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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 21:52:20 UTC

Update Date

2022-03-07 02:55:01 UTC

HMDB ID

HMDB0036705

Secondary Accession Numbers

HMDB36705

Metabolite Identification

Common Name

Ucriol

Description

Ucriol 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. Based on a literature review a small amount of articles have been published on Ucriol.

Structure

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

HMDB0036705
     RDKit          3D
Ucriol
 55 59  0  0  0  0  0  0  0  0999 V2000
   -3.5008   -0.1664   -1.2220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6573    0.4858   -0.1995 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8922    2.0007   -0.3156 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1132    2.6672    0.6350 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1562    0.0983    1.1719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0442   -0.4245    2.0632 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4443   -1.6058    1.2972 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7248   -1.1089    0.0981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0681   -2.0489   -1.0678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1888    0.2759   -0.3014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6054    0.7014   -1.6010 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7262    0.1368   -1.9328 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4516    1.1338   -2.6286 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4755   -0.1812   -0.7070 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8136   -0.8916   -0.9677 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4828   -0.6191    0.3797 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7587   -1.2675    1.5286 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3005   -0.7783    1.5995 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7530   -1.1110    0.2376 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2180    0.8834    0.4966 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8890    1.6541    1.5905 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2264    1.5485   -0.7449 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9549    1.0910   -0.0661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5449    0.2557   -1.0944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2458    0.0405   -2.2684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6549   -1.2681   -1.0219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9587    2.1981   -0.0419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7403    2.3639   -1.3329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7025    3.4384    0.1538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7296    0.9065    1.6716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8893   -0.7581    1.0884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5226   -0.8088    2.9835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3101    0.3222    2.3440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8766   -2.2815    1.9502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3481   -2.2059    0.9753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4516   -1.5134   -1.9363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8306   -2.8025   -0.7662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1696   -2.6682   -1.3569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7414    0.9528    0.4913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5481    1.8304   -1.5799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2722    0.4931   -2.4855 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7052   -0.7308   -2.6307 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8382    1.8082   -3.0140 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4117   -0.3756   -1.7224 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6800   -1.9665   -1.1208 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5326   -0.8726    0.3997 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2418   -0.9520    2.4501 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7091   -2.3637    1.4611 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2883    0.3102    1.7616 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8463   -1.3084    2.4277 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0682   -2.1867    0.0578 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3927    2.6462    1.6513 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9045    1.1379    2.5538 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9351    1.8825    1.2304 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3285    2.0027   -0.0534 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  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
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 16 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 10  2  1  0
 19 14  1  0
 23 20  1  0
 19  8  1  0
 23 14  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  6 33  1  0
  7 34  1  0
  7 35  1  0
  9 36  1  0
  9 37  1  0
  9 38  1  0
 10 39  1  0
 11 40  1  0
 11 41  1  0
 12 42  1  0
 13 43  1  0
 15 44  1  0
 15 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 18 49  1  0
 18 50  1  0
 19 51  1  0
 21 52  1  0
 21 53  1  0
 21 54  1  0
 23 55  1  0
M  END


  Mrv0541 05061309172D          

 23 27  0  0  0  0            999 V2000
    4.1140    3.6566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4372    1.0422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0425    1.2439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9930    1.5898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9409    0.3920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7355    0.7080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1450    2.4007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2148    1.3161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1166    3.2101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7162    1.5029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1565    3.4612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2548    0.9229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8008    1.5746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7407    2.6639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3283    2.9377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2306    2.3294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5188    2.9377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5886    1.8532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7593    1.6523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1038    2.1149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0220    4.2750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7259    3.5014    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4086    2.3991    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
 12  5  1  0  0  0  0
 12 10  1  0  0  0  0
 13  6  1  0  0  0  0
 14  9  1  0  0  0  0
 15  9  1  0  0  0  0
 17  1  1  0  0  0  0
 17  7  1  0  0  0  0
 17 11  1  0  0  0  0
 17 14  1  0  0  0  0
 18  2  1  0  0  0  0
 18  8  1  0  0  0  0
 18 13  1  0  0  0  0
 18 14  1  0  0  0  0
 19  3  1  0  0  0  0
 19 12  1  0  0  0  0
 19 16  1  0  0  0  0
 20 10  1  0  0  0  0
 20 13  1  0  0  0  0
 20 15  1  0  0  0  0
 20 16  1  0  0  0  0
 21 11  1  0  0  0  0
 22 15  1  0  0  0  0
 23 16  1  0  0  0  0
 23 19  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0036705

> <DATABASE_NAME>
hmdb

> <SMILES>
CC12OC1C13CC2CCC1C1(C)CCCC(C)(CO)C1CC3O

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O3/c1-17(11-21)7-4-8-18(2)13-6-5-12-10-20(13,15(22)9-14(17)18)16-19(12,3)23-16/h12-16,21-22H,4-11H2,1-3H3

> <INCHI_KEY>
BDWKHKXSYDEDRO-UHFFFAOYSA-N

> <FORMULA>
C20H32O3

> <MOLECULAR_WEIGHT>
320.4663

> <EXACT_MASS>
320.23514489

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
36.70859641271105

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-ol

> <ALOGPS_LOGP>
2.52

> <JCHEM_LOGP>
2.3797019530000005

> <ALOGPS_LOGS>
-3.96

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.592293023693387

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.598159159211487

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2271006680627279

> <JCHEM_POLAR_SURFACE_AREA>
52.99

> <JCHEM_REFRACTIVITY>
88.53859999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.49e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0036705
     RDKit          3D
Ucriol
 55 59  0  0  0  0  0  0  0  0999 V2000
   -3.5008   -0.1664   -1.2220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6573    0.4858   -0.1995 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8922    2.0007   -0.3156 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1132    2.6672    0.6350 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1562    0.0983    1.1719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0442   -0.4245    2.0632 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4443   -1.6058    1.2972 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7248   -1.1089    0.0981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0681   -2.0489   -1.0678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1888    0.2759   -0.3014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6054    0.7014   -1.6010 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7262    0.1368   -1.9328 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4516    1.1338   -2.6286 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4755   -0.1812   -0.7070 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8136   -0.8916   -0.9677 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4828   -0.6191    0.3797 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7587   -1.2675    1.5286 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3005   -0.7783    1.5995 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7530   -1.1110    0.2376 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2180    0.8834    0.4966 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8890    1.6541    1.5905 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2264    1.5485   -0.7449 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9549    1.0910   -0.0661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5449    0.2557   -1.0944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2458    0.0405   -2.2684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6549   -1.2681   -1.0219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9587    2.1981   -0.0419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7403    2.3639   -1.3329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7025    3.4384    0.1538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7296    0.9065    1.6716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8893   -0.7581    1.0884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5226   -0.8088    2.9835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3101    0.3222    2.3440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8766   -2.2815    1.9502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3481   -2.2059    0.9753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4516   -1.5134   -1.9363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8306   -2.8025   -0.7662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1696   -2.6682   -1.3569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7414    0.9528    0.4913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5481    1.8304   -1.5799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2722    0.4931   -2.4855 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7052   -0.7308   -2.6307 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8382    1.8082   -3.0140 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4117   -0.3756   -1.7224 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6800   -1.9665   -1.1208 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5326   -0.8726    0.3997 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2418   -0.9520    2.4501 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7091   -2.3637    1.4611 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2883    0.3102    1.7616 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8463   -1.3084    2.4277 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0682   -2.1867    0.0578 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3927    2.6462    1.6513 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9045    1.1379    2.5538 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9351    1.8825    1.2304 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3285    2.0027   -0.0534 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  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
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 16 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 10  2  1  0
 19 14  1  0
 23 20  1  0
 19  8  1  0
 23 14  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  6 33  1  0
  7 34  1  0
  7 35  1  0
  9 36  1  0
  9 37  1  0
  9 38  1  0
 10 39  1  0
 11 40  1  0
 11 41  1  0
 12 42  1  0
 13 43  1  0
 15 44  1  0
 15 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 18 49  1  0
 18 50  1  0
 19 51  1  0
 21 52  1  0
 21 53  1  0
 21 54  1  0
 23 55  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       7.680   6.826   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.416   1.946   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.079   2.322   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.320   2.968   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.623   0.732   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.106   1.322   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.604   4.481   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.868   2.457   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.818   5.992   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.204   2.805   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.625   6.461   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.342   1.723   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.228   2.939   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.983   4.973   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.346   5.484   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.297   4.348   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.435   5.484   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.699   3.459   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.417   3.084   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.927   3.948   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.374   7.980   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       3.222   6.536   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       0.763   4.478   0.000  0.00  0.00           O+0
CONECT    1   17                                                            
CONECT    2   18                                                            
CONECT    3   19                                                            
CONECT    4    7    8                                                       
CONECT    5    6   12                                                       
CONECT    6    5   13                                                       
CONECT    7    4   17                                                       
CONECT    8    4   18                                                       
CONECT    9   14   15                                                       
CONECT   10   12   20                                                       
CONECT   11   17   21                                                       
CONECT   12    5   10   19                                                  
CONECT   13    6   18   20                                                  
CONECT   14    9   17   18                                                  
CONECT   15    9   20   22                                                  
CONECT   16   19   20   23                                                  
CONECT   17    1    7   11   14                                             
CONECT   18    2    8   13   14                                             
CONECT   19    3   12   16   23                                             
CONECT   20   10   13   15   16                                             
CONECT   21   11                                                            
CONECT   22   15                                                            
CONECT   23   16   19                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   54    0
END

COMPND    HMDB0036705
HETATM    1  C1  UNL     1      -3.501  -0.166  -1.222  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.657   0.486  -0.200  1.00  0.00           C  
HETATM    3  C3  UNL     1      -2.892   2.001  -0.316  1.00  0.00           C  
HETATM    4  O1  UNL     1      -2.113   2.667   0.635  1.00  0.00           O  
HETATM    5  C4  UNL     1      -3.156   0.098   1.172  1.00  0.00           C  
HETATM    6  C5  UNL     1      -2.044  -0.425   2.063  1.00  0.00           C  
HETATM    7  C6  UNL     1      -1.444  -1.606   1.297  1.00  0.00           C  
HETATM    8  C7  UNL     1      -0.725  -1.109   0.098  1.00  0.00           C  
HETATM    9  C8  UNL     1      -1.068  -2.049  -1.068  1.00  0.00           C  
HETATM   10  C9  UNL     1      -1.189   0.276  -0.301  1.00  0.00           C  
HETATM   11  C10 UNL     1      -0.605   0.701  -1.601  1.00  0.00           C  
HETATM   12  C11 UNL     1       0.726   0.137  -1.933  1.00  0.00           C  
HETATM   13  O2  UNL     1       1.452   1.134  -2.629  1.00  0.00           O  
HETATM   14  C12 UNL     1       1.475  -0.181  -0.707  1.00  0.00           C  
HETATM   15  C13 UNL     1       2.814  -0.892  -0.968  1.00  0.00           C  
HETATM   16  C14 UNL     1       3.483  -0.619   0.380  1.00  0.00           C  
HETATM   17  C15 UNL     1       2.759  -1.267   1.529  1.00  0.00           C  
HETATM   18  C16 UNL     1       1.300  -0.778   1.600  1.00  0.00           C  
HETATM   19  C17 UNL     1       0.753  -1.111   0.238  1.00  0.00           C  
HETATM   20  C18 UNL     1       3.218   0.883   0.497  1.00  0.00           C  
HETATM   21  C19 UNL     1       3.889   1.654   1.590  1.00  0.00           C  
HETATM   22  O3  UNL     1       3.226   1.549  -0.745  1.00  0.00           O  
HETATM   23  C20 UNL     1       1.955   1.091  -0.066  1.00  0.00           C  
HETATM   24  H1  UNL     1      -4.545   0.256  -1.094  1.00  0.00           H  
HETATM   25  H2  UNL     1      -3.246   0.041  -2.268  1.00  0.00           H  
HETATM   26  H3  UNL     1      -3.655  -1.268  -1.022  1.00  0.00           H  
HETATM   27  H4  UNL     1      -3.959   2.198  -0.042  1.00  0.00           H  
HETATM   28  H5  UNL     1      -2.740   2.364  -1.333  1.00  0.00           H  
HETATM   29  H6  UNL     1      -1.702   3.438   0.154  1.00  0.00           H  
HETATM   30  H7  UNL     1      -3.730   0.906   1.672  1.00  0.00           H  
HETATM   31  H8  UNL     1      -3.889  -0.758   1.088  1.00  0.00           H  
HETATM   32  H9  UNL     1      -2.523  -0.809   2.983  1.00  0.00           H  
HETATM   33  H10 UNL     1      -1.310   0.322   2.344  1.00  0.00           H  
HETATM   34  H11 UNL     1      -0.877  -2.282   1.950  1.00  0.00           H  
HETATM   35  H12 UNL     1      -2.348  -2.206   0.975  1.00  0.00           H  
HETATM   36  H13 UNL     1      -1.452  -1.513  -1.936  1.00  0.00           H  
HETATM   37  H14 UNL     1      -1.831  -2.802  -0.766  1.00  0.00           H  
HETATM   38  H15 UNL     1      -0.170  -2.668  -1.357  1.00  0.00           H  
HETATM   39  H16 UNL     1      -0.741   0.953   0.491  1.00  0.00           H  
HETATM   40  H17 UNL     1      -0.548   1.830  -1.580  1.00  0.00           H  
HETATM   41  H18 UNL     1      -1.272   0.493  -2.486  1.00  0.00           H  
HETATM   42  H19 UNL     1       0.705  -0.731  -2.631  1.00  0.00           H  
HETATM   43  H20 UNL     1       0.838   1.808  -3.014  1.00  0.00           H  
HETATM   44  H21 UNL     1       3.412  -0.376  -1.722  1.00  0.00           H  
HETATM   45  H22 UNL     1       2.680  -1.966  -1.121  1.00  0.00           H  
HETATM   46  H23 UNL     1       4.533  -0.873   0.400  1.00  0.00           H  
HETATM   47  H24 UNL     1       3.242  -0.952   2.450  1.00  0.00           H  
HETATM   48  H25 UNL     1       2.709  -2.364   1.461  1.00  0.00           H  
HETATM   49  H26 UNL     1       1.288   0.310   1.762  1.00  0.00           H  
HETATM   50  H27 UNL     1       0.846  -1.308   2.428  1.00  0.00           H  
HETATM   51  H28 UNL     1       1.068  -2.187   0.058  1.00  0.00           H  
HETATM   52  H29 UNL     1       3.393   2.646   1.651  1.00  0.00           H  
HETATM   53  H30 UNL     1       3.904   1.138   2.554  1.00  0.00           H  
HETATM   54  H31 UNL     1       4.935   1.882   1.230  1.00  0.00           H  
HETATM   55  H32 UNL     1       1.329   2.003  -0.053  1.00  0.00           H  
CONECT    1    2   24   25   26
CONECT    2    3    5   10
CONECT    3    4   27   28
CONECT    4   29
CONECT    5    6   30   31
CONECT    6    7   32   33
CONECT    7    8   34   35
CONECT    8    9   10   19
CONECT    9   36   37   38
CONECT   10   11   39
CONECT   11   12   40   41
CONECT   12   13   14   42
CONECT   13   43
CONECT   14   15   19   23
CONECT   15   16   44   45
CONECT   16   17   20   46
CONECT   17   18   47   48
CONECT   18   19   49   50
CONECT   19   51
CONECT   20   21   22   23
CONECT   21   52   53   54
CONECT   22   23
CONECT   23   55
END

HMDB0036705
     RDKit          3D
Ucriol
 55 59  0  0  0  0  0  0  0  0999 V2000
   -3.5008   -0.1664   -1.2220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6573    0.4858   -0.1995 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8922    2.0007   -0.3156 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1132    2.6672    0.6350 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1562    0.0983    1.1719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0442   -0.4245    2.0632 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4443   -1.6058    1.2972 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7248   -1.1089    0.0981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0681   -2.0489   -1.0678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1888    0.2759   -0.3014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6054    0.7014   -1.6010 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7262    0.1368   -1.9328 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4516    1.1338   -2.6286 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4755   -0.1812   -0.7070 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8136   -0.8916   -0.9677 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4828   -0.6191    0.3797 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7587   -1.2675    1.5286 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3005   -0.7783    1.5995 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7530   -1.1110    0.2376 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2180    0.8834    0.4966 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8890    1.6541    1.5905 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2264    1.5485   -0.7449 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9549    1.0910   -0.0661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5449    0.2557   -1.0944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2458    0.0405   -2.2684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6549   -1.2681   -1.0219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9587    2.1981   -0.0419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7403    2.3639   -1.3329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7025    3.4384    0.1538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7296    0.9065    1.6716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8893   -0.7581    1.0884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5226   -0.8088    2.9835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3101    0.3222    2.3440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8766   -2.2815    1.9502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3481   -2.2059    0.9753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4516   -1.5134   -1.9363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8306   -2.8025   -0.7662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1696   -2.6682   -1.3569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7414    0.9528    0.4913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5481    1.8304   -1.5799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2722    0.4931   -2.4855 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7052   -0.7308   -2.6307 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8382    1.8082   -3.0140 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4117   -0.3756   -1.7224 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6800   -1.9665   -1.1208 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5326   -0.8726    0.3997 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2418   -0.9520    2.4501 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7091   -2.3637    1.4611 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2883    0.3102    1.7616 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8463   -1.3084    2.4277 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0682   -2.1867    0.0578 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3927    2.6462    1.6513 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9045    1.1379    2.5538 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9351    1.8825    1.2304 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3285    2.0027   -0.0534 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  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
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 16 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 10  2  1  0
 19 14  1  0
 23 20  1  0
 19  8  1  0
 23 14  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  6 33  1  0
  7 34  1  0
  7 35  1  0
  9 36  1  0
  9 37  1  0
  9 38  1  0
 10 39  1  0
 11 40  1  0
 11 41  1  0
 12 42  1  0
 13 43  1  0
 15 44  1  0
 15 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 18 49  1  0
 18 50  1  0
 19 51  1  0
 21 52  1  0
 21 53  1  0
 21 54  1  0
 23 55  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
ent-15b,16b-Epoxy-7b,18-kauranediol	HMDB

Chemical Formula

C₂₀H₃₂O₃

Average Molecular Weight

320.4663

Monoisotopic Molecular Weight

320.23514489

IUPAC Name

5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-ol

Traditional Name

5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-ol

CAS Registry Number

87376-64-5

SMILES

CC12OC1C13CC2CCC1C1(C)CCCC(C)(CO)C1CC3O

InChI Identifier

InChI=1S/C20H32O3/c1-17(11-21)7-4-8-18(2)13-6-5-12-10-20(13,15(22)9-14(17)18)16-19(12,3)23-16/h12-16,21-22H,4-11H2,1-3H3

InChI Key

BDWKHKXSYDEDRO-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

Substituents

Kaurane diterpenoid
Oxane
Cyclic alcohol
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cytoplasm (HMDB: HMDB0036705)
Cell membrane (HMDB: HMDB0036705)

Cellular substructure

Extracellular (HMDB: HMDB0036705)
Membrane (HMDB: HMDB0036705)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0036705)

Source

Endogenous

Endogenous (HMDB: HMDB0036705)

Plant

Plant (HMDB: HMDB0036705)

Animal

Animal (HMDB: HMDB0036705)

Exogenous

Food

Food (HMDB: HMDB0036705)

Tea

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0036705)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0036705)

Cellular process

Cell signaling (HMDB: HMDB0036705)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0036705)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0036705)

Nutrient

Nutrient (HMDB: HMDB0036705)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0036705)

Emulsifier (HMDB: HMDB0036705)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	185 - 186 °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	0.035 g/L	ALOGPS
logP	2.52	ALOGPS
logP	2.38	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	14.6	ChemAxon
pKa (Strongest Basic)	-1.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	52.99 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	88.54 m³·mol⁻¹	ChemAxon
Polarizability	36.71 Å³	ChemAxon
Number of Rings	5	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]+	172.736	31661259
DarkChem	[M-H]-	170.23	31661259
DeepCCS	[M-2H]-	207.826	30932474
DeepCCS	[M+Na]+	183.091	30932474
AllCCS	[M+H]+	181.0	32859911
AllCCS	[M+H-H2O]+	178.2	32859911
AllCCS	[M+NH4]+	183.6	32859911
AllCCS	[M+Na]+	184.3	32859911
AllCCS	[M-H]-	185.4	32859911
AllCCS	[M+Na-2H]-	185.5	32859911
AllCCS	[M+HCOO]-	185.8	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Ucriol	CC12OC1C13CC2CCC1C1(C)CCCC(C)(CO)C1CC3O	2542.3	Standard polar	33892256
Ucriol	CC12OC1C13CC2CCC1C1(C)CCCC(C)(CO)C1CC3O	2482.1	Standard non polar	33892256
Ucriol	CC12OC1C13CC2CCC1C1(C)CCCC(C)(CO)C1CC3O	2713.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Ucriol,1TMS,isomer #1	CC1(CO[Si](C)(C)C)CCCC2(C)C1CC(O)C13CC(CCC21)C1(C)OC13	2628.9	Semi standard non polar	33892256
Ucriol,1TMS,isomer #2	CC1(CO)CCCC2(C)C1CC(O[Si](C)(C)C)C13CC(CCC21)C1(C)OC13	2615.3	Semi standard non polar	33892256
Ucriol,2TMS,isomer #1	CC1(CO[Si](C)(C)C)CCCC2(C)C1CC(O[Si](C)(C)C)C13CC(CCC21)C1(C)OC13	2567.4	Semi standard non polar	33892256
Ucriol,1TBDMS,isomer #1	CC1(CO[Si](C)(C)C(C)(C)C)CCCC2(C)C1CC(O)C13CC(CCC21)C1(C)OC13	2899.1	Semi standard non polar	33892256
Ucriol,1TBDMS,isomer #2	CC1(CO)CCCC2(C)C1CC(O[Si](C)(C)C(C)(C)C)C13CC(CCC21)C1(C)OC13	2856.6	Semi standard non polar	33892256
Ucriol,2TBDMS,isomer #1	CC1(CO[Si](C)(C)C(C)(C)C)CCCC2(C)C1CC(O[Si](C)(C)C(C)(C)C)C13CC(CCC21)C1(C)OC13	3058.6	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 - Ucriol GC-MS (Non-derivatized) - 70eV, Positive	splash10-0nn9-3794000000-31f845a3c33c9d93d072	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Ucriol GC-MS (2 TMS) - 70eV, Positive	splash10-06xt-4128900000-f251d2fe9be5cd70db9d	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Ucriol 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 - Ucriol 10V, Negative-QTOF	splash10-014i-0019000000-9513089b4c9b0ad108ca	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ucriol 20V, Negative-QTOF	splash10-0gbi-0059000000-847a129bb1a6d1e59f2f	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ucriol 40V, Negative-QTOF	splash10-00dr-2091000000-bcd25ead5e57077aef17	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ucriol 10V, Negative-QTOF	splash10-014i-0009000000-e9172f49e67d0b8f9e55	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ucriol 20V, Negative-QTOF	splash10-014i-0009000000-e9172f49e67d0b8f9e55	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ucriol 40V, Negative-QTOF	splash10-014i-0049000000-613723b61b6a20669c2d	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ucriol 10V, Positive-QTOF	splash10-0uk9-0039000000-63d0276e3af417cb70eb	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ucriol 20V, Positive-QTOF	splash10-0udr-0196000000-12571c498c9b9a8f69f4	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ucriol 40V, Positive-QTOF	splash10-014u-6490000000-2d798d6cbec6718216fd	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ucriol 10V, Positive-QTOF	splash10-00dr-0039000000-0344b13128c97264123d	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ucriol 20V, Positive-QTOF	splash10-00di-0339000000-22f4567f87fa8b4d8b26	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ucriol 40V, Positive-QTOF	splash10-01b9-2922000000-a034fb3d7e88124467a3	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

FDB015641

KNApSAcK ID

C00058242

Chemspider ID

35014214

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

54275943

PDB ID

Not Available

ChEBI ID

175099

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 Ucriol (HMDB0036705)

MOL for HMDB0036705 (Ucriol)

3D MOL for HMDB0036705 (Ucriol)

3D SDF for HMDB0036705 (Ucriol)

3D-SDF for HMDB0036705 (Ucriol)

PDB for HMDB0036705 (Ucriol)

3D PDB for HMDB0036705 (Ucriol)

SMILES for HMDB0036705 (Ucriol)

INCHI for HMDB0036705 (Ucriol)

Structure for HMDB0036705 (Ucriol)

3D Structure for HMDB0036705 (Ucriol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra