Showing metabocard for PIP(18:1(12Z)-2OH(9,10)/18:1(9Z)) (HMDB0279092)
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Version | 5.0 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Status | Predicted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Creation Date | 2021-09-13 11:30:43 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Update Date | 2022-11-30 20:02:03 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
HMDB ID | HMDB0279092 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Secondary Accession Numbers | None | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Metabolite Identification | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Common Name | PIP(18:1(12Z)-2OH(9,10)/18:1(9Z)) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Description | PIP(18:1(12Z)-2OH(9,10)/18:1(9Z)) 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(18:1(12Z)-2OH(9,10)/18:1(9Z)), in particular, consists of one chain of 9,10-hydroxy-octadecenoyl at the C-1 position and one chain of 9Z-octadecenoyl 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 HMDB0279092 (PIP(18:1(12Z)-2OH(9,10)/18:1(9Z)))PIP(18:1(12Z)-2OH(9,10)/18:1(9Z)) Mrv1652309132113312D 66 66 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 -9.0669 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -9.7811 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -10.4952 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -11.2093 0.7694 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -11.2093 1.5408 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -11.9235 0.3563 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -11.9235 -0.4152 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -12.6376 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -13.3518 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -14.1768 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -14.8909 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -15.6050 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -16.3192 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -17.0333 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -17.7475 0.7694 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 -11.0583 -0.7691 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 -13.9149 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -14.6290 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -15.3432 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -16.0573 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -16.7714 -0.7691 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 1 0 0 0 0 33 34 1 0 0 0 0 34 35 1 0 0 0 0 35 36 1 0 0 0 0 36 37 1 6 0 0 0 36 38 1 0 0 0 0 38 39 1 6 0 0 0 38 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 1 0 0 0 0 44 45 1 0 0 0 0 45 46 1 0 0 0 0 46 47 1 0 0 0 0 48 5 1 0 0 0 0 48 49 2 0 0 0 0 48 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 1 0 0 0 0 61 62 1 0 0 0 0 62 63 1 0 0 0 0 63 64 1 0 0 0 0 64 65 1 0 0 0 0 65 66 1 0 0 0 0 M END 3D MOL for HMDB0279092 (PIP(18:1(12Z)-2OH(9,10)/18:1(9Z)))HMDB0279092 RDKit 3D PIP(18:1(12Z)-2OH(9,10)/18:1(9Z)) 149149 0 0 0 0 0 0 0 0999 V2000 -7.5395 -3.2373 2.4489 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.9506 -2.6069 3.7148 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.5978 -2.1028 3.3390 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.8496 -1.4361 4.4861 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.4861 -0.9638 3.9536 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.7721 -0.3146 5.0541 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6079 -0.6642 5.5592 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8530 -1.7949 5.0635 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.5609 -2.8842 6.1137 C 0 0 1 0 0 0 0 0 0 0 0 0 0.1848 -3.8930 5.4538 O 0 0 0 0 0 0 0 0 0 0 0 0 0.2951 -2.3473 7.2264 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.5126 -1.4262 7.9760 O 0 0 0 0 0 0 0 0 0 0 0 0 1.4996 -1.5883 6.7741 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4926 -2.3487 5.9480 C 0 0 0 0 0 0 0 0 0 0 0 0 3.6172 -1.3652 5.5204 C 0 0 0 0 0 0 0 0 0 0 0 0 4.6638 -2.0693 4.7037 C 0 0 0 0 0 0 0 0 0 0 0 0 5.7223 -1.0656 4.2116 C 0 0 0 0 0 0 0 0 0 0 0 0 5.0795 -0.0465 3.3432 C 0 0 0 0 0 0 0 0 0 0 0 0 6.0371 1.0028 2.7689 C 0 0 0 0 0 0 0 0 0 0 0 0 5.1793 1.9211 1.9184 C 0 0 0 0 0 0 0 0 0 0 0 0 4.6402 2.8851 2.4922 O 0 0 0 0 0 0 0 0 0 0 0 0 5.0152 1.6711 0.5747 O 0 0 0 0 0 0 0 0 0 0 0 0 4.1944 2.4908 -0.2237 C 0 0 0 0 0 0 0 0 0 0 0 0 4.1902 2.0064 -1.6760 C 0 0 2 0 0 0 0 0 0 0 0 0 3.3727 2.9165 -2.5375 C 0 0 0 0 0 0 0 0 0 0 0 0 2.0310 2.9659 -2.2453 O 0 0 0 0 0 0 0 0 0 0 0 0 1.3369 4.1157 -3.3004 P 0 0 0 0 0 5 0 0 0 0 0 0 1.9736 4.0175 -4.6667 O 0 0 0 0 0 0 0 0 0 0 0 0 1.7176 5.6830 -2.7246 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.3332 3.9320 -3.4382 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.9501 5.1192 -3.0841 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.6161 5.7726 -4.2745 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4073 4.8033 -4.8903 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.3454 7.0101 -3.9734 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.5418 8.1039 -4.3857 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.8755 7.2331 -2.6092 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.6070 8.5524 -2.2385 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.3272 6.3387 -1.5395 C 0 0 1 0 0 0 0 0 0 0 0 0 -3.2328 6.1908 -0.4876 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.6293 6.6745 0.9921 P 0 0 0 0 0 5 0 0 0 0 0 0 -1.8782 7.9828 0.9007 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.6417 5.5341 1.7298 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.9714 6.9255 2.0168 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.0530 4.9310 -2.0663 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.2501 4.5528 -2.6987 O 0 0 0 0 0 0 0 0 0 0 0 0 3.7916 0.6523 -1.7361 O 0 0 0 0 0 0 0 0 0 0 0 0 4.7081 -0.2637 -2.2008 C 0 0 0 0 0 0 0 0 0 0 0 0 5.8635 0.1883 -2.5762 O 0 0 0 0 0 0 0 0 0 0 0 0 4.5724 -1.7138 -2.3334 C 0 0 0 0 0 0 0 0 0 0 0 0 3.4301 -2.3653 -1.6770 C 0 0 0 0 0 0 0 0 0 0 0 0 2.0549 -2.0246 -2.1150 C 0 0 0 0 0 0 0 0 0 0 0 0 1.8404 -2.3296 -3.5950 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1764 -3.7538 -3.9045 C 0 0 0 0 0 0 0 0 0 0 0 0 1.9635 -4.1205 -5.3114 C 0 0 0 0 0 0 0 0 0 0 0 0 0.5611 -4.2526 -5.8457 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0873 -5.3409 -5.1420 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.2242 -5.4159 -4.5939 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.3015 -4.4263 -4.4921 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.5939 -4.1279 -3.0558 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6162 -3.2756 -2.3271 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.7914 -1.7891 -2.4939 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.9385 -1.2958 -3.8441 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.0242 0.1868 -4.0697 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.0869 0.9615 -3.4355 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.9902 0.9716 -1.9455 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.7913 -3.9874 2.1201 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.5178 -2.4337 1.6621 H 0 0 0 0 0 0 0 0 0 0 0 0 -8.5471 -3.6146 2.6029 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.6129 -1.7882 4.0706 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.8558 -3.4128 4.4534 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.6036 -1.3986 2.4971 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.9871 -2.9843 3.0232 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.4777 -0.5894 4.8071 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.7336 -2.1096 5.3381 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.7567 -0.1683 3.2112 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.0380 -1.8354 3.4996 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2918 0.5639 5.4896 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2500 -0.0143 6.3822 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2429 -2.2683 4.1437 H 0 0 0 0 0 0 0 0 0 0 0 0 0.1658 -1.4197 4.7524 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.4924 -3.2801 6.5333 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.3973 -4.3160 4.7494 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5829 -3.1845 7.8831 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.3726 -1.9045 8.1682 H 0 0 0 0 0 0 0 0 0 0 0 0 1.2486 -0.6466 6.2305 H 0 0 0 0 0 0 0 0 0 0 0 0 2.0325 -1.2439 7.7241 H 0 0 0 0 0 0 0 0 0 0 0 0 2.9951 -3.1024 6.5642 H 0 0 0 0 0 0 0 0 0 0 0 0 2.0918 -2.8071 5.0353 H 0 0 0 0 0 0 0 0 0 0 0 0 4.0709 -0.8989 6.4037 H 0 0 0 0 0 0 0 0 0 0 0 0 3.0966 -0.5584 4.9706 H 0 0 0 0 0 0 0 0 0 0 0 0 5.2225 -2.7518 5.3802 H 0 0 0 0 0 0 0 0 0 0 0 0 4.2732 -2.6513 3.8681 H 0 0 0 0 0 0 0 0 0 0 0 0 6.4942 -1.6649 3.7116 H 0 0 0 0 0 0 0 0 0 0 0 0 6.1647 -0.6163 5.1199 H 0 0 0 0 0 0 0 0 0 0 0 0 4.5604 -0.4726 2.4656 H 0 0 0 0 0 0 0 0 0 0 0 0 4.3487 0.5347 3.9707 H 0 0 0 0 0 0 0 0 0 0 0 0 6.7964 0.5681 2.1010 H 0 0 0 0 0 0 0 0 0 0 0 0 6.4925 1.6125 3.5649 H 0 0 0 0 0 0 0 0 0 0 0 0 3.1496 2.5329 0.1500 H 0 0 0 0 0 0 0 0 0 0 0 0 4.6101 3.5154 -0.1685 H 0 0 0 0 0 0 0 0 0 0 0 0 5.2339 2.0918 -2.0239 H 0 0 0 0 0 0 0 0 0 0 0 0 3.4773 2.5239 -3.5920 H 0 0 0 0 0 0 0 0 0 0 0 0 3.8544 3.9208 -2.5043 H 0 0 0 0 0 0 0 0 0 0 0 0 1.8464 5.5974 -1.7443 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.1891 5.8461 -2.7339 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.7800 5.9611 -5.0075 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.9552 3.9206 -4.8406 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2244 7.0734 -4.6879 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5834 7.9294 -4.2171 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.9928 7.1315 -2.5732 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.4073 9.0327 -1.9067 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.3518 6.7328 -1.1937 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.1543 4.8490 2.2367 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.6185 6.1944 1.7755 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.7847 4.2953 -1.2315 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.0282 5.0679 -2.3857 H 0 0 0 0 0 0 0 0 0 0 0 0 4.7162 -2.0488 -3.4019 H 0 0 0 0 0 0 0 0 0 0 0 0 5.5063 -2.1421 -1.8310 H 0 0 0 0 0 0 0 0 0 0 0 0 3.4851 -2.0772 -0.5741 H 0 0 0 0 0 0 0 0 0 0 0 0 3.6077 -3.4736 -1.6489 H 0 0 0 0 0 0 0 0 0 0 0 0 1.3427 -2.6609 -1.5543 H 0 0 0 0 0 0 0 0 0 0 0 0 1.8521 -0.9520 -1.9690 H 0 0 0 0 0 0 0 0 0 0 0 0 0.8084 -2.1075 -3.8152 H 0 0 0 0 0 0 0 0 0 0 0 0 2.4533 -1.6143 -4.2076 H 0 0 0 0 0 0 0 0 0 0 0 0 3.2328 -3.9839 -3.5772 H 0 0 0 0 0 0 0 0 0 0 0 0 1.5673 -4.3910 -3.1981 H 0 0 0 0 0 0 0 0 0 0 0 0 2.4685 -3.3735 -6.0023 H 0 0 0 0 0 0 0 0 0 0 0 0 2.5384 -5.0884 -5.5376 H 0 0 0 0 0 0 0 0 0 0 0 0 0.0847 -3.2712 -5.7276 H 0 0 0 0 0 0 0 0 0 0 0 0 0.6630 -4.5055 -6.9322 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5366 -6.2970 -5.0689 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.5182 -6.4029 -4.0667 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.2302 -3.6091 -5.1879 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2444 -4.9914 -4.8480 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.7247 -5.1021 -2.4955 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.5996 -3.6099 -2.9548 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5919 -3.6075 -2.6673 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.6215 -3.5591 -1.2380 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8940 -1.3335 -1.9494 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.6377 -1.5174 -1.7960 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2046 -1.6803 -4.5497 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.9430 -1.6992 -4.2913 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.0972 0.3242 -5.1934 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.0383 0.6829 -3.8210 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.9737 2.0352 -3.7845 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.1223 0.7079 -3.7878 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.0781 2.0556 -1.5673 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.7966 0.4660 -1.4070 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.9849 0.6937 -1.5631 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 1 0 9 11 1 0 11 12 1 0 11 13 1 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 2 0 20 22 1 0 22 23 1 0 23 24 1 0 24 25 1 0 25 26 1 0 26 27 1 0 27 28 2 0 27 29 1 0 27 30 1 0 30 31 1 0 31 32 1 0 32 33 1 0 32 34 1 0 34 35 1 0 34 36 1 0 36 37 1 0 36 38 1 0 38 39 1 0 39 40 1 0 40 41 2 0 40 42 1 0 40 43 1 0 38 44 1 0 44 45 1 0 24 46 1 0 46 47 1 0 47 48 2 0 47 49 1 0 49 50 1 0 50 51 1 0 51 52 1 0 52 53 1 0 53 54 1 0 54 55 1 0 55 56 1 0 56 57 2 0 57 58 1 0 58 59 1 0 59 60 1 0 60 61 1 0 61 62 1 0 62 63 1 0 63 64 1 0 64 65 1 0 44 31 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 1 10 82 1 0 11 83 1 1 12 84 1 0 13 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 18 95 1 0 18 96 1 0 19 97 1 0 19 98 1 0 23 99 1 0 23100 1 0 24101 1 6 25102 1 0 25103 1 0 29104 1 0 31105 1 1 32106 1 0 33107 1 0 34108 1 0 35109 1 0 36110 1 0 37111 1 0 38112 1 1 42113 1 0 43114 1 0 44115 1 0 45116 1 0 49117 1 0 49118 1 0 50119 1 0 50120 1 0 51121 1 0 51122 1 0 52123 1 0 52124 1 0 53125 1 0 53126 1 0 54127 1 0 54128 1 0 55129 1 0 55130 1 0 56131 1 0 57132 1 0 58133 1 0 58134 1 0 59135 1 0 59136 1 0 60137 1 0 60138 1 0 61139 1 0 61140 1 0 62141 1 0 62142 1 0 63143 1 0 63144 1 0 64145 1 0 64146 1 0 65147 1 0 65148 1 0 65149 1 0 M END 3D SDF for HMDB0279092 (PIP(18:1(12Z)-2OH(9,10)/18:1(9Z)))PIP(18:1(12Z)-2OH(9,10)/18:1(9Z)) Mrv1652309132113312D 66 66 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 -9.0669 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -9.7811 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -10.4952 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -11.2093 0.7694 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -11.2093 1.5408 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -11.9235 0.3563 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -11.9235 -0.4152 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -12.6376 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -13.3518 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -14.1768 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -14.8909 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -15.6050 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -16.3192 0.7694 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -17.0333 0.3563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -17.7475 0.7694 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 -11.0583 -0.7691 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 -13.9149 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -14.6290 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -15.3432 -0.7691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -16.0573 -0.3560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -16.7714 -0.7691 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 1 0 0 0 0 33 34 1 0 0 0 0 34 35 1 0 0 0 0 35 36 1 0 0 0 0 36 37 1 6 0 0 0 36 38 1 0 0 0 0 38 39 1 6 0 0 0 38 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 1 0 0 0 0 44 45 1 0 0 0 0 45 46 1 0 0 0 0 46 47 1 0 0 0 0 48 5 1 0 0 0 0 48 49 2 0 0 0 0 48 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 1 0 0 0 0 61 62 1 0 0 0 0 62 63 1 0 0 0 0 63 64 1 0 0 0 0 64 65 1 0 0 0 0 65 66 1 0 0 0 0 M END > <DATABASE_ID> HMDB0279092 > <DATABASE_NAME> hmdb > <SMILES> [H][C@@](COC(=O)CCCCCCC[C@@H](O)[C@H](O)C\C=C/CCCCC)(COP(O)(=O)O[C@H]1C(O)C(O)C(O)[C@@H](OP(O)(O)=O)C1O)OC(=O)CCCCCCC\C=C/CCCCCCCC > <INCHI_IDENTIFIER> InChI=1S/C45H84O18P2/c1-3-5-7-9-11-12-13-14-15-16-17-18-19-23-28-32-39(49)61-35(34-60-65(57,58)63-45-42(52)40(50)41(51)44(43(45)53)62-64(54,55)56)33-59-38(48)31-27-24-20-22-26-30-37(47)36(46)29-25-21-10-8-6-4-2/h14-15,21,25,35-37,40-47,50-53H,3-13,16-20,22-24,26-34H2,1-2H3,(H,57,58)(H2,54,55,56)/b15-14-,25-21-/t35-,36-,37-,40?,41?,42?,43?,44-,45+/m1/s1 > <INCHI_KEY> PZRXRBVHFWMQOY-BGUZILNVSA-N > <FORMULA> C45H84O18P2 > <MOLECULAR_WEIGHT> 975.097 > <EXACT_MASS> 974.513289861 > <JCHEM_ACCEPTOR_COUNT> 13 > <JCHEM_ATOM_COUNT> 149 > <JCHEM_AVERAGE_POLARIZABILITY> 107.26190820583875 > <JCHEM_BIOAVAILABILITY> 0 > <JCHEM_DONOR_COUNT> 9 > <JCHEM_FORMAL_CHARGE> 0 > <JCHEM_GHOSE_FILTER> 0 > <JCHEM_IUPAC> {[(1R,3S)-3-({[(2R)-3-{[(9R,10R,12Z)-9,10-dihydroxyoctadec-12-enoyl]oxy}-2-[(9Z)-octadec-9-enoyloxy]propoxy](hydroxy)phosphoryl}oxy)-2,4,5,6-tetrahydroxycyclohexyl]oxy}phosphonic acid > <ALOGPS_LOGP> 5.14 > <JCHEM_LOGP> 7.463299071333333 > <ALOGPS_LOGS> -4.66 > <JCHEM_MDDR_LIKE_RULE> 0 > <JCHEM_NUMBER_OF_RINGS> 1 > <JCHEM_PHYSIOLOGICAL_CHARGE> -3 > <JCHEM_PKA> 1.916652397772209 > <JCHEM_PKA_STRONGEST_ACIDIC> 1.0756803469746092 > <JCHEM_PKA_STRONGEST_BASIC> -3.169802256857242 > <JCHEM_POLAR_SURFACE_AREA> 296.49999999999994 > <JCHEM_REFRACTIVITY> 245.1089 > <JCHEM_ROTATABLE_BOND_COUNT> 42 > <JCHEM_RULE_OF_FIVE> 0 > <ALOGPS_SOLUBILITY> 2.12e-02 g/l > <JCHEM_TRADITIONAL_IUPAC> [(1R,3S)-3-{[(2R)-3-{[(9R,10R,12Z)-9,10-dihydroxyoctadec-12-enoyl]oxy}-2-[(9Z)-octadec-9-enoyloxy]propoxy(hydroxy)phosphoryl]oxy}-2,4,5,6-tetrahydroxycyclohexyl]oxyphosphonic acid > <JCHEM_VEBER_RULE> 0 $$$$ 3D-SDF for HMDB0279092 (PIP(18:1(12Z)-2OH(9,10)/18:1(9Z)))HMDB0279092 RDKit 3D PIP(18:1(12Z)-2OH(9,10)/18:1(9Z)) 149149 0 0 0 0 0 0 0 0999 V2000 -7.5395 -3.2373 2.4489 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.9506 -2.6069 3.7148 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.5978 -2.1028 3.3390 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.8496 -1.4361 4.4861 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.4861 -0.9638 3.9536 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.7721 -0.3146 5.0541 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6079 -0.6642 5.5592 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8530 -1.7949 5.0635 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.5609 -2.8842 6.1137 C 0 0 1 0 0 0 0 0 0 0 0 0 0.1848 -3.8930 5.4538 O 0 0 0 0 0 0 0 0 0 0 0 0 0.2951 -2.3473 7.2264 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.5126 -1.4262 7.9760 O 0 0 0 0 0 0 0 0 0 0 0 0 1.4996 -1.5883 6.7741 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4926 -2.3487 5.9480 C 0 0 0 0 0 0 0 0 0 0 0 0 3.6172 -1.3652 5.5204 C 0 0 0 0 0 0 0 0 0 0 0 0 4.6638 -2.0693 4.7037 C 0 0 0 0 0 0 0 0 0 0 0 0 5.7223 -1.0656 4.2116 C 0 0 0 0 0 0 0 0 0 0 0 0 5.0795 -0.0465 3.3432 C 0 0 0 0 0 0 0 0 0 0 0 0 6.0371 1.0028 2.7689 C 0 0 0 0 0 0 0 0 0 0 0 0 5.1793 1.9211 1.9184 C 0 0 0 0 0 0 0 0 0 0 0 0 4.6402 2.8851 2.4922 O 0 0 0 0 0 0 0 0 0 0 0 0 5.0152 1.6711 0.5747 O 0 0 0 0 0 0 0 0 0 0 0 0 4.1944 2.4908 -0.2237 C 0 0 0 0 0 0 0 0 0 0 0 0 4.1902 2.0064 -1.6760 C 0 0 2 0 0 0 0 0 0 0 0 0 3.3727 2.9165 -2.5375 C 0 0 0 0 0 0 0 0 0 0 0 0 2.0310 2.9659 -2.2453 O 0 0 0 0 0 0 0 0 0 0 0 0 1.3369 4.1157 -3.3004 P 0 0 0 0 0 5 0 0 0 0 0 0 1.9736 4.0175 -4.6667 O 0 0 0 0 0 0 0 0 0 0 0 0 1.7176 5.6830 -2.7246 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.3332 3.9320 -3.4382 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.9501 5.1192 -3.0841 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.6161 5.7726 -4.2745 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4073 4.8033 -4.8903 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.3454 7.0101 -3.9734 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.5418 8.1039 -4.3857 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.8755 7.2331 -2.6092 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.6070 8.5524 -2.2385 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.3272 6.3387 -1.5395 C 0 0 1 0 0 0 0 0 0 0 0 0 -3.2328 6.1908 -0.4876 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.6293 6.6745 0.9921 P 0 0 0 0 0 5 0 0 0 0 0 0 -1.8782 7.9828 0.9007 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.6417 5.5341 1.7298 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.9714 6.9255 2.0168 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.0530 4.9310 -2.0663 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.2501 4.5528 -2.6987 O 0 0 0 0 0 0 0 0 0 0 0 0 3.7916 0.6523 -1.7361 O 0 0 0 0 0 0 0 0 0 0 0 0 4.7081 -0.2637 -2.2008 C 0 0 0 0 0 0 0 0 0 0 0 0 5.8635 0.1883 -2.5762 O 0 0 0 0 0 0 0 0 0 0 0 0 4.5724 -1.7138 -2.3334 C 0 0 0 0 0 0 0 0 0 0 0 0 3.4301 -2.3653 -1.6770 C 0 0 0 0 0 0 0 0 0 0 0 0 2.0549 -2.0246 -2.1150 C 0 0 0 0 0 0 0 0 0 0 0 0 1.8404 -2.3296 -3.5950 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1764 -3.7538 -3.9045 C 0 0 0 0 0 0 0 0 0 0 0 0 1.9635 -4.1205 -5.3114 C 0 0 0 0 0 0 0 0 0 0 0 0 0.5611 -4.2526 -5.8457 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0873 -5.3409 -5.1420 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.2242 -5.4159 -4.5939 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.3015 -4.4263 -4.4921 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.5939 -4.1279 -3.0558 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6162 -3.2756 -2.3271 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.7914 -1.7891 -2.4939 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.9385 -1.2958 -3.8441 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.0242 0.1868 -4.0697 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.0869 0.9615 -3.4355 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.9902 0.9716 -1.9455 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.7913 -3.9874 2.1201 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.5178 -2.4337 1.6621 H 0 0 0 0 0 0 0 0 0 0 0 0 -8.5471 -3.6146 2.6029 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.6129 -1.7882 4.0706 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.8558 -3.4128 4.4534 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.6036 -1.3986 2.4971 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.9871 -2.9843 3.0232 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.4777 -0.5894 4.8071 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.7336 -2.1096 5.3381 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.7567 -0.1683 3.2112 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.0380 -1.8354 3.4996 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2918 0.5639 5.4896 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2500 -0.0143 6.3822 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2429 -2.2683 4.1437 H 0 0 0 0 0 0 0 0 0 0 0 0 0.1658 -1.4197 4.7524 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.4924 -3.2801 6.5333 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.3973 -4.3160 4.7494 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5829 -3.1845 7.8831 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.3726 -1.9045 8.1682 H 0 0 0 0 0 0 0 0 0 0 0 0 1.2486 -0.6466 6.2305 H 0 0 0 0 0 0 0 0 0 0 0 0 2.0325 -1.2439 7.7241 H 0 0 0 0 0 0 0 0 0 0 0 0 2.9951 -3.1024 6.5642 H 0 0 0 0 0 0 0 0 0 0 0 0 2.0918 -2.8071 5.0353 H 0 0 0 0 0 0 0 0 0 0 0 0 4.0709 -0.8989 6.4037 H 0 0 0 0 0 0 0 0 0 0 0 0 3.0966 -0.5584 4.9706 H 0 0 0 0 0 0 0 0 0 0 0 0 5.2225 -2.7518 5.3802 H 0 0 0 0 0 0 0 0 0 0 0 0 4.2732 -2.6513 3.8681 H 0 0 0 0 0 0 0 0 0 0 0 0 6.4942 -1.6649 3.7116 H 0 0 0 0 0 0 0 0 0 0 0 0 6.1647 -0.6163 5.1199 H 0 0 0 0 0 0 0 0 0 0 0 0 4.5604 -0.4726 2.4656 H 0 0 0 0 0 0 0 0 0 0 0 0 4.3487 0.5347 3.9707 H 0 0 0 0 0 0 0 0 0 0 0 0 6.7964 0.5681 2.1010 H 0 0 0 0 0 0 0 0 0 0 0 0 6.4925 1.6125 3.5649 H 0 0 0 0 0 0 0 0 0 0 0 0 3.1496 2.5329 0.1500 H 0 0 0 0 0 0 0 0 0 0 0 0 4.6101 3.5154 -0.1685 H 0 0 0 0 0 0 0 0 0 0 0 0 5.2339 2.0918 -2.0239 H 0 0 0 0 0 0 0 0 0 0 0 0 3.4773 2.5239 -3.5920 H 0 0 0 0 0 0 0 0 0 0 0 0 3.8544 3.9208 -2.5043 H 0 0 0 0 0 0 0 0 0 0 0 0 1.8464 5.5974 -1.7443 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.1891 5.8461 -2.7339 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.7800 5.9611 -5.0075 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.9552 3.9206 -4.8406 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2244 7.0734 -4.6879 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5834 7.9294 -4.2171 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.9928 7.1315 -2.5732 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.4073 9.0327 -1.9067 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.3518 6.7328 -1.1937 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.1543 4.8490 2.2367 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.6185 6.1944 1.7755 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.7847 4.2953 -1.2315 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.0282 5.0679 -2.3857 H 0 0 0 0 0 0 0 0 0 0 0 0 4.7162 -2.0488 -3.4019 H 0 0 0 0 0 0 0 0 0 0 0 0 5.5063 -2.1421 -1.8310 H 0 0 0 0 0 0 0 0 0 0 0 0 3.4851 -2.0772 -0.5741 H 0 0 0 0 0 0 0 0 0 0 0 0 3.6077 -3.4736 -1.6489 H 0 0 0 0 0 0 0 0 0 0 0 0 1.3427 -2.6609 -1.5543 H 0 0 0 0 0 0 0 0 0 0 0 0 1.8521 -0.9520 -1.9690 H 0 0 0 0 0 0 0 0 0 0 0 0 0.8084 -2.1075 -3.8152 H 0 0 0 0 0 0 0 0 0 0 0 0 2.4533 -1.6143 -4.2076 H 0 0 0 0 0 0 0 0 0 0 0 0 3.2328 -3.9839 -3.5772 H 0 0 0 0 0 0 0 0 0 0 0 0 1.5673 -4.3910 -3.1981 H 0 0 0 0 0 0 0 0 0 0 0 0 2.4685 -3.3735 -6.0023 H 0 0 0 0 0 0 0 0 0 0 0 0 2.5384 -5.0884 -5.5376 H 0 0 0 0 0 0 0 0 0 0 0 0 0.0847 -3.2712 -5.7276 H 0 0 0 0 0 0 0 0 0 0 0 0 0.6630 -4.5055 -6.9322 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5366 -6.2970 -5.0689 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.5182 -6.4029 -4.0667 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.2302 -3.6091 -5.1879 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2444 -4.9914 -4.8480 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.7247 -5.1021 -2.4955 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.5996 -3.6099 -2.9548 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5919 -3.6075 -2.6673 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.6215 -3.5591 -1.2380 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8940 -1.3335 -1.9494 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.6377 -1.5174 -1.7960 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2046 -1.6803 -4.5497 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.9430 -1.6992 -4.2913 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.0972 0.3242 -5.1934 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.0383 0.6829 -3.8210 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.9737 2.0352 -3.7845 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.1223 0.7079 -3.7878 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.0781 2.0556 -1.5673 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.7966 0.4660 -1.4070 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.9849 0.6937 -1.5631 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 1 0 9 11 1 0 11 12 1 0 11 13 1 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 2 0 20 22 1 0 22 23 1 0 23 24 1 0 24 25 1 0 25 26 1 0 26 27 1 0 27 28 2 0 27 29 1 0 27 30 1 0 30 31 1 0 31 32 1 0 32 33 1 0 32 34 1 0 34 35 1 0 34 36 1 0 36 37 1 0 36 38 1 0 38 39 1 0 39 40 1 0 40 41 2 0 40 42 1 0 40 43 1 0 38 44 1 0 44 45 1 0 24 46 1 0 46 47 1 0 47 48 2 0 47 49 1 0 49 50 1 0 50 51 1 0 51 52 1 0 52 53 1 0 53 54 1 0 54 55 1 0 55 56 1 0 56 57 2 0 57 58 1 0 58 59 1 0 59 60 1 0 60 61 1 0 61 62 1 0 62 63 1 0 63 64 1 0 64 65 1 0 44 31 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 1 10 82 1 0 11 83 1 1 12 84 1 0 13 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 18 95 1 0 18 96 1 0 19 97 1 0 19 98 1 0 23 99 1 0 23100 1 0 24101 1 6 25102 1 0 25103 1 0 29104 1 0 31105 1 1 32106 1 0 33107 1 0 34108 1 0 35109 1 0 36110 1 0 37111 1 0 38112 1 1 42113 1 0 43114 1 0 44115 1 0 45116 1 0 49117 1 0 49118 1 0 50119 1 0 50120 1 0 51121 1 0 51122 1 0 52123 1 0 52124 1 0 53125 1 0 53126 1 0 54127 1 0 54128 1 0 55129 1 0 55130 1 0 56131 1 0 57132 1 0 58133 1 0 58134 1 0 59135 1 0 59136 1 0 60137 1 0 60138 1 0 61139 1 0 61140 1 0 62141 1 0 62142 1 0 63143 1 0 63144 1 0 64145 1 0 64146 1 0 65147 1 0 65148 1 0 65149 1 0 M END PDB for HMDB0279092 (PIP(18:1(12Z)-2OH(9,10)/18:1(9Z)))HEADER PROTEIN 13-SEP-21 NONE TITLE NULL COMPND MOLECULE: PIP(18:1(12Z)-2OH(9,10)/18:1(9Z)) 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 -16.925 0.665 0.000 0.00 0.00 C+0 HETATM 34 C UNK 0 -18.258 1.436 0.000 0.00 0.00 C+0 HETATM 35 C UNK 0 -19.591 0.665 0.000 0.00 0.00 C+0 HETATM 36 C UNK 0 -20.924 1.436 0.000 0.00 0.00 C+0 HETATM 37 O UNK 0 -20.924 2.876 0.000 0.00 0.00 O+0 HETATM 38 C UNK 0 -22.257 0.665 0.000 0.00 0.00 C+0 HETATM 39 O UNK 0 -22.257 -0.775 0.000 0.00 0.00 O+0 HETATM 40 C UNK 0 -23.590 1.436 0.000 0.00 0.00 C+0 HETATM 41 C UNK 0 -24.923 0.665 0.000 0.00 0.00 C+0 HETATM 42 C UNK 0 -26.463 0.665 0.000 0.00 0.00 C+0 HETATM 43 C UNK 0 -27.796 1.436 0.000 0.00 0.00 C+0 HETATM 44 C UNK 0 -29.129 0.665 0.000 0.00 0.00 C+0 HETATM 45 C UNK 0 -30.463 1.436 0.000 0.00 0.00 C+0 HETATM 46 C UNK 0 -31.796 0.665 0.000 0.00 0.00 C+0 HETATM 47 C UNK 0 -33.129 1.436 0.000 0.00 0.00 C+0 HETATM 48 C UNK 0 -8.438 -1.436 0.000 0.00 0.00 C+0 HETATM 49 O UNK 0 -8.438 -2.876 0.000 0.00 0.00 O+0 HETATM 50 C UNK 0 -9.771 -0.665 0.000 0.00 0.00 C+0 HETATM 51 C UNK 0 -11.104 -1.436 0.000 0.00 0.00 C+0 HETATM 52 C UNK 0 -12.437 -0.665 0.000 0.00 0.00 C+0 HETATM 53 C UNK 0 -13.770 -1.436 0.000 0.00 0.00 C+0 HETATM 54 C UNK 0 -15.103 -0.665 0.000 0.00 0.00 C+0 HETATM 55 C UNK 0 -16.436 -1.436 0.000 0.00 0.00 C+0 HETATM 56 C UNK 0 -17.769 -0.665 0.000 0.00 0.00 C+0 HETATM 57 C UNK 0 -19.102 -1.436 0.000 0.00 0.00 C+0 HETATM 58 C UNK 0 -20.642 -1.436 0.000 0.00 0.00 C+0 HETATM 59 C UNK 0 -21.975 -0.665 0.000 0.00 0.00 C+0 HETATM 60 C UNK 0 -23.308 -1.436 0.000 0.00 0.00 C+0 HETATM 61 C UNK 0 -24.641 -0.665 0.000 0.00 0.00 C+0 HETATM 62 C UNK 0 -25.974 -1.436 0.000 0.00 0.00 C+0 HETATM 63 C UNK 0 -27.307 -0.665 0.000 0.00 0.00 C+0 HETATM 64 C UNK 0 -28.641 -1.436 0.000 0.00 0.00 C+0 HETATM 65 C UNK 0 -29.974 -0.665 0.000 0.00 0.00 C+0 HETATM 66 C UNK 0 -31.307 -1.436 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 48 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 CONECT 35 34 36 CONECT 36 35 37 38 CONECT 37 36 CONECT 38 36 39 40 CONECT 39 38 CONECT 40 38 41 CONECT 41 40 42 CONECT 42 41 43 CONECT 43 42 44 CONECT 44 43 45 CONECT 45 44 46 CONECT 46 45 47 CONECT 47 46 CONECT 48 5 49 50 CONECT 49 48 CONECT 50 48 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 MASTER 0 0 0 0 0 0 0 0 66 0 132 0 END 3D PDB for HMDB0279092 (PIP(18:1(12Z)-2OH(9,10)/18:1(9Z)))COMPND HMDB0279092 HETATM 1 C1 UNL 1 -7.539 -3.237 2.449 1.00 0.00 C HETATM 2 C2 UNL 1 -6.951 -2.607 3.715 1.00 0.00 C HETATM 3 C3 UNL 1 -5.598 -2.103 3.339 1.00 0.00 C HETATM 4 C4 UNL 1 -4.850 -1.436 4.486 1.00 0.00 C HETATM 5 C5 UNL 1 -3.486 -0.964 3.954 1.00 0.00 C HETATM 6 C6 UNL 1 -2.772 -0.315 5.054 1.00 0.00 C HETATM 7 C7 UNL 1 -1.608 -0.664 5.559 1.00 0.00 C HETATM 8 C8 UNL 1 -0.853 -1.795 5.063 1.00 0.00 C HETATM 9 C9 UNL 1 -0.561 -2.884 6.114 1.00 0.00 C HETATM 10 O1 UNL 1 0.185 -3.893 5.454 1.00 0.00 O HETATM 11 C10 UNL 1 0.295 -2.347 7.226 1.00 0.00 C HETATM 12 O2 UNL 1 -0.513 -1.426 7.976 1.00 0.00 O HETATM 13 C11 UNL 1 1.500 -1.588 6.774 1.00 0.00 C HETATM 14 C12 UNL 1 2.493 -2.349 5.948 1.00 0.00 C HETATM 15 C13 UNL 1 3.617 -1.365 5.520 1.00 0.00 C HETATM 16 C14 UNL 1 4.664 -2.069 4.704 1.00 0.00 C HETATM 17 C15 UNL 1 5.722 -1.066 4.212 1.00 0.00 C HETATM 18 C16 UNL 1 5.079 -0.047 3.343 1.00 0.00 C HETATM 19 C17 UNL 1 6.037 1.003 2.769 1.00 0.00 C HETATM 20 C18 UNL 1 5.179 1.921 1.918 1.00 0.00 C HETATM 21 O3 UNL 1 4.640 2.885 2.492 1.00 0.00 O HETATM 22 O4 UNL 1 5.015 1.671 0.575 1.00 0.00 O HETATM 23 C19 UNL 1 4.194 2.491 -0.224 1.00 0.00 C HETATM 24 C20 UNL 1 4.190 2.006 -1.676 1.00 0.00 C HETATM 25 C21 UNL 1 3.373 2.917 -2.538 1.00 0.00 C HETATM 26 O5 UNL 1 2.031 2.966 -2.245 1.00 0.00 O HETATM 27 P1 UNL 1 1.337 4.116 -3.300 1.00 0.00 P HETATM 28 O6 UNL 1 1.974 4.018 -4.667 1.00 0.00 O HETATM 29 O7 UNL 1 1.718 5.683 -2.725 1.00 0.00 O HETATM 30 O8 UNL 1 -0.333 3.932 -3.438 1.00 0.00 O HETATM 31 C22 UNL 1 -0.950 5.119 -3.084 1.00 0.00 C HETATM 32 C23 UNL 1 -1.616 5.773 -4.274 1.00 0.00 C HETATM 33 O9 UNL 1 -2.407 4.803 -4.890 1.00 0.00 O HETATM 34 C24 UNL 1 -2.345 7.010 -3.973 1.00 0.00 C HETATM 35 O10 UNL 1 -1.542 8.104 -4.386 1.00 0.00 O HETATM 36 C25 UNL 1 -2.876 7.233 -2.609 1.00 0.00 C HETATM 37 O11 UNL 1 -2.607 8.552 -2.238 1.00 0.00 O HETATM 38 C26 UNL 1 -2.327 6.339 -1.540 1.00 0.00 C HETATM 39 O12 UNL 1 -3.233 6.191 -0.488 1.00 0.00 O HETATM 40 P2 UNL 1 -2.629 6.674 0.992 1.00 0.00 P HETATM 41 O13 UNL 1 -1.878 7.983 0.901 1.00 0.00 O HETATM 42 O14 UNL 1 -1.642 5.534 1.730 1.00 0.00 O HETATM 43 O15 UNL 1 -3.971 6.926 2.017 1.00 0.00 O HETATM 44 C27 UNL 1 -2.053 4.931 -2.066 1.00 0.00 C HETATM 45 O16 UNL 1 -3.250 4.553 -2.699 1.00 0.00 O HETATM 46 O17 UNL 1 3.792 0.652 -1.736 1.00 0.00 O HETATM 47 C28 UNL 1 4.708 -0.264 -2.201 1.00 0.00 C HETATM 48 O18 UNL 1 5.863 0.188 -2.576 1.00 0.00 O HETATM 49 C29 UNL 1 4.572 -1.714 -2.333 1.00 0.00 C HETATM 50 C30 UNL 1 3.430 -2.365 -1.677 1.00 0.00 C HETATM 51 C31 UNL 1 2.055 -2.025 -2.115 1.00 0.00 C HETATM 52 C32 UNL 1 1.840 -2.330 -3.595 1.00 0.00 C HETATM 53 C33 UNL 1 2.176 -3.754 -3.905 1.00 0.00 C HETATM 54 C34 UNL 1 1.964 -4.121 -5.311 1.00 0.00 C HETATM 55 C35 UNL 1 0.561 -4.253 -5.846 1.00 0.00 C HETATM 56 C36 UNL 1 -0.087 -5.341 -5.142 1.00 0.00 C HETATM 57 C37 UNL 1 -1.224 -5.416 -4.594 1.00 0.00 C HETATM 58 C38 UNL 1 -2.302 -4.426 -4.492 1.00 0.00 C HETATM 59 C39 UNL 1 -2.594 -4.128 -3.056 1.00 0.00 C HETATM 60 C40 UNL 1 -1.616 -3.276 -2.327 1.00 0.00 C HETATM 61 C41 UNL 1 -1.791 -1.789 -2.494 1.00 0.00 C HETATM 62 C42 UNL 1 -1.938 -1.296 -3.844 1.00 0.00 C HETATM 63 C43 UNL 1 -2.024 0.187 -4.070 1.00 0.00 C HETATM 64 C44 UNL 1 -3.087 0.962 -3.435 1.00 0.00 C HETATM 65 C45 UNL 1 -2.990 0.972 -1.946 1.00 0.00 C HETATM 66 H1 UNL 1 -6.791 -3.987 2.120 1.00 0.00 H HETATM 67 H2 UNL 1 -7.518 -2.434 1.662 1.00 0.00 H HETATM 68 H3 UNL 1 -8.547 -3.615 2.603 1.00 0.00 H HETATM 69 H4 UNL 1 -7.613 -1.788 4.071 1.00 0.00 H HETATM 70 H5 UNL 1 -6.856 -3.413 4.453 1.00 0.00 H HETATM 71 H6 UNL 1 -5.604 -1.399 2.497 1.00 0.00 H HETATM 72 H7 UNL 1 -4.987 -2.984 3.023 1.00 0.00 H HETATM 73 H8 UNL 1 -5.478 -0.589 4.807 1.00 0.00 H HETATM 74 H9 UNL 1 -4.734 -2.110 5.338 1.00 0.00 H HETATM 75 H10 UNL 1 -3.757 -0.168 3.211 1.00 0.00 H HETATM 76 H11 UNL 1 -3.038 -1.835 3.500 1.00 0.00 H HETATM 77 H12 UNL 1 -3.292 0.564 5.490 1.00 0.00 H HETATM 78 H13 UNL 1 -1.250 -0.014 6.382 1.00 0.00 H HETATM 79 H14 UNL 1 -1.243 -2.268 4.144 1.00 0.00 H HETATM 80 H15 UNL 1 0.166 -1.420 4.752 1.00 0.00 H HETATM 81 H16 UNL 1 -1.492 -3.280 6.533 1.00 0.00 H HETATM 82 H17 UNL 1 -0.397 -4.316 4.749 1.00 0.00 H HETATM 83 H18 UNL 1 0.583 -3.184 7.883 1.00 0.00 H HETATM 84 H19 UNL 1 -1.373 -1.904 8.168 1.00 0.00 H HETATM 85 H20 UNL 1 1.249 -0.647 6.230 1.00 0.00 H HETATM 86 H21 UNL 1 2.033 -1.244 7.724 1.00 0.00 H HETATM 87 H22 UNL 1 2.995 -3.102 6.564 1.00 0.00 H HETATM 88 H23 UNL 1 2.092 -2.807 5.035 1.00 0.00 H HETATM 89 H24 UNL 1 4.071 -0.899 6.404 1.00 0.00 H HETATM 90 H25 UNL 1 3.097 -0.558 4.971 1.00 0.00 H HETATM 91 H26 UNL 1 5.222 -2.752 5.380 1.00 0.00 H HETATM 92 H27 UNL 1 4.273 -2.651 3.868 1.00 0.00 H HETATM 93 H28 UNL 1 6.494 -1.665 3.712 1.00 0.00 H HETATM 94 H29 UNL 1 6.165 -0.616 5.120 1.00 0.00 H HETATM 95 H30 UNL 1 4.560 -0.473 2.466 1.00 0.00 H HETATM 96 H31 UNL 1 4.349 0.535 3.971 1.00 0.00 H HETATM 97 H32 UNL 1 6.796 0.568 2.101 1.00 0.00 H HETATM 98 H33 UNL 1 6.493 1.612 3.565 1.00 0.00 H HETATM 99 H34 UNL 1 3.150 2.533 0.150 1.00 0.00 H HETATM 100 H35 UNL 1 4.610 3.515 -0.168 1.00 0.00 H HETATM 101 H36 UNL 1 5.234 2.092 -2.024 1.00 0.00 H HETATM 102 H37 UNL 1 3.477 2.524 -3.592 1.00 0.00 H HETATM 103 H38 UNL 1 3.854 3.921 -2.504 1.00 0.00 H HETATM 104 H39 UNL 1 1.846 5.597 -1.744 1.00 0.00 H HETATM 105 H40 UNL 1 -0.189 5.846 -2.734 1.00 0.00 H HETATM 106 H41 UNL 1 -0.780 5.961 -5.008 1.00 0.00 H HETATM 107 H42 UNL 1 -1.955 3.921 -4.841 1.00 0.00 H HETATM 108 H43 UNL 1 -3.224 7.073 -4.688 1.00 0.00 H HETATM 109 H44 UNL 1 -0.583 7.929 -4.217 1.00 0.00 H HETATM 110 H45 UNL 1 -3.993 7.132 -2.573 1.00 0.00 H HETATM 111 H46 UNL 1 -3.407 9.033 -1.907 1.00 0.00 H HETATM 112 H47 UNL 1 -1.352 6.733 -1.194 1.00 0.00 H HETATM 113 H48 UNL 1 -2.154 4.849 2.237 1.00 0.00 H HETATM 114 H49 UNL 1 -4.618 6.194 1.775 1.00 0.00 H HETATM 115 H50 UNL 1 -1.785 4.295 -1.231 1.00 0.00 H HETATM 116 H51 UNL 1 -4.028 5.068 -2.386 1.00 0.00 H HETATM 117 H52 UNL 1 4.716 -2.049 -3.402 1.00 0.00 H HETATM 118 H53 UNL 1 5.506 -2.142 -1.831 1.00 0.00 H HETATM 119 H54 UNL 1 3.485 -2.077 -0.574 1.00 0.00 H HETATM 120 H55 UNL 1 3.608 -3.474 -1.649 1.00 0.00 H HETATM 121 H56 UNL 1 1.343 -2.661 -1.554 1.00 0.00 H HETATM 122 H57 UNL 1 1.852 -0.952 -1.969 1.00 0.00 H HETATM 123 H58 UNL 1 0.808 -2.108 -3.815 1.00 0.00 H HETATM 124 H59 UNL 1 2.453 -1.614 -4.208 1.00 0.00 H HETATM 125 H60 UNL 1 3.233 -3.984 -3.577 1.00 0.00 H HETATM 126 H61 UNL 1 1.567 -4.391 -3.198 1.00 0.00 H HETATM 127 H62 UNL 1 2.469 -3.373 -6.002 1.00 0.00 H HETATM 128 H63 UNL 1 2.538 -5.088 -5.538 1.00 0.00 H HETATM 129 H64 UNL 1 0.085 -3.271 -5.728 1.00 0.00 H HETATM 130 H65 UNL 1 0.663 -4.505 -6.932 1.00 0.00 H HETATM 131 H66 UNL 1 0.537 -6.297 -5.069 1.00 0.00 H HETATM 132 H67 UNL 1 -1.518 -6.403 -4.067 1.00 0.00 H HETATM 133 H68 UNL 1 -2.230 -3.609 -5.188 1.00 0.00 H HETATM 134 H69 UNL 1 -3.244 -4.991 -4.848 1.00 0.00 H HETATM 135 H70 UNL 1 -2.725 -5.102 -2.496 1.00 0.00 H HETATM 136 H71 UNL 1 -3.600 -3.610 -2.955 1.00 0.00 H HETATM 137 H72 UNL 1 -0.592 -3.607 -2.667 1.00 0.00 H HETATM 138 H73 UNL 1 -1.621 -3.559 -1.238 1.00 0.00 H HETATM 139 H74 UNL 1 -0.894 -1.333 -1.949 1.00 0.00 H HETATM 140 H75 UNL 1 -2.638 -1.517 -1.796 1.00 0.00 H HETATM 141 H76 UNL 1 -1.205 -1.680 -4.550 1.00 0.00 H HETATM 142 H77 UNL 1 -2.943 -1.699 -4.291 1.00 0.00 H HETATM 143 H78 UNL 1 -2.097 0.324 -5.193 1.00 0.00 H HETATM 144 H79 UNL 1 -1.038 0.683 -3.821 1.00 0.00 H HETATM 145 H80 UNL 1 -2.974 2.035 -3.785 1.00 0.00 H HETATM 146 H81 UNL 1 -4.122 0.708 -3.788 1.00 0.00 H HETATM 147 H82 UNL 1 -3.078 2.056 -1.567 1.00 0.00 H HETATM 148 H83 UNL 1 -3.797 0.466 -1.407 1.00 0.00 H HETATM 149 H84 UNL 1 -1.985 0.694 -1.563 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 11 81 CONECT 10 82 CONECT 11 12 13 83 CONECT 12 84 CONECT 13 14 85 86 CONECT 14 15 87 88 CONECT 15 16 89 90 CONECT 16 17 91 92 CONECT 17 18 93 94 CONECT 18 19 95 96 CONECT 19 20 97 98 CONECT 20 21 21 22 CONECT 22 23 CONECT 23 24 99 100 CONECT 24 25 46 101 CONECT 25 26 102 103 CONECT 26 27 CONECT 27 28 28 29 30 CONECT 29 104 CONECT 30 31 CONECT 31 32 44 105 CONECT 32 33 34 106 CONECT 33 107 CONECT 34 35 36 108 CONECT 35 109 CONECT 36 37 38 110 CONECT 37 111 CONECT 38 39 44 112 CONECT 39 40 CONECT 40 41 41 42 43 CONECT 42 113 CONECT 43 114 CONECT 44 45 115 CONECT 45 116 CONECT 46 47 CONECT 47 48 48 49 CONECT 49 50 117 118 CONECT 50 51 119 120 CONECT 51 52 121 122 CONECT 52 53 123 124 CONECT 53 54 125 126 CONECT 54 55 127 128 CONECT 55 56 129 130 CONECT 56 57 57 131 CONECT 57 58 132 CONECT 58 59 133 134 CONECT 59 60 135 136 CONECT 60 61 137 138 CONECT 61 62 139 140 CONECT 62 63 141 142 CONECT 63 64 143 144 CONECT 64 65 145 146 CONECT 65 147 148 149 END SMILES for HMDB0279092 (PIP(18:1(12Z)-2OH(9,10)/18:1(9Z)))[H][C@@](COC(=O)CCCCCCC[C@@H](O)[C@H](O)C\C=C/CCCCC)(COP(O)(=O)O[C@H]1C(O)C(O)C(O)[C@@H](OP(O)(O)=O)C1O)OC(=O)CCCCCCC\C=C/CCCCCCCC INCHI for HMDB0279092 (PIP(18:1(12Z)-2OH(9,10)/18:1(9Z)))InChI=1S/C45H84O18P2/c1-3-5-7-9-11-12-13-14-15-16-17-18-19-23-28-32-39(49)61-35(34-60-65(57,58)63-45-42(52)40(50)41(51)44(43(45)53)62-64(54,55)56)33-59-38(48)31-27-24-20-22-26-30-37(47)36(46)29-25-21-10-8-6-4-2/h14-15,21,25,35-37,40-47,50-53H,3-13,16-20,22-24,26-34H2,1-2H3,(H,57,58)(H2,54,55,56)/b15-14-,25-21-/t35-,36-,37-,40?,41?,42?,43?,44-,45+/m1/s1 3D Structure for HMDB0279092 (PIP(18:1(12Z)-2OH(9,10)/18:1(9Z))) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms |
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Chemical Formula | C45H84O18P2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Average Molecular Weight | 975.097 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Monoisotopic Molecular Weight | 974.513289861 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
IUPAC Name | {[(1R,3S)-3-({[(2R)-3-{[(9R,10R,12Z)-9,10-dihydroxyoctadec-12-enoyl]oxy}-2-[(9Z)-octadec-9-enoyloxy]propoxy](hydroxy)phosphoryl}oxy)-2,4,5,6-tetrahydroxycyclohexyl]oxy}phosphonic acid | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Traditional Name | [(1R,3S)-3-{[(2R)-3-{[(9R,10R,12Z)-9,10-dihydroxyoctadec-12-enoyl]oxy}-2-[(9Z)-octadec-9-enoyloxy]propoxy(hydroxy)phosphoryl]oxy}-2,4,5,6-tetrahydroxycyclohexyl]oxyphosphonic acid | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
CAS Registry Number | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
SMILES | [H][C@@](COC(=O)CCCCCCC[C@@H](O)[C@H](O)C\C=C/CCCCC)(COP(O)(=O)O[C@H]1C(O)C(O)C(O)[C@@H](OP(O)(O)=O)C1O)OC(=O)CCCCCCC\C=C/CCCCCCCC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
InChI Identifier | InChI=1S/C45H84O18P2/c1-3-5-7-9-11-12-13-14-15-16-17-18-19-23-28-32-39(49)61-35(34-60-65(57,58)63-45-42(52)40(50)41(51)44(43(45)53)62-64(54,55)56)33-59-38(48)31-27-24-20-22-26-30-37(47)36(46)29-25-21-10-8-6-4-2/h14-15,21,25,35-37,40-47,50-53H,3-13,16-20,22-24,26-34H2,1-2H3,(H,57,58)(H2,54,55,56)/b15-14-,25-21-/t35-,36-,37-,40?,41?,42?,43?,44-,45+/m1/s1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
InChI Key | PZRXRBVHFWMQOY-BGUZILNVSA-N | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Chemical Taxonomy | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Classification | Not classified | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ontology | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Physiological effect | Health effect
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Disposition | Biological location
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Process | Naturally occurring process
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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 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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 |