NP-MRD: Showing NP-Card for (3ar,4s,6r,6ar,9ar,9br)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl acetate (NP0176943)

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Record Information

Version

2.0

Created at

2022-09-03 14:41:35 UTC

Updated at

2022-09-03 14:41:35 UTC

NP-MRD ID

NP0176943

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3ar,4s,6r,6ar,9ar,9br)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl acetate

Description

Cumambrin A 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. (3ar,4s,6r,6ar,9ar,9br)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl acetate is found in Ambrosia cumanensis, Anthemis carpatica, Artemisia cana, Artemisia tripartita, Glebionis coronaria, Chrysanthemum indicum, Chrysanthemum ornatum, Chrysanthemum lavandulifolium, Handelia trichophylla, Leucanthemopsis pallida, Plagius grandis, Polychrysum tadshikorum, Richteria pyrethroides, Tanacetum densum and Tanacetum santolina. (3ar,4s,6r,6ar,9ar,9br)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl acetate was first documented in 2013 (PMID: 23662902). Based on a literature review a small amount of articles have been published on cumambrin A (PMID: 26600718) (PMID: 30807230).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 46  0  0  0  0  0  0  0  0999 V2000
    2.5986    2.4819    0.4128 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4218    2.1392   -0.0764 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6232    2.9975   -0.9543 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9296    3.9817   -1.6476 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6882    2.4830   -0.8870 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5971    1.1027   -0.6302 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6908    0.8775    0.1537 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3685   -0.2692   -0.4942 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5419   -0.6085    0.2069 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8077   -0.5576   -0.3756 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0415   -0.9214    0.3843 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8467   -0.1865   -1.5802 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4671   -1.4632   -0.7042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5724   -1.6528    0.3243 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9770   -3.1399    0.2567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1104   -1.4791    1.6310 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8431   -0.8996    0.1796 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5994   -1.1711   -1.0839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4929    0.0133   -1.1682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0037    1.0120   -0.4471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6166    2.3711   -0.2809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7211    0.5929    0.1984 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0328    3.4407    0.1760 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1760    1.8435    1.0633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6004    0.5343   -1.5968 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4870    0.7432    1.2333 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6659    0.0391   -1.5234 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3336   -0.1192    1.1018 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8721   -0.9677   -0.3680 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9433   -1.9094    0.8758 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491   -2.3634   -0.6771 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0007   -1.4881   -1.7037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1610   -3.7784    0.6409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1130   -3.3542   -0.8246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9479   -3.3095    0.7388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9093   -1.6619    2.2173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5026   -1.1876    1.0274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9966   -1.2067   -1.9905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1651   -2.1140   -0.9454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4100    0.0683   -1.7302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4255    2.6837    0.7570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7015    2.3131   -0.4339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1729    3.0725   -1.0114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6703    1.0178    1.2298 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 10  1  0
 10 12  2  0
 10  9  1  0
  9  8  1  0
  8 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  1
 14 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 20 22  1  0
 22  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  2  3
  2  7  1  0
  7  8  1  0
 22 17  1  0
  7  6  1  0
 11 28  1  0
 11 29  1  0
 11 30  1  0
  8 27  1  6
 13 31  1  0
 13 32  1  0
 15 33  1  0
 15 34  1  0
 15 35  1  0
 16 36  1  0
 17 37  1  1
 18 38  1  0
 18 39  1  0
 19 40  1  0
 21 41  1  0
 21 42  1  0
 21 43  1  0
 22 44  1  1
  6 25  1  6
  1 23  1  0
  1 24  1  0
  7 26  1  1
M  END


  Mrv1652309032216412D          

 22 24  0  0  1  0            999 V2000
    5.6412   -1.0466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9527   -0.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9157    0.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5607    0.7464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1204    0.4515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6659   -0.2370    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1803   -0.8820    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9967   -1.6863    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6417   -2.2007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5188   -3.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1638   -3.5308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7508   -3.3179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2534   -2.0443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5101   -1.6863    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3265   -2.4906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6851   -1.6863    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3265   -0.8820    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5541   -0.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5912    0.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3864    0.4515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6763    1.2239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8409   -0.2370    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  2  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  1  0  0  0
 14 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 22 20  1  6  0  0  0
  6 22  1  0  0  0  0
 17 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0176943

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C17H22O5/c1-8-5-6-11-13(8)15-14(9(2)16(19)22-15)12(21-10(3)18)7-17(11,4)20/h5,11-15,20H,2,6-7H2,1,3-4H3/t11-,12+,13+,14-,15-,17-/m1/s1

> <INCHI_KEY>
XMJROHDIQQOWTO-NRPXGKOBSA-N

> <FORMULA>
C17H22O5

> <MOLECULAR_WEIGHT>
306.358

> <EXACT_MASS>
306.146723808

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
32.20326260637189

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3aR,4S,6R,6aR,9aR,9bR)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-2H,3H,3aH,4H,5H,6H,6aH,7H,9aH,9bH-azuleno[4,5-b]furan-4-yl acetate

> <JCHEM_LOGP>
1.0729297373333337

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.669974721206124

> <JCHEM_PKA_STRONGEST_BASIC>
-2.943153056944441

> <JCHEM_POLAR_SURFACE_AREA>
72.83

> <JCHEM_REFRACTIVITY>
79.6271

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3aR,4S,6R,6aR,9aR,9bR)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-3aH,4H,5H,6aH,7H,9aH,9bH-azuleno[4,5-b]furan-4-yl acetate

> <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      10.530  -1.954   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.245  -1.105   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.176   0.433   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      10.380   1.393   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       7.691   0.843   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       6.843  -0.442   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.803  -1.646   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.461  -3.148   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.665  -4.108   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       8.435  -5.631   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.639  -6.591   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       7.001  -6.193   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.073  -3.816   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.686  -3.148   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.343  -4.649   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       3.146  -3.148   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.343  -1.646   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.901  -1.105   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.970   0.433   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.455   0.843   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.996   2.285   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.303  -0.442   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   22                                                  
CONECT    7    6    2    8                                                  
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    8   14                                                       
CONECT   14   13   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   14   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20    6   17                                                  
MASTER        0    0    0    0    0    0    0    0   22    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₂₂O₅

Average Mass

306.3580 Da

Monoisotopic Mass

306.14672 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C17H22O5/c1-8-5-6-11-13(8)15-14(9(2)16(19)22-15)12(21-10(3)18)7-17(11,4)20/h5,11-15,20H,2,6-7H2,1,3-4H3/t11-,12+,13+,14-,15-,17-/m1/s1

InChI Key

XMJROHDIQQOWTO-NRPXGKOBSA-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
Ambrosia cumanensis	LOTUS Database	35616633
Anthemis carpatica	LOTUS Database	35616633
Artemisia cana	LOTUS Database	35616633
Artemisia tripartita	LOTUS Database	35616633
Chrysanthemum coronarium	LOTUS Database	35616633
Chrysanthemum indicum	LOTUS Database	35616633
Chrysanthemum ornatum	LOTUS Database	35616633
Dendranthema lavandulifolium	LOTUS Database	35616633
Handelia trichophylla	LOTUS Database	35616633
Leucanthemopsis pallida	LOTUS Database	35616633
Plagius grandis	LOTUS Database	35616633
Polychrysum tadshikorum	LOTUS Database	35616633
Pyrethrum pyrethroides	LOTUS Database	35616633
Tanacetum densum	LOTUS Database	35616633
Tanacetum santolina	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
Dicarboxylic acid or derivatives
Gamma butyrolactone
Cyclic alcohol
Tertiary alcohol
Tetrahydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
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	1.07	ChemAxon
pKa (Strongest Acidic)	14.67	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00020478

Chemspider ID

152487

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

174867

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Fu L, Wang P, Sun Y, Wang Y, Zhao J, Ye Y, Zhang Y, Bi Y: High performance liquid chromatography time of flight electrospray ionization mass spectrometry for quantification of sesquiterpenes in Chrysanthemi indici Flos active extract. Pharmacogn Mag. 2015 Oct-Dec;11(44):740-4. doi: 10.4103/0973-1296.165574. [PubMed:26600718 ]
Zhou L, Liu Q, Hong G, Song F, Zhao J, Yuan J, Xu J, Tan RX, Tickner J, Gu Q, Xu J: Cumambrin A prevents OVX-induced osteoporosis via the inhibition of osteoclastogenesis, bone resorption, and RANKL signaling pathways. FASEB J. 2019 Jun;33(6):6726-6735. doi: 10.1096/fj.201800883RRR. Epub 2019 Feb 26. [PubMed:30807230 ]
Wen B, Hexum JK, Widen JC, Harki DA, Brummond KM: A redox economical synthesis of bioactive 6,12-guaianolides. Org Lett. 2013 Jun 7;15(11):2644-7. doi: 10.1021/ol400904y. Epub 2013 May 10. [PubMed:23662902 ]
LOTUS database [Link]

Showing NP-Card for (3ar,4s,6r,6ar,9ar,9br)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl acetate (NP0176943)

MOL for NP0176943 ((3ar,4s,6r,6ar,9ar,9br)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl acetate)

3D MOL for NP0176943 ((3ar,4s,6r,6ar,9ar,9br)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl acetate)

3D SDF for NP0176943 ((3ar,4s,6r,6ar,9ar,9br)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl acetate)

3D-SDF for NP0176943 ((3ar,4s,6r,6ar,9ar,9br)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl acetate)

PDB for NP0176943 ((3ar,4s,6r,6ar,9ar,9br)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl acetate)

3D PDB for NP0176943 ((3ar,4s,6r,6ar,9ar,9br)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl acetate)

SMILES for NP0176943 ((3ar,4s,6r,6ar,9ar,9br)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl acetate)

INCHI for NP0176943 ((3ar,4s,6r,6ar,9ar,9br)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl acetate)

Structure for NP0176943 ((3ar,4s,6r,6ar,9ar,9br)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl acetate)

3D Structure for NP0176943 ((3ar,4s,6r,6ar,9ar,9br)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl acetate)