NP-MRD: Showing NP-Card for 12-(2,4-dimethyloxolan-2-yl)-4,7,15,18-tetramethyl-3,5,14,16-tetraoxapentacyclo[11.7.0.0²,¹⁰.0⁴,⁸.0¹⁵,¹⁹]icosa-1(13),2(10),11-trien-11-ol (NP0274299)

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Record Information

Version

2.0

Created at

2022-09-08 21:38:32 UTC

Updated at

2022-09-08 21:38:33 UTC

NP-MRD ID

NP0274299

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12-(2,4-dimethyloxolan-2-yl)-4,7,15,18-tetramethyl-3,5,14,16-tetraoxapentacyclo[11.7.0.0²,¹⁰.0⁴,⁸.0¹⁵,¹⁹]icosa-1(13),2(10),11-trien-11-ol

Description

12-(2,4-Dimethyloxolan-2-yl)-4,7,15,18-tetramethyl-3,5,14,16-tetraoxapentacyclo[11.7.0.0²,¹⁰.0⁴,⁸.0¹⁵,¹⁹]Icosa-1,10,12-trien-11-ol belongs to the class of organic compounds known as pyranochromenes. These are organic heterocyclic compounds containing a pyran ring fused to a chromene (1-benzopyran) moiety. Based on a literature review very few articles have been published on 12-(2,4-dimethyloxolan-2-yl)-4,7,15,18-tetramethyl-3,5,14,16-tetraoxapentacyclo[11.7.0.0²,¹⁰.0⁴,⁸.0¹⁵,¹⁹]Icosa-1,10,12-trien-11-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082223382D          

 32 37  0  0  0  0            999 V2000
    3.2480    1.3197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8611    0.7676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6681    0.9392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0806    0.2247    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5285   -0.3884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1960   -0.8733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1160   -1.1029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2910   -1.1029    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


  Mrv1652309082223382D          

 32 37  0  0  0  0            999 V2000
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M  END
> <DATABASE_ID>
NP0274299

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1COC(C)(C1)C1=C(O)C2=C(OC3(C)OCC(C)C3C2)C2=C1OC1(C)OCC(C)C1C2

> <INCHI_IDENTIFIER>
InChI=1S/C26H36O6/c1-13-9-24(4,28-10-13)20-21(27)16-7-18-14(2)11-29-25(18,5)31-22(16)17-8-19-15(3)12-30-26(19,6)32-23(17)20/h13-15,18-19,27H,7-12H2,1-6H3

> <INCHI_KEY>
ZNYRREFJIKRTIT-UHFFFAOYSA-N

> <FORMULA>
C26H36O6

> <MOLECULAR_WEIGHT>
444.568

> <EXACT_MASS>
444.251188879

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
49.89949074417315

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
12-(2,4-dimethyloxolan-2-yl)-4,7,15,18-tetramethyl-3,5,14,16-tetraoxapentacyclo[11.7.0.0^{2,10}.0^{4,8}.0^{15,19}]icosa-1(13),2(10),11-trien-11-ol

> <JCHEM_LOGP>
4.648197722

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.57349150262857

> <JCHEM_PKA_STRONGEST_BASIC>
-3.760852989355064

> <JCHEM_POLAR_SURFACE_AREA>
66.38000000000001

> <JCHEM_REFRACTIVITY>
120.81400000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
12-(2,4-dimethyloxolan-2-yl)-4,7,15,18-tetramethyl-3,5,14,16-tetraoxapentacyclo[11.7.0.0^{2,10}.0^{4,8}.0^{15,19}]icosa-1(13),2(10),11-trien-11-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       6.063   2.463   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.207   1.433   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.714   1.753   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       9.484   0.419   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       8.453  -0.725   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.699  -1.630   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.683  -2.059   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.143  -2.059   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.373  -0.725   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       5.373  -3.392   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.143  -4.726   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.683  -4.726   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.453  -3.392   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       9.993  -3.392   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      10.763  -4.726   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.668  -3.480   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      12.270  -5.046   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      12.431  -6.578   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.024  -7.204   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.704  -8.711   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.993  -6.060   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.453  -6.060   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.373  -6.060   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.833  -6.060   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.460  -7.467   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.803  -7.204   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       1.396  -6.578   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.557  -5.046   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.412  -4.016   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.063  -4.726   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.833  -3.392   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.046  -0.099   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   32                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7   32                                             
CONECT    6    5                                                            
CONECT    7    5    8   13                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   31                                                  
CONECT   11   10   12   23                                                  
CONECT   12   11   13   22                                                  
CONECT   13   12    7   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17   21                                             
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   15   22                                                  
CONECT   22   21   12                                                       
CONECT   23   11   24                                                       
CONECT   24   23   25   26   30                                             
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   24   31                                                  
CONECT   31   30   10                                                       
CONECT   32    5    2                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₃₆O₆

Average Mass

444.5680 Da

Monoisotopic Mass

444.25119 Da

IUPAC Name

12-(2,4-dimethyloxolan-2-yl)-4,7,15,18-tetramethyl-3,5,14,16-tetraoxapentacyclo[11.7.0.0^{2,10}.0^{4,8}.0^{15,19}]icosa-1(13),2(10),11-trien-11-ol

Traditional Name

12-(2,4-dimethyloxolan-2-yl)-4,7,15,18-tetramethyl-3,5,14,16-tetraoxapentacyclo[11.7.0.0^{2,10}.0^{4,8}.0^{15,19}]icosa-1(13),2(10),11-trien-11-ol

CAS Registry Number

Not Available

SMILES

CC1COC(C)(C1)C1=C(O)C2=C(OC3(C)OCC(C)C3C2)C2=C1OC1(C)OCC(C)C1C2

InChI Identifier

InChI=1S/C26H36O6/c1-13-9-24(4,28-10-13)20-21(27)16-7-18-14(2)11-29-25(18,5)31-22(16)17-8-19-15(3)12-30-26(19,6)32-23(17)20/h13-15,18-19,27H,7-12H2,1-6H3

InChI Key

ZNYRREFJIKRTIT-UHFFFAOYSA-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 pyranochromenes. These are organic heterocyclic compounds containing a pyran ring fused to a chromene (1-benzopyran) moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Pyranochromenes

Alternative Parents

Substituents

Pyranochromene
Furopyran
Ketal
Benzenoid
Pyran
Tetrahydrofuran
Furan
Oxacycle
Ether
Dialkyl ether
Acetal
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
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	4.65	ChemAxon
pKa (Strongest Acidic)	9.57	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	66.38 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	120.81 m³·mol⁻¹	ChemAxon
Polarizability	49.9 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

73837203

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 12-(2,4-dimethyloxolan-2-yl)-4,7,15,18-tetramethyl-3,5,14,16-tetraoxapentacyclo[11.7.0.0²,¹⁰.0⁴,⁸.0¹⁵,¹⁹]icosa-1(13),2(10),11-trien-11-ol (NP0274299)

MOL for NP0274299 (12-(2,4-dimethyloxolan-2-yl)-4,7,15,18-tetramethyl-3,5,14,16-tetraoxapentacyclo[11.7.0.0²,¹⁰.0⁴,⁸.0¹⁵,¹⁹]icosa-1(13),2(10),11-trien-11-ol)

3D MOL for NP0274299 (12-(2,4-dimethyloxolan-2-yl)-4,7,15,18-tetramethyl-3,5,14,16-tetraoxapentacyclo[11.7.0.0²,¹⁰.0⁴,⁸.0¹⁵,¹⁹]icosa-1(13),2(10),11-trien-11-ol)

3D SDF for NP0274299 (12-(2,4-dimethyloxolan-2-yl)-4,7,15,18-tetramethyl-3,5,14,16-tetraoxapentacyclo[11.7.0.0²,¹⁰.0⁴,⁸.0¹⁵,¹⁹]icosa-1(13),2(10),11-trien-11-ol)

3D-SDF for NP0274299 (12-(2,4-dimethyloxolan-2-yl)-4,7,15,18-tetramethyl-3,5,14,16-tetraoxapentacyclo[11.7.0.0²,¹⁰.0⁴,⁸.0¹⁵,¹⁹]icosa-1(13),2(10),11-trien-11-ol)

PDB for NP0274299 (12-(2,4-dimethyloxolan-2-yl)-4,7,15,18-tetramethyl-3,5,14,16-tetraoxapentacyclo[11.7.0.0²,¹⁰.0⁴,⁸.0¹⁵,¹⁹]icosa-1(13),2(10),11-trien-11-ol)

3D PDB for NP0274299 (12-(2,4-dimethyloxolan-2-yl)-4,7,15,18-tetramethyl-3,5,14,16-tetraoxapentacyclo[11.7.0.0²,¹⁰.0⁴,⁸.0¹⁵,¹⁹]icosa-1(13),2(10),11-trien-11-ol)

SMILES for NP0274299 (12-(2,4-dimethyloxolan-2-yl)-4,7,15,18-tetramethyl-3,5,14,16-tetraoxapentacyclo[11.7.0.0²,¹⁰.0⁴,⁸.0¹⁵,¹⁹]icosa-1(13),2(10),11-trien-11-ol)

INCHI for NP0274299 (12-(2,4-dimethyloxolan-2-yl)-4,7,15,18-tetramethyl-3,5,14,16-tetraoxapentacyclo[11.7.0.0²,¹⁰.0⁴,⁸.0¹⁵,¹⁹]icosa-1(13),2(10),11-trien-11-ol)

Structure for NP0274299 (12-(2,4-dimethyloxolan-2-yl)-4,7,15,18-tetramethyl-3,5,14,16-tetraoxapentacyclo[11.7.0.0²,¹⁰.0⁴,⁸.0¹⁵,¹⁹]icosa-1(13),2(10),11-trien-11-ol)

3D Structure for NP0274299 (12-(2,4-dimethyloxolan-2-yl)-4,7,15,18-tetramethyl-3,5,14,16-tetraoxapentacyclo[11.7.0.0²,¹⁰.0⁴,⁸.0¹⁵,¹⁹]icosa-1(13),2(10),11-trien-11-ol)