NP-MRD: Showing NP-Card for methyl 2-({9-oxo-1h,2h,3h-pyrrolo[2,1-b]quinazolin-3-yl}amino)benzoate (NP0167215)

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Record Information

Version

2.0

Created at

2022-09-03 02:45:23 UTC

Updated at

2022-09-03 02:45:23 UTC

NP-MRD ID

NP0167215

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-({9-oxo-1h,2h,3h-pyrrolo[2,1-b]quinazolin-3-yl}amino)benzoate

Description

Vasnetine belongs to the class of organic compounds known as quinazolines. Quinazolines are compounds containing a quinazoline moiety, which is made up of two fused six-member aromatic rings, a benzene ring and a pyrimidine ring. methyl 2-({9-oxo-1h,2h,3h-pyrrolo[2,1-b]quinazolin-3-yl}amino)benzoate is found in Justicia adhatoda. methyl 2-({9-oxo-1h,2h,3h-pyrrolo[2,1-b]quinazolin-3-yl}amino)benzoate was first documented in 2022 (PMID: 35207602). Based on a literature review very few articles have been published on Vasnetine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032204452D          

 25 28  0  0  0  0            999 V2000
    3.3454   -1.6527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6004   -2.4373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4073   -2.6088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6623   -3.3934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9594   -1.9957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7663   -2.1672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3184   -1.5541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0634   -0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2564   -0.5980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7044   -1.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8974   -1.0396    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1274    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    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
  3  4  2  0  0  0  0
  3  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  2  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  2  0  0  0  0
M  END

     RDKit          3D

 42 45  0  0  0  0  0  0  0  0999 V2000
   -4.0336    3.5327   -1.5006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1851    2.1717   -1.1405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0774    1.3548   -0.8470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9810    1.9161   -0.9289 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2587   -0.0394   -0.4798 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5809   -0.5221   -0.4163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9064   -1.7910   -0.0781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8937   -2.6636    0.2215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5838   -2.2112    0.1654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2475   -0.9080   -0.1816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8945   -0.5312   -0.2447 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1778   -1.4136    0.1956 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0819   -1.5731    1.6922 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7808   -0.2892    2.1611 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8342   -0.1568    1.1840 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5098   -0.7913    0.0456 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3789   -0.7687   -0.9783 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5541   -0.1584   -0.9542 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4390   -0.1461   -2.0226 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6590    0.4931   -1.9842 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0029    1.1477   -0.8205 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1408    1.1506    0.2563 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9232    0.5038    0.1963 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0373    0.4860    1.2524 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3418    1.0756    2.3068 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0291    3.9229   -1.2475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8410    4.1163   -0.9903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2540    3.6046   -2.5869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3739    0.1681   -0.6531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9432   -2.1208   -0.0419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1398   -3.6817    0.4939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8450   -2.9763    0.4090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5924    0.3725   -0.6076 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1041   -2.3874   -0.3345 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6754   -2.4499    1.9953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9524   -1.6069    2.0845 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1274   -0.4660    3.1786 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0380    0.5318    2.1020 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1438   -0.6663   -2.9203 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3103    0.4667   -2.8565 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9615    1.6461   -0.7996 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3915    1.6577    1.1770 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 10  5  1  0
 16 12  1  0
 23 18  1  0
 24 15  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  6 29  1  0
  7 30  1  0
  8 31  1  0
  9 32  1  0
 11 33  1  0
 12 34  1  6
 13 35  1  0
 13 36  1  0
 14 37  1  0
 14 38  1  0
 19 39  1  0
 20 40  1  0
 21 41  1  0
 22 42  1  0
M  END


  Mrv1652309032204452D          

 25 28  0  0  0  0            999 V2000
    3.3454   -1.6527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6004   -2.4373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4073   -2.6088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6623   -3.3934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9594   -1.9957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7663   -2.1672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3184   -1.5541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0634   -0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2564   -0.5980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7044   -1.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8974   -1.0396    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1274    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    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
  3  4  2  0  0  0  0
  3  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  2  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0167215

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CC=CC=C1NC1CCN2C1=NC1=CC=CC=C1C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H17N3O3/c1-25-19(24)13-7-3-5-9-15(13)20-16-10-11-22-17(16)21-14-8-4-2-6-12(14)18(22)23/h2-9,16,20H,10-11H2,1H3

> <INCHI_KEY>
XROLSYQINIGIQK-UHFFFAOYSA-N

> <FORMULA>
C19H17N3O3

> <MOLECULAR_WEIGHT>
335.363

> <EXACT_MASS>
335.126991419

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
35.22219864628504

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 2-({9-oxo-1H,2H,3H,9H-pyrrolo[2,1-b]quinazolin-3-yl}amino)benzoate

> <ALOGPS_LOGP>
2.60

> <JCHEM_LOGP>
2.898337580333333

> <ALOGPS_LOGS>
-3.22

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.727633156163758

> <JCHEM_PKA_STRONGEST_BASIC>
1.980269355929229

> <JCHEM_POLAR_SURFACE_AREA>
71.0

> <JCHEM_REFRACTIVITY>
96.64630000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.04e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 2-({9-oxo-1H,2H,3H-pyrrolo[2,1-b]quinazolin-3-yl}amino)benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       6.245  -3.085   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       6.721  -4.550   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.227  -4.870   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       8.703  -6.334   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       9.257  -3.725   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.764  -4.046   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.794  -2.901   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.318  -1.436   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.812  -1.116   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.782  -2.261   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       7.275  -1.941   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       6.799  -0.476   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.705   0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.799   2.016   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       5.335   1.540   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       4.001  -0.770   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    5   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   16                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   24                                                  
CONECT   16   15   12   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   18   24                                                  
CONECT   24   23   15   25                                                  
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₁₇N₃O₃

Average Mass

335.3630 Da

Monoisotopic Mass

335.12699 Da

IUPAC Name

methyl 2-({9-oxo-1H,2H,3H,9H-pyrrolo[2,1-b]quinazolin-3-yl}amino)benzoate

Traditional Name

methyl 2-({9-oxo-1H,2H,3H-pyrrolo[2,1-b]quinazolin-3-yl}amino)benzoate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CC=CC=C1NC1CCN2C1=NC1=CC=CC=C1C2=O

InChI Identifier

InChI=1S/C19H17N3O3/c1-25-19(24)13-7-3-5-9-15(13)20-16-10-11-22-17(16)21-14-8-4-2-6-12(14)18(22)23/h2-9,16,20H,10-11H2,1H3

InChI Key

XROLSYQINIGIQK-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
Adhatoda vasica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinazolines. Quinazolines are compounds containing a quinazoline moiety, which is made up of two fused six-member aromatic rings, a benzene ring and a pyrimidine ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazanaphthalenes

Sub Class

Benzodiazines

Direct Parent

Quinazolines

Alternative Parents

Substituents

Aminobenzoic acid or derivatives
Benzoate ester
Quinazoline
Benzoic acid or derivatives
Benzoyl
Aniline or substituted anilines
Phenylalkylamine
Aralkylamine
Secondary aliphatic/aromatic amine
Pyrimidone
Benzenoid
Pyrimidine
Monocyclic benzene moiety
Vinylogous amide
Methyl ester
Heteroaromatic compound
Amino acid or derivatives
Lactam
Carboxylic acid ester
Secondary amine
Azacycle
Carboxylic acid derivative
Hydrocarbon derivative
Amine
Organic oxide
Organic oxygen compound
Organonitrogen compound
Organic nitrogen compound
Organooxygen compound
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	2.6	ALOGPS
logP	2.9	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	13.73	ChemAxon
pKa (Strongest Basic)	1.98	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	71 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	96.65 m³·mol⁻¹	ChemAxon
Polarizability	35.22 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	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00029180

Chemspider ID

8172647

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

9997066

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Siva Kumar B, Anuragh S, Kammala AK, Ilango K: Computer Aided Drug Design Approach to Screen Phytoconstituents of Adhatoda vasica as Potential Inhibitors of SARS-CoV-2 Main Protease Enzyme. Life (Basel). 2022 Feb 20;12(2). pii: life12020315. doi: 10.3390/life12020315. [PubMed:35207602 ]
LOTUS database [Link]

Showing NP-Card for methyl 2-({9-oxo-1h,2h,3h-pyrrolo[2,1-b]quinazolin-3-yl}amino)benzoate (NP0167215)

MOL for NP0167215 (methyl 2-({9-oxo-1h,2h,3h-pyrrolo[2,1-b]quinazolin-3-yl}amino)benzoate)

3D MOL for NP0167215 (methyl 2-({9-oxo-1h,2h,3h-pyrrolo[2,1-b]quinazolin-3-yl}amino)benzoate)

3D SDF for NP0167215 (methyl 2-({9-oxo-1h,2h,3h-pyrrolo[2,1-b]quinazolin-3-yl}amino)benzoate)

3D-SDF for NP0167215 (methyl 2-({9-oxo-1h,2h,3h-pyrrolo[2,1-b]quinazolin-3-yl}amino)benzoate)

PDB for NP0167215 (methyl 2-({9-oxo-1h,2h,3h-pyrrolo[2,1-b]quinazolin-3-yl}amino)benzoate)

3D PDB for NP0167215 (methyl 2-({9-oxo-1h,2h,3h-pyrrolo[2,1-b]quinazolin-3-yl}amino)benzoate)

SMILES for NP0167215 (methyl 2-({9-oxo-1h,2h,3h-pyrrolo[2,1-b]quinazolin-3-yl}amino)benzoate)

INCHI for NP0167215 (methyl 2-({9-oxo-1h,2h,3h-pyrrolo[2,1-b]quinazolin-3-yl}amino)benzoate)

Structure for NP0167215 (methyl 2-({9-oxo-1h,2h,3h-pyrrolo[2,1-b]quinazolin-3-yl}amino)benzoate)

3D Structure for NP0167215 (methyl 2-({9-oxo-1h,2h,3h-pyrrolo[2,1-b]quinazolin-3-yl}amino)benzoate)