NP-MRD: Showing NP-Card for (1s,3s,3ar,5s,7ar)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-3a-propanoyl-hexahydro-1h-inden-4-one (NP0179853)

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Record Information

Version

2.0

Created at

2022-09-03 18:07:01 UTC

Updated at

2022-09-03 18:07:01 UTC

NP-MRD ID

NP0179853

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3s,3ar,5s,7ar)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-3a-propanoyl-hexahydro-1h-inden-4-one

Description

Elisabethin C belongs to the class of organic compounds known as elisabethane diterpenoids. These are diterpenoids with a structure based on the elisabethane skeleton, a tricyclic serrulatane derivative that is formed by connecting the C1 and C9 atom of serrulatane. This class of compounds also includes seco-elisabethane derivatives, nor-elisabethanes (resulting from the loss of one carbon atom), and bisnor-elisabethanes (resulting from the loss of two carbon atoms). (1s,3s,3ar,5s,7ar)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-3a-propanoyl-hexahydro-1h-inden-4-one is found in Antillogorgia elisabethae. (1s,3s,3ar,5s,7ar)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-3a-propanoyl-hexahydro-1h-inden-4-one was first documented in 2008 (PMID: 19148263). Based on a literature review very few articles have been published on Elisabethin C.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 48 49  0  0  0  0  0  0  0  0999 V2000
   -1.4470    3.4271   -1.0662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6121    2.0122   -0.5559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2865    1.3498   -0.4095 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7097    1.9868   -0.7015 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2870   -0.0387    0.0828 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9394   -0.0436    1.3993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5982    0.7863    2.2148 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9975   -0.9997    1.8101 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9322   -0.4225    2.8322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8267   -1.3664    0.5918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8804   -1.9368   -0.4188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9183   -0.9228   -0.9377 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2088   -1.7185   -1.6144 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0450   -1.8379   -3.0840 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4402   -0.8294   -1.2407 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1054   -0.6404    0.2017 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9875    0.0314    1.0911 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1513    0.5560    0.8767 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8615    0.5738   -0.4111 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9212    1.2363    2.0181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2897    4.1574   -0.2377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3272    3.7110   -1.7041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5576    3.4399   -1.7596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2809    1.4863   -1.2735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1258    2.1052    0.4425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5397   -1.9251    2.2144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4793   -1.2693    3.3004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7127    0.2054    2.3222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4142    0.1405    3.6273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5794   -2.1083    0.8794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2794   -0.4521    0.1588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3615   -2.7997    0.0669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4858   -2.2943   -1.2997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4572   -0.3215   -1.7104 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3977   -2.6698   -1.0824 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5029   -1.0114   -3.6643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0366   -1.9109   -3.3414 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5066   -2.7765   -3.4485 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3370   -1.4100   -1.4548 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3011    0.0710   -1.8802 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8787   -1.6988    0.5913 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6324    0.1315    2.1636 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7813    1.2269   -0.3723 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2409    1.0365   -1.1859 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2795   -0.4289   -0.6828 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9154    0.7435    2.0322 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3651    1.1533    2.9505 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0827    2.2651    1.6694 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  5  3  1  6
  5 16  1  0
 16 15  1  0
 15 13  1  0
 13 14  1  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  8  1  0
  8  9  1  0
  8  6  1  0
  6  7  2  0
 16 17  1  0
 17 18  2  3
 18 19  1  0
 18 20  1  0
 12  5  1  0
  6  5  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  2 24  1  0
  2 25  1  0
 16 41  1  1
 15 39  1  0
 15 40  1  0
 13 35  1  1
 14 36  1  0
 14 37  1  0
 14 38  1  0
 12 34  1  6
 11 32  1  0
 11 33  1  0
 10 30  1  0
 10 31  1  0
  8 26  1  1
  9 27  1  0
  9 28  1  0
  9 29  1  0
 17 42  1  0
 19 43  1  0
 19 44  1  0
 19 45  1  0
 20 46  1  0
 20 47  1  0
 20 48  1  0
M  END


  Mrv1652309032220072D          

 20 21  0  0  1  0            999 V2000
    1.6533    1.8805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4818    1.0736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0949    0.5215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8795    0.7765    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3053    0.6120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0668    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8838    0.7541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768    0.9256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4752    0.3126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781    1.7103    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  2  0  0  0  0
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  6  0  0  0
  5 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
  5 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0179853

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C18H28O2/c1-6-16(19)18-14(9-11(2)3)10-13(5)15(18)8-7-12(4)17(18)20/h9,12-15H,6-8,10H2,1-5H3/t12-,13-,14+,15+,18-/m0/s1

> <INCHI_KEY>
MPZCKSXAXSTSKM-YPIIOCQESA-N

> <FORMULA>
C18H28O2

> <MOLECULAR_WEIGHT>
276.42

> <EXACT_MASS>
276.208930142

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
32.51990030626757

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,3S,3aR,5S,7aR)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-3a-propanoyl-octahydro-1H-inden-4-one

> <JCHEM_LOGP>
4.964512088333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.13192076622575

> <JCHEM_PKA_STRONGEST_BASIC>
-7.361069459581838

> <JCHEM_POLAR_SURFACE_AREA>
34.14

> <JCHEM_REFRACTIVITY>
82.8378

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3S,3aR,5S,7aR)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-3a-propanoyl-hexahydro-1H-inden-4-one

> <JCHEM_VEBER_RULE>
1

$$$$

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       3.086   3.510   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.766   2.004   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.910   0.974   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       5.375   1.449   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       6.170   1.142   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.591   0.237   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.650  -4.013   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.126  -0.057   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.650   1.408   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.143   1.728   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.887   0.583   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.333   3.192   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   12   16                                             
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    5   13                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15    5   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   42    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₈O₂

Average Mass

276.4200 Da

Monoisotopic Mass

276.20893 Da

IUPAC Name

(1S,3S,3aR,5S,7aR)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-3a-propanoyl-octahydro-1H-inden-4-one

Traditional Name

(1S,3S,3aR,5S,7aR)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-3a-propanoyl-hexahydro-1H-inden-4-one

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C18H28O2/c1-6-16(19)18-14(9-11(2)3)10-13(5)15(18)8-7-12(4)17(18)20/h9,12-15H,6-8,10H2,1-5H3/t12-,13-,14+,15+,18-/m0/s1

InChI Key

MPZCKSXAXSTSKM-YPIIOCQESA-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
Antillogorgia elisabethae	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as elisabethane diterpenoids. These are diterpenoids with a structure based on the elisabethane skeleton, a tricyclic serrulatane derivative that is formed by connecting the C1 and C9 atom of serrulatane. This class of compounds also includes seco-elisabethane derivatives, nor-elisabethanes (resulting from the loss of one carbon atom), and bisnor-elisabethanes (resulting from the loss of two carbon atoms).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Elisabethane diterpenoids

Alternative Parents

Substituents

Elisabethane diterpenoid
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	4.96	ChemAxon
pKa (Strongest Acidic)	19.13	ChemAxon
pKa (Strongest Basic)	-7.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	34.14 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	82.84 m³·mol⁻¹	ChemAxon
Polarizability	32.52 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

358365

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

404630

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Manning JR, Davies HM: Efficient route to 4H-1,3-oxazines through ring expansion of isoxazoles by rhodium carbenoids. Tetrahedron. 2008 Jan 14;64(29):6901-6908. doi: 10.1016/j.tet.2008.03.010. [PubMed:19148263 ]
LOTUS database [Link]

Showing NP-Card for (1s,3s,3ar,5s,7ar)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-3a-propanoyl-hexahydro-1h-inden-4-one (NP0179853)

MOL for NP0179853 ((1s,3s,3ar,5s,7ar)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-3a-propanoyl-hexahydro-1h-inden-4-one)

3D MOL for NP0179853 ((1s,3s,3ar,5s,7ar)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-3a-propanoyl-hexahydro-1h-inden-4-one)

3D SDF for NP0179853 ((1s,3s,3ar,5s,7ar)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-3a-propanoyl-hexahydro-1h-inden-4-one)

3D-SDF for NP0179853 ((1s,3s,3ar,5s,7ar)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-3a-propanoyl-hexahydro-1h-inden-4-one)

PDB for NP0179853 ((1s,3s,3ar,5s,7ar)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-3a-propanoyl-hexahydro-1h-inden-4-one)

3D PDB for NP0179853 ((1s,3s,3ar,5s,7ar)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-3a-propanoyl-hexahydro-1h-inden-4-one)

SMILES for NP0179853 ((1s,3s,3ar,5s,7ar)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-3a-propanoyl-hexahydro-1h-inden-4-one)

INCHI for NP0179853 ((1s,3s,3ar,5s,7ar)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-3a-propanoyl-hexahydro-1h-inden-4-one)

Structure for NP0179853 ((1s,3s,3ar,5s,7ar)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-3a-propanoyl-hexahydro-1h-inden-4-one)

3D Structure for NP0179853 ((1s,3s,3ar,5s,7ar)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-3a-propanoyl-hexahydro-1h-inden-4-one)