NP-MRD: Showing NP-Card for methyl 2-[(3r,4r,6s)-4-ethyl-6-[(2r,3e)-2-ethylhex-3-en-1-yl]-6-methyl-1,2-dioxan-3-yl]acetate (NP0318744)

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Record Information

Version

2.0

Created at

2022-09-11 19:24:51 UTC

Updated at

2022-09-11 19:24:51 UTC

NP-MRD ID

NP0318744

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-[(3r,4r,6s)-4-ethyl-6-[(2r,3e)-2-ethylhex-3-en-1-yl]-6-methyl-1,2-dioxan-3-yl]acetate

Description

Plakortin belongs to the class of organic compounds known as 1,2-dioxanes. These are organic compounds containing 1,2-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 2. methyl 2-[(3r,4r,6s)-4-ethyl-6-[(2r,3e)-2-ethylhex-3-en-1-yl]-6-methyl-1,2-dioxan-3-yl]acetate is found in Plakortis angulospiculatus, Plakortis halichondrioides and Plakortis simplex. methyl 2-[(3r,4r,6s)-4-ethyl-6-[(2r,3e)-2-ethylhex-3-en-1-yl]-6-methyl-1,2-dioxan-3-yl]acetate was first documented in 2017 (PMID: 28383076). Based on a literature review a small amount of articles have been published on plakortin (PMID: 29314833) (PMID: 34723550) (PMID: 34549936) (PMID: 33185636).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 54 54  0  0  0  0  0  0  0  0999 V2000
    6.0879   -0.4336   -1.5485 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0388    0.1742   -0.1798 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6834    0.1176    0.4268 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6170   -0.4059   -0.1518 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2712   -0.4215    0.5404 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7838   -1.8490    0.6803 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7642   -2.6821    1.4901 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3229    0.3410   -0.3140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0749    0.4677    0.1639 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1859    1.1502    1.5102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7936    1.3506   -0.8846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1500    1.6350   -0.3345 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0304    2.3655   -1.3225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4235    3.6946   -1.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8038    0.4028    0.1965 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6495   -0.3040   -0.8432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2793   -1.5243   -0.2678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6133   -2.5649   -0.0228 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6430   -1.5721    0.0285 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1982   -2.7485    0.5730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9261   -0.4372    0.8231 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8197   -0.6895    0.2004 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1766   -0.5229   -1.8215 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5897    0.2629   -2.2673 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6456   -1.4364   -1.5350 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4694    1.1898   -0.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6965   -0.4490    0.4954 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5643    0.5386    1.4186 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7395   -0.8251   -1.1430 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4232   -0.0138    1.5399 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8375   -1.8392    1.2671 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5874   -2.2964   -0.2971 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4081   -2.0842    2.1416 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2211   -3.4225    2.1316 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3802   -3.2621    0.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6892    1.3752   -0.5392 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2803   -0.1690   -1.3141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1054    2.2497    1.3685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1228    0.8506    2.0027 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6473    0.8428    2.1522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8885    0.6975   -1.7834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1953    2.2309   -1.1195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0125    2.3407    0.5356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1785    1.7843   -2.2591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0297    2.5780   -0.9275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0728    4.1924   -2.4645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3987    3.5405   -2.1025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3294    4.3234   -0.7995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5388    0.7450    0.9861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4011    0.3486   -1.2915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9506   -0.6491   -1.6406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7550   -2.4898    1.5098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9213   -3.1836   -0.1473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4334   -3.5141    0.8029 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  5  8  1  0
  9  8  1  6
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 12 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 15 21  1  0
 21 22  1  0
 22  9  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  2 27  1  0
  3 28  1  0
  4 29  1  0
  5 30  1  1
  6 31  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  7 35  1  0
  8 36  1  0
  8 37  1  0
 10 38  1  0
 10 39  1  0
 10 40  1  0
 11 41  1  0
 11 42  1  0
 12 43  1  1
 13 44  1  0
 13 45  1  0
 14 46  1  0
 14 47  1  0
 14 48  1  0
 15 49  1  1
 16 50  1  0
 16 51  1  0
 20 52  1  0
 20 53  1  0
 20 54  1  0
M  END


  Mrv1652309112221242D          

 22 22  0  0  1  0            999 V2000
   -0.0299    5.4592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3121    4.6840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2182    4.0520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0640    3.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4663    2.6447    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2788    2.7880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5610    3.5632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2448    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    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
  3  4  2  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 15 21  1  0  0  0  0
 21 22  1  0  0  0  0
  9 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0318744

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC\C=C\[C@H](CC)C[C@@]1(C)C[C@@H](CC)[C@@H](CC(=O)OC)OO1

> <INCHI_IDENTIFIER>
InChI=1S/C18H32O4/c1-6-9-10-14(7-2)12-18(4)13-15(8-3)16(21-22-18)11-17(19)20-5/h9-10,14-16H,6-8,11-13H2,1-5H3/b10-9+/t14-,15+,16+,18-/m0/s1

> <INCHI_KEY>
CWUVZQMWRPJSFS-RUJCAILXSA-N

> <FORMULA>
C18H32O4

> <MOLECULAR_WEIGHT>
312.45

> <EXACT_MASS>
312.23005951

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
36.077450194048865

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 2-[(3R,4R,6S)-4-ethyl-6-[(2R,3E)-2-ethylhex-3-en-1-yl]-6-methyl-1,2-dioxan-3-yl]acetate

> <JCHEM_LOGP>
4.812330012666665

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.836225207791693

> <JCHEM_POLAR_SURFACE_AREA>
44.760000000000005

> <JCHEM_REFRACTIVITY>
88.18190000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl [(3R,4R,6S)-4-ethyl-6-[(2R,3E)-2-ethylhex-3-en-1-yl]-6-methyl-1,2-dioxan-3-yl]acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.056  10.191   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.583   8.743   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.407   7.564   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.119   6.117   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.870   4.937   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.387   5.204   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.914   6.651   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.344   3.490   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.324   3.490   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    8                                                  
CONECT    6    5    7                                                       
CONECT    7    6                                                            
CONECT    8    5    9                                                       
CONECT    9    8   10   11   22                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12   16   21                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19                                                            
CONECT   21   15   22                                                       
CONECT   22   21    9                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₃₂O₄

Average Mass

312.4500 Da

Monoisotopic Mass

312.23006 Da

IUPAC Name

methyl 2-[(3R,4R,6S)-4-ethyl-6-[(2R,3E)-2-ethylhex-3-en-1-yl]-6-methyl-1,2-dioxan-3-yl]acetate

Traditional Name

methyl [(3R,4R,6S)-4-ethyl-6-[(2R,3E)-2-ethylhex-3-en-1-yl]-6-methyl-1,2-dioxan-3-yl]acetate

CAS Registry Number

Not Available

SMILES

CC\C=C\[C@H](CC)C[C@@]1(C)C[C@@H](CC)[C@@H](CC(=O)OC)OO1

InChI Identifier

InChI=1S/C18H32O4/c1-6-9-10-14(7-2)12-18(4)13-15(8-3)16(21-22-18)11-17(19)20-5/h9-10,14-16H,6-8,11-13H2,1-5H3/b10-9+/t14-,15+,16+,18-/m0/s1

InChI Key

CWUVZQMWRPJSFS-RUJCAILXSA-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
Plakortis angulospiculatus	LOTUS Database	35616633
Plakortis halichondrioides	LOTUS Database	35616633
Plakortis simplex	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1,2-dioxanes. These are organic compounds containing 1,2-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 2.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dioxanes

Sub Class

1,2-dioxanes

Direct Parent

1,2-dioxanes

Alternative Parents

Substituents

Ortho-dioxane
Methyl ester
Dialkyl peroxide
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic 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	4.81	ChemAxon
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	44.76 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	88.18 m³·mol⁻¹	ChemAxon
Polarizability	36.08 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

23277150

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44417613

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Li Q, Zhao K, Peuronen A, Rissanen K, Enders D, Tang Y: Enantioselective Total Syntheses of (+)-Hippolachnin A, (+)-Gracilioether A, (-)-Gracilioether E, and (-)-Gracilioether F. J Am Chem Soc. 2018 Feb 7;140(5):1937-1944. doi: 10.1021/jacs.7b12903. Epub 2018 Jan 24. [PubMed:29314833 ]
Xue Z, Li Q, Zhang J, Tang Y: Unified Biomimetic Approach to (+)-Hippolachnin A: In-Depth Insights into Its Biosynthetic Origin. Org Lett. 2021 Nov 19;23(22):8783-8788. doi: 10.1021/acs.orglett.1c03280. Epub 2021 Nov 1. [PubMed:34723550 ]
Bao R, Zhang H, Tang Y: Biomimetic Synthesis of Natural Products: A Journey To Learn, To Mimic, and To Be Better. Acc Chem Res. 2021 Oct 5;54(19):3720-3733. doi: 10.1021/acs.accounts.1c00459. Epub 2021 Sep 22. [PubMed:34549936 ]
Li Q, Yang H, Tang Y: Recent advances in the synthesis of plakortin-type polyketides. Org Biomol Chem. 2020 Dec 7;18(46):9371-9384. doi: 10.1039/d0ob01930e. [PubMed:33185636 ]
Persico M, Fattorusso R, Taglialatela-Scafati O, Chianese G, de Paola I, Zaccaro L, Rondinelli F, Lombardo M, Quintavalla A, Trombini C, Fattorusso E, Fattorusso C, Farina B: The interaction of heme with plakortin and a synthetic endoperoxide analogue: new insights into the heme-activated antimalarial mechanism. Sci Rep. 2017 Apr 6;7:45485. doi: 10.1038/srep45485. [PubMed:28383076 ]
LOTUS database [Link]

Showing NP-Card for methyl 2-[(3r,4r,6s)-4-ethyl-6-[(2r,3e)-2-ethylhex-3-en-1-yl]-6-methyl-1,2-dioxan-3-yl]acetate (NP0318744)

MOL for NP0318744 (methyl 2-[(3r,4r,6s)-4-ethyl-6-[(2r,3e)-2-ethylhex-3-en-1-yl]-6-methyl-1,2-dioxan-3-yl]acetate)

3D MOL for NP0318744 (methyl 2-[(3r,4r,6s)-4-ethyl-6-[(2r,3e)-2-ethylhex-3-en-1-yl]-6-methyl-1,2-dioxan-3-yl]acetate)

3D SDF for NP0318744 (methyl 2-[(3r,4r,6s)-4-ethyl-6-[(2r,3e)-2-ethylhex-3-en-1-yl]-6-methyl-1,2-dioxan-3-yl]acetate)

3D-SDF for NP0318744 (methyl 2-[(3r,4r,6s)-4-ethyl-6-[(2r,3e)-2-ethylhex-3-en-1-yl]-6-methyl-1,2-dioxan-3-yl]acetate)

PDB for NP0318744 (methyl 2-[(3r,4r,6s)-4-ethyl-6-[(2r,3e)-2-ethylhex-3-en-1-yl]-6-methyl-1,2-dioxan-3-yl]acetate)

3D PDB for NP0318744 (methyl 2-[(3r,4r,6s)-4-ethyl-6-[(2r,3e)-2-ethylhex-3-en-1-yl]-6-methyl-1,2-dioxan-3-yl]acetate)

SMILES for NP0318744 (methyl 2-[(3r,4r,6s)-4-ethyl-6-[(2r,3e)-2-ethylhex-3-en-1-yl]-6-methyl-1,2-dioxan-3-yl]acetate)

INCHI for NP0318744 (methyl 2-[(3r,4r,6s)-4-ethyl-6-[(2r,3e)-2-ethylhex-3-en-1-yl]-6-methyl-1,2-dioxan-3-yl]acetate)

Structure for NP0318744 (methyl 2-[(3r,4r,6s)-4-ethyl-6-[(2r,3e)-2-ethylhex-3-en-1-yl]-6-methyl-1,2-dioxan-3-yl]acetate)

3D Structure for NP0318744 (methyl 2-[(3r,4r,6s)-4-ethyl-6-[(2r,3e)-2-ethylhex-3-en-1-yl]-6-methyl-1,2-dioxan-3-yl]acetate)