NP-MRD: Showing NP-Card for 3-{[7-hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-3ah-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid (NP0146870)

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Record Information

Version

2.0

Created at

2022-09-02 02:21:17 UTC

Updated at

2022-09-02 02:21:17 UTC

NP-MRD ID

NP0146870

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-{[7-hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-3ah-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid

Description

3-{[7-Hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-2,3,3a,4,5,7a-hexahydro-1-benzofuran-3-yl]-C-hydroxycarbonimidoyl}prop-2-enoic acid belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. N-acyl-alpha amino acids and derivatives are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen atom. 3-{[7-hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-3ah-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid is found in Penicillium chrysogenum. 3-{[7-Hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-2,3,3a,4,5,7a-hexahydro-1-benzofuran-3-yl]-C-hydroxycarbonimidoyl}prop-2-enoic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251512392D          

 30 31  0  0  0  0            999 V2000
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7846   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4491   -1.0086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4991   -0.6674    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4991   -1.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2136   -1.9049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7846   -1.9049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7846   -2.7299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4991   -3.1424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4991   -3.9674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2136   -2.7299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2695    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0945    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7846    1.0799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0862    1.6455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  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
  6  7  2  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
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 14 12  1  4  0  0  0
 14 15  2  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
  9 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
  8 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
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
  7 27  1  0  0  0  0
 27 28  2  0  0  0  0
 24 29  1  0  0  0  0
  6 30  1  4  0  0  0
M  END

     RDKit          3D

 55 56  0  0  0  0  0  0  0  0999 V2000
   -6.5923    1.6333   -1.9658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2730    1.1121   -1.5159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2317    0.9792   -2.2955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8932    0.4705   -1.9173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8663    0.1210   -0.4567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5669   -0.4096   -0.0160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1736   -1.6382   -0.6229 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7366    0.0951    0.8502 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9798    1.3459    1.5442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8640    2.1670    1.2086 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1740    1.7143    2.7035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4557    3.0283    3.4151 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7775    0.9311    3.1368 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5161    1.3180    4.2462 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1025   -0.3457    2.5003 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8699   -1.5123    3.4678 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5370   -0.3036    2.2918 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7318    0.2172    1.0040 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6647    1.0047    0.7141 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6411   -0.3695    0.1922 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2289    0.6478   -0.8662 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1072   -1.5717   -0.4369 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1687   -1.5830   -1.4062 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6599   -0.4753   -1.6648 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6184   -2.7964   -2.0230 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5296   -3.0499   -2.8964 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3995   -2.0966   -3.5260 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2540   -2.5734   -4.3858 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3981   -0.7441   -3.2938 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5427   -0.6071    1.1635 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.3405    0.8404   -2.1282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3857    2.2265   -2.8979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9500    2.3320   -1.1808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1871    0.8249   -0.4760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3987    1.2900   -3.3528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0752    1.1543   -2.2150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7359   -0.4563   -2.5387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6085   -0.7491   -0.3892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3299    0.8650    0.2079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7522   -2.4677   -0.4870 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0343    3.0318    4.3945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5411    3.0848    3.5384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0391    3.8382    2.7689 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9502    2.2192    4.3038 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6591   -1.4457    4.2629 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0020   -2.4360    2.9075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1190   -1.4109    3.9611 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7626    0.1237   -1.7216 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5071    1.3318   -0.3824 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1104    1.2119   -1.2667 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6737   -2.4757   -0.1954 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0657   -3.7257   -1.6782 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6958   -4.1119   -3.2292 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8101   -0.0933   -3.9308 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2515   -1.7109    1.1046 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
  6  7  1  0
  6  8  2  0
  8 30  1  0
 30 20  1  0
 20 21  1  0
 20 22  1  6
 22 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  2  0
 26 27  1  0
 27 29  1  0
 27 28  2  0
 20 18  1  0
 18 19  2  0
 18 17  1  0
 17 15  1  0
 15 16  1  1
 15 13  1  0
 13 14  1  0
 13 11  2  0
 11 12  1  0
 11  9  1  0
  9 10  2  0
  9  8  1  0
 15 30  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  5 38  1  0
  5 39  1  0
  7 40  1  0
 30 55  1  1
 21 48  1  0
 21 49  1  0
 21 50  1  0
 22 51  1  0
 25 52  1  0
 26 53  1  0
 29 54  1  0
 16 45  1  0
 16 46  1  0
 16 47  1  0
 14 44  1  0
 12 41  1  0
 12 42  1  0
 12 43  1  0
M  END


  Mrv1533004251512392D          

 30 31  0  0  0  0            999 V2000
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7846   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4491   -1.0086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4991   -0.6674    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4991   -1.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2136   -1.9049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7846   -1.9049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7846   -2.7299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4991   -3.1424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4991   -3.9674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2136   -2.7299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2695    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0945    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7846    1.0799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0862    1.6455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  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
  6  7  2  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
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 14 12  1  4  0  0  0
 14 15  2  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
  9 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
  8 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
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
  7 27  1  0  0  0  0
 27 28  2  0  0  0  0
 24 29  1  0  0  0  0
  6 30  1  4  0  0  0
M  END
> <DATABASE_ID>
NP0146870

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=CCCC(O)=C1C2C(C)(NC(=O)C=CC(O)=O)C(=O)OC2(C)C(O)=C(C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H25NO8/c1-5-6-7-8-12(23)15-16(27)11(2)18(28)21(4)17(15)20(3,19(29)30-21)22-13(24)9-10-14(25)26/h5-6,9-10,17,23,28H,7-8H2,1-4H3,(H,22,24)(H,25,26)

> <INCHI_KEY>
ZWCFJIDEAVJSER-UHFFFAOYSA-N

> <FORMULA>
C21H25NO8

> <MOLECULAR_WEIGHT>
419.43

> <EXACT_MASS>
419.158016769

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
42.30338807138611

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-{[7-hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-2,3,3a,4,5,7a-hexahydro-1-benzofuran-3-yl]carbamoyl}prop-2-enoic acid

> <ALOGPS_LOGP>
1.44

> <JCHEM_LOGP>
1.3394519669999996

> <ALOGPS_LOGS>
-3.30

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
3.5440733065941403

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.79037794523366

> <JCHEM_PKA_STRONGEST_BASIC>
-0.6437941386405791

> <JCHEM_POLAR_SURFACE_AREA>
150.23

> <JCHEM_REFRACTIVITY>
109.77919999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.13e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-{[7-hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-3aH-1-benzofuran-3-yl]carbamoyl}prop-2-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.465  -0.476   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.838  -1.883   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      -2.798  -1.246   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      -2.798  -2.786   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -4.132  -3.556   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -1.465  -3.556   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.465  -5.096   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.798  -5.866   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -2.798  -7.406   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -4.132  -5.096   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -2.370   0.770   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -3.910   0.770   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -1.465   2.016   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.161   3.072   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   30                                                  
CONECT    7    6    8   27                                                  
CONECT    8    7    9   22                                                  
CONECT    9    8   10   11   19                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19    9   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21    8   23   24                                             
CONECT   23   22                                                            
CONECT   24   22   25   29                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25    7   28                                                  
CONECT   28   27                                                            
CONECT   29   24                                                            
CONECT   30    6                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   62    0
END

View in JSmol

Synonyms

Value	Source
3-{[7-hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-2,3,3a,4,5,7a-hexahydro-1-benzofuran-3-yl]-C-hydroxycarbonimidoyl}prop-2-enoate	Generator

Chemical Formula

C₂₁H₂₅NO₈

Average Mass

419.4300 Da

Monoisotopic Mass

419.15802 Da

IUPAC Name

3-{[7-hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-2,3,3a,4,5,7a-hexahydro-1-benzofuran-3-yl]carbamoyl}prop-2-enoic acid

Traditional Name

3-{[7-hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-3aH-1-benzofuran-3-yl]carbamoyl}prop-2-enoic acid

CAS Registry Number

Not Available

SMILES

CC=CCCC(O)=C1C2C(C)(NC(=O)C=CC(O)=O)C(=O)OC2(C)C(O)=C(C)C1=O

InChI Identifier

InChI=1S/C21H25NO8/c1-5-6-7-8-12(23)15-16(27)11(2)18(28)21(4)17(15)20(3,19(29)30-21)22-13(24)9-10-14(25)26/h5-6,9-10,17,23,28H,7-8H2,1-4H3,(H,22,24)(H,25,26)

InChI Key

ZWCFJIDEAVJSER-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

Species Name	Source	Reference
Penicillium chrysogenum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. N-acyl-alpha amino acids and derivatives are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

N-acyl-alpha amino acids and derivatives

Alternative Parents

Substituents

N-acyl-alpha amino acid or derivatives
Benzofuran
O-quinomethane
Quinomethane
Heterocyclic fatty acid
Hydroxy fatty acid
Cyclohexenone
Dicarboxylic acid or derivatives
Gamma butyrolactone
N-acyl-amine
Unsaturated fatty acid
Fatty acid
Fatty acyl
Tetrahydrofuran
Vinylogous acid
Secondary carboxylic acid amide
Carboxylic acid ester
Cyclic ketone
Lactone
Ketone
Carboxamide group
Oxacycle
Carboxylic acid
Organoheterocyclic compound
Enol
Organooxygen compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Carbonyl group
Organic oxide
Hydrocarbon derivative
Organonitrogen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	1.44	ALOGPS
logP	1.34	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	2.79	ChemAxon
pKa (Strongest Basic)	-0.64	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	150.23 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	109.78 m³·mol⁻¹	ChemAxon
Polarizability	42.3 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

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 3-{[7-hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-3ah-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid (NP0146870)

MOL for NP0146870 (3-{[7-hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-3ah-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)

3D MOL for NP0146870 (3-{[7-hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-3ah-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)

3D SDF for NP0146870 (3-{[7-hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-3ah-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)

3D-SDF for NP0146870 (3-{[7-hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-3ah-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)

PDB for NP0146870 (3-{[7-hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-3ah-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)

3D PDB for NP0146870 (3-{[7-hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-3ah-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)

SMILES for NP0146870 (3-{[7-hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-3ah-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)

INCHI for NP0146870 (3-{[7-hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-3ah-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)

Structure for NP0146870 (3-{[7-hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-3ah-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)

3D Structure for NP0146870 (3-{[7-hydroxy-4-(1-hydroxyhex-4-en-1-ylidene)-3,6,7a-trimethyl-2,5-dioxo-3ah-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)