h1
h2
h3
  5  5
   -2.3166   -2.0393    0.0000 O   0  0  0  0  0
   -2.9838   -2.5241    0.0000 C   0  0  0  0  0
   -2.7289   -3.3084    0.0000 C   0  0  0  0  0
   -1.9042   -3.3084    0.0000 C   0  0  0  0  0
   -1.6493   -2.5241    0.0000 C   0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  1  1  0
M  END
>  <TEMPLATE_TYPE>
5-Membered Rings

>  <LABEL>
Furan

$$$$
h1
h2
h3
  5  5
   -2.3166   -2.0393    0.0000 S   0  0  0  0  0
   -2.9838   -2.5241    0.0000 C   0  0  0  0  0
   -2.7289   -3.3084    0.0000 C   0  0  0  0  0
   -1.9042   -3.3084    0.0000 C   0  0  0  0  0
   -1.6493   -2.5241    0.0000 C   0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  1  1  0
M  END
>  <TEMPLATE_TYPE>
5-Membered Rings

>  <LABEL>
Thiophene

$$$$
h1
h2
h3
  5  5
   -0.8920   -0.2025    0.0000 N   0  0  0  0  0
   -1.5593   -0.6872    0.0000 C   0  0  0  0  0
   -1.3044   -1.4716    0.0000 C   0  0  0  0  0
   -0.4797   -1.4716    0.0000 C   0  0  0  0  0
   -0.2248   -0.6872    0.0000 C   0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  1  1  0
M  END
>  <TEMPLATE_TYPE>
5-Membered Rings

>  <LABEL>
Pyrrole

$$$$
h1
h2
h3
  5  5
   -0.8920   -0.2025    0.0000 N   0  0  0  0  0
   -1.5593   -0.6872    0.0000 C   0  0  0  0  0
   -1.3044   -1.4716    0.0000 C   0  0  0  0  0
   -0.4797   -1.4716    0.0000 C   0  0  0  0  0
   -0.2248   -0.6872    0.0000 C   0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  1  1  0
M  END
>  <TEMPLATE_TYPE>
5-Membered Rings

>  <LABEL>
Pyrrolidine

$$$$
h1
h2
h3
  5  5
   -2.2041   -1.3645    0.0000 O   0  0  0  0  0
   -2.8713   -1.8493    0.0000 C   0  0  0  0  0
   -2.6164   -2.6336    0.0000 C   0  0  0  0  0
   -1.7917   -2.6336    0.0000 O   0  0  0  0  0
   -1.5369   -1.8493    0.0000 C   0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  1  1  0
M  END
>  <TEMPLATE_TYPE>
5-Membered Rings

>  <LABEL>
1,3-Dioxolane

$$$$
h1
h2
h3
  5  5
   -2.3166   -0.8022    0.0000 O   0  0  0  0  0
   -2.9838   -1.2870    0.0000 C   0  0  0  0  0
   -2.7289   -2.0713    0.0000 C   0  0  0  0  0
   -1.9042   -2.0713    0.0000 N   0  0  0  0  0
   -1.6493   -1.2870    0.0000 C   0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  1  1  0
M  END
>  <TEMPLATE_TYPE>
5-Membered Rings

>  <LABEL>
Oxazole

$$$$
h1
h2
h3
  5  5
   -2.3166   -0.8022    0.0000 S   0  0  0  0  0
   -2.9838   -1.2870    0.0000 C   0  0  0  0  0
   -2.7289   -2.0713    0.0000 C   0  0  0  0  0
   -1.9042   -2.0713    0.0000 N   0  0  0  0  0
   -1.6493   -1.2870    0.0000 C   0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  1  1  0
M  END
>  <TEMPLATE_TYPE>
5-Membered Rings

>  <LABEL>
Thiazole

$$$$
h1
h2
h3
  5  5
   -2.3166   -0.8022    0.0000 N   0  0  0  0  0
   -2.9838   -1.2870    0.0000 C   0  0  0  0  0
   -2.7289   -2.0713    0.0000 C   0  0  0  0  0
   -1.9042   -2.0713    0.0000 N   0  0  0  0  0
   -1.6493   -1.2870    0.0000 C   0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  1  1  0
M  END
>  <TEMPLATE_TYPE>
5-Membered Rings

>  <LABEL>
Imidazole

$$$$
h1
h2
h3
  5  5
   -2.3166   -0.8022    0.0000 N   0  0  0  0  0
   -2.9838   -1.2870    0.0000 C   0  0  0  0  0
   -2.7289   -2.0713    0.0000 C   0  0  0  0  0
   -1.9042   -2.0713    0.0000 C   0  0  0  0  0
   -1.6493   -1.2870    0.0000 N   0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  1  1  0
M  END
>  <TEMPLATE_TYPE>
5-Membered Rings

>  <LABEL>
Pyrazole

$$$$
h1
h2
h3
  5  5
   -2.3166   -0.8022    0.0000 O   0  0  0  0  0
   -2.9838   -1.2870    0.0000 C   0  0  0  0  0
   -2.7289   -2.0713    0.0000 C   0  0  0  0  0
   -1.9042   -2.0713    0.0000 C   0  0  0  0  0
   -1.6493   -1.2870    0.0000 N   0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  1  1  0
M  END
>  <TEMPLATE_TYPE>
5-Membered Rings

>  <LABEL>
Isoxazole

$$$$
h1
h2
h3
  5  5
   -2.3166   -0.8022    0.0000 S   0  0  0  0  0
   -2.9838   -1.2870    0.0000 C   0  0  0  0  0
   -2.7289   -2.0713    0.0000 C   0  0  0  0  0
   -1.9042   -2.0713    0.0000 C   0  0  0  0  0
   -1.6493   -1.2870    0.0000 N   0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  1  1  0
M  END
>  <TEMPLATE_TYPE>
5-Membered Rings

>  <LABEL>
Isothiazole

$$$$
h1
h2
h3
  5  5
   -2.3166   -0.8022    0.0000 O   0  0  0  0  0
   -2.9838   -1.2870    0.0000 C   0  0  0  0  0
   -2.7289   -2.0713    0.0000 C   0  0  0  0  0
   -1.9042   -2.0713    0.0000 N   0  0  0  0  0
   -1.6493   -1.2870    0.0000 N   0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  1  1  0
M  END
>  <TEMPLATE_TYPE>
5-Membered Rings

>  <LABEL>
1,2,3-Oxadiazole

$$$$
h1
h2
h3
  5  5
   -2.3166   -0.8022    0.0000 N   0  0  0  0  0
   -2.9838   -1.2870    0.0000 C   0  0  0  0  0
   -2.7289   -2.0713    0.0000 C   0  0  0  0  0
   -1.9042   -2.0713    0.0000 N   0  0  0  0  0
   -1.6493   -1.2870    0.0000 N   0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  1  1  0
M  END
>  <TEMPLATE_TYPE>
5-Membered Rings

>  <LABEL>
1,2,3-Triazole

$$$$
h1
h2
h3
  5  5
   -2.3166   -0.8022    0.0000 S   0  0  0  0  0
   -2.9838   -1.2870    0.0000 C   0  0  0  0  0
   -2.7289   -2.0713    0.0000 N   0  0  0  0  0
   -1.9042   -2.0713    0.0000 N   0  0  0  0  0
   -1.6493   -1.2870    0.0000 C   0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  1  1  0
M  END
>  <TEMPLATE_TYPE>
5-Membered Rings

>  <LABEL>
1,3,4-Thiadiazole

$$$$
MolHeader
  ELEMENTL01311315312D
Dotmatics Elemental
  5  5  0  0  0  0            999 V2000
   -4.6688    7.0205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3362    6.5356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3220    5.7135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9877    5.7135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0013    6.5356    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  1  1  0  0  0  0
M  END
>  <TEMPLATE_TYPE>
5-Membered Rings

>  <LABEL>
Cyclopentane

>  <ICONLABEL>
Cyclopentane-Up

$$$$
MolHeader
  ELEMENTL01311315322D
Dotmatics Elemental
  5  5  0  0  0  0            999 V2000
   -4.6576    5.5870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9902    6.0719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0044    6.8940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3387    6.8940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3251    6.0719    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  1  1  0  0  0  0
M  END
>  <TEMPLATE_TYPE>
5-Membered Rings

>  <LABEL>
Cyclopentane

>  <ICONLABEL>
Cyclopentane-Down

$$$$
MolHeader
  ELEMENTL02071319542D
Dotmatics Elemental
  5  5  0  0  0  0            999 V2000
   -9.0617   10.2471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8107    9.7029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5246    8.8225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5989    8.8225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3128    9.7029    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  2  0  0  0  0
  5  1  1  0  0  0  0
M  END
>  <TEMPLATE_TYPE>
5-Membered Rings

>  <LABEL>
Cyclopentadiene

>  <ICONLABEL>
Cyclopentadiene-Up

$$$$
MolHeader
  ELEMENTL02071319542D
Dotmatics Elemental
  5  5  0  0  0  0            999 V2000
   -9.0617    8.6721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3128    9.2162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5989   10.0967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5246   10.0967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8107    9.2162    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  2  0  0  0  0
  5  1  1  0  0  0  0
M  END
>  <TEMPLATE_TYPE>
5-Membered Rings

>  <LABEL>
Cyclopentadiene

>  <ICONLABEL>
Cyclopentadiene-Down

$$$$
h1
h2
h3
  6  6
   -1.6418   -1.5413    0.0000 N   0  0  0  0  0
   -2.3560   -1.9536    0.0000 C   0  0  0  0  0
   -2.3560   -2.7783    0.0000 C   0  0  0  0  0
   -1.6418   -3.1907    0.0000 C   0  0  0  0  0
   -0.9276   -2.7783    0.0000 C   0  0  0  0  0
   -0.9276   -1.9536    0.0000 C   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
M  END
>  <TEMPLATE_TYPE>
6-Membered Rings

>  <LABEL>
Pyridine

$$$$
h1
h2
h3
  6  6
   -0.6671    0.1831    0.0000 N   0  0  0  0  0
   -1.3813   -0.2292    0.0000 C   0  0  0  0  0
   -1.3813   -1.0539    0.0000 C   0  0  0  0  0
   -0.6671   -1.4663    0.0000 C   0  0  0  0  0
    0.0471   -1.0539    0.0000 C   0  0  0  0  0
    0.0471   -0.2292    0.0000 C   0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  1  1  0
M  END
>  <TEMPLATE_TYPE>
6-Membered Rings

>  <LABEL>
Piperidine

$$$$
h1
h2
h3
  6  6
   -0.6671    0.1831    0.0000 O   0  0  0  0  0
   -1.3813   -0.2292    0.0000 C   0  0  0  0  0
   -1.3813   -1.0539    0.0000 C   0  0  0  0  0
   -0.6671   -1.4663    0.0000 O   0  0  0  0  0
    0.0471   -1.0539    0.0000 C   0  0  0  0  0
    0.0471   -0.2292    0.0000 C   0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  1  1  0
M  END
>  <TEMPLATE_TYPE>
6-Membered Rings

>  <LABEL>
1,4-Dioxane

$$$$
h1
h2
h3
  6  6
   -0.6671    0.1831    0.0000 O   0  0  0  0  0
   -1.3813   -0.2292    0.0000 C   0  0  0  0  0
   -1.3813   -1.0539    0.0000 C   0  0  0  0  0
   -0.6671   -1.4663    0.0000 N   0  0  0  0  0
    0.0471   -1.0539    0.0000 C   0  0  0  0  0
    0.0471   -0.2292    0.0000 C   0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  1  1  0
M  END
>  <TEMPLATE_TYPE>
6-Membered Rings

>  <LABEL>
Morpholine

$$$$
h1
h2
h3
  6  6
   -0.6671    0.1831    0.0000 S   0  0  0  0  0
   -1.3813   -0.2292    0.0000 C   0  0  0  0  0
   -1.3813   -1.0539    0.0000 C   0  0  0  0  0
   -0.6671   -1.4663    0.0000 N   0  0  0  0  0
    0.0471   -1.0539    0.0000 C   0  0  0  0  0
    0.0471   -0.2292    0.0000 C   0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  1  1  0
M  END
>  <TEMPLATE_TYPE>
6-Membered Rings

>  <LABEL>
Thiomorpholine

$$$$
h1
h2
h3
  6  6
   -1.6793   -1.1289    0.0000 N   0  0  0  0  0
   -2.3935   -1.5413    0.0000 C   0  0  0  0  0
   -2.3935   -2.3660    0.0000 C   0  0  0  0  0
   -1.6793   -2.7783    0.0000 C   0  0  0  0  0
   -0.9651   -2.3660    0.0000 C   0  0  0  0  0
   -0.9651   -1.5413    0.0000 N   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
M  END
>  <TEMPLATE_TYPE>
6-Membered Rings

>  <LABEL>
Pyridazine

$$$$
h1
h2
h3
  6  6
   -1.6793   -1.1289    0.0000 N   0  0  0  0  0
   -2.3935   -1.5413    0.0000 C   0  0  0  0  0
   -2.3935   -2.3660    0.0000 C   0  0  0  0  0
   -1.6793   -2.7783    0.0000 C   0  0  0  0  0
   -0.9651   -2.3660    0.0000 N   0  0  0  0  0
   -0.9651   -1.5413    0.0000 C   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
M  END
>  <TEMPLATE_TYPE>
6-Membered Rings

>  <LABEL>
Pyrimidine

$$$$
h1
h2
h3
  6  6
   -1.6793   -1.1289    0.0000 N   0  0  0  0  0
   -2.3935   -1.5413    0.0000 C   0  0  0  0  0
   -2.3935   -2.3660    0.0000 C   0  0  0  0  0
   -1.6793   -2.7783    0.0000 N   0  0  0  0  0
   -0.9651   -2.3660    0.0000 C   0  0  0  0  0
   -0.9651   -1.5413    0.0000 C   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
M  END
>  <TEMPLATE_TYPE>
6-Membered Rings

>  <LABEL>
Pyrazine

$$$$
h1
h2
h3
  6  6
   -1.4544   -1.8412    0.0000 N   0  0  0  0  0
   -2.1686   -2.2535    0.0000 C   0  0  0  0  0
   -2.1686   -3.0782    0.0000 C   0  0  0  0  0
   -1.4544   -3.4906    0.0000 N   0  0  0  0  0
   -0.7401   -3.0782    0.0000 C   0  0  0  0  0
   -0.7401   -2.2535    0.0000 C   0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  1  1  0
M  END
>  <TEMPLATE_TYPE>
6-Membered Rings

>  <LABEL>
Piperazine

$$$$
h1
h2
h3
  6  6
   -0.1423    1.1953    0.0000 N   0  0  0  0  0
   -0.8565    0.7829    0.0000 C   0  0  0  0  0
   -0.8565   -0.0418    0.0000 N   0  0  0  0  0
   -0.1423   -0.4542    0.0000 C   0  0  0  0  0
    0.5719   -0.0418    0.0000 N   0  0  0  0  0
    0.5719    0.7829    0.0000 C   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
M  END
>  <TEMPLATE_TYPE>
6-Membered Rings

>  <LABEL>
1,3,5-Triazine

$$$$
h1
h2
h3
  6  6  0  0  0  0  0  0  0  0999 V2000
   -1.0019    0.3572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5894   -0.3572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2087   -0.1481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0019   -0.3572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5895    0.3572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2087    0.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0      
  2  3  1  0      
  3  4  1  0      
  4  5  1  0      
  5  6  1  0      
  6  1  1  0      
M  END
>  <TEMPLATE_TYPE>
6-Membered Rings

>  <LABEL>
Cyclohexane

>  <ICONLABEL>
Cyclohexane-Left

$$$$
h1
h2
h3
  6  6  0  0  0  0  0  0  0  0999 V2000
   -0.5895    0.3572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0020   -0.3572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2087   -0.1305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5894   -0.3572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0020    0.3572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2086    0.1306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0      
  2  3  1  0      
  3  4  1  0      
  4  5  1  0      
  5  6  1  0      
  6  1  1  0      
M  END
>  <TEMPLATE_TYPE>
6-Membered Rings

>  <LABEL>
Cyclohexane

>  <ICONLABEL>
Cyclohexane-Right

$$$$
h1
h2
h3
  9 10  0     0  0  0  0  0  0999 V2000 
   -3.6661   -0.1917    0.0000 C   0  0  0  0  0
   -4.3803   -0.6041    0.0000 C   0  0  0  0  0
   -4.3803   -1.4288    0.0000 C   0  0  0  0  0
   -3.6661   -1.8412    0.0000 C   0  0  0  0  0
   -2.9519   -1.4288    0.0000 C   0  0  0  0  0
   -2.9519   -0.6041    0.0000 N   0  0  0  0  0
   -2.1675   -1.6837    0.0000 C   0  0  0  0  0
   -1.6828   -1.0165    0.0000 C   0  0  0  0  0
   -2.1675   -0.3492    0.0000 C   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  1  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  9  6  1  0
M  END
> <LABEL>
Indolizine

> <TEMPLATE_TYPE>
Bicyclic Rings

$$$$
h1
h2
h3
  9 10  0     0  0  0  0  0  0999 V2000 
   -4.3408   -0.7540    0.0000 C   0  0  0  0  0
   -5.0551   -1.1664    0.0000 C   0  0  0  0  0
   -5.0551   -1.9911    0.0000 C   0  0  0  0  0
   -4.3408   -2.4035    0.0000 C   0  0  0  0  0
   -3.6266   -1.9911    0.0000 C   0  0  0  0  0
   -3.6266   -1.1664    0.0000 C   0  0  0  0  0
   -2.8423   -2.2460    0.0000 C   0  0  0  0  0
   -2.3575   -1.5788    0.0000 C   0  0  0  0  0
   -2.8423   -0.9116    0.0000 N   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9  6  1  0
M  END
>  <LABEL>
Indole

>  <TEMPLATE_TYPE>
Bicyclic Rings

$$$$
h1
h2
h3
  9 10  0     0  0  0  0  0  0999 V2000 
   -3.8535   -0.4916    0.0000 C   0  0  0  0  0
   -4.5677   -0.9040    0.0000 C   0  0  0  0  0
   -4.5677   -1.7287    0.0000 C   0  0  0  0  0
   -3.8535   -2.1411    0.0000 C   0  0  0  0  0
   -3.1393   -1.7287    0.0000 C   0  0  0  0  0
   -3.1393   -0.9040    0.0000 C   0  0  0  0  0
   -2.3549   -1.9836    0.0000 C   0  0  0  0  0
   -1.8702   -1.3164    0.0000 N   0  0  0  0  0
   -2.3549   -0.6491    0.0000 C   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  1  1  0
  5  7  2  0
  7  8  1  0
  8  9  1  0
  9  6  2  0
M  END
>  <LABEL>
Isoindole

>  <TEMPLATE_TYPE>
Bicyclic Rings

$$$$
h1
h2
h3
  9 10  0     0  0  0  0  0  0999 V2000 
   -5.3155   -0.8290    0.0000 C   0  0  0  0  0
   -6.0297   -1.2414    0.0000 C   0  0  0  0  0
   -6.0297   -2.0661    0.0000 C   0  0  0  0  0
   -5.3155   -2.4784    0.0000 C   0  0  0  0  0
   -4.6013   -2.0661    0.0000 C   0  0  0  0  0
   -4.6013   -1.2414    0.0000 C   0  0  0  0  0
   -3.8169   -2.3209    0.0000 C   0  0  0  0  0
   -3.3322   -1.6537    0.0000 C   0  0  0  0  0
   -3.8169   -0.9865    0.0000 N   0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  1  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9  6  1  0
M  END
>  <LABEL>
Indoline

>  <TEMPLATE_TYPE>
Bicyclic Rings

$$$$
h1
h2
h3
  9 10  0     0  0  0  0  0  0999 V2000 
   -4.0784    0.6330    0.0000 C   0  0  0  0  0
   -4.7927    0.2206    0.0000 C   0  0  0  0  0
   -4.7927   -0.6041    0.0000 C   0  0  0  0  0
   -4.0784   -1.0165    0.0000 C   0  0  0  0  0
   -3.3642   -0.6041    0.0000 C   0  0  0  0  0
   -3.3642    0.2206    0.0000 C   0  0  0  0  0
   -2.5799   -0.8589    0.0000 C   0  0  0  0  0
   -2.0951   -0.1917    0.0000 C   0  0  0  0  0
   -2.5799    0.4755    0.0000 O   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9  6  1  0
M  END
>  <LABEL>
Benzo[b]furan

>  <TEMPLATE_TYPE>
Bicyclic Rings

$$$$
h1
h2
h3
  9 10  0     0  0  0  0  0  0999 V2000 
   -4.0784    0.6330    0.0000 C   0  0  0  0  0
   -4.7927    0.2206    0.0000 C   0  0  0  0  0
   -4.7927   -0.6041    0.0000 C   0  0  0  0  0
   -4.0784   -1.0165    0.0000 C   0  0  0  0  0
   -3.3642   -0.6041    0.0000 C   0  0  0  0  0
   -3.3642    0.2206    0.0000 C   0  0  0  0  0
   -2.5799   -0.8589    0.0000 C   0  0  0  0  0
   -2.0951   -0.1917    0.0000 C   0  0  0  0  0
   -2.5799    0.4755    0.0000 S   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9  6  1  0
M  END
>  <LABEL>
Benzo[b]thiophene

>  <TEMPLATE_TYPE>
Bicyclic Rings

$$$$
h1
h2
h3
  9 10  0     0  0  0  0  0  0999 V2000 
   -4.0784    0.6330    0.0000 C   0  0  0  0  0
   -4.7927    0.2206    0.0000 C   0  0  0  0  0
   -4.7927   -0.6041    0.0000 C   0  0  0  0  0
   -4.0784   -1.0165    0.0000 C   0  0  0  0  0
   -3.3642   -0.6041    0.0000 C   0  0  0  0  0
   -3.3642    0.2206    0.0000 C   0  0  0  0  0
   -2.5799   -0.8589    0.0000 N   0  0  0  0  0
   -2.0951   -0.1917    0.0000 C   0  0  0  0  0
   -2.5799    0.4755    0.0000 N   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9  6  1  0
M  END
>  <LABEL>
Benzimidazole

>  <TEMPLATE_TYPE>
Bicyclic Rings

$$$$
h1
h2
h3
  9 10  0     0  0  0  0  0  0999 V2000 
   -4.0784    0.6330    0.0000 N   0  0  0  0  0
   -4.7927    0.2206    0.0000 C   0  0  0  0  0
   -4.7927   -0.6041    0.0000 N   0  0  0  0  0
   -4.0784   -1.0165    0.0000 C   0  0  0  0  0
   -3.3642   -0.6041    0.0000 C   0  0  0  0  0
   -3.3642    0.2206    0.0000 C   0  0  0  0  0
   -2.5799   -0.8589    0.0000 N   0  0  0  0  0
   -2.0951   -0.1917    0.0000 C   0  0  0  0  0
   -2.5799    0.4755    0.0000 N   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9  6  1  0
M  END
>  <LABEL>
Purine

>  <TEMPLATE_TYPE>
Bicyclic Rings

$$$$
h1
h2
h3
 10 11  0     0  0  0  0  0  0999 V2000 
   -3.9660   -0.1543    0.0000 C   0  0  0  0  0
   -4.6802   -0.5666    0.0000 C   0  0  0  0  0
   -4.6802   -1.3913    0.0000 C   0  0  0  0  0
   -3.9660   -1.8037    0.0000 N   0  0  0  0  0
   -3.2518   -1.3913    0.0000 C   0  0  0  0  0
   -3.2518   -0.5666    0.0000 C   0  0  0  0  0
   -2.5375   -1.8037    0.0000 C   0  0  0  0  0
   -1.8233   -1.3913    0.0000 C   0  0  0  0  0
   -1.8233   -0.5666    0.0000 C   0  0  0  0  0
   -2.5375   -0.1543    0.0000 C   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10  6  1  0
M  END
>  <LABEL>
Quinoline

>  <TEMPLATE_TYPE>
Bicyclic Rings
$$$$
h1
h2
h3
 10 11  0     0  0  0  0  0  0999 V2000 
   -3.9660   -0.1543    0.0000 C   0  0  0  0  0
   -4.6802   -0.5666    0.0000 C   0  0  0  0  0
   -4.6802   -1.3913    0.0000 N   0  0  0  0  0
   -3.9660   -1.8037    0.0000 C   0  0  0  0  0
   -3.2518   -1.3913    0.0000 C   0  0  0  0  0
   -3.2518   -0.5666    0.0000 C   0  0  0  0  0
   -2.5375   -1.8037    0.0000 C   0  0  0  0  0
   -1.8233   -1.3913    0.0000 C   0  0  0  0  0
   -1.8233   -0.5666    0.0000 C   0  0  0  0  0
   -2.5375   -0.1543    0.0000 C   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10  6  1  0
M  END
>  <LABEL>
Isoquinoline

>  <TEMPLATE_TYPE>
Bicyclic Rings

$$$$
h1
h2
h3
  9 10
   -0.4441    1.7576    0.0000 C   0  0  0  0  0
   -1.1584    1.3452    0.0000 C   0  0  0  0  0
   -1.1584    0.5205    0.0000 C   0  0  0  0  0
   -0.4441    0.1081    0.0000 C   0  0  0  0  0
    0.2700    0.5205    0.0000 C   0  0  0  0  0
    0.2700    1.3452    0.0000 C   0  0  0  0  0
    1.0543    0.2657    0.0000 N   0  0  0  0  0
    1.5391    0.9329    0.0000 C   0  0  0  0  0
    1.0543    1.6001    0.0000 S   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9  6  1  0
M  END
>  <TEMPLATE_TYPE>
Bicyclic Rings

>  <LABEL>
Benzthiazole

$$$$
h1
h2
h3
 10 11
   -3.5951    0.9704    0.0000 C   0  0  0  0  0
   -4.3093    0.5581    0.0000 C   0  0  0  0  0
   -4.3093   -0.2667    0.0000 N   0  0  0  0  0
   -3.5951   -0.6791    0.0000 N   0  0  0  0  0
   -2.8809   -0.2667    0.0000 C   0  0  0  0  0
   -2.8809    0.5581    0.0000 C   0  0  0  0  0
   -2.1666   -0.6791    0.0000 C   0  0  0  0  0
   -1.4524   -0.2667    0.0000 C   0  0  0  0  0
   -1.4524    0.5581    0.0000 C   0  0  0  0  0
   -2.1666    0.9704    0.0000 C   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10  6  1  0
M  END
>  <TEMPLATE_TYPE>
Bicyclic Rings

>  <LABEL>
Cinnoline

$$$$
h1
h2
h3
 10 11
   -3.5951    0.9704    0.0000 C   0  0  0  0  0
   -4.3093    0.5581    0.0000 N   0  0  0  0  0
   -4.3093   -0.2667    0.0000 N   0  0  0  0  0
   -3.5951   -0.6791    0.0000 C   0  0  0  0  0
   -2.8809   -0.2667    0.0000 C   0  0  0  0  0
   -2.8809    0.5581    0.0000 C   0  0  0  0  0
   -2.1666   -0.6791    0.0000 C   0  0  0  0  0
   -1.4524   -0.2667    0.0000 C   0  0  0  0  0
   -1.4524    0.5581    0.0000 C   0  0  0  0  0
   -2.1666    0.9704    0.0000 C   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10  6  1  0
M  END
>  <TEMPLATE_TYPE>
Bicyclic Rings

>  <LABEL>
Phthalazine

$$$$
h1
h2
h3
 10 11
   -3.5951    0.9704    0.0000 C   0  0  0  0  0
   -4.3093    0.5581    0.0000 N   0  0  0  0  0
   -4.3093   -0.2667    0.0000 C   0  0  0  0  0
   -3.5951   -0.6791    0.0000 N   0  0  0  0  0
   -2.8809   -0.2667    0.0000 C   0  0  0  0  0
   -2.8809    0.5581    0.0000 C   0  0  0  0  0
   -2.1666   -0.6791    0.0000 C   0  0  0  0  0
   -1.4524   -0.2667    0.0000 C   0  0  0  0  0
   -1.4524    0.5581    0.0000 C   0  0  0  0  0
   -2.1666    0.9704    0.0000 C   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10  6  1  0
M  END
>  <TEMPLATE_TYPE>
Bicyclic Rings

>  <LABEL>
Quinazoline

$$$$
h1
h2
h3
 10 11
   -3.5951    0.9704    0.0000 N   0  0  0  0  0
   -4.3093    0.5581    0.0000 C   0  0  0  0  0
   -4.3093   -0.2667    0.0000 C   0  0  0  0  0
   -3.5951   -0.6791    0.0000 N   0  0  0  0  0
   -2.8809   -0.2667    0.0000 C   0  0  0  0  0
   -2.8809    0.5581    0.0000 C   0  0  0  0  0
   -2.1666   -0.6791    0.0000 C   0  0  0  0  0
   -1.4524   -0.2667    0.0000 C   0  0  0  0  0
   -1.4524    0.5581    0.0000 C   0  0  0  0  0
   -2.1666    0.9704    0.0000 C   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10  6  1  0
M  END
>  <TEMPLATE_TYPE>
Bicyclic Rings

>  <LABEL>
Quinoxaline

$$$$
h1
h2
h3
 10 11
   -1.6793    0.2956    0.0000 N   0  0  0  0  0
   -2.3935   -0.1168    0.0000 C   0  0  0  0  0
   -2.3935   -0.9415    0.0000 C   0  0  0  0  0
   -1.6793   -1.3538    0.0000 N   0  0  0  0  0
   -0.9651   -0.9415    0.0000 C   0  0  0  0  0
   -0.9651   -0.1168    0.0000 C   0  0  0  0  0
   -0.2508   -1.3538    0.0000 C   0  0  0  0  0
    0.4634   -0.9415    0.0000 N   0  0  0  0  0
    0.4634   -0.1168    0.0000 C   0  0  0  0  0
   -0.2508    0.2956    0.0000 N   0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10  6  1  0
M  END
>  <TEMPLATE_TYPE>
Bicyclic Rings

>  <LABEL>
Pteridine

$$$$
h1
h2
h3
 10 11  0     0  0  0  0  0  0999 V2000 
   -5.2030   -0.9283    0.0000 C   0  0  0  0  0
   -5.9461   -1.2861    0.0000 C   0  0  0  0  0
   -6.1296   -2.0901    0.0000 C   0  0  0  0  0
   -5.6154   -2.7349    0.0000 C   0  0  0  0  0
   -4.7907   -2.7349    0.0000 C   0  0  0  0  0
   -4.2765   -2.0901    0.0000 C   0  0  0  0  0
   -4.4600   -1.2861    0.0000 C   0  0  0  0  0
   -3.4551   -2.1641    0.0000 C   0  0  0  0  0
   -3.1310   -1.4057    0.0000 C   0  0  0  0  0
   -3.7520   -0.8631    0.0000 C   0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  1  2  0
  6  8  2  0
  8  9  1  0
  9 10  2  0
 10  7  1  0
M  END
>  <LABEL>
Azulene

>  <TEMPLATE_TYPE>
Bicyclic Rings

$$$$
h1
h2
h3
  7  8
   -3.1788   -1.3538    0.0000 C   0  0  0  0  0
   -3.8930   -1.7662    0.0000 C   0  0  0  0  0
   -3.8930   -2.5909    0.0000 C   0  0  0  0  0
   -3.1788   -3.0033    0.0000 C   0  0  0  0  0
   -2.4645   -2.5909    0.0000 C   0  0  0  0  0
   -2.4645   -1.7662    0.0000 C   0  0  0  0  0
   -2.7664   -2.0681    0.0000 C   0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  1  1  0
  1  7  1  0
  7  4  1  0
M  END
>  <TEMPLATE_TYPE>
Complex Rings

>  <LABEL>
Norbornane

$$$$
h1
h2
h3
 10 12
   -1.7542   -0.3042    0.0000 C   0  0  0  0  0
   -2.4685   -0.7166    0.0000 C   0  0  0  0  0
   -2.4685   -1.5413    0.0000 C   0  0  0  0  0
   -1.7542   -1.9536    0.0000 C   0  0  0  0  0
   -1.0400   -1.5413    0.0000 C   0  0  0  0  0
   -1.0400   -0.7166    0.0000 C   0  0  0  0  0
   -2.2791   -1.0539    0.0000 C   0  0  0  0  0
   -3.1788   -2.2910    0.0000 C   0  0  0  0  0
   -1.7168   -2.5909    0.0000 C   0  0  0  0  0
   -2.3821   -2.0776    0.0000 C   0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  1  1  0
  1  7  1  0
  3  8  1  0
  5  9  1  0
  8 10  1  0
 10  9  1  0
  7 10  1  0
M  END
>  <TEMPLATE_TYPE>
Complex Rings

>  <LABEL>
Adamantane

$$$$
h1
h2
h3
 17 20
   -3.2912   -2.6659    0.0000 C   0  0  0  0  0
   -4.0054   -3.0782    0.0000 C   0  0  0  0  0
   -4.0054   -3.9029    0.0000 C   0  0  0  0  0
   -3.2912   -4.3153    0.0000 C   0  0  0  0  0
   -2.5770   -3.9029    0.0000 C   0  0  0  0  0
   -2.5770   -3.0782    0.0000 C   0  0  0  0  0
   -1.8628   -4.3153    0.0000 C   0  0  0  0  0
   -1.1485   -3.9029    0.0000 C   0  0  0  0  0
   -1.1485   -3.0782    0.0000 C   0  0  0  0  0
   -1.8628   -2.6659    0.0000 C   0  0  0  0  0
   -0.4343   -2.6659    0.0000 C   0  0  0  0  0
   -0.4343   -1.8412    0.0000 C   0  0  0  0  0
   -1.1485   -1.4288    0.0000 C   0  0  0  0  0
   -1.8628   -1.8412    0.0000 C   0  0  0  0  0
    0.3500   -2.9207    0.0000 C   0  0  0  0  0
    0.8348   -2.2535    0.0000 C   0  0  0  0  0
    0.3500   -1.5863    0.0000 C   0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  1  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10  6  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 10  1  0
 11 15  1  0
 15 16  1  0
 16 17  1  0
 17 12  1  0
M  END
>  <TEMPLATE_TYPE>
Complex Rings

>  <LABEL>
Steroid

$$$$
h1
h2
h3
  4  3
   -4.5283   -2.9283    0.0000 C   0  0  0  0  0
   -4.5283   -2.1036    0.0000 C   0  0  0  0  0
   -3.8141   -1.6912    0.0000 O   0  0  0  0  0
   -5.2425   -1.6912    0.0000 O   0  0  0  0  0
  2  1  1  0
  2  3  2  0
  2  4  1  0
M  END
>  <LABEL>
Carboxylate

>  <TEMPLATE_TYPE>
Functional Groups

$$$$
h1
h2
h3
  4  3
   -4.5283   -2.9283    0.0000 C   0  0  0  0  0
   -4.5283   -2.1036    0.0000 C   0  0  0  0  0
   -3.8141   -1.6912    0.0000 O   0  0  0  0  0
   -5.2425   -1.6912    0.0000 N   0  0  0  0  0
  2  1  1  0
  2  3  2  0
  2  4  1  0
M  END
>  <LABEL>
Carboxamide

>  <TEMPLATE_TYPE>
Functional Groups

$$$$
h1
h2
h3
  5  4
   -3.8910   -3.0782    0.0000 C   0  0  0  0  0
   -3.8910   -2.2535    0.0000 C   0  0  0  0  0
   -3.1768   -1.8412    0.0000 C   0  0  0  0  0
   -4.6052   -1.8412    0.0000 C   0  0  0  0  0
   -4.1045   -1.4569    0.0000 C   0  0  0  0  0
  2  1  1  0
  2  3  1  0
  2  4  1  0
  5  2  1  0
M  END
>  <LABEL>
t-butyl

>  <TEMPLATE_TYPE>
Functional Groups

$$$$
h1
h2
h3
  5  4
   -3.8910   -3.0782    0.0000 C   0  0  0  0  0
   -3.8910   -2.2535    0.0000 C   0  0  0  0  0
   -3.1768   -1.8412    0.0000 F   0  0  0  0  0
   -4.6052   -1.8412    0.0000 F   0  0  0  0  0
   -4.1045   -1.4569    0.0000 F   0  0  0  0  0
  2  1  1  0
  2  3  1  0
  2  4  1  0
  5  2  1  0
M  END
>  <LABEL>
CF3

>  <TEMPLATE_TYPE>
Functional Groups

$$$$
h1
h2
h3
  4  3
   -2.1291   -3.6031    0.0000 C   0  0  0  0  0
   -2.1291   -2.7783    0.0000 N   0  0  0  0  0
   -1.4149   -2.3660    0.0000 N   0  3  0  0  0
   -0.7007   -1.9536    0.0000 N   0  5  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  2  0
M  END
>  <TEMPLATE_TYPE>
Functional Groups

>  <LABEL>
Azide

$$$$
h1
h2
h3
  4  3
   -2.1291   -3.6031    0.0000 C   0  0  0  0  0
   -2.1291   -2.7783    0.0000 O   0  0  0  0  0
   -1.4149   -2.3660    0.0000 C   0  0  0  0  0
   -0.7007   -1.9536    0.0000 N   0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  3  0
M  END
>  <TEMPLATE_TYPE>
Functional Groups

>  <LABEL>
Cyanate

$$$$
h1
h2
h3
  3  2
   -2.2041   -3.1157    0.0000 C   0  0  0  0  0
   -2.2041   -2.2910    0.0000 N   0  3  0  0  0
   -2.2041   -1.4663    0.0000 C   0  5  0  0  0
  1  2  1  0
  2  3  3  0
M  END
>  <TEMPLATE_TYPE>
Functional Groups

>  <LABEL>
Isocyanide

$$$$
h1
h2
h3
  4  3
   -2.9163   -4.2778    0.0000 C   0  0  0  0  0
   -2.9163   -3.4531    0.0000 N   0  0  0  0  0
   -2.2021   -3.0408    0.0000 C   0  0  0  0  0
   -1.4879   -2.6284    0.0000 O   0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  2  0
M  END
>  <TEMPLATE_TYPE>
Functional Groups

>  <LABEL>
Isocyanate

$$$$
h1
h2
h3
  4  3
   -2.9163   -4.2778    0.0000 C   0  0  0  0  0
   -2.9163   -3.4531    0.0000 N   0  0  0  0  0
   -2.2021   -3.0408    0.0000 C   0  0  0  0  0
   -1.4879   -2.6284    0.0000 S   0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  2  0
M  END
>  <TEMPLATE_TYPE>
Functional Groups

>  <LABEL>
Isothiocyanate

$$$$
