NP-MRD: Showing NP-Card for farnesyl trihydrogen pyrophosphate (NP0244914)

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Record Information

Version

2.0

Created at

2022-09-07 05:48:52 UTC

Updated at

2022-09-07 05:48:53 UTC

NP-MRD ID

NP0244914

Secondary Accession Numbers

None

Natural Product Identification

Common Name

farnesyl trihydrogen pyrophosphate

Description

Farnesyl diphosphate belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. farnesyl trihydrogen pyrophosphate is found in Mus musculus, Pisum sativum and Streptomyces coelicolor. Farnesyl diphosphate is a moderately acidic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 52 51  0  0  0  0  0  0  0  0999 V2000
    4.9979   -1.3051   -1.4572 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8791   -0.4447   -0.6280 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3226   -0.3214   -1.0151 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3792    0.1783    0.4093 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9473    0.0380    0.7688 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3383    1.4282    0.7143 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8931    1.4307    1.0558 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5291    0.9301    2.4176 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9863    1.8550    0.1962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4575    1.9039    0.4199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2406    1.0727   -0.5564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8869   -0.3555   -0.4462 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5302   -0.7734   -0.7633 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7735   -1.2539   -0.1061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1706   -1.0155    0.2038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9157   -1.7767   -0.7465 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5381   -1.4844   -0.3672 P   0  0  2  0  0  5  0  0  0  0  0  0
   -5.8204   -1.9395    1.0566 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5868   -2.3134   -1.3768 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7848    0.1845   -0.4109 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3367    0.4557   -1.0300 P   0  0  0  0  0  5  0  0  0  0  0  0
   -7.3658    0.2863   -2.5364 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3749   -0.6518   -0.2760 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8046    2.0533   -0.7036 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1761   -0.6723   -1.8650 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5602   -2.0909   -0.8040 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5656   -1.7847   -2.2781 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6005    0.7625   -0.9330 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8928   -0.9403   -0.2923 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4691   -0.6770   -2.0414 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9725    0.8306    1.0665 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9120   -0.4080    1.7768 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4340   -0.6113    0.0337 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8954    2.1305    1.3746 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4474    1.7679   -0.3366 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5622    0.3860    2.4200 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5057    1.8138    3.0883 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2794    0.2197    2.8193 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3430    2.2197   -0.7814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7489    1.6175    1.4594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8502    2.9587    0.2899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0205    1.4474   -1.6129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3296    1.1902   -0.4301 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3935   -1.6976   -1.4043 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9838   -1.1228    0.1778 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0845   -0.0419   -1.3429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4337   -2.3081   -0.0450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4494   -1.5567    1.1836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5441   -0.0119    0.2918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0618   -3.0551   -0.9543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0455   -0.8982    0.6348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3401    2.3503    0.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  1  0
 17 16  1  6
 17 19  1  0
 17 18  2  0
 17 20  1  0
 20 21  1  0
 21 23  1  0
 21 24  1  0
 21 22  2  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  5 32  1  0
  5 33  1  0
  6 34  1  0
  6 35  1  0
  8 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  0
 11 43  1  0
 13 44  1  0
 13 45  1  0
 13 46  1  0
 14 47  1  0
 15 48  1  0
 15 49  1  0
 19 50  1  0
 23 51  1  0
 24 52  1  0
M  END


  Mrv1533005021512052D          

 24 23  0  0  0  0            999 V2000
    6.1875    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.4289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -2.1434    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1270   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250   -2.8579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -3.5724    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.2868    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1270   -3.9849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -3.1599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  4  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  4  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
 10 22  1  0  0  0  0
  6 23  1  0  0  0  0
  2 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0244914

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCCC(C)=CCCC(C)=CCOP(O)(=O)OP(O)(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H28O7P2/c1-13(2)7-5-8-14(3)9-6-10-15(4)11-12-21-24(19,20)22-23(16,17)18/h7,9,11H,5-6,8,10,12H2,1-4H3,(H,19,20)(H2,16,17,18)

> <INCHI_KEY>
VWFJDQUYCIWHTN-UHFFFAOYSA-N

> <FORMULA>
C15H28O7P2

> <MOLECULAR_WEIGHT>
382.33

> <EXACT_MASS>
382.131027238

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
37.860191852445155

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
({hydroxy[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phosphoryl}oxy)phosphonic acid

> <ALOGPS_LOGP>
2.40

> <JCHEM_LOGP>
3.6167330606666663

> <ALOGPS_LOGS>
-3.68

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
3.2043406094078315

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.7672186885241006

> <JCHEM_POLAR_SURFACE_AREA>
113.29000000000002

> <JCHEM_REFRACTIVITY>
96.73049999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.07e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
farnesyl diphosphate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-MAY-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-MAY-15         0                                  
HETATM    1  C   UNK     0      11.550   6.668   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.780   5.335   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.240   5.335   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.470   4.001   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.160   2.667   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.620   2.667   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.850   1.334   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.770  -1.334   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.000  -2.667   0.000  0.00  0.00           O+0
HETATM   14  P   UNK     0      -0.770  -4.001   0.000  0.00  0.00           P+0
HETATM   15  O   UNK     0      -2.104  -3.231   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       0.564  -4.771   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -1.540  -5.335   0.000  0.00  0.00           O+0
HETATM   18  P   UNK     0      -0.770  -6.668   0.000  0.00  0.00           P+0
HETATM   19  O   UNK     0       0.000  -8.002   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -2.104  -7.438   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       0.564  -5.898   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.310  -1.334   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.930   1.334   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.550   4.001   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   24                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   23                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   22                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   14   18                                                       
CONECT   18   17   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18                                                            
CONECT   22   10                                                            
CONECT   23    6                                                            
CONECT   24    2                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   46    0
END

View in JSmol

Synonyms

Value	Source
Farnesyl diphosphoric acid	Generator
Diphosphate,p-(3,7,11-trimethyl-2,6,10-dodecatrienyl) ester	Generator
Diphosphate,p-(3,7,11-trimethyl-2,6,10-dodecatrienyl) ester	Generator

Chemical Formula

C₁₅H₂₈O₇P₂

Average Mass

382.3300 Da

Monoisotopic Mass

382.13103 Da

IUPAC Name

({hydroxy[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phosphoryl}oxy)phosphonic acid

Traditional Name

farnesyl diphosphate

CAS Registry Number

Not Available

SMILES

CC(C)=CCCC(C)=CCCC(C)=CCOP(O)(=O)OP(O)(O)=O

InChI Identifier

InChI=1S/C15H28O7P2/c1-13(2)7-5-8-14(3)9-6-10-15(4)11-12-21-24(19,20)22-23(16,17)18/h7,9,11H,5-6,8,10,12H2,1-4H3,(H,19,20)(H2,16,17,18)

InChI Key

VWFJDQUYCIWHTN-UHFFFAOYSA-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
Mus musculus	LOTUS Database	35616633
Pisum sativum	LOTUS Database	35616633
Streptomyces coelicolor	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Farsesane sesquiterpenoid
Sesquiterpenoid
Organic pyrophosphate
Isoprenoid phosphate
Monoalkyl phosphate
Alkyl phosphate
Phosphoric acid ester
Organic phosphoric acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

polyprenol diphosphate (CHEBI:50277 )
farnesyl phosphate (CHEBI:50277 )

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	2.4	ALOGPS
logP	3.62	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	1.77	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	96.73 m³·mol⁻¹	ChemAxon
Polarizability	37.86 Å³	ChemAxon
Number of Rings	0	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

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Farnesyl pyrophosphate

METLIN ID

Not Available

PubChem Compound

706

PDB ID

Not Available

ChEBI ID

50277

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for farnesyl trihydrogen pyrophosphate (NP0244914)

MOL for NP0244914 (farnesyl trihydrogen pyrophosphate)

3D MOL for NP0244914 (farnesyl trihydrogen pyrophosphate)

3D SDF for NP0244914 (farnesyl trihydrogen pyrophosphate)

3D-SDF for NP0244914 (farnesyl trihydrogen pyrophosphate)

PDB for NP0244914 (farnesyl trihydrogen pyrophosphate)

3D PDB for NP0244914 (farnesyl trihydrogen pyrophosphate)

SMILES for NP0244914 (farnesyl trihydrogen pyrophosphate)

INCHI for NP0244914 (farnesyl trihydrogen pyrophosphate)

Structure for NP0244914 (farnesyl trihydrogen pyrophosphate)

3D Structure for NP0244914 (farnesyl trihydrogen pyrophosphate)