NP-MRD: Showing NP-Card for (1s,6s,8r,9s)-8-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodec-2-en-4-one (NP0176601)

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Record Information

Version

2.0

Created at

2022-09-03 14:17:38 UTC

Updated at

2022-09-03 14:17:39 UTC

NP-MRD ID

NP0176601

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,6s,8r,9s)-8-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodec-2-en-4-one

Description

Kandenol E belongs to the class of organic compounds known as agarofurans. These are organic compounds containing an agarofuran moiety( a three-ring system, with core fragment oxatricyclo[7.2.1.0^{1,6}]Dodec-2-ene). (1s,6s,8r,9s)-8-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodec-2-en-4-one was first documented in 2012 (PMID: 23234344). Based on a literature review very few articles have been published on Kandenol E.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          2D

 40 42  0  0  0  0  0  0  0  0999 V2000
   -1.9884   -2.2493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4980   -2.4192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1000   -3.7949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5903   -3.9648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1883   -5.3404    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4827   -2.7591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8943   -1.3846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3943   -1.3846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6443   -0.0855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8943    1.2135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6338    2.6907    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3943    1.2135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2760    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3943   -1.2135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0323   -0.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0323    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5241    0.5932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3442    2.2172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4787   -2.0794    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1583   -3.7397    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3639   -0.7971    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7924   -5.0006    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5151   -3.8472    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2609   -2.5867    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8943   -1.3846    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3943   -2.1817    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9320    0.0158    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6673    1.0115    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0626   -0.5738    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3038    1.7266    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7829    3.6549    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6805    2.6860    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6004    0.7041    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6004   -0.7041    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0159    0.4364    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8615    2.0548    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5503   -0.9066    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6560    3.6844    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8384    2.0865    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0741    2.7056    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  6
  7  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  1
 15 16  1  0
 16 17  1  0
 16 18  1  0
 14  2  1  0
 14  7  1  0
 16 12  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  3 22  1  0
  6 23  1  0
  6 24  1  0
  8 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
  9 29  1  0
 10 30  1  1
 11 31  1  0
 12 32  1  1
 13 33  1  0
 13 34  1  0
 17 35  1  0
 17 36  1  0
 17 37  1  0
 18 38  1  0
 18 39  1  0
 18 40  1  0
M  END


  Mrv1652309032216172D          

 18 20  0  0  1  0            999 V2000
    2.6419    2.3180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9588    1.5562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7894    1.4798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1332    0.7251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9548    0.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6590    0.0462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8281    0.1194    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2176   -0.6079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4117   -0.6435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5574   -0.6042    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1160   -1.3012    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1508    0.1622    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8101    0.5007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4154    0.8988    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7079    1.4538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9575    1.0058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4557    1.6606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1375    0.9156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  6  0  0  0
 14 13  1  1  0  0  0
  2 14  1  0  0  0  0
  7 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0176601

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC(=O)C[C@]2(C)C[C@@H](O)[C@@H]3C[C@@]12OC3(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O3/c1-9-5-10(16)6-14(4)8-12(17)11-7-15(9,14)18-13(11,2)3/h5,11-12,17H,6-8H2,1-4H3/t11-,12+,14+,15+/m0/s1

> <INCHI_KEY>
VSOIXBXUFYSVRL-CTHBEMJXSA-N

> <FORMULA>
C15H22O3

> <MOLECULAR_WEIGHT>
250.338

> <EXACT_MASS>
250.156894568

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
41.01378631169121

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,6S,8R,9S)-8-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodec-2-en-4-one

> <JCHEM_LOGP>
1.4674711359999995

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.759686538119396

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.83135851769342

> <JCHEM_PKA_STRONGEST_BASIC>
-2.872510855701301

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
69.4868

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,6S,8R,9S)-8-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodec-2-en-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       4.932   4.327   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.523   2.905   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.074   2.762   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.715   1.354   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       9.249   1.213   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       6.830   0.086   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.279   0.223   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.006  -1.135   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.502  -1.201   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.907  -1.128   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.083  -2.429   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.148   0.303   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.379   0.935   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.509   1.678   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.188   2.714   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.787   1.878   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.851   3.100   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.257   1.709   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   14                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8    9   14                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   16                                                  
CONECT   13   12   14                                                       
CONECT   14   13    2    7   15                                             
CONECT   15   14   16                                                       
CONECT   16   15   12   17   18                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   40    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₂O₃

Average Mass

250.3380 Da

Monoisotopic Mass

250.15689 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1=CC(=O)C[C@]2(C)C[C@@H](O)[C@@H]3C[C@@]12OC3(C)C

InChI Identifier

InChI=1S/C15H22O3/c1-9-5-10(16)6-14(4)8-12(17)11-7-15(9,14)18-13(11,2)3/h5,11-12,17H,6-8H2,1-4H3/t11-,12+,14+,15+/m0/s1

InChI Key

VSOIXBXUFYSVRL-CTHBEMJXSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as agarofurans. These are organic compounds containing an agarofuran moiety( a three-ring system, with core fragment oxatricyclo[7.2.1.0^{1,6}]Dodec-2-ene).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Agarofurans

Alternative Parents

Substituents

Agarofuran
Oxepane
Cyclohexenone
Cyclic alcohol
Tetrahydrofuran
Cyclic ketone
Secondary alcohol
Ketone
Organoheterocyclic compound
Ether
Dialkyl ether
Oxacycle
Alcohol
Organic oxide
Organooxygen compound
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
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

28649245

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71459822

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Ding L, Maier A, Fiebig HH, Lin WH, Peschel G, Hertweck C: Kandenols A-E, eudesmenes from an endophytic Streptomyces sp. of the mangrove tree Kandelia candel. J Nat Prod. 2012 Dec 28;75(12):2223-7. doi: 10.1021/np300387n. Epub 2012 Dec 12. [PubMed:23234344 ]
LOTUS database [Link]

Showing NP-Card for (1s,6s,8r,9s)-8-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodec-2-en-4-one (NP0176601)

MOL for NP0176601 ((1s,6s,8r,9s)-8-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodec-2-en-4-one)

3D MOL for NP0176601 ((1s,6s,8r,9s)-8-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodec-2-en-4-one)

3D SDF for NP0176601 ((1s,6s,8r,9s)-8-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodec-2-en-4-one)

3D-SDF for NP0176601 ((1s,6s,8r,9s)-8-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodec-2-en-4-one)

PDB for NP0176601 ((1s,6s,8r,9s)-8-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodec-2-en-4-one)

3D PDB for NP0176601 ((1s,6s,8r,9s)-8-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodec-2-en-4-one)

SMILES for NP0176601 ((1s,6s,8r,9s)-8-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodec-2-en-4-one)

INCHI for NP0176601 ((1s,6s,8r,9s)-8-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodec-2-en-4-one)

Structure for NP0176601 ((1s,6s,8r,9s)-8-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodec-2-en-4-one)

3D Structure for NP0176601 ((1s,6s,8r,9s)-8-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodec-2-en-4-one)