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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-10 23:44:19 UTC

Update Date

2021-09-26 22:55:59 UTC

HMDB ID

HMDB0246722

Secondary Accession Numbers

None

Metabolite Identification

Common Name

5-(4-Phenoxybutoxy)psoralen

Description

5-(4-Phenoxybutoxy)psoralen 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. Based on a literature review a significant number of articles have been published on 5-(4-Phenoxybutoxy)psoralen. This compound has been identified in human blood as reported by (PMID: 31557052 ). 5-(4-phenoxybutoxy)psoralen is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 5-(4-Phenoxybutoxy)psoralen is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

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

  Mrv1652309112101442D          

 26 29  0  0  0  0            999 V2000
   -4.2868   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5303   -5.9145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8659   -6.6682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6864   -6.5820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  4  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 13 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 22 26  1  0  0  0  0
M  END

HMDB0246722
     RDKit          3D
5-(4-Phenoxybutoxy)psoralen
 44 47  0  0  0  0  0  0  0  0999 V2000
   -4.1818    3.9829    1.8369 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7176    2.8545    1.5233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3684    2.5801    1.4983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9436    1.3266    1.1446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8529    0.3365    0.8109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4777   -0.9138    0.4646 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1913   -1.3554    0.3606 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4212   -1.6176   -0.7361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1247   -0.5737   -1.7047 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7323    0.5392   -1.2084 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0711    0.0480   -0.6759 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8284    1.1839   -0.2269 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0898    1.0410    0.3083 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6769   -0.1854    0.4362 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9503   -0.3063    0.9790 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6516    0.7946    1.3998 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0527    2.0304    1.2677 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7807    2.1581    0.7263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4701   -1.8555    0.1636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4798   -3.1794   -0.2127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7861   -3.5821   -0.3737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5448   -2.5371   -0.1039 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8056   -1.4968    0.2180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1705   -0.2280    0.5660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1992    0.7033    0.8677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5533    1.9096    1.2100 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6749    3.3852    1.7657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9026    1.0708    1.1616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7657   -2.5895   -1.2566 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5928   -1.9711   -0.3088 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2748   -0.9800   -2.6882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1249   -0.0675   -1.9830 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3122    1.2898   -0.5638 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0495    1.1682   -2.1328 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9377   -0.5650    0.2390 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6369   -0.5342   -1.4162 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1187   -1.0500    0.1024 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3927   -1.2767    1.0705 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6583    0.7074    1.8298 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6181    2.8863    1.6037 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3630    3.1597    0.6488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6199   -3.8073   -0.3597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1930   -4.5313   -0.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2190    0.0475    0.6053 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
  6 19  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26  2  1  0
 25  5  1  0
 18 13  1  0
 23 19  2  0
  3 27  1  0
  4 28  1  0
  8 29  1  0
  8 30  1  0
  9 31  1  0
  9 32  1  0
 10 33  1  0
 10 34  1  0
 11 35  1  0
 11 36  1  0
 14 37  1  0
 15 38  1  0
 16 39  1  0
 17 40  1  0
 18 41  1  0
 20 42  1  0
 21 43  1  0
 24 44  1  0
M  END

  Mrv1652309112101442D          

 26 29  0  0  0  0            999 V2000
   -4.2868   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5303   -5.9145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8659   -6.6682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6864   -6.5820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  4  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 13 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 22 26  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0246722

> <DATABASE_NAME>
hmdb

> <SMILES>
O=C1OC2=CC3=C(C=CO3)C(OCCCCOC3=CC=CC=C3)=C2C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H18O5/c22-20-9-8-16-19(26-20)14-18-17(10-13-24-18)21(16)25-12-5-4-11-23-15-6-2-1-3-7-15/h1-3,6-10,13-14H,4-5,11-12H2

> <INCHI_KEY>
KINMYBBFQRSVLL-UHFFFAOYSA-N

> <FORMULA>
C21H18O5

> <MOLECULAR_WEIGHT>
350.37

> <EXACT_MASS>
350.11542368

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
37.320804730055514

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-(4-phenoxybutoxy)-7H-furo[3,2-g]chromen-7-one

> <ALOGPS_LOGP>
4.51

> <JCHEM_LOGP>
4.006183767333333

> <ALOGPS_LOGS>
-4.66

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8270895503139957

> <JCHEM_POLAR_SURFACE_AREA>
57.900000000000006

> <JCHEM_REFRACTIVITY>
96.91510000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.69e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-(4-phenoxybutoxy)furo[3,2-g]chromen-7-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0246722
     RDKit          3D
5-(4-Phenoxybutoxy)psoralen
 44 47  0  0  0  0  0  0  0  0999 V2000
   -4.1818    3.9829    1.8369 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7176    2.8545    1.5233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3684    2.5801    1.4983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9436    1.3266    1.1446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8529    0.3365    0.8109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4777   -0.9138    0.4646 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1913   -1.3554    0.3606 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4212   -1.6176   -0.7361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1247   -0.5737   -1.7047 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7323    0.5392   -1.2084 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0711    0.0480   -0.6759 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8284    1.1839   -0.2269 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0898    1.0410    0.3083 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6769   -0.1854    0.4362 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9503   -0.3063    0.9790 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6516    0.7946    1.3998 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0527    2.0304    1.2677 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7807    2.1581    0.7263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4701   -1.8555    0.1636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4798   -3.1794   -0.2127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7861   -3.5821   -0.3737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5448   -2.5371   -0.1039 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8056   -1.4968    0.2180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1705   -0.2280    0.5660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1992    0.7033    0.8677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5533    1.9096    1.2100 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6749    3.3852    1.7657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9026    1.0708    1.1616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7657   -2.5895   -1.2566 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5928   -1.9711   -0.3088 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2748   -0.9800   -2.6882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1249   -0.0675   -1.9830 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3122    1.2898   -0.5638 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0495    1.1682   -2.1328 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9377   -0.5650    0.2390 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6369   -0.5342   -1.4162 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1187   -1.0500    0.1024 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3927   -1.2767    1.0705 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6583    0.7074    1.8298 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6181    2.8863    1.6037 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3630    3.1597    0.6488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6199   -3.8073   -0.3597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1930   -4.5313   -0.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2190    0.0475    0.6053 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
  6 19  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26  2  1  0
 25  5  1  0
 18 13  1  0
 23 19  2  0
  3 27  1  0
  4 28  1  0
  8 29  1  0
  8 30  1  0
  9 31  1  0
  9 32  1  0
 10 33  1  0
 10 34  1  0
 11 35  1  0
 11 36  1  0
 14 37  1  0
 15 38  1  0
 16 39  1  0
 17 40  1  0
 18 41  1  0
 20 42  1  0
 21 43  1  0
 24 44  1  0
M  END

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0      -8.002  -6.160   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.335  -6.160   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.668  -8.470   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.002  -7.700   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -4.001  -8.470   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334  -8.470   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -8.470   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.001  -8.470   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335  -6.160   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.002  -6.160   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       9.336  -5.390   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       8.002  -7.700   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.668  -8.470   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.335 -10.780   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.857 -11.040   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.483 -12.447   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.015 -12.286   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1                                                       
CONECT    7    4    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   23                                                  
CONECT   14   13   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   14   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   26                                                  
CONECT   23   22   13   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   22                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

COMPND    HMDB0246722
HETATM    1  O1  UNL     1      -4.182   3.983   1.837  1.00  0.00           O  
HETATM    2  C1  UNL     1      -3.718   2.854   1.523  1.00  0.00           C  
HETATM    3  C2  UNL     1      -2.368   2.580   1.498  1.00  0.00           C  
HETATM    4  C3  UNL     1      -1.944   1.327   1.145  1.00  0.00           C  
HETATM    5  C4  UNL     1      -2.853   0.336   0.811  1.00  0.00           C  
HETATM    6  C5  UNL     1      -2.478  -0.914   0.465  1.00  0.00           C  
HETATM    7  O2  UNL     1      -1.191  -1.355   0.361  1.00  0.00           O  
HETATM    8  C6  UNL     1      -0.421  -1.618  -0.736  1.00  0.00           C  
HETATM    9  C7  UNL     1      -0.125  -0.574  -1.705  1.00  0.00           C  
HETATM   10  C8  UNL     1       0.732   0.539  -1.208  1.00  0.00           C  
HETATM   11  C9  UNL     1       2.071   0.048  -0.676  1.00  0.00           C  
HETATM   12  O3  UNL     1       2.828   1.184  -0.227  1.00  0.00           O  
HETATM   13  C10 UNL     1       4.090   1.041   0.308  1.00  0.00           C  
HETATM   14  C11 UNL     1       4.677  -0.185   0.436  1.00  0.00           C  
HETATM   15  C12 UNL     1       5.950  -0.306   0.979  1.00  0.00           C  
HETATM   16  C13 UNL     1       6.652   0.795   1.400  1.00  0.00           C  
HETATM   17  C14 UNL     1       6.053   2.030   1.268  1.00  0.00           C  
HETATM   18  C15 UNL     1       4.781   2.158   0.726  1.00  0.00           C  
HETATM   19  C16 UNL     1      -3.470  -1.855   0.164  1.00  0.00           C  
HETATM   20  C17 UNL     1      -3.480  -3.179  -0.213  1.00  0.00           C  
HETATM   21  C18 UNL     1      -4.786  -3.582  -0.374  1.00  0.00           C  
HETATM   22  O4  UNL     1      -5.545  -2.537  -0.104  1.00  0.00           O  
HETATM   23  C19 UNL     1      -4.806  -1.497   0.218  1.00  0.00           C  
HETATM   24  C20 UNL     1      -5.170  -0.228   0.566  1.00  0.00           C  
HETATM   25  C21 UNL     1      -4.199   0.703   0.868  1.00  0.00           C  
HETATM   26  O5  UNL     1      -4.553   1.910   1.210  1.00  0.00           O  
HETATM   27  H1  UNL     1      -1.675   3.385   1.766  1.00  0.00           H  
HETATM   28  H2  UNL     1      -0.903   1.071   1.162  1.00  0.00           H  
HETATM   29  H3  UNL     1      -0.766  -2.590  -1.257  1.00  0.00           H  
HETATM   30  H4  UNL     1       0.593  -1.971  -0.309  1.00  0.00           H  
HETATM   31  H5  UNL     1       0.275  -0.980  -2.688  1.00  0.00           H  
HETATM   32  H6  UNL     1      -1.125  -0.067  -1.983  1.00  0.00           H  
HETATM   33  H7  UNL     1       0.312   1.290  -0.564  1.00  0.00           H  
HETATM   34  H8  UNL     1       1.049   1.168  -2.133  1.00  0.00           H  
HETATM   35  H9  UNL     1       1.938  -0.565   0.239  1.00  0.00           H  
HETATM   36  H10 UNL     1       2.637  -0.534  -1.416  1.00  0.00           H  
HETATM   37  H11 UNL     1       4.119  -1.050   0.102  1.00  0.00           H  
HETATM   38  H12 UNL     1       6.393  -1.277   1.071  1.00  0.00           H  
HETATM   39  H13 UNL     1       7.658   0.707   1.830  1.00  0.00           H  
HETATM   40  H14 UNL     1       6.618   2.886   1.604  1.00  0.00           H  
HETATM   41  H15 UNL     1       4.363   3.160   0.649  1.00  0.00           H  
HETATM   42  H16 UNL     1      -2.620  -3.807  -0.360  1.00  0.00           H  
HETATM   43  H17 UNL     1      -5.193  -4.531  -0.658  1.00  0.00           H  
HETATM   44  H18 UNL     1      -6.219   0.048   0.605  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   26
CONECT    3    4    4   27
CONECT    4    5   28
CONECT    5    6    6   25
CONECT    6    7   19
CONECT    7    8
CONECT    8    9   29   30
CONECT    9   10   31   32
CONECT   10   11   33   34
CONECT   11   12   35   36
CONECT   12   13
CONECT   13   14   14   18
CONECT   14   15   37
CONECT   15   16   16   38
CONECT   16   17   39
CONECT   17   18   18   40
CONECT   18   41
CONECT   19   20   23   23
CONECT   20   21   21   42
CONECT   21   22   43
CONECT   22   23
CONECT   23   24
CONECT   24   25   25   44
CONECT   25   26
END

HMDB0246722
     RDKit          3D
5-(4-Phenoxybutoxy)psoralen
 44 47  0  0  0  0  0  0  0  0999 V2000
   -4.1818    3.9829    1.8369 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7176    2.8545    1.5233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3684    2.5801    1.4983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9436    1.3266    1.1446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8529    0.3365    0.8109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4777   -0.9138    0.4646 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1913   -1.3554    0.3606 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4212   -1.6176   -0.7361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1247   -0.5737   -1.7047 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7323    0.5392   -1.2084 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0711    0.0480   -0.6759 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8284    1.1839   -0.2269 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0898    1.0410    0.3083 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6769   -0.1854    0.4362 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9503   -0.3063    0.9790 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6516    0.7946    1.3998 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0527    2.0304    1.2677 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7807    2.1581    0.7263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4701   -1.8555    0.1636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4798   -3.1794   -0.2127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7861   -3.5821   -0.3737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5448   -2.5371   -0.1039 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8056   -1.4968    0.2180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1705   -0.2280    0.5660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1992    0.7033    0.8677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5533    1.9096    1.2100 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6749    3.3852    1.7657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9026    1.0708    1.1616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7657   -2.5895   -1.2566 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5928   -1.9711   -0.3088 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2748   -0.9800   -2.6882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1249   -0.0675   -1.9830 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3122    1.2898   -0.5638 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0495    1.1682   -2.1328 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9377   -0.5650    0.2390 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6369   -0.5342   -1.4162 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1187   -1.0500    0.1024 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3927   -1.2767    1.0705 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6583    0.7074    1.8298 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6181    2.8863    1.6037 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3630    3.1597    0.6488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6199   -3.8073   -0.3597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1930   -4.5313   -0.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2190    0.0475    0.6053 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
  6 19  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26  2  1  0
 25  5  1  0
 18 13  1  0
 23 19  2  0
  3 27  1  0
  4 28  1  0
  8 29  1  0
  8 30  1  0
  9 31  1  0
  9 32  1  0
 10 33  1  0
 10 34  1  0
 11 35  1  0
 11 36  1  0
 14 37  1  0
 15 38  1  0
 16 39  1  0
 17 40  1  0
 18 41  1  0
 20 42  1  0
 21 43  1  0
 24 44  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₁H₁₈O₅

Average Molecular Weight

350.37

Monoisotopic Molecular Weight

350.11542368

IUPAC Name

4-(4-phenoxybutoxy)-7H-furo[3,2-g]chromen-7-one

Traditional Name

4-(4-phenoxybutoxy)furo[3,2-g]chromen-7-one

CAS Registry Number

Not Available

SMILES

O=C1OC2=CC3=C(C=CO3)C(OCCCCOC3=CC=CC=C3)=C2C=C1

InChI Identifier

InChI=1S/C21H18O5/c22-20-9-8-16-19(26-20)14-18-17(10-13-24-18)21(16)25-12-5-4-11-23-15-6-2-1-3-7-15/h1-3,6-10,13-14H,4-5,11-12H2

InChI Key

KINMYBBFQRSVLL-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
Phenoxy compound
Phenol ether
Alkyl aryl ether
Pyranone
Monocyclic benzene moiety
Benzenoid
Pyran
Heteroaromatic compound
Furan
Lactone
Oxacycle
Ether
Organoheterocyclic compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

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	4.51	ALOGPS
logP	4.01	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	57.9 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	96.92 m³·mol⁻¹	ChemAxon
Polarizability	37.32 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	187.892	30932474
DeepCCS	[M-H]-	185.534	30932474
DeepCCS	[M-2H]-	219.845	30932474
DeepCCS	[M+Na]+	195.196	30932474
AllCCS	[M+H]+	183.4	32859911
AllCCS	[M+H-H2O]+	180.3	32859911
AllCCS	[M+NH4]+	186.2	32859911
AllCCS	[M+Na]+	187.1	32859911
AllCCS	[M-H]-	185.6	32859911
AllCCS	[M+Na-2H]-	184.9	32859911
AllCCS	[M+HCOO]-	184.3	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
5-(4-Phenoxybutoxy)psoralen	O=C1OC2=CC3=C(C=CO3)C(OCCCCOC3=CC=CC=C3)=C2C=C1	4049.7	Standard polar	33892256
5-(4-Phenoxybutoxy)psoralen	O=C1OC2=CC3=C(C=CO3)C(OCCCCOC3=CC=CC=C3)=C2C=C1	3157.9	Standard non polar	33892256
5-(4-Phenoxybutoxy)psoralen	O=C1OC2=CC3=C(C=CO3)C(OCCCCOC3=CC=CC=C3)=C2C=C1	3270.5	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 - 5-(4-Phenoxybutoxy)psoralen GC-MS (Non-derivatized) - 70eV, Positive	splash10-0ac3-5974000000-67581cdbf5f6c395bb4b	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-(4-Phenoxybutoxy)psoralen 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 - 5-(4-Phenoxybutoxy)psoralen 10V, Positive-QTOF	splash10-0udi-0029000000-a87739fa842508a536a3	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(4-Phenoxybutoxy)psoralen 20V, Positive-QTOF	splash10-0udj-6359000000-5cfec2f8307fbb37d14b	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(4-Phenoxybutoxy)psoralen 40V, Positive-QTOF	splash10-0fba-9564000000-f190ec81819e7673a255	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(4-Phenoxybutoxy)psoralen 10V, Negative-QTOF	splash10-0002-1009000000-815d202a0c0416feb0e1	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(4-Phenoxybutoxy)psoralen 20V, Negative-QTOF	splash10-0006-9075000000-cdd0faf480fc69ca2ee6	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(4-Phenoxybutoxy)psoralen 40V, Negative-QTOF	splash10-0006-9210000000-bf0ffb02ea16ca6e2e7a	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

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

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9477516

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11302540

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

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for 5-(4-Phenoxybutoxy)psoralen (HMDB0246722)

MOL for HMDB0246722 (5-(4-Phenoxybutoxy)psoralen)

3D MOL for HMDB0246722 (5-(4-Phenoxybutoxy)psoralen)

3D SDF for HMDB0246722 (5-(4-Phenoxybutoxy)psoralen)

3D-SDF for HMDB0246722 (5-(4-Phenoxybutoxy)psoralen)

PDB for HMDB0246722 (5-(4-Phenoxybutoxy)psoralen)

3D PDB for HMDB0246722 (5-(4-Phenoxybutoxy)psoralen)

SMILES for HMDB0246722 (5-(4-Phenoxybutoxy)psoralen)

INCHI for HMDB0246722 (5-(4-Phenoxybutoxy)psoralen)

Structure for HMDB0246722 (5-(4-Phenoxybutoxy)psoralen)

3D Structure for HMDB0246722 (5-(4-Phenoxybutoxy)psoralen)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra