NP-MRD: Showing NP-Card for 12-hydroxy-4-methyl-7-(propan-2-ylidene)-3,14-dioxatetracyclo[10.2.1.0²,¹⁰.0⁴,⁸]pentadec-2(10)-en-11-one (NP0238366)

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Record Information

Version

2.0

Created at

2022-09-06 21:44:49 UTC

Updated at

2022-09-06 21:44:49 UTC

NP-MRD ID

NP0238366

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12-hydroxy-4-methyl-7-(propan-2-ylidene)-3,14-dioxatetracyclo[10.2.1.0²,¹⁰.0⁴,⁸]pentadec-2(10)-en-11-one

Description

12-Hydroxy-4-methyl-7-(propan-2-ylidene)-3,14-dioxatetracyclo[10.2.1.0²,¹⁰.0⁴,⁸]Pentadec-2(10)-en-11-one belongs to the class of organic compounds known as monoterpenoids. Monoterpenoids are compounds containing a chain of two isoprene units. 12-hydroxy-4-methyl-7-(propan-2-ylidene)-3,14-dioxatetracyclo[10.2.1.0²,¹⁰.0⁴,⁸]pentadec-2(10)-en-11-one is found in Phyllosticta capitalensis. Based on a literature review very few articles have been published on 12-hydroxy-4-methyl-7-(propan-2-ylidene)-3,14-dioxatetracyclo[10.2.1.0²,¹⁰.0⁴,⁸]Pentadec-2(10)-en-11-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 43 46  0  0  0  0  0  0  0  0999 V2000
   -4.5245    0.7203    0.7017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1090    0.8994    0.2836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6542    2.2417   -0.1211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3261   -0.1698    0.2982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6476   -1.5549    0.6760 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3551   -2.3002    0.6576 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5617   -1.5704   -0.3959 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9766   -1.9412   -1.7943 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8281   -1.8240   -0.2917 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7288   -0.7962   -0.2058 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3979    0.2432    0.5585 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0013    0.2976    1.0553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8953   -0.1297   -0.0947 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3874    1.2746    0.8805 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1111    2.1734    1.7152 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6863    1.1727    0.1691 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6696    1.9632    0.6821 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4013    1.4086   -1.2978 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0026    0.2250   -1.8522 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0439   -0.7723   -0.9097 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0634   -0.3118    0.1415 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8574   -0.2678    0.3405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1601    1.5360    0.2836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5511    0.7125    1.8245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1319    2.5802   -1.0820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8013    3.0147    0.6681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5578    2.2410   -0.3411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1479   -1.5654    1.6759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3354   -2.0494   -0.0574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8218   -2.3420    1.6068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5222   -3.3448    0.3242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0612   -1.9536   -1.9485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5030   -2.9294   -2.0270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4649   -1.2039   -2.4764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2718    1.2801    1.4652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0992   -0.4506    1.8622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7534    0.4609   -0.9999 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5752    2.0411    1.6535 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6065    2.2094   -1.3600 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3473    1.7396   -1.7546 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2957   -1.7361   -1.3420 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8741   -0.8094    1.0927 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0701   -0.4122   -0.2645 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  6
  7  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 11 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  1
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 13  4  1  0
 21 16  1  0
 13  7  1  0
 20 10  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  3 26  1  0
  3 27  1  0
  5 28  1  0
  5 29  1  0
  6 30  1  0
  6 31  1  0
  8 32  1  0
  8 33  1  0
  8 34  1  0
 12 35  1  0
 12 36  1  0
 13 37  1  6
 17 38  1  0
 18 39  1  0
 18 40  1  0
 20 41  1  6
 21 42  1  0
 21 43  1  0
M  END


  Mrv1652309062223442D          

 21 24  0  0  0  0            999 V2000
    4.3559    2.9813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8655    2.3325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6821    2.4493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5583    1.5668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9972    0.8682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4684    0.2349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7027    0.5421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7336   -0.2823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9621    0.1786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2770    0.6383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3326    1.4614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0732    1.8249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7583    1.3652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7236    2.0181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9610    2.8082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9088    1.8890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4390    2.5672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5016    1.1715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8087    0.4058    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5989    0.1685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0388    0.9425    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
  2  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
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  4 13  1  0  0  0  0
  7 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  2  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
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 10 20  1  0  0  0  0
 20 21  1  0  0  0  0
 16 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0238366

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=C1CCC2(C)OC3=C(CC12)C(=O)C1(O)COC3C1

> <INCHI_IDENTIFIER>
InChI=1S/C17H22O4/c1-9(2)10-4-5-16(3)12(10)6-11-14(21-16)13-7-17(19,8-20-13)15(11)18/h12-13,19H,4-8H2,1-3H3

> <INCHI_KEY>
XJTFQYOAMSEGKF-UHFFFAOYSA-N

> <FORMULA>
C17H22O4

> <MOLECULAR_WEIGHT>
290.359

> <EXACT_MASS>
290.151809188

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
30.88129026478901

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
12-hydroxy-4-methyl-7-(propan-2-ylidene)-3,14-dioxatetracyclo[10.2.1.0^{2,10}.0^{4,8}]pentadec-2(10)-en-11-one

> <JCHEM_LOGP>
1.3577635773333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.157837366633974

> <JCHEM_PKA_STRONGEST_BASIC>
-4.041961935834299

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
79.4537

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
12-hydroxy-4-methyl-7-(propan-2-ylidene)-3,14-dioxatetracyclo[10.2.1.0^{2,10}.0^{4,8}]pentadec-2(10)-en-11-one

> <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       8.131   5.565   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.082   4.354   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.607   4.572   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.509   2.925   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.328   1.621   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.341   0.439   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.912   1.012   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.969  -0.527   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.529   0.333   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       4.250   1.191   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.354   2.728   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.737   3.406   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.015   2.548   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.217   3.767   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.660   5.242   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.696   3.526   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.819   4.792   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.936   2.187   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.510   0.757   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.985   0.315   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.939   1.759   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   13                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   13                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   20                                                  
CONECT   11   10   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12    4    7                                                  
CONECT   14   11   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18   21                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   10   21                                                  
CONECT   21   20   16                                                       
MASTER        0    0    0    0    0    0    0    0   21    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₂₂O₄

Average Mass

290.3590 Da

Monoisotopic Mass

290.15181 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)=C1CCC2(C)OC3=C(CC12)C(=O)C1(O)COC3C1

InChI Identifier

InChI=1S/C17H22O4/c1-9(2)10-4-5-16(3)12(10)6-11-14(21-16)13-7-17(19,8-20-13)15(11)18/h12-13,19H,4-8H2,1-3H3

InChI Key

XJTFQYOAMSEGKF-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
Phyllosticta capitalensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as monoterpenoids. Monoterpenoids are compounds containing a chain of two isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Monoterpenoids

Alternative Parents

Substituents

Monoterpenoid
Cyclohexenone
Vinylogous ester
Tetrahydrofuran
Tertiary alcohol
Ketone
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
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

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

163075125

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-4-methyl-7-(propan-2-ylidene)-3,14-dioxatetracyclo[10.2.1.0²,¹⁰.0⁴,⁸]pentadec-2(10)-en-11-one (NP0238366)

MOL for NP0238366 (12-hydroxy-4-methyl-7-(propan-2-ylidene)-3,14-dioxatetracyclo[10.2.1.0²,¹⁰.0⁴,⁸]pentadec-2(10)-en-11-one)

3D MOL for NP0238366 (12-hydroxy-4-methyl-7-(propan-2-ylidene)-3,14-dioxatetracyclo[10.2.1.0²,¹⁰.0⁴,⁸]pentadec-2(10)-en-11-one)

3D SDF for NP0238366 (12-hydroxy-4-methyl-7-(propan-2-ylidene)-3,14-dioxatetracyclo[10.2.1.0²,¹⁰.0⁴,⁸]pentadec-2(10)-en-11-one)

3D-SDF for NP0238366 (12-hydroxy-4-methyl-7-(propan-2-ylidene)-3,14-dioxatetracyclo[10.2.1.0²,¹⁰.0⁴,⁸]pentadec-2(10)-en-11-one)

PDB for NP0238366 (12-hydroxy-4-methyl-7-(propan-2-ylidene)-3,14-dioxatetracyclo[10.2.1.0²,¹⁰.0⁴,⁸]pentadec-2(10)-en-11-one)

3D PDB for NP0238366 (12-hydroxy-4-methyl-7-(propan-2-ylidene)-3,14-dioxatetracyclo[10.2.1.0²,¹⁰.0⁴,⁸]pentadec-2(10)-en-11-one)

SMILES for NP0238366 (12-hydroxy-4-methyl-7-(propan-2-ylidene)-3,14-dioxatetracyclo[10.2.1.0²,¹⁰.0⁴,⁸]pentadec-2(10)-en-11-one)

INCHI for NP0238366 (12-hydroxy-4-methyl-7-(propan-2-ylidene)-3,14-dioxatetracyclo[10.2.1.0²,¹⁰.0⁴,⁸]pentadec-2(10)-en-11-one)

Structure for NP0238366 (12-hydroxy-4-methyl-7-(propan-2-ylidene)-3,14-dioxatetracyclo[10.2.1.0²,¹⁰.0⁴,⁸]pentadec-2(10)-en-11-one)

3D Structure for NP0238366 (12-hydroxy-4-methyl-7-(propan-2-ylidene)-3,14-dioxatetracyclo[10.2.1.0²,¹⁰.0⁴,⁸]pentadec-2(10)-en-11-one)