NP-MRD: Showing NP-Card for D-myo-Inositol 1,4-bisphosphate (NP0054980)

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Record Information

Version

2.0

Created at

2022-04-28 01:10:07 UTC

Updated at

2022-04-28 01:10:07 UTC

NP-MRD ID

NP0054980

Secondary Accession Numbers

None

Natural Product Identification

Common Name

D-myo-Inositol 1,4-bisphosphate

Description

D-myo-Inositol 1,4-bisphosphate is found in Arabidopsis thaliana.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 34 34  0  0  0  0  0  0  0  0999 V2000
   -4.3762    1.3592   -1.7792 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7888    0.6067   -0.6071 P   0  0  1  0  0  5  0  0  0  0  0  0
   -4.0437    1.5658    0.7840 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5862   -0.8617   -0.4870 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1372    0.4038   -0.9003 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4695   -0.0806    0.2140 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7453   -1.3664   -0.0352 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4238   -2.0248   -1.0735 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6737   -1.1870   -0.4919 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2360   -2.4715   -0.5911 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4969   -0.3443    0.4553 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1017    0.6497   -0.3111 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7636    0.5999   -0.2858 P   0  0  1  0  0  5  0  0  0  0  0  0
    4.3320   -0.3752    0.6873 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3581    0.1990   -1.8382 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3634    2.1635    0.0494 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5610    0.2239    1.4875 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1814    1.0340    2.4112 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5067    0.9923    0.6961 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0880    1.5317   -0.4525 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9019    2.0382    0.6527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9410   -0.9840    0.4481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2008   -0.2251    1.0626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7974   -2.0687    0.8369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0598   -2.6863   -0.7459 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6491   -0.7768   -1.5215 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0533   -2.9942    0.2466 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2945   -0.9494    0.9127 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2037    0.6920   -2.0331 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8656    2.1337    0.8934 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0909   -0.6374    2.0103 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2109    0.5846    3.3103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9810    1.7542    1.3113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5645    1.5013   -1.2135 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0
  9  7  1  0
  7  8  1  0
  7  6  1  0
  6  5  1  0
  2  5  1  6
  2  3  1  0
  2  4  1  0
  2  1  2  0
  6 19  1  0
 19 20  1  0
 19 17  1  0
 17 18  1  0
 17 11  1  0
 11 12  1  0
 13 12  1  6
 13 15  1  0
 13 16  1  0
 13 14  2  0
 11  9  1  0
 10 27  1  0
  9 26  1  6
  7 24  1  1
  8 25  1  0
  6 23  1  1
  3 21  1  0
  4 22  1  0
 19 33  1  1
 20 34  1  0
 17 31  1  1
 18 32  1  0
 11 28  1  1
 15 29  1  0
 16 30  1  0
M  END


  Mrv1652304282203102D          

 20 20  0  0  1  0            999 V2000
    0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.6500    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -2.3645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.9355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125    3.1895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    1.7605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  5  8  1  1  0  0  0
  4  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 10 13  1  0  0  0  0
  3 14  1  6  0  0  0
  2 15  1  6  0  0  0
  1 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0054980

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@H]1[C@H](O)[C@H](OP(O)(O)=O)[C@H](O)[C@H](O)[C@@H]1OP(O)(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C6H14O12P2/c7-1-2(8)6(18-20(14,15)16)4(10)3(9)5(1)17-19(11,12)13/h1-10H,(H2,11,12,13)(H2,14,15,16)/t1-,2-,3-,4+,5+,6-/m0/s1

> <INCHI_KEY>
PELZSPZCXGTUMR-NTNHSIQDSA-N

> <FORMULA>
C6H14O12P2

> <MOLECULAR_WEIGHT>
340.114

> <EXACT_MASS>
339.996049887

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
25.03268201429716

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(1S,2S,3R,4R,5S,6S)-2,3,5,6-tetrahydroxy-4-(phosphonooxy)cyclohexyl]oxy}phosphonic acid

> <ALOGPS_LOGP>
-1.33

> <JCHEM_LOGP>
-4.029141714666666

> <ALOGPS_LOGS>
-1.14

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-4

> <JCHEM_PKA>
1.4635394895369545

> <JCHEM_PKA_STRONGEST_ACIDIC>
0.8613145099702861

> <JCHEM_PKA_STRONGEST_BASIC>
-3.667896845422092

> <JCHEM_POLAR_SURFACE_AREA>
214.43999999999997

> <JCHEM_REFRACTIVITY>
57.520799999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.44e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(1S,2S,3R,4R,5S,6S)-2,3,5,6-tetrahydroxy-4-(phosphonooxy)cyclohexyl]oxyphosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   10  P   UNK     0      -0.000  -3.080   0.000  0.00  0.00           P+0
HETATM   11  O   UNK     0      -1.334  -3.850   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       0.770  -4.414   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      -0.770  -1.746   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   17  P   UNK     0       0.000   4.620   0.000  0.00  0.00           P+0
HETATM   18  O   UNK     0      -1.334   5.390   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       0.770   5.954   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -0.770   3.286   0.000  0.00  0.00           O+0
CONECT    1    2    6   16                                                  
CONECT    2    1    3   15                                                  
CONECT    3    2    4   14                                                  
CONECT    4    3    5    9                                                  
CONECT    5    4    6    8                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    5                                                            
CONECT    9    4   10                                                       
CONECT   10    9   11   12   13                                             
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13   10                                                            
CONECT   14    3                                                            
CONECT   15    2                                                            
CONECT   16    1   17                                                       
CONECT   17   16   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   17                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   40    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₆H₁₄O₁₂P₂

Average Mass

340.1140 Da

Monoisotopic Mass

339.99605 Da

IUPAC Name

{[(1S,2S,3R,4R,5S,6S)-2,3,5,6-tetrahydroxy-4-(phosphonooxy)cyclohexyl]oxy}phosphonic acid

Traditional Name

[(1S,2S,3R,4R,5S,6S)-2,3,5,6-tetrahydroxy-4-(phosphonooxy)cyclohexyl]oxyphosphonic acid

CAS Registry Number

Not Available

SMILES

O[C@H]1[C@H](O)[C@H](OP(O)(O)=O)[C@H](O)[C@H](O)[C@@H]1OP(O)(O)=O

InChI Identifier

InChI=1S/C6H14O12P2/c7-1-2(8)6(18-20(14,15)16)4(10)3(9)5(1)17-19(11,12)13/h1-10H,(H2,11,12,13)(H2,14,15,16)/t1-,2-,3-,4+,5+,6-/m0/s1

InChI Key

PELZSPZCXGTUMR-NTNHSIQDSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Arabidopsis thaliana	Plant	KNApSAcK

Chemical Taxonomy

Classification

Not classified

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	-1.3	ALOGPS
logP	-4	ChemAxon
logS	-1.1	ALOGPS
pKa (Strongest Acidic)	0.86	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-4	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	214.44 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	57.52 m³·mol⁻¹	ChemAxon
Polarizability	25.03 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

Not Available

Showing NP-Card for D-myo-Inositol 1,4-bisphosphate (NP0054980)

MOL for NP0054980 (D-myo-Inositol 1,4-bisphosphate)

3D MOL for NP0054980 (D-myo-Inositol 1,4-bisphosphate)

3D SDF for NP0054980 (D-myo-Inositol 1,4-bisphosphate)

3D-SDF for NP0054980 (D-myo-Inositol 1,4-bisphosphate)

PDB for NP0054980 (D-myo-Inositol 1,4-bisphosphate)

3D PDB for NP0054980 (D-myo-Inositol 1,4-bisphosphate)

SMILES for NP0054980 (D-myo-Inositol 1,4-bisphosphate)

INCHI for NP0054980 (D-myo-Inositol 1,4-bisphosphate)

Structure for NP0054980 (D-myo-Inositol 1,4-bisphosphate)

3D Structure for NP0054980 (D-myo-Inositol 1,4-bisphosphate)