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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2006-05-22 14:17:37 UTC

Update Date

2022-03-07 02:49:13 UTC

HMDB ID

HMDB0002122

Secondary Accession Numbers

HMDB02122

Metabolite Identification

Common Name

Prostaglandin F3a

Description

Prostaglandin F3alpha (PGF3a) is a prostanoid. Prostanoids is a term that collectively describes prostaglandins, prostacyclines and thromboxanes. Prostanoids are a subclass of the lipid mediator group known as eicosanoids. They derive from C-20 polyunsaturated fatty acids, mainly dihomo-gamma-linoleic (20:3n-6), arachidonic (20:4n-6), and eicosapentaenoic (20:5n-3) acids, through the action of cyclooxygenases-1 and -2 (COX-1 and COX-2). The reaction product of COX is the unstable endoperoxide prostaglandin H (PGH) that is further transformed into the individual prostanoids by a series of specific prostanoid synthases. Prostanoids are local-acting mediators formed and inactivated within the same or neighbouring cells prior to their release into circulation as inactive metabolites (15-keto- and 13,14-dihydroketo metabolites). Non-enzymatic peroxidation of arachidonic acid and other fatty acids in vivo can result in prostaglandin-like substances isomeric to the COX-derived prostaglandins that are termed isoprostanes. Prostanoids take part in many physiological and pathophysiological processes in practically every organ, tissue and cell, including the vascular, renal, gastrointestinal and reproductive systems. Their activities are mediated through prostanoid-specific receptors and intracellular signalling pathways, whilst their biosynthesis and action are blocked by nonsteroidal antiinflammatory drugs (NSAID). Isoprostanes are considered to be reliable markers of oxidant stress status and have been linked to inflammation, ischaemia-reperfusion, diabetes, cardiovascular disease, reproductive disorders and diabetes. (PMID: 16986207 )Prostaglandins are eicosanoids. The eicosanoids consist of the prostaglandins (PGs), thromboxanes (TXs), leukotrienes (LTs), and lipoxins (LXs). The PGs and TXs are collectively identified as prostanoids. Prostaglandins were originally shown to be synthesized in the prostate gland, thromboxanes from platelets (thrombocytes), and leukotrienes from leukocytes, hence the derivation of their names. All mammalian cells except erythrocytes synthesize eicosanoids. These molecules are extremely potent, able to cause profound physiological effects at very dilute concentrations. All eicosanoids function locally at the site of synthesis, through receptor-mediated G-protein linked signalling pathways.

Structure

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

HMDB0002122
     RDKit          3D
Prostaglandin F3a
 57 57  0  0  0  0  0  0  0  0999 V2000
    7.5933    0.3004   -0.4374 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2822   -0.0971   -1.1152 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1917   -1.5424   -1.3274 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2362   -2.2708   -0.7898 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1761   -1.7242    0.0673 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8206   -2.0061   -0.5941 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8285   -1.3824   -1.8338 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7615   -1.3740    0.2646 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4561   -0.0990    0.1811 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4127    0.4849    1.0388 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9638    1.7273    1.7516 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7937    1.3918    2.8022 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2697    2.4672    2.1500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4434    1.8313    1.3963 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0132    0.8506    2.2185 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7262    1.0872    0.2663 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6501    0.0568   -0.3579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6939    0.8046   -1.0704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9702    0.7180   -0.8279 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5163   -0.1677    0.2184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4550   -1.1625   -0.4616 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5975   -0.5423   -1.1733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5184    0.2385   -0.3413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3716    0.3284    0.8890 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6121    0.9258   -0.8785 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8497   -0.4805    0.2846 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4234    0.3826   -1.1682 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4692    1.2938    0.0251 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3899    0.3602   -2.1583 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4310    0.4109   -0.6885 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9357   -2.0681   -1.9556 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1935   -3.3694   -0.9705 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2236   -2.3233    1.0316 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2185   -0.6808    0.3282 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6367   -3.0846   -0.6801 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5090   -1.7679   -2.4169 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2455   -2.0117    0.9695 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9673    0.5479   -0.5218 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0715   -0.1893    1.8394 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5075    2.3061    0.9487 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5953    0.9576    2.4073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2149    3.5100    1.7766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4911    2.4130    3.2349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1504    2.5573    1.0038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6892    1.2366    2.8393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3141    1.7833   -0.4843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9529   -0.6091    0.4329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9851   -0.5132   -1.0802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3954    1.5051   -1.8841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6704    1.3459   -1.4396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8085   -0.6724    0.8580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1053    0.5095    0.9072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8029   -1.8336    0.3577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8826   -1.8156   -1.1501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1275   -1.3460   -1.7393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2137    0.1587   -1.9703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5421    0.6424   -0.5604 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  2  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  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 16 10  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
  3 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  6
  7 36  1  0
  8 37  1  0
  9 38  1  0
 10 39  1  1
 11 40  1  6
 12 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  6
 15 45  1  0
 16 46  1  6
 17 47  1  0
 17 48  1  0
 18 49  1  0
 19 50  1  0
 20 51  1  0
 20 52  1  0
 21 53  1  0
 21 54  1  0
 22 55  1  0
 22 56  1  0
 25 57  1  0
M  END


  Mrv0541 02231219222D          

 25 25  0  0  1  0            999 V2000
   17.3513   -9.0892    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.7007   -7.3823    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.2485   -4.6775    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.3151   -4.7486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8736   -6.1078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.5812   -7.6374    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.2485   -7.1524    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.8361   -8.4218    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.9161   -7.6374    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.6611   -8.4218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7965   -7.3823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.2485   -6.3274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1835   -7.9344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.9631   -5.9150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.9631   -5.0900    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.3990   -7.6795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2275   -6.8725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6775   -4.6775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4428   -6.6176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6775   -3.8524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2713   -5.8105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.3919   -3.4400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4867   -5.5557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.1065   -3.8524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.8209   -3.4400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  8  1  1  6  0  0  0
  9  2  1  6  0  0  0
 15  3  1  1  0  0  0
  4 23  1  0  0  0  0
  5 23  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  6 11  1  6  0  0  0
  7  9  1  0  0  0  0
  7 12  1  1  0  0  0
  8 10  1  0  0  0  0
  9 10  1  0  0  0  0
 11 13  1  0  0  0  0
 12 14  2  0  0  0  0
 13 16  2  0  0  0  0
 14 15  1  0  0  0  0
 15 18  1  0  0  0  0
 16 17  1  0  0  0  0
 17 19  1  0  0  0  0
 18 20  1  0  0  0  0
 19 21  1  0  0  0  0
 20 22  2  0  0  0  0
 21 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0002122

> <DATABASE_NAME>
hmdb

> <SMILES>
CC\C=C/C[C@H](O)\C=C\[C@H]1[C@H](O)C[C@H](O)[C@@H]1C\C=C/CCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O5/c1-2-3-6-9-15(21)12-13-17-16(18(22)14-19(17)23)10-7-4-5-8-11-20(24)25/h3-4,6-7,12-13,15-19,21-23H,2,5,8-11,14H2,1H3,(H,24,25)/b6-3-,7-4-,13-12+/t15-,16+,17+,18-,19+/m0/s1

> <INCHI_KEY>
SAKGBZWJAIABSY-SAMSIYEGSA-N

> <FORMULA>
C20H32O5

> <MOLECULAR_WEIGHT>
352.4651

> <EXACT_MASS>
352.224974134

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
40.19625456696345

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3S,5Z)-3-hydroxyocta-1,5-dien-1-yl]cyclopentyl]hept-5-enoic acid

> <ALOGPS_LOGP>
3.70

> <JCHEM_LOGP>
2.2491327606666656

> <ALOGPS_LOGS>
-3.52

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.513964223287505

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.355294009909431

> <JCHEM_PKA_STRONGEST_BASIC>
-1.6652743603062334

> <JCHEM_POLAR_SURFACE_AREA>
97.99000000000001

> <JCHEM_REFRACTIVITY>
101.5873

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.07e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
prostaglandin F3 α

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0002122
     RDKit          3D
Prostaglandin F3a
 57 57  0  0  0  0  0  0  0  0999 V2000
    7.5933    0.3004   -0.4374 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2822   -0.0971   -1.1152 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1917   -1.5424   -1.3274 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2362   -2.2708   -0.7898 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1761   -1.7242    0.0673 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8206   -2.0061   -0.5941 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8285   -1.3824   -1.8338 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7615   -1.3740    0.2646 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4561   -0.0990    0.1811 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4127    0.4849    1.0388 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9638    1.7273    1.7516 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7937    1.3918    2.8022 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2697    2.4672    2.1500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4434    1.8313    1.3963 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0132    0.8506    2.2185 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7262    1.0872    0.2663 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6501    0.0568   -0.3579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6939    0.8046   -1.0704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9702    0.7180   -0.8279 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5163   -0.1677    0.2184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4550   -1.1625   -0.4616 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5975   -0.5423   -1.1733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5184    0.2385   -0.3413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3716    0.3284    0.8890 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6121    0.9258   -0.8785 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8497   -0.4805    0.2846 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4234    0.3826   -1.1682 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4692    1.2938    0.0251 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3899    0.3602   -2.1583 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4310    0.4109   -0.6885 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9357   -2.0681   -1.9556 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1935   -3.3694   -0.9705 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2236   -2.3233    1.0316 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2185   -0.6808    0.3282 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6367   -3.0846   -0.6801 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5090   -1.7679   -2.4169 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2455   -2.0117    0.9695 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9673    0.5479   -0.5218 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0715   -0.1893    1.8394 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5075    2.3061    0.9487 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5953    0.9576    2.4073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2149    3.5100    1.7766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4911    2.4130    3.2349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1504    2.5573    1.0038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6892    1.2366    2.8393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3141    1.7833   -0.4843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9529   -0.6091    0.4329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9851   -0.5132   -1.0802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3954    1.5051   -1.8841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6704    1.3459   -1.4396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8085   -0.6724    0.8580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1053    0.5095    0.9072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8029   -1.8336    0.3577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8826   -1.8156   -1.1501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1275   -1.3460   -1.7393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2137    0.1587   -1.9703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5421    0.6424   -0.5604 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  2  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  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 16 10  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
  3 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  6
  7 36  1  0
  8 37  1  0
  9 38  1  0
 10 39  1  1
 11 40  1  6
 12 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  6
 15 45  1  0
 16 46  1  6
 17 47  1  0
 17 48  1  0
 18 49  1  0
 19 50  1  0
 20 51  1  0
 20 52  1  0
 21 53  1  0
 21 54  1  0
 22 55  1  0
 22 56  1  0
 25 57  1  0
M  END

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  O   UNK     0      32.389 -16.967   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0      36.775 -13.780   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0      34.064  -8.731   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      24.855  -8.864   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      24.031 -11.401   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      32.818 -14.256   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      34.064 -13.351   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      33.294 -15.721   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      35.310 -14.256   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      34.834 -15.721   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      31.354 -13.780   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      34.064 -11.811   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      30.209 -14.811   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      35.398 -11.041   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      35.398  -9.501   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      28.745 -14.335   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      28.425 -12.829   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      36.731  -8.731   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      26.960 -12.353   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      36.731  -7.191   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      26.640 -10.846   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      38.065  -6.421   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      25.175 -10.371   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      39.399  -7.191   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      40.732  -6.421   0.000  0.00  0.00           C+0
CONECT    1    8                                                            
CONECT    2    9                                                            
CONECT    3   15                                                            
CONECT    4   23                                                            
CONECT    5   23                                                            
CONECT    6    7    8   11                                                  
CONECT    7    6    9   12                                                  
CONECT    8    1    6   10                                                  
CONECT    9    2    7   10                                                  
CONECT   10    8    9                                                       
CONECT   11    6   13                                                       
CONECT   12    7   14                                                       
CONECT   13   11   16                                                       
CONECT   14   12   15                                                       
CONECT   15    3   14   18                                                  
CONECT   16   13   17                                                       
CONECT   17   16   19                                                       
CONECT   18   15   20                                                       
CONECT   19   17   21                                                       
CONECT   20   18   22                                                       
CONECT   21   19   23                                                       
CONECT   22   20   24                                                       
CONECT   23    4    5   21                                                  
CONECT   24   22   25                                                       
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   50    0
END

COMPND    HMDB0002122
HETATM    1  C1  UNL     1       7.593   0.300  -0.437  1.00  0.00           C  
HETATM    2  C2  UNL     1       6.282  -0.097  -1.115  1.00  0.00           C  
HETATM    3  C3  UNL     1       6.192  -1.542  -1.327  1.00  0.00           C  
HETATM    4  C4  UNL     1       5.236  -2.271  -0.790  1.00  0.00           C  
HETATM    5  C5  UNL     1       4.176  -1.724   0.067  1.00  0.00           C  
HETATM    6  C6  UNL     1       2.821  -2.006  -0.594  1.00  0.00           C  
HETATM    7  O1  UNL     1       2.829  -1.382  -1.834  1.00  0.00           O  
HETATM    8  C7  UNL     1       1.761  -1.374   0.265  1.00  0.00           C  
HETATM    9  C8  UNL     1       1.456  -0.099   0.181  1.00  0.00           C  
HETATM   10  C9  UNL     1       0.413   0.485   1.039  1.00  0.00           C  
HETATM   11  C10 UNL     1       0.964   1.727   1.752  1.00  0.00           C  
HETATM   12  O2  UNL     1       1.794   1.392   2.802  1.00  0.00           O  
HETATM   13  C11 UNL     1      -0.270   2.467   2.150  1.00  0.00           C  
HETATM   14  C12 UNL     1      -1.443   1.831   1.396  1.00  0.00           C  
HETATM   15  O3  UNL     1      -2.013   0.851   2.218  1.00  0.00           O  
HETATM   16  C13 UNL     1      -0.726   1.087   0.266  1.00  0.00           C  
HETATM   17  C14 UNL     1      -1.650   0.057  -0.358  1.00  0.00           C  
HETATM   18  C15 UNL     1      -2.694   0.805  -1.070  1.00  0.00           C  
HETATM   19  C16 UNL     1      -3.970   0.718  -0.828  1.00  0.00           C  
HETATM   20  C17 UNL     1      -4.516  -0.168   0.218  1.00  0.00           C  
HETATM   21  C18 UNL     1      -5.455  -1.162  -0.462  1.00  0.00           C  
HETATM   22  C19 UNL     1      -6.597  -0.542  -1.173  1.00  0.00           C  
HETATM   23  C20 UNL     1      -7.518   0.238  -0.341  1.00  0.00           C  
HETATM   24  O4  UNL     1      -7.372   0.328   0.889  1.00  0.00           O  
HETATM   25  O5  UNL     1      -8.612   0.926  -0.878  1.00  0.00           O  
HETATM   26  H1  UNL     1       7.850  -0.480   0.285  1.00  0.00           H  
HETATM   27  H2  UNL     1       8.423   0.383  -1.168  1.00  0.00           H  
HETATM   28  H3  UNL     1       7.469   1.294   0.025  1.00  0.00           H  
HETATM   29  H4  UNL     1       6.390   0.360  -2.158  1.00  0.00           H  
HETATM   30  H5  UNL     1       5.431   0.411  -0.689  1.00  0.00           H  
HETATM   31  H6  UNL     1       6.936  -2.068  -1.956  1.00  0.00           H  
HETATM   32  H7  UNL     1       5.193  -3.369  -0.970  1.00  0.00           H  
HETATM   33  H8  UNL     1       4.224  -2.323   1.032  1.00  0.00           H  
HETATM   34  H9  UNL     1       4.218  -0.681   0.328  1.00  0.00           H  
HETATM   35  H10 UNL     1       2.637  -3.085  -0.680  1.00  0.00           H  
HETATM   36  H11 UNL     1       3.509  -1.768  -2.417  1.00  0.00           H  
HETATM   37  H12 UNL     1       1.246  -2.012   0.969  1.00  0.00           H  
HETATM   38  H13 UNL     1       1.967   0.548  -0.522  1.00  0.00           H  
HETATM   39  H14 UNL     1       0.072  -0.189   1.839  1.00  0.00           H  
HETATM   40  H15 UNL     1       1.507   2.306   0.949  1.00  0.00           H  
HETATM   41  H16 UNL     1       2.595   0.958   2.407  1.00  0.00           H  
HETATM   42  H17 UNL     1      -0.215   3.510   1.777  1.00  0.00           H  
HETATM   43  H18 UNL     1      -0.491   2.413   3.235  1.00  0.00           H  
HETATM   44  H19 UNL     1      -2.150   2.557   1.004  1.00  0.00           H  
HETATM   45  H20 UNL     1      -2.689   1.237   2.839  1.00  0.00           H  
HETATM   46  H21 UNL     1      -0.314   1.783  -0.484  1.00  0.00           H  
HETATM   47  H22 UNL     1      -1.953  -0.609   0.433  1.00  0.00           H  
HETATM   48  H23 UNL     1      -0.985  -0.513  -1.080  1.00  0.00           H  
HETATM   49  H24 UNL     1      -2.395   1.505  -1.884  1.00  0.00           H  
HETATM   50  H25 UNL     1      -4.670   1.346  -1.440  1.00  0.00           H  
HETATM   51  H26 UNL     1      -3.809  -0.672   0.858  1.00  0.00           H  
HETATM   52  H27 UNL     1      -5.105   0.509   0.907  1.00  0.00           H  
HETATM   53  H28 UNL     1      -5.803  -1.834   0.358  1.00  0.00           H  
HETATM   54  H29 UNL     1      -4.883  -1.816  -1.150  1.00  0.00           H  
HETATM   55  H30 UNL     1      -7.128  -1.346  -1.739  1.00  0.00           H  
HETATM   56  H31 UNL     1      -6.214   0.159  -1.970  1.00  0.00           H  
HETATM   57  H32 UNL     1      -9.542   0.642  -0.560  1.00  0.00           H  
CONECT    1    2   26   27   28
CONECT    2    3   29   30
CONECT    3    4    4   31
CONECT    4    5   32
CONECT    5    6   33   34
CONECT    6    7    8   35
CONECT    7   36
CONECT    8    9    9   37
CONECT    9   10   38
CONECT   10   11   16   39
CONECT   11   12   13   40
CONECT   12   41
CONECT   13   14   42   43
CONECT   14   15   16   44
CONECT   15   45
CONECT   16   17   46
CONECT   17   18   47   48
CONECT   18   19   19   49
CONECT   19   20   50
CONECT   20   21   51   52
CONECT   21   22   53   54
CONECT   22   23   55   56
CONECT   23   24   24   25
CONECT   25   57
END

HMDB0002122
     RDKit          3D
Prostaglandin F3a
 57 57  0  0  0  0  0  0  0  0999 V2000
    7.5933    0.3004   -0.4374 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2822   -0.0971   -1.1152 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1917   -1.5424   -1.3274 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2362   -2.2708   -0.7898 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1761   -1.7242    0.0673 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8206   -2.0061   -0.5941 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8285   -1.3824   -1.8338 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7615   -1.3740    0.2646 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4561   -0.0990    0.1811 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4127    0.4849    1.0388 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9638    1.7273    1.7516 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7937    1.3918    2.8022 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2697    2.4672    2.1500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4434    1.8313    1.3963 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0132    0.8506    2.2185 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7262    1.0872    0.2663 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6501    0.0568   -0.3579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6939    0.8046   -1.0704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9702    0.7180   -0.8279 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5163   -0.1677    0.2184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4550   -1.1625   -0.4616 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5975   -0.5423   -1.1733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5184    0.2385   -0.3413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3716    0.3284    0.8890 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6121    0.9258   -0.8785 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8497   -0.4805    0.2846 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4234    0.3826   -1.1682 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4692    1.2938    0.0251 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3899    0.3602   -2.1583 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4310    0.4109   -0.6885 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9357   -2.0681   -1.9556 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1935   -3.3694   -0.9705 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2236   -2.3233    1.0316 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2185   -0.6808    0.3282 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6367   -3.0846   -0.6801 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5090   -1.7679   -2.4169 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2455   -2.0117    0.9695 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9673    0.5479   -0.5218 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0715   -0.1893    1.8394 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5075    2.3061    0.9487 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5953    0.9576    2.4073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2149    3.5100    1.7766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4911    2.4130    3.2349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1504    2.5573    1.0038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6892    1.2366    2.8393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3141    1.7833   -0.4843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9529   -0.6091    0.4329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9851   -0.5132   -1.0802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3954    1.5051   -1.8841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6704    1.3459   -1.4396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8085   -0.6724    0.8580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1053    0.5095    0.9072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8029   -1.8336    0.3577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8826   -1.8156   -1.1501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1275   -1.3460   -1.7393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2137    0.1587   -1.9703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5421    0.6424   -0.5604 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  2  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  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 16 10  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
  3 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  6
  7 36  1  0
  8 37  1  0
  9 38  1  0
 10 39  1  1
 11 40  1  6
 12 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  6
 15 45  1  0
 16 46  1  6
 17 47  1  0
 17 48  1  0
 18 49  1  0
 19 50  1  0
 20 51  1  0
 20 52  1  0
 21 53  1  0
 21 54  1  0
 22 55  1  0
 22 56  1  0
 25 57  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
PGF3alpha	ChEBI
PGF3a	Generator
PGF3Α	Generator
(5Z,13E,15S,17Z)-9alpha,11alpha,15-Trihydroxyprosta-5,13,17-trien-1-Oate	HMDB
(5Z,13E,15S,17Z)-9alpha,11alpha,15-Trihydroxyprosta-5,13,17-trien-1-Oic acid	HMDB
(5Z,9alpha,11alpha,13E,15S,17Z)-9,11,15-Trihydroxy-prosta-5,13,17-trien-1-Oate	HMDB
(5Z,9alpha,11alpha,13E,15S,17Z)-9,11,15-Trihydroxy-prosta-5,13,17-trien-1-Oic acid	HMDB
9S,11R,15S-Trihydroxy-5Z,13E,17Z-prostatrienoate	HMDB
9S,11R,15S-Trihydroxy-5Z,13E,17Z-prostatrienoic acid	HMDB
Prostaglandin F3alpha	HMDB
Prostaglandin F3 alpha	HMDB
Prostaglandin F3α	HMDB
Prostaglandin F3a	Generator

Chemical Formula

C₂₀H₃₂O₅

Average Molecular Weight

352.4651

Monoisotopic Molecular Weight

352.224974134

IUPAC Name

(5Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3S,5Z)-3-hydroxyocta-1,5-dien-1-yl]cyclopentyl]hept-5-enoic acid

Traditional Name

prostaglandin F3 α

CAS Registry Number

745-64-2

SMILES

CC\C=C/C[C@H](O)\C=C\[C@H]1[C@H](O)C[C@H](O)[C@@H]1C\C=C/CCCC(O)=O

InChI Identifier

InChI=1S/C20H32O5/c1-2-3-6-9-15(21)12-13-17-16(18(22)14-19(17)23)10-7-4-5-8-11-20(24)25/h3-4,6-7,12-13,15-19,21-23H,2,5,8-11,14H2,1H3,(H,24,25)/b6-3-,7-4-,13-12+/t15-,16+,17+,18-,19+/m0/s1

InChI Key

SAKGBZWJAIABSY-SAMSIYEGSA-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
Hydroxy fatty acid
Cyclopentanol
Fatty acid
Unsaturated fatty acid
Cyclic alcohol
Secondary alcohol
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Organic oxide
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

prostaglandins Falpha (CHEBI:36075 )
Prostaglandins (C06476 )
Prostaglandins (LMFA03010138 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0002122)
Membrane (HMDB: HMDB0002122)

Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)
Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)

Equine

Horse (FooDB: FOOD00378)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.11 g/L	ALOGPS
logP	3.7	ALOGPS
logP	2.25	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	4.36	ChemAxon
pKa (Strongest Basic)	-1.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	97.99 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	101.59 m³·mol⁻¹	ChemAxon
Polarizability	40.2 Å³	ChemAxon
Number of Rings	1	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
DarkChem	[M+H]+	188.901	31661259
DarkChem	[M-H]-	185.156	31661259
DeepCCS	[M+H]+	202.203	30932474
DeepCCS	[M-H]-	199.807	30932474
DeepCCS	[M-2H]-	233.061	30932474
DeepCCS	[M+Na]+	208.115	30932474
AllCCS	[M+H]+	193.1	32859911
AllCCS	[M+H-H2O]+	190.4	32859911
AllCCS	[M+NH4]+	195.6	32859911
AllCCS	[M+Na]+	196.3	32859911
AllCCS	[M-H]-	190.4	32859911
AllCCS	[M+Na-2H]-	191.8	32859911
AllCCS	[M+HCOO]-	193.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Prostaglandin F3a	CC\C=C/C[C@H](O)\C=C\[C@H]1[C@H](O)C[C@H](O)[C@@H]1C\C=C/CCCC(O)=O	4597.6	Standard polar	33892256
Prostaglandin F3a	CC\C=C/C[C@H](O)\C=C\[C@H]1[C@H](O)C[C@H](O)[C@@H]1C\C=C/CCCC(O)=O	2704.3	Standard non polar	33892256
Prostaglandin F3a	CC\C=C/C[C@H](O)\C=C\[C@H]1[C@H](O)C[C@H](O)[C@@H]1C\C=C/CCCC(O)=O	2970.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Prostaglandin F3a,1TMS,isomer #1	CC/C=C\C[C@@H](/C=C/[C@H]1[C@H](O)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	2931.6	Semi standard non polar	33892256
Prostaglandin F3a,1TMS,isomer #2	CC/C=C\C[C@H](O)/C=C/[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O	2826.6	Semi standard non polar	33892256
Prostaglandin F3a,1TMS,isomer #3	CC/C=C\C[C@H](O)/C=C/[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O	2807.9	Semi standard non polar	33892256
Prostaglandin F3a,1TMS,isomer #4	CC/C=C\C[C@H](O)/C=C/[C@H]1[C@H](O)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	2827.7	Semi standard non polar	33892256
Prostaglandin F3a,2TMS,isomer #1	CC/C=C\C[C@@H](/C=C/[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	2798.6	Semi standard non polar	33892256
Prostaglandin F3a,2TMS,isomer #2	CC/C=C\C[C@@H](/C=C/[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	2783.8	Semi standard non polar	33892256
Prostaglandin F3a,2TMS,isomer #3	CC/C=C\C[C@@H](/C=C/[C@H]1[C@H](O)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2844.7	Semi standard non polar	33892256
Prostaglandin F3a,2TMS,isomer #4	CC/C=C\C[C@H](O)/C=C/[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O	2777.9	Semi standard non polar	33892256
Prostaglandin F3a,2TMS,isomer #5	CC/C=C\C[C@H](O)/C=C/[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	2772.3	Semi standard non polar	33892256
Prostaglandin F3a,2TMS,isomer #6	CC/C=C\C[C@H](O)/C=C/[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	2753.0	Semi standard non polar	33892256
Prostaglandin F3a,3TMS,isomer #1	CC/C=C\C[C@@H](/C=C/[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	2736.7	Semi standard non polar	33892256
Prostaglandin F3a,3TMS,isomer #2	CC/C=C\C[C@@H](/C=C/[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2760.9	Semi standard non polar	33892256
Prostaglandin F3a,3TMS,isomer #3	CC/C=C\C[C@@H](/C=C/[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2741.9	Semi standard non polar	33892256
Prostaglandin F3a,3TMS,isomer #4	CC/C=C\C[C@H](O)/C=C/[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	2739.7	Semi standard non polar	33892256
Prostaglandin F3a,4TMS,isomer #1	CC/C=C\C[C@@H](/C=C/[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2750.1	Semi standard non polar	33892256
Prostaglandin F3a,1TBDMS,isomer #1	CC/C=C\C[C@@H](/C=C/[C@H]1[C@H](O)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C(C)(C)C	3179.6	Semi standard non polar	33892256
Prostaglandin F3a,1TBDMS,isomer #2	CC/C=C\C[C@H](O)/C=C/[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O	3046.5	Semi standard non polar	33892256
Prostaglandin F3a,1TBDMS,isomer #3	CC/C=C\C[C@H](O)/C=C/[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O	3026.2	Semi standard non polar	33892256
Prostaglandin F3a,1TBDMS,isomer #4	CC/C=C\C[C@H](O)/C=C/[C@H]1[C@H](O)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C	3097.2	Semi standard non polar	33892256
Prostaglandin F3a,2TBDMS,isomer #1	CC/C=C\C[C@@H](/C=C/[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C(C)(C)C	3264.5	Semi standard non polar	33892256
Prostaglandin F3a,2TBDMS,isomer #2	CC/C=C\C[C@@H](/C=C/[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C(C)(C)C	3255.7	Semi standard non polar	33892256
Prostaglandin F3a,2TBDMS,isomer #3	CC/C=C\C[C@@H](/C=C/[C@H]1[C@H](O)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3367.5	Semi standard non polar	33892256
Prostaglandin F3a,2TBDMS,isomer #4	CC/C=C\C[C@H](O)/C=C/[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O	3228.5	Semi standard non polar	33892256
Prostaglandin F3a,2TBDMS,isomer #5	CC/C=C\C[C@H](O)/C=C/[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C	3258.1	Semi standard non polar	33892256
Prostaglandin F3a,2TBDMS,isomer #6	CC/C=C\C[C@H](O)/C=C/[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C	3240.2	Semi standard non polar	33892256
Prostaglandin F3a,3TBDMS,isomer #1	CC/C=C\C[C@@H](/C=C/[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C(C)(C)C	3440.9	Semi standard non polar	33892256
Prostaglandin F3a,3TBDMS,isomer #2	CC/C=C\C[C@@H](/C=C/[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3487.0	Semi standard non polar	33892256
Prostaglandin F3a,3TBDMS,isomer #3	CC/C=C\C[C@@H](/C=C/[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3474.3	Semi standard non polar	33892256
Prostaglandin F3a,3TBDMS,isomer #4	CC/C=C\C[C@H](O)/C=C/[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C	3454.8	Semi standard non polar	33892256
Prostaglandin F3a,4TBDMS,isomer #1	CC/C=C\C[C@@H](/C=C/[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3625.5	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 - Prostaglandin F3a GC-MS (Non-derivatized) - 70eV, Positive	splash10-0690-5569000000-b6d9924bb1e1598b9d72	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Prostaglandin F3a GC-MS (4 TMS) - 70eV, Positive	splash10-004i-2300279000-9d3c59689b62b4e5a1ca	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Prostaglandin F3a GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Prostaglandin F3a 10V, Positive-QTOF	splash10-014r-0019000000-f98b94189569251d37a2	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Prostaglandin F3a 20V, Positive-QTOF	splash10-014r-3197000000-85761caed143126a0974	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Prostaglandin F3a 40V, Positive-QTOF	splash10-01bi-9170000000-9c3f2455a6d592ea0a4a	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Prostaglandin F3a 10V, Negative-QTOF	splash10-0ue9-0009000000-3b5070d3e2790d2cb20f	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Prostaglandin F3a 20V, Negative-QTOF	splash10-001i-1039000000-d00dd3f608a0e190f458	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Prostaglandin F3a 40V, Negative-QTOF	splash10-0a4i-9631000000-10bc983babf036749841	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Prostaglandin F3a 10V, Negative-QTOF	splash10-0uxr-0009000000-33af08865c9568c21f7a	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Prostaglandin F3a 20V, Negative-QTOF	splash10-0fs9-0097000000-18f214d33dfa137da432	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Prostaglandin F3a 40V, Negative-QTOF	splash10-007y-9162000000-31a96bbf479dad16df6e	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Prostaglandin F3a 10V, Positive-QTOF	splash10-014r-0019000000-40e30046291432c91b56	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Prostaglandin F3a 20V, Positive-QTOF	splash10-014i-9276000000-4e19df362ec1af060bb2	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Prostaglandin F3a 40V, Positive-QTOF	splash10-014l-9300000000-ba6ae7b1d6d0d6589c1f	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB022853

KNApSAcK ID

Not Available

Chemspider ID

4444442

KEGG Compound ID

C06476

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5280940

PDB ID

Not Available

ChEBI ID

36075

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

Masoodi M, Nicolaou A: Lipidomic analysis of twenty-seven prostanoids and isoprostanes by liquid chromatography/electrospray tandem mass spectrometry. Rapid Commun Mass Spectrom. 2006;20(20):3023-9. [PubMed:16986207 ]

Showing metabocard for Prostaglandin F3a (HMDB0002122)

MOL for HMDB0002122 (Prostaglandin F3a)

3D MOL for HMDB0002122 (Prostaglandin F3a)

3D SDF for HMDB0002122 (Prostaglandin F3a)

3D-SDF for HMDB0002122 (Prostaglandin F3a)

PDB for HMDB0002122 (Prostaglandin F3a)

3D PDB for HMDB0002122 (Prostaglandin F3a)

SMILES for HMDB0002122 (Prostaglandin F3a)

INCHI for HMDB0002122 (Prostaglandin F3a)

Structure for HMDB0002122 (Prostaglandin F3a)

3D Structure for HMDB0002122 (Prostaglandin F3a)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra