Showing metabocard for PIP(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/22:4(10Z,13Z,16Z,19Z)) (HMDB0280456)
| Record Information | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Version | 5.0 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Status | Predicted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Creation Date | 2021-09-13 14:34:25 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Update Date | 2022-11-30 20:02:42 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HMDB ID | HMDB0280456 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary Accession Numbers | None | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Metabolite Identification | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Common Name | PIP(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/22:4(10Z,13Z,16Z,19Z)) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Description | PIP(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/22:4(10Z,13Z,16Z,19Z)) is an oxidized phosphatidylinositol phosphate (PIP). As other PIPs, oxidized phosphatidylinositol phosphates are acidic (anionic) phospholipids that consist of a phosphatidic acid backbone, linked via the phosphate group to a phosphorylated inositol (hexahydroxycyclohexane). Phosphatidylinositol phosphates are generated from phosphatidylinositols, which are phosphorylated by a number of different kinases that place the phosphate moiety on positions 4 and 5 of the inositol ring, although position 3 can also be phosphorylated. Phosphatidylinositol phosphates can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. PIP(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/22:4(10Z,13Z,16Z,19Z)), in particular, consists of one chain of Resolvin D5 at the C-1 position and one chain of 10Z,13Z,16Z,19Z-docosatetraenoyl at the C-2 position. The most important phosphatidylinositol phosphate in both quantitative and biological terms is phosphatidylinositol 4-phosphate. Phosphatidylinositol and the phosphatidylinositol phosphates are the main source of diacylglycerols that serve as signaling molecules, via the action of phospholipase C enzymes. Phosphatidylinositol phosphates are usually present at low levels only in tissues, typically at about 1 to 3% of the concentration of phosphatidylinositol. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structure |  MOL for HMDB0280456 (PIP(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/22:4(10Z,13Z,16Z,19Z)))
PIP(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/22:4(10Z,13Z,16Z,19Z))
Mrv1652309132116342D
74 74 0 0 1 0 999 V2000
-3.3659 0.3605 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
-4.0760 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.7861 0.3605 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.9557 -0.3495 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.7764 -0.3495 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.6557 0.7706 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.9457 0.3605 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.0085 0.3393 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.7560 0.6437 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0
-1.1177 0.0167 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.7560 1.3914 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.7517 0.6614 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.4486 1.0094 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.7717 -0.1685 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
2.0764 0.1830 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.3830 -0.1685 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
4.0566 1.0094 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.6564 0.7973 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.0725 1.2225 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.2300 1.2547 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.2911 0.1292 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.7412 0.8366 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
5.4140 0.4301 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0
5.4140 1.2502 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
5.0039 -0.2801 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
6.2060 0.2178 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-5.4962 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.4962 1.5408 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-6.2104 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-6.9245 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.6387 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-8.3528 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.1778 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.8919 0.3563 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
-9.8919 -0.4152 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-10.6061 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-11.3202 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-12.0344 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-12.8594 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-13.5735 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.2877 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-15.1127 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-15.8268 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-16.5410 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-17.2551 0.3563 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
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-17.9693 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-18.6834 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-19.5084 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-20.2225 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-20.9367 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.5202 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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-5.2343 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.9485 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-6.6626 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.3768 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-8.0909 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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-9.5192 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-10.2333 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-10.9474 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-11.7724 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-12.4866 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-13.2008 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.0258 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.7399 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-15.4540 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-16.2790 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-16.9932 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-17.7073 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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-19.2465 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-19.9606 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1 2 1 0 0 0 0
1 5 1 0 0 0 0
1 4 1 1 0 0 0
2 3 1 0 0 0 0
3 27 1 0 0 0 0
6 1 1 0 0 0 0
7 6 1 0 0 0 0
7 9 1 0 0 0 0
9 8 1 0 0 0 0
9 10 1 0 0 0 0
9 11 2 0 0 0 0
12 13 1 0 0 0 0
12 17 1 0 0 0 0
12 20 1 0 0 0 0
13 14 1 0 0 0 0
13 18 1 0 0 0 0
14 15 1 0 0 0 0
14 8 1 1 0 0 0
15 19 1 0 0 0 0
16 17 1 0 0 0 0
16 15 1 0 0 0 0
16 21 1 1 0 0 0
17 22 1 0 0 0 0
21 23 1 0 0 0 0
23 24 2 0 0 0 0
23 25 1 0 0 0 0
23 26 1 0 0 0 0
27 28 2 0 0 0 0
27 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 2 0 0 0 0
33 34 1 0 0 0 0
34 35 1 6 0 0 0
34 36 1 0 0 0 0
36 37 2 0 0 0 0
37 38 1 0 0 0 0
38 39 2 0 0 0 0
39 40 1 0 0 0 0
40 41 1 0 0 0 0
41 42 2 0 0 0 0
42 43 1 0 0 0 0
43 44 2 0 0 0 0
44 45 1 0 0 0 0
45 46 1 6 0 0 0
45 47 1 0 0 0 0
47 48 1 0 0 0 0
48 49 2 0 0 0 0
49 50 1 0 0 0 0
50 51 1 0 0 0 0
52 5 1 0 0 0 0
52 53 2 0 0 0 0
52 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 1 0 0 0 0
58 59 1 0 0 0 0
59 60 1 0 0 0 0
60 61 1 0 0 0 0
61 62 1 0 0 0 0
62 63 2 0 0 0 0
63 64 1 0 0 0 0
64 65 1 0 0 0 0
65 66 2 0 0 0 0
66 67 1 0 0 0 0
67 68 1 0 0 0 0
68 69 2 0 0 0 0
69 70 1 0 0 0 0
70 71 1 0 0 0 0
71 72 2 0 0 0 0
72 73 1 0 0 0 0
73 74 1 0 0 0 0
M END
3D MOL for HMDB0280456 (PIP(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/22:4(10Z,13Z,16Z,19Z)))HMDB0280456
RDKit 3D
PIP(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/22:4(10Z,13Z,16Z,19Z))
157157 0 0 0 0 0 0 0 0999 V2000
-5.4367 -10.0315 -4.8242 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.4250 -10.7201 -3.4536 C 0 0 0 0 0 0 0 0 0 0 0 0
-6.1360 -9.8624 -2.4961 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.5702 -9.3687 -1.4339 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.1607 -9.5949 -1.0490 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.1769 -10.2256 0.2996 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.6219 -9.6685 1.3530 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.9461 -8.3552 1.2121 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.6521 -7.3865 2.0816 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.1370 -6.6460 3.0076 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.7043 -6.6377 3.3714 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.4721 -6.9202 4.8271 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.9248 -5.9736 5.5963 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.5636 -4.6835 5.0286 C 0 0 0 0 0 0 0 0 0 0 0 0
0.9262 -4.4134 5.2013 C 0 0 0 0 0 0 0 0 0 0 0 0
1.3032 -3.1448 4.4637 C 0 0 0 0 0 0 0 0 0 0 0 0
0.5062 -1.9859 4.9552 C 0 0 0 0 0 0 0 0 0 0 0 0
0.8019 -0.7390 4.1226 C 0 0 0 0 0 0 0 0 0 0 0 0
2.1932 -0.2590 4.1567 C 0 0 0 0 0 0 0 0 0 0 0 0
2.3413 0.9260 3.1837 C 0 0 0 0 0 0 0 0 0 0 0 0
2.1189 0.4483 1.7992 C 0 0 0 0 0 0 0 0 0 0 0 0
2.2079 1.5277 0.7987 C 0 0 0 0 0 0 0 0 0 0 0 0
1.0938 2.0916 0.4013 O 0 0 0 0 0 0 0 0 0 0 0 0
3.3170 2.0403 0.1976 O 0 0 0 0 0 0 0 0 0 0 0 0
3.2093 3.0559 -0.7803 C 0 0 2 0 0 0 0 0 0 0 0 0
3.9254 2.6738 -2.0489 C 0 0 0 0 0 0 0 0 0 0 0 0
3.6658 3.6246 -3.0577 O 0 0 0 0 0 0 0 0 0 0 0 0
2.3590 3.6813 -3.5183 C 0 0 0 0 0 0 0 0 0 0 0 0
1.5084 2.9197 -3.0300 O 0 0 0 0 0 0 0 0 0 0 0 0
1.9086 4.6147 -4.5846 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6442 4.2619 -5.8241 C 0 0 0 0 0 0 0 0 0 0 0 0
2.4070 2.8900 -6.4059 C 0 0 0 0 0 0 0 0 0 0 0 0
1.0523 2.6595 -6.8542 C 0 0 0 0 0 0 0 0 0 0 0 0
0.2445 1.7138 -6.5081 C 0 0 0 0 0 0 0 0 0 0 0 0
0.5053 0.6403 -5.5795 C 0 0 2 0 0 0 0 0 0 0 0 0
-0.1165 0.7978 -4.3192 O 0 0 0 0 0 0 0 0 0 0 0 0
1.8489 0.0691 -5.4990 C 0 0 0 0 0 0 0 0 0 0 0 0
2.3256 -0.2642 -4.2780 C 0 0 0 0 0 0 0 0 0 0 0 0
3.6412 -0.8293 -4.1697 C 0 0 0 0 0 0 0 0 0 0 0 0
4.2097 -1.1720 -3.0613 C 0 0 0 0 0 0 0 0 0 0 0 0
3.5486 -1.0141 -1.7502 C 0 0 0 0 0 0 0 0 0 0 0 0
3.4166 -2.2563 -0.9809 C 0 0 0 0 0 0 0 0 0 0 0 0
2.2602 -2.7321 -0.5950 C 0 0 0 0 0 0 0 0 0 0 0 0
0.9575 -2.1475 -0.8567 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.1092 -2.7223 -0.3621 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.5020 -2.2237 -0.5689 C 0 0 2 0 0 0 0 0 0 0 0 0
-1.5950 -1.4190 -1.6973 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.9047 -1.4512 0.6810 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.2684 -0.9039 0.6235 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.2323 -1.1949 1.4740 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.0872 -2.1119 2.6090 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.3582 -1.3829 3.9361 C 0 0 0 0 0 0 0 0 0 0 0 0
3.8284 4.3623 -0.3299 C 0 0 0 0 0 0 0 0 0 0 0 0
3.2053 4.8310 0.8303 O 0 0 0 0 0 0 0 0 0 0 0 0
3.8300 6.3177 1.3542 P 0 0 0 0 0 5 0 0 0 0 0 0
4.4831 6.2020 2.6990 O 0 0 0 0 0 0 0 0 0 0 0 0
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2.5396 7.4214 1.3601 O 0 0 0 0 0 0 0 0 0 0 0 0
1.3550 6.7686 1.7216 C 0 0 1 0 0 0 0 0 0 0 0 0
0.7672 7.4825 2.8906 C 0 0 0 0 0 0 0 0 0 0 0 0
1.2410 8.8147 2.9562 O 0 0 0 0 0 0 0 0 0 0 0 0
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2.4880 0.1483 5.1487 H 0 0 0 0 0 0 0 0 0 0 0 0
1.5902 1.6804 3.5050 H 0 0 0 0 0 0 0 0 0 0 0 0
3.3446 1.3930 3.3007 H 0 0 0 0 0 0 0 0 0 0 0 0
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-1.0388 8.2958 3.6310 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.8682 5.4804 3.3291 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.4265 8.3915 1.3054 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.1621 6.5315 1.3223 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.9837 5.3437 1.2463 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.4592 3.8604 0.6859 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.7164 3.3363 -2.1174 H 0 0 0 0 0 0 0 0 0 0 0 0
0.4448 7.7017 -0.0483 H 0 0 0 0 0 0 0 0 0 0 0 0
0.5823 4.8909 0.0153 H 0 0 0 0 0 0 0 0 0 0 0 0
1 2 1 0
2 3 1 0
3 4 2 0
4 5 1 0
5 6 1 0
6 7 2 0
7 8 1 0
8 9 1 0
9 10 2 0
10 11 1 0
11 12 1 0
12 13 2 0
13 14 1 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 2 0
22 24 1 0
24 25 1 0
25 26 1 0
26 27 1 0
27 28 1 0
28 29 2 0
28 30 1 0
30 31 1 0
31 32 1 0
32 33 1 0
33 34 2 0
34 35 1 0
35 36 1 0
35 37 1 0
37 38 2 0
38 39 1 0
39 40 2 0
40 41 1 0
41 42 1 0
42 43 2 0
43 44 1 0
44 45 2 0
45 46 1 0
46 47 1 0
46 48 1 0
48 49 1 0
49 50 2 0
50 51 1 0
51 52 1 0
25 53 1 0
53 54 1 0
54 55 1 0
55 56 2 0
55 57 1 0
55 58 1 0
58 59 1 0
59 60 1 0
60 61 1 0
60 62 1 0
62 63 1 0
62 64 1 0
64 65 1 0
64 66 1 0
66 67 1 0
67 68 1 0
68 69 2 0
68 70 1 0
68 71 1 0
66 72 1 0
72 73 1 0
72 59 1 0
1 74 1 0
1 75 1 0
1 76 1 0
2 77 1 0
2 78 1 0
3 79 1 0
4 80 1 0
5 81 1 0
5 82 1 0
6 83 1 0
7 84 1 0
8 85 1 0
8 86 1 0
9 87 1 0
10 88 1 0
11 89 1 0
11 90 1 0
12 91 1 0
13 92 1 0
14 93 1 0
14 94 1 0
15 95 1 0
15 96 1 0
16 97 1 0
16 98 1 0
17 99 1 0
17100 1 0
18101 1 0
18102 1 0
19103 1 0
19104 1 0
20105 1 0
20106 1 0
21107 1 0
21108 1 0
25109 1 6
26110 1 0
26111 1 0
30112 1 0
30113 1 0
31114 1 0
31115 1 0
32116 1 0
32117 1 0
33118 1 0
34119 1 0
35120 1 6
36121 1 0
37122 1 0
38123 1 0
39124 1 0
40125 1 0
41126 1 0
41127 1 0
42128 1 0
43129 1 0
44130 1 0
45131 1 0
46132 1 6
47133 1 0
48134 1 0
48135 1 0
49136 1 0
50137 1 0
51138 1 0
51139 1 0
52140 1 0
52141 1 0
52142 1 0
53143 1 0
53144 1 0
57145 1 0
59146 1 1
60147 1 0
61148 1 0
62149 1 0
63150 1 0
64151 1 0
65152 1 0
66153 1 1
70154 1 0
71155 1 0
72156 1 0
73157 1 0
M END
3D SDF for HMDB0280456 (PIP(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/22:4(10Z,13Z,16Z,19Z)))
PIP(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/22:4(10Z,13Z,16Z,19Z))
Mrv1652309132116342D
74 74 0 0 1 0 999 V2000
-3.3659 0.3605 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
-4.0760 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.7861 0.3605 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.9557 -0.3495 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.7764 -0.3495 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.6557 0.7706 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.9457 0.3605 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.0085 0.3393 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.7560 0.6437 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0
-1.1177 0.0167 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.7560 1.3914 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.7517 0.6614 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.4486 1.0094 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.7717 -0.1685 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
2.0764 0.1830 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.3830 -0.1685 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
4.0566 1.0094 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.6564 0.7973 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.0725 1.2225 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.2300 1.2547 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.2911 0.1292 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.7412 0.8366 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
5.4140 0.4301 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0
5.4140 1.2502 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
5.0039 -0.2801 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
6.2060 0.2178 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-5.4962 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.4962 1.5408 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-6.2104 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-6.9245 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.6387 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-8.3528 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.1778 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.8919 0.3563 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
-9.8919 -0.4152 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-10.6061 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-11.3202 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-12.0344 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-12.8594 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-13.5735 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.2877 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-15.1127 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-15.8268 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-16.5410 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-17.2551 0.3563 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
-17.2551 -0.4152 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-17.9693 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-18.6834 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-19.5084 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-20.2225 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-20.9367 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.5202 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.5202 -1.5406 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-5.2343 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.9485 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-6.6626 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.3768 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-8.0909 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-8.8051 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.5192 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-10.2333 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-10.9474 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-11.7724 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-12.4866 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-13.2008 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.0258 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.7399 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-15.4540 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-16.2790 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-16.9932 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-17.7073 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-18.5324 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-19.2465 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-19.9606 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1 2 1 0 0 0 0
1 5 1 0 0 0 0
1 4 1 1 0 0 0
2 3 1 0 0 0 0
3 27 1 0 0 0 0
6 1 1 0 0 0 0
7 6 1 0 0 0 0
7 9 1 0 0 0 0
9 8 1 0 0 0 0
9 10 1 0 0 0 0
9 11 2 0 0 0 0
12 13 1 0 0 0 0
12 17 1 0 0 0 0
12 20 1 0 0 0 0
13 14 1 0 0 0 0
13 18 1 0 0 0 0
14 15 1 0 0 0 0
14 8 1 1 0 0 0
15 19 1 0 0 0 0
16 17 1 0 0 0 0
16 15 1 0 0 0 0
16 21 1 1 0 0 0
17 22 1 0 0 0 0
21 23 1 0 0 0 0
23 24 2 0 0 0 0
23 25 1 0 0 0 0
23 26 1 0 0 0 0
27 28 2 0 0 0 0
27 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 2 0 0 0 0
33 34 1 0 0 0 0
34 35 1 6 0 0 0
34 36 1 0 0 0 0
36 37 2 0 0 0 0
37 38 1 0 0 0 0
38 39 2 0 0 0 0
39 40 1 0 0 0 0
40 41 1 0 0 0 0
41 42 2 0 0 0 0
42 43 1 0 0 0 0
43 44 2 0 0 0 0
44 45 1 0 0 0 0
45 46 1 6 0 0 0
45 47 1 0 0 0 0
47 48 1 0 0 0 0
48 49 2 0 0 0 0
49 50 1 0 0 0 0
50 51 1 0 0 0 0
52 5 1 0 0 0 0
52 53 2 0 0 0 0
52 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 1 0 0 0 0
58 59 1 0 0 0 0
59 60 1 0 0 0 0
60 61 1 0 0 0 0
61 62 1 0 0 0 0
62 63 2 0 0 0 0
63 64 1 0 0 0 0
64 65 1 0 0 0 0
65 66 2 0 0 0 0
66 67 1 0 0 0 0
67 68 1 0 0 0 0
68 69 2 0 0 0 0
69 70 1 0 0 0 0
70 71 1 0 0 0 0
71 72 2 0 0 0 0
72 73 1 0 0 0 0
73 74 1 0 0 0 0
M END
> <DATABASE_ID>
HMDB0280456
> <DATABASE_NAME>
hmdb
> <SMILES>
[H][C@@](COC(=O)CCC\C=C/[C@H](O)\C=C\C=C/C\C=C/C=C/[C@H](O)C\C=C/CC)(COP(O)(=O)O[C@H]1C(O)C(O)C(O)[C@@H](OP(O)(O)=O)C1O)OC(=O)CCCCCCCC\C=C/C\C=C/C\C=C/C\C=C/CC
> <INCHI_IDENTIFIER>
InChI=1S/C53H84O18P2/c1-3-5-7-8-9-10-11-12-13-14-15-16-17-18-19-20-24-27-33-40-47(57)69-45(42-68-73(65,66)71-53-50(60)48(58)49(59)52(51(53)61)70-72(62,63)64)41-67-46(56)39-34-28-32-38-44(55)37-31-26-23-21-22-25-30-36-43(54)35-29-6-4-2/h5-7,9-10,12-13,15-16,22-23,25-26,29-32,36-38,43-45,48-55,58-61H,3-4,8,11,14,17-21,24,27-28,33-35,39-42H2,1-2H3,(H,65,66)(H2,62,63,64)/b7-5-,10-9-,13-12-,16-15-,25-22-,26-23-,29-6-,36-30+,37-31+,38-32-/t43-,44-,45-,48?,49?,50?,51?,52-,53+/m1/s1
> <INCHI_KEY>
XQAJSFMFNPQERG-FLTJOHMYSA-N
> <FORMULA>
C53H84O18P2
> <MOLECULAR_WEIGHT>
1071.185
> <EXACT_MASS>
1070.513289861
> <JCHEM_ACCEPTOR_COUNT>
13
> <JCHEM_ATOM_COUNT>
157
> <JCHEM_AVERAGE_POLARIZABILITY>
114.28367660860093
> <JCHEM_BIOAVAILABILITY>
0
> <JCHEM_DONOR_COUNT>
9
> <JCHEM_FORMAL_CHARGE>
0
> <JCHEM_GHOSE_FILTER>
0
> <JCHEM_IUPAC>
{[(1R,3S)-3-({[(2R)-3-{[(5Z,7S,8E,10Z,13Z,15E,17R,19Z)-7,17-dihydroxydocosa-5,8,10,13,15,19-hexaenoyl]oxy}-2-[(10Z,13Z,16Z,19Z)-docosa-10,13,16,19-tetraenoyloxy]propoxy](hydroxy)phosphoryl}oxy)-2,4,5,6-tetrahydroxycyclohexyl]oxy}phosphonic acid
> <ALOGPS_LOGP>
5.99
> <JCHEM_LOGP>
8.280382598000001
> <ALOGPS_LOGS>
-5.41
> <JCHEM_MDDR_LIKE_RULE>
0
> <JCHEM_NUMBER_OF_RINGS>
1
> <JCHEM_PHYSIOLOGICAL_CHARGE>
-3
> <JCHEM_PKA>
1.916781916784089
> <JCHEM_PKA_STRONGEST_ACIDIC>
1.076448135630991
> <JCHEM_PKA_STRONGEST_BASIC>
-1.6096078290895006
> <JCHEM_POLAR_SURFACE_AREA>
296.49999999999994
> <JCHEM_REFRACTIVITY>
290.69569999999993
> <JCHEM_ROTATABLE_BOND_COUNT>
42
> <JCHEM_RULE_OF_FIVE>
0
> <ALOGPS_SOLUBILITY>
4.17e-03 g/l
> <JCHEM_TRADITIONAL_IUPAC>
[(1R,3S)-3-{[(2R)-3-{[(5Z,7S,8E,10Z,13Z,15E,17R,19Z)-7,17-dihydroxydocosa-5,8,10,13,15,19-hexaenoyl]oxy}-2-[(10Z,13Z,16Z,19Z)-docosa-10,13,16,19-tetraenoyloxy]propoxy(hydroxy)phosphoryl]oxy}-2,4,5,6-tetrahydroxycyclohexyl]oxyphosphonic acid
> <JCHEM_VEBER_RULE>
0
$$$$
3D-SDF for HMDB0280456 (PIP(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/22:4(10Z,13Z,16Z,19Z)))HMDB0280456
RDKit 3D
PIP(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/22:4(10Z,13Z,16Z,19Z))
157157 0 0 0 0 0 0 0 0999 V2000
-5.4367 -10.0315 -4.8242 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.4250 -10.7201 -3.4536 C 0 0 0 0 0 0 0 0 0 0 0 0
-6.1360 -9.8624 -2.4961 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.5702 -9.3687 -1.4339 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.1607 -9.5949 -1.0490 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.1769 -10.2256 0.2996 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.6219 -9.6685 1.3530 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.9461 -8.3552 1.2121 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.6521 -7.3865 2.0816 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.1370 -6.6460 3.0076 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.7043 -6.6377 3.3714 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.4721 -6.9202 4.8271 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.9248 -5.9736 5.5963 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.5636 -4.6835 5.0286 C 0 0 0 0 0 0 0 0 0 0 0 0
0.9262 -4.4134 5.2013 C 0 0 0 0 0 0 0 0 0 0 0 0
1.3032 -3.1448 4.4637 C 0 0 0 0 0 0 0 0 0 0 0 0
0.5062 -1.9859 4.9552 C 0 0 0 0 0 0 0 0 0 0 0 0
0.8019 -0.7390 4.1226 C 0 0 0 0 0 0 0 0 0 0 0 0
2.1932 -0.2590 4.1567 C 0 0 0 0 0 0 0 0 0 0 0 0
2.3413 0.9260 3.1837 C 0 0 0 0 0 0 0 0 0 0 0 0
2.1189 0.4483 1.7992 C 0 0 0 0 0 0 0 0 0 0 0 0
2.2079 1.5277 0.7987 C 0 0 0 0 0 0 0 0 0 0 0 0
1.0938 2.0916 0.4013 O 0 0 0 0 0 0 0 0 0 0 0 0
3.3170 2.0403 0.1976 O 0 0 0 0 0 0 0 0 0 0 0 0
3.2093 3.0559 -0.7803 C 0 0 2 0 0 0 0 0 0 0 0 0
3.9254 2.6738 -2.0489 C 0 0 0 0 0 0 0 0 0 0 0 0
3.6658 3.6246 -3.0577 O 0 0 0 0 0 0 0 0 0 0 0 0
2.3590 3.6813 -3.5183 C 0 0 0 0 0 0 0 0 0 0 0 0
1.5084 2.9197 -3.0300 O 0 0 0 0 0 0 0 0 0 0 0 0
1.9086 4.6147 -4.5846 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6442 4.2619 -5.8241 C 0 0 0 0 0 0 0 0 0 0 0 0
2.4070 2.8900 -6.4059 C 0 0 0 0 0 0 0 0 0 0 0 0
1.0523 2.6595 -6.8542 C 0 0 0 0 0 0 0 0 0 0 0 0
0.2445 1.7138 -6.5081 C 0 0 0 0 0 0 0 0 0 0 0 0
0.5053 0.6403 -5.5795 C 0 0 2 0 0 0 0 0 0 0 0 0
-0.1165 0.7978 -4.3192 O 0 0 0 0 0 0 0 0 0 0 0 0
1.8489 0.0691 -5.4990 C 0 0 0 0 0 0 0 0 0 0 0 0
2.3256 -0.2642 -4.2780 C 0 0 0 0 0 0 0 0 0 0 0 0
3.6412 -0.8293 -4.1697 C 0 0 0 0 0 0 0 0 0 0 0 0
4.2097 -1.1720 -3.0613 C 0 0 0 0 0 0 0 0 0 0 0 0
3.5486 -1.0141 -1.7502 C 0 0 0 0 0 0 0 0 0 0 0 0
3.4166 -2.2563 -0.9809 C 0 0 0 0 0 0 0 0 0 0 0 0
2.2602 -2.7321 -0.5950 C 0 0 0 0 0 0 0 0 0 0 0 0
0.9575 -2.1475 -0.8567 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.1092 -2.7223 -0.3621 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.5020 -2.2237 -0.5689 C 0 0 2 0 0 0 0 0 0 0 0 0
-1.5950 -1.4190 -1.6973 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.9047 -1.4512 0.6810 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.2684 -0.9039 0.6235 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.2323 -1.1949 1.4740 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.0872 -2.1119 2.6090 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.3582 -1.3829 3.9361 C 0 0 0 0 0 0 0 0 0 0 0 0
3.8284 4.3623 -0.3299 C 0 0 0 0 0 0 0 0 0 0 0 0
3.2053 4.8310 0.8303 O 0 0 0 0 0 0 0 0 0 0 0 0
3.8300 6.3177 1.3542 P 0 0 0 0 0 5 0 0 0 0 0 0
4.4831 6.2020 2.6990 O 0 0 0 0 0 0 0 0 0 0 0 0
4.9193 6.8225 0.1498 O 0 0 0 0 0 0 0 0 0 0 0 0
2.5396 7.4214 1.3601 O 0 0 0 0 0 0 0 0 0 0 0 0
1.3550 6.7686 1.7216 C 0 0 1 0 0 0 0 0 0 0 0 0
0.7672 7.4825 2.8906 C 0 0 0 0 0 0 0 0 0 0 0 0
1.2410 8.8147 2.9562 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.7089 7.3858 3.0429 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.0766 6.3089 3.8662 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.5032 7.3994 1.7810 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.8156 7.0561 2.1017 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.9559 6.3651 0.8417 C 0 0 1 0 0 0 0 0 0 0 0 0
-1.6651 6.4578 -0.3798 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.3218 4.9809 -0.8263 P 0 0 0 0 0 5 0 0 0 0 0 0
-3.6719 5.2329 -1.4708 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.4978 3.9217 0.4632 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.3112 4.2481 -1.9776 O 0 0 0 0 0 0 0 0 0 0 0 0
0.4601 6.7571 0.5041 C 0 0 0 0 0 0 0 0 0 0 0 0
0.9449 5.7427 -0.3487 O 0 0 0 0 0 0 0 0 0 0 0 0
-6.4490 -9.7842 -5.1537 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.8244 -9.0895 -4.7444 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.9577 -10.6597 -5.5943 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.0923 -11.6357 -3.6050 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.4322 -11.0456 -3.2188 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.2097 -9.6112 -2.6724 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.1382 -8.7268 -0.7296 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.6676 -8.6269 -1.1285 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.6473 -10.3191 -1.7404 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.6910 -11.2010 0.3372 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.6437 -10.1414 2.3167 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.8857 -8.5504 1.5398 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.9055 -7.9187 0.2272 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.7469 -7.2988 1.9043 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.7930 -5.9599 3.5898 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.2276 -7.5799 2.8933 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.1258 -5.8234 2.9534 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.7577 -7.8975 5.2155 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.7743 -6.2383 6.6424 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.0948 -3.8697 5.6875 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.8845 -4.4237 4.0350 H 0 0 0 0 0 0 0 0 0 0 0 0
1.1231 -4.3423 6.2952 H 0 0 0 0 0 0 0 0 0 0 0 0
1.4660 -5.2439 4.7177 H 0 0 0 0 0 0 0 0 0 0 0 0
1.1296 -3.3409 3.3867 H 0 0 0 0 0 0 0 0 0 0 0 0
2.4010 -2.9951 4.6700 H 0 0 0 0 0 0 0 0 0 0 0 0
0.6367 -1.8243 6.0236 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.5669 -2.1905 4.7716 H 0 0 0 0 0 0 0 0 0 0 0 0
0.1524 0.0606 4.6039 H 0 0 0 0 0 0 0 0 0 0 0 0
0.3840 -0.8847 3.1289 H 0 0 0 0 0 0 0 0 0 0 0 0
2.9695 -0.9758 3.8395 H 0 0 0 0 0 0 0 0 0 0 0 0
2.4880 0.1483 5.1487 H 0 0 0 0 0 0 0 0 0 0 0 0
1.5902 1.6804 3.5050 H 0 0 0 0 0 0 0 0 0 0 0 0
3.3446 1.3930 3.3007 H 0 0 0 0 0 0 0 0 0 0 0 0
1.0871 -0.0045 1.7114 H 0 0 0 0 0 0 0 0 0 0 0 0
2.8431 -0.3451 1.4900 H 0 0 0 0 0 0 0 0 0 0 0 0
2.1516 3.2702 -0.9411 H 0 0 0 0 0 0 0 0 0 0 0 0
3.5027 1.7144 -2.4437 H 0 0 0 0 0 0 0 0 0 0 0 0
5.0151 2.5797 -1.8503 H 0 0 0 0 0 0 0 0 0 0 0 0
0.7958 4.5697 -4.7115 H 0 0 0 0 0 0 0 0 0 0 0 0
2.1046 5.6469 -4.2383 H 0 0 0 0 0 0 0 0 0 0 0 0
2.4068 5.0657 -6.5847 H 0 0 0 0 0 0 0 0 0 0 0 0
3.7611 4.3574 -5.7049 H 0 0 0 0 0 0 0 0 0 0 0 0
2.8724 2.1488 -5.7479 H 0 0 0 0 0 0 0 0 0 0 0 0
3.0633 2.8733 -7.3411 H 0 0 0 0 0 0 0 0 0 0 0 0
0.6893 3.4327 -7.6036 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.7994 1.7229 -6.9835 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.1103 -0.2816 -5.9853 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.7005 1.6226 -4.4164 H 0 0 0 0 0 0 0 0 0 0 0 0
2.4944 -0.1050 -6.3396 H 0 0 0 0 0 0 0 0 0 0 0 0
1.6750 -0.0952 -3.4387 H 0 0 0 0 0 0 0 0 0 0 0 0
4.2307 -0.9783 -5.0894 H 0 0 0 0 0 0 0 0 0 0 0 0
5.2385 -1.6079 -3.0551 H 0 0 0 0 0 0 0 0 0 0 0 0
2.6287 -0.4243 -1.7885 H 0 0 0 0 0 0 0 0 0 0 0 0
4.3247 -0.3741 -1.1590 H 0 0 0 0 0 0 0 0 0 0 0 0
4.3290 -2.8284 -0.7018 H 0 0 0 0 0 0 0 0 0 0 0 0
2.2601 -3.6777 -0.0049 H 0 0 0 0 0 0 0 0 0 0 0 0
0.8883 -1.2608 -1.4483 H 0 0 0 0 0 0 0 0 0 0 0 0
0.0265 -3.6221 0.2415 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.2006 -3.0662 -0.6701 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.4484 -0.9531 -1.7744 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.7232 -2.0394 1.5878 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.1766 -0.5794 0.7186 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.5318 -0.2020 -0.1769 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.2257 -0.7396 1.3524 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.1505 -2.6303 2.7222 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.8830 -2.9095 2.5024 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.2746 -0.7847 3.7715 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.4826 -0.7189 4.1304 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.4794 -2.1154 4.7372 H 0 0 0 0 0 0 0 0 0 0 0 0
4.9289 4.3260 -0.2620 H 0 0 0 0 0 0 0 0 0 0 0 0
3.5983 5.1054 -1.1285 H 0 0 0 0 0 0 0 0 0 0 0 0
5.6740 7.3051 0.5763 H 0 0 0 0 0 0 0 0 0 0 0 0
1.6417 5.7076 1.9679 H 0 0 0 0 0 0 0 0 0 0 0 0
1.2111 7.0053 3.8154 H 0 0 0 0 0 0 0 0 0 0 0 0
0.5044 9.4601 2.9644 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.0388 8.2958 3.6310 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.8682 5.4804 3.3291 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.4265 8.3915 1.3054 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.1621 6.5315 1.3223 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.9837 5.3437 1.2463 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.4592 3.8604 0.6859 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.7164 3.3363 -2.1174 H 0 0 0 0 0 0 0 0 0 0 0 0
0.4448 7.7017 -0.0483 H 0 0 0 0 0 0 0 0 0 0 0 0
0.5823 4.8909 0.0153 H 0 0 0 0 0 0 0 0 0 0 0 0
1 2 1 0
2 3 1 0
3 4 2 0
4 5 1 0
5 6 1 0
6 7 2 0
7 8 1 0
8 9 1 0
9 10 2 0
10 11 1 0
11 12 1 0
12 13 2 0
13 14 1 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 2 0
22 24 1 0
24 25 1 0
25 26 1 0
26 27 1 0
27 28 1 0
28 29 2 0
28 30 1 0
30 31 1 0
31 32 1 0
32 33 1 0
33 34 2 0
34 35 1 0
35 36 1 0
35 37 1 0
37 38 2 0
38 39 1 0
39 40 2 0
40 41 1 0
41 42 1 0
42 43 2 0
43 44 1 0
44 45 2 0
45 46 1 0
46 47 1 0
46 48 1 0
48 49 1 0
49 50 2 0
50 51 1 0
51 52 1 0
25 53 1 0
53 54 1 0
54 55 1 0
55 56 2 0
55 57 1 0
55 58 1 0
58 59 1 0
59 60 1 0
60 61 1 0
60 62 1 0
62 63 1 0
62 64 1 0
64 65 1 0
64 66 1 0
66 67 1 0
67 68 1 0
68 69 2 0
68 70 1 0
68 71 1 0
66 72 1 0
72 73 1 0
72 59 1 0
1 74 1 0
1 75 1 0
1 76 1 0
2 77 1 0
2 78 1 0
3 79 1 0
4 80 1 0
5 81 1 0
5 82 1 0
6 83 1 0
7 84 1 0
8 85 1 0
8 86 1 0
9 87 1 0
10 88 1 0
11 89 1 0
11 90 1 0
12 91 1 0
13 92 1 0
14 93 1 0
14 94 1 0
15 95 1 0
15 96 1 0
16 97 1 0
16 98 1 0
17 99 1 0
17100 1 0
18101 1 0
18102 1 0
19103 1 0
19104 1 0
20105 1 0
20106 1 0
21107 1 0
21108 1 0
25109 1 6
26110 1 0
26111 1 0
30112 1 0
30113 1 0
31114 1 0
31115 1 0
32116 1 0
32117 1 0
33118 1 0
34119 1 0
35120 1 6
36121 1 0
37122 1 0
38123 1 0
39124 1 0
40125 1 0
41126 1 0
41127 1 0
42128 1 0
43129 1 0
44130 1 0
45131 1 0
46132 1 6
47133 1 0
48134 1 0
48135 1 0
49136 1 0
50137 1 0
51138 1 0
51139 1 0
52140 1 0
52141 1 0
52142 1 0
53143 1 0
53144 1 0
57145 1 0
59146 1 1
60147 1 0
61148 1 0
62149 1 0
63150 1 0
64151 1 0
65152 1 0
66153 1 1
70154 1 0
71155 1 0
72156 1 0
73157 1 0
M END
PDB for HMDB0280456 (PIP(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/22:4(10Z,13Z,16Z,19Z)))HEADER PROTEIN 13-SEP-21 NONE TITLE NULL COMPND MOLECULE: PIP(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/22:4( SOURCE NULL KEYWDS NULL EXPDTA NULL AUTHOR Marvin REVDAT 1 13-SEP-21 0 HETATM 1 C UNK 0 -6.283 0.673 0.000 0.00 0.00 C+0 HETATM 2 C UNK 0 -7.609 1.436 0.000 0.00 0.00 C+0 HETATM 3 O UNK 0 -8.934 0.673 0.000 0.00 0.00 O+0 HETATM 4 H UNK 0 -5.517 -0.652 0.000 0.00 0.00 H+0 HETATM 5 O UNK 0 -7.049 -0.652 0.000 0.00 0.00 O+0 HETATM 6 C UNK 0 -4.957 1.439 0.000 0.00 0.00 C+0 HETATM 7 O UNK 0 -3.632 0.673 0.000 0.00 0.00 O+0 HETATM 8 O UNK 0 -0.016 0.633 0.000 0.00 0.00 O+0 HETATM 9 P UNK 0 -1.411 1.202 0.000 0.00 0.00 P+0 HETATM 10 O UNK 0 -2.086 0.031 0.000 0.00 0.00 O+0 HETATM 11 O UNK 0 -1.411 2.597 0.000 0.00 0.00 O+0 HETATM 12 C UNK 0 5.136 1.235 0.000 0.00 0.00 C+0 HETATM 13 C UNK 0 2.704 1.884 0.000 0.00 0.00 C+0 HETATM 14 C UNK 0 1.440 -0.315 0.000 0.00 0.00 C+0 HETATM 15 C UNK 0 3.876 0.342 0.000 0.00 0.00 C+0 HETATM 16 C UNK 0 6.315 -0.315 0.000 0.00 0.00 C+0 HETATM 17 C UNK 0 7.572 1.884 0.000 0.00 0.00 C+0 HETATM 18 O UNK 0 1.225 1.488 0.000 0.00 0.00 O+0 HETATM 19 O UNK 0 3.869 2.282 0.000 0.00 0.00 O+0 HETATM 20 O UNK 0 6.029 2.342 0.000 0.00 0.00 O+0 HETATM 21 O UNK 0 8.010 0.241 0.000 0.00 0.00 O+0 HETATM 22 O UNK 0 8.850 1.562 0.000 0.00 0.00 O+0 HETATM 23 P UNK 0 10.106 0.803 0.000 0.00 0.00 P+0 HETATM 24 O UNK 0 10.106 2.334 0.000 0.00 0.00 O+0 HETATM 25 O UNK 0 9.341 -0.523 0.000 0.00 0.00 O+0 HETATM 26 O UNK 0 11.585 0.407 0.000 0.00 0.00 O+0 HETATM 27 C UNK 0 -10.260 1.436 0.000 0.00 0.00 C+0 HETATM 28 O UNK 0 -10.260 2.876 0.000 0.00 0.00 O+0 HETATM 29 C UNK 0 -11.593 0.665 0.000 0.00 0.00 C+0 HETATM 30 C UNK 0 -12.926 1.436 0.000 0.00 0.00 C+0 HETATM 31 C UNK 0 -14.259 0.665 0.000 0.00 0.00 C+0 HETATM 32 C UNK 0 -15.592 1.436 0.000 0.00 0.00 C+0 HETATM 33 C UNK 0 -17.132 1.436 0.000 0.00 0.00 C+0 HETATM 34 C UNK 0 -18.465 0.665 0.000 0.00 0.00 C+0 HETATM 35 O UNK 0 -18.465 -0.775 0.000 0.00 0.00 O+0 HETATM 36 C UNK 0 -19.798 1.436 0.000 0.00 0.00 C+0 HETATM 37 C UNK 0 -21.131 0.665 0.000 0.00 0.00 C+0 HETATM 38 C UNK 0 -22.464 1.436 0.000 0.00 0.00 C+0 HETATM 39 C UNK 0 -24.004 1.436 0.000 0.00 0.00 C+0 HETATM 40 C UNK 0 -25.337 0.665 0.000 0.00 0.00 C+0 HETATM 41 C UNK 0 -26.670 1.436 0.000 0.00 0.00 C+0 HETATM 42 C UNK 0 -28.210 1.436 0.000 0.00 0.00 C+0 HETATM 43 C UNK 0 -29.543 0.665 0.000 0.00 0.00 C+0 HETATM 44 C UNK 0 -30.876 1.436 0.000 0.00 0.00 C+0 HETATM 45 C UNK 0 -32.209 0.665 0.000 0.00 0.00 C+0 HETATM 46 O UNK 0 -32.209 -0.775 0.000 0.00 0.00 O+0 HETATM 47 C UNK 0 -33.543 1.436 0.000 0.00 0.00 C+0 HETATM 48 C UNK 0 -34.876 0.665 0.000 0.00 0.00 C+0 HETATM 49 C UNK 0 -36.416 0.665 0.000 0.00 0.00 C+0 HETATM 50 C UNK 0 -37.749 1.436 0.000 0.00 0.00 C+0 HETATM 51 C UNK 0 -39.082 0.665 0.000 0.00 0.00 C+0 HETATM 52 C UNK 0 -8.438 -1.436 0.000 0.00 0.00 C+0 HETATM 53 O UNK 0 -8.438 -2.876 0.000 0.00 0.00 O+0 HETATM 54 C UNK 0 -9.771 -0.665 0.000 0.00 0.00 C+0 HETATM 55 C UNK 0 -11.104 -1.436 0.000 0.00 0.00 C+0 HETATM 56 C UNK 0 -12.437 -0.665 0.000 0.00 0.00 C+0 HETATM 57 C UNK 0 -13.770 -1.436 0.000 0.00 0.00 C+0 HETATM 58 C UNK 0 -15.103 -0.665 0.000 0.00 0.00 C+0 HETATM 59 C UNK 0 -16.436 -1.436 0.000 0.00 0.00 C+0 HETATM 60 C UNK 0 -17.769 -0.665 0.000 0.00 0.00 C+0 HETATM 61 C UNK 0 -19.102 -1.436 0.000 0.00 0.00 C+0 HETATM 62 C UNK 0 -20.435 -0.665 0.000 0.00 0.00 C+0 HETATM 63 C UNK 0 -21.975 -0.665 0.000 0.00 0.00 C+0 HETATM 64 C UNK 0 -23.308 -1.436 0.000 0.00 0.00 C+0 HETATM 65 C UNK 0 -24.641 -0.665 0.000 0.00 0.00 C+0 HETATM 66 C UNK 0 -26.181 -0.665 0.000 0.00 0.00 C+0 HETATM 67 C UNK 0 -27.514 -1.436 0.000 0.00 0.00 C+0 HETATM 68 C UNK 0 -28.848 -0.665 0.000 0.00 0.00 C+0 HETATM 69 C UNK 0 -30.388 -0.665 0.000 0.00 0.00 C+0 HETATM 70 C UNK 0 -31.721 -1.436 0.000 0.00 0.00 C+0 HETATM 71 C UNK 0 -33.054 -0.665 0.000 0.00 0.00 C+0 HETATM 72 C UNK 0 -34.594 -0.665 0.000 0.00 0.00 C+0 HETATM 73 C UNK 0 -35.927 -1.436 0.000 0.00 0.00 C+0 HETATM 74 C UNK 0 -37.260 -0.665 0.000 0.00 0.00 C+0 CONECT 1 2 5 4 6 CONECT 2 1 3 CONECT 3 2 27 CONECT 4 1 CONECT 5 1 52 CONECT 6 1 7 CONECT 7 6 9 CONECT 8 9 14 CONECT 9 7 8 10 11 CONECT 10 9 CONECT 11 9 CONECT 12 13 17 20 CONECT 13 12 14 18 CONECT 14 13 15 8 CONECT 15 14 19 16 CONECT 16 17 15 21 CONECT 17 12 16 22 CONECT 18 13 CONECT 19 15 CONECT 20 12 CONECT 21 16 23 CONECT 22 17 CONECT 23 21 24 25 26 CONECT 24 23 CONECT 25 23 CONECT 26 23 CONECT 27 3 28 29 CONECT 28 27 CONECT 29 27 30 CONECT 30 29 31 CONECT 31 30 32 CONECT 32 31 33 CONECT 33 32 34 CONECT 34 33 35 36 CONECT 35 34 CONECT 36 34 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 47 CONECT 46 45 CONECT 47 45 48 CONECT 48 47 49 CONECT 49 48 50 CONECT 50 49 51 CONECT 51 50 CONECT 52 5 53 54 CONECT 53 52 CONECT 54 52 55 CONECT 55 54 56 CONECT 56 55 57 CONECT 57 56 58 CONECT 58 57 59 CONECT 59 58 60 CONECT 60 59 61 CONECT 61 60 62 CONECT 62 61 63 CONECT 63 62 64 CONECT 64 63 65 CONECT 65 64 66 CONECT 66 65 67 CONECT 67 66 68 CONECT 68 67 69 CONECT 69 68 70 CONECT 70 69 71 CONECT 71 70 72 CONECT 72 71 73 CONECT 73 72 74 CONECT 74 73 MASTER 0 0 0 0 0 0 0 0 74 0 148 0 END 3D PDB for HMDB0280456 (PIP(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/22:4(10Z,13Z,16Z,19Z)))COMPND HMDB0280456 HETATM 1 C1 UNL 1 -5.437 -10.032 -4.824 1.00 0.00 C HETATM 2 C2 UNL 1 -5.425 -10.720 -3.454 1.00 0.00 C HETATM 3 C3 UNL 1 -6.136 -9.862 -2.496 1.00 0.00 C HETATM 4 C4 UNL 1 -5.570 -9.369 -1.434 1.00 0.00 C HETATM 5 C5 UNL 1 -4.161 -9.595 -1.049 1.00 0.00 C HETATM 6 C6 UNL 1 -4.177 -10.226 0.300 1.00 0.00 C HETATM 7 C7 UNL 1 -3.622 -9.669 1.353 1.00 0.00 C HETATM 8 C8 UNL 1 -2.946 -8.355 1.212 1.00 0.00 C HETATM 9 C9 UNL 1 -3.652 -7.387 2.082 1.00 0.00 C HETATM 10 C10 UNL 1 -3.137 -6.646 3.008 1.00 0.00 C HETATM 11 C11 UNL 1 -1.704 -6.638 3.371 1.00 0.00 C HETATM 12 C12 UNL 1 -1.472 -6.920 4.827 1.00 0.00 C HETATM 13 C13 UNL 1 -0.925 -5.974 5.596 1.00 0.00 C HETATM 14 C14 UNL 1 -0.564 -4.684 5.029 1.00 0.00 C HETATM 15 C15 UNL 1 0.926 -4.413 5.201 1.00 0.00 C HETATM 16 C16 UNL 1 1.303 -3.145 4.464 1.00 0.00 C HETATM 17 C17 UNL 1 0.506 -1.986 4.955 1.00 0.00 C HETATM 18 C18 UNL 1 0.802 -0.739 4.123 1.00 0.00 C HETATM 19 C19 UNL 1 2.193 -0.259 4.157 1.00 0.00 C HETATM 20 C20 UNL 1 2.341 0.926 3.184 1.00 0.00 C HETATM 21 C21 UNL 1 2.119 0.448 1.799 1.00 0.00 C HETATM 22 C22 UNL 1 2.208 1.528 0.799 1.00 0.00 C HETATM 23 O1 UNL 1 1.094 2.092 0.401 1.00 0.00 O HETATM 24 O2 UNL 1 3.317 2.040 0.198 1.00 0.00 O HETATM 25 C23 UNL 1 3.209 3.056 -0.780 1.00 0.00 C HETATM 26 C24 UNL 1 3.925 2.674 -2.049 1.00 0.00 C HETATM 27 O3 UNL 1 3.666 3.625 -3.058 1.00 0.00 O HETATM 28 C25 UNL 1 2.359 3.681 -3.518 1.00 0.00 C HETATM 29 O4 UNL 1 1.508 2.920 -3.030 1.00 0.00 O HETATM 30 C26 UNL 1 1.909 4.615 -4.585 1.00 0.00 C HETATM 31 C27 UNL 1 2.644 4.262 -5.824 1.00 0.00 C HETATM 32 C28 UNL 1 2.407 2.890 -6.406 1.00 0.00 C HETATM 33 C29 UNL 1 1.052 2.660 -6.854 1.00 0.00 C HETATM 34 C30 UNL 1 0.244 1.714 -6.508 1.00 0.00 C HETATM 35 C31 UNL 1 0.505 0.640 -5.580 1.00 0.00 C HETATM 36 O5 UNL 1 -0.116 0.798 -4.319 1.00 0.00 O HETATM 37 C32 UNL 1 1.849 0.069 -5.499 1.00 0.00 C HETATM 38 C33 UNL 1 2.326 -0.264 -4.278 1.00 0.00 C HETATM 39 C34 UNL 1 3.641 -0.829 -4.170 1.00 0.00 C HETATM 40 C35 UNL 1 4.210 -1.172 -3.061 1.00 0.00 C HETATM 41 C36 UNL 1 3.549 -1.014 -1.750 1.00 0.00 C HETATM 42 C37 UNL 1 3.417 -2.256 -0.981 1.00 0.00 C HETATM 43 C38 UNL 1 2.260 -2.732 -0.595 1.00 0.00 C HETATM 44 C39 UNL 1 0.958 -2.148 -0.857 1.00 0.00 C HETATM 45 C40 UNL 1 -0.109 -2.722 -0.362 1.00 0.00 C HETATM 46 C41 UNL 1 -1.502 -2.224 -0.569 1.00 0.00 C HETATM 47 O6 UNL 1 -1.595 -1.419 -1.697 1.00 0.00 O HETATM 48 C42 UNL 1 -1.905 -1.451 0.681 1.00 0.00 C HETATM 49 C43 UNL 1 -3.268 -0.904 0.624 1.00 0.00 C HETATM 50 C44 UNL 1 -4.232 -1.195 1.474 1.00 0.00 C HETATM 51 C45 UNL 1 -4.087 -2.112 2.609 1.00 0.00 C HETATM 52 C46 UNL 1 -4.358 -1.383 3.936 1.00 0.00 C HETATM 53 C47 UNL 1 3.828 4.362 -0.330 1.00 0.00 C HETATM 54 O7 UNL 1 3.205 4.831 0.830 1.00 0.00 O HETATM 55 P1 UNL 1 3.830 6.318 1.354 1.00 0.00 P HETATM 56 O8 UNL 1 4.483 6.202 2.699 1.00 0.00 O HETATM 57 O9 UNL 1 4.919 6.822 0.150 1.00 0.00 O HETATM 58 O10 UNL 1 2.540 7.421 1.360 1.00 0.00 O HETATM 59 C48 UNL 1 1.355 6.769 1.722 1.00 0.00 C HETATM 60 C49 UNL 1 0.767 7.482 2.891 1.00 0.00 C HETATM 61 O11 UNL 1 1.241 8.815 2.956 1.00 0.00 O HETATM 62 C50 UNL 1 -0.709 7.386 3.043 1.00 0.00 C HETATM 63 O12 UNL 1 -1.077 6.309 3.866 1.00 0.00 O HETATM 64 C51 UNL 1 -1.503 7.399 1.781 1.00 0.00 C HETATM 65 O13 UNL 1 -2.816 7.056 2.102 1.00 0.00 O HETATM 66 C52 UNL 1 -0.956 6.365 0.842 1.00 0.00 C HETATM 67 O14 UNL 1 -1.665 6.458 -0.380 1.00 0.00 O HETATM 68 P2 UNL 1 -2.322 4.981 -0.826 1.00 0.00 P HETATM 69 O15 UNL 1 -3.672 5.233 -1.471 1.00 0.00 O HETATM 70 O16 UNL 1 -2.498 3.922 0.463 1.00 0.00 O HETATM 71 O17 UNL 1 -1.311 4.248 -1.978 1.00 0.00 O HETATM 72 C53 UNL 1 0.460 6.757 0.504 1.00 0.00 C HETATM 73 O18 UNL 1 0.945 5.743 -0.349 1.00 0.00 O HETATM 74 H1 UNL 1 -6.449 -9.784 -5.154 1.00 0.00 H HETATM 75 H2 UNL 1 -4.824 -9.090 -4.744 1.00 0.00 H HETATM 76 H3 UNL 1 -4.958 -10.660 -5.594 1.00 0.00 H HETATM 77 H4 UNL 1 -6.092 -11.636 -3.605 1.00 0.00 H HETATM 78 H5 UNL 1 -4.432 -11.046 -3.219 1.00 0.00 H HETATM 79 H6 UNL 1 -7.210 -9.611 -2.672 1.00 0.00 H HETATM 80 H7 UNL 1 -6.138 -8.727 -0.730 1.00 0.00 H HETATM 81 H8 UNL 1 -3.668 -8.627 -1.129 1.00 0.00 H HETATM 82 H9 UNL 1 -3.647 -10.319 -1.740 1.00 0.00 H HETATM 83 H10 UNL 1 -4.691 -11.201 0.337 1.00 0.00 H HETATM 84 H11 UNL 1 -3.644 -10.141 2.317 1.00 0.00 H HETATM 85 H12 UNL 1 -1.886 -8.550 1.540 1.00 0.00 H HETATM 86 H13 UNL 1 -2.905 -7.919 0.227 1.00 0.00 H HETATM 87 H14 UNL 1 -4.747 -7.299 1.904 1.00 0.00 H HETATM 88 H15 UNL 1 -3.793 -5.960 3.590 1.00 0.00 H HETATM 89 H16 UNL 1 -1.228 -7.580 2.893 1.00 0.00 H HETATM 90 H17 UNL 1 -1.126 -5.823 2.953 1.00 0.00 H HETATM 91 H18 UNL 1 -1.758 -7.898 5.216 1.00 0.00 H HETATM 92 H19 UNL 1 -0.774 -6.238 6.642 1.00 0.00 H HETATM 93 H20 UNL 1 -1.095 -3.870 5.688 1.00 0.00 H HETATM 94 H21 UNL 1 -0.885 -4.424 4.035 1.00 0.00 H HETATM 95 H22 UNL 1 1.123 -4.342 6.295 1.00 0.00 H HETATM 96 H23 UNL 1 1.466 -5.244 4.718 1.00 0.00 H HETATM 97 H24 UNL 1 1.130 -3.341 3.387 1.00 0.00 H HETATM 98 H25 UNL 1 2.401 -2.995 4.670 1.00 0.00 H HETATM 99 H26 UNL 1 0.637 -1.824 6.024 1.00 0.00 H HETATM 100 H27 UNL 1 -0.567 -2.190 4.772 1.00 0.00 H HETATM 101 H28 UNL 1 0.152 0.061 4.604 1.00 0.00 H HETATM 102 H29 UNL 1 0.384 -0.885 3.129 1.00 0.00 H HETATM 103 H30 UNL 1 2.970 -0.976 3.839 1.00 0.00 H HETATM 104 H31 UNL 1 2.488 0.148 5.149 1.00 0.00 H HETATM 105 H32 UNL 1 1.590 1.680 3.505 1.00 0.00 H HETATM 106 H33 UNL 1 3.345 1.393 3.301 1.00 0.00 H HETATM 107 H34 UNL 1 1.087 -0.004 1.711 1.00 0.00 H HETATM 108 H35 UNL 1 2.843 -0.345 1.490 1.00 0.00 H HETATM 109 H36 UNL 1 2.152 3.270 -0.941 1.00 0.00 H HETATM 110 H37 UNL 1 3.503 1.714 -2.444 1.00 0.00 H HETATM 111 H38 UNL 1 5.015 2.580 -1.850 1.00 0.00 H HETATM 112 H39 UNL 1 0.796 4.570 -4.711 1.00 0.00 H HETATM 113 H40 UNL 1 2.105 5.647 -4.238 1.00 0.00 H HETATM 114 H41 UNL 1 2.407 5.066 -6.585 1.00 0.00 H HETATM 115 H42 UNL 1 3.761 4.357 -5.705 1.00 0.00 H HETATM 116 H43 UNL 1 2.872 2.149 -5.748 1.00 0.00 H HETATM 117 H44 UNL 1 3.063 2.873 -7.341 1.00 0.00 H HETATM 118 H45 UNL 1 0.689 3.433 -7.604 1.00 0.00 H HETATM 119 H46 UNL 1 -0.799 1.723 -6.983 1.00 0.00 H HETATM 120 H47 UNL 1 -0.110 -0.282 -5.985 1.00 0.00 H HETATM 121 H48 UNL 1 -0.701 1.623 -4.416 1.00 0.00 H HETATM 122 H49 UNL 1 2.494 -0.105 -6.340 1.00 0.00 H HETATM 123 H50 UNL 1 1.675 -0.095 -3.439 1.00 0.00 H HETATM 124 H51 UNL 1 4.231 -0.978 -5.089 1.00 0.00 H HETATM 125 H52 UNL 1 5.239 -1.608 -3.055 1.00 0.00 H HETATM 126 H53 UNL 1 2.629 -0.424 -1.788 1.00 0.00 H HETATM 127 H54 UNL 1 4.325 -0.374 -1.159 1.00 0.00 H HETATM 128 H55 UNL 1 4.329 -2.828 -0.702 1.00 0.00 H HETATM 129 H56 UNL 1 2.260 -3.678 -0.005 1.00 0.00 H HETATM 130 H57 UNL 1 0.888 -1.261 -1.448 1.00 0.00 H HETATM 131 H58 UNL 1 0.027 -3.622 0.242 1.00 0.00 H HETATM 132 H59 UNL 1 -2.201 -3.066 -0.670 1.00 0.00 H HETATM 133 H60 UNL 1 -2.448 -0.953 -1.774 1.00 0.00 H HETATM 134 H61 UNL 1 -1.723 -2.039 1.588 1.00 0.00 H HETATM 135 H62 UNL 1 -1.177 -0.579 0.719 1.00 0.00 H HETATM 136 H63 UNL 1 -3.532 -0.202 -0.177 1.00 0.00 H HETATM 137 H64 UNL 1 -5.226 -0.740 1.352 1.00 0.00 H HETATM 138 H65 UNL 1 -3.151 -2.630 2.722 1.00 0.00 H HETATM 139 H66 UNL 1 -4.883 -2.910 2.502 1.00 0.00 H HETATM 140 H67 UNL 1 -5.275 -0.785 3.771 1.00 0.00 H HETATM 141 H68 UNL 1 -3.483 -0.719 4.130 1.00 0.00 H HETATM 142 H69 UNL 1 -4.479 -2.115 4.737 1.00 0.00 H HETATM 143 H70 UNL 1 4.929 4.326 -0.262 1.00 0.00 H HETATM 144 H71 UNL 1 3.598 5.105 -1.128 1.00 0.00 H HETATM 145 H72 UNL 1 5.674 7.305 0.576 1.00 0.00 H HETATM 146 H73 UNL 1 1.642 5.708 1.968 1.00 0.00 H HETATM 147 H74 UNL 1 1.211 7.005 3.815 1.00 0.00 H HETATM 148 H75 UNL 1 0.504 9.460 2.964 1.00 0.00 H HETATM 149 H76 UNL 1 -1.039 8.296 3.631 1.00 0.00 H HETATM 150 H77 UNL 1 -0.868 5.480 3.329 1.00 0.00 H HETATM 151 H78 UNL 1 -1.426 8.391 1.305 1.00 0.00 H HETATM 152 H79 UNL 1 -3.162 6.531 1.322 1.00 0.00 H HETATM 153 H80 UNL 1 -0.984 5.344 1.246 1.00 0.00 H HETATM 154 H81 UNL 1 -3.459 3.860 0.686 1.00 0.00 H HETATM 155 H82 UNL 1 -1.716 3.336 -2.117 1.00 0.00 H HETATM 156 H83 UNL 1 0.445 7.702 -0.048 1.00 0.00 H HETATM 157 H84 UNL 1 0.582 4.891 0.015 1.00 0.00 H CONECT 1 2 74 75 76 CONECT 2 3 77 78 CONECT 3 4 4 79 CONECT 4 5 80 CONECT 5 6 81 82 CONECT 6 7 7 83 CONECT 7 8 84 CONECT 8 9 85 86 CONECT 9 10 10 87 CONECT 10 11 88 CONECT 11 12 89 90 CONECT 12 13 13 91 CONECT 13 14 92 CONECT 14 15 93 94 CONECT 15 16 95 96 CONECT 16 17 97 98 CONECT 17 18 99 100 CONECT 18 19 101 102 CONECT 19 20 103 104 CONECT 20 21 105 106 CONECT 21 22 107 108 CONECT 22 23 23 24 CONECT 24 25 CONECT 25 26 53 109 CONECT 26 27 110 111 CONECT 27 28 CONECT 28 29 29 30 CONECT 30 31 112 113 CONECT 31 32 114 115 CONECT 32 33 116 117 CONECT 33 34 34 118 CONECT 34 35 119 CONECT 35 36 37 120 CONECT 36 121 CONECT 37 38 38 122 CONECT 38 39 123 CONECT 39 40 40 124 CONECT 40 41 125 CONECT 41 42 126 127 CONECT 42 43 43 128 CONECT 43 44 129 CONECT 44 45 45 130 CONECT 45 46 131 CONECT 46 47 48 132 CONECT 47 133 CONECT 48 49 134 135 CONECT 49 50 50 136 CONECT 50 51 137 CONECT 51 52 138 139 CONECT 52 140 141 142 CONECT 53 54 143 144 CONECT 54 55 CONECT 55 56 56 57 58 CONECT 57 145 CONECT 58 59 CONECT 59 60 72 146 CONECT 60 61 62 147 CONECT 61 148 CONECT 62 63 64 149 CONECT 63 150 CONECT 64 65 66 151 CONECT 65 152 CONECT 66 67 72 153 CONECT 67 68 CONECT 68 69 69 70 71 CONECT 70 154 CONECT 71 155 CONECT 72 73 156 CONECT 73 157 END SMILES for HMDB0280456 (PIP(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/22:4(10Z,13Z,16Z,19Z)))[H][C@@](COC(=O)CCC\C=C/[C@H](O)\C=C\C=C/C\C=C/C=C/[C@H](O)C\C=C/CC)(COP(O)(=O)O[C@H]1C(O)C(O)C(O)[C@@H](OP(O)(O)=O)C1O)OC(=O)CCCCCCCC\C=C/C\C=C/C\C=C/C\C=C/CC INCHI for HMDB0280456 (PIP(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/22:4(10Z,13Z,16Z,19Z)))InChI=1S/C53H84O18P2/c1-3-5-7-8-9-10-11-12-13-14-15-16-17-18-19-20-24-27-33-40-47(57)69-45(42-68-73(65,66)71-53-50(60)48(58)49(59)52(51(53)61)70-72(62,63)64)41-67-46(56)39-34-28-32-38-44(55)37-31-26-23-21-22-25-30-36-43(54)35-29-6-4-2/h5-7,9-10,12-13,15-16,22-23,25-26,29-32,36-38,43-45,48-55,58-61H,3-4,8,11,14,17-21,24,27-28,33-35,39-42H2,1-2H3,(H,65,66)(H2,62,63,64)/b7-5-,10-9-,13-12-,16-15-,25-22-,26-23-,29-6-,36-30+,37-31+,38-32-/t43-,44-,45-,48?,49?,50?,51?,52-,53+/m1/s1 Structure for HMDB0280456 (PIP(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/22:4(10Z,13Z,16Z,19Z)))
3D Structure for HMDB0280456 (PIP(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/22:4(10Z,13Z,16Z,19Z))) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Synonyms |
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| Chemical Formula | C53H84O18P2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Average Molecular Weight | 1071.185 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Monoisotopic Molecular Weight | 1070.513289861 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| IUPAC Name | {[(1R,3S)-3-({[(2R)-3-{[(5Z,7S,8E,10Z,13Z,15E,17R,19Z)-7,17-dihydroxydocosa-5,8,10,13,15,19-hexaenoyl]oxy}-2-[(10Z,13Z,16Z,19Z)-docosa-10,13,16,19-tetraenoyloxy]propoxy](hydroxy)phosphoryl}oxy)-2,4,5,6-tetrahydroxycyclohexyl]oxy}phosphonic acid | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Traditional Name | [(1R,3S)-3-{[(2R)-3-{[(5Z,7S,8E,10Z,13Z,15E,17R,19Z)-7,17-dihydroxydocosa-5,8,10,13,15,19-hexaenoyl]oxy}-2-[(10Z,13Z,16Z,19Z)-docosa-10,13,16,19-tetraenoyloxy]propoxy(hydroxy)phosphoryl]oxy}-2,4,5,6-tetrahydroxycyclohexyl]oxyphosphonic acid | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| CAS Registry Number | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| SMILES | [H][C@@](COC(=O)CCC\C=C/[C@H](O)\C=C\C=C/C\C=C/C=C/[C@H](O)C\C=C/CC)(COP(O)(=O)O[C@H]1C(O)C(O)C(O)[C@@H](OP(O)(O)=O)C1O)OC(=O)CCCCCCCC\C=C/C\C=C/C\C=C/C\C=C/CC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Identifier | InChI=1S/C53H84O18P2/c1-3-5-7-8-9-10-11-12-13-14-15-16-17-18-19-20-24-27-33-40-47(57)69-45(42-68-73(65,66)71-53-50(60)48(58)49(59)52(51(53)61)70-72(62,63)64)41-67-46(56)39-34-28-32-38-44(55)37-31-26-23-21-22-25-30-36-43(54)35-29-6-4-2/h5-7,9-10,12-13,15-16,22-23,25-26,29-32,36-38,43-45,48-55,58-61H,3-4,8,11,14,17-21,24,27-28,33-35,39-42H2,1-2H3,(H,65,66)(H2,62,63,64)/b7-5-,10-9-,13-12-,16-15-,25-22-,26-23-,29-6-,36-30+,37-31+,38-32-/t43-,44-,45-,48?,49?,50?,51?,52-,53+/m1/s1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Key | XQAJSFMFNPQERG-FLTJOHMYSA-N | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chemical Taxonomy | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Classification | Not classified | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ontology | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Physiological effect | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Disposition | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Process | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Role | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Physical Properties | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| State | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Experimental Molecular Properties |
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| Experimental Chromatographic Properties | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Predicted Molecular Properties |
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| 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 | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
