NP-MRD: Showing NP-Card for (1as,5s,6r,7r,7br)-5,6-dihydroxy-3,3,5,7b-tetramethyl-1h,1ah,2h,4h,6h,7h-cyclopropa[e]azulen-7-yl acetate (NP0215433)

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Record Information

Version

2.0

Created at

2022-09-05 15:03:34 UTC

Updated at

2022-09-05 15:03:34 UTC

NP-MRD ID

NP0215433

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1as,5s,6r,7r,7br)-5,6-dihydroxy-3,3,5,7b-tetramethyl-1h,1ah,2h,4h,6h,7h-cyclopropa[e]azulen-7-yl acetate

Description

(1AR,2R,3R,4S,7aS)-3,4-dihydroxy-1a,4,6,6-tetramethyl-1H,1aH,2H,3H,4H,5H,6H,7H,7aH-cyclopropa[e]azulen-2-yl acetate belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. (1as,5s,6r,7r,7br)-5,6-dihydroxy-3,3,5,7b-tetramethyl-1h,1ah,2h,4h,6h,7h-cyclopropa[e]azulen-7-yl acetate is found in Porella swartziana. Based on a literature review very few articles have been published on (1aR,2R,3R,4S,7aS)-3,4-dihydroxy-1a,4,6,6-tetramethyl-1H,1aH,2H,3H,4H,5H,6H,7H,7aH-cyclopropa[e]azulen-2-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
    3.6273    0.5679    2.3858 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1902    0.9227    1.0092 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6550    1.8863    0.3687 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2143    0.1304    0.4225 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7054    0.3362   -0.8550 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2070    0.5081   -0.7172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3112   -0.6976   -0.8493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7429   -1.0230   -0.6554 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1832   -0.3685    0.6422 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2831   -0.7139    1.7966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5142   -1.0901    0.9601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5350    1.0484    0.5133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5374    2.0614    0.2110 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2857    2.2705    0.9893 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3339    1.8308   -0.4893 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1514    2.8715   -1.5126 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6752   -1.7183   -1.2154 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1778   -2.6610   -2.2900 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0869   -2.5128   -0.1453 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8617   -0.9175   -1.6641 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0473   -1.5424   -1.2407 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3839    1.2853    2.7630 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0058   -0.4689    2.3498 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7101    0.5452    3.0348 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1416    1.2005   -1.3935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9098   -2.1129   -0.5559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3896   -0.6465   -1.4539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5648   -1.7117    2.2498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2280   -0.7930    1.5471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5100    0.0185    2.6137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4391   -2.1629    0.6906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7853   -0.9336    2.0256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3233   -0.6424    0.3243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0634    1.3488    1.4699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3640    1.1140   -0.2554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0507    3.0587    0.0046 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0868    1.5741    1.7325 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1390    3.3074    1.1362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5855    3.7100   -1.5401 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1605    2.3659   -2.4834 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1260    3.2966   -1.2071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1694   -3.6293   -1.8570 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0376   -2.9236   -2.9465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6473   -2.2362   -2.8767 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4717   -3.2910   -0.0033 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8919   -0.7471   -2.7548 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0026   -1.7147   -0.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5 20  1  0
 20 21  1  0
 20 17  1  0
 17 18  1  0
 17 19  1  1
 17  7  1  0
  7  6  2  0
  6 15  1  0
 15 16  1  6
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12  9  1  0
  9 10  1  0
  9 11  1  0
  9  8  1  0
  6  5  1  0
 13 15  1  0
  8  7  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  5 25  1  6
 20 46  1  6
 21 47  1  0
 18 42  1  0
 18 43  1  0
 18 44  1  0
 19 45  1  0
 16 39  1  0
 16 40  1  0
 16 41  1  0
 14 37  1  0
 14 38  1  0
 13 36  1  6
 12 34  1  0
 12 35  1  0
 10 28  1  0
 10 29  1  0
 10 30  1  0
 11 31  1  0
 11 32  1  0
 11 33  1  0
  8 26  1  0
  8 27  1  0
M  END


  Mrv1652309052217032D          

 21 23  0  0  1  0            999 V2000
    3.8169    2.7926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0251    1.9943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8205    1.7754    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4378    1.4149    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6460    0.6166    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1225   -0.0210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5671   -0.7159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3011   -1.4969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5246   -1.7758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9693   -2.4707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9461   -2.3639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8225   -1.3426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7234   -0.5236    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5033    0.2715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3019    0.0646    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4486    0.8764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3654   -0.5078    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4890   -1.3235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1896   -0.4702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4142    0.3158    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1091    0.7604    0.0000 O   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
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  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
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
  6 15  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
  7 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  1  0  0  0
 17 20  1  0  0  0  0
  5 20  1  0  0  0  0
 20 21  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0215433

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1[C@@H](O)[C@@](C)(O)C2=C1[C@]1(C)C[C@@H]1CC(C)(C)C2

> <INCHI_IDENTIFIER>
InChI=1S/C17H26O4/c1-9(18)21-13-12-11(17(5,20)14(13)19)8-15(2,3)6-10-7-16(10,12)4/h10,13-14,19-20H,6-8H2,1-5H3/t10-,13+,14+,16+,17-/m0/s1

> <INCHI_KEY>
KPVVUSNUSZMDQB-OHGMZSHCSA-N

> <FORMULA>
C17H26O4

> <MOLECULAR_WEIGHT>
294.391

> <EXACT_MASS>
294.183109317

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
32.372082411363756

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1aR,2R,3R,4S,7aS)-3,4-dihydroxy-1a,4,6,6-tetramethyl-1H,1aH,2H,3H,4H,5H,6H,7H,7aH-cyclopropa[e]azulen-2-yl acetate

> <JCHEM_LOGP>
1.267472522999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.302590812397565

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.780423081438524

> <JCHEM_PKA_STRONGEST_BASIC>
-3.508830273761852

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
78.75340000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1aR,2R,3R,4S,7aS)-3,4-dihydroxy-1a,4,6,6-tetramethyl-1H,2H,3H,5H,7H,7aH-cyclopropa[e]azulen-2-yl acetate

> <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       7.125   5.213   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.513   3.723   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       8.998   3.314   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.417   2.641   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.806   1.151   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.829  -0.039   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.659  -1.336   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.162  -2.794   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.713  -3.315   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.543  -4.612   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.633  -4.413   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.402  -2.506   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.217  -0.977   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.806   0.507   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.297   0.121   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.571   1.636   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.149  -0.948   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.379  -2.471   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.687  -0.878   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.240   0.589   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.537   1.419   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   20                                                  
CONECT    6    5    7   15                                                  
CONECT    7    6    8   17                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11   12                                             
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    9   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13   15                                                       
CONECT   15   14    6   13   16                                             
CONECT   16   15                                                            
CONECT   17    7   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   17    5   21                                                  
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Value	Source
(1AR,2R,3R,4S,7as)-3,4-dihydroxy-1a,4,6,6-tetramethyl-1H,1ah,2H,3H,4H,5H,6H,7H,7ah-cyclopropa[e]azulen-2-yl acetic acid	Generator

Chemical Formula

C₁₇H₂₆O₄

Average Mass

294.3910 Da

Monoisotopic Mass

294.18311 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1[C@@H](O)[C@@](C)(O)C2=C1[C@]1(C)C[C@@H]1CC(C)(C)C2

InChI Identifier

InChI=1S/C17H26O4/c1-9(18)21-13-12-11(17(5,20)14(13)19)8-15(2,3)6-10-7-16(10,12)4/h10,13-14,19-20H,6-8H2,1-5H3/t10-,13+,14+,16+,17-/m0/s1

InChI Key

KPVVUSNUSZMDQB-OHGMZSHCSA-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
Porella swartziana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Africanane sesquiterpenoid
Sesquiterpenoid
Tertiary alcohol
Secondary alcohol
Carboxylic acid ester
1,2-diol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	1.27	ChemAxon
pKa (Strongest Acidic)	12.78	ChemAxon

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PubChem Compound

162849132

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References

General References

LOTUS database [Link]

Showing NP-Card for (1as,5s,6r,7r,7br)-5,6-dihydroxy-3,3,5,7b-tetramethyl-1h,1ah,2h,4h,6h,7h-cyclopropa[e]azulen-7-yl acetate (NP0215433)

MOL for NP0215433 ((1as,5s,6r,7r,7br)-5,6-dihydroxy-3,3,5,7b-tetramethyl-1h,1ah,2h,4h,6h,7h-cyclopropa[e]azulen-7-yl acetate)

3D MOL for NP0215433 ((1as,5s,6r,7r,7br)-5,6-dihydroxy-3,3,5,7b-tetramethyl-1h,1ah,2h,4h,6h,7h-cyclopropa[e]azulen-7-yl acetate)

3D SDF for NP0215433 ((1as,5s,6r,7r,7br)-5,6-dihydroxy-3,3,5,7b-tetramethyl-1h,1ah,2h,4h,6h,7h-cyclopropa[e]azulen-7-yl acetate)

3D-SDF for NP0215433 ((1as,5s,6r,7r,7br)-5,6-dihydroxy-3,3,5,7b-tetramethyl-1h,1ah,2h,4h,6h,7h-cyclopropa[e]azulen-7-yl acetate)

PDB for NP0215433 ((1as,5s,6r,7r,7br)-5,6-dihydroxy-3,3,5,7b-tetramethyl-1h,1ah,2h,4h,6h,7h-cyclopropa[e]azulen-7-yl acetate)

3D PDB for NP0215433 ((1as,5s,6r,7r,7br)-5,6-dihydroxy-3,3,5,7b-tetramethyl-1h,1ah,2h,4h,6h,7h-cyclopropa[e]azulen-7-yl acetate)

SMILES for NP0215433 ((1as,5s,6r,7r,7br)-5,6-dihydroxy-3,3,5,7b-tetramethyl-1h,1ah,2h,4h,6h,7h-cyclopropa[e]azulen-7-yl acetate)

INCHI for NP0215433 ((1as,5s,6r,7r,7br)-5,6-dihydroxy-3,3,5,7b-tetramethyl-1h,1ah,2h,4h,6h,7h-cyclopropa[e]azulen-7-yl acetate)

Structure for NP0215433 ((1as,5s,6r,7r,7br)-5,6-dihydroxy-3,3,5,7b-tetramethyl-1h,1ah,2h,4h,6h,7h-cyclopropa[e]azulen-7-yl acetate)

3D Structure for NP0215433 ((1as,5s,6r,7r,7br)-5,6-dihydroxy-3,3,5,7b-tetramethyl-1h,1ah,2h,4h,6h,7h-cyclopropa[e]azulen-7-yl acetate)