NP-MRD: Showing NP-Card for 3-[2-[2-hydroxy-3-methylphenyl-5-(hydroxymethyl)]-2-oxoethyl]glutarimide (NP0012970)

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Record Information

Version

2.0

Created at

2021-01-05 22:29:16 UTC

Updated at

2021-07-15 17:13:13 UTC

NP-MRD ID

NP0012970

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[2-[2-hydroxy-3-methylphenyl-5-(hydroxymethyl)]-2-oxoethyl]glutarimide

Provided By

NPAtlas

Description

3-[2-[2-Hydroxy-3-methylphenyl-5-(hydroxymethyl)]-2-oxoethyl]glutarimide belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. 3-[2-[2-hydroxy-3-methylphenyl-5-(hydroxymethyl)]-2-oxoethyl]glutarimide is found in Streptomyces and Streptomyces anulatus. Based on a literature review very few articles have been published on 3-[2-[2-hydroxy-3-methylphenyl-5-(hydroxymethyl)]-2-oxoethyl]glutarimide.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242119323D          

 38 39  0  0  0  0            999 V2000
    3.5753   -1.9853   -1.3327 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0156   -0.7995   -0.6270 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8204    0.1546   -0.0474 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2819    1.2362    0.5957 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0992    2.2965    1.2388 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4526    2.0888    1.1264 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9235    1.3682    0.6618 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0907    0.4069    0.0777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3657    0.5671    0.1629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8355    1.5926    0.7703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2556   -0.4420   -0.4443 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6924   -0.0702   -0.1721 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6525   -1.0719   -0.8040 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0147   -0.4626   -0.6541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9347   -0.7620   -1.4487 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2876    0.4782    0.4078 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3181    0.6538    1.4259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5067    1.4016    2.4021 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0387   -0.0859    1.3110 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6206   -0.6788   -0.5681 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8390   -1.6763   -1.1738 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1066   -2.9057   -0.9075 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3017   -1.9809   -2.4155 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6568   -2.0542   -1.1950 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8890    0.0665   -0.0899 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8583    3.2572    0.7101 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7477    2.4192    2.2745 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7844    1.2818    1.5477 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4336    2.2085    1.1608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1089   -1.4508    0.0066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0718   -0.4325   -1.5348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9456    0.9193   -0.5812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5758   -1.9915   -0.1745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3866   -1.2374   -1.8537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1869    1.0104    0.4098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2587    0.2879    1.9661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3121   -1.1571    1.5702 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2515   -2.4507   -1.6343 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 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  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  8 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20  2  1  0  0  0  0
 19 12  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  3 25  1  0  0  0  0
  5 26  1  0  0  0  0
  5 27  1  0  0  0  0
  6 28  1  0  0  0  0
  7 29  1  0  0  0  0
 11 30  1  0  0  0  0
 11 31  1  0  0  0  0
 12 32  1  0  0  0  0
 13 33  1  0  0  0  0
 13 34  1  0  0  0  0
 16 35  1  0  0  0  0
 19 36  1  0  0  0  0
 19 37  1  0  0  0  0
 21 38  1  0  0  0  0
M  END

     RDKit          3D

 38 39  0  0  0  0  0  0  0  0999 V2000
    3.5753   -1.9853   -1.3327 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0156   -0.7995   -0.6270 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8204    0.1546   -0.0474 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2819    1.2362    0.5957 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0992    2.2965    1.2388 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4526    2.0888    1.1264 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9235    1.3682    0.6618 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0907    0.4069    0.0777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3657    0.5671    0.1629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8355    1.5926    0.7703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2556   -0.4420   -0.4443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6924   -0.0702   -0.1721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6525   -1.0719   -0.8040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0147   -0.4626   -0.6541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9347   -0.7620   -1.4487 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2876    0.4782    0.4078 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3181    0.6538    1.4259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5067    1.4016    2.4021 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0387   -0.0859    1.3110 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6206   -0.6788   -0.5681 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8390   -1.6763   -1.1738 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1066   -2.9057   -0.9075 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3017   -1.9809   -2.4155 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6568   -2.0542   -1.1950 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8890    0.0665   -0.0899 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8583    3.2572    0.7101 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7477    2.4192    2.2745 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7844    1.2818    1.5477 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4336    2.2085    1.1608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1089   -1.4508    0.0066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0718   -0.4325   -1.5348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9456    0.9193   -0.5812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5758   -1.9915   -0.1745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3866   -1.2374   -1.8537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1869    1.0104    0.4098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2587    0.2879    1.9661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3121   -1.1571    1.5702 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2515   -2.4507   -1.6343 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  4  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
  8 20  2  0
 20 21  1  0
 20  2  1  0
 19 12  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  5 26  1  0
  5 27  1  0
  6 28  1  0
  7 29  1  0
 11 30  1  0
 11 31  1  0
 12 32  1  0
 13 33  1  0
 13 34  1  0
 16 35  1  0
 19 36  1  0
 19 37  1  0
 21 38  1  0
M  END


  Mrv1652306242119323D          

 38 39  0  0  0  0            999 V2000
    3.5753   -1.9853   -1.3327 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0156   -0.7995   -0.6270 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8204    0.1546   -0.0474 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2819    1.2362    0.5957 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0992    2.2965    1.2388 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4526    2.0888    1.1264 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9235    1.3682    0.6618 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0907    0.4069    0.0777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3657    0.5671    0.1629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8355    1.5926    0.7703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2556   -0.4420   -0.4443 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6924   -0.0702   -0.1721 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6525   -1.0719   -0.8040 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0147   -0.4626   -0.6541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9347   -0.7620   -1.4487 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2876    0.4782    0.4078 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3181    0.6538    1.4259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5067    1.4016    2.4021 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0387   -0.0859    1.3110 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6206   -0.6788   -0.5681 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8390   -1.6763   -1.1738 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1066   -2.9057   -0.9075 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3017   -1.9809   -2.4155 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6568   -2.0542   -1.1950 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8890    0.0665   -0.0899 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8583    3.2572    0.7101 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7477    2.4192    2.2745 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7844    1.2818    1.5477 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4336    2.2085    1.1608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1089   -1.4508    0.0066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0718   -0.4325   -1.5348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9456    0.9193   -0.5812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5758   -1.9915   -0.1745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3866   -1.2374   -1.8537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1869    1.0104    0.4098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2587    0.2879    1.9661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3121   -1.1571    1.5702 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2515   -2.4507   -1.6343 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 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  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  8 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20  2  1  0  0  0  0
 19 12  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  3 25  1  0  0  0  0
  5 26  1  0  0  0  0
  5 27  1  0  0  0  0
  6 28  1  0  0  0  0
  7 29  1  0  0  0  0
 11 30  1  0  0  0  0
 11 31  1  0  0  0  0
 12 32  1  0  0  0  0
 13 33  1  0  0  0  0
 13 34  1  0  0  0  0
 16 35  1  0  0  0  0
 19 36  1  0  0  0  0
 19 37  1  0  0  0  0
 21 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0012970

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(C([H])=C(C([H])=C1C([H])([H])[H])C([H])([H])O[H])C(=O)C([H])([H])C1([H])C([H])([H])C(=O)N([H])C(=O)C1([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H17NO5/c1-8-2-10(7-17)3-11(15(8)21)12(18)4-9-5-13(19)16-14(20)6-9/h2-3,9,17,21H,4-7H2,1H3,(H,16,19,20)

> <INCHI_KEY>
TWNICLRZGUUHCS-UHFFFAOYSA-N

> <FORMULA>
C15H17NO5

> <MOLECULAR_WEIGHT>
291.303

> <EXACT_MASS>
291.110672651

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
30.092599544132575

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-{2-[2-hydroxy-5-(hydroxymethyl)-3-methylphenyl]-2-oxoethyl}piperidine-2,6-dione

> <ALOGPS_LOGP>
0.22

> <JCHEM_LOGP>
0.7091884496666665

> <ALOGPS_LOGS>
-2.51

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.801768227308019

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.4478675101224

> <JCHEM_PKA_STRONGEST_BASIC>
-2.838824590679705

> <JCHEM_POLAR_SURFACE_AREA>
103.7

> <JCHEM_REFRACTIVITY>
75.35249999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.09e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-{2-[2-hydroxy-5-(hydroxymethyl)-3-methylphenyl]-2-oxoethyl}piperidine-2,6-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 38 39  0  0  0  0  0  0  0  0999 V2000
    3.5753   -1.9853   -1.3327 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0156   -0.7995   -0.6270 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8204    0.1546   -0.0474 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2819    1.2362    0.5957 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0992    2.2965    1.2388 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4526    2.0888    1.1264 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9235    1.3682    0.6618 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0907    0.4069    0.0777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3657    0.5671    0.1629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8355    1.5926    0.7703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2556   -0.4420   -0.4443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6924   -0.0702   -0.1721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6525   -1.0719   -0.8040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0147   -0.4626   -0.6541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9347   -0.7620   -1.4487 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2876    0.4782    0.4078 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3181    0.6538    1.4259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5067    1.4016    2.4021 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0387   -0.0859    1.3110 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6206   -0.6788   -0.5681 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8390   -1.6763   -1.1738 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1066   -2.9057   -0.9075 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3017   -1.9809   -2.4155 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6568   -2.0542   -1.1950 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8890    0.0665   -0.0899 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8583    3.2572    0.7101 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7477    2.4192    2.2745 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7844    1.2818    1.5477 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4336    2.2085    1.1608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1089   -1.4508    0.0066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0718   -0.4325   -1.5348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9456    0.9193   -0.5812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5758   -1.9915   -0.1745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3866   -1.2374   -1.8537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1869    1.0104    0.4098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2587    0.2879    1.9661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3121   -1.1571    1.5702 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2515   -2.4507   -1.6343 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  4  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
  8 20  2  0
 20 21  1  0
 20  2  1  0
 19 12  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  5 26  1  0
  5 27  1  0
  6 28  1  0
  7 29  1  0
 11 30  1  0
 11 31  1  0
 12 32  1  0
 13 33  1  0
 13 34  1  0
 16 35  1  0
 19 36  1  0
 19 37  1  0
 21 38  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       3.575  -1.985  -1.333  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.016  -0.800  -0.627  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.820   0.155  -0.047  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.282   1.236   0.596  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.099   2.297   1.239  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.453   2.089   1.126  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.924   1.368   0.662  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.091   0.407   0.078  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.366   0.567   0.163  0.00  0.00           C+0
HETATM   10  O   UNK     0      -0.836   1.593   0.770  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.256  -0.442  -0.444  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.692  -0.070  -0.172  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.652  -1.072  -0.804  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.015  -0.463  -0.654  0.00  0.00           C+0
HETATM   15  O   UNK     0      -5.935  -0.762  -1.449  0.00  0.00           O+0
HETATM   16  N   UNK     0      -5.288   0.478   0.408  0.00  0.00           N+0
HETATM   17  C   UNK     0      -4.318   0.654   1.426  0.00  0.00           C+0
HETATM   18  O   UNK     0      -4.507   1.402   2.402  0.00  0.00           O+0
HETATM   19  C   UNK     0      -3.039  -0.086   1.311  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.621  -0.679  -0.568  0.00  0.00           C+0
HETATM   21  O   UNK     0       0.839  -1.676  -1.174  0.00  0.00           O+0
HETATM   22  H   UNK     0       3.107  -2.906  -0.908  0.00  0.00           H+0
HETATM   23  H   UNK     0       3.302  -1.981  -2.416  0.00  0.00           H+0
HETATM   24  H   UNK     0       4.657  -2.054  -1.195  0.00  0.00           H+0
HETATM   25  H   UNK     0       4.889   0.067  -0.090  0.00  0.00           H+0
HETATM   26  H   UNK     0       3.858   3.257   0.710  0.00  0.00           H+0
HETATM   27  H   UNK     0       3.748   2.419   2.275  0.00  0.00           H+0
HETATM   28  H   UNK     0       5.784   1.282   1.548  0.00  0.00           H+0
HETATM   29  H   UNK     0       1.434   2.208   1.161  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.109  -1.451   0.007  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.072  -0.433  -1.535  0.00  0.00           H+0
HETATM   32  H   UNK     0      -2.946   0.919  -0.581  0.00  0.00           H+0
HETATM   33  H   UNK     0      -3.576  -1.992  -0.175  0.00  0.00           H+0
HETATM   34  H   UNK     0      -3.387  -1.237  -1.854  0.00  0.00           H+0
HETATM   35  H   UNK     0      -6.187   1.010   0.410  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.259   0.288   1.966  0.00  0.00           H+0
HETATM   37  H   UNK     0      -3.312  -1.157   1.570  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.252  -2.451  -1.634  0.00  0.00           H+0
CONECT    1    2   22   23   24                                             
CONECT    2    1    3   20                                                  
CONECT    3    2    4   25                                                  
CONECT    4    3    5    7                                                  
CONECT    5    4    6   26   27                                             
CONECT    6    5   28                                                       
CONECT    7    4    8   29                                                  
CONECT    8    7    9   20                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   30   31                                             
CONECT   12   11   13   19   32                                             
CONECT   13   12   14   33   34                                             
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   35                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   12   36   37                                             
CONECT   20    8   21    2                                                  
CONECT   21   20   38                                                       
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    3                                                            
CONECT   26    5                                                            
CONECT   27    5                                                            
CONECT   28    6                                                            
CONECT   29    7                                                            
CONECT   30   11                                                            
CONECT   31   11                                                            
CONECT   32   12                                                            
CONECT   33   13                                                            
CONECT   34   13                                                            
CONECT   35   16                                                            
CONECT   36   19                                                            
CONECT   37   19                                                            
CONECT   38   21                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   78    0
END

RDKit          3D

38 39  0  0  0  0  0  0  0  0999 V2000
    3.5753   -1.9853   -1.3327 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0156   -0.7995   -0.6270 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8204    0.1546   -0.0474 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2819    1.2362    0.5957 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0992    2.2965    1.2388 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4526    2.0888    1.1264 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9235    1.3682    0.6618 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0907    0.4069    0.0777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3657    0.5671    0.1629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8355    1.5926    0.7703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2556   -0.4420   -0.4443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6924   -0.0702   -0.1721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6525   -1.0719   -0.8040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0147   -0.4626   -0.6541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9347   -0.7620   -1.4487 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2876    0.4782    0.4078 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3181    0.6538    1.4259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5067    1.4016    2.4021 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0387   -0.0859    1.3110 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6206   -0.6788   -0.5681 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8390   -1.6763   -1.1738 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1066   -2.9057   -0.9075 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3017   -1.9809   -2.4155 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6568   -2.0542   -1.1950 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8890    0.0665   -0.0899 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8583    3.2572    0.7101 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7477    2.4192    2.2745 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7844    1.2818    1.5477 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4336    2.2085    1.1608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1089   -1.4508    0.0066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0718   -0.4325   -1.5348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9456    0.9193   -0.5812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5758   -1.9915   -0.1745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3866   -1.2374   -1.8537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1869    1.0104    0.4098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2587    0.2879    1.9661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3121   -1.1571    1.5702 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2515   -2.4507   -1.6343 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  4  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
  8 20  2  0
 20 21  1  0
 20  2  1  0
 19 12  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  5 26  1  0
  5 27  1  0
  6 28  1  0
  7 29  1  0
 11 30  1  0
 11 31  1  0
 12 32  1  0
 13 33  1  0
 13 34  1  0
 16 35  1  0
 19 36  1  0
 19 37  1  0
 21 38  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₅H₁₇NO₅

Average Mass

291.3030 Da

Monoisotopic Mass

291.11067 Da

IUPAC Name

4-{2-[2-hydroxy-5-(hydroxymethyl)-3-methylphenyl]-2-oxoethyl}piperidine-2,6-dione

Traditional Name

4-{2-[2-hydroxy-5-(hydroxymethyl)-3-methylphenyl]-2-oxoethyl}piperidine-2,6-dione

CAS Registry Number

Not Available

SMILES

CC1=C(O)C(=CC(CO)=C1)C(=O)CC1CC(=O)NC(=O)C1

InChI Identifier

InChI=1S/C15H17NO5/c1-8-2-10(7-17)3-11(15(8)21)12(18)4-9-5-13(19)16-14(20)6-9/h2-3,9,17,21H,4-7H2,1H3,(H,16,19,20)

InChI Key

TWNICLRZGUUHCS-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, 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
Streptomyces	NPAtlas	24949797
Streptomyces anulatus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Alkyl-phenylketones

Alternative Parents

Substituents

Alkyl-phenylketone
Aryl alkyl ketone
O-cresol
Benzyl alcohol
Benzoyl
Toluene
Tetrahydropyridine
Phenol
Benzenoid
Hydropyridine
Monocyclic benzene moiety
Vinylogous acid
Lactim
N-acylimine
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Carboxylic acid derivative
Organic nitrogen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Aromatic alcohol
Primary alcohol
Organonitrogen compound
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	0.22	ALOGPS
logP	0.71	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	9.45	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	103.7 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	75.35 m³·mol⁻¹	ChemAxon
Polarizability	30.09 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

NPA020172

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

34981493

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139588714

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 3-[2-[2-hydroxy-3-methylphenyl-5-(hydroxymethyl)]-2-oxoethyl]glutarimide (NP0012970)

MOL for NP0012970 (3-[2-[2-hydroxy-3-methylphenyl-5-(hydroxymethyl)]-2-oxoethyl]glutarimide)

3D MOL for NP0012970 (3-[2-[2-hydroxy-3-methylphenyl-5-(hydroxymethyl)]-2-oxoethyl]glutarimide)

3D SDF for NP0012970 (3-[2-[2-hydroxy-3-methylphenyl-5-(hydroxymethyl)]-2-oxoethyl]glutarimide)

3D-SDF for NP0012970 (3-[2-[2-hydroxy-3-methylphenyl-5-(hydroxymethyl)]-2-oxoethyl]glutarimide)

PDB for NP0012970 (3-[2-[2-hydroxy-3-methylphenyl-5-(hydroxymethyl)]-2-oxoethyl]glutarimide)

3D PDB for NP0012970 (3-[2-[2-hydroxy-3-methylphenyl-5-(hydroxymethyl)]-2-oxoethyl]glutarimide)

SMILES for NP0012970 (3-[2-[2-hydroxy-3-methylphenyl-5-(hydroxymethyl)]-2-oxoethyl]glutarimide)

INCHI for NP0012970 (3-[2-[2-hydroxy-3-methylphenyl-5-(hydroxymethyl)]-2-oxoethyl]glutarimide)

Structure for NP0012970 (3-[2-[2-hydroxy-3-methylphenyl-5-(hydroxymethyl)]-2-oxoethyl]glutarimide)

3D Structure for NP0012970 (3-[2-[2-hydroxy-3-methylphenyl-5-(hydroxymethyl)]-2-oxoethyl]glutarimide)