NP-MRD: Showing NP-Card for 1-O-Deacetylkhayanolide E (NP0081747)

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Record Information

Version

2.0

Created at

2022-04-29 02:49:30 UTC

Updated at

2022-04-29 02:49:30 UTC

NP-MRD ID

NP0081747

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-O-Deacetylkhayanolide E

Description

Methyl (2S)-2-[(1S,2R,3S,4S,5R,6R,8S,10S,13R,14R,17R,18S)-13-(furan-3-yl)-1,3-dihydroxy-4,6,14-trimethyl-7,11-dioxo-9,12-dioxahexacyclo[8.7.1.1³,⁶.0²,⁸.0⁴,¹⁷.0¹⁴,¹⁸]Nonadecan-5-yl]-2-hydroxyacetate belongs to the class of organic compounds known as delta valerolactones. These are cyclic organic compounds containing an oxan-2- one moiety. 1-O-Deacetylkhayanolide E is found in Khaya senegalensis . Based on a literature review very few articles have been published on methyl (2S)-2-[(1S,2R,3S,4S,5R,6R,8S,10S,13R,14R,17R,18S)-13-(furan-3-yl)-1,3-dihydroxy-4,6,14-trimethyl-7,11-dioxo-9,12-dioxahexacyclo[8.7.1.1³,⁶.0²,⁸.0⁴,¹⁷.0¹⁴,¹⁸]Nonadecan-5-yl]-2-hydroxyacetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292204492D          

 37 43  0  0  1  0            999 V2000
    1.1904   -0.6933    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0907    0.0282    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    3.3451    0.8967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.2318   -0.5440    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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  6 35  1  6  0  0  0
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  1 37  1  6  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652304292204492D          

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 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
  2 15  1  0  0  0  0
 15 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
 19 20  1  0  0  0  0
 16 21  1  1  0  0  0
 14 22  1  1  0  0  0
 14 23  1  0  0  0  0
  1 23  1  0  0  0  0
 11 24  1  6  0  0  0
 25 24  1  1  0  0  0
  7 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
  6 29  1  0  0  0  0
 29 30  1  6  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 30 34  1  0  0  0  0
  6 35  1  6  0  0  0
  2 36  1  6  0  0  0
  1 37  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0081747

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@H](O)[C@H]1[C@@]2(C)C[C@]3(O)[C@@H]4[C@H](O[C@H]5[C@H]6[C@@]4(O)[C@H](CC[C@@]6(C)[C@@H](OC5=O)C4=COC=C4)[C@]13C)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C27H32O10/c1-23-7-5-12-25(3)16(13(28)21(30)34-4)24(2)10-26(25,32)18-14(19(24)29)36-15(17(23)27(12,18)33)22(31)37-20(23)11-6-8-35-9-11/h6,8-9,12-18,20,28,32-33H,5,7,10H2,1-4H3/t12-,13+,14+,15+,16+,17-,18+,20+,23-,24-,25-,26+,27+/m1/s1

> <INCHI_KEY>
TYWPPOPXVDAORZ-FRUWVUPKSA-N

> <FORMULA>
C27H32O10

> <MOLECULAR_WEIGHT>
516.543

> <EXACT_MASS>
516.19954723

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
51.45969717791602

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (2S)-2-[(1S,2R,3S,4S,5R,6R,8S,10S,13R,14R,17R,18S)-13-(furan-3-yl)-1,3-dihydroxy-4,6,14-trimethyl-7,11-dioxo-9,12-dioxahexacyclo[8.7.1.1^{3,6}.0^{2,8}.0^{4,17}.0^{14,18}]nonadecan-5-yl]-2-hydroxyacetate

> <ALOGPS_LOGP>
1.16

> <JCHEM_LOGP>
0.4141413546666664

> <ALOGPS_LOGS>
-2.91

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.607181544127304

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.389023680705339

> <JCHEM_PKA_STRONGEST_BASIC>
-2.872104380896693

> <JCHEM_POLAR_SURFACE_AREA>
152.73

> <JCHEM_REFRACTIVITY>
122.14819999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.33e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(S)-(methyl [(1S,2R,3S,4S,5R,6R,8S,10S,13R,14R,17R,18S)-13-(furan-3-yl)-1,3-dihydroxy-4,6,14-trimethyl-7,11-dioxo-9,12-dioxahexacyclo[8.7.1.1^{3,6}.0^{2,8}.0^{4,17}.0^{14,18}]nonadecan-5-yl](hydroxy)acetate)

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       2.222  -1.294   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.036   0.053   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.689   0.580   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.670   1.823   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.244   1.674   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.967   0.239   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.033  -1.015   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.522  -0.738   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.384   0.538   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       3.580  -1.894   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.769  -3.363   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.248  -3.944   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.936  -5.452   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.022  -2.749   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.557  -0.741   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.846  -0.106   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.098  -1.003   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.946  -2.536   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -3.501  -0.368   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -4.752  -1.265   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.997   1.426   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.320  -3.504   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.516  -1.820   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.382  -3.672   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.507  -2.532   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.051  -2.793   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.576  -4.241   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       9.058  -1.614   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       8.520  -0.145   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.548   1.001   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.224   2.507   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      10.556   3.280   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      11.703   2.252   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      11.080   0.843   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       7.928   1.443   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       1.435   1.471   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       2.132  -2.832   0.000  0.00  0.00           O+0
CONECT    1    2   10   23   37                                             
CONECT    2    1    3   15   36                                             
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   29   35                                             
CONECT    7    6    8   25                                                  
CONECT    8    7    3    9   10                                             
CONECT    9    8                                                            
CONECT   10    8    1   11                                                  
CONECT   11   10   12   24                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   22   23                                             
CONECT   15   14    2   16                                                  
CONECT   16   15   17   21                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19                                                            
CONECT   21   16                                                            
CONECT   22   14                                                            
CONECT   23   14    1                                                       
CONECT   24   11   25                                                       
CONECT   25   24    7   26                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28    6   30                                                  
CONECT   30   29   31   34                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   30                                                       
CONECT   35    6                                                            
CONECT   36    2                                                            
CONECT   37    1                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   86    0
END

View in JSmol

Synonyms

Value	Source
Methyl (2S)-2-[(1S,2R,3S,4S,5R,6R,8S,10S,13R,14R,17R,18S)-13-(furan-3-yl)-1,3-dihydroxy-4,6,14-trimethyl-7,11-dioxo-9,12-dioxahexacyclo[8.7.1.1,.0,.0,.0,]nonadecan-5-yl]-2-hydroxyacetic acid	Generator

Chemical Formula

C₂₇H₃₂O₁₀

Average Mass

516.5430 Da

Monoisotopic Mass

516.19955 Da

IUPAC Name

methyl (2S)-2-[(1S,2R,3S,4S,5R,6R,8S,10S,13R,14R,17R,18S)-13-(furan-3-yl)-1,3-dihydroxy-4,6,14-trimethyl-7,11-dioxo-9,12-dioxahexacyclo[8.7.1.1^{3,6}.0^{2,8}.0^{4,17}.0^{14,18}]nonadecan-5-yl]-2-hydroxyacetate

Traditional Name

(S)-(methyl [(1S,2R,3S,4S,5R,6R,8S,10S,13R,14R,17R,18S)-13-(furan-3-yl)-1,3-dihydroxy-4,6,14-trimethyl-7,11-dioxo-9,12-dioxahexacyclo[8.7.1.1^{3,6}.0^{2,8}.0^{4,17}.0^{14,18}]nonadecan-5-yl](hydroxy)acetate)

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@H](O)[C@H]1[C@@]2(C)C[C@]3(O)[C@@H]4[C@H](O[C@H]5[C@H]6[C@@]4(O)[C@H](CC[C@@]6(C)[C@@H](OC5=O)C4=COC=C4)[C@]13C)C2=O

InChI Identifier

InChI=1S/C27H32O10/c1-23-7-5-12-25(3)16(13(28)21(30)34-4)24(2)10-26(25,32)18-14(19(24)29)36-15(17(23)27(12,18)33)22(31)37-20(23)11-6-8-35-9-11/h6,8-9,12-18,20,28,32-33H,5,7,10H2,1-4H3/t12-,13+,14+,15+,16+,17-,18+,20+,23-,24-,25-,26+,27+/m1/s1

InChI Key

TYWPPOPXVDAORZ-FRUWVUPKSA-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
Khaya senegalensis	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as delta valerolactones. These are cyclic organic compounds containing an oxan-2- one moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Delta valerolactones

Direct Parent

Delta valerolactones

Alternative Parents

Substituents

Delta_valerolactone
Delta valerolactone
Oxane
Dicarboxylic acid or derivatives
Heteroaromatic compound
Methyl ester
Tertiary alcohol
Furan
Cyclic alcohol
Secondary alcohol
Ketone
Carboxylic acid ester
Oxacycle
Ether
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	1.16	ALOGPS
logP	0.41	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	12.39	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	152.73 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	122.15 m³·mol⁻¹	ChemAxon
Polarizability	51.46 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

Not Available

METLIN ID

Not Available

PubChem Compound

163106115

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 1-O-Deacetylkhayanolide E (NP0081747)

MOL for NP0081747 (1-O-Deacetylkhayanolide E)

3D MOL for NP0081747 (1-O-Deacetylkhayanolide E)

3D SDF for NP0081747 (1-O-Deacetylkhayanolide E)

3D-SDF for NP0081747 (1-O-Deacetylkhayanolide E)

PDB for NP0081747 (1-O-Deacetylkhayanolide E)

3D PDB for NP0081747 (1-O-Deacetylkhayanolide E)

SMILES for NP0081747 (1-O-Deacetylkhayanolide E)

INCHI for NP0081747 (1-O-Deacetylkhayanolide E)

Structure for NP0081747 (1-O-Deacetylkhayanolide E)

3D Structure for NP0081747 (1-O-Deacetylkhayanolide E)