NP-MRD: Showing NP-Card for (1r,2s,3s,5r,8r,9z,11s)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate (NP0322698)

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Record Information

Version

2.0

Created at

2022-09-12 01:37:27 UTC

Updated at

2022-09-12 01:37:27 UTC

NP-MRD ID

NP0322698

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,3s,5r,8r,9z,11s)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate

Description

(1R,2S,3S,5R,8R,9Z,11S)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]Tetradec-9-en-2-yl (2Z)-2-methylbut-2-enoate belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. (1r,2s,3s,5r,8r,9z,11s)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate is found in Gochnatia vernonioides. Based on a literature review very few articles have been published on (1R,2S,3S,5R,8R,9Z,11S)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]Tetradec-9-en-2-yl (2Z)-2-methylbut-2-enoate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309122203372D          

 26 28  0  0  1  0            999 V2000
    3.6734    0.2816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1931    0.9523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3681    0.9580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8786    0.2940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1186    1.7444    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7894    2.2247    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8813    3.0446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6373    3.3749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7292    4.1948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3013    2.8854    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3932    3.7053    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0573    3.2157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7214    2.7262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6295    1.9063    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4493    1.8144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5376    1.0865    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8735    1.5760    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2094    2.0655    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1175    1.2457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7816    0.7561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5874    0.5790    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6897   -0.0637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9337   -0.3941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3538   -0.5533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1097   -0.2229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4534    1.7352    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 17 16  1  1  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 24 25  1  0  0  0  0
 18 26  1  0  0  0  0
 26  2  1  6  0  0  0
  6 26  1  0  0  0  0
M  END


  Mrv1652309122203372D          

 26 28  0  0  1  0            999 V2000
    3.6734    0.2816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1931    0.9523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3681    0.9580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8786    0.2940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1186    1.7444    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7894    2.2247    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8813    3.0446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6373    3.3749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7292    4.1948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3013    2.8854    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3932    3.7053    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0573    3.2157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7214    2.7262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6295    1.9063    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4493    1.8144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5376    1.0865    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8735    1.5760    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2094    2.0655    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1175    1.2457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7816    0.7561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5874    0.5790    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6897   -0.0637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9337   -0.3941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3538   -0.5533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1097   -0.2229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4534    1.7352    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 17 16  1  1  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 24 25  1  0  0  0  0
 18 26  1  0  0  0  0
 26  2  1  6  0  0  0
  6 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0322698

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(\C)C(=O)O[C@@H]1[C@@H]2O[C@]2(C)CC[C@@H](O)\C(C)=C/[C@@H]2OC(=O)C(=C)[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C20H26O6/c1-6-10(2)18(22)25-16-15-12(4)19(23)24-14(15)9-11(3)13(21)7-8-20(5)17(16)26-20/h6,9,13-17,21H,4,7-8H2,1-3,5H3/b10-6-,11-9-/t13-,14+,15-,16+,17+,20-/m1/s1

> <INCHI_KEY>
GICGZKVUKMMVJE-DAQYVPLLSA-N

> <FORMULA>
C20H26O6

> <MOLECULAR_WEIGHT>
362.422

> <EXACT_MASS>
362.172938557

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
37.82360060373771

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,3S,5R,8R,9Z,11S)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0^{3,5}]tetradec-9-en-2-yl (2Z)-2-methylbut-2-enoate

> <JCHEM_LOGP>
2.8641644260000003

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.609038597516033

> <JCHEM_PKA_STRONGEST_BASIC>
-2.969806517446443

> <JCHEM_POLAR_SURFACE_AREA>
85.36000000000001

> <JCHEM_REFRACTIVITY>
95.3149

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,3S,5R,8R,9Z,11S)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0^{3,5}]tetradec-9-en-2-yl (2Z)-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       6.857   0.526   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.960   1.778   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.420   1.788   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.507   0.549   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       3.955   3.256   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       5.207   4.153   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.378   5.683   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.790   6.300   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.961   7.830   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.029   5.386   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.201   6.916   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       9.440   6.003   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.680   5.089   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.508   3.559   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.039   3.387   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      10.337   2.028   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       9.097   2.942   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.858   3.856   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       7.686   2.325   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.926   1.411   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      10.430   1.081   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.754  -0.119   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.343  -0.736   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.994  -1.033   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.405  -0.416   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.446   3.239   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   26                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   26                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   14   18                                                  
CONECT   18   17   19   26                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24                                                            
CONECT   26   18    2    6                                                  
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Value	Source
(1R,2S,3S,5R,8R,9Z,11S)-8-Hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0,]tetradec-9-en-2-yl (2Z)-2-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₀H₂₆O₆

Average Mass

362.4220 Da

Monoisotopic Mass

362.17294 Da

IUPAC Name

(1R,2S,3S,5R,8R,9Z,11S)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0^{3,5}]tetradec-9-en-2-yl (2Z)-2-methylbut-2-enoate

Traditional Name

(1R,2S,3S,5R,8R,9Z,11S)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0^{3,5}]tetradec-9-en-2-yl (2Z)-2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

C\C=C(\C)C(=O)O[C@@H]1[C@@H]2O[C@]2(C)CC[C@@H](O)\C(C)=C/[C@@H]2OC(=O)C(=C)[C@@H]12

InChI Identifier

InChI=1S/C20H26O6/c1-6-10(2)18(22)25-16-15-12(4)19(23)24-14(15)9-11(3)13(21)7-8-20(5)17(16)26-20/h6,9,13-17,21H,4,7-8H2,1-3,5H3/b10-6-,11-9-/t13-,14+,15-,16+,17+,20-/m1/s1

InChI Key

GICGZKVUKMMVJE-DAQYVPLLSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Gochnatia vernonioides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Germacrane sesquiterpenoid
Sesquiterpenoid
Fatty acid ester
Dicarboxylic acid or derivatives
Gamma butyrolactone
Fatty acyl
Alpha,beta-unsaturated carboxylic ester
Tetrahydrofuran
Enoate ester
Secondary alcohol
Lactone
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
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	2.86	ChemAxon
pKa (Strongest Acidic)	14.61	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	85.36 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	95.31 m³·mol⁻¹	ChemAxon
Polarizability	37.82 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

162922111

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,3s,5r,8r,9z,11s)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate (NP0322698)

MOL for NP0322698 ((1r,2s,3s,5r,8r,9z,11s)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)

3D MOL for NP0322698 ((1r,2s,3s,5r,8r,9z,11s)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)

3D SDF for NP0322698 ((1r,2s,3s,5r,8r,9z,11s)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)

3D-SDF for NP0322698 ((1r,2s,3s,5r,8r,9z,11s)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)

PDB for NP0322698 ((1r,2s,3s,5r,8r,9z,11s)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)

3D PDB for NP0322698 ((1r,2s,3s,5r,8r,9z,11s)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)

SMILES for NP0322698 ((1r,2s,3s,5r,8r,9z,11s)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)

INCHI for NP0322698 ((1r,2s,3s,5r,8r,9z,11s)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)

Structure for NP0322698 ((1r,2s,3s,5r,8r,9z,11s)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)

3D Structure for NP0322698 ((1r,2s,3s,5r,8r,9z,11s)-8-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)