NP-MRD: Showing NP-Card for 10-hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]dodec-1(12)-en-2-one (NP0183917)

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Record Information

Version

2.0

Created at

2022-09-03 22:54:48 UTC

Updated at

2022-09-03 22:54:48 UTC

NP-MRD ID

NP0183917

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10-hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]dodec-1(12)-en-2-one

Description

10-Hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-2H-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]Dodec-1(12)-en-2-one belongs to the class of organic compounds known as 1-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 1-position. 10-hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]dodec-1(12)-en-2-one is found in Cystoseira mediterranea. 10-Hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-2H-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]Dodec-1(12)-en-2-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171514162D          

 32 35  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004171514162D          

 32 35  0  0  0  0            999 V2000
    0.1993    5.1877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0183917

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC(O)=CC2=C1OC(C)(CC1=C3CC(O)C(C)(C)OC1C(C)(C)CCCC3=O)CC2

> <INCHI_IDENTIFIER>
InChI=1S/C27H38O5/c1-16-12-18(28)13-17-9-11-27(6,31-23(16)17)15-20-19-14-22(30)26(4,5)32-24(20)25(2,3)10-7-8-21(19)29/h12-13,22,24,28,30H,7-11,14-15H2,1-6H3

> <INCHI_KEY>
ZTHCYPHYCZDHSI-UHFFFAOYSA-N

> <FORMULA>
C27H38O5

> <MOLECULAR_WEIGHT>
442.596

> <EXACT_MASS>
442.271924324

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
49.23885849999244

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
10-hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-2H-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]dodec-1(12)-en-2-one

> <ALOGPS_LOGP>
4.90

> <JCHEM_LOGP>
5.1393384709999985

> <ALOGPS_LOGS>
-4.89

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.92078887894948

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.140536812304681

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2708784594772427

> <JCHEM_POLAR_SURFACE_AREA>
75.99

> <JCHEM_REFRACTIVITY>
125.63679999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.76e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10-hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]dodec-1(12)-en-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       0.372   9.684   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.372   8.144   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.962   7.374   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.962   5.834   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -2.295   5.064   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       0.372   5.064   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.706   5.834   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.039   5.064   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.373   5.834   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.373   7.374   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.153   6.423   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.931   7.825   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.416   9.088   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.703   7.678   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.346   7.676   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.453   8.832   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      10.968   8.297   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       9.182  10.367   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.780  10.616   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.566  11.931   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       7.747  11.075   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.203  10.512   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.580  10.778   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.879  12.364   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.771  12.222   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.182   9.966   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.677   8.606   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.677   7.157   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.269   6.872   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       4.968   4.933   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       3.039   8.144   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       1.706   7.374   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   32                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   32                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   31                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   22                                                  
CONECT   14   13   15   29                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18   22                                                       
CONECT   22   21   13   23                                                  
CONECT   23   22   24   25   26                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   23   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   14   30                                                  
CONECT   30   29                                                            
CONECT   31   10   32                                                       
CONECT   32   31    2    7                                                  
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₈O₅

Average Mass

442.5960 Da

Monoisotopic Mass

442.27192 Da

IUPAC Name

10-hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-2H-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]dodec-1(12)-en-2-one

Traditional Name

10-hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]dodec-1(12)-en-2-one

CAS Registry Number

Not Available

SMILES

CC1=CC(O)=CC2=C1OC(C)(CC1=C3CC(O)C(C)(C)OC1C(C)(C)CCCC3=O)CC2

InChI Identifier

InChI=1S/C27H38O5/c1-16-12-18(28)13-17-9-11-27(6,31-23(16)17)15-20-19-14-22(30)26(4,5)32-24(20)25(2,3)10-7-8-21(19)29/h12-13,22,24,28,30H,7-11,14-15H2,1-6H3

InChI Key

ZTHCYPHYCZDHSI-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

Species Name	Source	Reference
Ericaria mediterranea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 1-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

1-benzopyrans

Alternative Parents

Substituents

1-benzopyran
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Ketone
Secondary alcohol
Dialkyl ether
Ether
Oxacycle
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
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	4.9	ALOGPS
logP	5.14	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	10.14	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.99 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	125.64 m³·mol⁻¹	ChemAxon
Polarizability	49.24 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

74051611

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 10-hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]dodec-1(12)-en-2-one (NP0183917)

MOL for NP0183917 (10-hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]dodec-1(12)-en-2-one)

3D MOL for NP0183917 (10-hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]dodec-1(12)-en-2-one)

3D SDF for NP0183917 (10-hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]dodec-1(12)-en-2-one)

3D-SDF for NP0183917 (10-hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]dodec-1(12)-en-2-one)

PDB for NP0183917 (10-hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]dodec-1(12)-en-2-one)

3D PDB for NP0183917 (10-hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]dodec-1(12)-en-2-one)

SMILES for NP0183917 (10-hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]dodec-1(12)-en-2-one)

INCHI for NP0183917 (10-hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]dodec-1(12)-en-2-one)

Structure for NP0183917 (10-hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]dodec-1(12)-en-2-one)

3D Structure for NP0183917 (10-hydroxy-12-[(6-hydroxy-2,8-dimethyl-3,4-dihydro-1-benzopyran-2-yl)methyl]-6,6,9,9-tetramethyl-8-oxabicyclo[5.4.1]dodec-1(12)-en-2-one)