NP-MRD: Showing NP-Card for 5-{[2-imino-5-(4-methoxyphenyl)-3-methyl-1h-imidazol-4-yl]sulfanyl}-4-(4-methoxyphenyl)-1-methyl-3h-imidazol-2-imine (NP0210185)

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Record Information

Version

2.0

Created at

2022-09-05 07:53:23 UTC

Updated at

2022-09-05 07:53:23 UTC

NP-MRD ID

NP0210185

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-{[2-imino-5-(4-methoxyphenyl)-3-methyl-1h-imidazol-4-yl]sulfanyl}-4-(4-methoxyphenyl)-1-methyl-3h-imidazol-2-imine

Description

921987-37-3 Belongs to the class of organic compounds known as phenylimidazoles. These are polycyclic aromatic compounds containing a benzene ring linked to an imidazole ring through a CC or CN bond. 5-{[2-imino-5-(4-methoxyphenyl)-3-methyl-1h-imidazol-4-yl]sulfanyl}-4-(4-methoxyphenyl)-1-methyl-3h-imidazol-2-imine is found in Polycarpa aurata. 921987-37-3 Is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231521462D          

 31 34  0  0  0  0            999 V2000
    2.5867    1.9252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3012    1.5127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3012    0.6877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0156    0.2752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0156   -0.5498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3012   -0.9623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5867   -0.5498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5867    0.2752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3012   -1.7873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9686   -2.2722    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7137   -3.0569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1986   -3.7243    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8887   -3.0569    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4037   -3.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6337   -2.2722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8491   -2.0173    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.2360   -2.5693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4290   -2.3978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0165   -3.1123    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5686   -3.7254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3970   -4.5323    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3222   -3.3898    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -3.8023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0935   -1.6441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7270   -1.5579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0626   -0.8042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5776   -0.1368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9132    0.6169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7337    0.7031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2428   -0.2230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5784   -0.9767    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
  3  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
  9 15  2  0  0  0  0
 15 16  1  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  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  2  0  0  0  0
 24 31  1  0  0  0  0
M  END

     RDKit          3D

 55 58  0  0  0  0  0  0  0  0999 V2000
   -6.4569    2.2802   -3.0727 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9033    1.0927   -2.6074 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9508    1.0029   -1.6018 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4749   -0.2349   -1.2246 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5275   -0.3747   -0.2296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0084    0.7170    0.4381 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0070    0.5889    1.4920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0048    1.2322    2.6982 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9076    0.8266    3.3568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5460    1.2689    4.6512 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2318   -0.0639    2.5641 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9954   -0.7080    2.9411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8939   -0.2184    1.4198 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4826   -1.2370    0.0405 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.9890   -2.1693    0.2091 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2874   -1.7869   -0.1422 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7148   -0.5246   -0.7190 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0771    0.1185   -1.7567 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5246    1.3177   -2.2685 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6456    1.9293   -1.7531 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0570    3.1318   -2.2988 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1843    3.8422   -1.8521 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2981    1.3058   -0.7172 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8317    0.1139   -0.2274 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0520   -2.8577    0.1769 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3256   -3.8410    0.6856 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8330   -5.0888    1.1154 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0505   -3.4278    0.7106 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0372   -4.2511    1.2089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4902    1.9527    0.0544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4376    2.0973   -0.9400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0094    2.0860   -4.0085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7432    3.1192   -3.1558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2275    2.6129   -2.3234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8696   -1.1198   -1.7379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1446   -1.3450    0.0767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8629    0.7570    5.4726 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0414    2.1144    4.7556 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9497   -1.8057    2.9511 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2124   -0.4247    4.0149 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8607   -0.3476    2.3113 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1976   -0.3123   -2.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9810    1.7771   -3.0864 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2241    4.8130   -2.3834 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0745    3.1960   -2.0796 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1355    4.0679   -0.7601 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1773    1.8004   -0.3242 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3749   -0.3556    0.5979 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6154   -5.3914    2.0881 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4078   -5.7294    0.5345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2064   -4.0970    2.2999 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1784   -5.3270    1.0526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9835   -4.0195    0.6778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0813    2.8232    0.5815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8080    3.0735   -1.2323 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 30  1  0
 30 31  2  0
  6  7  1  0
  7 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 25  1  0
 25 26  2  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 20 23  1  0
 23 24  2  0
 13 11  1  0
 11 12  1  0
 11  9  1  0
  9 10  1  0
  9  8  2  0
 31  3  1  0
  8  7  1  0
 28 15  1  0
 24 17  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  4 35  1  0
  5 36  1  0
 30 54  1  0
 31 55  1  0
 27 49  1  0
 27 50  1  0
 29 51  1  0
 29 52  1  0
 29 53  1  0
 18 42  1  0
 19 43  1  0
 22 44  1  0
 22 45  1  0
 22 46  1  0
 23 47  1  0
 24 48  1  0
 12 39  1  0
 12 40  1  0
 12 41  1  0
 10 37  1  0
 10 38  1  0
M  END


  Mrv1533004231521462D          

 31 34  0  0  0  0            999 V2000
    2.5867    1.9252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3012    1.5127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3012    0.6877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0156    0.2752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0156   -0.5498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3012   -0.9623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5867   -0.5498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5867    0.2752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3012   -1.7873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9686   -2.2722    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7137   -3.0569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1986   -3.7243    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8887   -3.0569    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4037   -3.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6337   -2.2722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8491   -2.0173    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.2360   -2.5693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4290   -2.3978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0165   -3.1123    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5686   -3.7254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3970   -4.5323    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3222   -3.3898    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -3.8023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0935   -1.6441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7270   -1.5579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0626   -0.8042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5776   -0.1368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9132    0.6169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7337    0.7031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2428   -0.2230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5784   -0.9767    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
  3  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
  9 15  2  0  0  0  0
 15 16  1  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  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  2  0  0  0  0
 24 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0210185

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C=C1)C1=C(SC2=C(N=C(N)N2C)C2=CC=C(OC)C=C2)N(C)C(N)=N1

> <INCHI_IDENTIFIER>
InChI=1S/C22H24N6O2S/c1-27-19(17(25-21(27)23)13-5-9-15(29-3)10-6-13)31-20-18(26-22(24)28(20)2)14-7-11-16(30-4)12-8-14/h5-12H,1-4H3,(H2,23,25)(H2,24,26)

> <INCHI_KEY>
MFYQKLYRRCYHIK-UHFFFAOYSA-N

> <FORMULA>
C22H24N6O2S

> <MOLECULAR_WEIGHT>
436.53

> <EXACT_MASS>
436.168145211

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
46.249668827942585

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-{[2-amino-4-(4-methoxyphenyl)-1-methyl-1H-imidazol-5-yl]sulfanyl}-4-(4-methoxyphenyl)-1-methyl-1H-imidazol-2-amine

> <ALOGPS_LOGP>
3.83

> <JCHEM_LOGP>
4.012446328333333

> <ALOGPS_LOGS>
-3.82

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
7.242044310238688

> <JCHEM_POLAR_SURFACE_AREA>
106.14

> <JCHEM_REFRACTIVITY>
123.75389999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.59e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-{[2-amino-5-(4-methoxyphenyl)-3-methylimidazol-4-yl]sulfanyl}-4-(4-methoxyphenyl)-1-methylimidazol-2-amine

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0       4.828   3.594   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       6.162   2.824   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.162   1.284   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.496   0.514   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.496  -1.026   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.162  -1.796   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.828  -1.026   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.828   0.514   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.162  -3.336   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       7.408  -4.242   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       6.932  -5.706   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       7.837  -6.952   0.000  0.00  0.00           N+0
HETATM   13  N   UNK     0       5.392  -5.706   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0       4.487  -6.952   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.916  -4.242   0.000  0.00  0.00           C+0
HETATM   16  S   UNK     0       3.452  -3.766   0.000  0.00  0.00           S+0
HETATM   17  C   UNK     0       2.307  -4.796   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.801  -4.476   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       0.031  -5.810   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       1.061  -6.954   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       0.741  -8.460   0.000  0.00  0.00           N+0
HETATM   22  N   UNK     0       2.468  -6.328   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       3.802  -7.098   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.174  -3.069   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.357  -2.908   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.983  -1.501   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.078  -0.255   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -1.705   1.152   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -3.236   1.313   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.453  -0.416   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.080  -1.823   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3                                                       
CONECT    9    6   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    9   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19   24                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   17   23                                                  
CONECT   23   22                                                            
CONECT   24   18   25   31                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   30                                                  
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   27   31                                                       
CONECT   31   30   24                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₄N₆O₂S

Average Mass

436.5300 Da

Monoisotopic Mass

436.16815 Da

IUPAC Name

5-{[2-amino-4-(4-methoxyphenyl)-1-methyl-1H-imidazol-5-yl]sulfanyl}-4-(4-methoxyphenyl)-1-methyl-1H-imidazol-2-amine

Traditional Name

5-{[2-amino-5-(4-methoxyphenyl)-3-methylimidazol-4-yl]sulfanyl}-4-(4-methoxyphenyl)-1-methylimidazol-2-amine

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=C1)C1=C(SC2=C(N=C(N)N2C)C2=CC=C(OC)C=C2)N(C)C(N)=N1

InChI Identifier

InChI=1S/C22H24N6O2S/c1-27-19(17(25-21(27)23)13-5-9-15(29-3)10-6-13)31-20-18(26-22(24)28(20)2)14-7-11-16(30-4)12-8-14/h5-12H,1-4H3,(H2,23,25)(H2,24,26)

InChI Key

MFYQKLYRRCYHIK-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
Polycarpa aurata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylimidazoles. These are polycyclic aromatic compounds containing a benzene ring linked to an imidazole ring through a CC or CN bond.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Azoles

Sub Class

Imidazoles

Direct Parent

Phenylimidazoles

Alternative Parents

Substituents

Diarylthioether
4-phenylimidazole
5-phenylimidazole
1,2,4,5-tetrasubstituted imidazole
Phenoxy compound
Aryl thioether
Anisole
Methoxybenzene
Phenol ether
Alkyl aryl ether
Aminoimidazole
Benzenoid
Monocyclic benzene moiety
N-substituted imidazole
Heteroaromatic compound
Azacycle
Sulfenyl compound
Ether
Thioether
Hydrocarbon derivative
Amine
Organic oxygen compound
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Organosulfur compound
Primary amine
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	3.83	ALOGPS
logP	4.01	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Basic)	7.24	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	106.14 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	123.75 m³·mol⁻¹	ChemAxon
Polarizability	46.25 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

16104600

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-{[2-imino-5-(4-methoxyphenyl)-3-methyl-1h-imidazol-4-yl]sulfanyl}-4-(4-methoxyphenyl)-1-methyl-3h-imidazol-2-imine (NP0210185)

MOL for NP0210185 (5-{[2-imino-5-(4-methoxyphenyl)-3-methyl-1h-imidazol-4-yl]sulfanyl}-4-(4-methoxyphenyl)-1-methyl-3h-imidazol-2-imine)

3D MOL for NP0210185 (5-{[2-imino-5-(4-methoxyphenyl)-3-methyl-1h-imidazol-4-yl]sulfanyl}-4-(4-methoxyphenyl)-1-methyl-3h-imidazol-2-imine)

3D SDF for NP0210185 (5-{[2-imino-5-(4-methoxyphenyl)-3-methyl-1h-imidazol-4-yl]sulfanyl}-4-(4-methoxyphenyl)-1-methyl-3h-imidazol-2-imine)

3D-SDF for NP0210185 (5-{[2-imino-5-(4-methoxyphenyl)-3-methyl-1h-imidazol-4-yl]sulfanyl}-4-(4-methoxyphenyl)-1-methyl-3h-imidazol-2-imine)

PDB for NP0210185 (5-{[2-imino-5-(4-methoxyphenyl)-3-methyl-1h-imidazol-4-yl]sulfanyl}-4-(4-methoxyphenyl)-1-methyl-3h-imidazol-2-imine)

3D PDB for NP0210185 (5-{[2-imino-5-(4-methoxyphenyl)-3-methyl-1h-imidazol-4-yl]sulfanyl}-4-(4-methoxyphenyl)-1-methyl-3h-imidazol-2-imine)

SMILES for NP0210185 (5-{[2-imino-5-(4-methoxyphenyl)-3-methyl-1h-imidazol-4-yl]sulfanyl}-4-(4-methoxyphenyl)-1-methyl-3h-imidazol-2-imine)

INCHI for NP0210185 (5-{[2-imino-5-(4-methoxyphenyl)-3-methyl-1h-imidazol-4-yl]sulfanyl}-4-(4-methoxyphenyl)-1-methyl-3h-imidazol-2-imine)

Structure for NP0210185 (5-{[2-imino-5-(4-methoxyphenyl)-3-methyl-1h-imidazol-4-yl]sulfanyl}-4-(4-methoxyphenyl)-1-methyl-3h-imidazol-2-imine)

3D Structure for NP0210185 (5-{[2-imino-5-(4-methoxyphenyl)-3-methyl-1h-imidazol-4-yl]sulfanyl}-4-(4-methoxyphenyl)-1-methyl-3h-imidazol-2-imine)