NP-MRD: Showing NP-Card for 4-{1-hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]ethyl}-5h-furan-2-one (NP0153501)

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Record Information

Version

2.0

Created at

2022-09-02 10:10:35 UTC

Updated at

2022-09-02 10:10:35 UTC

NP-MRD ID

NP0153501

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-{1-hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]ethyl}-5h-furan-2-one

Description

4-{1-Hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-5-yl]ethyl}-2,5-dihydrofuran-2-one belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom. 4-{1-hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]ethyl}-5h-furan-2-one is found in Teucrium massiliense. 4-{1-Hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-5-yl]ethyl}-2,5-dihydrofuran-2-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004241504212D          

 26 29  0  0  0  0            999 V2000
    5.3861    0.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5801   -0.0621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0246    0.5479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2186    0.3718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6632    0.9818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9681   -0.4142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4127    0.1957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6571    0.5270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5236   -1.0242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2731   -1.8103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4671   -1.9863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9116   -1.3764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1622   -0.5903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3761   -0.3398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9861    0.2157    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3296   -0.8481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1064   -1.1259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5337   -1.6475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3280   -1.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9182   -1.2940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5321   -2.6697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2988   -2.9745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2459   -3.7978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8809   -4.3245    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4465   -4.0019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0054   -3.3047    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
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 13 15  1  0  0  0  0
  9 16  1  0  0  0  0
  2 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 21 26  1  0  0  0  0
M  END


  Mrv1533004241504212D          

 26 29  0  0  0  0            999 V2000
    5.3861    0.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5801   -0.0621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0246    0.5479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2186    0.3718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6632    0.9818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9681   -0.4142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4127    0.1957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6571    0.5270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5236   -1.0242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2731   -1.8103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4671   -1.9863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9116   -1.3764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1622   -0.5903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3761   -0.3398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9861    0.2157    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3296   -0.8481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1064   -1.1259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5337   -1.6475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3280   -1.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9182   -1.2940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5321   -2.6697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2988   -2.9745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2459   -3.7978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8809   -4.3245    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4465   -4.0019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0054   -3.3047    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
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 13 15  1  0  0  0  0
  9 16  1  0  0  0  0
  2 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 21 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0153501

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC(O)C2(CO)C(CCCC22CO2)C1(C)CC(O)C1=CC(=O)OC1

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O6/c1-12-6-16(23)20(10-21)15(4-3-5-19(20)11-26-19)18(12,2)8-14(22)13-7-17(24)25-9-13/h7,12,14-16,21-23H,3-6,8-11H2,1-2H3

> <INCHI_KEY>
CYUUYGRZAYHVCT-UHFFFAOYSA-N

> <FORMULA>
C20H30O6

> <MOLECULAR_WEIGHT>
366.454

> <EXACT_MASS>
366.204238686

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
38.853135699838965

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-{1-hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-5-yl]ethyl}-2,5-dihydrofuran-2-one

> <ALOGPS_LOGP>
0.50

> <JCHEM_LOGP>
0.5794109166666663

> <ALOGPS_LOGS>
-2.74

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.293608909446245

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.766996782841458

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8296358912397723

> <JCHEM_POLAR_SURFACE_AREA>
99.52

> <JCHEM_REFRACTIVITY>
94.87059999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.74e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-{1-hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2H-spiro[naphthalene-1,2'-oxirane]-5-yl]ethyl}-5H-furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      10.054   0.213   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.550  -0.116   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.513   1.023   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.008   0.694   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       4.971   1.833   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       5.541  -0.773   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.504   0.365   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       3.093   0.984   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       6.577  -1.912   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.110  -3.379   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.605  -3.708   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.568  -2.569   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.036  -1.102   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.569  -0.634   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.707   0.403   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.082  -1.583   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.532  -2.102   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.463  -3.075   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.946  -3.491   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      11.047  -2.415   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      10.327  -4.984   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.758  -5.552   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.659  -7.089   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      12.844  -8.072   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      10.167  -7.470   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       9.343  -6.169   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   16                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    9   13                                             
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    6   10   16                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    6   14   15                                             
CONECT   14   13   15                                                       
CONECT   15   14   13                                                       
CONECT   16    9    2   17   18                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   21                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₀O₆

Average Mass

366.4540 Da

Monoisotopic Mass

366.20424 Da

IUPAC Name

4-{1-hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-5-yl]ethyl}-2,5-dihydrofuran-2-one

Traditional Name

4-{1-hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2H-spiro[naphthalene-1,2'-oxirane]-5-yl]ethyl}-5H-furan-2-one

CAS Registry Number

Not Available

SMILES

CC1CC(O)C2(CO)C(CCCC22CO2)C1(C)CC(O)C1=CC(=O)OC1

InChI Identifier

InChI=1S/C20H30O6/c1-12-6-16(23)20(10-21)15(4-3-5-19(20)11-26-19)18(12,2)8-14(22)13-7-17(24)25-9-13/h7,12,14-16,21-23H,3-6,8-11H2,1-2H3

InChI Key

CYUUYGRZAYHVCT-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Teucrium massiliense	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dihydrofurans

Sub Class

Furanones

Direct Parent

Butenolides

Alternative Parents

Substituents

2-furanone
Cyclic alcohol
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Lactone
Secondary alcohol
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Primary alcohol
Organooxygen compound
Organic oxide
Alcohol
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
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	0.5	ALOGPS
logP	0.58	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	5.77	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	99.52 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	94.87 m³·mol⁻¹	ChemAxon
Polarizability	38.85 Å³	ChemAxon
Number of Rings	4	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-{1-hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]ethyl}-5h-furan-2-one (NP0153501)

MOL for NP0153501 (4-{1-hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]ethyl}-5h-furan-2-one)

3D MOL for NP0153501 (4-{1-hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]ethyl}-5h-furan-2-one)

3D SDF for NP0153501 (4-{1-hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]ethyl}-5h-furan-2-one)

3D-SDF for NP0153501 (4-{1-hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]ethyl}-5h-furan-2-one)

PDB for NP0153501 (4-{1-hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]ethyl}-5h-furan-2-one)

3D PDB for NP0153501 (4-{1-hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]ethyl}-5h-furan-2-one)

SMILES for NP0153501 (4-{1-hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]ethyl}-5h-furan-2-one)

INCHI for NP0153501 (4-{1-hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]ethyl}-5h-furan-2-one)

Structure for NP0153501 (4-{1-hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]ethyl}-5h-furan-2-one)

3D Structure for NP0153501 (4-{1-hydroxy-2-[8-hydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]ethyl}-5h-furan-2-one)