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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 20:03:18 UTC

Update Date

2022-03-07 02:54:22 UTC

HMDB ID

HMDB0035111

Secondary Accession Numbers

HMDB35111

Metabolite Identification

Common Name

(3beta,21alphaH)-22(30)-Hopene-3,29-diol

Description

(3beta,21alphaH)-22(30)-Hopene-3,29-diol belongs to the class of organic compounds known as hopanoids. These are terpenoids containing hopane skeleton(A'-Neogammacerane), a pentacyclic structure with four cyclohexane rings and one cyclopentane ring (and often, a side chain emerging from C30) (3beta,21alphaH)-22(30)-Hopene-3,29-diol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

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


  Mrv0541 05061308142D          

 32 36  0  0  0  0            999 V2000
    6.8034    1.2031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4137   -1.5822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3531   -1.5983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7271    2.4579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5568    1.1148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7001    0.0014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9834    1.0600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9731    1.9615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2649    1.5382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3801    2.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.3025   -0.9365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1406    0.2682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5610    2.7927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8487    0.6916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4269    0.3334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.5550   -0.9800    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0  0  0  0
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 30 29  1  0  0  0  0
 31 18  1  0  0  0  0
 32 25  1  0  0  0  0
M  END

HMDB0035111
     RDKit          3D
(3beta,21alphaH)-22(30)-Hopene-3,29-diol
 82 86  0  0  0  0  0  0  0  0999 V2000
    6.3782    0.8980   -0.0116 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv0541 05061308142D          

 32 36  0  0  0  0            999 V2000
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 27 14  1  0  0  0  0
 27 21  1  0  0  0  0
 27 23  1  0  0  0  0
 28  5  1  0  0  0  0
 28 15  1  0  0  0  0
 28 22  1  0  0  0  0
 28 24  1  0  0  0  0
 29  6  1  0  0  0  0
 29 16  1  0  0  0  0
 29 23  1  0  0  0  0
 30  7  1  0  0  0  0
 30 17  1  0  0  0  0
 30 24  1  0  0  0  0
 30 29  1  0  0  0  0
 31 18  1  0  0  0  0
 32 25  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0035111

> <DATABASE_NAME>
hmdb

> <SMILES>
CC12CCC(C1CCC1(C)C2CCC2C3(C)CCC(O)C(C)(C)C3CCC12C)C(=C)CO

> <INCHI_IDENTIFIER>
InChI=1S/C30H50O2/c1-19(18-31)20-10-14-27(4)21(20)11-16-29(6)23(27)8-9-24-28(5)15-13-25(32)26(2,3)22(28)12-17-30(24,29)7/h20-25,31-32H,1,8-18H2,2-7H3

> <INCHI_KEY>
SUMUIPKPDFCHLW-UHFFFAOYSA-N

> <FORMULA>
C30H50O2

> <MOLECULAR_WEIGHT>
442.7168

> <EXACT_MASS>
442.381080844

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
55.24387079747561

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-(3-hydroxyprop-1-en-2-yl)-1,2,9,14,18,18-hexamethylpentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-17-ol

> <ALOGPS_LOGP>
5.79

> <JCHEM_LOGP>
6.167275324333334

> <ALOGPS_LOGS>
-6.13

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.48943339017772

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.881471159352557

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8047961541041347

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
132.68299999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.29e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-(3-hydroxyprop-1-en-2-yl)-1,2,9,14,18,18-hexamethylpentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-17-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0035111
     RDKit          3D
(3beta,21alphaH)-22(30)-Hopene-3,29-diol
 82 86  0  0  0  0  0  0  0  0999 V2000
    6.3782    0.8980   -0.0116 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2160    1.4395    0.4432 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3818    2.1850    1.7142 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6956    1.7773    2.7995 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9786    1.3907   -0.2897 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1367    0.8645   -1.7327 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7263    0.3448   -2.0863 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5339   -0.4782   -0.7759 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5216   -1.5431   -0.8235 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7608    0.7171    0.1356 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3344    0.5764    1.5187 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8232    0.2321    1.4900 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6137   -1.0948    0.7654 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4905   -2.0452    1.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1113   -0.8541   -0.6202 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6583   -1.9276   -1.5734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8300   -1.6851   -1.7395 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5844   -1.6478   -0.4492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8005   -0.7265   -0.4958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0456   -1.3930    0.0668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0602   -0.2749   -1.9455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4231    0.3756   -2.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7295    1.2952   -0.9330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9104    0.9297   -0.2345 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5985    1.6104   -0.0140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2628    1.9999    1.3231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9564    2.9468   -0.4471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5706    0.5849    0.2190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1992    0.3269    1.6463 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6157   -0.9900    1.9285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7798   -1.6091    0.7961 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7256   -3.0787    1.3069 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4986    0.3289   -0.8918 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2572    1.0843    0.6125 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1304    3.2935    1.5388 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4850    2.2546    1.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1671    1.7666    3.6472 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7589    2.5155   -0.5239 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8595    0.0578   -1.7760 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4454    1.6349   -2.4372 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7673   -0.3026   -2.9549 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0509    1.1955   -2.1190 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9877   -2.5362   -0.6806 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4103   -1.4562   -0.1873 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9490   -1.7299   -1.8620 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9178    1.4097   -0.2823 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8733   -0.0080    2.2283 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2771    1.6357    1.9406 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5293    0.2459    2.5245 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4343    1.0234    0.8422 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5570   -1.8356    1.5409 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2031   -1.8756    2.6373 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3848   -3.0996    1.2478 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5551    0.0826   -0.9483 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1440   -1.7142   -2.5513 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9201   -2.9362   -1.2924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8608   -0.7197   -2.3167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1689   -2.4429   -2.4780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1143   -2.6616   -0.4778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3984   -0.9824    1.0059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7367   -2.4589    0.3029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8382   -1.5543   -0.6906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9893   -1.0887   -2.6565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3596    0.5876   -2.1681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3885    0.9284   -3.0537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2433   -0.3686   -2.2657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0518    2.2805   -1.3973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4735    0.3696   -0.8306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5398    2.4036    2.0347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9147    2.8802    1.0367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9488    1.2422    1.6918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7179    3.7328   -0.4795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2164    3.1764    0.3538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4344    2.8585   -1.3941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6266    0.9680   -0.2825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6156    1.2049    2.0596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1677    0.4143    2.2306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0198   -0.9961    2.8677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4597   -1.7028    2.1857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8273   -3.3306    1.4191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3359   -3.1594    2.3064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3840   -3.7628    0.5406 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 25 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 10  5  1  0
 31 13  1  0
 15  8  1  0
 31 18  1  0
 28 19  1  0
  1 33  1  0
  1 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  5 38  1  0
  6 39  1  0
  6 40  1  0
  7 41  1  0
  7 42  1  0
  9 43  1  0
  9 44  1  0
  9 45  1  0
 10 46  1  0
 11 47  1  0
 11 48  1  0
 12 49  1  0
 12 50  1  0
 14 51  1  0
 14 52  1  0
 14 53  1  0
 15 54  1  0
 16 55  1  0
 16 56  1  0
 17 57  1  0
 17 58  1  0
 18 59  1  0
 20 60  1  0
 20 61  1  0
 20 62  1  0
 21 63  1  0
 21 64  1  0
 22 65  1  0
 22 66  1  0
 23 67  1  0
 24 68  1  0
 26 69  1  0
 26 70  1  0
 26 71  1  0
 27 72  1  0
 27 73  1  0
 27 74  1  0
 28 75  1  0
 29 76  1  0
 29 77  1  0
 30 78  1  0
 30 79  1  0
 32 80  1  0
 32 81  1  0
 32 82  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      12.700   2.246   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.639  -2.953   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.659  -2.983   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.957   4.588   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.906   2.081   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.907   0.003   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.569   1.979   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.550   3.661   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.228   2.871   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.043   5.397   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.585   1.413   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.298  -1.748   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.262   0.501   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.514   5.213   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.584   1.291   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.264   0.622   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.620  -0.958   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      13.215   4.863   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.202   3.703   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.691   4.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.562   2.952   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.953  -0.999   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.895   2.912   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.251   1.331   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.286  -1.039   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.631  -1.789   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.217   3.702   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.930   0.541   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.918   1.372   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.596   0.582   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      14.726   4.566   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      -1.036  -1.829   0.000  0.00  0.00           O+0
CONECT    1   19                                                            
CONECT    2   26                                                            
CONECT    3   26                                                            
CONECT    4   27                                                            
CONECT    5   28                                                            
CONECT    6   29                                                            
CONECT    7   30                                                            
CONECT    8    9   23                                                       
CONECT    9    8   24                                                       
CONECT   10   14   20                                                       
CONECT   11   16   21                                                       
CONECT   12   17   22                                                       
CONECT   13   15   25                                                       
CONECT   14   10   27                                                       
CONECT   15   13   28                                                       
CONECT   16   11   29                                                       
CONECT   17   12   30                                                       
CONECT   18   19   31                                                       
CONECT   19    1   18   20                                                  
CONECT   20   10   19   21                                                  
CONECT   21   11   20   27                                                  
CONECT   22   12   26   28                                                  
CONECT   23    8   27   29                                                  
CONECT   24    9   28   30                                                  
CONECT   25   13   26   32                                                  
CONECT   26    2    3   22   25                                             
CONECT   27    4   14   21   23                                             
CONECT   28    5   15   22   24                                             
CONECT   29    6   16   23   30                                             
CONECT   30    7   17   24   29                                             
CONECT   31   18                                                            
CONECT   32   25                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

COMPND    HMDB0035111
HETATM    1  C1  UNL     1       6.378   0.898  -0.012  1.00  0.00           C  
HETATM    2  C2  UNL     1       5.216   1.440   0.443  1.00  0.00           C  
HETATM    3  C3  UNL     1       5.382   2.185   1.714  1.00  0.00           C  
HETATM    4  O1  UNL     1       4.696   1.777   2.799  1.00  0.00           O  
HETATM    5  C4  UNL     1       3.979   1.391  -0.290  1.00  0.00           C  
HETATM    6  C5  UNL     1       4.137   0.865  -1.733  1.00  0.00           C  
HETATM    7  C6  UNL     1       2.726   0.345  -2.086  1.00  0.00           C  
HETATM    8  C7  UNL     1       2.534  -0.478  -0.776  1.00  0.00           C  
HETATM    9  C8  UNL     1       3.522  -1.543  -0.823  1.00  0.00           C  
HETATM   10  C9  UNL     1       2.761   0.717   0.136  1.00  0.00           C  
HETATM   11  C10 UNL     1       2.334   0.576   1.519  1.00  0.00           C  
HETATM   12  C11 UNL     1       0.823   0.232   1.490  1.00  0.00           C  
HETATM   13  C12 UNL     1       0.614  -1.095   0.765  1.00  0.00           C  
HETATM   14  C13 UNL     1       1.491  -2.045   1.572  1.00  0.00           C  
HETATM   15  C14 UNL     1       1.111  -0.854  -0.620  1.00  0.00           C  
HETATM   16  C15 UNL     1       0.658  -1.928  -1.573  1.00  0.00           C  
HETATM   17  C16 UNL     1      -0.830  -1.685  -1.739  1.00  0.00           C  
HETATM   18  C17 UNL     1      -1.584  -1.648  -0.449  1.00  0.00           C  
HETATM   19  C18 UNL     1      -2.801  -0.727  -0.496  1.00  0.00           C  
HETATM   20  C19 UNL     1      -4.046  -1.393   0.067  1.00  0.00           C  
HETATM   21  C20 UNL     1      -3.060  -0.275  -1.945  1.00  0.00           C  
HETATM   22  C21 UNL     1      -4.423   0.376  -2.061  1.00  0.00           C  
HETATM   23  C22 UNL     1      -4.730   1.295  -0.933  1.00  0.00           C  
HETATM   24  O2  UNL     1      -5.910   0.930  -0.234  1.00  0.00           O  
HETATM   25  C23 UNL     1      -3.598   1.610  -0.014  1.00  0.00           C  
HETATM   26  C24 UNL     1      -4.263   2.000   1.323  1.00  0.00           C  
HETATM   27  C25 UNL     1      -2.956   2.947  -0.447  1.00  0.00           C  
HETATM   28  C26 UNL     1      -2.571   0.585   0.219  1.00  0.00           C  
HETATM   29  C27 UNL     1      -2.199   0.327   1.646  1.00  0.00           C  
HETATM   30  C28 UNL     1      -1.616  -0.990   1.929  1.00  0.00           C  
HETATM   31  C29 UNL     1      -0.780  -1.609   0.796  1.00  0.00           C  
HETATM   32  C30 UNL     1      -0.726  -3.079   1.307  1.00  0.00           C  
HETATM   33  H1  UNL     1       6.499   0.329  -0.892  1.00  0.00           H  
HETATM   34  H2  UNL     1       7.257   1.084   0.612  1.00  0.00           H  
HETATM   35  H3  UNL     1       5.130   3.293   1.539  1.00  0.00           H  
HETATM   36  H4  UNL     1       6.485   2.255   1.997  1.00  0.00           H  
HETATM   37  H5  UNL     1       5.167   1.767   3.647  1.00  0.00           H  
HETATM   38  H6  UNL     1       3.759   2.516  -0.524  1.00  0.00           H  
HETATM   39  H7  UNL     1       4.860   0.058  -1.776  1.00  0.00           H  
HETATM   40  H8  UNL     1       4.445   1.635  -2.437  1.00  0.00           H  
HETATM   41  H9  UNL     1       2.767  -0.303  -2.955  1.00  0.00           H  
HETATM   42  H10 UNL     1       2.051   1.196  -2.119  1.00  0.00           H  
HETATM   43  H11 UNL     1       2.988  -2.536  -0.681  1.00  0.00           H  
HETATM   44  H12 UNL     1       4.410  -1.456  -0.187  1.00  0.00           H  
HETATM   45  H13 UNL     1       3.949  -1.730  -1.862  1.00  0.00           H  
HETATM   46  H14 UNL     1       1.918   1.410  -0.282  1.00  0.00           H  
HETATM   47  H15 UNL     1       2.873  -0.008   2.228  1.00  0.00           H  
HETATM   48  H16 UNL     1       2.277   1.636   1.941  1.00  0.00           H  
HETATM   49  H17 UNL     1       0.529   0.246   2.524  1.00  0.00           H  
HETATM   50  H18 UNL     1       0.434   1.023   0.842  1.00  0.00           H  
HETATM   51  H19 UNL     1       2.557  -1.836   1.541  1.00  0.00           H  
HETATM   52  H20 UNL     1       1.203  -1.876   2.637  1.00  0.00           H  
HETATM   53  H21 UNL     1       1.385  -3.100   1.248  1.00  0.00           H  
HETATM   54  H22 UNL     1       0.555   0.083  -0.948  1.00  0.00           H  
HETATM   55  H23 UNL     1       1.144  -1.714  -2.551  1.00  0.00           H  
HETATM   56  H24 UNL     1       0.920  -2.936  -1.292  1.00  0.00           H  
HETATM   57  H25 UNL     1      -0.861  -0.720  -2.317  1.00  0.00           H  
HETATM   58  H26 UNL     1      -1.169  -2.443  -2.478  1.00  0.00           H  
HETATM   59  H27 UNL     1      -2.114  -2.662  -0.478  1.00  0.00           H  
HETATM   60  H28 UNL     1      -4.398  -0.982   1.006  1.00  0.00           H  
HETATM   61  H29 UNL     1      -3.737  -2.459   0.303  1.00  0.00           H  
HETATM   62  H30 UNL     1      -4.838  -1.554  -0.691  1.00  0.00           H  
HETATM   63  H31 UNL     1      -2.989  -1.089  -2.657  1.00  0.00           H  
HETATM   64  H32 UNL     1      -2.360   0.588  -2.168  1.00  0.00           H  
HETATM   65  H33 UNL     1      -4.388   0.928  -3.054  1.00  0.00           H  
HETATM   66  H34 UNL     1      -5.243  -0.369  -2.266  1.00  0.00           H  
HETATM   67  H35 UNL     1      -5.052   2.281  -1.397  1.00  0.00           H  
HETATM   68  H36 UNL     1      -6.473   0.370  -0.831  1.00  0.00           H  
HETATM   69  H37 UNL     1      -3.540   2.404   2.035  1.00  0.00           H  
HETATM   70  H38 UNL     1      -4.915   2.880   1.037  1.00  0.00           H  
HETATM   71  H39 UNL     1      -4.949   1.242   1.692  1.00  0.00           H  
HETATM   72  H40 UNL     1      -3.718   3.733  -0.479  1.00  0.00           H  
HETATM   73  H41 UNL     1      -2.216   3.176   0.354  1.00  0.00           H  
HETATM   74  H42 UNL     1      -2.434   2.859  -1.394  1.00  0.00           H  
HETATM   75  H43 UNL     1      -1.627   0.968  -0.283  1.00  0.00           H  
HETATM   76  H44 UNL     1      -1.616   1.205   2.060  1.00  0.00           H  
HETATM   77  H45 UNL     1      -3.168   0.414   2.231  1.00  0.00           H  
HETATM   78  H46 UNL     1      -1.020  -0.996   2.868  1.00  0.00           H  
HETATM   79  H47 UNL     1      -2.460  -1.703   2.186  1.00  0.00           H  
HETATM   80  H48 UNL     1      -1.827  -3.331   1.419  1.00  0.00           H  
HETATM   81  H49 UNL     1      -0.336  -3.159   2.306  1.00  0.00           H  
HETATM   82  H50 UNL     1      -0.384  -3.763   0.541  1.00  0.00           H  
CONECT    1    2    2   33   34
CONECT    2    3    5
CONECT    3    4   35   36
CONECT    4   37
CONECT    5    6   10   38
CONECT    6    7   39   40
CONECT    7    8   41   42
CONECT    8    9   10   15
CONECT    9   43   44   45
CONECT   10   11   46
CONECT   11   12   47   48
CONECT   12   13   49   50
CONECT   13   14   15   31
CONECT   14   51   52   53
CONECT   15   16   54
CONECT   16   17   55   56
CONECT   17   18   57   58
CONECT   18   19   31   59
CONECT   19   20   21   28
CONECT   20   60   61   62
CONECT   21   22   63   64
CONECT   22   23   65   66
CONECT   23   24   25   67
CONECT   24   68
CONECT   25   26   27   28
CONECT   26   69   70   71
CONECT   27   72   73   74
CONECT   28   29   75
CONECT   29   30   76   77
CONECT   30   31   78   79
CONECT   31   32
CONECT   32   80   81   82
END

HMDB0035111
     RDKit          3D
(3beta,21alphaH)-22(30)-Hopene-3,29-diol
 82 86  0  0  0  0  0  0  0  0999 V2000
    6.3782    0.8980   -0.0116 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2160    1.4395    0.4432 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3818    2.1850    1.7142 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6956    1.7773    2.7995 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9786    1.3907   -0.2897 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1367    0.8645   -1.7327 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7263    0.3448   -2.0863 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5339   -0.4782   -0.7759 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5216   -1.5431   -0.8235 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7608    0.7171    0.1356 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3344    0.5764    1.5187 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8232    0.2321    1.4900 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6137   -1.0948    0.7654 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4905   -2.0452    1.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1113   -0.8541   -0.6202 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6583   -1.9276   -1.5734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8300   -1.6851   -1.7395 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5844   -1.6478   -0.4492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8005   -0.7265   -0.4958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0456   -1.3930    0.0668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0602   -0.2749   -1.9455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4231    0.3756   -2.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7295    1.2952   -0.9330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9104    0.9297   -0.2345 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5985    1.6104   -0.0140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2628    1.9999    1.3231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9564    2.9468   -0.4471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5706    0.5849    0.2190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1992    0.3269    1.6463 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6157   -0.9900    1.9285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7798   -1.6091    0.7961 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7256   -3.0787    1.3069 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4986    0.3289   -0.8918 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2572    1.0843    0.6125 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1304    3.2935    1.5388 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4850    2.2546    1.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1671    1.7666    3.6472 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7589    2.5155   -0.5239 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8595    0.0578   -1.7760 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4454    1.6349   -2.4372 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7673   -0.3026   -2.9549 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0509    1.1955   -2.1190 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9877   -2.5362   -0.6806 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4103   -1.4562   -0.1873 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9490   -1.7299   -1.8620 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9178    1.4097   -0.2823 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8733   -0.0080    2.2283 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2771    1.6357    1.9406 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5293    0.2459    2.5245 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4343    1.0234    0.8422 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5570   -1.8356    1.5409 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2031   -1.8756    2.6373 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3848   -3.0996    1.2478 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5551    0.0826   -0.9483 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1440   -1.7142   -2.5513 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9201   -2.9362   -1.2924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8608   -0.7197   -2.3167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1689   -2.4429   -2.4780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1143   -2.6616   -0.4778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3984   -0.9824    1.0059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7367   -2.4589    0.3029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8382   -1.5543   -0.6906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9893   -1.0887   -2.6565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3596    0.5876   -2.1681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3885    0.9284   -3.0537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2433   -0.3686   -2.2657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0518    2.2805   -1.3973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4735    0.3696   -0.8306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5398    2.4036    2.0347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9147    2.8802    1.0367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9488    1.2422    1.6918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7179    3.7328   -0.4795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2164    3.1764    0.3538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4344    2.8585   -1.3941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6266    0.9680   -0.2825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6156    1.2049    2.0596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1677    0.4143    2.2306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0198   -0.9961    2.8677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4597   -1.7028    2.1857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8273   -3.3306    1.4191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3359   -3.1594    2.3064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3840   -3.7628    0.5406 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 25 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 10  5  1  0
 31 13  1  0
 15  8  1  0
 31 18  1  0
 28 19  1  0
  1 33  1  0
  1 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  5 38  1  0
  6 39  1  0
  6 40  1  0
  7 41  1  0
  7 42  1  0
  9 43  1  0
  9 44  1  0
  9 45  1  0
 10 46  1  0
 11 47  1  0
 11 48  1  0
 12 49  1  0
 12 50  1  0
 14 51  1  0
 14 52  1  0
 14 53  1  0
 15 54  1  0
 16 55  1  0
 16 56  1  0
 17 57  1  0
 17 58  1  0
 18 59  1  0
 20 60  1  0
 20 61  1  0
 20 62  1  0
 21 63  1  0
 21 64  1  0
 22 65  1  0
 22 66  1  0
 23 67  1  0
 24 68  1  0
 26 69  1  0
 26 70  1  0
 26 71  1  0
 27 72  1  0
 27 73  1  0
 27 74  1  0
 28 75  1  0
 29 76  1  0
 29 77  1  0
 30 78  1  0
 30 79  1  0
 32 80  1  0
 32 81  1  0
 32 82  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(3b,21AlphaH)-22(30)-hopene-3,29-diol	Generator
(3Β,21alphah)-22(30)-hopene-3,29-diol	Generator

Chemical Formula

C₃₀H₅₀O₂

Average Molecular Weight

442.7168

Monoisotopic Molecular Weight

442.381080844

IUPAC Name

6-(3-hydroxyprop-1-en-2-yl)-1,2,9,14,18,18-hexamethylpentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-17-ol

Traditional Name

6-(3-hydroxyprop-1-en-2-yl)-1,2,9,14,18,18-hexamethylpentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-17-ol

CAS Registry Number

62498-82-2

SMILES

CC12CCC(C1CCC1(C)C2CCC2C3(C)CCC(O)C(C)(C)C3CCC12C)C(=C)CO

InChI Identifier

InChI=1S/C30H50O2/c1-19(18-31)20-10-14-27(4)21(20)11-16-29(6)23(27)8-9-24-28(5)15-13-25(32)26(2,3)22(28)12-17-30(24,29)7/h20-25,31-32H,1,8-18H2,2-7H3

InChI Key

SUMUIPKPDFCHLW-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hopanoids. These are terpenoids containing hopane skeleton(A'-Neogammacerane), a pentacyclic structure with four cyclohexane rings and one cyclopentane ring (and often, a side chain emerging from C30).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Hopanoids

Direct Parent

Hopanoids

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: HMDB0035111)
Cell membrane (HMDB: HMDB0035111)

Cellular substructure

Extracellular (HMDB: HMDB0035111)
Membrane (HMDB: HMDB0035111)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0035111)

Source

Endogenous

Endogenous (HMDB: HMDB0035111)

Plant

Plant (HMDB: HMDB0035111)

Animal

Animal (HMDB: HMDB0035111)

Exogenous

Food

Food (HMDB: HMDB0035111)

Fruit

Fruits (FooDB: FOOD00871)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0035111)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0035111)

Cellular process

Cell signaling (HMDB: HMDB0035111)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0035111)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0035111)

Nutrient

Nutrient (HMDB: HMDB0035111)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0035111)

Emulsifier (HMDB: HMDB0035111)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	253 - 254 °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	0.00033 g/L	ALOGPS
logP	5.79	ALOGPS
logP	6.17	ChemAxon
logS	-6.1	ALOGPS
pKa (Strongest Acidic)	16.88	ChemAxon
pKa (Strongest Basic)	-0.8	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	2	ChemAxon
Refractivity	132.68 m³·mol⁻¹	ChemAxon
Polarizability	55.24 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	202.404	31661259
DarkChem	[M-H]-	196.786	31661259
DeepCCS	[M-2H]-	241.831	30932474
DeepCCS	[M+Na]+	217.059	30932474
AllCCS	[M+H]+	216.0	32859911
AllCCS	[M+H-H2O]+	214.3	32859911
AllCCS	[M+NH4]+	217.6	32859911
AllCCS	[M+Na]+	218.0	32859911
AllCCS	[M-H]-	209.7	32859911
AllCCS	[M+Na-2H]-	211.8	32859911
AllCCS	[M+HCOO]-	214.2	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(3beta,21alphaH)-22(30)-Hopene-3,29-diol	CC12CCC(C1CCC1(C)C2CCC2C3(C)CCC(O)C(C)(C)C3CCC12C)C(=C)CO	2421.4	Standard polar	33892256
(3beta,21alphaH)-22(30)-Hopene-3,29-diol	CC12CCC(C1CCC1(C)C2CCC2C3(C)CCC(O)C(C)(C)C3CCC12C)C(=C)CO	3450.5	Standard non polar	33892256
(3beta,21alphaH)-22(30)-Hopene-3,29-diol	CC12CCC(C1CCC1(C)C2CCC2C3(C)CCC(O)C(C)(C)C3CCC12C)C(=C)CO	3764.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
(3beta,21alphaH)-22(30)-Hopene-3,29-diol,1TMS,isomer #1	C=C(CO)C1CCC2(C)C1CCC1(C)C2CCC2C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3CCC21C	3648.3	Semi standard non polar	33892256
(3beta,21alphaH)-22(30)-Hopene-3,29-diol,1TMS,isomer #2	C=C(CO[Si](C)(C)C)C1CCC2(C)C1CCC1(C)C2CCC2C3(C)CCC(O)C(C)(C)C3CCC21C	3691.5	Semi standard non polar	33892256
(3beta,21alphaH)-22(30)-Hopene-3,29-diol,2TMS,isomer #1	C=C(CO[Si](C)(C)C)C1CCC2(C)C1CCC1(C)C2CCC2C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3CCC21C	3639.7	Semi standard non polar	33892256
(3beta,21alphaH)-22(30)-Hopene-3,29-diol,1TBDMS,isomer #1	C=C(CO)C1CCC2(C)C1CCC1(C)C2CCC2C3(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C3CCC21C	3866.7	Semi standard non polar	33892256
(3beta,21alphaH)-22(30)-Hopene-3,29-diol,1TBDMS,isomer #2	C=C(CO[Si](C)(C)C(C)(C)C)C1CCC2(C)C1CCC1(C)C2CCC2C3(C)CCC(O)C(C)(C)C3CCC21C	3917.5	Semi standard non polar	33892256
(3beta,21alphaH)-22(30)-Hopene-3,29-diol,2TBDMS,isomer #1	C=C(CO[Si](C)(C)C(C)(C)C)C1CCC2(C)C1CCC1(C)C2CCC2C3(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C3CCC21C	4127.4	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 - (3beta,21alphaH)-22(30)-Hopene-3,29-diol GC-MS (Non-derivatized) - 70eV, Positive	splash10-03fr-0115900000-5c0ba017218a5693f9be	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (3beta,21alphaH)-22(30)-Hopene-3,29-diol GC-MS (2 TMS) - 70eV, Positive	splash10-00di-1021390000-180be04482a37cc09b6e	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (3beta,21alphaH)-22(30)-Hopene-3,29-diol 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 - (3beta,21alphaH)-22(30)-Hopene-3,29-diol 10V, Positive-QTOF	splash10-004l-0001900000-1fd9a3d27ae4d00de50b	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,21alphaH)-22(30)-Hopene-3,29-diol 20V, Positive-QTOF	splash10-056r-0125900000-ac24cf5e8fdb5133c924	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,21alphaH)-22(30)-Hopene-3,29-diol 40V, Positive-QTOF	splash10-014s-1589200000-78edcc9133d754b89057	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,21alphaH)-22(30)-Hopene-3,29-diol 10V, Negative-QTOF	splash10-0006-0000900000-b541eaebee1498f7074d	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,21alphaH)-22(30)-Hopene-3,29-diol 20V, Negative-QTOF	splash10-006x-0001900000-ca18f2035f17a5f8cad2	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,21alphaH)-22(30)-Hopene-3,29-diol 40V, Negative-QTOF	splash10-06tb-2009700000-e7a4892385c646923f6e	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,21alphaH)-22(30)-Hopene-3,29-diol 10V, Positive-QTOF	splash10-0006-0033900000-3f89ab240b3b8c01a626	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,21alphaH)-22(30)-Hopene-3,29-diol 20V, Positive-QTOF	splash10-0ku2-6379400000-7970d8cd8a45866b86ae	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,21alphaH)-22(30)-Hopene-3,29-diol 40V, Positive-QTOF	splash10-00ls-9422000000-66ab1b893fce1a9a4871	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,21alphaH)-22(30)-Hopene-3,29-diol 10V, Negative-QTOF	splash10-0006-0000900000-849799f7ece1fdb1b84b	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,21alphaH)-22(30)-Hopene-3,29-diol 20V, Negative-QTOF	splash10-0006-0000900000-72d806996a9d634a63d3	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,21alphaH)-22(30)-Hopene-3,29-diol 40V, Negative-QTOF	splash10-052f-0000900000-9c41beaf630cfa958375	2021-09-22	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

FDB013742

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

131751667

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 (3beta,21alphaH)-22(30)-Hopene-3,29-diol (HMDB0035111)

MOL for HMDB0035111 ((3beta,21alphaH)-22(30)-Hopene-3,29-diol)

3D MOL for HMDB0035111 ((3beta,21alphaH)-22(30)-Hopene-3,29-diol)

3D SDF for HMDB0035111 ((3beta,21alphaH)-22(30)-Hopene-3,29-diol)

3D-SDF for HMDB0035111 ((3beta,21alphaH)-22(30)-Hopene-3,29-diol)

PDB for HMDB0035111 ((3beta,21alphaH)-22(30)-Hopene-3,29-diol)

3D PDB for HMDB0035111 ((3beta,21alphaH)-22(30)-Hopene-3,29-diol)

SMILES for HMDB0035111 ((3beta,21alphaH)-22(30)-Hopene-3,29-diol)

INCHI for HMDB0035111 ((3beta,21alphaH)-22(30)-Hopene-3,29-diol)

Structure for HMDB0035111 ((3beta,21alphaH)-22(30)-Hopene-3,29-diol)

3D Structure for HMDB0035111 ((3beta,21alphaH)-22(30)-Hopene-3,29-diol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra