NP-MRD: Showing NP-Card for {4-[(1z,3z)-4-(4-methoxyphenyl)-2,3-bis[(2-oxoethyl)amino]buta-1,3-dien-1-yl]phenyl}oxidanesulfonic acid (NP0317643)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-11 17:38:48 UTC

Updated at

2022-09-11 17:38:48 UTC

NP-MRD ID

NP0317643

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{4-[(1z,3z)-4-(4-methoxyphenyl)-2,3-bis[(2-oxoethyl)amino]buta-1,3-dien-1-yl]phenyl}oxidanesulfonic acid

Description

{4-[(1z,3z)-4-(4-methoxyphenyl)-2,3-bis[(2-oxoethyl)amino]buta-1,3-dien-1-yl]phenyl}oxidanesulfonic acid is found in Streptomyces peucetius.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112219382D          

 31 32  0  0  0  0            999 V2000
    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 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -11.5500    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434  -11.9625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164  -12.2645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414  -10.8355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.8375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    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  2  0  0  0  0
  8  9  1  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
  8 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  2  0  0  0  0
 20 23  1  0  0  0  0
 18 24  1  0  0  0  0
 24 25  2  0  0  0  0
 15 25  1  0  0  0  0
 13 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  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 54  0  0  0  0  0  0  0  0999 V2000
   -8.0335    1.6754   -1.6298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2029    0.5371   -1.6708 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8329    0.5712   -1.4705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1744    1.7695   -1.2077 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8093    1.7727   -1.0123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0563    0.5971   -1.0701 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6197    0.6701   -0.8600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9017   -0.2202   -0.2088 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4931   -1.3543    0.3564 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2454   -1.3727    1.5803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7215   -2.7545    1.8621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4525   -3.6650    1.0924 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5571   -0.0455   -0.0609 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2917   -0.9276    0.5889 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7265   -0.8459    0.7892 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2909    0.3609    1.1130 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6762    0.4541    1.3031 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4837   -0.6548    1.1693 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8646   -0.5647    1.3586 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5940   -0.7969    2.8639 S   0  0  0  0  0  6  0  0  0  0  0  0
    6.5235   -0.7773    3.9463 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2281   -2.1685    2.9532 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7539    0.3552    3.2083 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8739   -1.8464    0.8432 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5325   -1.9604    0.6537 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1787    1.0864   -0.6415 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0318    1.0220   -1.8157 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5352    2.3721   -2.1869 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2238    3.3447   -1.5333 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7570   -0.5574   -1.3329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1252   -0.5890   -1.5328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0274    1.3783   -2.0550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1972    1.9960   -0.5820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5824    2.4834   -2.2600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7950    2.6541   -1.1732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3136    2.7157   -0.8088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0492    1.5246   -1.2633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3665   -2.2555   -0.1592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6065   -1.0446    2.4272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1285   -0.6904    1.4846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3102   -3.0056    2.7374 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7110   -1.7803    0.9925 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7015    1.2514    1.2337 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1212    1.4152    1.5605 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7690    1.0962    2.5662 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4981   -2.7301    0.7341 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0410   -2.8927    0.3957 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0087    2.0174   -0.2089 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4217    0.6654   -2.6929 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8514    0.2882   -1.7282 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1818    2.4478   -3.0523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2410   -1.4849   -1.3928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6285   -1.5370   -1.7381 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  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
  8 13  1  0
 13 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  2  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 20 23  1  0
 20 21  2  0
 20 22  2  0
 18 24  1  0
 24 25  2  0
  6 30  1  0
 30 31  2  0
 31  3  1  0
 25 15  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
  9 38  1  0
 10 39  1  0
 10 40  1  0
 11 41  1  0
 26 48  1  0
 27 49  1  0
 27 50  1  0
 28 51  1  0
 14 42  1  0
 16 43  1  0
 17 44  1  0
 23 45  1  0
 24 46  1  0
 25 47  1  0
 30 52  1  0
 31 53  1  0
M  END


  Mrv1652309112219382D          

 31 32  0  0  0  0            999 V2000
    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 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -11.5500    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434  -11.9625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164  -12.2645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414  -10.8355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.8375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    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  2  0  0  0  0
  8  9  1  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
  8 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  2  0  0  0  0
 20 23  1  0  0  0  0
 18 24  1  0  0  0  0
 24 25  2  0  0  0  0
 15 25  1  0  0  0  0
 13 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  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>
NP0317643

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(\C=C(/NCC=O)\C(\NCC=O)=C\C2=CC=C(OS(O)(=O)=O)C=C2)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H22N2O7S/c1-29-18-6-2-16(3-7-18)14-20(22-10-12-24)21(23-11-13-25)15-17-4-8-19(9-5-17)30-31(26,27)28/h2-9,12-15,22-23H,10-11H2,1H3,(H,26,27,28)/b20-14-,21-15-

> <INCHI_KEY>
NPWQFYPSSPCBMG-SIBCGJTDSA-N

> <FORMULA>
C21H22N2O7S

> <MOLECULAR_WEIGHT>
446.47

> <EXACT_MASS>
446.11477223

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
45.047239508704024

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{4-[(1Z,3Z)-4-(4-methoxyphenyl)-2,3-bis[(2-oxoethyl)amino]buta-1,3-dien-1-yl]phenyl}oxidanesulfonic acid

> <JCHEM_LOGP>
-0.43013253144796687

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
16.84997031614529

> <JCHEM_PKA_STRONGEST_ACIDIC>
-2.200587457101583

> <JCHEM_PKA_STRONGEST_BASIC>
6.242870408590733

> <JCHEM_POLAR_SURFACE_AREA>
131.03

> <JCHEM_REFRACTIVITY>
117.23449999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
{4-[(1Z,3Z)-4-(4-methoxyphenyl)-2,3-bis[(2-oxoethyl)amino]buta-1,3-dien-1-yl]phenyl}oxidanesulfonic 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       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334 -11.550   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000 -12.320   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      -1.334 -11.550   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      -2.667 -12.320   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -4.001 -14.630   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.000 -13.860   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334 -14.630   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334 -16.170   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667 -16.940   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667 -18.480   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.334 -19.250   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.334 -20.790   0.000  0.00  0.00           O+0
HETATM   20  S   UNK     0       2.667 -21.560   0.000  0.00  0.00           S+0
HETATM   21  O   UNK     0       4.001 -22.330   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       1.897 -22.894   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       3.437 -20.226   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -0.000 -18.480   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.000 -16.940   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0      -1.334 -14.630   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0      -1.334 -16.170   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.667 -16.940   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -4.001 -16.170   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.000  -7.700   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   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13    8   14   26                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   25                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   24                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20                                                            
CONECT   24   18   25                                                       
CONECT   25   24   15                                                       
CONECT   26   13   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30    6   31                                                       
CONECT   31   30    3                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₂N₂O₇S

Average Mass

446.4700 Da

Monoisotopic Mass

446.11477 Da

IUPAC Name

{4-[(1Z,3Z)-4-(4-methoxyphenyl)-2,3-bis[(2-oxoethyl)amino]buta-1,3-dien-1-yl]phenyl}oxidanesulfonic acid

Traditional Name

{4-[(1Z,3Z)-4-(4-methoxyphenyl)-2,3-bis[(2-oxoethyl)amino]buta-1,3-dien-1-yl]phenyl}oxidanesulfonic acid

CAS Registry Number

Not Available

SMILES

COC1=CC=C(\C=C(/NCC=O)\C(\NCC=O)=C\C2=CC=C(OS(O)(=O)=O)C=C2)C=C1

InChI Identifier

InChI=1S/C21H22N2O7S/c1-29-18-6-2-16(3-7-18)14-20(22-10-12-24)21(23-11-13-25)15-17-4-8-19(9-5-17)30-31(26,27)28/h2-9,12-15,22-23H,10-11H2,1H3,(H,26,27,28)/b20-14-,21-15-

InChI Key

NPWQFYPSSPCBMG-SIBCGJTDSA-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
Streptomyces peucetius	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	-0.43	ChemAxon
pKa (Strongest Acidic)	-2.2	ChemAxon
pKa (Strongest Basic)	6.24	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	131.03 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	117.23 m³·mol⁻¹	ChemAxon
Polarizability	45.05 Å³	ChemAxon
Number of Rings	2	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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for {4-[(1z,3z)-4-(4-methoxyphenyl)-2,3-bis[(2-oxoethyl)amino]buta-1,3-dien-1-yl]phenyl}oxidanesulfonic acid (NP0317643)

MOL for NP0317643 ({4-[(1z,3z)-4-(4-methoxyphenyl)-2,3-bis[(2-oxoethyl)amino]buta-1,3-dien-1-yl]phenyl}oxidanesulfonic acid)

3D MOL for NP0317643 ({4-[(1z,3z)-4-(4-methoxyphenyl)-2,3-bis[(2-oxoethyl)amino]buta-1,3-dien-1-yl]phenyl}oxidanesulfonic acid)

3D SDF for NP0317643 ({4-[(1z,3z)-4-(4-methoxyphenyl)-2,3-bis[(2-oxoethyl)amino]buta-1,3-dien-1-yl]phenyl}oxidanesulfonic acid)

3D-SDF for NP0317643 ({4-[(1z,3z)-4-(4-methoxyphenyl)-2,3-bis[(2-oxoethyl)amino]buta-1,3-dien-1-yl]phenyl}oxidanesulfonic acid)

PDB for NP0317643 ({4-[(1z,3z)-4-(4-methoxyphenyl)-2,3-bis[(2-oxoethyl)amino]buta-1,3-dien-1-yl]phenyl}oxidanesulfonic acid)

3D PDB for NP0317643 ({4-[(1z,3z)-4-(4-methoxyphenyl)-2,3-bis[(2-oxoethyl)amino]buta-1,3-dien-1-yl]phenyl}oxidanesulfonic acid)

SMILES for NP0317643 ({4-[(1z,3z)-4-(4-methoxyphenyl)-2,3-bis[(2-oxoethyl)amino]buta-1,3-dien-1-yl]phenyl}oxidanesulfonic acid)

INCHI for NP0317643 ({4-[(1z,3z)-4-(4-methoxyphenyl)-2,3-bis[(2-oxoethyl)amino]buta-1,3-dien-1-yl]phenyl}oxidanesulfonic acid)

Structure for NP0317643 ({4-[(1z,3z)-4-(4-methoxyphenyl)-2,3-bis[(2-oxoethyl)amino]buta-1,3-dien-1-yl]phenyl}oxidanesulfonic acid)

3D Structure for NP0317643 ({4-[(1z,3z)-4-(4-methoxyphenyl)-2,3-bis[(2-oxoethyl)amino]buta-1,3-dien-1-yl]phenyl}oxidanesulfonic acid)