NP-MRD: Showing NP-Card for Tensyuic acid A (NP0007250)

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Record Information

Version

2.0

Created at

2020-12-09 04:05:32 UTC

Updated at

2021-07-15 16:57:04 UTC

NP-MRD ID

NP0007250

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Tensyuic acid A

Provided By

NPAtlas

Description

Tensyuic acid a is also known as tensyuate a. Tensyuic acid a 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 A is found in Aspergillus. Based on a literature review very few articles have been published on Tensyuic acid a.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118383D          

 33 32  0  0  0  0            999 V2000
   -3.7448   -0.6145   -0.4462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7486   -1.1922    0.1846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8446   -2.6169    0.4522 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9353   -3.2325    1.0492 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9406   -3.3330    0.0562 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5592   -0.4568    0.6263 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2819   -0.9844   -0.0508 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8497   -0.1374    0.4966 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1602   -0.5621   -0.0965 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2629    0.2527    0.4278 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0125    1.1646    1.2662 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5815    0.0905    0.0625 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6553    0.8484    0.5421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5904    0.9764    0.3066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5647    1.7982    1.2563 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6467    1.4874   -0.9791 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6723    2.8903   -1.1602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6195   -1.1470   -0.7697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6930    0.4373   -0.6517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5941   -3.7687    0.6713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4322   -0.5693    1.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3471   -0.8264   -1.1467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1635   -2.0446    0.1573 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6077    0.9191    0.2328 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8879   -0.1886    1.5978 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0565   -0.5095   -1.2008 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2754   -1.6574    0.1339 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3917    1.8885    0.8094 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1797    0.3718    1.3990 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4111    0.9151   -0.2930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3707    3.1977   -1.9595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6385    3.2057   -1.4201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9444    3.3972   -0.1929 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  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
  6 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  5 20  1  0  0  0  0
  6 21  1  1  0  0  0
  7 22  1  0  0  0  0
  7 23  1  0  0  0  0
  8 24  1  0  0  0  0
  8 25  1  0  0  0  0
  9 26  1  0  0  0  0
  9 27  1  0  0  0  0
 13 28  1  0  0  0  0
 13 29  1  0  0  0  0
 13 30  1  0  0  0  0
 17 31  1  0  0  0  0
 17 32  1  0  0  0  0
 17 33  1  0  0  0  0
M  END

     RDKit          3D

 33 32  0  0  0  0  0  0  0  0999 V2000
   -3.7448   -0.6145   -0.4462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7486   -1.1922    0.1846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8446   -2.6169    0.4522 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9353   -3.2325    1.0492 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9406   -3.3330    0.0562 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5592   -0.4568    0.6263 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2819   -0.9844   -0.0508 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8497   -0.1374    0.4966 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1602   -0.5621   -0.0965 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2629    0.2527    0.4278 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0125    1.1646    1.2662 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5815    0.0905    0.0625 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6553    0.8484    0.5421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5904    0.9764    0.3066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5647    1.7982    1.2563 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6467    1.4874   -0.9791 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6723    2.8903   -1.1602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6195   -1.1470   -0.7697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6930    0.4373   -0.6517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5941   -3.7687    0.6713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4322   -0.5693    1.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3471   -0.8264   -1.1467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1635   -2.0446    0.1573 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6077    0.9191    0.2328 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8879   -0.1886    1.5978 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0565   -0.5095   -1.2008 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2754   -1.6574    0.1339 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3917    1.8885    0.8094 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1797    0.3718    1.3990 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4111    0.9151   -0.2930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3707    3.1977   -1.9595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6385    3.2057   -1.4201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9444    3.3972   -0.1929 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  2  0
 10 12  1  0
 12 13  1  0
  6 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
  1 18  1  0
  1 19  1  0
  5 20  1  0
  6 21  1  1
  7 22  1  0
  7 23  1  0
  8 24  1  0
  8 25  1  0
  9 26  1  0
  9 27  1  0
 13 28  1  0
 13 29  1  0
 13 30  1  0
 17 31  1  0
 17 32  1  0
 17 33  1  0
M  END


  Mrv1652306242118383D          

 33 32  0  0  0  0            999 V2000
   -3.7448   -0.6145   -0.4462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7486   -1.1922    0.1846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8446   -2.6169    0.4522 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9353   -3.2325    1.0492 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9406   -3.3330    0.0562 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5592   -0.4568    0.6263 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2819   -0.9844   -0.0508 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8497   -0.1374    0.4966 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1602   -0.5621   -0.0965 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2629    0.2527    0.4278 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0125    1.1646    1.2662 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5815    0.0905    0.0625 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6553    0.8484    0.5421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5904    0.9764    0.3066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5647    1.7982    1.2563 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6467    1.4874   -0.9791 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6723    2.8903   -1.1602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6195   -1.1470   -0.7697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6930    0.4373   -0.6517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5941   -3.7687    0.6713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4322   -0.5693    1.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3471   -0.8264   -1.1467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1635   -2.0446    0.1573 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6077    0.9191    0.2328 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8879   -0.1886    1.5978 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0565   -0.5095   -1.2008 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2754   -1.6574    0.1339 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3917    1.8885    0.8094 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1797    0.3718    1.3990 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4111    0.9151   -0.2930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3707    3.1977   -1.9595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6385    3.2057   -1.4201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9444    3.3972   -0.1929 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  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
  6 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  5 20  1  0  0  0  0
  6 21  1  1  0  0  0
  7 22  1  0  0  0  0
  7 23  1  0  0  0  0
  8 24  1  0  0  0  0
  8 25  1  0  0  0  0
  9 26  1  0  0  0  0
  9 27  1  0  0  0  0
 13 28  1  0  0  0  0
 13 29  1  0  0  0  0
 13 30  1  0  0  0  0
 17 31  1  0  0  0  0
 17 32  1  0  0  0  0
 17 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0007250

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C11H16O6/c1-7(10(13)14)8(11(15)17-3)5-4-6-9(12)16-2/h8H,1,4-6H2,2-3H3,(H,13,14)/t8-/m1/s1

> <INCHI_KEY>
MDFIHAYHEBXNCC-UHFFFAOYSA-N

> <FORMULA>
C11H16O6

> <MOLECULAR_WEIGHT>
244.243

> <EXACT_MASS>
244.094688235

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
24.521972144610224

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R)-7-methoxy-3-(methyl carboxy)-2-methylidene-7-oxoheptanoic acid

> <ALOGPS_LOGP>
1.21

> <JCHEM_LOGP>
0.9010633023333334

> <ALOGPS_LOGS>
-1.85

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.244243775625321

> <JCHEM_PKA_STRONGEST_BASIC>
-6.767713059356172

> <JCHEM_POLAR_SURFACE_AREA>
89.89999999999999

> <JCHEM_REFRACTIVITY>
57.49600000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.45e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R)-7-methoxy-3-(methyl carboxy)-2-methylidene-7-oxoheptanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 33 32  0  0  0  0  0  0  0  0999 V2000
   -3.7448   -0.6145   -0.4462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7486   -1.1922    0.1846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8446   -2.6169    0.4522 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9353   -3.2325    1.0492 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9406   -3.3330    0.0562 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5592   -0.4568    0.6263 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2819   -0.9844   -0.0508 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8497   -0.1374    0.4966 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1602   -0.5621   -0.0965 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2629    0.2527    0.4278 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0125    1.1646    1.2662 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5815    0.0905    0.0625 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6553    0.8484    0.5421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5904    0.9764    0.3066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5647    1.7982    1.2563 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6467    1.4874   -0.9791 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6723    2.8903   -1.1602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6195   -1.1470   -0.7697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6930    0.4373   -0.6517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5941   -3.7687    0.6713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4322   -0.5693    1.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3471   -0.8264   -1.1467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1635   -2.0446    0.1573 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6077    0.9191    0.2328 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8879   -0.1886    1.5978 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0565   -0.5095   -1.2008 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2754   -1.6574    0.1339 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3917    1.8885    0.8094 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1797    0.3718    1.3990 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4111    0.9151   -0.2930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3707    3.1977   -1.9595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6385    3.2057   -1.4201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9444    3.3972   -0.1929 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  2  0
 10 12  1  0
 12 13  1  0
  6 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
  1 18  1  0
  1 19  1  0
  5 20  1  0
  6 21  1  1
  7 22  1  0
  7 23  1  0
  8 24  1  0
  8 25  1  0
  9 26  1  0
  9 27  1  0
 13 28  1  0
 13 29  1  0
 13 30  1  0
 17 31  1  0
 17 32  1  0
 17 33  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -3.745  -0.615  -0.446  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.749  -1.192   0.185  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.845  -2.617   0.452  0.00  0.00           C+0
HETATM    4  O   UNK     0      -1.935  -3.232   1.049  0.00  0.00           O+0
HETATM    5  O   UNK     0      -3.941  -3.333   0.056  0.00  0.00           O+0
HETATM    6  C   UNK     0      -1.559  -0.457   0.626  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.282  -0.984  -0.051  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.850  -0.137   0.497  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.160  -0.562  -0.097  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.263   0.253   0.428  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.013   1.165   1.266  0.00  0.00           O+0
HETATM   12  O   UNK     0       4.582   0.091   0.063  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.655   0.848   0.542  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.590   0.976   0.307  0.00  0.00           C+0
HETATM   15  O   UNK     0      -1.565   1.798   1.256  0.00  0.00           O+0
HETATM   16  O   UNK     0      -1.647   1.487  -0.979  0.00  0.00           O+0
HETATM   17  C   UNK     0      -1.672   2.890  -1.160  0.00  0.00           C+0
HETATM   18  H   UNK     0      -4.620  -1.147  -0.770  0.00  0.00           H+0
HETATM   19  H   UNK     0      -3.693   0.437  -0.652  0.00  0.00           H+0
HETATM   20  H   UNK     0      -4.594  -3.769   0.671  0.00  0.00           H+0
HETATM   21  H   UNK     0      -1.432  -0.569   1.721  0.00  0.00           H+0
HETATM   22  H   UNK     0      -0.347  -0.826  -1.147  0.00  0.00           H+0
HETATM   23  H   UNK     0      -0.164  -2.045   0.157  0.00  0.00           H+0
HETATM   24  H   UNK     0       0.608   0.919   0.233  0.00  0.00           H+0
HETATM   25  H   UNK     0       0.888  -0.189   1.598  0.00  0.00           H+0
HETATM   26  H   UNK     0       2.057  -0.509  -1.201  0.00  0.00           H+0
HETATM   27  H   UNK     0       2.275  -1.657   0.134  0.00  0.00           H+0
HETATM   28  H   UNK     0       5.392   1.889   0.809  0.00  0.00           H+0
HETATM   29  H   UNK     0       6.180   0.372   1.399  0.00  0.00           H+0
HETATM   30  H   UNK     0       6.411   0.915  -0.293  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.371   3.198  -1.960  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.639   3.206  -1.420  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.944   3.397  -0.193  0.00  0.00           H+0
CONECT    1    2   18   19                                                  
CONECT    2    1    3    6                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3   20                                                       
CONECT    6    2    7   14   21                                             
CONECT    7    6    8   22   23                                             
CONECT    8    7    9   24   25                                             
CONECT    9    8   10   26   27                                             
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   28   29   30                                             
CONECT   14    6   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   31   32   33                                             
CONECT   18    1                                                            
CONECT   19    1                                                            
CONECT   20    5                                                            
CONECT   21    6                                                            
CONECT   22    7                                                            
CONECT   23    7                                                            
CONECT   24    8                                                            
CONECT   25    8                                                            
CONECT   26    9                                                            
CONECT   27    9                                                            
CONECT   28   13                                                            
CONECT   29   13                                                            
CONECT   30   13                                                            
CONECT   31   17                                                            
CONECT   32   17                                                            
CONECT   33   17                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   64    0
END

RDKit          3D

33 32  0  0  0  0  0  0  0  0999 V2000
   -3.7448   -0.6145   -0.4462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7486   -1.1922    0.1846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8446   -2.6169    0.4522 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9353   -3.2325    1.0492 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9406   -3.3330    0.0562 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5592   -0.4568    0.6263 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2819   -0.9844   -0.0508 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8497   -0.1374    0.4966 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1602   -0.5621   -0.0965 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2629    0.2527    0.4278 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0125    1.1646    1.2662 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5815    0.0905    0.0625 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6553    0.8484    0.5421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5904    0.9764    0.3066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5647    1.7982    1.2563 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6467    1.4874   -0.9791 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6723    2.8903   -1.1602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6195   -1.1470   -0.7697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6930    0.4373   -0.6517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5941   -3.7687    0.6713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4322   -0.5693    1.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3471   -0.8264   -1.1467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1635   -2.0446    0.1573 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6077    0.9191    0.2328 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8879   -0.1886    1.5978 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0565   -0.5095   -1.2008 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2754   -1.6574    0.1339 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3917    1.8885    0.8094 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1797    0.3718    1.3990 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4111    0.9151   -0.2930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3707    3.1977   -1.9595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6385    3.2057   -1.4201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9444    3.3972   -0.1929 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  2  0
 10 12  1  0
 12 13  1  0
  6 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
  1 18  1  0
  1 19  1  0
  5 20  1  0
  6 21  1  1
  7 22  1  0
  7 23  1  0
  8 24  1  0
  8 25  1  0
  9 26  1  0
  9 27  1  0
 13 28  1  0
 13 29  1  0
 13 30  1  0
 17 31  1  0
 17 32  1  0
 17 33  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
(+)-7-Methoxy-3-(methoxycarbonyl)-2-methylene-7-oxoheptanoic acid	ChEBI
(+)-7-Methoxy-3-(methoxycarbonyl)-2-methylidene-7-oxoheptanoic acid	ChEBI
(+)-Tensyuic acid a	ChEBI
(+)-7-Methoxy-3-(methoxycarbonyl)-2-methylene-7-oxoheptanoate	Generator
(+)-7-Methoxy-3-(methoxycarbonyl)-2-methylidene-7-oxoheptanoate	Generator
(+)-Tensyuate a	Generator
Tensyuate a	Generator

Chemical Formula

C₁₁H₁₆O₆

Average Mass

244.2430 Da

Monoisotopic Mass

244.09469 Da

IUPAC Name

(3R)-7-methoxy-3-(methyl carboxy)-2-methylidene-7-oxoheptanoic acid

Traditional Name

(3R)-7-methoxy-3-(methyl carboxy)-2-methylidene-7-oxoheptanoic acid

CAS Registry Number

Not Available

SMILES

COC(=O)CCCC(C(=O)OC)C(=C)C(O)=O

InChI Identifier

InChI=1S/C11H16O6/c1-7(10(13)14)8(11(15)17-3)5-4-6-9(12)16-2/h8H,1,4-6H2,2-3H3,(H,13,14)

InChI Key

MDFIHAYHEBXNCC-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

Species Where Detected

Species Name	Source	Reference
Aspergillus niger EKI-2342	KNApSAcK Database	22123792

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 methyl ester
Fatty acid ester
Fatty acyl
Methyl ester
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	1.21	ALOGPS
logP	0.9	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	4.24	ChemAxon
pKa (Strongest Basic)	-6.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	89.9 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	57.5 m³·mol⁻¹	ChemAxon
Polarizability	24.52 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

NPA002347

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00032299

Chemspider ID

28284444

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23651872

PDB ID

Not Available

ChEBI ID

133826

Good Scents ID

Not Available

References

General References

Showing NP-Card for Tensyuic acid A (NP0007250)

MOL for NP0007250 (Tensyuic acid A)

3D MOL for NP0007250 (Tensyuic acid A)

3D SDF for NP0007250 (Tensyuic acid A)

3D-SDF for NP0007250 (Tensyuic acid A)

PDB for NP0007250 (Tensyuic acid A)

3D PDB for NP0007250 (Tensyuic acid A)

SMILES for NP0007250 (Tensyuic acid A)

INCHI for NP0007250 (Tensyuic acid A)

Structure for NP0007250 (Tensyuic acid A)

3D Structure for NP0007250 (Tensyuic acid A)