NP-MRD: Showing NP-Card for (1s,2s,3r,4r,5s,6r)-3-(acetyloxy)-4,6-dihydroxy-2,5-bis[(2-methylbut-2-enoyl)oxy]cyclohexyl (2z)-2-methylbut-2-enoate (NP0227896)

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Record Information

Version

2.0

Created at

2022-09-06 07:22:28 UTC

Updated at

2022-09-06 07:22:28 UTC

NP-MRD ID

NP0227896

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,3r,4r,5s,6r)-3-(acetyloxy)-4,6-dihydroxy-2,5-bis[(2-methylbut-2-enoyl)oxy]cyclohexyl (2z)-2-methylbut-2-enoate

Description

(1S,2R,3R,4S,5R,6S)-2-(acetyloxy)-3,5-dihydroxy-4-[(2-methylbut-2-enoyl)oxy]-6-{[(2Z)-2-methylbut-2-enoyl]oxy}cyclohexyl 2-methylbut-2-enoate belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups. (1s,2s,3r,4r,5s,6r)-3-(acetyloxy)-4,6-dihydroxy-2,5-bis[(2-methylbut-2-enoyl)oxy]cyclohexyl (2z)-2-methylbut-2-enoate is found in Duhaldea cappa. Based on a literature review very few articles have been published on (1S,2R,3R,4S,5R,6S)-2-(acetyloxy)-3,5-dihydroxy-4-[(2-methylbut-2-enoyl)oxy]-6-{[(2Z)-2-methylbut-2-enoyl]oxy}cyclohexyl 2-methylbut-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062209222D          

 33 33  0  0  1  0            999 V2000
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    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
    0.7145    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
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  2  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
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  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
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   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
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 O   0  0  0  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
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
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  9 10  1  1  0  0  0
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 27 32  1  0  0  0  0
  8 32  1  0  0  0  0
 32 33  1  6  0  0  0
M  END

     RDKit          3D

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    1.9342   -2.0707   -1.8680 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309062209222D          

 33 33  0  0  1  0            999 V2000
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0227896

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C23H32O10/c1-8-11(4)21(27)31-17-15(25)18(30-14(7)24)20(33-23(29)13(6)10-3)19(16(17)26)32-22(28)12(5)9-2/h8-10,15-20,25-26H,1-7H3/b11-8?,12-9-,13-10?/t15-,16-,17+,18-,19+,20+/m1/s1

> <INCHI_KEY>
ODTBYXFKNHAVFE-IPAZESSSSA-N

> <FORMULA>
C23H32O10

> <MOLECULAR_WEIGHT>
468.499

> <EXACT_MASS>
468.19954723

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
47.441828653207565

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,3R,4R,5S,6R)-3-(acetyloxy)-4,6-dihydroxy-2,5-bis[(2-methylbut-2-enoyl)oxy]cyclohexyl (2Z)-2-methylbut-2-enoate

> <JCHEM_LOGP>
3.297927462333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.39424360274656

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.692332915571672

> <JCHEM_PKA_STRONGEST_BASIC>
-3.676364493493364

> <JCHEM_POLAR_SURFACE_AREA>
145.66000000000003

> <JCHEM_REFRACTIVITY>
116.41590000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3R,4R,5S,6R)-3-(acetyloxy)-4,6-dihydroxy-2,5-bis[(2-methylbut-2-enoyl)oxy]cyclohexyl (2Z)-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.001   6.930   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   32                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   19                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17                                                            
CONECT   19   11   20   27                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25                                                            
CONECT   27   19   28   32                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   27    8   33                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   66    0
END

View in JSmol

Synonyms

Value	Source
(1S,2R,3R,4S,5R,6S)-2-(Acetyloxy)-3,5-dihydroxy-4-[(2-methylbut-2-enoyl)oxy]-6-{[(2Z)-2-methylbut-2-enoyl]oxy}cyclohexyl 2-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₃H₃₂O₁₀

Average Mass

468.4990 Da

Monoisotopic Mass

468.19955 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C23H32O10/c1-8-11(4)21(27)31-17-15(25)18(30-14(7)24)20(33-23(29)13(6)10-3)19(16(17)26)32-22(28)12(5)9-2/h8-10,15-20,25-26H,1-7H3/b11-8?,12-9-,13-10?/t15-,16-,17+,18-,19+,20+/m1/s1

InChI Key

ODTBYXFKNHAVFE-IPAZESSSSA-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
Duhaldea cappa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tetracarboxylic acids and derivatives

Direct Parent

Tetracarboxylic acids and derivatives

Alternative Parents

Substituents

Tetracarboxylic acid or derivatives
Fatty acid ester
Cyclohexanol
Fatty acyl
Cyclitol or derivatives
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

Not Available

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	3.3	ChemAxon
pKa (Strongest Acidic)	12.69	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	145.66 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	116.42 m³·mol⁻¹	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

Not Available

METLIN ID

Not Available

PubChem Compound

162818868

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,3r,4r,5s,6r)-3-(acetyloxy)-4,6-dihydroxy-2,5-bis[(2-methylbut-2-enoyl)oxy]cyclohexyl (2z)-2-methylbut-2-enoate (NP0227896)

MOL for NP0227896 ((1s,2s,3r,4r,5s,6r)-3-(acetyloxy)-4,6-dihydroxy-2,5-bis[(2-methylbut-2-enoyl)oxy]cyclohexyl (2z)-2-methylbut-2-enoate)

3D MOL for NP0227896 ((1s,2s,3r,4r,5s,6r)-3-(acetyloxy)-4,6-dihydroxy-2,5-bis[(2-methylbut-2-enoyl)oxy]cyclohexyl (2z)-2-methylbut-2-enoate)

3D SDF for NP0227896 ((1s,2s,3r,4r,5s,6r)-3-(acetyloxy)-4,6-dihydroxy-2,5-bis[(2-methylbut-2-enoyl)oxy]cyclohexyl (2z)-2-methylbut-2-enoate)

3D-SDF for NP0227896 ((1s,2s,3r,4r,5s,6r)-3-(acetyloxy)-4,6-dihydroxy-2,5-bis[(2-methylbut-2-enoyl)oxy]cyclohexyl (2z)-2-methylbut-2-enoate)

PDB for NP0227896 ((1s,2s,3r,4r,5s,6r)-3-(acetyloxy)-4,6-dihydroxy-2,5-bis[(2-methylbut-2-enoyl)oxy]cyclohexyl (2z)-2-methylbut-2-enoate)

3D PDB for NP0227896 ((1s,2s,3r,4r,5s,6r)-3-(acetyloxy)-4,6-dihydroxy-2,5-bis[(2-methylbut-2-enoyl)oxy]cyclohexyl (2z)-2-methylbut-2-enoate)

SMILES for NP0227896 ((1s,2s,3r,4r,5s,6r)-3-(acetyloxy)-4,6-dihydroxy-2,5-bis[(2-methylbut-2-enoyl)oxy]cyclohexyl (2z)-2-methylbut-2-enoate)

INCHI for NP0227896 ((1s,2s,3r,4r,5s,6r)-3-(acetyloxy)-4,6-dihydroxy-2,5-bis[(2-methylbut-2-enoyl)oxy]cyclohexyl (2z)-2-methylbut-2-enoate)

Structure for NP0227896 ((1s,2s,3r,4r,5s,6r)-3-(acetyloxy)-4,6-dihydroxy-2,5-bis[(2-methylbut-2-enoyl)oxy]cyclohexyl (2z)-2-methylbut-2-enoate)

3D Structure for NP0227896 ((1s,2s,3r,4r,5s,6r)-3-(acetyloxy)-4,6-dihydroxy-2,5-bis[(2-methylbut-2-enoyl)oxy]cyclohexyl (2z)-2-methylbut-2-enoate)