NP-MRD: Showing NP-Card for 3-Oxa-achillicin (NP0073809)

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Record Information

Version

2.0

Created at

2022-04-28 19:02:08 UTC

Updated at

2022-04-28 19:02:08 UTC

NP-MRD ID

NP0073809

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-Oxa-achillicin

Description

(3S)-2-Oxo-3beta,6,9-trimethyl-2,3,3abeta,5,6,9balpha-hexahydro-4H-cyclohepta[2,1-b:3,4-C']difuran-4beta,6alpha-diol 4-acetate belongs to the class of organic compounds known as cycloheptafurans. These are organic heterocyclic compounds containing a cycloheptane derivative fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. 3-Oxa-achillicin is found in Achillea collina and Achillea millefolium . Based on a literature review very few articles have been published on (3S)-2-Oxo-3beta,6,9-trimethyl-2,3,3abeta,5,6,9balpha-hexahydro-4H-cyclohepta[2,1-b:3,4-C']difuran-4beta,6alpha-diol 4-acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
    4.2581    1.9602   -0.9695 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9928    1.1951   -1.1627 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5735    0.9852   -2.3094 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2369    0.6923   -0.1399 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0625   -0.0127   -0.3894 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1676   -1.4346    0.0783 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0271   -2.3028   -0.3264 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3908   -3.7588   -0.1688 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1732   -2.1010   -1.7129 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2524   -1.9778    0.3499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0301   -2.8385    1.0930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0682   -2.1654    1.5125 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0242   -0.9275    1.0969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0135    0.1431    1.3619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8892   -0.7602    0.3544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4179    0.4669   -0.3171 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1521    1.6200    0.0189 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3288    2.7285   -0.1132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6819    3.9283   -0.1631 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0886    2.2190   -0.1867 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0012    2.9950    0.7125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0405    0.7674    0.2284 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4806    2.6214   -1.8113 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0831    1.2303   -0.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2265    2.5216    0.0010 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8814   -0.0561   -1.4989 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2474   -1.4489    1.1738 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0626   -1.8711   -0.4273 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5483   -4.0672    0.8641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4639   -4.3572   -0.5730 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2466   -3.9700   -0.8412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1094   -2.4289   -1.8904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7853   -3.8895    1.2744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5331    1.0441    1.8363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4824    0.4730    0.4049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8340   -0.2260    2.0083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3249    0.2976   -1.3928 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4229    2.2868   -1.2398 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4068    3.7383    1.2873 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6889    3.6149    0.0704 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5473    2.3873    1.4449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0365    0.6777    1.3345 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 22  1  0
 22 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 16 15  1  0
 15 13  2  0
 13 14  1  0
 13 12  1  0
 12 11  1  0
 11 10  2  0
 10  7  1  0
  7  8  1  0
  7  9  1  6
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
 18 20  1  0
 10 15  1  0
  5 22  1  0
 21 39  1  0
 21 40  1  0
 21 41  1  0
 20 38  1  6
 22 42  1  1
 16 37  1  6
 14 34  1  0
 14 35  1  0
 14 36  1  0
 11 33  1  0
  8 29  1  0
  8 30  1  0
  8 31  1  0
  9 32  1  0
  6 27  1  0
  6 28  1  0
  5 26  1  6
  1 23  1  0
  1 24  1  0
  1 25  1  0
M  END


  Mrv1652304282221022D          

 22 24  0  0  1  0            999 V2000
    1.8746   -1.0076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6996   -1.0076    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2140   -1.6526    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0304   -2.4569    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2871   -2.8149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5438   -2.4569    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3602   -1.6526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5878   -1.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6248   -0.5386    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4201   -0.3191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7100    0.4533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2026   -3.2081    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7356   -2.6224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6754   -2.9713    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5524   -3.7871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1974   -4.3015    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -4.0885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9864   -1.3627    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9493   -0.5386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5944   -0.0242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1541   -0.3191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6749   -1.8172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  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
  1  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
  1 10  2  0  0  0  0
 10 11  1  0  0  0  0
  6 12  1  6  0  0  0
  6 13  1  1  0  0  0
  4 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
  3 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
  2 21  1  1  0  0  0
 18 22  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0073809

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1[C@H]2[C@H](OC1=O)C1=C(C)OC=C1[C@@](C)(O)C[C@@H]2OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H20O6/c1-7-12-11(21-9(3)17)5-16(4,19)10-6-20-8(2)13(10)14(12)22-15(7)18/h6-7,11-12,14,19H,5H2,1-4H3/t7-,11-,12+,14-,16-/m0/s1

> <INCHI_KEY>
KOUVNGDGNNAPQW-LWFZOEDRSA-N

> <FORMULA>
C16H20O6

> <MOLECULAR_WEIGHT>
308.33

> <EXACT_MASS>
308.125988364

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
31.392662528584868

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,5S,6R,7S,9S)-9-hydroxy-5,9,13-trimethyl-4-oxo-3,12-dioxatricyclo[8.3.0.0^{2,6}]trideca-1(13),10-dien-7-yl acetate

> <ALOGPS_LOGP>
1.72

> <JCHEM_LOGP>
0.7487567983333341

> <ALOGPS_LOGS>
-2.90

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.80574782262265

> <JCHEM_PKA_STRONGEST_BASIC>
-2.840326269724325

> <JCHEM_POLAR_SURFACE_AREA>
85.97000000000001

> <JCHEM_REFRACTIVITY>
75.9724

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.90e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,5S,6R,7S,9S)-9-hydroxy-5,9,13-trimethyl-4-oxo-3,12-dioxatricyclo[8.3.0.0^{2,6}]trideca-1(13),10-dien-7-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       3.499  -1.881   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.039  -1.881   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.999  -3.085   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.657  -4.586   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.269  -5.254   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.882  -4.586   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.539  -3.085   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.097  -2.544   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.166  -1.005   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.651  -0.596   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.192   0.846   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.245  -5.988   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.373  -4.895   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       6.861  -5.546   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.631  -7.069   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.835  -8.029   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.198  -7.632   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.441  -2.544   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.372  -1.005   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.576  -0.045   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       5.888  -0.596   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.726  -3.392   0.000  0.00  0.00           C+0
CONECT    1    2    7   10                                                  
CONECT    2    1    3   21                                                  
CONECT    3    2    4   18                                                  
CONECT    4    3    5   14                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   12   13                                             
CONECT    7    6    1    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    1   11                                                  
CONECT   11   10                                                            
CONECT   12    6                                                            
CONECT   13    6                                                            
CONECT   14    4   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18    3   19   22                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19    2                                                       
CONECT   22   18                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   48    0
END

View in JSmol

Synonyms

Value	Source
(3S)-2-oxo-3b,6,9-Trimethyl-2,3,3abeta,5,6,9balpha-hexahydro-4H-cyclohepta[2,1-b:3,4-c']difuran-4b,6a-diol 4-acetate	Generator
(3S)-2-oxo-3b,6,9-Trimethyl-2,3,3abeta,5,6,9balpha-hexahydro-4H-cyclohepta[2,1-b:3,4-c']difuran-4b,6a-diol 4-acetic acid	Generator
(3S)-2-oxo-3beta,6,9-Trimethyl-2,3,3abeta,5,6,9balpha-hexahydro-4H-cyclohepta[2,1-b:3,4-c']difuran-4beta,6alpha-diol 4-acetic acid	Generator
(3S)-2-oxo-3Β,6,9-trimethyl-2,3,3abeta,5,6,9balpha-hexahydro-4H-cyclohepta[2,1-b:3,4-c']difuran-4β,6α-diol 4-acetate	Generator
(3S)-2-oxo-3Β,6,9-trimethyl-2,3,3abeta,5,6,9balpha-hexahydro-4H-cyclohepta[2,1-b:3,4-c']difuran-4β,6α-diol 4-acetic acid	Generator

Chemical Formula

C₁₆H₂₀O₆

Average Mass

308.3300 Da

Monoisotopic Mass

308.12599 Da

IUPAC Name

(2S,5S,6R,7S,9S)-9-hydroxy-5,9,13-trimethyl-4-oxo-3,12-dioxatricyclo[8.3.0.0^{2,6}]trideca-1(13),10-dien-7-yl acetate

Traditional Name

(2S,5S,6R,7S,9S)-9-hydroxy-5,9,13-trimethyl-4-oxo-3,12-dioxatricyclo[8.3.0.0^{2,6}]trideca-1(13),10-dien-7-yl acetate

CAS Registry Number

Not Available

SMILES

C[C@H]1[C@H]2[C@H](OC1=O)C1=C(C)OC=C1[C@@](C)(O)C[C@@H]2OC(C)=O

InChI Identifier

InChI=1S/C16H20O6/c1-7-12-11(21-9(3)17)5-16(4,19)10-6-20-8(2)13(10)14(12)22-15(7)18/h6-7,11-12,14,19H,5H2,1-4H3/t7-,11-,12+,14-,16-/m0/s1

InChI Key

KOUVNGDGNNAPQW-LWFZOEDRSA-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
Achillea collina	Plant	KNApSAcK
Achillea millefolium	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cycloheptafurans. These are organic heterocyclic compounds containing a cycloheptane derivative fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Cycloheptafurans

Sub Class

Not Available

Direct Parent

Cycloheptafurans

Alternative Parents

Substituents

Cycloheptafuran
Dicarboxylic acid or derivatives
Gamma butyrolactone
Furan
Heteroaromatic compound
Tetrahydrofuran
Tertiary alcohol
Carboxylic acid ester
Lactone
Oxacycle
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	1.72	ALOGPS
logP	0.75	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	13.81	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	85.97 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	75.97 m³·mol⁻¹	ChemAxon
Polarizability	31.39 Å³	ChemAxon
Number of Rings	3	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

103885070

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15127111

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 3-Oxa-achillicin (NP0073809)

MOL for NP0073809 (3-Oxa-achillicin)

3D MOL for NP0073809 (3-Oxa-achillicin)

3D SDF for NP0073809 (3-Oxa-achillicin)

3D-SDF for NP0073809 (3-Oxa-achillicin)

PDB for NP0073809 (3-Oxa-achillicin)

3D PDB for NP0073809 (3-Oxa-achillicin)

SMILES for NP0073809 (3-Oxa-achillicin)

INCHI for NP0073809 (3-Oxa-achillicin)

Structure for NP0073809 (3-Oxa-achillicin)

3D Structure for NP0073809 (3-Oxa-achillicin)