NP-MRD: Showing NP-Card for (1s)-2-[(4ar,5s,6r,8s,8ar)-8-(acetyloxy)-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(5-oxo-2h-furan-3-yl)ethyl (2s)-2-methylbutanoate (NP0314130)

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Record Information

Version

2.0

Created at

2022-09-11 12:04:27 UTC

Updated at

2022-09-11 12:04:27 UTC

NP-MRD ID

NP0314130

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s)-2-[(4ar,5s,6r,8s,8ar)-8-(acetyloxy)-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(5-oxo-2h-furan-3-yl)ethyl (2s)-2-methylbutanoate

Description

Ajugamarin F 2 belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. (1s)-2-[(4ar,5s,6r,8s,8ar)-8-(acetyloxy)-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(5-oxo-2h-furan-3-yl)ethyl (2s)-2-methylbutanoate is found in Ajuga ciliata. Based on a literature review very few articles have been published on Ajugamarin F 2.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112214042D          

 35 38  0  0  1  0            999 V2000
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   -3.9004    1.7873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

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M  END


  Mrv1652309112214042D          

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 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 10 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 20 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 27 29  1  0  0  0  0
  8 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 30 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0314130

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](C)C(=O)O[C@@H](C[C@@]1(C)[C@H](C)C[C@H](OC(C)=O)[C@]2(CO)[C@@H]1CCCC21CO1)C1=CC(=O)OC1

> <INCHI_IDENTIFIER>
InChI=1S/C27H40O8/c1-6-16(2)24(31)35-20(19-11-23(30)32-13-19)12-25(5)17(3)10-22(34-18(4)29)27(14-28)21(25)8-7-9-26(27)15-33-26/h11,16-17,20-22,28H,6-10,12-15H2,1-5H3/t16-,17+,20-,21+,22-,25-,26?,27-/m0/s1

> <INCHI_KEY>
QHHXLQKFECWSRR-XGYWGJSESA-N

> <FORMULA>
C27H40O8

> <MOLECULAR_WEIGHT>
492.609

> <EXACT_MASS>
492.272318248

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
52.9175930249711

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S)-2-[(4aR,5S,6R,8S,8aR)-8-(acetyloxy)-8a-(hydroxymethyl)-5,6-dimethyl-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-5-yl]-1-(5-oxo-2,5-dihydrofuran-3-yl)ethyl (2S)-2-methylbutanoate

> <JCHEM_LOGP>
3.149752527666667

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.927934138731072

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.593896837697931

> <JCHEM_PKA_STRONGEST_BASIC>
-2.830321613285671

> <JCHEM_POLAR_SURFACE_AREA>
111.66000000000001

> <JCHEM_REFRACTIVITY>
126.97599999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S)-2-[(4aR,5S,6R,8S,8aR)-8-(acetyloxy)-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2H-spiro[naphthalene-1,2'-oxirane]-5-yl]-1-(5-oxo-2H-furan-3-yl)ethyl (2S)-2-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -8.614   4.106   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -7.281   3.336   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.947   4.106   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.947   5.646   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.613   3.336   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -4.613   1.796   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      -3.280   4.106   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -1.946   3.336   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.612   4.106   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.721   3.336   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.269   2.157   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.711   2.157   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.185   0.709   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.228   2.424   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.755   3.871   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.271   4.138   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.261   2.959   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.778   3.226   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.734   1.512   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.765   5.051   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.281   5.318   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       5.558   6.179   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.248   4.783   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.258   5.963   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.785   7.410   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.302   7.678   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.291   6.498   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.471   7.488   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.739   5.971   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -1.946   1.796   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -0.700   0.891   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -1.176  -0.574   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -0.271  -1.819   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      -2.716  -0.574   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -3.192   0.891   0.000  0.00  0.00           C+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   30                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12   23                                             
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   15   21   23   27                                             
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   10   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   20   28   29                                             
CONECT   28   27   29                                                       
CONECT   29   28   27                                                       
CONECT   30    8   31   35                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   30                                                       
MASTER        0    0    0    0    0    0    0    0   35    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₄₀O₈

Average Mass

492.6090 Da

Monoisotopic Mass

492.27232 Da

IUPAC Name

(1S)-2-[(4aR,5S,6R,8S,8aR)-8-(acetyloxy)-8a-(hydroxymethyl)-5,6-dimethyl-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-5-yl]-1-(5-oxo-2,5-dihydrofuran-3-yl)ethyl (2S)-2-methylbutanoate

Traditional Name

(1S)-2-[(4aR,5S,6R,8S,8aR)-8-(acetyloxy)-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2H-spiro[naphthalene-1,2'-oxirane]-5-yl]-1-(5-oxo-2H-furan-3-yl)ethyl (2S)-2-methylbutanoate

CAS Registry Number

Not Available

SMILES

CC[C@H](C)C(=O)O[C@@H](C[C@@]1(C)[C@H](C)C[C@H](OC(C)=O)[C@]2(CO)[C@@H]1CCCC21CO1)C1=CC(=O)OC1

InChI Identifier

InChI=1S/C27H40O8/c1-6-16(2)24(31)35-20(19-11-23(30)32-13-19)12-25(5)17(3)10-22(34-18(4)29)27(14-28)21(25)8-7-9-26(27)15-33-26/h11,16-17,20-22,28H,6-10,12-15H2,1-5H3/t16-,17+,20-,21+,22-,25-,26?,27-/m0/s1

InChI Key

QHHXLQKFECWSRR-XGYWGJSESA-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
Ajuga ciliata	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
2-furanone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Dihydrofuran
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	3.15	ChemAxon
pKa (Strongest Acidic)	5.59	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	111.66 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	126.98 m³·mol⁻¹	ChemAxon
Polarizability	52.92 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

156793

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

180166

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s)-2-[(4ar,5s,6r,8s,8ar)-8-(acetyloxy)-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(5-oxo-2h-furan-3-yl)ethyl (2s)-2-methylbutanoate (NP0314130)

MOL for NP0314130 ((1s)-2-[(4ar,5s,6r,8s,8ar)-8-(acetyloxy)-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(5-oxo-2h-furan-3-yl)ethyl (2s)-2-methylbutanoate)

3D MOL for NP0314130 ((1s)-2-[(4ar,5s,6r,8s,8ar)-8-(acetyloxy)-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(5-oxo-2h-furan-3-yl)ethyl (2s)-2-methylbutanoate)

3D SDF for NP0314130 ((1s)-2-[(4ar,5s,6r,8s,8ar)-8-(acetyloxy)-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(5-oxo-2h-furan-3-yl)ethyl (2s)-2-methylbutanoate)

3D-SDF for NP0314130 ((1s)-2-[(4ar,5s,6r,8s,8ar)-8-(acetyloxy)-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(5-oxo-2h-furan-3-yl)ethyl (2s)-2-methylbutanoate)

PDB for NP0314130 ((1s)-2-[(4ar,5s,6r,8s,8ar)-8-(acetyloxy)-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(5-oxo-2h-furan-3-yl)ethyl (2s)-2-methylbutanoate)

3D PDB for NP0314130 ((1s)-2-[(4ar,5s,6r,8s,8ar)-8-(acetyloxy)-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(5-oxo-2h-furan-3-yl)ethyl (2s)-2-methylbutanoate)

SMILES for NP0314130 ((1s)-2-[(4ar,5s,6r,8s,8ar)-8-(acetyloxy)-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(5-oxo-2h-furan-3-yl)ethyl (2s)-2-methylbutanoate)

INCHI for NP0314130 ((1s)-2-[(4ar,5s,6r,8s,8ar)-8-(acetyloxy)-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(5-oxo-2h-furan-3-yl)ethyl (2s)-2-methylbutanoate)

Structure for NP0314130 ((1s)-2-[(4ar,5s,6r,8s,8ar)-8-(acetyloxy)-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(5-oxo-2h-furan-3-yl)ethyl (2s)-2-methylbutanoate)

3D Structure for NP0314130 ((1s)-2-[(4ar,5s,6r,8s,8ar)-8-(acetyloxy)-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(5-oxo-2h-furan-3-yl)ethyl (2s)-2-methylbutanoate)