NP-MRD: Showing NP-Card for (2r,3s)-4-[(1r,7as)-hexahydro-1h-pyrrolizin-1-ylmethoxy]-3-hydroxy-3-methyl-4-oxobutan-2-yl (2e)-2-methylbut-2-enoate (NP0237342)

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Record Information

Version

2.0

Created at

2022-09-06 20:27:27 UTC

Updated at

2022-09-06 20:27:28 UTC

NP-MRD ID

NP0237342

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3s)-4-[(1r,7as)-hexahydro-1h-pyrrolizin-1-ylmethoxy]-3-hydroxy-3-methyl-4-oxobutan-2-yl (2e)-2-methylbut-2-enoate

Description

Minalobine O belongs to the class of organic compounds known as pyrrolizidines. Pyrrolizidines are compounds containing a pyrrolizidine, which is a bicyclic ring system made up of two fused pyrrolidine ring sharing a nitrogen atom. (2r,3s)-4-[(1r,7as)-hexahydro-1h-pyrrolizin-1-ylmethoxy]-3-hydroxy-3-methyl-4-oxobutan-2-yl (2e)-2-methylbut-2-enoate is found in Ipomoea cristulata. Based on a literature review very few articles have been published on Minalobine O.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 53 54  0  0  0  0  0  0  0  0999 V2000
    5.0438    2.7611   -1.8724 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3478    1.4596   -1.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2548    0.9762   -0.3641 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8589    1.7386    0.7590 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5742   -0.2893   -0.0972 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5049   -0.7256    1.0886 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9874   -1.0620   -1.0678 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3308   -2.2694   -0.8607 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9494   -3.4400   -1.5589 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8652   -2.2276   -1.2156 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2275   -3.5706   -0.9538 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7349   -1.9012   -2.5646 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1292   -1.2116   -0.4122 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0983   -1.2881    0.8332 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5336   -0.1658   -1.0194 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2533    0.8404   -0.3694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3902    0.2549    0.4331 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3595   -0.5150   -0.4819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7616   -0.1211    0.0165 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4678    0.4422    1.2836 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3622    1.4103    1.8014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4417    2.1910    2.7565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0191    1.9073    2.2412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3164    1.3023    0.9314 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1284    2.6066   -1.8450 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6671    3.2269   -2.7872 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7670    3.4448   -1.0284 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8966    0.8813   -2.3770 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4021    2.7471    0.8584 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9452    1.8591    0.5862 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7475    1.1527    1.7149 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3738   -2.4868    0.2443 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7571   -3.9073   -0.9476 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3072   -3.1871   -2.5836 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1731   -4.2174   -1.6936 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1309   -4.1861   -1.8663 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7957   -4.1589   -0.1864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8028   -3.4633   -0.5421 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5238   -1.3761   -2.9023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6232    1.5462   -1.1396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6049    1.3758    0.3623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0176   -0.3907    1.2262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1964   -1.5899   -0.4374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2392   -0.0661   -1.4858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2700    0.5392   -0.6884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3132   -1.0911    0.1682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7045    2.1158    1.0427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2031    0.9630    2.3764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5348    1.8290    3.7808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5975    3.2828    2.6457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4413    2.8413    2.1303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4871    1.2025    2.8827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5816    2.0100    0.1298 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  6
 10 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 17  1  0
 24 20  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  4 29  1  0
  4 30  1  0
  4 31  1  0
  8 32  1  1
  9 33  1  0
  9 34  1  0
  9 35  1  0
 11 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  0
 16 40  1  0
 16 41  1  0
 17 42  1  1
 18 43  1  0
 18 44  1  0
 19 45  1  0
 19 46  1  0
 21 47  1  0
 21 48  1  0
 22 49  1  0
 22 50  1  0
 23 51  1  0
 23 52  1  0
 24 53  1  6
M  END


  Mrv1652309062222272D          

 24 25  0  0  1  0            999 V2000
   -4.0400   -5.7031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7851   -4.9185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9781   -4.7470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4261   -5.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7232   -3.9624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2752   -3.3493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9162   -3.7908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6612   -3.0062    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2133   -2.3931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8543   -2.8347    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6827   -3.6416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0258   -2.0277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0473   -2.6631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5047   -3.2762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2076   -1.8785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0146   -1.7070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695   -0.9224    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542    0.1576    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8388    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3237   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8388   -0.9224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542   -0.6674    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  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  1  0  0  0
 10 12  1  1  0  0  0
 10 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 17 16  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 17 24  1  0  0  0  0
 24 20  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0237342

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(/C)C(=O)O[C@H](C)[C@](C)(O)C(=O)OC[C@@H]1CCN2CCC[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C18H29NO5/c1-5-12(2)16(20)24-13(3)18(4,22)17(21)23-11-14-8-10-19-9-6-7-15(14)19/h5,13-15,22H,6-11H2,1-4H3/b12-5+/t13-,14+,15+,18+/m1/s1

> <INCHI_KEY>
QWLVLKBPONBFQZ-BPIFGQDUSA-N

> <FORMULA>
C18H29NO5

> <MOLECULAR_WEIGHT>
339.432

> <EXACT_MASS>
339.204573038

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
36.48905200741568

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3S)-4-{[(1R,7aS)-hexahydro-1H-pyrrolizin-1-yl]methoxy}-3-hydroxy-3-methyl-4-oxobutan-2-yl (2E)-2-methylbut-2-enoate

> <JCHEM_LOGP>
2.0865514732618697

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.656815850135104

> <JCHEM_PKA_STRONGEST_BASIC>
10.183480948176333

> <JCHEM_POLAR_SURFACE_AREA>
76.07

> <JCHEM_REFRACTIVITY>
90.89499999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3S)-4-[(1R,7aS)-hexahydro-1H-pyrrolizin-1-ylmethoxy]-3-hydroxy-3-methyl-4-oxobutan-2-yl (2E)-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -7.541 -10.646   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -7.065  -9.181   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.559  -8.861   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.529 -10.005   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.083  -7.396   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -6.114  -6.252   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      -3.577  -7.076   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -3.101  -5.612   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.131  -4.467   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.595  -5.291   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.274  -6.798   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.915  -3.785   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.088  -4.971   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       0.942  -6.116   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       0.388  -3.507   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.894  -3.186   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.370  -1.722   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.465  -0.476   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.370   0.770   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       3.834   0.294   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       5.299   0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.204  -0.476   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.299  -1.722   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.834  -1.246   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12   13                                             
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13   10   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   24                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   24                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   17   20                                                  
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₉NO₅

Average Mass

339.4320 Da

Monoisotopic Mass

339.20457 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C\C=C(/C)C(=O)O[C@H](C)[C@](C)(O)C(=O)OC[C@@H]1CCN2CCC[C@@H]12

InChI Identifier

InChI=1S/C18H29NO5/c1-5-12(2)16(20)24-13(3)18(4,22)17(21)23-11-14-8-10-19-9-6-7-15(14)19/h5,13-15,22H,6-11H2,1-4H3/b12-5+/t13-,14+,15+,18+/m1/s1

InChI Key

QWLVLKBPONBFQZ-BPIFGQDUSA-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
Ipomoea cristulata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrrolizidines. Pyrrolizidines are compounds containing a pyrrolizidine, which is a bicyclic ring system made up of two fused pyrrolidine ring sharing a nitrogen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrrolizidines

Sub Class

Not Available

Direct Parent

Pyrrolizidines

Alternative Parents

Substituents

Pyrrolizidine
Fatty acid ester
Dicarboxylic acid or derivatives
N-alkylpyrrolidine
Fatty acyl
Pyrrolidine
Tertiary alcohol
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Tertiary aliphatic amine
Tertiary amine
Carboxylic acid ester
Amino acid or derivatives
Carboxylic acid derivative
Azacycle
Organic oxide
Alcohol
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organic nitrogen compound
Carbonyl group
Hydrocarbon derivative
Amine
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

91749900

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3s)-4-[(1r,7as)-hexahydro-1h-pyrrolizin-1-ylmethoxy]-3-hydroxy-3-methyl-4-oxobutan-2-yl (2e)-2-methylbut-2-enoate (NP0237342)

MOL for NP0237342 ((2r,3s)-4-[(1r,7as)-hexahydro-1h-pyrrolizin-1-ylmethoxy]-3-hydroxy-3-methyl-4-oxobutan-2-yl (2e)-2-methylbut-2-enoate)

3D MOL for NP0237342 ((2r,3s)-4-[(1r,7as)-hexahydro-1h-pyrrolizin-1-ylmethoxy]-3-hydroxy-3-methyl-4-oxobutan-2-yl (2e)-2-methylbut-2-enoate)

3D SDF for NP0237342 ((2r,3s)-4-[(1r,7as)-hexahydro-1h-pyrrolizin-1-ylmethoxy]-3-hydroxy-3-methyl-4-oxobutan-2-yl (2e)-2-methylbut-2-enoate)

3D-SDF for NP0237342 ((2r,3s)-4-[(1r,7as)-hexahydro-1h-pyrrolizin-1-ylmethoxy]-3-hydroxy-3-methyl-4-oxobutan-2-yl (2e)-2-methylbut-2-enoate)

PDB for NP0237342 ((2r,3s)-4-[(1r,7as)-hexahydro-1h-pyrrolizin-1-ylmethoxy]-3-hydroxy-3-methyl-4-oxobutan-2-yl (2e)-2-methylbut-2-enoate)

3D PDB for NP0237342 ((2r,3s)-4-[(1r,7as)-hexahydro-1h-pyrrolizin-1-ylmethoxy]-3-hydroxy-3-methyl-4-oxobutan-2-yl (2e)-2-methylbut-2-enoate)

SMILES for NP0237342 ((2r,3s)-4-[(1r,7as)-hexahydro-1h-pyrrolizin-1-ylmethoxy]-3-hydroxy-3-methyl-4-oxobutan-2-yl (2e)-2-methylbut-2-enoate)

INCHI for NP0237342 ((2r,3s)-4-[(1r,7as)-hexahydro-1h-pyrrolizin-1-ylmethoxy]-3-hydroxy-3-methyl-4-oxobutan-2-yl (2e)-2-methylbut-2-enoate)

Structure for NP0237342 ((2r,3s)-4-[(1r,7as)-hexahydro-1h-pyrrolizin-1-ylmethoxy]-3-hydroxy-3-methyl-4-oxobutan-2-yl (2e)-2-methylbut-2-enoate)

3D Structure for NP0237342 ((2r,3s)-4-[(1r,7as)-hexahydro-1h-pyrrolizin-1-ylmethoxy]-3-hydroxy-3-methyl-4-oxobutan-2-yl (2e)-2-methylbut-2-enoate)