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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 21:52:09 UTC

Update Date

2022-03-07 02:55:01 UTC

HMDB ID

HMDB0036702

Secondary Accession Numbers

HMDB36702

Metabolite Identification

Common Name

Sideridiol

Description

Sideridiol belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D. Sideridiol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0036702
     RDKit          3D
Sideridiol
 54 57  0  0  0  0  0  0  0  0999 V2000
    5.2782    0.5467    0.7171 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8297    0.4246    0.3917 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7843    0.4739    1.2089 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5063    0.5383    0.4046 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0540    1.0869   -0.9058 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3171    0.2156   -0.9908 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9073   -1.2225   -1.1084 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4139   -1.4299   -1.0212 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9363   -0.8305    0.2616 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5602   -0.8935    0.4437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8846   -1.0876    1.8844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0477   -2.1186   -0.3062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5662   -2.1730   -0.3524 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1422   -0.9627   -1.0194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6752    0.2665   -0.2721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4167    0.3496    1.0074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1095    1.4653   -1.1302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4839    1.4755   -1.2858 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1925    0.3128   -0.1839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7026    1.6159    0.3757 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6150    1.5223    1.0811 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2579    2.7809    1.0027 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7630    1.3524    0.0988 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4506    0.8165    1.7714 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8136   -0.3894    0.4218 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8806    0.4667    2.2847 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3051    2.1348   -0.7492 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4306    0.8870   -1.7648 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9990    0.5560   -1.7682 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2742   -1.6450   -2.0635 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3864   -1.8454   -0.2966 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9172   -1.0793   -1.9211 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2699   -2.5470   -0.9362 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3683   -1.4668    1.0903 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0531   -1.3763    2.4460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5673   -1.9719    2.0545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2925   -0.2266    2.4044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7172   -3.0335    0.2344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6955   -2.1778   -1.3331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8075   -3.0508   -1.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0227   -2.3859    0.6153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2537   -1.0079   -0.8694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8893   -0.9165   -2.0804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1153    1.1580    1.6882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4948    0.5796    0.7461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4967   -0.6378    1.5519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8375    2.3626   -0.5244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5595    1.4249   -2.0971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9010    2.3123   -0.9723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8387    0.2926   -1.2619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5627    2.3758   -0.4502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4175    2.1001    1.0741 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5354    1.3078    2.1630 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9036    3.2742    0.2272 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 15 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
  6  2  1  0
 19 10  1  0
  9  4  1  0
 21  4  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  5 27  1  0
  5 28  1  0
  6 29  1  0
  7 30  1  0
  7 31  1  0
  8 32  1  0
  8 33  1  0
  9 34  1  0
 11 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 12 39  1  0
 13 40  1  0
 13 41  1  0
 14 42  1  0
 14 43  1  0
 16 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 18 49  1  0
 19 50  1  0
 20 51  1  0
 20 52  1  0
 21 53  1  0
 22 54  1  0
M  END


  Mrv0541 05061309172D          

 22 25  0  0  0  0            999 V2000
   -0.6778    1.4980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7827    2.9325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7366    0.4428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3550    0.7608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1623    0.0148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9942    0.2131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6222    1.5413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5455    0.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7314    2.6342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7382    2.0342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0998    1.1465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7862    2.5891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1409    1.3963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5599    0.6390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1835    1.0613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704    2.0040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9121    2.4782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0798    2.1629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0032    1.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5715    1.6963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7703    3.4139    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3971    3.1227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
  7  4  1  0  0  0  0
  8  4  1  0  0  0  0
 13  1  1  0  0  0  0
 13 10  2  0  0  0  0
 14  5  1  0  0  0  0
 14 11  1  0  0  0  0
 14 13  1  0  0  0  0
 15  6  1  0  0  0  0
 16  9  1  0  0  0  0
 17  9  1  0  0  0  0
 18  2  1  0  0  0  0
 18  7  1  0  0  0  0
 18 12  1  0  0  0  0
 18 16  1  0  0  0  0
 19  3  1  0  0  0  0
 19  8  1  0  0  0  0
 19 15  1  0  0  0  0
 19 16  1  0  0  0  0
 20 10  1  0  0  0  0
 20 11  1  0  0  0  0
 20 15  1  0  0  0  0
 20 17  1  0  0  0  0
 21 12  1  0  0  0  0
 22 17  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0036702

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1=CC23CC1CCC2C1(C)CCCC(C)(CO)C1CC3O

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O2/c1-13-10-20-11-14(13)5-6-15(20)19(3)8-4-7-18(2,12-21)16(19)9-17(20)22/h10,14-17,21-22H,4-9,11-12H2,1-3H3

> <INCHI_KEY>
BATFJLLEMUIAJD-UHFFFAOYSA-N

> <FORMULA>
C20H32O2

> <MOLECULAR_WEIGHT>
304.4669

> <EXACT_MASS>
304.240230268

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
36.27424654049962

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-(hydroxymethyl)-5,9,14-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-14-en-2-ol

> <ALOGPS_LOGP>
3.24

> <JCHEM_LOGP>
3.0466222713333346

> <ALOGPS_LOGS>
-3.85

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.59229292401227

> <JCHEM_PKA_STRONGEST_BASIC>
-0.3865207416888933

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
90.00909999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.26e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-(hydroxymethyl)-5,9,14-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-14-en-2-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0036702
     RDKit          3D
Sideridiol
 54 57  0  0  0  0  0  0  0  0999 V2000
    5.2782    0.5467    0.7171 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8297    0.4246    0.3917 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7843    0.4739    1.2089 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5063    0.5383    0.4046 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0540    1.0869   -0.9058 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3171    0.2156   -0.9908 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9073   -1.2225   -1.1084 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4139   -1.4299   -1.0212 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9363   -0.8305    0.2616 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5602   -0.8935    0.4437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8846   -1.0876    1.8844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0477   -2.1186   -0.3062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5662   -2.1730   -0.3524 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1422   -0.9627   -1.0194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6752    0.2665   -0.2721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4167    0.3496    1.0074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1095    1.4653   -1.1302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4839    1.4755   -1.2858 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1925    0.3128   -0.1839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7026    1.6159    0.3757 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6150    1.5223    1.0811 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2579    2.7809    1.0027 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7630    1.3524    0.0988 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4506    0.8165    1.7714 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8136   -0.3894    0.4218 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8806    0.4667    2.2847 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3051    2.1348   -0.7492 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4306    0.8870   -1.7648 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9990    0.5560   -1.7682 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2742   -1.6450   -2.0635 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3864   -1.8454   -0.2966 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9172   -1.0793   -1.9211 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2699   -2.5470   -0.9362 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3683   -1.4668    1.0903 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0531   -1.3763    2.4460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5673   -1.9719    2.0545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2925   -0.2266    2.4044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7172   -3.0335    0.2344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6955   -2.1778   -1.3331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8075   -3.0508   -1.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0227   -2.3859    0.6153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2537   -1.0079   -0.8694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8893   -0.9165   -2.0804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1153    1.1580    1.6882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4948    0.5796    0.7461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4967   -0.6378    1.5519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8375    2.3626   -0.5244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5595    1.4249   -2.0971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9010    2.3123   -0.9723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8387    0.2926   -1.2619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5627    2.3758   -0.4502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4175    2.1001    1.0741 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5354    1.3078    2.1630 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9036    3.2742    0.2272 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 15 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
  6  2  1  0
 19 10  1  0
  9  4  1  0
 21  4  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  5 27  1  0
  5 28  1  0
  6 29  1  0
  7 30  1  0
  7 31  1  0
  8 32  1  0
  8 33  1  0
  9 34  1  0
 11 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 12 39  1  0
 13 40  1  0
 13 41  1  0
 14 42  1  0
 14 43  1  0
 16 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 18 49  1  0
 19 50  1  0
 20 51  1  0
 20 52  1  0
 21 53  1  0
 22 54  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -1.265   2.796   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.061   5.474   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.108   0.826   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.129   1.420   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.170   0.028   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.722   0.398   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.628   2.877   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.618   1.124   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.099   4.917   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.378   3.797   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.053   2.140   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.934   4.833   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.263   2.606   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.045   1.193   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.076   1.981   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.105   3.741   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.569   4.626   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.616   4.037   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.606   2.284   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.933   3.166   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.904   6.373   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       2.608   5.829   0.000  0.00  0.00           O+0
CONECT    1   13                                                            
CONECT    2   18                                                            
CONECT    3   19                                                            
CONECT    4    7    8                                                       
CONECT    5    6   14                                                       
CONECT    6    5   15                                                       
CONECT    7    4   18                                                       
CONECT    8    4   19                                                       
CONECT    9   16   17                                                       
CONECT   10   13   20                                                       
CONECT   11   14   20                                                       
CONECT   12   18   21                                                       
CONECT   13    1   10   14                                                  
CONECT   14    5   11   13                                                  
CONECT   15    6   19   20                                                  
CONECT   16    9   18   19                                                  
CONECT   17    9   20   22                                                  
CONECT   18    2    7   12   16                                             
CONECT   19    3    8   15   16                                             
CONECT   20   10   11   15   17                                             
CONECT   21   12                                                            
CONECT   22   17                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   50    0
END

COMPND    HMDB0036702
HETATM    1  C1  UNL     1       5.278   0.547   0.717  1.00  0.00           C  
HETATM    2  C2  UNL     1       3.830   0.425   0.392  1.00  0.00           C  
HETATM    3  C3  UNL     1       2.784   0.474   1.209  1.00  0.00           C  
HETATM    4  C4  UNL     1       1.506   0.538   0.405  1.00  0.00           C  
HETATM    5  C5  UNL     1       2.054   1.087  -0.906  1.00  0.00           C  
HETATM    6  C6  UNL     1       3.317   0.216  -0.991  1.00  0.00           C  
HETATM    7  C7  UNL     1       2.907  -1.223  -1.108  1.00  0.00           C  
HETATM    8  C8  UNL     1       1.414  -1.430  -1.021  1.00  0.00           C  
HETATM    9  C9  UNL     1       0.936  -0.830   0.262  1.00  0.00           C  
HETATM   10  C10 UNL     1      -0.560  -0.893   0.444  1.00  0.00           C  
HETATM   11  C11 UNL     1      -0.885  -1.088   1.884  1.00  0.00           C  
HETATM   12  C12 UNL     1      -1.048  -2.119  -0.306  1.00  0.00           C  
HETATM   13  C13 UNL     1      -2.566  -2.173  -0.352  1.00  0.00           C  
HETATM   14  C14 UNL     1      -3.142  -0.963  -1.019  1.00  0.00           C  
HETATM   15  C15 UNL     1      -2.675   0.267  -0.272  1.00  0.00           C  
HETATM   16  C16 UNL     1      -3.417   0.350   1.007  1.00  0.00           C  
HETATM   17  C17 UNL     1      -3.110   1.465  -1.130  1.00  0.00           C  
HETATM   18  O1  UNL     1      -4.484   1.476  -1.286  1.00  0.00           O  
HETATM   19  C18 UNL     1      -1.192   0.313  -0.184  1.00  0.00           C  
HETATM   20  C19 UNL     1      -0.703   1.616   0.376  1.00  0.00           C  
HETATM   21  C20 UNL     1       0.615   1.522   1.081  1.00  0.00           C  
HETATM   22  O2  UNL     1       1.258   2.781   1.003  1.00  0.00           O  
HETATM   23  H1  UNL     1       5.763   1.352   0.099  1.00  0.00           H  
HETATM   24  H2  UNL     1       5.451   0.816   1.771  1.00  0.00           H  
HETATM   25  H3  UNL     1       5.814  -0.389   0.422  1.00  0.00           H  
HETATM   26  H4  UNL     1       2.881   0.467   2.285  1.00  0.00           H  
HETATM   27  H5  UNL     1       2.305   2.135  -0.749  1.00  0.00           H  
HETATM   28  H6  UNL     1       1.431   0.887  -1.765  1.00  0.00           H  
HETATM   29  H7  UNL     1       3.999   0.556  -1.768  1.00  0.00           H  
HETATM   30  H8  UNL     1       3.274  -1.645  -2.063  1.00  0.00           H  
HETATM   31  H9  UNL     1       3.386  -1.845  -0.297  1.00  0.00           H  
HETATM   32  H10 UNL     1       0.917  -1.079  -1.921  1.00  0.00           H  
HETATM   33  H11 UNL     1       1.270  -2.547  -0.936  1.00  0.00           H  
HETATM   34  H12 UNL     1       1.368  -1.467   1.090  1.00  0.00           H  
HETATM   35  H13 UNL     1       0.053  -1.376   2.446  1.00  0.00           H  
HETATM   36  H14 UNL     1      -1.567  -1.972   2.055  1.00  0.00           H  
HETATM   37  H15 UNL     1      -1.292  -0.227   2.404  1.00  0.00           H  
HETATM   38  H16 UNL     1      -0.717  -3.034   0.234  1.00  0.00           H  
HETATM   39  H17 UNL     1      -0.696  -2.178  -1.333  1.00  0.00           H  
HETATM   40  H18 UNL     1      -2.808  -3.051  -1.016  1.00  0.00           H  
HETATM   41  H19 UNL     1      -3.023  -2.386   0.615  1.00  0.00           H  
HETATM   42  H20 UNL     1      -4.254  -1.008  -0.869  1.00  0.00           H  
HETATM   43  H21 UNL     1      -2.889  -0.917  -2.080  1.00  0.00           H  
HETATM   44  H22 UNL     1      -3.115   1.158   1.688  1.00  0.00           H  
HETATM   45  H23 UNL     1      -4.495   0.580   0.746  1.00  0.00           H  
HETATM   46  H24 UNL     1      -3.497  -0.638   1.552  1.00  0.00           H  
HETATM   47  H25 UNL     1      -2.837   2.363  -0.524  1.00  0.00           H  
HETATM   48  H26 UNL     1      -2.560   1.425  -2.097  1.00  0.00           H  
HETATM   49  H27 UNL     1      -4.901   2.312  -0.972  1.00  0.00           H  
HETATM   50  H28 UNL     1      -0.839   0.293  -1.262  1.00  0.00           H  
HETATM   51  H29 UNL     1      -0.563   2.376  -0.450  1.00  0.00           H  
HETATM   52  H30 UNL     1      -1.418   2.100   1.074  1.00  0.00           H  
HETATM   53  H31 UNL     1       0.535   1.308   2.163  1.00  0.00           H  
HETATM   54  H32 UNL     1       0.904   3.274   0.227  1.00  0.00           H  
CONECT    1    2   23   24   25
CONECT    2    3    3    6
CONECT    3    4   26
CONECT    4    5    9   21
CONECT    5    6   27   28
CONECT    6    7   29
CONECT    7    8   30   31
CONECT    8    9   32   33
CONECT    9   10   34
CONECT   10   11   12   19
CONECT   11   35   36   37
CONECT   12   13   38   39
CONECT   13   14   40   41
CONECT   14   15   42   43
CONECT   15   16   17   19
CONECT   16   44   45   46
CONECT   17   18   47   48
CONECT   18   49
CONECT   19   20   50
CONECT   20   21   51   52
CONECT   21   22   53
CONECT   22   54
END

HMDB0036702
     RDKit          3D
Sideridiol
 54 57  0  0  0  0  0  0  0  0999 V2000
    5.2782    0.5467    0.7171 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8297    0.4246    0.3917 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7843    0.4739    1.2089 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5063    0.5383    0.4046 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0540    1.0869   -0.9058 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3171    0.2156   -0.9908 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9073   -1.2225   -1.1084 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4139   -1.4299   -1.0212 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9363   -0.8305    0.2616 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5602   -0.8935    0.4437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8846   -1.0876    1.8844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0477   -2.1186   -0.3062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5662   -2.1730   -0.3524 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1422   -0.9627   -1.0194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6752    0.2665   -0.2721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4167    0.3496    1.0074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1095    1.4653   -1.1302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4839    1.4755   -1.2858 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1925    0.3128   -0.1839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7026    1.6159    0.3757 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6150    1.5223    1.0811 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2579    2.7809    1.0027 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7630    1.3524    0.0988 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4506    0.8165    1.7714 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8136   -0.3894    0.4218 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8806    0.4667    2.2847 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3051    2.1348   -0.7492 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4306    0.8870   -1.7648 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9990    0.5560   -1.7682 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2742   -1.6450   -2.0635 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3864   -1.8454   -0.2966 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9172   -1.0793   -1.9211 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2699   -2.5470   -0.9362 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3683   -1.4668    1.0903 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0531   -1.3763    2.4460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5673   -1.9719    2.0545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2925   -0.2266    2.4044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7172   -3.0335    0.2344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6955   -2.1778   -1.3331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8075   -3.0508   -1.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0227   -2.3859    0.6153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2537   -1.0079   -0.8694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8893   -0.9165   -2.0804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1153    1.1580    1.6882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4948    0.5796    0.7461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4967   -0.6378    1.5519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8375    2.3626   -0.5244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5595    1.4249   -2.0971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9010    2.3123   -0.9723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8387    0.2926   -1.2619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5627    2.3758   -0.4502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4175    2.1001    1.0741 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5354    1.3078    2.1630 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9036    3.2742    0.2272 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 15 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
  6  2  1  0
 19 10  1  0
  9  4  1  0
 21  4  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  5 27  1  0
  5 28  1  0
  6 29  1  0
  7 30  1  0
  7 31  1  0
  8 32  1  0
  8 33  1  0
  9 34  1  0
 11 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 12 39  1  0
 13 40  1  0
 13 41  1  0
 14 42  1  0
 14 43  1  0
 16 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 18 49  1  0
 19 50  1  0
 20 51  1  0
 20 52  1  0
 21 53  1  0
 22 54  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₀H₃₂O₂

Average Molecular Weight

304.4669

Monoisotopic Molecular Weight

304.240230268

IUPAC Name

5-(hydroxymethyl)-5,9,14-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-14-en-2-ol

Traditional Name

5-(hydroxymethyl)-5,9,14-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-14-en-2-ol

CAS Registry Number

19891-25-9

SMILES

CC1=CC23CC1CCC2C1(C)CCCC(C)(CO)C1CC3O

InChI Identifier

InChI=1S/C20H32O2/c1-13-10-20-11-14(13)5-6-15(20)19(3)8-4-7-18(2,12-21)16(19)9-17(20)22/h10,14-17,21-22H,4-9,11-12H2,1-3H3

InChI Key

BATFJLLEMUIAJD-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Kaurane diterpenoids

Alternative Parents

Not Available

Substituents

Not Available

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cytoplasm (HMDB: HMDB0036702)
Cell membrane (HMDB: HMDB0036702)

Cellular substructure

Extracellular (HMDB: HMDB0036702)
Membrane (HMDB: HMDB0036702)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0036702)

Source

Endogenous

Endogenous (HMDB: HMDB0036702)

Animal

Animal (HMDB: HMDB0036702)

Exogenous

Food

Food (HMDB: HMDB0036702)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0036702)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0036702)

Cellular process

Cell signaling (HMDB: HMDB0036702)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0036702)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0036702)

Nutrient

Nutrient (HMDB: HMDB0036702)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0036702)

Emulsifier (HMDB: HMDB0036702)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	196 - 197 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.043 g/L	ALOGPS
logP	3.24	ALOGPS
logP	3.05	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	18.59	ChemAxon
pKa (Strongest Basic)	-0.39	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.46 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	90.01 m³·mol⁻¹	ChemAxon
Polarizability	36.27 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	169.752	31661259
DarkChem	[M-H]-	167.017	31661259
DeepCCS	[M-2H]-	204.563	30932474
DeepCCS	[M+Na]+	180.087	30932474
AllCCS	[M+H]+	177.4	32859911
AllCCS	[M+H-H2O]+	174.4	32859911
AllCCS	[M+NH4]+	180.2	32859911
AllCCS	[M+Na]+	180.9	32859911
AllCCS	[M-H]-	182.4	32859911
AllCCS	[M+Na-2H]-	182.7	32859911
AllCCS	[M+HCOO]-	183.2	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Sideridiol	CC1=CC23CC1CCC2C1(C)CCCC(C)(CO)C1CC3O	2784.0	Standard polar	33892256
Sideridiol	CC1=CC23CC1CCC2C1(C)CCCC(C)(CO)C1CC3O	2499.6	Standard non polar	33892256
Sideridiol	CC1=CC23CC1CCC2C1(C)CCCC(C)(CO)C1CC3O	2575.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Sideridiol,1TMS,isomer #1	CC1=CC23CC1CCC2C1(C)CCCC(C)(CO[Si](C)(C)C)C1CC3O	2565.7	Semi standard non polar	33892256
Sideridiol,1TMS,isomer #2	CC1=CC23CC1CCC2C1(C)CCCC(C)(CO)C1CC3O[Si](C)(C)C	2567.5	Semi standard non polar	33892256
Sideridiol,2TMS,isomer #1	CC1=CC23CC1CCC2C1(C)CCCC(C)(CO[Si](C)(C)C)C1CC3O[Si](C)(C)C	2483.3	Semi standard non polar	33892256
Sideridiol,1TBDMS,isomer #1	CC1=CC23CC1CCC2C1(C)CCCC(C)(CO[Si](C)(C)C(C)(C)C)C1CC3O	2826.3	Semi standard non polar	33892256
Sideridiol,1TBDMS,isomer #2	CC1=CC23CC1CCC2C1(C)CCCC(C)(CO)C1CC3O[Si](C)(C)C(C)(C)C	2800.4	Semi standard non polar	33892256
Sideridiol,2TBDMS,isomer #1	CC1=CC23CC1CCC2C1(C)CCCC(C)(CO[Si](C)(C)C(C)(C)C)C1CC3O[Si](C)(C)C(C)(C)C	2987.9	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Sideridiol GC-MS (Non-derivatized) - 70eV, Positive	splash10-000i-0590000000-91bb8ba8b72e91180d72	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Sideridiol GC-MS (2 TMS) - 70eV, Positive	splash10-0089-4257900000-41beaf433288cdf22c6d	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Sideridiol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Sideridiol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Sideridiol 10V, Positive-QTOF	splash10-052r-0093000000-30ffd985077cc5756881	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Sideridiol 20V, Positive-QTOF	splash10-00kr-0190000000-58ca6562fd16642180d3	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Sideridiol 40V, Positive-QTOF	splash10-06dl-5690000000-8b2b3a453f906d6c3041	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Sideridiol 10V, Negative-QTOF	splash10-0udi-0059000000-b2b1a05bef1a9ea2e377	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Sideridiol 20V, Negative-QTOF	splash10-0uki-0094000000-c4a83de10f63f78a1fbb	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Sideridiol 40V, Negative-QTOF	splash10-0ab9-0090000000-acd2b0b4cb58b0ffbf4a	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Sideridiol 10V, Negative-QTOF	splash10-0udi-0009000000-f9d10b76ade80bd401ad	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Sideridiol 20V, Negative-QTOF	splash10-0udi-0009000000-f9d10b76ade80bd401ad	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Sideridiol 40V, Negative-QTOF	splash10-0udi-0029000000-a6d4533d8c8f1e2c9d58	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Sideridiol 10V, Positive-QTOF	splash10-0abi-0097000000-f0bd5296cd651471ba2f	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Sideridiol 20V, Positive-QTOF	splash10-0ab9-0897000000-4b4a0c4d66412c97a0dd	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Sideridiol 40V, Positive-QTOF	splash10-00dl-4943000000-84fceb022f7afbd8f031	2021-09-23	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB015638

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

12315540

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for Sideridiol (HMDB0036702)

MOL for HMDB0036702 (Sideridiol)

3D MOL for HMDB0036702 (Sideridiol)

3D SDF for HMDB0036702 (Sideridiol)

3D-SDF for HMDB0036702 (Sideridiol)

PDB for HMDB0036702 (Sideridiol)

3D PDB for HMDB0036702 (Sideridiol)

SMILES for HMDB0036702 (Sideridiol)

INCHI for HMDB0036702 (Sideridiol)

Structure for HMDB0036702 (Sideridiol)

3D Structure for HMDB0036702 (Sideridiol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra