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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 22:50:45 UTC

Update Date

2021-09-26 23:17:43 UTC

HMDB ID

HMDB0259889

Secondary Accession Numbers

None

Metabolite Identification

Common Name

N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide

Description

N-tert-butyl-3-[4-(2-methoxyphenyl)piperazin-1-yl]-2-phenylpropanimidic acid belongs to the class of organic compounds known as phenylpiperazines. Phenylpiperazines are compounds containing a phenylpiperazine skeleton, which consists of a piperazine bound to a phenyl group. Based on a literature review very few articles have been published on N-tert-butyl-3-[4-(2-methoxyphenyl)piperazin-1-yl]-2-phenylpropanimidic acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). N-tert-butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv1533004241523542D          

 29 31  0  0  0  0            999 V2000
   -2.8579    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6829    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0329    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 O   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
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 N   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
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 N   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   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   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
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   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
   -3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    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
  2  4  1  0  0  0  0
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  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
 10 15  1  0  0  0  0
 13 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
 16 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  8 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  2  0  0  0  0
 24 29  1  0  0  0  0
M  END

HMDB0259889
     RDKit          3D
N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide
 62 64  0  0  0  0  0  0  0  0999 V2000
    6.6345   -1.9873   -0.4324 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3936   -1.4423   -0.0810 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3020   -0.1093    0.2479 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4260    0.6753    0.2285 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2891    2.0044    0.5644 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0649    2.5292    0.9085 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9299    1.7128    0.9226 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0731    0.3988    0.5891 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9454   -0.4486    0.5963 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5552   -1.1088   -0.6075 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0729   -1.3205   -0.7273 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2794   -0.5970    0.1756 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4666    0.5102   -0.3222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5750    0.1020   -1.2337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5356   -0.7850   -0.5328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6856   -1.9793   -0.9524 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2824   -0.3548    0.5728 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2265   -1.2608    1.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3132   -1.7309    0.3172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8688   -0.6002    2.4159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4333   -2.4457    1.7694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3010    1.2711   -1.8052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7260    1.2729   -3.1252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3823    2.3312   -3.6829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6459    3.4552   -2.9270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2447    3.5018   -1.6141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5818    2.4123   -1.0799 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6951   -0.4781    1.5126 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1435   -0.6902    1.7814 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3963   -1.8621    0.3700 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5133   -3.0828   -0.6529 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9813   -1.5526   -1.4086 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3922    0.2668   -0.0417 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1599    2.6643    0.5614 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9266    3.5575    1.1748 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9800    2.1652    1.2001 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0448   -2.1040   -0.6204 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9572   -0.5455   -1.4827 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7896   -1.0579   -1.7762 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8174   -2.4147   -0.6409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8838    1.0571    0.5635 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2717    1.1935   -0.8261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1598   -0.4490   -2.1321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2081    0.6038    0.9731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9958   -1.9513   -0.7122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0432   -0.8804    0.2290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7809   -2.6243    0.7652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5924   -1.2887    2.8636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3507    0.3540    2.0581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1171   -0.3502    3.1931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0349   -2.8681    2.6066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2877   -3.2090    0.9587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4903   -2.0785    2.1802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5211    0.3991   -3.7147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7184    2.3315   -4.7275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1722    4.2915   -3.3886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4629    4.3926   -1.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2845    2.5058   -0.0537 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3774    0.5310    1.8934 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1173   -1.2048    2.1382 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4773    0.0531    2.5340 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3656   -1.6815    2.2429 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  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 18 21  1  0
 14 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 12 28  1  0
 28 29  1  0
  8  3  1  0
 29  9  1  0
 27 22  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 33  1  0
  5 34  1  0
  6 35  1  0
  7 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 13 41  1  0
 13 42  1  0
 14 43  1  0
 17 44  1  0
 19 45  1  0
 19 46  1  0
 19 47  1  0
 20 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  0
 21 52  1  0
 21 53  1  0
 23 54  1  0
 24 55  1  0
 25 56  1  0
 26 57  1  0
 27 58  1  0
 28 59  1  0
 28 60  1  0
 29 61  1  0
 29 62  1  0
M  END


  Mrv1533004241523542D          

 29 31  0  0  0  0            999 V2000
   -2.8579    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6829    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0329    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 O   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
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 N   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
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 N   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   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   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
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   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
   -3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    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
  2  4  1  0  0  0  0
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  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
 10 15  1  0  0  0  0
 13 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
 16 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  8 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  2  0  0  0  0
 24 29  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0259889

> <DATABASE_NAME>
hmdb

> <SMILES>
COC1=CC=CC=C1N1CCN(CC(C(=O)NC(C)(C)C)C2=CC=CC=C2)CC1

> <INCHI_IDENTIFIER>
InChI=1S/C24H33N3O2/c1-24(2,3)25-23(28)20(19-10-6-5-7-11-19)18-26-14-16-27(17-15-26)21-12-8-9-13-22(21)29-4/h5-13,20H,14-18H2,1-4H3,(H,25,28)

> <INCHI_KEY>
UMTDAKAAYOXIKU-UHFFFAOYSA-N

> <FORMULA>
C24H33N3O2

> <MOLECULAR_WEIGHT>
395.547

> <EXACT_MASS>
395.257277315

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
45.84487596273189

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-tert-butyl-3-[4-(2-methoxyphenyl)piperazin-1-yl]-2-phenylpropanamide

> <ALOGPS_LOGP>
3.71

> <JCHEM_LOGP>
3.633217383333333

> <ALOGPS_LOGS>
-3.86

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.47737102557468

> <JCHEM_PKA_STRONGEST_BASIC>
8.118598551755763

> <JCHEM_POLAR_SURFACE_AREA>
44.81

> <JCHEM_REFRACTIVITY>
118.97790000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.49e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-tert-butyl-3-[4-(2-methoxyphenyl)piperazin-1-yl]-2-phenylpropanamide

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0259889
     RDKit          3D
N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide
 62 64  0  0  0  0  0  0  0  0999 V2000
    6.6345   -1.9873   -0.4324 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3936   -1.4423   -0.0810 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3020   -0.1093    0.2479 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4260    0.6753    0.2285 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2891    2.0044    0.5644 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0649    2.5292    0.9085 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9299    1.7128    0.9226 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0731    0.3988    0.5891 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9454   -0.4486    0.5963 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5552   -1.1088   -0.6075 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0729   -1.3205   -0.7273 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2794   -0.5970    0.1756 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4666    0.5102   -0.3222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5750    0.1020   -1.2337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5356   -0.7850   -0.5328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6856   -1.9793   -0.9524 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2824   -0.3548    0.5728 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2265   -1.2608    1.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3132   -1.7309    0.3172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8688   -0.6002    2.4159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4333   -2.4457    1.7694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3010    1.2711   -1.8052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7260    1.2729   -3.1252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3823    2.3312   -3.6829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6459    3.4552   -2.9270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2447    3.5018   -1.6141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5818    2.4123   -1.0799 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6951   -0.4781    1.5126 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1435   -0.6902    1.7814 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3963   -1.8621    0.3700 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5133   -3.0828   -0.6529 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9813   -1.5526   -1.4086 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3922    0.2668   -0.0417 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1599    2.6643    0.5614 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9266    3.5575    1.1748 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9800    2.1652    1.2001 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0448   -2.1040   -0.6204 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9572   -0.5455   -1.4827 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7896   -1.0579   -1.7762 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8174   -2.4147   -0.6409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8838    1.0571    0.5635 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2717    1.1935   -0.8261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1598   -0.4490   -2.1321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2081    0.6038    0.9731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9958   -1.9513   -0.7122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0432   -0.8804    0.2290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7809   -2.6243    0.7652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5924   -1.2887    2.8636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3507    0.3540    2.0581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1171   -0.3502    3.1931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0349   -2.8681    2.6066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2877   -3.2090    0.9587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4903   -2.0785    2.1802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5211    0.3991   -3.7147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7184    2.3315   -4.7275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1722    4.2915   -3.3886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4629    4.3926   -1.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2845    2.5058   -0.0537 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3774    0.5310    1.8934 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1173   -1.2048    2.1382 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4773    0.0531    2.5340 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3656   -1.6815    2.2429 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  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 18 21  1  0
 14 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 12 28  1  0
 28 29  1  0
  8  3  1  0
 29  9  1  0
 27 22  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 33  1  0
  5 34  1  0
  6 35  1  0
  7 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 13 41  1  0
 13 42  1  0
 14 43  1  0
 17 44  1  0
 19 45  1  0
 19 46  1  0
 19 47  1  0
 20 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  0
 21 52  1  0
 21 53  1  0
 23 54  1  0
 24 55  1  0
 25 56  1  0
 26 57  1  0
 27 58  1  0
 28 59  1  0
 28 60  1  0
 29 61  1  0
 29 62  1  0
M  END

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -5.335   7.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.335   6.160   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -6.875   6.160   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.795   6.160   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0      -5.335   4.620   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -2.667   4.620   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      -2.667  -0.000   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      -2.667  -3.080   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -5.335   1.540   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -8.002   0.000   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -8.002   1.540   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -6.668   2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4    5                                             
CONECT    3    2                                                            
CONECT    4    2                                                            
CONECT    5    2    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   24                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14   10                                                       
CONECT   16   13   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   16   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24    8   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   24                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

COMPND    HMDB0259889
HETATM    1  C1  UNL     1       6.635  -1.987  -0.432  1.00  0.00           C  
HETATM    2  O1  UNL     1       5.394  -1.442  -0.081  1.00  0.00           O  
HETATM    3  C2  UNL     1       5.302  -0.109   0.248  1.00  0.00           C  
HETATM    4  C3  UNL     1       6.426   0.675   0.228  1.00  0.00           C  
HETATM    5  C4  UNL     1       6.289   2.004   0.564  1.00  0.00           C  
HETATM    6  C5  UNL     1       5.065   2.529   0.909  1.00  0.00           C  
HETATM    7  C6  UNL     1       3.930   1.713   0.923  1.00  0.00           C  
HETATM    8  C7  UNL     1       4.073   0.399   0.589  1.00  0.00           C  
HETATM    9  N1  UNL     1       2.945  -0.449   0.596  1.00  0.00           N  
HETATM   10  C8  UNL     1       2.555  -1.109  -0.607  1.00  0.00           C  
HETATM   11  C9  UNL     1       1.073  -1.320  -0.727  1.00  0.00           C  
HETATM   12  N2  UNL     1       0.279  -0.597   0.176  1.00  0.00           N  
HETATM   13  C10 UNL     1      -0.467   0.510  -0.322  1.00  0.00           C  
HETATM   14  C11 UNL     1      -1.575   0.102  -1.234  1.00  0.00           C  
HETATM   15  C12 UNL     1      -2.536  -0.785  -0.533  1.00  0.00           C  
HETATM   16  O2  UNL     1      -2.686  -1.979  -0.952  1.00  0.00           O  
HETATM   17  N3  UNL     1      -3.282  -0.355   0.573  1.00  0.00           N  
HETATM   18  C13 UNL     1      -4.226  -1.261   1.237  1.00  0.00           C  
HETATM   19  C14 UNL     1      -5.313  -1.731   0.317  1.00  0.00           C  
HETATM   20  C15 UNL     1      -4.869  -0.600   2.416  1.00  0.00           C  
HETATM   21  C16 UNL     1      -3.433  -2.446   1.769  1.00  0.00           C  
HETATM   22  C17 UNL     1      -2.301   1.271  -1.805  1.00  0.00           C  
HETATM   23  C18 UNL     1      -2.726   1.273  -3.125  1.00  0.00           C  
HETATM   24  C19 UNL     1      -3.382   2.331  -3.683  1.00  0.00           C  
HETATM   25  C20 UNL     1      -3.646   3.455  -2.927  1.00  0.00           C  
HETATM   26  C21 UNL     1      -3.245   3.502  -1.614  1.00  0.00           C  
HETATM   27  C22 UNL     1      -2.582   2.412  -1.080  1.00  0.00           C  
HETATM   28  C23 UNL     1       0.695  -0.478   1.513  1.00  0.00           C  
HETATM   29  C24 UNL     1       2.144  -0.690   1.781  1.00  0.00           C  
HETATM   30  H1  UNL     1       7.396  -1.862   0.370  1.00  0.00           H  
HETATM   31  H2  UNL     1       6.513  -3.083  -0.653  1.00  0.00           H  
HETATM   32  H3  UNL     1       6.981  -1.553  -1.409  1.00  0.00           H  
HETATM   33  H4  UNL     1       7.392   0.267  -0.042  1.00  0.00           H  
HETATM   34  H5  UNL     1       7.160   2.664   0.561  1.00  0.00           H  
HETATM   35  H6  UNL     1       4.927   3.557   1.175  1.00  0.00           H  
HETATM   36  H7  UNL     1       2.980   2.165   1.200  1.00  0.00           H  
HETATM   37  H8  UNL     1       3.045  -2.104  -0.620  1.00  0.00           H  
HETATM   38  H9  UNL     1       2.957  -0.545  -1.483  1.00  0.00           H  
HETATM   39  H10 UNL     1       0.790  -1.058  -1.776  1.00  0.00           H  
HETATM   40  H11 UNL     1       0.817  -2.415  -0.641  1.00  0.00           H  
HETATM   41  H12 UNL     1      -0.884   1.057   0.564  1.00  0.00           H  
HETATM   42  H13 UNL     1       0.272   1.193  -0.826  1.00  0.00           H  
HETATM   43  H14 UNL     1      -1.160  -0.449  -2.132  1.00  0.00           H  
HETATM   44  H15 UNL     1      -3.208   0.604   0.973  1.00  0.00           H  
HETATM   45  H16 UNL     1      -4.996  -1.951  -0.712  1.00  0.00           H  
HETATM   46  H17 UNL     1      -6.043  -0.880   0.229  1.00  0.00           H  
HETATM   47  H18 UNL     1      -5.781  -2.624   0.765  1.00  0.00           H  
HETATM   48  H19 UNL     1      -5.592  -1.289   2.864  1.00  0.00           H  
HETATM   49  H20 UNL     1      -5.351   0.354   2.058  1.00  0.00           H  
HETATM   50  H21 UNL     1      -4.117  -0.350   3.193  1.00  0.00           H  
HETATM   51  H22 UNL     1      -4.035  -2.868   2.607  1.00  0.00           H  
HETATM   52  H23 UNL     1      -3.288  -3.209   0.959  1.00  0.00           H  
HETATM   53  H24 UNL     1      -2.490  -2.078   2.180  1.00  0.00           H  
HETATM   54  H25 UNL     1      -2.521   0.399  -3.715  1.00  0.00           H  
HETATM   55  H26 UNL     1      -3.718   2.332  -4.728  1.00  0.00           H  
HETATM   56  H27 UNL     1      -4.172   4.291  -3.389  1.00  0.00           H  
HETATM   57  H28 UNL     1      -3.463   4.393  -1.043  1.00  0.00           H  
HETATM   58  H29 UNL     1      -2.285   2.506  -0.054  1.00  0.00           H  
HETATM   59  H30 UNL     1       0.377   0.531   1.893  1.00  0.00           H  
HETATM   60  H31 UNL     1       0.117  -1.205   2.138  1.00  0.00           H  
HETATM   61  H32 UNL     1       2.477   0.053   2.534  1.00  0.00           H  
HETATM   62  H33 UNL     1       2.366  -1.682   2.243  1.00  0.00           H  
CONECT    1    2   30   31   32
CONECT    2    3
CONECT    3    4    4    8
CONECT    4    5   33
CONECT    5    6    6   34
CONECT    6    7   35
CONECT    7    8    8   36
CONECT    8    9
CONECT    9   10   29
CONECT   10   11   37   38
CONECT   11   12   39   40
CONECT   12   13   28
CONECT   13   14   41   42
CONECT   14   15   22   43
CONECT   15   16   16   17
CONECT   17   18   44
CONECT   18   19   20   21
CONECT   19   45   46   47
CONECT   20   48   49   50
CONECT   21   51   52   53
CONECT   22   23   23   27
CONECT   23   24   54
CONECT   24   25   25   55
CONECT   25   26   56
CONECT   26   27   27   57
CONECT   27   58
CONECT   28   29   59   60
CONECT   29   61   62
END

HMDB0259889
     RDKit          3D
N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide
 62 64  0  0  0  0  0  0  0  0999 V2000
    6.6345   -1.9873   -0.4324 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3936   -1.4423   -0.0810 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3020   -0.1093    0.2479 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4260    0.6753    0.2285 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2891    2.0044    0.5644 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0649    2.5292    0.9085 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9299    1.7128    0.9226 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0731    0.3988    0.5891 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9454   -0.4486    0.5963 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5552   -1.1088   -0.6075 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0729   -1.3205   -0.7273 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2794   -0.5970    0.1756 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4666    0.5102   -0.3222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5750    0.1020   -1.2337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5356   -0.7850   -0.5328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6856   -1.9793   -0.9524 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2824   -0.3548    0.5728 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2265   -1.2608    1.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3132   -1.7309    0.3172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8688   -0.6002    2.4159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4333   -2.4457    1.7694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3010    1.2711   -1.8052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7260    1.2729   -3.1252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3823    2.3312   -3.6829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6459    3.4552   -2.9270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2447    3.5018   -1.6141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5818    2.4123   -1.0799 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6951   -0.4781    1.5126 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1435   -0.6902    1.7814 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3963   -1.8621    0.3700 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5133   -3.0828   -0.6529 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9813   -1.5526   -1.4086 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3922    0.2668   -0.0417 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1599    2.6643    0.5614 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9266    3.5575    1.1748 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9800    2.1652    1.2001 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0448   -2.1040   -0.6204 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9572   -0.5455   -1.4827 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7896   -1.0579   -1.7762 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8174   -2.4147   -0.6409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8838    1.0571    0.5635 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2717    1.1935   -0.8261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1598   -0.4490   -2.1321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2081    0.6038    0.9731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9958   -1.9513   -0.7122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0432   -0.8804    0.2290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7809   -2.6243    0.7652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5924   -1.2887    2.8636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3507    0.3540    2.0581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1171   -0.3502    3.1931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0349   -2.8681    2.6066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2877   -3.2090    0.9587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4903   -2.0785    2.1802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5211    0.3991   -3.7147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7184    2.3315   -4.7275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1722    4.2915   -3.3886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4629    4.3926   -1.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2845    2.5058   -0.0537 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3774    0.5310    1.8934 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1173   -1.2048    2.1382 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4773    0.0531    2.5340 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3656   -1.6815    2.2429 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  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
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 18 19  1  0
 18 20  1  0
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 14 22  1  0
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  8  3  1  0
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  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 33  1  0
  5 34  1  0
  6 35  1  0
  7 36  1  0
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 28 59  1  0
 28 60  1  0
 29 61  1  0
 29 62  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
N-Tert-butyl-3-[4-(2-methoxyphenyl)piperazin-1-yl]-2-phenylpropanimidate	Generator
N-Tert-butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide	MeSH

Chemical Formula

C₂₄H₃₃N₃O₂

Average Molecular Weight

395.547

Monoisotopic Molecular Weight

395.257277315

IUPAC Name

N-tert-butyl-3-[4-(2-methoxyphenyl)piperazin-1-yl]-2-phenylpropanamide

Traditional Name

N-tert-butyl-3-[4-(2-methoxyphenyl)piperazin-1-yl]-2-phenylpropanamide

CAS Registry Number

Not Available

SMILES

COC1=CC=CC=C1N1CCN(CC(C(=O)NC(C)(C)C)C2=CC=CC=C2)CC1

InChI Identifier

InChI=1S/C24H33N3O2/c1-24(2,3)25-23(28)20(19-10-6-5-7-11-19)18-26-14-16-27(17-15-26)21-12-8-9-13-22(21)29-4/h5-13,20H,14-18H2,1-4H3,(H,25,28)

InChI Key

UMTDAKAAYOXIKU-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylpiperazines. Phenylpiperazines are compounds containing a phenylpiperazine skeleton, which consists of a piperazine bound to a phenyl group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazinanes

Sub Class

Piperazines

Direct Parent

Phenylpiperazines

Alternative Parents

Substituents

Phenylpiperazine
N-arylpiperazine
Aminophenyl ether
Methoxyaniline
Anisole
Phenol ether
Tertiary aliphatic/aromatic amine
Phenoxy compound
Dialkylarylamine
Aniline or substituted anilines
Methoxybenzene
Aralkylamine
Alkyl aryl ether
N-alkylpiperazine
Monocyclic benzene moiety
Benzenoid
Tertiary amine
Tertiary aliphatic amine
Azacycle
Carboximidic acid derivative
Carboximidic acid
Organic 1,3-dipolar compound
Ether
Propargyl-type 1,3-dipolar organic compound
Organic oxygen compound
Hydrocarbon derivative
Organonitrogen compound
Organooxygen compound
Amine
Organic nitrogen compound
Organopnictogen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular 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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	3.71	ALOGPS
logP	3.63	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	15.48	ChemAxon
pKa (Strongest Basic)	8.12	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	44.81 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	118.98 m³·mol⁻¹	ChemAxon
Polarizability	45.84 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
AllCCS	[M+H]+	197.746	32859911
AllCCS	[M+H-H2O]+	195.222	32859911
AllCCS	[M+Na]+	200.738	32859911
AllCCS	[M+NH4]+	200.072	32859911
AllCCS	[M-H]-	201.732	32859911
AllCCS	[M+Na-2H]-	202.169	32859911
AllCCS	[M+HCOO]-	202.795	32859911
DeepCCS	[M+H]+	192.128	30932474
DeepCCS	[M-H]-	189.695	30932474
DeepCCS	[M-2H]-	224.061	30932474
DeepCCS	[M+Na]+	199.29	30932474

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	4.16 minutes	32390414
Predicted by Siyang on May 30, 2022	12.4838 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	2.17 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	1843.8 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	197.0 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	198.9 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	161.4 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	113.6 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	507.9 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	485.4 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	112.5 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	1092.6 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	472.7 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1516.0 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	339.5 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	357.9 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	189.2 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	247.4 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	8.4 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide	COC1=CC=CC=C1N1CCN(CC(C(=O)NC(C)(C)C)C2=CC=CC=C2)CC1	3531.6	Standard polar	33892256
N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide	COC1=CC=CC=C1N1CCN(CC(C(=O)NC(C)(C)C)C2=CC=CC=C2)CC1	2545.2	Standard non polar	33892256
N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide	COC1=CC=CC=C1N1CCN(CC(C(=O)NC(C)(C)C)C2=CC=CC=C2)CC1	2980.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide,1TMS,isomer #1	COC1=CC=CC=C1N1CCN(CC(C(=O)N(C(C)(C)C)[Si](C)(C)C)C2=CC=CC=C2)CC1	2901.0	Semi standard non polar	33892256
N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide,1TMS,isomer #1	COC1=CC=CC=C1N1CCN(CC(C(=O)N(C(C)(C)C)[Si](C)(C)C)C2=CC=CC=C2)CC1	2919.6	Standard non polar	33892256
N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide,1TMS,isomer #1	COC1=CC=CC=C1N1CCN(CC(C(=O)N(C(C)(C)C)[Si](C)(C)C)C2=CC=CC=C2)CC1	3827.5	Standard polar	33892256
N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide,1TBDMS,isomer #1	COC1=CC=CC=C1N1CCN(CC(C(=O)N(C(C)(C)C)[Si](C)(C)C(C)(C)C)C2=CC=CC=C2)CC1	3089.0	Semi standard non polar	33892256
N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide,1TBDMS,isomer #1	COC1=CC=CC=C1N1CCN(CC(C(=O)N(C(C)(C)C)[Si](C)(C)C(C)(C)C)C2=CC=CC=C2)CC1	3133.7	Standard non polar	33892256
N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide,1TBDMS,isomer #1	COC1=CC=CC=C1N1CCN(CC(C(=O)N(C(C)(C)C)[Si](C)(C)C(C)(C)C)C2=CC=CC=C2)CC1	3851.4	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a5a-6589000000-e938b98f4aa3b9d35b89	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

103008

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

115111

PDB ID

Not Available

ChEBI ID

104131

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide (HMDB0259889)

MOL for HMDB0259889 (N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide)

3D MOL for HMDB0259889 (N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide)

3D SDF for HMDB0259889 (N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide)

3D-SDF for HMDB0259889 (N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide)

PDB for HMDB0259889 (N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide)

3D PDB for HMDB0259889 (N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide)

SMILES for HMDB0259889 (N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide)

INCHI for HMDB0259889 (N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide)

Structure for HMDB0259889 (N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide)

3D Structure for HMDB0259889 (N-Tert-Butyl-3-(4-(2-methoxyphenyl)-piperazin-1-yl)-2-phenylpropanamide)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra