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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2021-09-22 21:18:08 UTC

Update Date

2021-09-22 21:18:08 UTC

HMDB ID

HMDB0301811

Secondary Accession Numbers

None

Metabolite Identification

Common Name

(-)-Olivil

Description

(-)-olivil is a member of the class of compounds known as 7,9'-epoxylignans. 7,9'-epoxylignans are lignans that contain the 7,9'-epoxylignan skeleton, which consists of a tetrahydrofuran that carries a phenyl group, a methyl group, and a benzyl group at the 2-, 3-, 4-position, respectively (-)-olivil is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). (-)-olivil can be found in olive, which makes (-)-olivil a potential biomarker for the consumption of this food product.

Structure

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


  Mrv0541 02241221392D          

 27 29  0  0  1  0            999 V2000
    1.2665   -0.6244    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1624   -0.6244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6445   -0.7959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8995   -1.5806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7064   -1.7521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9614   -2.5367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7684   -2.7082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2585   -1.1390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0654   -1.3105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0035   -0.3544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1966   -0.1828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3819   -1.7224    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1270   -2.5070    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3020   -2.5070    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470   -1.7224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6119   -3.1745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4324   -3.0882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9173   -3.7557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5817   -4.5094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0667   -5.1768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7613   -4.5956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4257   -5.3493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6052   -5.4355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2763   -3.9282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1665   -1.4675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7796   -2.0195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  6  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
  4 12  1  0  0  0  0
  2 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
  2 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  2  0  0  0  0
 17 25  1  0  0  0  0
 13 26  1  6  0  0  0
 26 27  1  0  0  0  0
M  END

HMDB0301811
     RDKit          3D
(-)-Olivil
 51 53  0  0  0  0  0  0  0  0999 V2000
   -6.4088   -0.7344    0.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1263    0.2887   -0.5594 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8627    0.8488   -0.6657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8288    0.4185    0.1347 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5482    0.9750    0.0382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4432    0.5164    0.9153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7465   -0.6596    0.3252 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5969   -1.7514    0.1437 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.2402   -1.0147 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9938    0.4657   -0.7032 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5019   -0.0443    0.4842 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8810   -0.5547    0.2692 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2928   -1.7749    0.7518 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6015   -2.1751    0.5061 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4817   -1.3836   -0.2022 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7850   -1.7890   -0.4434 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0689   -0.1571   -0.6878 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9730    0.6120   -1.3929 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5908    1.8861   -1.9134 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7732    0.2251   -0.4373 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5401   -1.0231    1.0320 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4141   -1.0209    2.5224 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0555    0.1687    3.0919 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4052    1.9712   -0.9049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4439    2.4041   -1.7098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6819    1.8465   -1.5971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7436    2.2553   -2.3861 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9306   -0.5263    1.3507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0722   -1.6887   -0.0733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5075   -0.7137    0.5415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9524   -0.3683    0.8760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9163    0.3012    1.8990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7144    1.3320    1.1124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1432   -1.6742   -0.6766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8416    0.2587   -1.6701 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0975   -1.2227   -1.5228 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5580    0.8202    1.2151 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6511   -2.4395    1.3115 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9074   -3.1375    0.8934 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0826   -2.6830   -0.0882 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0751    2.4597   -1.0885 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4553    2.4898   -2.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8676    1.7802   -2.7208 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4789    1.2044   -0.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7511   -2.0822    0.7199 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3426   -1.3643    2.9785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3678   -1.7870    2.7845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4232   -0.0393    3.9477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4515    2.4613   -1.0439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2678    3.1919   -2.4333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6527    1.8537   -2.3113 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  6
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 17 20  2  0
 11 21  1  0
 21 22  1  0
 22 23  1  0
  5 24  2  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 26  3  1  0
 21  7  1  0
 20 12  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  4 31  1  0
  6 32  1  0
  6 33  1  0
  8 34  1  0
  9 35  1  0
  9 36  1  0
 11 37  1  1
 13 38  1  0
 14 39  1  0
 16 40  1  0
 19 41  1  0
 19 42  1  0
 19 43  1  0
 20 44  1  0
 21 45  1  6
 22 46  1  0
 22 47  1  0
 23 48  1  0
 24 49  1  0
 25 50  1  0
 27 51  1  0
M  END


  Mrv0541 02241221392D          

 27 29  0  0  1  0            999 V2000
    1.2665   -0.6244    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1624   -0.6244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6445   -0.7959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8995   -1.5806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7064   -1.7521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9614   -2.5367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7684   -2.7082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2585   -1.1390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0654   -1.3105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0035   -0.3544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1966   -0.1828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3819   -1.7224    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1270   -2.5070    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3020   -2.5070    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470   -1.7224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6119   -3.1745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4324   -3.0882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9173   -3.7557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5817   -4.5094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0667   -5.1768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7613   -4.5956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4257   -5.3493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6052   -5.4355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2763   -3.9282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1665   -1.4675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7796   -2.0195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  6  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
  4 12  1  0  0  0  0
  2 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
  2 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  2  0  0  0  0
 17 25  1  0  0  0  0
 13 26  1  6  0  0  0
 26 27  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0301811

> <DATABASE_NAME>
hmdb

> <SMILES>
COC1=CC(=CC=C1O)[C@H]1OC[C@](O)(CC2=CC(OC)=C(O)C=C2)[C@@H]1CO

> <INCHI_IDENTIFIER>
InChI=1S/C20H24O7/c1-25-17-7-12(3-5-15(17)22)9-20(24)11-27-19(14(20)10-21)13-4-6-16(23)18(8-13)26-2/h3-8,14,19,21-24H,9-11H2,1-2H3/t14-,19-,20-/m1/s1

> <INCHI_KEY>
BVHIKUCXNBQDEM-JSNMRZPZSA-N

> <FORMULA>
C20H24O7

> <MOLECULAR_WEIGHT>
376.4004

> <EXACT_MASS>
376.152203122

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_AVERAGE_POLARIZABILITY>
39.2290193016116

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-4-(hydroxymethyl)oxolan-3-ol

> <ALOGPS_LOGP>
1.45

> <JCHEM_LOGP>
1.4850434310000002

> <ALOGPS_LOGS>
-3.57

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.34598115809029

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.712118497707058

> <JCHEM_PKA_STRONGEST_BASIC>
-2.6753338846636074

> <JCHEM_POLAR_SURFACE_AREA>
108.61000000000001

> <JCHEM_REFRACTIVITY>
98.28389999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.00e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-4-(hydroxymethyl)oxolan-3-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0301811
     RDKit          3D
(-)-Olivil
 51 53  0  0  0  0  0  0  0  0999 V2000
   -6.4088   -0.7344    0.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1263    0.2887   -0.5594 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8627    0.8488   -0.6657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8288    0.4185    0.1347 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5482    0.9750    0.0382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4432    0.5164    0.9153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7465   -0.6596    0.3252 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5969   -1.7514    0.1437 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.2402   -1.0147 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9938    0.4657   -0.7032 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5019   -0.0443    0.4842 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8810   -0.5547    0.2692 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2928   -1.7749    0.7518 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6015   -2.1751    0.5061 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4817   -1.3836   -0.2022 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7850   -1.7890   -0.4434 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0689   -0.1571   -0.6878 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9730    0.6120   -1.3929 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5908    1.8861   -1.9134 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7732    0.2251   -0.4373 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5401   -1.0231    1.0320 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4141   -1.0209    2.5224 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0555    0.1687    3.0919 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4052    1.9712   -0.9049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4439    2.4041   -1.7098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6819    1.8465   -1.5971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7436    2.2553   -2.3861 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9306   -0.5263    1.3507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0722   -1.6887   -0.0733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5075   -0.7137    0.5415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9524   -0.3683    0.8760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9163    0.3012    1.8990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7144    1.3320    1.1124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1432   -1.6742   -0.6766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8416    0.2587   -1.6701 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0975   -1.2227   -1.5228 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5580    0.8202    1.2151 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6511   -2.4395    1.3115 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9074   -3.1375    0.8934 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0826   -2.6830   -0.0882 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0751    2.4597   -1.0885 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4553    2.4898   -2.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8676    1.7802   -2.7208 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4789    1.2044   -0.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7511   -2.0822    0.7199 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3426   -1.3643    2.9785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3678   -1.7870    2.7845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4232   -0.0393    3.9477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4515    2.4613   -1.0439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2678    3.1919   -2.4333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6527    1.8537   -2.3113 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  6
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 17 20  2  0
 11 21  1  0
 21 22  1  0
 22 23  1  0
  5 24  2  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 26  3  1  0
 21  7  1  0
 20 12  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  4 31  1  0
  6 32  1  0
  6 33  1  0
  8 34  1  0
  9 35  1  0
  9 36  1  0
 11 37  1  1
 13 38  1  0
 14 39  1  0
 16 40  1  0
 19 41  1  0
 19 42  1  0
 19 43  1  0
 20 44  1  0
 21 45  1  6
 22 46  1  0
 22 47  1  0
 23 48  1  0
 24 49  1  0
 25 50  1  0
 27 51  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  O   UNK     0       2.364  -1.166   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.303  -1.166   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.203  -1.486   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.679  -2.950   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.185  -3.271   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -3.661  -4.735   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -5.168  -5.055   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.216  -2.126   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -5.722  -2.446   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -3.740  -0.662   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.234  -0.341   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.580  -3.215   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.104  -4.680   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.564  -4.680   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.088  -3.215   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.009  -5.926   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.540  -5.765   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.446  -7.011   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.819  -8.418   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       5.725  -9.663   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       3.288  -8.578   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.661  -9.985   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.130 -10.146   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.382  -7.333   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.044  -2.739   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.189  -3.770   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   13   16                                             
CONECT    3    2    4                                                       
CONECT    4    3    5   12                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    6   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11    4                                                       
CONECT   13    2   14   26                                                  
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15    2                                                       
CONECT   17   14   18   25                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   17                                                       
CONECT   26   13   27                                                       
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

COMPND    HMDB0301811
HETATM    1  C1  UNL     1      -6.409  -0.734   0.361  1.00  0.00           C  
HETATM    2  O1  UNL     1      -6.126   0.289  -0.559  1.00  0.00           O  
HETATM    3  C2  UNL     1      -4.863   0.849  -0.666  1.00  0.00           C  
HETATM    4  C3  UNL     1      -3.829   0.419   0.135  1.00  0.00           C  
HETATM    5  C4  UNL     1      -2.548   0.975   0.038  1.00  0.00           C  
HETATM    6  C5  UNL     1      -1.443   0.516   0.915  1.00  0.00           C  
HETATM    7  C6  UNL     1      -0.746  -0.660   0.325  1.00  0.00           C  
HETATM    8  O2  UNL     1      -1.597  -1.751   0.144  1.00  0.00           O  
HETATM    9  C7  UNL     1      -0.144  -0.240  -1.015  1.00  0.00           C  
HETATM   10  O3  UNL     1       0.994   0.466  -0.703  1.00  0.00           O  
HETATM   11  C8  UNL     1       1.502  -0.044   0.484  1.00  0.00           C  
HETATM   12  C9  UNL     1       2.881  -0.555   0.269  1.00  0.00           C  
HETATM   13  C10 UNL     1       3.293  -1.775   0.752  1.00  0.00           C  
HETATM   14  C11 UNL     1       4.602  -2.175   0.506  1.00  0.00           C  
HETATM   15  C12 UNL     1       5.482  -1.384  -0.202  1.00  0.00           C  
HETATM   16  O4  UNL     1       6.785  -1.789  -0.443  1.00  0.00           O  
HETATM   17  C13 UNL     1       5.069  -0.157  -0.688  1.00  0.00           C  
HETATM   18  O5  UNL     1       5.973   0.612  -1.393  1.00  0.00           O  
HETATM   19  C14 UNL     1       5.591   1.886  -1.913  1.00  0.00           C  
HETATM   20  C15 UNL     1       3.773   0.225  -0.437  1.00  0.00           C  
HETATM   21  C16 UNL     1       0.540  -1.023   1.032  1.00  0.00           C  
HETATM   22  C17 UNL     1       0.414  -1.021   2.522  1.00  0.00           C  
HETATM   23  O6  UNL     1       0.055   0.169   3.092  1.00  0.00           O  
HETATM   24  C18 UNL     1      -2.405   1.971  -0.905  1.00  0.00           C  
HETATM   25  C19 UNL     1      -3.444   2.404  -1.710  1.00  0.00           C  
HETATM   26  C20 UNL     1      -4.682   1.847  -1.597  1.00  0.00           C  
HETATM   27  O7  UNL     1      -5.744   2.255  -2.386  1.00  0.00           O  
HETATM   28  H1  UNL     1      -5.931  -0.526   1.351  1.00  0.00           H  
HETATM   29  H2  UNL     1      -6.072  -1.689  -0.073  1.00  0.00           H  
HETATM   30  H3  UNL     1      -7.508  -0.714   0.542  1.00  0.00           H  
HETATM   31  H4  UNL     1      -3.952  -0.368   0.876  1.00  0.00           H  
HETATM   32  H5  UNL     1      -1.916   0.301   1.899  1.00  0.00           H  
HETATM   33  H6  UNL     1      -0.714   1.332   1.112  1.00  0.00           H  
HETATM   34  H7  UNL     1      -2.143  -1.674  -0.677  1.00  0.00           H  
HETATM   35  H8  UNL     1      -0.842   0.259  -1.670  1.00  0.00           H  
HETATM   36  H9  UNL     1       0.098  -1.223  -1.523  1.00  0.00           H  
HETATM   37  H10 UNL     1       1.558   0.820   1.215  1.00  0.00           H  
HETATM   38  H11 UNL     1       2.651  -2.440   1.311  1.00  0.00           H  
HETATM   39  H12 UNL     1       4.907  -3.137   0.893  1.00  0.00           H  
HETATM   40  H13 UNL     1       7.083  -2.683  -0.088  1.00  0.00           H  
HETATM   41  H14 UNL     1       5.075   2.460  -1.088  1.00  0.00           H  
HETATM   42  H15 UNL     1       6.455   2.490  -2.199  1.00  0.00           H  
HETATM   43  H16 UNL     1       4.868   1.780  -2.721  1.00  0.00           H  
HETATM   44  H17 UNL     1       3.479   1.204  -0.837  1.00  0.00           H  
HETATM   45  H18 UNL     1       0.751  -2.082   0.720  1.00  0.00           H  
HETATM   46  H19 UNL     1       1.343  -1.364   2.978  1.00  0.00           H  
HETATM   47  H20 UNL     1      -0.368  -1.787   2.784  1.00  0.00           H  
HETATM   48  H21 UNL     1      -0.423  -0.039   3.948  1.00  0.00           H  
HETATM   49  H22 UNL     1      -1.452   2.461  -1.044  1.00  0.00           H  
HETATM   50  H23 UNL     1      -3.268   3.192  -2.433  1.00  0.00           H  
HETATM   51  H24 UNL     1      -6.653   1.854  -2.311  1.00  0.00           H  
CONECT    1    2   28   29   30
CONECT    2    3
CONECT    3    4    4   26
CONECT    4    5   31
CONECT    5    6   24   24
CONECT    6    7   32   33
CONECT    7    8    9   21
CONECT    8   34
CONECT    9   10   35   36
CONECT   10   11
CONECT   11   12   21   37
CONECT   12   13   13   20
CONECT   13   14   38
CONECT   14   15   15   39
CONECT   15   16   17
CONECT   16   40
CONECT   17   18   20   20
CONECT   18   19
CONECT   19   41   42   43
CONECT   20   44
CONECT   21   22   45
CONECT   22   23   46   47
CONECT   23   48
CONECT   24   25   49
CONECT   25   26   26   50
CONECT   26   27
CONECT   27   51
END

HMDB0301811
     RDKit          3D
(-)-Olivil
 51 53  0  0  0  0  0  0  0  0999 V2000
   -6.4088   -0.7344    0.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1263    0.2887   -0.5594 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8627    0.8488   -0.6657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8288    0.4185    0.1347 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5482    0.9750    0.0382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4432    0.5164    0.9153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7465   -0.6596    0.3252 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5969   -1.7514    0.1437 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.2402   -1.0147 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9938    0.4657   -0.7032 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5019   -0.0443    0.4842 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8810   -0.5547    0.2692 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2928   -1.7749    0.7518 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6015   -2.1751    0.5061 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4817   -1.3836   -0.2022 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7850   -1.7890   -0.4434 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0689   -0.1571   -0.6878 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9730    0.6120   -1.3929 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5908    1.8861   -1.9134 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7732    0.2251   -0.4373 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5401   -1.0231    1.0320 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4141   -1.0209    2.5224 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0555    0.1687    3.0919 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4052    1.9712   -0.9049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4439    2.4041   -1.7098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6819    1.8465   -1.5971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7436    2.2553   -2.3861 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9306   -0.5263    1.3507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0722   -1.6887   -0.0733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5075   -0.7137    0.5415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9524   -0.3683    0.8760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9163    0.3012    1.8990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7144    1.3320    1.1124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1432   -1.6742   -0.6766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8416    0.2587   -1.6701 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0975   -1.2227   -1.5228 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5580    0.8202    1.2151 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6511   -2.4395    1.3115 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9074   -3.1375    0.8934 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0826   -2.6830   -0.0882 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0751    2.4597   -1.0885 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4553    2.4898   -2.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8676    1.7802   -2.7208 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4789    1.2044   -0.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7511   -2.0822    0.7199 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3426   -1.3643    2.9785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3678   -1.7870    2.7845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4232   -0.0393    3.9477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4515    2.4613   -1.0439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2678    3.1919   -2.4333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6527    1.8537   -2.3113 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  6
  7  9  1  0
  9 10  1  0
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 12 13  2  0
 13 14  1  0
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 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 17 20  2  0
 11 21  1  0
 21 22  1  0
 22 23  1  0
  5 24  2  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 26  3  1  0
 21  7  1  0
 20 12  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  4 31  1  0
  6 32  1  0
  6 33  1  0
  8 34  1  0
  9 35  1  0
  9 36  1  0
 11 37  1  1
 13 38  1  0
 14 39  1  0
 16 40  1  0
 19 41  1  0
 19 42  1  0
 19 43  1  0
 20 44  1  0
 21 45  1  6
 22 46  1  0
 22 47  1  0
 23 48  1  0
 24 49  1  0
 25 50  1  0
 27 51  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₀H₂₄O₇

Average Molecular Weight

376.4004

Monoisotopic Molecular Weight

376.152203122

IUPAC Name

(3S,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-4-(hydroxymethyl)oxolan-3-ol

Traditional Name

(3S,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-4-(hydroxymethyl)oxolan-3-ol

CAS Registry Number

2955-23-9

SMILES

COC1=CC(=CC=C1O)[C@H]1OC[C@](O)(CC2=CC(OC)=C(O)C=C2)[C@@H]1CO

InChI Identifier

InChI=1S/C20H24O7/c1-25-17-7-12(3-5-15(17)22)9-20(24)11-27-19(14(20)10-21)13-4-6-16(23)18(8-13)26-2/h3-8,14,19,21-24H,9-11H2,1-2H3/t14-,19-,20-/m1/s1

InChI Key

BVHIKUCXNBQDEM-JSNMRZPZSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 7,9'-epoxylignans. These are lignans that contain the 7,9'-epoxylignan skeleton, which consists of a tetrahydrofuran that carries a phenyl group, a methyl group, and a benzyl group at the 2-, 3-, 4-position, respectively.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Furanoid lignans

Sub Class

Tetrahydrofuran lignans

Direct Parent

7,9'-epoxylignans

Alternative Parents

Substituents

7,9p-epoxylignan
Methoxyphenol
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Benzenoid
Tetrahydrofuran
Tertiary alcohol
Oxacycle
Dialkyl ether
Ether
Organoheterocyclic compound
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Organooxygen compound
Primary alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Olive (FooDB: FOOD00121)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	1.45	ALOGPS
logP	1.49	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	9.71	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	108.61 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	98.28 m³·mol⁻¹	ChemAxon
Polarizability	39.23 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
AllCCS	[M+H]+	190.602	32859911
AllCCS	[M+H-H2O]+	187.623	32859911
AllCCS	[M+Na]+	194.144	32859911
AllCCS	[M+NH4]+	193.354	32859911
AllCCS	[M-H]-	191.909	32859911
AllCCS	[M+Na-2H]-	192.326	32859911
AllCCS	[M+HCOO]-	192.935	32859911
DeepCCS	[M+H]+	182.576	30932474
DeepCCS	[M-H]-	180.181	30932474
DeepCCS	[M-2H]-	213.483	30932474
DeepCCS	[M+Na]+	188.489	30932474

Predicted Kovats Retention Indices

Not Available

Spectra

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Olivil 10V, Positive-QTOF	splash10-056r-0219000000-3b9716e65ae36b442ee1	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Olivil 20V, Positive-QTOF	splash10-052r-0859000000-263898aeb5b36f658f8f	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Olivil 40V, Positive-QTOF	splash10-000i-1921000000-646e34bd4efebb53bb88	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Olivil 10V, Negative-QTOF	splash10-004i-0129000000-bc34842025a2a8439494	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Olivil 20V, Negative-QTOF	splash10-0a6r-0259000000-8843dcd1915985ee5e86	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Olivil 40V, Negative-QTOF	splash10-0007-1900000000-6112a309a86aa47f5434	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Olivil 10V, Positive-QTOF	splash10-004i-0009000000-c6e598923dcadfb0b8e5	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Olivil 20V, Positive-QTOF	splash10-000i-0932000000-4a7acb7b564bd502eba7	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Olivil 40V, Positive-QTOF	splash10-052r-3900000000-462118f6128714de228d	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Olivil 10V, Negative-QTOF	splash10-00b9-0089000000-83dbe4297f2e188386e4	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Olivil 20V, Negative-QTOF	splash10-05i0-0197000000-da1a53664a9f14112fa0	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Olivil 40V, Negative-QTOF	splash10-0ab9-2978000000-31fc35c16233c0fb6ba9	2021-10-21	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

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

FDB001448

KNApSAcK ID

Not Available

Chemspider ID

4437973

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5273570

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

Not Available

Showing metabocard for (-)-Olivil (HMDB0301811)

MOL for HMDB0301811 ((-)-Olivil)

3D MOL for HMDB0301811 ((-)-Olivil)

3D SDF for HMDB0301811 ((-)-Olivil)

3D-SDF for HMDB0301811 ((-)-Olivil)

PDB for HMDB0301811 ((-)-Olivil)

3D PDB for HMDB0301811 ((-)-Olivil)

SMILES for HMDB0301811 ((-)-Olivil)

INCHI for HMDB0301811 ((-)-Olivil)

Structure for HMDB0301811 ((-)-Olivil)

3D Structure for HMDB0301811 ((-)-Olivil)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

MS/MS Spectra