NP-MRD: Showing NP-Card for (3s,3ar,4s,4as,7as,8s,9r,9as)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2e)-2-methylbut-2-enoate (NP0241630)

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Record Information

Version

2.0

Created at

2022-09-07 01:45:40 UTC

Updated at

2022-09-07 01:45:40 UTC

NP-MRD ID

NP0241630

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,3ar,4s,4as,7as,8s,9r,9as)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2e)-2-methylbut-2-enoate

Description

(3S,3aR,4S,4aS,7aS,8S,9R,9aS)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-2H,3H,3aH,4H,4aH,5H,7aH,8H,9H,9aH-azuleno[6,5-b]furan-4-yl (2E)-2-methylbut-2-enoate belongs to the class of organic compounds known as sesquiterpene lactones. These are sesquiterpenoids containing a lactone ring. (3s,3ar,4s,4as,7as,8s,9r,9as)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2e)-2-methylbut-2-enoate is found in Gaillardia aestivalis. Based on a literature review very few articles have been published on (3S,3aR,4S,4aS,7aS,8S,9R,9aS)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-2H,3H,3aH,4H,4aH,5H,7aH,8H,9H,9aH-azuleno[6,5-b]furan-4-yl (2E)-2-methylbut-2-enoate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309072203452D          

 26 28  0  0  1  0            999 V2000
    4.9574    3.7283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9574    2.9033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2429    2.4908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5284    2.9033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2429    1.6658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9574    1.2533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5284    1.2533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5284    0.4283    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2717    0.0703    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9800    0.4935    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3042    1.2521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6013   -0.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4056    0.1343    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2770   -0.8079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4553   -0.7340    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9409   -1.3790    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2989   -2.1223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1159   -1.3790    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7580   -2.1223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6016   -0.7340    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7799   -0.8079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4556   -0.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0769    0.4935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0030    1.3152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7851    0.0703    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8222    0.8945    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  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
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 15 14  1  6  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 20 25  1  0  0  0  0
  8 25  1  0  0  0  0
 25 26  1  1  0  0  0
M  END


  Mrv1652309072203452D          

 26 28  0  0  1  0            999 V2000
    4.9574    3.7283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9574    2.9033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2429    2.4908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5284    2.9033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2429    1.6658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9574    1.2533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5284    1.2533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5284    0.4283    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2717    0.0703    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9800    0.4935    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3042    1.2521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6013   -0.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4056    0.1343    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2770   -0.8079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4553   -0.7340    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9409   -1.3790    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2989   -2.1223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1159   -1.3790    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7580   -2.1223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6016   -0.7340    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7799   -0.8079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4556   -0.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0769    0.4935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0030    1.3152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7851    0.0703    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8222    0.8945    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  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
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 15 14  1  6  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 20 25  1  0  0  0  0
  8 25  1  0  0  0  0
 25 26  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0241630

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C20H26O6/c1-6-9(2)18(23)26-17-14-11(4)19(24)25-16(14)15(22)10(3)12-7-8-13(21)20(12,17)5/h6-8,10-12,14-17,22H,1-5H3/b9-6+/t10-,11-,12-,14-,15+,16-,17-,20+/m0/s1

> <INCHI_KEY>
NOASRRBRAULRFQ-UIJMQGGWSA-N

> <FORMULA>
C20H26O6

> <MOLECULAR_WEIGHT>
362.422

> <EXACT_MASS>
362.172938557

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
37.14385457557621

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,3aR,4S,4aS,7aS,8S,9R,9aS)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-2H,3H,3aH,4H,4aH,5H,7aH,8H,9H,9aH-azuleno[6,5-b]furan-4-yl (2E)-2-methylbut-2-enoate

> <JCHEM_LOGP>
2.9212395746666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.993679373313071

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.885857799888264

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2777841462943664

> <JCHEM_POLAR_SURFACE_AREA>
89.9

> <JCHEM_REFRACTIVITY>
94.93399999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3S,3aR,4S,4aS,7aS,8S,9R,9aS)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3H,3aH,4H,7aH,8H,9H,9aH-azuleno[6,5-b]furan-4-yl (2E)-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       9.254   6.959   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.254   5.419   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.920   4.649   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.586   5.419   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.920   3.109   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       9.254   2.339   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       6.586   2.339   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.586   0.799   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.974   0.131   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.296   0.921   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.901   2.337   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.456  -0.092   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      11.957   0.251   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       9.850  -1.508   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       8.317  -1.370   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.356  -2.574   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       8.025  -3.962   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.816  -2.574   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.148  -3.962   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.856  -1.370   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.322  -1.508   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.717  -0.092   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.877   0.921   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       3.739   2.455   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.199   0.131   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.268   1.670   0.000  0.00  0.00           C+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   25                                                  
CONECT    9    8   10   15                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14    9   16                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   20    8   26                                             
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Value	Source
(3S,3AR,4S,4as,7as,8S,9R,9as)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-2H,3H,3ah,4H,4ah,5H,7ah,8H,9H,9ah-azuleno[6,5-b]furan-4-yl (2E)-2-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₀H₂₆O₆

Average Mass

362.4220 Da

Monoisotopic Mass

362.17294 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C20H26O6/c1-6-9(2)18(23)26-17-14-11(4)19(24)25-16(14)15(22)10(3)12-7-8-13(21)20(12,17)5/h6-8,10-12,14-17,22H,1-5H3/b9-6+/t10-,11-,12-,14-,15+,16-,17-,20+/m0/s1

InChI Key

NOASRRBRAULRFQ-UIJMQGGWSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Gaillardia aestivalis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpene lactones. These are sesquiterpenoids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Sesquiterpene lactones

Alternative Parents

Substituents

Helenalin-skeleton
Ambrosanolide
Pseudoguaiane sesquiterpenoid
Sesquiterpenoid
Fatty acid ester
Dicarboxylic acid or derivatives
Gamma butyrolactone
Fatty acyl
Cyclic alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Lactone
Ketone
Carboxylic acid ester
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen compound
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

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

162884425

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,3ar,4s,4as,7as,8s,9r,9as)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2e)-2-methylbut-2-enoate (NP0241630)

MOL for NP0241630 ((3s,3ar,4s,4as,7as,8s,9r,9as)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2e)-2-methylbut-2-enoate)

3D MOL for NP0241630 ((3s,3ar,4s,4as,7as,8s,9r,9as)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2e)-2-methylbut-2-enoate)

3D SDF for NP0241630 ((3s,3ar,4s,4as,7as,8s,9r,9as)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2e)-2-methylbut-2-enoate)

3D-SDF for NP0241630 ((3s,3ar,4s,4as,7as,8s,9r,9as)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2e)-2-methylbut-2-enoate)

PDB for NP0241630 ((3s,3ar,4s,4as,7as,8s,9r,9as)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2e)-2-methylbut-2-enoate)

3D PDB for NP0241630 ((3s,3ar,4s,4as,7as,8s,9r,9as)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2e)-2-methylbut-2-enoate)

SMILES for NP0241630 ((3s,3ar,4s,4as,7as,8s,9r,9as)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2e)-2-methylbut-2-enoate)

INCHI for NP0241630 ((3s,3ar,4s,4as,7as,8s,9r,9as)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2e)-2-methylbut-2-enoate)

Structure for NP0241630 ((3s,3ar,4s,4as,7as,8s,9r,9as)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2e)-2-methylbut-2-enoate)

3D Structure for NP0241630 ((3s,3ar,4s,4as,7as,8s,9r,9as)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2e)-2-methylbut-2-enoate)