NP-MRD: Showing NP-Card for n-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide (NP0206269)

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Record Information

Version

2.0

Created at

2022-09-05 02:27:27 UTC

Updated at

2022-09-05 02:27:27 UTC

NP-MRD ID

NP0206269

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide

Description

N-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide belongs to the class of organic compounds known as benzamides. These are organic compounds containing a carboxamido substituent attached to a benzene ring. n-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide is found in Agelenopsis aperta. N-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171504552D          

 28 28  0  0  0  0            999 V2000
    5.0013  -11.1375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737  -11.5500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315  -11.5500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894  -11.5500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894  -12.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -11.5500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -12.7875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -12.3750    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  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
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  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  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 22 28  1  0  0  0  0
M  END

     RDKit          3D

 65 65  0  0  0  0  0  0  0  0999 V2000
    9.4777    2.4013    2.1595 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.2754    1.7165    0.8963 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6243    0.3613    1.0792 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2687    0.4516    1.7352 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7469   -0.9747    1.8447 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6120   -1.6015    0.5720 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5938   -1.0708   -0.2668 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2235   -1.3492    0.2681 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1577   -0.7554   -0.6704 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9028   -1.0958   -0.0352 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7358   -0.5995   -0.7669 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5579   -1.3186   -2.0631 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5428   -0.9044   -2.9542 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8767   -0.9549   -2.6066 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2927   -2.2422   -2.3637 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4866   -0.1189   -1.6666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0277   -0.3430   -1.6334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5402    0.6174   -0.5926 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9674    0.4638   -0.4744 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6687    1.2790    0.4435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0414    2.1202    1.1247 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1332    1.1231    0.5836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7492   -0.0273    0.1354 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1296   -0.1350    0.2746 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8233    0.9080    0.8523 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1968    0.7824    0.9825 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2077    2.0618    1.3020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8348    2.1587    1.1589 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5318    3.4225    1.9102 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4283    2.1493    2.5274 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2442    1.5593    0.4018 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6337    2.3410    0.2197 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4542   -0.0626    0.0601 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2855   -0.3400    1.6176 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3176    0.9416    2.7265 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5843    1.0763    1.1102 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8676   -0.9833    2.4872 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5442   -1.5450    2.4086 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6291   -2.6399    0.6200 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7228    0.0200   -0.4777 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6846   -1.5614   -1.2682 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0502   -2.4535    0.2218 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0372   -0.9236    1.2494 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2861   -1.1822   -1.6740 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2806    0.3519   -0.7698 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8263   -2.1426   -0.0262 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7721    0.4810   -0.9209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1006   -0.7969   -0.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5318   -1.1313   -2.6309 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5894   -2.4355   -1.9014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4449   -1.5049   -3.9425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3190    0.1418   -3.3642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4955   -2.3391   -1.4165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3550    0.9452   -1.8648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1520   -0.3105   -0.6129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2840   -1.3822   -1.4637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4564   -0.0042   -2.6077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2468    1.6667   -0.8202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0964    0.4122    0.4132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4445   -0.2403   -1.0727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2117   -0.8537   -0.3147 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5885   -1.0436   -0.0828 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7511    1.5073    1.3954 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7275    2.8739    1.7480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2850    3.0327    1.4875 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 25 27  1  0
 27 28  2  0
 28 22  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  6 39  1  0
  7 40  1  0
  7 41  1  0
  8 42  1  0
  8 43  1  0
  9 44  1  0
  9 45  1  0
 10 46  1  0
 11 47  1  0
 11 48  1  0
 12 49  1  0
 12 50  1  0
 13 51  1  0
 13 52  1  0
 15 53  1  0
 16 54  1  0
 16 55  1  0
 17 56  1  0
 17 57  1  0
 18 58  1  0
 18 59  1  0
 19 60  1  0
 23 61  1  0
 24 62  1  0
 26 63  1  0
 27 64  1  0
 28 65  1  0
M  END


  Mrv1533004171504552D          

 28 28  0  0  0  0            999 V2000
    5.0013  -11.1375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737  -11.5500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315  -11.5500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894  -11.5500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894  -12.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -11.5500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -12.7875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -12.3750    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  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
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  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  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 22 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0206269

> <DATABASE_NAME>
NP-MRD

> <SMILES>
NCCCCNCCCNCCCN(O)CCCNC(=O)C1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H37N5O3/c21-10-1-2-11-22-12-3-13-23-14-4-16-25(28)17-5-15-24-20(27)18-6-8-19(26)9-7-18/h6-9,22-23,26,28H,1-5,10-17,21H2,(H,24,27)

> <INCHI_KEY>
DRGTWDCOBHOVSL-UHFFFAOYSA-N

> <FORMULA>
C20H37N5O3

> <MOLECULAR_WEIGHT>
395.548

> <EXACT_MASS>
395.289640071

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
47.259674058215154

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide

> <ALOGPS_LOGP>
0.54

> <JCHEM_LOGP>
-2.1677952481085647

> <ALOGPS_LOGS>
-3.61

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
3

> <JCHEM_PKA>
15.441541213489899

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.205858180827553

> <JCHEM_PKA_STRONGEST_BASIC>
10.929560857163711

> <JCHEM_POLAR_SURFACE_AREA>
122.88000000000001

> <JCHEM_REFRACTIVITY>
114.00779999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
17

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.80e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  N   UNK     0       9.336 -20.790   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0      10.669 -21.560   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.003 -20.790   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.337 -21.560   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      14.670 -20.790   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      16.004 -21.560   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      17.338 -20.790   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      18.672 -21.560   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      20.005 -20.790   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      21.339 -21.560   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      22.673 -20.790   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      24.006 -21.560   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      25.340 -20.790   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0      26.674 -21.560   0.000  0.00  0.00           N+0
HETATM   15  O   UNK     0      26.674 -23.100   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      28.007 -20.790   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      29.341 -21.560   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      30.675 -20.790   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0      32.008 -21.560   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0      33.342 -20.790   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      33.342 -19.250   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      34.676 -21.560   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      36.009 -20.790   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      37.343 -21.560   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      37.343 -23.100   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      38.677 -23.870   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      36.009 -23.870   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      34.676 -23.100   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   28                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   22                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₇N₅O₃

Average Mass

395.5480 Da

Monoisotopic Mass

395.28964 Da

IUPAC Name

N-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide

Traditional Name

N-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide

CAS Registry Number

Not Available

SMILES

NCCCCNCCCNCCCN(O)CCCNC(=O)C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C20H37N5O3/c21-10-1-2-11-22-12-3-13-23-14-4-16-25(28)17-5-15-24-20(27)18-6-8-19(26)9-7-18/h6-9,22-23,26,28H,1-5,10-17,21H2,(H,24,27)

InChI Key

DRGTWDCOBHOVSL-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
Agelenopsis aperta	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzamides. These are organic compounds containing a carboxamido substituent attached to a benzene ring.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Benzamides

Alternative Parents

Substituents

Benzamide
Benzoyl
1-hydroxy-2-unsubstituted benzenoid
Phenol
Amino acid or derivatives
Carboxamide group
Secondary carboxylic acid amide
Carboxylic acid derivative
Secondary aliphatic amine
N-organohydroxylamine
Secondary amine
Organonitrogen compound
Primary aliphatic amine
Organic nitrogen compound
Amine
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Primary amine
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	0.54	ALOGPS
logP	-2.2	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	8.21	ChemAxon
pKa (Strongest Basic)	10.93	ChemAxon
Physiological Charge	3	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	122.88 Å²	ChemAxon
Rotatable Bond Count	17	ChemAxon
Refractivity	114.01 m³·mol⁻¹	ChemAxon
Polarizability	47.26 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

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

102304251

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide (NP0206269)

MOL for NP0206269 (n-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide)

3D MOL for NP0206269 (n-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide)

3D SDF for NP0206269 (n-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide)

3D-SDF for NP0206269 (n-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide)

PDB for NP0206269 (n-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide)

3D PDB for NP0206269 (n-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide)

SMILES for NP0206269 (n-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide)

INCHI for NP0206269 (n-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide)

Structure for NP0206269 (n-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide)

3D Structure for NP0206269 (n-(3-{[3-({3-[(4-aminobutyl)amino]propyl}amino)propyl](hydroxy)amino}propyl)-4-hydroxybenzamide)