NP-MRD: Showing NP-Card for 8-(acetyloxy)-3,6,9-trimethylidene-2-oxo-octahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoate (NP0194432)

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Record Information

Version

2.0

Created at

2022-09-04 12:05:12 UTC

Updated at

2022-09-04 12:05:12 UTC

NP-MRD ID

NP0194432

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8-(acetyloxy)-3,6,9-trimethylidene-2-oxo-octahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoate

Description

8-(Acetyloxy)-3,6,9-trimethylidene-2-oxo-dodecahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoate belongs to the class of organic compounds known as guaianolides and derivatives. These are diterpene lactones with a structure characterized by the presence of a gamma-lactone fused to a guaiane, forming 3,6,9-trimethyl-azuleno[4,5-b]furan-2-one or a derivative. 8-(Acetyloxy)-3,6,9-trimethylidene-2-oxo-dodecahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161513402D          

 32 34  0  0  0  0            999 V2000
    3.9114   -0.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2664   -0.2416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4984   -0.5430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3894    0.5741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7444    1.0885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7814    1.9127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0090    2.2026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4946    1.5576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6696    1.5576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2151    0.8690    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5802    1.0885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2252    0.5741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6172    1.9127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3057    2.3672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1552    2.2026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3388    3.0069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0821    3.3648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8254    3.0069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4704    3.5213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3062    3.5213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1833    4.3371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5847    4.6385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8283    4.8514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3139    5.4964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3426    4.2064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1584    4.3294    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -1.4733    5.3658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3503    6.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9953    6.6960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5823    6.4830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9491    0.8690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6592    0.0966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  7 18  1  0  0  0  0
 18 19  2  0  0  0  0
 16 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 23 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
  8 31  1  0  0  0  0
  5 31  1  0  0  0  0
 31 32  2  0  0  0  0
M  END

     RDKit          3D

 59 61  0  0  0  0  0  0  0  0999 V2000
    4.3944   -1.9642    0.0243 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8015   -0.8198   -0.2407 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4406    0.5116   -0.1936 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7490    0.5348   -0.6568 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7592    1.0046    0.1660 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1942    1.0496   -0.2912 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4295    1.3934    1.3136 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5047    1.3708   -1.0536 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1793    0.8664   -0.5866 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0685    1.1496   -1.5245 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1728    2.2092   -2.3037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1546    0.3015   -1.6310 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6638    0.0910   -0.2237 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0057   -0.3856   -0.2395 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0882    0.3621    0.1910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8137    1.5170    0.6163 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4957   -0.0855    0.1855 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8621   -0.3040   -1.2839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6173   -1.4145    0.8721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6010   -2.5771   -0.0455 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -5.3130    0.9220    0.7401 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6704    0.8314    0.8764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4443    1.9515    1.4775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2689   -0.1882    0.4989 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2370   -0.6084    0.7021 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5055   -1.7363    1.3349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2809   -1.7032    2.4034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1737   -2.8904    0.5006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6543   -4.0546    0.6437 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7615   -2.4670   -0.4703 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3974   -1.3632    0.1451 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4014   -0.6475   -0.6313 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4352   -1.9815    0.3043 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8596   -2.8925   -0.0324 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3559    0.8955    0.8425 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8791    0.9801    0.5801 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3921    0.2590   -1.0350 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3504    2.0786   -0.7168 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5937    2.4377   -0.7931 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6146    1.1542   -2.1203 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9176    1.1925    0.4383 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0566    2.8290   -2.2323 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3594    2.4199   -2.9932 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1452   -0.6293   -2.1320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9377    0.8677   -2.1717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7554    1.1466    0.1871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8684   -0.7621   -1.3141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0707   -0.9768   -1.6868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8960    0.6369   -1.8384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2990   -1.3630    1.9381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6419   -1.8085    0.7926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0785    1.5498    2.2966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1435    2.3904    0.7311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7739    2.7225    1.8799 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6119    0.0129    1.5499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4069   -0.7372    2.8948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7822   -2.5491    2.8075 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9165   -1.8114    1.0476 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2884   -0.9191   -1.7202 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0
  5  7  2  0
  5  4  1  0
  4  3  1  0
  3  8  1  0
  8  9  1  0
  9 32  1  0
 32 31  1  0
 31 30  1  0
 30 28  1  0
 28 29  2  0
 28 26  1  0
 26 27  2  3
 26 25  1  0
 25 13  1  0
 13 12  1  0
 12 10  1  0
 10 11  2  3
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 17 21  1  1
 21 22  1  0
 22 23  1  0
 22 24  2  0
 32  2  1  0
  2  1  2  3
  2  3  1  0
 10  9  1  0
 25 31  1  0
  6 36  1  0
  6 37  1  0
  6 38  1  0
  3 35  1  1
  8 39  1  0
  8 40  1  0
  9 41  1  1
 32 59  1  6
 31 58  1  1
 27 56  1  0
 27 57  1  0
 25 55  1  1
 13 46  1  1
 12 44  1  0
 12 45  1  0
 11 42  1  0
 11 43  1  0
 18 47  1  0
 18 48  1  0
 18 49  1  0
 19 50  1  0
 19 51  1  0
 23 52  1  0
 23 53  1  0
 23 54  1  0
  1 33  1  0
  1 34  1  0
M  END


  Mrv1533004161513402D          

 32 34  0  0  0  0            999 V2000
    3.9114   -0.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2664   -0.2416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4984   -0.5430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3894    0.5741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7444    1.0885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7814    1.9127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0090    2.2026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4946    1.5576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6696    1.5576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2151    0.8690    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5802    1.0885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2252    0.5741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6172    1.9127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3057    2.3672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1552    2.2026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3388    3.0069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0821    3.3648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8254    3.0069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4704    3.5213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3062    3.5213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1833    4.3371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5847    4.6385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8283    4.8514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3139    5.4964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3426    4.2064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1584    4.3294    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -1.4733    5.3658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3503    6.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9953    6.6960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5823    6.4830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9491    0.8690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6592    0.0966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  7 18  1  0  0  0  0
 18 19  2  0  0  0  0
 16 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 23 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
  8 31  1  0  0  0  0
  5 31  1  0  0  0  0
 31 32  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0194432

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1CC2C(C3OC(=O)C(=C)C3C(CC2=C)OC(=O)C(C)(CCl)OC(C)=O)C1=C

> <INCHI_IDENTIFIER>
InChI=1S/C23H27ClO8/c1-10-7-17(30-22(28)23(6,9-24)32-14(5)26)19-12(3)21(27)31-20(19)18-11(2)16(8-15(10)18)29-13(4)25/h15-20H,1-3,7-9H2,4-6H3

> <INCHI_KEY>
QOFSCUKKFCFXNG-UHFFFAOYSA-N

> <FORMULA>
C23H27ClO8

> <MOLECULAR_WEIGHT>
466.91

> <EXACT_MASS>
466.1394455

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
46.64854328539014

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8-(acetyloxy)-3,6,9-trimethylidene-2-oxo-dodecahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoate

> <ALOGPS_LOGP>
2.48

> <JCHEM_LOGP>
2.3146225529999995

> <ALOGPS_LOGS>
-3.85

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.999980478451295

> <JCHEM_PKA_STRONGEST_BASIC>
-6.447459115012383

> <JCHEM_POLAR_SURFACE_AREA>
105.20000000000002

> <JCHEM_REFRACTIVITY>
112.01619999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.64e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8-(acetyloxy)-3,6,9-trimethylidene-2-oxo-octahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoate

> <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       7.301  -1.411   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.097  -0.451   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.664  -1.014   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.327   1.072   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.123   2.032   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.192   3.570   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.750   4.111   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.790   2.907   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.250   2.907   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.402   1.622   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.083   2.032   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -2.287   1.072   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -1.152   3.570   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.437   4.419   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.290   4.111   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.632   5.613   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.020   6.281   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.407   5.613   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.611   6.573   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -0.572   6.573   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -0.342   8.096   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.091   8.658   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -1.546   9.056   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.586  10.260   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.506   7.852   0.000  0.00  0.00           C+0
HETATM   26 Cl   UNK     0      -4.029   8.082   0.000  0.00  0.00          Cl+0
HETATM   27  O   UNK     0      -2.750  10.016   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -2.521  11.539   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -3.725  12.499   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -1.087  12.102   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.638   1.622   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.097   0.180   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   31                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   18                                                  
CONECT    8    7    9   31                                                  
CONECT    9    8   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    9   16                                                  
CONECT   16   15   17   20                                                  
CONECT   17   16   18                                                       
CONECT   18   17    7   19                                                  
CONECT   19   18                                                            
CONECT   20   16   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25   27                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25                                                            
CONECT   27   23   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31    8    5   32                                                  
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

View in JSmol

Synonyms

Value	Source
8-(Acetyloxy)-3,6,9-trimethylidene-2-oxo-dodecahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoic acid	Generator

Chemical Formula

C₂₃H₂₇ClO₈

Average Mass

466.9100 Da

Monoisotopic Mass

466.13945 Da

IUPAC Name

8-(acetyloxy)-3,6,9-trimethylidene-2-oxo-dodecahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoate

Traditional Name

8-(acetyloxy)-3,6,9-trimethylidene-2-oxo-octahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1CC2C(C3OC(=O)C(=C)C3C(CC2=C)OC(=O)C(C)(CCl)OC(C)=O)C1=C

InChI Identifier

InChI=1S/C23H27ClO8/c1-10-7-17(30-22(28)23(6,9-24)32-14(5)26)19-12(3)21(27)31-20(19)18-11(2)16(8-15(10)18)29-13(4)25/h15-20H,1-3,7-9H2,4-6H3

InChI Key

QOFSCUKKFCFXNG-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as guaianolides and derivatives. These are diterpene lactones with a structure characterized by the presence of a gamma-lactone fused to a guaiane, forming 3,6,9-trimethyl-azuleno[4,5-b]furan-2-one or a derivative.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Guaianolides and derivatives

Alternative Parents

Substituents

Guaianolide-skeleton
Guaiane sesquiterpenoid
Sesquiterpenoid
Tetracarboxylic acid or derivatives
Gamma butyrolactone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Organooxygen compound
Organochloride
Organohalogen compound
Alkyl chloride
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Alkyl halide
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	2.48	ALOGPS
logP	2.31	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	20	ChemAxon
pKa (Strongest Basic)	-6.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	105.2 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	112.02 m³·mol⁻¹	ChemAxon
Polarizability	46.65 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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 8-(acetyloxy)-3,6,9-trimethylidene-2-oxo-octahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoate (NP0194432)

MOL for NP0194432 (8-(acetyloxy)-3,6,9-trimethylidene-2-oxo-octahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoate)

3D MOL for NP0194432 (8-(acetyloxy)-3,6,9-trimethylidene-2-oxo-octahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoate)

3D SDF for NP0194432 (8-(acetyloxy)-3,6,9-trimethylidene-2-oxo-octahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoate)

3D-SDF for NP0194432 (8-(acetyloxy)-3,6,9-trimethylidene-2-oxo-octahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoate)

PDB for NP0194432 (8-(acetyloxy)-3,6,9-trimethylidene-2-oxo-octahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoate)

3D PDB for NP0194432 (8-(acetyloxy)-3,6,9-trimethylidene-2-oxo-octahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoate)

SMILES for NP0194432 (8-(acetyloxy)-3,6,9-trimethylidene-2-oxo-octahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoate)

INCHI for NP0194432 (8-(acetyloxy)-3,6,9-trimethylidene-2-oxo-octahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoate)

Structure for NP0194432 (8-(acetyloxy)-3,6,9-trimethylidene-2-oxo-octahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoate)

3D Structure for NP0194432 (8-(acetyloxy)-3,6,9-trimethylidene-2-oxo-octahydroazuleno[4,5-b]furan-4-yl 2-(acetyloxy)-3-chloro-2-methylpropanoate)