NP-MRD: Showing NP-Card for Strychnistenolide acetate (NP0080905)

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Record Information

Version

2.0

Created at

2022-04-29 01:52:52 UTC

Updated at

2022-04-29 01:52:52 UTC

NP-MRD ID

NP0080905

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Strychnistenolide acetate

Description

(4R)-3,6bbeta-Dimethyl-4alpha-acetoxy-5-methylene-7abeta-hydroxy-2,4,4aalpha,5,5aalpha,6,6aalpha,6b,7,7a-decahydrocyclopropa[2,3]indeno[5,6-b]furan-2-one belongs to the class of organic compounds known as eudesmanolides, secoeudesmanolides, and derivatives. These are terpenoids with a structure based on the eudesmanolide (a 3,5a,9-trimethyl-naphtho[1,2-b]furan-2-one derivative) or secoeudesmanolide (a 3,6-dimethyl-5-(pentan-2-yl)-1-benzofuran-2-one derivative) skeleton. Strychnistenolide acetate is found in Lindera strychnifolia . Based on a literature review very few articles have been published on (4R)-3,6bbeta-Dimethyl-4alpha-acetoxy-5-methylene-7abeta-hydroxy-2,4,4aalpha,5,5aalpha,6,6aalpha,6b,7,7a-decahydrocyclopropa[2,3]indeno[5,6-b]furan-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 45  0  0  0  0  0  0  0  0999 V2000
   -0.9420   -2.8417   -0.2430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2735   -1.6435   -0.6691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5552   -1.3225   -1.4171 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7743   -1.0093   -0.6604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8872    0.1331   -0.9468 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7640    0.4671    0.0464 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1894   -0.1176    1.3576 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4829    1.9459    0.0890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1336    2.2477    0.6681 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2087    2.0632    2.0835 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3833    3.5043    0.4915 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6860    3.4214    0.0619 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5015    4.3832   -0.1457 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9508    1.9911   -0.1111 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2619    1.4225   -0.5795 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8928    1.3059    0.1989 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5978   -0.1866    0.1982 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7012   -0.8953   -0.2952 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4885   -1.7786    0.4206 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6492   -2.5090   -0.1410 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2002   -1.9740    1.6259 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6392   -0.3177   -0.6001 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6291   -3.6864   -0.4400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0482   -3.0843    0.2927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5282   -1.4918   -2.4922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9119   -1.3678    0.3777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7175   -1.0410   -1.2431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0620    0.8387   -1.7601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0901   -1.2295    1.2806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2486    0.1824    1.5257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5930    0.1990    2.2268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2561    2.4205    0.7181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5495    2.3526   -0.9290 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7371    2.2348    2.3917 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0778    0.8403   -1.5037 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7537    0.8210    0.1880 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9663    2.2428   -0.8492 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4055   -0.4349    1.2511 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8762   -2.2164   -1.1796 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5357   -2.3859    0.5144 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3763   -3.5861   -0.1725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5576    0.1026   -1.6300 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 19  1  0
 19 21  2  0
 19 18  1  0
 18 17  1  0
 17 22  1  0
 22  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  1
  6  8  1  0
  8  9  1  0
  9 10  1  1
  9 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
  6 22  1  0
 16  9  1  0
  5  3  1  0
 20 39  1  0
 20 40  1  0
 20 41  1  0
 17 38  1  1
 22 42  1  6
  1 23  1  0
  1 24  1  0
  3 25  1  6
  4 26  1  0
  4 27  1  0
  5 28  1  6
  7 29  1  0
  7 30  1  0
  7 31  1  0
  8 32  1  0
  8 33  1  0
 10 34  1  0
 15 35  1  0
 15 36  1  0
 15 37  1  0
M  END


  Mrv1652304292203522D          

 22 25  0  0  1  0            999 V2000
    4.5870    1.0470    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2045    1.7780    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3911    1.6401    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2709    0.8239    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0100    0.4574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1479   -0.3560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5039    0.5199    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8572    1.0321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0438    0.8942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6613    1.6252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1549    1.7454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2383    2.2149    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9774    1.8483    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7443    2.1523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0116    2.6726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6772    0.1551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3837   -0.2963    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0305   -0.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7974   -0.5045    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9103   -1.6247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5959    2.4393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0288    1.7438    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
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  1  5  1  0  0  0  0
  5  6  2  0  0  0  0
  4  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
  3 14  1  0  0  0  0
 13 15  1  6  0  0  0
  9 16  1  0  0  0  0
  7 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
  3 21  1  6  0  0  0
  2 22  1  6  0  0  0
  1 22  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0080905

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@@H]1[C@H]2C(=C)[C@H]3C[C@H]3[C@]2(C)C[C@]2(O)OC(=O)C(C)=C12

> <INCHI_IDENTIFIER>
InChI=1S/C17H20O5/c1-7-10-5-11(10)16(4)6-17(20)13(8(2)15(19)22-17)14(12(7)16)21-9(3)18/h10-12,14,20H,1,5-6H2,2-4H3/t10-,11-,12-,14-,16+,17+/m1/s1

> <INCHI_KEY>
CEEKQDNVMHWRJZ-ZGYPGPFKSA-N

> <FORMULA>
C17H20O5

> <MOLECULAR_WEIGHT>
304.342

> <EXACT_MASS>
304.131073744

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
31.316040646135036

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2R,7S,9S,10R,12S)-7-hydroxy-4,9-dimethyl-13-methylidene-5-oxo-6-oxatetracyclo[7.4.0.0^{3,7}.0^{10,12}]tridec-3-en-2-yl acetate

> <ALOGPS_LOGP>
1.71

> <JCHEM_LOGP>
1.4253950826666681

> <ALOGPS_LOGS>
-2.48

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.17618732113974

> <JCHEM_PKA_STRONGEST_BASIC>
-4.471335665733478

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
77.18700000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.00e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,7S,9S,10R,12S)-7-hydroxy-4,9-dimethyl-13-methylidene-5-oxo-6-oxatetracyclo[7.4.0.0^{3,7}.0^{10,12}]tridec-3-en-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

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  C   UNK     0       8.562   1.954   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.848   3.319   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.330   3.062   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.106   1.538   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.485   0.854   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.743  -0.665   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.674   0.971   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.467   1.927   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.948   1.669   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.234   3.034   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.289   3.258   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       2.311   4.134   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       3.691   3.450   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.123   4.018   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.755   4.989   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.264   0.290   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       4.450  -0.553   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.657  -1.509   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       7.089  -0.942   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.432  -3.033   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.712   4.553   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.387   3.255   0.000  0.00  0.00           C+0
CONECT    1    2    5   22                                                  
CONECT    2    1    3   22                                                  
CONECT    3    2    4   14   21                                             
CONECT    4    3    5    7                                                  
CONECT    5    4    1    6                                                  
CONECT    6    5                                                            
CONECT    7    4    8   17                                                  
CONECT    8    7    9   13                                                  
CONECT    9    8   10   16                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12    8   14   15                                             
CONECT   14   13    3                                                       
CONECT   15   13                                                            
CONECT   16    9                                                            
CONECT   17    7   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21    3                                                            
CONECT   22    2    1                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   50    0
END

View in JSmol

Synonyms

Value	Source
(4R)-3,6Bbeta-dimethyl-4a-acetoxy-5-methylene-7abeta-hydroxy-2,4,4aalpha,5,5aalpha,6,6aalpha,6b,7,7a-decahydrocyclopropa[2,3]indeno[5,6-b]furan-2-one	Generator
(4R)-3,6Bbeta-dimethyl-4α-acetoxy-5-methylene-7abeta-hydroxy-2,4,4aalpha,5,5aalpha,6,6aalpha,6b,7,7a-decahydrocyclopropa[2,3]indeno[5,6-b]furan-2-one	Generator

Chemical Formula

C₁₇H₂₀O₅

Average Mass

304.3420 Da

Monoisotopic Mass

304.13107 Da

IUPAC Name

(1S,2R,7S,9S,10R,12S)-7-hydroxy-4,9-dimethyl-13-methylidene-5-oxo-6-oxatetracyclo[7.4.0.0^{3,7}.0^{10,12}]tridec-3-en-2-yl acetate

Traditional Name

(1S,2R,7S,9S,10R,12S)-7-hydroxy-4,9-dimethyl-13-methylidene-5-oxo-6-oxatetracyclo[7.4.0.0^{3,7}.0^{10,12}]tridec-3-en-2-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1[C@H]2C(=C)[C@H]3C[C@H]3[C@]2(C)C[C@]2(O)OC(=O)C(C)=C12

InChI Identifier

InChI=1S/C17H20O5/c1-7-10-5-11(10)16(4)6-17(20)13(8(2)15(19)22-17)14(12(7)16)21-9(3)18/h10-12,14,20H,1,5-6H2,2-4H3/t10-,11-,12-,14-,16+,17+/m1/s1

InChI Key

CEEKQDNVMHWRJZ-ZGYPGPFKSA-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
Lindera aggregata	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eudesmanolides, secoeudesmanolides, and derivatives. These are terpenoids with a structure based on the eudesmanolide (a 3,5a,9-trimethyl-naphtho[1,2-b]furan-2-one derivative) or secoeudesmanolide (a 3,6-dimethyl-5-(pentan-2-yl)-1-benzofuran-2-one derivative) skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Eudesmanolides, secoeudesmanolides, and derivatives

Alternative Parents

Substituents

Eudesmanolide
Sesquiterpenoid
Naphthofuran
2-furanone
Dicarboxylic acid or derivatives
Cyclic alcohol
Dihydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Lactone
Hemiacetal
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Organooxygen compound
Carbonyl group
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	1.71	ALOGPS
logP	1.43	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	11.18	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	77.19 m³·mol⁻¹	ChemAxon
Polarizability	31.32 Å³	ChemAxon
Number of Rings	4	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

2275646

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3005473

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Strychnistenolide acetate (NP0080905)

MOL for NP0080905 (Strychnistenolide acetate)

3D MOL for NP0080905 (Strychnistenolide acetate)

3D SDF for NP0080905 (Strychnistenolide acetate)

3D-SDF for NP0080905 (Strychnistenolide acetate)

PDB for NP0080905 (Strychnistenolide acetate)

3D PDB for NP0080905 (Strychnistenolide acetate)

SMILES for NP0080905 (Strychnistenolide acetate)

INCHI for NP0080905 (Strychnistenolide acetate)

Structure for NP0080905 (Strychnistenolide acetate)

3D Structure for NP0080905 (Strychnistenolide acetate)