NP-MRD: Showing NP-Card for {7-[(2,3-dihydroxy-2-methylbutanoyl)oxy]-5,6,7,7a-tetrahydro-3h-pyrrolizin-1-yl}methyl 2,3-dihydroxy-2-isopropylbutanoate (NP0322400)

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Record Information

Version

1.0

Created at

2022-09-12 01:09:00 UTC

Updated at

2022-09-12 01:09:01 UTC

NP-MRD ID

NP0322400

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{7-[(2,3-dihydroxy-2-methylbutanoyl)oxy]-5,6,7,7a-tetrahydro-3h-pyrrolizin-1-yl}methyl 2,3-dihydroxy-2-isopropylbutanoate

Description

{1-[(2,3-Dihydroxy-2-methylbutanoyl)oxy]-2,3,5,7a-tetrahydro-1H-pyrrolizin-7-yl}methyl 2,3-dihydroxy-2-(propan-2-yl)butanoate belongs to the class of organic compounds known as alkaloids and derivatives. These are naturally occurring chemical compounds that contain mostly basic nitrogen atoms. This group also includes some related compounds with neutral and even weakly acidic properties. Also some synthetic compounds of similar structure are attributed to alkaloids. In addition to carbon, hydrogen and nitrogen, alkaloids may also contain oxygen, sulfur and more rarely other elements such as chlorine, bromine, and phosphorus. {7-[(2,3-dihydroxy-2-methylbutanoyl)oxy]-5,6,7,7a-tetrahydro-3h-pyrrolizin-1-yl}methyl 2,3-dihydroxy-2-isopropylbutanoate is found in Cryptantha leiocarpa. {1-[(2,3-Dihydroxy-2-methylbutanoyl)oxy]-2,3,5,7a-tetrahydro-1H-pyrrolizin-7-yl}methyl 2,3-dihydroxy-2-(propan-2-yl)butanoate is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161523032D          

 29 30  0  0  0  0            999 V2000
   -1.9162   -3.7908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6612   -3.0062    0.0000 C   0  0  0  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  0  0  0  0  0  0  0  0  0  0
   -0.6827   -3.6416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0258   -2.0277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4127   -1.4757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8104   -1.7728    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  0  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
    3.0937   -1.7070    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9007   -1.8785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4527   -1.2654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1556   -2.6631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3710   -2.9181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9403   -2.4082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4106   -3.4478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2175   -3.6193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8585   -4.0609    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542   -0.6674    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  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  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 19 29  1  0  0  0  0
 13 29  1  0  0  0  0
 16 29  1  0  0  0  0
M  END

     RDKit          3D

 62 63  0  0  0  0  0  0  0  0999 V2000
   -5.4097   -1.4427    0.4341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6063   -1.9678   -0.7118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5268   -2.6523   -1.6880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6440   -1.0278   -1.3334 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9865   -1.6826   -2.3884 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5742   -0.6753   -0.3645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8835   -0.0611    0.6831 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2395   -0.9921   -0.5584 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2316   -0.6618    0.3418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0240    0.7778    0.5725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6300    1.8413    0.0684 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0139    3.0886    0.6575 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4170    2.5428    1.9544 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4793    3.3757    2.4479 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6361    3.0316    1.5501 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2542    1.7646    0.8043 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3462    0.8456    0.9644 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0181    0.3364   -0.1391 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6167    0.7239   -1.2627 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1365   -0.6013   -0.0488 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3250   -0.0315    0.6957 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5802   -0.9124   -1.3313 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7678   -1.9081    0.6143 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5051   -1.7632    2.0884 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7673   -2.5898   -0.0610 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0179    1.3003    1.5108 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2073    0.2301   -1.8944 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9963    0.0101   -3.1672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8997    1.0198   -0.9848 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4969   -2.1913    1.2673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1504   -0.4470    0.7935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4797   -1.3474    0.0764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9810   -2.8083   -0.2779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3393   -2.0304   -2.0579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0085   -3.4984   -1.1143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9478   -3.1747   -2.4963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4713   -2.4475   -1.9878 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7401   -1.1115   -0.0188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4147   -1.1988    1.3183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4346    1.7937   -0.6557 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6617    3.1064    3.5110 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8647    3.8598    0.8493 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5327    2.8818    2.1944 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1176    1.9293   -0.2705 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9271    0.6192    1.5092 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0001   -0.8067    1.0734 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8894    0.6584    0.0221 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1162   -0.1987   -1.7171 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6877   -2.5590    0.5270 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7563   -0.9992    2.3381 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0725   -2.7520    2.4196 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4469   -1.6581    2.6603 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6880   -2.2581   -1.0113 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2176    0.5963    2.3359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3187    0.8587   -2.2046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7356   -1.0188   -3.5289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0731    0.1627   -3.0330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6797    0.6904   -3.9918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3833    1.7077   -1.5443 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  6
  4 27  1  0
 27 28  1  0
 27 29  1  0
  4  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
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 20 22  1  6
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 23 24  1  0
 23 25  1  0
 16 26  1  0
 26 10  1  0
 26 13  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  3 34  1  0
  3 35  1  0
  3 36  1  0
  5 37  1  0
 27 58  1  6
 28 59  1  0
 28 60  1  0
 28 61  1  0
 29 62  1  0
  9 38  1  0
  9 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 14 43  1  0
 14 44  1  0
 15 45  1  0
 15 46  1  0
 16 47  1  6
 21 48  1  0
 21 49  1  0
 21 50  1  0
 22 51  1  0
 23 52  1  1
 24 53  1  0
 24 54  1  0
 24 55  1  0
 25 56  1  0
 26 57  1  1
M  END


  Mrv1533004161523032D          

 29 30  0  0  0  0            999 V2000
   -1.9162   -3.7908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6612   -3.0062    0.0000 C   0  0  0  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  0  0  0  0  0  0  0  0  0  0
   -0.6827   -3.6416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0258   -2.0277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4127   -1.4757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8104   -1.7728    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  0  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
    3.0937   -1.7070    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9007   -1.8785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.1556   -2.6631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3710   -2.9181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9403   -2.4082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4106   -3.4478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2175   -3.6193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8585   -4.0609    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542   -0.6674    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  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  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 19 29  1  0  0  0  0
 13 29  1  0  0  0  0
 16 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0322400

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C(O)(C(C)O)C(=O)OCC1=CCN2CCC(OC(=O)C(C)(O)C(C)O)C12

> <INCHI_IDENTIFIER>
InChI=1S/C20H33NO8/c1-11(2)20(27,13(4)23)18(25)28-10-14-6-8-21-9-7-15(16(14)21)29-17(24)19(5,26)12(3)22/h6,11-13,15-16,22-23,26-27H,7-10H2,1-5H3

> <INCHI_KEY>
JRIDDIGGYCXEIK-UHFFFAOYSA-N

> <FORMULA>
C20H33NO8

> <MOLECULAR_WEIGHT>
415.483

> <EXACT_MASS>
415.220617027

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
42.636877285378965

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
{1-[(2,3-dihydroxy-2-methylbutanoyl)oxy]-2,3,5,7a-tetrahydro-1H-pyrrolizin-7-yl}methyl 2,3-dihydroxy-2-(propan-2-yl)butanoate

> <ALOGPS_LOGP>
0.60

> <JCHEM_LOGP>
-0.296042443

> <ALOGPS_LOGS>
-1.89

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
11.83834385308712

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.175733984090124

> <JCHEM_PKA_STRONGEST_BASIC>
6.922769774430446

> <JCHEM_POLAR_SURFACE_AREA>
136.76000000000002

> <JCHEM_REFRACTIVITY>
103.96590000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.32e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{7-[(2,3-dihydroxy-2-methylbutanoyl)oxy]-5,6,7,7a-tetrahydro-3H-pyrrolizin-1-yl}methyl 2,3-dihydroxy-2-isopropylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      -3.577  -7.076   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.101  -5.612   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.131  -4.467   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.595  -5.291   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -1.274  -6.798   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -1.915  -3.785   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.770  -2.755   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -3.379  -3.309   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.088  -4.971   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.942  -6.116   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       0.388  -3.507   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.894  -3.186   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.370  -1.722   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.465  -0.476   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.370   0.770   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       3.834   0.294   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       5.299   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.204  -0.476   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.299  -1.722   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.775  -3.186   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.281  -3.507   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.312  -2.362   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       7.757  -4.971   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.293  -5.447   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       9.222  -4.495   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.233  -6.436   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.739  -6.756   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       7.203  -7.580   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       3.834  -1.246   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6    9                                             
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    4   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   29                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   29                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   29                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25   26                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   23   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   19   13   16                                                  
MASTER        0    0    0    0    0    0    0    0   29    0   60    0
END

View in JSmol

Synonyms

Value	Source
{1-[(2,3-dihydroxy-2-methylbutanoyl)oxy]-2,3,5,7a-tetrahydro-1H-pyrrolizin-7-yl}methyl 2,3-dihydroxy-2-(propan-2-yl)butanoic acid	Generator

Chemical Formula

C₂₀H₃₃NO₈

Average Mass

415.4830 Da

Monoisotopic Mass

415.22062 Da

IUPAC Name

{1-[(2,3-dihydroxy-2-methylbutanoyl)oxy]-2,3,5,7a-tetrahydro-1H-pyrrolizin-7-yl}methyl 2,3-dihydroxy-2-(propan-2-yl)butanoate

Traditional Name

{7-[(2,3-dihydroxy-2-methylbutanoyl)oxy]-5,6,7,7a-tetrahydro-3H-pyrrolizin-1-yl}methyl 2,3-dihydroxy-2-isopropylbutanoate

CAS Registry Number

Not Available

SMILES

CC(C)C(O)(C(C)O)C(=O)OCC1=CCN2CCC(OC(=O)C(C)(O)C(C)O)C12

InChI Identifier

InChI=1S/C20H33NO8/c1-11(2)20(27,13(4)23)18(25)28-10-14-6-8-21-9-7-15(16(14)21)29-17(24)19(5,26)12(3)22/h6,11-13,15-16,22-23,26-27H,7-10H2,1-5H3

InChI Key

JRIDDIGGYCXEIK-UHFFFAOYSA-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
Cryptantha leiocarpa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkaloids and derivatives. These are naturally occurring chemical compounds that contain mostly basic nitrogen atoms. This group also includes some related compounds with neutral and even weakly acidic properties. Also some synthetic compounds of similar structure are attributed to alkaloids. In addition to carbon, hydrogen and nitrogen, alkaloids may also contain oxygen, sulfur and more rarely other elements such as chlorine, bromine, and phosphorus.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Not Available

Sub Class

Not Available

Direct Parent

Alkaloids and derivatives

Alternative Parents

Substituents

Alkaloid or derivatives
Pyrrolizine
Beta-hydroxy acid
Fatty acid ester
Dicarboxylic acid or derivatives
Hydroxy acid
N-alkylpyrrolidine
Fatty acyl
Tertiary alcohol
Pyrroline
Pyrrolidine
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Amino acid or derivatives
Carboxylic acid ester
Organoheterocyclic compound
Azacycle
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxygen compound
Alcohol
Organonitrogen compound
Organooxygen compound
Carbonyl group
Organic nitrogen compound
Organopnictogen compound
Organic oxide
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
logP	0.6	ALOGPS
logP	-0.3	ChemAxon
logS	-1.9	ALOGPS
pKa (Strongest Acidic)	11.18	ChemAxon
pKa (Strongest Basic)	6.92	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	136.76 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	103.97 m³·mol⁻¹	ChemAxon
Polarizability	42.64 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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for {7-[(2,3-dihydroxy-2-methylbutanoyl)oxy]-5,6,7,7a-tetrahydro-3h-pyrrolizin-1-yl}methyl 2,3-dihydroxy-2-isopropylbutanoate (NP0322400)

MOL for NP0322400 ({7-[(2,3-dihydroxy-2-methylbutanoyl)oxy]-5,6,7,7a-tetrahydro-3h-pyrrolizin-1-yl}methyl 2,3-dihydroxy-2-isopropylbutanoate)

3D MOL for NP0322400 ({7-[(2,3-dihydroxy-2-methylbutanoyl)oxy]-5,6,7,7a-tetrahydro-3h-pyrrolizin-1-yl}methyl 2,3-dihydroxy-2-isopropylbutanoate)

3D SDF for NP0322400 ({7-[(2,3-dihydroxy-2-methylbutanoyl)oxy]-5,6,7,7a-tetrahydro-3h-pyrrolizin-1-yl}methyl 2,3-dihydroxy-2-isopropylbutanoate)

3D-SDF for NP0322400 ({7-[(2,3-dihydroxy-2-methylbutanoyl)oxy]-5,6,7,7a-tetrahydro-3h-pyrrolizin-1-yl}methyl 2,3-dihydroxy-2-isopropylbutanoate)

PDB for NP0322400 ({7-[(2,3-dihydroxy-2-methylbutanoyl)oxy]-5,6,7,7a-tetrahydro-3h-pyrrolizin-1-yl}methyl 2,3-dihydroxy-2-isopropylbutanoate)

3D PDB for NP0322400 ({7-[(2,3-dihydroxy-2-methylbutanoyl)oxy]-5,6,7,7a-tetrahydro-3h-pyrrolizin-1-yl}methyl 2,3-dihydroxy-2-isopropylbutanoate)

SMILES for NP0322400 ({7-[(2,3-dihydroxy-2-methylbutanoyl)oxy]-5,6,7,7a-tetrahydro-3h-pyrrolizin-1-yl}methyl 2,3-dihydroxy-2-isopropylbutanoate)

INCHI for NP0322400 ({7-[(2,3-dihydroxy-2-methylbutanoyl)oxy]-5,6,7,7a-tetrahydro-3h-pyrrolizin-1-yl}methyl 2,3-dihydroxy-2-isopropylbutanoate)

Structure for NP0322400 ({7-[(2,3-dihydroxy-2-methylbutanoyl)oxy]-5,6,7,7a-tetrahydro-3h-pyrrolizin-1-yl}methyl 2,3-dihydroxy-2-isopropylbutanoate)

3D Structure for NP0322400 ({7-[(2,3-dihydroxy-2-methylbutanoyl)oxy]-5,6,7,7a-tetrahydro-3h-pyrrolizin-1-yl}methyl 2,3-dihydroxy-2-isopropylbutanoate)