NP-MRD: Showing NP-Card for 4,6-dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),9,12,14-tetraene (NP0246370)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 07:49:12 UTC

Updated at

2022-09-07 07:49:12 UTC

NP-MRD ID

NP0246370

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,6-dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),9,12,14-tetraene

Description

4,6-Dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]Hexadeca-1(16),9,12,14-tetraene belongs to the class of organic compounds known as clavines and derivatives. These are hydroxy and dehydro derivatives of 6,8-dimethylergolenes and the corresponding ergolines. 4,6-dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),9,12,14-tetraene is found in Aspergillus fumigatus. 4,6-Dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]Hexadeca-1(16),9,12,14-tetraene is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 54  0  0  0  0  0  0  0  0999 V2000
   -3.3150   -0.2714   -1.6984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5457   -1.1717   -0.7506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2991   -0.8421    0.6811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6495   -0.3669    1.2327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9753   -2.1208    1.3788 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3141    0.2071    0.7608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5037    1.4217    1.3158 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3643    2.1614    1.2130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9414    3.4150    1.5689 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3704    3.8197    1.2710 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2370    2.9655    0.6226 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8053    1.7117    0.2696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4590    1.3436    0.5661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0130    0.1344    0.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2204   -0.8683   -0.3958 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9738   -0.3379   -1.1170 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6959    0.7762   -0.4305 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7359    0.2970    0.5614 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8128   -0.5243   -0.1299 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0899    0.2607   -0.2983 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2740   -0.9628   -1.4748 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9350   -1.4206   -1.2918 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5005   -2.4213   -2.2073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4794   -0.4657   -2.7504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9469    0.6991   -1.4105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9207   -2.1704   -0.9782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8011    0.6432    0.7902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4040   -1.0354    0.7771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6582   -0.3571    2.3298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8263   -2.0195    2.4662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1708   -2.6824    0.8658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8878   -2.7729    1.2744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3530    1.8194    1.7739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6380    4.0609    2.0736 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6920    4.8161    1.5591 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2367    3.2694    0.3936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7668   -1.5057   -1.1191 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1982   -1.6298    0.3369 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6479   -0.0223   -2.1357 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2432    1.3525   -1.2063 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1974   -0.2978    1.3213 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1950    1.2036    1.0079 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0205   -1.4098    0.4715 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0634    0.8591   -1.2451 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9314   -0.4556   -0.3630 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2071    0.9460    0.5609 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8821   -1.7594   -1.9143 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2618   -0.1134   -2.1937 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7587   -2.0601   -2.9493 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4088   -2.8464   -2.7072 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0789   -3.2718   -1.5981 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
  6  3  1  0
  3  4  1  0
  3  5  1  0
  3  2  1  0
  2  1  2  3
 16 22  1  0
 22 23  1  0
 22 21  1  0
 21 19  1  0
 12 17  1  0
 13 14  1  0
 13  8  1  0
 20 44  1  0
 20 45  1  0
 20 46  1  0
 19 43  1  1
 18 41  1  0
 18 42  1  0
 17 40  1  6
 16 39  1  6
 15 37  1  0
 15 38  1  0
  7 33  1  0
  9 34  1  0
 10 35  1  0
 11 36  1  0
  4 27  1  0
  4 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  5 32  1  0
  2 26  1  0
  1 24  1  0
  1 25  1  0
 23 49  1  0
 23 50  1  0
 23 51  1  0
 21 47  1  0
 21 48  1  0
M  END


  Mrv1533004181501112D          

 23 26  0  0  0  0            999 V2000
    4.7079    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8500   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1355   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3509   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1340    0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3509    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1794    1.8869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7925    2.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5771    2.1840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8500    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1355    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0960   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6887   -0.7846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8806   -1.2945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1590   -1.8242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3930   -2.4373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -0.0000    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  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
  4 14  1  0  0  0  0
 14 15  2  0  0  0  0
  7 15  1  0  0  0  0
 10 15  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  2  0  0  0  0
  5 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
  2 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0246370

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC2C(CC3=C(NC4=CC=CC2=C34)C(C)(C)C=C)N(C)C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H28N2/c1-6-21(3,4)20-16-11-18-15(10-13(2)12-23(18)5)14-8-7-9-17(22-20)19(14)16/h6-9,13,15,18,22H,1,10-12H2,2-5H3

> <INCHI_KEY>
GXEMWNLJOIOIIM-UHFFFAOYSA-N

> <FORMULA>
C21H28N2

> <MOLECULAR_WEIGHT>
308.469

> <EXACT_MASS>
308.22524891

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
37.479412401740944

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4,6-dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),9,12,14-tetraene

> <ALOGPS_LOGP>
5.14

> <JCHEM_LOGP>
4.708340865

> <ALOGPS_LOGS>
-4.98

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.74710750460866

> <JCHEM_PKA_STRONGEST_BASIC>
8.747083710648313

> <JCHEM_POLAR_SURFACE_AREA>
19.03

> <JCHEM_REFRACTIVITY>
98.4231

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.24e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,6-dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),9,12,14-tetraene

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 18-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   18-APR-15         0                                  
HETATM    1  C   UNK     0       8.788   2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.453  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.120  -0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.655  -0.476   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      -0.250   0.770   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       0.655   2.016   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.335   3.522   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.479   4.553   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.944   4.077   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.453   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.120   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.179  -1.941   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.286  -1.465   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.644  -2.416   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.297  -3.405   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.734  -4.550   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       6.121  -0.770   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       6.121  -2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.454  -0.000   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   23                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   14                                                  
CONECT    5    4    6   21                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   15                                                  
CONECT    8    7    9   16                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    4   15                                                  
CONECT   15   14    7   10                                                  
CONECT   16    8   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   16   20                                                       
CONECT   20   19                                                            
CONECT   21    5   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21    2                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₈N₂

Average Mass

308.4690 Da

Monoisotopic Mass

308.22525 Da

IUPAC Name

4,6-dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),9,12,14-tetraene

Traditional Name

4,6-dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),9,12,14-tetraene

CAS Registry Number

Not Available

SMILES

CC1CC2C(CC3=C(NC4=CC=CC2=C34)C(C)(C)C=C)N(C)C1

InChI Identifier

InChI=1S/C21H28N2/c1-6-21(3,4)20-16-11-18-15(10-13(2)12-23(18)5)14-8-7-9-17(22-20)19(14)16/h6-9,13,15,18,22H,1,10-12H2,2-5H3

InChI Key

GXEMWNLJOIOIIM-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
Aspergillus fumigatus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as clavines and derivatives. These are hydroxy and dehydro derivatives of 6,8-dimethylergolenes and the corresponding ergolines.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Ergoline and derivatives

Sub Class

Clavines and derivatives

Direct Parent

Clavines and derivatives

Alternative Parents

Substituents

Clavine skeleton
Indoloquinoline
Benzoquinoline
Pyrroloquinoline
Quinoline
3-alkylindole
Indole
Indole or derivatives
Isoindole or derivatives
Aralkylamine
Benzenoid
Piperidine
Substituted pyrrole
Pyrrole
Heteroaromatic compound
Tertiary amine
Tertiary aliphatic amine
Organoheterocyclic compound
Azacycle
Organonitrogen compound
Hydrocarbon derivative
Amine
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	5.14	ALOGPS
logP	4.71	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	16.75	ChemAxon
pKa (Strongest Basic)	8.75	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	19.03 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	98.42 m³·mol⁻¹	ChemAxon
Polarizability	37.48 Å³	ChemAxon
Number of Rings	4	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

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

44715304

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,6-dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),9,12,14-tetraene (NP0246370)

MOL for NP0246370 (4,6-dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),9,12,14-tetraene)

3D MOL for NP0246370 (4,6-dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),9,12,14-tetraene)

3D SDF for NP0246370 (4,6-dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),9,12,14-tetraene)

3D-SDF for NP0246370 (4,6-dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),9,12,14-tetraene)

PDB for NP0246370 (4,6-dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),9,12,14-tetraene)

3D PDB for NP0246370 (4,6-dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),9,12,14-tetraene)

SMILES for NP0246370 (4,6-dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),9,12,14-tetraene)

INCHI for NP0246370 (4,6-dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),9,12,14-tetraene)

Structure for NP0246370 (4,6-dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),9,12,14-tetraene)

3D Structure for NP0246370 (4,6-dimethyl-10-(2-methylbut-3-en-2-yl)-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),9,12,14-tetraene)