NP-MRD: Showing NP-Card for 6-[(acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate (NP0204884)

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Record Information

Version

2.0

Created at

2022-09-05 00:40:24 UTC

Updated at

2022-09-05 00:40:24 UTC

NP-MRD ID

NP0204884

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-[(acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate

Description

6-[(Acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]Tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. 6-[(acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate is found in Stilpnopappus tomentosus, Vernonanthura nudiflora and Vernonanthura pinguis. 6-[(Acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]Tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161522062D          

 30 32  0  0  0  0            999 V2000
   -1.4178   -0.6346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2444   -1.4412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4592   -1.6944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2859   -2.5009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1526   -1.1409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9378   -1.3941    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0207   -0.3344    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5911    0.2190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3065   -0.1918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1268   -0.1038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4641   -0.8567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7387    0.4496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4541    0.0387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9084    1.2570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5711    2.0099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8557    2.4208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0255    3.2282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0508    1.3249    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0355    2.3327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4236    1.7793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2918    2.1902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9036    1.6368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7110    1.8065    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5664    0.8839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2539    0.9720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9773    0.1685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8023    0.1666    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2132   -0.5488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7991   -1.2623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0382   -0.5506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 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
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 12 18  1  0  0  0  0
 19 16  1  4  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
  8 25  1  0  0  0  0
 20 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
M  END

     RDKit          3D

 58 60  0  0  0  0  0  0  0  0999 V2000
    5.5491   -1.3354   -1.1310 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1444   -1.0613   -0.7792 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1861   -1.6840   -1.3933 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5313   -2.6833   -2.4626 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7691   -1.4848   -1.1201 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9178   -2.1359   -1.7687 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2647   -0.6226   -0.1885 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0826   -0.3810    0.1264 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3992   -0.7404    1.5441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7897   -0.5501    1.9787 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8254   -0.6614    3.5084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7847   -1.5373    1.4491 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6385   -2.8059    2.0387 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1659   -0.9807    1.7324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2643    0.0671    0.6435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4838   -0.5922   -0.4750 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5591   -1.3098   -1.3084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7508    0.3385   -1.3086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8064    1.2083   -0.9473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8726    2.5791   -1.1615 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7206    3.2006   -0.6658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5056    4.4456   -0.7180 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0986    2.1424   -0.1172 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4174    2.2683    0.5628 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4771    2.7455   -0.0880 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9319    3.8856   -0.6072 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2754    3.9530   -1.3209 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2529    4.9256   -0.5133 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5634    0.9640   -0.2912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7706   -1.6146    0.0865 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0216   -0.4924   -1.6726 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6082   -2.2098   -1.8085 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1235   -1.6134   -0.2224 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9263   -0.3429   -0.0117 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1617   -2.2270   -3.2543 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6467   -3.1058   -2.9443 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0509   -3.5216   -1.9465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5986   -1.0930   -0.6010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0398   -1.8049    1.6712 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2325   -0.1140    2.2013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1262    0.4573    1.7396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6566   -0.1090    3.9464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7937   -1.7420    3.8105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8878   -0.2141    3.9364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3400   -3.4815    1.3693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2488   -0.5421    2.7469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9359   -1.7592    1.6288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8942    1.0485    0.9277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3506    0.1736    0.4166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3562   -0.5554   -1.4700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1251   -1.6365   -2.2760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9345   -2.1622   -0.7018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0521    0.2797   -2.3775 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2647    2.9337    1.4933 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7032    1.2741    1.0414 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7388    2.9633   -1.3532 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1107    4.4235   -2.3020 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9184    4.6301   -0.7271 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  1
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  6
 16 30  1  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  2  0
 23 29  2  0
 29  8  1  0
 30 12  1  0
 29 19  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  0
  4 35  1  0
  4 36  1  0
  4 37  1  0
  8 38  1  6
  9 39  1  0
  9 40  1  0
 10 41  1  1
 11 42  1  0
 11 43  1  0
 11 44  1  0
 13 45  1  0
 14 46  1  0
 14 47  1  0
 15 48  1  0
 15 49  1  0
 17 50  1  0
 17 51  1  0
 17 52  1  0
 18 53  1  0
 24 54  1  0
 24 55  1  0
 27 56  1  0
 27 57  1  0
 27 58  1  0
M  END


  Mrv1533004161522062D          

 30 32  0  0  0  0            999 V2000
   -1.4178   -0.6346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2444   -1.4412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4592   -1.6944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2859   -2.5009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1526   -1.1409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9378   -1.3941    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0207   -0.3344    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5911    0.2190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3065   -0.1918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1268   -0.1038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4641   -0.8567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7387    0.4496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4541    0.0387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9084    1.2570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5711    2.0099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8557    2.4208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0255    3.2282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0508    1.3249    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0355    2.3327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4236    1.7793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2918    2.1902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9036    1.6368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7110    1.8065    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5664    0.8839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2539    0.9720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9773    0.1685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8023    0.1666    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2132   -0.5488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7991   -1.2623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0382   -0.5506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 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
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 12 18  1  0  0  0  0
 19 16  1  4  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
  8 25  1  0  0  0  0
 20 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0204884

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=C(C)C(=O)OC1CC(C)C2(O)CCC(C)(O2)C=C2OC(=O)C(COC(C)=O)=C12

> <INCHI_IDENTIFIER>
InChI=1S/C22H28O8/c1-6-12(2)19(24)28-16-9-13(3)22(26)8-7-21(5,30-22)10-17-18(16)15(20(25)29-17)11-27-14(4)23/h6,10,13,16,26H,7-9,11H2,1-5H3

> <INCHI_KEY>
NPUVRWFJDAPMIA-UHFFFAOYSA-N

> <FORMULA>
C22H28O8

> <MOLECULAR_WEIGHT>
420.458

> <EXACT_MASS>
420.178417862

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
43.10521874837593

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-[(acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate

> <ALOGPS_LOGP>
1.83

> <JCHEM_LOGP>
2.340953242333333

> <ALOGPS_LOGS>
-3.96

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.829859671977818

> <JCHEM_PKA_STRONGEST_BASIC>
-4.185419379476902

> <JCHEM_POLAR_SURFACE_AREA>
108.36000000000001

> <JCHEM_REFRACTIVITY>
108.21459999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.64e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-[(acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      -2.646  -1.185   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.323  -2.690   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.857  -3.163   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.534  -4.668   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.285  -2.130   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.751  -2.602   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      -0.039  -0.624   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.103   0.409   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.439  -0.358   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.970  -0.194   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.600  -1.599   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.112   0.839   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.448   0.072   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       5.429   2.346   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.799   3.752   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.464   4.519   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.781   6.026   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.828   2.473   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.933   4.354   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.791   3.321   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.545   4.088   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -1.687   3.055   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -3.194   3.372   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -1.057   1.650   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.474   1.814   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.824   0.315   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -3.364   0.311   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -4.131  -1.024   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -3.358  -2.356   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -5.671  -1.028   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   25                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14   18                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16   12                                                       
CONECT   19   16   20                                                       
CONECT   20   19   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24    8   20                                                  
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Value	Source
6-[(Acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0,]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoic acid	Generator
6-[(Acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoic acid	Generator
8a-Tigloyloxyhirsutinolide 13-O-acetate	Generator
8a-Tigloyloxyhirsutinolide 13-O-acetic acid	Generator
8alpha-Tigloyloxyhirsutinolide 13-O-acetic acid	Generator
8Α-tigloyloxyhirsutinolide 13-O-acetate	Generator
8Α-tigloyloxyhirsutinolide 13-O-acetic acid	Generator

Chemical Formula

C₂₂H₂₈O₈

Average Mass

420.4580 Da

Monoisotopic Mass

420.17842 Da

IUPAC Name

6-[(acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate

Traditional Name

6-[(acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

CC=C(C)C(=O)OC1CC(C)C2(O)CCC(C)(O2)C=C2OC(=O)C(COC(C)=O)=C12

InChI Identifier

InChI=1S/C22H28O8/c1-6-12(2)19(24)28-16-9-13(3)22(26)8-7-21(5,30-22)10-17-18(16)15(20(25)29-17)11-27-14(4)23/h6,10,13,16,26H,7-9,11H2,1-5H3

InChI Key

NPUVRWFJDAPMIA-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
Stilpnopappus tomentosus	LOTUS Database	35616633
Vernonanthura nudiflora	LOTUS Database	35616633
Vernonanthura pinguis	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Fatty acid ester
2-furanone
Fatty acyl
Dihydrofuran
Enol ester
Tetrahydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Lactone
Hemiacetal
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Carbonyl group
Organooxygen compound
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	1.83	ALOGPS
logP	2.34	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	11.83	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	108.36 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	108.21 m³·mol⁻¹	ChemAxon
Polarizability	43.11 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	Yes	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

85088728

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-[(acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate (NP0204884)

MOL for NP0204884 (6-[(acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate)

3D MOL for NP0204884 (6-[(acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate)

3D SDF for NP0204884 (6-[(acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate)

3D-SDF for NP0204884 (6-[(acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate)

PDB for NP0204884 (6-[(acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate)

3D PDB for NP0204884 (6-[(acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate)

SMILES for NP0204884 (6-[(acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate)

INCHI for NP0204884 (6-[(acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate)

Structure for NP0204884 (6-[(acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate)

3D Structure for NP0204884 (6-[(acetyloxy)methyl]-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-8-yl 2-methylbut-2-enoate)