NP-MRD: Showing NP-Card for Agaridoxin (NP0023602)

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Record Information

Version

2.0

Created at

2021-01-06 08:39:36 UTC

Updated at

2021-07-15 17:42:11 UTC

NP-MRD ID

NP0023602

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Agaridoxin

Provided By

NPAtlas

Description

Agaridoxin is found in Agaricus bisporus and Agaricus campestris. Agaridoxin was first documented in 1976 (PMID: 944247). Based on a literature review very few articles have been published on (2S)-2-amino-4-[(3,4-dihydroxyphenyl)-C-hydroxycarbonimidoyl]butanoic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI

  Mrv1652306242120433D          

 32 32  0  0  0  0            999 V2000
    4.1945   -1.7305    0.2197 N   0  0  2  0  0  0  0  0  0  0  0  0
    4.0413   -0.8315   -0.8887 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5705   -0.7708   -1.2402 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7810   -0.2720   -0.0601 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3264   -0.2353   -0.4762 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0813   -0.6012   -1.6392 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6364    0.1913    0.4295 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0083    0.2868    0.2074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5530    0.0733   -1.0300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9472    0.1781   -1.1818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7555    0.4888   -0.1134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1476    0.5915   -0.2740 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2356    0.7095    1.1446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0721    1.0220    2.2079 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8755    0.6018    1.2682 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5595    0.5153   -0.5891 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0758    0.7956    0.5442 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5088    1.5229   -1.5139 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1305   -2.1494    0.2225 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4429   -2.4603    0.2540 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5660   -1.2511   -1.7747 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1983   -1.7607   -1.5248 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3874   -0.0554   -2.0788 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1053    0.7299    0.2726 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8375   -0.9946    0.7967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2962    0.4795    1.3999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9974   -0.1696   -1.9246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3708    0.0083   -2.1606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7480    0.8152    0.4867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6358    1.1769    3.1233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4353    0.7695    2.2462 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9079    2.3259   -1.4885 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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  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
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
  2 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 15  8  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  2 21  1  6  0  0  0
  3 22  1  0  0  0  0
  3 23  1  0  0  0  0
  4 24  1  0  0  0  0
  4 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
 12 29  1  0  0  0  0
 14 30  1  0  0  0  0
 15 31  1  0  0  0  0
 18 32  1  0  0  0  0
M  END

     RDKit          3D

 32 32  0  0  0  0  0  0  0  0999 V2000
    4.1945   -1.7305    0.2197 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0413   -0.8315   -0.8887 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5705   -0.7708   -1.2402 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7810   -0.2720   -0.0601 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3264   -0.2353   -0.4762 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0813   -0.6012   -1.6392 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6364    0.1913    0.4295 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0083    0.2868    0.2074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5530    0.0733   -1.0300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9472    0.1781   -1.1818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7555    0.4888   -0.1134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1476    0.5915   -0.2740 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2356    0.7095    1.1446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0721    1.0220    2.2079 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8755    0.6018    1.2682 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5595    0.5153   -0.5891 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0758    0.7956    0.5442 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5088    1.5229   -1.5139 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1305   -2.1494    0.2225 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4429   -2.4603    0.2540 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5660   -1.2511   -1.7747 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1983   -1.7607   -1.5248 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3874   -0.0554   -2.0788 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1053    0.7299    0.2726 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8375   -0.9946    0.7967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2962    0.4795    1.3999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9974   -0.1696   -1.9246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3708    0.0083   -2.1606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7480    0.8152    0.4867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6358    1.1769    3.1233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4353    0.7695    2.2462 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9079    2.3259   -1.4885 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  2  0
  2 16  1  0
 16 17  2  0
 16 18  1  0
 15  8  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  6
  3 22  1  0
  3 23  1  0
  4 24  1  0
  4 25  1  0
  7 26  1  0
  9 27  1  0
 10 28  1  0
 12 29  1  0
 14 30  1  0
 15 31  1  0
 18 32  1  0
M  END

  Mrv1652306242120433D          

 32 32  0  0  0  0            999 V2000
    4.1945   -1.7305    0.2197 N   0  0  2  0  0  0  0  0  0  0  0  0
    4.0413   -0.8315   -0.8887 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5705   -0.7708   -1.2402 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7810   -0.2720   -0.0601 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3264   -0.2353   -0.4762 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0813   -0.6012   -1.6392 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6364    0.1913    0.4295 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0083    0.2868    0.2074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5530    0.0733   -1.0300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9472    0.1781   -1.1818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7555    0.4888   -0.1134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1476    0.5915   -0.2740 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2356    0.7095    1.1446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0721    1.0220    2.2079 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8755    0.6018    1.2682 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5595    0.5153   -0.5891 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0758    0.7956    0.5442 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5088    1.5229   -1.5139 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1305   -2.1494    0.2225 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4429   -2.4603    0.2540 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5660   -1.2511   -1.7747 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1983   -1.7607   -1.5248 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3874   -0.0554   -2.0788 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1053    0.7299    0.2726 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8375   -0.9946    0.7967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2962    0.4795    1.3999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9974   -0.1696   -1.9246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3708    0.0083   -2.1606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7480    0.8152    0.4867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6358    1.1769    3.1233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4353    0.7695    2.2462 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9079    2.3259   -1.4885 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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  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
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
  2 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 15  8  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  2 21  1  6  0  0  0
  3 22  1  0  0  0  0
  3 23  1  0  0  0  0
  4 24  1  0  0  0  0
  4 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
 12 29  1  0  0  0  0
 14 30  1  0  0  0  0
 15 31  1  0  0  0  0
 18 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0023602

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C11H14N2O5/c12-7(11(17)18)2-4-10(16)13-6-1-3-8(14)9(15)5-6/h1,3,5,7,14-15H,2,4,12H2,(H,13,16)(H,17,18)/t7-/m0/s1

> <INCHI_KEY>
HJLNKWYSKFDHDG-ZETCQYMHSA-N

> <FORMULA>
C11H14N2O5

> <MOLECULAR_WEIGHT>
254.242

> <EXACT_MASS>
254.090271559

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
24.988380039024676

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-amino-4-[(3,4-dihydroxyphenyl)carbamoyl]butanoic acid

> <ALOGPS_LOGP>
-2.25

> <JCHEM_LOGP>
-2.3673271254945236

> <ALOGPS_LOGS>
-1.93

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.530832989189687

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.5348931251407034

> <JCHEM_PKA_STRONGEST_BASIC>
8.909722884986966

> <JCHEM_POLAR_SURFACE_AREA>
132.88

> <JCHEM_REFRACTIVITY>
63.52680000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.96e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-amino-4-[(3,4-dihydroxyphenyl)carbamoyl]butanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 32 32  0  0  0  0  0  0  0  0999 V2000
    4.1945   -1.7305    0.2197 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0413   -0.8315   -0.8887 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5705   -0.7708   -1.2402 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7810   -0.2720   -0.0601 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3264   -0.2353   -0.4762 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0813   -0.6012   -1.6392 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6364    0.1913    0.4295 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0083    0.2868    0.2074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5530    0.0733   -1.0300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9472    0.1781   -1.1818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7555    0.4888   -0.1134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1476    0.5915   -0.2740 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2356    0.7095    1.1446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0721    1.0220    2.2079 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8755    0.6018    1.2682 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5595    0.5153   -0.5891 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0758    0.7956    0.5442 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5088    1.5229   -1.5139 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1305   -2.1494    0.2225 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4429   -2.4603    0.2540 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5660   -1.2511   -1.7747 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1983   -1.7607   -1.5248 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3874   -0.0554   -2.0788 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1053    0.7299    0.2726 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8375   -0.9946    0.7967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2962    0.4795    1.3999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9974   -0.1696   -1.9246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3708    0.0083   -2.1606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7480    0.8152    0.4867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6358    1.1769    3.1233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4353    0.7695    2.2462 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9079    2.3259   -1.4885 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  2  0
  2 16  1  0
 16 17  2  0
 16 18  1  0
 15  8  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  6
  3 22  1  0
  3 23  1  0
  4 24  1  0
  4 25  1  0
  7 26  1  0
  9 27  1  0
 10 28  1  0
 12 29  1  0
 14 30  1  0
 15 31  1  0
 18 32  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  N   UNK     0       4.194  -1.730   0.220  0.00  0.00           N+0
HETATM    2  C   UNK     0       4.041  -0.832  -0.889  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.571  -0.771  -1.240  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.781  -0.272  -0.060  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.326  -0.235  -0.476  0.00  0.00           C+0
HETATM    6  O   UNK     0       0.081  -0.601  -1.639  0.00  0.00           O+0
HETATM    7  N   UNK     0      -0.636   0.191   0.430  0.00  0.00           N+0
HETATM    8  C   UNK     0      -2.008   0.287   0.207  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.553   0.073  -1.030  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.947   0.178  -1.182  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.755   0.489  -0.113  0.00  0.00           C+0
HETATM   12  O   UNK     0      -6.148   0.592  -0.274  0.00  0.00           O+0
HETATM   13  C   UNK     0      -4.236   0.710   1.145  0.00  0.00           C+0
HETATM   14  O   UNK     0      -5.072   1.022   2.208  0.00  0.00           O+0
HETATM   15  C   UNK     0      -2.876   0.602   1.268  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.559   0.515  -0.589  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.076   0.796   0.544  0.00  0.00           O+0
HETATM   18  O   UNK     0       4.509   1.523  -1.514  0.00  0.00           O+0
HETATM   19  H   UNK     0       5.130  -2.149   0.223  0.00  0.00           H+0
HETATM   20  H   UNK     0       3.443  -2.460   0.254  0.00  0.00           H+0
HETATM   21  H   UNK     0       4.566  -1.251  -1.775  0.00  0.00           H+0
HETATM   22  H   UNK     0       2.198  -1.761  -1.525  0.00  0.00           H+0
HETATM   23  H   UNK     0       2.387  -0.055  -2.079  0.00  0.00           H+0
HETATM   24  H   UNK     0       2.105   0.730   0.273  0.00  0.00           H+0
HETATM   25  H   UNK     0       1.837  -0.995   0.797  0.00  0.00           H+0
HETATM   26  H   UNK     0      -0.296   0.480   1.400  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.997  -0.170  -1.925  0.00  0.00           H+0
HETATM   28  H   UNK     0      -4.371   0.008  -2.161  0.00  0.00           H+0
HETATM   29  H   UNK     0      -6.748   0.815   0.487  0.00  0.00           H+0
HETATM   30  H   UNK     0      -4.636   1.177   3.123  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.435   0.770   2.246  0.00  0.00           H+0
HETATM   32  H   UNK     0       3.908   2.326  -1.488  0.00  0.00           H+0
CONECT    1    2   19   20                                                  
CONECT    2    1    3   16   21                                             
CONECT    3    2    4   22   23                                             
CONECT    4    3    5   24   25                                             
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   26                                                  
CONECT    8    7    9   15                                                  
CONECT    9    8   10   27                                                  
CONECT   10    9   11   28                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11   29                                                       
CONECT   13   11   14   15                                                  
CONECT   14   13   30                                                       
CONECT   15   13    8   31                                                  
CONECT   16    2   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   32                                                       
CONECT   19    1                                                            
CONECT   20    1                                                            
CONECT   21    2                                                            
CONECT   22    3                                                            
CONECT   23    3                                                            
CONECT   24    4                                                            
CONECT   25    4                                                            
CONECT   26    7                                                            
CONECT   27    9                                                            
CONECT   28   10                                                            
CONECT   29   12                                                            
CONECT   30   14                                                            
CONECT   31   15                                                            
CONECT   32   18                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   64    0
END

RDKit          3D

32 32  0  0  0  0  0  0  0  0999 V2000
    4.1945   -1.7305    0.2197 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0413   -0.8315   -0.8887 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5705   -0.7708   -1.2402 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7810   -0.2720   -0.0601 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3264   -0.2353   -0.4762 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0813   -0.6012   -1.6392 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6364    0.1913    0.4295 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0083    0.2868    0.2074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5530    0.0733   -1.0300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9472    0.1781   -1.1818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7555    0.4888   -0.1134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1476    0.5915   -0.2740 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2356    0.7095    1.1446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0721    1.0220    2.2079 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8755    0.6018    1.2682 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5595    0.5153   -0.5891 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0758    0.7956    0.5442 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5088    1.5229   -1.5139 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1305   -2.1494    0.2225 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4429   -2.4603    0.2540 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5660   -1.2511   -1.7747 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1983   -1.7607   -1.5248 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3874   -0.0554   -2.0788 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1053    0.7299    0.2726 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8375   -0.9946    0.7967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2962    0.4795    1.3999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9974   -0.1696   -1.9246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3708    0.0083   -2.1606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7480    0.8152    0.4867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6358    1.1769    3.1233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4353    0.7695    2.2462 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9079    2.3259   -1.4885 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  2  0
  2 16  1  0
 16 17  2  0
 16 18  1  0
 15  8  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  6
  3 22  1  0
  3 23  1  0
  4 24  1  0
  4 25  1  0
  7 26  1  0
  9 27  1  0
 10 28  1  0
 12 29  1  0
 14 30  1  0
 15 31  1  0
 18 32  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
(2S)-2-Amino-4-[(3,4-dihydroxyphenyl)-C-hydroxycarbonimidoyl]butanoate	Generator

Chemical Formula

C₁₁H₁₄N₂O₅

Average Mass

254.2420 Da

Monoisotopic Mass

254.09027 Da

IUPAC Name

(2S)-2-amino-4-[(3,4-dihydroxyphenyl)carbamoyl]butanoic acid

Traditional Name

(2S)-2-amino-4-[(3,4-dihydroxyphenyl)carbamoyl]butanoic acid

CAS Registry Number

Not Available

SMILES

N[C@@H](CCC(=O)NC1=CC(O)=C(O)C=C1)C(O)=O

InChI Identifier

InChI=1S/C11H14N2O5/c12-7(11(17)18)2-4-10(16)13-6-1-3-8(14)9(15)5-6/h1,3,5,7,14-15H,2,4,12H2,(H,13,16)(H,17,18)/t7-/m0/s1

InChI Key

HJLNKWYSKFDHDG-ZETCQYMHSA-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
Agaricus bisporus	LOTUS Database	35616633
Agaricus campestris	NPAtlas	944247

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	-2.2	ALOGPS
logP	-2.4	ChemAxon
logS	-1.9	ALOGPS
pKa (Strongest Acidic)	1.53	ChemAxon
pKa (Strongest Basic)	8.91	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	132.88 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	63.53 m³·mol⁻¹	ChemAxon
Polarizability	24.99 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

NPAtlas ID

NPA019766

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

29365425

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15382847

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Szent-Gyorgyi A, Chung RH, Boyajian MJ, Tishler M, Arison BH, Schoenewaldt EF, Wittick JJ: Agaridoxin, a mushroom metabolite. Isolation, structure, and synthesis. J Org Chem. 1976 Apr 30;41(9):1603-6. doi: 10.1021/jo00871a027. [PubMed:944247 ]

Showing NP-Card for Agaridoxin (NP0023602)

MOL for NP0023602 (Agaridoxin)

3D MOL for NP0023602 (Agaridoxin)

3D SDF for NP0023602 (Agaridoxin)

3D-SDF for NP0023602 (Agaridoxin)

PDB for NP0023602 (Agaridoxin)

3D PDB for NP0023602 (Agaridoxin)

SMILES for NP0023602 (Agaridoxin)

INCHI for NP0023602 (Agaridoxin)

Structure for NP0023602 (Agaridoxin)

3D Structure for NP0023602 (Agaridoxin)