NP-MRD: Showing NP-Card for Methoxycarboxylic acid 42 (NP0003766)

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Record Information

Version

1.0

Created at

2020-12-09 00:55:40 UTC

Updated at

2021-07-15 16:47:19 UTC

NP-MRD ID

NP0003766

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Methoxycarboxylic acid 42

Provided By

NPAtlas

Description

(4E)-3-methoxy-4-methyl-5-(2-methyl-1,3-thiazol-4-yl)pent-4-enoic acid belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms. Methoxycarboxylic acid 42 is found in Sorangium cellulosum. It was first documented in 2001 (PMID: 11473410). Based on a literature review very few articles have been published on (4E)-3-methoxy-4-methyl-5-(2-methyl-1,3-thiazol-4-yl)pent-4-enoic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242117493D          

 31 31  0  0  0  0            999 V2000
   -3.4159   -1.4325   -0.6196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4935   -0.7334    0.1444 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6452   -0.0154   -0.6889 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8051    1.4728   -0.4614 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2126    1.8963   -0.7439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5525    2.1143   -1.9189 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1306    2.0471    0.2705 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2125   -0.4461   -0.5309 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1617   -1.8626   -0.7260 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6530    0.4550   -0.2006 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1020    0.1338   -0.0209 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7296   -0.6649   -0.9485 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3180   -0.7527   -0.3284 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.1012    0.2190    1.0590 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1099    0.6014    2.1243 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8314    0.5569    0.9743 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8740   -2.1261   -1.2879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0036   -0.6990   -1.2085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0910   -2.0493   -0.0054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9216   -0.1937   -1.7480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1739    2.0151   -1.2217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5661    1.7919    0.5649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1225    1.8739    0.1466 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0273   -2.2038   -0.1618 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1927   -2.1615   -1.8071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7192   -2.4512   -0.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3642    1.5070   -0.0321 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3089   -1.1228   -1.8611 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6460    0.6777    3.1046 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9528   -0.0840    2.0437 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4410    1.6369    1.8304 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
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 11  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  3 20  1  6  0  0  0
  4 21  1  0  0  0  0
  4 22  1  0  0  0  0
  7 23  1  0  0  0  0
  9 24  1  0  0  0  0
  9 25  1  0  0  0  0
  9 26  1  0  0  0  0
 10 27  1  0  0  0  0
 12 28  1  0  0  0  0
 15 29  1  0  0  0  0
 15 30  1  0  0  0  0
 15 31  1  0  0  0  0
M  END

     RDKit          3D

 31 31  0  0  0  0  0  0  0  0999 V2000
   -3.4159   -1.4325   -0.6196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4935   -0.7334    0.1444 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6452   -0.0154   -0.6889 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8051    1.4728   -0.4614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2126    1.8963   -0.7439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5525    2.1143   -1.9189 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1306    2.0471    0.2705 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2125   -0.4461   -0.5309 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1617   -1.8626   -0.7260 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6530    0.4550   -0.2006 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1020    0.1338   -0.0209 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7296   -0.6649   -0.9485 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3180   -0.7527   -0.3284 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.1012    0.2190    1.0590 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1099    0.6014    2.1243 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8314    0.5569    0.9743 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8740   -2.1261   -1.2879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0036   -0.6990   -1.2085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0910   -2.0493   -0.0054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9216   -0.1937   -1.7480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1739    2.0151   -1.2217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5661    1.7919    0.5649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1225    1.8739    0.1466 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0273   -2.2038   -0.1618 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1927   -2.1615   -1.8071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7192   -2.4512   -0.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3642    1.5070   -0.0321 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3089   -1.1228   -1.8611 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6460    0.6777    3.1046 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9528   -0.0840    2.0437 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4410    1.6369    1.8304 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
  3  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 11  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  6
  4 21  1  0
  4 22  1  0
  7 23  1  0
  9 24  1  0
  9 25  1  0
  9 26  1  0
 10 27  1  0
 12 28  1  0
 15 29  1  0
 15 30  1  0
 15 31  1  0
M  END


  Mrv1652306242117493D          

 31 31  0  0  0  0            999 V2000
   -3.4159   -1.4325   -0.6196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4935   -0.7334    0.1444 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6452   -0.0154   -0.6889 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8051    1.4728   -0.4614 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2126    1.8963   -0.7439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5525    2.1143   -1.9189 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1306    2.0471    0.2705 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2125   -0.4461   -0.5309 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1617   -1.8626   -0.7260 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6530    0.4550   -0.2006 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1020    0.1338   -0.0209 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7296   -0.6649   -0.9485 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3180   -0.7527   -0.3284 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.1012    0.2190    1.0590 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1099    0.6014    2.1243 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8314    0.5569    0.9743 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8740   -2.1261   -1.2879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0036   -0.6990   -1.2085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0910   -2.0493   -0.0054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9216   -0.1937   -1.7480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1739    2.0151   -1.2217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5661    1.7919    0.5649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1225    1.8739    0.1466 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0273   -2.2038   -0.1618 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1927   -2.1615   -1.8071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7192   -2.4512   -0.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3642    1.5070   -0.0321 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3089   -1.1228   -1.8611 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6460    0.6777    3.1046 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9528   -0.0840    2.0437 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4410    1.6369    1.8304 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
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 11  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  3 20  1  6  0  0  0
  4 21  1  0  0  0  0
  4 22  1  0  0  0  0
  7 23  1  0  0  0  0
  9 24  1  0  0  0  0
  9 25  1  0  0  0  0
  9 26  1  0  0  0  0
 10 27  1  0  0  0  0
 12 28  1  0  0  0  0
 15 29  1  0  0  0  0
 15 30  1  0  0  0  0
 15 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0003766

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)C([H])([H])[C@]([H])(OC([H])([H])[H])C(=C(/[H])C1=C([H])SC(=N1)C([H])([H])[H])\C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C11H15NO3S/c1-7(10(15-3)5-11(13)14)4-9-6-16-8(2)12-9/h4,6,10H,5H2,1-3H3,(H,13,14)/b7-4+/t10-/m0/s1

> <INCHI_KEY>
MTNLUIZVDKCAMF-QPJJXVBHSA-N

> <FORMULA>
C11H15NO3S

> <MOLECULAR_WEIGHT>
241.31

> <EXACT_MASS>
241.077264521

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
25.801154772114067

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,4E)-3-methoxy-4-methyl-5-(2-methyl-1,3-thiazol-4-yl)pent-4-enoic acid

> <ALOGPS_LOGP>
1.91

> <JCHEM_LOGP>
1.3624423771404495

> <ALOGPS_LOGS>
-2.90

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.638949873263845

> <JCHEM_PKA_STRONGEST_BASIC>
2.7023271381058795

> <JCHEM_POLAR_SURFACE_AREA>
59.42

> <JCHEM_REFRACTIVITY>
61.881899999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.03e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4E)-3-methoxy-4-methyl-5-(2-methyl-1,3-thiazol-4-yl)pent-4-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 31 31  0  0  0  0  0  0  0  0999 V2000
   -3.4159   -1.4325   -0.6196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4935   -0.7334    0.1444 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6452   -0.0154   -0.6889 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8051    1.4728   -0.4614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2126    1.8963   -0.7439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5525    2.1143   -1.9189 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1306    2.0471    0.2705 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2125   -0.4461   -0.5309 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1617   -1.8626   -0.7260 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6530    0.4550   -0.2006 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1020    0.1338   -0.0209 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7296   -0.6649   -0.9485 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3180   -0.7527   -0.3284 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.1012    0.2190    1.0590 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1099    0.6014    2.1243 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8314    0.5569    0.9743 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8740   -2.1261   -1.2879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0036   -0.6990   -1.2085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0910   -2.0493   -0.0054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9216   -0.1937   -1.7480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1739    2.0151   -1.2217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5661    1.7919    0.5649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1225    1.8739    0.1466 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0273   -2.2038   -0.1618 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1927   -2.1615   -1.8071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7192   -2.4512   -0.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3642    1.5070   -0.0321 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3089   -1.1228   -1.8611 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6460    0.6777    3.1046 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9528   -0.0840    2.0437 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4410    1.6369    1.8304 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
  3  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 11  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  6
  4 21  1  0
  4 22  1  0
  7 23  1  0
  9 24  1  0
  9 25  1  0
  9 26  1  0
 10 27  1  0
 12 28  1  0
 15 29  1  0
 15 30  1  0
 15 31  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      -3.416  -1.433  -0.620  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.494  -0.733   0.144  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.645  -0.015  -0.689  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.805   1.473  -0.461  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.213   1.896  -0.744  0.00  0.00           C+0
HETATM    6  O   UNK     0      -3.553   2.114  -1.919  0.00  0.00           O+0
HETATM    7  O   UNK     0      -4.131   2.047   0.271  0.00  0.00           O+0
HETATM    8  C   UNK     0      -0.213  -0.446  -0.531  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.162  -1.863  -0.726  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.653   0.455  -0.201  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.102   0.134  -0.021  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.730  -0.665  -0.949  0.00  0.00           C+0
HETATM   13  S   UNK     0       4.318  -0.753  -0.328  0.00  0.00           S+0
HETATM   14  C   UNK     0       4.101   0.219   1.059  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.110   0.601   2.124  0.00  0.00           C+0
HETATM   16  N   UNK     0       2.831   0.557   0.974  0.00  0.00           N+0
HETATM   17  H   UNK     0      -2.874  -2.126  -1.288  0.00  0.00           H+0
HETATM   18  H   UNK     0      -4.004  -0.699  -1.208  0.00  0.00           H+0
HETATM   19  H   UNK     0      -4.091  -2.049  -0.005  0.00  0.00           H+0
HETATM   20  H   UNK     0      -1.922  -0.194  -1.748  0.00  0.00           H+0
HETATM   21  H   UNK     0      -1.174   2.015  -1.222  0.00  0.00           H+0
HETATM   22  H   UNK     0      -1.566   1.792   0.565  0.00  0.00           H+0
HETATM   23  H   UNK     0      -5.122   1.874   0.147  0.00  0.00           H+0
HETATM   24  H   UNK     0       1.027  -2.204  -0.162  0.00  0.00           H+0
HETATM   25  H   UNK     0       0.193  -2.162  -1.807  0.00  0.00           H+0
HETATM   26  H   UNK     0      -0.719  -2.451  -0.304  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.364   1.507  -0.032  0.00  0.00           H+0
HETATM   28  H   UNK     0       2.309  -1.123  -1.861  0.00  0.00           H+0
HETATM   29  H   UNK     0       4.646   0.678   3.105  0.00  0.00           H+0
HETATM   30  H   UNK     0       5.953  -0.084   2.044  0.00  0.00           H+0
HETATM   31  H   UNK     0       5.441   1.637   1.830  0.00  0.00           H+0
CONECT    1    2   17   18   19                                             
CONECT    2    1    3                                                       
CONECT    3    2    4    8   20                                             
CONECT    4    3    5   21   22                                             
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5   23                                                       
CONECT    8    3    9   10                                                  
CONECT    9    8   24   25   26                                             
CONECT   10    8   11   27                                                  
CONECT   11   10   12   16                                                  
CONECT   12   11   13   28                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14   29   30   31                                             
CONECT   16   14   11                                                       
CONECT   17    1                                                            
CONECT   18    1                                                            
CONECT   19    1                                                            
CONECT   20    3                                                            
CONECT   21    4                                                            
CONECT   22    4                                                            
CONECT   23    7                                                            
CONECT   24    9                                                            
CONECT   25    9                                                            
CONECT   26    9                                                            
CONECT   27   10                                                            
CONECT   28   12                                                            
CONECT   29   15                                                            
CONECT   30   15                                                            
CONECT   31   15                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   62    0
END

RDKit          3D

31 31  0  0  0  0  0  0  0  0999 V2000
   -3.4159   -1.4325   -0.6196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4935   -0.7334    0.1444 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6452   -0.0154   -0.6889 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8051    1.4728   -0.4614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2126    1.8963   -0.7439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5525    2.1143   -1.9189 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1306    2.0471    0.2705 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2125   -0.4461   -0.5309 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1617   -1.8626   -0.7260 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6530    0.4550   -0.2006 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1020    0.1338   -0.0209 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7296   -0.6649   -0.9485 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3180   -0.7527   -0.3284 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.1012    0.2190    1.0590 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1099    0.6014    2.1243 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8314    0.5569    0.9743 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8740   -2.1261   -1.2879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0036   -0.6990   -1.2085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0910   -2.0493   -0.0054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9216   -0.1937   -1.7480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1739    2.0151   -1.2217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5661    1.7919    0.5649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1225    1.8739    0.1466 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0273   -2.2038   -0.1618 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1927   -2.1615   -1.8071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7192   -2.4512   -0.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3642    1.5070   -0.0321 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3089   -1.1228   -1.8611 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6460    0.6777    3.1046 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9528   -0.0840    2.0437 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4410    1.6369    1.8304 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
  3  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 11  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  6
  4 21  1  0
  4 22  1  0
  7 23  1  0
  9 24  1  0
  9 25  1  0
  9 26  1  0
 10 27  1  0
 12 28  1  0
 15 29  1  0
 15 30  1  0
 15 31  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
(4E)-3-Methoxy-4-methyl-5-(2-methyl-1,3-thiazol-4-yl)pent-4-enoate	Generator
Methoxycarboxylate 42	Generator

Chemical Formula

C₁₁H₁₅NO₃S

Average Mass

241.3100 Da

Monoisotopic Mass

241.07726 Da

IUPAC Name

(3S,4E)-3-methoxy-4-methyl-5-(2-methyl-1,3-thiazol-4-yl)pent-4-enoic acid

Traditional Name

(3S,4E)-3-methoxy-4-methyl-5-(2-methyl-1,3-thiazol-4-yl)pent-4-enoic acid

CAS Registry Number

Not Available

SMILES

COC(CC(O)=O)C(\C)=C\C1=CSC(C)=N1

InChI Identifier

InChI=1S/C11H15NO3S/c1-7(10(15-3)5-11(13)14)4-9-6-16-8(2)12-9/h4,6,10H,5H2,1-3H3,(H,13,14)/b7-4+

InChI Key

MTNLUIZVDKCAMF-QPJJXVBHSA-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
Sorangium cellulosum	NPAtlas	11473410

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Medium-chain fatty acids

Alternative Parents

Substituents

Medium-chain fatty acid
2,4-disubstituted 1,3-thiazole
Branched fatty acid
Heterocyclic fatty acid
Methyl-branched fatty acid
Unsaturated fatty acid
Azole
Heteroaromatic compound
Thiazole
Carboxylic acid derivative
Carboxylic acid
Dialkyl ether
Ether
Monocarboxylic acid or derivatives
Azacycle
Organoheterocyclic compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organonitrogen compound
Organooxygen compound
Organic nitrogen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.91	ALOGPS
logP	1.36	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	4.64	ChemAxon
pKa (Strongest Basic)	2.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	59.42 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	61.88 m³·mol⁻¹	ChemAxon
Polarizability	25.8 Å³	ChemAxon
Number of Rings	1	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

NPA003358

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9921483

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11746779

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Hardt IH, Steinmetz H, Gerth K, Sasse F, Reichenbach H, Hofle G: New natural epothilones from Sorangium cellulosum, strains So ce90/B2 and So ce90/D13: isolation, structure elucidation, and SAR studies. J Nat Prod. 2001 Jul;64(7):847-56. doi: 10.1021/np000629f. [PubMed:11473410 ]

Showing NP-Card for Methoxycarboxylic acid 42 (NP0003766)

MOL for NP0003766 (Methoxycarboxylic acid 42)

3D MOL for NP0003766 (Methoxycarboxylic acid 42)

3D SDF for NP0003766 (Methoxycarboxylic acid 42)

3D-SDF for NP0003766 (Methoxycarboxylic acid 42)

PDB for NP0003766 (Methoxycarboxylic acid 42)

3D PDB for NP0003766 (Methoxycarboxylic acid 42)

SMILES for NP0003766 (Methoxycarboxylic acid 42)

INCHI for NP0003766 (Methoxycarboxylic acid 42)

Structure for NP0003766 (Methoxycarboxylic acid 42)

3D Structure for NP0003766 (Methoxycarboxylic acid 42)