NP-MRD: Showing NP-Card for 4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-6-isopropyl-5-methyloxan-4-yl}oxy)-4-oxobut-2-enimidic acid (NP0232902)

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Record Information

Version

2.0

Created at

2022-09-06 14:17:45 UTC

Updated at

2022-09-06 14:17:45 UTC

NP-MRD ID

NP0232902

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-6-isopropyl-5-methyloxan-4-yl}oxy)-4-oxobut-2-enimidic acid

Description

4-({2-Hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-5-methyl-6-(propan-2-yl)oxan-4-yl}oxy)-4-oxobut-2-enimidic acid belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. 4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-6-isopropyl-5-methyloxan-4-yl}oxy)-4-oxobut-2-enimidic acid is found in Kitasatospora cheerisanensis. Based on a literature review very few articles have been published on 4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-5-methyl-6-(propan-2-yl)oxan-4-yl}oxy)-4-oxobut-2-enimidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062216172D          

 51 52  0  0  0  0            999 V2000
   -2.0391   -1.0505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2267   -1.1937    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6964   -0.5618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5088   -0.4185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7910    0.3567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6035    0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2607    0.9887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4482    0.8455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1661    0.0702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0821    1.4775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2001    2.2527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8945    1.3342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1767    0.5590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4248    1.9662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2373    1.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7676    2.4549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5195    1.0477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9892    0.4157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2713   -0.3596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7410   -0.9915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0232   -1.7668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8357   -1.9100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9286   -0.8483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2107   -1.6235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7838   -2.2170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6804   -2.2555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1320   -2.1123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9626   -3.0308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7751   -3.1740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4323   -3.6627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0980   -3.0308    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1468   -4.0752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1468   -4.9002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8612   -5.3127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8612   -6.1377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1468   -6.5502    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5757   -6.5502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5757   -7.3752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2902   -7.7877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2902   -8.6127    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0047   -7.3752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4323   -5.3127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4323   -6.1377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822   -4.9002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9966   -5.3127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7111   -4.9002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9966   -6.1377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822   -4.0752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3983   -1.4803    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4142   -1.3370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9445   -1.9690    0.0000 O   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  2  0  0  0  0
  4  5  1  4  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  4  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  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
 15 17  2  0  0  0  0
 17 18  1  4  0  0  0
 18 19  2  0  0  0  0
 19 20  1  4  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 37 35  1  4  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 33 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 47  1  0  0  0  0
 44 48  1  0  0  0  0
 30 48  1  0  0  0  0
 23 49  1  0  0  0  0
 49 50  1  0  0  0  0
  3 50  1  0  0  0  0
 50 51  2  0  0  0  0
M  END

     RDKit          3D

112113  0  0  0  0  0  0  0  0999 V2000
   10.5381    0.2405    1.4789 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4926   -0.5328    2.2774 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.2115   -1.0566    2.4298 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5740   -0.2470    1.2082 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3380   -1.7892    2.9502 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4499   -2.5434    3.4936 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0647   -2.8376    2.9753 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0836   -3.0001    2.5302 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3279   -1.8493    1.5323 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1287   -1.6179    0.9215 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8208   -1.9856    1.7332 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8661   -0.8342    1.2393 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6882    0.2914    0.9109 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8862   -0.5183    2.2614 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9025   -1.2136    3.6053 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8113    0.4151    1.9919 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9438    1.6694    2.5367 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5670   -0.0973    2.2028 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8398   -1.4988    2.5245 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7329    0.6035    1.6424 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6187    0.0660    0.7787 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8110   -0.4487    0.5377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6400   -1.7816    0.3078 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1738    0.0239    0.4666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0288   -1.1566    0.6717 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0297   -1.8457    1.8938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8202    1.1191    0.2916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7650    2.5393    0.0538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5105    3.4366    1.1261 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2706    3.2902   -0.8706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4988    3.1190   -2.1240 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0919    3.6967   -1.9451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5021    1.8033   -2.8204 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2709    1.8918   -4.0144 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1797    1.2108   -3.1375 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1036    1.2189   -4.7082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0805   -0.2096   -2.7586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8646   -0.7350   -2.1149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8418   -2.2569   -2.2621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9025   -0.1271   -1.4613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5791    1.2362   -1.1057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7575    2.0586   -0.1399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4337    2.0018    1.1554 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6861    2.6037    1.0447 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7574    3.7080    1.9091 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4414   -1.1702   -0.0195 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5961   -0.9924   -0.9418 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9865   -1.5840   -2.1878 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2716   -2.9021   -1.9496 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0768   -0.6148   -2.8969 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7756   -1.7347   -0.4368 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8485   -3.1958   -0.8766 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8830   -0.6815    0.3429 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9569   -1.7529    4.2829 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.9982   -0.4729    1.3404 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4673   -2.9316    1.3553 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8803   -1.7248    2.7787 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1257    1.0970    0.8332 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6546    0.4505    2.7666 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.6555   -0.8448    4.3358 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6275    0.3362    3.3976 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.4439    0.8839    2.5705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7622   -2.6826    1.7532 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0142   -2.3106    2.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0078    0.8870    0.3629 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.5846    3.4579    0.7927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4923    3.0100    2.0991 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.0374    4.5595   -1.2740 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0827    1.7024   -1.9133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2851    3.0740   -0.2610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9295    2.5487    1.9485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5547    3.4263    2.9423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8561    4.0381    1.9339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1642    4.5158    1.4770 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7558    0.0616   -1.0699 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8025   -1.8748   -2.9477 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6985   -3.7804   -2.3930 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0694   -3.0367   -0.8416 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1752   -2.8601   -2.3282 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1056   -1.0671   -3.2084 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8597    0.2046   -2.1745 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5069   -0.1982   -3.8421 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.8297   -3.3132   -1.9664 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1389   -3.8459   -0.4163 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8719   -3.5504   -0.5247 H   0  0  0  0  0  0  0  0  0  0  0  0
 45 44  1  0
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 30 28  2  0
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 12 13  1  6
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  6  5  2  0
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 31 79  1  6
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 29 77  1  0
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 16 64  1  6
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 14 60  1  1
 15 61  1  0
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 15 63  1  0
 13 59  1  0
 11 57  1  0
 11 58  1  0
 10 56  1  6
  6 55  1  0
  5 54  1  0
  4 53  1  0
  2  1  1  0
 51109  1  6
 52110  1  0
 52111  1  0
 52112  1  0
 47101  1  6
 48102  1  0
 49103  1  0
 49104  1  0
 49105  1  0
 50106  1  0
 50107  1  0
 50108  1  0
M  END


  Mrv1652309062216172D          

 51 52  0  0  0  0            999 V2000
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   -1.2607    0.9887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4482    0.8455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1661    0.0702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0821    1.4775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2001    2.2527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.1767    0.5590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4248    1.9662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2373    1.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7410   -0.9915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0232   -1.7668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9286   -0.8483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2107   -1.6235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7838   -2.2170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6804   -2.2555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1320   -2.1123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9626   -3.0308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7751   -3.1740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4323   -3.6627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0980   -3.0308    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1468   -4.0752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1468   -4.9002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8612   -5.3127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8612   -6.1377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1468   -6.5502    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5757   -6.5502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5757   -7.3752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2902   -7.7877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2902   -8.6127    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0047   -7.3752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4323   -5.3127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4323   -6.1377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822   -4.9002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9966   -5.3127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7111   -4.9002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9966   -6.1377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822   -4.0752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3983   -1.4803    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4142   -1.3370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9445   -1.9690    0.0000 O   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  2  0  0  0  0
  4  5  1  4  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  4  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  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
 15 17  2  0  0  0  0
 17 18  1  4  0  0  0
 18 19  2  0  0  0  0
 19 20  1  4  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 37 35  1  4  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 33 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 47  1  0  0  0  0
 44 48  1  0  0  0  0
 30 48  1  0  0  0  0
 23 49  1  0  0  0  0
 49 50  1  0  0  0  0
  3 50  1  0  0  0  0
 50 51  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0232902

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1C=CC=C(C)CC(C)C(O)C(C)C=C(C)C=C(OC)C(=O)OC1C(C)C(O)C(C)C1(O)CC(OC(=O)C=CC(O)=N)C(C)C(O1)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C39H61NO11/c1-21(2)36-26(7)31(49-33(42)16-15-32(40)41)20-39(46,51-36)28(9)35(44)27(8)37-29(47-10)14-12-13-22(3)17-24(5)34(43)25(6)18-23(4)19-30(48-11)38(45)50-37/h12-16,18-19,21,24-29,31,34-37,43-44,46H,17,20H2,1-11H3,(H2,40,41)

> <INCHI_KEY>
FVEPTFOBWXDHAK-UHFFFAOYSA-N

> <FORMULA>
C39H61NO11

> <MOLECULAR_WEIGHT>
719.913

> <EXACT_MASS>
719.424461788

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
112

> <JCHEM_AVERAGE_POLARIZABILITY>
77.88975661988955

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-5-methyl-6-(propan-2-yl)oxan-4-yl}oxy)-4-oxobut-2-enimidic acid

> <JCHEM_LOGP>
3.306192048931046

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.446049750295293

> <JCHEM_PKA_STRONGEST_ACIDIC>
-0.050872762490425494

> <JCHEM_PKA_STRONGEST_BASIC>
12.056572834382884

> <JCHEM_POLAR_SURFACE_AREA>
185.05999999999997

> <JCHEM_REFRACTIVITY>
208.4018000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-6-isopropyl-5-methyloxan-4-yl}oxy)-4-oxobut-2-enimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.806  -1.961   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.290  -2.228   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.300  -1.049   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.816  -0.781   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.343   0.666   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.860   0.933   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.353   1.846   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.837   1.578   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.310   0.131   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.153   2.758   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.374   4.205   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.670   2.491   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.197   1.043   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.660   3.670   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.176   3.403   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.166   4.583   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.703   1.956   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.713   0.776   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.240  -0.671   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.250  -1.851   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       3.777  -3.298   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.293  -3.565   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.733  -1.583   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.260  -3.031   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.330  -4.138   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.270  -4.210   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -0.246  -3.943   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       1.797  -5.657   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.313  -5.925   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.807  -6.837   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -0.183  -5.657   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       2.141  -7.607   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.141  -9.147   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       3.474  -9.917   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       3.474 -11.457   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       2.141 -12.227   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       4.808 -12.227   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       4.808 -13.767   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       6.142 -14.537   0.000  0.00  0.00           C+0
HETATM   40  N   UNK     0       6.142 -16.077   0.000  0.00  0.00           N+0
HETATM   41  O   UNK     0       7.475 -13.767   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       0.807  -9.917   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       0.807 -11.457   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -0.527  -9.147   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -1.860  -9.917   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -3.194  -9.147   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -1.860 -11.457   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      -0.527  -7.607   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0       0.743  -2.763   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      -0.773  -2.496   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0      -1.763  -3.675   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   50                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24   49                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32   48                                             
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34   42                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42   33   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45   48                                                  
CONECT   45   44   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45                                                            
CONECT   48   44   30                                                       
CONECT   49   23   50                                                       
CONECT   50   49    3   51                                                  
CONECT   51   50                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  104    0
END

View in JSmol

Synonyms

Value	Source
4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-5-methyl-6-(propan-2-yl)oxan-4-yl}oxy)-4-oxobut-2-enimidate	Generator

Chemical Formula

C₃₉H₆₁NO₁₁

Average Mass

719.9130 Da

Monoisotopic Mass

719.42446 Da

IUPAC Name

4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-5-methyl-6-(propan-2-yl)oxan-4-yl}oxy)-4-oxobut-2-enimidic acid

Traditional Name

4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-6-isopropyl-5-methyloxan-4-yl}oxy)-4-oxobut-2-enimidic acid

CAS Registry Number

Not Available

SMILES

COC1C=CC=C(C)CC(C)C(O)C(C)C=C(C)C=C(OC)C(=O)OC1C(C)C(O)C(C)C1(O)CC(OC(=O)C=CC(O)=N)C(C)C(O1)C(C)C

InChI Identifier

InChI=1S/C39H61NO11/c1-21(2)36-26(7)31(49-33(42)16-15-32(40)41)20-39(46,51-36)28(9)35(44)27(8)37-29(47-10)14-12-13-22(3)17-24(5)34(43)25(6)18-23(4)19-30(48-11)38(45)50-37/h12-16,18-19,21,24-29,31,34-37,43-44,46H,17,20H2,1-11H3,(H2,40,41)

InChI Key

FVEPTFOBWXDHAK-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
Kitasatospora cheerisanensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Fatty acid ester
Dicarboxylic acid or derivatives
Oxane
Fatty acyl
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Secondary alcohol
Carboxylic acid ester
Lactone
Hemiacetal
Oxacycle
Organoheterocyclic compound
Carboximidic acid
Carboximidic acid derivative
Carboxylic acid derivative
Dialkyl ether
Ether
Alcohol
Organic nitrogen compound
Organic oxygen compound
Organic oxide
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic 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	3.31	ChemAxon
pKa (Strongest Acidic)	-0.051	ChemAxon
pKa (Strongest Basic)	12.06	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	185.06 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	208.4 m³·mol⁻¹	ChemAxon
Polarizability	77.89 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

72951193

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-6-isopropyl-5-methyloxan-4-yl}oxy)-4-oxobut-2-enimidic acid (NP0232902)

MOL for NP0232902 (4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-6-isopropyl-5-methyloxan-4-yl}oxy)-4-oxobut-2-enimidic acid)

3D MOL for NP0232902 (4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-6-isopropyl-5-methyloxan-4-yl}oxy)-4-oxobut-2-enimidic acid)

3D SDF for NP0232902 (4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-6-isopropyl-5-methyloxan-4-yl}oxy)-4-oxobut-2-enimidic acid)

3D-SDF for NP0232902 (4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-6-isopropyl-5-methyloxan-4-yl}oxy)-4-oxobut-2-enimidic acid)

PDB for NP0232902 (4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-6-isopropyl-5-methyloxan-4-yl}oxy)-4-oxobut-2-enimidic acid)

3D PDB for NP0232902 (4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-6-isopropyl-5-methyloxan-4-yl}oxy)-4-oxobut-2-enimidic acid)

SMILES for NP0232902 (4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-6-isopropyl-5-methyloxan-4-yl}oxy)-4-oxobut-2-enimidic acid)

INCHI for NP0232902 (4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-6-isopropyl-5-methyloxan-4-yl}oxy)-4-oxobut-2-enimidic acid)

Structure for NP0232902 (4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-6-isopropyl-5-methyloxan-4-yl}oxy)-4-oxobut-2-enimidic acid)

3D Structure for NP0232902 (4-({2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-6-isopropyl-5-methyloxan-4-yl}oxy)-4-oxobut-2-enimidic acid)