MiMeDB: Showing metabocard for zymosteryl palmitoleate (MMDBc0033032)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-19 04:31:52 UTC

Update Date

2022-08-31 22:20:58 UTC

Metabolite ID

MMDBc0033032

Metabolite Identification

Common Name

zymosteryl palmitoleate

Description

zymosteryl palmitoleate belongs to the class of organic compounds known as cholestane steroids. These are steroids with a structure containing the 27-carbon cholestane skeleton. zymosteryl palmitoleate is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL SDF PDB SMILES InChI

  Mrv0541 02241222252D          

 48 51  0  0  1  0            999 V2000
   -3.4228   -0.4181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1454   -0.8144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1454   -1.6535    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4228   -2.0653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7235   -1.6535    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0086   -2.0653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2782   -1.6535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2782   -0.8144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0086   -0.4181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7235   -0.8144    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0086    0.3900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2782    0.8096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5789    0.3900    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5789   -0.4181    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2058   -0.6745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6721   -0.0218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2058    0.6464    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5789    1.2370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7235   -0.0063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5789   -1.2495    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9285    1.0505    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7256   -2.4322    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8782   -2.0840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6348    1.4934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3493    1.9059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0637    1.4934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0637    0.6684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7782    1.9059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9203    1.9059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2058    1.4934    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5086    1.9059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8782   -2.9090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1663   -3.3259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5952   -3.3173    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1715   -4.1508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4596   -4.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4648   -5.3928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7529   -5.8096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7580   -6.6346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0462   -7.0515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0513   -7.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3394   -8.2935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6225   -7.8854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0894   -8.3023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8064   -7.8943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5183   -8.3112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2353   -7.9032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9472   -8.3201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 14 13  1  0  0  0  0
 17 13  1  0  0  0  0
 12 13  1  0  0  0  0
 13 18  1  1  0  0  0
  8 14  1  0  0  0  0
 15 14  1  0  0  0  0
 14 20  1  6  0  0  0
 11  9  1  0  0  0  0
 10  9  1  0  0  0  0
  8  9  2  0  0  0  0
  7  8  1  0  0  0  0
  5 10  1  0  0  0  0
 10 19  1  1  0  0  0
  1 10  1  0  0  0  0
 16 17  1  0  0  0  0
 30 17  1  0  0  0  0
 17 21  1  6  0  0  0
 11 12  1  0  0  0  0
 16 15  1  0  0  0  0
  6  7  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  0  0  0  0
  2  1  1  0  0  0  0
  3  4  1  0  0  0  0
  3  2  1  0  0  0  0
  5 22  1  6  0  0  0
  3 23  1  1  0  0  0
 29 24  1  0  0  0  0
 25 24  1  0  0  0  0
 26 25  2  0  0  0  0
 27 26  1  0  0  0  0
 28 26  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  6  0  0  0
 23 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 35  1  0  0  0  0
 32 34  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 43 42  1  0  0  0  0
 44 43  1  0  0  0  0
 45 44  1  0  0  0  0
 46 45  1  0  0  0  0
 47 46  1  0  0  0  0
 48 47  1  0  0  0  0
M  END

  Mrv0541 02241222252D          

 48 51  0  0  1  0            999 V2000
   -3.4228   -0.4181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1454   -0.8144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1454   -1.6535    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4228   -2.0653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7235   -1.6535    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0086   -2.0653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2782   -1.6535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2782   -0.8144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0086   -0.4181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7235   -0.8144    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0086    0.3900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2782    0.8096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5789    0.3900    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5789   -0.4181    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2058   -0.6745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6721   -0.0218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2058    0.6464    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5789    1.2370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7235   -0.0063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5789   -1.2495    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9285    1.0505    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7256   -2.4322    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8782   -2.0840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6348    1.4934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3493    1.9059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0637    1.4934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0637    0.6684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7782    1.9059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9203    1.9059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2058    1.4934    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5086    1.9059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8782   -2.9090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1663   -3.3259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5952   -3.3173    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1715   -4.1508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4596   -4.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4648   -5.3928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7529   -5.8096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7580   -6.6346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0462   -7.0515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0513   -7.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3394   -8.2935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6225   -7.8854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0894   -8.3023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8064   -7.8943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5183   -8.3112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2353   -7.9032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9472   -8.3201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 14 13  1  0  0  0  0
 17 13  1  0  0  0  0
 12 13  1  0  0  0  0
 13 18  1  1  0  0  0
  8 14  1  0  0  0  0
 15 14  1  0  0  0  0
 14 20  1  6  0  0  0
 11  9  1  0  0  0  0
 10  9  1  0  0  0  0
  8  9  2  0  0  0  0
  7  8  1  0  0  0  0
  5 10  1  0  0  0  0
 10 19  1  1  0  0  0
  1 10  1  0  0  0  0
 16 17  1  0  0  0  0
 30 17  1  0  0  0  0
 17 21  1  6  0  0  0
 11 12  1  0  0  0  0
 16 15  1  0  0  0  0
  6  7  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  0  0  0  0
  2  1  1  0  0  0  0
  3  4  1  0  0  0  0
  3  2  1  0  0  0  0
  5 22  1  6  0  0  0
  3 23  1  1  0  0  0
 29 24  1  0  0  0  0
 25 24  1  0  0  0  0
 26 25  2  0  0  0  0
 27 26  1  0  0  0  0
 28 26  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  6  0  0  0
 23 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 35  1  0  0  0  0
 32 34  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 43 42  1  0  0  0  0
 44 43  1  0  0  0  0
 45 44  1  0  0  0  0
 46 45  1  0  0  0  0
 47 46  1  0  0  0  0
 48 47  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0033032

> <DATABASE_NAME>
MIME

> <SMILES>
CCCCCC\C=C/CCCCCCCC(=O)O[C@H]1CC[C@]2(C)C3=C(CC[C@@]2([H])C1)[C@]1([H])CC[C@]([H])([C@H](C)CCC=C(C)C)[C@@]1(C)CC3

> <INCHI_IDENTIFIER>
InChI=1S/C43H72O2/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-23-41(44)45-36-28-30-42(5)35(32-36)24-25-37-39-27-26-38(34(4)22-20-21-33(2)3)43(39,6)31-29-40(37)42/h12-13,21,34-36,38-39H,7-11,14-20,22-32H2,1-6H3/b13-12-/t34-,35+,36+,38-,39+,42+,43-/m1/s1

> <INCHI_KEY>
RKBOCYGCMVZAEZ-MMBTXPDKSA-N

> <FORMULA>
C43H72O2

> <MOLECULAR_WEIGHT>
621.0306

> <EXACT_MASS>
620.553231548

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
82.55724792977392

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,5S,7S,11R,14R,15R)-2,15-dimethyl-14-[(2R)-6-methylhept-5-en-2-yl]tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-5-yl (9Z)-hexadec-9-enoate

> <ALOGPS_LOGP>
10.54

> <JCHEM_LOGP>
13.222783970333333

> <ALOGPS_LOGS>
-7.51

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.041520418194966

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
195.9079

> <JCHEM_ROTATABLE_BOND_COUNT>
19

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.91e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
zymosteryl palmitoleate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -6.389  -0.780   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -7.738  -1.520   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.738  -3.087   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.389  -3.855   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.084  -3.087   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.749  -3.855   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.386  -3.087   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.386  -1.520   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.749  -0.780   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.084  -1.520   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.749   0.728   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.386   1.511   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.081   0.728   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.081  -0.780   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.384  -1.259   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.255  -0.041   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.384   1.207   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.081   2.309   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -5.084  -0.012   0.000  0.00  0.00           C+0
HETATM   20  H   UNK     0      -1.081  -2.332   0.000  0.00  0.00           H+0
HETATM   21  H   UNK     0       1.733   1.961   0.000  0.00  0.00           H+0
HETATM   22  H   UNK     0      -5.088  -4.540   0.000  0.00  0.00           H+0
HETATM   23  O   UNK     0      -9.106  -3.890   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.052   2.788   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.385   3.558   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.719   2.788   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.719   1.248   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.053   3.558   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.718   3.558   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.384   2.788   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -0.949   3.558   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -9.106  -5.430   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -7.777  -6.208   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0     -10.444  -6.192   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -7.787  -7.748   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -6.458  -8.527   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -6.468 -10.067   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -5.139 -10.845   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -5.148 -12.385   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -3.820 -13.163   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -3.829 -14.703   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -2.500 -15.481   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -1.162 -14.719   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       0.167 -15.498   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       1.505 -14.736   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       2.834 -15.514   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       4.173 -14.753   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       5.501 -15.531   0.000  0.00  0.00           C+0
CONECT    1   10    2                                                       
CONECT    2    1    3                                                       
CONECT    3    4    2   23                                                  
CONECT    4    5    3                                                       
CONECT    5   10    4    6   22                                             
CONECT    6    7    5                                                       
CONECT    7    8    6                                                       
CONECT    8   14    9    7                                                  
CONECT    9   11   10    8                                                  
CONECT   10    9    5   19    1                                             
CONECT   11    9   12                                                       
CONECT   12   13   11                                                       
CONECT   13   14   17   12   18                                             
CONECT   14   13    8   15   20                                             
CONECT   15   14   16                                                       
CONECT   16   17   15                                                       
CONECT   17   13   16   30   21                                             
CONECT   18   13                                                            
CONECT   19   10                                                            
CONECT   20   14                                                            
CONECT   21   17                                                            
CONECT   22    5                                                            
CONECT   23    3   32                                                       
CONECT   24   29   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   24   30                                                       
CONECT   30   17   29   31                                                  
CONECT   31   30                                                            
CONECT   32   23   33   34                                                  
CONECT   33   32   35                                                       
CONECT   34   32                                                            
CONECT   35   33   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  102    0
END

Synonyms

Value	Source
Zymosteryl palmitoleic acid	Generator

Molecular Formula

C₄₃H₇₂O₂

Average Mass

621.0306

Monoisotopic Mass

620.553231548

IUPAC Name

(2S,5S,7S,11R,14R,15R)-2,15-dimethyl-14-[(2R)-6-methylhept-5-en-2-yl]tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-5-yl (9Z)-hexadec-9-enoate

Traditional Name

zymosteryl palmitoleate

CAS Registry Number

Not Available

SMILES

CCCCCC\C=C/CCCCCCCC(=O)O[C@H]1CC[C@]2(C)C3=C(CC[C@@]2([H])C1)[C@]1([H])CC[C@]([H])([C@H](C)CCC=C(C)C)[C@@]1(C)CC3

InChI Identifier

InChI=1S/C43H72O2/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-23-41(44)45-36-28-30-42(5)35(32-36)24-25-37-39-27-26-38(34(4)22-20-21-33(2)3)43(39,6)31-29-40(37)42/h12-13,21,34-36,38-39H,7-11,14-20,22-32H2,1-6H3/b13-12-/t34-,35+,36+,38-,39+,42+,43-/m1/s1

InChI Key

RKBOCYGCMVZAEZ-MMBTXPDKSA-N

Chemical Taxonomy

Functional Ontology

Physical Properties

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-00dr-1256049000-2d9c65af4a1a00ce7e3b	2016-09-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-014r-4659040000-7271a4e05ccffa452d86	2016-09-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-07do-4819240000-d24fd5679fff49f331d3	2016-09-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-014i-0024009000-10728694041bebcf1a86	2016-09-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-00lr-0049103000-7867c03f0d278193203f	2016-09-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-015c-2029000000-c58a083015235ec11379	2016-09-12	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-21	View Spectrum

Biological Properties

Human Proteins and Enzymes

Human Pathways

Metabolic Reactions

Health Effects and Bioactivity

Microbial Sources

Exposure Sources

Host Biospecimen and Location

External Links

References

Showing metabocard for zymosteryl palmitoleate (MMDBc0033032)

MOL for #<Metabolite:0x00007fd5ac01cbb8>

3D MOL for #<Metabolite:0x00007fd5ac01cbb8>

3D SDF for #<Metabolite:0x00007fd5ac01cbb8>

3D-SDF for #<Metabolite:0x00007fd5ac01cbb8>

PDB for #<Metabolite:0x00007fd5ac01cbb8>

3D PDB for #<Metabolite:0x00007fd5ac01cbb8>

SMILES for #<Metabolite:0x00007fd5ac01cbb8>

INCHI for #<Metabolite:0x00007fd5ac01cbb8>

Structure for #<Metabolite:0x00007fd5ac01cbb8>

3D Structure for #<Metabolite:0x00007fd5ac01cbb8>