Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Predicted

Creation Date

2021-09-21 20:22:56 UTC

Update Date

2021-10-01 16:52:14 UTC

HMDB ID

HMDB0300997

Secondary Accession Numbers

None

Metabolite Identification

Common Name

(5E,7E)-Undeca-2,5,7-trienedioyl-CoA

Description

(5e,7e)-undeca-2,5,7-trienedioyl-coa is an acyl-CoA or acyl-coenzyme A. More specifically, it is a (5E_7E)-undeca-2_5_7-trienedioic acid thioester of coenzyme A. (5e,7e)-undeca-2,5,7-trienedioyl-coa is an acyl-CoA with 11 fatty acid group as the acyl moiety attached to coenzyme A. Coenzyme A was discovered in 1946 by Fritz Lipmann (Journal of Biological Chemistry (1946) 162 (3): 743–744) and its structure was determined in the early 1950s at the Lister Institute in London. Coenzyme A is a complex, thiol-containing molecule that is naturally synthesized from pantothenate (vitamin B5), which is found in various foods such as meat, vegetables, cereal grains, legumes, eggs, and milk. More specifically, coenzyme A (CoASH or CoA) consists of a beta-mercaptoethylamine group linked to the vitamin pantothenic acid (B5) through an amide linkage and 3'-phosphorylated ADP. Coenzyme A is synthesized in a five-step process that requires four molecules of ATP, pantothenate and cysteine. It is believed that there are more than 1100 types of acyl-CoA’s in the human body, which also corresponds to the number of acylcarnitines in the human body. Acyl-CoAs exists in all living species, ranging from bacteria to plants to humans. The general role of acyl-CoA’s is to assist in transferring fatty acids from the cytoplasm to mitochondria. This process facilitates the production of fatty acids in cells, which are essential in cell membrane structure. Acyl-CoA's are also susceptible to beta oxidation, forming, ultimately, acetyl-CoA. Acetyl-CoA can enter the citric acid cycle, eventually forming several equivalents of ATP. In this way, fats are converted to ATP -- or biochemical energy. Acyl-CoAs can be classified into 9 different categories depending on the size of their acyl-group: 1) short-chain acyl-CoAs; 2) medium-chain acyl-CoAs; 3) long-chain acyl-CoAs; and 4) very long-chain acyl-CoAs; 5) hydroxy acyl-CoAs; 6) branched chain acyl-CoAs; 7) unsaturated acyl-CoAs; 8) dicarboxylic acyl-CoAs and 9) miscellaneous acyl-CoAs. Short-chain acyl-CoAs have acyl-groups with two to four carbons (C2-C4), medium-chain acyl-CoAs have acyl-groups with five to eleven carbons (C5-C11), long-chain acyl-CoAs have acyl-groups with twelve to twenty carbons (C12-C20) while very long-chain acyl-CoAs have acyl groups with more than 20 carbons. (5e,7e)-undeca-2,5,7-trienedioyl-coa is therefore classified as a medium chain acyl-CoA. The oxidative degradation of fatty acids is a two-step process, catalyzed by acyl-CoA synthetase/synthase. Fatty acids are first converted to their acyl phosphate, the precursor to acyl-CoA. The latter conversion is mediated by acyl-CoA synthase. Three types of acyl-CoA synthases are employed, depending on the chain length of the fatty acid. (5e,7e)-undeca-2,5,7-trienedioyl-coa, being a medium chain acyl-CoA is a substrate for medium chain acyl-CoA synthase. The second step of fatty acid degradation is beta oxidation. Beta oxidation occurs in mitochondria and, in the case of very long chain acyl-CoAs, the peroxisome. After its formation in the cytosol, (5E,7E)-Undeca-2,5,7-trienedioyl-CoA is transported into the mitochondria, the locus of beta oxidation. Transport of (5E,7E)-Undeca-2,5,7-trienedioyl-CoA into the mitochondria requires carnitine palmitoyltransferase 1 (CPT1), which converts (5E,7E)-Undeca-2,5,7-trienedioyl-CoA into (5E_7E)-Undeca-2_5_7-trienedioylcarnitine, which gets transported into the mitochondrial matrix. Once in the matrix, (5E_7E)-Undeca-2_5_7-trienedioylcarnitine is converted back to (5E,7E)-Undeca-2,5,7-trienedioyl-CoA by CPT2, whereupon beta-oxidation can begin. Beta oxidation of (5E,7E)-Undeca-2,5,7-trienedioyl-CoA occurs in four steps. First, since (5E,7E)-Undeca-2,5,7-trienedioyl-CoA is a medium chain acyl-CoA it is the substrate for a medium chain acyl-CoA dehydrogenase, which catalyzes dehydrogenation of (5E,7E)-Undeca-2,5,7-trienedioyl-CoA, creating a double bond between the alpha and beta carbons. FAD is the hydrogen acceptor, yielding FADH2. Second, Enoyl-CoA hydrase catalyzes the addition of water across the newly formed double bond to make an alcohol. Third, 3-hydroxyacyl-CoA dehydrogenase oxidizes the alcohol group to a ketone and NADH is produced from NAD+. Finally, Thiolase cleaves between the alpha carbon and ketone to release one molecule of acetyl-CoA and a new acyl-CoA which is now 2 carbons shorter. This four-step process repeats until (5E,7E)-Undeca-2,5,7-trienedioyl-CoA has had all its carbons removed from the chain, leaving only acetyl-CoA. Beta oxidation, as well as alpha-oxidation, also occurs in the peroxisome. The peroxisome handles beta oxidation of fatty acids that have more than 20 carbons in their chain because the peroxisome contains very-long-chain Acyl-CoA synthetases and dehydrogenases. The heart primarily metabolizes fat for energy and Acyl-CoA metabolism has been identified as a critical molecule in early-stage heart muscle pump failure. Cellular acyl-CoA content also correlates with insulin resistance, suggesting that it can mediate lipotoxicity in non-adipose tissues. Acyl-CoA: diacylglycerol acyltransferase (DGAT) plays an important role in energy metabolism on account of key enzyme in triglyceride biosynthesis. The study of acyl-CoAs is an active area of research and it is likely that many novel acyl-CoAs will be discovered in the coming years. It is also likely that many novel roles in health and disease will be uncovered for these molecules.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

  Mrv1652304102100562D          

 62 64  0  0  0  0            999 V2000
   19.0630    7.9092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.3485    7.4967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6340    7.9092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.3485    6.6717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6340    6.2592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6340    5.4342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9196    5.0217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9196    4.1967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2051    3.7842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2051    2.9592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9196    2.5467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9196    1.7217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6340    1.3092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6340    0.4842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.3485    1.7217    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   19.0630    1.3092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.7775    1.7217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.4919    1.3092    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   21.2064    1.7217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.2064    2.5467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.9209    1.3092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.6353    1.7217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.3498    1.3092    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   24.0643    1.7217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.0643    2.5467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.7787    1.3092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.7787    0.4842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.4932    1.7217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.9057    1.0072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0807    2.4361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.2077    2.1342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.9222    1.7217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.6366    2.1342    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   28.0491    1.4197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.2241    2.8486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.3511    2.5467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.0656    2.1342    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   28.6531    1.4197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.4781    2.8486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.7800    1.7217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   30.4945    2.1342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.2090    1.7217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.9627    2.0572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   32.5147    1.4441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.3352    1.5304    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   33.7477    2.2448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.5546    2.0733    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   34.6409    1.2528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.3083    0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.2221   -0.0526    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   34.4684   -0.3881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.8010    0.0968    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   33.8872    0.9173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.0620    1.1035    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   32.1022    0.7297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.4378   -0.0240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   31.2952    0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.6821    0.3492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.8975    0.6041    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   30.1524    1.3887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.6426   -0.1805    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.1129    0.8590    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  8  7  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  4  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
 33 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
 37 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  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  2  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
 50 51  1  0  0  0  0
 51 52  2  0  0  0  0
 52 53  1  0  0  0  0
 48 53  2  0  0  0  0
 45 53  1  0  0  0  0
 49 54  1  0  0  0  0
 44 55  1  0  0  0  0
 55 56  1  0  0  0  0
 55 57  1  0  0  0  0
 42 57  1  0  0  0  0
 57 58  1  0  0  0  0
 58 59  1  0  0  0  0
 59 60  2  0  0  0  0
 59 61  1  0  0  0  0
 59 62  1  0  0  0  0
M  END

HMDB0300997
     RDKit          3D
(5E,7E)-Undeca-2,5,7-trienedioyl-CoA
110112  0  0  0  0  0  0  0  0999 V2000
    0.5714   -0.0400   -1.3648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1995    0.8016   -0.4275 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4467    2.1663   -0.2265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5429    1.1873   -1.1023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1787    1.9287   -0.1224 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6669    2.5629   -0.4882 P   0  0  0  0  0  5  0  0  0  0  0  0
   -3.6125    4.1024   -0.5899 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3273    2.0435   -1.9411 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7078    2.2647    0.8294 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3078    0.7028    0.6803 P   0  0  0  0  0  5  0  0  0  0  0  0
   -4.4001   -0.0224   -0.3323 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2206   -0.0990    2.1752 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8774    0.6056    0.1274 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8311    0.3960    1.1023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2008    0.2862    0.4426 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2299    0.0833    1.3264 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0986   -0.8280    0.8134 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4531   -0.3441    0.6725 N   0  0  0  0  0  0  0  0  0  0  0  0
  -13.4333   -1.0289    0.0602 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.5648   -0.2954    0.0879 N   0  0  0  0  0  0  0  0  0  0  0  0
  -14.3017    0.8727    0.7330 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.0891    1.9390    1.0268 C   0  0  0  0  0  0  0  0  0  0  0  0
  -16.4556    1.9323    0.6370 N   0  0  0  0  0  0  0  0  0  0  0  0
  -14.5026    2.9691    1.6849 N   0  0  0  0  0  0  0  0  0  0  0  0
  -13.2141    2.9285    2.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4263    1.8788    1.7590 N   0  0  0  0  0  0  0  0  0  0  0  0
  -12.9570    0.8116    1.0902 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5707   -1.3359   -0.5245 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7341   -2.6923   -0.6713 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1276   -0.9246   -0.4675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3686   -1.8997    0.1780 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2733   -2.6729   -0.8163 P   0  0  0  0  0  5  0  0  0  0  0  0
   -5.8951   -2.6952   -0.1921 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2380   -2.1035   -2.3888 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7791   -4.3136   -0.8949 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5574    0.1853    0.8667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2868   -0.9562    0.7868 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4858    0.1119    1.9055 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1189   -0.2638    3.0474 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8171    0.4426    1.6894 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9025    0.4842    2.6535 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1705    0.9070    1.9130 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7460   -0.0885    1.0502 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2643   -1.1107    1.6602 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8381   -0.1407   -0.3544 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5319   -1.1474   -1.1257 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2852   -2.5508   -0.7569 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3117   -3.6759   -1.7621 S   0  0  0  0  0  0  0  0  0  0  0  0
    8.0378   -3.1634   -1.4823 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8738   -3.7028   -2.1811 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2891   -2.1648   -0.5078 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3839   -1.5189   -0.2922 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6555   -1.6895   -1.0229 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8139   -1.6060   -0.0071 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6384   -0.6662   -0.1538 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5134    0.3668   -0.3454 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5944    0.7131    0.3750 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3116    1.9188   -0.1448 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7296    1.6455   -0.5124 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6034    1.2594    0.6454 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4406    2.0876    1.0799 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.4850    0.0198    1.2236 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0088   -0.3679   -2.2667 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4525    0.5056   -1.8078 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9030   -1.0307   -0.9050 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5952    2.4254    0.8243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2068    2.9466   -0.6585 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3661    2.1698   -0.8619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2979    1.7891   -2.0039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0236    0.2612   -1.3890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5989    1.6066   -2.4643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4076   -0.6763    2.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5980   -0.5512    1.5933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9046    1.1953    1.8690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3878    1.2226   -0.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1306   -1.7138    1.4963 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.2710   -2.0152   -0.3639 H   0  0  0  0  0  0  0  0  0  0  0  0
  -16.7799    2.6622   -0.0238 H   0  0  0  0  0  0  0  0  0  0  0  0
  -17.0955    1.2290    0.9839 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7472    3.7530    2.5682 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0367   -0.7222   -1.3313 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5937   -2.9529   -1.6240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7368   -0.6559   -1.4651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0183   -1.1447   -2.4741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4677   -4.5103   -0.2295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3593    0.9470    1.3133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0570   -1.0515    1.3871 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1109    0.6523    0.6991 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0297   -0.4317    3.2196 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6949    1.2934    3.3741 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9459    1.8769    1.4392 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9104    1.1210    2.7389 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3661    0.6472   -0.8806 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0121   -1.0535   -2.1854 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5359   -0.7938   -1.3063 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2058   -2.7668   -0.9534 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4638   -2.7641    0.2861 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4752   -1.8957    0.2425 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3960   -0.7421    0.5188 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7549   -0.9327   -1.8064 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7413   -2.6914   -1.4941 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8077   -2.3688    0.7419 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1990   -0.5471   -1.4820 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.3680    1.1318   -1.1968 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.8770    0.1552    1.2251 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.7550    2.3261   -1.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.2655    2.7402    0.6117 H   0  0  0  0  0  0  0  0  0  0  0  0
   17.1998    2.5249   -1.0252 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.8195    0.8166   -1.2693 H   0  0  0  0  0  0  0  0  0  0  0  0
   18.2467   -0.4829    1.6617 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  6  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 10 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  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 17 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  2  0
 32 34  1  0
 32 35  1  0
  2 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  2  0
 38 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  2  0
 43 45  1  0
 45 46  1  0
 46 47  1  0
 47 48  1  0
 48 49  1  0
 49 50  2  0
 49 51  1  0
 51 52  2  3
 52 53  1  0
 53 54  1  0
 54 55  2  3
 55 56  1  0
 56 57  2  3
 57 58  1  0
 58 59  1  0
 59 60  1  0
 60 61  2  0
 60 62  1  0
 30 15  1  0
 27 18  1  0
 27 21  1  0
  1 63  1  0
  1 64  1  0
  1 65  1  0
  3 66  1  0
  3 67  1  0
  3 68  1  0
  4 69  1  0
  4 70  1  0
  8 71  1  0
 12 72  1  0
 14 73  1  0
 14 74  1  0
 15 75  1  0
 17 76  1  0
 19 77  1  0
 23 78  1  0
 23 79  1  0
 25 80  1  0
 28 81  1  0
 29 82  1  0
 30 83  1  0
 34 84  1  0
 35 85  1  0
 36 86  1  0
 37 87  1  0
 40 88  1  0
 41 89  1  0
 41 90  1  0
 42 91  1  0
 42 92  1  0
 45 93  1  0
 46 94  1  0
 46 95  1  0
 47 96  1  0
 47 97  1  0
 51 98  1  0
 52 99  1  0
 53100  1  0
 53101  1  0
 54102  1  0
 55103  1  0
 56104  1  0
 57105  1  0
 58106  1  0
 58107  1  0
 59108  1  0
 59109  1  0
 62110  1  0
M  END

  Mrv1652304102100562D          

 62 64  0  0  0  0            999 V2000
   19.0630    7.9092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.3485    7.4967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6340    7.9092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.3485    6.6717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6340    6.2592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6340    5.4342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9196    5.0217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9196    4.1967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2051    3.7842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2051    2.9592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9196    2.5467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9196    1.7217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6340    1.3092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6340    0.4842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.3485    1.7217    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   19.0630    1.3092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.7775    1.7217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.4919    1.3092    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   21.2064    1.7217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.2064    2.5467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.9209    1.3092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.6353    1.7217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.3498    1.3092    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   24.0643    1.7217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.0643    2.5467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.7787    1.3092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.7787    0.4842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.4932    1.7217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.9057    1.0072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0807    2.4361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.2077    2.1342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.9222    1.7217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.6366    2.1342    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   28.0491    1.4197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.2241    2.8486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.3511    2.5467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.0656    2.1342    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   28.6531    1.4197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.4781    2.8486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.7800    1.7217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   30.4945    2.1342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.2090    1.7217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.9627    2.0572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   32.5147    1.4441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.3352    1.5304    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   33.7477    2.2448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.5546    2.0733    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   34.6409    1.2528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.3083    0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.2221   -0.0526    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   34.4684   -0.3881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.8010    0.0968    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   33.8872    0.9173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.0620    1.1035    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   32.1022    0.7297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.4378   -0.0240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   31.2952    0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.6821    0.3492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.8975    0.6041    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   30.1524    1.3887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.6426   -0.1805    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.1129    0.8590    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  8  7  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  4  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
 33 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
 37 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  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  2  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
 50 51  1  0  0  0  0
 51 52  2  0  0  0  0
 52 53  1  0  0  0  0
 48 53  2  0  0  0  0
 45 53  1  0  0  0  0
 49 54  1  0  0  0  0
 44 55  1  0  0  0  0
 55 56  1  0  0  0  0
 55 57  1  0  0  0  0
 42 57  1  0  0  0  0
 57 58  1  0  0  0  0
 58 59  1  0  0  0  0
 59 60  2  0  0  0  0
 59 61  1  0  0  0  0
 59 62  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0300997

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)(COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N)C(O)C(=O)NCCC(=O)NCCSC(=O)C=CCC=CC=CCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C32H48N7O19P3S/c1-32(2,27(45)30(46)35-13-12-21(40)34-14-15-62-23(43)11-9-7-5-3-4-6-8-10-22(41)42)17-55-61(52,53)58-60(50,51)54-16-20-26(57-59(47,48)49)25(44)31(56-20)39-19-38-24-28(33)36-18-37-29(24)39/h3-6,9,11,18-20,25-27,31,44-45H,7-8,10,12-17H2,1-2H3,(H,34,40)(H,35,46)(H,41,42)(H,50,51)(H,52,53)(H2,33,36,37)(H2,47,48,49)

> <INCHI_KEY>
LPZQUELDLFEGRQ-UHFFFAOYSA-N

> <FORMULA>
C32H48N7O19P3S

> <MOLECULAR_WEIGHT>
959.75

> <EXACT_MASS>
959.193854522

> <JCHEM_ACCEPTOR_COUNT>
19

> <JCHEM_ATOM_COUNT>
110

> <JCHEM_AVERAGE_POLARIZABILITY>
89.8530582096538

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
11-{[2-(3-{3-[({[({[5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)methyl]-2-hydroxy-3-methylbutanamido}propanamido)ethyl]sulfanyl}-11-oxoundeca-4,6,9-trienoic acid

> <ALOGPS_LOGP>
0.66

> <JCHEM_LOGP>
-3.4374933886469194

> <ALOGPS_LOGS>
-2.78

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-5

> <JCHEM_PKA>
1.8996771381132902

> <JCHEM_PKA_STRONGEST_ACIDIC>
0.82093848397056

> <JCHEM_PKA_STRONGEST_BASIC>
3.9577179725649576

> <JCHEM_POLAR_SURFACE_AREA>
400.92999999999995

> <JCHEM_REFRACTIVITY>
218.63480000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
27

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.58e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
11-({2-[3-(3-{[({[5-(6-aminopurin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)oxy]methyl}-2-hydroxy-3-methylbutanamido)propanamido]ethyl}sulfanyl)-11-oxoundeca-4,6,9-trienoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0300997
     RDKit          3D
(5E,7E)-Undeca-2,5,7-trienedioyl-CoA
110112  0  0  0  0  0  0  0  0999 V2000
    0.5714   -0.0400   -1.3648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1995    0.8016   -0.4275 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4467    2.1663   -0.2265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5429    1.1873   -1.1023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1787    1.9287   -0.1224 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6669    2.5629   -0.4882 P   0  0  0  0  0  5  0  0  0  0  0  0
   -3.6125    4.1024   -0.5899 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3273    2.0435   -1.9411 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7078    2.2647    0.8294 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3078    0.7028    0.6803 P   0  0  0  0  0  5  0  0  0  0  0  0
   -4.4001   -0.0224   -0.3323 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2206   -0.0990    2.1752 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8774    0.6056    0.1274 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8311    0.3960    1.1023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2008    0.2862    0.4426 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2299    0.0833    1.3264 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0986   -0.8280    0.8134 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4531   -0.3441    0.6725 N   0  0  0  0  0  0  0  0  0  0  0  0
  -13.4333   -1.0289    0.0602 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.5648   -0.2954    0.0879 N   0  0  0  0  0  0  0  0  0  0  0  0
  -14.3017    0.8727    0.7330 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.0891    1.9390    1.0268 C   0  0  0  0  0  0  0  0  0  0  0  0
  -16.4556    1.9323    0.6370 N   0  0  0  0  0  0  0  0  0  0  0  0
  -14.5026    2.9691    1.6849 N   0  0  0  0  0  0  0  0  0  0  0  0
  -13.2141    2.9285    2.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4263    1.8788    1.7590 N   0  0  0  0  0  0  0  0  0  0  0  0
  -12.9570    0.8116    1.0902 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5707   -1.3359   -0.5245 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7341   -2.6923   -0.6713 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1276   -0.9246   -0.4675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3686   -1.8997    0.1780 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2733   -2.6729   -0.8163 P   0  0  0  0  0  5  0  0  0  0  0  0
   -5.8951   -2.6952   -0.1921 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2380   -2.1035   -2.3888 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7791   -4.3136   -0.8949 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5574    0.1853    0.8667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2868   -0.9562    0.7868 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4858    0.1119    1.9055 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1189   -0.2638    3.0474 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8171    0.4426    1.6894 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9025    0.4842    2.6535 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1705    0.9070    1.9130 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7460   -0.0885    1.0502 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2643   -1.1107    1.6602 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8381   -0.1407   -0.3544 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5319   -1.1474   -1.1257 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2852   -2.5508   -0.7569 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3117   -3.6759   -1.7621 S   0  0  0  0  0  0  0  0  0  0  0  0
    8.0378   -3.1634   -1.4823 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8738   -3.7028   -2.1811 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2891   -2.1648   -0.5078 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3839   -1.5189   -0.2922 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6555   -1.6895   -1.0229 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8139   -1.6060   -0.0071 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6384   -0.6662   -0.1538 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5134    0.3668   -0.3454 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5944    0.7131    0.3750 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3116    1.9188   -0.1448 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7296    1.6455   -0.5124 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6034    1.2594    0.6454 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4406    2.0876    1.0799 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.4850    0.0198    1.2236 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0088   -0.3679   -2.2667 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4525    0.5056   -1.8078 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9030   -1.0307   -0.9050 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5952    2.4254    0.8243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2068    2.9466   -0.6585 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3661    2.1698   -0.8619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2979    1.7891   -2.0039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0236    0.2612   -1.3890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5989    1.6066   -2.4643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4076   -0.6763    2.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5980   -0.5512    1.5933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9046    1.1953    1.8690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3878    1.2226   -0.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1306   -1.7138    1.4963 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.2710   -2.0152   -0.3639 H   0  0  0  0  0  0  0  0  0  0  0  0
  -16.7799    2.6622   -0.0238 H   0  0  0  0  0  0  0  0  0  0  0  0
  -17.0955    1.2290    0.9839 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7472    3.7530    2.5682 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0367   -0.7222   -1.3313 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5937   -2.9529   -1.6240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7368   -0.6559   -1.4651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0183   -1.1447   -2.4741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4677   -4.5103   -0.2295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3593    0.9470    1.3133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0570   -1.0515    1.3871 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1109    0.6523    0.6991 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0297   -0.4317    3.2196 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6949    1.2934    3.3741 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9459    1.8769    1.4392 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9104    1.1210    2.7389 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3661    0.6472   -0.8806 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0121   -1.0535   -2.1854 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5359   -0.7938   -1.3063 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2058   -2.7668   -0.9534 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4638   -2.7641    0.2861 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4752   -1.8957    0.2425 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3960   -0.7421    0.5188 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7549   -0.9327   -1.8064 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7413   -2.6914   -1.4941 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8077   -2.3688    0.7419 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1990   -0.5471   -1.4820 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.3680    1.1318   -1.1968 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.8770    0.1552    1.2251 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.7550    2.3261   -1.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.2655    2.7402    0.6117 H   0  0  0  0  0  0  0  0  0  0  0  0
   17.1998    2.5249   -1.0252 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.8195    0.8166   -1.2693 H   0  0  0  0  0  0  0  0  0  0  0  0
   18.2467   -0.4829    1.6617 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  6  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 10 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  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 17 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  2  0
 32 34  1  0
 32 35  1  0
  2 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  2  0
 38 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  2  0
 43 45  1  0
 45 46  1  0
 46 47  1  0
 47 48  1  0
 48 49  1  0
 49 50  2  0
 49 51  1  0
 51 52  2  3
 52 53  1  0
 53 54  1  0
 54 55  2  3
 55 56  1  0
 56 57  2  3
 57 58  1  0
 58 59  1  0
 59 60  1  0
 60 61  2  0
 60 62  1  0
 30 15  1  0
 27 18  1  0
 27 21  1  0
  1 63  1  0
  1 64  1  0
  1 65  1  0
  3 66  1  0
  3 67  1  0
  3 68  1  0
  4 69  1  0
  4 70  1  0
  8 71  1  0
 12 72  1  0
 14 73  1  0
 14 74  1  0
 15 75  1  0
 17 76  1  0
 19 77  1  0
 23 78  1  0
 23 79  1  0
 25 80  1  0
 28 81  1  0
 29 82  1  0
 30 83  1  0
 34 84  1  0
 35 85  1  0
 36 86  1  0
 37 87  1  0
 40 88  1  0
 41 89  1  0
 41 90  1  0
 42 91  1  0
 42 92  1  0
 45 93  1  0
 46 94  1  0
 46 95  1  0
 47 96  1  0
 47 97  1  0
 51 98  1  0
 52 99  1  0
 53100  1  0
 53101  1  0
 54102  1  0
 55103  1  0
 56104  1  0
 57105  1  0
 58106  1  0
 58107  1  0
 59108  1  0
 59109  1  0
 62110  1  0
M  END

HEADER    PROTEIN                                 10-APR-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-APR-21         0                                  
HETATM    1  O   UNK     0      35.584  14.764   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      34.251  13.994   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      32.917  14.764   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      34.251  12.454   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      32.917  11.684   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      32.917  10.144   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      31.583   9.374   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      31.583   7.834   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      30.250   7.064   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      30.250   5.524   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      31.583   4.754   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      31.583   3.214   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      32.917   2.444   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      32.917   0.904   0.000  0.00  0.00           O+0
HETATM   15  S   UNK     0      34.251   3.214   0.000  0.00  0.00           S+0
HETATM   16  C   UNK     0      35.584   2.444   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      36.918   3.214   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0      38.252   2.444   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0      39.585   3.214   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      39.585   4.754   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      40.919   2.444   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      42.253   3.214   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0      43.586   2.444   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0      44.920   3.214   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      44.920   4.754   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      46.254   2.444   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      46.254   0.904   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      47.587   3.214   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      48.357   1.880   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      46.817   4.547   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      48.921   3.984   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      50.255   3.214   0.000  0.00  0.00           O+0
HETATM   33  P   UNK     0      51.588   3.984   0.000  0.00  0.00           P+0
HETATM   34  O   UNK     0      52.358   2.650   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      50.818   5.317   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      52.922   4.754   0.000  0.00  0.00           O+0
HETATM   37  P   UNK     0      54.256   3.984   0.000  0.00  0.00           P+0
HETATM   38  O   UNK     0      53.486   2.650   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      55.026   5.317   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      55.589   3.214   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      56.923   3.984   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      58.257   3.214   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      59.664   3.840   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      60.694   2.696   0.000  0.00  0.00           C+0
HETATM   45  N   UNK     0      62.226   2.857   0.000  0.00  0.00           N+0
HETATM   46  C   UNK     0      62.996   4.190   0.000  0.00  0.00           C+0
HETATM   47  N   UNK     0      64.502   3.870   0.000  0.00  0.00           N+0
HETATM   48  C   UNK     0      64.663   2.339   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      65.909   1.433   0.000  0.00  0.00           C+0
HETATM   50  N   UNK     0      65.748  -0.098   0.000  0.00  0.00           N+0
HETATM   51  C   UNK     0      64.341  -0.725   0.000  0.00  0.00           C+0
HETATM   52  N   UNK     0      63.095   0.181   0.000  0.00  0.00           N+0
HETATM   53  C   UNK     0      63.256   1.712   0.000  0.00  0.00           C+0
HETATM   54  N   UNK     0      67.316   2.060   0.000  0.00  0.00           N+0
HETATM   55  C   UNK     0      59.924   1.362   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0      60.550  -0.045   0.000  0.00  0.00           O+0
HETATM   57  C   UNK     0      58.418   1.682   0.000  0.00  0.00           C+0
HETATM   58  O   UNK     0      57.273   0.652   0.000  0.00  0.00           O+0
HETATM   59  P   UNK     0      55.809   1.128   0.000  0.00  0.00           P+0
HETATM   60  O   UNK     0      56.285   2.592   0.000  0.00  0.00           O+0
HETATM   61  O   UNK     0      55.333  -0.337   0.000  0.00  0.00           O+0
HETATM   62  O   UNK     0      54.344   1.604   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30   31                                             
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   28   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35   36                                             
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   33   37                                                       
CONECT   37   36   38   39   40                                             
CONECT   38   37                                                            
CONECT   39   37                                                            
CONECT   40   37   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43   57                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45   55                                                  
CONECT   45   44   46   53                                                  
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49   53                                                  
CONECT   49   48   50   54                                                  
CONECT   50   49   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52   48   45                                                  
CONECT   54   49                                                            
CONECT   55   44   56   57                                                  
CONECT   56   55                                                            
CONECT   57   55   42   58                                                  
CONECT   58   57   59                                                       
CONECT   59   58   60   61   62                                             
CONECT   60   59                                                            
CONECT   61   59                                                            
CONECT   62   59                                                            
MASTER        0    0    0    0    0    0    0    0   62    0  128    0
END

COMPND    HMDB0300997
HETATM    1  C1  UNL     1       0.571  -0.040  -1.365  1.00  0.00           C  
HETATM    2  C2  UNL     1      -0.199   0.802  -0.427  1.00  0.00           C  
HETATM    3  C3  UNL     1       0.447   2.166  -0.226  1.00  0.00           C  
HETATM    4  C4  UNL     1      -1.543   1.187  -1.102  1.00  0.00           C  
HETATM    5  O1  UNL     1      -2.179   1.929  -0.122  1.00  0.00           O  
HETATM    6  P1  UNL     1      -3.667   2.563  -0.488  1.00  0.00           P  
HETATM    7  O2  UNL     1      -3.612   4.102  -0.590  1.00  0.00           O  
HETATM    8  O3  UNL     1      -4.327   2.043  -1.941  1.00  0.00           O  
HETATM    9  O4  UNL     1      -4.708   2.265   0.829  1.00  0.00           O  
HETATM   10  P2  UNL     1      -5.308   0.703   0.680  1.00  0.00           P  
HETATM   11  O5  UNL     1      -4.400  -0.022  -0.332  1.00  0.00           O  
HETATM   12  O6  UNL     1      -5.221  -0.099   2.175  1.00  0.00           O  
HETATM   13  O7  UNL     1      -6.877   0.606   0.127  1.00  0.00           O  
HETATM   14  C5  UNL     1      -7.831   0.396   1.102  1.00  0.00           C  
HETATM   15  C6  UNL     1      -9.201   0.286   0.443  1.00  0.00           C  
HETATM   16  O8  UNL     1     -10.230   0.083   1.326  1.00  0.00           O  
HETATM   17  C7  UNL     1     -11.099  -0.828   0.813  1.00  0.00           C  
HETATM   18  N1  UNL     1     -12.453  -0.344   0.673  1.00  0.00           N  
HETATM   19  C8  UNL     1     -13.433  -1.029   0.060  1.00  0.00           C  
HETATM   20  N2  UNL     1     -14.565  -0.295   0.088  1.00  0.00           N  
HETATM   21  C9  UNL     1     -14.302   0.873   0.733  1.00  0.00           C  
HETATM   22  C10 UNL     1     -15.089   1.939   1.027  1.00  0.00           C  
HETATM   23  N3  UNL     1     -16.456   1.932   0.637  1.00  0.00           N  
HETATM   24  N4  UNL     1     -14.503   2.969   1.685  1.00  0.00           N  
HETATM   25  C11 UNL     1     -13.214   2.928   2.033  1.00  0.00           C  
HETATM   26  N5  UNL     1     -12.426   1.879   1.759  1.00  0.00           N  
HETATM   27  C12 UNL     1     -12.957   0.812   1.090  1.00  0.00           C  
HETATM   28  C13 UNL     1     -10.571  -1.336  -0.525  1.00  0.00           C  
HETATM   29  O9  UNL     1     -10.734  -2.692  -0.671  1.00  0.00           O  
HETATM   30  C14 UNL     1      -9.128  -0.925  -0.467  1.00  0.00           C  
HETATM   31  O10 UNL     1      -8.369  -1.900   0.178  1.00  0.00           O  
HETATM   32  P3  UNL     1      -7.273  -2.673  -0.816  1.00  0.00           P  
HETATM   33  O11 UNL     1      -5.895  -2.695  -0.192  1.00  0.00           O  
HETATM   34  O12 UNL     1      -7.238  -2.104  -2.389  1.00  0.00           O  
HETATM   35  O13 UNL     1      -7.779  -4.314  -0.895  1.00  0.00           O  
HETATM   36  C15 UNL     1      -0.557   0.185   0.867  1.00  0.00           C  
HETATM   37  O14 UNL     1      -1.287  -0.956   0.787  1.00  0.00           O  
HETATM   38  C16 UNL     1       0.486   0.112   1.905  1.00  0.00           C  
HETATM   39  O15 UNL     1       0.119  -0.264   3.047  1.00  0.00           O  
HETATM   40  N6  UNL     1       1.817   0.443   1.689  1.00  0.00           N  
HETATM   41  C17 UNL     1       2.902   0.484   2.654  1.00  0.00           C  
HETATM   42  C18 UNL     1       4.171   0.907   1.913  1.00  0.00           C  
HETATM   43  C19 UNL     1       4.746  -0.088   1.050  1.00  0.00           C  
HETATM   44  O16 UNL     1       5.264  -1.111   1.660  1.00  0.00           O  
HETATM   45  N7  UNL     1       4.838  -0.141  -0.354  1.00  0.00           N  
HETATM   46  C20 UNL     1       5.532  -1.147  -1.126  1.00  0.00           C  
HETATM   47  C21 UNL     1       5.285  -2.551  -0.757  1.00  0.00           C  
HETATM   48  S1  UNL     1       6.312  -3.676  -1.762  1.00  0.00           S  
HETATM   49  C22 UNL     1       8.038  -3.163  -1.482  1.00  0.00           C  
HETATM   50  O17 UNL     1       8.874  -3.703  -2.181  1.00  0.00           O  
HETATM   51  C23 UNL     1       8.289  -2.165  -0.508  1.00  0.00           C  
HETATM   52  C24 UNL     1       9.384  -1.519  -0.292  1.00  0.00           C  
HETATM   53  C25 UNL     1      10.655  -1.689  -1.023  1.00  0.00           C  
HETATM   54  C26 UNL     1      11.814  -1.606  -0.007  1.00  0.00           C  
HETATM   55  C27 UNL     1      12.638  -0.666  -0.154  1.00  0.00           C  
HETATM   56  C28 UNL     1      13.513   0.367  -0.345  1.00  0.00           C  
HETATM   57  C29 UNL     1      14.594   0.713   0.375  1.00  0.00           C  
HETATM   58  C30 UNL     1      15.312   1.919  -0.145  1.00  0.00           C  
HETATM   59  C31 UNL     1      16.730   1.646  -0.512  1.00  0.00           C  
HETATM   60  C32 UNL     1      17.603   1.259   0.645  1.00  0.00           C  
HETATM   61  O18 UNL     1      18.441   2.088   1.080  1.00  0.00           O  
HETATM   62  O19 UNL     1      17.485   0.020   1.224  1.00  0.00           O  
HETATM   63  H1  UNL     1      -0.009  -0.368  -2.267  1.00  0.00           H  
HETATM   64  H2  UNL     1       1.452   0.506  -1.808  1.00  0.00           H  
HETATM   65  H3  UNL     1       0.903  -1.031  -0.905  1.00  0.00           H  
HETATM   66  H4  UNL     1       0.595   2.425   0.824  1.00  0.00           H  
HETATM   67  H5  UNL     1      -0.207   2.947  -0.659  1.00  0.00           H  
HETATM   68  H6  UNL     1       1.366   2.170  -0.862  1.00  0.00           H  
HETATM   69  H7  UNL     1      -1.298   1.789  -2.004  1.00  0.00           H  
HETATM   70  H8  UNL     1      -2.024   0.261  -1.389  1.00  0.00           H  
HETATM   71  H9  UNL     1      -3.599   1.607  -2.464  1.00  0.00           H  
HETATM   72  H10 UNL     1      -4.408  -0.676   2.153  1.00  0.00           H  
HETATM   73  H11 UNL     1      -7.598  -0.551   1.593  1.00  0.00           H  
HETATM   74  H12 UNL     1      -7.905   1.195   1.869  1.00  0.00           H  
HETATM   75  H13 UNL     1      -9.388   1.223  -0.100  1.00  0.00           H  
HETATM   76  H14 UNL     1     -11.131  -1.714   1.496  1.00  0.00           H  
HETATM   77  H15 UNL     1     -13.271  -2.015  -0.364  1.00  0.00           H  
HETATM   78  H16 UNL     1     -16.780   2.662  -0.024  1.00  0.00           H  
HETATM   79  H17 UNL     1     -17.096   1.229   0.984  1.00  0.00           H  
HETATM   80  H18 UNL     1     -12.747   3.753   2.568  1.00  0.00           H  
HETATM   81  H19 UNL     1     -11.037  -0.722  -1.331  1.00  0.00           H  
HETATM   82  H20 UNL     1     -10.594  -2.953  -1.624  1.00  0.00           H  
HETATM   83  H21 UNL     1      -8.737  -0.656  -1.465  1.00  0.00           H  
HETATM   84  H22 UNL     1      -7.018  -1.145  -2.474  1.00  0.00           H  
HETATM   85  H23 UNL     1      -8.468  -4.510  -0.230  1.00  0.00           H  
HETATM   86  H24 UNL     1      -1.359   0.947   1.313  1.00  0.00           H  
HETATM   87  H25 UNL     1      -2.057  -1.052   1.387  1.00  0.00           H  
HETATM   88  H26 UNL     1       2.111   0.652   0.699  1.00  0.00           H  
HETATM   89  H27 UNL     1       3.030  -0.432   3.220  1.00  0.00           H  
HETATM   90  H28 UNL     1       2.695   1.293   3.374  1.00  0.00           H  
HETATM   91  H29 UNL     1       3.946   1.877   1.439  1.00  0.00           H  
HETATM   92  H30 UNL     1       4.910   1.121   2.739  1.00  0.00           H  
HETATM   93  H31 UNL     1       4.366   0.647  -0.881  1.00  0.00           H  
HETATM   94  H32 UNL     1       5.012  -1.054  -2.185  1.00  0.00           H  
HETATM   95  H33 UNL     1       6.536  -0.794  -1.306  1.00  0.00           H  
HETATM   96  H34 UNL     1       4.206  -2.767  -0.953  1.00  0.00           H  
HETATM   97  H35 UNL     1       5.464  -2.764   0.286  1.00  0.00           H  
HETATM   98  H36 UNL     1       7.475  -1.896   0.242  1.00  0.00           H  
HETATM   99  H37 UNL     1       9.396  -0.742   0.519  1.00  0.00           H  
HETATM  100  H38 UNL     1      10.755  -0.933  -1.806  1.00  0.00           H  
HETATM  101  H39 UNL     1      10.741  -2.691  -1.494  1.00  0.00           H  
HETATM  102  H40 UNL     1      11.808  -2.369   0.742  1.00  0.00           H  
HETATM  103  H41 UNL     1      12.199  -0.547  -1.482  1.00  0.00           H  
HETATM  104  H42 UNL     1      13.368   1.132  -1.197  1.00  0.00           H  
HETATM  105  H43 UNL     1      14.877   0.155   1.225  1.00  0.00           H  
HETATM  106  H44 UNL     1      14.755   2.326  -1.014  1.00  0.00           H  
HETATM  107  H45 UNL     1      15.266   2.740   0.612  1.00  0.00           H  
HETATM  108  H46 UNL     1      17.200   2.525  -1.025  1.00  0.00           H  
HETATM  109  H47 UNL     1      16.819   0.817  -1.269  1.00  0.00           H  
HETATM  110  H48 UNL     1      18.247  -0.483   1.662  1.00  0.00           H  
CONECT    1    2   63   64   65
CONECT    2    3    4   36
CONECT    3   66   67   68
CONECT    4    5   69   70
CONECT    5    6
CONECT    6    7    7    8    9
CONECT    8   71
CONECT    9   10
CONECT   10   11   11   12   13
CONECT   12   72
CONECT   13   14
CONECT   14   15   73   74
CONECT   15   16   30   75
CONECT   16   17
CONECT   17   18   28   76
CONECT   18   19   27
CONECT   19   20   20   77
CONECT   20   21
CONECT   21   22   22   27
CONECT   22   23   24
CONECT   23   78   79
CONECT   24   25   25
CONECT   25   26   80
CONECT   26   27   27
CONECT   28   29   30   81
CONECT   29   82
CONECT   30   31   83
CONECT   31   32
CONECT   32   33   33   34   35
CONECT   34   84
CONECT   35   85
CONECT   36   37   38   86
CONECT   37   87
CONECT   38   39   39   40
CONECT   40   41   88
CONECT   41   42   89   90
CONECT   42   43   91   92
CONECT   43   44   44   45
CONECT   45   46   93
CONECT   46   47   94   95
CONECT   47   48   96   97
CONECT   48   49
CONECT   49   50   50   51
CONECT   51   52   52   98
CONECT   52   53   99
CONECT   53   54  100  101
CONECT   54   55   55  102
CONECT   55   56  103
CONECT   56   57   57  104
CONECT   57   58  105
CONECT   58   59  106  107
CONECT   59   60  108  109
CONECT   60   61   61   62
CONECT   62  110
END

HMDB0300997
     RDKit          3D
(5E,7E)-Undeca-2,5,7-trienedioyl-CoA
110112  0  0  0  0  0  0  0  0999 V2000
    0.5714   -0.0400   -1.3648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1995    0.8016   -0.4275 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4467    2.1663   -0.2265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5429    1.1873   -1.1023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1787    1.9287   -0.1224 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6669    2.5629   -0.4882 P   0  0  0  0  0  5  0  0  0  0  0  0
   -3.6125    4.1024   -0.5899 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3273    2.0435   -1.9411 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7078    2.2647    0.8294 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3078    0.7028    0.6803 P   0  0  0  0  0  5  0  0  0  0  0  0
   -4.4001   -0.0224   -0.3323 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2206   -0.0990    2.1752 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8774    0.6056    0.1274 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8311    0.3960    1.1023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2008    0.2862    0.4426 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2299    0.0833    1.3264 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0986   -0.8280    0.8134 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4531   -0.3441    0.6725 N   0  0  0  0  0  0  0  0  0  0  0  0
  -13.4333   -1.0289    0.0602 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.5648   -0.2954    0.0879 N   0  0  0  0  0  0  0  0  0  0  0  0
  -14.3017    0.8727    0.7330 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.0891    1.9390    1.0268 C   0  0  0  0  0  0  0  0  0  0  0  0
  -16.4556    1.9323    0.6370 N   0  0  0  0  0  0  0  0  0  0  0  0
  -14.5026    2.9691    1.6849 N   0  0  0  0  0  0  0  0  0  0  0  0
  -13.2141    2.9285    2.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4263    1.8788    1.7590 N   0  0  0  0  0  0  0  0  0  0  0  0
  -12.9570    0.8116    1.0902 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5707   -1.3359   -0.5245 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7341   -2.6923   -0.6713 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1276   -0.9246   -0.4675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3686   -1.8997    0.1780 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2733   -2.6729   -0.8163 P   0  0  0  0  0  5  0  0  0  0  0  0
   -5.8951   -2.6952   -0.1921 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2380   -2.1035   -2.3888 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7791   -4.3136   -0.8949 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5574    0.1853    0.8667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2868   -0.9562    0.7868 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4858    0.1119    1.9055 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1189   -0.2638    3.0474 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8171    0.4426    1.6894 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9025    0.4842    2.6535 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1705    0.9070    1.9130 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7460   -0.0885    1.0502 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2643   -1.1107    1.6602 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8381   -0.1407   -0.3544 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5319   -1.1474   -1.1257 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2852   -2.5508   -0.7569 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3117   -3.6759   -1.7621 S   0  0  0  0  0  0  0  0  0  0  0  0
    8.0378   -3.1634   -1.4823 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8738   -3.7028   -2.1811 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2891   -2.1648   -0.5078 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3839   -1.5189   -0.2922 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6555   -1.6895   -1.0229 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8139   -1.6060   -0.0071 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6384   -0.6662   -0.1538 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5134    0.3668   -0.3454 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5944    0.7131    0.3750 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3116    1.9188   -0.1448 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7296    1.6455   -0.5124 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6034    1.2594    0.6454 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4406    2.0876    1.0799 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.4850    0.0198    1.2236 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0088   -0.3679   -2.2667 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4525    0.5056   -1.8078 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9030   -1.0307   -0.9050 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5952    2.4254    0.8243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2068    2.9466   -0.6585 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3661    2.1698   -0.8619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2979    1.7891   -2.0039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0236    0.2612   -1.3890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5989    1.6066   -2.4643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4076   -0.6763    2.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5980   -0.5512    1.5933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9046    1.1953    1.8690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3878    1.2226   -0.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1306   -1.7138    1.4963 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.2710   -2.0152   -0.3639 H   0  0  0  0  0  0  0  0  0  0  0  0
  -16.7799    2.6622   -0.0238 H   0  0  0  0  0  0  0  0  0  0  0  0
  -17.0955    1.2290    0.9839 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7472    3.7530    2.5682 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0367   -0.7222   -1.3313 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5937   -2.9529   -1.6240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7368   -0.6559   -1.4651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0183   -1.1447   -2.4741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4677   -4.5103   -0.2295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3593    0.9470    1.3133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0570   -1.0515    1.3871 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1109    0.6523    0.6991 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0297   -0.4317    3.2196 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6949    1.2934    3.3741 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9459    1.8769    1.4392 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9104    1.1210    2.7389 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3661    0.6472   -0.8806 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0121   -1.0535   -2.1854 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5359   -0.7938   -1.3063 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2058   -2.7668   -0.9534 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4638   -2.7641    0.2861 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4752   -1.8957    0.2425 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3960   -0.7421    0.5188 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7549   -0.9327   -1.8064 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7413   -2.6914   -1.4941 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8077   -2.3688    0.7419 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1990   -0.5471   -1.4820 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.3680    1.1318   -1.1968 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.8770    0.1552    1.2251 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.7550    2.3261   -1.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.2655    2.7402    0.6117 H   0  0  0  0  0  0  0  0  0  0  0  0
   17.1998    2.5249   -1.0252 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.8195    0.8166   -1.2693 H   0  0  0  0  0  0  0  0  0  0  0  0
   18.2467   -0.4829    1.6617 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  6  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 10 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  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 17 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  2  0
 32 34  1  0
 32 35  1  0
  2 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  2  0
 38 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  2  0
 43 45  1  0
 45 46  1  0
 46 47  1  0
 47 48  1  0
 48 49  1  0
 49 50  2  0
 49 51  1  0
 51 52  2  3
 52 53  1  0
 53 54  1  0
 54 55  2  3
 55 56  1  0
 56 57  2  3
 57 58  1  0
 58 59  1  0
 59 60  1  0
 60 61  2  0
 60 62  1  0
 30 15  1  0
 27 18  1  0
 27 21  1  0
  1 63  1  0
  1 64  1  0
  1 65  1  0
  3 66  1  0
  3 67  1  0
  3 68  1  0
  4 69  1  0
  4 70  1  0
  8 71  1  0
 12 72  1  0
 14 73  1  0
 14 74  1  0
 15 75  1  0
 17 76  1  0
 19 77  1  0
 23 78  1  0
 23 79  1  0
 25 80  1  0
 28 81  1  0
 29 82  1  0
 30 83  1  0
 34 84  1  0
 35 85  1  0
 36 86  1  0
 37 87  1  0
 40 88  1  0
 41 89  1  0
 41 90  1  0
 42 91  1  0
 42 92  1  0
 45 93  1  0
 46 94  1  0
 46 95  1  0
 47 96  1  0
 47 97  1  0
 51 98  1  0
 52 99  1  0
 53100  1  0
 53101  1  0
 54102  1  0
 55103  1  0
 56104  1  0
 57105  1  0
 58106  1  0
 58107  1  0
 59108  1  0
 59109  1  0
 62110  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
11-({2-[(3-{[4-({[({[5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)-1,2-dihydroxy-3,3-dimethylbutylidene]amino}-1-hydroxypropylidene)amino]ethyl}sulfanyl)-11-oxoundeca-4,6,9-trienoate	HMDB
11-({2-[(3-{[4-({[({[5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)-1,2-dihydroxy-3,3-dimethylbutylidene]amino}-1-hydroxypropylidene)amino]ethyl}sulphanyl)-11-oxoundeca-4,6,9-trienoate	HMDB
11-({2-[(3-{[4-({[({[5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)-1,2-dihydroxy-3,3-dimethylbutylidene]amino}-1-hydroxypropylidene)amino]ethyl}sulphanyl)-11-oxoundeca-4,6,9-trienoic acid	HMDB

Chemical Formula

C₃₂H₄₈N₇O₁₉P₃S

Average Molecular Weight

959.75

Monoisotopic Molecular Weight

959.193854522

IUPAC Name

11-{[2-(3-{3-[({[({[5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)methyl]-2-hydroxy-3-methylbutanamido}propanamido)ethyl]sulfanyl}-11-oxoundeca-4,6,9-trienoic acid

Traditional Name

11-({2-[3-(3-{[({[5-(6-aminopurin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)oxy]methyl}-2-hydroxy-3-methylbutanamido)propanamido]ethyl}sulfanyl)-11-oxoundeca-4,6,9-trienoic acid

CAS Registry Number

Not Available

SMILES

CC(C)(COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N)C(O)C(=O)NCCC(=O)NCCSC(=O)C=CCC=CC=CCCC(O)=O

InChI Identifier

InChI=1S/C32H48N7O19P3S/c1-32(2,27(45)30(46)35-13-12-21(40)34-14-15-62-23(43)11-9-7-5-3-4-6-8-10-22(41)42)17-55-61(52,53)58-60(50,51)54-16-20-26(57-59(47,48)49)25(44)31(56-20)39-19-38-24-28(33)36-18-37-29(24)39/h3-6,9,11,18-20,25-27,31,44-45H,7-8,10,12-17H2,1-2H3,(H,34,40)(H,35,46)(H,41,42)(H,50,51)(H,52,53)(H2,33,36,37)(H2,47,48,49)

InChI Key

LPZQUELDLFEGRQ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as medium-chain 2-enoyl coas. These are organic compounds containing a coenzyme A substructure linked to a medium-chain 2-enoyl chain of 5 to 12 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl thioesters

Direct Parent

Medium-chain 2-enoyl CoAs

Alternative Parents

Substituents

Coenzyme a or derivatives
Purine ribonucleoside diphosphate
Purine ribonucleoside bisphosphate
Purine ribonucleoside 3',5'-bisphosphate
Ribonucleoside 3'-phosphate
Pentose-5-phosphate
Pentose phosphate
N-glycosyl compound
Glycosyl compound
Beta amino acid or derivatives
Pentose monosaccharide
Organic pyrophosphate
Monosaccharide phosphate
6-aminopurine
Purine
Imidazopyrimidine
Medium-chain fatty acid
Monoalkyl phosphate
Hydroxy fatty acid
Aminopyrimidine
Fatty acid
Imidolactam
Alkyl phosphate
Unsaturated fatty acid
Pyrimidine
Phosphoric acid ester
Organic phosphoric acid derivative
N-substituted imidazole
N-acyl-amine
Monosaccharide
Fatty amide
Heteroaromatic compound
Tetrahydrofuran
Imidazole
Azole
Amino acid
Carbothioic s-ester
Thiocarboxylic acid ester
Secondary carboxylic acid amide
Secondary alcohol
Carboxamide group
Amino acid or derivatives
Oxacycle
Azacycle
Organoheterocyclic compound
Sulfenyl compound
Thiocarboxylic acid or derivatives
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary amine
Organosulfur compound
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Not Available

Not Available

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	0.66	ALOGPS
logP	-3.4	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	0.82	ChemAxon
pKa (Strongest Basic)	3.96	ChemAxon
Physiological Charge	-5	ChemAxon
Hydrogen Acceptor Count	19	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	400.93 Å²	ChemAxon
Rotatable Bond Count	27	ChemAxon
Refractivity	218.63 m³·mol⁻¹	ChemAxon
Polarizability	89.85 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
AllCCS	[M+H]+	278.08	32859911
AllCCS	[M+H-H2O]+	278.7	32859911
AllCCS	[M+Na]+	277.271	32859911
AllCCS	[M+NH4]+	277.458	32859911
AllCCS	[M-H]-	284.289	32859911
AllCCS	[M+Na-2H]-	289.707	32859911
AllCCS	[M+HCOO]-	295.64	32859911
DeepCCS	[M+H]+	272.151	30932474
DeepCCS	[M-H]-	270.418	30932474
DeepCCS	[M-2H]-	304.452	30932474
DeepCCS	[M+Na]+	278.615	30932474

Predicted Kovats Retention Indices

Not Available

Spectra

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (5E,7E)-Undeca-2,5,7-trienedioyl-CoA 10V, Negative-QTOF	splash10-0a4i-0000000009-18cec7cfe84719f662d5	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (5E,7E)-Undeca-2,5,7-trienedioyl-CoA 20V, Negative-QTOF	splash10-052f-2100000149-4b4a0310a288e2841ad0	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (5E,7E)-Undeca-2,5,7-trienedioyl-CoA 40V, Negative-QTOF	splash10-03fr-5221200090-83a7cfad2660faa2b0a4	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (5E,7E)-Undeca-2,5,7-trienedioyl-CoA 10V, Positive-QTOF	splash10-01vx-0200000019-41f2a3182e1bb4d8243e	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (5E,7E)-Undeca-2,5,7-trienedioyl-CoA 20V, Positive-QTOF	splash10-000i-1900100014-28055326bc9f490a0ce5	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (5E,7E)-Undeca-2,5,7-trienedioyl-CoA 40V, Positive-QTOF	splash10-0udi-1100900000-060316d1ee93778317cb	2021-10-21	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

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

Abe T, Fujino T, Fukuyama R, Minoshima S, Shimizu N, Toh H, Suzuki H, Yamamoto T: Human long-chain acyl-CoA synthetase: structure and chromosomal location. J Biochem. 1992 Jan;111(1):123-8. [PubMed:1607358 ]
Wishart DS, Li C, Marcu A, Badran H, Pon A, Budinski Z, Patron J, Lipton D, Cao X, Oler E, Li K, Paccoud M, Hong C, Guo AC, Chan C, Wei W, Ramirez-Gaona M: PathBank: a comprehensive pathway database for model organisms. Nucleic Acids Res. 2020 Jan 8;48(D1):D470-D478. doi: 10.1093/nar/gkz861. [PubMed:31602464 ]

Showing metabocard for (5E,7E)-Undeca-2,5,7-trienedioyl-CoA (HMDB0300997)

MOL for HMDB0300997 ((5E,7E)-Undeca-2,5,7-trienedioyl-CoA)

3D MOL for HMDB0300997 ((5E,7E)-Undeca-2,5,7-trienedioyl-CoA)

3D SDF for HMDB0300997 ((5E,7E)-Undeca-2,5,7-trienedioyl-CoA)

3D-SDF for HMDB0300997 ((5E,7E)-Undeca-2,5,7-trienedioyl-CoA)

PDB for HMDB0300997 ((5E,7E)-Undeca-2,5,7-trienedioyl-CoA)

3D PDB for HMDB0300997 ((5E,7E)-Undeca-2,5,7-trienedioyl-CoA)

SMILES for HMDB0300997 ((5E,7E)-Undeca-2,5,7-trienedioyl-CoA)

INCHI for HMDB0300997 ((5E,7E)-Undeca-2,5,7-trienedioyl-CoA)

Structure for HMDB0300997 ((5E,7E)-Undeca-2,5,7-trienedioyl-CoA)

3D Structure for HMDB0300997 ((5E,7E)-Undeca-2,5,7-trienedioyl-CoA)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

MS/MS Spectra