Showing metabocard for PI(18:3(6Z,9Z,12Z)/TXB2) (HMDB0276793)
| Record Information | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Version | 5.0 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Status | Predicted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Creation Date | 2021-09-13 06:25:43 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Update Date | 2022-11-30 20:00:55 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HMDB ID | HMDB0276793 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary Accession Numbers | None | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Metabolite Identification | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Common Name | PI(18:3(6Z,9Z,12Z)/TXB2) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Description | PI(18:3(6Z,9Z,12Z)/TXB2) 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(18:3(6Z,9Z,12Z)/TXB2), in particular, consists of one chain of 6Z,9Z,12Z-octadecatrienoyl at the C-1 position and one chain of Thromboxane B2 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 HMDB0276793 (PI(18:3(6Z,9Z,12Z)/TXB2))
Mrv1652309132108262D
65 66 0 0 1 0 999 V2000
0.1948 -0.6000 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.6299 -0.4590 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
-1.0084 0.4182 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
-0.7819 1.0850 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.6578 0.9862 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
-2.5254 1.0069 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.3221 1.7502 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
-1.4773 2.5510 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.7665 2.9997 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0
-0.9479 3.9208 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.5643 3.4374 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
0.0786 3.1007 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
0.8951 2.8235 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.5962 2.3278 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
2.2339 3.0387 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.9882 3.4921 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.6239 4.0727 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.3385 4.8728 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.4624 3.8678 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.2116 4.2632 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.9620 3.8407 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.3023 3.0387 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.0935 2.7087 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.7399 3.2507 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.5968 4.0632 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.2289 4.5934 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.0859 5.4059 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.3107 5.6882 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.1676 6.5008 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.3924 6.7831 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.7603 6.2530 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.9851 6.5353 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.3530 6.0052 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.5779 6.2875 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.9457 5.7574 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.1769 1.7018 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.5104 0.9347 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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0.5384 0.0513 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
0.9435 0.7810 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
1.8642 0.7186 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.8429 0.5001 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.7077 0.1191 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
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-0.4761 1.6542 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
-0.3616 2.5399 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
0.3233 1.3700 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
0.8892 2.0912 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
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7 8 1 6 0 0 0
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9 11 2 0 0 0 0
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15 16 1 0 0 0 0
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17 18 2 0 0 0 0
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64 65 1 6 0 0 0
M END
3D MOL for HMDB0276793 (PI(18:3(6Z,9Z,12Z)/TXB2))HMDB0276793
RDKit 3D
PI(18:3(6Z,9Z,12Z)/TXB2)
144145 0 0 0 0 0 0 0 0999 V2000
15.2952 -1.6343 2.5322 C 0 0 0 0 0 0 0 0 0 0 0 0
13.8673 -1.4571 1.9162 C 0 0 0 0 0 0 0 0 0 0 0 0
13.8771 -0.2560 1.0320 C 0 0 0 0 0 0 0 0 0 0 0 0
12.6626 0.1892 0.3675 C 0 0 0 0 0 0 0 0 0 0 0 0
11.9219 -0.6321 -0.6084 C 0 0 0 0 0 0 0 0 0 0 0 0
11.3218 -1.8818 -0.1894 C 0 0 0 0 0 0 0 0 0 0 0 0
10.0302 -2.1442 -0.2161 C 0 0 0 0 0 0 0 0 0 0 0 0
8.9923 -1.2210 -0.6729 C 0 0 0 0 0 0 0 0 0 0 0 0
8.2021 -1.7810 -1.8109 C 0 0 0 0 0 0 0 0 0 0 0 0
8.0846 -1.2350 -2.9979 C 0 0 0 0 0 0 0 0 0 0 0 0
8.6934 0.0088 -3.4335 C 0 0 0 0 0 0 0 0 0 0 0 0
7.8820 1.1468 -3.7990 C 0 0 0 0 0 0 0 0 0 0 0 0
6.6063 1.2928 -3.7283 C 0 0 0 0 0 0 0 0 0 0 0 0
5.5995 0.3685 -3.2586 C 0 0 0 0 0 0 0 0 0 0 0 0
4.8309 0.9775 -2.0518 C 0 0 0 0 0 0 0 0 0 0 0 0
5.7987 1.2829 -0.9534 C 0 0 0 0 0 0 0 0 0 0 0 0
5.2086 1.8714 0.2660 C 0 0 0 0 0 0 0 0 0 0 0 0
4.2204 0.9784 0.9644 C 0 0 0 0 0 0 0 0 0 0 0 0
4.0289 -0.1639 0.5259 O 0 0 0 0 0 0 0 0 0 0 0 0
3.5340 1.3845 2.0583 O 0 0 0 0 0 0 0 0 0 0 0 0
2.6020 0.7535 2.8452 C 0 0 0 0 0 0 0 0 0 0 0 0
1.3344 0.3378 2.0982 C 0 0 2 0 0 0 0 0 0 0 0 0
0.2332 0.0993 3.0639 C 0 0 0 0 0 0 0 0 0 0 0 0
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-4.1949 1.0013 1.1268 C 0 0 2 0 0 0 0 0 0 0 0 0
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0.3181 -0.9711 3.3860 H 0 0 0 0 0 0 0 0 0 0 0 0
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4 74 1 0
5 75 1 0
5 76 1 0
6 77 1 0
7 78 1 0
8 79 1 0
8 80 1 0
9 81 1 0
10 82 1 0
11 83 1 0
11 84 1 0
12 85 1 0
13 86 1 0
14 87 1 0
14 88 1 0
15 89 1 0
15 90 1 0
16 91 1 0
16 92 1 0
17 93 1 0
17 94 1 0
21 95 1 0
21 96 1 0
22 97 1 6
23 98 1 0
23 99 1 0
27100 1 0
29101 1 1
30102 1 1
31103 1 0
32104 1 6
33105 1 0
34106 1 1
35107 1 0
36108 1 0
37109 1 1
38110 1 0
39111 1 0
39112 1 0
40113 1 0
40114 1 0
41115 1 0
41116 1 0
42117 1 0
42118 1 0
43119 1 0
43120 1 0
43121 1 0
45122 1 0
46123 1 0
47124 1 0
47125 1 0
48126 1 1
49127 1 0
50128 1 6
51129 1 0
51130 1 0
52131 1 0
53132 1 0
54133 1 0
54134 1 0
55135 1 0
55136 1 0
56137 1 0
56138 1 0
60139 1 6
61140 1 0
62141 1 6
63142 1 0
64143 1 6
65144 1 0
M END
3D SDF for HMDB0276793 (PI(18:3(6Z,9Z,12Z)/TXB2))
Mrv1652309132108262D
65 66 0 0 1 0 999 V2000
0.1948 -0.6000 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.6299 -0.4590 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
-1.0084 0.4182 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
-0.7819 1.0850 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.6578 0.9862 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
-2.5254 1.0069 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.3221 1.7502 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
-1.4773 2.5510 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.7665 2.9997 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0
-0.9479 3.9208 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.5643 3.4374 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
0.0786 3.1007 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
0.8951 2.8235 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.5962 2.3278 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
2.2339 3.0387 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.9882 3.4921 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.6239 4.0727 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.3385 4.8728 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.4624 3.8678 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.2116 4.2632 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.9620 3.8407 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.3023 3.0387 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.0935 2.7087 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.7399 3.2507 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.5968 4.0632 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.2289 4.5934 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.0859 5.4059 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.3107 5.6882 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.1676 6.5008 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.3924 6.7831 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.7603 6.2530 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.9851 6.5353 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.3530 6.0052 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.5779 6.2875 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.9457 5.7574 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.1769 1.7018 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.5104 0.9347 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.4259 1.1881 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.6043 0.0921 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.2288 -0.7049 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.2213 -1.5540 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.6825 -2.2053 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.8430 -2.0996 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.0903 -1.6666 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.6981 -1.3091 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
-1.5213 -1.0094 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
-2.2247 -1.5407 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.1981 -0.2278 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.3174 0.0864 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.1996 1.0385 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
0.5384 0.0513 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
0.9435 0.7810 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
1.8642 0.7186 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.8429 0.5001 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.7077 0.1191 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
4.1712 0.7931 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.4690 -0.4073 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.5105 -1.2764 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.8174 -2.1082 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.4367 -2.8692 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.8912 -3.5578 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.4761 1.6542 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
-0.3616 2.5399 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
0.3233 1.3700 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
0.8892 2.0912 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2 1 1 6 0 0 0
2 3 1 0 0 0 0
3 4 1 1 0 0 0
3 5 1 0 0 0 0
5 6 1 1 0 0 0
5 7 1 0 0 0 0
7 8 1 6 0 0 0
8 9 1 0 0 0 0
9 10 1 0 0 0 0
9 11 2 0 0 0 0
9 12 1 0 0 0 0
12 13 1 0 0 0 0
13 14 1 0 0 0 0
14 15 1 1 0 0 0
15 16 1 0 0 0 0
16 17 1 0 0 0 0
17 18 2 0 0 0 0
17 19 1 0 0 0 0
19 20 1 0 0 0 0
20 21 1 0 0 0 0
21 22 1 0 0 0 0
22 23 1 0 0 0 0
23 24 2 0 0 0 0
24 25 1 0 0 0 0
25 26 1 0 0 0 0
26 27 2 0 0 0 0
27 28 1 0 0 0 0
28 29 1 0 0 0 0
29 30 2 0 0 0 0
30 31 1 0 0 0 0
31 32 1 0 0 0 0
32 33 1 0 0 0 0
33 34 1 0 0 0 0
34 35 1 0 0 0 0
14 36 1 0 0 0 0
36 37 1 0 0 0 0
37 38 2 0 0 0 0
37 39 1 0 0 0 0
39 40 1 0 0 0 0
40 41 1 0 0 0 0
41 42 1 0 0 0 0
42 43 2 0 0 0 0
43 44 1 0 0 0 0
45 44 1 1 0 0 0
2 45 1 0 0 0 0
45 46 1 0 0 0 0
46 47 1 1 0 0 0
46 48 1 0 0 0 0
48 49 1 0 0 0 0
49 50 1 0 0 0 0
49 51 1 0 0 0 0
51 52 1 0 0 0 0
52 53 1 1 0 0 0
53 54 2 0 0 0 0
54 55 1 0 0 0 0
55 56 1 1 0 0 0
55 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
7 62 1 0 0 0 0
62 63 1 6 0 0 0
62 64 1 0 0 0 0
52 64 1 0 0 0 0
64 65 1 6 0 0 0
M END
> <DATABASE_ID>
HMDB0276793
> <DATABASE_NAME>
hmdb
> <SMILES>
CCCCC\C=C/C\C=C/C\C=C/CCCCC(=O)OC[C@@H]1COP(O)(=O)O[C@H]2[C@H](O)[C@@H](O)[C@H](O)[C@@H](C\C=C/CCCC(=O)O1)[C@@H](O)CC(O)O[C@H](\C=C/[C@@H](O)CCCCC)[C@@H](O)[C@H]2O
> <INCHI_IDENTIFIER>
InChI=1S/C47H79O17P/c1-3-5-7-8-9-10-11-12-13-14-15-16-17-18-23-27-39(50)60-32-35-33-61-65(58,59)64-47-45(56)43(54)38(30-29-34(48)25-21-6-4-2)63-41(52)31-37(49)36(42(53)44(55)46(47)57)26-22-19-20-24-28-40(51)62-35/h9-10,12-13,15-16,19,22,29-30,34-38,41-49,52-57H,3-8,11,14,17-18,20-21,23-28,31-33H2,1-2H3,(H,58,59)/b10-9-,13-12-,16-15-,22-19-,30-29-/t34-,35+,36-,37-,38+,41?,42+,43+,44-,45+,46+,47+/m0/s1
> <INCHI_KEY>
UNXGOMINZXBOTN-KKGHAOFHSA-N
> <FORMULA>
C47H79O17P
> <MOLECULAR_WEIGHT>
947.106
> <EXACT_MASS>
946.505488082
> <JCHEM_ACCEPTOR_COUNT>
13
> <JCHEM_ATOM_COUNT>
144
> <JCHEM_AVERAGE_POLARIZABILITY>
101.59361422130402
> <JCHEM_BIOAVAILABILITY>
0
> <JCHEM_DONOR_COUNT>
9
> <JCHEM_FORMAL_CHARGE>
0
> <JCHEM_GHOSE_FILTER>
0
> <JCHEM_IUPAC>
[(1S,6R,12Z,15S,16S,20R,21S,22R,23R,24S,25R)-3,16,18,21,22,23,24,25-octahydroxy-20-[(1E,3S)-3-hydroxyoct-1-en-1-yl]-3,8-dioxo-2,4,7,19-tetraoxa-3lambda5-phosphabicyclo[13.7.3]pentacos-12-en-6-yl]methyl (6Z,9Z,12Z)-octadeca-6,9,12-trienoate
> <ALOGPS_LOGP>
3.78
> <JCHEM_LOGP>
5.463830213999998
> <ALOGPS_LOGS>
-4.42
> <JCHEM_MDDR_LIKE_RULE>
0
> <JCHEM_NUMBER_OF_RINGS>
2
> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1
> <JCHEM_PKA>
12.109484732936078
> <JCHEM_PKA_STRONGEST_ACIDIC>
1.83325345150097
> <JCHEM_PKA_STRONGEST_BASIC>
-2.9342614914749285
> <JCHEM_POLAR_SURFACE_AREA>
279.42999999999995
> <JCHEM_REFRACTIVITY>
247.2204000000001
> <JCHEM_ROTATABLE_BOND_COUNT>
22
> <JCHEM_RULE_OF_FIVE>
0
> <ALOGPS_SOLUBILITY>
3.61e-02 g/l
> <JCHEM_TRADITIONAL_IUPAC>
[(1S,6R,12Z,15S,16S,20R,21S,22R,23R,24S,25R)-3,16,18,21,22,23,24,25-octahydroxy-20-[(1E,3S)-3-hydroxyoct-1-en-1-yl]-3,8-dioxo-2,4,7,19-tetraoxa-3lambda5-phosphabicyclo[13.7.3]pentacos-12-en-6-yl]methyl (6Z,9Z,12Z)-octadeca-6,9,12-trienoate
> <JCHEM_VEBER_RULE>
0
$$$$
3D-SDF for HMDB0276793 (PI(18:3(6Z,9Z,12Z)/TXB2))HMDB0276793
RDKit 3D
PI(18:3(6Z,9Z,12Z)/TXB2)
144145 0 0 0 0 0 0 0 0999 V2000
15.2952 -1.6343 2.5322 C 0 0 0 0 0 0 0 0 0 0 0 0
13.8673 -1.4571 1.9162 C 0 0 0 0 0 0 0 0 0 0 0 0
13.8771 -0.2560 1.0320 C 0 0 0 0 0 0 0 0 0 0 0 0
12.6626 0.1892 0.3675 C 0 0 0 0 0 0 0 0 0 0 0 0
11.9219 -0.6321 -0.6084 C 0 0 0 0 0 0 0 0 0 0 0 0
11.3218 -1.8818 -0.1894 C 0 0 0 0 0 0 0 0 0 0 0 0
10.0302 -2.1442 -0.2161 C 0 0 0 0 0 0 0 0 0 0 0 0
8.9923 -1.2210 -0.6729 C 0 0 0 0 0 0 0 0 0 0 0 0
8.2021 -1.7810 -1.8109 C 0 0 0 0 0 0 0 0 0 0 0 0
8.0846 -1.2350 -2.9979 C 0 0 0 0 0 0 0 0 0 0 0 0
8.6934 0.0088 -3.4335 C 0 0 0 0 0 0 0 0 0 0 0 0
7.8820 1.1468 -3.7990 C 0 0 0 0 0 0 0 0 0 0 0 0
6.6063 1.2928 -3.7283 C 0 0 0 0 0 0 0 0 0 0 0 0
5.5995 0.3685 -3.2586 C 0 0 0 0 0 0 0 0 0 0 0 0
4.8309 0.9775 -2.0518 C 0 0 0 0 0 0 0 0 0 0 0 0
5.7987 1.2829 -0.9534 C 0 0 0 0 0 0 0 0 0 0 0 0
5.2086 1.8714 0.2660 C 0 0 0 0 0 0 0 0 0 0 0 0
4.2204 0.9784 0.9644 C 0 0 0 0 0 0 0 0 0 0 0 0
4.0289 -0.1639 0.5259 O 0 0 0 0 0 0 0 0 0 0 0 0
3.5340 1.3845 2.0583 O 0 0 0 0 0 0 0 0 0 0 0 0
2.6020 0.7535 2.8452 C 0 0 0 0 0 0 0 0 0 0 0 0
1.3344 0.3378 2.0982 C 0 0 2 0 0 0 0 0 0 0 0 0
0.2332 0.0993 3.0639 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.0410 0.3013 2.6683 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.5024 1.8359 2.2274 P 0 0 0 0 0 5 0 0 0 0 0 0
-0.3515 2.8566 2.3225 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.6897 2.5033 3.2608 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.9531 1.7935 0.6338 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.2828 1.8482 0.3325 C 0 0 2 0 0 0 0 0 0 0 0 0
-4.1949 1.0013 1.1268 C 0 0 2 0 0 0 0 0 0 0 0 0
-4.4227 -0.2736 0.7076 O 0 0 0 0 0 0 0 0 0 0 0 0
-5.4834 1.7045 1.5649 C 0 0 2 0 0 0 0 0 0 0 0 0
-5.6499 1.6484 2.9551 O 0 0 0 0 0 0 0 0 0 0 0 0
-6.7037 1.1183 0.8540 C 0 0 1 0 0 0 0 0 0 0 0 0
-7.4357 2.2614 0.2886 C 0 0 0 0 0 0 0 0 0 0 0 0
-8.4576 2.8146 0.8532 C 0 0 0 0 0 0 0 0 0 0 0 0
-8.9737 2.3275 2.1329 C 0 0 1 0 0 0 0 0 0 0 0 0
-8.3747 3.0394 3.1907 O 0 0 0 0 0 0 0 0 0 0 0 0
-10.4555 2.7409 2.2071 C 0 0 0 0 0 0 0 0 0 0 0 0
-11.1473 2.0976 1.0335 C 0 0 0 0 0 0 0 0 0 0 0 0
-11.0721 0.6048 1.0189 C 0 0 0 0 0 0 0 0 0 0 0 0
-11.8060 0.0289 -0.1978 C 0 0 0 0 0 0 0 0 0 0 0 0
-11.1211 0.6024 -1.4308 C 0 0 0 0 0 0 0 0 0 0 0 0
-6.3472 0.1783 -0.0955 O 0 0 0 0 0 0 0 0 0 0 0 0
-7.1503 -0.9081 -0.2517 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.4956 -1.5586 0.9249 O 0 0 0 0 0 0 0 0 0 0 0 0
-6.4145 -1.8687 -1.2164 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.8037 -1.0164 -2.2629 C 0 0 2 0 0 0 0 0 0 0 0 0
-6.6523 -1.0869 -3.3791 O 0 0 0 0 0 0 0 0 0 0 0 0
-4.4206 -1.3040 -2.7204 C 0 0 2 0 0 0 0 0 0 0 0 0
-3.6981 -2.3688 -1.9529 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.3600 -2.5923 -2.5308 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.5397 -3.4505 -1.9354 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.5137 -3.6973 -0.4737 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.0762 -3.6499 0.0348 C 0 0 0 0 0 0 0 0 0 0 0 0
0.0667 -2.6154 1.1502 C 0 0 0 0 0 0 0 0 0 0 0 0
1.3859 -1.9504 1.0947 C 0 0 0 0 0 0 0 0 0 0 0 0
2.3862 -2.7333 1.0009 O 0 0 0 0 0 0 0 0 0 0 0 0
1.5785 -0.6186 1.1353 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.6878 -0.0215 -2.9250 C 0 0 1 0 0 0 0 0 0 0 0 0
-4.6575 0.9420 -3.3004 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.8868 0.5605 -1.8337 C 0 0 2 0 0 0 0 0 0 0 0 0
-2.4440 -0.3211 -0.8645 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.3675 1.8059 -1.1734 C 0 0 1 0 0 0 0 0 0 0 0 0
-4.5312 2.3650 -1.6809 O 0 0 0 0 0 0 0 0 0 0 0 0
15.2653 -2.6266 3.0299 H 0 0 0 0 0 0 0 0 0 0 0 0
16.0499 -1.5988 1.7402 H 0 0 0 0 0 0 0 0 0 0 0 0
15.4632 -0.8603 3.2909 H 0 0 0 0 0 0 0 0 0 0 0 0
13.7511 -2.4221 1.3726 H 0 0 0 0 0 0 0 0 0 0 0 0
13.1969 -1.3333 2.7733 H 0 0 0 0 0 0 0 0 0 0 0 0
14.7051 -0.3639 0.2557 H 0 0 0 0 0 0 0 0 0 0 0 0
14.2543 0.6103 1.6650 H 0 0 0 0 0 0 0 0 0 0 0 0
11.8862 0.4982 1.1545 H 0 0 0 0 0 0 0 0 0 0 0 0
12.8941 1.2145 -0.1048 H 0 0 0 0 0 0 0 0 0 0 0 0
11.1639 -0.0079 -1.1662 H 0 0 0 0 0 0 0 0 0 0 0 0
12.6579 -0.8909 -1.4700 H 0 0 0 0 0 0 0 0 0 0 0 0
11.9988 -2.6895 0.1570 H 0 0 0 0 0 0 0 0 0 0 0 0
9.7035 -3.1379 0.1359 H 0 0 0 0 0 0 0 0 0 0 0 0
8.2184 -1.1827 0.1782 H 0 0 0 0 0 0 0 0 0 0 0 0
9.2909 -0.1843 -0.8126 H 0 0 0 0 0 0 0 0 0 0 0 0
7.6594 -2.7419 -1.6599 H 0 0 0 0 0 0 0 0 0 0 0 0
7.4872 -1.8315 -3.7446 H 0 0 0 0 0 0 0 0 0 0 0 0
9.4080 -0.2646 -4.2958 H 0 0 0 0 0 0 0 0 0 0 0 0
9.4299 0.3713 -2.6638 H 0 0 0 0 0 0 0 0 0 0 0 0
8.4693 2.0364 -4.2072 H 0 0 0 0 0 0 0 0 0 0 0 0
6.1916 2.2981 -4.0860 H 0 0 0 0 0 0 0 0 0 0 0 0
5.8379 -0.6330 -2.9584 H 0 0 0 0 0 0 0 0 0 0 0 0
4.8236 0.2781 -4.0896 H 0 0 0 0 0 0 0 0 0 0 0 0
4.3078 1.8637 -2.4291 H 0 0 0 0 0 0 0 0 0 0 0 0
4.0858 0.2357 -1.7251 H 0 0 0 0 0 0 0 0 0 0 0 0
6.6076 1.9919 -1.2971 H 0 0 0 0 0 0 0 0 0 0 0 0
6.3594 0.3500 -0.6579 H 0 0 0 0 0 0 0 0 0 0 0 0
4.6156 2.7777 -0.0598 H 0 0 0 0 0 0 0 0 0 0 0 0
5.9501 2.2715 0.9784 H 0 0 0 0 0 0 0 0 0 0 0 0
3.0235 -0.1270 3.3964 H 0 0 0 0 0 0 0 0 0 0 0 0
2.2303 1.5107 3.6001 H 0 0 0 0 0 0 0 0 0 0 0 0
1.0542 1.3026 1.5465 H 0 0 0 0 0 0 0 0 0 0 0 0
0.3181 -0.9711 3.3860 H 0 0 0 0 0 0 0 0 0 0 0 0
0.4125 0.6757 4.0043 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.2595 2.4984 4.1723 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.5878 2.9228 0.5993 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.6425 0.8372 2.1140 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.1255 -1.0072 1.2622 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.3240 2.7733 1.3298 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.8519 0.6738 3.1358 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.2585 0.5556 1.6285 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.0677 2.6483 -0.6762 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.9890 3.6830 0.4050 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.9742 1.2575 2.3038 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.2094 3.9561 2.7991 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.8990 2.4169 3.1639 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.4688 3.8314 2.0493 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.2245 2.4035 1.0217 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.7203 2.5326 0.0974 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.5713 0.2024 1.9050 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.0457 0.2115 0.9540 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.7258 -1.0678 -0.2241 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.8526 0.3967 -0.2052 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.0487 0.8393 -1.2330 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.5893 1.5501 -1.7708 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.1459 -0.0876 -2.2843 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.1124 -0.6540 -0.7520 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.8799 -1.4485 1.6662 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.6820 -2.3900 -0.5762 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.1659 -2.5967 -1.6227 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.7704 0.0186 -1.8593 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.5053 -1.5273 -3.1528 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.5286 -1.7640 -3.7648 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.2754 -3.3233 -2.1669 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.7132 -2.2899 -0.8714 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.0622 -2.0751 -3.4076 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.8191 -4.0365 -2.5240 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.0339 -2.8655 0.0315 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.9804 -4.6663 -0.1874 H 0 0 0 0 0 0 0 0 0 0 0 0
0.2168 -4.6389 0.3828 H 0 0 0 0 0 0 0 0 0 0 0 0
0.5704 -3.2979 -0.7929 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.7886 -1.9301 1.1642 H 0 0 0 0 0 0 0 0 0 0 0 0
0.0446 -3.2123 2.1089 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.1019 -0.1396 -3.8903 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.0689 0.6445 -4.1692 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.8898 0.8228 -2.3562 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.5080 -0.2866 -0.6288 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.6269 2.6496 -1.4371 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.5876 3.3302 -1.6274 H 0 0 0 0 0 0 0 0 0 0 0 0
1 2 1 0
2 3 1 0
3 4 1 0
4 5 1 0
5 6 1 0
6 7 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 2 0
18 20 1 0
20 21 1 0
21 22 1 0
22 23 1 0
23 24 1 0
24 25 1 0
25 26 2 0
25 27 1 0
25 28 1 0
28 29 1 0
29 30 1 0
30 31 1 0
30 32 1 0
32 33 1 0
32 34 1 0
34 35 1 0
35 36 2 0
36 37 1 0
37 38 1 0
37 39 1 0
39 40 1 0
40 41 1 0
41 42 1 0
42 43 1 0
34 44 1 0
44 45 1 0
45 46 1 0
45 47 1 0
47 48 1 0
48 49 1 0
48 50 1 0
50 51 1 0
51 52 1 0
52 53 2 0
53 54 1 0
54 55 1 0
55 56 1 0
56 57 1 0
57 58 2 0
57 59 1 0
50 60 1 0
60 61 1 0
60 62 1 0
62 63 1 0
62 64 1 0
64 65 1 0
59 22 1 0
64 29 1 0
1 66 1 0
1 67 1 0
1 68 1 0
2 69 1 0
2 70 1 0
3 71 1 0
3 72 1 0
4 73 1 0
4 74 1 0
5 75 1 0
5 76 1 0
6 77 1 0
7 78 1 0
8 79 1 0
8 80 1 0
9 81 1 0
10 82 1 0
11 83 1 0
11 84 1 0
12 85 1 0
13 86 1 0
14 87 1 0
14 88 1 0
15 89 1 0
15 90 1 0
16 91 1 0
16 92 1 0
17 93 1 0
17 94 1 0
21 95 1 0
21 96 1 0
22 97 1 6
23 98 1 0
23 99 1 0
27100 1 0
29101 1 1
30102 1 1
31103 1 0
32104 1 6
33105 1 0
34106 1 1
35107 1 0
36108 1 0
37109 1 1
38110 1 0
39111 1 0
39112 1 0
40113 1 0
40114 1 0
41115 1 0
41116 1 0
42117 1 0
42118 1 0
43119 1 0
43120 1 0
43121 1 0
45122 1 0
46123 1 0
47124 1 0
47125 1 0
48126 1 1
49127 1 0
50128 1 6
51129 1 0
51130 1 0
52131 1 0
53132 1 0
54133 1 0
54134 1 0
55135 1 0
55136 1 0
56137 1 0
56138 1 0
60139 1 6
61140 1 0
62141 1 6
63142 1 0
64143 1 6
65144 1 0
M END
PDB for HMDB0276793 (PI(18:3(6Z,9Z,12Z)/TXB2))HEADER PROTEIN 13-SEP-21 NONE TITLE NULL COMPND NULL SOURCE NULL KEYWDS NULL EXPDTA NULL AUTHOR Marvin REVDAT 1 13-SEP-21 0 HETATM 1 O UNK 0 0.364 -1.120 0.000 0.00 0.00 O+0 HETATM 2 C UNK 0 -1.176 -0.857 0.000 0.00 0.00 C+0 HETATM 3 C UNK 0 -1.882 0.781 0.000 0.00 0.00 C+0 HETATM 4 O UNK 0 -1.460 2.025 0.000 0.00 0.00 O+0 HETATM 5 C UNK 0 -3.094 1.841 0.000 0.00 0.00 C+0 HETATM 6 O UNK 0 -4.714 1.880 0.000 0.00 0.00 O+0 HETATM 7 C UNK 0 -2.468 3.267 0.000 0.00 0.00 C+0 HETATM 8 O UNK 0 -2.758 4.762 0.000 0.00 0.00 O+0 HETATM 9 P UNK 0 -1.431 5.599 0.000 0.00 0.00 P+0 HETATM 10 O UNK 0 -1.770 7.319 0.000 0.00 0.00 O+0 HETATM 11 O UNK 0 -2.920 6.417 0.000 0.00 0.00 O+0 HETATM 12 O UNK 0 0.147 5.788 0.000 0.00 0.00 O+0 HETATM 13 C UNK 0 1.671 5.271 0.000 0.00 0.00 C+0 HETATM 14 C UNK 0 2.980 4.345 0.000 0.00 0.00 C+0 HETATM 15 C UNK 0 4.170 5.672 0.000 0.00 0.00 C+0 HETATM 16 O UNK 0 5.578 6.519 0.000 0.00 0.00 O+0 HETATM 17 C UNK 0 6.765 7.602 0.000 0.00 0.00 C+0 HETATM 18 O UNK 0 6.232 9.096 0.000 0.00 0.00 O+0 HETATM 19 C UNK 0 8.330 7.220 0.000 0.00 0.00 C+0 HETATM 20 C UNK 0 9.728 7.958 0.000 0.00 0.00 C+0 HETATM 21 C UNK 0 11.129 7.169 0.000 0.00 0.00 C+0 HETATM 22 C UNK 0 11.764 5.672 0.000 0.00 0.00 C+0 HETATM 23 C UNK 0 13.241 5.056 0.000 0.00 0.00 C+0 HETATM 24 C UNK 0 14.448 6.068 0.000 0.00 0.00 C+0 HETATM 25 C UNK 0 14.181 7.585 0.000 0.00 0.00 C+0 HETATM 26 C UNK 0 15.361 8.574 0.000 0.00 0.00 C+0 HETATM 27 C UNK 0 15.094 10.091 0.000 0.00 0.00 C+0 HETATM 28 C UNK 0 13.647 10.618 0.000 0.00 0.00 C+0 HETATM 29 C UNK 0 13.380 12.135 0.000 0.00 0.00 C+0 HETATM 30 C UNK 0 11.933 12.662 0.000 0.00 0.00 C+0 HETATM 31 C UNK 0 10.753 11.672 0.000 0.00 0.00 C+0 HETATM 32 C UNK 0 9.306 12.199 0.000 0.00 0.00 C+0 HETATM 33 C UNK 0 8.126 11.210 0.000 0.00 0.00 C+0 HETATM 34 C UNK 0 6.679 11.737 0.000 0.00 0.00 C+0 HETATM 35 C UNK 0 5.499 10.747 0.000 0.00 0.00 C+0 HETATM 36 O UNK 0 4.064 3.177 0.000 0.00 0.00 O+0 HETATM 37 C UNK 0 4.686 1.745 0.000 0.00 0.00 C+0 HETATM 38 O UNK 0 6.395 2.218 0.000 0.00 0.00 O+0 HETATM 39 C UNK 0 4.861 0.172 0.000 0.00 0.00 C+0 HETATM 40 C UNK 0 4.160 -1.316 0.000 0.00 0.00 C+0 HETATM 41 C UNK 0 4.146 -2.901 0.000 0.00 0.00 C+0 HETATM 42 C UNK 0 3.141 -4.117 0.000 0.00 0.00 C+0 HETATM 43 C UNK 0 1.574 -3.919 0.000 0.00 0.00 C+0 HETATM 44 C UNK 0 0.169 -3.111 0.000 0.00 0.00 C+0 HETATM 45 C UNK 0 -1.303 -2.444 0.000 0.00 0.00 C+0 HETATM 46 C UNK 0 -2.840 -1.884 0.000 0.00 0.00 C+0 HETATM 47 O UNK 0 -4.153 -2.876 0.000 0.00 0.00 O+0 HETATM 48 C UNK 0 -2.236 -0.425 0.000 0.00 0.00 C+0 HETATM 49 C UNK 0 -0.593 0.161 0.000 0.00 0.00 C+0 HETATM 50 O UNK 0 -0.373 1.939 0.000 0.00 0.00 O+0 HETATM 51 O UNK 0 1.005 0.096 0.000 0.00 0.00 O+0 HETATM 52 C UNK 0 1.761 1.458 0.000 0.00 0.00 C+0 HETATM 53 C UNK 0 3.480 1.341 0.000 0.00 0.00 C+0 HETATM 54 C UNK 0 5.307 0.934 0.000 0.00 0.00 C+0 HETATM 55 C UNK 0 6.921 0.222 0.000 0.00 0.00 C+0 HETATM 56 O UNK 0 7.786 1.480 0.000 0.00 0.00 O+0 HETATM 57 C UNK 0 8.342 -0.760 0.000 0.00 0.00 C+0 HETATM 58 C UNK 0 8.420 -2.383 0.000 0.00 0.00 C+0 HETATM 59 C UNK 0 8.992 -3.935 0.000 0.00 0.00 C+0 HETATM 60 C UNK 0 8.282 -5.356 0.000 0.00 0.00 C+0 HETATM 61 C UNK 0 9.130 -6.641 0.000 0.00 0.00 C+0 HETATM 62 C UNK 0 -0.889 3.088 0.000 0.00 0.00 C+0 HETATM 63 O UNK 0 -0.675 4.741 0.000 0.00 0.00 O+0 HETATM 64 C UNK 0 0.604 2.557 0.000 0.00 0.00 C+0 HETATM 65 O UNK 0 1.660 3.903 0.000 0.00 0.00 O+0 CONECT 1 2 CONECT 2 1 3 45 CONECT 3 2 4 5 CONECT 4 3 CONECT 5 3 6 7 CONECT 6 5 CONECT 7 5 8 62 CONECT 8 7 9 CONECT 9 8 10 11 12 CONECT 10 9 CONECT 11 9 CONECT 12 9 13 CONECT 13 12 14 CONECT 14 13 15 36 CONECT 15 14 16 CONECT 16 15 17 CONECT 17 16 18 19 CONECT 18 17 CONECT 19 17 20 CONECT 20 19 21 CONECT 21 20 22 CONECT 22 21 23 CONECT 23 22 24 CONECT 24 23 25 CONECT 25 24 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 CONECT 36 14 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 2 46 CONECT 46 45 47 48 CONECT 47 46 CONECT 48 46 49 CONECT 49 48 50 51 CONECT 50 49 CONECT 51 49 52 CONECT 52 51 53 64 CONECT 53 52 54 CONECT 54 53 55 CONECT 55 54 56 57 CONECT 56 55 CONECT 57 55 58 CONECT 58 57 59 CONECT 59 58 60 CONECT 60 59 61 CONECT 61 60 CONECT 62 7 63 64 CONECT 63 62 CONECT 64 62 52 65 CONECT 65 64 MASTER 0 0 0 0 0 0 0 0 65 0 132 0 END 3D PDB for HMDB0276793 (PI(18:3(6Z,9Z,12Z)/TXB2))COMPND HMDB0276793 HETATM 1 C1 UNL 1 15.295 -1.634 2.532 1.00 0.00 C HETATM 2 C2 UNL 1 13.867 -1.457 1.916 1.00 0.00 C HETATM 3 C3 UNL 1 13.877 -0.256 1.032 1.00 0.00 C HETATM 4 C4 UNL 1 12.663 0.189 0.368 1.00 0.00 C HETATM 5 C5 UNL 1 11.922 -0.632 -0.608 1.00 0.00 C HETATM 6 C6 UNL 1 11.322 -1.882 -0.189 1.00 0.00 C HETATM 7 C7 UNL 1 10.030 -2.144 -0.216 1.00 0.00 C HETATM 8 C8 UNL 1 8.992 -1.221 -0.673 1.00 0.00 C HETATM 9 C9 UNL 1 8.202 -1.781 -1.811 1.00 0.00 C HETATM 10 C10 UNL 1 8.085 -1.235 -2.998 1.00 0.00 C HETATM 11 C11 UNL 1 8.693 0.009 -3.434 1.00 0.00 C HETATM 12 C12 UNL 1 7.882 1.147 -3.799 1.00 0.00 C HETATM 13 C13 UNL 1 6.606 1.293 -3.728 1.00 0.00 C HETATM 14 C14 UNL 1 5.600 0.369 -3.259 1.00 0.00 C HETATM 15 C15 UNL 1 4.831 0.978 -2.052 1.00 0.00 C HETATM 16 C16 UNL 1 5.799 1.283 -0.953 1.00 0.00 C HETATM 17 C17 UNL 1 5.209 1.871 0.266 1.00 0.00 C HETATM 18 C18 UNL 1 4.220 0.978 0.964 1.00 0.00 C HETATM 19 O1 UNL 1 4.029 -0.164 0.526 1.00 0.00 O HETATM 20 O2 UNL 1 3.534 1.384 2.058 1.00 0.00 O HETATM 21 C19 UNL 1 2.602 0.753 2.845 1.00 0.00 C HETATM 22 C20 UNL 1 1.334 0.338 2.098 1.00 0.00 C HETATM 23 C21 UNL 1 0.233 0.099 3.064 1.00 0.00 C HETATM 24 O3 UNL 1 -1.041 0.301 2.668 1.00 0.00 O HETATM 25 P1 UNL 1 -1.502 1.836 2.227 1.00 0.00 P HETATM 26 O4 UNL 1 -0.351 2.857 2.322 1.00 0.00 O HETATM 27 O5 UNL 1 -2.690 2.503 3.261 1.00 0.00 O HETATM 28 O6 UNL 1 -1.953 1.794 0.634 1.00 0.00 O HETATM 29 C22 UNL 1 -3.283 1.848 0.333 1.00 0.00 C HETATM 30 C23 UNL 1 -4.195 1.001 1.127 1.00 0.00 C HETATM 31 O7 UNL 1 -4.423 -0.274 0.708 1.00 0.00 O HETATM 32 C24 UNL 1 -5.483 1.704 1.565 1.00 0.00 C HETATM 33 O8 UNL 1 -5.650 1.648 2.955 1.00 0.00 O HETATM 34 C25 UNL 1 -6.704 1.118 0.854 1.00 0.00 C HETATM 35 C26 UNL 1 -7.436 2.261 0.289 1.00 0.00 C HETATM 36 C27 UNL 1 -8.458 2.815 0.853 1.00 0.00 C HETATM 37 C28 UNL 1 -8.974 2.327 2.133 1.00 0.00 C HETATM 38 O9 UNL 1 -8.375 3.039 3.191 1.00 0.00 O HETATM 39 C29 UNL 1 -10.456 2.741 2.207 1.00 0.00 C HETATM 40 C30 UNL 1 -11.147 2.098 1.033 1.00 0.00 C HETATM 41 C31 UNL 1 -11.072 0.605 1.019 1.00 0.00 C HETATM 42 C32 UNL 1 -11.806 0.029 -0.198 1.00 0.00 C HETATM 43 C33 UNL 1 -11.121 0.602 -1.431 1.00 0.00 C HETATM 44 O10 UNL 1 -6.347 0.178 -0.096 1.00 0.00 O HETATM 45 C34 UNL 1 -7.150 -0.908 -0.252 1.00 0.00 C HETATM 46 O11 UNL 1 -7.496 -1.559 0.925 1.00 0.00 O HETATM 47 C35 UNL 1 -6.414 -1.869 -1.216 1.00 0.00 C HETATM 48 C36 UNL 1 -5.804 -1.016 -2.263 1.00 0.00 C HETATM 49 O12 UNL 1 -6.652 -1.087 -3.379 1.00 0.00 O HETATM 50 C37 UNL 1 -4.421 -1.304 -2.720 1.00 0.00 C HETATM 51 C38 UNL 1 -3.698 -2.369 -1.953 1.00 0.00 C HETATM 52 C39 UNL 1 -2.360 -2.592 -2.531 1.00 0.00 C HETATM 53 C40 UNL 1 -1.540 -3.450 -1.935 1.00 0.00 C HETATM 54 C41 UNL 1 -1.514 -3.697 -0.474 1.00 0.00 C HETATM 55 C42 UNL 1 -0.076 -3.650 0.035 1.00 0.00 C HETATM 56 C43 UNL 1 0.067 -2.615 1.150 1.00 0.00 C HETATM 57 C44 UNL 1 1.386 -1.950 1.095 1.00 0.00 C HETATM 58 O13 UNL 1 2.386 -2.733 1.001 1.00 0.00 O HETATM 59 O14 UNL 1 1.578 -0.619 1.135 1.00 0.00 O HETATM 60 C45 UNL 1 -3.688 -0.021 -2.925 1.00 0.00 C HETATM 61 O15 UNL 1 -4.657 0.942 -3.300 1.00 0.00 O HETATM 62 C46 UNL 1 -2.887 0.560 -1.834 1.00 0.00 C HETATM 63 O16 UNL 1 -2.444 -0.321 -0.864 1.00 0.00 O HETATM 64 C47 UNL 1 -3.368 1.806 -1.173 1.00 0.00 C HETATM 65 O17 UNL 1 -4.531 2.365 -1.681 1.00 0.00 O HETATM 66 H1 UNL 1 15.265 -2.627 3.030 1.00 0.00 H HETATM 67 H2 UNL 1 16.050 -1.599 1.740 1.00 0.00 H HETATM 68 H3 UNL 1 15.463 -0.860 3.291 1.00 0.00 H HETATM 69 H4 UNL 1 13.751 -2.422 1.373 1.00 0.00 H HETATM 70 H5 UNL 1 13.197 -1.333 2.773 1.00 0.00 H HETATM 71 H6 UNL 1 14.705 -0.364 0.256 1.00 0.00 H HETATM 72 H7 UNL 1 14.254 0.610 1.665 1.00 0.00 H HETATM 73 H8 UNL 1 11.886 0.498 1.154 1.00 0.00 H HETATM 74 H9 UNL 1 12.894 1.214 -0.105 1.00 0.00 H HETATM 75 H10 UNL 1 11.164 -0.008 -1.166 1.00 0.00 H HETATM 76 H11 UNL 1 12.658 -0.891 -1.470 1.00 0.00 H HETATM 77 H12 UNL 1 11.999 -2.690 0.157 1.00 0.00 H HETATM 78 H13 UNL 1 9.703 -3.138 0.136 1.00 0.00 H HETATM 79 H14 UNL 1 8.218 -1.183 0.178 1.00 0.00 H HETATM 80 H15 UNL 1 9.291 -0.184 -0.813 1.00 0.00 H HETATM 81 H16 UNL 1 7.659 -2.742 -1.660 1.00 0.00 H HETATM 82 H17 UNL 1 7.487 -1.832 -3.745 1.00 0.00 H HETATM 83 H18 UNL 1 9.408 -0.265 -4.296 1.00 0.00 H HETATM 84 H19 UNL 1 9.430 0.371 -2.664 1.00 0.00 H HETATM 85 H20 UNL 1 8.469 2.036 -4.207 1.00 0.00 H HETATM 86 H21 UNL 1 6.192 2.298 -4.086 1.00 0.00 H HETATM 87 H22 UNL 1 5.838 -0.633 -2.958 1.00 0.00 H HETATM 88 H23 UNL 1 4.824 0.278 -4.090 1.00 0.00 H HETATM 89 H24 UNL 1 4.308 1.864 -2.429 1.00 0.00 H HETATM 90 H25 UNL 1 4.086 0.236 -1.725 1.00 0.00 H HETATM 91 H26 UNL 1 6.608 1.992 -1.297 1.00 0.00 H HETATM 92 H27 UNL 1 6.359 0.350 -0.658 1.00 0.00 H HETATM 93 H28 UNL 1 4.616 2.778 -0.060 1.00 0.00 H HETATM 94 H29 UNL 1 5.950 2.271 0.978 1.00 0.00 H HETATM 95 H30 UNL 1 3.023 -0.127 3.396 1.00 0.00 H HETATM 96 H31 UNL 1 2.230 1.511 3.600 1.00 0.00 H HETATM 97 H32 UNL 1 1.054 1.303 1.546 1.00 0.00 H HETATM 98 H33 UNL 1 0.318 -0.971 3.386 1.00 0.00 H HETATM 99 H34 UNL 1 0.412 0.676 4.004 1.00 0.00 H HETATM 100 H35 UNL 1 -2.259 2.498 4.172 1.00 0.00 H HETATM 101 H36 UNL 1 -3.588 2.923 0.599 1.00 0.00 H HETATM 102 H37 UNL 1 -3.642 0.837 2.114 1.00 0.00 H HETATM 103 H38 UNL 1 -4.126 -1.007 1.262 1.00 0.00 H HETATM 104 H39 UNL 1 -5.324 2.773 1.330 1.00 0.00 H HETATM 105 H40 UNL 1 -5.852 0.674 3.136 1.00 0.00 H HETATM 106 H41 UNL 1 -7.258 0.556 1.628 1.00 0.00 H HETATM 107 H42 UNL 1 -7.068 2.648 -0.676 1.00 0.00 H HETATM 108 H43 UNL 1 -8.989 3.683 0.405 1.00 0.00 H HETATM 109 H44 UNL 1 -8.974 1.258 2.304 1.00 0.00 H HETATM 110 H45 UNL 1 -8.209 3.956 2.799 1.00 0.00 H HETATM 111 H46 UNL 1 -10.899 2.417 3.164 1.00 0.00 H HETATM 112 H47 UNL 1 -10.469 3.831 2.049 1.00 0.00 H HETATM 113 H48 UNL 1 -12.224 2.404 1.022 1.00 0.00 H HETATM 114 H49 UNL 1 -10.720 2.533 0.097 1.00 0.00 H HETATM 115 H50 UNL 1 -11.571 0.202 1.905 1.00 0.00 H HETATM 116 H51 UNL 1 -10.046 0.211 0.954 1.00 0.00 H HETATM 117 H52 UNL 1 -11.726 -1.068 -0.224 1.00 0.00 H HETATM 118 H53 UNL 1 -12.853 0.397 -0.205 1.00 0.00 H HETATM 119 H54 UNL 1 -10.049 0.839 -1.233 1.00 0.00 H HETATM 120 H55 UNL 1 -11.589 1.550 -1.771 1.00 0.00 H HETATM 121 H56 UNL 1 -11.146 -0.088 -2.284 1.00 0.00 H HETATM 122 H57 UNL 1 -8.112 -0.654 -0.752 1.00 0.00 H HETATM 123 H58 UNL 1 -6.880 -1.448 1.666 1.00 0.00 H HETATM 124 H59 UNL 1 -5.682 -2.390 -0.576 1.00 0.00 H HETATM 125 H60 UNL 1 -7.166 -2.597 -1.623 1.00 0.00 H HETATM 126 H61 UNL 1 -5.770 0.019 -1.859 1.00 0.00 H HETATM 127 H62 UNL 1 -7.505 -1.527 -3.153 1.00 0.00 H HETATM 128 H63 UNL 1 -4.529 -1.764 -3.765 1.00 0.00 H HETATM 129 H64 UNL 1 -4.275 -3.323 -2.167 1.00 0.00 H HETATM 130 H65 UNL 1 -3.713 -2.290 -0.871 1.00 0.00 H HETATM 131 H66 UNL 1 -2.062 -2.075 -3.408 1.00 0.00 H HETATM 132 H67 UNL 1 -0.819 -4.036 -2.524 1.00 0.00 H HETATM 133 H68 UNL 1 -2.034 -2.865 0.032 1.00 0.00 H HETATM 134 H69 UNL 1 -1.980 -4.666 -0.187 1.00 0.00 H HETATM 135 H70 UNL 1 0.217 -4.639 0.383 1.00 0.00 H HETATM 136 H71 UNL 1 0.570 -3.298 -0.793 1.00 0.00 H HETATM 137 H72 UNL 1 -0.789 -1.930 1.164 1.00 0.00 H HETATM 138 H73 UNL 1 0.045 -3.212 2.109 1.00 0.00 H HETATM 139 H74 UNL 1 -3.102 -0.140 -3.890 1.00 0.00 H HETATM 140 H75 UNL 1 -5.069 0.644 -4.169 1.00 0.00 H HETATM 141 H76 UNL 1 -1.890 0.823 -2.356 1.00 0.00 H HETATM 142 H77 UNL 1 -1.508 -0.287 -0.629 1.00 0.00 H HETATM 143 H78 UNL 1 -2.627 2.650 -1.437 1.00 0.00 H HETATM 144 H79 UNL 1 -4.588 3.330 -1.627 1.00 0.00 H CONECT 1 2 66 67 68 CONECT 2 3 69 70 CONECT 3 4 71 72 CONECT 4 5 73 74 CONECT 5 6 75 76 CONECT 6 7 7 77 CONECT 7 8 78 CONECT 8 9 79 80 CONECT 9 10 10 81 CONECT 10 11 82 CONECT 11 12 83 84 CONECT 12 13 13 85 CONECT 13 14 86 CONECT 14 15 87 88 CONECT 15 16 89 90 CONECT 16 17 91 92 CONECT 17 18 93 94 CONECT 18 19 19 20 CONECT 20 21 CONECT 21 22 95 96 CONECT 22 23 59 97 CONECT 23 24 98 99 CONECT 24 25 CONECT 25 26 26 27 28 CONECT 27 100 CONECT 28 29 CONECT 29 30 64 101 CONECT 30 31 32 102 CONECT 31 103 CONECT 32 33 34 104 CONECT 33 105 CONECT 34 35 44 106 CONECT 35 36 36 107 CONECT 36 37 108 CONECT 37 38 39 109 CONECT 38 110 CONECT 39 40 111 112 CONECT 40 41 113 114 CONECT 41 42 115 116 CONECT 42 43 117 118 CONECT 43 119 120 121 CONECT 44 45 CONECT 45 46 47 122 CONECT 46 123 CONECT 47 48 124 125 CONECT 48 49 50 126 CONECT 49 127 CONECT 50 51 60 128 CONECT 51 52 129 130 CONECT 52 53 53 131 CONECT 53 54 132 CONECT 54 55 133 134 CONECT 55 56 135 136 CONECT 56 57 137 138 CONECT 57 58 58 59 CONECT 60 61 62 139 CONECT 61 140 CONECT 62 63 64 141 CONECT 63 142 CONECT 64 65 143 CONECT 65 144 END SMILES for HMDB0276793 (PI(18:3(6Z,9Z,12Z)/TXB2))CCCCC\C=C/C\C=C/C\C=C/CCCCC(=O)OC[C@@H]1COP(O)(=O)O[C@H]2[C@H](O)[C@@H](O)[C@H](O)[C@@H](C\C=C/CCCC(=O)O1)[C@@H](O)CC(O)O[C@H](\C=C/[C@@H](O)CCCCC)[C@@H](O)[C@H]2O INCHI for HMDB0276793 (PI(18:3(6Z,9Z,12Z)/TXB2))InChI=1S/C47H79O17P/c1-3-5-7-8-9-10-11-12-13-14-15-16-17-18-23-27-39(50)60-32-35-33-61-65(58,59)64-47-45(56)43(54)38(30-29-34(48)25-21-6-4-2)63-41(52)31-37(49)36(42(53)44(55)46(47)57)26-22-19-20-24-28-40(51)62-35/h9-10,12-13,15-16,19,22,29-30,34-38,41-49,52-57H,3-8,11,14,17-18,20-21,23-28,31-33H2,1-2H3,(H,58,59)/b10-9-,13-12-,16-15-,22-19-,30-29-/t34-,35+,36-,37-,38+,41?,42+,43+,44-,45+,46+,47+/m0/s1 3D Structure for HMDB0276793 (PI(18:3(6Z,9Z,12Z)/TXB2)) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Synonyms |
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| Chemical Formula | C47H79O17P | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Average Molecular Weight | 947.106 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Monoisotopic Molecular Weight | 946.505488082 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| IUPAC Name | [(1S,6R,12Z,15S,16S,20R,21S,22R,23R,24S,25R)-3,16,18,21,22,23,24,25-octahydroxy-20-[(1E,3S)-3-hydroxyoct-1-en-1-yl]-3,8-dioxo-2,4,7,19-tetraoxa-3lambda5-phosphabicyclo[13.7.3]pentacos-12-en-6-yl]methyl (6Z,9Z,12Z)-octadeca-6,9,12-trienoate | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Traditional Name | [(1S,6R,12Z,15S,16S,20R,21S,22R,23R,24S,25R)-3,16,18,21,22,23,24,25-octahydroxy-20-[(1E,3S)-3-hydroxyoct-1-en-1-yl]-3,8-dioxo-2,4,7,19-tetraoxa-3lambda5-phosphabicyclo[13.7.3]pentacos-12-en-6-yl]methyl (6Z,9Z,12Z)-octadeca-6,9,12-trienoate | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| CAS Registry Number | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| SMILES | CCCCC\C=C/C\C=C/C\C=C/CCCCC(=O)OC[C@@H]1COP(O)(=O)O[C@H]2[C@H](O)[C@@H](O)[C@H](O)[C@@H](C\C=C/CCCC(=O)O1)[C@@H](O)CC(O)O[C@H](\C=C/[C@@H](O)CCCCC)[C@@H](O)[C@H]2O | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Identifier | InChI=1S/C47H79O17P/c1-3-5-7-8-9-10-11-12-13-14-15-16-17-18-23-27-39(50)60-32-35-33-61-65(58,59)64-47-45(56)43(54)38(30-29-34(48)25-21-6-4-2)63-41(52)31-37(49)36(42(53)44(55)46(47)57)26-22-19-20-24-28-40(51)62-35/h9-10,12-13,15-16,19,22,29-30,34-38,41-49,52-57H,3-8,11,14,17-18,20-21,23-28,31-33H2,1-2H3,(H,58,59)/b10-9-,13-12-,16-15-,22-19-,30-29-/t34-,35+,36-,37-,38+,41?,42+,43+,44-,45+,46+,47+/m0/s1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Key | UNXGOMINZXBOTN-KKGHAOFHSA-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 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
