NP-MRD: Showing NP-Card for 4-[(3ar,7s,8as)-7-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,8ah-cyclohepta[b]furan-6-yl]-4-hydroxybutan-2-yl acetate (NP0328545)

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Record Information

Version

1.0

Created at

2022-09-12 12:06:53 UTC

Updated at

2022-09-12 12:06:53 UTC

NP-MRD ID

NP0328545

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-[(3ar,7s,8as)-7-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,8ah-cyclohepta[b]furan-6-yl]-4-hydroxybutan-2-yl acetate

Description

4-[(3AR,7S,8aS)-7-methyl-3-methylidene-2-oxo-2H,3H,3aH,4H,7H,8H,8aH-cyclohepta[b]furan-6-yl]-4-hydroxybutan-2-yl acetate belongs to the class of organic compounds known as xanthanolides. These are sesquiterpenoids with a structure based on the xanthanolide skeleton consistsing of a cycloheptane ring usually attached to a four-carbon chain (at carbon 1 ) and a methyl group (at carbon 10), and fused to a five-member lactone ring (sharing carbons 7 and 8). The lactone ring can be conjugated with a methyl or methylene group at position 11. 4-[(3ar,7s,8as)-7-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,8ah-cyclohepta[b]furan-6-yl]-4-hydroxybutan-2-yl acetate is found in Xanthium spinosum. Based on a literature review very few articles have been published on 4-[(3aR,7S,8aS)-7-methyl-3-methylidene-2-oxo-2H,3H,3aH,4H,7H,8H,8aH-cyclohepta[b]furan-6-yl]-4-hydroxybutan-2-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 47  0  0  0  0  0  0  0  0999 V2000
    5.3557    1.7089    0.4367 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6829    0.5882    0.4669 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2349   -0.7585    0.2658 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4439   -1.0681    0.0570 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1845   -1.6765    0.3430 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0192   -0.9559    0.0117 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7504   -1.6346    0.4666 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6422   -1.1600   -0.4434 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0629   -1.1894   -1.8988 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2256    0.2346   -0.1483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2435    0.4240   -0.0816 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8551    0.0833   -1.3034 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9179   -0.3906    0.9773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4070   -0.0310    0.9765 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1368   -0.8158    2.0181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9579   -0.1322   -0.3075 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4647    0.9594   -1.0162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0459    0.8185   -2.3835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4005    2.0762   -0.4269 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0041    1.2686    0.0497 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4621    1.4902    0.0679 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2302    0.3569    0.7023 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8565    2.6540    0.5973 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4004    1.7104    0.2546 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0336   -0.7675   -1.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8260   -2.7295    0.3825 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5345   -1.2935    1.4936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2035   -1.8490   -0.3419 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7817   -2.0045   -2.1135 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4302   -0.1917   -2.2044 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1538   -1.3845   -2.5258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4818    1.5206    0.0459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8941   -0.9249   -1.2958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8758   -1.4574    0.7411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5402   -0.2449    1.9875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4715    1.0552    1.2668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6119   -1.7053    1.5287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9124   -0.1825    2.4882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4186   -1.2290    2.7497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7704    1.6784   -3.0261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6954   -0.1487   -2.7947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1455    0.7544   -2.2843 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4336    2.1889    0.2493 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8940    1.6562   -0.9536 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7141    2.4041    0.6439 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0932    0.2943    1.7980 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 13  1  0
 13 11  1  0
 11 12  1  0
 11 10  1  0
 10 20  2  0
 20 21  1  0
 21 22  1  0
 22  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  6  5  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  2  3
 14 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
  8 10  1  0
  2 22  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
 14 36  1  1
 13 34  1  0
 13 35  1  0
 11 32  1  1
 12 33  1  0
 20 43  1  0
 21 44  1  0
 21 45  1  0
 22 46  1  1
  6 25  1  6
  7 26  1  0
  7 27  1  0
  8 28  1  6
  9 29  1  0
  9 30  1  0
  9 31  1  0
  1 23  1  0
  1 24  1  0
 18 40  1  0
 18 41  1  0
 18 42  1  0
M  END


  Mrv1652309122214062D          

 22 23  0  0  1  0            999 V2000
   -3.4445    2.7221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8314    3.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9176    4.0946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6321    4.5071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1640    4.4302    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6119    3.8171    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7962    3.9400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1914    3.3789    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5766    3.6803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2530    2.5562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4614    2.1437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4614    1.3187    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1759    2.5562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8904    2.1437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8904    1.3187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    2.5562    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3193    2.1437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0338    2.5562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3193    1.3187    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9347    2.0915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7230    2.3346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0244    3.1026    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 10 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22  2  1  6  0  0  0
  6 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0328545

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CC(O)C1=CC[C@H]2[C@H](C[C@@H]1C)OC(=O)C2=C)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H24O5/c1-9-7-16-14(11(3)17(20)22-16)6-5-13(9)15(19)8-10(2)21-12(4)18/h5,9-10,14-16,19H,3,6-8H2,1-2,4H3/t9-,10?,14+,15?,16-/m0/s1

> <INCHI_KEY>
IQAWVYINTAIBSH-HPJQFELNSA-N

> <FORMULA>
C17H24O5

> <MOLECULAR_WEIGHT>
308.374

> <EXACT_MASS>
308.162373873

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
33.326724660406114

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-[(3aR,7S,8aS)-7-methyl-3-methylidene-2-oxo-2H,3H,3aH,4H,7H,8H,8aH-cyclohepta[b]furan-6-yl]-4-hydroxybutan-2-yl acetate

> <JCHEM_LOGP>
1.738686748333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.52797611023859

> <JCHEM_PKA_STRONGEST_BASIC>
-3.00526324938164

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
81.6203

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4-[(3aR,7S,8aS)-7-methyl-3-methylidene-2-oxo-3aH,4H,7H,8H,8aH-cyclohepta[b]furan-6-yl]-4-hydroxybutan-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      -6.430   5.081   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.285   6.112   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.446   7.643   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -6.780   8.413   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      -4.039   8.270   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -3.009   7.125   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.486   7.355   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.357   6.307   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.076   6.870   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.472   4.772   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.861   4.002   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       0.861   2.462   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.195   4.772   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.529   4.002   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.529   2.462   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.862   4.772   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.196   4.002   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.530   4.772   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.196   2.462   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -1.745   3.904   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.216   4.358   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.779   5.792   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   22                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   20                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   10   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    2    6                                                  
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Value	Source
4-[(3AR,7S,8as)-7-methyl-3-methylidene-2-oxo-2H,3H,3ah,4H,7H,8H,8ah-cyclohepta[b]furan-6-yl]-4-hydroxybutan-2-yl acetic acid	Generator

Chemical Formula

C₁₇H₂₄O₅

Average Mass

308.3740 Da

Monoisotopic Mass

308.16237 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(CC(O)C1=CC[C@H]2[C@H](C[C@@H]1C)OC(=O)C2=C)OC(C)=O

InChI Identifier

InChI=1S/C17H24O5/c1-9-7-16-14(11(3)17(20)22-16)6-5-13(9)15(19)8-10(2)21-12(4)18/h5,9-10,14-16,19H,3,6-8H2,1-2,4H3/t9-,10?,14+,15?,16-/m0/s1

InChI Key

IQAWVYINTAIBSH-HPJQFELNSA-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
Xanthium spinosum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as xanthanolides. These are sesquiterpenoids with a structure based on the xanthanolide skeleton consistsing of a cycloheptane ring usually attached to a four-carbon chain (at carbon 1 ) and a methyl group (at carbon 10), and fused to a five-member lactone ring (sharing carbons 7 and 8). The lactone ring can be conjugated with a methyl or methylene group at position 11.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Xanthanolides

Alternative Parents

Substituents

Xanthanolide-skeleton
Xanthane sesquiterpenoid
Sesquiterpenoid
Gamma butyrolactone
Dicarboxylic acid or derivatives
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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

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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

12310003

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-[(3ar,7s,8as)-7-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,8ah-cyclohepta[b]furan-6-yl]-4-hydroxybutan-2-yl acetate (NP0328545)

MOL for NP0328545 (4-[(3ar,7s,8as)-7-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,8ah-cyclohepta[b]furan-6-yl]-4-hydroxybutan-2-yl acetate)

3D MOL for NP0328545 (4-[(3ar,7s,8as)-7-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,8ah-cyclohepta[b]furan-6-yl]-4-hydroxybutan-2-yl acetate)

3D SDF for NP0328545 (4-[(3ar,7s,8as)-7-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,8ah-cyclohepta[b]furan-6-yl]-4-hydroxybutan-2-yl acetate)

3D-SDF for NP0328545 (4-[(3ar,7s,8as)-7-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,8ah-cyclohepta[b]furan-6-yl]-4-hydroxybutan-2-yl acetate)

PDB for NP0328545 (4-[(3ar,7s,8as)-7-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,8ah-cyclohepta[b]furan-6-yl]-4-hydroxybutan-2-yl acetate)

3D PDB for NP0328545 (4-[(3ar,7s,8as)-7-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,8ah-cyclohepta[b]furan-6-yl]-4-hydroxybutan-2-yl acetate)

SMILES for NP0328545 (4-[(3ar,7s,8as)-7-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,8ah-cyclohepta[b]furan-6-yl]-4-hydroxybutan-2-yl acetate)

INCHI for NP0328545 (4-[(3ar,7s,8as)-7-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,8ah-cyclohepta[b]furan-6-yl]-4-hydroxybutan-2-yl acetate)

Structure for NP0328545 (4-[(3ar,7s,8as)-7-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,8ah-cyclohepta[b]furan-6-yl]-4-hydroxybutan-2-yl acetate)

3D Structure for NP0328545 (4-[(3ar,7s,8as)-7-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,8ah-cyclohepta[b]furan-6-yl]-4-hydroxybutan-2-yl acetate)