NP-MRD: Showing NP-Card for [(e)-(6-methanesulfinyl-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}hexylidene)amino]oxysulfonic acid (NP0309765)

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Record Information

Version

2.0

Created at

2022-09-11 04:35:14 UTC

Updated at

2022-09-11 04:35:14 UTC

NP-MRD ID

NP0309765

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(e)-(6-methanesulfinyl-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}hexylidene)amino]oxysulfonic acid

Description

Glucoalyssin belongs to the class of organic compounds known as alkylglucosinolates. These are organic compounds containing a glucosinolate moiety that carries an alkyl chain. [(e)-(6-methanesulfinyl-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}hexylidene)amino]oxysulfonic acid is found in Lepidium meyenii. [(e)-(6-methanesulfinyl-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}hexylidene)amino]oxysulfonic acid was first documented in 2017 (PMID: 30174493). Based on a literature review a small amount of articles have been published on Glucoalyssin (PMID: 29379360) (PMID: 35696949) (PMID: 34500612) (PMID: 32784853).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112206352D          

 27 27  0  0  1  0            999 V2000
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 S   0  3  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    1.2375    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    8.6842    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0342    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -1.2375    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.0026   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -3.3000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.7171   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.2881   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -3.3000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.8592   -2.0625    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
  2  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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  2  0  0  0  0
 12 15  1  0  0  0  0
  9 16  1  0  0  0  0
 17 16  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  0  0  0  0
 19 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
 17 26  1  0  0  0  0
 26 27  1  1  0  0  0
M  CHG  2   2   1   3  -1
M  END

     RDKit          3D

 52 52  0  0  0  0  0  0  0  0999 V2000
    6.4186   -1.5017   -1.9219 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3522   -1.3957   -0.1418 S   0  0  0  0  0  3  0  0  0  0  0  0
    7.1377   -0.0023    0.3418 O   0  0  0  0  0  1  0  0  0  0  0  0
    4.6861   -1.4585    0.4151 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8526   -0.3198   -0.1445 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4247   -0.3931    0.3470 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6780    0.7979   -0.2786 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2616    0.7925    0.1606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6014    1.8510   -0.3323 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1610    2.7612   -1.1059 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1297    2.8576   -1.5557 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7314    4.3584   -2.0101 S   0  0  0  0  0  6  0  0  0  0  0  0
    0.6839    5.2422   -2.6338 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8335    4.1841   -3.0175 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3402    5.2171   -0.6812 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3236    1.8393    0.1866 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6693    0.4401    1.2799 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5289   -0.7147    0.5515 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1246   -1.8272    1.0846 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9588   -2.9531    0.0536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5963   -2.5327   -1.1267 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5896   -1.6976    1.3530 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9320   -1.9345    2.6774 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0069   -0.2866    1.0069 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7859   -0.1261   -0.3619 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0910    0.6368    1.8027 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1975    0.2833    3.1453 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5733   -2.1104   -2.2858 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3402   -0.4550   -2.3045 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3611   -1.9874   -2.2363 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2588   -2.4356    0.1481 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7025   -1.4052    1.5337 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3436    0.6335    0.1575 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8998   -0.3863   -1.2468 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4742   -0.2564    1.4635 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9816   -1.3391    0.0408 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8298    0.6570   -1.3707 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1964    1.6846    0.1393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1952   -0.1863   -0.1746 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2586    0.7358    1.2766 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9045    5.9441   -1.0732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0136    0.4460    2.1781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6195   -2.1910    2.0267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9077   -3.2014   -0.1052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5308   -3.8560    0.3861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9706   -3.2999   -1.6258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2189   -2.3800    0.7283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7835   -1.4383    2.8417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0421   -0.0707    1.3050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0623    0.7757   -0.6036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4546    1.6603    1.6200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2890    0.3441    3.5304 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  6
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 15  1  0
 12 13  2  0
 12 14  2  0
 26 17  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  6 36  1  0
  7 37  1  0
  7 38  1  0
  8 39  1  0
  8 40  1  0
 17 42  1  1
 19 43  1  1
 20 44  1  0
 20 45  1  0
 21 46  1  0
 22 47  1  6
 23 48  1  0
 24 49  1  6
 25 50  1  0
 26 51  1  1
 27 52  1  0
 15 41  1  0
M  CHG  2   2   1   3  -1
M  END


  Mrv1652309112206352D          

 27 27  0  0  1  0            999 V2000
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 S   0  3  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    1.2375    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    8.6842    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0342    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -1.2375    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.0026   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -3.3000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.7171   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.2881   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -3.3000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.8592   -2.0625    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
  2  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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  2  0  0  0  0
 12 15  1  0  0  0  0
  9 16  1  0  0  0  0
 17 16  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  0  0  0  0
 19 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
 17 26  1  0  0  0  0
 26 27  1  1  0  0  0
M  CHG  2   2   1   3  -1
M  END
> <DATABASE_ID>
NP0309765

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[S+]([O-])CCCCC\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/C13H25NO10S3/c1-26(19)6-4-2-3-5-9(14-24-27(20,21)22)25-13-12(18)11(17)10(16)8(7-15)23-13/h8,10-13,15-18H,2-7H2,1H3,(H,20,21,22)/b14-9+/t8-,10-,11+,12-,13+,26?/m1/s1

> <INCHI_KEY>
HUCGRJSHMZWRQQ-LPXZBHKBSA-N

> <FORMULA>
C13H25NO10S3

> <MOLECULAR_WEIGHT>
451.52

> <EXACT_MASS>
451.064059531

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
43.50095763053828

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <JCHEM_LOGP>
-4.183237105370589

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.447675813477716

> <JCHEM_PKA_STRONGEST_ACIDIC>
-3.6043695808153524

> <JCHEM_PKA_STRONGEST_BASIC>
-0.37943718192965636

> <JCHEM_POLAR_SURFACE_AREA>
183.17999999999998

> <JCHEM_REFRACTIVITY>
98.22000000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[(E)-(6-methanesulfinyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}hexylidene)amino]oxysulfonic acid

> <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       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    2  S   UNK     0       8.002  -1.540   0.000  0.00  0.00           S+1
HETATM    3  O   UNK     0       8.002   0.000   0.000  0.00  0.00           O-1
HETATM    4  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.669  -1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.337  -1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      14.670  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      16.004  -1.540   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      16.004   0.000   0.000  0.00  0.00           N+0
HETATM   11  O   UNK     0      14.670   0.770   0.000  0.00  0.00           O+0
HETATM   12  S   UNK     0      14.670   2.310   0.000  0.00  0.00           S+0
HETATM   13  O   UNK     0      16.210   2.310   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      13.130   2.310   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0      14.670   3.850   0.000  0.00  0.00           O+0
HETATM   16  S   UNK     0      17.338  -2.310   0.000  0.00  0.00           S+0
HETATM   17  C   UNK     0      17.338  -3.850   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      18.672  -4.620   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      18.672  -6.160   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      20.005  -6.930   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      21.339  -6.160   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      17.338  -6.930   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      17.338  -8.470   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      16.004  -6.160   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      14.670  -6.930   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      16.004  -4.620   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      14.670  -3.850   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   16                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12                                                            
CONECT   16    9   17                                                       
CONECT   17   16   18   26                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   17   27                                                  
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₃H₂₅NO₁₀S₃

Average Mass

451.5200 Da

Monoisotopic Mass

451.06406 Da

IUPAC Name

{[(E)-(6-methanesulfinyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}hexylidene)amino]oxy}sulfonic acid

Traditional Name

[(E)-(6-methanesulfinyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}hexylidene)amino]oxysulfonic acid

CAS Registry Number

Not Available

SMILES

C[S+]([O-])CCCCC\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/C13H25NO10S3/c1-26(19)6-4-2-3-5-9(14-24-27(20,21)22)25-13-12(18)11(17)10(16)8(7-15)23-13/h8,10-13,15-18H,2-7H2,1H3,(H,20,21,22)/b14-9+/t8-,10-,11+,12-,13+,26?/m1/s1

InChI Key

HUCGRJSHMZWRQQ-LPXZBHKBSA-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
Lepidium meyenii	LOTUS Database	35616633

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
Glycosyl compound
S-glycosyl compound
Oxane
Monothioacetal
Organic sulfuric acid or derivatives
Secondary alcohol
Sulfoxide
Sulfinyl compound
Oxacycle
Polyol
Sulfenyl compound
Organoheterocyclic compound
Alcohol
Primary alcohol
Hydrocarbon derivative
Organosulfur compound
Organonitrogen compound
Organic oxide
Organopnictogen compound
Organic nitrogen compound
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	-4.2	ChemAxon
pKa (Strongest Acidic)	-3.6	ChemAxon
pKa (Strongest Basic)	-0.38	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	183.18 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	98.22 m³·mol⁻¹	ChemAxon
Polarizability	43.5 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

C00007345

Chemspider ID

4678001

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5748529

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Chun JH, Kim NH, Seo MS, Jin M, Park SU, Arasu MV, Kim SJ, Al-Dhabi NA: Molecular characterization of glucosinolates and carotenoid biosynthetic genes in Chinese cabbage (Brassica rapa L. ssp. pekinensis). Saudi J Biol Sci. 2018 Jan;25(1):71-82. doi: 10.1016/j.sjbs.2016.04.004. Epub 2016 Apr 25. [PubMed:29379360 ]
Zhou B, Huang W, Feng X, Liu Q, Ibrahim SA, Liu Y: Identification and quantification of intact glucosinolates at different vegetative growth periods in Chinese cabbage cultivars by UHPLC-Q-TOF-MS. Food Chem. 2022 Nov 1;393:133414. doi: 10.1016/j.foodchem.2022.133414. Epub 2022 Jun 8. [PubMed:35696949 ]
Wu W, Chen J, Yu D, Chen S, Ye X, Zhang Z: Analysis of Processing Effects on Glucosinolate Profiles in Red Cabbage by LC-MS/MS in Multiple Reaction Monitoring Mode. Molecules. 2021 Aug 26;26(17):5171. doi: 10.3390/molecules26175171. [PubMed:34500612 ]
Li M, Xie F, Li J, Sun B, Luo Y, Zhang Y, Chen Q, Wang Y, Zhang F, Zhang Y, Lin Y, Wang X, Tang H: Tumorous Stem Development of Brassica Juncea: A Complex Regulatory Network of Stem Formation and Identification of Key Genes in Glucosinolate Biosynthesis. Plants (Basel). 2020 Aug 9;9(8):1006. doi: 10.3390/plants9081006. [PubMed:32784853 ]
Arasu MV, Kim NH, Antonisamy P, Yoon YH, Kim SJ: Variation of glucosinolates on position orders of flower buds in turnip rape (Brassica rapa). Saudi J Biol Sci. 2017 Nov;24(7):1562-1566. doi: 10.1016/j.sjbs.2017.04.009. Epub 2017 Apr 26. [PubMed:30174493 ]
LOTUS database [Link]

Showing NP-Card for [(e)-(6-methanesulfinyl-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}hexylidene)amino]oxysulfonic acid (NP0309765)

MOL for NP0309765 ([(e)-(6-methanesulfinyl-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}hexylidene)amino]oxysulfonic acid)

3D MOL for NP0309765 ([(e)-(6-methanesulfinyl-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}hexylidene)amino]oxysulfonic acid)

3D SDF for NP0309765 ([(e)-(6-methanesulfinyl-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}hexylidene)amino]oxysulfonic acid)

3D-SDF for NP0309765 ([(e)-(6-methanesulfinyl-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}hexylidene)amino]oxysulfonic acid)

PDB for NP0309765 ([(e)-(6-methanesulfinyl-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}hexylidene)amino]oxysulfonic acid)

3D PDB for NP0309765 ([(e)-(6-methanesulfinyl-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}hexylidene)amino]oxysulfonic acid)

SMILES for NP0309765 ([(e)-(6-methanesulfinyl-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}hexylidene)amino]oxysulfonic acid)

INCHI for NP0309765 ([(e)-(6-methanesulfinyl-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}hexylidene)amino]oxysulfonic acid)

Structure for NP0309765 ([(e)-(6-methanesulfinyl-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}hexylidene)amino]oxysulfonic acid)

3D Structure for NP0309765 ([(e)-(6-methanesulfinyl-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}hexylidene)amino]oxysulfonic acid)