NP-MRD: Showing NP-Card for prostaglandin b2 (NP0187620)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 03:49:10 UTC

Updated at

2022-09-04 03:49:10 UTC

NP-MRD ID

NP0187620

Secondary Accession Numbers

None

Natural Product Identification

Common Name

prostaglandin b2

Description

Prostaglandin B2, also known as PGB2, 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. Thus, prostaglandin B2 is considered to be an eicosanoid lipid molecule. Prostaglandin B2 is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. prostaglandin b2 is found in Homo sapiens, Larix sibirica and Sarcophyton crassocaule. In humans, prostaglandin B2 is involved in mefenamic acid action pathway.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 54 54  0  0  0  0  0  0  0  0999 V2000
   -6.8456    2.7262   -0.7620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9745    1.2399   -0.4405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5786    0.8064    0.0070 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6507   -0.6489    0.3355 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3229   -1.1457    0.7903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2146   -1.0002   -0.2230 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5378   -1.7178   -1.3727 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9379   -1.5627    0.3271 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7591   -1.0304   -0.0058 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4895   -1.5670    0.5226 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6964   -1.1040    0.2478 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9977    0.0465   -0.6496 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6994    1.1264    0.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8979    1.5881   -0.2580 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7008    1.1000   -1.3558 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0090    0.4833   -0.9862 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9514    1.3208   -0.1938 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4982    1.5771    1.1739 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6383    0.8235    1.7072 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0076    2.6415    1.8848 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7008   -1.9014    0.9696 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9070   -2.0430    0.7315 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9305   -2.5240    2.0879 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5728   -2.7230    1.4501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2283    3.2319    0.0194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3193    2.8442   -1.7289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8486    3.1767   -0.7609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2318    0.6596   -1.3269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6551    1.0841    0.4168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3266    1.4180    0.8858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8362    0.9790   -0.7784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9813   -1.2671   -0.5173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3709   -0.8577    1.1676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0226   -0.7624    1.7862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4318   -2.2607    0.9446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0503    0.0853   -0.4952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5570   -2.6799   -1.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9420   -2.3986    0.9943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8270   -0.1908   -0.6834 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4886   -0.3625   -1.5278 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0374    0.4873   -1.0102 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1957    1.5924    0.9280 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2386    2.4379    0.3642 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1811    0.3890   -2.0494 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8902    2.0212   -2.0266 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5718    0.2191   -1.9409 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8350   -0.5144   -0.4676 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9447    0.7701   -0.1672 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1189    2.2799   -0.7518 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7297    2.8538    2.8145 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3781   -3.4919    2.3972 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8113   -1.8211    2.9279 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5759   -3.7040    0.8967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2438   -2.7302    2.1988 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  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  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 20  1  0
 18 19  2  0
 11 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  0
 24 10  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  6
  7 37  1  0
  8 38  1  0
  9 39  1  0
 12 40  1  0
 12 41  1  0
 13 42  1  0
 14 43  1  0
 15 44  1  0
 15 45  1  0
 16 46  1  0
 16 47  1  0
 17 48  1  0
 17 49  1  0
 20 50  1  0
 23 51  1  0
 23 52  1  0
 24 53  1  0
 24 54  1  0
M  END

  Mrv1652305301723412D          

 24 24  0  0  1  0            999 V2000
    6.3118  -19.5337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0420  -19.9453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3112  -20.3587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5265  -20.6131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0252  -19.1195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0258  -20.7709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7401  -20.3581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1691  -20.3576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8838  -20.7698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5980  -20.3570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3126  -20.7692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0270  -20.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4548  -20.7703    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.4548  -21.5953    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5273  -19.2782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3138  -18.4814    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9150  -16.6831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6232  -17.1080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7335  -19.5445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4701  -19.1478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9256  -15.8713    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2067  -17.0797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4701  -18.3263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2067  -17.9296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1 15  1  0  0  0  0
 15  2  1  0  0  0  0
  3  1  2  0  0  0  0
  4  2  1  0  0  0  0
  4  3  1  0  0  0  0
  1  5  1  0  0  0  0
  3  6  1  0  0  0  0
  7  6  2  0  0  0  0
 13  7  1  0  0  0  0
  8 13  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  1  0  0  0  0
 11 10  1  0  0  0  0
 12 11  1  0  0  0  0
 13 14  1  6  0  0  0
 15 16  2  0  0  0  0
 22 17  1  0  0  0  0
 18 17  1  0  0  0  0
 21 17  2  0  0  0  0
  5 19  1  0  0  0  0
 20 19  2  0  0  0  0
 23 20  1  0  0  0  0
 24 22  1  0  0  0  0
 24 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0187620

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCC[C@H](O)\C=C\C1=C(C\C=C/CCCC(O)=O)C(=O)CC1

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O4/c1-2-3-6-9-17(21)14-12-16-13-15-19(22)18(16)10-7-4-5-8-11-20(23)24/h4,7,12,14,17,21H,2-3,5-6,8-11,13,15H2,1H3,(H,23,24)/b7-4-,14-12+/t17-/m0/s1

> <INCHI_KEY>
PRFXRIUZNKLRHM-HKVRTXJWSA-N

> <FORMULA>
C20H30O4

> <MOLECULAR_WEIGHT>
334.456

> <EXACT_MASS>
334.214409446

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
39.32241125285137

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5Z)-7-{2-[(1E,3S)-3-hydroxyoct-1-en-1-yl]-5-oxocyclopent-1-en-1-yl}hept-5-enoic acid

> <ALOGPS_LOGP>
4.07

> <JCHEM_LOGP>
4.18485735

> <ALOGPS_LOGS>
-4.05

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
17.769121310332174

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.25375476006069

> <JCHEM_PKA_STRONGEST_BASIC>
-1.587391578492345

> <JCHEM_POLAR_SURFACE_AREA>
74.6

> <JCHEM_REFRACTIVITY>
98.60589999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.99e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
prostaglandin B2

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 30-MAY-17   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   30-MAY-17         0                                  
HETATM    1  C   UNK     0      11.782 -36.463   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.412 -37.231   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.781 -38.003   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.316 -38.478   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.114 -35.690   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.115 -38.772   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.448 -38.002   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      17.116 -38.001   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      18.450 -38.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      19.783 -38.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      21.117 -38.769   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      22.450 -37.999   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      15.782 -38.771   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      15.782 -40.311   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      10.318 -35.986   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       9.919 -34.499   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      18.508 -31.142   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      19.830 -31.935   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      14.436 -36.483   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      15.811 -35.743   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      18.528 -29.626   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      17.186 -31.882   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      15.811 -34.209   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      17.186 -33.469   0.000  0.00  0.00           C+0
CONECT    1   15    3    5                                                  
CONECT    2   15    4                                                       
CONECT    3    1    4    6                                                  
CONECT    4    2    3                                                       
CONECT    5    1   19                                                       
CONECT    6    3    7                                                       
CONECT    7    6   13                                                       
CONECT    8   13    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13    7    8   14                                                  
CONECT   14   13                                                            
CONECT   15    1    2   16                                                  
CONECT   16   15                                                            
CONECT   17   22   18   21                                                  
CONECT   18   17                                                            
CONECT   19    5   20                                                       
CONECT   20   19   23                                                       
CONECT   21   17                                                            
CONECT   22   17   24                                                       
CONECT   23   20   24                                                       
CONECT   24   22   23                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   48    0
END

View in JSmol

Synonyms

Value	Source
(5Z,13E,15R)-15-Hydroxy-9-oxoprosta-5,8(12),13-trien-1-Oic acid	ChEBI
PGB2	ChEBI
(5Z,13E,15R)-15-Hydroxy-9-oxoprosta-5,8(12),13-trien-1-Oate	Generator

Chemical Formula

C₂₀H₃₀O₄

Average Mass

334.4560 Da

Monoisotopic Mass

334.21441 Da

IUPAC Name

(5Z)-7-{2-[(1E,3S)-3-hydroxyoct-1-en-1-yl]-5-oxocyclopent-1-en-1-yl}hept-5-enoic acid

Traditional Name

prostaglandin B2

CAS Registry Number

Not Available

SMILES

CCCCC[C@H](O)\C=C\C1=C(C\C=C/CCCC(O)=O)C(=O)CC1

InChI Identifier

InChI=1S/C20H30O4/c1-2-3-6-9-17(21)14-12-16-13-15-19(22)18(16)10-7-4-5-8-11-20(23)24/h4,7,12,14,17,21H,2-3,5-6,8-11,13,15H2,1H3,(H,23,24)/b7-4-,14-12+/t17-/m0/s1

InChI Key

PRFXRIUZNKLRHM-HKVRTXJWSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Homo sapiens	LOTUS Database	35616633
Larix sibirica	LOTUS Database	35616633
Sarcophyton crassocaule	LOTUS Database	35616633

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
Fatty acid
Unsaturated fatty acid
Ketone
Cyclic ketone
Secondary alcohol
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Organic oxide
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

prostaglandins B (CHEBI:28099 )
Prostaglandins (C05954 )
Prostaglandins (LMFA03010018 )

Physical Properties

State

Not Available

Experimental 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

Predicted Properties

Property	Value	Source
logP	4.07	ALOGPS
logP	4.18	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	4.25	ChemAxon
pKa (Strongest Basic)	-1.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	98.61 m³·mol⁻¹	ChemAxon
Polarizability	39.32 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

External Links

HMDB ID

Not Available

DrugBank ID

DB02304

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

C05954

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5280881

PDB ID

Not Available

ChEBI ID

28099

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for prostaglandin b2 (NP0187620)

MOL for NP0187620 (prostaglandin b2)

3D MOL for NP0187620 (prostaglandin b2)

3D SDF for NP0187620 (prostaglandin b2)

3D-SDF for NP0187620 (prostaglandin b2)

PDB for NP0187620 (prostaglandin b2)

3D PDB for NP0187620 (prostaglandin b2)

SMILES for NP0187620 (prostaglandin b2)

INCHI for NP0187620 (prostaglandin b2)

Structure for NP0187620 (prostaglandin b2)

3D Structure for NP0187620 (prostaglandin b2)