NP-MRD: Showing NP-Card for 8-(Methylsulfonyl)octyl glucosinolate (NP0055223)

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Record Information

Version

2.0

Created at

2022-04-28 01:21:00 UTC

Updated at

2022-04-28 01:21:00 UTC

NP-MRD ID

NP0055223

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8-(Methylsulfonyl)octyl glucosinolate

Description

{[(Z)-(9-methanesulfonyl-1-{[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}nonylidene)amino]oxy}sulfonic acid belongs to the class of organic compounds known as alkylglucosinolates. These are organic compounds containing a glucosinolate moiety that carries an alkyl chain. 8-(Methylsulfonyl)octyl glucosinolate is found in Arabis turrita, Heliophila amplexicaulis and Sinapis arvensis . Based on a literature review very few articles have been published on {[(Z)-(9-methanesulfonyl-1-{[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}nonylidene)amino]oxy}sulfonic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282203212D          

 31 31  0  0  1  0            999 V2000
   -3.5724    6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    5.3625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579    4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579    4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724    3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868    4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0013    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    2.8875    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    1.6500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    1.6500    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8743    2.3645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6993    0.9355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.8875    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9849    2.1730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1599    3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  5 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  2  0  0  0  0
 14 17  1  0  0  0  0
 11 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
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  2  0  0  0  0
 26 29  1  0  0  0  0
  4 30  1  1  0  0  0
  3 31  1  1  0  0  0
M  END

     RDKit          3D

 62 62  0  0  0  0  0  0  0  0999 V2000
    8.7093    0.1516    1.1237 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1398    0.6628    1.7747 S   0  0  2  0  0  6  0  0  0  0  0  0
    7.2667    1.8989    2.5919 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6191   -0.4780    2.6109 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0473    0.8973    0.3906 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9292   -0.4155   -0.3479 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0349   -0.3504   -1.5419 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6073    0.0481   -1.2097 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9543   -0.9014   -0.2699 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5519   -0.4531    0.0423 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6759   -0.3774   -1.1659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7305    0.0643   -0.8560 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4860   -0.8109    0.0331 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0019   -1.9452    0.3941 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6945   -2.8068    1.2417 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9499   -2.3464    2.8610 S   0  0  2  0  0  6  0  0  0  0  0  0
   -1.5929   -3.5066    3.7640 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4014   -2.0100    3.0151 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0067   -1.0141    3.2511 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1081   -0.4136    0.6638 S   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7199    1.1632    0.0701 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9834    1.2367   -1.2561 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0994    0.6435   -1.7477 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7296   -0.6101   -2.5464 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0689   -1.5474   -1.7856 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2385    0.4085   -0.8300 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.4046    1.1196   -1.2011 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0010    0.6136    0.6181 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.6456   -0.5940    1.2319 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8967    1.6151    0.8978 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5514    1.5246    2.2271 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5186    0.2041    1.8790 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6347   -0.9227    0.8005 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0184    0.7495    0.2498 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4257    1.6936   -0.2752 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0290    1.1224    0.7919 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9402   -0.6830   -0.7028 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5483   -1.1805    0.3786 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4351    0.4198   -2.2346 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0248   -1.3377   -2.0202 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5504    1.0680   -0.8180 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0667   -0.0030   -2.1965 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9411   -1.9052   -0.7471 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5031   -0.9892    0.6936 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1293   -1.1781    0.7772 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5843    0.5320    0.5796 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6052   -1.4354   -1.5629 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1130    0.2110   -2.0002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6998    1.0740   -0.3566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2288    0.2181   -1.8395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5936   -0.2178    3.2484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9079    1.9224    0.2785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4865    1.3445   -2.5531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1422   -0.3389   -3.4474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6619   -1.1066   -2.9296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3299   -1.9192   -2.3322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5454   -0.6732   -0.9544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3672    1.4230   -2.1382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9376    0.9520    1.1029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2977   -1.2976    1.0662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2131    2.6439    0.6133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8813    0.6740    2.6044 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  2  0
  2  4  2  0
  2  5  1  0
  5  6  1  0
  6  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 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 23 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 13 14  2  0
 14 15  1  0
 16 15  1  6
 16 19  1  0
 16 17  2  0
 16 18  2  0
 30 21  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  5 35  1  0
  5 36  1  0
  6 37  1  0
  6 38  1  0
  7 39  1  0
  7 40  1  0
  8 41  1  0
  8 42  1  0
  9 43  1  0
  9 44  1  0
 10 45  1  0
 10 46  1  0
 11 47  1  0
 11 48  1  0
 12 49  1  0
 12 50  1  0
 21 52  1  6
 23 53  1  6
 24 54  1  0
 24 55  1  0
 25 56  1  0
 26 57  1  1
 27 58  1  0
 28 59  1  1
 29 60  1  0
 30 61  1  6
 31 62  1  0
 19 51  1  0
M  END


  Mrv1652304282203212D          

 31 31  0  0  1  0            999 V2000
   -3.5724    6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    5.3625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579    4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579    4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724    3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868    4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0013    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    2.8875    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    1.6500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    1.6500    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8743    2.3645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6993    0.9355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.8875    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9849    2.1730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1599    3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  5 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  2  0  0  0  0
 14 17  1  0  0  0  0
 11 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
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  2  0  0  0  0
 26 29  1  0  0  0  0
  4 30  1  1  0  0  0
  3 31  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0055223

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CS(=O)(=O)CCCCCCCC\C(S[C@H]1O[C@@H](CO)[C@H](O)[C@@H](O)[C@H]1O)=N\OS(O)(=O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H31NO11S3/c1-30(22,23)9-7-5-3-2-4-6-8-12(17-28-31(24,25)26)29-16-15(21)14(20)13(19)11(10-18)27-16/h11,13-16,18-21H,2-10H2,1H3,(H,24,25,26)/b17-12-/t11-,13-,14+,15+,16+/m0/s1

> <INCHI_KEY>
OZKVQSNRAFPWMK-GWCOOYRESA-N

> <FORMULA>
C16H31NO11S3

> <MOLECULAR_WEIGHT>
509.6

> <EXACT_MASS>
509.105924344

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
50.61120894048443

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(Z)-(9-methanesulfonyl-1-{[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}nonylidene)amino]oxy}sulfonic acid

> <ALOGPS_LOGP>
-0.95

> <JCHEM_LOGP>
-2.675484218021112

> <ALOGPS_LOGS>
-2.55

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.447675813619416

> <JCHEM_PKA_STRONGEST_ACIDIC>
-3.4995284312952464

> <JCHEM_PKA_STRONGEST_BASIC>
-0.24002097073290096

> <JCHEM_POLAR_SURFACE_AREA>
200.24999999999997

> <JCHEM_REFRACTIVITY>
111.77539999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.43e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(Z)-(9-methanesulfonyl-1-{[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}nonylidene)amino]oxysulfonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  O   UNK     0      -6.668  11.550   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -6.668  10.010   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.335   9.240   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.335   7.700   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.668   6.930   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -8.002   7.700   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -8.002   9.240   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -9.336  10.010   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -9.336  11.550   0.000  0.00  0.00           O+0
HETATM   10  S   UNK     0      -6.668   5.390   0.000  0.00  0.00           S+0
HETATM   11  C   UNK     0      -5.335   4.620   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0      -5.335   3.080   0.000  0.00  0.00           N+0
HETATM   13  O   UNK     0      -6.668   2.310   0.000  0.00  0.00           O+0
HETATM   14  S   UNK     0      -8.002   3.080   0.000  0.00  0.00           S+0
HETATM   15  O   UNK     0      -7.232   4.414   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      -8.772   1.746   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -9.336   3.850   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -4.001   5.390   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.334   5.390   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334   5.390   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.001   5.390   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   26  S   UNK     0       6.668   5.390   0.000  0.00  0.00           S+0
HETATM   27  O   UNK     0       8.002   6.160   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       7.438   4.056   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       5.898   6.724   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -4.001   6.930   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -4.001  10.010   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4   31                                                  
CONECT    4    3    5   30                                                  
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    2    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    5   11                                                       
CONECT   11   10   12   18                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   14                                                            
CONECT   18   11   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28   29                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   26                                                            
CONECT   30    4                                                            
CONECT   31    3                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   62    0
END

View in JSmol

Synonyms

Value	Source
{[(Z)-(9-methanesulfonyl-1-{[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}nonylidene)amino]oxy}sulfonate	Generator
{[(Z)-(9-methanesulphonyl-1-{[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulphanyl}nonylidene)amino]oxy}sulphonate	Generator
{[(Z)-(9-methanesulphonyl-1-{[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulphanyl}nonylidene)amino]oxy}sulphonic acid	Generator

Chemical Formula

C₁₆H₃₁NO₁₁S₃

Average Mass

509.6000 Da

Monoisotopic Mass

509.10592 Da

IUPAC Name

{[(Z)-(9-methanesulfonyl-1-{[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}nonylidene)amino]oxy}sulfonic acid

Traditional Name

[(Z)-(9-methanesulfonyl-1-{[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}nonylidene)amino]oxysulfonic acid

CAS Registry Number

Not Available

SMILES

CS(=O)(=O)CCCCCCCC\C(S[C@H]1O[C@@H](CO)[C@H](O)[C@@H](O)[C@H]1O)=N\OS(O)(=O)=O

InChI Identifier

InChI=1S/C16H31NO11S3/c1-30(22,23)9-7-5-3-2-4-6-8-12(17-28-31(24,25)26)29-16-15(21)14(20)13(19)11(10-18)27-16/h11,13-16,18-21H,2-10H2,1H3,(H,24,25,26)/b17-12-/t11-,13-,14+,15+,16+/m0/s1

InChI Key

OZKVQSNRAFPWMK-GWCOOYRESA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Arabis turrita	Plant	KNApSAcK
Heliophila amplexicaulis	Plant	KNApSAcK
Sinapis arvensis	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkylglucosinolates. These are organic compounds containing a glucosinolate moiety that carries an alkyl chain.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Alkylglucosinolates

Alternative Parents

Substituents

Alkylglucosinolate
S-glycosyl compound
Glycosyl compound
Oxane
Sulfonyl
Sulfone
Organic sulfuric acid or derivatives
Monothioacetal
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Sulfenyl compound
Polyol
Organic nitrogen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organosulfur compound
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	-0.95	ALOGPS
logP	-2.7	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	-3.5	ChemAxon
pKa (Strongest Basic)	-0.24	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	200.25 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	111.78 m³·mol⁻¹	ChemAxon
Polarizability	50.61 Å³	ChemAxon
Number of Rings	1	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

154496080

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 8-(Methylsulfonyl)octyl glucosinolate (NP0055223)

MOL for NP0055223 (8-(Methylsulfonyl)octyl glucosinolate)

3D MOL for NP0055223 (8-(Methylsulfonyl)octyl glucosinolate)

3D SDF for NP0055223 (8-(Methylsulfonyl)octyl glucosinolate)

3D-SDF for NP0055223 (8-(Methylsulfonyl)octyl glucosinolate)

PDB for NP0055223 (8-(Methylsulfonyl)octyl glucosinolate)

3D PDB for NP0055223 (8-(Methylsulfonyl)octyl glucosinolate)

SMILES for NP0055223 (8-(Methylsulfonyl)octyl glucosinolate)

INCHI for NP0055223 (8-(Methylsulfonyl)octyl glucosinolate)

Structure for NP0055223 (8-(Methylsulfonyl)octyl glucosinolate)

3D Structure for NP0055223 (8-(Methylsulfonyl)octyl glucosinolate)