site-specific Her-SG3249
     RDKit          2D

107114  0  0  1  0  0  0  0  0999 V2000
   13.5136    4.9321    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.1739    0.6998    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4736    3.8354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.3708   -2.5182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3071    1.2426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.2468   -3.3718    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1531   -9.9902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0383  -16.6248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9758  -12.0541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6444   10.4614    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1518   14.5908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8293   13.6308    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6657    9.8858    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4913    8.8297    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6516    6.4292    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4771    5.3731    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -26.4488   -1.5401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -15.6374    2.9726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -31.7712   -2.5001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -22.6232   -0.4840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -32.3010   -8.0568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -36.6953   -5.1292    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -19.4629    1.9165    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.9630    2.9328    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.6357    2.3948    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.5776  -16.6927    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.7754  -13.5422    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.3158    9.3092    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.9853   11.9980    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9915   12.1902    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  -34.2663   -6.2450    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  -29.6091   -3.9406    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   15.8526    3.9412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4685    5.3089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3718    3.7018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9596    5.1457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.2652    3.6772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8669    1.4358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1986    1.0045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6366    0.5777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.9681    6.2561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1100   -0.0275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1388    2.4909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9860   -0.8811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4594   -1.4862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8974   -1.9130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9767    3.9315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7202   -3.9769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6315   -5.0089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3114    5.2759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9809   -6.4676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.6848   -3.7986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8923   -7.4996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0062  -16.2353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8826  -17.4526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1431    6.5242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8145    5.3720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9958  -18.6623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2417   -8.9583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5712  -18.1927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5392  -14.8332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3293  -15.8610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4779    7.8686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1493    6.7164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2012  -14.3665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9810    7.9648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2898  -13.3345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4532  -20.0909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5025  -11.4490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9405  -11.8758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7632  -13.9397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4138  -12.4809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1475   10.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4822   11.9019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8232   13.4386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1579   14.7830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3201   13.3424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3139   13.1502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6610   14.8791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9896   16.0313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6265  -10.5954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4946   12.2864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6629   11.0380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8341   11.1342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1627    9.9820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9944    8.7336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3230    7.5814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8199    7.6775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1485    6.5253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9802    5.2770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -33.4346   -4.9967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -31.9377   -5.0928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -31.1060   -3.8445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -28.7774   -2.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -33.7452   -7.6516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -35.7651   -6.3059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.3088    4.1248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -27.2805   -2.7884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -34.9220   -8.5818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -36.1703   -7.7501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.8057    4.2209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -24.9519   -1.6362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -24.1202   -0.3879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -17.1343    3.0687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -17.9660    1.8204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -21.7915    0.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -20.2946    0.6682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1 35  1  0
  2 38  2  0
  3 43  1  0
  3 47  1  0
  4 45  1  0
  4 48  1  0
  5 43  2  0
  6 46  1  0
  6 52  1  0
  7 59  1  0
  7 69  1  0
  8 62  2  0
  9 72  1  0
  9 81  1  0
 10 73  2  0
 11 77  2  0
 12 82  2  0
 13 84  1  0
 13 85  1  0
 14 86  1  0
 14 87  1  0
 15 88  1  0
 15 89  1  0
 16 90  1  0
 16 97  1  0
 17 98  1  0
 17102  1  0
 18101  1  0
 18104  1  0
 19 93  2  0
 20103  1  0
 20106  1  0
 21 95  2  0
 22 96  2  0
 23105  1  0
 23107  1  0
 24 33  1  0
 24 37  1  0
 24 38  1  0
 25 35  1  0
 25 39  1  0
 25 43  1  0
 26 54  1  0
 26 60  1  0
 26 62  1  0
 27 61  2  0
 27 67  1  0
 28 66  1  0
 28 73  1  0
 29 74  1  0
 29 77  1  0
 30 75  1  0
 30 82  1  0
 31 91  1  0
 31 95  1  0
 31 96  1  0
 32 93  1  0
 32 94  1  0
 33 34  1  0
 33 35  1  0
 34 36  1  0
 36 37  2  0
 36 41  1  0
 38 40  1  0
 39 40  2  0
 39 42  1  0
 40 44  1  0
 42 45  2  0
 44 46  2  0
 45 46  1  0
 47 50  1  0
 48 49  1  0
 49 51  1  0
 50 56  2  0
 50 57  1  0
 51 53  1  0
 53 59  1  0
 54 55  1  0
 54 61  1  0
 55 58  1  0
 56 63  1  0
 57 64  2  0
 58 60  2  0
 58 68  1  0
 62 65  1  0
 63 66  2  0
 64 66  1  0
 65 67  2  0
 65 71  1  0
 67 70  1  0
 69 70  2  0
 69 72  1  0
 71 72  2  0
 73 74  1  0
 74 78  1  0
 75 76  1  0
 75 77  1  0
 76 79  1  0
 76 80  1  0
 82 83  1  0
 83 84  1  0
 85 86  1  0
 87 88  1  0
 89 90  1  0
 91 92  1  0
 92 93  1  0
 94 98  1  0
 95 99  1  0
 96100  1  0
 97101  1  0
 99100  2  0
102103  1  0
104105  1  0
106107  1  0
M  END
>  <i_m_stars>  (1) 
0

>  <s_m_entry_id>  (1) 
31

>  <s_m_entry_name>  (1) 
Structure31

>  <PUBCHEM_COMPOUND_CID>  (1) 
73672523

>  <PUBCHEM_HEAVY_ATOM_COUNT>  (1) 
107

>  <PUBCHEM_ATOM_DEF_STEREO_COUNT>  (1) 
5

>  <PUBCHEM_ATOM_UDEF_STEREO_COUNT>  (1) 
0

>  <PUBCHEM_BOND_DEF_STEREO_COUNT>  (1) 
0

>  <PUBCHEM_BOND_UDEF_STEREO_COUNT>  (1) 
0

>  <PUBCHEM_ISOTOPIC_ATOM_COUNT>  (1) 
0

>  <PUBCHEM_COMPONENT_COUNT>  (1) 
1

>  <PUBCHEM_CACTVS_TAUTO_COUNT>  (1) 
-1

>  <PUBCHEM_COORDINATE_TYPE>  (1) 
1
5
255

>  <chiral flag>  (1) 
1

>  <version>  (1) 
0

>  <s_m_Source_Path>  (1) 
D:\Project\ADC\linker_payload

>  <s_m_Source_File>  (1) 
tesirine_Mal-PEG8-Val-Ala-PABC-SG3199.sdf

>  <i_m_Source_File_Index>  (1) 
1

>  <i_lp_mmshare_version>  (1) 
61128

>  <r_lp_tautomer_probability>  (1) 
0.999601159137504

>  <s_lp_Force_Field>  (1) 
S-OPLS

>  <r_lp_Energy>  (1) 
108.130425

>  <b_lp_Chiralities_Consistent>  (1) 
1

>  <s_lp_Variant>  (1) 
tesirine-1

>  <s_m_job_name>  (1) 
ligprep_9

>  <i_f3d_flags>  (1) 
0

>  <PUBCHEM_COMPOUND_CANONICALIZED>  (1) 
1

>  <PUBCHEM_CACTVS_COMPLEXITY>  (1) 
2970

>  <PUBCHEM_CACTVS_HBOND_ACCEPTOR>  (1) 
24

>  <PUBCHEM_CACTVS_HBOND_DONOR>  (1) 
5

>  <PUBCHEM_CACTVS_ROTATABLE_BOND>  (1) 
49

>  <PUBCHEM_CACTVS_SUBSKEYS>  (1) 
AAADcfB//gAAAAAAAAAAAAAAAAAAAQIEAAAwYMAABYgAAACBUAAAHgAQCAAADSzhmAYyzoPABgCoAjV3XACCCAAlIgAIiIG+7MgPdj7E9bufearm9jna6ce6/DvOKEABAgACQABQgAIEAASAAAAAAAAAAA==

>  <PUBCHEM_IUPAC_OPENEYE_NAME>  (1) 
[4-[[(2S)-2-[[(2S)-2-[3-[2-[2-[2-[2-[2-[2-[2-[2-[3-(2,5-dioxopyrrol-1-yl)propanoylamino]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]propanoylamino]-3-methyl-butanoyl]amino]propanoyl]amino]phenyl]methyl (6S,6aS)-3-[5-[[(6aS)-2-methoxy-8-methyl-11-oxo-6a,7-dihydropyrrolo[2,1-c][1,4]benzodiazepin-3-yl]oxy]pentoxy]-6-hydroxy-2-methoxy-8-methyl-11-oxo-6a,7-dihydro-6H-pyrrolo[2,1-c][1,4]benzodiazepine-5-carboxylate

>  <PUBCHEM_IUPAC_CAS_NAME>  (1) 
(6S,6aS)-3-[5-[[(6aS)-2-methoxy-8-methyl-11-oxo-6a,7-dihydropyrrolo[2,1-c][1,4]benzodiazepin-3-yl]oxy]pentoxy]-6-hydroxy-2-methoxy-8-methyl-11-oxo-6a,7-dihydro-6H-pyrrolo[2,1-c][1,4]benzodiazepine-5-carboxylic acid [4-[[(2S)-2-[[(2S)-2-[[3-[2-[2-[2-[2-[2-[2-[2-[2-[[3-(2,5-dioxo-1-pyrrolyl)-1-oxopropyl]amino]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]-1-oxopropyl]amino]-3-methyl-1-oxobutyl]amino]-1-oxopropyl]amino]phenyl]methyl ester

>  <PUBCHEM_IUPAC_NAME_MARKUP>  (1) 
[4-[[(2<I>S</I>)-2-[[(2<I>S</I>)-2-[3-[2-[2-[2-[2-[2-[2-[2-[2-[3-(2,5-dioxopyrrol-1-yl)propanoylamino]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]propanoylamino]-3-methylbutanoyl]amino]propanoyl]amino]phenyl]methyl (6<I>S</I>,6<I>a</I><I>S</I>)-3-[5-[[(6<I>a</I><I>S</I>)-2-methoxy-8-methyl-11-oxo-6<I>a</I>,7-dihydropyrrolo[2,1-c][1,4]benzodiazepin-3-yl]oxy]pentoxy]-6-hydroxy-2-methoxy-8-methyl-11-oxo-6<I>a</I>,7-dihydro-6<I>H</I>-pyrrolo[2,1-c][1,4]benzodiazepine-5-carboxylate

>  <PUBCHEM_IUPAC_NAME>  (1) 
[4-[[(2S)-2-[[(2S)-2-[3-[2-[2-[2-[2-[2-[2-[2-[2-[3-(2,5-dioxopyrrol-1-yl)propanoylamino]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]propanoylamino]-3-methylbutanoyl]amino]propanoyl]amino]phenyl]methyl (6S,6aS)-3-[5-[[(6aS)-2-methoxy-8-methyl-11-oxo-6a,7-dihydropyrrolo[2,1-c][1,4]benzodiazepin-3-yl]oxy]pentoxy]-6-hydroxy-2-methoxy-8-methyl-11-oxo-6a,7-dihydro-6H-pyrrolo[2,1-c][1,4]benzodiazepine-5-carboxylate

>  <PUBCHEM_IUPAC_SYSTEMATIC_NAME>  (1) 
[4-[[(2S)-2-[[(2S)-2-[3-[2-[2-[2-[2-[2-[2-[2-[2-[3-[2,5-bis(oxidanylidene)pyrrol-1-yl]propanoylamino]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]propanoylamino]-3-methyl-butanoyl]amino]propanoyl]amino]phenyl]methyl (6S,6aS)-3-[5-[[(6aS)-2-methoxy-8-methyl-11-oxidanylidene-6a,7-dihydropyrrolo[2,1-c][1,4]benzodiazepin-3-yl]oxy]pentoxy]-2-methoxy-8-methyl-6-oxidanyl-11-oxidanylidene-6a,7-dihydro-6H-pyrrolo[2,1-c][1,4]benzodiazepine-5-carboxylate

>  <PUBCHEM_IUPAC_TRADITIONAL_NAME>  (1) 
(6S,6aS)-3-[5-[[(6aS)-11-keto-2-methoxy-8-methyl-6a,7-dihydropyrrolo[2,1-c][1,4]benzodiazepin-3-yl]oxy]pentoxy]-6-hydroxy-11-keto-2-methoxy-8-methyl-6a,7-dihydro-6H-pyrrolo[2,1-c][1,4]benzodiazepine-5-carboxylic acid [4-[[(2S)-2-[[(2S)-2-[3-[2-[2-[2-[2-[2-[2-[2-[2-(3-maleimidopropanoylamino)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]propanoylamino]-3-methyl-butanoyl]amino]propanoyl]amino]benzyl] ester

>  <PUBCHEM_IUPAC_INCHI>  (1) 
InChI=1S/C75H101N9O23/c1-49(2)69(80-66(86)18-23-97-25-27-99-29-31-101-33-35-103-37-38-104-36-34-102-32-30-100-28-26-98-24-19-76-65(85)17-20-81-67(87)15-16-68(81)88)71(90)78-52(5)70(89)79-54-13-11-53(12-14-54)48-107-75(94)84-59-44-64(62(96-7)42-57(59)73(92)83-47-51(4)40-60(83)74(84)93)106-22-10-8-9-21-105-63-43-58-56(41-61(63)95-6)72(91)82-46-50(3)39-55(82)45-77-58/h11-16,41-47,49,52,55,60,69,74,93H,8-10,17-40,48H2,1-7H3,(H,76,85)(H,78,90)(H,79,89)(H,80,86)/t52-,55-,60-,69-,74-/m0/s1

>  <PUBCHEM_IUPAC_INCHIKEY>  (1) 
HKGATZAPXCCEJR-OWRSNIELSA-N

>  <PUBCHEM_XLOGP3_AA>  (1) 
1.6

>  <PUBCHEM_EXACT_MASS>  (1) 
1495.7010305

>  <PUBCHEM_MOLECULAR_FORMULA>  (1) 
C75H101N9O23

>  <PUBCHEM_MOLECULAR_WEIGHT>  (1) 
1496.6

>  <PUBCHEM_OPENEYE_CAN_SMILES>  (1) 
CC1=CN2C(C1)C=NC3=CC(=C(C=C3C2=O)OC)OCCCCCOC4=C(C=C5C(=C4)N(C(C6CC(=CN6C5=O)C)O)C(=O)OCC7=CC=C(C=C7)NC(=O)C(C)NC(=O)C(C(C)C)NC(=O)CCOCCOCCOCCOCCOCCOCCOCCOCCNC(=O)CCN8C(=O)C=CC8=O)OC

>  <PUBCHEM_OPENEYE_ISO_SMILES>  (1) 
CC1=CN2[C@@H](C1)C=NC3=CC(=C(C=C3C2=O)OC)OCCCCCOC4=C(C=C5C(=C4)N([C@H]([C@@H]6CC(=CN6C5=O)C)O)C(=O)OCC7=CC=C(C=C7)NC(=O)[C@H](C)NC(=O)[C@H](C(C)C)NC(=O)CCOCCOCCOCCOCCOCCOCCOCCOCCNC(=O)CCN8C(=O)C=CC8=O)OC

>  <PUBCHEM_CACTVS_TPSA>  (1) 
367

>  <PUBCHEM_MONOISOTOPIC_WEIGHT>  (1) 
1495.7010305

>  <PUBCHEM_TOTAL_CHARGE>  (1) 
0

>  <PUBCHEM_BONDANNOTATIONS>  (1) 
35  1  6
74  29  6
75  30  5
33  108  6
39  40  8
39  42  8
40  44  8
42  45  8
44  46  8
45  46  8
50  56  8
50  57  8
54  132  5
56  63  8
57  64  8
63  66  8
64  66  8
65  67  8
65  71  8
67  70  8
69  70  8
69  72  8
71  72  8

$$$$
