NP-MRD: Showing NP-Card for (10r,11s,12r)-12-butoxy-6,6,10,11-tetramethyl-4-phenyl-11,12-dihydro-10h-1,5,9-trioxatriphenylen-2-one (NP0195537)

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Record Information

Version

2.0

Created at

2022-09-04 13:25:15 UTC

Updated at

2022-09-04 13:25:16 UTC

NP-MRD ID

NP0195537

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(10r,11s,12r)-12-butoxy-6,6,10,11-tetramethyl-4-phenyl-11,12-dihydro-10h-1,5,9-trioxatriphenylen-2-one

Description

4-Phenyl-6,6,10alpha,11alpha-tetramethyl-12beta-butoxy-11,12-dihydro-2H,6H,10H-benzo[1,2-b:3,4-B':5,6-B'']tripyran-2-one belongs to the class of organic compounds known as prenylated neoflavonoids. These are neoflavonoids that features a C5-isoprenoid substituent at any position of the A, B, or C ring. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone. (10r,11s,12r)-12-butoxy-6,6,10,11-tetramethyl-4-phenyl-11,12-dihydro-10h-1,5,9-trioxatriphenylen-2-one is found in Calophyllum inophyllum. Based on a literature review very few articles have been published on 4-Phenyl-6,6,10alpha,11alpha-tetramethyl-12beta-butoxy-11,12-dihydro-2H,6H,10H-benzo[1,2-b:3,4-B':5,6-B'']tripyran-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042215252D          

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> <DATABASE_ID>
NP0195537

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCO[C@@H]1[C@@H](C)[C@@H](C)OC2=C3C=CC(C)(C)OC3=C3C(OC(=O)C=C3C3=CC=CC=C3)=C12

> <INCHI_IDENTIFIER>
InChI=1S/C29H32O5/c1-6-7-15-31-25-17(2)18(3)32-26-20-13-14-29(4,5)34-27(20)23-21(19-11-9-8-10-12-19)16-22(30)33-28(23)24(25)26/h8-14,16-18,25H,6-7,15H2,1-5H3/t17-,18+,25+/m0/s1

> <INCHI_KEY>
ZHFUOBRTYSARSE-YYULODDRSA-N

> <FORMULA>
C29H32O5

> <MOLECULAR_WEIGHT>
460.57

> <EXACT_MASS>
460.22497413

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
52.12077751073713

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(10R,11S,12R)-12-butoxy-6,6,10,11-tetramethyl-4-phenyl-6,10,11,12-tetrahydro-2H-1,5,9-trioxatriphenylen-2-one

> <JCHEM_LOGP>
6.003286529999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.0473174555280185

> <JCHEM_POLAR_SURFACE_AREA>
53.99000000000001

> <JCHEM_REFRACTIVITY>
142.80040000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(10R,11S,12R)-12-butoxy-6,6,10,11-tetramethyl-4-phenyl-11,12-dihydro-10H-1,5,9-trioxatriphenylen-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.825  -6.875   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.055  -5.541   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.485  -5.541   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.255  -4.207   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       3.795  -4.207   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.565  -2.874   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.105  -2.874   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.875  -1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.415  -1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.185  -2.874   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.415  -4.207   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.185  -5.541   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.725  -5.541   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.495  -4.207   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.035  -4.207   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.805  -5.541   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.035  -6.875   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.495  -6.875   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.415  -6.875   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.875  -6.875   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.105  -8.208   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       6.105  -5.541   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.875  -4.207   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      10.725  -2.874   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      11.495  -1.540   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      12.674  -2.530   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.674  -0.550   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.725  -0.206   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.185  -0.206   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       6.105  -0.206   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       4.565  -0.206   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.795   1.127   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       3.795  -1.540   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.255  -1.540   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   33                                                  
CONECT    7    6    8   23                                                  
CONECT    8    7    9   30                                                  
CONECT    9    8   10   29                                                  
CONECT   10    9   11   24                                                  
CONECT   11   10   12   23                                                  
CONECT   12   11   13   19                                                  
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   13                                                       
CONECT   19   12   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22    7   11                                                  
CONECT   24   10   25                                                       
CONECT   25   24   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25   29                                                       
CONECT   29   28    9                                                       
CONECT   30    8   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31    6   34                                                  
CONECT   34   33                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   76    0
END

View in JSmol

Synonyms

Value	Source
4-Phenyl-6,6,10a,11a-tetramethyl-12b-butoxy-11,12-dihydro-2H,6H,10H-benzo[1,2-b:3,4-b':5,6-b'']tripyran-2-one	Generator
4-Phenyl-6,6,10α,11α-tetramethyl-12β-butoxy-11,12-dihydro-2H,6H,10H-benzo[1,2-b:3,4-b':5,6-b'']tripyran-2-one	Generator

Chemical Formula

C₂₉H₃₂O₅

Average Mass

460.5700 Da

Monoisotopic Mass

460.22497 Da

IUPAC Name

(10R,11S,12R)-12-butoxy-6,6,10,11-tetramethyl-4-phenyl-6,10,11,12-tetrahydro-2H-1,5,9-trioxatriphenylen-2-one

Traditional Name

(10R,11S,12R)-12-butoxy-6,6,10,11-tetramethyl-4-phenyl-11,12-dihydro-10H-1,5,9-trioxatriphenylen-2-one

CAS Registry Number

Not Available

SMILES

CCCCO[C@@H]1[C@@H](C)[C@@H](C)OC2=C3C=CC(C)(C)OC3=C3C(OC(=O)C=C3C3=CC=CC=C3)=C12

InChI Identifier

InChI=1S/C29H32O5/c1-6-7-15-31-25-17(2)18(3)32-26-20-13-14-29(4,5)34-27(20)23-21(19-11-9-8-10-12-19)16-22(30)33-28(23)24(25)26/h8-14,16-18,25H,6-7,15H2,1-5H3/t17-,18+,25+/m0/s1

InChI Key

ZHFUOBRTYSARSE-YYULODDRSA-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
Calophyllum inophyllum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as prenylated neoflavonoids. These are neoflavonoids that features a C5-isoprenoid substituent at any position of the A, B, or C ring. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Neoflavonoids

Sub Class

Prenylated neoflavonoids

Direct Parent

Prenylated neoflavonoids

Alternative Parents

Substituents

Prenylated neoflavonoid
Pyranoneoflavonoid
4-phenylcoumarin
Pyranocoumarin
Angular pyranocoumarin
Pyranochromene
2,2-dimethyl-1-benzopyran
Coumarin
Chromane
Benzopyran
1-benzopyran
Pyranone
Alkyl aryl ether
Monocyclic benzene moiety
Pyran
Benzenoid
Heteroaromatic compound
Lactone
Ether
Dialkyl ether
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen 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	6	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	53.99 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	142.8 m³·mol⁻¹	ChemAxon
Polarizability	52.12 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

28288013

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102052114

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (10r,11s,12r)-12-butoxy-6,6,10,11-tetramethyl-4-phenyl-11,12-dihydro-10h-1,5,9-trioxatriphenylen-2-one (NP0195537)

MOL for NP0195537 ((10r,11s,12r)-12-butoxy-6,6,10,11-tetramethyl-4-phenyl-11,12-dihydro-10h-1,5,9-trioxatriphenylen-2-one)

3D MOL for NP0195537 ((10r,11s,12r)-12-butoxy-6,6,10,11-tetramethyl-4-phenyl-11,12-dihydro-10h-1,5,9-trioxatriphenylen-2-one)

3D SDF for NP0195537 ((10r,11s,12r)-12-butoxy-6,6,10,11-tetramethyl-4-phenyl-11,12-dihydro-10h-1,5,9-trioxatriphenylen-2-one)

3D-SDF for NP0195537 ((10r,11s,12r)-12-butoxy-6,6,10,11-tetramethyl-4-phenyl-11,12-dihydro-10h-1,5,9-trioxatriphenylen-2-one)

PDB for NP0195537 ((10r,11s,12r)-12-butoxy-6,6,10,11-tetramethyl-4-phenyl-11,12-dihydro-10h-1,5,9-trioxatriphenylen-2-one)

3D PDB for NP0195537 ((10r,11s,12r)-12-butoxy-6,6,10,11-tetramethyl-4-phenyl-11,12-dihydro-10h-1,5,9-trioxatriphenylen-2-one)

SMILES for NP0195537 ((10r,11s,12r)-12-butoxy-6,6,10,11-tetramethyl-4-phenyl-11,12-dihydro-10h-1,5,9-trioxatriphenylen-2-one)

INCHI for NP0195537 ((10r,11s,12r)-12-butoxy-6,6,10,11-tetramethyl-4-phenyl-11,12-dihydro-10h-1,5,9-trioxatriphenylen-2-one)

Structure for NP0195537 ((10r,11s,12r)-12-butoxy-6,6,10,11-tetramethyl-4-phenyl-11,12-dihydro-10h-1,5,9-trioxatriphenylen-2-one)

3D Structure for NP0195537 ((10r,11s,12r)-12-butoxy-6,6,10,11-tetramethyl-4-phenyl-11,12-dihydro-10h-1,5,9-trioxatriphenylen-2-one)