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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 00:24:41 UTC

Update Date

2022-03-07 02:56:03 UTC

HMDB ID

HMDB0039058

Secondary Accession Numbers

HMDB39058

Metabolite Identification

Common Name

(R)-Heraclenol 2'-(3-methyl-2-butenoate)

Description

(R)-Heraclenol 2'-(3-methyl-2-butenoate) belongs to the class of organic compounds known as psoralens. These are organic compounds containing a psoralen moiety, which consists of a furan fused to a chromenone to for 7H-furo[3,2-g]chromen-7-one (R)-Heraclenol 2'-(3-methyl-2-butenoate) has been detected, but not quantified in, a few different foods, such as fats and oils, green vegetables, and herbs and spices. This could make (R)-heraclenol 2'-(3-methyl-2-butenoate) a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on (R)-Heraclenol 2'-(3-methyl-2-butenoate).

Structure

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

  Mrv0541 02241209092D          

 28 30  0  0  0  0            999 V2000
   -0.7133   -1.7041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.2918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.4672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7146   -0.0550    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7146    0.7696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.1818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.0065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7834    2.2607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2685    1.5941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7834    0.9276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4279   -0.4672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4279   -1.2918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1411   -1.7041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1425    0.7696    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4292    1.1818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4292    2.0065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7146    2.4187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1425    2.4187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8572    2.0065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8572    1.1818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5704    0.7696    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4292   -2.1164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7146   -1.7041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3023   -2.4187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1268   -0.9895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8558   -1.2918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5704   -1.7041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8558   -0.4672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1 12  1  0  0  0  0
  2  3  1  0  0  0  0
  2 23  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5 15  2  0  0  0  0
  6  7  2  0  0  0  0
  6 10  1  0  0  0  0
  7  8  1  0  0  0  0
  7 17  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 26  2  0  0  0  0
 14 15  1  0  0  0  0
 14 20  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
M  END

HMDB0039058
     RDKit          3D
(R)-Heraclenol 2'-(3-methyl-2-butenoate)
 50 52  0  0  0  0  0  0  0  0999 V2000
   -3.3366    1.4188   -2.0948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3091    2.2201   -1.3219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2803    3.0747   -2.0657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3017    2.1668   -0.0066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3382    1.3215    0.6695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3759    1.3078    1.9475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3882    0.5329    0.0924 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4721   -0.2742    0.8236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0837    0.2298    0.5044 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9126   -0.5086    1.1844 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2609   -0.2221    1.0420 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9353    0.6682    1.8522 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5204    1.4045    2.8690 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5060    2.1177    3.3593 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6564    1.8608    2.6462 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2768    0.9335    1.6872 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9738    0.2935    0.6835 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3338   -0.6051   -0.1488 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0380   -1.2397   -1.1487 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3675   -2.1284   -1.9584 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0258   -2.3444   -1.7351 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3975   -3.1602   -2.4739 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3953   -1.7215   -0.7754 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9900   -0.8522    0.0385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6860   -1.6951    0.4021 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4932   -1.8868   -1.0818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8183   -2.6672    1.1741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0082   -2.0234    0.7020 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5020    1.5824   -3.1939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3006    1.7430   -1.8896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4882    0.3105   -1.9434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9545    2.4287   -2.6703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7859    3.8651   -2.6495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9249    3.5777   -1.3150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0207    2.7609    0.5190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6109   -0.1956    1.9032 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1364    0.1941   -0.5759 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0327    1.2856    0.8224 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4544    2.8134    4.1988 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6467    2.2519    2.7547 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0211    0.4697    0.5182 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0949   -1.0356   -1.2845 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8510   -2.6584   -2.7563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5573   -2.4525   -1.2811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4570   -0.9266   -1.6341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3258   -2.4819   -1.5041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3567   -3.6401    1.2146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7143   -2.3097    2.2096 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1491   -2.8618    0.6750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0860   -2.9422    1.0729 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  0
  8 25  1  0
 25 26  1  0
 25 27  1  0
 25 28  1  0
 24 11  1  0
 16 12  1  0
 24 18  2  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  8 36  1  0
  9 37  1  0
  9 38  1  0
 14 39  1  0
 15 40  1  0
 17 41  1  0
 19 42  1  0
 20 43  1  0
 26 44  1  0
 26 45  1  0
 26 46  1  0
 27 47  1  0
 27 48  1  0
 27 49  1  0
 28 50  1  0
M  END

  Mrv0541 02241209092D          

 28 30  0  0  0  0            999 V2000
   -0.7133   -1.7041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.2918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.4672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7146   -0.0550    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7146    0.7696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.1818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.0065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7834    2.2607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2685    1.5941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7834    0.9276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4279   -0.4672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4279   -1.2918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1411   -1.7041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1425    0.7696    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4292    1.1818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4292    2.0065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7146    2.4187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1425    2.4187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8572    2.0065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8572    1.1818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5704    0.7696    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4292   -2.1164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7146   -1.7041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3023   -2.4187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1268   -0.9895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8558   -1.2918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5704   -1.7041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8558   -0.4672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1 12  1  0  0  0  0
  2  3  1  0  0  0  0
  2 23  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5 15  2  0  0  0  0
  6  7  2  0  0  0  0
  6 10  1  0  0  0  0
  7  8  1  0  0  0  0
  7 17  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 26  2  0  0  0  0
 14 15  1  0  0  0  0
 14 20  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0039058

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)=CC(=O)OC(COC1=C2OC(=O)C=CC2=CC2=C1OC=C2)C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C21H22O7/c1-12(2)9-17(23)27-15(21(3,4)24)11-26-20-18-14(7-8-25-18)10-13-5-6-16(22)28-19(13)20/h5-10,15,24H,11H2,1-4H3

> <INCHI_KEY>
YFMSPAAEUUQLDI-UHFFFAOYSA-N

> <FORMULA>
C21H22O7

> <MOLECULAR_WEIGHT>
386.3952

> <EXACT_MASS>
386.136553058

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
39.610553474967034

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-hydroxy-3-methyl-1-({7-oxo-7H-furo[3,2-g]chromen-9-yl}oxy)butan-2-yl 3-methylbut-2-enoate

> <ALOGPS_LOGP>
3.13

> <JCHEM_LOGP>
3.222274506333334

> <ALOGPS_LOGS>
-3.99

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.226874826135873

> <JCHEM_PKA_STRONGEST_BASIC>
-3.136964951048168

> <JCHEM_POLAR_SURFACE_AREA>
95.2

> <JCHEM_REFRACTIVITY>
101.91940000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.94e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-hydroxy-3-methyl-1-({7-oxofuro[3,2-g]chromen-9-yl}oxy)butan-2-yl 3-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0039058
     RDKit          3D
(R)-Heraclenol 2'-(3-methyl-2-butenoate)
 50 52  0  0  0  0  0  0  0  0999 V2000
   -3.3366    1.4188   -2.0948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3091    2.2201   -1.3219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2803    3.0747   -2.0657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3017    2.1668   -0.0066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3382    1.3215    0.6695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3759    1.3078    1.9475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3882    0.5329    0.0924 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4721   -0.2742    0.8236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0837    0.2298    0.5044 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9126   -0.5086    1.1844 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2609   -0.2221    1.0420 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9353    0.6682    1.8522 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5204    1.4045    2.8690 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5060    2.1177    3.3593 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6564    1.8608    2.6462 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2768    0.9335    1.6872 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9738    0.2935    0.6835 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3338   -0.6051   -0.1488 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0380   -1.2397   -1.1487 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3675   -2.1284   -1.9584 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0258   -2.3444   -1.7351 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3975   -3.1602   -2.4739 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3953   -1.7215   -0.7754 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9900   -0.8522    0.0385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6860   -1.6951    0.4021 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4932   -1.8868   -1.0818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8183   -2.6672    1.1741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0082   -2.0234    0.7020 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5020    1.5824   -3.1939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3006    1.7430   -1.8896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4882    0.3105   -1.9434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9545    2.4287   -2.6703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7859    3.8651   -2.6495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9249    3.5777   -1.3150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0207    2.7609    0.5190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6109   -0.1956    1.9032 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1364    0.1941   -0.5759 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0327    1.2856    0.8224 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4544    2.8134    4.1988 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6467    2.2519    2.7547 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0211    0.4697    0.5182 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0949   -1.0356   -1.2845 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8510   -2.6584   -2.7563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5573   -2.4525   -1.2811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4570   -0.9266   -1.6341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3258   -2.4819   -1.5041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3567   -3.6401    1.2146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7143   -2.3097    2.2096 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1491   -2.8618    0.6750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0860   -2.9422    1.0729 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  0
  8 25  1  0
 25 26  1  0
 25 27  1  0
 25 28  1  0
 24 11  1  0
 16 12  1  0
 24 18  2  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  8 36  1  0
  9 37  1  0
  9 38  1  0
 14 39  1  0
 15 40  1  0
 17 41  1  0
 19 42  1  0
 20 43  1  0
 26 44  1  0
 26 45  1  0
 26 46  1  0
 27 47  1  0
 27 48  1  0
 27 49  1  0
 28 50  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      -1.331  -3.181   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       0.000  -2.411   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -0.872   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.334  -0.103   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.334   1.437   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   2.206   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   3.745   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.462   4.220   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.368   2.976   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -1.462   1.732   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      -2.665  -0.872   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -2.665  -2.411   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.997  -3.181   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.999   1.437   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.668   2.206   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.668   3.745   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334   4.515   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.999   4.515   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.333   3.745   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.333   2.206   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.665   1.437   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.668  -3.951   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.334  -3.181   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.564  -4.515   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.103  -1.847   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -5.331  -2.411   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -6.665  -3.181   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -5.331  -0.872   0.000  0.00  0.00           C+0
CONECT    1    2   12                                                       
CONECT    2    1    3   23                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   15                                                  
CONECT    6    5    7   10                                                  
CONECT    7    6    8   17                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    6    9                                                       
CONECT   11   12                                                            
CONECT   12    1   11   13                                                  
CONECT   13   12   26                                                       
CONECT   14   15   20                                                       
CONECT   15    5   14   16                                                  
CONECT   16   15   17   18                                                  
CONECT   17    7   16                                                       
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   14   19   21                                                  
CONECT   21   20                                                            
CONECT   22   23                                                            
CONECT   23    2   22   24   25                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   13   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

COMPND    HMDB0039058
HETATM    1  C1  UNL     1      -3.337   1.419  -2.095  1.00  0.00           C  
HETATM    2  C2  UNL     1      -4.309   2.220  -1.322  1.00  0.00           C  
HETATM    3  C3  UNL     1      -5.280   3.075  -2.066  1.00  0.00           C  
HETATM    4  C4  UNL     1      -4.302   2.167  -0.007  1.00  0.00           C  
HETATM    5  C5  UNL     1      -3.338   1.322   0.669  1.00  0.00           C  
HETATM    6  O1  UNL     1      -3.376   1.308   1.948  1.00  0.00           O  
HETATM    7  O2  UNL     1      -2.388   0.533   0.092  1.00  0.00           O  
HETATM    8  C6  UNL     1      -1.472  -0.274   0.824  1.00  0.00           C  
HETATM    9  C7  UNL     1      -0.084   0.230   0.504  1.00  0.00           C  
HETATM   10  O3  UNL     1       0.913  -0.509   1.184  1.00  0.00           O  
HETATM   11  C8  UNL     1       2.261  -0.222   1.042  1.00  0.00           C  
HETATM   12  C9  UNL     1       2.935   0.668   1.852  1.00  0.00           C  
HETATM   13  O4  UNL     1       2.520   1.405   2.869  1.00  0.00           O  
HETATM   14  C10 UNL     1       3.506   2.118   3.359  1.00  0.00           C  
HETATM   15  C11 UNL     1       4.656   1.861   2.646  1.00  0.00           C  
HETATM   16  C12 UNL     1       4.277   0.933   1.687  1.00  0.00           C  
HETATM   17  C13 UNL     1       4.974   0.293   0.683  1.00  0.00           C  
HETATM   18  C14 UNL     1       4.334  -0.605  -0.149  1.00  0.00           C  
HETATM   19  C15 UNL     1       5.038  -1.240  -1.149  1.00  0.00           C  
HETATM   20  C16 UNL     1       4.368  -2.128  -1.958  1.00  0.00           C  
HETATM   21  C17 UNL     1       3.026  -2.344  -1.735  1.00  0.00           C  
HETATM   22  O5  UNL     1       2.397  -3.160  -2.474  1.00  0.00           O  
HETATM   23  O6  UNL     1       2.395  -1.722  -0.775  1.00  0.00           O  
HETATM   24  C18 UNL     1       2.990  -0.852   0.038  1.00  0.00           C  
HETATM   25  C19 UNL     1      -1.686  -1.695   0.402  1.00  0.00           C  
HETATM   26  C20 UNL     1      -1.493  -1.887  -1.082  1.00  0.00           C  
HETATM   27  C21 UNL     1      -0.818  -2.667   1.174  1.00  0.00           C  
HETATM   28  O7  UNL     1      -3.008  -2.023   0.702  1.00  0.00           O  
HETATM   29  H1  UNL     1      -3.502   1.582  -3.194  1.00  0.00           H  
HETATM   30  H2  UNL     1      -2.301   1.743  -1.890  1.00  0.00           H  
HETATM   31  H3  UNL     1      -3.488   0.310  -1.943  1.00  0.00           H  
HETATM   32  H4  UNL     1      -5.955   2.429  -2.670  1.00  0.00           H  
HETATM   33  H5  UNL     1      -4.786   3.865  -2.650  1.00  0.00           H  
HETATM   34  H6  UNL     1      -5.925   3.578  -1.315  1.00  0.00           H  
HETATM   35  H7  UNL     1      -5.021   2.761   0.519  1.00  0.00           H  
HETATM   36  H8  UNL     1      -1.611  -0.196   1.903  1.00  0.00           H  
HETATM   37  H9  UNL     1       0.136   0.194  -0.576  1.00  0.00           H  
HETATM   38  H10 UNL     1       0.033   1.286   0.822  1.00  0.00           H  
HETATM   39  H11 UNL     1       3.454   2.813   4.199  1.00  0.00           H  
HETATM   40  H12 UNL     1       5.647   2.252   2.755  1.00  0.00           H  
HETATM   41  H13 UNL     1       6.021   0.470   0.518  1.00  0.00           H  
HETATM   42  H14 UNL     1       6.095  -1.036  -1.285  1.00  0.00           H  
HETATM   43  H15 UNL     1       4.851  -2.658  -2.756  1.00  0.00           H  
HETATM   44  H16 UNL     1      -0.557  -2.453  -1.281  1.00  0.00           H  
HETATM   45  H17 UNL     1      -1.457  -0.927  -1.634  1.00  0.00           H  
HETATM   46  H18 UNL     1      -2.326  -2.482  -1.504  1.00  0.00           H  
HETATM   47  H19 UNL     1      -1.357  -3.640   1.215  1.00  0.00           H  
HETATM   48  H20 UNL     1      -0.714  -2.310   2.210  1.00  0.00           H  
HETATM   49  H21 UNL     1       0.149  -2.862   0.675  1.00  0.00           H  
HETATM   50  H22 UNL     1      -3.086  -2.942   1.073  1.00  0.00           H  
CONECT    1    2   29   30   31
CONECT    2    3    4    4
CONECT    3   32   33   34
CONECT    4    5   35
CONECT    5    6    6    7
CONECT    7    8
CONECT    8    9   25   36
CONECT    9   10   37   38
CONECT   10   11
CONECT   11   12   12   24
CONECT   12   13   16
CONECT   13   14
CONECT   14   15   15   39
CONECT   15   16   40
CONECT   16   17   17
CONECT   17   18   41
CONECT   18   19   24   24
CONECT   19   20   20   42
CONECT   20   21   43
CONECT   21   22   22   23
CONECT   23   24
CONECT   25   26   27   28
CONECT   26   44   45   46
CONECT   27   47   48   49
CONECT   28   50
END

HMDB0039058
     RDKit          3D
(R)-Heraclenol 2'-(3-methyl-2-butenoate)
 50 52  0  0  0  0  0  0  0  0999 V2000
   -3.3366    1.4188   -2.0948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3091    2.2201   -1.3219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2803    3.0747   -2.0657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3017    2.1668   -0.0066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3382    1.3215    0.6695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3759    1.3078    1.9475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3882    0.5329    0.0924 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4721   -0.2742    0.8236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0837    0.2298    0.5044 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9126   -0.5086    1.1844 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2609   -0.2221    1.0420 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9353    0.6682    1.8522 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5204    1.4045    2.8690 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5060    2.1177    3.3593 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6564    1.8608    2.6462 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2768    0.9335    1.6872 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9738    0.2935    0.6835 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3338   -0.6051   -0.1488 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0380   -1.2397   -1.1487 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3675   -2.1284   -1.9584 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0258   -2.3444   -1.7351 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3975   -3.1602   -2.4739 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3953   -1.7215   -0.7754 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9900   -0.8522    0.0385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6860   -1.6951    0.4021 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4932   -1.8868   -1.0818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8183   -2.6672    1.1741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0082   -2.0234    0.7020 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5020    1.5824   -3.1939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3006    1.7430   -1.8896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4882    0.3105   -1.9434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9545    2.4287   -2.6703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7859    3.8651   -2.6495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9249    3.5777   -1.3150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0207    2.7609    0.5190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6109   -0.1956    1.9032 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1364    0.1941   -0.5759 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0327    1.2856    0.8224 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4544    2.8134    4.1988 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6467    2.2519    2.7547 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0211    0.4697    0.5182 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0949   -1.0356   -1.2845 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8510   -2.6584   -2.7563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5573   -2.4525   -1.2811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4570   -0.9266   -1.6341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3258   -2.4819   -1.5041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3567   -3.6401    1.2146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7143   -2.3097    2.2096 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1491   -2.8618    0.6750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0860   -2.9422    1.0729 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  0
  8 25  1  0
 25 26  1  0
 25 27  1  0
 25 28  1  0
 24 11  1  0
 16 12  1  0
 24 18  2  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
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M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(R)-Heraclenol 2'-(3-methyl-2-butenoic acid)	Generator
3-Hydroxy-3-methyl-1-({7-oxo-7H-furo[3,2-g]chromen-9-yl}oxy)butan-2-yl 3-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₁H₂₂O₇

Average Molecular Weight

386.3952

Monoisotopic Molecular Weight

386.136553058

IUPAC Name

3-hydroxy-3-methyl-1-({7-oxo-7H-furo[3,2-g]chromen-9-yl}oxy)butan-2-yl 3-methylbut-2-enoate

Traditional Name

3-hydroxy-3-methyl-1-({7-oxofuro[3,2-g]chromen-9-yl}oxy)butan-2-yl 3-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

CC(C)=CC(=O)OC(COC1=C2OC(=O)C=CC2=CC2=C1OC=C2)C(C)(C)O

InChI Identifier

InChI=1S/C21H22O7/c1-12(2)9-17(23)27-15(21(3,4)24)11-26-20-18-14(7-8-25-18)10-13-5-6-16(22)28-19(13)20/h5-10,15,24H,11H2,1-4H3

InChI Key

YFMSPAAEUUQLDI-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as psoralens. These are organic compounds containing a psoralen moiety, which consists of a furan fused to a chromenone to for 7H-furo[3,2-g]chromen-7-one.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Furanocoumarins

Direct Parent

Psoralens

Alternative Parents

Substituents

Psoralen
Benzopyran
1-benzopyran
Benzofuran
Alkyl aryl ether
Fatty acid ester
Pyranone
Fatty acyl
Pyran
Benzenoid
Tertiary alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Furan
Heteroaromatic compound
Lactone
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Ether
Organic oxygen compound
Organooxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Membrane (HMDB: HMDB0039058)
Cell membrane (HMDB: HMDB0039058)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0039058)

Source

Exogenous

Exogenous (HMDB: HMDB0039058)

Food

Food (HMDB: HMDB0039058)

Herb and spice

Herbs and Spices (FooDB: FOOD00866)

Vegetable

Leaf vegetable

Green vegetables (FooDB: FOOD00872)

Fat and oil

Fats and oils (FooDB: FOOD00864)

Endogenous

Plant

Plant (HMDB: HMDB0039058)

Process

Not Available

Role

Biological role

Nutrient (HMDB: HMDB0039058)

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
Water Solubility	0.039 g/L	ALOGPS
logP	3.13	ALOGPS
logP	3.22	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	14.23	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	95.2 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	101.92 m³·mol⁻¹	ChemAxon
Polarizability	39.61 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
DarkChem	[M+H]+	190.767	31661259
DarkChem	[M-H]-	186.994	31661259
DeepCCS	[M+H]+	188.707	30932474
DeepCCS	[M-H]-	186.349	30932474
DeepCCS	[M-2H]-	220.706	30932474
DeepCCS	[M+Na]+	195.852	30932474
AllCCS	[M+H]+	189.6	32859911
AllCCS	[M+H-H2O]+	186.9	32859911
AllCCS	[M+NH4]+	192.0	32859911
AllCCS	[M+Na]+	192.7	32859911
AllCCS	[M-H]-	194.6	32859911
AllCCS	[M+Na-2H]-	194.5	32859911
AllCCS	[M+HCOO]-	194.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(R)-Heraclenol 2'-(3-methyl-2-butenoate)	CC(C)=CC(=O)OC(COC1=C2OC(=O)C=CC2=CC2=C1OC=C2)C(C)(C)O	4499.7	Standard polar	33892256
(R)-Heraclenol 2'-(3-methyl-2-butenoate)	CC(C)=CC(=O)OC(COC1=C2OC(=O)C=CC2=CC2=C1OC=C2)C(C)(C)O	2878.7	Standard non polar	33892256
(R)-Heraclenol 2'-(3-methyl-2-butenoate)	CC(C)=CC(=O)OC(COC1=C2OC(=O)C=CC2=CC2=C1OC=C2)C(C)(C)O	3025.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
(R)-Heraclenol 2'-(3-methyl-2-butenoate),1TMS,isomer #1	CC(C)=CC(=O)OC(COC1=C2OC=CC2=CC2=C1OC(=O)C=C2)C(C)(C)O[Si](C)(C)C	3047.4	Semi standard non polar	33892256
(R)-Heraclenol 2'-(3-methyl-2-butenoate),1TBDMS,isomer #1	CC(C)=CC(=O)OC(COC1=C2OC=CC2=CC2=C1OC(=O)C=C2)C(C)(C)O[Si](C)(C)C(C)(C)C	3285.0	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 - (R)-Heraclenol 2'-(3-methyl-2-butenoate) GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4i-9101000000-a8fc860cbcc48fa4617d	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (R)-Heraclenol 2'-(3-methyl-2-butenoate) GC-MS (1 TMS) - 70eV, Positive	splash10-001i-9610100000-9e7b6570218445b99074	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (R)-Heraclenol 2'-(3-methyl-2-butenoate) 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 - (R)-Heraclenol 2'-(3-methyl-2-butenoate) 10V, Positive-QTOF	splash10-00kr-3039000000-91bbd97d0fa8a67de43c	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-Heraclenol 2'-(3-methyl-2-butenoate) 20V, Positive-QTOF	splash10-0006-9132000000-41293de2efbb3e7dd3c1	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-Heraclenol 2'-(3-methyl-2-butenoate) 40V, Positive-QTOF	splash10-0udl-7490000000-c1360936b8869699d2e9	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-Heraclenol 2'-(3-methyl-2-butenoate) 10V, Negative-QTOF	splash10-0f79-2049000000-1af58b744a5d63516441	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-Heraclenol 2'-(3-methyl-2-butenoate) 20V, Negative-QTOF	splash10-0udi-2392000000-83e03775569dab61c807	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-Heraclenol 2'-(3-methyl-2-butenoate) 40V, Negative-QTOF	splash10-0a4i-4940000000-df5c8d3b07e7c024fadc	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-Heraclenol 2'-(3-methyl-2-butenoate) 10V, Positive-QTOF	splash10-000i-0092000000-27810d94210a5dc2e6f4	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-Heraclenol 2'-(3-methyl-2-butenoate) 20V, Positive-QTOF	splash10-0zg3-9140000000-a85986e6270593cfcf89	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-Heraclenol 2'-(3-methyl-2-butenoate) 40V, Positive-QTOF	splash10-000l-9220000000-ff173073ec7e35b370db	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-Heraclenol 2'-(3-methyl-2-butenoate) 10V, Negative-QTOF	splash10-000i-0094000000-6a8c5a0f98fd7298c731	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-Heraclenol 2'-(3-methyl-2-butenoate) 20V, Negative-QTOF	splash10-0udi-9661000000-3eea7ae35ad994131271	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-Heraclenol 2'-(3-methyl-2-butenoate) 40V, Negative-QTOF	splash10-0uk9-5690000000-1f5537d05c09c2d623d2	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

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

FDB018556

KNApSAcK ID

Not Available

Chemspider ID

35014731

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

78173139

PDB ID

Not Available

ChEBI ID

175918

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

(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

Enzymes

Enzyme Details

1. Liver carboxylesterase 1

General function:: Lipid transport and metabolism
Specific function:: Involved in the detoxification of xenobiotics and in the activation of ester and amide prodrugs. Hydrolyzes aromatic and aliphatic esters, but has no catalytic activity toward amides or a fatty acyl-CoA ester. Hydrolyzes the methyl ester group of cocaine to form benzoylecgonine. Catalyzes the transesterification of cocaine to form cocaethylene. Displays fatty acid ethyl ester synthase activity, catalyzing the ethyl esterification of oleic acid to ethyloleate.
Gene Name:: CES1
Uniprot ID:: P23141
Molecular weight:: 62520.62

Reactions

(R)-Heraclenol 2'-(3-methyl-2-butenoate) → (R)-Heraclenol	details

Showing metabocard for (R)-Heraclenol 2'-(3-methyl-2-butenoate) (HMDB0039058)

MOL for HMDB0039058 ((R)-Heraclenol 2'-(3-methyl-2-butenoate))

3D MOL for HMDB0039058 ((R)-Heraclenol 2'-(3-methyl-2-butenoate))

3D SDF for HMDB0039058 ((R)-Heraclenol 2'-(3-methyl-2-butenoate))

3D-SDF for HMDB0039058 ((R)-Heraclenol 2'-(3-methyl-2-butenoate))

PDB for HMDB0039058 ((R)-Heraclenol 2'-(3-methyl-2-butenoate))

3D PDB for HMDB0039058 ((R)-Heraclenol 2'-(3-methyl-2-butenoate))

SMILES for HMDB0039058 ((R)-Heraclenol 2'-(3-methyl-2-butenoate))

INCHI for HMDB0039058 ((R)-Heraclenol 2'-(3-methyl-2-butenoate))

Structure for HMDB0039058 ((R)-Heraclenol 2'-(3-methyl-2-butenoate))

3D Structure for HMDB0039058 ((R)-Heraclenol 2'-(3-methyl-2-butenoate))

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

Enzymes

Reactions