NP-MRD: Showing NP-Card for N-Benzoyl-L-phenyalaninol (NP0023213)

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Record Information

Version

2.0

Created at

2021-01-06 08:19:29 UTC

Updated at

2021-07-15 17:41:08 UTC

NP-MRD ID

NP0023213

Secondary Accession Numbers

None

Natural Product Identification

Common Name

N-Benzoyl-L-phenyalaninol

Provided By

NPAtlas

Description

N-benzoylphenylalaninol is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. N-Benzoyl-L-phenyalaninol is found in Aspergillus flavipes, Houttuynia cordata and Penicillium brevicompactum. N-Benzoyl-L-phenyalaninol was first documented in 1977 (PMID: 875642). Based on a literature review a small amount of articles have been published on N-benzoylphenylalaninol (PMID: 19035573) (PMID: 19938546) (PMID: 29493149).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242105403D          

 36 37  0  0  0  0            999 V2000
   -1.3992   -0.8936    1.8028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7819   -0.2836    0.7753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8065    0.3694   -0.0091 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6123    0.3384    0.3619 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0173    1.7821    0.5865 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8454    2.5578   -0.5412 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3479   -0.2923   -0.7788 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7983   -0.3973   -0.5585 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3367   -1.5166    0.0396 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6801   -1.6674    0.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5318   -0.6601   -0.1122 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0144    0.4706   -0.7133 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6605    0.6082   -0.9379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1900   -0.2638    0.4242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7113    0.3749   -0.6777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0789    0.3475   -0.9470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9686   -0.3142   -0.1308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4618   -0.9585    0.9766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1112   -0.9308    1.2414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0759    0.8881   -0.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7670   -0.2320    1.2762 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3918    2.2247    1.3885 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0676    1.8772    0.9051 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5062    2.0934   -1.3232 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0997    0.1908   -1.7573 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9587   -1.3372   -0.8734 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6829   -2.3444    0.3586 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0650   -2.5552    0.7387 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5922   -0.7784    0.0687 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6890    1.2631   -1.0129 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3199    1.5202   -1.4137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0346    0.9028   -1.3363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4541    0.8654   -1.8298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0409   -0.3249   -0.3584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1507   -1.4820    1.6257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7192   -1.4422    2.1181 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  4  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  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
  2 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 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
 13  8  1  0  0  0  0
 19 14  1  0  0  0  0
  3 20  1  0  0  0  0
  4 21  1  1  0  0  0
  5 22  1  0  0  0  0
  5 23  1  0  0  0  0
  6 24  1  0  0  0  0
  7 25  1  0  0  0  0
  7 26  1  0  0  0  0
  9 27  1  0  0  0  0
 10 28  1  0  0  0  0
 11 29  1  0  0  0  0
 12 30  1  0  0  0  0
 13 31  1  0  0  0  0
 15 32  1  0  0  0  0
 16 33  1  0  0  0  0
 17 34  1  0  0  0  0
 18 35  1  0  0  0  0
 19 36  1  0  0  0  0
M  END

     RDKit          3D

 36 37  0  0  0  0  0  0  0  0999 V2000
   -1.3992   -0.8936    1.8028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7819   -0.2836    0.7753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8065    0.3694   -0.0091 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6123    0.3384    0.3619 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0173    1.7821    0.5865 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8454    2.5578   -0.5412 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3479   -0.2923   -0.7788 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7983   -0.3973   -0.5585 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3367   -1.5166    0.0396 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6801   -1.6674    0.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5318   -0.6601   -0.1122 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0144    0.4706   -0.7133 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6605    0.6082   -0.9379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1900   -0.2638    0.4242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7113    0.3749   -0.6777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0789    0.3475   -0.9470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9686   -0.3142   -0.1308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4618   -0.9585    0.9766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1112   -0.9308    1.2414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0759    0.8881   -0.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7670   -0.2320    1.2762 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3918    2.2247    1.3885 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0676    1.8772    0.9051 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5062    2.0934   -1.3232 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0997    0.1908   -1.7573 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9587   -1.3372   -0.8734 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6829   -2.3444    0.3586 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0650   -2.5552    0.7387 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5922   -0.7784    0.0687 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6890    1.2631   -1.0129 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3199    1.5202   -1.4137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0346    0.9028   -1.3363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4541    0.8654   -1.8298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0409   -0.3249   -0.3584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1507   -1.4820    1.6257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7192   -1.4422    2.1181 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  4  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
  2 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 13  8  1  0
 19 14  1  0
  3 20  1  0
  4 21  1  1
  5 22  1  0
  5 23  1  0
  6 24  1  0
  7 25  1  0
  7 26  1  0
  9 27  1  0
 10 28  1  0
 11 29  1  0
 12 30  1  0
 13 31  1  0
 15 32  1  0
 16 33  1  0
 17 34  1  0
 18 35  1  0
 19 36  1  0
M  END


  Mrv1652306242105403D          

 36 37  0  0  0  0            999 V2000
   -1.3992   -0.8936    1.8028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7819   -0.2836    0.7753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8065    0.3694   -0.0091 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6123    0.3384    0.3619 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0173    1.7821    0.5865 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8454    2.5578   -0.5412 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3479   -0.2923   -0.7788 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7983   -0.3973   -0.5585 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3367   -1.5166    0.0396 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6801   -1.6674    0.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5318   -0.6601   -0.1122 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0144    0.4706   -0.7133 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6605    0.6082   -0.9379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1900   -0.2638    0.4242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7113    0.3749   -0.6777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0789    0.3475   -0.9470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9686   -0.3142   -0.1308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4618   -0.9585    0.9766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1112   -0.9308    1.2414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0759    0.8881   -0.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7670   -0.2320    1.2762 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3918    2.2247    1.3885 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0676    1.8772    0.9051 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5062    2.0934   -1.3232 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0997    0.1908   -1.7573 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9587   -1.3372   -0.8734 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6829   -2.3444    0.3586 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0650   -2.5552    0.7387 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5922   -0.7784    0.0687 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6890    1.2631   -1.0129 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3199    1.5202   -1.4137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0346    0.9028   -1.3363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4541    0.8654   -1.8298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0409   -0.3249   -0.3584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1507   -1.4820    1.6257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7192   -1.4422    2.1181 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  4  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  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
  2 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 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
 13  8  1  0  0  0  0
 19 14  1  0  0  0  0
  3 20  1  0  0  0  0
  4 21  1  1  0  0  0
  5 22  1  0  0  0  0
  5 23  1  0  0  0  0
  6 24  1  0  0  0  0
  7 25  1  0  0  0  0
  7 26  1  0  0  0  0
  9 27  1  0  0  0  0
 10 28  1  0  0  0  0
 11 29  1  0  0  0  0
 12 30  1  0  0  0  0
 13 31  1  0  0  0  0
 15 32  1  0  0  0  0
 16 33  1  0  0  0  0
 17 34  1  0  0  0  0
 18 35  1  0  0  0  0
 19 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0023213

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C16H17NO2/c18-12-15(11-13-7-3-1-4-8-13)17-16(19)14-9-5-2-6-10-14/h1-10,15,18H,11-12H2,(H,17,19)/t15-/m0/s1

> <INCHI_KEY>
RFYNAVYPYXLVOM-HNNXBMFYSA-N

> <FORMULA>
C16H17NO2

> <MOLECULAR_WEIGHT>
255.317

> <EXACT_MASS>
255.125928791

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
28.37861815966861

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-[(2S)-1-hydroxy-3-phenylpropan-2-yl]benzamide

> <ALOGPS_LOGP>
2.32

> <JCHEM_LOGP>
2.4303615563333336

> <ALOGPS_LOGS>
-3.94

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.340870117535609

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.775432046100878

> <JCHEM_PKA_STRONGEST_BASIC>
-0.971362033997225

> <JCHEM_POLAR_SURFACE_AREA>
49.33

> <JCHEM_REFRACTIVITY>
75.36320000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.92e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-[(2S)-1-hydroxy-3-phenylpropan-2-yl]benzamide

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 36 37  0  0  0  0  0  0  0  0999 V2000
   -1.3992   -0.8936    1.8028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7819   -0.2836    0.7753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8065    0.3694   -0.0091 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6123    0.3384    0.3619 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0173    1.7821    0.5865 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8454    2.5578   -0.5412 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3479   -0.2923   -0.7788 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7983   -0.3973   -0.5585 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3367   -1.5166    0.0396 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6801   -1.6674    0.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5318   -0.6601   -0.1122 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0144    0.4706   -0.7133 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6605    0.6082   -0.9379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1900   -0.2638    0.4242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7113    0.3749   -0.6777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0789    0.3475   -0.9470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9686   -0.3142   -0.1308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4618   -0.9585    0.9766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1112   -0.9308    1.2414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0759    0.8881   -0.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7670   -0.2320    1.2762 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3918    2.2247    1.3885 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0676    1.8772    0.9051 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5062    2.0934   -1.3232 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0997    0.1908   -1.7573 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9587   -1.3372   -0.8734 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6829   -2.3444    0.3586 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0650   -2.5552    0.7387 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5922   -0.7784    0.0687 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6890    1.2631   -1.0129 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3199    1.5202   -1.4137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0346    0.9028   -1.3363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4541    0.8654   -1.8298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0409   -0.3249   -0.3584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1507   -1.4820    1.6257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7192   -1.4422    2.1181 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  4  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
  2 14  1  0
 14 15  2  0
 15 16  1  0
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 17 18  1  0
 18 19  2  0
 13  8  1  0
 19 14  1  0
  3 20  1  0
  4 21  1  1
  5 22  1  0
  5 23  1  0
  6 24  1  0
  7 25  1  0
  7 26  1  0
  9 27  1  0
 10 28  1  0
 11 29  1  0
 12 30  1  0
 13 31  1  0
 15 32  1  0
 16 33  1  0
 17 34  1  0
 18 35  1  0
 19 36  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  O   UNK     0      -1.399  -0.894   1.803  0.00  0.00           O+0
HETATM    2  C   UNK     0      -1.782  -0.284   0.775  0.00  0.00           C+0
HETATM    3  N   UNK     0      -0.807   0.369  -0.009  0.00  0.00           N+0
HETATM    4  C   UNK     0       0.612   0.338   0.362  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.017   1.782   0.587  0.00  0.00           C+0
HETATM    6  O   UNK     0       0.845   2.558  -0.541  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.348  -0.292  -0.779  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.798  -0.397  -0.559  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.337  -1.517   0.040  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.680  -1.667   0.269  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.532  -0.660  -0.112  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.014   0.471  -0.713  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.660   0.608  -0.938  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.190  -0.264   0.424  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.711   0.375  -0.678  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.079   0.348  -0.947  0.00  0.00           C+0
HETATM   17  C   UNK     0      -5.969  -0.314  -0.131  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.462  -0.959   0.977  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.111  -0.931   1.241  0.00  0.00           C+0
HETATM   20  H   UNK     0      -1.076   0.888  -0.870  0.00  0.00           H+0
HETATM   21  H   UNK     0       0.767  -0.232   1.276  0.00  0.00           H+0
HETATM   22  H   UNK     0       0.392   2.225   1.389  0.00  0.00           H+0
HETATM   23  H   UNK     0       2.068   1.877   0.905  0.00  0.00           H+0
HETATM   24  H   UNK     0       0.506   2.093  -1.323  0.00  0.00           H+0
HETATM   25  H   UNK     0       1.100   0.191  -1.757  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.959  -1.337  -0.873  0.00  0.00           H+0
HETATM   27  H   UNK     0       2.683  -2.344   0.359  0.00  0.00           H+0
HETATM   28  H   UNK     0       5.065  -2.555   0.739  0.00  0.00           H+0
HETATM   29  H   UNK     0       6.592  -0.778   0.069  0.00  0.00           H+0
HETATM   30  H   UNK     0       5.689   1.263  -1.013  0.00  0.00           H+0
HETATM   31  H   UNK     0       3.320   1.520  -1.414  0.00  0.00           H+0
HETATM   32  H   UNK     0      -3.035   0.903  -1.336  0.00  0.00           H+0
HETATM   33  H   UNK     0      -5.454   0.865  -1.830  0.00  0.00           H+0
HETATM   34  H   UNK     0      -7.041  -0.325  -0.358  0.00  0.00           H+0
HETATM   35  H   UNK     0      -6.151  -1.482   1.626  0.00  0.00           H+0
HETATM   36  H   UNK     0      -3.719  -1.442   2.118  0.00  0.00           H+0
CONECT    1    2                                                            
CONECT    2    1    3   14                                                  
CONECT    3    2    4   20                                                  
CONECT    4    3    5    7   21                                             
CONECT    5    4    6   22   23                                             
CONECT    6    5   24                                                       
CONECT    7    4    8   25   26                                             
CONECT    8    7    9   13                                                  
CONECT    9    8   10   27                                                  
CONECT   10    9   11   28                                                  
CONECT   11   10   12   29                                                  
CONECT   12   11   13   30                                                  
CONECT   13   12    8   31                                                  
CONECT   14    2   15   19                                                  
CONECT   15   14   16   32                                                  
CONECT   16   15   17   33                                                  
CONECT   17   16   18   34                                                  
CONECT   18   17   19   35                                                  
CONECT   19   18   14   36                                                  
CONECT   20    3                                                            
CONECT   21    4                                                            
CONECT   22    5                                                            
CONECT   23    5                                                            
CONECT   24    6                                                            
CONECT   25    7                                                            
CONECT   26    7                                                            
CONECT   27    9                                                            
CONECT   28   10                                                            
CONECT   29   11                                                            
CONECT   30   12                                                            
CONECT   31   13                                                            
CONECT   32   15                                                            
CONECT   33   16                                                            
CONECT   34   17                                                            
CONECT   35   18                                                            
CONECT   36   19                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   74    0
END

RDKit          3D

36 37  0  0  0  0  0  0  0  0999 V2000
   -1.3992   -0.8936    1.8028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7819   -0.2836    0.7753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8065    0.3694   -0.0091 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6123    0.3384    0.3619 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0173    1.7821    0.5865 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8454    2.5578   -0.5412 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3479   -0.2923   -0.7788 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7983   -0.3973   -0.5585 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3367   -1.5166    0.0396 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6801   -1.6674    0.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5318   -0.6601   -0.1122 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0144    0.4706   -0.7133 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6605    0.6082   -0.9379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1900   -0.2638    0.4242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7113    0.3749   -0.6777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0789    0.3475   -0.9470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9686   -0.3142   -0.1308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4618   -0.9585    0.9766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1112   -0.9308    1.2414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0759    0.8881   -0.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7670   -0.2320    1.2762 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3918    2.2247    1.3885 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0676    1.8772    0.9051 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5062    2.0934   -1.3232 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0997    0.1908   -1.7573 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9587   -1.3372   -0.8734 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6829   -2.3444    0.3586 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0650   -2.5552    0.7387 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5922   -0.7784    0.0687 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6890    1.2631   -1.0129 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3199    1.5202   -1.4137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0346    0.9028   -1.3363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4541    0.8654   -1.8298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0409   -0.3249   -0.3584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1507   -1.4820    1.6257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7192   -1.4422    2.1181 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  4  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
  2 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 13  8  1  0
 19 14  1  0
  3 20  1  0
  4 21  1  1
  5 22  1  0
  5 23  1  0
  6 24  1  0
  7 25  1  0
  7 26  1  0
  9 27  1  0
 10 28  1  0
 11 29  1  0
 12 30  1  0
 13 31  1  0
 15 32  1  0
 16 33  1  0
 17 34  1  0
 18 35  1  0
 19 36  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
N-Benzoyl-L-phenylalaninol	MeSH

Chemical Formula

C₁₆H₁₇NO₂

Average Mass

255.3170 Da

Monoisotopic Mass

255.12593 Da

IUPAC Name

N-[(2S)-1-hydroxy-3-phenylpropan-2-yl]benzamide

Traditional Name

N-[(2S)-1-hydroxy-3-phenylpropan-2-yl]benzamide

CAS Registry Number

Not Available

SMILES

OC[C@H](CC1=CC=CC=C1)NC(=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C16H17NO2/c18-12-15(11-13-7-3-1-4-8-13)17-16(19)14-9-5-2-6-10-14/h1-10,15,18H,11-12H2,(H,17,19)/t15-/m0/s1

InChI Key

RFYNAVYPYXLVOM-HNNXBMFYSA-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, 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

Not Available

Species

Species of Origin

Species Name	Source	Reference
Aspergillus flavipes	NPAtlas	875642
Begonia nantoensis	KNApSAcK Database	22123792
Houttuynia cordata	LOTUS Database	35616633
Penicillium brevicompactum	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	2.32	ALOGPS
logP	2.43	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	14.78	ChemAxon
pKa (Strongest Basic)	-0.97	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	49.33 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	75.36 m³·mol⁻¹	ChemAxon
Polarizability	28.38 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA008537

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00031476

Chemspider ID

745307

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

852848

PDB ID

Not Available

ChEBI ID

145107

Good Scents ID

Not Available

References

General References

Clark AM, Hufford CD, Robertson LW: Two metabolites from Aspergillus flavipes. Lloydia. 1977 Mar-Apr;40(2):146-51. [PubMed:875642 ]
Ma CY, Musoke SF, Tan GT, Sydara K, Bouamanivong S, Southavong B, Soejarto DD, Fong HH, Zhang HJ: Study of antimalarial activity of chemical constituents from Diospyros quaesita. Chem Biodivers. 2008 Nov;5(11):2442-8. doi: 10.1002/cbdv.200890209. [PubMed:19035573 ]
Zhang W, Kong L: [Chemical constituents in the introduced Coleus forskohlii]. Zhongguo Zhong Yao Za Zhi. 2009 Aug;34(16):2060-2. [PubMed:19938546 ]
Du DS, Cheng ZH, Chen DF: [Anti-complement alkaloids from whole plants of Viola yedoensis]. Zhongguo Zhong Yao Za Zhi. 2017 Dec;42(24):4794-4800. doi: 10.19540/j.cnki.cjcmm.20170928.012. [PubMed:29493149 ]

Showing NP-Card for N-Benzoyl-L-phenyalaninol (NP0023213)

MOL for NP0023213 (N-Benzoyl-L-phenyalaninol)

3D MOL for NP0023213 (N-Benzoyl-L-phenyalaninol)

3D SDF for NP0023213 (N-Benzoyl-L-phenyalaninol)

3D-SDF for NP0023213 (N-Benzoyl-L-phenyalaninol)

PDB for NP0023213 (N-Benzoyl-L-phenyalaninol)

3D PDB for NP0023213 (N-Benzoyl-L-phenyalaninol)

SMILES for NP0023213 (N-Benzoyl-L-phenyalaninol)

INCHI for NP0023213 (N-Benzoyl-L-phenyalaninol)

Structure for NP0023213 (N-Benzoyl-L-phenyalaninol)

3D Structure for NP0023213 (N-Benzoyl-L-phenyalaninol)