NP-MRD: Showing NP-Card for 12-hydroxy-5a,8,8,11a-tetramethyl-1-oxo-3-phenyl-6,7,7a,9,10,11,11b,12-octahydro-2,5-dioxatetraphen-9-yl acetate (NP0228266)

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Record Information

Version

2.0

Created at

2022-09-06 07:51:11 UTC

Updated at

2022-09-06 07:51:11 UTC

NP-MRD ID

NP0228266

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12-hydroxy-5a,8,8,11a-tetramethyl-1-oxo-3-phenyl-6,7,7a,9,10,11,11b,12-octahydro-2,5-dioxatetraphen-9-yl acetate

Description

12-Hydroxy-5a,8,8,11a-tetramethyl-1-oxo-3-phenyl-1,5a,6,7,7a,8,9,10,11,11a,11b,12-dodecahydro-2,5-dioxatetraphen-9-yl acetate belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. 12-hydroxy-5a,8,8,11a-tetramethyl-1-oxo-3-phenyl-6,7,7a,9,10,11,11b,12-octahydro-2,5-dioxatetraphen-9-yl acetate is found in Penicillium concentricum. Based on a literature review very few articles have been published on 12-hydroxy-5a,8,8,11a-tetramethyl-1-oxo-3-phenyl-1,5a,6,7,7a,8,9,10,11,11a,11b,12-dodecahydro-2,5-dioxatetraphen-9-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062209512D          

 34 38  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309062209512D          

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 30 31  1  0  0  0  0
  8 31  1  0  0  0  0
 31 32  1  0  0  0  0
  5 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0228266

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1CCC2(C)C(CCC3(C)OC4=C(C(O)C23)C(=O)OC(=C4)C2=CC=CC=C2)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C28H34O6/c1-16(29)32-21-12-13-27(4)20(26(21,2)3)11-14-28(5)24(27)23(30)22-19(34-28)15-18(33-25(22)31)17-9-7-6-8-10-17/h6-10,15,20-21,23-24,30H,11-14H2,1-5H3

> <INCHI_KEY>
AVKUBALSSZDALG-UHFFFAOYSA-N

> <FORMULA>
C28H34O6

> <MOLECULAR_WEIGHT>
466.574

> <EXACT_MASS>
466.235538815

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
51.8771096000925

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
12-hydroxy-5a,8,8,11a-tetramethyl-1-oxo-3-phenyl-1,5a,6,7,7a,8,9,10,11,11a,11b,12-dodecahydro-2,5-dioxatetraphen-9-yl acetate

> <JCHEM_LOGP>
3.5974397759999985

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.844016971353557

> <JCHEM_PKA_STRONGEST_BASIC>
-3.304426976729954

> <JCHEM_POLAR_SURFACE_AREA>
82.06000000000002

> <JCHEM_REFRACTIVITY>
128.5795

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
12-hydroxy-5a,8,8,11a-tetramethyl-1-oxo-3-phenyl-6,7,7a,9,10,11,11b,12-octahydro-2,5-dioxatetraphen-9-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -5.545  -5.869   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.033  -5.578   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -3.529  -4.123   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -3.024  -6.742   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -1.512  -6.451   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.504  -7.615   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.008  -7.324   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.512  -5.869   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.520  -7.033   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.024  -5.578   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.033  -6.742   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.529  -8.197   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.545  -6.451   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.049  -4.996   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.561  -4.705   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.569  -5.869   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.082  -5.578   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.586  -4.123   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.098  -3.832   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      13.106  -4.996   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.602  -6.451   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.090  -6.742   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.065  -7.324   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.553  -7.615   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       6.049  -9.070   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       5.041  -3.832   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.529  -4.123   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.033  -2.668   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.520  -2.959   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.008  -3.250   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.504  -4.705   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -1.008  -4.996   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -1.352  -3.495   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -2.445  -4.441   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   32                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10   31                                             
CONECT    9    8                                                            
CONECT   10    8   11   27                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   24                                                  
CONECT   14   13   15   26                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   23                                                  
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17                                                       
CONECT   23   16   24                                                       
CONECT   24   23   13   25                                                  
CONECT   25   24                                                            
CONECT   26   14   27                                                       
CONECT   27   26   10   28   29                                             
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30    8   32                                                  
CONECT   32   31    5   33   34                                             
CONECT   33   32                                                            
CONECT   34   32                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   76    0
END

View in JSmol

Synonyms

Value	Source
12-Hydroxy-5a,8,8,11a-tetramethyl-1-oxo-3-phenyl-1,5a,6,7,7a,8,9,10,11,11a,11b,12-dodecahydro-2,5-dioxatetraphen-9-yl acetic acid	Generator

Chemical Formula

C₂₈H₃₄O₆

Average Mass

466.5740 Da

Monoisotopic Mass

466.23554 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)OC1CCC2(C)C(CCC3(C)OC4=C(C(O)C23)C(=O)OC(=C4)C2=CC=CC=C2)C1(C)C

InChI Identifier

InChI=1S/C28H34O6/c1-16(29)32-21-12-13-27(4)20(26(21,2)3)11-14-28(5)24(27)23(30)22-19(34-28)15-18(33-25(22)31)17-9-7-6-8-10-17/h6-10,15,20-21,23-24,30H,11-14H2,1-5H3

InChI Key

AVKUBALSSZDALG-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
Penicillium concentricum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Naphthalene
Pyranone
Alkyl aryl ether
Benzenoid
Pyran
Monocyclic benzene moiety
Heteroaromatic compound
Vinylogous ester
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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

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

162896787

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 12-hydroxy-5a,8,8,11a-tetramethyl-1-oxo-3-phenyl-6,7,7a,9,10,11,11b,12-octahydro-2,5-dioxatetraphen-9-yl acetate (NP0228266)

MOL for NP0228266 (12-hydroxy-5a,8,8,11a-tetramethyl-1-oxo-3-phenyl-6,7,7a,9,10,11,11b,12-octahydro-2,5-dioxatetraphen-9-yl acetate)

3D MOL for NP0228266 (12-hydroxy-5a,8,8,11a-tetramethyl-1-oxo-3-phenyl-6,7,7a,9,10,11,11b,12-octahydro-2,5-dioxatetraphen-9-yl acetate)

3D SDF for NP0228266 (12-hydroxy-5a,8,8,11a-tetramethyl-1-oxo-3-phenyl-6,7,7a,9,10,11,11b,12-octahydro-2,5-dioxatetraphen-9-yl acetate)

3D-SDF for NP0228266 (12-hydroxy-5a,8,8,11a-tetramethyl-1-oxo-3-phenyl-6,7,7a,9,10,11,11b,12-octahydro-2,5-dioxatetraphen-9-yl acetate)

PDB for NP0228266 (12-hydroxy-5a,8,8,11a-tetramethyl-1-oxo-3-phenyl-6,7,7a,9,10,11,11b,12-octahydro-2,5-dioxatetraphen-9-yl acetate)

3D PDB for NP0228266 (12-hydroxy-5a,8,8,11a-tetramethyl-1-oxo-3-phenyl-6,7,7a,9,10,11,11b,12-octahydro-2,5-dioxatetraphen-9-yl acetate)

SMILES for NP0228266 (12-hydroxy-5a,8,8,11a-tetramethyl-1-oxo-3-phenyl-6,7,7a,9,10,11,11b,12-octahydro-2,5-dioxatetraphen-9-yl acetate)

INCHI for NP0228266 (12-hydroxy-5a,8,8,11a-tetramethyl-1-oxo-3-phenyl-6,7,7a,9,10,11,11b,12-octahydro-2,5-dioxatetraphen-9-yl acetate)

Structure for NP0228266 (12-hydroxy-5a,8,8,11a-tetramethyl-1-oxo-3-phenyl-6,7,7a,9,10,11,11b,12-octahydro-2,5-dioxatetraphen-9-yl acetate)

3D Structure for NP0228266 (12-hydroxy-5a,8,8,11a-tetramethyl-1-oxo-3-phenyl-6,7,7a,9,10,11,11b,12-octahydro-2,5-dioxatetraphen-9-yl acetate)