NP-MRD: Showing NP-Card for burrodin (NP0169226)

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Record Information

Version

2.0

Created at

2022-09-03 05:08:47 UTC

Updated at

2022-09-03 05:08:47 UTC

NP-MRD ID

NP0169226

Secondary Accession Numbers

None

Natural Product Identification

Common Name

burrodin

Description

Burrodin belongs to the class of organic compounds known as ambrosanolides and secoambrosanolides. These are sesquiterpene lactones from the Ambrosia family, with a backbone derivative of azuleno[6,5-b]furan-2-one (ambrosanolides) or azuleno[4,5-b]furan-2-one (secoambrosanolides). burrodin is found in Inula hupehensis. burrodin was first documented in 1989 (PMID: 24272182). Based on a literature review very few articles have been published on burrodin.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
    3.8223   -1.2958   -1.2650 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0302   -0.5646   -0.5399 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2811    0.1247    0.7260 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2941   -0.0685    1.4734 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2152    1.0253    0.9623 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6782    1.2008   -0.3307 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5456    2.0789   -0.4754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7890    1.6543    0.0219 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8986    1.9872    1.4769 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1708    0.3155   -0.4016 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6708    0.0376   -0.3980 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2773    0.4842   -1.5718 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7997   -1.4738   -0.3848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3978   -1.9382   -0.4318 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9809   -2.9401   -0.9202 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6122   -0.8805    0.2657 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0178   -1.0108    1.7344 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8233   -1.1407    0.0838 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5764   -0.2054   -0.8050 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4943   -1.7430   -2.1828 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8454   -1.4854   -0.9759 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5346    1.6564   -0.9237 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4383    2.3580   -1.5650 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7833    3.0608    0.0205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5283    2.3662   -0.4716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5714    3.0701    1.5648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2369    1.4393    2.1414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9701    2.0317    1.8346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8824    0.2183   -1.4921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1545    0.4971    0.4943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0466   -0.1776   -2.2778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4128   -1.8519   -1.2250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2746   -1.8120    0.5801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1080   -0.9336    2.4017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8299   -0.3497    2.0197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3879   -2.0575    1.9596 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3090   -1.1838    1.0879 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0028   -2.1728   -0.3450 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3443   -0.3207   -1.8657 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8  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 19  1  0
 19 18  1  0
 18 16  1  0
 16 17  1  1
 16 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  2  0
 10  8  1  0
 19  6  1  0
 14 16  1  0
  9 26  1  0
  9 27  1  0
  9 28  1  0
  8 25  1  6
  7 23  1  0
  7 24  1  0
  6 22  1  6
  1 20  1  0
  1 21  1  0
 19 39  1  6
 18 37  1  0
 18 38  1  0
 17 34  1  0
 17 35  1  0
 17 36  1  0
 10 29  1  6
 11 30  1  1
 12 31  1  0
 13 32  1  0
 13 33  1  0
M  END


  Mrv1652309032207082D          

 19 21  0  0  1  0            999 V2000
    1.0366   -2.4968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1106   -1.6751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4893   -1.1323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3150   -1.3159    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8136   -0.3737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6352   -0.4476    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1496    0.1974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9746    0.1974    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3326    0.9407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4890   -0.4476    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3107   -0.3737    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7338    0.3346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6349   -1.1323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0136   -1.6751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0876   -2.4968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3054   -1.2519    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2684   -2.0761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5621   -1.6099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8188   -1.2519    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  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19  2  1  6  0  0  0
  6 19  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0169226

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1C[C@H]2OC(=O)C(=C)[C@H]2C[C@@]2(C)[C@H]1[C@@H](O)CC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H20O4/c1-7-4-11-9(8(2)14(18)19-11)6-15(3)12(17)5-10(16)13(7)15/h7,9-11,13,16H,2,4-6H2,1,3H3/t7-,9+,10-,11+,13+,15+/m0/s1

> <INCHI_KEY>
HSNYUOAAQCCKRP-UGKIOTTESA-N

> <FORMULA>
C15H20O4

> <MOLECULAR_WEIGHT>
264.321

> <EXACT_MASS>
264.136159124

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
27.954434268399417

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3aR,4aS,7S,7aS,8S,9aR)-7-hydroxy-4a,8-dimethyl-3-methylidene-dodecahydroazuleno[6,5-b]furan-2,5-dione

> <ALOGPS_LOGP>
0.42

> <JCHEM_LOGP>
1.8854804346666656

> <ALOGPS_LOGS>
-1.78

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.521697667521774

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.719630334733495

> <JCHEM_PKA_STRONGEST_BASIC>
-2.918091049925649

> <JCHEM_POLAR_SURFACE_AREA>
63.6

> <JCHEM_REFRACTIVITY>
68.55160000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.39e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3aR,4aS,7S,7aS,8S,9aR)-7-hydroxy-4a,8-dimethyl-3-methylidene-octahydroazuleno[6,5-b]furan-2,5-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       1.935  -4.661   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.073  -3.127   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.913  -2.114   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.588  -2.456   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       1.519  -0.698   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       3.052  -0.836   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.013   0.368   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.553   0.368   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.221   1.756   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.513  -0.836   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.047  -0.698   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.836   0.625   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       8.652  -2.114   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.492  -3.127   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       7.630  -4.661   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.170  -2.337   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.101  -3.875   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.783  -3.005   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.395  -2.337   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   19                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   16                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   10   17   18                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18    2    6                                                  
MASTER        0    0    0    0    0    0    0    0   19    0   42    0
END

View in JSmol

Synonyms

Value	Source
(3AR,4as,7S,7as,8S,9ar)-7-hydroxy-4a,8-dimethyl-3-methylene-decahydroazuleno(6,5-b)furan-2,5-dione	ChEBI
2alpha,8beta-Dihydroxy-4-oxo-10alphah-ambros-11(13)-en-12-Oic acid gamma-lactone	ChEBI
2a,8b-Dihydroxy-4-oxo-10alphah-ambros-11(13)-en-12-Oate g-lactone	Generator
2a,8b-Dihydroxy-4-oxo-10alphah-ambros-11(13)-en-12-Oic acid g-lactone	Generator
2alpha,8beta-Dihydroxy-4-oxo-10alphah-ambros-11(13)-en-12-Oate gamma-lactone	Generator
2Α,8β-dihydroxy-4-oxo-10alphah-ambros-11(13)-en-12-Oate γ-lactone	Generator
2Α,8β-dihydroxy-4-oxo-10alphah-ambros-11(13)-en-12-Oic acid γ-lactone	Generator

Chemical Formula

C₁₅H₂₀O₄

Average Mass

264.3210 Da

Monoisotopic Mass

264.13616 Da

IUPAC Name

(3aR,4aS,7S,7aS,8S,9aR)-7-hydroxy-4a,8-dimethyl-3-methylidene-dodecahydroazuleno[6,5-b]furan-2,5-dione

Traditional Name

(3aR,4aS,7S,7aS,8S,9aR)-7-hydroxy-4a,8-dimethyl-3-methylidene-octahydroazuleno[6,5-b]furan-2,5-dione

CAS Registry Number

Not Available

SMILES

C[C@H]1C[C@H]2OC(=O)C(=C)[C@H]2C[C@@]2(C)[C@H]1[C@@H](O)CC2=O

InChI Identifier

InChI=1S/C15H20O4/c1-7-4-11-9(8(2)14(18)19-11)6-15(3)12(17)5-10(16)13(7)15/h7,9-11,13,16H,2,4-6H2,1,3H3/t7-,9+,10-,11+,13+,15+/m0/s1

InChI Key

HSNYUOAAQCCKRP-UGKIOTTESA-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
Inula hupehensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ambrosanolides and secoambrosanolides. These are sesquiterpene lactones from the Ambrosia family, with a backbone derivative of azuleno[6,5-b]furan-2-one (ambrosanolides) or azuleno[4,5-b]furan-2-one (secoambrosanolides).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Ambrosanolides and secoambrosanolides

Alternative Parents

Substituents

Ambrosanolide
Pseudoguaiane sesquiterpenoid
Sesquiterpenoid
Gamma butyrolactone
Cyclic alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Carboxylic acid ester
Ketone
Lactone
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

cyclic ketone (CHEBI:69343 )
organic heterotricyclic compound (CHEBI:69343 )
secondary alcohol (CHEBI:69343 )
gamma-lactone (CHEBI:69343 )
pseudoguaianolide (CHEBI:69343 )

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	0.42	ALOGPS
logP	1.89	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	14.72	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	68.55 m³·mol⁻¹	ChemAxon
Polarizability	27.95 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

154259

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

177140

PDB ID

Not Available

ChEBI ID

69343

Good Scents ID

Not Available

References

General References

Fischer NH, Weidenhamer JD, Bradow JM: Inhibition and promotion of germination by several sesquiterpenes. J Chem Ecol. 1989 Jun;15(6):1785-93. doi: 10.1007/BF01012266. [PubMed:24272182 ]
LOTUS database [Link]

Showing NP-Card for burrodin (NP0169226)

MOL for NP0169226 (burrodin)

3D MOL for NP0169226 (burrodin)

3D SDF for NP0169226 (burrodin)

3D-SDF for NP0169226 (burrodin)

PDB for NP0169226 (burrodin)

3D PDB for NP0169226 (burrodin)

SMILES for NP0169226 (burrodin)

INCHI for NP0169226 (burrodin)

Structure for NP0169226 (burrodin)

3D Structure for NP0169226 (burrodin)