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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 20:22:07 UTC

Update Date

2021-09-26 23:15:47 UTC

HMDB ID

HMDB0258679

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Tafluprost acid

Description

Tafluprost acid belongs to the class of organic compounds known as prostaglandins and related compounds. These are unsaturated carboxylic acids consisting of a 20 carbon skeleton that also contains a five member ring, and are based upon the fatty acid arachidonic acid. Based on a literature review a significant number of articles have been published on Tafluprost acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). Tafluprost acid is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Tafluprost acid 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


  Mrv1652309112122222D          

 29 30  0  0  0  0            999 V2000
   -9.4275   -3.9572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6206   -4.1287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5343   -4.9492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2880   -5.2847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8400   -4.6716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6605   -4.7579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4595   -6.0917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2441   -6.3466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4157   -7.1536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5872   -7.9606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3718   -8.2155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5433   -9.0225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9303   -9.5745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1018  -10.3815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.8864  -10.6364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4995  -10.0844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.3280   -9.2774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6087   -7.3251    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2226   -6.9821    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8198   -5.3617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1054   -4.9492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3909   -5.3617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6764   -4.9492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9620   -5.3617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2475   -4.9492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5330   -5.3617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8186   -4.9492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5330   -6.1867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0075   -3.5767    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
  1  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  4  1  4  0  0  0
  7  8  2  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  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
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
  9 18  1  0  0  0  0
  9 19  1  0  0  0  0
  3 20  1  0  0  0  0
 21 20  1  4  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
  2 29  1  0  0  0  0
M  END

HMDB0258679
     RDKit          3D
Tafluprost acid
 57 58  0  0  0  0  0  0  0  0999 V2000
    7.5688   -1.4998   -0.4895 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8886   -0.3135   -0.2064 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2352   -0.0606    0.0784 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8466    0.7261   -0.1888 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7359    0.3099    0.7410 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6500    1.3584    0.7809 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0126    1.6035   -0.5179 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7390    1.4659   -0.8253 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7293    1.0271    0.1317 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0260   -0.2722   -0.3088 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1701   -1.3006   -0.3956 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6019   -1.4704   -1.6845 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5725   -2.5370    0.2427 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5471   -2.0376    1.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6091   -2.8529    1.2130 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1086   -0.6730    0.7604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3457   -0.6155    0.4644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9280   -0.2604   -0.6296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4010   -0.2484   -0.7941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8024   -1.3385   -1.5928 F   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8141    0.8600   -1.5044 F   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1018   -0.4609    0.5148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4444   -0.4620    0.5320 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4992    0.3063    0.3081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4783    1.6210   -0.0687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6360    2.3709   -0.2917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8262    1.7202   -0.1119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9128    0.3965    0.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7630   -0.3018    0.4764 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5971    0.8442    0.2748 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2258    1.7078    0.1247 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4475    0.8001   -1.2335 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1874    0.3128    1.7746 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3643   -0.7138    0.5533 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9671    1.2092    1.6238 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2019    2.3191    1.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6737    1.9480   -1.3530 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4097    1.6877   -1.8395 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9297    1.7770    0.3325 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1357    0.7678    1.1287 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5981   -0.1487   -1.3164 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0260   -0.9978    0.2314 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8778   -1.6380   -2.3386 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1454   -3.2192   -0.4998 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3248   -3.1044    0.8366 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9728   -1.9876    2.2599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8729   -2.9543    2.1520 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2265    0.0304    1.6459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9658   -0.9161    1.3186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3517    0.0505   -1.4894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7638   -1.4949    0.8487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6650    0.2918    1.2228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5461    2.1862   -0.1986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5711    3.4139   -0.5915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7572    2.2427   -0.2664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8744   -0.1159    0.4136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8135   -1.3592    0.7831 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  3
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  2  3
 18 19  1  0
 19 20  1  0
 19 21  1  0
 19 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 16 10  1  0
 29 24  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 11 42  1  0
 12 43  1  0
 13 44  1  0
 13 45  1  0
 14 46  1  0
 15 47  1  0
 16 48  1  0
 17 49  1  0
 18 50  1  0
 22 51  1  0
 22 52  1  0
 25 53  1  0
 26 54  1  0
 27 55  1  0
 28 56  1  0
 29 57  1  0
M  END


  Mrv1652309112122222D          

 29 30  0  0  0  0            999 V2000
   -9.4275   -3.9572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6206   -4.1287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5343   -4.9492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2880   -5.2847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8400   -4.6716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6605   -4.7579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4595   -6.0917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2441   -6.3466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4157   -7.1536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5872   -7.9606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3718   -8.2155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5433   -9.0225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9303   -9.5745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1018  -10.3815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.8864  -10.6364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4995  -10.0844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.3280   -9.2774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6087   -7.3251    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2226   -6.9821    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8198   -5.3617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1054   -4.9492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3909   -5.3617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6764   -4.9492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9620   -5.3617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2475   -4.9492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5330   -5.3617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8186   -4.9492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5330   -6.1867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0075   -3.5767    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
  1  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  4  1  4  0  0  0
  7  8  2  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  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
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
  9 18  1  0  0  0  0
  9 19  1  0  0  0  0
  3 20  1  0  0  0  0
 21 20  1  4  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
  2 29  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0258679

> <DATABASE_NAME>
hmdb

> <SMILES>
OC1CC(O)C(C=CC(F)(F)COC2=CC=CC=C2)C1CC=CCCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H28F2O5/c23-22(24,15-29-16-8-4-3-5-9-16)13-12-18-17(19(25)14-20(18)26)10-6-1-2-7-11-21(27)28/h1,3-6,8-9,12-13,17-20,25-26H,2,7,10-11,14-15H2,(H,27,28)

> <INCHI_KEY>
KIQXRQVVYTYYAZ-UHFFFAOYSA-N

> <FORMULA>
C22H28F2O5

> <MOLECULAR_WEIGHT>
410.458

> <EXACT_MASS>
410.190480328

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
41.911222907225124

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-[2-(3,3-difluoro-4-phenoxybut-1-en-1-yl)-3,5-dihydroxycyclopentyl]hept-5-enoic acid

> <ALOGPS_LOGP>
3.42

> <JCHEM_LOGP>
3.3730453359999992

> <ALOGPS_LOGS>
-4.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.51387749215359

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.3552935959611325

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8720050891706874

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
106.65280000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.39e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-[2-(3,3-difluoro-4-phenoxybut-1-en-1-yl)-3,5-dihydroxycyclopentyl]hept-5-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0258679
     RDKit          3D
Tafluprost acid
 57 58  0  0  0  0  0  0  0  0999 V2000
    7.5688   -1.4998   -0.4895 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8886   -0.3135   -0.2064 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2352   -0.0606    0.0784 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8466    0.7261   -0.1888 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7359    0.3099    0.7410 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6500    1.3584    0.7809 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0126    1.6035   -0.5179 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7390    1.4659   -0.8253 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7293    1.0271    0.1317 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0260   -0.2722   -0.3088 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1701   -1.3006   -0.3956 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6019   -1.4704   -1.6845 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5725   -2.5370    0.2427 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5471   -2.0376    1.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6091   -2.8529    1.2130 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1086   -0.6730    0.7604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3457   -0.6155    0.4644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9280   -0.2604   -0.6296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4010   -0.2484   -0.7941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8024   -1.3385   -1.5928 F   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8141    0.8600   -1.5044 F   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1018   -0.4609    0.5148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4444   -0.4620    0.5320 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4992    0.3063    0.3081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4783    1.6210   -0.0687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6360    2.3709   -0.2917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8262    1.7202   -0.1119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9128    0.3965    0.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7630   -0.3018    0.4764 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5971    0.8442    0.2748 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2258    1.7078    0.1247 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4475    0.8001   -1.2335 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1874    0.3128    1.7746 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3643   -0.7138    0.5533 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9671    1.2092    1.6238 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2019    2.3191    1.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6737    1.9480   -1.3530 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4097    1.6877   -1.8395 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9297    1.7770    0.3325 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1357    0.7678    1.1287 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5981   -0.1487   -1.3164 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0260   -0.9978    0.2314 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8778   -1.6380   -2.3386 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1454   -3.2192   -0.4998 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3248   -3.1044    0.8366 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9728   -1.9876    2.2599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8729   -2.9543    2.1520 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2265    0.0304    1.6459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9658   -0.9161    1.3186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3517    0.0505   -1.4894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7638   -1.4949    0.8487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6650    0.2918    1.2228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5461    2.1862   -0.1986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5711    3.4139   -0.5915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7572    2.2427   -0.2664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8744   -0.1159    0.4136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8135   -1.3592    0.7831 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  3
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  2  3
 18 19  1  0
 19 20  1  0
 19 21  1  0
 19 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 16 10  1  0
 29 24  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 11 42  1  0
 12 43  1  0
 13 44  1  0
 13 45  1  0
 14 46  1  0
 15 47  1  0
 16 48  1  0
 17 49  1  0
 18 50  1  0
 22 51  1  0
 22 52  1  0
 25 53  1  0
 26 54  1  0
 27 55  1  0
 28 56  1  0
 29 57  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     -17.598  -7.387   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -16.092  -7.707   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -15.931  -9.238   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -17.338  -9.865   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -18.368  -8.720   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0     -19.900  -8.881   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0     -17.658 -11.371   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -19.122 -11.847   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -19.443 -13.353   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -19.763 -14.860   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0     -21.227 -15.336   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0     -21.548 -16.842   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -20.403 -17.872   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -20.723 -19.379   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -22.188 -19.855   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -23.332 -18.824   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -23.012 -17.318   0.000  0.00  0.00           C+0
HETATM   18  F   UNK     0     -17.936 -13.674   0.000  0.00  0.00           F+0
HETATM   19  F   UNK     0     -20.949 -13.033   0.000  0.00  0.00           F+0
HETATM   20  C   UNK     0     -14.597 -10.008   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0     -13.263  -9.238   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0     -11.930 -10.008   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0     -10.596  -9.238   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -9.262 -10.008   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -7.929  -9.238   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -6.595 -10.008   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -5.261  -9.238   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -6.595 -11.548   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0     -14.947  -6.676   0.000  0.00  0.00           O+0
CONECT    1    2    5                                                       
CONECT    2    1    3   29                                                  
CONECT    3    2    4   20                                                  
CONECT    4    3    5    7                                                  
CONECT    5    4    1    6                                                  
CONECT    6    5                                                            
CONECT    7    4    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   18   19                                             
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18    9                                                            
CONECT   19    9                                                            
CONECT   20    3   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29    2                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   60    0
END

COMPND    HMDB0258679
HETATM    1  O1  UNL     1       7.569  -1.500  -0.490  1.00  0.00           O  
HETATM    2  C1  UNL     1       7.889  -0.313  -0.206  1.00  0.00           C  
HETATM    3  O2  UNL     1       9.235  -0.061   0.078  1.00  0.00           O  
HETATM    4  C2  UNL     1       6.847   0.726  -0.189  1.00  0.00           C  
HETATM    5  C3  UNL     1       5.736   0.310   0.741  1.00  0.00           C  
HETATM    6  C4  UNL     1       4.650   1.358   0.781  1.00  0.00           C  
HETATM    7  C5  UNL     1       4.013   1.604  -0.518  1.00  0.00           C  
HETATM    8  C6  UNL     1       2.739   1.466  -0.825  1.00  0.00           C  
HETATM    9  C7  UNL     1       1.729   1.027   0.132  1.00  0.00           C  
HETATM   10  C8  UNL     1       1.026  -0.272  -0.309  1.00  0.00           C  
HETATM   11  C9  UNL     1       2.170  -1.301  -0.396  1.00  0.00           C  
HETATM   12  O3  UNL     1       2.602  -1.470  -1.685  1.00  0.00           O  
HETATM   13  C10 UNL     1       1.572  -2.537   0.243  1.00  0.00           C  
HETATM   14  C11 UNL     1       0.547  -2.038   1.218  1.00  0.00           C  
HETATM   15  O4  UNL     1      -0.609  -2.853   1.213  1.00  0.00           O  
HETATM   16  C12 UNL     1       0.109  -0.673   0.760  1.00  0.00           C  
HETATM   17  C13 UNL     1      -1.346  -0.616   0.464  1.00  0.00           C  
HETATM   18  C14 UNL     1      -1.928  -0.260  -0.630  1.00  0.00           C  
HETATM   19  C15 UNL     1      -3.401  -0.248  -0.794  1.00  0.00           C  
HETATM   20  F1  UNL     1      -3.802  -1.339  -1.593  1.00  0.00           F  
HETATM   21  F2  UNL     1      -3.814   0.860  -1.504  1.00  0.00           F  
HETATM   22  C16 UNL     1      -4.102  -0.461   0.515  1.00  0.00           C  
HETATM   23  O5  UNL     1      -5.444  -0.462   0.532  1.00  0.00           O  
HETATM   24  C17 UNL     1      -6.499   0.306   0.308  1.00  0.00           C  
HETATM   25  C18 UNL     1      -6.478   1.621  -0.069  1.00  0.00           C  
HETATM   26  C19 UNL     1      -7.636   2.371  -0.292  1.00  0.00           C  
HETATM   27  C20 UNL     1      -8.826   1.720  -0.112  1.00  0.00           C  
HETATM   28  C21 UNL     1      -8.913   0.396   0.269  1.00  0.00           C  
HETATM   29  C22 UNL     1      -7.763  -0.302   0.476  1.00  0.00           C  
HETATM   30  H1  UNL     1       9.597   0.844   0.275  1.00  0.00           H  
HETATM   31  H2  UNL     1       7.226   1.708   0.125  1.00  0.00           H  
HETATM   32  H3  UNL     1       6.448   0.800  -1.233  1.00  0.00           H  
HETATM   33  H4  UNL     1       6.187   0.313   1.775  1.00  0.00           H  
HETATM   34  H5  UNL     1       5.364  -0.714   0.553  1.00  0.00           H  
HETATM   35  H6  UNL     1       3.967   1.209   1.624  1.00  0.00           H  
HETATM   36  H7  UNL     1       5.202   2.319   1.030  1.00  0.00           H  
HETATM   37  H8  UNL     1       4.674   1.948  -1.353  1.00  0.00           H  
HETATM   38  H9  UNL     1       2.410   1.688  -1.840  1.00  0.00           H  
HETATM   39  H10 UNL     1       0.930   1.777   0.333  1.00  0.00           H  
HETATM   40  H11 UNL     1       2.136   0.768   1.129  1.00  0.00           H  
HETATM   41  H12 UNL     1       0.598  -0.149  -1.316  1.00  0.00           H  
HETATM   42  H13 UNL     1       3.026  -0.998   0.231  1.00  0.00           H  
HETATM   43  H14 UNL     1       1.878  -1.638  -2.339  1.00  0.00           H  
HETATM   44  H15 UNL     1       1.145  -3.219  -0.500  1.00  0.00           H  
HETATM   45  H16 UNL     1       2.325  -3.104   0.837  1.00  0.00           H  
HETATM   46  H17 UNL     1       0.973  -1.988   2.260  1.00  0.00           H  
HETATM   47  H18 UNL     1      -0.873  -2.954   2.152  1.00  0.00           H  
HETATM   48  H19 UNL     1       0.227   0.030   1.646  1.00  0.00           H  
HETATM   49  H20 UNL     1      -1.966  -0.916   1.319  1.00  0.00           H  
HETATM   50  H21 UNL     1      -1.352   0.050  -1.489  1.00  0.00           H  
HETATM   51  H22 UNL     1      -3.764  -1.495   0.849  1.00  0.00           H  
HETATM   52  H23 UNL     1      -3.665   0.292   1.223  1.00  0.00           H  
HETATM   53  H24 UNL     1      -5.546   2.186  -0.199  1.00  0.00           H  
HETATM   54  H25 UNL     1      -7.571   3.414  -0.591  1.00  0.00           H  
HETATM   55  H26 UNL     1      -9.757   2.243  -0.266  1.00  0.00           H  
HETATM   56  H27 UNL     1      -9.874  -0.116   0.414  1.00  0.00           H  
HETATM   57  H28 UNL     1      -7.813  -1.359   0.783  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3    4
CONECT    3   30
CONECT    4    5   31   32
CONECT    5    6   33   34
CONECT    6    7   35   36
CONECT    7    8    8   37
CONECT    8    9   38
CONECT    9   10   39   40
CONECT   10   11   16   41
CONECT   11   12   13   42
CONECT   12   43
CONECT   13   14   44   45
CONECT   14   15   16   46
CONECT   15   47
CONECT   16   17   48
CONECT   17   18   18   49
CONECT   18   19   50
CONECT   19   20   21   22
CONECT   22   23   51   52
CONECT   23   24
CONECT   24   25   25   29
CONECT   25   26   53
CONECT   26   27   27   54
CONECT   27   28   55
CONECT   28   29   29   56
CONECT   29   57
END

HMDB0258679
     RDKit          3D
Tafluprost acid
 57 58  0  0  0  0  0  0  0  0999 V2000
    7.5688   -1.4998   -0.4895 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8886   -0.3135   -0.2064 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2352   -0.0606    0.0784 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8466    0.7261   -0.1888 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7359    0.3099    0.7410 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6500    1.3584    0.7809 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0126    1.6035   -0.5179 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7390    1.4659   -0.8253 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7293    1.0271    0.1317 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0260   -0.2722   -0.3088 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1701   -1.3006   -0.3956 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6019   -1.4704   -1.6845 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5725   -2.5370    0.2427 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5471   -2.0376    1.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6091   -2.8529    1.2130 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1086   -0.6730    0.7604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3457   -0.6155    0.4644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9280   -0.2604   -0.6296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4010   -0.2484   -0.7941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8024   -1.3385   -1.5928 F   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8141    0.8600   -1.5044 F   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1018   -0.4609    0.5148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4444   -0.4620    0.5320 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4992    0.3063    0.3081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4783    1.6210   -0.0687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6360    2.3709   -0.2917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8262    1.7202   -0.1119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9128    0.3965    0.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7630   -0.3018    0.4764 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5971    0.8442    0.2748 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2258    1.7078    0.1247 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4475    0.8001   -1.2335 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1874    0.3128    1.7746 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3643   -0.7138    0.5533 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9671    1.2092    1.6238 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2019    2.3191    1.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6737    1.9480   -1.3530 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4097    1.6877   -1.8395 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9297    1.7770    0.3325 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1357    0.7678    1.1287 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5981   -0.1487   -1.3164 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0260   -0.9978    0.2314 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8778   -1.6380   -2.3386 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1454   -3.2192   -0.4998 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3248   -3.1044    0.8366 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9728   -1.9876    2.2599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8729   -2.9543    2.1520 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2265    0.0304    1.6459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9658   -0.9161    1.3186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3517    0.0505   -1.4894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7638   -1.4949    0.8487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6650    0.2918    1.2228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5461    2.1862   -0.1986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5711    3.4139   -0.5915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7572    2.2427   -0.2664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8744   -0.1159    0.4136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8135   -1.3592    0.7831 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  3
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  2  3
 18 19  1  0
 19 20  1  0
 19 21  1  0
 19 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 16 10  1  0
 29 24  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 11 42  1  0
 12 43  1  0
 13 44  1  0
 13 45  1  0
 14 46  1  0
 15 47  1  0
 16 48  1  0
 17 49  1  0
 18 50  1  0
 22 51  1  0
 22 52  1  0
 25 53  1  0
 26 54  1  0
 27 55  1  0
 28 56  1  0
 29 57  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
7-[2-(3,3-Difluoro-4-phenoxybut-1-en-1-yl)-3,5-dihydroxycyclopentyl]hept-5-enoate	HMDB

Chemical Formula

C₂₂H₂₈F₂O₅

Average Molecular Weight

410.458

Monoisotopic Molecular Weight

410.190480328

IUPAC Name

7-[2-(3,3-difluoro-4-phenoxybut-1-en-1-yl)-3,5-dihydroxycyclopentyl]hept-5-enoic acid

Traditional Name

7-[2-(3,3-difluoro-4-phenoxybut-1-en-1-yl)-3,5-dihydroxycyclopentyl]hept-5-enoic acid

CAS Registry Number

Not Available

SMILES

OC1CC(O)C(C=CC(F)(F)COC2=CC=CC=C2)C1CC=CCCCC(O)=O

InChI Identifier

InChI=1S/C22H28F2O5/c23-22(24,15-29-16-8-4-3-5-9-16)13-12-18-17(19(25)14-20(18)26)10-6-1-2-7-11-21(27)28/h1,3-6,8-9,12-13,17-20,25-26H,2,7,10-11,14-15H2,(H,27,28)

InChI Key

KIQXRQVVYTYYAZ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as prostaglandins and related compounds. These are unsaturated carboxylic acids consisting of a 20 carbon skeleton that also contains a five member ring, and are based upon the fatty acid arachidonic acid.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Eicosanoids

Direct Parent

Prostaglandins and related compounds

Alternative Parents

Substituents

Prostaglandin skeleton
Long-chain fatty acid
Phenoxy compound
Phenol ether
Alkyl aryl ether
Halogenated fatty acid
Hydroxy fatty acid
Monocyclic benzene moiety
Fatty acid
Benzenoid
Unsaturated fatty acid
Cyclopentanol
Cyclic alcohol
Secondary alcohol
Ether
Carboxylic acid
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organohalogen compound
Organofluoride
Organooxygen compound
Alcohol
Hydrocarbon derivative
Carbonyl group
Organic oxide
Alkyl halide
Alkyl fluoride
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	3.42	ALOGPS
logP	3.37	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	4.36	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	106.65 m³·mol⁻¹	ChemAxon
Polarizability	41.91 Å³	ChemAxon
Number of Rings	2	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+H]+	190.851	30932474
DeepCCS	[M-H]-	188.493	30932474
DeepCCS	[M-2H]-	222.367	30932474
DeepCCS	[M+Na]+	197.594	30932474
AllCCS	[M+H]+	198.8	32859911
AllCCS	[M+H-H2O]+	196.3	32859911
AllCCS	[M+NH4]+	201.0	32859911
AllCCS	[M+Na]+	201.6	32859911
AllCCS	[M-H]-	196.3	32859911
AllCCS	[M+Na-2H]-	197.4	32859911
AllCCS	[M+HCOO]-	198.8	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.	6.59 minutes	32390414
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.	7.04 minutes	32390414
Predicted by Siyang on May 30, 2022	13.6012 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	1.39 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	2629.0 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	226.2 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	187.4 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	190.6 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	199.0 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	602.1 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	505.2 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	132.3 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	1246.6 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	536.2 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	1298.6 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	387.1 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	409.1 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	316.4 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	215.9 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	9.1 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Tafluprost acid	OC1CC(O)C(C=CC(F)(F)COC2=CC=CC=C2)C1CC=CCCCC(O)=O	4130.2	Standard polar	33892256
Tafluprost acid	OC1CC(O)C(C=CC(F)(F)COC2=CC=CC=C2)C1CC=CCCCC(O)=O	2890.4	Standard non polar	33892256
Tafluprost acid	OC1CC(O)C(C=CC(F)(F)COC2=CC=CC=C2)C1CC=CCCCC(O)=O	2960.5	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 - Tafluprost acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-014r-1219000000-8e1ec65ae01361e172d1	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tafluprost acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tafluprost acid GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tafluprost acid GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tafluprost acid GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tafluprost acid GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tafluprost acid GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tafluprost acid GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tafluprost acid GC-MS (TMS_3_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tafluprost acid GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tafluprost acid GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tafluprost acid GC-MS (TBDMS_1_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tafluprost acid GC-MS (TBDMS_2_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tafluprost acid GC-MS (TBDMS_2_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tafluprost acid GC-MS (TBDMS_2_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tafluprost acid GC-MS (TBDMS_3_1) - 70eV, Positive	Not Available	2021-11-05	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

26458449

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53394479

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 Tafluprost acid (HMDB0258679)

MOL for HMDB0258679 (Tafluprost acid)

3D MOL for HMDB0258679 (Tafluprost acid)

3D SDF for HMDB0258679 (Tafluprost acid)

3D-SDF for HMDB0258679 (Tafluprost acid)

PDB for HMDB0258679 (Tafluprost acid)

3D PDB for HMDB0258679 (Tafluprost acid)

SMILES for HMDB0258679 (Tafluprost acid)

INCHI for HMDB0258679 (Tafluprost acid)

Structure for HMDB0258679 (Tafluprost acid)

3D Structure for HMDB0258679 (Tafluprost acid)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra