NP-MRD: Showing NP-Card for {[2-(5-methoxy-1h-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino}oxysulfonic acid (NP0315583)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2022-09-11 14:17:25 UTC

Updated at

2022-09-11 14:17:25 UTC

NP-MRD ID

NP0315583

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{[2-(5-methoxy-1h-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino}oxysulfonic acid

Description

({[2-(5-Methoxy-1H-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]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. {[2-(5-methoxy-1h-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino}oxysulfonic acid is found in Brassica oleracea. Based on a literature review very few articles have been published on ({[2-(5-methoxy-1H-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino}oxy)sulfonic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112216172D          

 31 33  0  0  0  0            999 V2000
    4.7812    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    2.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768    3.1465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4752    2.5334    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2822    2.7050    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5371    3.4896    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7525    3.7445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3218    3.2346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7921    4.2742    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781    3.9312    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.3739    4.5442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1190    5.3289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6710    5.9420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4161    6.7266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3909    6.8981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4780    5.7704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0300    6.3835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7329    4.9858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5399    4.8143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1809    4.3727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358    3.5881    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    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
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  4  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
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 19 28  1  0  0  0  0
 28 29  1  0  0  0  0
  9 30  1  0  0  0  0
  6 30  1  0  0  0  0
 30 31  2  0  0  0  0
  3 31  1  0  0  0  0
M  END

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
    6.3852    0.7747   -1.9279 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2442    0.8406   -1.1380 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6621   -0.1661   -0.4114 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1961   -1.4582   -0.3895 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5850   -2.4442    0.3514 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4405   -2.1873    1.0857 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6658   -2.9439    1.8729 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6501   -2.2291    2.3738 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7943   -0.9536    1.8743 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8990    0.1897    2.1548 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0007    0.4763    1.0200 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0304    1.6121    0.4360 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8737    2.6153    0.8108 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5279    3.7543   -0.2655 S   0  0  0  0  0  6  0  0  0  0  0  0
    1.4677    3.2911   -1.6866 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9936    3.9176    0.0772 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8067    5.2436   -0.0414 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1355   -0.7667    0.4610 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1203   -0.1597   -0.9572 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9512    0.8689   -0.6104 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2997    0.5508   -0.5597 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0901    1.7138   -0.0583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7655    2.1613    1.1959 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4564   -0.7082    0.2391 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8210   -0.6635    1.4541 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9194   -1.8440   -0.6255 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9438   -2.4544   -1.3210 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8144   -1.3748   -1.5262 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2588   -1.1622   -2.8361 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9198   -0.8925    1.0535 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5228    0.0972    0.3170 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0857    1.0124   -2.9905 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9592   -0.1491   -1.8972 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0756    1.6055   -1.6211 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0871   -1.7090   -0.9453 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9711   -3.4696    0.3958 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7996   -3.9703    2.0969 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8787   -2.6138    3.0431 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5120    1.0696    2.4438 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2391   -0.0877    3.0143 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0765    5.4035   -0.6650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3770    0.1922   -1.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7026    0.3385   -1.5966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1790    1.4217   -0.1379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9836    2.5307   -0.8241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4936    1.9248    1.8225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5516   -0.8536    0.4202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6181    0.2328    1.8074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4970   -2.5858    0.0820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3719   -3.2017   -0.8033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0579   -2.1835   -1.5915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0418   -1.6940   -3.0731 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1000    1.0874    0.3100 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 21 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 17  1  0
 14 15  2  0
 14 16  2  0
  9 30  1  0
 30 31  2  0
 31  3  1  0
 30  6  1  0
 28 19  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  4 35  1  0
  5 36  1  0
  7 37  1  0
  8 38  1  0
 10 39  1  0
 10 40  1  0
 19 42  1  6
 21 43  1  6
 22 44  1  0
 22 45  1  0
 23 46  1  0
 24 47  1  1
 25 48  1  0
 26 49  1  1
 27 50  1  0
 28 51  1  6
 29 52  1  0
 17 41  1  0
 31 53  1  0
M  END


  Mrv1652309112216172D          

 31 33  0  0  0  0            999 V2000
    4.7812    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    2.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768    3.1465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4752    2.5334    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2822    2.7050    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5371    3.4896    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7525    3.7445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3218    3.2346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7921    4.2742    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781    3.9312    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.3739    4.5442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1190    5.3289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6710    5.9420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4161    6.7266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3909    6.8981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4780    5.7704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0300    6.3835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7329    4.9858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5399    4.8143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1809    4.3727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358    3.5881    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    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
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  4  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
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 19 28  1  0  0  0  0
 28 29  1  0  0  0  0
  9 30  1  0  0  0  0
  6 30  1  0  0  0  0
 30 31  2  0  0  0  0
  3 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0315583

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C2NC=C(CC(SC3OC(CO)C(O)C(O)C3O)=NOS(O)(=O)=O)C2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C17H22N2O10S2/c1-27-9-2-3-11-10(5-9)8(6-18-11)4-13(19-29-31(24,25)26)30-17-16(23)15(22)14(21)12(7-20)28-17/h2-3,5-6,12,14-18,20-23H,4,7H2,1H3,(H,24,25,26)

> <INCHI_KEY>
VGSOGNUJYYDTSG-UHFFFAOYSA-N

> <FORMULA>
C17H22N2O10S2

> <MOLECULAR_WEIGHT>
478.49

> <EXACT_MASS>
478.071587264

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
45.09615857256178

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
({[2-(5-methoxy-1H-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino}oxy)sulfonic acid

> <JCHEM_LOGP>
-2.2620010533046377

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.446669951297498

> <JCHEM_PKA_STRONGEST_ACIDIC>
-3.5720319275935823

> <JCHEM_PKA_STRONGEST_BASIC>
-0.3866756152847538

> <JCHEM_POLAR_SURFACE_AREA>
191.12999999999997

> <JCHEM_REFRACTIVITY>
107.6967

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
{[2-(5-methoxy-1H-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]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       8.925   3.613   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.591   4.383   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       2.126   1.597   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.126   4.089   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.650   5.553   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.143   5.874   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0      -0.887   4.729   0.000  0.00  0.00           N+0
HETATM   13  O   UNK     0      -2.393   5.049   0.000  0.00  0.00           O+0
HETATM   14  S   UNK     0      -2.869   6.514   0.000  0.00  0.00           S+0
HETATM   15  O   UNK     0      -1.405   6.990   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      -4.334   6.038   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -3.345   7.979   0.000  0.00  0.00           O+0
HETATM   18  S   UNK     0      -0.333   7.338   0.000  0.00  0.00           S+0
HETATM   19  C   UNK     0       0.698   8.483   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.222   9.947   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.253  11.092   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.777  12.556   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.730  12.876   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.759  10.771   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       3.789  11.916   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       3.235   9.307   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       4.741   8.987   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.204   8.162   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       2.680   6.698   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   31                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   30                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   30                                                  
CONECT   10    9   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   28                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   19   29                                                  
CONECT   29   28                                                            
CONECT   30    9    6   31                                                  
CONECT   31   30    3                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Value	Source
({[2-(5-methoxy-1H-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino}oxy)sulfonate	Generator
({[2-(5-methoxy-1H-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulphanyl}ethylidene]amino}oxy)sulphonate	Generator
({[2-(5-methoxy-1H-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulphanyl}ethylidene]amino}oxy)sulphonic acid	Generator

Chemical Formula

C₁₇H₂₂N₂O₁₀S₂

Average Mass

478.4900 Da

Monoisotopic Mass

478.07159 Da

IUPAC Name

({[2-(5-methoxy-1H-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino}oxy)sulfonic acid

Traditional Name

{[2-(5-methoxy-1H-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino}oxysulfonic acid

CAS Registry Number

Not Available

SMILES

COC1=CC=C2NC=C(CC(SC3OC(CO)C(O)C(O)C3O)=NOS(O)(=O)=O)C2=C1

InChI Identifier

InChI=1S/C17H22N2O10S2/c1-27-9-2-3-11-10(5-9)8(6-18-11)4-13(19-29-31(24,25)26)30-17-16(23)15(22)14(21)12(7-20)28-17/h2-3,5-6,12,14-18,20-23H,4,7H2,1H3,(H,24,25,26)

InChI Key

VGSOGNUJYYDTSG-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
Brassica oleracea	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
3-alkylindole
Indole
Indole or derivatives
Anisole
Alkyl aryl ether
Oxane
Substituted pyrrole
Benzenoid
Heteroaromatic compound
Monothioacetal
Organic sulfuric acid or derivatives
Pyrrole
Secondary alcohol
Polyol
Oxacycle
Ether
Azacycle
Organoheterocyclic compound
Sulfenyl compound
Primary alcohol
Organosulfur compound
Organonitrogen compound
Organopnictogen compound
Organic nitrogen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	-2.3	ChemAxon
pKa (Strongest Acidic)	-3.6	ChemAxon
pKa (Strongest Basic)	-0.39	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	191.13 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	107.7 m³·mol⁻¹	ChemAxon
Polarizability	45.1 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

163083717

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for {[2-(5-methoxy-1h-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino}oxysulfonic acid (NP0315583)

MOL for NP0315583 ({[2-(5-methoxy-1h-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino}oxysulfonic acid)

3D MOL for NP0315583 ({[2-(5-methoxy-1h-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino}oxysulfonic acid)

3D SDF for NP0315583 ({[2-(5-methoxy-1h-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino}oxysulfonic acid)

3D-SDF for NP0315583 ({[2-(5-methoxy-1h-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino}oxysulfonic acid)

PDB for NP0315583 ({[2-(5-methoxy-1h-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino}oxysulfonic acid)

3D PDB for NP0315583 ({[2-(5-methoxy-1h-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino}oxysulfonic acid)

SMILES for NP0315583 ({[2-(5-methoxy-1h-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino}oxysulfonic acid)

INCHI for NP0315583 ({[2-(5-methoxy-1h-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino}oxysulfonic acid)

Structure for NP0315583 ({[2-(5-methoxy-1h-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino}oxysulfonic acid)

3D Structure for NP0315583 ({[2-(5-methoxy-1h-indol-3-yl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino}oxysulfonic acid)