NP-MRD: Showing NP-Card for Trans-1-hydroxy-3-(4-hydroxyphenyl)-4-isobutylpyrrolidine-2,5-dione (NP0007866)

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Record Information

Version

2.0

Created at

2020-12-09 05:26:17 UTC

Updated at

2021-07-15 16:58:46 UTC

NP-MRD ID

NP0007866

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Trans-1-hydroxy-3-(4-hydroxyphenyl)-4-isobutylpyrrolidine-2,5-dione

Provided By

NPAtlas

Description

(3S,4R)-1-hydroxy-3-(4-hydroxyphenyl)-4-(2-methylpropyl)pyrrolidine-2,5-dione belongs to the class of organic compounds known as phenylpyrrolidines. These are polycyclic aromatic compounds containing a benzene ring linked to a pyrrolidine ring through a CC or CN bond. Pyrrolidine is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms. Trans-1-hydroxy-3-(4-hydroxyphenyl)-4-isobutylpyrrolidine-2,5-dione is found in Antrodia and Taiwanofungus camphoratus. Trans-1-hydroxy-3-(4-hydroxyphenyl)-4-isobutylpyrrolidine-2,5-dione was first documented in 2008 (PMID: 18642845). Based on a literature review very few articles have been published on (3S,4R)-1-hydroxy-3-(4-hydroxyphenyl)-4-(2-methylpropyl)pyrrolidine-2,5-dione.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106043D          

 36 37  0  0  0  0            999 V2000
   -3.7567    1.0296    1.6424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8437    0.2022    0.6912 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9285    0.8897   -0.6476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4952    0.1313    1.2807 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4290   -0.6156    0.6043 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7272   -2.0480    0.3719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1082   -2.8799    1.2065 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4953   -2.3068   -1.0033 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6855   -3.5156   -1.6168 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0372   -1.1301   -1.6515 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1858   -0.9629   -2.8662 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1563   -0.0474   -0.6261 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6173    0.2241   -0.4801 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0875    1.4867   -0.7243 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4324    1.7905   -0.6033 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3131    0.8091   -0.2316 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6732    1.0523   -0.0934 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8706   -0.4767    0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5081   -0.7528   -0.1081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1163    1.7843    2.1043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1610    0.3425    2.4183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5513    1.4822    1.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3252   -0.7810    0.5845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5062    0.2822   -1.4605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0275    1.1208   -0.8844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3824    1.8493   -0.6040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6089   -0.2037    2.3675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1183    1.2005    1.4378 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4423   -0.6515    1.3653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5734   -4.2134   -0.9308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3074    0.8809   -0.9239 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4250    2.2814   -1.0178 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7894    2.7869   -0.7980 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0135    1.9778   -0.2730 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5303   -1.2849    0.3189 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1395   -1.7338    0.0812 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  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 12  5  1  0  0  0  0
 19 13  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  2 23  1  6  0  0  0
  3 24  1  0  0  0  0
  3 25  1  0  0  0  0
  3 26  1  0  0  0  0
  4 27  1  0  0  0  0
  4 28  1  0  0  0  0
  5 29  1  1  0  0  0
  9 30  1  0  0  0  0
 12 31  1  6  0  0  0
 14 32  1  0  0  0  0
 15 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
   -3.7567    1.0296    1.6424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8437    0.2022    0.6912 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9285    0.8897   -0.6476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4952    0.1313    1.2807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4290   -0.6156    0.6043 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7272   -2.0480    0.3719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1082   -2.8799    1.2065 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4953   -2.3068   -1.0033 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6855   -3.5156   -1.6168 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0372   -1.1301   -1.6515 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1858   -0.9629   -2.8662 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1563   -0.0474   -0.6261 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6173    0.2241   -0.4801 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0875    1.4867   -0.7243 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4324    1.7905   -0.6033 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3131    0.8091   -0.2316 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6732    1.0523   -0.0934 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8706   -0.4767    0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5081   -0.7528   -0.1081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1163    1.7843    2.1043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1610    0.3425    2.4183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5513    1.4822    1.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3252   -0.7810    0.5845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5062    0.2822   -1.4605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0275    1.1208   -0.8844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3824    1.8493   -0.6040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6089   -0.2037    2.3675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1183    1.2005    1.4378 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4423   -0.6515    1.3653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5734   -4.2134   -0.9308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3074    0.8809   -0.9239 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4250    2.2814   -1.0178 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7894    2.7869   -0.7980 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0135    1.9778   -0.2730 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5303   -1.2849    0.3189 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1395   -1.7338    0.0812 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  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 12  5  1  0
 19 13  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  6
  3 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  1
  9 30  1  0
 12 31  1  6
 14 32  1  0
 15 33  1  0
 17 34  1  0
 18 35  1  0
 19 36  1  0
M  END


  Mrv1652306242106043D          

 36 37  0  0  0  0            999 V2000
   -3.7567    1.0296    1.6424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8437    0.2022    0.6912 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9285    0.8897   -0.6476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4952    0.1313    1.2807 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4290   -0.6156    0.6043 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7272   -2.0480    0.3719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1082   -2.8799    1.2065 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4953   -2.3068   -1.0033 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6855   -3.5156   -1.6168 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0372   -1.1301   -1.6515 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1858   -0.9629   -2.8662 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1563   -0.0474   -0.6261 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6173    0.2241   -0.4801 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0875    1.4867   -0.7243 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4324    1.7905   -0.6033 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3131    0.8091   -0.2316 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6732    1.0523   -0.0934 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8706   -0.4767    0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5081   -0.7528   -0.1081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1163    1.7843    2.1043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1610    0.3425    2.4183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5513    1.4822    1.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3252   -0.7810    0.5845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5062    0.2822   -1.4605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0275    1.1208   -0.8844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3824    1.8493   -0.6040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6089   -0.2037    2.3675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1183    1.2005    1.4378 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4423   -0.6515    1.3653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5734   -4.2134   -0.9308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3074    0.8809   -0.9239 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4250    2.2814   -1.0178 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7894    2.7869   -0.7980 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0135    1.9778   -0.2730 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5303   -1.2849    0.3189 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1395   -1.7338    0.0812 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  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 12  5  1  0  0  0  0
 19 13  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  2 23  1  6  0  0  0
  3 24  1  0  0  0  0
  3 25  1  0  0  0  0
  3 26  1  0  0  0  0
  4 27  1  0  0  0  0
  4 28  1  0  0  0  0
  5 29  1  1  0  0  0
  9 30  1  0  0  0  0
 12 31  1  6  0  0  0
 14 32  1  0  0  0  0
 15 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>
NP0007866

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]ON1C(=O)[C@]([H])(C2=C([H])C([H])=C(O[H])C([H])=C2[H])[C@]([H])(C1=O)C([H])([H])C([H])(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C14H17NO4/c1-8(2)7-11-12(14(18)15(19)13(11)17)9-3-5-10(16)6-4-9/h3-6,8,11-12,16,19H,7H2,1-2H3/t11-,12-/m1/s1

> <INCHI_KEY>
MHPDCPMZYWJSJJ-VXGBXAGGSA-N

> <FORMULA>
C14H17NO4

> <MOLECULAR_WEIGHT>
263.293

> <EXACT_MASS>
263.115758031

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
27.17833276969808

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,4R)-1-hydroxy-3-(4-hydroxyphenyl)-4-(2-methylpropyl)pyrrolidine-2,5-dione

> <ALOGPS_LOGP>
2.06

> <JCHEM_LOGP>
2.095714345666667

> <ALOGPS_LOGS>
-2.83

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.50026785181814

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.16241998684901

> <JCHEM_PKA_STRONGEST_BASIC>
-5.958671666532891

> <JCHEM_POLAR_SURFACE_AREA>
77.84

> <JCHEM_REFRACTIVITY>
69.02150000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.90e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4R)-1-hydroxy-3-(4-hydroxyphenyl)-4-(2-methylpropyl)pyrrolidine-2,5-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 36 37  0  0  0  0  0  0  0  0999 V2000
   -3.7567    1.0296    1.6424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8437    0.2022    0.6912 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9285    0.8897   -0.6476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4952    0.1313    1.2807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4290   -0.6156    0.6043 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7272   -2.0480    0.3719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1082   -2.8799    1.2065 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4953   -2.3068   -1.0033 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6855   -3.5156   -1.6168 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0372   -1.1301   -1.6515 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1858   -0.9629   -2.8662 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1563   -0.0474   -0.6261 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6173    0.2241   -0.4801 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0875    1.4867   -0.7243 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4324    1.7905   -0.6033 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3131    0.8091   -0.2316 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6732    1.0523   -0.0934 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8706   -0.4767    0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5081   -0.7528   -0.1081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1163    1.7843    2.1043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1610    0.3425    2.4183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5513    1.4822    1.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3252   -0.7810    0.5845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5062    0.2822   -1.4605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0275    1.1208   -0.8844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3824    1.8493   -0.6040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6089   -0.2037    2.3675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1183    1.2005    1.4378 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4423   -0.6515    1.3653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5734   -4.2134   -0.9308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3074    0.8809   -0.9239 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4250    2.2814   -1.0178 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7894    2.7869   -0.7980 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0135    1.9778   -0.2730 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5303   -1.2849    0.3189 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1395   -1.7338    0.0812 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  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  2  0
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 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 12  5  1  0
 19 13  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  6
  3 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  1
  9 30  1  0
 12 31  1  6
 14 32  1  0
 15 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  C   UNK     0      -3.757   1.030   1.642  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.844   0.202   0.691  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.929   0.890  -0.648  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.495   0.131   1.281  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.429  -0.616   0.604  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.727  -2.048   0.372  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.108  -2.880   1.206  0.00  0.00           O+0
HETATM    8  N   UNK     0      -0.495  -2.307  -1.003  0.00  0.00           N+0
HETATM    9  O   UNK     0      -0.686  -3.516  -1.617  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.037  -1.130  -1.652  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.186  -0.963  -2.866  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.156  -0.047  -0.626  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.617   0.224  -0.480  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.087   1.487  -0.724  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.432   1.791  -0.603  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.313   0.809  -0.232  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.673   1.052  -0.093  0.00  0.00           O+0
HETATM   18  C   UNK     0       3.871  -0.477   0.022  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.508  -0.753  -0.108  0.00  0.00           C+0
HETATM   20  H   UNK     0      -3.116   1.784   2.104  0.00  0.00           H+0
HETATM   21  H   UNK     0      -4.161   0.343   2.418  0.00  0.00           H+0
HETATM   22  H   UNK     0      -4.551   1.482   1.048  0.00  0.00           H+0
HETATM   23  H   UNK     0      -3.325  -0.781   0.585  0.00  0.00           H+0
HETATM   24  H   UNK     0      -2.506   0.282  -1.460  0.00  0.00           H+0
HETATM   25  H   UNK     0      -4.027   1.121  -0.884  0.00  0.00           H+0
HETATM   26  H   UNK     0      -2.382   1.849  -0.604  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.609  -0.204   2.368  0.00  0.00           H+0
HETATM   28  H   UNK     0      -1.118   1.200   1.438  0.00  0.00           H+0
HETATM   29  H   UNK     0       0.442  -0.652   1.365  0.00  0.00           H+0
HETATM   30  H   UNK     0      -0.573  -4.213  -0.931  0.00  0.00           H+0
HETATM   31  H   UNK     0      -0.307   0.881  -0.924  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.425   2.281  -1.018  0.00  0.00           H+0
HETATM   33  H   UNK     0       3.789   2.787  -0.798  0.00  0.00           H+0
HETATM   34  H   UNK     0       6.013   1.978  -0.273  0.00  0.00           H+0
HETATM   35  H   UNK     0       4.530  -1.285   0.319  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.139  -1.734   0.081  0.00  0.00           H+0
CONECT    1    2   20   21   22                                             
CONECT    2    1    3    4   23                                             
CONECT    3    2   24   25   26                                             
CONECT    4    2    5   27   28                                             
CONECT    5    4    6   12   29                                             
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8   30                                                       
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13    5   31                                             
CONECT   13   12   14   19                                                  
CONECT   14   13   15   32                                                  
CONECT   15   14   16   33                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16   34                                                       
CONECT   18   16   19   35                                                  
CONECT   19   18   13   36                                                  
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    2                                                            
CONECT   24    3                                                            
CONECT   25    3                                                            
CONECT   26    3                                                            
CONECT   27    4                                                            
CONECT   28    4                                                            
CONECT   29    5                                                            
CONECT   30    9                                                            
CONECT   31   12                                                            
CONECT   32   14                                                            
CONECT   33   15                                                            
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
   -3.7567    1.0296    1.6424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8437    0.2022    0.6912 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9285    0.8897   -0.6476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4952    0.1313    1.2807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4290   -0.6156    0.6043 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7272   -2.0480    0.3719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1082   -2.8799    1.2065 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4953   -2.3068   -1.0033 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6855   -3.5156   -1.6168 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0372   -1.1301   -1.6515 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1858   -0.9629   -2.8662 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1563   -0.0474   -0.6261 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6173    0.2241   -0.4801 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0875    1.4867   -0.7243 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4324    1.7905   -0.6033 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3131    0.8091   -0.2316 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6732    1.0523   -0.0934 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8706   -0.4767    0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5081   -0.7528   -0.1081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1163    1.7843    2.1043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1610    0.3425    2.4183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5513    1.4822    1.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3252   -0.7810    0.5845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5062    0.2822   -1.4605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0275    1.1208   -0.8844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3824    1.8493   -0.6040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6089   -0.2037    2.3675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1183    1.2005    1.4378 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4423   -0.6515    1.3653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5734   -4.2134   -0.9308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3074    0.8809   -0.9239 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4250    2.2814   -1.0178 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7894    2.7869   -0.7980 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0135    1.9778   -0.2730 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5303   -1.2849    0.3189 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1395   -1.7338    0.0812 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  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 12  5  1  0
 19 13  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  6
  3 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  1
  9 30  1  0
 12 31  1  6
 14 32  1  0
 15 33  1  0
 17 34  1  0
 18 35  1  0
 19 36  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₄H₁₇NO₄

Average Mass

263.2930 Da

Monoisotopic Mass

263.11576 Da

IUPAC Name

(3S,4R)-1-hydroxy-3-(4-hydroxyphenyl)-4-(2-methylpropyl)pyrrolidine-2,5-dione

Traditional Name

(3S,4R)-1-hydroxy-3-(4-hydroxyphenyl)-4-(2-methylpropyl)pyrrolidine-2,5-dione

CAS Registry Number

Not Available

SMILES

CC(C)C[C@@H]1[C@H](C(=O)N(O)C1=O)C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C14H17NO4/c1-8(2)7-11-12(14(18)15(19)13(11)17)9-3-5-10(16)6-4-9/h3-6,8,11-12,16,19H,7H2,1-2H3/t11-,12-/m1/s1

InChI Key

MHPDCPMZYWJSJJ-VXGBXAGGSA-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
Antrodia	NPAtlas	18642845
Taiwanofungus camphoratus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylpyrrolidines. These are polycyclic aromatic compounds containing a benzene ring linked to a pyrrolidine ring through a CC or CN bond. Pyrrolidine is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrrolidines

Sub Class

Phenylpyrrolidines

Direct Parent

Phenylpyrrolidines

Alternative Parents

Substituents

3-phenylpyrrolidine
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
2-pyrrolidone
Pyrrolidone
Dicarboximide
Pyrrole
Hydroxamic acid
Lactam
Carboxylic acid derivative
Azacycle
Organic oxide
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
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	2.06	ALOGPS
logP	2.1	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	7.16	ChemAxon
pKa (Strongest Basic)	-6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	77.84 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	69.02 m³·mol⁻¹	ChemAxon
Polarizability	27.18 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

NPA004637

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78440872

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

25067896

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Chien SC, Chen ML, Kuo HT, Tsai YC, Lin BF, Kuo YH: Anti-inflammatory activities of new succinic and maleic derivatives from the fruiting body of Antrodia camphorata. J Agric Food Chem. 2008 Aug 27;56(16):7017-22. doi: 10.1021/jf801171x. Epub 2008 Jul 19. [PubMed:18642845 ]

Showing NP-Card for Trans-1-hydroxy-3-(4-hydroxyphenyl)-4-isobutylpyrrolidine-2,5-dione (NP0007866)

MOL for NP0007866 (Trans-1-hydroxy-3-(4-hydroxyphenyl)-4-isobutylpyrrolidine-2,5-dione)

3D MOL for NP0007866 (Trans-1-hydroxy-3-(4-hydroxyphenyl)-4-isobutylpyrrolidine-2,5-dione)

3D SDF for NP0007866 (Trans-1-hydroxy-3-(4-hydroxyphenyl)-4-isobutylpyrrolidine-2,5-dione)

3D-SDF for NP0007866 (Trans-1-hydroxy-3-(4-hydroxyphenyl)-4-isobutylpyrrolidine-2,5-dione)

PDB for NP0007866 (Trans-1-hydroxy-3-(4-hydroxyphenyl)-4-isobutylpyrrolidine-2,5-dione)

3D PDB for NP0007866 (Trans-1-hydroxy-3-(4-hydroxyphenyl)-4-isobutylpyrrolidine-2,5-dione)

SMILES for NP0007866 (Trans-1-hydroxy-3-(4-hydroxyphenyl)-4-isobutylpyrrolidine-2,5-dione)

INCHI for NP0007866 (Trans-1-hydroxy-3-(4-hydroxyphenyl)-4-isobutylpyrrolidine-2,5-dione)

Structure for NP0007866 (Trans-1-hydroxy-3-(4-hydroxyphenyl)-4-isobutylpyrrolidine-2,5-dione)

3D Structure for NP0007866 (Trans-1-hydroxy-3-(4-hydroxyphenyl)-4-isobutylpyrrolidine-2,5-dione)