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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 12:39:42 UTC

Update Date

2022-09-22 17:44:24 UTC

HMDB ID

HMDB0253803

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Kirenol

Description

Hallol belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. Based on a literature review a significant number of articles have been published on Hallol. This compound has been identified in human blood as reported by (PMID: 31557052 ). Kirenol is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Kirenol 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

HMDB0253803
     RDKit          3D
Kirenol
 58 60  0  0  0  0  0  0  0  0999 V2000
    3.8354    1.4622   -1.3653 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1117    0.6353   -0.3197 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1213    0.3260    0.7680 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6088   -0.4238    1.7943 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2835   -0.4409    0.1605 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2758   -0.6708    1.1078 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9938    1.4547    0.1933 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7507    1.0277    0.3655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2259    2.0191    0.8959 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3968    1.1973    1.4555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8917    0.3808    0.2850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3454    0.0155    0.4497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6880   -0.3432    1.8881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1212    1.3137    0.2191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8328    1.7594   -1.0703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7977   -1.0056   -0.5137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8543   -1.3811   -1.5982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1628   -0.6290   -2.7615 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4208   -1.2912   -1.3623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9839   -0.7626   -0.0037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1417   -1.9286    0.9508 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4505   -0.3708    0.0232 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1865   -0.6531   -1.2856 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6697   -0.6439   -0.9581 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1575    2.2440   -1.8115 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6631    2.0642   -0.8876 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2246    0.8657   -2.1942 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5070    1.2874    1.1885 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7754   -0.0962    2.6924 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7430    0.1875   -0.6418 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9181   -1.4061   -0.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0846   -1.4958    1.6529 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2594    2.4999    0.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2073    2.6794    1.6620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6254    2.5690    0.0191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9682    0.5866    2.2649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1206    1.9184    1.8275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8564    1.0491   -0.6053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8088   -0.2188    1.9604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4861   -1.3833    2.1362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2598    0.3959    2.5644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9680    2.0554    0.9995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2046    1.0042    0.3019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9285    2.7416   -1.0638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7511   -0.6536   -1.0150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1611   -1.8969    0.0728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1228   -2.4351   -1.9017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6834   -1.0778   -3.5230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9304   -2.2939   -1.5577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9077   -0.6163   -2.1074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9682   -2.5903    0.7239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2093   -2.5514    0.7926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0818   -1.6106    2.0135 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0326   -0.9769    0.7835 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9867   -1.6710   -1.6776 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9837    0.1259   -2.0504 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8546   -1.4985   -0.2789 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2196   -0.8492   -1.9006 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  1  0
  2  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 12 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24  2  1  0
 22  8  1  0
 20 11  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  7 33  1  0
  9 34  1  0
  9 35  1  0
 10 36  1  0
 10 37  1  0
 11 38  1  0
 13 39  1  0
 13 40  1  0
 13 41  1  0
 14 42  1  0
 14 43  1  0
 15 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 18 48  1  0
 19 49  1  0
 19 50  1  0
 21 51  1  0
 21 52  1  0
 21 53  1  0
 22 54  1  0
 23 55  1  0
 23 56  1  0
 24 57  1  0
 24 58  1  0
M  END

  Mrv1533004191521112D          

 24 26  0  0  0  0            999 V2000
   -0.4733   -3.0591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4452   -3.5894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1868   -4.1197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -0.6336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465   -1.5322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465   -2.5928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4217   -2.3106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5032   -3.4053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1352   -3.9356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  2 20  1  0  0  0  0
  9 20  1  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0253803

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1(CO)CC(O)CC2(C)C3CCC(C)(C=C3CCC12)C(O)CO

> <INCHI_IDENTIFIER>
InChI=1S/C20H34O4/c1-18(17(24)11-21)7-6-15-13(8-18)4-5-16-19(2,12-22)9-14(23)10-20(15,16)3/h8,14-17,21-24H,4-7,9-12H2,1-3H3

> <INCHI_KEY>
NRYNTARIOIRWAB-UHFFFAOYSA-N

> <FORMULA>
C20H34O4

> <MOLECULAR_WEIGHT>
338.488

> <EXACT_MASS>
338.245709575

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
39.15278637039489

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-[6-hydroxy-8-(hydroxymethyl)-2,4b,8-trimethyl-2,3,4,4a,4b,5,6,7,8,8a,9,10-dodecahydrophenanthren-2-yl]ethane-1,2-diol

> <ALOGPS_LOGP>
1.39

> <JCHEM_LOGP>
1.156315519

> <ALOGPS_LOGS>
-3.24

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.820654982878462

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.789102009510437

> <JCHEM_PKA_STRONGEST_BASIC>
-2.70225922385033

> <JCHEM_POLAR_SURFACE_AREA>
80.92

> <JCHEM_REFRACTIVITY>
95.1539

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.96e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-[6-hydroxy-8-(hydroxymethyl)-2,4b,8-trimethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl]ethane-1,2-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0253803
     RDKit          3D
Kirenol
 58 60  0  0  0  0  0  0  0  0999 V2000
    3.8354    1.4622   -1.3653 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1117    0.6353   -0.3197 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1213    0.3260    0.7680 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6088   -0.4238    1.7943 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2835   -0.4409    0.1605 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2758   -0.6708    1.1078 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9938    1.4547    0.1933 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7507    1.0277    0.3655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2259    2.0191    0.8959 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3968    1.1973    1.4555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8917    0.3808    0.2850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3454    0.0155    0.4497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6880   -0.3432    1.8881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1212    1.3137    0.2191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8328    1.7594   -1.0703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7977   -1.0056   -0.5137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8543   -1.3811   -1.5982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1628   -0.6290   -2.7615 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4208   -1.2912   -1.3623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9839   -0.7626   -0.0037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1417   -1.9286    0.9508 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4505   -0.3708    0.0232 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1865   -0.6531   -1.2856 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6697   -0.6439   -0.9581 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1575    2.2440   -1.8115 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6631    2.0642   -0.8876 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2246    0.8657   -2.1942 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5070    1.2874    1.1885 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7754   -0.0962    2.6924 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7430    0.1875   -0.6418 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9181   -1.4061   -0.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0846   -1.4958    1.6529 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2594    2.4999    0.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2073    2.6794    1.6620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6254    2.5690    0.0191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9682    0.5866    2.2649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1206    1.9184    1.8275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8564    1.0491   -0.6053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8088   -0.2188    1.9604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4861   -1.3833    2.1362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2598    0.3959    2.5644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9680    2.0554    0.9995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2046    1.0042    0.3019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9285    2.7416   -1.0638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7511   -0.6536   -1.0150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1611   -1.8969    0.0728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1228   -2.4351   -1.9017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6834   -1.0778   -3.5230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9304   -2.2939   -1.5577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9077   -0.6163   -2.1074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9682   -2.5903    0.7239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2093   -2.5514    0.7926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0818   -1.6106    2.0135 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0326   -0.9769    0.7835 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9867   -1.6710   -1.6776 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9837    0.1259   -2.0504 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8546   -1.4985   -0.2789 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2196   -0.8492   -1.9006 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  1  0
  2  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 12 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24  2  1  0
 22  8  1  0
 20 11  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  7 33  1  0
  9 34  1  0
  9 35  1  0
 10 36  1  0
 10 37  1  0
 11 38  1  0
 13 39  1  0
 13 40  1  0
 13 41  1  0
 14 42  1  0
 14 43  1  0
 15 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 18 48  1  0
 19 49  1  0
 19 50  1  0
 21 51  1  0
 21 52  1  0
 21 53  1  0
 22 54  1  0
 23 55  1  0
 23 56  1  0
 24 57  1  0
 24 58  1  0
M  END

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0      -0.883  -5.710   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.564  -5.184   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.831  -6.700   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.349  -7.690   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.206  -3.850   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.564  -2.516   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -0.206  -1.183   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.104  -2.516   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.874  -3.850   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.644  -2.516   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.414  -3.850   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.184  -2.516   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.724  -2.516   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.494  -3.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.673  -2.860   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.724  -5.184   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.184  -5.184   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.414  -6.517   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.874  -6.517   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.104  -5.184   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.673  -4.840   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      10.121  -4.313   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       8.406  -6.356   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       9.586  -7.346   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    5   20                                             
CONECT    3    2    4                                                       
CONECT    4    3                                                            
CONECT    5    2    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   11   20                                             
CONECT   10    9                                                            
CONECT   11    9   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   21                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   11   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19    2    9                                                  
CONECT   21   14   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

COMPND    HMDB0253803
HETATM    1  C1  UNL     1       3.835   1.462  -1.365  1.00  0.00           C  
HETATM    2  C2  UNL     1       3.112   0.635  -0.320  1.00  0.00           C  
HETATM    3  C3  UNL     1       4.121   0.326   0.768  1.00  0.00           C  
HETATM    4  O1  UNL     1       3.609  -0.424   1.794  1.00  0.00           O  
HETATM    5  C4  UNL     1       5.284  -0.441   0.160  1.00  0.00           C  
HETATM    6  O2  UNL     1       6.276  -0.671   1.108  1.00  0.00           O  
HETATM    7  C5  UNL     1       1.994   1.455   0.193  1.00  0.00           C  
HETATM    8  C6  UNL     1       0.751   1.028   0.366  1.00  0.00           C  
HETATM    9  C7  UNL     1      -0.226   2.019   0.896  1.00  0.00           C  
HETATM   10  C8  UNL     1      -1.397   1.197   1.456  1.00  0.00           C  
HETATM   11  C9  UNL     1      -1.892   0.381   0.285  1.00  0.00           C  
HETATM   12  C10 UNL     1      -3.345   0.016   0.450  1.00  0.00           C  
HETATM   13  C11 UNL     1      -3.688  -0.343   1.888  1.00  0.00           C  
HETATM   14  C12 UNL     1      -4.121   1.314   0.219  1.00  0.00           C  
HETATM   15  O3  UNL     1      -3.833   1.759  -1.070  1.00  0.00           O  
HETATM   16  C13 UNL     1      -3.798  -1.006  -0.514  1.00  0.00           C  
HETATM   17  C14 UNL     1      -2.854  -1.381  -1.598  1.00  0.00           C  
HETATM   18  O4  UNL     1      -3.163  -0.629  -2.761  1.00  0.00           O  
HETATM   19  C15 UNL     1      -1.421  -1.291  -1.362  1.00  0.00           C  
HETATM   20  C16 UNL     1      -0.984  -0.763  -0.004  1.00  0.00           C  
HETATM   21  C17 UNL     1      -1.142  -1.929   0.951  1.00  0.00           C  
HETATM   22  C18 UNL     1       0.450  -0.371   0.023  1.00  0.00           C  
HETATM   23  C19 UNL     1       1.187  -0.653  -1.286  1.00  0.00           C  
HETATM   24  C20 UNL     1       2.670  -0.644  -0.958  1.00  0.00           C  
HETATM   25  H1  UNL     1       3.157   2.244  -1.812  1.00  0.00           H  
HETATM   26  H2  UNL     1       4.663   2.064  -0.888  1.00  0.00           H  
HETATM   27  H3  UNL     1       4.225   0.866  -2.194  1.00  0.00           H  
HETATM   28  H4  UNL     1       4.507   1.287   1.188  1.00  0.00           H  
HETATM   29  H5  UNL     1       3.775  -0.096   2.692  1.00  0.00           H  
HETATM   30  H6  UNL     1       5.743   0.188  -0.642  1.00  0.00           H  
HETATM   31  H7  UNL     1       4.918  -1.406  -0.198  1.00  0.00           H  
HETATM   32  H8  UNL     1       6.085  -1.496   1.653  1.00  0.00           H  
HETATM   33  H9  UNL     1       2.259   2.500   0.440  1.00  0.00           H  
HETATM   34  H10 UNL     1       0.207   2.679   1.662  1.00  0.00           H  
HETATM   35  H11 UNL     1      -0.625   2.569   0.019  1.00  0.00           H  
HETATM   36  H12 UNL     1      -0.968   0.587   2.265  1.00  0.00           H  
HETATM   37  H13 UNL     1      -2.121   1.918   1.827  1.00  0.00           H  
HETATM   38  H14 UNL     1      -1.856   1.049  -0.605  1.00  0.00           H  
HETATM   39  H15 UNL     1      -4.809  -0.219   1.960  1.00  0.00           H  
HETATM   40  H16 UNL     1      -3.486  -1.383   2.136  1.00  0.00           H  
HETATM   41  H17 UNL     1      -3.260   0.396   2.564  1.00  0.00           H  
HETATM   42  H18 UNL     1      -3.968   2.055   0.999  1.00  0.00           H  
HETATM   43  H19 UNL     1      -5.205   1.004   0.302  1.00  0.00           H  
HETATM   44  H20 UNL     1      -3.928   2.742  -1.064  1.00  0.00           H  
HETATM   45  H21 UNL     1      -4.751  -0.654  -1.015  1.00  0.00           H  
HETATM   46  H22 UNL     1      -4.161  -1.897   0.073  1.00  0.00           H  
HETATM   47  H23 UNL     1      -3.123  -2.435  -1.902  1.00  0.00           H  
HETATM   48  H24 UNL     1      -2.683  -1.078  -3.523  1.00  0.00           H  
HETATM   49  H25 UNL     1      -0.930  -2.294  -1.558  1.00  0.00           H  
HETATM   50  H26 UNL     1      -0.908  -0.616  -2.107  1.00  0.00           H  
HETATM   51  H27 UNL     1      -1.968  -2.590   0.724  1.00  0.00           H  
HETATM   52  H28 UNL     1      -0.209  -2.551   0.793  1.00  0.00           H  
HETATM   53  H29 UNL     1      -1.082  -1.611   2.014  1.00  0.00           H  
HETATM   54  H30 UNL     1       1.033  -0.977   0.783  1.00  0.00           H  
HETATM   55  H31 UNL     1       0.987  -1.671  -1.678  1.00  0.00           H  
HETATM   56  H32 UNL     1       0.984   0.126  -2.050  1.00  0.00           H  
HETATM   57  H33 UNL     1       2.855  -1.498  -0.279  1.00  0.00           H  
HETATM   58  H34 UNL     1       3.220  -0.849  -1.901  1.00  0.00           H  
CONECT    1    2   25   26   27
CONECT    2    3    7   24
CONECT    3    4    5   28
CONECT    4   29
CONECT    5    6   30   31
CONECT    6   32
CONECT    7    8    8   33
CONECT    8    9   22
CONECT    9   10   34   35
CONECT   10   11   36   37
CONECT   11   12   20   38
CONECT   12   13   14   16
CONECT   13   39   40   41
CONECT   14   15   42   43
CONECT   15   44
CONECT   16   17   45   46
CONECT   17   18   19   47
CONECT   18   48
CONECT   19   20   49   50
CONECT   20   21   22
CONECT   21   51   52   53
CONECT   22   23   54
CONECT   23   24   55   56
CONECT   24   57   58
END

HMDB0253803
     RDKit          3D
Kirenol
 58 60  0  0  0  0  0  0  0  0999 V2000
    3.8354    1.4622   -1.3653 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1117    0.6353   -0.3197 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1213    0.3260    0.7680 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6088   -0.4238    1.7943 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2835   -0.4409    0.1605 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2758   -0.6708    1.1078 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9938    1.4547    0.1933 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7507    1.0277    0.3655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2259    2.0191    0.8959 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3968    1.1973    1.4555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8917    0.3808    0.2850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3454    0.0155    0.4497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6880   -0.3432    1.8881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1212    1.3137    0.2191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8328    1.7594   -1.0703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7977   -1.0056   -0.5137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8543   -1.3811   -1.5982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1628   -0.6290   -2.7615 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4208   -1.2912   -1.3623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9839   -0.7626   -0.0037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1417   -1.9286    0.9508 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4505   -0.3708    0.0232 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1865   -0.6531   -1.2856 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6697   -0.6439   -0.9581 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1575    2.2440   -1.8115 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6631    2.0642   -0.8876 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2246    0.8657   -2.1942 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5070    1.2874    1.1885 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7754   -0.0962    2.6924 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7430    0.1875   -0.6418 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9181   -1.4061   -0.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0846   -1.4958    1.6529 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2594    2.4999    0.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2073    2.6794    1.6620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6254    2.5690    0.0191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9682    0.5866    2.2649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1206    1.9184    1.8275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8564    1.0491   -0.6053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8088   -0.2188    1.9604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4861   -1.3833    2.1362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2598    0.3959    2.5644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9680    2.0554    0.9995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2046    1.0042    0.3019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9285    2.7416   -1.0638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7511   -0.6536   -1.0150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1611   -1.8969    0.0728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1228   -2.4351   -1.9017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6834   -1.0778   -3.5230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9304   -2.2939   -1.5577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9077   -0.6163   -2.1074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9682   -2.5903    0.7239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2093   -2.5514    0.7926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0818   -1.6106    2.0135 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0326   -0.9769    0.7835 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9867   -1.6710   -1.6776 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9837    0.1259   -2.0504 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8546   -1.4985   -0.2789 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2196   -0.8492   -1.9006 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  1  0
  2  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 12 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24  2  1  0
 22  8  1  0
 20 11  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  7 33  1  0
  9 34  1  0
  9 35  1  0
 10 36  1  0
 10 37  1  0
 11 38  1  0
 13 39  1  0
 13 40  1  0
 13 41  1  0
 14 42  1  0
 14 43  1  0
 15 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 18 48  1  0
 19 49  1  0
 19 50  1  0
 21 51  1  0
 21 52  1  0
 21 53  1  0
 22 54  1  0
 23 55  1  0
 23 56  1  0
 24 57  1  0
 24 58  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₀H₃₄O₄

Average Molecular Weight

338.488

Monoisotopic Molecular Weight

338.245709575

IUPAC Name

1-[6-hydroxy-8-(hydroxymethyl)-2,4b,8-trimethyl-2,3,4,4a,4b,5,6,7,8,8a,9,10-dodecahydrophenanthren-2-yl]ethane-1,2-diol

Traditional Name

1-[6-hydroxy-8-(hydroxymethyl)-2,4b,8-trimethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl]ethane-1,2-diol

CAS Registry Number

Not Available

SMILES

CC1(CO)CC(O)CC2(C)C3CCC(C)(C=C3CCC12)C(O)CO

InChI Identifier

InChI=1S/C20H34O4/c1-18(17(24)11-21)7-6-15-13(8-18)4-5-16-19(2,12-22)9-14(23)10-20(15,16)3/h8,14-17,21-24H,4-7,9-12H2,1-3H3

InChI Key

NRYNTARIOIRWAB-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Pimarane diterpenoid
Diterpenoid
Abietane diterpenoid
Phenanthrene
Hydrophenanthrene
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	1.39	ALOGPS
logP	1.16	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	13.79	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	80.92 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	95.15 m³·mol⁻¹	ChemAxon
Polarizability	39.15 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	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M-2H]-	215.869	30932474
DeepCCS	[M+Na]+	191.096	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Kirenol	CC1(CO)CC(O)CC2(C)C3CCC(C)(C=C3CCC12)C(O)CO	2778.6	Standard polar	33892256
Kirenol	CC1(CO)CC(O)CC2(C)C3CCC(C)(C=C3CCC12)C(O)CO	2634.3	Standard non polar	33892256
Kirenol	CC1(CO)CC(O)CC2(C)C3CCC(C)(C=C3CCC12)C(O)CO	2991.6	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (Non-derivatized) - 70eV, Positive	splash10-05g0-1296000000-004dd1da4d719b711782	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TMS_3_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TMS_3_2) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TMS_3_3) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TMS_3_4) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TMS_4_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TBDMS_1_3) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TBDMS_1_4) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TBDMS_2_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TBDMS_2_2) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TBDMS_2_3) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kirenol GC-MS (TBDMS_2_4) - 70eV, Positive	Not Available	2021-11-04	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 - Kirenol 10V, Negative-QTOF	splash10-000i-0009000000-9e7e1f1199ccd979487c	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kirenol 20V, Negative-QTOF	splash10-0a4r-2079000000-7de50d340da6b208bfcf	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kirenol 40V, Negative-QTOF	splash10-00kr-2049000000-0fffd5b13f06c2c9ec73	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kirenol 10V, Positive-QTOF	splash10-000i-0019000000-bb5b204508f01413a08d	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kirenol 20V, Positive-QTOF	splash10-0w90-0397000000-ab98f5a50b4b2bc686e5	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kirenol 40V, Positive-QTOF	splash10-01oy-9540000000-d9811a0c3b3fc8860fc4	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood
Urine

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

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Urine	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Cancer patients undergoing total body irradiation	31424920	details

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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

45934421

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 Kirenol (HMDB0253803)

MOL for HMDB0253803 (Kirenol)

3D MOL for HMDB0253803 (Kirenol)

3D SDF for HMDB0253803 (Kirenol)

3D-SDF for HMDB0253803 (Kirenol)

PDB for HMDB0253803 (Kirenol)

3D PDB for HMDB0253803 (Kirenol)

SMILES for HMDB0253803 (Kirenol)

INCHI for HMDB0253803 (Kirenol)

Structure for HMDB0253803 (Kirenol)

3D Structure for HMDB0253803 (Kirenol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra