NP-MRD: Showing NP-Card for 11-(acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate (NP0224264)

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Record Information

Version

2.0

Created at

2022-09-06 02:35:02 UTC

Updated at

2022-09-06 02:35:02 UTC

NP-MRD ID

NP0224264

Secondary Accession Numbers

None

Natural Product Identification

Common Name

11-(acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate

Description

11-(Acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]Tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate 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. 11-(acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate is found in Eupatorium chinense. 11-(Acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]Tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171519132D          

 32 35  0  0  0  0            999 V2000
   -0.9959   -4.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4776   -3.4524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7743   -2.6826    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3374   -3.5803    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8557   -2.9385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -2.1419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5968   -1.3181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3324   -1.6916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7808   -0.9991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9742   -2.2099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7604   -1.9597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9847   -1.1658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8091   -1.1339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2678   -0.4481    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0943   -1.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8882   -2.1323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4461   -2.4184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5151   -3.2405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9153   -3.8070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0985   -3.6913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1674   -4.5134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3123   -3.9414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1359   -4.7474    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.6797   -2.9805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2857   -3.5351    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4159   -4.3498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7754   -4.8699    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1865   -4.6444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3167   -5.4591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0873   -5.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7277   -5.2336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8269   -4.1243    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
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 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
 15 17  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 20 24  1  0  0  0  0
  5 24  1  0  0  0  0
 10 24  1  0  0  0  0
 18 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  4  0  0  0
 30 31  1  0  0  0  0
 28 32  1  0  0  0  0
M  END

     RDKit          3D

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    0.7279    3.3999    0.9737 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2953    3.0088    2.3025 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4233    3.6469    3.3654 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2965    1.7727    2.1692 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9092    1.7701    0.8758 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0142    2.5378    0.0144 C   0  0  2  0  0  0  0  0  0  0  0  0
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    3.6564   -0.0996    0.9892 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1079    0.0151    1.2130 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9759   -1.1047    1.5246 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6487   -2.1197    2.3498 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1253   -2.1657    3.6523 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3610    1.2008   -2.0932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4443   -0.0900   -1.7954 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4347   -0.9134   -1.1009 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7780   -0.7792   -3.0851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7738    0.2173   -4.1669 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -1.5818    0.3449   -1.0249 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2308    0.3825    0.4745 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3903   -0.2460    1.1233 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3019   -1.7374    1.2666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5784    0.1788    1.4641 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4768    0.3650    0.1877 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8886   -0.3299   -1.0137 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9849   -1.6890   -0.9976 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8142   -2.3774   -1.8767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9227   -3.8707   -1.8626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4720   -1.6774   -2.6889 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.6673   -0.9183    0.9341 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3802    0.2504    2.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9155   -1.2064    1.3709 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7216   -1.8712    2.4477 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5475   -3.1556    1.9222 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7837   -3.0561    3.8745 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0660    1.0365   -2.9063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4228    1.9007   -2.5006 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8225   -1.6200   -1.6634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3212   -1.7082   -2.8766 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1667   -1.0801   -3.6291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8163    1.4309   -1.2965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3261   -0.2418    0.6238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9646   -1.8947    2.3425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2512   -2.2842    1.2235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4824   -2.2102    0.6902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3973    1.4721   -0.0079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5112    0.0656   -1.8751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0057   -4.1150   -1.9375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4417   -4.3291   -2.7475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5781   -4.2925   -0.9100 H   0  0  0  0  0  0  0  0  0  0  0  0
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 31 57  1  0
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M  END


  Mrv1533004171519132D          

 32 35  0  0  0  0            999 V2000
   -0.9959   -4.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4776   -3.4524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7743   -2.6826    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3374   -3.5803    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8557   -2.9385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -2.1419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5968   -1.3181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3324   -1.6916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7808   -0.9991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9742   -2.2099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7604   -1.9597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9847   -1.1658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8091   -1.1339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2678   -0.4481    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0943   -1.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8882   -2.1323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4461   -2.4184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.3123   -3.9414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1359   -4.7474    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.6797   -2.9805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2857   -3.5351    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4159   -4.3498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7754   -4.8699    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1865   -4.6444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3167   -5.4591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0873   -5.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7277   -5.2336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8269   -4.1243    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
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 28 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0224264

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1C2OC2(C)C2C3OC(=O)C(=C)C3C(CC(O)(CCl)C12)OC(=O)C(C)=CCO

> <INCHI_IDENTIFIER>
InChI=1S/C22H27ClO9/c1-9(5-6-24)19(26)30-12-7-22(28,8-23)15-14(16-13(12)10(2)20(27)31-16)21(4)18(32-21)17(15)29-11(3)25/h5,12-18,24,28H,2,6-8H2,1,3-4H3

> <INCHI_KEY>
CXXLXCCCYXUUOP-UHFFFAOYSA-N

> <FORMULA>
C22H27ClO9

> <MOLECULAR_WEIGHT>
470.9

> <EXACT_MASS>
470.1343601

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
45.63688657971694

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
11-(acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate

> <ALOGPS_LOGP>
1.22

> <JCHEM_LOGP>
0.42020604333333456

> <ALOGPS_LOGS>
-2.95

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.568651325497726

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.610335969618653

> <JCHEM_PKA_STRONGEST_BASIC>
-2.5521985964827456

> <JCHEM_POLAR_SURFACE_AREA>
131.89

> <JCHEM_REFRACTIVITY>
109.7507

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.28e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
11-(acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      -1.859  -7.643   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.892  -6.444   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -1.445  -5.008   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       0.630  -6.683   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.597  -5.485   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.197  -3.998   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.114  -2.460   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.487  -3.158   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.324  -1.865   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.685  -4.125   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.153  -3.658   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.572  -2.176   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       7.110  -2.117   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       7.967  -0.836   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       7.643  -3.562   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.125  -3.980   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.433  -4.514   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.561  -6.049   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.442  -7.106   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.917  -6.890   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.046  -8.425   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.450  -7.357   0.000  0.00  0.00           C+0
HETATM   23 Cl   UNK     0       2.120  -8.862   0.000  0.00  0.00          Cl+0
HETATM   24  C   UNK     0       3.135  -5.564   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.000  -6.599   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.243  -8.120   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.047  -9.090   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       9.681  -8.670   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.924 -10.190   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      11.363 -10.740   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      12.558  -9.769   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      10.877  -7.699   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   24                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6    8                                                       
CONECT    8    7    6    9   10                                             
CONECT    9    8                                                            
CONECT   10    8   11   24                                                  
CONECT   11   10   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   11   18                                                  
CONECT   18   17   19   25                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22   24                                             
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22                                                            
CONECT   24   20    5   10                                                  
CONECT   25   18   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   32                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30                                                            
CONECT   32   28                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Value	Source
11-(Acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0,.0,]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoic acid	Generator
11-(Acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₂H₂₇ClO₉

Average Mass

470.9000 Da

Monoisotopic Mass

470.13436 Da

IUPAC Name

11-(acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate

Traditional Name

11-(acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1C2OC2(C)C2C3OC(=O)C(=C)C3C(CC(O)(CCl)C12)OC(=O)C(C)=CCO

InChI Identifier

InChI=1S/C22H27ClO9/c1-9(5-6-24)19(26)30-12-7-22(28,8-23)15-14(16-13(12)10(2)20(27)31-16)21(4)18(32-21)17(15)29-11(3)25/h5,12-18,24,28H,2,6-8H2,1,3-4H3

InChI Key

CXXLXCCCYXUUOP-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
Eupatorium chinense	LOTUS Database	35616633

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
Tricarboxylic acid or derivatives
Fatty acid ester
Gamma butyrolactone
Fatty acyl
Oxane
Cyclic alcohol
Alpha,beta-unsaturated carboxylic ester
Tertiary alcohol
Tetrahydrofuran
Enoate ester
Carboxylic acid ester
Chlorohydrin
Halohydrin
Lactone
Carboxylic acid derivative
Organoheterocyclic compound
Dialkyl ether
Oxirane
Ether
Oxacycle
Primary alcohol
Alkyl chloride
Alcohol
Organooxygen compound
Alkyl halide
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organochloride
Organohalogen compound
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	1.22	ALOGPS
logP	0.42	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	13.61	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	131.89 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	109.75 m³·mol⁻¹	ChemAxon
Polarizability	45.64 Å³	ChemAxon
Number of Rings	4	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

73803358

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 11-(acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate (NP0224264)

MOL for NP0224264 (11-(acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate)

3D MOL for NP0224264 (11-(acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate)

3D SDF for NP0224264 (11-(acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate)

3D-SDF for NP0224264 (11-(acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate)

PDB for NP0224264 (11-(acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate)

3D PDB for NP0224264 (11-(acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate)

SMILES for NP0224264 (11-(acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate)

INCHI for NP0224264 (11-(acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate)

Structure for NP0224264 (11-(acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate)

3D Structure for NP0224264 (11-(acetyloxy)-9-(chloromethyl)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.0²,⁶.0¹²,¹⁴]tetradecan-7-yl 4-hydroxy-2-methylbut-2-enoate)