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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 21:57:14 UTC

Update Date

2021-09-26 23:16:55 UTC

HMDB ID

HMDB0259397

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Ulinastatin

Description

Ulinastatin, also known as MR 20 or miraclid, belongs to the class of organic compounds known as 1,3-dioxanes. These are organic compounds containing 1,3-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 3. Based on a literature review a significant number of articles have been published on Ulinastatin. This compound has been identified in human blood as reported by (PMID: 31557052 ). Ulinastatin is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Ulinastatin 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

HMDB0259397
     RDKit          3D
Ulinastatin
 32 34  0  0  0  0  0  0  0  0999 V2000
   -3.5736   -0.3950    0.9745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2486    0.8781    0.7295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4113    1.1242   -0.4772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1997    0.2299   -0.3746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5782   -1.2107   -0.2386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0621   -1.4075    0.0166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3761    0.6250    0.8450 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8018   -0.1205    0.7928 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4765    0.2910   -0.3568 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9168   -0.0390   -0.3225 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7318    0.1676    0.7713 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0114   -0.2600    0.4347 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8991   -0.7088   -0.8644 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6542   -0.5677   -1.2878 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8253   -0.2906   -1.4370 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3649    0.4447   -1.6169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1815   -0.6503    1.8361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5624    1.6944    1.3542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0900    2.1707   -0.5673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0009    0.8311   -1.3674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0494   -1.7111    0.6199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2598   -1.7527   -1.1411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2249   -2.4319    0.4088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5564   -1.2709   -0.9860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0513    1.7018    0.7395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9395    0.4565    1.7737 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3444    1.4017   -0.4744 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4402    0.5860    1.7248 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9083   -0.2519    1.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7023   -1.1192   -1.4634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0872    1.4998   -1.6540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8944    0.0856   -2.5052 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  4  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
  9 15  1  0
 15 16  1  0
  6  1  1  0
 14 10  1  0
 16  4  1  0
  1 17  1  0
  2 18  1  0
  3 19  1  0
  3 20  1  0
  5 21  1  0
  5 22  1  0
  6 23  1  0
  6 24  1  0
  7 25  1  0
  7 26  1  0
  9 27  1  0
 11 28  1  0
 12 29  1  0
 13 30  1  0
 16 31  1  0
 16 32  1  0
M  END


  Mrv1652309112123572D          

 16 18  0  0  0  0            999 V2000
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4994    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2840    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2840   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4994   -0.2549    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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  3  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
  3 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 12 16  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0259397

> <DATABASE_NAME>
hmdb

> <SMILES>
C1CC2(COC(OC2)C2=CC=CO2)CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C13H16O3/c1-2-6-13(7-3-1)9-15-12(16-10-13)11-5-4-8-14-11/h1-2,4-5,8,12H,3,6-7,9-10H2

> <INCHI_KEY>
ODVKSTFPQDVPJZ-UHFFFAOYSA-N

> <FORMULA>
C13H16O3

> <MOLECULAR_WEIGHT>
220.268

> <EXACT_MASS>
220.109944375

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
23.93171805949217

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-(furan-2-yl)-2,4-dioxaspiro[5.5]undec-8-ene

> <ALOGPS_LOGP>
2.43

> <JCHEM_LOGP>
2.556340132

> <ALOGPS_LOGS>
-3.45

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-2.933997330755027

> <JCHEM_POLAR_SURFACE_AREA>
31.6

> <JCHEM_REFRACTIVITY>
60.570200000000014

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.90e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-(furan-2-yl)-2,4-dioxaspiro[5.5]undec-8-ene

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0259397
     RDKit          3D
Ulinastatin
 32 34  0  0  0  0  0  0  0  0999 V2000
   -3.5736   -0.3950    0.9745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2486    0.8781    0.7295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4113    1.1242   -0.4772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1997    0.2299   -0.3746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5782   -1.2107   -0.2386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0621   -1.4075    0.0166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3761    0.6250    0.8450 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8018   -0.1205    0.7928 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4765    0.2910   -0.3568 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9168   -0.0390   -0.3225 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7318    0.1676    0.7713 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0114   -0.2600    0.4347 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8991   -0.7088   -0.8644 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6542   -0.5677   -1.2878 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8253   -0.2906   -1.4370 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3649    0.4447   -1.6169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1815   -0.6503    1.8361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5624    1.6944    1.3542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0900    2.1707   -0.5673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0009    0.8311   -1.3674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0494   -1.7111    0.6199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2598   -1.7527   -1.1411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2249   -2.4319    0.4088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5564   -1.2709   -0.9860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0513    1.7018    0.7395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9395    0.4565    1.7737 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3444    1.4017   -0.4744 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4402    0.5860    1.7248 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9083   -0.2519    1.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7023   -1.1192   -1.4634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0872    1.4998   -1.6540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8944    0.0856   -2.5052 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  4  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
  9 15  1  0
 15 16  1  0
  6  1  1  0
 14 10  1  0
 16  4  1  0
  1 17  1  0
  2 18  1  0
  3 19  1  0
  3 20  1  0
  5 21  1  0
  5 22  1  0
  6 23  1  0
  6 24  1  0
  7 25  1  0
  7 26  1  0
  9 27  1  0
 11 28  1  0
 12 29  1  0
 13 30  1  0
 16 31  1  0
 16 32  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       0.564   2.104   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       5.184   2.104   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       5.954   0.770   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       5.184  -0.564   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.644  -0.564   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.399   2.016   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.863   1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.863  -0.000   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.399  -0.476   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4    7   11                                             
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    1                                                       
CONECT    7    3    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10    3                                                       
CONECT   12    9   13   16                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   12                                                       
MASTER        0    0    0    0    0    0    0    0   16    0   36    0
END

COMPND    HMDB0259397
HETATM    1  C1  UNL     1      -3.574  -0.395   0.975  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.249   0.878   0.730  1.00  0.00           C  
HETATM    3  C3  UNL     1      -2.411   1.124  -0.477  1.00  0.00           C  
HETATM    4  C4  UNL     1      -1.200   0.230  -0.375  1.00  0.00           C  
HETATM    5  C5  UNL     1      -1.578  -1.211  -0.239  1.00  0.00           C  
HETATM    6  C6  UNL     1      -3.062  -1.408   0.017  1.00  0.00           C  
HETATM    7  C7  UNL     1      -0.376   0.625   0.845  1.00  0.00           C  
HETATM    8  O1  UNL     1       0.802  -0.120   0.793  1.00  0.00           O  
HETATM    9  C8  UNL     1       1.476   0.291  -0.357  1.00  0.00           C  
HETATM   10  C9  UNL     1       2.917  -0.039  -0.323  1.00  0.00           C  
HETATM   11  C10 UNL     1       3.732   0.168   0.771  1.00  0.00           C  
HETATM   12  C11 UNL     1       5.011  -0.260   0.435  1.00  0.00           C  
HETATM   13  C12 UNL     1       4.899  -0.709  -0.864  1.00  0.00           C  
HETATM   14  O2  UNL     1       3.654  -0.568  -1.288  1.00  0.00           O  
HETATM   15  O3  UNL     1       0.825  -0.291  -1.437  1.00  0.00           O  
HETATM   16  C13 UNL     1      -0.365   0.445  -1.617  1.00  0.00           C  
HETATM   17  H1  UNL     1      -4.182  -0.650   1.836  1.00  0.00           H  
HETATM   18  H2  UNL     1      -3.562   1.694   1.354  1.00  0.00           H  
HETATM   19  H3  UNL     1      -2.090   2.171  -0.567  1.00  0.00           H  
HETATM   20  H4  UNL     1      -3.001   0.831  -1.367  1.00  0.00           H  
HETATM   21  H5  UNL     1      -1.049  -1.711   0.620  1.00  0.00           H  
HETATM   22  H6  UNL     1      -1.260  -1.753  -1.141  1.00  0.00           H  
HETATM   23  H7  UNL     1      -3.225  -2.432   0.409  1.00  0.00           H  
HETATM   24  H8  UNL     1      -3.556  -1.271  -0.986  1.00  0.00           H  
HETATM   25  H9  UNL     1      -0.051   1.702   0.740  1.00  0.00           H  
HETATM   26  H10 UNL     1      -0.940   0.456   1.774  1.00  0.00           H  
HETATM   27  H11 UNL     1       1.344   1.402  -0.474  1.00  0.00           H  
HETATM   28  H12 UNL     1       3.440   0.586   1.725  1.00  0.00           H  
HETATM   29  H13 UNL     1       5.908  -0.252   1.040  1.00  0.00           H  
HETATM   30  H14 UNL     1       5.702  -1.119  -1.463  1.00  0.00           H  
HETATM   31  H15 UNL     1      -0.087   1.500  -1.654  1.00  0.00           H  
HETATM   32  H16 UNL     1      -0.894   0.086  -2.505  1.00  0.00           H  
CONECT    1    2    2    6   17
CONECT    2    3   18
CONECT    3    4   19   20
CONECT    4    5    7   16
CONECT    5    6   21   22
CONECT    6   23   24
CONECT    7    8   25   26
CONECT    8    9
CONECT    9   10   15   27
CONECT   10   11   11   14
CONECT   11   12   28
CONECT   12   13   13   29
CONECT   13   14   30
CONECT   15   16
CONECT   16   31   32
END

HMDB0259397
     RDKit          3D
Ulinastatin
 32 34  0  0  0  0  0  0  0  0999 V2000
   -3.5736   -0.3950    0.9745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2486    0.8781    0.7295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4113    1.1242   -0.4772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1997    0.2299   -0.3746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5782   -1.2107   -0.2386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0621   -1.4075    0.0166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3761    0.6250    0.8450 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8018   -0.1205    0.7928 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4765    0.2910   -0.3568 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9168   -0.0390   -0.3225 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7318    0.1676    0.7713 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0114   -0.2600    0.4347 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8991   -0.7088   -0.8644 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6542   -0.5677   -1.2878 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8253   -0.2906   -1.4370 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3649    0.4447   -1.6169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1815   -0.6503    1.8361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5624    1.6944    1.3542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0900    2.1707   -0.5673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0009    0.8311   -1.3674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0494   -1.7111    0.6199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2598   -1.7527   -1.1411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2249   -2.4319    0.4088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5564   -1.2709   -0.9860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0513    1.7018    0.7395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9395    0.4565    1.7737 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3444    1.4017   -0.4744 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4402    0.5860    1.7248 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9083   -0.2519    1.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7023   -1.1192   -1.4634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0872    1.4998   -1.6540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8944    0.0856   -2.5052 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  4  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
  9 15  1  0
 15 16  1  0
  6  1  1  0
 14 10  1  0
 16  4  1  0
  1 17  1  0
  2 18  1  0
  3 19  1  0
  3 20  1  0
  5 21  1  0
  5 22  1  0
  6 23  1  0
  6 24  1  0
  7 25  1  0
  7 26  1  0
  9 27  1  0
 11 28  1  0
 12 29  1  0
 13 30  1  0
 16 31  1  0
 16 32  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
MR 20	HMDB
MR 20 (Magnetic powder) OF urinastatin	HMDB
MR-20 (Magnetic powder)	HMDB
Miraclid	HMDB
UTI(68)	HMDB
UTI68	HMDB
Acid-stable protease inhibitor	HMDB
Trypsin inhibitor MR-20	HMDB
Urinary trypsin inhibitor	HMDB
Urinary trypsin inhibitor (68)	HMDB
Urinary trypsin inhibitor-like inhibitor (43)	HMDB
Urinastatin	HMDB

Chemical Formula

C₁₃H₁₆O₃

Average Molecular Weight

220.268

Monoisotopic Molecular Weight

220.109944375

IUPAC Name

3-(furan-2-yl)-2,4-dioxaspiro[5.5]undec-8-ene

Traditional Name

3-(furan-2-yl)-2,4-dioxaspiro[5.5]undec-8-ene

CAS Registry Number

Not Available

SMILES

C1CC2(COC(OC2)C2=CC=CO2)CC=C1

InChI Identifier

InChI=1S/C13H16O3/c1-2-6-13(7-3-1)9-15-12(16-10-13)11-5-4-8-14-11/h1-2,4-5,8,12H,3,6-7,9-10H2

InChI Key

ODVKSTFPQDVPJZ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1,3-dioxanes. These are organic compounds containing 1,3-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 3.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dioxanes

Sub Class

1,3-dioxanes

Direct Parent

1,3-dioxanes

Alternative Parents

Substituents

Meta-dioxane
Heteroaromatic compound
Furan
Oxacycle
Acetal
Organic oxygen compound
Hydrocarbon derivative
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 (HMDB: HMDB0259397)

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	2.43	ALOGPS
logP	2.56	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	31.6 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	60.57 m³·mol⁻¹	ChemAxon
Polarizability	23.93 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	152.356	30932474
DeepCCS	[M-H]-	149.998	30932474
DeepCCS	[M-2H]-	183.717	30932474
DeepCCS	[M+Na]+	158.652	30932474
AllCCS	[M+H]+	151.9	32859911
AllCCS	[M+H-H2O]+	147.9	32859911
AllCCS	[M+NH4]+	155.6	32859911
AllCCS	[M+Na]+	156.7	32859911
AllCCS	[M-H]-	154.5	32859911
AllCCS	[M+Na-2H]-	154.5	32859911
AllCCS	[M+HCOO]-	154.5	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	5.56 minutes	32390414
Predicted by Siyang on May 30, 2022	13.8949 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	1.48 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	1936.4 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	388.7 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	170.4 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	236.6 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	268.0 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	494.4 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	520.1 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	111.4 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	1277.2 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	430.7 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1194.4 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	444.6 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	381.7 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	427.8 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	365.0 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	8.0 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Ulinastatin	C1CC2(COC(OC2)C2=CC=CO2)CC=C1	2412.7	Standard polar	33892256
Ulinastatin	C1CC2(COC(OC2)C2=CC=CO2)CC=C1	1714.8	Standard non polar	33892256
Ulinastatin	C1CC2(COC(OC2)C2=CC=CO2)CC=C1	1637.7	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 - Ulinastatin GC-MS (Non-derivatized) - 70eV, Positive	splash10-054x-9810000000-2d4b064feac9f9c15af3	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Ulinastatin GC-MS (Non-derivatized) - 70eV, Positive	Not Available	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

94826

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Ulinastatin

METLIN ID

Not Available

PubChem Compound

105102

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 Ulinastatin (HMDB0259397)

MOL for HMDB0259397 (Ulinastatin)

3D MOL for HMDB0259397 (Ulinastatin)

3D SDF for HMDB0259397 (Ulinastatin)

3D-SDF for HMDB0259397 (Ulinastatin)

PDB for HMDB0259397 (Ulinastatin)

3D PDB for HMDB0259397 (Ulinastatin)

SMILES for HMDB0259397 (Ulinastatin)

INCHI for HMDB0259397 (Ulinastatin)

Structure for HMDB0259397 (Ulinastatin)

3D Structure for HMDB0259397 (Ulinastatin)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra