Chemical Components in the PDB

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JXD : Summary

Code

JXD

One-letter code

X

Molecule name

2-(acetylamino)-4-O-[2-(acetylamino)-2-deoxy-beta-D-mannopyranosyl]-2-deoxy-1-O-[(S)-{[(R)-{[(2Z,6Z,10Z,14E,18E)-3,7,11,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaen-1-yl]oxy}(hydroxy)phosphoryl]oxy}(hydroxy)phosphoryl]-alpha-D-glucopyranose

Systematic names

ProgramVersionName
ACDLabs 12.01 2-(acetylamino)-4-O-[2-(acetylamino)-2-deoxy-beta-D-mannopyranosyl]-2-deoxy-1-O-[(S)-{[(R)-{[(2Z,6Z,10Z,14E,18E)-3,7,11,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaen-1-yl]oxy}(hydroxy)phosphoryl]oxy}(hydroxy)phosphoryl]-alpha-D-glucopyranose
OpenEye OEToolkits 2.0.6 [(2~{R},3~{R},4~{R},5~{S},6~{R})-3-acetamido-5-[(2~{S},3~{S},4~{R},5~{S},6~{R})-3-acetamido-6-(hydroxymethyl)-4,5-bis(oxidanyl)oxan-2-yl]oxy-6-(hydroxymethyl)-4-oxidanyl-oxan-2-yl] [[(2~{Z},6~{Z},10~{Z},14~{E},18~{E})-3,7,11,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaenoxy]-oxidanyl-phosphoryl] hydrogen phosphate

Formula

C46 H78 N2 O17 P2

Formal charge

0

Molecular weight

993.062 Da

SMILES

TypeProgramVersionDescriptor
SMILES ACDLabs 12.01 C1(O)C(O)C(C(OC1CO)OC2C(O)C(C(OC2CO)OP(=O)(OP(O)(OC[C@H]=C(CC[C@H]=C(C)CC[C@H]=C(CC\C=C(\CC\C=C(/C)CC[C@H]=C(C)C)C)C)C)=O)O)NC(C)=O)NC(C)=O
SMILES CACTVS 3.385 CC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCO[P](O)(=O)O[P](O)(=O)O[CH]1O[CH](CO)[CH](O[CH]2O[CH](CO)[CH](O)[CH](O)[CH]2NC(C)=O)[CH](O)[CH]1NC(C)=O
SMILES OpenEye OEToolkits 2.0.6 CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCOP(=O)(O)OP(=O)(O)OC1C(C(C(C(O1)CO)OC2C(C(C(C(O2)CO)O)O)NC(=O)C)O)NC(=O)C)C)C)C)C)C)C
Canonical SMILES CACTVS 3.385 CC(C)=CCC/C(C)=C/CC/C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CO[P](O)(=O)O[P](O)(=O)O[C@H]1O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]2NC(C)=O)[C@H](O)[C@H]1NC(C)=O
Canonical SMILES OpenEye OEToolkits 2.0.6 CC(=CCC/C(=C/CC/C(=C/CC/C(=C\CC/C(=C\CC/C(=C\COP(=O)(O)OP(=O)(O)O[C@@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O[C@H]2[C@H]([C@H]([C@@H]([C@H](O2)CO)O)O)NC(=O)C)O)NC(=O)C)/C)/C)/C)/C)/C)C

IUPAC InChI

InChI=1S/C46H78N2O17P2/c1-29(2)15-10-16-30(3)17-11-18-31(4)19-12-20-32(5)21-13-22-33(6)23-14-24-34(7)25-26-60-66(56,57)65-67(58,59)64-46-40(48-36(9)52)43(55)44(38(28-50)62-46)63-45-39(47-35(8)51)42(54)41(53)37(27-49)61-45/h15,17,19,21,23,25,37-46,49-50,53-55H,10-14,16,18,20,22,24,26-28H2,1-9H3,(H,47,51)(H,48,52)(H,56,57)(H,58,59)/b30-17+,31-19+,32-21-,33-23-,34-25-/t37-,38-,39+,40-,41-,42-,43-,44-,45+,46-/m1/s1

IUPAC InChI key

MUXGVGLOWSLCMK-NSGWRCNHSA-N
JXD

wwPDB Information

Atom count

145 (67 without Hydrogen)

Polymer type

Bound ligand

Type description

NON-POLYMER

Type code

HETAIN

Is modified

No

Standard parent

Not Assigned

Defined at

2018-10-09

Last modified at

2018-10-12

Status

Released

Obsoleted

Not Assigned



JXD : Atoms of Molecule

Total Number of Atoms: 145
Record Atom Name Symbol PDB Name Stereochemistry Is Aromatic Is Leaving Atom Charge X-Coordinate Y-Coordinate Z-Coordinate
1 C10 C C1 S N N 0 -10.478 3.876 0.139
2 C12 C C2 R N N 0 -9.932 3.6 1.543
3 C14 C C3 S N N 0 -8.498 3.072 1.426
4 C16 C C4 N N N 0 -6.319 4.097 1.057
5 C20 C C5 N N N 0 -7.744 -1.092 1.837
6 C02 C C6 R N N 0 -5.984 0.147 -1.354
7 C03 C C7 S N N 0 -7.051 0.083 -0.257
8 C05 C C8 S N N 0 -8.494 1.821 0.545
9 C07 C C9 R N N 0 -10.397 2.594 -0.694
10 C08 C C10 N N N 0 -10.884 2.878 -2.116
11 C17 C C11 N N N 0 -5.442 5.154 0.436
12 C19 C C12 R N N 0 -6.653 -0.98 0.77
13 C23 C C13 R N N 0 -5.476 -2.252 -0.889
14 C31 C C14 N N N 0 2.063 -1.633 1.243
15 C32 C C15 N N N 0 2.696 -0.266 1.242
16 C33 C C16 N N N 0 3.633 0.023 2.111
17 C34 C C17 N N N 0 4.14 -1.039 3.053
18 C35 C C18 N N N 0 5.394 -1.688 2.463
19 C36 C C19 N N N 0 5.901 -2.749 3.404
20 C37 C C20 N N N 0 5.988 -3.993 3.003
21 C41 C C24 N N N 0 6.429 -3.885 -1.719
22 C38 C C21 N N N 0 5.531 -4.372 1.618
23 C39 C C22 N N N 0 6.725 -4.343 0.661
24 C40 C C23 N N N 0 6.268 -4.722 -0.724
25 C42 C C25 N N N 0 6.998 -2.512 -1.464
26 C43 C C26 N N N 0 8.517 -2.548 -1.648
27 C44 C C27 N N N 0 9.085 -1.176 -1.393
28 C45 C C28 N N N 0 9.823 -0.593 -2.306
29 C46 C C29 N N N 0 10.285 0.828 -2.106
30 C47 C C30 N N N 0 11.688 0.826 -1.495
31 C48 C C31 N N N 0 12.151 2.247 -1.296
32 C49 C C32 N N N 0 12.439 2.679 -0.093
33 C50 C C33 N N N 0 13.017 4.058 0.093
34 C51 C C34 N N N 0 11.89 5.045 0.405
35 C52 C C35 N N N 0 12.468 6.425 0.591
36 C53 C C36 N N N 0 12.088 7.405 -0.19
37 C54 C C37 N N N 0 11.108 7.144 -1.304
38 C55 C C38 N N N 0 12.632 8.794 0.026
39 C56 C C39 N N N 0 12.193 1.797 1.104
40 C57 C C40 N N N 0 10.209 -1.343 -3.554
41 C58 C C41 N N N 0 6.046 -4.294 -3.118
42 C59 C C42 N N N 0 6.546 -5.045 3.926
43 C60 C C43 N N N 0 4.203 1.416 2.17
44 C63 C C44 R N N 0 -5.827 -1.241 -1.983
45 C65 C C45 N N N 0 -4.748 -2.102 -3.991
46 C66 C C46 N N N 0 -3.646 -2.069 -5.019
47 N15 N N1 N N N 0 -7.646 4.1 0.822
48 N64 N N2 N N N 0 -4.756 -1.209 -2.982
49 O01 O O1 N N N 0 -6.383 1.084 -2.356
50 O04 O O2 N N N 0 -7.152 1.355 0.386
51 O06 O O3 N N N 0 -9.043 2.14 -0.735
52 O09 O O4 N N N 0 -10.919 1.659 -2.861
53 O11 O O5 N N N 0 -11.839 4.3 0.231
54 O13 O O6 N N N 0 -9.935 4.81 2.303
55 O18 O O7 N N N 0 -5.83 3.245 1.768
56 O21 O O8 N N N 0 -7.307 -1.972 2.875
57 O22 O O9 N N N 0 -6.496 -2.24 0.115
58 O24 O O10 N N N 0 -4.223 -1.901 -0.3
59 O26 O O11 N N N 0 -2.902 -4.015 -0.697
60 O27 O O12 N N N 0 -1.85 -2.257 0.776
61 O29 O O13 N N N 0 -0.31 -3.524 2.489
62 O30 O O14 N N N 0 0.647 -1.503 1.107
63 O61 O O15 N N N 0 0.072 -3.697 -0.001
64 O62 O O16 N N N 0 -3.895 -3.688 1.6
65 O67 O O17 N N N 0 -5.628 -2.933 -4.073
66 P25 P P1 N N N 0 -3.211 -2.988 0.322
67 P28 P P2 N N N 0 -0.351 -2.765 1.069
68 H101 H H1 N N N 0 -9.884 4.657 -0.336
69 H121 H H2 N N N 0 -10.556 2.857 2.038
70 H141 H H3 N N N 0 -8.121 2.821 2.418
71 H201 H H4 N N N 0 -7.944 -0.106 2.257
72 H202 H H5 N N N 0 -8.654 -1.486 1.386
73 H021 H H6 N N N 0 -5.034 0.46 -0.92
74 H031 H H7 N N N 0 -8.012 -0.179 -0.7
75 H173 H H13 N N N 0 -4.407 4.991 0.737
76 H051 H H8 N N N 0 -9.095 1.043 1.015
77 H071 H H9 N N N 0 -11.024 1.826 -0.242
78 H082 H H10 N N N 0 -11.885 3.309 -2.078
79 H081 H H11 N N N 0 -10.205 3.58 -2.6
80 H172 H H12 N N N 0 -5.767 6.139 0.771
81 H171 H H14 N N N 0 -5.517 5.097 -0.65
82 H191 H H15 N N N 0 -5.712 -0.695 1.241
83 H231 H H16 N N N 0 -5.406 -3.249 -1.324
84 H312 H H17 N N N 0 2.456 -2.216 0.41
85 H311 H H18 N N N 0 2.293 -2.14 2.18
86 H321 H H19 N N N 0 2.378 0.476 0.525
87 H342 H H20 N N N 0 4.384 -0.586 4.014
88 H341 H H21 N N N 0 3.37 -1.798 3.194
89 H351 H H22 N N N 0 5.15 -2.141 1.502
90 H352 H H23 N N N 0 6.163 -0.929 2.322
91 H361 H H24 N N N 0 6.192 -2.485 4.41
92 H381 H H25 N N N 0 5.106 -5.375 1.637
93 H382 H H26 N N N 0 4.776 -3.663 1.278
94 H391 H H27 N N N 0 7.151 -3.34 0.642
95 H392 H H28 N N N 0 7.48 -5.051 1.001
96 H401 H H29 N N N 0 5.808 -5.683 -0.897
97 H422 H H30 N N N 0 6.563 -1.803 -2.168
98 H421 H H31 N N N 0 6.762 -2.205 -0.445
99 H431 H H32 N N N 0 8.951 -3.257 -0.944
100 H432 H H33 N N N 0 8.752 -2.855 -2.667
101 H441 H H34 N N N 0 8.885 -0.673 -0.459
102 H461 H H35 N N N 0 10.309 1.341 -3.068
103 H462 H H36 N N N 0 9.598 1.343 -1.436
104 H471 H H37 N N N 0 11.665 0.313 -0.534
105 H472 H H38 N N N 0 12.376 0.311 -2.166
106 H481 H H39 N N N 0 12.244 2.908 -2.144
107 H502 H H40 N N N 0 13.728 4.046 0.919
108 H501 H H41 N N N 0 13.527 4.365 -0.82
109 H512 H H42 N N N 0 11.179 5.058 -0.422
110 H511 H H43 N N N 0 11.381 4.739 1.318
111 H521 H H44 N N N 0 13.196 6.605 1.369
112 H543 H H45 N N N 0 10.092 7.19 -0.913
113 H541 H H46 N N N 0 11.232 7.898 -2.082
114 H542 H H47 N N N 0 11.291 6.155 -1.725
115 H553 H H48 N N N 0 13.321 8.788 0.87
116 H551 H H49 N N N 0 13.158 9.122 -0.871
117 H552 H H50 N N N 0 11.809 9.478 0.234
118 H561 H H51 N N N 0 13.032 1.113 1.23
119 H563 H H52 N N N 0 12.09 2.415 1.995
120 H562 H H53 N N N 0 11.277 1.225 0.951
121 H573 H H54 N N N 0 9.411 -1.257 -4.291
122 H571 H H55 N N N 0 11.127 -0.92 -3.963
123 H572 H H56 N N N 0 10.369 -2.393 -3.312
124 H582 H H57 N N N 0 5.005 -4.027 -3.302
125 H581 H H58 N N N 0 6.685 -3.778 -3.835
126 H583 H H59 N N N 0 6.17 -5.371 -3.228
127 H593 H H60 N N N 0 5.736 -5.482 4.511
128 H592 H H61 N N N 0 7.031 -5.825 3.338
129 H591 H H62 N N N 0 7.274 -4.59 4.598
130 H602 H H63 N N N 0 5.059 1.487 1.498
131 H601 H H64 N N N 0 3.441 2.134 1.865
132 H603 H H65 N N N 0 4.522 1.636 3.189
133 H631 H H66 N N N 0 -6.762 -1.532 -2.462
134 H663 H H67 N N N 0 -2.954 -1.261 -4.782
135 H662 H H68 N N N 0 -3.113 -3.019 -5.01
136 H661 H H69 N N N 0 -4.076 -1.902 -6.007
137 H151 H H70 N N N 0 -8.037 4.781 0.254
138 H641 H H71 N N N 0 -4.052 -0.544 -2.917
139 H011 H H72 N N N 0 -5.753 1.173 -3.084
140 H091 H H73 N N N 0 -11.22 1.764 -3.774
141 H111 H H74 N N N 0 -12.251 4.491 -0.623
142 H131 H H75 N N N 0 -10.811 5.204 2.411
143 H211 H H76 N N N 0 -7.95 -2.091 3.587
144 H1 H H77 N N N 0 -0.576 -2.973 3.237
145 H2 H H78 N N N 0 -4.125 -3.073 2.31



JXD : Chemical Bonds

Total Number of Bonds: 146
Record First Atom Second Atom First Element Second Element Bond Order Type Bond Length Bond Stereochemistry Is Aromatic
1 C54 C53 C C sing 1.51 N N
2 C55 C53 C C sing 1.51 N N
3 C53 C52 C C doub 1.31 N N
4 C52 C51 C C sing 1.51 N N
5 C51 C50 C C sing 1.53 N N
6 C43 C42 C C sing 1.53 N N
7 C43 C44 C C sing 1.51 N N
8 C42 C41 C C sing 1.51 N N
9 C44 C45 C C doub 1.31 E N
10 C50 C49 C C sing 1.51 N N
11 C57 C45 C C sing 1.51 N N
12 C58 C41 C C sing 1.51 N N
13 C41 C40 C C doub 1.31 Z N
14 C45 C46 C C sing 1.51 N N
15 C48 C49 C C doub 1.31 E N
16 C48 C47 C C sing 1.51 N N
17 C49 C56 C C sing 1.51 N N
18 C46 C47 C C sing 1.53 N N
19 C40 C39 C C sing 1.51 N N
20 C60 C33 C C sing 1.51 N N
21 C39 C38 C C sing 1.53 N N
22 O26 P25 O P doub 1.48 N N
23 C33 C34 C C sing 1.51 N N
24 C33 C32 C C doub 1.31 Z N
25 C34 C35 C C sing 1.53 N N
26 O62 P25 O P sing 1.61 N N
27 C38 C37 C C sing 1.51 N N
28 P25 O24 P O sing 1.61 N N
29 P25 O27 P O sing 1.61 N N
30 C32 C31 C C sing 1.51 N N
31 C35 C36 C C sing 1.51 N N
32 C37 C36 C C doub 1.31 Z N
33 C37 C59 C C sing 1.51 N N
34 O24 C23 O C sing 1.43 N N
35 O27 P28 O P sing 1.61 N N
36 O22 C23 O C sing 1.43 N N
37 O22 C19 O C sing 1.43 N N
38 C23 C63 C C sing 1.53 N N
39 C31 O30 C O sing 1.43 N N
40 C20 O21 C O sing 1.43 N N
41 C20 C19 C C sing 1.53 N N
42 C19 C03 C C sing 1.53 N N
43 O61 P28 O P doub 1.48 N N
44 P28 O30 P O sing 1.61 N N
45 P28 O29 P O sing 1.61 N N
46 O67 C65 O C doub 1.21 N N
47 C63 N64 C N sing 1.46 N N
48 C63 C02 C C sing 1.53 N N
49 C65 N64 C N sing 1.35 N N
50 C65 C66 C C sing 1.51 N N
51 C17 C16 C C sing 1.51 N N
52 C03 C02 C C sing 1.53 N N
53 C03 O04 C O sing 1.43 N N
54 C02 O01 C O sing 1.43 N N
55 O18 C16 O C doub 1.21 N N
56 C16 N15 C N sing 1.35 N N
57 O04 C05 O C sing 1.43 N N
58 N15 C14 N C sing 1.47 N N
59 C14 C05 C C sing 1.53 N N
60 C14 C12 C C sing 1.53 N N
61 C05 O06 C O sing 1.43 N N
62 O06 C07 O C sing 1.43 N N
63 C12 O13 C O sing 1.43 N N
64 C12 C10 C C sing 1.53 N N
65 C07 C10 C C sing 1.53 N N
66 C07 C08 C C sing 1.53 N N
67 C10 O11 C O sing 1.43 N N
68 O09 C08 O C sing 1.43 N N
69 C10 H101 C H sing 1.09 N N
70 C12 H121 C H sing 1.09 N N
71 C14 H141 C H sing 1.09 N N
72 C20 H201 C H sing 1.09 N N
73 C20 H202 C H sing 1.09 N N
74 C02 H021 C H sing 1.09 N N
75 C03 H031 C H sing 1.09 N N
76 C05 H051 C H sing 1.09 N N
77 C07 H071 C H sing 1.09 N N
78 C08 H082 C H sing 1.09 N N
79 C08 H081 C H sing 1.09 N N
80 C17 H172 C H sing 1.09 N N
81 C17 H173 C H sing 1.09 N N
82 C17 H171 C H sing 1.09 N N
83 C19 H191 C H sing 1.09 N N
84 C23 H231 C H sing 1.09 N N
85 C31 H312 C H sing 1.09 N N
86 C31 H311 C H sing 1.09 N N
87 C32 H321 C H sing 1.08 N N
88 C34 H342 C H sing 1.09 N N
89 C34 H341 C H sing 1.09 N N
90 C35 H351 C H sing 1.09 N N
91 C35 H352 C H sing 1.09 N N
92 C36 H361 C H sing 1.08 N N
93 C38 H381 C H sing 1.09 N N
94 C38 H382 C H sing 1.09 N N
95 C39 H391 C H sing 1.09 N N
96 C39 H392 C H sing 1.09 N N
97 C40 H401 C H sing 1.08 N N
98 C42 H422 C H sing 1.09 N N
99 C42 H421 C H sing 1.09 N N
100 C43 H431 C H sing 1.09 N N
101 C43 H432 C H sing 1.09 N N
102 C44 H441 C H sing 1.08 N N
103 C46 H461 C H sing 1.09 N N
104 C46 H462 C H sing 1.09 N N
105 C47 H471 C H sing 1.09 N N
106 C47 H472 C H sing 1.09 N N
107 C48 H481 C H sing 1.08 N N
108 C50 H502 C H sing 1.09 N N
109 C50 H501 C H sing 1.09 N N
110 C51 H512 C H sing 1.09 N N
111 C51 H511 C H sing 1.09 N N
112 C52 H521 C H sing 1.08 N N
113 C54 H543 C H sing 1.09 N N
114 C54 H541 C H sing 1.09 N N
115 C54 H542 C H sing 1.09 N N
116 C55 H553 C H sing 1.09 N N
117 C55 H551 C H sing 1.09 N N
118 C55 H552 C H sing 1.09 N N
119 C56 H561 C H sing 1.09 N N
120 C56 H563 C H sing 1.09 N N
121 C56 H562 C H sing 1.09 N N
122 C57 H573 C H sing 1.09 N N
123 C57 H571 C H sing 1.09 N N
124 C57 H572 C H sing 1.09 N N
125 C58 H582 C H sing 1.09 N N
126 C58 H581 C H sing 1.09 N N
127 C58 H583 C H sing 1.09 N N
128 C59 H593 C H sing 1.09 N N
129 C59 H592 C H sing 1.09 N N
130 C59 H591 C H sing 1.09 N N
131 C60 H602 C H sing 1.09 N N
132 C60 H601 C H sing 1.09 N N
133 C60 H603 C H sing 1.09 N N
134 C63 H631 C H sing 1.09 N N
135 C66 H663 C H sing 1.09 N N
136 C66 H662 C H sing 1.09 N N
137 C66 H661 C H sing 1.09 N N
138 N15 H151 N H sing 0.97 N N
139 N64 H641 N H sing 0.97 N N
140 O01 H011 O H sing 0.97 N N
141 O09 H091 O H sing 0.97 N N
142 O11 H111 O H sing 0.97 N N
143 O13 H131 O H sing 0.97 N N
144 O21 H211 O H sing 0.97 N N
145 O29 H1 O H sing 0.97 N N
146 O62 H2 O H sing 0.97 N N



JXD : Used in PDB Entries

Total Number of PDB Entries: 1
Ligand Code PDB Entry ID Type Total Distinct
JXD 6mps Open in New Window Bound ligand 1 1