NP-MRD: Showing NP-Card for n'-{7-isopropyl-2,10-dimethylspiro[4.5]dec-1-en-6-yl}-n,n-dimethylcarbamimidothioic acid (NP0197801)

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Record Information

Version

2.0

Created at

2022-09-04 16:07:47 UTC

Updated at

2022-09-04 16:07:47 UTC

NP-MRD ID

NP0197801

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n'-{7-isopropyl-2,10-dimethylspiro[4.5]dec-1-en-6-yl}-n,n-dimethylcarbamimidothioic acid

Description

N'-[2,10-dimethyl-7-(propan-2-yl)spiro[4.5]Dec-1-en-6-yl]-N,N-dimethylcarbamimidothioic acid belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. n'-{7-isopropyl-2,10-dimethylspiro[4.5]dec-1-en-6-yl}-n,n-dimethylcarbamimidothioic acid is found in Axinella cannabina. Based on a literature review very few articles have been published on N'-[2,10-dimethyl-7-(propan-2-yl)spiro[4.5]Dec-1-en-6-yl]-N,N-dimethylcarbamimidothioic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 53 54  0  0  0  0  0  0  0  0999 V2000
   -0.9217    4.4400   -0.1188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5884    3.0478   -0.6127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9781    1.9044   -0.1036 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4204    0.7931   -0.9014 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6487    1.3936   -1.7308 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2580    2.8345   -1.7852 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0924   -0.2270    0.1239 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0968    0.3661    0.9226 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2757    0.0877    1.2293 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2613    1.1598    2.3292 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.0758   -1.0127    0.8556 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5456   -1.9113    1.8901 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4354   -1.2568   -0.4997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0924   -0.7364    0.8639 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0105   -2.2487    1.1385 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2759   -2.7282    1.6394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1837   -2.5823    2.0238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4509   -0.5130    0.3815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6882    0.1906   -0.8918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4235    0.0666   -1.7184 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6594    0.5260   -3.1049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0559    4.9075    0.3478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3001    5.0547   -0.9599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7504    4.3567    0.6183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6140    1.8807    0.7767 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6800    1.2239   -1.3721 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6114    1.0015   -2.7651 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2121    3.4172   -1.5931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2143    3.1658   -2.7262 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4888   -1.0712   -0.5079 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5765    2.2873    1.5292 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6234   -1.6456    2.0730 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5582   -2.9732    1.5632 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0221   -1.7635    2.8575 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7400   -0.8958   -1.2655 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4349   -0.8348   -0.7705 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5549   -2.3637   -0.7014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9795   -0.3034    1.9104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2368   -2.7148    0.1347 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1333   -3.7429    2.0627 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9765   -2.8414    0.7681 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6802   -2.0172    2.3859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9059   -3.2435    2.8689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6441   -1.6692    2.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0030   -3.1221    1.4754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0648   -1.4687    0.2969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0493    0.0364    1.1748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9194    1.2808   -0.7877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5081   -0.2334   -1.5027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1939   -1.0314   -1.7602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9231    1.5843   -3.2138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5896   -0.0243   -3.4549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8886    0.1692   -3.8366 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 17  1  0
 15 14  1  0
 14 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20  4  1  0
  4  5  1  0
  5  6  1  0
  6  2  1  0
  2  1  1  0
  2  3  2  0
  4  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 11 13  1  0
  7 14  1  0
  4  3  1  1
 16 40  1  0
 16 41  1  0
 16 42  1  0
 15 39  1  0
 17 43  1  0
 17 44  1  0
 17 45  1  0
 14 38  1  1
 18 46  1  0
 18 47  1  0
 19 48  1  0
 19 49  1  0
 20 50  1  6
 21 51  1  0
 21 52  1  0
 21 53  1  0
  5 26  1  0
  5 27  1  0
  6 28  1  0
  6 29  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  7 30  1  6
 10 31  1  0
 12 32  1  0
 12 33  1  0
 12 34  1  0
 13 35  1  0
 13 36  1  0
 13 37  1  0
M  END


  Mrv1652309042218072D          

 21 22  0  0  0  0            999 V2000
   -0.6674    1.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6820    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5070    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9195    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5070   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9195   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5070   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7445   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6820   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695   -1.0164    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6820   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3495   -2.2158    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695   -2.4454    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6820   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4445   -2.4454    0.0000 C   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  2  6  1  0  0  0  0
  4  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 11 15  1  0  0  0  0
  4 15  1  0  0  0  0
 16 15  1  4  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0197801

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1CCC(C)C2(CCC(C)=C2)C1N=C(S)N(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C18H32N2S/c1-12(2)15-8-7-14(4)18(10-9-13(3)11-18)16(15)19-17(21)20(5)6/h11-12,14-16H,7-10H2,1-6H3,(H,19,21)

> <INCHI_KEY>
RMJRFNRHHMOKTF-UHFFFAOYSA-N

> <FORMULA>
C18H32N2S

> <MOLECULAR_WEIGHT>
308.53

> <EXACT_MASS>
308.228620212

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
36.98728723458821

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N'-[2,10-dimethyl-7-(propan-2-yl)spiro[4.5]dec-1-en-6-yl]-N,N-dimethylcarbamimidothioic acid

> <JCHEM_LOGP>
5.663946740363303

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.65146602875696

> <JCHEM_PKA_STRONGEST_BASIC>
14.956170816084343

> <JCHEM_POLAR_SURFACE_AREA>
15.6

> <JCHEM_REFRACTIVITY>
95.73149999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
N'-{7-isopropyl-2,10-dimethylspiro[4.5]dec-1-en-6-yl}-N,N-dimethylcarbamimidothioic acid

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.246   2.445   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.465   2.016   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.370   0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.465  -0.476   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.140   2.104   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.370   3.437   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.680   2.104   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.450   0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.680  -0.564   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.450  -1.897   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.680  -3.231   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.990  -1.897   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.140  -0.564   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       2.370  -1.897   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       3.140  -3.231   0.000  0.00  0.00           C+0
HETATM   18  S   UNK     0       4.386  -4.136   0.000  0.00  0.00           S+0
HETATM   19  N   UNK     0       2.370  -4.565   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       3.140  -5.898   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.830  -4.565   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    6                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    7   15                                             
CONECT    5    4    6                                                       
CONECT    6    5    2                                                       
CONECT    7    4    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   15                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   11    4   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

View in JSmol

Synonyms

Value	Source
N'-[2,10-dimethyl-7-(propan-2-yl)spiro[4.5]dec-1-en-6-yl]-N,N-dimethylcarbamimidothioate	Generator

Chemical Formula

C₁₈H₃₂N₂S

Average Mass

308.5300 Da

Monoisotopic Mass

308.22862 Da

IUPAC Name

N'-[2,10-dimethyl-7-(propan-2-yl)spiro[4.5]dec-1-en-6-yl]-N,N-dimethylcarbamimidothioic acid

Traditional Name

N'-{7-isopropyl-2,10-dimethylspiro[4.5]dec-1-en-6-yl}-N,N-dimethylcarbamimidothioic acid

CAS Registry Number

Not Available

SMILES

CC(C)C1CCC(C)C2(CCC(C)=C2)C1N=C(S)N(C)C

InChI Identifier

InChI=1S/C18H32N2S/c1-12(2)15-8-7-14(4)18(10-9-13(3)11-18)16(15)19-17(21)20(5)6/h11-12,14-16H,7-10H2,1-6H3,(H,19,21)

InChI Key

RMJRFNRHHMOKTF-UHFFFAOYSA-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
Axinella cannabina	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Menthane monoterpenoids

Alternative Parents

Substituents

P-menthane monoterpenoid
Isothiourea
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Carboximidamide
Organic nitrogen compound
Organopnictogen compound
Hydrocarbon derivative
Organosulfur compound
Organonitrogen compound
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	5.66	ChemAxon
pKa (Strongest Acidic)	1.65	ChemAxon
pKa (Strongest Basic)	14.96	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	15.6 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	95.73 m³·mol⁻¹	ChemAxon
Polarizability	36.99 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162936359

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n'-{7-isopropyl-2,10-dimethylspiro[4.5]dec-1-en-6-yl}-n,n-dimethylcarbamimidothioic acid (NP0197801)

MOL for NP0197801 (n'-{7-isopropyl-2,10-dimethylspiro[4.5]dec-1-en-6-yl}-n,n-dimethylcarbamimidothioic acid)

3D MOL for NP0197801 (n'-{7-isopropyl-2,10-dimethylspiro[4.5]dec-1-en-6-yl}-n,n-dimethylcarbamimidothioic acid)

3D SDF for NP0197801 (n'-{7-isopropyl-2,10-dimethylspiro[4.5]dec-1-en-6-yl}-n,n-dimethylcarbamimidothioic acid)

3D-SDF for NP0197801 (n'-{7-isopropyl-2,10-dimethylspiro[4.5]dec-1-en-6-yl}-n,n-dimethylcarbamimidothioic acid)

PDB for NP0197801 (n'-{7-isopropyl-2,10-dimethylspiro[4.5]dec-1-en-6-yl}-n,n-dimethylcarbamimidothioic acid)

3D PDB for NP0197801 (n'-{7-isopropyl-2,10-dimethylspiro[4.5]dec-1-en-6-yl}-n,n-dimethylcarbamimidothioic acid)

SMILES for NP0197801 (n'-{7-isopropyl-2,10-dimethylspiro[4.5]dec-1-en-6-yl}-n,n-dimethylcarbamimidothioic acid)

INCHI for NP0197801 (n'-{7-isopropyl-2,10-dimethylspiro[4.5]dec-1-en-6-yl}-n,n-dimethylcarbamimidothioic acid)

Structure for NP0197801 (n'-{7-isopropyl-2,10-dimethylspiro[4.5]dec-1-en-6-yl}-n,n-dimethylcarbamimidothioic acid)

3D Structure for NP0197801 (n'-{7-isopropyl-2,10-dimethylspiro[4.5]dec-1-en-6-yl}-n,n-dimethylcarbamimidothioic acid)