NP-MRD: Showing NP-Card for 3-methyl-N-(2-phenylethyl)butanamide (NP0006821)

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Record Information

Version

2.0

Created at

2020-12-09 03:44:47 UTC

Updated at

2025-02-11 15:45:17 UTC

NP-MRD ID

NP0006821

Natural Product DOI

https://doi.org/10.57994/1123

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-methyl-N-(2-phenylethyl)butanamide

Provided By

NPAtlas

Description

3-methyl-N-(2-phenylethyl)butanamide is found in Letendraea helminthicola and Streptomyces olivaceus. 3-methyl-N-(2-phenylethyl)butanamide was first documented in 2023 (PMID: 37794774). Based on a literature review very few articles have been published on 3-methyl-N-(2-phenylethyl)butanimidic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118353D          

 34 34  0  0  0  0            999 V2000
   -3.2528    2.6350    0.7810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7222    1.4462    0.0039 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8634    0.2783    0.9528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7791    1.0615   -1.1085 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4318    0.7183   -0.6225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1872    0.7696    0.5964 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4324    0.3371   -1.5227 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8705    0.0017   -1.0758 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9589   -1.1638   -0.1214 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3888   -1.3415    0.2123 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9435   -0.6764    1.2967 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2679   -0.8221    1.6302 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0617   -1.6421    0.8769 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5495   -2.3327   -0.2240 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1985   -2.1525   -0.5231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6138    2.3484    1.6459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1400    3.1441    1.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7378    3.3920    0.1458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7181    1.6768   -0.4017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1653    0.4408    1.7941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6486   -0.6779    0.4127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9159    0.2138    1.2947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2264    0.2688   -1.7316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6484    1.9411   -1.8018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6467    0.2984   -2.5384 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3928    0.8560   -0.5511 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5750   -0.2468   -1.9193 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5729   -2.0884   -0.6270 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3693   -0.9400    0.7902 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3110   -0.0314    1.8862 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6737   -0.3035    2.4653 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0905   -1.7543    1.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1405   -2.9800   -0.8329 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7651   -2.6744   -1.3734 H   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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  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  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 10  1  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  2 19  1  0  0  0  0
  3 20  1  0  0  0  0
  3 21  1  0  0  0  0
  3 22  1  0  0  0  0
  4 23  1  0  0  0  0
  4 24  1  0  0  0  0
  7 25  1  0  0  0  0
  8 26  1  0  0  0  0
  8 27  1  0  0  0  0
  9 28  1  0  0  0  0
  9 29  1  0  0  0  0
 11 30  1  0  0  0  0
 12 31  1  0  0  0  0
 13 32  1  0  0  0  0
 14 33  1  0  0  0  0
 15 34  1  0  0  0  0
M  END

     RDKit          3D

 34 34  0  0  0  0  0  0  0  0999 V2000
   -3.2528    2.6350    0.7810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7222    1.4462    0.0039 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8634    0.2783    0.9528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7791    1.0615   -1.1085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4318    0.7183   -0.6225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1872    0.7696    0.5964 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4324    0.3371   -1.5227 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8705    0.0017   -1.0758 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9589   -1.1638   -0.1214 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3888   -1.3415    0.2123 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9435   -0.6764    1.2967 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2679   -0.8221    1.6302 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0617   -1.6421    0.8769 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5495   -2.3327   -0.2240 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1985   -2.1525   -0.5231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6138    2.3484    1.6459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1400    3.1441    1.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7378    3.3920    0.1458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7181    1.6768   -0.4017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1653    0.4408    1.7941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6486   -0.6779    0.4127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9159    0.2138    1.2947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2264    0.2688   -1.7316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6484    1.9411   -1.8018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6467    0.2984   -2.5384 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3928    0.8560   -0.5511 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5750   -0.2468   -1.9193 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5729   -2.0884   -0.6270 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3693   -0.9400    0.7902 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3110   -0.0314    1.8862 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6737   -0.3035    2.4653 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0905   -1.7543    1.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1405   -2.9800   -0.8329 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7651   -2.6744   -1.3734 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 10  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  0
  3 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  7 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
  9 29  1  0
 11 30  1  0
 12 31  1  0
 13 32  1  0
 14 33  1  0
 15 34  1  0
M  END


  Mrv1652306242118353D          

 34 34  0  0  0  0            999 V2000
   -3.2528    2.6350    0.7810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7222    1.4462    0.0039 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8634    0.2783    0.9528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7791    1.0615   -1.1085 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4318    0.7183   -0.6225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1872    0.7696    0.5964 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4324    0.3371   -1.5227 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8705    0.0017   -1.0758 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9589   -1.1638   -0.1214 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3888   -1.3415    0.2123 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9435   -0.6764    1.2967 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2679   -0.8221    1.6302 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0617   -1.6421    0.8769 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5495   -2.3327   -0.2240 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1985   -2.1525   -0.5231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6138    2.3484    1.6459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1400    3.1441    1.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7378    3.3920    0.1458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7181    1.6768   -0.4017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1653    0.4408    1.7941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6486   -0.6779    0.4127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9159    0.2138    1.2947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2264    0.2688   -1.7316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6484    1.9411   -1.8018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6467    0.2984   -2.5384 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3928    0.8560   -0.5511 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5750   -0.2468   -1.9193 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5729   -2.0884   -0.6270 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3693   -0.9400    0.7902 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3110   -0.0314    1.8862 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6737   -0.3035    2.4653 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0905   -1.7543    1.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1405   -2.9800   -0.8329 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7651   -2.6744   -1.3734 H   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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  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  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 10  1  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  2 19  1  0  0  0  0
  3 20  1  0  0  0  0
  3 21  1  0  0  0  0
  3 22  1  0  0  0  0
  4 23  1  0  0  0  0
  4 24  1  0  0  0  0
  7 25  1  0  0  0  0
  8 26  1  0  0  0  0
  8 27  1  0  0  0  0
  9 28  1  0  0  0  0
  9 29  1  0  0  0  0
 11 30  1  0  0  0  0
 12 31  1  0  0  0  0
 13 32  1  0  0  0  0
 14 33  1  0  0  0  0
 15 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0006821

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]N(C(=O)C([H])([H])C([H])(C([H])([H])[H])C([H])([H])[H])C([H])([H])C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C13H19NO/c1-11(2)10-13(15)14-9-8-12-6-4-3-5-7-12/h3-7,11H,8-10H2,1-2H3,(H,14,15)

> <INCHI_KEY>
GIOFEZBLCNCEBN-UHFFFAOYSA-N

> <FORMULA>
C13H19NO

> <MOLECULAR_WEIGHT>
205.301

> <EXACT_MASS>
205.146664236

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
24.339541737389766

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-methyl-N-(2-phenylethyl)butanamide

> <ALOGPS_LOGP>
2.59

> <JCHEM_LOGP>
2.638645668333333

> <ALOGPS_LOGS>
-3.28

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.292975050599704

> <JCHEM_PKA_STRONGEST_BASIC>
-1.321850871649957

> <JCHEM_POLAR_SURFACE_AREA>
29.1

> <JCHEM_REFRACTIVITY>
62.50670000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.07e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-methyl-N-(2-phenylethyl)butanamide

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 34 34  0  0  0  0  0  0  0  0999 V2000
   -3.2528    2.6350    0.7810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7222    1.4462    0.0039 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8634    0.2783    0.9528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7791    1.0615   -1.1085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4318    0.7183   -0.6225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1872    0.7696    0.5964 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4324    0.3371   -1.5227 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8705    0.0017   -1.0758 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9589   -1.1638   -0.1214 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3888   -1.3415    0.2123 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9435   -0.6764    1.2967 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2679   -0.8221    1.6302 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0617   -1.6421    0.8769 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5495   -2.3327   -0.2240 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1985   -2.1525   -0.5231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6138    2.3484    1.6459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1400    3.1441    1.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7378    3.3920    0.1458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7181    1.6768   -0.4017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1653    0.4408    1.7941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6486   -0.6779    0.4127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9159    0.2138    1.2947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2264    0.2688   -1.7316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6484    1.9411   -1.8018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6467    0.2984   -2.5384 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3928    0.8560   -0.5511 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5750   -0.2468   -1.9193 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5729   -2.0884   -0.6270 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3693   -0.9400    0.7902 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3110   -0.0314    1.8862 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6737   -0.3035    2.4653 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0905   -1.7543    1.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1405   -2.9800   -0.8329 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7651   -2.6744   -1.3734 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 10  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  0
  3 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  7 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
  9 29  1  0
 11 30  1  0
 12 31  1  0
 13 32  1  0
 14 33  1  0
 15 34  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -3.253   2.635   0.781  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.722   1.446   0.004  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.863   0.278   0.953  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.779   1.062  -1.109  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.432   0.718  -0.623  0.00  0.00           C+0
HETATM    6  O   UNK     0      -1.187   0.770   0.596  0.00  0.00           O+0
HETATM    7  N   UNK     0      -0.432   0.337  -1.523  0.00  0.00           N+0
HETATM    8  C   UNK     0       0.871   0.002  -1.076  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.959  -1.164  -0.121  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.389  -1.341   0.212  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.943  -0.676   1.297  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.268  -0.822   1.630  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.062  -1.642   0.877  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.550  -2.333  -0.224  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.199  -2.152  -0.523  0.00  0.00           C+0
HETATM   16  H   UNK     0      -2.614   2.348   1.646  0.00  0.00           H+0
HETATM   17  H   UNK     0      -4.140   3.144   1.212  0.00  0.00           H+0
HETATM   18  H   UNK     0      -2.738   3.392   0.146  0.00  0.00           H+0
HETATM   19  H   UNK     0      -4.718   1.677  -0.402  0.00  0.00           H+0
HETATM   20  H   UNK     0      -3.165   0.441   1.794  0.00  0.00           H+0
HETATM   21  H   UNK     0      -3.649  -0.678   0.413  0.00  0.00           H+0
HETATM   22  H   UNK     0      -4.916   0.214   1.295  0.00  0.00           H+0
HETATM   23  H   UNK     0      -3.226   0.269  -1.732  0.00  0.00           H+0
HETATM   24  H   UNK     0      -2.648   1.941  -1.802  0.00  0.00           H+0
HETATM   25  H   UNK     0      -0.647   0.298  -2.538  0.00  0.00           H+0
HETATM   26  H   UNK     0       1.393   0.856  -0.551  0.00  0.00           H+0
HETATM   27  H   UNK     0       1.575  -0.247  -1.919  0.00  0.00           H+0
HETATM   28  H   UNK     0       0.573  -2.088  -0.627  0.00  0.00           H+0
HETATM   29  H   UNK     0       0.369  -0.940   0.790  0.00  0.00           H+0
HETATM   30  H   UNK     0       2.311  -0.031   1.886  0.00  0.00           H+0
HETATM   31  H   UNK     0       4.674  -0.304   2.465  0.00  0.00           H+0
HETATM   32  H   UNK     0       6.090  -1.754   1.137  0.00  0.00           H+0
HETATM   33  H   UNK     0       5.141  -2.980  -0.833  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.765  -2.674  -1.373  0.00  0.00           H+0
CONECT    1    2   16   17   18                                             
CONECT    2    1    3    4   19                                             
CONECT    3    2   20   21   22                                             
CONECT    4    2    5   23   24                                             
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   25                                                  
CONECT    8    7    9   26   27                                             
CONECT    9    8   10   28   29                                             
CONECT   10    9   11   15                                                  
CONECT   11   10   12   30                                                  
CONECT   12   11   13   31                                                  
CONECT   13   12   14   32                                                  
CONECT   14   13   15   33                                                  
CONECT   15   14   10   34                                                  
CONECT   16    1                                                            
CONECT   17    1                                                            
CONECT   18    1                                                            
CONECT   19    2                                                            
CONECT   20    3                                                            
CONECT   21    3                                                            
CONECT   22    3                                                            
CONECT   23    4                                                            
CONECT   24    4                                                            
CONECT   25    7                                                            
CONECT   26    8                                                            
CONECT   27    8                                                            
CONECT   28    9                                                            
CONECT   29    9                                                            
CONECT   30   11                                                            
CONECT   31   12                                                            
CONECT   32   13                                                            
CONECT   33   14                                                            
CONECT   34   15                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   68    0
END

RDKit          3D

34 34  0  0  0  0  0  0  0  0999 V2000
   -3.2528    2.6350    0.7810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7222    1.4462    0.0039 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8634    0.2783    0.9528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7791    1.0615   -1.1085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4318    0.7183   -0.6225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1872    0.7696    0.5964 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4324    0.3371   -1.5227 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8705    0.0017   -1.0758 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9589   -1.1638   -0.1214 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3888   -1.3415    0.2123 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9435   -0.6764    1.2967 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2679   -0.8221    1.6302 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0617   -1.6421    0.8769 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5495   -2.3327   -0.2240 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1985   -2.1525   -0.5231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6138    2.3484    1.6459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1400    3.1441    1.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7378    3.3920    0.1458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7181    1.6768   -0.4017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1653    0.4408    1.7941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6486   -0.6779    0.4127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9159    0.2138    1.2947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2264    0.2688   -1.7316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6484    1.9411   -1.8018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6467    0.2984   -2.5384 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3928    0.8560   -0.5511 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5750   -0.2468   -1.9193 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5729   -2.0884   -0.6270 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3693   -0.9400    0.7902 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3110   -0.0314    1.8862 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6737   -0.3035    2.4653 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0905   -1.7543    1.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1405   -2.9800   -0.8329 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7651   -2.6744   -1.3734 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 10  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  0
  3 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  7 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
  9 29  1  0
 11 30  1  0
 12 31  1  0
 13 32  1  0
 14 33  1  0
 15 34  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
3-Methyl-N-(2-phenylethyl)butanimidate	Generator

Chemical Formula

C₁₃H₁₉NO

Average Mass

205.3010 Da

Monoisotopic Mass

205.14666 Da

IUPAC Name

3-methyl-N-(2-phenylethyl)butanamide

Traditional Name

3-methyl-N-(2-phenylethyl)butanamide

CAS Registry Number

Not Available

SMILES

CC(C)CC(=O)NCCC1=CC=CC=C1

InChI Identifier

InChI=1S/C13H19NO/c1-11(2)10-13(15)14-9-8-12-6-4-3-5-7-12/h3-7,11H,8-10H2,1-2H3,(H,14,15)

InChI Key

GIOFEZBLCNCEBN-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 400, C2D6OS, simulated)	zhanglihua200061@163.com	Tianjin University of Traditional Chinese Medicine	zhanglihua	2024-05-09	View Spectrum

Species

Species of Origin

Species Name	Source	Reference
Letendraea helminthicola	NPAtlas	17216446
Paraconiothyrium sp. YK-03		Not Available
Streptomyces olivaceus	LOTUS Database	35616633

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as n-acyl amines. These are compounds containing a fatty acid moiety linked to an amine group through an ester linkage.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty amides

Direct Parent

N-acyl amines

Alternative Parents

Substituents

Benzenoid
N-acyl-amine
Monocyclic benzene moiety
Secondary carboxylic acid amide
Carboxamide group
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
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	2.59	ALOGPS
logP	2.64	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	16.29	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	29.1 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	62.51 m³·mol⁻¹	ChemAxon
Polarizability	24.34 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA003074

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

2789010

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3551002

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Gao WK, Song XY, Li SW, Xue BX, Wu HH, Zhang LH, Pei YH: A rare tetrahydroimidazopyridine from the marine-derived fungus Paraconiothyrium sp. YK-03. Nat Prod Res. 2023 Oct 5:1-7. doi: 10.1080/14786419.2023.2262720. [PubMed:37794774 ]
DOI: 10.1080/14786419.2023.2262720

Showing NP-Card for 3-methyl-N-(2-phenylethyl)butanamide (NP0006821)

MOL for NP0006821 (3-methyl-N-(2-phenylethyl)butanamide)

3D MOL for NP0006821 (3-methyl-N-(2-phenylethyl)butanamide)

3D SDF for NP0006821 (3-methyl-N-(2-phenylethyl)butanamide)

3D-SDF for NP0006821 (3-methyl-N-(2-phenylethyl)butanamide)

PDB for NP0006821 (3-methyl-N-(2-phenylethyl)butanamide)

3D PDB for NP0006821 (3-methyl-N-(2-phenylethyl)butanamide)

SMILES for NP0006821 (3-methyl-N-(2-phenylethyl)butanamide)

INCHI for NP0006821 (3-methyl-N-(2-phenylethyl)butanamide)

Structure for NP0006821 (3-methyl-N-(2-phenylethyl)butanamide)

3D Structure for NP0006821 (3-methyl-N-(2-phenylethyl)butanamide)