NP-MRD: Showing NP-Card for D-quinovitol (NP0031480)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2021-06-19 22:33:11 UTC

Updated at

2021-06-30 00:00:05 UTC

NP-MRD ID

NP0031480

Secondary Accession Numbers

None

Natural Product Identification

Common Name

D-quinovitol

Provided By

JEOL Database JEOL Logo

Description

D-quinovitol is found in Averrhoa carambola , Carum carvi L. and Cnidium monnieri. D-quinovitol was first documented in 2001 (Kitajima, J., et al.). Based on a literature review very few articles have been published on (2S,3R,4R,5R)-hexane-1,2,3,4,5-pentol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI

  Mrv1652306202100333D          

 25 24  0  0  0  0            999 V2000
    2.1784   -1.0673   -2.2560 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5346   -0.0057   -3.1398 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3443   -0.5823   -4.4427 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1521    0.4627   -2.6521 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7777   -0.6427   -2.7247 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0919    1.0092   -1.2151 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2758    1.4068   -0.9609 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0446    2.1925   -0.9563 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8984    3.1688   -1.9954 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7816    2.8783    0.3927 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4888    3.5334    0.3806 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5383   -1.9516   -2.1669 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1199   -1.4098   -2.6996 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3943   -0.6866   -1.2542 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2073    0.8516   -3.2483 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2286   -0.7467   -4.8168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2477    1.2053   -3.3538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5901   -1.0508   -3.5969 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2955    0.2097   -0.4934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8119    0.6906   -1.3677 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0810    1.8408   -0.9844 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1169    3.7026   -1.7390 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8074    2.1639    1.2211 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5332    3.6531    0.5730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1379    2.8572    0.0802 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
 10  8  1  0  0  0  0
 10 11  1  0  0  0  0
  6  4  1  0  0  0  0
  8  9  1  0  0  0  0
  6  7  1  0  0  0  0
  4  2  1  0  0  0  0
  4  5  1  0  0  0  0
  8  6  1  0  0  0  0
  2  3  1  0  0  0  0
 10 23  1  0  0  0  0
 10 24  1  0  0  0  0
  8 21  1  1  0  0  0
  6 19  1  1  0  0  0
  4 17  1  6  0  0  0
  2 15  1  6  0  0  0
  1 12  1  0  0  0  0
  1 13  1  0  0  0  0
  1 14  1  0  0  0  0
 11 25  1  0  0  0  0
  9 22  1  0  0  0  0
  7 20  1  0  0  0  0
  5 18  1  0  0  0  0
  3 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0031480

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])[C@]([H])(O[H])[C@@]([H])(O[H])[C@]([H])(O[H])[C@]([H])(O[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C6H14O5/c1-3(8)5(10)6(11)4(9)2-7/h3-11H,2H2,1H3/t3-,4+,5-,6-/m1/s1

> <INCHI_KEY>
SKCKOFZKJLZSFA-JGWLITMVSA-N

> <FORMULA>
C6H14O5

> <MOLECULAR_WEIGHT>
166.173

> <EXACT_MASS>
166.084123551

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
25

> <JCHEM_AVERAGE_POLARIZABILITY>
15.922378469133514

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,4R,5R)-hexane-1,2,3,4,5-pentol

> <ALOGPS_LOGP>
-2.25

> <JCHEM_LOGP>
-2.683108882

> <ALOGPS_LOGS>
0.46

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.642051755496475

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.69525446645461

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9742106409022417

> <JCHEM_POLAR_SURFACE_AREA>
101.15

> <JCHEM_REFRACTIVITY>
36.859899999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.76e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4R,5R)-hexane-1,2,3,4,5-pentol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0       2.178  -1.067  -2.256  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.535  -0.006  -3.140  0.00  0.00           C+0
HETATM    3  O   UNK     0       1.344  -0.582  -4.443  0.00  0.00           O+0
HETATM    4  C   UNK     0       0.152   0.463  -2.652  0.00  0.00           C+0
HETATM    5  O   UNK     0      -0.778  -0.643  -2.725  0.00  0.00           O+0
HETATM    6  C   UNK     0       0.092   1.009  -1.215  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.276   1.407  -0.961  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.045   2.192  -0.956  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.898   3.169  -1.995  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.782   2.878   0.393  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.489   3.533   0.381  0.00  0.00           O+0
HETATM   12  H   UNK     0       1.538  -1.952  -2.167  0.00  0.00           H+0
HETATM   13  H   UNK     0       3.120  -1.410  -2.700  0.00  0.00           H+0
HETATM   14  H   UNK     0       2.394  -0.687  -1.254  0.00  0.00           H+0
HETATM   15  H   UNK     0       2.207   0.852  -3.248  0.00  0.00           H+0
HETATM   16  H   UNK     0       2.229  -0.747  -4.817  0.00  0.00           H+0
HETATM   17  H   UNK     0      -0.248   1.205  -3.354  0.00  0.00           H+0
HETATM   18  H   UNK     0      -0.590  -1.051  -3.597  0.00  0.00           H+0
HETATM   19  H   UNK     0       0.296   0.210  -0.493  0.00  0.00           H+0
HETATM   20  H   UNK     0      -1.812   0.691  -1.368  0.00  0.00           H+0
HETATM   21  H   UNK     0       2.081   1.841  -0.984  0.00  0.00           H+0
HETATM   22  H   UNK     0       0.117   3.703  -1.739  0.00  0.00           H+0
HETATM   23  H   UNK     0       0.807   2.164   1.221  0.00  0.00           H+0
HETATM   24  H   UNK     0       1.533   3.653   0.573  0.00  0.00           H+0
HETATM   25  H   UNK     0      -1.138   2.857   0.080  0.00  0.00           H+0
CONECT    1    2   12   13   14                                             
CONECT    2    1    4    3   15                                             
CONECT    3    2   16                                                       
CONECT    4    6    2    5   17                                             
CONECT    5    4   18                                                       
CONECT    6    4    7    8   19                                             
CONECT    7    6   20                                                       
CONECT    8   10    9    6   21                                             
CONECT    9    8   22                                                       
CONECT   10    8   11   23   24                                             
CONECT   11   10   25                                                       
CONECT   12    1                                                            
CONECT   13    1                                                            
CONECT   14    1                                                            
CONECT   15    2                                                            
CONECT   16    3                                                            
CONECT   17    4                                                            
CONECT   18    5                                                            
CONECT   19    6                                                            
CONECT   20    7                                                            
CONECT   21    8                                                            
CONECT   22    9                                                            
CONECT   23   10                                                            
CONECT   24   10                                                            
CONECT   25   11                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   48    0
END

View in JSmol

Synonyms

Value	Source
6-Deoxyglucitol, (D)-isomer	MeSH
6-Deoxyglucitol, (L)-isomer	MeSH

Chemical Formula

C₆H₁₄O₅

Average Mass

166.1730 Da

Monoisotopic Mass

166.08412 Da

IUPAC Name

(2S,3R,4R,5R)-hexane-1,2,3,4,5-pentol

Traditional Name

(2S,3R,4R,5R)-hexane-1,2,3,4,5-pentol

CAS Registry Number

Not Available

SMILES

[H]OC([H])([H])[C@]([H])(O[H])[C@@]([H])(O[H])[C@]([H])(O[H])[C@]([H])(O[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C6H14O5/c1-3(8)5(10)6(11)4(9)2-7/h3-11H,2H2,1H3/t3-,4+,5-,6-/m1/s1

InChI Key

SKCKOFZKJLZSFA-JGWLITMVSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Averrhoa carambola	Plant	KNApSAcK
Carum carvi	Plant	KNApSAcK
Cnidium monnieri	JEOL database	Kitajima, J., et al, Phytochemistry 58, 641 (2001)

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	-2.2	ALOGPS
logP	-2.7	ChemAxon
logS	0.46	ALOGPS
pKa (Strongest Acidic)	12.7	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	101.15 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	36.86 m³·mol⁻¹	ChemAxon
Polarizability	15.92 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0240352

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

133321

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

151266

PDB ID

Not Available

ChEBI ID

166507

Good Scents ID

Not Available

References

General References

Kitajima, J., et al. (2001). Kitajima, J., et al, Phytochemistry 58, 641 (2001) . Phytochem..

Showing NP-Card for D-quinovitol (NP0031480)

MOL for NP0031480 (D-quinovitol)

3D MOL for NP0031480 (D-quinovitol)

3D SDF for NP0031480 (D-quinovitol)

3D-SDF for NP0031480 (D-quinovitol)

PDB for NP0031480 (D-quinovitol)

3D PDB for NP0031480 (D-quinovitol)

SMILES for NP0031480 (D-quinovitol)

INCHI for NP0031480 (D-quinovitol)

Structure for NP0031480 (D-quinovitol)

3D Structure for NP0031480 (D-quinovitol)