PC-Compounds ::= {
{
id {
id cid 66539917
},
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,
65,
66
},
element {
cl,
s,
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,
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,
2,
2,
3,
3,
4,
5,
5,
6,
6,
6,
7,
7,
7,
8,
8,
9,
9,
9,
10,
10,
10,
11,
11,
11,
12,
12,
12,
13,
14,
14,
15,
15,
15,
16,
16,
17,
17,
18,
18,
19,
20,
21,
22,
22,
22,
23,
25,
25,
26,
27,
27,
28,
28,
29,
30,
31,
31,
32,
32,
33,
33,
34,
35,
35,
35,
36,
36,
36
},
aid2 {
21,
24,
25,
14,
17,
13,
19,
36,
9,
13,
46,
16,
18,
51,
24,
26,
10,
11,
12,
37,
38,
39,
40,
41,
42,
43,
44,
45,
14,
47,
48,
16,
20,
21,
49,
50,
19,
23,
27,
28,
20,
52,
23,
24,
29,
30,
53,
26,
31,
33,
29,
54,
30,
55,
56,
57,
32,
58,
34,
35,
34,
59,
60,
61,
62,
63,
64,
65,
66
},
order {
single,
single,
single,
single,
single,
double,
single,
single,
single,
single,
single,
single,
single,
single,
double,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
single,
double,
single,
single,
single,
double,
single,
double,
single,
single,
single,
double,
single,
double,
single,
single,
double,
single,
single,
single,
single,
double,
single,
single,
single,
double,
single,
single,
single,
double,
single,
single,
single,
single,
single,
single,
single,
single
}
},
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,
65,
66
},
conformers {
{
x {
{ 116279, 10, -4 },
{ 55443, 10, -4 },
{ 146279, 10, -4 },
{ 166279, 10, -4 },
{ 136279, 10, -4 },
{ 166279, 10, -4 },
{ 101279, 10, -4 },
{ 55443, 10, -4 },
{ 176279, 10, -4 },
{ 186279, 10, -4 },
{ 176279, 10, -4 },
{ 176279, 10, -4 },
{ 161279, 10, -4 },
{ 151279, 10, -4 },
{ 116279, 10, -4 },
{ 106279, 10, -4 },
{ 136279, 10, -4 },
{ 91279, 10, -4 },
{ 131279, 10, -4 },
{ 121279, 10, -4 },
{ 121279, 10, -4 },
{ 71279, 10, -4 },
{ 131279, 10, -4 },
{ 61279, 10, -4 },
{ 45981, 10, -4 },
{ 45981, 10, -4 },
{ 86279, 10, -4 },
{ 86279, 10, -4 },
{ 76279, 10, -4 },
{ 76279, 10, -4 },
{ 3732, 10, -3 },
{ 2866, 10, -3 },
{ 3732, 10, -3 },
{ 2866, 10, -3 },
{ 2, 10, 0 },
{ 131279, 10, -4 },
{ 186279, 10, -4 },
{ 192479, 10, -4 },
{ 186279, 10, -4 },
{ 182479, 10, -4 },
{ 176279, 10, -4 },
{ 170079, 10, -4 },
{ 170079, 10, -4 },
{ 176279, 10, -4 },
{ 182479, 10, -4 },
{ 163179, 10, -4 },
{ 152356, 10, -4 },
{ 145453, 10, -4 },
{ 100453, 10, -4 },
{ 107356, 10, -4 },
{ 104379, 10, -4 },
{ 118179, 10, -4 },
{ 134379, 10, -4 },
{ 89379, 10, -4 },
{ 89379, 10, -4 },
{ 73179, 10, -4 },
{ 73179, 10, -4 },
{ 3732, 10, -3 },
{ 3732, 10, -3 },
{ 23291, 10, -4 },
{ 231, 10, -2 },
{ 14631, 10, -4 },
{ 169, 10, -2 },
{ 12591, 10, -3 },
{ 128179, 10, -4 },
{ 136648, 10, -4 }
},
y {
{ 16651, 10, -4 },
{ 16038, 10, -4 },
{ -67, 10, -3 },
{ -67, 10, -3 },
{ -1799, 10, -3 },
{ 16651, 10, -4 },
{ 799, 10, -3 },
{ -57, 10, -4 },
{ 16651, 10, -4 },
{ 16651, 10, -4 },
{ 26651, 10, -4 },
{ 6651, 10, -4 },
{ 799, 10, -3 },
{ 799, 10, -3 },
{ -67, 10, -3 },
{ -67, 10, -3 },
{ -67, 10, -3 },
{ 799, 10, -3 },
{ -933, 10, -3 },
{ -933, 10, -3 },
{ 799, 10, -3 },
{ 799, 10, -3 },
{ 799, 10, -3 },
{ 799, 10, -3 },
{ 1299, 10, -3 },
{ 299, 10, -3 },
{ -67, 10, -3 },
{ 16651, 10, -4 },
{ -67, 10, -3 },
{ 16651, 10, -4 },
{ 1799, 10, -3 },
{ 1299, 10, -3 },
{ -201, 10, -3 },
{ 299, 10, -3 },
{ 1799, 10, -3 },
{ -26651, 10, -4 },
{ 10451, 10, -4 },
{ 16651, 10, -4 },
{ 22851, 10, -4 },
{ 26651, 10, -4 },
{ 32851, 10, -4 },
{ 26651, 10, -4 },
{ 6651, 10, -4 },
{ 451, 10, -4 },
{ 6651, 10, -4 },
{ 2202, 10, -3 },
{ 14096, 10, -4 },
{ 10111, 10, -4 },
{ -279, 10, -3 },
{ -6776, 10, -4 },
{ 1336, 10, -3 },
{ -147, 10, -2 },
{ 1336, 10, -3 },
{ -6039, 10, -4 },
{ 2202, 10, -3 },
{ -6039, 10, -4 },
{ 2202, 10, -3 },
{ 2419, 10, -3 },
{ -821, 10, -3 },
{ -11, 10, -3 },
{ 2336, 10, -3 },
{ 2109, 10, -3 },
{ 12621, 10, -4 },
{ -23551, 10, -4 },
{ -3202, 10, -3 },
{ -29751, 10, -4 }
},
style {
annotation {
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic,
aromatic
},
aid1 {
2,
2,
8,
8,
15,
15,
17,
17,
18,
18,
19,
21,
22,
22,
25,
25,
26,
27,
28,
31,
32,
33
},
aid2 {
24,
25,
24,
26,
20,
21,
19,
23,
27,
28,
20,
23,
29,
30,
26,
31,
33,
29,
30,
32,
34,
34
}
}
}
}
}
},
charge 0,
props {
{
urn {
label "Compound",
name "Canonicalized",
datatype uint,
release "2021.05.07"
},
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 { 715, 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 6
},
{
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 9
},
{
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 '00000371E07B30004400000000000000000000000001600000003060
C000000000005801F400001E06100000000C8EE1DE2632C7B2C81408AC032572540283F8A0612F
384898BC7EEE980F26A2E5B39F87382AE4D411FAE807B0D0120E28200181000141005040030200
028200000000000000'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 "N-tert-butyl-2-[5-chloro-2-methoxy-4-[[4-(6-methyl-1,3-ben
zothiazol-2-yl)anilino]methyl]phenoxy]acetamide"
},
{
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 "N-tert-butyl-2-[5-chloro-2-methoxy-4-[[4-(6-methyl-1,3-ben
zothiazol-2-yl)anilino]methyl]phenoxy]acetamide"
},
{
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 "N-tert-butyl-2-[5-chloro-2-methoxy-4-[[4-(6-
methyl-1,3-benzothiazol-2-yl)anilino]methyl]phenoxy]acetamide"
},
{
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 "N-tert-butyl-2-[5-chloro-2-methoxy-4-[[4-(6-methyl-1,3-ben
zothiazol-2-yl)anilino]methyl]phenoxy]acetamide"
},
{
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 "N-tert-butyl-2-[5-chloranyl-2-methoxy-4-[[[4-(6-methyl-1,3
-benzothiazol-2-yl)phenyl]amino]methyl]phenoxy]ethanamide"
},
{
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 "N-tert-butyl-2-[5-chloro-2-methoxy-4-[[4-(6-methyl-1,3-ben
zothiazol-2-yl)anilino]methyl]phenoxy]acetamide"
},
{
urn {
label "InChI",
name "Standard",
datatype string,
version "1.0.6",
software "InChI",
source "iupac.org",
release "2021.05.07"
},
value sval "InChI=1S/C28H30ClN3O3S/c1-17-6-11-22-25(12-17)36-27(31-22)
18-7-9-20(10-8-18)30-15-19-13-23(34-5)24(14-21(19)29)35-16-26(33)32-28(2,3)4/h
6-14,30H,15-16H2,1-5H3,(H,32,33)"
},
{
urn {
label "InChIKey",
name "Standard",
datatype string,
version "1.0.6",
software "InChI",
source "iupac.org",
release "2021.05.07"
},
value sval "YQBWVZPEANBFDN-UHFFFAOYSA-N"
},
{
urn {
label "Log P",
name "XLogP3-AA",
datatype double,
version "3.0",
source "sioc-ccbg.ac.cn",
release "2021.05.07"
},
value fval { 68, 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 "523.1696407"
},
{
urn {
label "Molecular Formula",
datatype string,
version "2.1",
software "PubChem",
source "ncbi.nlm.nih.gov",
release "2021.05.07"
},
value sval "C28H30ClN3O3S"
},
{
urn {
label "Molecular Weight",
datatype string,
version "2.1",
software "PubChem",
source "ncbi.nlm.nih.gov",
release "2021.05.07"
},
value sval "524.1"
},
{
urn {
label "SMILES",
name "Canonical",
datatype string,
version "2.3.0",
software "OEChem",
source "OpenEye Scientific Software",
release "2021.05.07"
},
value sval "CC1=CC2=C(C=C1)N=C(S2)C3=CC=C(C=C3)NCC4=CC(=C(C=C4Cl)OCC(=
O)NC(C)(C)C)OC"
},
{
urn {
label "SMILES",
name "Isomeric",
datatype string,
version "2.3.0",
software "OEChem",
source "OpenEye Scientific Software",
release "2021.05.07"
},
value sval "CC1=CC2=C(C=C1)N=C(S2)C3=CC=C(C=C3)NCC4=CC(=C(C=C4Cl)OCC(=
O)NC(C)(C)C)OC"
},
{
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 { 101, 10, 0 }
},
{
urn {
label "Weight",
name "MonoIsotopic",
datatype string,
version "2.1",
software "PubChem",
source "ncbi.nlm.nih.gov",
release "2021.05.07"
},
value sval "523.1696407"
}
},
count {
heavy-atom 36,
atom-chiral 0,
atom-chiral-def 0,
atom-chiral-undef 0,
bond-chiral 0,
bond-chiral-def 0,
bond-chiral-undef 0,
isotope-atom 0,
covalent-unit 1,
tautomers -1
}
}
}