NP-MRD: Showing NP-Card for 4-hydroxy-6-[(1e,7e,9e,11e)-14-hydroxy-9,13,15-trimethyl-17-phenylheptadeca-1,7,9,11-tetraen-1-yl]-3,5-dimethylpyran-2-one (NP0273659)

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Record Information

Version

2.0

Created at

2022-09-08 20:46:32 UTC

Updated at

2022-09-08 20:46:32 UTC

NP-MRD ID

NP0273659

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-hydroxy-6-[(1e,7e,9e,11e)-14-hydroxy-9,13,15-trimethyl-17-phenylheptadeca-1,7,9,11-tetraen-1-yl]-3,5-dimethylpyran-2-one

Description

Hyapyrone B belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms. 4-hydroxy-6-[(1e,7e,9e,11e)-14-hydroxy-9,13,15-trimethyl-17-phenylheptadeca-1,7,9,11-tetraen-1-yl]-3,5-dimethylpyran-2-one is found in Hyalangium minutum. 4-hydroxy-6-[(1e,7e,9e,11e)-14-hydroxy-9,13,15-trimethyl-17-phenylheptadeca-1,7,9,11-tetraen-1-yl]-3,5-dimethylpyran-2-one was first documented in 2014 (PMID: 24848583). Based on a literature review very few articles have been published on Hyapyrone B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082222462D          

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M  END

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M  END


  Mrv1652309082222462D          

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    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    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  2  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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  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
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 11 19  2  0  0  0  0
 19 20  1  0  0  0  0
  2 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 32 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0273659

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CCC1=CC=CC=C1)C(O)C(C)\C=C\C=C(/C)\C=C\CCCC\C=C\C1=C(C)C(O)=C(C)C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C33H44O4/c1-24(17-15-18-25(2)31(34)26(3)22-23-29-19-12-10-13-20-29)16-11-8-6-7-9-14-21-30-27(4)32(35)28(5)33(36)37-30/h10-21,25-26,31,34-35H,6-9,22-23H2,1-5H3/b16-11+,18-15+,21-14+,24-17+

> <INCHI_KEY>
GPQHHXQFVXQFFW-QCSLTFAHSA-N

> <FORMULA>
C33H44O4

> <MOLECULAR_WEIGHT>
504.711

> <EXACT_MASS>
504.323959897

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
62.03166211461704

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-hydroxy-6-[(1E,7E,9E,11E)-14-hydroxy-9,13,15-trimethyl-17-phenylheptadeca-1,7,9,11-tetraen-1-yl]-3,5-dimethyl-2H-pyran-2-one

> <JCHEM_LOGP>
8.252227649000002

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.654297073088166

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.641596980766099

> <JCHEM_PKA_STRONGEST_BASIC>
-2.950010478679821

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
159.88809999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
4-hydroxy-6-[(1E,7E,9E,11E)-14-hydroxy-9,13,15-trimethyl-17-phenylheptadeca-1,7,9,11-tetraen-1-yl]-3,5-dimethylpyran-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -8.002  -7.700   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -9.336  -6.930   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -12.003 -10.010   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0     -12.003 -11.550   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0     -13.337 -12.320   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0     -13.337 -13.860   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0     -14.670 -11.550   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -16.004 -12.320   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -14.670 -10.010   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0     -16.004  -9.240   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0     -13.337  -9.240   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -13.337  -7.700   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      13.337  -7.700   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      13.337  -9.240   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      12.003 -10.010   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   19                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   11   20                                                  
CONECT   20   19                                                            
CONECT   21    2   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   37                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   32                                                       
MASTER        0    0    0    0    0    0    0    0   37    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₃H₄₄O₄

Average Mass

504.7110 Da

Monoisotopic Mass

504.32396 Da

IUPAC Name

4-hydroxy-6-[(1E,7E,9E,11E)-14-hydroxy-9,13,15-trimethyl-17-phenylheptadeca-1,7,9,11-tetraen-1-yl]-3,5-dimethyl-2H-pyran-2-one

Traditional Name

4-hydroxy-6-[(1E,7E,9E,11E)-14-hydroxy-9,13,15-trimethyl-17-phenylheptadeca-1,7,9,11-tetraen-1-yl]-3,5-dimethylpyran-2-one

CAS Registry Number

Not Available

SMILES

CC(CCC1=CC=CC=C1)C(O)C(C)\C=C\C=C(/C)\C=C\CCCC\C=C\C1=C(C)C(O)=C(C)C(=O)O1

InChI Identifier

InChI=1S/C33H44O4/c1-24(17-15-18-25(2)31(34)26(3)22-23-29-19-12-10-13-20-29)16-11-8-6-7-9-14-21-30-27(4)32(35)28(5)33(36)37-30/h10-21,25-26,31,34-35H,6-9,22-23H2,1-5H3/b16-11+,18-15+,21-14+,24-17+

InChI Key

GPQHHXQFVXQFFW-QCSLTFAHSA-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
Hyalangium minutum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Long-chain fatty alcohols

Alternative Parents

Substituents

Long chain fatty alcohol
Pyranone
Monocyclic benzene moiety
Pyran
Benzenoid
Heteroaromatic compound
Vinylogous acid
Lactone
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Alcohol
Organic oxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	8.25	ChemAxon
pKa (Strongest Acidic)	7.64	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	159.89 m³·mol⁻¹	ChemAxon
Polarizability	62.03 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	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

34217216

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

90681743

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Okanya PW, Mohr KI, Gerth K, Kessler W, Jansen R, Stadler M, Muller R: Hyafurones, hyapyrrolines, and hyapyrones: polyketides from Hyalangium minutum. J Nat Prod. 2014 Jun 27;77(6):1420-9. doi: 10.1021/np500145f. Epub 2014 May 21. [PubMed:24848583 ]
LOTUS database [Link]

Showing NP-Card for 4-hydroxy-6-[(1e,7e,9e,11e)-14-hydroxy-9,13,15-trimethyl-17-phenylheptadeca-1,7,9,11-tetraen-1-yl]-3,5-dimethylpyran-2-one (NP0273659)

MOL for NP0273659 (4-hydroxy-6-[(1e,7e,9e,11e)-14-hydroxy-9,13,15-trimethyl-17-phenylheptadeca-1,7,9,11-tetraen-1-yl]-3,5-dimethylpyran-2-one)

3D MOL for NP0273659 (4-hydroxy-6-[(1e,7e,9e,11e)-14-hydroxy-9,13,15-trimethyl-17-phenylheptadeca-1,7,9,11-tetraen-1-yl]-3,5-dimethylpyran-2-one)

3D SDF for NP0273659 (4-hydroxy-6-[(1e,7e,9e,11e)-14-hydroxy-9,13,15-trimethyl-17-phenylheptadeca-1,7,9,11-tetraen-1-yl]-3,5-dimethylpyran-2-one)

3D-SDF for NP0273659 (4-hydroxy-6-[(1e,7e,9e,11e)-14-hydroxy-9,13,15-trimethyl-17-phenylheptadeca-1,7,9,11-tetraen-1-yl]-3,5-dimethylpyran-2-one)

PDB for NP0273659 (4-hydroxy-6-[(1e,7e,9e,11e)-14-hydroxy-9,13,15-trimethyl-17-phenylheptadeca-1,7,9,11-tetraen-1-yl]-3,5-dimethylpyran-2-one)

3D PDB for NP0273659 (4-hydroxy-6-[(1e,7e,9e,11e)-14-hydroxy-9,13,15-trimethyl-17-phenylheptadeca-1,7,9,11-tetraen-1-yl]-3,5-dimethylpyran-2-one)

SMILES for NP0273659 (4-hydroxy-6-[(1e,7e,9e,11e)-14-hydroxy-9,13,15-trimethyl-17-phenylheptadeca-1,7,9,11-tetraen-1-yl]-3,5-dimethylpyran-2-one)

INCHI for NP0273659 (4-hydroxy-6-[(1e,7e,9e,11e)-14-hydroxy-9,13,15-trimethyl-17-phenylheptadeca-1,7,9,11-tetraen-1-yl]-3,5-dimethylpyran-2-one)

Structure for NP0273659 (4-hydroxy-6-[(1e,7e,9e,11e)-14-hydroxy-9,13,15-trimethyl-17-phenylheptadeca-1,7,9,11-tetraen-1-yl]-3,5-dimethylpyran-2-one)

3D Structure for NP0273659 (4-hydroxy-6-[(1e,7e,9e,11e)-14-hydroxy-9,13,15-trimethyl-17-phenylheptadeca-1,7,9,11-tetraen-1-yl]-3,5-dimethylpyran-2-one)