NP-MRD: Showing NP-Card for (1'r,2r,2's,4'r,5's,6'r,8'r,9'r,11'r)-5'-[(2s,3ar,6as)-hexahydrofuro[2,3-b]furan-2-yl]-2'-(acetyloxy)-9'-hydroxy-4',5'-dimethyl-12'-oxaspiro[oxirane-2,10'-tricyclo[6.2.2.0¹,⁶]dodecan]-11'-yl 2-methylpropanoate (NP0291158)

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Record Information

Version

1.0

Created at

2022-09-09 22:08:50 UTC

Updated at

2022-09-09 22:08:50 UTC

NP-MRD ID

NP0291158

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1'r,2r,2's,4'r,5's,6'r,8'r,9'r,11'r)-5'-[(2s,3ar,6as)-hexahydrofuro[2,3-b]furan-2-yl]-2'-(acetyloxy)-9'-hydroxy-4',5'-dimethyl-12'-oxaspiro[oxirane-2,10'-tricyclo[6.2.2.0¹,⁶]dodecan]-11'-yl 2-methylpropanoate

Description

Scupolin G belongs to the class of organic compounds known as furofurans. These are organic compounds containing a two furan rings fused to each other. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. It was first documented in 2015 (PMID: 25920210). Based on a literature review very few articles have been published on Scupolin G.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102200082D          

 35 40  0  0  1  0            999 V2000
    1.5571   -2.2738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2914    0.7529    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0717    0.2658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309102200082D          

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 17 18  1  0  0  0  0
 11 18  1  1  0  0  0
  9 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 23 30  1  0  0  0  0
  5 30  1  0  0  0  0
 19 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 33  1  1  0  0  0
 31 34  1  0  0  0  0
 21 34  1  0  0  0  0
 34 35  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0291158

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C(=O)O[C@H]1O[C@@H]2C[C@@H]3[C@@](C)([C@@H]4C[C@H]5CCO[C@H]5O4)[C@H](C)C[C@H](OC(C)=O)[C@]13[C@@]1(CO1)[C@@H]2O

> <INCHI_IDENTIFIER>
InChI=1S/C26H38O9/c1-12(2)21(29)35-23-26-17(10-16(33-23)20(28)25(26)11-31-25)24(5,13(3)8-19(26)32-14(4)27)18-9-15-6-7-30-22(15)34-18/h12-13,15-20,22-23,28H,6-11H2,1-5H3/t13-,15-,16-,17-,18+,19+,20-,22+,23-,24+,25-,26+/m1/s1

> <INCHI_KEY>
JRFTYJRNDOQDQK-PRCXJLFBSA-N

> <FORMULA>
C26H38O9

> <MOLECULAR_WEIGHT>
494.581

> <EXACT_MASS>
494.251582804

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
51.84099018182866

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1'R,2R,2'S,4'R,5'S,6'R,8'R,9'R,11'R)-5'-[(2S,3aR,6aS)-hexahydrofuro[2,3-b]furan-2-yl]-2'-(acetyloxy)-9'-hydroxy-4',5'-dimethyl-12'-oxaspiro[oxirane-2,10'-tricyclo[6.2.2.0^{1,6}]dodecane]-11'-yl 2-methylpropanoate

> <JCHEM_LOGP>
2.1513280446666645

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.94909597181886

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6958654219264293

> <JCHEM_POLAR_SURFACE_AREA>
113.05000000000003

> <JCHEM_REFRACTIVITY>
119.68849999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1'R,2R,2'S,4'R,5'S,6'R,8'R,9'R,11'R)-5'-[(2S,3aR,6aS)-hexahydrofuro[2,3-b]furan-2-yl]-2'-(acetyloxy)-9'-hydroxy-4',5'-dimethyl-12'-oxaspiro[oxirane-2,10'-tricyclo[6.2.2.0^{1,6}]dodecane]-11'-yl 2-methylpropanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       2.907  -4.244   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.840  -3.028   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       0.567  -3.980   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       2.069  -1.349   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.931   0.395   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.405   0.137   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.544   1.405   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.001   0.496   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.190   2.813   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.249   4.448   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.296   3.218   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.842   4.658   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.380   4.584   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.668   5.429   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.869   4.465   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -5.323   3.025   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -3.785   3.099   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -2.497   2.254   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.578   2.951   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.195   4.741   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.875   5.244   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.212   4.095   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       3.711   2.839   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.310   3.574   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.016   1.926   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.607   1.223   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.858   1.301   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.386   2.583   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.145  -0.378   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.842   1.721   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.570   2.165   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.077   1.845   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       5.047   0.701   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       4.916   3.853   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       6.034   5.078   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   30                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11   19                                             
CONECT   10    9                                                            
CONECT   11    9   12   18                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   13   18                                                  
CONECT   18   17   11                                                       
CONECT   19    9   20   30                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   34                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   30                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   23    5   19   31                                             
CONECT   31   30   32   33   34                                             
CONECT   32   31   33                                                       
CONECT   33   32   31                                                       
CONECT   34   31   21   35                                                  
CONECT   35   34                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₃₈O₉

Average Mass

494.5810 Da

Monoisotopic Mass

494.25158 Da

IUPAC Name

(1'R,2R,2'S,4'R,5'S,6'R,8'R,9'R,11'R)-5'-[(2S,3aR,6aS)-hexahydrofuro[2,3-b]furan-2-yl]-2'-(acetyloxy)-9'-hydroxy-4',5'-dimethyl-12'-oxaspiro[oxirane-2,10'-tricyclo[6.2.2.0^{1,6}]dodecane]-11'-yl 2-methylpropanoate

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(C)C(=O)O[C@H]1O[C@@H]2C[C@@H]3[C@@](C)([C@@H]4C[C@H]5CCO[C@H]5O4)[C@H](C)C[C@H](OC(C)=O)[C@]13[C@@]1(CO1)[C@@H]2O

InChI Identifier

InChI=1S/C26H38O9/c1-12(2)21(29)35-23-26-17(10-16(33-23)20(28)25(26)11-31-25)24(5,13(3)8-19(26)32-14(4)27)18-9-15-6-7-30-22(15)34-18/h12-13,15-20,22-23,28H,6-11H2,1-5H3/t13-,15-,16-,17-,18+,19+,20-,22+,23-,24+,25-,26+/m1/s1

InChI Key

JRFTYJRNDOQDQK-PRCXJLFBSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as furofurans. These are organic compounds containing a two furan rings fused to each other. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Furofurans

Sub Class

Not Available

Direct Parent

Furofurans

Alternative Parents

Substituents

Furofuran
Oxane
Monosaccharide
Dicarboxylic acid or derivatives
Tetrahydrofuran
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Oxacycle
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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	2.15	ChemAxon
pKa (Strongest Acidic)	12.95	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	113.05 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	119.69 m³·mol⁻¹	ChemAxon
Polarizability	51.84 Å³	ChemAxon
Number of Rings	6	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

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

102092519

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Bozov PI, Coll J: Neo-Clerodane diterpenoids from Scutellaria altissima. Nat Prod Commun. 2015 Jan;10(1):13-6. [PubMed:25920210 ]
LOTUS database [Link]

Showing NP-Card for (1'r,2r,2's,4'r,5's,6'r,8'r,9'r,11'r)-5'-[(2s,3ar,6as)-hexahydrofuro[2,3-b]furan-2-yl]-2'-(acetyloxy)-9'-hydroxy-4',5'-dimethyl-12'-oxaspiro[oxirane-2,10'-tricyclo[6.2.2.0¹,⁶]dodecan]-11'-yl 2-methylpropanoate (NP0291158)

MOL for NP0291158 ((1'r,2r,2's,4'r,5's,6'r,8'r,9'r,11'r)-5'-[(2s,3ar,6as)-hexahydrofuro[2,3-b]furan-2-yl]-2'-(acetyloxy)-9'-hydroxy-4',5'-dimethyl-12'-oxaspiro[oxirane-2,10'-tricyclo[6.2.2.0¹,⁶]dodecan]-11'-yl 2-methylpropanoate)

3D MOL for NP0291158 ((1'r,2r,2's,4'r,5's,6'r,8'r,9'r,11'r)-5'-[(2s,3ar,6as)-hexahydrofuro[2,3-b]furan-2-yl]-2'-(acetyloxy)-9'-hydroxy-4',5'-dimethyl-12'-oxaspiro[oxirane-2,10'-tricyclo[6.2.2.0¹,⁶]dodecan]-11'-yl 2-methylpropanoate)

3D SDF for NP0291158 ((1'r,2r,2's,4'r,5's,6'r,8'r,9'r,11'r)-5'-[(2s,3ar,6as)-hexahydrofuro[2,3-b]furan-2-yl]-2'-(acetyloxy)-9'-hydroxy-4',5'-dimethyl-12'-oxaspiro[oxirane-2,10'-tricyclo[6.2.2.0¹,⁶]dodecan]-11'-yl 2-methylpropanoate)

3D-SDF for NP0291158 ((1'r,2r,2's,4'r,5's,6'r,8'r,9'r,11'r)-5'-[(2s,3ar,6as)-hexahydrofuro[2,3-b]furan-2-yl]-2'-(acetyloxy)-9'-hydroxy-4',5'-dimethyl-12'-oxaspiro[oxirane-2,10'-tricyclo[6.2.2.0¹,⁶]dodecan]-11'-yl 2-methylpropanoate)

PDB for NP0291158 ((1'r,2r,2's,4'r,5's,6'r,8'r,9'r,11'r)-5'-[(2s,3ar,6as)-hexahydrofuro[2,3-b]furan-2-yl]-2'-(acetyloxy)-9'-hydroxy-4',5'-dimethyl-12'-oxaspiro[oxirane-2,10'-tricyclo[6.2.2.0¹,⁶]dodecan]-11'-yl 2-methylpropanoate)

3D PDB for NP0291158 ((1'r,2r,2's,4'r,5's,6'r,8'r,9'r,11'r)-5'-[(2s,3ar,6as)-hexahydrofuro[2,3-b]furan-2-yl]-2'-(acetyloxy)-9'-hydroxy-4',5'-dimethyl-12'-oxaspiro[oxirane-2,10'-tricyclo[6.2.2.0¹,⁶]dodecan]-11'-yl 2-methylpropanoate)

SMILES for NP0291158 ((1'r,2r,2's,4'r,5's,6'r,8'r,9'r,11'r)-5'-[(2s,3ar,6as)-hexahydrofuro[2,3-b]furan-2-yl]-2'-(acetyloxy)-9'-hydroxy-4',5'-dimethyl-12'-oxaspiro[oxirane-2,10'-tricyclo[6.2.2.0¹,⁶]dodecan]-11'-yl 2-methylpropanoate)

INCHI for NP0291158 ((1'r,2r,2's,4'r,5's,6'r,8'r,9'r,11'r)-5'-[(2s,3ar,6as)-hexahydrofuro[2,3-b]furan-2-yl]-2'-(acetyloxy)-9'-hydroxy-4',5'-dimethyl-12'-oxaspiro[oxirane-2,10'-tricyclo[6.2.2.0¹,⁶]dodecan]-11'-yl 2-methylpropanoate)

Structure for NP0291158 ((1'r,2r,2's,4'r,5's,6'r,8'r,9'r,11'r)-5'-[(2s,3ar,6as)-hexahydrofuro[2,3-b]furan-2-yl]-2'-(acetyloxy)-9'-hydroxy-4',5'-dimethyl-12'-oxaspiro[oxirane-2,10'-tricyclo[6.2.2.0¹,⁶]dodecan]-11'-yl 2-methylpropanoate)

3D Structure for NP0291158 ((1'r,2r,2's,4'r,5's,6'r,8'r,9'r,11'r)-5'-[(2s,3ar,6as)-hexahydrofuro[2,3-b]furan-2-yl]-2'-(acetyloxy)-9'-hydroxy-4',5'-dimethyl-12'-oxaspiro[oxirane-2,10'-tricyclo[6.2.2.0¹,⁶]dodecan]-11'-yl 2-methylpropanoate)