NP-MRD: Showing NP-Card for 9-(chloromethyl)-9,11-dihydroxy-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 (NP0266552)

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Record Information

Version

2.0

Created at

2022-09-08 10:55:54 UTC

Updated at

2022-09-08 10:55:54 UTC

NP-MRD ID

NP0266552

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9-(chloromethyl)-9,11-dihydroxy-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

9-(Chloromethyl)-9,11-dihydroxy-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. 9-(chloromethyl)-9,11-dihydroxy-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. 9-(Chloromethyl)-9,11-dihydroxy-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


  Mrv1533004231522502D          

 29 32  0  0  0  0            999 V2000
   -0.2681    2.2017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3723    2.7217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2421    3.5364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5285    3.8310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6587    4.6457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1429    2.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7833    2.9472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2731    1.6125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0437    1.3179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6435    1.8844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4603    1.7686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3914    2.5907    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2465    2.0188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4229    2.8247    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.8791    1.0578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7030    1.0158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2214    1.6577    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9177    0.2192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9620   -0.6046    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2264   -0.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7780   -0.9236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5845    0.2872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7984    0.0371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5740   -0.7568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7497   -0.7888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2910   -1.4745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4645   -0.0147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6706    0.2097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1126    0.4958    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
  3  4  1  4  0  0  0
  4  5  1  0  0  0  0
  2  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  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  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 11 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
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 15 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
  9 29  1  0  0  0  0
 23 29  1  0  0  0  0
M  END

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
   -0.3276   -4.2085   -0.5651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9736   -3.0868   -0.3149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3406   -3.0108    0.1877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0278   -4.0038    0.5460 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7376   -1.6546    0.1969 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8669   -1.0264   -0.6963 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8913    0.4542   -0.6821 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0710    1.0792    0.6501 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5260    2.4618    0.3404 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0892    3.1285    1.4239 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5730    2.2025   -0.7533 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1037    2.1688   -2.0546 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1106    0.9393   -1.4461 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1617   -0.0676   -1.8539 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8197    1.0035    1.4876 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1770    1.5738    2.7385 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3004    1.8297    0.9634 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6234    1.7866    2.1764 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.5121   -0.4206    1.7473 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2129   -1.1928    0.7299 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3956   -0.5652    0.2681 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6703   -1.0766    0.4637 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7238   -2.1749    1.1004 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8736   -0.4201   -0.0166 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1837   -1.0587    0.2502 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8324    0.7079   -0.6715 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0355    1.4129   -1.1802 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0979    2.6727   -0.6006 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5536   -1.6650   -0.4523 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7778   -5.1588   -0.4111 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7052   -4.1711   -0.9437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1954   -1.3485   -1.7309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9901    0.8465   -1.1637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8581    0.5203    1.1981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7414    3.0556   -0.1435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9589    2.7244    1.6044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6288    2.3167   -0.5191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0613    0.5414   -2.1619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4997   -0.6828   -1.0106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8500   -0.6670   -2.7379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4084    2.0514    3.1350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0530    2.9035    0.9841 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6383    1.6161   -0.0453 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0999   -0.4540    2.6997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4455   -0.9517    2.0091 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5793   -2.1330    1.2513 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1003   -1.8423    1.0470 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8374   -0.2652    0.7053 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6613   -1.4567   -0.6498 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8707    1.1673   -0.8619 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9518    0.8243   -1.0154 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9713    1.5588   -2.2977 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9200    2.7781   -0.0524 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0463   -1.5619   -1.4053 H   0  0  0  0  0  0  0  0  0  0  0  0
 25 24  1  0
 24 26  2  0
 26 27  1  0
 27 28  1  0
 24 22  1  0
 22 23  2  0
 22 21  1  0
 21 20  1  0
 20 19  1  0
 19 15  1  0
 15 16  1  1
 15 17  1  0
 17 18  1  0
 15  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  6
 13  7  1  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  2  3
  2 29  1  0
 29 20  1  0
  7  8  1  0
 29  6  1  0
 13 11  1  0
 25 47  1  0
 25 48  1  0
 25 49  1  0
 26 50  1  0
 27 51  1  0
 27 52  1  0
 28 53  1  0
 20 46  1  1
 19 44  1  0
 19 45  1  0
 16 41  1  0
 17 42  1  0
 17 43  1  0
  8 34  1  1
  9 35  1  6
 10 36  1  0
 11 37  1  6
 14 38  1  0
 14 39  1  0
 14 40  1  0
  7 33  1  6
  6 32  1  6
  1 30  1  0
  1 31  1  0
 29 54  1  6
M  END


  Mrv1533004231522502D          

 29 32  0  0  0  0            999 V2000
   -0.2681    2.2017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3723    2.7217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2421    3.5364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5285    3.8310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6587    4.6457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1429    2.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7833    2.9472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2731    1.6125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0437    1.3179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6435    1.8844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4603    1.7686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3914    2.5907    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2465    2.0188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4229    2.8247    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.8791    1.0578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7030    1.0158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2214    1.6577    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9177    0.2192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9620   -0.6046    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2264   -0.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7780   -0.9236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5845    0.2872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7984    0.0371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5740   -0.7568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7497   -0.7888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2910   -1.4745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4645   -0.0147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6706    0.2097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1126    0.4958    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
  3  4  1  4  0  0  0
  4  5  1  0  0  0  0
  2  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  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  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 11 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
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 15 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
  9 29  1  0  0  0  0
 23 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0266552

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=CCO)C(=O)OC1CC(O)(CCl)C2C(O)C3OC3(C)C2C2OC(=O)C(=C)C12

> <INCHI_IDENTIFIER>
InChI=1S/C20H25ClO8/c1-8(4-5-22)17(24)27-10-6-20(26,7-21)12-13(19(3)16(29-19)14(12)23)15-11(10)9(2)18(25)28-15/h4,10-16,22-23,26H,2,5-7H2,1,3H3

> <INCHI_KEY>
JNLCQVGOEVZPLZ-UHFFFAOYSA-N

> <FORMULA>
C20H25ClO8

> <MOLECULAR_WEIGHT>
428.86

> <EXACT_MASS>
428.1237955

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
42.44820746267577

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
9-(chloromethyl)-9,11-dihydroxy-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>
0.73

> <JCHEM_LOGP>
-0.02091936699999901

> <ALOGPS_LOGS>
-2.30

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.075945812313282

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.374519297620328

> <JCHEM_PKA_STRONGEST_BASIC>
-2.5521985964827207

> <JCHEM_POLAR_SURFACE_AREA>
125.82000000000002

> <JCHEM_REFRACTIVITY>
100.59920000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.15e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
9-(chloromethyl)-9,11-dihydroxy-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                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0      -0.501   4.110   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.695   5.081   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.452   6.601   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.987   7.151   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -1.230   8.672   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       2.133   4.531   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       3.329   5.501   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       2.376   3.010   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       3.815   2.460   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.934   3.517   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.459   3.301   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.331   4.836   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       7.927   3.768   0.000  0.00  0.00           C+0
HETATM   14 Cl   UNK     0       8.256   5.273   0.000  0.00  0.00          Cl+0
HETATM   15  C   UNK     0       7.241   1.975   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.779   1.896   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       9.747   3.094   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       9.180   0.409   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.262  -1.129   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.889  -0.431   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.052  -1.724   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.691   0.536   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.224   0.069   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       4.805  -1.413   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.266  -1.472   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.410  -2.752   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.734  -0.027   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.252   0.391   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.944   0.925   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    6                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4                                                            
CONECT    6    2    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   29                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13   15                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13                                                            
CONECT   15   11   16   22                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18   20                                                       
CONECT   20   19   18   21   22                                             
CONECT   21   20                                                            
CONECT   22   20   15   23                                                  
CONECT   23   22   24   29                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27    9   23                                                  
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Value	Source
9-(Chloromethyl)-9,11-dihydroxy-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
9-(Chloromethyl)-9,11-dihydroxy-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

C₂₀H₂₅ClO₈

Average Mass

428.8600 Da

Monoisotopic Mass

428.12380 Da

IUPAC Name

9-(chloromethyl)-9,11-dihydroxy-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

9-(chloromethyl)-9,11-dihydroxy-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(=CCO)C(=O)OC1CC(O)(CCl)C2C(O)C3OC3(C)C2C2OC(=O)C(=C)C12

InChI Identifier

InChI=1S/C20H25ClO8/c1-8(4-5-22)17(24)27-10-6-20(26,7-21)12-13(19(3)16(29-19)14(12)23)15-11(10)9(2)18(25)28-15/h4,10-16,22-23,26H,2,5-7H2,1,3H3

InChI Key

JNLCQVGOEVZPLZ-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
Fatty acid ester
Dicarboxylic acid or derivatives
Gamma butyrolactone
Fatty acyl
Oxane
Cyclic alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Tertiary alcohol
Carboxylic acid ester
Chlorohydrin
Secondary alcohol
Halohydrin
Lactone
Carboxylic acid derivative
Dialkyl ether
Organoheterocyclic compound
Oxacycle
Oxirane
Ether
Primary alcohol
Hydrocarbon derivative
Organic oxide
Alkyl chloride
Organic oxygen compound
Alcohol
Alkyl halide
Carbonyl group
Organohalogen compound
Organochloride
Organooxygen 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	0.73	ALOGPS
logP	-0.021	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	13.37	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	125.82 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	100.6 m³·mol⁻¹	ChemAxon
Polarizability	42.45 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	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

73803357

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 9-(chloromethyl)-9,11-dihydroxy-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 (NP0266552)

MOL for NP0266552 (9-(chloromethyl)-9,11-dihydroxy-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 NP0266552 (9-(chloromethyl)-9,11-dihydroxy-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 NP0266552 (9-(chloromethyl)-9,11-dihydroxy-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 NP0266552 (9-(chloromethyl)-9,11-dihydroxy-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 NP0266552 (9-(chloromethyl)-9,11-dihydroxy-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 NP0266552 (9-(chloromethyl)-9,11-dihydroxy-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 NP0266552 (9-(chloromethyl)-9,11-dihydroxy-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 NP0266552 (9-(chloromethyl)-9,11-dihydroxy-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 NP0266552 (9-(chloromethyl)-9,11-dihydroxy-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 NP0266552 (9-(chloromethyl)-9,11-dihydroxy-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)