NP-MRD: Showing NP-Card for 2,9-dihydroxy-1,1,4a,8,8,13a,13b-heptamethyl-2h,3h,4h,4bh,7h,9h,9ah,12h,13h,14h,15h,15ah-piceno[4,4a-b]oxet-11-one (NP0279895)

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Record Information

Version

2.0

Created at

2022-09-09 05:26:55 UTC

Updated at

2022-09-09 05:26:55 UTC

NP-MRD ID

NP0279895

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2,9-dihydroxy-1,1,4a,8,8,13a,13b-heptamethyl-2h,3h,4h,4bh,7h,9h,9ah,12h,13h,14h,15h,15ah-piceno[4,4a-b]oxet-11-one

Description

7,18-Dihydroxy-1,2,6,6,10,17,17-heptamethyl-20-oxahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁹,²²]Tetracosa-12,14-dien-21-one belongs to the class of organic compounds known as beta propiolactones. These are organic compounds containing a four-member lactone (a cyclic ester). 2,9-dihydroxy-1,1,4a,8,8,13a,13b-heptamethyl-2h,3h,4h,4bh,7h,9h,9ah,12h,13h,14h,15h,15ah-piceno[4,4a-b]oxet-11-one is found in Tetrapanax papyrifer. 7,18-Dihydroxy-1,2,6,6,10,17,17-heptamethyl-20-oxahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁹,²²]Tetracosa-12,14-dien-21-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251508172D          

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M  END

     RDKit          3D

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M  END


  Mrv1533004251508172D          

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   -0.0807    2.8536    0.0000 O   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 16 19  1  0  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  9 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
  6 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
 27 28  1  0  0  0  0
  5 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  2  0  0  0  0
 29 33  1  0  0  0  0
  2 33  1  0  0  0  0
 33 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0279895

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)CC2=C3C=CC4C5(C)CCC(O)C(C)(C)C5CCC4(C)C3(C)CCC22C(OC2=O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C30H44O4/c1-25(2)16-18-17-8-9-20-27(5)12-11-21(31)26(3,4)19(27)10-13-29(20,7)28(17,6)14-15-30(18)23(22(25)32)34-24(30)33/h8-9,19-23,31-32H,10-16H2,1-7H3

> <INCHI_KEY>
GGPUTPVILFAMBK-UHFFFAOYSA-N

> <FORMULA>
C30H44O4

> <MOLECULAR_WEIGHT>
468.678

> <EXACT_MASS>
468.323959897

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
54.356734858033896

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7,18-dihydroxy-1,2,6,6,10,17,17-heptamethyl-20-oxahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁹,²²]tetracosa-12,14-dien-21-one

> <ALOGPS_LOGP>
5.25

> <JCHEM_LOGP>
4.703917862666666

> <ALOGPS_LOGS>
-5.05

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.489420328243167

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.688096305939482

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8351273648352805

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
133.7053

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.21e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7,18-dihydroxy-1,2,6,6,10,17,17-heptamethyl-20-oxahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁹,²²]tetracosa-12,14-dien-21-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       2.995   7.534   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.398   6.114   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.104   6.949   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.899   5.772   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.354   4.301   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.856   3.959   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.903   5.089   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.404   4.747   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.859   3.276   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.360   2.934   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.906   4.405   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.407   4.063   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.909   3.721   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.364   2.250   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      14.865   1.908   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      12.317   1.121   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.719  -0.299   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      13.611   0.286   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.815   1.462   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.768   0.333   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.267   0.675   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.812   2.146   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.765   1.017   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.310   2.488   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.813   1.030   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.264   1.358   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.762   1.700   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.307   3.172   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.806   3.514   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       1.464   2.012   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       2.965   1.670   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       3.785   0.367   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       1.351   4.985   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -0.151   5.327   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   33                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   28                                                  
CONECT    6    5    7   24                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   22                                                  
CONECT   10    9   11   12   19                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   16   10   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    9   23   24                                             
CONECT   23   22                                                            
CONECT   24   22    6   25   26                                             
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27    5   29   31                                             
CONECT   29   28   30   33                                                  
CONECT   30   29   31                                                       
CONECT   31   30   28   32                                                  
CONECT   32   31                                                            
CONECT   33   29    2   34                                                  
CONECT   34   33                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₄O₄

Average Mass

468.6780 Da

Monoisotopic Mass

468.32396 Da

IUPAC Name

7,18-dihydroxy-1,2,6,6,10,17,17-heptamethyl-20-oxahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁹,²²]tetracosa-12,14-dien-21-one

Traditional Name

7,18-dihydroxy-1,2,6,6,10,17,17-heptamethyl-20-oxahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁵,²².0¹⁹,²²]tetracosa-12,14-dien-21-one

CAS Registry Number

Not Available

SMILES

CC1(C)CC2=C3C=CC4C5(C)CCC(O)C(C)(C)C5CCC4(C)C3(C)CCC22C(OC2=O)C1O

InChI Identifier

InChI=1S/C30H44O4/c1-25(2)16-18-17-8-9-20-27(5)12-11-21(31)26(3,4)19(27)10-13-29(20,7)28(17,6)14-15-30(18)23(22(25)32)34-24(30)33/h8-9,19-23,31-32H,10-16H2,1-7H3

InChI Key

GGPUTPVILFAMBK-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
Tetrapanax papyrifer	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as beta propiolactones. These are organic compounds containing a four-member lactone (a cyclic ester).

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Beta propiolactones

Direct Parent

Beta propiolactones

Alternative Parents

Substituents

Cyclic alcohol
Beta_propiolactone
Secondary alcohol
Oxetane
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	5.25	ALOGPS
logP	4.7	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	13.69	ChemAxon
pKa (Strongest Basic)	-0.84	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	0	ChemAxon
Refractivity	133.71 m³·mol⁻¹	ChemAxon
Polarizability	54.36 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

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 2,9-dihydroxy-1,1,4a,8,8,13a,13b-heptamethyl-2h,3h,4h,4bh,7h,9h,9ah,12h,13h,14h,15h,15ah-piceno[4,4a-b]oxet-11-one (NP0279895)

MOL for NP0279895 (2,9-dihydroxy-1,1,4a,8,8,13a,13b-heptamethyl-2h,3h,4h,4bh,7h,9h,9ah,12h,13h,14h,15h,15ah-piceno[4,4a-b]oxet-11-one)

3D MOL for NP0279895 (2,9-dihydroxy-1,1,4a,8,8,13a,13b-heptamethyl-2h,3h,4h,4bh,7h,9h,9ah,12h,13h,14h,15h,15ah-piceno[4,4a-b]oxet-11-one)

3D SDF for NP0279895 (2,9-dihydroxy-1,1,4a,8,8,13a,13b-heptamethyl-2h,3h,4h,4bh,7h,9h,9ah,12h,13h,14h,15h,15ah-piceno[4,4a-b]oxet-11-one)

3D-SDF for NP0279895 (2,9-dihydroxy-1,1,4a,8,8,13a,13b-heptamethyl-2h,3h,4h,4bh,7h,9h,9ah,12h,13h,14h,15h,15ah-piceno[4,4a-b]oxet-11-one)

PDB for NP0279895 (2,9-dihydroxy-1,1,4a,8,8,13a,13b-heptamethyl-2h,3h,4h,4bh,7h,9h,9ah,12h,13h,14h,15h,15ah-piceno[4,4a-b]oxet-11-one)

3D PDB for NP0279895 (2,9-dihydroxy-1,1,4a,8,8,13a,13b-heptamethyl-2h,3h,4h,4bh,7h,9h,9ah,12h,13h,14h,15h,15ah-piceno[4,4a-b]oxet-11-one)

SMILES for NP0279895 (2,9-dihydroxy-1,1,4a,8,8,13a,13b-heptamethyl-2h,3h,4h,4bh,7h,9h,9ah,12h,13h,14h,15h,15ah-piceno[4,4a-b]oxet-11-one)

INCHI for NP0279895 (2,9-dihydroxy-1,1,4a,8,8,13a,13b-heptamethyl-2h,3h,4h,4bh,7h,9h,9ah,12h,13h,14h,15h,15ah-piceno[4,4a-b]oxet-11-one)

Structure for NP0279895 (2,9-dihydroxy-1,1,4a,8,8,13a,13b-heptamethyl-2h,3h,4h,4bh,7h,9h,9ah,12h,13h,14h,15h,15ah-piceno[4,4a-b]oxet-11-one)

3D Structure for NP0279895 (2,9-dihydroxy-1,1,4a,8,8,13a,13b-heptamethyl-2h,3h,4h,4bh,7h,9h,9ah,12h,13h,14h,15h,15ah-piceno[4,4a-b]oxet-11-one)