NP-MRD: Showing NP-Card for 6beta-Isobutyroyloxy-10alphaH-9-oxofuranoeremophilane (NP0061786)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 06:30:25 UTC

Updated at

2022-04-28 06:30:25 UTC

NP-MRD ID

NP0061786

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6beta-Isobutyroyloxy-10alphaH-9-oxofuranoeremophilane

Description

(4S,4aR,5S,8aR)-3,4a,5-trimethyl-9-oxo-4,4a,5,6,7,8,8a,9-octahydronaphtho[2,3-b]furan-4-yl isobutyrate belongs to the class of organic compounds known as eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids. These are sesquiterpenoids with a structure based either on the eremophilane skeleton, its 8,9-seco derivative, or the furoeremophilane skeleton. Eremophilanes have been shown to be derived from eudesmanes by migration of the methyl group at C-10 to C-5. 6beta-Isobutyroyloxy-10alphaH-9-oxofuranoeremophilane is found in Pittocaulon praecox, Jacobaea auricula, Senecio rosmarinifolius and Senecio umbellatus. Based on a literature review very few articles have been published on (4S,4aR,5S,8aR)-3,4a,5-trimethyl-9-oxo-4,4a,5,6,7,8,8a,9-octahydronaphtho[2,3-b]furan-4-yl isobutyrate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 49 51  0  0  0  0  0  0  0  0999 V2000
    1.3600    3.4425   -1.3602 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4985    3.2728   -0.1835 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1234    4.2818    0.6768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6432    3.7626    1.6054 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7814    2.4496    1.3804 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0822    2.0851    0.2649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0403    0.6948   -0.2248 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2555    0.2066    0.1304 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2260   -0.0983   -0.7705 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9895    0.0507   -1.9935 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5393   -0.5984   -0.2946 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4190   -0.8537   -1.4862 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3635   -1.9408    0.4164 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0803   -0.2268    0.2708 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3830   -1.4510    0.8931 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9238   -0.8309   -0.8561 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3364   -2.1133   -1.3887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3417   -1.0752   -0.4668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5641   -1.5451    0.9356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8128   -0.7386    1.9733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0855    0.3484    1.2264 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5133    1.4009    2.0866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6133    1.4487    3.3380 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4461    3.4670   -1.1038 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2045    2.6823   -2.1466 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1503    4.4685   -1.7801 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3799    5.3298    0.6472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1036    0.7761   -1.3582 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0109    0.0827    0.4450 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9594   -1.8191   -1.4333 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8373   -0.8822   -2.4491 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1837   -0.0284   -1.5241 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8190   -1.7169    1.3582 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6691   -2.5290   -0.2383 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3151   -2.4451    0.5759 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0339   -1.0937    1.8771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0429   -2.2998    1.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4816   -1.6771    0.2584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9002   -0.0919   -1.6839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6159   -3.0055   -0.8075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2515   -2.0404   -1.6073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8154   -2.2652   -2.4014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0149   -0.2053   -0.7264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7301   -1.9004   -1.1358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6655   -1.3924    1.1444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4143   -2.6351    1.0379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1336   -1.3627    2.5836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5006   -0.2392    2.6872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8757    0.8505    0.5921 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  1  0
 11 13  1  0
 11  9  1  0
  9 10  2  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  2  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  5 22  1  0
 22 23  2  0
 22 21  1  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18 16  1  0
 16 17  1  0
 16 14  1  0
 14 15  1  1
 14  7  1  0
  2  6  1  0
 14 21  1  0
 12 30  1  0
 12 31  1  0
 12 32  1  0
 11 29  1  1
 13 33  1  0
 13 34  1  0
 13 35  1  0
  7 28  1  6
  3 27  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
 21 49  1  6
 20 47  1  0
 20 48  1  0
 19 45  1  0
 19 46  1  0
 18 43  1  0
 18 44  1  0
 16 39  1  6
 17 40  1  0
 17 41  1  0
 17 42  1  0
 15 36  1  0
 15 37  1  0
 15 38  1  0
M  END


  Mrv1652304282208302D          

 23 25  0  0  1  0            999 V2000
    4.7812    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0668    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6378    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089    4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    2.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
  4 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 10 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
  9 20  1  0  0  0  0
 18 21  1  0  0  0  0
  4 22  1  1  0  0  0
  3 23  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0061786

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C(=O)O[C@@H]1C2=C(OC=C2C)C(=O)[C@@H]2CCC[C@H](C)[C@@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C19H26O4/c1-10(2)18(21)23-17-14-11(3)9-22-16(14)15(20)13-8-6-7-12(4)19(13,17)5/h9-10,12-13,17H,6-8H2,1-5H3/t12-,13-,17+,19+/m0/s1

> <INCHI_KEY>
QCRWAFVWZAWSSH-CLKWJJAWSA-N

> <FORMULA>
C19H26O4

> <MOLECULAR_WEIGHT>
318.413

> <EXACT_MASS>
318.183109317

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
35.05140943714831

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4S,4aR,5S,8aR)-3,4a,5-trimethyl-9-oxo-4H,4aH,5H,6H,7H,8H,8aH,9H-naphtho[2,3-b]furan-4-yl 2-methylpropanoate

> <ALOGPS_LOGP>
3.98

> <JCHEM_LOGP>
4.307019648666666

> <ALOGPS_LOGS>
-4.16

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.645538215553895

> <JCHEM_PKA_STRONGEST_BASIC>
-2.946859052978433

> <JCHEM_POLAR_SURFACE_AREA>
56.510000000000005

> <JCHEM_REFRACTIVITY>
87.0198

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.20e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4S,4aR,5S,8aR)-3,4a,5-trimethyl-9-oxo-4H,5H,6H,7H,8H,8aH-naphtho[2,3-b]furan-4-yl 2-methylpropanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       8.925   2.073   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.925   3.613   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.591   4.383   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.591   1.303   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.924  -0.237   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.924   5.923   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       3.590   6.693   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.257   5.923   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.590   8.233   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.257   9.003   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.924   9.003   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.126   4.089   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.126   1.597   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.650   5.553   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.258   5.153   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.591   5.923   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   23                                                  
CONECT    4    3    5   11   22                                             
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   20                                                  
CONECT   10    9   11   18                                                  
CONECT   11   10    4   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   10   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19    9                                                       
CONECT   21   18                                                            
CONECT   22    4                                                            
CONECT   23    3                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Value	Source
(4S,4AR,5S,8ar)-3,4a,5-trimethyl-9-oxo-4,4a,5,6,7,8,8a,9-octahydronaphtho[2,3-b]furan-4-yl isobutyric acid	Generator

Chemical Formula

C₁₉H₂₆O₄

Average Mass

318.4130 Da

Monoisotopic Mass

318.18311 Da

IUPAC Name

(4S,4aR,5S,8aR)-3,4a,5-trimethyl-9-oxo-4H,4aH,5H,6H,7H,8H,8aH,9H-naphtho[2,3-b]furan-4-yl 2-methylpropanoate

Traditional Name

(4S,4aR,5S,8aR)-3,4a,5-trimethyl-9-oxo-4H,5H,6H,7H,8H,8aH-naphtho[2,3-b]furan-4-yl 2-methylpropanoate

CAS Registry Number

Not Available

SMILES

CC(C)C(=O)O[C@@H]1C2=C(OC=C2C)C(=O)[C@@H]2CCC[C@H](C)[C@@]12C

InChI Identifier

InChI=1S/C19H26O4/c1-10(2)18(21)23-17-14-11(3)9-22-16(14)15(20)13-8-6-7-12(4)19(13,17)5/h9-10,12-13,17H,6-8H2,1-5H3/t12-,13-,17+,19+/m0/s1

InChI Key

QCRWAFVWZAWSSH-CLKWJJAWSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Pittocaulon praecox	LOTUS Database	35616633
Senecio auricula	LOTUS Database	35616633
Senecio rosmarinifolius	LOTUS Database	35616633
Senecio umbellatus	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids. These are sesquiterpenoids with a structure based either on the eremophilane skeleton, its 8,9-seco derivative, or the furoeremophilane skeleton. Eremophilanes have been shown to be derived from eudesmanes by migration of the methyl group at C-10 to C-5.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids

Alternative Parents

Substituents

Furoeremophilane sesquiterpenoid
Naphthofuran
Benzofuran
Aryl alkyl ketone
Aryl ketone
Furan
Heteroaromatic compound
Carboxylic acid ester
Ketone
Carboxylic acid derivative
Oxacycle
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

sesquiterpenoid (CHEBI:69894 )

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	3.98	ALOGPS
logP	4.31	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	14.65	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	56.51 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	87.02 m³·mol⁻¹	ChemAxon
Polarizability	35.05 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

35518327

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

70698241

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 6beta-Isobutyroyloxy-10alphaH-9-oxofuranoeremophilane (NP0061786)

MOL for NP0061786 (6beta-Isobutyroyloxy-10alphaH-9-oxofuranoeremophilane)

3D MOL for NP0061786 (6beta-Isobutyroyloxy-10alphaH-9-oxofuranoeremophilane)

3D SDF for NP0061786 (6beta-Isobutyroyloxy-10alphaH-9-oxofuranoeremophilane)

3D-SDF for NP0061786 (6beta-Isobutyroyloxy-10alphaH-9-oxofuranoeremophilane)

PDB for NP0061786 (6beta-Isobutyroyloxy-10alphaH-9-oxofuranoeremophilane)

3D PDB for NP0061786 (6beta-Isobutyroyloxy-10alphaH-9-oxofuranoeremophilane)

SMILES for NP0061786 (6beta-Isobutyroyloxy-10alphaH-9-oxofuranoeremophilane)

INCHI for NP0061786 (6beta-Isobutyroyloxy-10alphaH-9-oxofuranoeremophilane)

Structure for NP0061786 (6beta-Isobutyroyloxy-10alphaH-9-oxofuranoeremophilane)

3D Structure for NP0061786 (6beta-Isobutyroyloxy-10alphaH-9-oxofuranoeremophilane)