NP-MRD: Showing NP-Card for Tensyuic acid C (NP0007252)

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Record Information

Version

2.0

Created at

2020-12-09 04:05:37 UTC

Updated at

2021-07-15 16:57:05 UTC

NP-MRD ID

NP0007252

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Tensyuic acid C

Provided By

NPAtlas

Description

Tensyuic acid c is also known as tensyuate c. Tensyuic acid c is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. Tensyuic acid C is found in Aspergillus. Based on a literature review very few articles have been published on Tensyuic acid c.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI

  Mrv1652306242118383D          

 39 38  0  0  0  0            999 V2000
   -4.5692   -1.4096    1.0948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5744   -0.3656    0.2932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8272    0.1803   -0.1560 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9060    1.1694   -0.9176 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0466   -0.3909    0.2556 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3092    0.2841   -0.1682 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1025   -0.4590    0.3689 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8431    0.2237   -0.1202 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3787   -0.5036    0.4102 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6523    0.1639   -0.0759 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8028   -0.6194    0.5243 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1334   -0.1034    0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4719    0.0206   -1.0675 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0950    0.2793    1.0845 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3637    0.7640    0.6937 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3114    1.9796   -0.1838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2269    0.2371   -1.6470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1572    1.3112   -2.2666 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2272   -0.9550   -2.3210 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4825   -1.8626    1.4192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6369   -1.8100    1.4236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4334   -1.0683   -0.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2997    1.3035    0.2266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1198   -0.3820    1.4681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1746   -1.5066    0.0237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7720    0.2704   -1.2165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8093    1.2336    0.3546 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3139   -0.6118    1.4916 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3392   -1.5270   -0.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6456    0.1313   -1.1811 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6245    1.1998    0.3404 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7082   -1.6499    0.1124 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6612   -0.6674    1.6088 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8552    1.0806    1.6656 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0325   -0.0460    0.3082 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3076    2.4154   -0.3084 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0203    2.7557    0.1691 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7527    1.6541   -1.1788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9526   -1.6577   -2.2123 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  2  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  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  6 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  5 22  1  0  0  0  0
  6 23  1  1  0  0  0
  7 24  1  0  0  0  0
  7 25  1  0  0  0  0
  8 26  1  0  0  0  0
  8 27  1  0  0  0  0
  9 28  1  0  0  0  0
  9 29  1  0  0  0  0
 10 30  1  0  0  0  0
 10 31  1  0  0  0  0
 11 32  1  0  0  0  0
 11 33  1  0  0  0  0
 15 34  1  0  0  0  0
 15 35  1  0  0  0  0
 16 36  1  0  0  0  0
 16 37  1  0  0  0  0
 16 38  1  0  0  0  0
 19 39  1  0  0  0  0
M  END

     RDKit          3D

 39 38  0  0  0  0  0  0  0  0999 V2000
   -4.5692   -1.4096    1.0948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5744   -0.3656    0.2932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8272    0.1803   -0.1560 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9060    1.1694   -0.9176 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0466   -0.3909    0.2556 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3092    0.2841   -0.1682 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1025   -0.4590    0.3689 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8431    0.2237   -0.1202 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3787   -0.5036    0.4102 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6523    0.1639   -0.0759 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8028   -0.6194    0.5243 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1334   -0.1034    0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4719    0.0206   -1.0675 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0950    0.2793    1.0845 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3637    0.7640    0.6937 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3114    1.9796   -0.1838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2269    0.2371   -1.6470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1572    1.3112   -2.2666 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2272   -0.9550   -2.3210 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4825   -1.8626    1.4192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6369   -1.8100    1.4236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4334   -1.0683   -0.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2997    1.3035    0.2266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1198   -0.3820    1.4681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1746   -1.5066    0.0237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7720    0.2704   -1.2165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8093    1.2336    0.3546 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3139   -0.6118    1.4916 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3392   -1.5270   -0.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6456    0.1313   -1.1811 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6245    1.1998    0.3404 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7082   -1.6499    0.1124 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6612   -0.6674    1.6088 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8552    1.0806    1.6656 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0325   -0.0460    0.3082 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3076    2.4154   -0.3084 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0203    2.7557    0.1691 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7527    1.6541   -1.1788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9526   -1.6577   -2.2123 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  0
  3  5  1  0
  2  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
  6 17  1  0
 17 18  2  0
 17 19  1  0
  1 20  1  0
  1 21  1  0
  5 22  1  0
  6 23  1  1
  7 24  1  0
  7 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
  9 29  1  0
 10 30  1  0
 10 31  1  0
 11 32  1  0
 11 33  1  0
 15 34  1  0
 15 35  1  0
 16 36  1  0
 16 37  1  0
 16 38  1  0
 19 39  1  0
M  END

  Mrv1652306242118383D          

 39 38  0  0  0  0            999 V2000
   -4.5692   -1.4096    1.0948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5744   -0.3656    0.2932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8272    0.1803   -0.1560 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9060    1.1694   -0.9176 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0466   -0.3909    0.2556 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3092    0.2841   -0.1682 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1025   -0.4590    0.3689 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8431    0.2237   -0.1202 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3787   -0.5036    0.4102 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6523    0.1639   -0.0759 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8028   -0.6194    0.5243 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1334   -0.1034    0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4719    0.0206   -1.0675 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0950    0.2793    1.0845 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3637    0.7640    0.6937 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3114    1.9796   -0.1838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2269    0.2371   -1.6470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1572    1.3112   -2.2666 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2272   -0.9550   -2.3210 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4825   -1.8626    1.4192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6369   -1.8100    1.4236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4334   -1.0683   -0.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2997    1.3035    0.2266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1198   -0.3820    1.4681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1746   -1.5066    0.0237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7720    0.2704   -1.2165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8093    1.2336    0.3546 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3139   -0.6118    1.4916 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3392   -1.5270   -0.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6456    0.1313   -1.1811 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6245    1.1998    0.3404 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7082   -1.6499    0.1124 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6612   -0.6674    1.6088 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8552    1.0806    1.6656 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0325   -0.0460    0.3082 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3076    2.4154   -0.3084 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0203    2.7557    0.1691 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7527    1.6541   -1.1788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9526   -1.6577   -2.2123 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  2  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  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  6 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  5 22  1  0  0  0  0
  6 23  1  1  0  0  0
  7 24  1  0  0  0  0
  7 25  1  0  0  0  0
  8 26  1  0  0  0  0
  8 27  1  0  0  0  0
  9 28  1  0  0  0  0
  9 29  1  0  0  0  0
 10 30  1  0  0  0  0
 10 31  1  0  0  0  0
 11 32  1  0  0  0  0
 11 33  1  0  0  0  0
 15 34  1  0  0  0  0
 15 35  1  0  0  0  0
 16 36  1  0  0  0  0
 16 37  1  0  0  0  0
 16 38  1  0  0  0  0
 19 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0007252

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C13H20O6/c1-3-19-11(14)8-6-4-5-7-10(13(17)18)9(2)12(15)16/h10H,2-8H2,1H3,(H,15,16)(H,17,18)/t10-/m1/s1

> <INCHI_KEY>
STUMFFBVBKIJSG-UHFFFAOYSA-N

> <FORMULA>
C13H20O6

> <MOLECULAR_WEIGHT>
272.297

> <EXACT_MASS>
272.125988364

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
28.557917088772104

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R)-2-(6-ethoxy-6-oxohexyl)-3-methylidenebutanedioic acid

> <ALOGPS_LOGP>
2.12

> <JCHEM_LOGP>
2.001114531

> <ALOGPS_LOGS>
-2.49

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
4.515787022393785

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.756919296781257

> <JCHEM_PKA_STRONGEST_BASIC>
-7.032123337165571

> <JCHEM_POLAR_SURFACE_AREA>
100.89999999999999

> <JCHEM_REFRACTIVITY>
66.67750000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.86e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-2-(6-ethoxy-6-oxohexyl)-3-methylidenebutanedioic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 39 38  0  0  0  0  0  0  0  0999 V2000
   -4.5692   -1.4096    1.0948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5744   -0.3656    0.2932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8272    0.1803   -0.1560 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9060    1.1694   -0.9176 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0466   -0.3909    0.2556 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3092    0.2841   -0.1682 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1025   -0.4590    0.3689 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8431    0.2237   -0.1202 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3787   -0.5036    0.4102 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6523    0.1639   -0.0759 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8028   -0.6194    0.5243 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1334   -0.1034    0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4719    0.0206   -1.0675 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0950    0.2793    1.0845 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3637    0.7640    0.6937 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3114    1.9796   -0.1838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2269    0.2371   -1.6470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1572    1.3112   -2.2666 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2272   -0.9550   -2.3210 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4825   -1.8626    1.4192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6369   -1.8100    1.4236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4334   -1.0683   -0.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2997    1.3035    0.2266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1198   -0.3820    1.4681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1746   -1.5066    0.0237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7720    0.2704   -1.2165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8093    1.2336    0.3546 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3139   -0.6118    1.4916 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3392   -1.5270   -0.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6456    0.1313   -1.1811 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6245    1.1998    0.3404 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7082   -1.6499    0.1124 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6612   -0.6674    1.6088 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8552    1.0806    1.6656 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0325   -0.0460    0.3082 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3076    2.4154   -0.3084 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0203    2.7557    0.1691 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7527    1.6541   -1.1788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9526   -1.6577   -2.2123 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  0
  3  5  1  0
  2  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
  6 17  1  0
 17 18  2  0
 17 19  1  0
  1 20  1  0
  1 21  1  0
  5 22  1  0
  6 23  1  1
  7 24  1  0
  7 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
  9 29  1  0
 10 30  1  0
 10 31  1  0
 11 32  1  0
 11 33  1  0
 15 34  1  0
 15 35  1  0
 16 36  1  0
 16 37  1  0
 16 38  1  0
 19 39  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      -4.569  -1.410   1.095  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.574  -0.366   0.293  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.827   0.180  -0.156  0.00  0.00           C+0
HETATM    4  O   UNK     0      -5.906   1.169  -0.918  0.00  0.00           O+0
HETATM    5  O   UNK     0      -7.047  -0.391   0.256  0.00  0.00           O+0
HETATM    6  C   UNK     0      -3.309   0.284  -0.168  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.103  -0.459   0.369  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.843   0.224  -0.120  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.379  -0.504   0.410  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.652   0.164  -0.076  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.803  -0.619   0.524  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.133  -0.103   0.133  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.472   0.021  -1.067  0.00  0.00           O+0
HETATM   14  O   UNK     0       5.095   0.279   1.085  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.364   0.764   0.694  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.311   1.980  -0.184  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.227   0.237  -1.647  0.00  0.00           C+0
HETATM   18  O   UNK     0      -3.157   1.311  -2.267  0.00  0.00           O+0
HETATM   19  O   UNK     0      -3.227  -0.955  -2.321  0.00  0.00           O+0
HETATM   20  H   UNK     0      -5.482  -1.863   1.419  0.00  0.00           H+0
HETATM   21  H   UNK     0      -3.637  -1.810   1.424  0.00  0.00           H+0
HETATM   22  H   UNK     0      -7.433  -1.068  -0.407  0.00  0.00           H+0
HETATM   23  H   UNK     0      -3.300   1.304   0.227  0.00  0.00           H+0
HETATM   24  H   UNK     0      -2.120  -0.382   1.468  0.00  0.00           H+0
HETATM   25  H   UNK     0      -2.175  -1.507   0.024  0.00  0.00           H+0
HETATM   26  H   UNK     0      -0.772   0.270  -1.216  0.00  0.00           H+0
HETATM   27  H   UNK     0      -0.809   1.234   0.355  0.00  0.00           H+0
HETATM   28  H   UNK     0       0.314  -0.612   1.492  0.00  0.00           H+0
HETATM   29  H   UNK     0       0.339  -1.527  -0.043  0.00  0.00           H+0
HETATM   30  H   UNK     0       1.646   0.131  -1.181  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.625   1.200   0.340  0.00  0.00           H+0
HETATM   32  H   UNK     0       2.708  -1.650   0.112  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.661  -0.667   1.609  0.00  0.00           H+0
HETATM   34  H   UNK     0       6.855   1.081   1.666  0.00  0.00           H+0
HETATM   35  H   UNK     0       7.032  -0.046   0.308  0.00  0.00           H+0
HETATM   36  H   UNK     0       5.308   2.415  -0.308  0.00  0.00           H+0
HETATM   37  H   UNK     0       7.020   2.756   0.169  0.00  0.00           H+0
HETATM   38  H   UNK     0       6.753   1.654  -1.179  0.00  0.00           H+0
HETATM   39  H   UNK     0      -3.953  -1.658  -2.212  0.00  0.00           H+0
CONECT    1    2   20   21                                                  
CONECT    2    1    3    6                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3   22                                                       
CONECT    6    2    7   17   23                                             
CONECT    7    6    8   24   25                                             
CONECT    8    7    9   26   27                                             
CONECT    9    8   10   28   29                                             
CONECT   10    9   11   30   31                                             
CONECT   11   10   12   32   33                                             
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   34   35                                             
CONECT   16   15   36   37   38                                             
CONECT   17    6   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   39                                                       
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    5                                                            
CONECT   23    6                                                            
CONECT   24    7                                                            
CONECT   25    7                                                            
CONECT   26    8                                                            
CONECT   27    8                                                            
CONECT   28    9                                                            
CONECT   29    9                                                            
CONECT   30   10                                                            
CONECT   31   10                                                            
CONECT   32   11                                                            
CONECT   33   11                                                            
CONECT   34   15                                                            
CONECT   35   15                                                            
CONECT   36   16                                                            
CONECT   37   16                                                            
CONECT   38   16                                                            
CONECT   39   19                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   76    0
END

RDKit          3D

39 38  0  0  0  0  0  0  0  0999 V2000
   -4.5692   -1.4096    1.0948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5744   -0.3656    0.2932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8272    0.1803   -0.1560 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9060    1.1694   -0.9176 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0466   -0.3909    0.2556 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3092    0.2841   -0.1682 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1025   -0.4590    0.3689 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8431    0.2237   -0.1202 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3787   -0.5036    0.4102 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6523    0.1639   -0.0759 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8028   -0.6194    0.5243 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1334   -0.1034    0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4719    0.0206   -1.0675 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0950    0.2793    1.0845 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3637    0.7640    0.6937 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3114    1.9796   -0.1838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2269    0.2371   -1.6470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1572    1.3112   -2.2666 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2272   -0.9550   -2.3210 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4825   -1.8626    1.4192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6369   -1.8100    1.4236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4334   -1.0683   -0.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2997    1.3035    0.2266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1198   -0.3820    1.4681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1746   -1.5066    0.0237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7720    0.2704   -1.2165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8093    1.2336    0.3546 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3139   -0.6118    1.4916 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3392   -1.5270   -0.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6456    0.1313   -1.1811 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6245    1.1998    0.3404 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7082   -1.6499    0.1124 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6612   -0.6674    1.6088 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8552    1.0806    1.6656 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0325   -0.0460    0.3082 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3076    2.4154   -0.3084 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0203    2.7557    0.1691 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7527    1.6541   -1.1788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9526   -1.6577   -2.2123 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  0
  3  5  1  0
  2  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
  6 17  1  0
 17 18  2  0
 17 19  1  0
  1 20  1  0
  1 21  1  0
  5 22  1  0
  6 23  1  1
  7 24  1  0
  7 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
  9 29  1  0
 10 30  1  0
 10 31  1  0
 11 32  1  0
 11 33  1  0
 15 34  1  0
 15 35  1  0
 16 36  1  0
 16 37  1  0
 16 38  1  0
 19 39  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
(-)-2-(6-Ethoxy-6-oxohexyl)-3-methylenesuccinic acid	ChEBI
(-)-2-(6-Ethoxy-6-oxohexyl)-3-methylidenebutanedioic acid	ChEBI
(-)-Tensyuic acid C	ChEBI
(-)-2-(6-Ethoxy-6-oxohexyl)-3-methylenesuccinate	Generator
(-)-2-(6-Ethoxy-6-oxohexyl)-3-methylidenebutanedioate	Generator
(-)-Tensyuate C	Generator
Tensyuate c	Generator

Chemical Formula

C₁₃H₂₀O₆

Average Mass

272.2970 Da

Monoisotopic Mass

272.12599 Da

IUPAC Name

(2R)-2-(6-ethoxy-6-oxohexyl)-3-methylidenebutanedioic acid

Traditional Name

(2R)-2-(6-ethoxy-6-oxohexyl)-3-methylidenebutanedioic acid

CAS Registry Number

Not Available

SMILES

CCOC(=O)CCCCCC(C(O)=O)C(=C)C(O)=O

InChI Identifier

InChI=1S/C13H20O6/c1-3-19-11(14)8-6-4-5-7-10(13(17)18)9(2)12(15)16/h10H,2-8H2,1H3,(H,15,16)(H,17,18)

InChI Key

STUMFFBVBKIJSG-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Aspergillus	NPAtlas	17827758

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
Carboxylic acid ester
Carboxylic acid
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	2.12	ALOGPS
logP	2	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	3.76	ChemAxon
pKa (Strongest Basic)	-7	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	100.9 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	66.68 m³·mol⁻¹	ChemAxon
Polarizability	28.56 Å³	ChemAxon
Number of Rings	0	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

NPA000140

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

28285426

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

17757653

PDB ID

Not Available

ChEBI ID

133829

Good Scents ID

Not Available

References

General References

Showing NP-Card for Tensyuic acid C (NP0007252)

MOL for NP0007252 (Tensyuic acid C)

3D MOL for NP0007252 (Tensyuic acid C)

3D SDF for NP0007252 (Tensyuic acid C)

3D-SDF for NP0007252 (Tensyuic acid C)

PDB for NP0007252 (Tensyuic acid C)

3D PDB for NP0007252 (Tensyuic acid C)

SMILES for NP0007252 (Tensyuic acid C)

INCHI for NP0007252 (Tensyuic acid C)

Structure for NP0007252 (Tensyuic acid C)

3D Structure for NP0007252 (Tensyuic acid C)