Showing metabocard for CDP-DG(22:3(10Z,13Z,16Z)/6 keto-PGF1alpha) (HMDB0292351)
| Record Information | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Version | 5.0 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Status | Predicted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Creation Date | 2021-09-17 06:40:01 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Update Date | 2022-11-30 20:08:03 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HMDB ID | HMDB0292351 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary Accession Numbers | None | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Metabolite Identification | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Common Name | CDP-DG(22:3(10Z,13Z,16Z)/6 keto-PGF1alpha) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Description | CDP-DG(22:3(10Z,13Z,16Z)/6 keto-PGF1alpha) is an oxidized CDP-diacylglycerol (CDP-DG). Oxidized CDP-diacylglycerols are glycerophospholipids in which a cytidine diphosphate moiety occupies a glycerol substitution site and at least one of the fatty acyl chains has undergone oxidation. As all oxidized lipids, oxidized CDP-diacylglycerols belong to a group of biomolecules that have a role as signaling molecules. The biosynthesis of oxidized lipids is mediated by several enzymatic families, including cyclooxygenases (COX), lipoxygenases (LOX) and cytochrome P450s (CYP). Non-enzymatically oxidized lipids are produced by uncontrolled oxidation through free radicals and are considered harmful to human health (PMID: 33329396 ). As is the case with diacylglycerols, CDP-diacylglycerols can have many different combinations of fatty acids of varying lengths, saturation and degrees of oxidation attached at the C-1 and C-2 positions. CDP-DG(22:3(10Z,13Z,16Z)/6 keto-PGF1alpha), in particular, consists of one chain of one 10Z,13Z,16Z-docosenoyl at the C-1 position and one chain of 6-Keto-prostaglandin F1alpha at the C-2 position. Phospholipids are ubiquitous in nature and are key components of the lipid bilayer of cells, as well as being involved in metabolism and signaling. Similarly to what occurs with phospholipids, the fatty acid distribution at the C-1 and C-2 positions of glycerol within oxidized phospholipids is continually in flux, owing to phospholipid degradation and the continuous phospholipid remodeling that occurs while these molecules are in membranes. Oxidized CDP-DGs can be synthesized via three different routes. In one route, the oxidized CDP-DG is synthetized de novo following the same mechanisms as for CDP-DGs but incorporating oxidized acyl chains (PMID: 33329396 ). An alternative is the transacylation of one of the non-oxidized acyl chains with an oxidized acylCoA (PMID: 33329396 ). The third pathway results from the oxidation of the acyl chain while still attached to the CDP-DG backbone, mainly through the action of LOX (PMID: 33329396 ). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structure |  MOL for HMDB0292351 (CDP-DG(22:3(10Z,13Z,16Z)/6 keto-PGF1alpha))
Mrv1652309172108402D
79 81 0 0 1 0 999 V2000
-2.6865 -1.9837 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
-1.9678 -1.5284 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.9993 -0.7040 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
-1.3011 -0.2646 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.8459 0.4142 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.5714 -0.6495 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
-0.5399 -1.4739 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.2381 -1.9134 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.1268 -0.2100 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
-0.2315 0.5700 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
0.0573 1.3852 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
0.4284 2.1714 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.2062 2.5853 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.0537 2.8481 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0
1.3991 3.4519 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.0729 3.7474 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.8993 2.6108 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.6417 2.1352 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0
3.6535 3.0434 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.3987 2.7972 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.5420 1.7405 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
5.2455 1.4514 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.9488 0.9566 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
6.7968 1.1709 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.6089 0.9327 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
8.2839 1.4454 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.2804 2.2994 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
8.9012 0.8586 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.6122 1.3108 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.2856 0.8019 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.9934 1.2662 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.6900 0.7850 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.4194 1.2158 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
13.1429 0.7730 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
13.8953 1.1709 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
14.6171 0.7214 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
15.3789 1.0779 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
15.4498 1.8999 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
16.1970 2.2495 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
16.2678 3.0714 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
15.5914 3.5438 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
15.6623 4.3657 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
14.9858 4.8380 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
14.2386 4.4884 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
13.5622 4.9607 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.8149 4.6111 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.1385 5.0834 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.3913 4.7338 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.7148 5.2061 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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6.2269 -1.2144 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
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2.6389 -2.0851 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.7777 -2.1447 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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2.9646 0.1069 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
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2.5628 0.8402 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
3.3121 1.0636 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9809 1.4819 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.3522 2.3162 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
5.2043 2.2041 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.3522 3.3624 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.8841 4.0934 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.5461 4.8920 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.0698 5.5336 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.7772 6.3050 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.8814 1.1681 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
0.4418 0.5402 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1.7307 1.0410 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
1.2656 1.7511 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
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73 74 1 0 0 0 0
74 75 1 0 0 0 0
11 76 1 0 0 0 0
76 77 1 6 0 0 0
76 78 1 0 0 0 0
66 78 1 0 0 0 0
78 79 1 1 0 0 0
M END
3D MOL for HMDB0292351 (CDP-DG(22:3(10Z,13Z,16Z)/6 keto-PGF1alpha))HMDB0292351
RDKit 3D
CDP-DG(22:3(10Z,13Z,16Z)/6 keto-PGF1alpha)
170172 0 0 0 0 0 0 0 0999 V2000
20.6768 2.4632 -2.1978 C 0 0 0 0 0 0 0 0 0 0 0 0
19.4643 3.3084 -1.9312 C 0 0 0 0 0 0 0 0 0 0 0 0
18.2889 2.3316 -1.6444 C 0 0 0 0 0 0 0 0 0 0 0 0
18.6756 1.5685 -0.4512 C 0 0 0 0 0 0 0 0 0 0 0 0
17.8691 0.4831 0.0995 C 0 0 0 0 0 0 0 0 0 0 0 0
16.4493 0.7602 0.4575 C 0 0 0 0 0 0 0 0 0 0 0 0
15.5102 1.0387 -0.6131 C 0 0 0 0 0 0 0 0 0 0 0 0
14.4909 0.2730 -0.9038 C 0 0 0 0 0 0 0 0 0 0 0 0
14.0549 -0.9624 -0.2958 C 0 0 0 0 0 0 0 0 0 0 0 0
14.7905 -1.5525 0.7954 C 0 0 0 0 0 0 0 0 0 0 0 0
14.3463 -1.7967 1.9905 C 0 0 0 0 0 0 0 0 0 0 0 0
12.9845 -1.5226 2.4839 C 0 0 0 0 0 0 0 0 0 0 0 0
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9.0883 -2.5766 2.0014 C 0 0 0 0 0 0 0 0 0 0 0 0
8.0274 -2.1721 1.0807 C 0 0 0 0 0 0 0 0 0 0 0 0
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5.4689 0.3409 1.1987 C 0 0 0 0 0 0 0 0 0 0 0 0
4.3002 0.1739 2.1233 C 0 0 0 0 0 0 0 0 0 0 0 0
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-9.3437 -3.5787 0.8653 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.6275 -2.5212 2.1675 H 0 0 0 0 0 0 0 0 0 0 0 0
-9.8481 -3.1612 -1.2614 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.9171 -1.6595 -1.2147 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.7519 -1.9590 -1.4251 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.5194 -1.4381 0.4459 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.7833 0.3247 -1.6690 H 0 0 0 0 0 0 0 0 0 0 0 0
-9.2063 -0.8947 -3.0543 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.3719 -0.4808 -4.9587 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.5870 0.3101 -5.1341 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.2568 -1.1828 -3.7275 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.7342 2.2662 -2.9371 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.7755 2.4629 -4.6774 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.3088 1.8203 -3.1196 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.1768 2.1215 -4.8699 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.9742 4.0968 -3.6623 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.3769 4.4553 -4.3738 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.6212 5.2822 -2.1361 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.3165 3.9899 -2.1181 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.0697 3.9994 -0.2372 H 0 0 0 0 0 0 0 0 0 0 0 0
-15.1827 3.2229 -1.4524 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.6062 2.4574 -0.9741 H 0 0 0 0 0 0 0 0 0 0 0 0
-9.8281 0.3748 0.2314 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.1754 2.7543 -0.1653 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.5359 2.4018 -1.0378 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.7068 1.8524 -2.8983 H 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 7 1 0
7 8 2 0
8 9 1 0
9 10 1 0
10 11 2 0
11 12 1 0
12 13 1 0
13 14 2 0
14 15 1 0
15 16 1 0
16 17 1 0
17 18 1 0
18 19 1 0
19 20 1 0
20 21 1 0
21 22 1 0
22 23 1 0
23 24 2 0
23 25 1 0
25 26 1 0
26 27 1 0
27 28 1 0
28 29 1 0
29 30 1 0
30 31 2 0
30 32 1 0
30 33 1 0
33 34 1 0
34 35 2 0
34 36 1 0
34 37 1 0
37 38 1 0
38 39 1 0
39 40 1 0
40 41 1 0
41 42 1 0
42 43 1 0
43 44 2 0
44 45 1 0
45 46 1 0
45 47 2 0
47 48 1 0
48 49 2 0
41 50 1 0
50 51 1 0
51 52 1 0
52 53 2 0
52 54 1 0
54 55 1 0
55 56 1 0
56 57 1 0
57 58 1 0
58 59 2 0
58 60 1 0
50 61 1 0
61 62 1 0
61 63 1 0
63 64 1 0
64 65 1 0
64 66 1 0
66 67 1 0
67 68 2 0
68 69 1 0
69 70 1 0
69 71 1 0
71 72 1 0
72 73 1 0
73 74 1 0
74 75 1 0
66 76 1 0
76 77 1 0
76 78 1 0
78 79 1 0
60 27 1 0
78 39 1 0
48 42 1 0
1 80 1 0
1 81 1 0
1 82 1 0
2 83 1 0
2 84 1 0
3 85 1 0
3 86 1 0
4 87 1 0
4 88 1 0
5 89 1 0
5 90 1 0
6 91 1 0
6 92 1 0
7 93 1 0
8 94 1 0
9 95 1 0
9 96 1 0
10 97 1 0
11 98 1 0
12 99 1 0
12100 1 0
13101 1 0
14102 1 0
15103 1 0
15104 1 0
16105 1 0
16106 1 0
17107 1 0
17108 1 0
18109 1 0
18110 1 0
19111 1 0
19112 1 0
20113 1 0
20114 1 0
21115 1 0
21116 1 0
22117 1 0
22118 1 0
26119 1 0
26120 1 0
27121 1 6
28122 1 0
28123 1 0
32124 1 0
36125 1 0
38126 1 0
38127 1 0
39128 1 6
41129 1 6
43130 1 0
44131 1 0
46132 1 0
46133 1 0
50134 1 6
51135 1 0
51136 1 0
54137 1 0
54138 1 0
55139 1 0
55140 1 0
56141 1 0
56142 1 0
57143 1 0
57144 1 0
61145 1 1
62146 1 0
63147 1 0
63148 1 0
64149 1 6
65150 1 0
66151 1 6
67152 1 0
68153 1 0
69154 1 6
70155 1 0
71156 1 0
71157 1 0
72158 1 0
72159 1 0
73160 1 0
73161 1 0
74162 1 0
74163 1 0
75164 1 0
75165 1 0
75166 1 0
76167 1 1
77168 1 0
78169 1 1
79170 1 0
M END
3D SDF for HMDB0292351 (CDP-DG(22:3(10Z,13Z,16Z)/6 keto-PGF1alpha))
Mrv1652309172108402D
79 81 0 0 1 0 999 V2000
-2.6865 -1.9837 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
-1.9678 -1.5284 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.9993 -0.7040 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
-1.3011 -0.2646 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.8459 0.4142 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.5714 -0.6495 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
-0.5399 -1.4739 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.2381 -1.9134 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.1268 -0.2100 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
-0.2315 0.5700 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
0.0573 1.3852 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
0.4284 2.1714 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.2062 2.5853 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.0537 2.8481 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0
1.3991 3.4519 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.0729 3.7474 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.8993 2.6108 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.6417 2.1352 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0
3.6535 3.0434 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.3987 2.7972 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.5420 1.7405 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
5.2455 1.4514 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.9488 0.9566 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
6.7968 1.1709 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.6089 0.9327 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
8.2839 1.4454 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.2804 2.2994 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
8.9012 0.8586 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.6122 1.3108 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.2856 0.8019 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.9934 1.2662 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.6900 0.7850 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.4194 1.2158 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
13.1429 0.7730 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
13.8953 1.1709 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
14.6171 0.7214 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
15.3789 1.0779 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
15.4498 1.8999 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
16.1970 2.2495 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
16.2678 3.0714 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
15.5914 3.5438 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
15.6623 4.3657 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
14.9858 4.8380 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
14.2386 4.4884 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
13.5622 4.9607 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.8149 4.6111 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.1385 5.0834 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.3913 4.7338 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.7148 5.2061 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.9810 0.0975 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
5.5739 -0.6659 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.2269 -1.2144 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
5.0956 -1.3799 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.3303 -1.7772 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.5046 -2.0460 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6389 -2.0851 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.7777 -2.1447 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.6199 -2.9937 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1.0669 -1.6520 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.6793 -0.8755 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
1.4498 -0.5356 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
1.1108 0.2836 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.2699 -0.3596 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.9646 0.1069 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
3.4208 -0.6160 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.5628 0.8402 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
3.3121 1.0636 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9809 1.4819 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.3522 2.3162 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
5.2043 2.2041 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.3522 3.3624 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.8841 4.0934 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.5461 4.8920 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.0698 5.5336 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.7772 6.3050 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.8814 1.1681 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
0.4418 0.5402 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1.7307 1.0410 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
1.2656 1.7511 0.0000 O 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
4 6 1 0 0 0 0
6 7 1 0 0 0 0
7 8 2 0 0 0 0
2 8 1 0 0 0 0
9 6 1 6 0 0 0
9 10 1 0 0 0 0
11 10 1 6 0 0 0
11 12 1 0 0 0 0
12 13 1 0 0 0 0
13 14 1 0 0 0 0
14 15 1 0 0 0 0
14 16 2 0 0 0 0
14 17 1 0 0 0 0
17 18 1 0 0 0 0
18 19 1 0 0 0 0
18 20 2 0 0 0 0
18 21 1 0 0 0 0
21 22 1 0 0 0 0
22 23 1 0 0 0 0
23 24 1 1 0 0 0
24 25 1 0 0 0 0
25 26 1 0 0 0 0
26 27 2 0 0 0 0
26 28 1 0 0 0 0
28 29 1 0 0 0 0
29 30 1 0 0 0 0
30 31 1 0 0 0 0
31 32 1 0 0 0 0
32 33 1 0 0 0 0
33 34 1 0 0 0 0
34 35 1 0 0 0 0
35 36 1 0 0 0 0
36 37 2 0 0 0 0
37 38 1 0 0 0 0
38 39 1 0 0 0 0
39 40 2 0 0 0 0
40 41 1 0 0 0 0
41 42 1 0 0 0 0
42 43 2 0 0 0 0
43 44 1 0 0 0 0
44 45 1 0 0 0 0
45 46 1 0 0 0 0
46 47 1 0 0 0 0
47 48 1 0 0 0 0
48 49 1 0 0 0 0
23 50 1 0 0 0 0
50 51 1 0 0 0 0
51 52 2 0 0 0 0
51 53 1 0 0 0 0
53 54 1 0 0 0 0
54 55 1 0 0 0 0
55 56 1 0 0 0 0
56 57 1 0 0 0 0
57 58 2 0 0 0 0
57 59 1 0 0 0 0
60 59 1 6 0 0 0
9 60 1 0 0 0 0
60 61 1 0 0 0 0
61 62 1 1 0 0 0
61 63 1 0 0 0 0
63 64 1 0 0 0 0
64 65 1 6 0 0 0
64 66 1 0 0 0 0
66 67 1 1 0 0 0
67 68 2 0 0 0 0
68 69 1 0 0 0 0
69 70 1 6 0 0 0
69 71 1 0 0 0 0
71 72 1 0 0 0 0
72 73 1 0 0 0 0
73 74 1 0 0 0 0
74 75 1 0 0 0 0
11 76 1 0 0 0 0
76 77 1 6 0 0 0
76 78 1 0 0 0 0
66 78 1 0 0 0 0
78 79 1 1 0 0 0
M END
> <DATABASE_ID>
HMDB0292351
> <DATABASE_NAME>
hmdb
> <SMILES>
CCCCCC\C=C/C\C=C/C\C=C/CCCCCCCCC(=O)OC[C@@H]1COP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@@H](CC(=O)CCCCC(=O)O1)[C@@H](O)C[C@@H](O)[C@H](\C=C/[C@@H](O)CCCCC)[C@H](O)[C@@H]2O)N1C=CC(N)=NC1=O
> <INCHI_IDENTIFIER>
InChI=1S/C55H91N3O19P2/c1-3-5-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-25-30-50(63)72-38-43-39-73-78(68,69)77-79(70,71)74-40-48-53(66)52(65)44(33-32-41(59)28-24-6-4-2)46(61)37-47(62)45(36-42(60)29-26-27-31-51(64)75-43)54(76-48)58-35-34-49(56)57-55(58)67/h10-11,13-14,16-17,32-35,41,43-48,52-54,59,61-62,65-66H,3-9,12,15,18-31,36-40H2,1-2H3,(H,68,69)(H,70,71)(H2,56,57,67)/b11-10-,14-13-,17-16-,33-32-/t41-,43+,44-,45-,46+,47-,48+,52?,53+,54+/m0/s1
> <INCHI_KEY>
BOFFZDCAMXZVKR-HIWTVLOPSA-N
> <FORMULA>
C55H91N3O19P2
> <MOLECULAR_WEIGHT>
1160.283
> <EXACT_MASS>
1159.572201718
> <JCHEM_ACCEPTOR_COUNT>
16
> <JCHEM_ATOM_COUNT>
170
> <JCHEM_AVERAGE_POLARIZABILITY>
122.5563442437498
> <JCHEM_BIOAVAILABILITY>
0
> <JCHEM_DONOR_COUNT>
8
> <JCHEM_FORMAL_CHARGE>
0
> <JCHEM_GHOSE_FILTER>
0
> <JCHEM_IUPAC>
[(1R,9R,18S,19S,21R,22S,23S,24S,26R)-26-(4-amino-2-oxo-1,2-dihydropyrimidin-1-yl)-4,6,19,21,23,24-hexahydroxy-22-[(1E,3S)-3-hydroxyoct-1-en-1-yl]-4,6,11,16-tetraoxo-3,5,7,10,25-pentaoxa-4lambda5,6lambda5-diphosphabicyclo[16.6.2]hexacosan-9-yl]methyl (10Z,13Z,16Z)-tricosa-10,13,16-trienoate
> <ALOGPS_LOGP>
4.14
> <JCHEM_LOGP>
6.858925904902307
> <ALOGPS_LOGS>
-4.56
> <JCHEM_MDDR_LIKE_RULE>
1
> <JCHEM_NUMBER_OF_RINGS>
3
> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2
> <JCHEM_PKA>
3.271902101828823
> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8697802094369766
> <JCHEM_PKA_STRONGEST_BASIC>
0.306545982232454
> <JCHEM_POLAR_SURFACE_AREA>
341.03000000000003
> <JCHEM_REFRACTIVITY>
298.58279999999996
> <JCHEM_ROTATABLE_BOND_COUNT>
28
> <JCHEM_RULE_OF_FIVE>
0
> <ALOGPS_SOLUBILITY>
3.17e-02 g/l
> <JCHEM_TRADITIONAL_IUPAC>
[(1R,9R,18S,19S,21R,22S,23S,24S,26R)-26-(4-amino-2-oxopyrimidin-1-yl)-4,6,19,21,23,24-hexahydroxy-22-[(1E,3S)-3-hydroxyoct-1-en-1-yl]-4,6,11,16-tetraoxo-3,5,7,10,25-pentaoxa-4lambda5,6lambda5-diphosphabicyclo[16.6.2]hexacosan-9-yl]methyl (10Z,13Z,16Z)-tricosa-10,13,16-trienoate
> <JCHEM_VEBER_RULE>
0
$$$$
3D-SDF for HMDB0292351 (CDP-DG(22:3(10Z,13Z,16Z)/6 keto-PGF1alpha))HMDB0292351
RDKit 3D
CDP-DG(22:3(10Z,13Z,16Z)/6 keto-PGF1alpha)
170172 0 0 0 0 0 0 0 0999 V2000
20.6768 2.4632 -2.1978 C 0 0 0 0 0 0 0 0 0 0 0 0
19.4643 3.3084 -1.9312 C 0 0 0 0 0 0 0 0 0 0 0 0
18.2889 2.3316 -1.6444 C 0 0 0 0 0 0 0 0 0 0 0 0
18.6756 1.5685 -0.4512 C 0 0 0 0 0 0 0 0 0 0 0 0
17.8691 0.4831 0.0995 C 0 0 0 0 0 0 0 0 0 0 0 0
16.4493 0.7602 0.4575 C 0 0 0 0 0 0 0 0 0 0 0 0
15.5102 1.0387 -0.6131 C 0 0 0 0 0 0 0 0 0 0 0 0
14.4909 0.2730 -0.9038 C 0 0 0 0 0 0 0 0 0 0 0 0
14.0549 -0.9624 -0.2958 C 0 0 0 0 0 0 0 0 0 0 0 0
14.7905 -1.5525 0.7954 C 0 0 0 0 0 0 0 0 0 0 0 0
14.3463 -1.7967 1.9905 C 0 0 0 0 0 0 0 0 0 0 0 0
12.9845 -1.5226 2.4839 C 0 0 0 0 0 0 0 0 0 0 0 0
12.3681 -2.7749 2.9720 C 0 0 0 0 0 0 0 0 0 0 0 0
11.3073 -3.2968 2.5162 C 0 0 0 0 0 0 0 0 0 0 0 0
10.4690 -2.7743 1.4169 C 0 0 0 0 0 0 0 0 0 0 0 0
9.0883 -2.5766 2.0014 C 0 0 0 0 0 0 0 0 0 0 0 0
8.0274 -2.1721 1.0807 C 0 0 0 0 0 0 0 0 0 0 0 0
8.1241 -0.8831 0.3492 C 0 0 0 0 0 0 0 0 0 0 0 0
6.9174 -0.7207 -0.5885 C 0 0 0 0 0 0 0 0 0 0 0 0
5.6611 -0.7764 0.2250 C 0 0 0 0 0 0 0 0 0 0 0 0
5.4689 0.3409 1.1987 C 0 0 0 0 0 0 0 0 0 0 0 0
4.3002 0.1739 2.1233 C 0 0 0 0 0 0 0 0 0 0 0 0
3.0007 -0.0840 1.5267 C 0 0 0 0 0 0 0 0 0 0 0 0
2.8980 -1.0124 0.6773 O 0 0 0 0 0 0 0 0 0 0 0 0
1.8044 0.5909 1.7974 O 0 0 0 0 0 0 0 0 0 0 0 0
0.5958 0.2116 1.1788 C 0 0 0 0 0 0 0 0 0 0 0 0
0.5636 0.3573 -0.2871 C 0 0 2 0 0 0 0 0 0 0 0 0
0.3649 1.8365 -0.7007 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.8988 2.2621 -0.3509 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.9145 2.3629 -1.6840 P 0 0 0 0 0 5 0 0 0 0 0 0
-1.0764 2.8490 -2.8612 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.5905 0.8847 -2.1289 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.2068 3.4329 -1.4528 O 0 0 0 0 0 0 0 0 0 0 0 0
-4.2318 2.9275 -0.2476 P 0 0 0 0 0 5 0 0 0 0 0 0
-5.0730 4.1079 0.2587 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.3099 2.4116 1.0722 O 0 0 0 0 0 0 0 0 0 0 0 0
-5.3484 1.7515 -0.7249 O 0 0 0 0 0 0 0 0 0 0 0 0
-6.5020 1.8032 0.0479 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.4771 0.7052 -0.3218 C 0 0 1 0 0 0 0 0 0 0 0 0
-8.0158 0.1888 0.8463 O 0 0 0 0 0 0 0 0 0 0 0 0
-7.3334 -0.8967 1.3804 C 0 0 1 0 0 0 0 0 0 0 0 0
-7.3582 -0.7440 2.8302 N 0 0 0 0 0 0 0 0 0 0 0 0
-6.4788 -1.4243 3.5758 C 0 0 0 0 0 0 0 0 0 0 0 0
-6.4770 -1.3004 4.9451 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.3833 -0.4705 5.5709 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.3948 -0.3305 6.9897 N 0 0 0 0 0 0 0 0 0 0 0 0
-8.2350 0.1849 4.7685 N 0 0 0 0 0 0 0 0 0 0 0 0
-8.2407 0.0676 3.4331 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.0944 0.7424 2.7529 O 0 0 0 0 0 0 0 0 0 0 0 0
-7.7560 -2.1827 0.8195 C 0 0 1 0 0 0 0 0 0 0 0 0
-7.0296 -3.4086 1.2455 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.6914 -3.5456 0.6779 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.8569 -4.1259 1.3969 O 0 0 0 0 0 0 0 0 0 0 0 0
-5.2156 -3.0881 -0.6209 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.7130 -2.7405 -0.5081 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.5315 -1.6554 0.5013 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.1086 -1.2747 0.7837 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.2206 -1.3794 -0.3824 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.0928 -2.5489 -0.8873 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.5871 -0.2674 -0.8663 O 0 0 0 0 0 0 0 0 0 0 0 0
-9.2536 -2.4432 0.7098 C 0 0 1 0 0 0 0 0 0 0 0 0
-9.9697 -1.9107 1.7341 O 0 0 0 0 0 0 0 0 0 0 0 0
-9.7610 -2.1995 -0.6787 C 0 0 0 0 0 0 0 0 0 0 0 0
-10.9838 -1.3943 -0.8228 C 0 0 1 0 0 0 0 0 0 0 0 0
-11.6129 -1.0135 0.3472 O 0 0 0 0 0 0 0 0 0 0 0 0
-10.7360 -0.0796 -1.6046 C 0 0 2 0 0 0 0 0 0 0 0 0
-10.1975 -0.4204 -2.9090 C 0 0 0 0 0 0 0 0 0 0 0 0
-10.8872 -0.1830 -4.0182 C 0 0 0 0 0 0 0 0 0 0 0 0
-12.2225 0.4237 -4.0564 C 0 0 1 0 0 0 0 0 0 0 0 0
-13.2054 -0.2843 -3.3569 O 0 0 0 0 0 0 0 0 0 0 0 0
-12.2742 1.9041 -3.8231 C 0 0 0 0 0 0 0 0 0 0 0 0
-13.7234 2.3669 -3.8895 C 0 0 0 0 0 0 0 0 0 0 0 0
-13.8934 3.8289 -3.6412 C 0 0 0 0 0 0 0 0 0 0 0 0
-13.3806 4.2106 -2.2558 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.1379 3.4243 -1.1865 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.9588 0.8886 -0.7720 C 0 0 2 0 0 0 0 0 0 0 0 0
-10.7520 2.0138 -0.3994 O 0 0 0 0 0 0 0 0 0 0 0 0
-8.6035 1.2783 -1.2080 C 0 0 2 0 0 0 0 0 0 0 0 0
-8.2917 1.1325 -2.5345 O 0 0 0 0 0 0 0 0 0 0 0 0
20.3619 1.4732 -2.5410 H 0 0 0 0 0 0 0 0 0 0 0 0
21.2836 3.0035 -2.9721 H 0 0 0 0 0 0 0 0 0 0 0 0
21.2600 2.4137 -1.2360 H 0 0 0 0 0 0 0 0 0 0 0 0
19.1745 3.9832 -2.7306 H 0 0 0 0 0 0 0 0 0 0 0 0
19.5557 3.8898 -0.9833 H 0 0 0 0 0 0 0 0 0 0 0 0
17.9814 1.7953 -2.5341 H 0 0 0 0 0 0 0 0 0 0 0 0
17.4689 3.0851 -1.4137 H 0 0 0 0 0 0 0 0 0 0 0 0
19.7534 1.2069 -0.6458 H 0 0 0 0 0 0 0 0 0 0 0 0
18.8728 2.3322 0.3779 H 0 0 0 0 0 0 0 0 0 0 0 0
18.3912 0.1750 1.0784 H 0 0 0 0 0 0 0 0 0 0 0 0
17.9514 -0.4883 -0.4920 H 0 0 0 0 0 0 0 0 0 0 0 0
16.1059 0.2661 1.3596 H 0 0 0 0 0 0 0 0 0 0 0 0
16.5737 1.8714 0.9348 H 0 0 0 0 0 0 0 0 0 0 0 0
15.6368 1.9669 -1.2330 H 0 0 0 0 0 0 0 0 0 0 0 0
13.8645 0.6557 -1.7623 H 0 0 0 0 0 0 0 0 0 0 0 0
13.9790 -1.7477 -1.1531 H 0 0 0 0 0 0 0 0 0 0 0 0
12.9548 -0.8933 -0.0161 H 0 0 0 0 0 0 0 0 0 0 0 0
15.8564 -1.8609 0.5852 H 0 0 0 0 0 0 0 0 0 0 0 0
15.0572 -2.2581 2.7226 H 0 0 0 0 0 0 0 0 0 0 0 0
13.0855 -0.8781 3.4309 H 0 0 0 0 0 0 0 0 0 0 0 0
12.3924 -0.9154 1.8197 H 0 0 0 0 0 0 0 0 0 0 0 0
12.9216 -3.2579 3.8100 H 0 0 0 0 0 0 0 0 0 0 0 0
10.9564 -4.2563 2.9890 H 0 0 0 0 0 0 0 0 0 0 0 0
10.8066 -1.8353 0.9803 H 0 0 0 0 0 0 0 0 0 0 0 0
10.3738 -3.5115 0.5672 H 0 0 0 0 0 0 0 0 0 0 0 0
8.8023 -3.5253 2.5283 H 0 0 0 0 0 0 0 0 0 0 0 0
9.1386 -1.8218 2.8468 H 0 0 0 0 0 0 0 0 0 0 0 0
7.0641 -2.1618 1.7016 H 0 0 0 0 0 0 0 0 0 0 0 0
7.8612 -3.0250 0.3554 H 0 0 0 0 0 0 0 0 0 0 0 0
9.0262 -0.9114 -0.3236 H 0 0 0 0 0 0 0 0 0 0 0 0
8.1465 -0.0065 1.0024 H 0 0 0 0 0 0 0 0 0 0 0 0
6.9445 -1.4626 -1.4046 H 0 0 0 0 0 0 0 0 0 0 0 0
7.0055 0.3296 -0.9949 H 0 0 0 0 0 0 0 0 0 0 0 0
5.4549 -1.7403 0.7146 H 0 0 0 0 0 0 0 0 0 0 0 0
4.7597 -0.6923 -0.5140 H 0 0 0 0 0 0 0 0 0 0 0 0
5.2801 1.3174 0.6556 H 0 0 0 0 0 0 0 0 0 0 0 0
6.4159 0.5341 1.7897 H 0 0 0 0 0 0 0 0 0 0 0 0
4.6120 -0.6670 2.8245 H 0 0 0 0 0 0 0 0 0 0 0 0
4.2659 1.0604 2.8235 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.1656 0.9109 1.6821 H 0 0 0 0 0 0 0 0 0 0 0 0
0.3976 -0.8413 1.4760 H 0 0 0 0 0 0 0 0 0 0 0 0
1.4530 -0.0078 -0.7800 H 0 0 0 0 0 0 0 0 0 0 0 0
0.5746 1.8655 -1.7872 H 0 0 0 0 0 0 0 0 0 0 0 0
1.1867 2.3871 -0.1977 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.4038 0.6019 -3.0413 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.7749 3.1280 1.4515 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.2264 1.7131 1.1216 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.0068 2.7865 -0.0763 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.9412 -0.0234 -0.9299 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.2176 -0.8097 1.1449 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.7163 -2.0839 3.1023 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.7469 -1.8709 5.5293 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.5718 -0.0793 7.5717 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.3108 -0.4950 7.4631 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.4658 -2.1058 -0.3091 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.0936 -3.6851 2.3000 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.6278 -4.2725 0.7452 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.2419 -3.8781 -1.4091 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.6672 -2.1889 -1.0404 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.1922 -3.6629 -0.2018 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.3248 -2.4686 -1.5096 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.0476 -0.7170 0.1278 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.0748 -1.9527 1.4232 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.0922 -0.2165 1.1657 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.7679 -1.8966 1.6541 H 0 0 0 0 0 0 0 0 0 0 0 0
-9.3437 -3.5787 0.8653 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.6275 -2.5212 2.1675 H 0 0 0 0 0 0 0 0 0 0 0 0
-9.8481 -3.1612 -1.2614 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.9171 -1.6595 -1.2147 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.7519 -1.9590 -1.4251 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.5194 -1.4381 0.4459 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.7833 0.3247 -1.6690 H 0 0 0 0 0 0 0 0 0 0 0 0
-9.2063 -0.8947 -3.0543 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.3719 -0.4808 -4.9587 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.5870 0.3101 -5.1341 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.2568 -1.1828 -3.7275 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.7342 2.2662 -2.9371 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.7755 2.4629 -4.6774 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.3088 1.8203 -3.1196 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.1768 2.1215 -4.8699 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.9742 4.0968 -3.6623 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.3769 4.4553 -4.3738 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.6212 5.2822 -2.1361 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.3165 3.9899 -2.1181 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.0697 3.9994 -0.2372 H 0 0 0 0 0 0 0 0 0 0 0 0
-15.1827 3.2229 -1.4524 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.6062 2.4574 -0.9741 H 0 0 0 0 0 0 0 0 0 0 0 0
-9.8281 0.3748 0.2314 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.1754 2.7543 -0.1653 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.5359 2.4018 -1.0378 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.7068 1.8524 -2.8983 H 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 7 1 0
7 8 2 0
8 9 1 0
9 10 1 0
10 11 2 0
11 12 1 0
12 13 1 0
13 14 2 0
14 15 1 0
15 16 1 0
16 17 1 0
17 18 1 0
18 19 1 0
19 20 1 0
20 21 1 0
21 22 1 0
22 23 1 0
23 24 2 0
23 25 1 0
25 26 1 0
26 27 1 0
27 28 1 0
28 29 1 0
29 30 1 0
30 31 2 0
30 32 1 0
30 33 1 0
33 34 1 0
34 35 2 0
34 36 1 0
34 37 1 0
37 38 1 0
38 39 1 0
39 40 1 0
40 41 1 0
41 42 1 0
42 43 1 0
43 44 2 0
44 45 1 0
45 46 1 0
45 47 2 0
47 48 1 0
48 49 2 0
41 50 1 0
50 51 1 0
51 52 1 0
52 53 2 0
52 54 1 0
54 55 1 0
55 56 1 0
56 57 1 0
57 58 1 0
58 59 2 0
58 60 1 0
50 61 1 0
61 62 1 0
61 63 1 0
63 64 1 0
64 65 1 0
64 66 1 0
66 67 1 0
67 68 2 0
68 69 1 0
69 70 1 0
69 71 1 0
71 72 1 0
72 73 1 0
73 74 1 0
74 75 1 0
66 76 1 0
76 77 1 0
76 78 1 0
78 79 1 0
60 27 1 0
78 39 1 0
48 42 1 0
1 80 1 0
1 81 1 0
1 82 1 0
2 83 1 0
2 84 1 0
3 85 1 0
3 86 1 0
4 87 1 0
4 88 1 0
5 89 1 0
5 90 1 0
6 91 1 0
6 92 1 0
7 93 1 0
8 94 1 0
9 95 1 0
9 96 1 0
10 97 1 0
11 98 1 0
12 99 1 0
12100 1 0
13101 1 0
14102 1 0
15103 1 0
15104 1 0
16105 1 0
16106 1 0
17107 1 0
17108 1 0
18109 1 0
18110 1 0
19111 1 0
19112 1 0
20113 1 0
20114 1 0
21115 1 0
21116 1 0
22117 1 0
22118 1 0
26119 1 0
26120 1 0
27121 1 6
28122 1 0
28123 1 0
32124 1 0
36125 1 0
38126 1 0
38127 1 0
39128 1 6
41129 1 6
43130 1 0
44131 1 0
46132 1 0
46133 1 0
50134 1 6
51135 1 0
51136 1 0
54137 1 0
54138 1 0
55139 1 0
55140 1 0
56141 1 0
56142 1 0
57143 1 0
57144 1 0
61145 1 1
62146 1 0
63147 1 0
63148 1 0
64149 1 6
65150 1 0
66151 1 6
67152 1 0
68153 1 0
69154 1 6
70155 1 0
71156 1 0
71157 1 0
72158 1 0
72159 1 0
73160 1 0
73161 1 0
74162 1 0
74163 1 0
75164 1 0
75165 1 0
75166 1 0
76167 1 1
77168 1 0
78169 1 1
79170 1 0
M END
PDB for HMDB0292351 (CDP-DG(22:3(10Z,13Z,16Z)/6 keto-PGF1alpha))HEADER PROTEIN 17-SEP-21 NONE TITLE NULL COMPND NULL SOURCE NULL KEYWDS NULL EXPDTA NULL AUTHOR Marvin REVDAT 1 17-SEP-21 0 HETATM 1 N UNK 0 -5.015 -3.703 0.000 0.00 0.00 N+0 HETATM 2 C UNK 0 -3.673 -2.853 0.000 0.00 0.00 C+0 HETATM 3 N UNK 0 -3.732 -1.314 0.000 0.00 0.00 N+0 HETATM 4 C UNK 0 -2.429 -0.494 0.000 0.00 0.00 C+0 HETATM 5 O UNK 0 -3.446 0.773 0.000 0.00 0.00 O+0 HETATM 6 N UNK 0 -1.067 -1.212 0.000 0.00 0.00 N+0 HETATM 7 C UNK 0 -1.008 -2.751 0.000 0.00 0.00 C+0 HETATM 8 C UNK 0 -2.311 -3.572 0.000 0.00 0.00 C+0 HETATM 9 C UNK 0 0.237 -0.392 0.000 0.00 0.00 C+0 HETATM 10 O UNK 0 -0.432 1.064 0.000 0.00 0.00 O+0 HETATM 11 C UNK 0 0.107 2.586 0.000 0.00 0.00 C+0 HETATM 12 C UNK 0 0.800 4.053 0.000 0.00 0.00 C+0 HETATM 13 O UNK 0 2.252 4.826 0.000 0.00 0.00 O+0 HETATM 14 P UNK 0 3.834 5.316 0.000 0.00 0.00 P+0 HETATM 15 O UNK 0 2.612 6.444 0.000 0.00 0.00 O+0 HETATM 16 O UNK 0 3.869 6.995 0.000 0.00 0.00 O+0 HETATM 17 O UNK 0 5.412 4.873 0.000 0.00 0.00 O+0 HETATM 18 P UNK 0 6.798 3.986 0.000 0.00 0.00 P+0 HETATM 19 O UNK 0 6.820 5.681 0.000 0.00 0.00 O+0 HETATM 20 O UNK 0 8.211 5.222 0.000 0.00 0.00 O+0 HETATM 21 O UNK 0 8.478 3.249 0.000 0.00 0.00 O+0 HETATM 22 C UNK 0 9.792 2.709 0.000 0.00 0.00 C+0 HETATM 23 C UNK 0 11.104 1.786 0.000 0.00 0.00 C+0 HETATM 24 C UNK 0 12.687 2.186 0.000 0.00 0.00 C+0 HETATM 25 O UNK 0 14.203 1.741 0.000 0.00 0.00 O+0 HETATM 26 C UNK 0 15.463 2.698 0.000 0.00 0.00 C+0 HETATM 27 O UNK 0 15.457 4.292 0.000 0.00 0.00 O+0 HETATM 28 C UNK 0 16.615 1.603 0.000 0.00 0.00 C+0 HETATM 29 C UNK 0 17.943 2.447 0.000 0.00 0.00 C+0 HETATM 30 C UNK 0 19.200 1.497 0.000 0.00 0.00 C+0 HETATM 31 C UNK 0 20.521 2.364 0.000 0.00 0.00 C+0 HETATM 32 C UNK 0 21.821 1.465 0.000 0.00 0.00 C+0 HETATM 33 C UNK 0 23.183 2.269 0.000 0.00 0.00 C+0 HETATM 34 C UNK 0 24.533 1.443 0.000 0.00 0.00 C+0 HETATM 35 C UNK 0 25.938 2.186 0.000 0.00 0.00 C+0 HETATM 36 C UNK 0 27.285 1.347 0.000 0.00 0.00 C+0 HETATM 37 C UNK 0 28.707 2.012 0.000 0.00 0.00 C+0 HETATM 38 C UNK 0 28.840 3.546 0.000 0.00 0.00 C+0 HETATM 39 C UNK 0 30.234 4.199 0.000 0.00 0.00 C+0 HETATM 40 C UNK 0 30.367 5.733 0.000 0.00 0.00 C+0 HETATM 41 C UNK 0 29.104 6.615 0.000 0.00 0.00 C+0 HETATM 42 C UNK 0 29.236 8.149 0.000 0.00 0.00 C+0 HETATM 43 C UNK 0 27.974 9.031 0.000 0.00 0.00 C+0 HETATM 44 C UNK 0 26.579 8.378 0.000 0.00 0.00 C+0 HETATM 45 C UNK 0 25.316 9.260 0.000 0.00 0.00 C+0 HETATM 46 C UNK 0 23.921 8.607 0.000 0.00 0.00 C+0 HETATM 47 C UNK 0 22.659 9.489 0.000 0.00 0.00 C+0 HETATM 48 C UNK 0 21.264 8.836 0.000 0.00 0.00 C+0 HETATM 49 C UNK 0 20.001 9.718 0.000 0.00 0.00 C+0 HETATM 50 O UNK 0 11.165 0.182 0.000 0.00 0.00 O+0 HETATM 51 C UNK 0 10.405 -1.243 0.000 0.00 0.00 C+0 HETATM 52 O UNK 0 11.624 -2.267 0.000 0.00 0.00 O+0 HETATM 53 C UNK 0 9.512 -2.576 0.000 0.00 0.00 C+0 HETATM 54 C UNK 0 8.083 -3.317 0.000 0.00 0.00 C+0 HETATM 55 C UNK 0 6.542 -3.819 0.000 0.00 0.00 C+0 HETATM 56 C UNK 0 4.926 -3.892 0.000 0.00 0.00 C+0 HETATM 57 C UNK 0 3.318 -4.003 0.000 0.00 0.00 C+0 HETATM 58 O UNK 0 3.024 -5.588 0.000 0.00 0.00 O+0 HETATM 59 C UNK 0 1.992 -3.084 0.000 0.00 0.00 C+0 HETATM 60 C UNK 0 1.268 -1.634 0.000 0.00 0.00 C+0 HETATM 61 C UNK 0 2.706 -1.000 0.000 0.00 0.00 C+0 HETATM 62 O UNK 0 2.074 0.529 0.000 0.00 0.00 O+0 HETATM 63 C UNK 0 4.237 -0.671 0.000 0.00 0.00 C+0 HETATM 64 C UNK 0 5.534 0.199 0.000 0.00 0.00 C+0 HETATM 65 O UNK 0 6.386 -1.150 0.000 0.00 0.00 O+0 HETATM 66 C UNK 0 4.784 1.568 0.000 0.00 0.00 C+0 HETATM 67 C UNK 0 6.183 1.985 0.000 0.00 0.00 C+0 HETATM 68 C UNK 0 7.431 2.766 0.000 0.00 0.00 C+0 HETATM 69 C UNK 0 8.124 4.324 0.000 0.00 0.00 C+0 HETATM 70 O UNK 0 9.715 4.114 0.000 0.00 0.00 O+0 HETATM 71 C UNK 0 8.124 6.276 0.000 0.00 0.00 C+0 HETATM 72 C UNK 0 9.117 7.641 0.000 0.00 0.00 C+0 HETATM 73 C UNK 0 8.486 9.132 0.000 0.00 0.00 C+0 HETATM 74 C UNK 0 9.464 10.329 0.000 0.00 0.00 C+0 HETATM 75 C UNK 0 8.917 11.769 0.000 0.00 0.00 C+0 HETATM 76 C UNK 0 1.645 2.180 0.000 0.00 0.00 C+0 HETATM 77 O UNK 0 0.825 1.008 0.000 0.00 0.00 O+0 HETATM 78 C UNK 0 3.231 1.943 0.000 0.00 0.00 C+0 HETATM 79 O UNK 0 2.363 3.269 0.000 0.00 0.00 O+0 CONECT 1 2 CONECT 2 1 3 8 CONECT 3 2 4 CONECT 4 3 5 6 CONECT 5 4 CONECT 6 4 7 9 CONECT 7 6 8 CONECT 8 7 2 CONECT 9 6 10 60 CONECT 10 9 11 CONECT 11 10 12 76 CONECT 12 11 13 CONECT 13 12 14 CONECT 14 13 15 16 17 CONECT 15 14 CONECT 16 14 CONECT 17 14 18 CONECT 18 17 19 20 21 CONECT 19 18 CONECT 20 18 CONECT 21 18 22 CONECT 22 21 23 CONECT 23 22 24 50 CONECT 24 23 25 CONECT 25 24 26 CONECT 26 25 27 28 CONECT 27 26 CONECT 28 26 29 CONECT 29 28 30 CONECT 30 29 31 CONECT 31 30 32 CONECT 32 31 33 CONECT 33 32 34 CONECT 34 33 35 CONECT 35 34 36 CONECT 36 35 37 CONECT 37 36 38 CONECT 38 37 39 CONECT 39 38 40 CONECT 40 39 41 CONECT 41 40 42 CONECT 42 41 43 CONECT 43 42 44 CONECT 44 43 45 CONECT 45 44 46 CONECT 46 45 47 CONECT 47 46 48 CONECT 48 47 49 CONECT 49 48 CONECT 50 23 51 CONECT 51 50 52 53 CONECT 52 51 CONECT 53 51 54 CONECT 54 53 55 CONECT 55 54 56 CONECT 56 55 57 CONECT 57 56 58 59 CONECT 58 57 CONECT 59 57 60 CONECT 60 59 9 61 CONECT 61 60 62 63 CONECT 62 61 CONECT 63 61 64 CONECT 64 63 65 66 CONECT 65 64 CONECT 66 64 67 78 CONECT 67 66 68 CONECT 68 67 69 CONECT 69 68 70 71 CONECT 70 69 CONECT 71 69 72 CONECT 72 71 73 CONECT 73 72 74 CONECT 74 73 75 CONECT 75 74 CONECT 76 11 77 78 CONECT 77 76 CONECT 78 76 66 79 CONECT 79 78 MASTER 0 0 0 0 0 0 0 0 79 0 162 0 END 3D PDB for HMDB0292351 (CDP-DG(22:3(10Z,13Z,16Z)/6 keto-PGF1alpha))COMPND HMDB0292351 HETATM 1 C1 UNL 1 20.677 2.463 -2.198 1.00 0.00 C HETATM 2 C2 UNL 1 19.464 3.308 -1.931 1.00 0.00 C HETATM 3 C3 UNL 1 18.289 2.332 -1.644 1.00 0.00 C HETATM 4 C4 UNL 1 18.676 1.569 -0.451 1.00 0.00 C HETATM 5 C5 UNL 1 17.869 0.483 0.099 1.00 0.00 C HETATM 6 C6 UNL 1 16.449 0.760 0.458 1.00 0.00 C HETATM 7 C7 UNL 1 15.510 1.039 -0.613 1.00 0.00 C HETATM 8 C8 UNL 1 14.491 0.273 -0.904 1.00 0.00 C HETATM 9 C9 UNL 1 14.055 -0.962 -0.296 1.00 0.00 C HETATM 10 C10 UNL 1 14.791 -1.552 0.795 1.00 0.00 C HETATM 11 C11 UNL 1 14.346 -1.797 1.990 1.00 0.00 C HETATM 12 C12 UNL 1 12.985 -1.523 2.484 1.00 0.00 C HETATM 13 C13 UNL 1 12.368 -2.775 2.972 1.00 0.00 C HETATM 14 C14 UNL 1 11.307 -3.297 2.516 1.00 0.00 C HETATM 15 C15 UNL 1 10.469 -2.774 1.417 1.00 0.00 C HETATM 16 C16 UNL 1 9.088 -2.577 2.001 1.00 0.00 C HETATM 17 C17 UNL 1 8.027 -2.172 1.081 1.00 0.00 C HETATM 18 C18 UNL 1 8.124 -0.883 0.349 1.00 0.00 C HETATM 19 C19 UNL 1 6.917 -0.721 -0.588 1.00 0.00 C HETATM 20 C20 UNL 1 5.661 -0.776 0.225 1.00 0.00 C HETATM 21 C21 UNL 1 5.469 0.341 1.199 1.00 0.00 C HETATM 22 C22 UNL 1 4.300 0.174 2.123 1.00 0.00 C HETATM 23 C23 UNL 1 3.001 -0.084 1.527 1.00 0.00 C HETATM 24 O1 UNL 1 2.898 -1.012 0.677 1.00 0.00 O HETATM 25 O2 UNL 1 1.804 0.591 1.797 1.00 0.00 O HETATM 26 C24 UNL 1 0.596 0.212 1.179 1.00 0.00 C HETATM 27 C25 UNL 1 0.564 0.357 -0.287 1.00 0.00 C HETATM 28 C26 UNL 1 0.365 1.837 -0.701 1.00 0.00 C HETATM 29 O3 UNL 1 -0.899 2.262 -0.351 1.00 0.00 O HETATM 30 P1 UNL 1 -1.914 2.363 -1.684 1.00 0.00 P HETATM 31 O4 UNL 1 -1.076 2.849 -2.861 1.00 0.00 O HETATM 32 O5 UNL 1 -2.591 0.885 -2.129 1.00 0.00 O HETATM 33 O6 UNL 1 -3.207 3.433 -1.453 1.00 0.00 O HETATM 34 P2 UNL 1 -4.232 2.928 -0.248 1.00 0.00 P HETATM 35 O7 UNL 1 -5.073 4.108 0.259 1.00 0.00 O HETATM 36 O8 UNL 1 -3.310 2.412 1.072 1.00 0.00 O HETATM 37 O9 UNL 1 -5.348 1.752 -0.725 1.00 0.00 O HETATM 38 C27 UNL 1 -6.502 1.803 0.048 1.00 0.00 C HETATM 39 C28 UNL 1 -7.477 0.705 -0.322 1.00 0.00 C HETATM 40 O10 UNL 1 -8.016 0.189 0.846 1.00 0.00 O HETATM 41 C29 UNL 1 -7.333 -0.897 1.380 1.00 0.00 C HETATM 42 N1 UNL 1 -7.358 -0.744 2.830 1.00 0.00 N HETATM 43 C30 UNL 1 -6.479 -1.424 3.576 1.00 0.00 C HETATM 44 C31 UNL 1 -6.477 -1.300 4.945 1.00 0.00 C HETATM 45 C32 UNL 1 -7.383 -0.471 5.571 1.00 0.00 C HETATM 46 N2 UNL 1 -7.395 -0.331 6.990 1.00 0.00 N HETATM 47 N3 UNL 1 -8.235 0.185 4.769 1.00 0.00 N HETATM 48 C33 UNL 1 -8.241 0.068 3.433 1.00 0.00 C HETATM 49 O11 UNL 1 -9.094 0.742 2.753 1.00 0.00 O HETATM 50 C34 UNL 1 -7.756 -2.183 0.819 1.00 0.00 C HETATM 51 C35 UNL 1 -7.030 -3.409 1.245 1.00 0.00 C HETATM 52 C36 UNL 1 -5.691 -3.546 0.678 1.00 0.00 C HETATM 53 O12 UNL 1 -4.857 -4.126 1.397 1.00 0.00 O HETATM 54 C37 UNL 1 -5.216 -3.088 -0.621 1.00 0.00 C HETATM 55 C38 UNL 1 -3.713 -2.741 -0.508 1.00 0.00 C HETATM 56 C39 UNL 1 -3.532 -1.655 0.501 1.00 0.00 C HETATM 57 C40 UNL 1 -2.109 -1.275 0.784 1.00 0.00 C HETATM 58 C41 UNL 1 -1.221 -1.379 -0.382 1.00 0.00 C HETATM 59 O13 UNL 1 -1.093 -2.549 -0.887 1.00 0.00 O HETATM 60 O14 UNL 1 -0.587 -0.267 -0.866 1.00 0.00 O HETATM 61 C42 UNL 1 -9.254 -2.443 0.710 1.00 0.00 C HETATM 62 O15 UNL 1 -9.970 -1.911 1.734 1.00 0.00 O HETATM 63 C43 UNL 1 -9.761 -2.199 -0.679 1.00 0.00 C HETATM 64 C44 UNL 1 -10.984 -1.394 -0.823 1.00 0.00 C HETATM 65 O16 UNL 1 -11.613 -1.014 0.347 1.00 0.00 O HETATM 66 C45 UNL 1 -10.736 -0.080 -1.605 1.00 0.00 C HETATM 67 C46 UNL 1 -10.198 -0.420 -2.909 1.00 0.00 C HETATM 68 C47 UNL 1 -10.887 -0.183 -4.018 1.00 0.00 C HETATM 69 C48 UNL 1 -12.223 0.424 -4.056 1.00 0.00 C HETATM 70 O17 UNL 1 -13.205 -0.284 -3.357 1.00 0.00 O HETATM 71 C49 UNL 1 -12.274 1.904 -3.823 1.00 0.00 C HETATM 72 C50 UNL 1 -13.723 2.367 -3.890 1.00 0.00 C HETATM 73 C51 UNL 1 -13.893 3.829 -3.641 1.00 0.00 C HETATM 74 C52 UNL 1 -13.381 4.211 -2.256 1.00 0.00 C HETATM 75 C53 UNL 1 -14.138 3.424 -1.187 1.00 0.00 C HETATM 76 C54 UNL 1 -9.959 0.889 -0.772 1.00 0.00 C HETATM 77 O18 UNL 1 -10.752 2.014 -0.399 1.00 0.00 O HETATM 78 C55 UNL 1 -8.604 1.278 -1.208 1.00 0.00 C HETATM 79 O19 UNL 1 -8.292 1.132 -2.535 1.00 0.00 O HETATM 80 H1 UNL 1 20.362 1.473 -2.541 1.00 0.00 H HETATM 81 H2 UNL 1 21.284 3.003 -2.972 1.00 0.00 H HETATM 82 H3 UNL 1 21.260 2.414 -1.236 1.00 0.00 H HETATM 83 H4 UNL 1 19.174 3.983 -2.731 1.00 0.00 H HETATM 84 H5 UNL 1 19.556 3.890 -0.983 1.00 0.00 H HETATM 85 H6 UNL 1 17.981 1.795 -2.534 1.00 0.00 H HETATM 86 H7 UNL 1 17.469 3.085 -1.414 1.00 0.00 H HETATM 87 H8 UNL 1 19.753 1.207 -0.646 1.00 0.00 H HETATM 88 H9 UNL 1 18.873 2.332 0.378 1.00 0.00 H HETATM 89 H10 UNL 1 18.391 0.175 1.078 1.00 0.00 H HETATM 90 H11 UNL 1 17.951 -0.488 -0.492 1.00 0.00 H HETATM 91 H12 UNL 1 16.106 0.266 1.360 1.00 0.00 H HETATM 92 H13 UNL 1 16.574 1.871 0.935 1.00 0.00 H HETATM 93 H14 UNL 1 15.637 1.967 -1.233 1.00 0.00 H HETATM 94 H15 UNL 1 13.865 0.656 -1.762 1.00 0.00 H HETATM 95 H16 UNL 1 13.979 -1.748 -1.153 1.00 0.00 H HETATM 96 H17 UNL 1 12.955 -0.893 -0.016 1.00 0.00 H HETATM 97 H18 UNL 1 15.856 -1.861 0.585 1.00 0.00 H HETATM 98 H19 UNL 1 15.057 -2.258 2.723 1.00 0.00 H HETATM 99 H20 UNL 1 13.085 -0.878 3.431 1.00 0.00 H HETATM 100 H21 UNL 1 12.392 -0.915 1.820 1.00 0.00 H HETATM 101 H22 UNL 1 12.922 -3.258 3.810 1.00 0.00 H HETATM 102 H23 UNL 1 10.956 -4.256 2.989 1.00 0.00 H HETATM 103 H24 UNL 1 10.807 -1.835 0.980 1.00 0.00 H HETATM 104 H25 UNL 1 10.374 -3.512 0.567 1.00 0.00 H HETATM 105 H26 UNL 1 8.802 -3.525 2.528 1.00 0.00 H HETATM 106 H27 UNL 1 9.139 -1.822 2.847 1.00 0.00 H HETATM 107 H28 UNL 1 7.064 -2.162 1.702 1.00 0.00 H HETATM 108 H29 UNL 1 7.861 -3.025 0.355 1.00 0.00 H HETATM 109 H30 UNL 1 9.026 -0.911 -0.324 1.00 0.00 H HETATM 110 H31 UNL 1 8.146 -0.006 1.002 1.00 0.00 H HETATM 111 H32 UNL 1 6.944 -1.463 -1.405 1.00 0.00 H HETATM 112 H33 UNL 1 7.006 0.330 -0.995 1.00 0.00 H HETATM 113 H34 UNL 1 5.455 -1.740 0.715 1.00 0.00 H HETATM 114 H35 UNL 1 4.760 -0.692 -0.514 1.00 0.00 H HETATM 115 H36 UNL 1 5.280 1.317 0.656 1.00 0.00 H HETATM 116 H37 UNL 1 6.416 0.534 1.790 1.00 0.00 H HETATM 117 H38 UNL 1 4.612 -0.667 2.824 1.00 0.00 H HETATM 118 H39 UNL 1 4.266 1.060 2.824 1.00 0.00 H HETATM 119 H40 UNL 1 -0.166 0.911 1.682 1.00 0.00 H HETATM 120 H41 UNL 1 0.398 -0.841 1.476 1.00 0.00 H HETATM 121 H42 UNL 1 1.453 -0.008 -0.780 1.00 0.00 H HETATM 122 H43 UNL 1 0.575 1.865 -1.787 1.00 0.00 H HETATM 123 H44 UNL 1 1.187 2.387 -0.198 1.00 0.00 H HETATM 124 H45 UNL 1 -2.404 0.602 -3.041 1.00 0.00 H HETATM 125 H46 UNL 1 -2.775 3.128 1.452 1.00 0.00 H HETATM 126 H47 UNL 1 -6.226 1.713 1.122 1.00 0.00 H HETATM 127 H48 UNL 1 -7.007 2.786 -0.076 1.00 0.00 H HETATM 128 H49 UNL 1 -6.941 -0.023 -0.930 1.00 0.00 H HETATM 129 H50 UNL 1 -6.218 -0.810 1.145 1.00 0.00 H HETATM 130 H51 UNL 1 -5.716 -2.084 3.102 1.00 0.00 H HETATM 131 H52 UNL 1 -5.747 -1.871 5.529 1.00 0.00 H HETATM 132 H53 UNL 1 -6.572 -0.079 7.572 1.00 0.00 H HETATM 133 H54 UNL 1 -8.311 -0.495 7.463 1.00 0.00 H HETATM 134 H55 UNL 1 -7.466 -2.106 -0.309 1.00 0.00 H HETATM 135 H56 UNL 1 -7.094 -3.685 2.300 1.00 0.00 H HETATM 136 H57 UNL 1 -7.628 -4.272 0.745 1.00 0.00 H HETATM 137 H58 UNL 1 -5.242 -3.878 -1.409 1.00 0.00 H HETATM 138 H59 UNL 1 -5.667 -2.189 -1.040 1.00 0.00 H HETATM 139 H60 UNL 1 -3.192 -3.663 -0.202 1.00 0.00 H HETATM 140 H61 UNL 1 -3.325 -2.469 -1.510 1.00 0.00 H HETATM 141 H62 UNL 1 -4.048 -0.717 0.128 1.00 0.00 H HETATM 142 H63 UNL 1 -4.075 -1.953 1.423 1.00 0.00 H HETATM 143 H64 UNL 1 -2.092 -0.216 1.166 1.00 0.00 H HETATM 144 H65 UNL 1 -1.768 -1.897 1.654 1.00 0.00 H HETATM 145 H66 UNL 1 -9.344 -3.579 0.865 1.00 0.00 H HETATM 146 H67 UNL 1 -10.628 -2.521 2.168 1.00 0.00 H HETATM 147 H68 UNL 1 -9.848 -3.161 -1.261 1.00 0.00 H HETATM 148 H69 UNL 1 -8.917 -1.659 -1.215 1.00 0.00 H HETATM 149 H70 UNL 1 -11.752 -1.959 -1.425 1.00 0.00 H HETATM 150 H71 UNL 1 -12.519 -1.438 0.446 1.00 0.00 H HETATM 151 H72 UNL 1 -11.783 0.325 -1.669 1.00 0.00 H HETATM 152 H73 UNL 1 -9.206 -0.895 -3.054 1.00 0.00 H HETATM 153 H74 UNL 1 -10.372 -0.481 -4.959 1.00 0.00 H HETATM 154 H75 UNL 1 -12.587 0.310 -5.134 1.00 0.00 H HETATM 155 H76 UNL 1 -13.257 -1.183 -3.727 1.00 0.00 H HETATM 156 H77 UNL 1 -11.734 2.266 -2.937 1.00 0.00 H HETATM 157 H78 UNL 1 -11.776 2.463 -4.677 1.00 0.00 H HETATM 158 H79 UNL 1 -14.309 1.820 -3.120 1.00 0.00 H HETATM 159 H80 UNL 1 -14.177 2.122 -4.870 1.00 0.00 H HETATM 160 H81 UNL 1 -14.974 4.097 -3.662 1.00 0.00 H HETATM 161 H82 UNL 1 -13.377 4.455 -4.374 1.00 0.00 H HETATM 162 H83 UNL 1 -13.621 5.282 -2.136 1.00 0.00 H HETATM 163 H84 UNL 1 -12.316 3.990 -2.118 1.00 0.00 H HETATM 164 H85 UNL 1 -14.070 3.999 -0.237 1.00 0.00 H HETATM 165 H86 UNL 1 -15.183 3.223 -1.452 1.00 0.00 H HETATM 166 H87 UNL 1 -13.606 2.457 -0.974 1.00 0.00 H HETATM 167 H88 UNL 1 -9.828 0.375 0.231 1.00 0.00 H HETATM 168 H89 UNL 1 -10.175 2.754 -0.165 1.00 0.00 H HETATM 169 H90 UNL 1 -8.536 2.402 -1.038 1.00 0.00 H HETATM 170 H91 UNL 1 -7.707 1.852 -2.898 1.00 0.00 H CONECT 1 2 80 81 82 CONECT 2 3 83 84 CONECT 3 4 85 86 CONECT 4 5 87 88 CONECT 5 6 89 90 CONECT 6 7 91 92 CONECT 7 8 8 93 CONECT 8 9 94 CONECT 9 10 95 96 CONECT 10 11 11 97 CONECT 11 12 98 CONECT 12 13 99 100 CONECT 13 14 14 101 CONECT 14 15 102 CONECT 15 16 103 104 CONECT 16 17 105 106 CONECT 17 18 107 108 CONECT 18 19 109 110 CONECT 19 20 111 112 CONECT 20 21 113 114 CONECT 21 22 115 116 CONECT 22 23 117 118 CONECT 23 24 24 25 CONECT 25 26 CONECT 26 27 119 120 CONECT 27 28 60 121 CONECT 28 29 122 123 CONECT 29 30 CONECT 30 31 31 32 33 CONECT 32 124 CONECT 33 34 CONECT 34 35 35 36 37 CONECT 36 125 CONECT 37 38 CONECT 38 39 126 127 CONECT 39 40 78 128 CONECT 40 41 CONECT 41 42 50 129 CONECT 42 43 48 CONECT 43 44 44 130 CONECT 44 45 131 CONECT 45 46 47 47 CONECT 46 132 133 CONECT 47 48 CONECT 48 49 49 CONECT 50 51 61 134 CONECT 51 52 135 136 CONECT 52 53 53 54 CONECT 54 55 137 138 CONECT 55 56 139 140 CONECT 56 57 141 142 CONECT 57 58 143 144 CONECT 58 59 59 60 CONECT 61 62 63 145 CONECT 62 146 CONECT 63 64 147 148 CONECT 64 65 66 149 CONECT 65 150 CONECT 66 67 76 151 CONECT 67 68 68 152 CONECT 68 69 153 CONECT 69 70 71 154 CONECT 70 155 CONECT 71 72 156 157 CONECT 72 73 158 159 CONECT 73 74 160 161 CONECT 74 75 162 163 CONECT 75 164 165 166 CONECT 76 77 78 167 CONECT 77 168 CONECT 78 79 169 CONECT 79 170 END SMILES for HMDB0292351 (CDP-DG(22:3(10Z,13Z,16Z)/6 keto-PGF1alpha))CCCCCC\C=C/C\C=C/C\C=C/CCCCCCCCC(=O)OC[C@@H]1COP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@@H](CC(=O)CCCCC(=O)O1)[C@@H](O)C[C@@H](O)[C@H](\C=C/[C@@H](O)CCCCC)[C@H](O)[C@@H]2O)N1C=CC(N)=NC1=O INCHI for HMDB0292351 (CDP-DG(22:3(10Z,13Z,16Z)/6 keto-PGF1alpha))InChI=1S/C55H91N3O19P2/c1-3-5-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-25-30-50(63)72-38-43-39-73-78(68,69)77-79(70,71)74-40-48-53(66)52(65)44(33-32-41(59)28-24-6-4-2)46(61)37-47(62)45(36-42(60)29-26-27-31-51(64)75-43)54(76-48)58-35-34-49(56)57-55(58)67/h10-11,13-14,16-17,32-35,41,43-48,52-54,59,61-62,65-66H,3-9,12,15,18-31,36-40H2,1-2H3,(H,68,69)(H,70,71)(H2,56,57,67)/b11-10-,14-13-,17-16-,33-32-/t41-,43+,44-,45-,46+,47-,48+,52?,53+,54+/m0/s1 3D Structure for HMDB0292351 (CDP-DG(22:3(10Z,13Z,16Z)/6 keto-PGF1alpha)) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Synonyms |
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| Chemical Formula | C55H91N3O19P2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Average Molecular Weight | 1160.283 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Monoisotopic Molecular Weight | 1159.572201718 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| IUPAC Name | [(1R,9R,18S,19S,21R,22S,23S,24S,26R)-26-(4-amino-2-oxo-1,2-dihydropyrimidin-1-yl)-4,6,19,21,23,24-hexahydroxy-22-[(1E,3S)-3-hydroxyoct-1-en-1-yl]-4,6,11,16-tetraoxo-3,5,7,10,25-pentaoxa-4lambda5,6lambda5-diphosphabicyclo[16.6.2]hexacosan-9-yl]methyl (10Z,13Z,16Z)-tricosa-10,13,16-trienoate | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Traditional Name | [(1R,9R,18S,19S,21R,22S,23S,24S,26R)-26-(4-amino-2-oxopyrimidin-1-yl)-4,6,19,21,23,24-hexahydroxy-22-[(1E,3S)-3-hydroxyoct-1-en-1-yl]-4,6,11,16-tetraoxo-3,5,7,10,25-pentaoxa-4lambda5,6lambda5-diphosphabicyclo[16.6.2]hexacosan-9-yl]methyl (10Z,13Z,16Z)-tricosa-10,13,16-trienoate | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| CAS Registry Number | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| SMILES | CCCCCC\C=C/C\C=C/C\C=C/CCCCCCCCC(=O)OC[C@@H]1COP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@@H](CC(=O)CCCCC(=O)O1)[C@@H](O)C[C@@H](O)[C@H](\C=C/[C@@H](O)CCCCC)[C@H](O)[C@@H]2O)N1C=CC(N)=NC1=O | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Identifier | InChI=1S/C55H91N3O19P2/c1-3-5-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-25-30-50(63)72-38-43-39-73-78(68,69)77-79(70,71)74-40-48-53(66)52(65)44(33-32-41(59)28-24-6-4-2)46(61)37-47(62)45(36-42(60)29-26-27-31-51(64)75-43)54(76-48)58-35-34-49(56)57-55(58)67/h10-11,13-14,16-17,32-35,41,43-48,52-54,59,61-62,65-66H,3-9,12,15,18-31,36-40H2,1-2H3,(H,68,69)(H,70,71)(H2,56,57,67)/b11-10-,14-13-,17-16-,33-32-/t41-,43+,44-,45-,46+,47-,48+,52?,53+,54+/m0/s1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Key | BOFFZDCAMXZVKR-HIWTVLOPSA-N | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chemical Taxonomy | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Classification | Not classified | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ontology | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Physiological effect | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Disposition | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Process | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Role | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Physical Properties | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| State | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Experimental Molecular Properties |
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| Experimental Chromatographic Properties | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Predicted Molecular Properties |
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Predicted Chromatographic Properties | Predicted Collision Cross Sections
Predicted Kovats Retention IndicesNot Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
MS/MS Spectra
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| Biological Properties | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cellular Locations | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Biospecimen Locations | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Tissue Locations | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Pathways |
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| Normal Concentrations | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Abnormal Concentrations | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Associated Disorders and Diseases | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Disease References | None | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Associated OMIM IDs | None | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| External Links | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| DrugBank ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Phenol Explorer Compound ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| FooDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| KNApSAcK ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chemspider ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| KEGG Compound ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BioCyc ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BiGG ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Wikipedia Link | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| METLIN ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| PubChem Compound | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| PDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| ChEBI ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Food Biomarker Ontology | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| VMH ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| MarkerDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Good Scents ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| References | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Synthesis Reference | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Material Safety Data Sheet (MSDS) | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| General References |
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