NP-MRD: Showing NP-Card for Palisadin D (NP0084311)

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Record Information

Version

2.0

Created at

2022-04-29 05:04:56 UTC

Updated at

2022-04-29 05:04:56 UTC

NP-MRD ID

NP0084311

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Palisadin D

Description

(1S,3R,10S,11R,12R)-1,11,12-trimethyl-2,5-dioxatricyclo[8.4.0.0³,⁷]Tetradec-7-en-12-ol belongs to the class of organic compounds known as tetrahydrofurans. These are heterocyclic compounds containing a saturated, aliphatic, five-membered ring where a carbon is replaced by an oxygen. Palisadin D is found in Laurencia snackeyi. Based on a literature review very few articles have been published on (1S,3R,10S,11R,12R)-1,11,12-trimethyl-2,5-dioxatricyclo[8.4.0.0³,⁷]Tetradec-7-en-12-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
   -2.2495   -1.1460   -1.1580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6658    0.1221   -0.5852 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1805    0.0752   -0.4100 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4987   -0.2524   -1.7391 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8078    0.4454   -1.7795 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5831    0.8083   -0.7729 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8741    1.4946   -0.7633 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5238    1.1062    0.3657 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6761    0.4902    1.2314 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2695    0.5704    0.6806 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6690   -0.6482    0.8797 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3159   -0.7223    0.7351 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0173   -2.2211    0.5826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4434   -0.2787    1.9708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3188    0.9278    1.6934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3638    0.6112    0.6336 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3748   -0.3420    1.2003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0575    1.8271    0.4211 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8716   -0.9554   -2.0825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4125   -1.7798   -1.5160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9279   -1.6723   -0.4686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8389    0.9121   -1.3824 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1341    1.1428   -0.2022 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5879   -1.3411   -1.8815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1721    0.1038   -2.5655 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2103    0.7065   -2.7433 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4377    1.3187   -1.7037 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6774    2.6003   -0.6897 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7348    0.8685    2.2775 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9961   -0.5907    1.3067 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7701    1.4235    1.1458 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4782   -2.6439   -0.3207 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5854   -2.6925    1.4411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0231   -2.4639    0.7499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1148   -1.0636    2.3743 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2336    0.0083    2.7982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7605    1.8403    1.4928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8959    1.1041    2.6360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8202    0.1779    2.0994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2379   -0.4417    0.4942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9671   -1.2977    1.5356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3839    1.8678   -0.5163 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  2  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  1  0
  2 16  1  0
 16 17  1  0
 16 18  1  6
 16 15  1  0
 15 14  1  0
 14 12  1  0
 12 13  1  6
 12 11  1  0
  6 10  1  0
 12  3  1  0
 11 10  1  0
 10 31  1  1
  9 29  1  0
  9 30  1  0
  7 27  1  0
  7 28  1  0
  5 26  1  0
  4 24  1  0
  4 25  1  0
  3 23  1  1
  2 22  1  6
  1 19  1  0
  1 20  1  0
  1 21  1  0
 17 39  1  0
 17 40  1  0
 17 41  1  0
 18 42  1  0
 15 37  1  0
 15 38  1  0
 14 35  1  0
 14 36  1  0
 13 32  1  0
 13 33  1  0
 13 34  1  0
M  END


  Mrv1652304292207042D          

 20 22  0  0  1  0            999 V2000
    1.8681    0.1162    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8219   -0.7075    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5691   -0.3579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3084   -0.7241    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1945    0.0930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4829   -1.5305    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2685   -1.7824    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4431   -2.5887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8795   -1.2281    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3194   -1.9261    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6433   -0.9161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7050   -0.4218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9194   -0.1698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6807   -1.3379    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9614   -2.1697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1364   -2.1605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6293   -1.5097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8068   -1.5745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4911   -0.8123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1184   -0.2765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  6  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
  4 13  1  0  0  0  0
  6 14  1  1  0  0  0
  6 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
  2 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  2 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0084311

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@]12COCC1=CC[C@@]1([H])[C@@H](C)[C@](C)(O)CC[C@]1(C)O2

> <INCHI_IDENTIFIER>
InChI=1S/C15H24O3/c1-10-12-5-4-11-8-17-9-13(11)18-15(12,3)7-6-14(10,2)16/h4,10,12-13,16H,5-9H2,1-3H3/t10-,12+,13+,14-,15+/m1/s1

> <INCHI_KEY>
COJIKWHAFLDDBV-NZNQWUEYSA-N

> <FORMULA>
C15H24O3

> <MOLECULAR_WEIGHT>
252.354

> <EXACT_MASS>
252.172544633

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
28.50974686160541

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,3R,10S,11R,12R)-1,11,12-trimethyl-2,5-dioxatricyclo[8.4.0.0^{3,7}]tetradec-7-en-12-ol

> <ALOGPS_LOGP>
1.80

> <JCHEM_LOGP>
1.5317494246666667

> <ALOGPS_LOGS>
-2.63

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.780052110701138

> <JCHEM_PKA_STRONGEST_BASIC>
-2.895005206779321

> <JCHEM_POLAR_SURFACE_AREA>
38.69

> <JCHEM_REFRACTIVITY>
70.8579

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.93e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,10S,11R,12R)-1,11,12-trimethyl-2,5-dioxatricyclo[8.4.0.0^{3,7}]tetradec-7-en-12-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  H   UNK     0       3.487   0.217   0.000  0.00  0.00           H+0
HETATM    2  C   UNK     0       3.401  -1.321   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.796  -0.668   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       6.176  -1.352   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.963   0.174   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.501  -2.857   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.968  -3.327   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.294  -4.832   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.108  -2.292   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       9.929  -3.595   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      10.534  -1.710   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.783  -0.787   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.316  -0.317   0.000  0.00  0.00           C+0
HETATM   14  H   UNK     0       5.004  -2.497   0.000  0.00  0.00           H+0
HETATM   15  C   UNK     0       5.528  -4.050   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.988  -4.033   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.041  -2.818   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.506  -2.939   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.917  -1.516   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.088  -0.516   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   17   20                                             
CONECT    3    2    4                                                       
CONECT    4    3    5    6   13                                             
CONECT    5    4                                                            
CONECT    6    4    7   14   15                                             
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11   12                                             
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    9   13                                                       
CONECT   13   12    4                                                       
CONECT   14    6                                                            
CONECT   15    6   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16    2   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19    2                                                       
MASTER        0    0    0    0    0    0    0    0   20    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₄O₃

Average Mass

252.3540 Da

Monoisotopic Mass

252.17254 Da

IUPAC Name

(1S,3R,10S,11R,12R)-1,11,12-trimethyl-2,5-dioxatricyclo[8.4.0.0^{3,7}]tetradec-7-en-12-ol

Traditional Name

(1S,3R,10S,11R,12R)-1,11,12-trimethyl-2,5-dioxatricyclo[8.4.0.0^{3,7}]tetradec-7-en-12-ol

CAS Registry Number

Not Available

SMILES

[H][C@]12COCC1=CC[C@@]1([H])[C@@H](C)[C@](C)(O)CC[C@]1(C)O2

InChI Identifier

InChI=1S/C15H24O3/c1-10-12-5-4-11-8-17-9-13(11)18-15(12,3)7-6-14(10,2)16/h4,10,12-13,16H,5-9H2,1-3H3/t10-,12+,13+,14-,15+/m1/s1

InChI Key

COJIKWHAFLDDBV-NZNQWUEYSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Laurencia snackeyi	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetrahydrofurans. These are heterocyclic compounds containing a saturated, aliphatic, five-membered ring where a carbon is replaced by an oxygen.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Tetrahydrofurans

Sub Class

Not Available

Direct Parent

Tetrahydrofurans

Alternative Parents

Substituents

Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Oxacycle
Ether
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
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	1.8	ALOGPS
logP	1.53	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	14.78	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	38.69 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	70.86 m³·mol⁻¹	ChemAxon
Polarizability	28.51 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

C00053622

Chemspider ID

60958474

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163123995

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Palisadin D (NP0084311)

MOL for NP0084311 (Palisadin D)

3D MOL for NP0084311 (Palisadin D)

3D SDF for NP0084311 (Palisadin D)

3D-SDF for NP0084311 (Palisadin D)

PDB for NP0084311 (Palisadin D)

3D PDB for NP0084311 (Palisadin D)

SMILES for NP0084311 (Palisadin D)

INCHI for NP0084311 (Palisadin D)

Structure for NP0084311 (Palisadin D)

3D Structure for NP0084311 (Palisadin D)