-19-21(25-19)18(22)15-12-9-7-8-11-14-17-20(23)24-2/h4-5,7-8,10,12-13,15,18-19,21-22H,3,6,9,11,14,16-17H2,1-2H3/b5-4-,8-7-,13-10-,15-12-/t18-,19-,21-/m0/s1

InChI Key

TZZBJXZCAVSJCY-XMRHUZDPSA-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
Murrayella periclados	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Fatty alcohols

Alternative Parents

Substituents

Fatty alcohol
Fatty acid ester
Fatty acid methyl ester
Methyl ester
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Alcohol
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Carbonyl group
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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

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

8535847

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10360398

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (5z,8z,10s)-10-hydroxy-10-[(2s,3s)-3-[(2z,5z)-octa-2,5-dien-1-yl]oxiran-2-yl]deca-5,8-dienoate (NP0244428)

MOL for NP0244428 (methyl (5z,8z,10s)-10-hydroxy-10-[(2s,3s)-3-[(2z,5z)-octa-2,5-dien-1-yl]oxiran-2-yl]deca-5,8-dienoate)

3D MOL for NP0244428 (methyl (5z,8z,10s)-10-hydroxy-10-[(2s,3s)-3-[(2z,5z)-octa-2,5-dien-1-yl]oxiran-2-yl]deca-5,8-dienoate)

3D SDF for NP0244428 (methyl (5z,8z,10s)-10-hydroxy-10-[(2s,3s)-3-[(2z,5z)-octa-2,5-dien-1-yl]oxiran-2-yl]deca-5,8-dienoate)

3D-SDF for NP0244428 (methyl (5z,8z,10s)-10-hydroxy-10-[(2s,3s)-3-[(2z,5z)-octa-2,5-dien-1-yl]oxiran-2-yl]deca-5,8-dienoate)

PDB for NP0244428 (methyl (5z,8z,10s)-10-hydroxy-10-[(2s,3s)-3-[(2z,5z)-octa-2,5-dien-1-yl]oxiran-2-yl]deca-5,8-dienoate)

3D PDB for NP0244428 (methyl (5z,8z,10s)-10-hydroxy-10-[(2s,3s)-3-[(2z,5z)-octa-2,5-dien-1-yl]oxiran-2-yl]deca-5,8-dienoate)

SMILES for NP0244428 (methyl (5z,8z,10s)-10-hydroxy-10-[(2s,3s)-3-[(2z,5z)-octa-2,5-dien-1-yl]oxiran-2-yl]deca-5,8-dienoate)

INCHI for NP0244428 (methyl (5z,8z,10s)-10-hydroxy-10-[(2s,3s)-3-[(2z,5z)-octa-2,5-dien-1-yl]oxiran-2-yl]deca-5,8-dienoate)

Structure for NP0244428 (methyl (5z,8z,10s)-10-hydroxy-10-[(2s,3s)-3-[(2z,5z)-octa-2,5-dien-1-yl]oxiran-2-yl]deca-5,8-dienoate)

3D Structure for NP0244428 (methyl (5z,8z,10s)-10-hydroxy-10-[(2s,3s)-3-[(2z,5z)-octa-2,5-dien-1-yl]oxiran-2-yl]deca-5,8-dienoate)