Showing metabocard for PI(22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)/22:4(10Z,13Z,16Z,19Z)) (HMDB0277979)
| Record Information | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Version | 5.0 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Status | Predicted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Creation Date | 2021-09-13 08:57:18 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Update Date | 2022-11-30 20:01:31 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HMDB ID | HMDB0277979 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary Accession Numbers | None | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Metabolite Identification | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Common Name | PI(22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)/22:4(10Z,13Z,16Z,19Z)) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Description | PI(22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)/22:4(10Z,13Z,16Z,19Z)) is an oxidized phosphatidylinositol (PI). Phosphatidylinositols are important lipids, both as a key membrane constituent and as a participant in essential metabolic processes, both directly and via a number of metabolites. Phosphatidylinositols are acidic (anionic) phospholipids that consist of a phosphatidic acid backbone, linked via the phosphate group to inositol (hexahydroxycyclohexane). Phosphatidylinositols can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. PI(22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)/22:4(10Z,13Z,16Z,19Z)), in particular, consists of one chain of 14-hydroxy-docosahexaenoyl at the C-1 position and one chain of 10Z,13Z,16Z,19Z-docosatetraenoyl at the C-2 position. The inositol group that is part of every phosphatidylinositol lipid is covalently linked to the phosphate group that acts as a bridge to the lipid tail. In most organisms, the stereochemical form of this inositol is myo-D-inositol (with one axial hydroxyl in position 2 with the remainder equatorial), although other forms can be found in certain plant phosphatidylinositols. Phosphatidylinositol is especially abundant in brain tissue, where it can amount to 10% of the phospholipids, but it is present in all tissues and cell types. There is usually less of it than of phosphatidylcholine, phosphatidylethanolamine and phosphatidylserine. In animal tissues, phosphatidylinositol is the primary source of the arachidonic acid required for biosynthesis of eicosanoids, including prostaglandins, via the action of the enzyme phospholipase A2. Phosphatidylinositol can be 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 by a specific kinase. Seven different isomers are known, but the most important in both quantitative and biological terms are phosphatidylinositol 4-phosphate and phosphatidylinositol 4,5-bisphosphate. Phosphatidylinositol and the phosphatidylinositol phosphates are the main source of diacylglycerols that serve as signaling molecules, via the action of phospholipase C enzymes. While most phospholipids have a saturated fatty acid on C-1 and an unsaturated fatty acid on C-2 of the glycerol backbone, the fatty acid distribution at the C-1 and C-2 positions of glycerol within phospholipids is continually in flux, owing to phospholipid degradation and the continuous phospholipid remodeling that occurs while these molecules are in membranes. PIs composed exclusively of non-phosphorylated inositol exhibit a net charge of -1 at physiological pH. Molecules with phosphorylated inositol (such as PIP, PIP2, PIP3, etc.) are termed polyphosphoinositides. The polyphosphoinositides are important intracellular transducers of signals emanating from the plasma membrane. The synthesis of PI involves CDP-activated 1,2-diacylglycerol condensation with myo-inositol. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structure |  MOL for HMDB0277979 (PI(22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)/22:4(10Z,13Z,16Z,19Z)))
PI(22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)/22:4(10Z,13Z,16Z,19Z))
Mrv1652309132110572D
69 69 0 0 1 0 999 V2000
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M END
3D MOL for HMDB0277979 (PI(22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)/22:4(10Z,13Z,16Z,19Z)))HMDB0277979
RDKit 3D
PI(22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)/22:4(10Z,13Z,16Z,19Z))
151151 0 0 0 0 0 0 0 0999 V2000
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0.8545 1.0417 -4.0693 H 0 0 0 0 0 0 0 0 0 0 0 0
1.1775 -1.3138 -6.6752 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.3338 0.3754 -6.8571 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.3698 -2.7558 -5.8074 H 0 0 0 0 0 0 0 0 0 0 0 0
0.8327 -3.5070 -7.5186 H 0 0 0 0 0 0 0 0 0 0 0 0
0.0724 -4.6246 -5.1781 H 0 0 0 0 0 0 0 0 0 0 0 0
2.1588 -4.5871 -5.7243 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 2 0
33 34 1 0
34 35 1 0
35 36 2 0
36 37 1 0
37 38 1 0
38 39 2 0
39 40 1 0
40 41 2 0
41 42 1 0
42 43 1 0
42 44 1 0
44 45 1 0
45 46 2 0
46 47 1 0
47 48 1 0
48 49 2 0
49 50 1 0
50 51 1 0
25 52 1 0
52 53 1 0
53 54 1 0
54 55 2 0
54 56 1 0
54 57 1 0
57 58 1 0
58 59 1 0
59 60 1 0
59 61 1 0
61 62 1 0
61 63 1 0
63 64 1 0
63 65 1 0
65 66 1 0
65 67 1 0
67 68 1 0
67 58 1 0
1 69 1 0
1 70 1 0
1 71 1 0
2 72 1 0
2 73 1 0
3 74 1 0
4 75 1 0
5 76 1 0
5 77 1 0
6 78 1 0
7 79 1 0
8 80 1 0
8 81 1 0
9 82 1 0
10 83 1 0
11 84 1 0
11 85 1 0
12 86 1 0
13 87 1 0
14 88 1 0
14 89 1 0
15 90 1 0
15 91 1 0
16 92 1 0
16 93 1 0
17 94 1 0
17 95 1 0
18 96 1 0
18 97 1 0
19 98 1 0
19 99 1 0
20100 1 0
20101 1 0
21102 1 0
21103 1 0
25104 1 1
26105 1 0
26106 1 0
30107 1 0
30108 1 0
31109 1 0
31110 1 0
32111 1 0
33112 1 0
34113 1 0
34114 1 0
35115 1 0
36116 1 0
37117 1 0
37118 1 0
38119 1 0
39120 1 0
40121 1 0
41122 1 0
42123 1 0
43124 1 0
44125 1 0
44126 1 0
45127 1 0
46128 1 0
47129 1 0
47130 1 0
48131 1 0
49132 1 0
50133 1 0
50134 1 0
51135 1 0
51136 1 0
51137 1 0
52138 1 0
52139 1 0
56140 1 0
58141 1 1
59142 1 6
60143 1 0
61144 1 1
62145 1 0
63146 1 6
64147 1 0
65148 1 1
66149 1 0
67150 1 1
68151 1 0
M END
3D SDF for HMDB0277979 (PI(22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)/22:4(10Z,13Z,16Z,19Z)))
PI(22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)/22:4(10Z,13Z,16Z,19Z))
Mrv1652309132110572D
69 69 0 0 1 0 999 V2000
-3.8021 0.3608 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.0970 0.7716 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.3824 0.3590 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
-1.6679 0.7716 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.9699 -0.3554 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.7950 -0.3554 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
0.4706 0.3596 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.2454 0.7696 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0
-0.9591 0.3596 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
0.1678 1.4840 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.6563 1.4840 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1.8961 -0.4662 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.3257 0.3596 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
0.4706 2.0076 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1.8961 2.8318 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.3257 2.0076 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1.8974 0.3577 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
2.6117 0.7702 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
2.6117 1.5950 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
1.8974 2.0073 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
1.1831 1.5950 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
1.1831 0.7702 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
-4.5122 0.7696 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.5122 1.5410 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-5.2263 0.3564 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.9404 0.7696 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-6.6545 0.3564 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.4795 0.3564 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-8.1936 0.7696 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-8.9078 0.3564 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.7328 0.3564 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-10.4469 0.7696 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-11.1610 0.3564 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-11.9860 0.3564 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-12.7001 0.7696 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-13.4142 0.3564 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.1283 0.7696 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.1283 1.5410 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-14.8424 0.3564 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-15.5566 0.7696 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-16.3816 0.7696 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-17.0957 0.3564 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-17.8098 0.7696 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-18.6348 0.7696 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-19.3490 0.3564 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-20.0631 0.7696 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.5096 -0.7679 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.5096 -1.5394 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-4.2237 -0.3549 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.9378 -0.7679 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.6519 -0.3549 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-6.3661 -0.7679 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.0802 -0.3549 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.7943 -0.7679 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-8.5084 -0.3549 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.2225 -0.7679 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.9366 -0.3549 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-10.7616 -0.3549 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-11.4758 -0.7679 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-12.1899 -0.3549 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-13.0149 -0.3549 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-13.7290 -0.7679 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.4431 -0.3549 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-15.2681 -0.3549 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-15.9822 -0.7679 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-16.6963 -0.3549 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-17.5213 -0.3549 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-18.2355 -0.7679 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-18.9496 -0.3549 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1 23 1 0 0 0 0
2 1 1 0 0 0 0
3 2 1 0 0 0 0
3 5 1 1 0 0 0
3 6 1 0 0 0 0
4 3 1 0 0 0 0
6 47 1 0 0 0 0
7 8 1 0 0 0 0
8 9 1 0 0 0 0
8 10 2 0 0 0 0
8 11 1 0 0 0 0
9 4 1 0 0 0 0
17 18 1 0 0 0 0
17 22 1 0 0 0 0
17 12 1 1 0 0 0
18 19 1 0 0 0 0
18 13 1 6 0 0 0
19 20 1 0 0 0 0
19 16 1 1 0 0 0
20 21 1 0 0 0 0
20 15 1 6 0 0 0
21 22 1 0 0 0 0
21 14 1 6 0 0 0
22 7 1 6 0 0 0
23 24 2 0 0 0 0
23 25 1 0 0 0 0
25 26 1 0 0 0 0
26 27 1 0 0 0 0
27 28 2 0 0 0 0
28 29 1 0 0 0 0
29 30 1 0 0 0 0
30 31 2 0 0 0 0
31 32 1 0 0 0 0
32 33 1 0 0 0 0
33 34 2 0 0 0 0
34 35 1 0 0 0 0
35 36 2 0 0 0 0
36 37 1 0 0 0 0
37 38 1 0 0 0 0
37 39 1 0 0 0 0
39 40 1 0 0 0 0
40 41 2 0 0 0 0
41 42 1 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 0 0 0 0
47 48 2 0 0 0 0
47 49 1 0 0 0 0
49 50 1 0 0 0 0
50 51 1 0 0 0 0
51 52 1 0 0 0 0
52 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
58 59 1 0 0 0 0
59 60 1 0 0 0 0
60 61 2 0 0 0 0
61 62 1 0 0 0 0
62 63 1 0 0 0 0
63 64 2 0 0 0 0
64 65 1 0 0 0 0
65 66 1 0 0 0 0
66 67 2 0 0 0 0
67 68 1 0 0 0 0
68 69 1 0 0 0 0
M END
> <DATABASE_ID>
HMDB0277979
> <DATABASE_NAME>
hmdb
> <SMILES>
[H][C@@](COC(=O)CC\C=C/C\C=C/C\C=C/C=C/C(O)C\C=C/C\C=C/CC)(COP(O)(=O)O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O)OC(=O)CCCCCCCC\C=C/C\C=C/C\C=C/C\C=C/CC
> <INCHI_IDENTIFIER>
InChI=1S/C53H83O14P/c1-3-5-7-9-11-12-13-14-15-16-17-18-19-20-21-26-29-33-37-41-47(56)66-45(43-65-68(62,63)67-53-51(60)49(58)48(57)50(59)52(53)61)42-64-46(55)40-36-32-28-25-23-22-24-27-31-35-39-44(54)38-34-30-10-8-6-4-2/h5-8,11-12,14-15,17-18,22-23,27-28,30-32,34-35,39,44-45,48-54,57-61H,3-4,9-10,13,16,19-21,24-26,29,33,36-38,40-43H2,1-2H3,(H,62,63)/b7-5-,8-6-,12-11-,15-14-,18-17-,23-22-,31-27-,32-28-,34-30-,39-35+/t44?,45-,48-,49-,50+,51-,52-,53-/m1/s1
> <INCHI_KEY>
GALMLXWDSDRPCW-BEFVJYSJSA-N
> <FORMULA>
C53H83O14P
> <MOLECULAR_WEIGHT>
975.207
> <EXACT_MASS>
974.552044351
> <JCHEM_ACCEPTOR_COUNT>
10
> <JCHEM_ATOM_COUNT>
151
> <JCHEM_AVERAGE_POLARIZABILITY>
107.81602550123927
> <JCHEM_BIOAVAILABILITY>
0
> <JCHEM_DONOR_COUNT>
7
> <JCHEM_FORMAL_CHARGE>
0
> <JCHEM_GHOSE_FILTER>
0
> <JCHEM_IUPAC>
[(2R)-2-[(10Z,13Z,16Z,19Z)-docosa-10,13,16,19-tetraenoyloxy]-3-{[(4Z,7Z,10Z,12E,16Z,19Z)-14-hydroxydocosa-4,7,10,12,16,19-hexaenoyl]oxy}propoxy]({[(1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl]oxy})phosphinic acid
> <ALOGPS_LOGP>
6.76
> <JCHEM_LOGP>
9.478852236333333
> <ALOGPS_LOGS>
-6.10
> <JCHEM_MDDR_LIKE_RULE>
0
> <JCHEM_NUMBER_OF_RINGS>
1
> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1
> <JCHEM_PKA>
12.360530531715526
> <JCHEM_PKA_STRONGEST_ACIDIC>
1.833412186910805
> <JCHEM_PKA_STRONGEST_BASIC>
-1.6088687030986915
> <JCHEM_POLAR_SURFACE_AREA>
229.73999999999995
> <JCHEM_REFRACTIVITY>
278.4613
> <JCHEM_ROTATABLE_BOND_COUNT>
40
> <JCHEM_RULE_OF_FIVE>
0
> <ALOGPS_SOLUBILITY>
7.76e-04 g/l
> <JCHEM_TRADITIONAL_IUPAC>
(2R)-2-[(10Z,13Z,16Z,19Z)-docosa-10,13,16,19-tetraenoyloxy]-3-{[(4Z,7Z,10Z,12E,16Z,19Z)-14-hydroxydocosa-4,7,10,12,16,19-hexaenoyl]oxy}propoxy([(1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl]oxy)phosphinic acid
> <JCHEM_VEBER_RULE>
0
$$$$
3D-SDF for HMDB0277979 (PI(22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)/22:4(10Z,13Z,16Z,19Z)))HMDB0277979
RDKit 3D
PI(22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)/22:4(10Z,13Z,16Z,19Z))
151151 0 0 0 0 0 0 0 0999 V2000
1.3529 20.4020 -5.2825 C 0 0 0 0 0 0 0 0 0 0 0 0
0.3127 19.4856 -5.9560 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.2303 18.5669 -4.9332 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.1106 17.2746 -5.0127 C 0 0 0 0 0 0 0 0 0 0 0 0
0.6070 16.6148 -6.1694 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.3063 15.7434 -6.9142 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.0858 14.4783 -7.0538 C 0 0 0 0 0 0 0 0 0 0 0 0
1.0429 13.6771 -6.5462 C 0 0 0 0 0 0 0 0 0 0 0 0
1.6938 13.0240 -7.7091 C 0 0 0 0 0 0 0 0 0 0 0 0
1.6996 11.7278 -7.8337 C 0 0 0 0 0 0 0 0 0 0 0 0
1.0276 10.8740 -6.7867 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.0294 10.1421 -7.5847 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.1507 8.8590 -7.6445 C 0 0 0 0 0 0 0 0 0 0 0 0
0.7384 7.9089 -6.9249 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.1398 7.1160 -5.9867 C 0 0 0 0 0 0 0 0 0 0 0 0
0.5874 6.0355 -5.1961 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.4640 5.4107 -4.3423 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.0421 4.2242 -3.5187 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.2574 3.7937 -2.7636 C 0 0 0 0 0 0 0 0 0 0 0 0
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-1.1765 -10.2618 5.6444 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.1040 -10.6846 4.2875 C 0 0 0 0 0 0 0 0 0 0 0 0
0.0943 -11.1881 3.6511 C 0 0 0 0 0 0 0 0 0 0 0 0
1.2624 -11.3496 4.1534 C 0 0 0 0 0 0 0 0 0 0 0 0
1.6332 -11.0507 5.5005 C 0 0 0 0 0 0 0 0 0 0 0 0
2.8827 -11.2624 5.9559 C 0 0 0 0 0 0 0 0 0 0 0 0
3.2764 -10.9624 7.3535 C 0 0 0 0 0 0 0 0 0 0 0 0
3.6006 -9.6280 7.4381 O 0 0 0 0 0 0 0 0 0 0 0 0
2.1359 -11.3039 8.3498 C 0 0 0 0 0 0 0 0 0 0 0 0
1.8677 -12.7319 8.1325 C 0 0 0 0 0 0 0 0 0 0 0 0
1.9805 -13.6164 9.0674 C 0 0 0 0 0 0 0 0 0 0 0 0
2.3776 -13.3950 10.4822 C 0 0 0 0 0 0 0 0 0 0 0 0
1.2991 -13.8573 11.3863 C 0 0 0 0 0 0 0 0 0 0 0 0
1.5151 -14.8099 12.2465 C 0 0 0 0 0 0 0 0 0 0 0 0
2.7732 -15.5287 12.4491 C 0 0 0 0 0 0 0 0 0 0 0 0
2.5899 -17.0251 12.1627 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.9695 -2.2989 -0.3369 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.6257 -2.4993 -0.6912 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.5192 -3.8939 -1.6466 P 0 0 0 0 0 5 0 0 0 0 0 0
-1.8276 -4.1715 -2.3488 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.2133 -5.1975 -0.6192 O 0 0 0 0 0 0 0 0 0 0 0 0
0.7617 -3.7263 -2.7039 O 0 0 0 0 0 0 0 0 0 0 0 0
0.4972 -2.9568 -3.8038 C 0 0 1 0 0 0 0 0 0 0 0 0
1.3327 -1.6991 -3.9129 C 0 0 2 0 0 0 0 0 0 0 0 0
1.6149 -1.1607 -2.6669 O 0 0 0 0 0 0 0 0 0 0 0 0
0.4709 -0.7204 -4.7186 C 0 0 1 0 0 0 0 0 0 0 0 0
1.0931 0.4978 -4.8564 O 0 0 0 0 0 0 0 0 0 0 0 0
0.2543 -1.3228 -6.0724 C 0 0 2 0 0 0 0 0 0 0 0 0
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-0.2756 -2.7254 -6.0710 C 0 0 1 0 0 0 0 0 0 0 0 0
-0.1246 -3.2676 -7.3441 O 0 0 0 0 0 0 0 0 0 0 0 0
0.5247 -3.6403 -5.1255 C 0 0 1 0 0 0 0 0 0 0 0 0
1.8004 -3.6932 -5.6859 O 0 0 0 0 0 0 0 0 0 0 0 0
1.8036 21.0852 -6.0384 H 0 0 0 0 0 0 0 0 0 0 0 0
0.8954 21.0370 -4.5065 H 0 0 0 0 0 0 0 0 0 0 0 0
2.1036 19.7499 -4.8232 H 0 0 0 0 0 0 0 0 0 0 0 0
0.7437 19.0658 -6.8427 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.5168 20.2159 -6.2325 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.7629 18.9927 -4.0619 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.5155 16.5834 -4.2545 H 0 0 0 0 0 0 0 0 0 0 0 0
1.3546 15.9675 -5.6258 H 0 0 0 0 0 0 0 0 0 0 0 0
1.1718 17.3053 -6.7759 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.2024 16.2049 -7.3587 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.8419 13.9080 -7.6312 H 0 0 0 0 0 0 0 0 0 0 0 0
1.8819 14.3769 -6.1814 H 0 0 0 0 0 0 0 0 0 0 0 0
0.8121 13.0690 -5.6872 H 0 0 0 0 0 0 0 0 0 0 0 0
2.1638 13.6461 -8.4527 H 0 0 0 0 0 0 0 0 0 0 0 0
2.1740 11.2035 -8.6735 H 0 0 0 0 0 0 0 0 0 0 0 0
1.8147 10.2202 -6.4098 H 0 0 0 0 0 0 0 0 0 0 0 0
0.4808 11.4172 -6.0337 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.7601 10.7410 -8.1607 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.9372 8.3773 -8.2397 H 0 0 0 0 0 0 0 0 0 0 0 0
1.1113 7.1936 -7.7211 H 0 0 0 0 0 0 0 0 0 0 0 0
1.5937 8.3525 -6.4254 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.9252 6.5993 -6.6186 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.6884 7.8140 -5.3114 H 0 0 0 0 0 0 0 0 0 0 0 0
0.9865 5.3170 -5.9195 H 0 0 0 0 0 0 0 0 0 0 0 0
1.3735 6.5509 -4.6004 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.2736 5.0506 -5.0326 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.9039 6.2192 -3.7115 H 0 0 0 0 0 0 0 0 0 0 0 0
0.2597 3.4209 -4.2353 H 0 0 0 0 0 0 0 0 0 0 0 0
0.7686 4.4740 -2.8181 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.0710 3.6422 -3.5210 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.5787 4.6426 -2.1018 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.2866 2.5511 -1.2457 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.9670 1.7110 -2.6730 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.5838 3.1677 -0.5660 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.2501 2.4848 -2.0594 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.2468 -1.0406 0.7547 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.3773 -1.3131 1.7019 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.6589 -0.4089 2.5414 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.5839 -4.8665 2.9528 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.7072 -3.9162 3.9235 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.2441 -5.3362 5.0178 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.5070 -4.4200 5.9881 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.3340 -5.8197 5.2744 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.8946 -8.1650 5.1343 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.3678 -8.3019 3.9442 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.9181 -7.1753 5.2132 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.4853 -8.6930 7.0589 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.0787 -10.9885 6.4739 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.8568 -11.6226 4.2493 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.6909 -10.0427 3.5466 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.0543 -11.4689 2.5501 H 0 0 0 0 0 0 0 0 0 0 0 0
2.0296 -11.7659 3.4410 H 0 0 0 0 0 0 0 0 0 0 0 0
0.9941 -10.6243 6.2211 H 0 0 0 0 0 0 0 0 0 0 0 0
3.6026 -11.6582 5.2603 H 0 0 0 0 0 0 0 0 0 0 0 0
4.1484 -11.5752 7.5789 H 0 0 0 0 0 0 0 0 0 0 0 0
3.7876 -9.4429 8.4122 H 0 0 0 0 0 0 0 0 0 0 0 0
2.6055 -11.0601 9.3349 H 0 0 0 0 0 0 0 0 0 0 0 0
1.2393 -10.7229 8.1579 H 0 0 0 0 0 0 0 0 0 0 0 0
1.5566 -13.0646 7.1273 H 0 0 0 0 0 0 0 0 0 0 0 0
1.7637 -14.6669 8.8173 H 0 0 0 0 0 0 0 0 0 0 0 0
2.5907 -12.3577 10.7537 H 0 0 0 0 0 0 0 0 0 0 0 0
3.3250 -13.9484 10.6087 H 0 0 0 0 0 0 0 0 0 0 0 0
0.3272 -13.3909 11.3182 H 0 0 0 0 0 0 0 0 0 0 0 0
0.6703 -15.1051 12.8864 H 0 0 0 0 0 0 0 0 0 0 0 0
2.9512 -15.5134 13.5748 H 0 0 0 0 0 0 0 0 0 0 0 0
3.6773 -15.1390 12.0192 H 0 0 0 0 0 0 0 0 0 0 0 0
1.6035 -17.3118 12.5815 H 0 0 0 0 0 0 0 0 0 0 0 0
2.6081 -17.2331 11.0816 H 0 0 0 0 0 0 0 0 0 0 0 0
3.3624 -17.5807 12.7260 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.5690 -2.1655 -1.2502 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.3431 -3.1965 0.1826 H 0 0 0 0 0 0 0 0 0 0 0 0
0.7470 -5.4414 -0.6075 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.5698 -2.5988 -3.6664 H 0 0 0 0 0 0 0 0 0 0 0 0
2.2457 -1.8610 -4.5232 H 0 0 0 0 0 0 0 0 0 0 0 0
2.0371 -0.2890 -2.8258 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.5027 -0.6851 -4.1985 H 0 0 0 0 0 0 0 0 0 0 0 0
0.8545 1.0417 -4.0693 H 0 0 0 0 0 0 0 0 0 0 0 0
1.1775 -1.3138 -6.6752 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.3338 0.3754 -6.8571 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.3698 -2.7558 -5.8074 H 0 0 0 0 0 0 0 0 0 0 0 0
0.8327 -3.5070 -7.5186 H 0 0 0 0 0 0 0 0 0 0 0 0
0.0724 -4.6246 -5.1781 H 0 0 0 0 0 0 0 0 0 0 0 0
2.1588 -4.5871 -5.7243 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 2 0
33 34 1 0
34 35 1 0
35 36 2 0
36 37 1 0
37 38 1 0
38 39 2 0
39 40 1 0
40 41 2 0
41 42 1 0
42 43 1 0
42 44 1 0
44 45 1 0
45 46 2 0
46 47 1 0
47 48 1 0
48 49 2 0
49 50 1 0
50 51 1 0
25 52 1 0
52 53 1 0
53 54 1 0
54 55 2 0
54 56 1 0
54 57 1 0
57 58 1 0
58 59 1 0
59 60 1 0
59 61 1 0
61 62 1 0
61 63 1 0
63 64 1 0
63 65 1 0
65 66 1 0
65 67 1 0
67 68 1 0
67 58 1 0
1 69 1 0
1 70 1 0
1 71 1 0
2 72 1 0
2 73 1 0
3 74 1 0
4 75 1 0
5 76 1 0
5 77 1 0
6 78 1 0
7 79 1 0
8 80 1 0
8 81 1 0
9 82 1 0
10 83 1 0
11 84 1 0
11 85 1 0
12 86 1 0
13 87 1 0
14 88 1 0
14 89 1 0
15 90 1 0
15 91 1 0
16 92 1 0
16 93 1 0
17 94 1 0
17 95 1 0
18 96 1 0
18 97 1 0
19 98 1 0
19 99 1 0
20100 1 0
20101 1 0
21102 1 0
21103 1 0
25104 1 1
26105 1 0
26106 1 0
30107 1 0
30108 1 0
31109 1 0
31110 1 0
32111 1 0
33112 1 0
34113 1 0
34114 1 0
35115 1 0
36116 1 0
37117 1 0
37118 1 0
38119 1 0
39120 1 0
40121 1 0
41122 1 0
42123 1 0
43124 1 0
44125 1 0
44126 1 0
45127 1 0
46128 1 0
47129 1 0
47130 1 0
48131 1 0
49132 1 0
50133 1 0
50134 1 0
51135 1 0
51136 1 0
51137 1 0
52138 1 0
52139 1 0
56140 1 0
58141 1 1
59142 1 6
60143 1 0
61144 1 1
62145 1 0
63146 1 6
64147 1 0
65148 1 1
66149 1 0
67150 1 1
68151 1 0
M END
PDB for HMDB0277979 (PI(22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)/22:4(10Z,13Z,16Z,19Z)))HEADER PROTEIN 13-SEP-21 NONE TITLE NULL COMPND MOLECULE: PI(22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)/22:4(10Z,13Z SOURCE NULL KEYWDS NULL EXPDTA NULL AUTHOR Marvin REVDAT 1 13-SEP-21 0 HETATM 1 O UNK 0 -7.097 0.673 0.000 0.00 0.00 O+0 HETATM 2 C UNK 0 -5.781 1.440 0.000 0.00 0.00 C+0 HETATM 3 C UNK 0 -4.447 0.670 0.000 0.00 0.00 C+0 HETATM 4 C UNK 0 -3.114 1.440 0.000 0.00 0.00 C+0 HETATM 5 H UNK 0 -3.677 -0.664 0.000 0.00 0.00 H+0 HETATM 6 O UNK 0 -5.217 -0.664 0.000 0.00 0.00 O+0 HETATM 7 O UNK 0 0.879 0.671 0.000 0.00 0.00 O+0 HETATM 8 P UNK 0 -0.458 1.437 0.000 0.00 0.00 P+0 HETATM 9 O UNK 0 -1.790 0.671 0.000 0.00 0.00 O+0 HETATM 10 O UNK 0 0.313 2.770 0.000 0.00 0.00 O+0 HETATM 11 O UNK 0 -1.225 2.770 0.000 0.00 0.00 O+0 HETATM 12 O UNK 0 3.539 -0.870 0.000 0.00 0.00 O+0 HETATM 13 O UNK 0 6.208 0.671 0.000 0.00 0.00 O+0 HETATM 14 O UNK 0 0.879 3.748 0.000 0.00 0.00 O+0 HETATM 15 O UNK 0 3.539 5.286 0.000 0.00 0.00 O+0 HETATM 16 O UNK 0 6.208 3.748 0.000 0.00 0.00 O+0 HETATM 17 C UNK 0 3.542 0.668 0.000 0.00 0.00 C+0 HETATM 18 C UNK 0 4.875 1.438 0.000 0.00 0.00 C+0 HETATM 19 C UNK 0 4.875 2.977 0.000 0.00 0.00 C+0 HETATM 20 C UNK 0 3.542 3.747 0.000 0.00 0.00 C+0 HETATM 21 C UNK 0 2.209 2.977 0.000 0.00 0.00 C+0 HETATM 22 C UNK 0 2.209 1.438 0.000 0.00 0.00 C+0 HETATM 23 C UNK 0 -8.423 1.437 0.000 0.00 0.00 C+0 HETATM 24 O UNK 0 -8.423 2.877 0.000 0.00 0.00 O+0 HETATM 25 C UNK 0 -9.756 0.665 0.000 0.00 0.00 C+0 HETATM 26 C UNK 0 -11.089 1.437 0.000 0.00 0.00 C+0 HETATM 27 C UNK 0 -12.422 0.665 0.000 0.00 0.00 C+0 HETATM 28 C UNK 0 -13.962 0.665 0.000 0.00 0.00 C+0 HETATM 29 C UNK 0 -15.295 1.437 0.000 0.00 0.00 C+0 HETATM 30 C UNK 0 -16.628 0.665 0.000 0.00 0.00 C+0 HETATM 31 C UNK 0 -18.168 0.665 0.000 0.00 0.00 C+0 HETATM 32 C UNK 0 -19.501 1.437 0.000 0.00 0.00 C+0 HETATM 33 C UNK 0 -20.834 0.665 0.000 0.00 0.00 C+0 HETATM 34 C UNK 0 -22.374 0.665 0.000 0.00 0.00 C+0 HETATM 35 C UNK 0 -23.707 1.437 0.000 0.00 0.00 C+0 HETATM 36 C UNK 0 -25.040 0.665 0.000 0.00 0.00 C+0 HETATM 37 C UNK 0 -26.373 1.437 0.000 0.00 0.00 C+0 HETATM 38 O UNK 0 -26.373 2.877 0.000 0.00 0.00 O+0 HETATM 39 C UNK 0 -27.706 0.665 0.000 0.00 0.00 C+0 HETATM 40 C UNK 0 -29.039 1.437 0.000 0.00 0.00 C+0 HETATM 41 C UNK 0 -30.579 1.437 0.000 0.00 0.00 C+0 HETATM 42 C UNK 0 -31.912 0.665 0.000 0.00 0.00 C+0 HETATM 43 C UNK 0 -33.245 1.437 0.000 0.00 0.00 C+0 HETATM 44 C UNK 0 -34.785 1.437 0.000 0.00 0.00 C+0 HETATM 45 C UNK 0 -36.118 0.665 0.000 0.00 0.00 C+0 HETATM 46 C UNK 0 -37.451 1.437 0.000 0.00 0.00 C+0 HETATM 47 C UNK 0 -6.551 -1.434 0.000 0.00 0.00 C+0 HETATM 48 O UNK 0 -6.551 -2.874 0.000 0.00 0.00 O+0 HETATM 49 C UNK 0 -7.884 -0.662 0.000 0.00 0.00 C+0 HETATM 50 C UNK 0 -9.217 -1.434 0.000 0.00 0.00 C+0 HETATM 51 C UNK 0 -10.550 -0.662 0.000 0.00 0.00 C+0 HETATM 52 C UNK 0 -11.883 -1.434 0.000 0.00 0.00 C+0 HETATM 53 C UNK 0 -13.216 -0.662 0.000 0.00 0.00 C+0 HETATM 54 C UNK 0 -14.549 -1.434 0.000 0.00 0.00 C+0 HETATM 55 C UNK 0 -15.882 -0.662 0.000 0.00 0.00 C+0 HETATM 56 C UNK 0 -17.215 -1.434 0.000 0.00 0.00 C+0 HETATM 57 C UNK 0 -18.548 -0.662 0.000 0.00 0.00 C+0 HETATM 58 C UNK 0 -20.088 -0.662 0.000 0.00 0.00 C+0 HETATM 59 C UNK 0 -21.421 -1.434 0.000 0.00 0.00 C+0 HETATM 60 C UNK 0 -22.754 -0.662 0.000 0.00 0.00 C+0 HETATM 61 C UNK 0 -24.294 -0.662 0.000 0.00 0.00 C+0 HETATM 62 C UNK 0 -25.628 -1.434 0.000 0.00 0.00 C+0 HETATM 63 C UNK 0 -26.961 -0.662 0.000 0.00 0.00 C+0 HETATM 64 C UNK 0 -28.501 -0.662 0.000 0.00 0.00 C+0 HETATM 65 C UNK 0 -29.834 -1.434 0.000 0.00 0.00 C+0 HETATM 66 C UNK 0 -31.167 -0.662 0.000 0.00 0.00 C+0 HETATM 67 C UNK 0 -32.707 -0.662 0.000 0.00 0.00 C+0 HETATM 68 C UNK 0 -34.040 -1.434 0.000 0.00 0.00 C+0 HETATM 69 C UNK 0 -35.373 -0.662 0.000 0.00 0.00 C+0 CONECT 1 23 2 CONECT 2 1 3 CONECT 3 2 5 6 4 CONECT 4 3 9 CONECT 5 3 CONECT 6 3 47 CONECT 7 8 22 CONECT 8 7 9 10 11 CONECT 9 8 4 CONECT 10 8 CONECT 11 8 CONECT 12 17 CONECT 13 18 CONECT 14 21 CONECT 15 20 CONECT 16 19 CONECT 17 18 22 12 CONECT 18 17 19 13 CONECT 19 18 20 16 CONECT 20 19 21 15 CONECT 21 20 22 14 CONECT 22 17 21 7 CONECT 23 1 24 25 CONECT 24 23 CONECT 25 23 26 CONECT 26 25 27 CONECT 27 26 28 CONECT 28 27 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 39 CONECT 38 37 CONECT 39 37 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 CONECT 47 6 48 49 CONECT 48 47 CONECT 49 47 50 CONECT 50 49 51 CONECT 51 50 52 CONECT 52 51 53 CONECT 53 52 54 CONECT 54 53 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 MASTER 0 0 0 0 0 0 0 0 69 0 138 0 END 3D PDB for HMDB0277979 (PI(22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)/22:4(10Z,13Z,16Z,19Z)))COMPND HMDB0277979 HETATM 1 C1 UNL 1 1.353 20.402 -5.282 1.00 0.00 C HETATM 2 C2 UNL 1 0.313 19.486 -5.956 1.00 0.00 C HETATM 3 C3 UNL 1 -0.230 18.567 -4.933 1.00 0.00 C HETATM 4 C4 UNL 1 -0.111 17.275 -5.013 1.00 0.00 C HETATM 5 C5 UNL 1 0.607 16.615 -6.169 1.00 0.00 C HETATM 6 C6 UNL 1 -0.306 15.743 -6.914 1.00 0.00 C HETATM 7 C7 UNL 1 -0.086 14.478 -7.054 1.00 0.00 C HETATM 8 C8 UNL 1 1.043 13.677 -6.546 1.00 0.00 C HETATM 9 C9 UNL 1 1.694 13.024 -7.709 1.00 0.00 C HETATM 10 C10 UNL 1 1.700 11.728 -7.834 1.00 0.00 C HETATM 11 C11 UNL 1 1.028 10.874 -6.787 1.00 0.00 C HETATM 12 C12 UNL 1 -0.029 10.142 -7.585 1.00 0.00 C HETATM 13 C13 UNL 1 -0.151 8.859 -7.645 1.00 0.00 C HETATM 14 C14 UNL 1 0.738 7.909 -6.925 1.00 0.00 C HETATM 15 C15 UNL 1 -0.140 7.116 -5.987 1.00 0.00 C HETATM 16 C16 UNL 1 0.587 6.035 -5.196 1.00 0.00 C HETATM 17 C17 UNL 1 -0.464 5.411 -4.342 1.00 0.00 C HETATM 18 C18 UNL 1 -0.042 4.224 -3.519 1.00 0.00 C HETATM 19 C19 UNL 1 -1.257 3.794 -2.764 1.00 0.00 C HETATM 20 C20 UNL 1 -1.127 2.538 -1.945 1.00 0.00 C HETATM 21 C21 UNL 1 -2.461 2.290 -1.285 1.00 0.00 C HETATM 22 C22 UNL 1 -2.635 1.078 -0.541 1.00 0.00 C HETATM 23 O1 UNL 1 -3.832 0.815 -0.105 1.00 0.00 O HETATM 24 O2 UNL 1 -1.718 0.082 -0.190 1.00 0.00 O HETATM 25 C23 UNL 1 -2.144 -1.046 0.512 1.00 0.00 C HETATM 26 C24 UNL 1 -1.473 -1.273 1.877 1.00 0.00 C HETATM 27 O3 UNL 1 -2.044 -2.389 2.441 1.00 0.00 O HETATM 28 C25 UNL 1 -1.793 -3.059 3.615 1.00 0.00 C HETATM 29 O4 UNL 1 -0.874 -2.608 4.332 1.00 0.00 O HETATM 30 C26 UNL 1 -2.639 -4.236 3.893 1.00 0.00 C HETATM 31 C27 UNL 1 -2.277 -5.073 5.096 1.00 0.00 C HETATM 32 C28 UNL 1 -3.274 -6.178 5.154 1.00 0.00 C HETATM 33 C29 UNL 1 -3.028 -7.436 5.079 1.00 0.00 C HETATM 34 C30 UNL 1 -1.664 -7.998 4.928 1.00 0.00 C HETATM 35 C31 UNL 1 -1.434 -9.019 6.025 1.00 0.00 C HETATM 36 C32 UNL 1 -1.177 -10.262 5.644 1.00 0.00 C HETATM 37 C33 UNL 1 -1.104 -10.685 4.288 1.00 0.00 C HETATM 38 C34 UNL 1 0.094 -11.188 3.651 1.00 0.00 C HETATM 39 C35 UNL 1 1.262 -11.350 4.153 1.00 0.00 C HETATM 40 C36 UNL 1 1.633 -11.051 5.500 1.00 0.00 C HETATM 41 C37 UNL 1 2.883 -11.262 5.956 1.00 0.00 C HETATM 42 C38 UNL 1 3.276 -10.962 7.354 1.00 0.00 C HETATM 43 O5 UNL 1 3.601 -9.628 7.438 1.00 0.00 O HETATM 44 C39 UNL 1 2.136 -11.304 8.350 1.00 0.00 C HETATM 45 C40 UNL 1 1.868 -12.732 8.133 1.00 0.00 C HETATM 46 C41 UNL 1 1.980 -13.616 9.067 1.00 0.00 C HETATM 47 C42 UNL 1 2.378 -13.395 10.482 1.00 0.00 C HETATM 48 C43 UNL 1 1.299 -13.857 11.386 1.00 0.00 C HETATM 49 C44 UNL 1 1.515 -14.810 12.246 1.00 0.00 C HETATM 50 C45 UNL 1 2.773 -15.529 12.449 1.00 0.00 C HETATM 51 C46 UNL 1 2.590 -17.025 12.163 1.00 0.00 C HETATM 52 C47 UNL 1 -1.970 -2.299 -0.337 1.00 0.00 C HETATM 53 O6 UNL 1 -0.626 -2.499 -0.691 1.00 0.00 O HETATM 54 P1 UNL 1 -0.519 -3.894 -1.647 1.00 0.00 P HETATM 55 O7 UNL 1 -1.828 -4.172 -2.349 1.00 0.00 O HETATM 56 O8 UNL 1 -0.213 -5.198 -0.619 1.00 0.00 O HETATM 57 O9 UNL 1 0.762 -3.726 -2.704 1.00 0.00 O HETATM 58 C48 UNL 1 0.497 -2.957 -3.804 1.00 0.00 C HETATM 59 C49 UNL 1 1.333 -1.699 -3.913 1.00 0.00 C HETATM 60 O10 UNL 1 1.615 -1.161 -2.667 1.00 0.00 O HETATM 61 C50 UNL 1 0.471 -0.720 -4.719 1.00 0.00 C HETATM 62 O11 UNL 1 1.093 0.498 -4.856 1.00 0.00 O HETATM 63 C51 UNL 1 0.254 -1.323 -6.072 1.00 0.00 C HETATM 64 O12 UNL 1 -0.698 -0.545 -6.748 1.00 0.00 O HETATM 65 C52 UNL 1 -0.276 -2.725 -6.071 1.00 0.00 C HETATM 66 O13 UNL 1 -0.125 -3.268 -7.344 1.00 0.00 O HETATM 67 C53 UNL 1 0.525 -3.640 -5.126 1.00 0.00 C HETATM 68 O14 UNL 1 1.800 -3.693 -5.686 1.00 0.00 O HETATM 69 H1 UNL 1 1.804 21.085 -6.038 1.00 0.00 H HETATM 70 H2 UNL 1 0.895 21.037 -4.507 1.00 0.00 H HETATM 71 H3 UNL 1 2.104 19.750 -4.823 1.00 0.00 H HETATM 72 H4 UNL 1 0.744 19.066 -6.843 1.00 0.00 H HETATM 73 H5 UNL 1 -0.517 20.216 -6.233 1.00 0.00 H HETATM 74 H6 UNL 1 -0.763 18.993 -4.062 1.00 0.00 H HETATM 75 H7 UNL 1 -0.516 16.583 -4.255 1.00 0.00 H HETATM 76 H8 UNL 1 1.355 15.967 -5.626 1.00 0.00 H HETATM 77 H9 UNL 1 1.172 17.305 -6.776 1.00 0.00 H HETATM 78 H10 UNL 1 -1.202 16.205 -7.359 1.00 0.00 H HETATM 79 H11 UNL 1 -0.842 13.908 -7.631 1.00 0.00 H HETATM 80 H12 UNL 1 1.882 14.377 -6.181 1.00 0.00 H HETATM 81 H13 UNL 1 0.812 13.069 -5.687 1.00 0.00 H HETATM 82 H14 UNL 1 2.164 13.646 -8.453 1.00 0.00 H HETATM 83 H15 UNL 1 2.174 11.204 -8.673 1.00 0.00 H HETATM 84 H16 UNL 1 1.815 10.220 -6.410 1.00 0.00 H HETATM 85 H17 UNL 1 0.481 11.417 -6.034 1.00 0.00 H HETATM 86 H18 UNL 1 -0.760 10.741 -8.161 1.00 0.00 H HETATM 87 H19 UNL 1 -0.937 8.377 -8.240 1.00 0.00 H HETATM 88 H20 UNL 1 1.111 7.194 -7.721 1.00 0.00 H HETATM 89 H21 UNL 1 1.594 8.353 -6.425 1.00 0.00 H HETATM 90 H22 UNL 1 -0.925 6.599 -6.619 1.00 0.00 H HETATM 91 H23 UNL 1 -0.688 7.814 -5.311 1.00 0.00 H HETATM 92 H24 UNL 1 0.987 5.317 -5.920 1.00 0.00 H HETATM 93 H25 UNL 1 1.373 6.551 -4.600 1.00 0.00 H HETATM 94 H26 UNL 1 -1.274 5.051 -5.033 1.00 0.00 H HETATM 95 H27 UNL 1 -0.904 6.219 -3.711 1.00 0.00 H HETATM 96 H28 UNL 1 0.260 3.421 -4.235 1.00 0.00 H HETATM 97 H29 UNL 1 0.769 4.474 -2.818 1.00 0.00 H HETATM 98 H30 UNL 1 -2.071 3.642 -3.521 1.00 0.00 H HETATM 99 H31 UNL 1 -1.579 4.643 -2.102 1.00 0.00 H HETATM 100 H32 UNL 1 -0.287 2.551 -1.246 1.00 0.00 H HETATM 101 H33 UNL 1 -0.967 1.711 -2.673 1.00 0.00 H HETATM 102 H34 UNL 1 -2.584 3.168 -0.566 1.00 0.00 H HETATM 103 H35 UNL 1 -3.250 2.485 -2.059 1.00 0.00 H HETATM 104 H36 UNL 1 -3.247 -1.041 0.755 1.00 0.00 H HETATM 105 H37 UNL 1 -0.377 -1.313 1.702 1.00 0.00 H HETATM 106 H38 UNL 1 -1.659 -0.409 2.541 1.00 0.00 H HETATM 107 H39 UNL 1 -2.584 -4.866 2.953 1.00 0.00 H HETATM 108 H40 UNL 1 -3.707 -3.916 3.924 1.00 0.00 H HETATM 109 H41 UNL 1 -1.244 -5.336 5.018 1.00 0.00 H HETATM 110 H42 UNL 1 -2.507 -4.420 5.988 1.00 0.00 H HETATM 111 H43 UNL 1 -4.334 -5.820 5.274 1.00 0.00 H HETATM 112 H44 UNL 1 -3.895 -8.165 5.134 1.00 0.00 H HETATM 113 H45 UNL 1 -1.368 -8.302 3.944 1.00 0.00 H HETATM 114 H46 UNL 1 -0.918 -7.175 5.213 1.00 0.00 H HETATM 115 H47 UNL 1 -1.485 -8.693 7.059 1.00 0.00 H HETATM 116 H48 UNL 1 -1.079 -10.989 6.474 1.00 0.00 H HETATM 117 H49 UNL 1 -1.857 -11.623 4.249 1.00 0.00 H HETATM 118 H50 UNL 1 -1.691 -10.043 3.547 1.00 0.00 H HETATM 119 H51 UNL 1 -0.054 -11.469 2.550 1.00 0.00 H HETATM 120 H52 UNL 1 2.030 -11.766 3.441 1.00 0.00 H HETATM 121 H53 UNL 1 0.994 -10.624 6.221 1.00 0.00 H HETATM 122 H54 UNL 1 3.603 -11.658 5.260 1.00 0.00 H HETATM 123 H55 UNL 1 4.148 -11.575 7.579 1.00 0.00 H HETATM 124 H56 UNL 1 3.788 -9.443 8.412 1.00 0.00 H HETATM 125 H57 UNL 1 2.605 -11.060 9.335 1.00 0.00 H HETATM 126 H58 UNL 1 1.239 -10.723 8.158 1.00 0.00 H HETATM 127 H59 UNL 1 1.557 -13.065 7.127 1.00 0.00 H HETATM 128 H60 UNL 1 1.764 -14.667 8.817 1.00 0.00 H HETATM 129 H61 UNL 1 2.591 -12.358 10.754 1.00 0.00 H HETATM 130 H62 UNL 1 3.325 -13.948 10.609 1.00 0.00 H HETATM 131 H63 UNL 1 0.327 -13.391 11.318 1.00 0.00 H HETATM 132 H64 UNL 1 0.670 -15.105 12.886 1.00 0.00 H HETATM 133 H65 UNL 1 2.951 -15.513 13.575 1.00 0.00 H HETATM 134 H66 UNL 1 3.677 -15.139 12.019 1.00 0.00 H HETATM 135 H67 UNL 1 1.603 -17.312 12.582 1.00 0.00 H HETATM 136 H68 UNL 1 2.608 -17.233 11.082 1.00 0.00 H HETATM 137 H69 UNL 1 3.362 -17.581 12.726 1.00 0.00 H HETATM 138 H70 UNL 1 -2.569 -2.165 -1.250 1.00 0.00 H HETATM 139 H71 UNL 1 -2.343 -3.196 0.183 1.00 0.00 H HETATM 140 H72 UNL 1 0.747 -5.441 -0.607 1.00 0.00 H HETATM 141 H73 UNL 1 -0.570 -2.599 -3.666 1.00 0.00 H HETATM 142 H74 UNL 1 2.246 -1.861 -4.523 1.00 0.00 H HETATM 143 H75 UNL 1 2.037 -0.289 -2.826 1.00 0.00 H HETATM 144 H76 UNL 1 -0.503 -0.685 -4.199 1.00 0.00 H HETATM 145 H77 UNL 1 0.854 1.042 -4.069 1.00 0.00 H HETATM 146 H78 UNL 1 1.178 -1.314 -6.675 1.00 0.00 H HETATM 147 H79 UNL 1 -0.334 0.375 -6.857 1.00 0.00 H HETATM 148 H80 UNL 1 -1.370 -2.756 -5.807 1.00 0.00 H HETATM 149 H81 UNL 1 0.833 -3.507 -7.519 1.00 0.00 H HETATM 150 H82 UNL 1 0.072 -4.625 -5.178 1.00 0.00 H HETATM 151 H83 UNL 1 2.159 -4.587 -5.724 1.00 0.00 H CONECT 1 2 69 70 71 CONECT 2 3 72 73 CONECT 3 4 4 74 CONECT 4 5 75 CONECT 5 6 76 77 CONECT 6 7 7 78 CONECT 7 8 79 CONECT 8 9 80 81 CONECT 9 10 10 82 CONECT 10 11 83 CONECT 11 12 84 85 CONECT 12 13 13 86 CONECT 13 14 87 CONECT 14 15 88 89 CONECT 15 16 90 91 CONECT 16 17 92 93 CONECT 17 18 94 95 CONECT 18 19 96 97 CONECT 19 20 98 99 CONECT 20 21 100 101 CONECT 21 22 102 103 CONECT 22 23 23 24 CONECT 24 25 CONECT 25 26 52 104 CONECT 26 27 105 106 CONECT 27 28 CONECT 28 29 29 30 CONECT 30 31 107 108 CONECT 31 32 109 110 CONECT 32 33 33 111 CONECT 33 34 112 CONECT 34 35 113 114 CONECT 35 36 36 115 CONECT 36 37 116 CONECT 37 38 117 118 CONECT 38 39 39 119 CONECT 39 40 120 CONECT 40 41 41 121 CONECT 41 42 122 CONECT 42 43 44 123 CONECT 43 124 CONECT 44 45 125 126 CONECT 45 46 46 127 CONECT 46 47 128 CONECT 47 48 129 130 CONECT 48 49 49 131 CONECT 49 50 132 CONECT 50 51 133 134 CONECT 51 135 136 137 CONECT 52 53 138 139 CONECT 53 54 CONECT 54 55 55 56 57 CONECT 56 140 CONECT 57 58 CONECT 58 59 67 141 CONECT 59 60 61 142 CONECT 60 143 CONECT 61 62 63 144 CONECT 62 145 CONECT 63 64 65 146 CONECT 64 147 CONECT 65 66 67 148 CONECT 66 149 CONECT 67 68 150 CONECT 68 151 END SMILES for HMDB0277979 (PI(22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)/22:4(10Z,13Z,16Z,19Z)))[H][C@@](COC(=O)CC\C=C/C\C=C/C\C=C/C=C/C(O)C\C=C/C\C=C/CC)(COP(O)(=O)O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O)OC(=O)CCCCCCCC\C=C/C\C=C/C\C=C/C\C=C/CC INCHI for HMDB0277979 (PI(22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)/22:4(10Z,13Z,16Z,19Z)))InChI=1S/C53H83O14P/c1-3-5-7-9-11-12-13-14-15-16-17-18-19-20-21-26-29-33-37-41-47(56)66-45(43-65-68(62,63)67-53-51(60)49(58)48(57)50(59)52(53)61)42-64-46(55)40-36-32-28-25-23-22-24-27-31-35-39-44(54)38-34-30-10-8-6-4-2/h5-8,11-12,14-15,17-18,22-23,27-28,30-32,34-35,39,44-45,48-54,57-61H,3-4,9-10,13,16,19-21,24-26,29,33,36-38,40-43H2,1-2H3,(H,62,63)/b7-5-,8-6-,12-11-,15-14-,18-17-,23-22-,31-27-,32-28-,34-30-,39-35+/t44?,45-,48-,49-,50+,51-,52-,53-/m1/s1 3D Structure for HMDB0277979 (PI(22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)/22:4(10Z,13Z,16Z,19Z))) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Synonyms |
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chemical Formula | C53H83O14P | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Average Molecular Weight | 975.207 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Monoisotopic Molecular Weight | 974.552044351 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| IUPAC Name | [(2R)-2-[(10Z,13Z,16Z,19Z)-docosa-10,13,16,19-tetraenoyloxy]-3-{[(4Z,7Z,10Z,12E,16Z,19Z)-14-hydroxydocosa-4,7,10,12,16,19-hexaenoyl]oxy}propoxy]({[(1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl]oxy})phosphinic acid | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Traditional Name | (2R)-2-[(10Z,13Z,16Z,19Z)-docosa-10,13,16,19-tetraenoyloxy]-3-{[(4Z,7Z,10Z,12E,16Z,19Z)-14-hydroxydocosa-4,7,10,12,16,19-hexaenoyl]oxy}propoxy([(1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl]oxy)phosphinic acid | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| CAS Registry Number | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| SMILES | [H][C@@](COC(=O)CC\C=C/C\C=C/C\C=C/C=C/C(O)C\C=C/C\C=C/CC)(COP(O)(=O)O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O)OC(=O)CCCCCCCC\C=C/C\C=C/C\C=C/C\C=C/CC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Identifier | InChI=1S/C53H83O14P/c1-3-5-7-9-11-12-13-14-15-16-17-18-19-20-21-26-29-33-37-41-47(56)66-45(43-65-68(62,63)67-53-51(60)49(58)48(57)50(59)52(53)61)42-64-46(55)40-36-32-28-25-23-22-24-27-31-35-39-44(54)38-34-30-10-8-6-4-2/h5-8,11-12,14-15,17-18,22-23,27-28,30-32,34-35,39,44-45,48-54,57-61H,3-4,9-10,13,16,19-21,24-26,29,33,36-38,40-43H2,1-2H3,(H,62,63)/b7-5-,8-6-,12-11-,15-14-,18-17-,23-22-,31-27-,32-28-,34-30-,39-35+/t44?,45-,48-,49-,50+,51-,52-,53-/m1/s1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Key | GALMLXWDSDRPCW-BEFVJYSJSA-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 |
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 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 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
