NP-MRD: Showing NP-Card for 2-{[(2s,3r,4s,5s,6s)-6-{[(2s,3s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile (NP0256040)

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Record Information

Version

2.0

Created at

2022-09-07 20:44:52 UTC

Updated at

2022-09-07 20:44:52 UTC

NP-MRD ID

NP0256040

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{[(2s,3r,4s,5s,6s)-6-{[(2s,3s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile

Description

2-{[(2S,3R,4S,5S,6S)-6-{[(2S,3S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile belongs to the class of organic compounds known as cyanogenic glycosides. These are glycosides in which the aglycone moiety contains a cyanide group. 2-{[(2s,3r,4s,5s,6s)-6-{[(2s,3s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile is found in Manihot esculenta. Based on a literature review very few articles have been published on 2-{[(2S,3R,4S,5S,6S)-6-{[(2S,3S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072222442D          

 27 28  0  0  1  0            999 V2000
   -4.9430   -4.0345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1225   -3.9483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7869   -3.1946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0332   -3.5301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5406   -2.8590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2943   -2.5235    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4514   -2.4409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6309   -2.3547    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2953   -1.6010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4748   -1.5148    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1393   -0.7611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3188   -0.6749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6242   -0.0937    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4492   -0.0937    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7041    0.6910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367    1.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5887    1.7890    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4847    1.7890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7396    2.5736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3693    0.6910    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5846    0.9459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9899   -2.1822    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1694   -2.0960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3255   -2.9359    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8406   -3.6033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1460   -3.0221    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4815   -3.7758    0.0000 O   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
  3  5  1  0  0  0  0
  5  6  3  0  0  0  0
  3  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  6  0  0  0
 11 12  1  0  0  0  0
 13 11  1  6  0  0  0
 13 14  1  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
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 16 20  1  0  0  0  0
 13 20  1  0  0  0  0
 20 21  1  1  0  0  0
 10 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
  8 26  1  0  0  0  0
 26 27  1  1  0  0  0
M  END

     RDKit          3D

 54 55  0  0  0  0  0  0  0  0999 V2000
   -6.2552    0.7195    1.1427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9996    1.3346    0.5617 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0459    0.1907    0.1886 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7588   -0.5632    1.4690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6648   -0.7031   -0.7679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1745   -1.4040   -1.5291 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9125    0.7898   -0.3331 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9433   -0.1230   -0.7224 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7913    0.0565    0.0512 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2059   -0.7927   -0.4216 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3484   -0.9554    0.5135 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2774   -1.8169   -0.0659 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0185    0.3161    0.9290 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6150    1.0152   -0.0789 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9264    0.6465   -0.2190 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3507   -0.0762    1.0142 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7411   -1.4025    0.7684 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5629    0.6102    1.6263 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5956    0.5254    0.6857 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1447    0.0210    1.8927 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2243    1.0522    2.8143 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6722   -0.4680   -1.8023 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5099   -1.5421   -2.6873 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2135    0.6792   -2.3102 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0392    1.8037   -1.5293 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6406    0.1255   -2.1914 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6043   -1.1008   -2.8909 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3353   -0.3477    0.8158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1687    1.2558    0.7564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2510    0.8267    2.2368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5620    1.9942    1.3083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3123    1.8865   -0.3603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7034   -1.6523    1.2106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6293   -0.4666    2.1652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8024   -0.2580    1.9305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2866   -1.1570   -0.5310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2949   -1.8057   -0.4843 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0002   -1.5003    1.4405 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8311   -2.6786   -0.3114 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2896    0.9597    1.4643 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1352    0.0696   -1.1603 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5243    1.5952   -0.3404 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1723   -1.7113    1.6276 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3866    1.6929    1.7919 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8885    0.0855    2.5513 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2216    0.3863   -0.2290 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9398   -0.9115    2.4575 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0925    1.9541    2.4049 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6999   -0.1314   -1.8956 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0794   -1.4195   -3.4850 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0367    0.8166   -3.3701 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6132    2.3941   -1.9857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3024    0.8552   -2.6534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4121   -1.1150   -3.4632 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  6
 16 18  1  0
 18 19  1  0
 16 20  1  0
 20 21  1  0
 10 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
  3  5  1  6
  5  6  3  0
 26  8  1  0
 20 13  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  4 33  1  0
  4 34  1  0
  4 35  1  0
  8 36  1  6
 10 37  1  6
 11 38  1  1
 12 39  1  0
 13 40  1  1
 15 41  1  0
 15 42  1  0
 17 43  1  0
 18 44  1  0
 18 45  1  0
 19 46  1  0
 20 47  1  1
 21 48  1  0
 22 49  1  1
 23 50  1  0
 24 51  1  6
 25 52  1  0
 26 53  1  6
 27 54  1  0
M  END


  Mrv1652309072222442D          

 27 28  0  0  1  0            999 V2000
   -4.9430   -4.0345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1225   -3.9483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7869   -3.1946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0332   -3.5301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5406   -2.8590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2943   -2.5235    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4514   -2.4409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6309   -2.3547    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2953   -1.6010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4748   -1.5148    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1393   -0.7611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3188   -0.6749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6242   -0.0937    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4492   -0.0937    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7041    0.6910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367    1.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5887    1.7890    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4847    1.7890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7396    2.5736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3693    0.6910    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5846    0.9459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9899   -2.1822    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1694   -2.0960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3255   -2.9359    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8406   -3.6033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1460   -3.0221    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4815   -3.7758    0.0000 O   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
  3  5  1  0  0  0  0
  5  6  3  0  0  0  0
  3  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  6  0  0  0
 11 12  1  0  0  0  0
 13 11  1  6  0  0  0
 13 14  1  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
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 16 20  1  0  0  0  0
 13 20  1  0  0  0  0
 20 21  1  1  0  0  0
 10 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
  8 26  1  0  0  0  0
 26 27  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0256040

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)(O[C@@H]1O[C@H](C(O)[C@@H]2OCC(O)(CO)[C@H]2O)[C@@H](O)[C@H](O)[C@H]1O)C#N

> <INCHI_IDENTIFIER>
InChI=1S/C16H27NO10/c1-3-15(2,4-17)27-14-9(21)7(19)8(20)11(26-14)10(22)12-13(23)16(24,5-18)6-25-12/h7-14,18-24H,3,5-6H2,1-2H3/t7-,8-,9+,10?,11-,12-,13-,14-,15?,16?/m0/s1

> <INCHI_KEY>
MIRNGICCHAQGMM-ULPCSGKVSA-N

> <FORMULA>
C16H27NO10

> <MOLECULAR_WEIGHT>
393.389

> <EXACT_MASS>
393.163496073

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
38.04677770214826

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-{[(2S,3R,4S,5S,6S)-6-{[(2S,3S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile

> <JCHEM_LOGP>
-3.355397510000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.367762993237303

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.847769097145214

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1403738988538183

> <JCHEM_POLAR_SURFACE_AREA>
193.08999999999997

> <JCHEM_REFRACTIVITY>
85.99150000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-{[(2S,3R,4S,5S,6S)-6-{[(2S,3S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -9.227  -7.531   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -7.695  -7.370   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.069  -5.963   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.662  -6.590   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -8.476  -5.337   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      -9.883  -4.710   0.000  0.00  0.00           N+0
HETATM    7  O   UNK     0      -6.443  -4.556   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -4.911  -4.395   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -4.285  -2.989   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -2.753  -2.828   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.127  -1.421   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.595  -1.260   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -3.032  -0.175   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -4.572  -0.175   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -5.048   1.290   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.802   2.195   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -4.832   3.339   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -2.771   3.339   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -3.247   4.804   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -2.556   1.290   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.091   1.766   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -1.848  -4.073   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.316  -3.912   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -2.474  -5.480   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -1.569  -6.726   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -4.006  -5.641   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -4.632  -7.048   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5    7                                             
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5                                                            
CONECT    7    3    8                                                       
CONECT    8    7    9   26                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   22                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   20                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   20                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18                                                            
CONECT   20   16   13   21                                                  
CONECT   21   20                                                            
CONECT   22   10   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24    8   27                                                  
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₇NO₁₀

Average Mass

393.3890 Da

Monoisotopic Mass

393.16350 Da

IUPAC Name

2-{[(2S,3R,4S,5S,6S)-6-{[(2S,3S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile

Traditional Name

2-{[(2S,3R,4S,5S,6S)-6-{[(2S,3S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile

CAS Registry Number

Not Available

SMILES

CCC(C)(O[C@@H]1O[C@H](C(O)[C@@H]2OCC(O)(CO)[C@H]2O)[C@@H](O)[C@H](O)[C@H]1O)C#N

InChI Identifier

InChI=1S/C16H27NO10/c1-3-15(2,4-17)27-14-9(21)7(19)8(20)11(26-14)10(22)12-13(23)16(24,5-18)6-25-12/h7-14,18-24H,3,5-6H2,1-2H3/t7-,8-,9+,10?,11-,12-,13-,14-,15?,16?/m0/s1

InChI Key

MIRNGICCHAQGMM-ULPCSGKVSA-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
Manihot esculenta	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyanogenic glycosides. These are glycosides in which the aglycone moiety contains a cyanide group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Cyanogenic glycosides

Alternative Parents

Substituents

Cyanogenic glycoside
O-glycosyl compound
Oxane
Monosaccharide
Tetrahydrofuran
Tertiary alcohol
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Polyol
Nitrile
Carbonitrile
Ether
Dialkyl ether
Acetal
Organic nitrogen compound
Organopnictogen compound
Hydrocarbon derivative
Primary alcohol
Organonitrogen compound
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	-3.4	ChemAxon
pKa (Strongest Acidic)	11.85	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	193.09 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	85.99 m³·mol⁻¹	ChemAxon
Polarizability	38.05 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

163190440

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{[(2s,3r,4s,5s,6s)-6-{[(2s,3s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile (NP0256040)

MOL for NP0256040 (2-{[(2s,3r,4s,5s,6s)-6-{[(2s,3s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile)

3D MOL for NP0256040 (2-{[(2s,3r,4s,5s,6s)-6-{[(2s,3s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile)

3D SDF for NP0256040 (2-{[(2s,3r,4s,5s,6s)-6-{[(2s,3s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile)

3D-SDF for NP0256040 (2-{[(2s,3r,4s,5s,6s)-6-{[(2s,3s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile)

PDB for NP0256040 (2-{[(2s,3r,4s,5s,6s)-6-{[(2s,3s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile)

3D PDB for NP0256040 (2-{[(2s,3r,4s,5s,6s)-6-{[(2s,3s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile)

SMILES for NP0256040 (2-{[(2s,3r,4s,5s,6s)-6-{[(2s,3s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile)

INCHI for NP0256040 (2-{[(2s,3r,4s,5s,6s)-6-{[(2s,3s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile)

Structure for NP0256040 (2-{[(2s,3r,4s,5s,6s)-6-{[(2s,3s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile)

3D Structure for NP0256040 (2-{[(2s,3r,4s,5s,6s)-6-{[(2s,3s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl](hydroxy)methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-2-methylbutanenitrile)