NP-MRD: Showing NP-Card for 7-(chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-1(13)-en-9-yl 2-methylbut-2-enoate (NP0214849)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 14:16:01 UTC

Updated at

2022-09-05 14:16:01 UTC

NP-MRD ID

NP0214849

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-(chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-1(13)-en-9-yl 2-methylbut-2-enoate

Description

7-(Chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]Tetradec-1(13)-en-9-yl 2-methylbut-2-enoate belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid. 7-(chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-1(13)-en-9-yl 2-methylbut-2-enoate is found in Bejaranoa balansae. Based on a literature review very few articles have been published on 7-(chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]Tetradec-1(13)-en-9-yl 2-methylbut-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052216162D          

 30 32  0  0  0  0            999 V2000
    4.0481   -3.2978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5632   -2.6303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8988   -1.8767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7192   -1.7904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4138   -1.2092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5934   -1.2954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7494   -0.4555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2645    0.2119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7494    0.8793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7494    1.7043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5340    1.9593    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0189    1.2918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8439    1.2918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5340    0.6244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1413    0.0660    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3710   -0.1843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9898   -0.7299    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.2645    2.3718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7494    3.0392    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4799    2.6267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4799    3.4517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6952    2.3718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2103    1.7043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2103    0.8793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4257    0.6244    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6952    0.2119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2103   -0.4555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9652    1.2918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4799   -0.0430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4799   -0.8680    0.0000 O   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
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 10 18  1  0  0  0  0
 18 19  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
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 22 28  1  0  0  0  0
 26 29  1  0  0  0  0
  8 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END

     RDKit          3D

 55 57  0  0  0  0  0  0  0  0999 V2000
    3.5526   -0.0210    2.0134 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4431    0.4407    0.9227 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0115    0.6648   -0.3007 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0408    1.1309   -1.3006 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6368    0.4926   -0.6994 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2198    0.6995   -1.8709 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7032    0.0842    0.2129 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3173   -0.1061   -0.1334 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0203   -1.5679    0.0508 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2237   -2.2717    0.2147 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6534   -2.1954   -1.1417 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2466   -2.4908   -2.2889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6610   -1.3000   -1.5890 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8110   -1.6001   -0.8118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8098   -2.8984   -0.5696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4564   -3.3921   -0.7582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9657   -4.5407   -0.6498 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6747   -0.4464   -0.4852 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3164   -0.6834    0.8592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7486    0.7717   -0.3163 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0381    1.0019   -1.4912 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9243    0.5505    0.8889 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2266    1.6553    1.7741 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6389    2.7437    1.1403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0704    3.9450    1.0386 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3405    2.2333    0.5666 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1468    2.6330   -0.7398 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7363    2.8900    1.4423 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2966    2.5842    3.1368 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.4527    0.7648    0.7789 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1558   -1.0108    1.6891 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7295    0.6887    2.2225 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1251   -0.2453    2.9480 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4958    0.5879    1.1939 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6814    0.9798   -2.3332 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3428    2.1717   -1.1060 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9329    0.4979   -1.1265 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2334    0.1232   -1.2015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5476   -1.7668    0.9943 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0888   -3.2294    0.3094 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7664   -3.4662   -2.2121 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9313   -1.6504   -2.4810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4022   -2.5672   -3.2084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6505   -3.4895   -0.2843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4321   -0.2422   -1.2650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2144    0.2100    1.5024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7919   -1.5017    1.3555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3771   -1.0083    0.7625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4624    1.6354   -0.2391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7122    1.2025   -2.1926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1238   -0.3464    1.4696 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5530    3.5062   -0.9595 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5770    3.9988    1.2769 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7422    2.5784    1.1703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0485    0.5715    1.8209 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 30  1  0
 30 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  1  6
 26 28  1  0
 28 29  1  0
 22 20  1  0
 20 21  1  0
 20 18  1  0
 18 19  1  0
 18 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 16 11  1  0
 11 12  1  6
 11 13  1  0
 11  9  1  0
  9 10  1  0
  9  8  1  0
 26 30  1  0
 13 14  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
 30 55  1  1
 22 51  1  1
 27 52  1  0
 28 53  1  0
 28 54  1  0
 20 49  1  1
 21 50  1  0
 18 45  1  6
 19 46  1  0
 19 47  1  0
 19 48  1  0
 15 44  1  0
 12 41  1  0
 12 42  1  0
 12 43  1  0
  9 39  1  1
 10 40  1  0
M  END


  Mrv1652309052216162D          

 30 32  0  0  0  0            999 V2000
    4.0481   -3.2978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5632   -2.6303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8988   -1.8767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7192   -1.7904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4138   -1.2092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5934   -1.2954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7494   -0.4555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2645    0.2119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7494    0.8793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7494    1.7043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5340    1.9593    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0189    1.2918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8439    1.2918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5340    0.6244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1413    0.0660    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3710   -0.1843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9898   -0.7299    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.2645    2.3718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7494    3.0392    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4799    2.6267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4799    3.4517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6952    2.3718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2103    1.7043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2103    0.8793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4257    0.6244    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6952    0.2119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2103   -0.4555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9652    1.2918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4799   -0.0430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4799   -0.8680    0.0000 O   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
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 10 18  1  0  0  0  0
 18 19  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
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 22 28  1  0  0  0  0
 26 29  1  0  0  0  0
  8 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0214849

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=C(C)C(=O)OC1C2C(OC(=O)C2(O)CCl)C(O)C(C)C2=CC(=O)C(C)(O2)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H25ClO9/c1-5-8(2)17(25)28-15-12-14(29-18(26)20(12,27)7-21)13(23)9(3)10-6-11(22)19(4,30-10)16(15)24/h5-6,9,12-16,23-24,27H,7H2,1-4H3

> <INCHI_KEY>
NGOAHMYLNDMUGV-UHFFFAOYSA-N

> <FORMULA>
C20H25ClO9

> <MOLECULAR_WEIGHT>
444.86

> <EXACT_MASS>
444.1187101

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
42.12872738435013

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-(chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0^{4,8}]tetradec-1(13)-en-9-yl 2-methylbut-2-enoate

> <JCHEM_LOGP>
0.9644685023333335

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.79114633930958

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.28736611732026

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3338668643055334

> <JCHEM_POLAR_SURFACE_AREA>
139.59

> <JCHEM_REFRACTIVITY>
104.0294

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
7-(chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0^{4,8}]tetradec-1(13)-en-9-yl 2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       7.557  -6.156   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.651  -4.910   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.278  -3.503   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.809  -3.342   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.373  -2.257   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.841  -2.418   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       6.999  -0.850   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.094   0.396   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.999   1.641   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.999   3.181   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.464   3.657   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       9.369   2.411   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      10.909   2.411   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       8.464   1.166   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       9.597   0.123   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.159  -0.344   0.000  0.00  0.00           C+0
HETATM   17 Cl   UNK     0       9.314  -1.362   0.000  0.00  0.00          Cl+0
HETATM   18  C   UNK     0       6.094   4.427   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.999   5.673   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.629   4.903   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.629   6.443   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.164   4.427   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.259   3.181   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.259   1.641   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       0.795   1.166   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       3.164   0.396   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.259  -0.850   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       3.668   2.411   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       4.629  -0.080   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       4.629  -1.620   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   29                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11   18                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    9   15   16                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16                                                            
CONECT   18   10   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   28                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28   29                                             
CONECT   27   26                                                            
CONECT   28   26   22                                                       
CONECT   29   26    8   30                                                  
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Value	Source
7-(Chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0,]tetradec-1(13)-en-9-yl 2-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₀H₂₅ClO₉

Average Mass

444.8600 Da

Monoisotopic Mass

444.11871 Da

IUPAC Name

7-(chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0^{4,8}]tetradec-1(13)-en-9-yl 2-methylbut-2-enoate

Traditional Name

7-(chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0^{4,8}]tetradec-1(13)-en-9-yl 2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

CC=C(C)C(=O)OC1C2C(OC(=O)C2(O)CCl)C(O)C(C)C2=CC(=O)C(C)(O2)C1O

InChI Identifier

InChI=1S/C20H25ClO9/c1-5-8(2)17(25)28-15-12-14(29-18(26)20(12,27)7-21)13(23)9(3)10-6-11(22)19(4,30-10)16(15)24/h5-6,9,12-16,23-24,27H,7H2,1-4H3

InChI Key

NGOAHMYLNDMUGV-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
Bejaranoa balansae	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acid esters

Direct Parent

Fatty acid esters

Alternative Parents

Substituents

Fatty acid ester
Dicarboxylic acid or derivatives
3-furanone
Gamma butyrolactone
Dihydrofuran
Vinylogous ester
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Tertiary alcohol
Carboxylic acid ester
Chlorohydrin
Halohydrin
Ketone
Lactone
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Polyol
Carboxylic acid derivative
Alkyl halide
Alkyl chloride
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
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	0.96	ChemAxon
pKa (Strongest Acidic)	11.29	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	139.59 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	104.03 m³·mol⁻¹	ChemAxon
Polarizability	42.13 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163054938

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-(chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-1(13)-en-9-yl 2-methylbut-2-enoate (NP0214849)

MOL for NP0214849 (7-(chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-1(13)-en-9-yl 2-methylbut-2-enoate)

3D MOL for NP0214849 (7-(chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-1(13)-en-9-yl 2-methylbut-2-enoate)

3D SDF for NP0214849 (7-(chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-1(13)-en-9-yl 2-methylbut-2-enoate)

3D-SDF for NP0214849 (7-(chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-1(13)-en-9-yl 2-methylbut-2-enoate)

PDB for NP0214849 (7-(chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-1(13)-en-9-yl 2-methylbut-2-enoate)

3D PDB for NP0214849 (7-(chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-1(13)-en-9-yl 2-methylbut-2-enoate)

SMILES for NP0214849 (7-(chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-1(13)-en-9-yl 2-methylbut-2-enoate)

INCHI for NP0214849 (7-(chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-1(13)-en-9-yl 2-methylbut-2-enoate)

Structure for NP0214849 (7-(chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-1(13)-en-9-yl 2-methylbut-2-enoate)

3D Structure for NP0214849 (7-(chloromethyl)-3,7,10-trihydroxy-2,11-dimethyl-6,12-dioxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-1(13)-en-9-yl 2-methylbut-2-enoate)