PC-Compounds ::= {
{
id {
id cid 60192335
},
atoms {
aid {
1,
2,
3,
4,
5,
6,
7,
8,
9,
10,
11,
12,
13,
14,
15,
16,
17,
18,
19,
20,
21,
22,
23,
24,
25,
26,
27,
28,
29,
30,
31,
32,
33,
34,
35,
36,
37,
38,
39,
40,
41,
42,
43,
44,
45,
46,
47,
48,
49,
50,
51,
52,
53,
54,
55,
56,
57,
58,
59,
60,
61,
62,
63,
64
},
element {
s,
f,
o,
o,
o,
o,
n,
n,
n,
c,
c,
c,
c,
c,
c,
c,
c,
c,
c,
c,
c,
c,
c,
c,
c,
c,
c,
c,
c,
c,
c,
c,
c,
c,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h,
h
}
},
bonds {
aid1 {
1,
1,
1,
1,
2,
3,
3,
6,
6,
7,
7,
7,
8,
8,
9,
9,
9,
10,
10,
10,
10,
11,
11,
12,
12,
12,
13,
13,
13,
14,
14,
15,
15,
15,
17,
17,
18,
18,
19,
19,
20,
20,
20,
21,
22,
22,
23,
23,
24,
24,
25,
25,
26,
26,
26,
27,
27,
29,
30,
30,
31,
31,
32,
32,
33,
34,
34,
34
},
aid2 {
4,
5,
8,
26,
29,
22,
57,
28,
34,
11,
15,
20,
17,
18,
16,
21,
46,
11,
12,
13,
14,
35,
36,
17,
37,
38,
18,
39,
40,
16,
19,
16,
22,
41,
42,
43,
44,
45,
21,
23,
25,
47,
48,
24,
49,
50,
27,
51,
28,
52,
29,
30,
53,
54,
55,
28,
56,
31,
32,
58,
33,
59,
33,
60,
61,
62,
63,
64
},
order {
double,
double,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
double,
single,
single,
single,
single,
single,
single,
single,
single,
double,
single,
single,
single,
single,
single,
single,
single,
double,
single,
double,
single,
single,
double,
single,
single,
single,
single,
single,
double,
single,
single,
single,
single,
double,
single,
single,
single,
single,
single
}
},
stereo {
tetrahedral {
center 15,
above 7,
top 16,
bottom 22,
below 41,
parity clockwise,
type tetrahedral
}
},
coords {
{
type {
twod,
computed,
units-unknown
},
aid {
1,
2,
3,
4,
5,
6,
7,
8,
9,
10,
11,
12,
13,
14,
15,
16,
17,
18,
19,
20,
21,
22,
23,
24,
25,
26,
27,
28,
29,
30,
31,
32,
33,
34,
35,
36,
37,
38,
39,
40,
41,
42,
43,
44,
45,
46,
47,
48,
49,
50,
51,
52,
53,
54,
55,
56,
57,
58,
59,
60,
61,
62,
63,
64
},
conformers {
{
x {
{ 72626, 10, -4 },
{ 89946, 10, -4 },
{ 81286, 10, -4 },
{ 82626, 10, -4 },
{ 62626, 10, -4 },
{ 2411, 10, -3 },
{ 81286, 10, -4 },
{ 72626, 10, -4 },
{ 54503, 10, -4 },
{ 72626, 10, -4 },
{ 81286, 10, -4 },
{ 63966, 10, -4 },
{ 81286, 10, -4 },
{ 63966, 10, -4 },
{ 72626, 10, -4 },
{ 63966, 10, -4 },
{ 63966, 10, -4 },
{ 81286, 10, -4 },
{ 54503, 10, -4 },
{ 89946, 10, -4 },
{ 48667, 10, -4 },
{ 72626, 10, -4 },
{ 5043, 10, -3 },
{ 38353, 10, -4 },
{ 98606, 10, -4 },
{ 72626, 10, -4 },
{ 4014, 10, -3 },
{ 3406, 10, -3 },
{ 98606, 10, -4 },
{ 107267, 10, -4 },
{ 107267, 10, -4 },
{ 115927, 10, -4 },
{ 115927, 10, -4 },
{ 2, 10, 0 },
{ 83406, 10, -4 },
{ 87392, 10, -4 },
{ 61845, 10, -4 },
{ 5786, 10, -3 },
{ 87392, 10, -4 },
{ 83406, 10, -4 },
{ 77995, 10, -4 },
{ 5786, 10, -3 },
{ 61845, 10, -4 },
{ 83406, 10, -4 },
{ 87392, 10, -4 },
{ 52577, 10, -4 },
{ 93932, 10, -4 },
{ 85961, 10, -4 },
{ 70505, 10, -4 },
{ 6652, 10, -3 },
{ 54128, 10, -4 },
{ 34771, 10, -4 },
{ 66426, 10, -4 },
{ 72626, 10, -4 },
{ 78826, 10, -4 },
{ 37635, 10, -4 },
{ 81286, 10, -4 },
{ 107267, 10, -4 },
{ 107267, 10, -4 },
{ 121296, 10, -4 },
{ 121296, 10, -4 },
{ 14348, 10, -4 },
{ 17452, 10, -4 },
{ 25652, 10, -4 }
},
y {
{ -306, 10, -2 },
{ -6, 10, -2 },
{ 344, 10, -2 },
{ -306, 10, -2 },
{ -306, 10, -2 },
{ -1936, 10, -4 },
{ 144, 10, -2 },
{ -206, 10, -2 },
{ 17447, 10, -4 },
{ -6, 10, -2 },
{ 44, 10, -2 },
{ -56, 10, -2 },
{ -56, 10, -2 },
{ 44, 10, -2 },
{ 194, 10, -2 },
{ 144, 10, -2 },
{ -156, 10, -2 },
{ -156, 10, -2 },
{ 1353, 10, -4 },
{ 194, 10, -2 },
{ 94, 10, -2 },
{ 294, 10, -2 },
{ -8167, 10, -4 },
{ 8485, 10, -4 },
{ 144, 10, -2 },
{ -406, 10, -2 },
{ -932, 10, -3 },
{ -938, 10, -4 },
{ 44, 10, -2 },
{ 194, 10, -2 },
{ -6, 10, -2 },
{ 144, 10, -2 },
{ 44, 10, -2 },
{ -11052, 10, -4 },
{ -1426, 10, -4 },
{ 5477, 10, -4 },
{ 226, 10, -4 },
{ -6677, 10, -4 },
{ -6677, 10, -4 },
{ 226, 10, -4 },
{ 225, 10, -2 },
{ -14523, 10, -4 },
{ -21426, 10, -4 },
{ -21426, 10, -4 },
{ -14523, 10, -4 },
{ 2334, 10, -3 },
{ 2415, 10, -3 },
{ 2415, 10, -3 },
{ 35226, 10, -4 },
{ 28323, 10, -4 },
{ -13144, 10, -4 },
{ 13546, 10, -4 },
{ -406, 10, -2 },
{ -468, 10, -2 },
{ -406, 10, -2 },
{ -14991, 10, -4 },
{ 406, 10, -2 },
{ 256, 10, -2 },
{ -68, 10, -2 },
{ 175, 10, -2 },
{ 13, 10, -2 },
{ -8504, 10, -4 },
{ -16704, 10, -4 },
{ -136, 10, -2 }
},
style {
annotation {
aromatic,
aromatic,
aromatic,
aromatic,
wedge-up,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic
},
aid1 {
9,
9,
14,
14,
15,
19,
19,
21,
23,
24,
25,
25,
27,
29,
30,
31,
32
},
aid2 {
16,
21,
16,
19,
22,
21,
23,
24,
27,
28,
29,
30,
28,
31,
32,
33,
33
}
}
}
}
}
},
charge 0,
props {
{
urn {
label "Compound",
name "Canonicalized",
datatype uint,
release "2012.05.21"
},
value ival 1
},
{
urn {
label "Compound Complexity",
datatype double,
implementation "E_COMPLEXITY",
version "3.4.8.18",
software "Cactvs",
source "Xemistry GmbH",
release "2021.05.07"
},
value fval { 816, 10, 0 }
},
{
urn {
label "Count",
name "Hydrogen Bond Acceptor",
datatype uint,
implementation "E_NHACCEPTORS",
version "3.4.8.18",
software "Cactvs",
source "Xemistry GmbH",
release "2021.05.07"
},
value ival 7
},
{
urn {
label "Count",
name "Hydrogen Bond Donor",
datatype uint,
implementation "E_NHDONORS",
version "3.4.8.18",
software "Cactvs",
source "Xemistry GmbH",
release "2021.05.07"
},
value ival 2
},
{
urn {
label "Count",
name "Rotatable Bond",
datatype uint,
implementation "E_NROTBONDS",
version "3.4.8.18",
software "Cactvs",
source "Xemistry GmbH",
release "2021.05.07"
},
value ival 5
},
{
urn {
label "Fingerprint",
name "SubStructure Keys",
datatype fingerprint,
parameters "extended 2",
implementation "E_SCREEN",
version "3.4.8.18",
software "Cactvs",
source "Xemistry GmbH",
release "2021.05.07"
},
value binary '00000371E07B39004000000000000000000000000001600000003C78
8100000000005801F400001F04104800000E2CE19E0EB2C6F3C99602A003246244708288202122
200899203E6C980E76E2C4B19B94702866D019D8E80790D0F30FA0000002000200004000000400
040000000000000000'H
},
{
urn {
label "IUPAC Name",
name "Allowed",
datatype string,
version "2.7.0",
software "Lexichem TK",
source "OpenEye Scientific Software",
release "2021.05.07"
},
value sval "[(1S)-2-[(2-fluorophenyl)methyl]-7-methoxy-1
'-methylsulfonyl-spiro[3,9-dihydro-1H-pyrido[3,4-b]indole-4,4
'-piperidine]-1-yl]methanol"
},
{
urn {
label "IUPAC Name",
name "CAS-like Style",
datatype string,
version "2.7.0",
software "Lexichem TK",
source "OpenEye Scientific Software",
release "2021.05.07"
},
value sval "[(1S)-2-[(2-fluorophenyl)methyl]-7-methoxy-1
'-methylsulfonyl-1-spiro[3,9-dihydro-1H-pyrido[3,4-b]indole-4,4
'-piperidine]yl]methanol"
},
{
urn {
label "IUPAC Name",
name "Markup",
datatype string,
version "2.7.0",
software "Lexichem TK",
source "OpenEye Scientific Software",
release "2021.05.07"
},
value sval "[(1S)-2-[(2-fluorophenyl)methyl]-7-methoxy-1'-
methylsulfonylspiro[3,9-dihydro-1H-pyrido[3,4-b]indole-4,4'-piperi
dine]-1-yl]methanol"
},
{
urn {
label "IUPAC Name",
name "Preferred",
datatype string,
version "2.7.0",
software "Lexichem TK",
source "OpenEye Scientific Software",
release "2021.05.07"
},
value sval "[(1S)-2-[(2-fluorophenyl)methyl]-7-methoxy-1
'-methylsulfonylspiro[3,9-dihydro-1H-pyrido[3,4-b]indole-4,4
'-piperidine]-1-yl]methanol"
},
{
urn {
label "IUPAC Name",
name "Systematic",
datatype string,
version "2.7.0",
software "Lexichem TK",
source "OpenEye Scientific Software",
release "2021.05.07"
},
value sval "[(1S)-2-[(2-fluorophenyl)methyl]-7-methoxy-1
'-methylsulfonyl-spiro[3,9-dihydro-1H-pyrido[3,4-b]indole-4,4
'-piperidine]-1-yl]methanol"
},
{
urn {
label "IUPAC Name",
name "Traditional",
datatype string,
version "2.7.0",
software "Lexichem TK",
source "OpenEye Scientific Software",
release "2021.05.07"
},
value sval "[(1S)-2-(2-fluorobenzyl)-1
'-mesyl-7-methoxy-spiro[3,9-dihydro-1H-beta-carboline-4,4
'-piperidine]-1-yl]methanol"
},
{
urn {
label "InChI",
name "Standard",
datatype string,
version "1.0.6",
software "InChI",
source "iupac.org",
release "2021.05.07"
},
value sval "InChI=1S/C25H30FN3O4S/c1-33-18-7-8-19-21(13-18)27-24-22(15
-30)28(14-17-5-3-4-6-20(17)26)16-25(23(19)24)9-11-29(12-10-25)34(2,31)32/h3-8,
13,22,27,30H,9-12,14-16H2,1-2H3/t22-/m1/s1"
},
{
urn {
label "InChIKey",
name "Standard",
datatype string,
version "1.0.6",
software "InChI",
source "iupac.org",
release "2021.05.07"
},
value sval "SHWWIPFIIYYIHM-JOCHJYFZSA-N"
},
{
urn {
label "Log P",
name "XLogP3-AA",
datatype double,
version "3.0",
source "sioc-ccbg.ac.cn",
release "2021.05.07"
},
value fval { 24, 10, -1 }
},
{
urn {
label "Mass",
name "Exact",
datatype string,
version "2.1",
software "PubChem",
source "ncbi.nlm.nih.gov",
release "2021.05.07"
},
value sval "487.19410578"
},
{
urn {
label "Molecular Formula",
datatype string,
version "2.1",
software "PubChem",
source "ncbi.nlm.nih.gov",
release "2021.05.07"
},
value sval "C25H30FN3O4S"
},
{
urn {
label "Molecular Weight",
datatype string,
version "2.1",
software "PubChem",
source "ncbi.nlm.nih.gov",
release "2021.05.07"
},
value sval "487.6"
},
{
urn {
label "SMILES",
name "Canonical",
datatype string,
version "2.3.0",
software "OEChem",
source "OpenEye Scientific Software",
release "2021.05.07"
},
value sval "COC1=CC2=C(C=C1)C3=C(N2)C(N(CC34CCN(CC4)S(=O)(=O)C)CC5=CC=
CC=C5F)CO"
},
{
urn {
label "SMILES",
name "Isomeric",
datatype string,
version "2.3.0",
software "OEChem",
source "OpenEye Scientific Software",
release "2021.05.07"
},
value sval "COC1=CC2=C(C=C1)C3=C(N2)[C@H](N(CC34CCN(CC4)S(=O)(=O)C)CC5
=CC=CC=C5F)CO"
},
{
urn {
label "Topological",
name "Polar Surface Area",
datatype double,
implementation "E_TPSA",
version "3.4.8.18",
software "Cactvs",
source "Xemistry GmbH",
release "2021.05.07"
},
value fval { 942, 10, -1 }
},
{
urn {
label "Weight",
name "MonoIsotopic",
datatype string,
version "2.1",
software "PubChem",
source "ncbi.nlm.nih.gov",
release "2021.05.07"
},
value sval "487.19410578"
}
},
count {
heavy-atom 34,
atom-chiral 1,
atom-chiral-def 1,
atom-chiral-undef 0,
bond-chiral 0,
bond-chiral-def 0,
bond-chiral-undef 0,
isotope-atom 0,
covalent-unit 1,
tautomers -1
}
}
}