NP-MRD: Showing NP-Card for Furanether B (NP0064528)

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Record Information

Version

2.0

Created at

2022-04-28 08:44:35 UTC

Updated at

2022-04-28 08:44:36 UTC

NP-MRD ID

NP0064528

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Furanether B

Description

Furanether B belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Furanether B is found in Lactarius scrobiculatus . Based on a literature review very few articles have been published on Furanether B.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 40  0  0  0  0  0  0  0  0999 V2000
   -3.0992    0.8309   -1.2175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2854   -0.0100   -0.2646 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2488   -0.8377    0.5744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2624   -0.8518   -0.9582 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0837   -0.2141   -0.7462 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1477    1.0526    0.0501 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5193    0.8769    0.6683 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8624    0.9248    1.1655 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8454   -0.4337    1.4187 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9893   -0.9979    0.1479 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6206   -2.4685    0.2047 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4341   -0.9252   -0.2954 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9818    0.4060    0.0003 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2053    1.0223   -0.2994 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1237    2.2041    0.2188 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9884    2.4337    0.8234 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2166    1.3005    0.7092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3477    1.7781   -0.6949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0682    0.3150   -1.4124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5559    1.0354   -2.1710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0774   -1.2493   -0.0131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6901   -1.6102    1.1541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7212   -0.1233    1.3086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3390   -1.8766   -0.5711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5395   -0.9014   -2.0511 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5295   -0.0169   -1.7356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0466    1.9641   -0.5409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0161    1.8463    0.8739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4525    0.3598    1.6694 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5033    1.5424    2.0106 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5345   -3.0282    0.5606 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4344   -2.8548   -0.8176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1813   -2.6548    0.9174 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5075   -1.0605   -1.4081 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0419   -1.6690    0.2459 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0058    0.5448   -0.8543 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6902    3.3465    1.3295 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  1  0
  2  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  5 10  1  0
 10 11  1  1
 10 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17  8  1  0
  8  9  1  0
  4  2  1  0
  9 10  1  0
  8  6  1  0
 17 13  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  7 28  1  0
  7 29  1  0
  6 27  1  6
  5 26  1  6
  4 24  1  0
  4 25  1  0
 11 31  1  0
 11 32  1  0
 11 33  1  0
 12 34  1  0
 12 35  1  0
 14 36  1  0
 16 37  1  0
  8 30  1  1
M  END


  Mrv1652304282210442D          

 17 20  0  0  1  0            999 V2000
    4.4553    1.5590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9409    2.2040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1159    2.2040    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6016    1.5590    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7851    0.7547    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5284    0.3967    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2717    0.7547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9800    0.3315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6013    0.8743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2770    1.6329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0963    1.2488    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0769    0.3315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4556    0.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7799    1.6329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8450    0.3195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6648    1.1092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7580    2.9473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  1 10  2  0  0  0  0
  6 11  1  6  0  0  0
  3 11  1  0  0  0  0
  5 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  4 14  1  6  0  0  0
 13 15  1  0  0  0  0
 13 16  1  0  0  0  0
  3 17  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0064528

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)C[C@@H]2[C@H](C1)[C@@]1(C)CC3=COC=C3[C@@H]2O1

> <INCHI_IDENTIFIER>
InChI=1S/C15H20O2/c1-14(2)5-10-12(6-14)15(3)4-9-7-16-8-11(9)13(10)17-15/h7-8,10,12-13H,4-6H2,1-3H3/t10-,12+,13-,15-/m1/s1

> <INCHI_KEY>
ILACEZQKVDMRMW-CQROYNQRSA-N

> <FORMULA>
C15H20O2

> <MOLECULAR_WEIGHT>
232.323

> <EXACT_MASS>
232.146329884

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
26.3158395761916

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,8R,9S,13R)-8,11,11-trimethyl-4,14-dioxatetracyclo[6.5.1.0^{2,6}.0^{9,13}]tetradeca-2,5-diene

> <ALOGPS_LOGP>
3.44

> <JCHEM_LOGP>
3.132919485333333

> <ALOGPS_LOGS>
-4.00

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8077765569794932

> <JCHEM_POLAR_SURFACE_AREA>
22.37

> <JCHEM_REFRACTIVITY>
65.7334

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.31e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,8R,9S,13R)-8,11,11-trimethyl-4,14-dioxatetracyclo[6.5.1.0^{2,6}.0^{9,13}]tetradeca-2,5-diene

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       8.317   2.910   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.356   4.114   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.816   4.114   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.856   2.910   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.199   1.409   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.586   0.741   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.974   1.409   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.296   0.619   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      10.456   1.632   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       9.850   3.048   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.780   2.331   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.877   0.619   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.717   1.632   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.322   3.048   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.577   0.596   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.241   2.071   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.148   5.502   0.000  0.00  0.00           C+0
CONECT    1    2    7   10                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   11   17                                             
CONECT    4    3    5   14                                                  
CONECT    5    4    6   12                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    1    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    1                                                       
CONECT   11    6    3                                                       
CONECT   12    5   13                                                       
CONECT   13   12   14   15   16                                             
CONECT   14   13    4                                                       
CONECT   15   13                                                            
CONECT   16   13                                                            
CONECT   17    3                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   40    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₀O₂

Average Mass

232.3230 Da

Monoisotopic Mass

232.14633 Da

IUPAC Name

(1R,8R,9S,13R)-8,11,11-trimethyl-4,14-dioxatetracyclo[6.5.1.0^{2,6}.0^{9,13}]tetradeca-2,5-diene

Traditional Name

(1R,8R,9S,13R)-8,11,11-trimethyl-4,14-dioxatetracyclo[6.5.1.0^{2,6}.0^{9,13}]tetradeca-2,5-diene

CAS Registry Number

Not Available

SMILES

CC1(C)C[C@@H]2[C@H](C1)[C@@]1(C)CC3=COC=C3[C@@H]2O1

InChI Identifier

InChI=1S/C15H20O2/c1-14(2)5-10-12(6-14)15(3)4-9-7-16-8-11(9)13(10)17-15/h7-8,10,12-13H,4-6H2,1-3H3/t10-,12+,13-,15-/m1/s1

InChI Key

ILACEZQKVDMRMW-CQROYNQRSA-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
Lactarius scrobiculatus	Fungi	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Lactarane sesquiterpenoid
Cycloheptafuran
Furopyran
Pyran
Furan
Oxolane
Heteroaromatic compound
Ether
Dialkyl ether
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
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	3.44	ALOGPS
logP	3.13	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	22.37 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	65.73 m³·mol⁻¹	ChemAxon
Polarizability	26.32 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

C00021528

Chemspider ID

9945024

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11770341

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Furanether B (NP0064528)

MOL for NP0064528 (Furanether B)

3D MOL for NP0064528 (Furanether B)

3D SDF for NP0064528 (Furanether B)

3D-SDF for NP0064528 (Furanether B)

PDB for NP0064528 (Furanether B)

3D PDB for NP0064528 (Furanether B)

SMILES for NP0064528 (Furanether B)

INCHI for NP0064528 (Furanether B)

Structure for NP0064528 (Furanether B)

3D Structure for NP0064528 (Furanether B)