NP-MRD: Showing NP-Card for 2-{3-hydroxy-1-[3-(n-hydroxyacetamido)propyl]-2,5-dioxopyrrolidin-3-yl}-n-[3-(n-hydroxyacetamido)propyl]ethanimidic acid (NP0317852)

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Record Information

Version

2.0

Created at

2022-09-11 17:58:54 UTC

Updated at

2022-09-11 17:58:54 UTC

NP-MRD ID

NP0317852

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{3-hydroxy-1-[3-(n-hydroxyacetamido)propyl]-2,5-dioxopyrrolidin-3-yl}-n-[3-(n-hydroxyacetamido)propyl]ethanimidic acid

Description

2-{3-Hydroxy-1-[3-(N-hydroxyacetamido)propyl]-2,5-dioxopyrrolidin-3-yl}-N-[3-(N-hydroxyacetamido)propyl]ethanimidic acid belongs to the class of organic compounds known as n-substituted carboxylic acid imides. N-substituted carboxylic acid imides are compounds comprising an N-substituted carboxylic acid imide group, with the general structure R1N(C(R2)=O)C(R3)=O (R2,R3=H, alkyl, aryl; R1=Anything but H). 2-{3-Hydroxy-1-[3-(N-hydroxyacetamido)propyl]-2,5-dioxopyrrolidin-3-yl}-N-[3-(N-hydroxyacetamido)propyl]ethanimidic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241500252D          

 28 28  0  0  0  0            999 V2000
   -0.5318   -5.2720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -5.6845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -6.5095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8972   -5.2720    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8972   -4.4470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6116   -5.6845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3261   -5.2720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0406   -5.6845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7550   -5.2720    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4695   -5.6845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4695   -6.5095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1840   -5.2720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8985   -5.6845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4135   -6.3519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2340   -4.9308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0545   -5.0170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6065   -4.4039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2260   -5.8240    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.9797   -6.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6471   -5.6746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4008   -6.0102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0682   -5.5253    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.9820   -4.7048    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8219   -5.8608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4894   -5.3759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.9082   -6.6813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5116   -6.2365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4253   -7.0570    0.0000 O   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 18 27  1  0  0  0  0
 13 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END

     RDKit          3D

 54 54  0  0  0  0  0  0  0  0999 V2000
   -6.2737   -3.4429   -1.1485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8037   -2.2355   -1.8510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4610   -1.7926   -2.8147 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6211   -1.5932   -1.4323 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2167   -0.4864   -2.1115 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8382   -2.0774   -0.3036 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3050   -1.4304    0.9638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4967   -1.9309    2.1366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0976   -1.6777    2.0521 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6010   -0.3434    1.9660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4309    0.5923    1.9674 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1424   -0.0762    1.8779 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0622    1.4023    1.7878 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4575    2.0569    2.9042 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3935    1.9887    0.4859 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7737    1.6897   -0.4153 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6840    1.5604   -1.6597 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9331    1.5927    0.4152 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2777    1.3525   -0.0913 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6244   -0.0791   -0.1747 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0215   -0.2727   -0.7051 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2696    0.2443   -2.0047 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9971   -0.6317   -3.0399 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7471    1.5067   -2.3565 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1068    2.5079   -1.3393 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8896    1.8328   -3.5600 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5145    1.7696    1.7642 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2540    2.1527    2.6831 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4381   -4.2014   -1.0993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5642   -3.2717   -0.1018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1445   -3.8976   -1.7079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0164    0.2722   -1.5005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7695   -1.7618   -0.4626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9230   -3.1724   -0.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2583   -0.3261    0.8644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3660   -1.6633    1.1822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9445   -1.4232    3.0427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6756   -3.0186    2.2404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4363   -2.5028    2.0547 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2871   -0.4495    2.8438 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2661   -0.6143    1.0196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3989    3.0298    2.7197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3028    1.5007    0.1467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4599    3.0888    0.5298 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0364    1.8703    0.5298 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3359    1.7858   -1.1094 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5966   -0.6172    0.7974 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8992   -0.6280   -0.8463 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1873   -1.3987   -0.6601 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7785    0.1037    0.0478 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7938   -1.2485   -3.0671 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0173    3.0841   -1.6460 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2380    3.2094   -1.2254 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2457    2.0153   -0.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  2  0
 18 27  1  0
 27 28  2  0
 27 13  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  5 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  0
 12 40  1  0
 12 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 19 45  1  0
 19 46  1  0
 20 47  1  0
 20 48  1  0
 21 49  1  0
 21 50  1  0
 23 51  1  0
 25 52  1  0
 25 53  1  0
 25 54  1  0
M  END


  Mrv1533004241500252D          

 28 28  0  0  0  0            999 V2000
   -0.5318   -5.2720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -5.6845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -6.5095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8972   -5.2720    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8972   -4.4470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6116   -5.6845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3261   -5.2720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0406   -5.6845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7550   -5.2720    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4695   -5.6845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4695   -6.5095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1840   -5.2720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8985   -5.6845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4135   -6.3519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2340   -4.9308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0545   -5.0170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6065   -4.4039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2260   -5.8240    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.9797   -6.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6471   -5.6746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4008   -6.0102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0682   -5.5253    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.9820   -4.7048    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8219   -5.8608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4894   -5.3759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.9082   -6.6813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5116   -6.2365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4253   -7.0570    0.0000 O   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 18 27  1  0  0  0  0
 13 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0317852

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)N(O)CCCNC(=O)CC1(O)CC(=O)N(CCCN(O)C(C)=O)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H26N4O8/c1-11(21)19(27)7-3-5-17-13(23)9-16(26)10-14(24)18(15(16)25)6-4-8-20(28)12(2)22/h26-28H,3-10H2,1-2H3,(H,17,23)

> <INCHI_KEY>
YFPAMFCNJAVQBF-UHFFFAOYSA-N

> <FORMULA>
C16H26N4O8

> <MOLECULAR_WEIGHT>
402.404

> <EXACT_MASS>
402.175063813

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
39.97770228811066

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-hydroxy-N-{3-[3-hydroxy-3-({[3-(N-hydroxyacetamido)propyl]carbamoyl}methyl)-2,5-dioxopyrrolidin-1-yl]propyl}acetamide

> <ALOGPS_LOGP>
-0.78

> <JCHEM_LOGP>
-4.119984916

> <ALOGPS_LOGS>
-2.16

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.701342656158184

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.09933955456833

> <JCHEM_PKA_STRONGEST_BASIC>
-2.1615796394662885

> <JCHEM_POLAR_SURFACE_AREA>
167.79

> <JCHEM_REFRACTIVITY>
94.03109999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.80e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-hydroxy-N-{3-[3-hydroxy-3-({[3-(N-hydroxyacetamido)propyl]carbamoyl}methyl)-2,5-dioxopyrrolidin-1-yl]propyl}acetamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -0.993  -9.841   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.341 -10.611   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       0.341 -12.151   0.000  0.00  0.00           O+0
HETATM    4  N   UNK     0       1.675  -9.841   0.000  0.00  0.00           N+0
HETATM    5  O   UNK     0       1.675  -8.301   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       3.008 -10.611   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.342  -9.841   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.676 -10.611   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       7.009  -9.841   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       8.343 -10.611   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.343 -12.151   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       9.677  -9.841   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.010 -10.611   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      10.105 -11.857   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      11.637  -9.204   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.168  -9.365   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      14.199  -8.221   0.000  0.00  0.00           O+0
HETATM   18  N   UNK     0      13.489 -10.871   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0      14.895 -11.498   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      16.141 -10.593   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      17.548 -11.219   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0      18.794 -10.314   0.000  0.00  0.00           N+0
HETATM   23  O   UNK     0      18.633  -8.782   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      20.201 -10.940   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      21.447 -10.035   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      20.362 -12.472   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.155 -11.641   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      11.994 -13.173   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15   27                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   27                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   18   13   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   56    0
END

View in JSmol

Synonyms

Value	Source
2-{3-hydroxy-1-[3-(N-hydroxyacetamido)propyl]-2,5-dioxopyrrolidin-3-yl}-N-[3-(N-hydroxyacetamido)propyl]ethanimidate	Generator

Chemical Formula

C₁₆H₂₆N₄O₈

Average Mass

402.4040 Da

Monoisotopic Mass

402.17506 Da

IUPAC Name

N-hydroxy-N-{3-[3-hydroxy-3-({[3-(N-hydroxyacetamido)propyl]carbamoyl}methyl)-2,5-dioxopyrrolidin-1-yl]propyl}acetamide

Traditional Name

N-hydroxy-N-{3-[3-hydroxy-3-({[3-(N-hydroxyacetamido)propyl]carbamoyl}methyl)-2,5-dioxopyrrolidin-1-yl]propyl}acetamide

CAS Registry Number

Not Available

SMILES

CC(=O)N(O)CCCNC(=O)CC1(O)CC(=O)N(CCCN(O)C(C)=O)C1=O

InChI Identifier

InChI=1S/C16H26N4O8/c1-11(21)19(27)7-3-5-17-13(23)9-16(26)10-14(24)18(15(16)25)6-4-8-20(28)12(2)22/h26-28H,3-10H2,1-2H3,(H,17,23)

InChI Key

YFPAMFCNJAVQBF-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-substituted carboxylic acid imides. N-substituted carboxylic acid imides are compounds comprising an N-substituted carboxylic acid imide group, with the general structure R1N(C(R2)=O)C(R3)=O (R2,R3=H, alkyl, aryl; R1=Anything but H).

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Carboxylic acid derivatives

Direct Parent

N-substituted carboxylic acid imides

Alternative Parents

Substituents

Carboxylic acid imide, n-substituted
Pyrrolidone
2-pyrrolidone
N-alkylpyrrolidine
Dicarboximide
Pyrrolidine
Tertiary alcohol
Acetamide
Acetohydroxamic acid
Secondary carboxylic acid amide
Lactam
Hydroxamic acid
Carboxamide group
Organoheterocyclic compound
Azacycle
Organic oxide
Carbonyl group
Organopnictogen compound
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Alcohol
Hydrocarbon derivative
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic 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	-0.78	ALOGPS
logP	-4.1	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	8.1	ChemAxon
pKa (Strongest Basic)	-2.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	167.79 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	94.03 m³·mol⁻¹	ChemAxon
Polarizability	39.98 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{3-hydroxy-1-[3-(n-hydroxyacetamido)propyl]-2,5-dioxopyrrolidin-3-yl}-n-[3-(n-hydroxyacetamido)propyl]ethanimidic acid (NP0317852)

MOL for NP0317852 (2-{3-hydroxy-1-[3-(n-hydroxyacetamido)propyl]-2,5-dioxopyrrolidin-3-yl}-n-[3-(n-hydroxyacetamido)propyl]ethanimidic acid)

3D MOL for NP0317852 (2-{3-hydroxy-1-[3-(n-hydroxyacetamido)propyl]-2,5-dioxopyrrolidin-3-yl}-n-[3-(n-hydroxyacetamido)propyl]ethanimidic acid)

3D SDF for NP0317852 (2-{3-hydroxy-1-[3-(n-hydroxyacetamido)propyl]-2,5-dioxopyrrolidin-3-yl}-n-[3-(n-hydroxyacetamido)propyl]ethanimidic acid)

3D-SDF for NP0317852 (2-{3-hydroxy-1-[3-(n-hydroxyacetamido)propyl]-2,5-dioxopyrrolidin-3-yl}-n-[3-(n-hydroxyacetamido)propyl]ethanimidic acid)

PDB for NP0317852 (2-{3-hydroxy-1-[3-(n-hydroxyacetamido)propyl]-2,5-dioxopyrrolidin-3-yl}-n-[3-(n-hydroxyacetamido)propyl]ethanimidic acid)

3D PDB for NP0317852 (2-{3-hydroxy-1-[3-(n-hydroxyacetamido)propyl]-2,5-dioxopyrrolidin-3-yl}-n-[3-(n-hydroxyacetamido)propyl]ethanimidic acid)

SMILES for NP0317852 (2-{3-hydroxy-1-[3-(n-hydroxyacetamido)propyl]-2,5-dioxopyrrolidin-3-yl}-n-[3-(n-hydroxyacetamido)propyl]ethanimidic acid)

INCHI for NP0317852 (2-{3-hydroxy-1-[3-(n-hydroxyacetamido)propyl]-2,5-dioxopyrrolidin-3-yl}-n-[3-(n-hydroxyacetamido)propyl]ethanimidic acid)

Structure for NP0317852 (2-{3-hydroxy-1-[3-(n-hydroxyacetamido)propyl]-2,5-dioxopyrrolidin-3-yl}-n-[3-(n-hydroxyacetamido)propyl]ethanimidic acid)

3D Structure for NP0317852 (2-{3-hydroxy-1-[3-(n-hydroxyacetamido)propyl]-2,5-dioxopyrrolidin-3-yl}-n-[3-(n-hydroxyacetamido)propyl]ethanimidic acid)