NP-MRD: Showing NP-Card for methyl (2r,4r,6s,7r,8e,11s)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0²,⁴]octadeca-1(18),8,14,16-tetraene-7-carboxylate (NP0242476)

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Record Information

Version

2.0

Created at

2022-09-07 02:48:02 UTC

Updated at

2022-09-07 02:48:02 UTC

NP-MRD ID

NP0242476

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2r,4r,6s,7r,8e,11s)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0²,⁴]octadeca-1(18),8,14,16-tetraene-7-carboxylate

Description

Methyl (2R,4R,6S,7R,8E,11S)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0²,⁴]Octadeca-1(14),8,15,17-tetraene-7-carboxylate 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. methyl (2r,4r,6s,7r,8e,11s)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0²,⁴]octadeca-1(18),8,14,16-tetraene-7-carboxylate is found in Aigialus parvus. Based on a literature review very few articles have been published on methyl (2R,4R,6S,7R,8E,11S)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0²,⁴]Octadeca-1(14),8,15,17-tetraene-7-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072204482D          

 29 31  0  0  1  0            999 V2000
   -2.0232   -0.1426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2778   -0.4962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5989   -0.0276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6653    0.7947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1465   -0.3813    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3491   -1.0408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3439    0.4198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1465    1.2208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6935    1.8383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4649    2.1309    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3655    2.9499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2839    2.0314    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9629    1.5628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5804    2.1098    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3463    0.8323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0607    1.2448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0607    2.0698    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7752    0.8323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7752    0.0073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4897   -0.4052    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2042    0.0073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0607   -0.4052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3463    0.0073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9629   -0.7232    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0293   -1.5456    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2839   -1.1919    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4649   -1.2913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6935   -0.9988    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2249   -1.6777    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
  5  3  1  1  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  2  0  0  0  0
 15 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 26 25  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
  5 28  1  0  0  0  0
 28 29  1  6  0  0  0
M  END

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
    6.1123    2.1857   -0.7125 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8214    1.6094   -0.6391 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2891    1.0717    0.5058 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9570    1.0734    1.5694 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8975    0.4894    0.4403 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4484    0.6405   -0.8415 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9397   -0.8998    0.9256 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3836   -1.9733    0.4401 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5315   -2.1106   -0.7638 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2625   -2.9210   -0.4392 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7063   -2.8133   -1.5949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2429   -2.4372    0.7573 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5180   -2.1505    1.1497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0177   -2.8668    2.0959 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3997   -1.1201    0.6266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7439   -1.4450    0.4974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2357   -2.6924    0.8545 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6630   -0.5285    0.0018 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2102    0.7175   -0.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0953    1.6905   -0.8707 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4598    1.4387   -1.0302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8779    1.0469   -0.2350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9604    0.1473    0.2544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5570    0.5679    0.3687 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1364    1.1220   -0.9456 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2356    1.9050    0.3403 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1673    2.3044    0.7079 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9843    1.2789    1.4014 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8803    1.9793    2.2500 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0714    3.2876   -0.6932 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5256    1.8972   -1.7195 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7905    1.7881    0.0460 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0248    1.1696   -1.4296 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5448   -1.0315    1.8502 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5270   -2.9687    0.9534 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2875   -1.1954   -1.2921 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1649   -2.7069   -1.4909 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5892   -3.9857   -0.3985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7340   -2.8735   -1.2169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4380   -3.5442   -2.3561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5378   -1.7875   -2.0351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2142   -2.8757    0.7414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7054   -0.7891   -0.0955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8924    2.2775   -1.6097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9508    1.4471   -0.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6414    0.5079   -1.5985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5917    2.0641   -0.5494 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1568   -0.1682    0.7888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8954    2.7904    0.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1422    3.2603    1.3116 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7322    2.6107   -0.2217 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4446    0.6104    2.0960 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9846    2.9055    1.9787 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  6
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 19 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28  5  1  0
 23 15  1  0
 26 24  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  6 33  1  0
  7 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  1
 11 39  1  0
 11 40  1  0
 11 41  1  0
 17 42  1  0
 18 43  1  0
 21 44  1  0
 21 45  1  0
 21 46  1  0
 22 47  1  0
 24 48  1  1
 26 49  1  6
 27 50  1  0
 27 51  1  0
 28 52  1  1
 29 53  1  0
M  END


  Mrv1652309072204482D          

 29 31  0  0  1  0            999 V2000
   -2.0232   -0.1426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2778   -0.4962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5989   -0.0276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6653    0.7947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1465   -0.3813    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3491   -1.0408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3439    0.4198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1465    1.2208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6935    1.8383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4649    2.1309    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3655    2.9499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2839    2.0314    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9629    1.5628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5804    2.1098    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3463    0.8323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0607    1.2448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0607    2.0698    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7752    0.8323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7752    0.0073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4897   -0.4052    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2042    0.0073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0607   -0.4052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3463    0.0073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9629   -0.7232    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0293   -1.5456    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2839   -1.1919    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4649   -1.2913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6935   -0.9988    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2249   -1.6777    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
  5  3  1  1  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  2  0  0  0  0
 15 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 26 25  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
  5 28  1  0  0  0  0
 28 29  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0242476

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@]1(O)\C=C\C[C@H](C)OC(=O)C2=C(O)C=C(OC)C=C2[C@H]2O[C@@H]2C[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H24O9/c1-10-5-4-6-20(25,19(24)27-3)15(22)9-14-17(29-14)12-7-11(26-2)8-13(21)16(12)18(23)28-10/h4,6-8,10,14-15,17,21-22,25H,5,9H2,1-3H3/b6-4+/t10-,14+,15-,17+,20+/m0/s1

> <INCHI_KEY>
KFYHMUXHQAGCDJ-QSQJCSDYSA-N

> <FORMULA>
C20H24O9

> <MOLECULAR_WEIGHT>
408.403

> <EXACT_MASS>
408.142032353

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
40.4202488478452

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (2R,4R,6S,8E,11S)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0^{2,4}]octadeca-1(14),8,15,17-tetraene-7-carboxylate

> <JCHEM_LOGP>
1.5015134536666668

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.107666905154005

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.464985439260044

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4115692371027944

> <JCHEM_POLAR_SURFACE_AREA>
135.05

> <JCHEM_REFRACTIVITY>
100.67319999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2R,4R,6S,8E,11S)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0^{2,4}]octadeca-1(14),8,15,17-tetraene-7-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.777  -0.266   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.385  -0.926   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.118  -0.051   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -1.242   1.484   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.273  -0.712   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -0.652  -1.943   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.642   0.784   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.273   2.279   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.295   3.432   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.735   3.978   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.549   5.506   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.263   3.792   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.531   2.917   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       6.683   3.938   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.246   1.554   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.580   2.324   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       7.580   3.864   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       8.914   1.554   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.914   0.014   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      10.247  -0.756   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      11.581   0.014   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.580  -0.756   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.246   0.014   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.531  -1.350   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.655  -2.885   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.263  -2.225   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.735  -2.410   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.295  -1.864   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       0.420  -3.132   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7   28                                             
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   23                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   23                                                       
CONECT   23   22   15   24                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24   26                                                       
CONECT   26   25   24   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27    5   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Value	Source
Methyl (2R,4R,6S,7R,8E,11S)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0,]octadeca-1(14),8,15,17-tetraene-7-carboxylic acid	Generator

Chemical Formula

C₂₀H₂₄O₉

Average Mass

408.4030 Da

Monoisotopic Mass

408.14203 Da

IUPAC Name

methyl (2R,4R,6S,8E,11S)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0^{2,4}]octadeca-1(14),8,15,17-tetraene-7-carboxylate

Traditional Name

methyl (2R,4R,6S,8E,11S)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0^{2,4}]octadeca-1(14),8,15,17-tetraene-7-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@]1(O)\C=C\C[C@H](C)OC(=O)C2=C(O)C=C(OC)C=C2[C@H]2O[C@@H]2C[C@@H]1O

InChI Identifier

InChI=1S/C20H24O9/c1-10-5-4-6-20(25,19(24)27-3)15(22)9-14-17(29-14)12-7-11(26-2)8-13(21)16(12)18(23)28-10/h4,6-8,10,14-15,17,21-22,25H,5,9H2,1-3H3/b6-4+/t10-,14+,15-,17+,20+/m0/s1

InChI Key

KFYHMUXHQAGCDJ-QSQJCSDYSA-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
Aigialus parvus	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
Anisole
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Beta-hydroxy acid
Dicarboxylic acid or derivatives
Hydroxy acid
Benzenoid
Vinylogous acid
Tertiary alcohol
Methyl ester
Secondary alcohol
Carboxylic acid ester
1,2-diol
Lactone
Polyol
Carboxylic acid derivative
Dialkyl ether
Oxacycle
Oxirane
Ether
Organoheterocyclic compound
Alcohol
Organooxygen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	1.5	ChemAxon
pKa (Strongest Acidic)	9.46	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	135.05 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	100.67 m³·mol⁻¹	ChemAxon
Polarizability	40.42 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163193234

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (2r,4r,6s,7r,8e,11s)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0²,⁴]octadeca-1(18),8,14,16-tetraene-7-carboxylate (NP0242476)

MOL for NP0242476 (methyl (2r,4r,6s,7r,8e,11s)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0²,⁴]octadeca-1(18),8,14,16-tetraene-7-carboxylate)

3D MOL for NP0242476 (methyl (2r,4r,6s,7r,8e,11s)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0²,⁴]octadeca-1(18),8,14,16-tetraene-7-carboxylate)

3D SDF for NP0242476 (methyl (2r,4r,6s,7r,8e,11s)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0²,⁴]octadeca-1(18),8,14,16-tetraene-7-carboxylate)

3D-SDF for NP0242476 (methyl (2r,4r,6s,7r,8e,11s)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0²,⁴]octadeca-1(18),8,14,16-tetraene-7-carboxylate)

PDB for NP0242476 (methyl (2r,4r,6s,7r,8e,11s)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0²,⁴]octadeca-1(18),8,14,16-tetraene-7-carboxylate)

3D PDB for NP0242476 (methyl (2r,4r,6s,7r,8e,11s)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0²,⁴]octadeca-1(18),8,14,16-tetraene-7-carboxylate)

SMILES for NP0242476 (methyl (2r,4r,6s,7r,8e,11s)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0²,⁴]octadeca-1(18),8,14,16-tetraene-7-carboxylate)

INCHI for NP0242476 (methyl (2r,4r,6s,7r,8e,11s)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0²,⁴]octadeca-1(18),8,14,16-tetraene-7-carboxylate)

Structure for NP0242476 (methyl (2r,4r,6s,7r,8e,11s)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0²,⁴]octadeca-1(18),8,14,16-tetraene-7-carboxylate)

3D Structure for NP0242476 (methyl (2r,4r,6s,7r,8e,11s)-6,7,15-trihydroxy-17-methoxy-11-methyl-13-oxo-3,12-dioxatricyclo[12.4.0.0²,⁴]octadeca-1(18),8,14,16-tetraene-7-carboxylate)