NP-MRD: Showing NP-Card for (1r,7s,7as)-7-({[(2s)-2-hydroxy-2-[(1s)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1h-pyrrolizin-1-yl (2z)-2-methylbut-2-enoate (NP0309163)

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Record Information

Version

1.0

Created at

2022-09-11 03:33:06 UTC

Updated at

2022-09-11 03:33:06 UTC

NP-MRD ID

NP0309163

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,7s,7as)-7-({[(2s)-2-hydroxy-2-[(1s)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1h-pyrrolizin-1-yl (2z)-2-methylbut-2-enoate

Description

(1R,7S,7aS)-7-({[(2S)-2-hydroxy-2-[(1S)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1H-pyrrolizin-1-yl (2Z)-2-methylbut-2-enoate 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. (1r,7s,7as)-7-({[(2s)-2-hydroxy-2-[(1s)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1h-pyrrolizin-1-yl (2z)-2-methylbut-2-enoate is found in Liatris punctata. Based on a literature review very few articles have been published on (1R,7S,7aS)-7-({[(2S)-2-hydroxy-2-[(1S)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1H-pyrrolizin-1-yl (2Z)-2-methylbut-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112205332D          

 27 28  0  0  1  0            999 V2000
   -1.4063   -2.2216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8543   -2.8347    0.0000 C   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 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2076   -1.8785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3444   -1.2654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0146   -1.7070    0.0000 O   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  2  0  0  0  0  0  0  0  0  0
    3.0937   -1.7070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5417   -2.3201    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7966   -3.1047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2446   -3.7178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6036   -3.2762    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7751   -2.4693    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4321   -4.0832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0452   -4.6352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6475   -4.3382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4106   -3.4478    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9626   -2.8347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6655   -4.2324    0.0000 O   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
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 19 17  1  1  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  6  0  0  0
 14 27  1  0  0  0  0
  8 27  1  0  0  0  0
 27 11  1  1  0  0  0
M  END

     RDKit          3D

 60 61  0  0  0  0  0  0  0  0999 V2000
    5.9650    1.2949   -0.3313 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3678    0.8650    1.0102 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6687    0.0062    1.7288 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2165   -0.3342    3.0894 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4466   -0.5732    1.2352 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7254   -1.3927    1.8505 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9533   -0.2612   -0.0002 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8095   -0.7369   -0.5885 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2380   -1.5425   -1.8004 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0510   -0.5632   -2.9280 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0147    0.3422   -2.5335 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8076   -0.0052   -3.2147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3190   -0.0117   -2.2377 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3990   -0.3245   -0.9358 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3401    0.4479    0.1398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6835   -0.0357    0.1192 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6424    0.4618    0.9866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2571    1.3565    1.7839 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0340   -0.0600    0.9434 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0824   -1.0342   -0.0632 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9199    1.0730    0.5672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4447    1.5574   -0.8103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3788    0.7425    0.4546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3608   -0.7175    2.2631 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5547   -1.6214    2.2199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3524    0.1586    3.3379 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8141    0.2036   -1.1236 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7272    2.0137   -0.7296 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9214    0.4139   -1.0311 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9847    1.7882   -0.3567 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2920    1.2714    1.4441 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9117    0.4513    3.4386 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3555   -0.4025    3.7931 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7382   -1.3099    3.0187 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3086   -1.4460    0.1042 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3118   -1.8097   -1.7647 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6728   -2.4709   -1.9177 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9945    0.0393   -3.0154 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8331   -1.0906   -3.8613 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5493    0.7145   -4.0238 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8892   -1.0072   -3.6852 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8157    0.9833   -2.1954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1105   -0.7511   -2.4632 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3966   -1.4108   -0.7170 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1216    0.3330    1.1304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3353    1.5175   -0.1855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1964   -1.4401   -0.1409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8274    1.9339    1.2525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8746    0.7769   -1.3402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7662    2.4450   -0.6759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2777    1.8692   -1.4442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8986    1.6967    0.1396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6164   -0.0180   -0.3047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8478    0.4669    1.4002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4775   -1.4052    2.4582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9662   -1.7542    1.2047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3215   -2.6752    2.5608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3588   -1.3022    2.9315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2329    1.0701    2.9850 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8081    1.2132   -0.6778 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
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  6
 19 21  1  0
 21 22  1  0
 21 23  1  0
 19 24  1  0
 24 25  1  0
 24 26  1  0
 14 27  1  0
 27  8  1  0
 27 11  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  4 32  1  0
  4 33  1  0
  4 34  1  0
  8 35  1  1
  9 36  1  0
  9 37  1  0
 10 38  1  0
 10 39  1  0
 12 40  1  0
 12 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  1
 15 45  1  0
 15 46  1  0
 20 47  1  0
 21 48  1  0
 22 49  1  0
 22 50  1  0
 22 51  1  0
 23 52  1  0
 23 53  1  0
 23 54  1  0
 24 55  1  1
 25 56  1  0
 25 57  1  0
 25 58  1  0
 26 59  1  0
 27 60  1  1
M  END


  Mrv1652309112205332D          

 27 28  0  0  1  0            999 V2000
   -1.4063   -2.2216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8543   -2.8347    0.0000 C   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 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2076   -1.8785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3444   -1.2654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0146   -1.7070    0.0000 O   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  2  0  0  0  0  0  0  0  0  0
    3.0937   -1.7070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5417   -2.3201    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7966   -3.1047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2446   -3.7178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6036   -3.2762    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7751   -2.4693    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4321   -4.0832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0452   -4.6352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6475   -4.3382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4106   -3.4478    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9626   -2.8347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6655   -4.2324    0.0000 O   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
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 19 17  1  1  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  6  0  0  0
 14 27  1  0  0  0  0
  8 27  1  0  0  0  0
 27 11  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0309163

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(\C)C(=O)O[C@@H]1CCN2CC[C@H](COC(=O)[C@](O)(C(C)C)[C@H](C)O)[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C20H33NO6/c1-6-13(4)18(23)27-16-8-10-21-9-7-15(17(16)21)11-26-19(24)20(25,12(2)3)14(5)22/h6,12,14-17,22,25H,7-11H2,1-5H3/b13-6-/t14-,15+,16+,17-,20-/m0/s1

> <INCHI_KEY>
YPKVTWPOGHRQRB-BSQCWQGTSA-N

> <FORMULA>
C20H33NO6

> <MOLECULAR_WEIGHT>
383.485

> <EXACT_MASS>
383.230787787

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
41.06006451647248

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,7S,7aS)-7-({[(2S)-2-hydroxy-2-[(1S)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1H-pyrrolizin-1-yl (2Z)-2-methylbut-2-enoate

> <JCHEM_LOGP>
1.9791897993333336

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.800919445712896

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.34591283068262

> <JCHEM_PKA_STRONGEST_BASIC>
8.989782568415162

> <JCHEM_POLAR_SURFACE_AREA>
96.3

> <JCHEM_REFRACTIVITY>
101.20850000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,7S,7aS)-7-({[(2S)-2-hydroxy-2-[(1S)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1H-pyrrolizin-1-yl (2Z)-2-methylbut-2-enoate

> <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      -2.625  -4.147   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.595  -5.291   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.088  -4.971   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.942  -6.116   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.388  -3.507   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -0.643  -2.362   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       1.894  -3.186   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.370  -1.722   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.465  -0.476   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.370   0.770   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       3.834   0.294   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       5.299   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.204  -0.476   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.299  -1.722   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.775  -3.186   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.744  -4.331   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.220  -5.795   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.190  -6.940   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.727  -6.116   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       7.047  -4.609   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.407  -7.622   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.551  -8.652   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.942  -8.098   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.233  -6.436   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.264  -5.291   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       8.709  -7.900   0.000  0.00  0.00           O+0
HETATM   27  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   27                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   27                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   27                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21   24                                             
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   19   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   14    8   11                                                  
MASTER        0    0    0    0    0    0    0    0   27    0   56    0
END

View in JSmol

Synonyms

Value	Source
(1R,7S,7AS)-7-({[(2S)-2-hydroxy-2-[(1S)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1H-pyrrolizin-1-yl (2Z)-2-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₀H₃₃NO₆

Average Mass

383.4850 Da

Monoisotopic Mass

383.23079 Da

IUPAC Name

(1R,7S,7aS)-7-({[(2S)-2-hydroxy-2-[(1S)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1H-pyrrolizin-1-yl (2Z)-2-methylbut-2-enoate

Traditional Name

(1R,7S,7aS)-7-({[(2S)-2-hydroxy-2-[(1S)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1H-pyrrolizin-1-yl (2Z)-2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

C\C=C(\C)C(=O)O[C@@H]1CCN2CC[C@H](COC(=O)[C@](O)(C(C)C)[C@H](C)O)[C@@H]12

InChI Identifier

InChI=1S/C20H33NO6/c1-6-13(4)18(23)27-16-8-10-21-9-7-15(17(16)21)11-26-19(24)20(25,12(2)3)14(5)22/h6,12,14-17,22,25H,7-11H2,1-5H3/b13-6-/t14-,15+,16+,17-,20-/m0/s1

InChI Key

YPKVTWPOGHRQRB-BSQCWQGTSA-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
Liatris punctata	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
Beta-hydroxy acid
Fatty acid ester
Dicarboxylic acid or derivatives
Hydroxy acid
N-alkylpyrrolidine
Fatty acyl
Pyrrolidine
Tertiary alcohol
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Tertiary amine
Secondary alcohol
Tertiary aliphatic amine
1,2-diol
Amino acid or derivatives
Carboxylic acid ester
Azacycle
Carboxylic acid derivative
Amine
Organopnictogen compound
Organic oxygen compound
Organic oxide
Organonitrogen compound
Carbonyl group
Organic nitrogen compound
Organooxygen compound
Hydrocarbon derivative
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
logP	1.98	ChemAxon
pKa (Strongest Acidic)	11.35	ChemAxon
pKa (Strongest Basic)	8.99	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	96.3 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	101.21 m³·mol⁻¹	ChemAxon
Polarizability	41.06 Å³	ChemAxon
Number of Rings	2	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

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

162995081

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,7s,7as)-7-({[(2s)-2-hydroxy-2-[(1s)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1h-pyrrolizin-1-yl (2z)-2-methylbut-2-enoate (NP0309163)

MOL for NP0309163 ((1r,7s,7as)-7-({[(2s)-2-hydroxy-2-[(1s)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1h-pyrrolizin-1-yl (2z)-2-methylbut-2-enoate)

3D MOL for NP0309163 ((1r,7s,7as)-7-({[(2s)-2-hydroxy-2-[(1s)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1h-pyrrolizin-1-yl (2z)-2-methylbut-2-enoate)

3D SDF for NP0309163 ((1r,7s,7as)-7-({[(2s)-2-hydroxy-2-[(1s)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1h-pyrrolizin-1-yl (2z)-2-methylbut-2-enoate)

3D-SDF for NP0309163 ((1r,7s,7as)-7-({[(2s)-2-hydroxy-2-[(1s)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1h-pyrrolizin-1-yl (2z)-2-methylbut-2-enoate)

PDB for NP0309163 ((1r,7s,7as)-7-({[(2s)-2-hydroxy-2-[(1s)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1h-pyrrolizin-1-yl (2z)-2-methylbut-2-enoate)

3D PDB for NP0309163 ((1r,7s,7as)-7-({[(2s)-2-hydroxy-2-[(1s)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1h-pyrrolizin-1-yl (2z)-2-methylbut-2-enoate)

SMILES for NP0309163 ((1r,7s,7as)-7-({[(2s)-2-hydroxy-2-[(1s)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1h-pyrrolizin-1-yl (2z)-2-methylbut-2-enoate)

INCHI for NP0309163 ((1r,7s,7as)-7-({[(2s)-2-hydroxy-2-[(1s)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1h-pyrrolizin-1-yl (2z)-2-methylbut-2-enoate)

Structure for NP0309163 ((1r,7s,7as)-7-({[(2s)-2-hydroxy-2-[(1s)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1h-pyrrolizin-1-yl (2z)-2-methylbut-2-enoate)

3D Structure for NP0309163 ((1r,7s,7as)-7-({[(2s)-2-hydroxy-2-[(1s)-1-hydroxyethyl]-3-methylbutanoyl]oxy}methyl)-hexahydro-1h-pyrrolizin-1-yl (2z)-2-methylbut-2-enoate)