Showing NP-Card for Ganglioside GQ1c (d18:1/18:1(11Z)) (NP0338896)
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Version | 2.0 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Created at | 2024-09-11 18:35:52 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Updated at | 2024-09-11 18:35:52 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
NP-MRD ID | NP0338896 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Secondary Accession Numbers | None | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Natural Product Identification | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Common Name | Ganglioside GQ1c (d18:1/18:1(11Z)) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Description | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structure | MOL for NP0338896 (Ganglioside GQ1c (d18:1/18:1(11Z)))Mrv0541 02251204572D 205212 0 0 1 0 999 V2000 3.3317 -19.4160 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.8846 -18.7229 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2613 -17.9889 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.8141 -17.2958 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.1907 -16.5620 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.7435 -15.8688 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.1201 -15.1350 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.6729 -14.4418 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.0496 -13.7080 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.6023 -13.0147 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.9790 -12.2810 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5318 -11.5878 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.9084 -10.8539 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4611 -10.1607 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.8378 -9.4268 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.3784 -8.7149 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 1.6658 -9.1619 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 2.5018 -7.8358 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 1.8399 -7.3169 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.0488 -7.5793 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.2808 -7.2359 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 0.2885 -6.4111 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.4219 -5.9918 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 0.3754 -5.5697 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.2123 -5.4258 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.1402 -6.3974 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.8887 -6.2440 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.1444 -5.3812 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -1.5577 -4.8013 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.7550 -4.1194 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -1.1929 -3.3822 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.3265 -3.7397 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.5620 -3.7850 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.7950 -3.0253 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.1361 -2.4798 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -1.3461 -2.7171 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.7455 -2.1514 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 0.0929 -1.9506 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8386 -1.5744 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.9353 -1.3486 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.2101 -0.9131 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.7254 -1.1114 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -1.9118 -0.2961 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.3144 0.2570 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.5296 0.0033 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.0826 0.5563 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 0.9663 0.4765 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.7528 0.7615 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.0901 1.3629 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 0.4963 1.9585 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.8750 1.6166 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -1.0668 2.4423 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.4357 2.9761 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.0260 3.6920 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7989 3.6951 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 1.2086 4.4112 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 1.2141 2.9825 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 2.0390 2.9856 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 2.4487 3.7016 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.0335 4.4144 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2736 3.7048 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.8045 2.2664 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0204 2.2632 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 1.2196 1.5536 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 0.8100 0.8377 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 2.0445 1.5568 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 2.4598 0.8441 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 2.4543 2.2728 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2791 2.2760 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.0696 3.5038 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.9295 4.3169 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.8438 3.2186 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.4873 1.0636 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -2.2734 1.3643 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.3258 -1.6770 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -2.7520 -0.9889 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.6549 -0.9474 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.4033 -1.1744 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.1885 -1.6533 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.1487 -4.3648 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -3.8549 -4.1743 0.0000 O 0 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6 0 0 0 146205 1 1 0 0 0 M END > <DATABASE_ID> NP0338896 > <DATABASE_NAME> NP-MRD > <SMILES> [H][C@@](O)(CO)[C@@]([H])(O)C1O[C@@](C[C@]([H])(O)[C@@]1([H])NC(C)=O)(O[C@]([H])(CO)[C@@]([H])(O)C1O[C@@](C[C@]([H])(O)[C@@]1([H])NC(C)=O)(O[C@]([H])(CO)[C@@]([H])(O)C1O[C@@](C[C@]([H])(O)[C@@]1([H])NC(C)=O)(O[C@]1([H])[C@@]([H])(O)[C@]([H])(O[C@]2([H])[C@@]([H])(CO)O[C@@]([H])(OC[C@]([H])(NC(=O)CCCCCCCCCC=CCCCCCC)[C@]([H])(O)C=CCCCCCCCCCCCCC)[C@]([H])(O)[C@@]2([H])O)O[C@]([H])(CO)[C@]1([H])O[C@]1([H])O[C@]([H])(CO)[C@]([H])(O)[C@]([H])(O[C@]2([H])O[C@]([H])(CO)[C@]([H])(O)[C@]([H])(O[C@@]3(C[C@]([H])(O)[C@@]([H])(NC(C)=O)C(O3)[C@]([H])(O)[C@]([H])(O)CO)C(O)=O)[C@@]2([H])O)[C@@]1([H])CC(C)=O)C(O)=O)C(O)=O)C(O)=O > <INCHI_IDENTIFIER> InChI=1S/C107H181N5O55/c1-8-10-12-14-16-18-20-22-23-25-27-29-31-33-35-37-72(133)112-58(59(126)36-34-32-30-28-26-24-21-19-17-15-13-11-9-2)51-152-97-84(141)83(140)88(70(49-119)155-97)158-99-86(143)95(89(71(50-120)156-99)159-96-57(38-52(3)121)87(79(136)66(45-115)153-96)157-98-85(142)94(80(137)67(46-116)154-98)166-106(102(148)149)41-62(129)74(109-54(5)123)91(163-106)78(135)65(132)44-114)167-107(103(150)151)42-63(130)76(111-56(7)125)93(165-107)82(139)69(48-118)161-105(101(146)147)40-61(128)75(110-55(6)124)92(164-105)81(138)68(47-117)160-104(100(144)145)39-60(127)73(108-53(4)122)90(162-104)77(134)64(131)43-113/h18,20,34,36,57-71,73-99,113-120,126-132,134-143H,8-17,19,21-33,35,37-51H2,1-7H3,(H,108,122)(H,109,123)(H,110,124)(H,111,125)(H,112,133)(H,144,145)(H,146,147)(H,148,149)(H,150,151)/t57-,58+,59-,60+,61+,62+,63+,64-,65-,66-,67-,68-,69-,70-,71-,73-,74-,75-,76-,77-,78-,79+,80+,81?,82-,83-,84-,85-,86?,87-,88-,89+,90?,91?,92?,93?,94+,95-,96+,97-,98+,99+,104-,105-,106+,107+/m1/s1 > <INCHI_KEY> OIQDHZKSBJYFLC-HCRJAZJVSA-N > <FORMULA> C107H181N5O55 > <MOLECULAR_WEIGHT> 2417.5825 > <EXACT_MASS> 2416.152005027 > <JCHEM_ACCEPTOR_COUNT> 55 > <JCHEM_AVERAGE_POLARIZABILITY> 252.80595160532317 > <JCHEM_BIOAVAILABILITY> 0 > <JCHEM_DONOR_COUNT> 34 > <JCHEM_FORMAL_CHARGE> 0 > <JCHEM_GHOSE_FILTER> 0 > <JCHEM_IUPAC> (2S,4S,5R)-2-{[(1S,2R)-1-[(3R,4S,6S)-6-carboxy-6-{[(1S,2R)-1-[(3R,4S,6S)-6-carboxy-6-{[(2R,3S,4R,5R,6S)-3-{[(2S,3R,4R,5R,6R)-4-{[(2R,3R,4S,5S,6R)-4-{[(2S,4S,5R)-2-carboxy-5-acetamido-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxan-2-yl]oxy}-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-hydroxy-6-(hydroxymethyl)-3-(2-oxopropyl)oxan-2-yl]oxy}-6-{[(2R,3S,4R,5R,6R)-4,5-dihydroxy-6-{[(2S,3R)-3-hydroxy-2-(octadec-11-enamido)octadec-4-en-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxy}-5-hydroxy-2-(hydroxymethyl)oxan-4-yl]oxy}-3-acetamido-4-hydroxyoxan-2-yl]-1,3-dihydroxypropan-2-yl]oxy}-3-acetamido-4-hydroxyoxan-2-yl]-1,3-dihydroxypropan-2-yl]oxy}-5-acetamido-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid > <ALOGPS_LOGP> 0.31 > <JCHEM_LOGP> -4.570965198333335 > <ALOGPS_LOGS> -3.09 > <JCHEM_MDDR_LIKE_RULE> 1 > <JCHEM_NUMBER_OF_RINGS> 8 > <JCHEM_PHYSIOLOGICAL_CHARGE> -4 > <JCHEM_PKA> 2.611851049980949 > <JCHEM_PKA_STRONGEST_ACIDIC> 2.1619347183861306 > <JCHEM_PKA_STRONGEST_BASIC> -3.9476121977780165 > <JCHEM_POLAR_SURFACE_AREA> 965.2000000000006 > <JCHEM_REFRACTIVITY> 559.7627 > <JCHEM_ROTATABLE_BOND_COUNT> 73 > <JCHEM_RULE_OF_FIVE> 0 > <ALOGPS_SOLUBILITY> 1.97e+00 g/l > <JCHEM_TRADITIONAL_IUPAC> (2S,4S,5R)-2-{[(1S,2R)-1-[(3R,4S,6S)-6-carboxy-6-{[(1S,2R)-1-[(3R,4S,6S)-6-carboxy-6-{[(2R,3S,4R,5R,6S)-3-{[(2S,3R,4R,5R,6R)-4-{[(2R,3R,4S,5S,6R)-4-{[(2S,4S,5R)-2-carboxy-5-acetamido-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxan-2-yl]oxy}-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-hydroxy-6-(hydroxymethyl)-3-(2-oxopropyl)oxan-2-yl]oxy}-6-{[(2R,3S,4R,5R,6R)-4,5-dihydroxy-6-{[(2S,3R)-3-hydroxy-2-(octadec-11-enamido)octadec-4-en-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxy}-5-hydroxy-2-(hydroxymethyl)oxan-4-yl]oxy}-3-acetamido-4-hydroxyoxan-2-yl]-1,3-dihydroxypropan-2-yl]oxy}-3-acetamido-4-hydroxyoxan-2-yl]-1,3-dihydroxypropan-2-yl]oxy}-5-acetamido-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid > <JCHEM_VEBER_RULE> 0 $$$$ PDB for NP0338896 (Ganglioside GQ1c (d18:1/18:1(11Z)))HEADER PROTEIN 25-FEB-12 NONE TITLE NULL COMPND NULL SOURCE NULL KEYWDS NULL EXPDTA NULL AUTHOR Marvin REVDAT 1 25-FEB-12 0 HETATM 1 C UNK 0 6.219 -36.243 0.000 0.00 0.00 C+0 HETATM 2 C UNK 0 5.385 -34.949 0.000 0.00 0.00 C+0 HETATM 3 C UNK 0 6.088 -33.579 0.000 0.00 0.00 C+0 HETATM 4 C UNK 0 5.253 -32.286 0.000 0.00 0.00 C+0 HETATM 5 C UNK 0 5.956 -30.916 0.000 0.00 0.00 C+0 HETATM 6 C UNK 0 5.121 -29.622 0.000 0.00 0.00 C+0 HETATM 7 C UNK 0 5.824 -28.252 0.000 0.00 0.00 C+0 HETATM 8 C UNK 0 4.989 -26.958 0.000 0.00 0.00 C+0 HETATM 9 C UNK 0 5.693 -25.588 0.000 0.00 0.00 C+0 HETATM 10 C UNK 0 4.858 -24.294 0.000 0.00 0.00 C+0 HETATM 11 C UNK 0 5.561 -22.924 0.000 0.00 0.00 C+0 HETATM 12 C UNK 0 4.726 -21.630 0.000 0.00 0.00 C+0 HETATM 13 C UNK 0 5.429 -20.261 0.000 0.00 0.00 C+0 HETATM 14 C UNK 0 4.594 -18.967 0.000 0.00 0.00 C+0 HETATM 15 C UNK 0 5.297 -17.597 0.000 0.00 0.00 C+0 HETATM 16 C UNK 0 4.440 -16.268 0.000 0.00 0.00 C+0 HETATM 17 O UNK 0 3.110 -17.102 0.000 0.00 0.00 O+0 HETATM 18 C UNK 0 4.670 -14.627 0.000 0.00 0.00 C+0 HETATM 19 C UNK 0 3.434 -13.658 0.000 0.00 0.00 C+0 HETATM 20 O UNK 0 1.958 -14.148 0.000 0.00 0.00 O+0 HETATM 21 C UNK 0 0.524 -13.507 0.000 0.00 0.00 C+0 HETATM 22 O UNK 0 0.539 -11.967 0.000 0.00 0.00 O+0 HETATM 23 C UNK 0 -0.787 -11.185 0.000 0.00 0.00 C+0 HETATM 24 C UNK 0 0.701 -10.397 0.000 0.00 0.00 C+0 HETATM 25 O UNK 0 2.263 -10.128 0.000 0.00 0.00 O+0 HETATM 26 C UNK 0 -2.128 -11.942 0.000 0.00 0.00 C+0 HETATM 27 O UNK 0 -3.526 -11.655 0.000 0.00 0.00 O+0 HETATM 28 C UNK 0 -4.003 -10.045 0.000 0.00 0.00 C+0 HETATM 29 O UNK 0 -2.908 -8.962 0.000 0.00 0.00 O+0 HETATM 30 C UNK 0 -3.276 -7.690 0.000 0.00 0.00 C+0 HETATM 31 C UNK 0 -2.227 -6.313 0.000 0.00 0.00 C+0 HETATM 32 O UNK 0 -0.609 -6.981 0.000 0.00 0.00 O+0 HETATM 33 C UNK 0 -4.782 -7.065 0.000 0.00 0.00 C+0 HETATM 34 O UNK 0 -5.217 -5.647 0.000 0.00 0.00 O+0 HETATM 35 C UNK 0 -3.987 -4.629 0.000 0.00 0.00 C+0 HETATM 36 O UNK 0 -2.513 -5.072 0.000 0.00 0.00 O+0 HETATM 37 C UNK 0 -1.392 -4.016 0.000 0.00 0.00 C+0 HETATM 38 C UNK 0 0.173 -3.641 0.000 0.00 0.00 C+0 HETATM 39 O UNK 0 1.565 -2.939 0.000 0.00 0.00 O+0 HETATM 40 C UNK 0 -1.746 -2.517 0.000 0.00 0.00 C+0 HETATM 41 O UNK 0 -0.392 -1.704 0.000 0.00 0.00 O+0 HETATM 42 C UNK 0 -3.221 -2.075 0.000 0.00 0.00 C+0 HETATM 43 O UNK 0 -3.569 -0.553 0.000 0.00 0.00 O+0 HETATM 44 C UNK 0 -2.454 0.480 0.000 0.00 0.00 C+0 HETATM 45 O UNK 0 -0.988 0.006 0.000 0.00 0.00 O+0 HETATM 46 C UNK 0 0.154 1.038 0.000 0.00 0.00 C+0 HETATM 47 C UNK 0 1.804 0.889 0.000 0.00 0.00 C+0 HETATM 48 O UNK 0 3.272 1.422 0.000 0.00 0.00 O+0 HETATM 49 C UNK 0 -0.168 2.544 0.000 0.00 0.00 C+0 HETATM 50 O UNK 0 0.926 3.656 0.000 0.00 0.00 O+0 HETATM 51 C UNK 0 -1.633 3.018 0.000 0.00 0.00 C+0 HETATM 52 O UNK 0 -1.991 4.559 0.000 0.00 0.00 O+0 HETATM 53 C UNK 0 -0.813 5.555 0.000 0.00 0.00 C+0 HETATM 54 C UNK 0 -0.049 6.892 0.000 0.00 0.00 C+0 HETATM 55 C UNK 0 1.491 6.898 0.000 0.00 0.00 C+0 HETATM 56 O UNK 0 2.256 8.234 0.000 0.00 0.00 O+0 HETATM 57 C UNK 0 2.266 5.567 0.000 0.00 0.00 C+0 HETATM 58 N UNK 0 3.806 5.573 0.000 0.00 0.00 N+0 HETATM 59 C UNK 0 4.571 6.910 0.000 0.00 0.00 C+0 HETATM 60 C UNK 0 3.796 8.240 0.000 0.00 0.00 C+0 HETATM 61 O UNK 0 6.111 6.916 0.000 0.00 0.00 O+0 HETATM 62 C UNK 0 1.502 4.231 0.000 0.00 0.00 C+0 HETATM 63 O UNK 0 -0.038 4.225 0.000 0.00 0.00 O+0 HETATM 64 C UNK 0 2.277 2.900 0.000 0.00 0.00 C+0 HETATM 65 O UNK 0 1.512 1.564 0.000 0.00 0.00 O+0 HETATM 66 C UNK 0 3.816 2.906 0.000 0.00 0.00 C+0 HETATM 67 O UNK 0 4.592 1.576 0.000 0.00 0.00 O+0 HETATM 68 C UNK 0 4.581 4.243 0.000 0.00 0.00 C+0 HETATM 69 O UNK 0 6.121 4.249 0.000 0.00 0.00 O+0 HETATM 70 C UNK 0 -1.997 6.540 0.000 0.00 0.00 C+0 HETATM 71 O UNK 0 -1.735 8.058 0.000 0.00 0.00 O+0 HETATM 72 O UNK 0 -3.442 6.008 0.000 0.00 0.00 O+0 HETATM 73 C UNK 0 -2.776 1.985 0.000 0.00 0.00 C+0 HETATM 74 O UNK 0 -4.244 2.547 0.000 0.00 0.00 O+0 HETATM 75 C UNK 0 -4.341 -3.130 0.000 0.00 0.00 C+0 HETATM 76 C UNK 0 -5.137 -1.846 0.000 0.00 0.00 C+0 HETATM 77 C UNK 0 -6.823 -1.768 0.000 0.00 0.00 C+0 HETATM 78 C UNK 0 -8.220 -2.192 0.000 0.00 0.00 C+0 HETATM 79 O UNK 0 -7.818 -3.086 0.000 0.00 0.00 O+0 HETATM 80 C UNK 0 -5.878 -8.148 0.000 0.00 0.00 C+0 HETATM 81 O UNK 0 -7.196 -7.792 0.000 0.00 0.00 O+0 HETATM 82 C UNK 0 -8.477 -8.857 0.000 0.00 0.00 C+0 HETATM 83 C UNK 0 -9.918 -9.400 0.000 0.00 0.00 C+0 HETATM 84 C UNK 0 -10.169 -10.919 0.000 0.00 0.00 C+0 HETATM 85 O UNK 0 -11.696 -11.311 0.000 0.00 0.00 O+0 HETATM 86 C UNK 0 -8.978 -11.896 0.000 0.00 0.00 C+0 HETATM 87 N UNK 0 -9.945 -13.203 0.000 0.00 0.00 N+0 HETATM 88 C UNK 0 -11.111 -14.293 0.000 0.00 0.00 C+0 HETATM 89 C UNK 0 -12.666 -14.147 0.000 0.00 0.00 C+0 HETATM 90 O UNK 0 -11.139 -15.865 0.000 0.00 0.00 O+0 HETATM 91 C UNK 0 -7.537 -11.353 0.000 0.00 0.00 C+0 HETATM 92 O UNK 0 -7.287 -9.834 0.000 0.00 0.00 O+0 HETATM 93 C UNK 0 -6.851 -12.904 0.000 0.00 0.00 C+0 HETATM 94 O UNK 0 -7.488 -14.415 0.000 0.00 0.00 O+0 HETATM 95 C UNK 0 -5.186 -12.812 0.000 0.00 0.00 C+0 HETATM 96 C UNK 0 -5.128 -14.418 0.000 0.00 0.00 C+0 HETATM 97 O UNK 0 -5.213 -16.031 0.000 0.00 0.00 O+0 HETATM 98 O UNK 0 -4.444 -11.188 0.000 0.00 0.00 O+0 HETATM 99 C UNK 0 -3.214 -9.724 0.000 0.00 0.00 C+0 HETATM 100 C UNK 0 -1.675 -9.707 0.000 0.00 0.00 C+0 HETATM 101 C UNK 0 -0.920 -8.365 0.000 0.00 0.00 C+0 HETATM 102 O UNK 0 0.691 -8.385 0.000 0.00 0.00 O+0 HETATM 103 C UNK 0 -1.704 -7.040 0.000 0.00 0.00 C+0 HETATM 104 N UNK 0 -0.262 -5.933 0.000 0.00 0.00 N+0 HETATM 105 C UNK 0 1.413 -5.813 0.000 0.00 0.00 C+0 HETATM 106 C UNK 0 3.037 -5.992 0.000 0.00 0.00 C+0 HETATM 107 O UNK 0 2.974 -5.413 0.000 0.00 0.00 O+0 HETATM 108 C UNK 0 -3.244 -7.058 0.000 0.00 0.00 C+0 HETATM 109 O UNK 0 -3.999 -8.399 0.000 0.00 0.00 O+0 HETATM 110 C UNK 0 -4.073 -5.538 0.000 0.00 0.00 C+0 HETATM 111 O UNK 0 -3.113 -4.049 0.000 0.00 0.00 O+0 HETATM 112 C UNK 0 -5.646 -4.568 0.000 0.00 0.00 C+0 HETATM 113 C UNK 0 -5.982 -2.852 0.000 0.00 0.00 C+0 HETATM 114 O UNK 0 -5.974 -1.048 0.000 0.00 0.00 O+0 HETATM 115 O UNK 0 -6.527 -6.067 0.000 0.00 0.00 O+0 HETATM 116 C UNK 0 -7.863 -7.109 0.000 0.00 0.00 C+0 HETATM 117 C UNK 0 -9.262 -8.086 0.000 0.00 0.00 C+0 HETATM 118 C UNK 0 -10.495 -6.676 0.000 0.00 0.00 C+0 HETATM 119 O UNK 0 -12.124 -6.699 0.000 0.00 0.00 O+0 HETATM 120 C UNK 0 -10.245 -5.156 0.000 0.00 0.00 C+0 HETATM 121 N UNK 0 -11.771 -4.669 0.000 0.00 0.00 N+0 HETATM 122 C UNK 0 -13.280 -4.256 0.000 0.00 0.00 C+0 HETATM 123 C UNK 0 -14.397 -5.411 0.000 0.00 0.00 C+0 HETATM 124 O UNK 0 -14.278 -2.996 0.000 0.00 0.00 O+0 HETATM 125 C UNK 0 -8.803 -4.613 0.000 0.00 0.00 C+0 HETATM 126 O UNK 0 -7.613 -5.590 0.000 0.00 0.00 O+0 HETATM 127 C UNK 0 -9.720 -3.150 0.000 0.00 0.00 C+0 HETATM 128 O UNK 0 -9.840 -1.548 0.000 0.00 0.00 O+0 HETATM 129 C UNK 0 -10.483 -1.615 0.000 0.00 0.00 C+0 HETATM 130 O UNK 0 -12.013 -1.151 0.000 0.00 0.00 O+0 HETATM 131 C UNK 0 -10.267 0.022 0.000 0.00 0.00 C+0 HETATM 132 O UNK 0 -10.380 1.593 0.000 0.00 0.00 O+0 HETATM 133 C UNK 0 -7.365 -8.832 0.000 0.00 0.00 C+0 HETATM 134 O UNK 0 -6.436 -10.220 0.000 0.00 0.00 O+0 HETATM 135 O UNK 0 -8.468 -10.164 0.000 0.00 0.00 O+0 HETATM 136 C UNK 0 -1.937 -10.961 0.000 0.00 0.00 C+0 HETATM 137 O UNK 0 -1.673 -12.489 0.000 0.00 0.00 O+0 HETATM 138 O UNK 0 -1.000 -12.432 0.000 0.00 0.00 O+0 HETATM 139 C UNK 0 -10.292 -8.239 0.000 0.00 0.00 C+0 HETATM 140 O UNK 0 -11.882 -8.754 0.000 0.00 0.00 O+0 HETATM 141 O UNK 0 -9.387 -6.797 0.000 0.00 0.00 O+0 HETATM 142 C UNK 0 -5.488 -9.638 0.000 0.00 0.00 C+0 HETATM 143 O UNK 0 -5.763 -11.301 0.000 0.00 0.00 O+0 HETATM 144 C UNK 0 -2.143 -13.482 0.000 0.00 0.00 C+0 HETATM 145 O UNK 0 -2.551 -15.062 0.000 0.00 0.00 O+0 HETATM 146 C UNK 0 -0.817 -14.264 0.000 0.00 0.00 C+0 HETATM 147 O UNK 0 -0.503 -15.820 0.000 0.00 0.00 O+0 HETATM 148 N UNK 0 5.870 -13.515 0.000 0.00 0.00 N+0 HETATM 149 C UNK 0 7.304 -14.141 0.000 0.00 0.00 C+0 HETATM 150 O UNK 0 7.977 -15.548 0.000 0.00 0.00 O+0 HETATM 151 C UNK 0 8.783 -13.508 0.000 0.00 0.00 C+0 HETATM 152 C UNK 0 10.036 -14.410 0.000 0.00 0.00 C+0 HETATM 153 C UNK 0 11.267 -13.408 0.000 0.00 0.00 C+0 HETATM 154 C UNK 0 12.572 -14.224 0.000 0.00 0.00 C+0 HETATM 155 C UNK 0 14.002 -13.649 0.000 0.00 0.00 C+0 HETATM 156 C UNK 0 15.203 -14.612 0.000 0.00 0.00 C+0 HETATM 157 C UNK 0 16.504 -13.694 0.000 0.00 0.00 C+0 HETATM 158 C UNK 0 17.970 -14.339 0.000 0.00 0.00 C+0 HETATM 159 C UNK 0 19.350 -13.658 0.000 0.00 0.00 C+0 HETATM 160 C UNK 0 20.770 -14.389 0.000 0.00 0.00 C+0 HETATM 161 C UNK 0 22.188 -13.787 0.000 0.00 0.00 C+0 HETATM 162 C UNK 0 23.418 -14.715 0.000 0.00 0.00 C+0 HETATM 163 C UNK 0 23.230 -16.243 0.000 0.00 0.00 C+0 HETATM 164 C UNK 0 24.459 -17.170 0.000 0.00 0.00 C+0 HETATM 165 C UNK 0 24.271 -18.698 0.000 0.00 0.00 C+0 HETATM 166 C UNK 0 25.501 -19.625 0.000 0.00 0.00 C+0 HETATM 167 C UNK 0 25.313 -21.154 0.000 0.00 0.00 C+0 HETATM 168 H UNK 0 5.944 -15.937 0.000 0.00 0.00 H+0 HETATM 169 H UNK 0 6.035 -15.340 0.000 0.00 0.00 H+0 HETATM 170 H UNK 0 0.596 -15.045 0.000 0.00 0.00 H+0 HETATM 171 H UNK 0 -1.526 -9.834 0.000 0.00 0.00 H+0 HETATM 172 H UNK 0 -4.250 -12.258 0.000 0.00 0.00 H+0 HETATM 173 H UNK 0 -2.382 -10.169 0.000 0.00 0.00 H+0 HETATM 174 H UNK 0 -6.000 -9.194 0.000 0.00 0.00 H+0 HETATM 175 H UNK 0 -4.832 -4.514 0.000 0.00 0.00 H+0 HETATM 176 H UNK 0 -5.944 -6.274 0.000 0.00 0.00 H+0 HETATM 177 H UNK 0 0.260 -4.848 0.000 0.00 0.00 H+0 HETATM 178 H UNK 0 -0.988 -0.918 0.000 0.00 0.00 H+0 HETATM 179 H UNK 0 -5.990 -2.169 0.000 0.00 0.00 H+0 HETATM 180 H UNK 0 -2.008 -1.306 0.000 0.00 0.00 H+0 HETATM 181 H UNK 0 1.492 -0.001 0.000 0.00 0.00 H+0 HETATM 182 H UNK 0 1.377 2.888 0.000 0.00 0.00 H+0 HETATM 183 H UNK 0 -3.018 3.994 0.000 0.00 0.00 H+0 HETATM 184 H UNK 0 3.006 7.903 0.000 0.00 0.00 H+0 HETATM 185 H UNK 0 3.684 4.545 0.000 0.00 0.00 H+0 HETATM 186 H UNK 0 3.997 2.239 0.000 0.00 0.00 H+0 HETATM 187 H UNK 0 2.525 1.536 0.000 0.00 0.00 H+0 HETATM 188 H UNK 0 -3.988 3.377 0.000 0.00 0.00 H+0 HETATM 189 H UNK 0 -4.491 -1.423 0.000 0.00 0.00 H+0 HETATM 190 H UNK 0 -5.077 -9.131 0.000 0.00 0.00 H+0 HETATM 191 H UNK 0 -10.754 -12.277 0.000 0.00 0.00 H+0 HETATM 192 H UNK 0 -9.089 -13.860 0.000 0.00 0.00 H+0 HETATM 193 H UNK 0 -8.224 -11.527 0.000 0.00 0.00 H+0 HETATM 194 H UNK 0 -2.408 -11.421 0.000 0.00 0.00 H+0 HETATM 195 H UNK 0 0.445 -7.449 0.000 0.00 0.00 H+0 HETATM 196 H UNK 0 -3.961 -7.169 0.000 0.00 0.00 H+0 HETATM 197 H UNK 0 -3.633 -6.448 0.000 0.00 0.00 H+0 HETATM 198 H UNK 0 -8.215 -5.275 0.000 0.00 0.00 H+0 HETATM 199 H UNK 0 -11.877 -5.753 0.000 0.00 0.00 H+0 HETATM 200 H UNK 0 -11.481 -3.716 0.000 0.00 0.00 H+0 HETATM 201 H UNK 0 -9.418 -5.263 0.000 0.00 0.00 H+0 HETATM 202 H UNK 0 -11.940 -0.130 0.000 0.00 0.00 H+0 HETATM 203 H UNK 0 -6.165 -7.314 0.000 0.00 0.00 H+0 HETATM 204 H UNK 0 -3.850 -14.346 0.000 0.00 0.00 H+0 HETATM 205 H UNK 0 1.177 -14.961 0.000 0.00 0.00 H+0 CONECT 1 2 CONECT 2 1 3 CONECT 3 2 4 CONECT 4 3 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 CONECT 14 13 15 CONECT 15 14 16 CONECT 16 15 17 18 168 CONECT 17 16 CONECT 18 16 19 148 169 CONECT 19 18 20 CONECT 20 19 21 CONECT 21 20 22 146 170 CONECT 22 21 23 CONECT 23 22 24 26 171 CONECT 24 23 25 CONECT 25 24 CONECT 26 23 27 144 172 CONECT 27 26 28 CONECT 28 27 29 142 173 CONECT 29 28 30 CONECT 30 29 31 33 174 CONECT 31 30 32 CONECT 32 31 CONECT 33 30 34 80 175 CONECT 34 33 35 CONECT 35 34 36 75 176 CONECT 36 35 37 CONECT 37 36 38 40 177 CONECT 38 37 39 CONECT 39 38 CONECT 40 37 41 42 178 CONECT 41 40 CONECT 42 40 43 75 179 CONECT 43 42 44 CONECT 44 43 45 73 180 CONECT 45 44 46 CONECT 46 45 47 49 181 CONECT 47 46 48 CONECT 48 47 CONECT 49 46 50 51 182 CONECT 50 49 CONECT 51 49 52 73 183 CONECT 52 51 53 CONECT 53 52 54 63 70 CONECT 54 53 55 CONECT 55 54 56 57 184 CONECT 56 55 CONECT 57 55 58 62 185 CONECT 58 57 59 CONECT 59 58 60 61 CONECT 60 59 CONECT 61 59 CONECT 62 57 63 64 CONECT 63 62 53 CONECT 64 62 65 66 186 CONECT 65 64 CONECT 66 64 67 68 187 CONECT 67 66 CONECT 68 66 69 CONECT 69 68 CONECT 70 53 71 72 CONECT 71 70 CONECT 72 70 CONECT 73 51 44 74 188 CONECT 74 73 CONECT 75 42 35 76 189 CONECT 76 75 77 CONECT 77 76 78 79 CONECT 78 77 CONECT 79 77 CONECT 80 33 81 142 190 CONECT 81 80 82 CONECT 82 81 83 92 139 CONECT 83 82 84 CONECT 84 83 85 86 191 CONECT 85 84 CONECT 86 84 87 91 192 CONECT 87 86 88 CONECT 88 87 89 90 CONECT 89 88 CONECT 90 88 CONECT 91 86 92 93 CONECT 92 91 82 CONECT 93 91 94 95 193 CONECT 94 93 CONECT 95 93 96 98 194 CONECT 96 95 97 CONECT 97 96 CONECT 98 95 99 CONECT 99 98 100 109 136 CONECT 100 99 101 CONECT 101 100 102 103 195 CONECT 102 101 CONECT 103 101 104 108 196 CONECT 104 103 105 CONECT 105 104 106 107 CONECT 106 105 CONECT 107 105 CONECT 108 103 109 110 CONECT 109 108 99 CONECT 110 108 111 112 197 CONECT 111 110 CONECT 112 110 113 115 198 CONECT 113 112 114 CONECT 114 113 CONECT 115 112 116 CONECT 116 115 117 126 133 CONECT 117 116 118 CONECT 118 117 119 120 199 CONECT 119 118 CONECT 120 118 121 125 200 CONECT 121 120 122 CONECT 122 121 123 124 CONECT 123 122 CONECT 124 122 CONECT 125 120 126 127 CONECT 126 125 116 CONECT 127 125 128 129 201 CONECT 128 127 CONECT 129 127 130 131 202 CONECT 130 129 CONECT 131 129 132 CONECT 132 131 CONECT 133 116 134 135 CONECT 134 133 CONECT 135 133 CONECT 136 99 137 138 CONECT 137 136 CONECT 138 136 CONECT 139 82 140 141 CONECT 140 139 CONECT 141 139 CONECT 142 80 28 143 203 CONECT 143 142 CONECT 144 26 145 146 204 CONECT 145 144 CONECT 146 144 21 147 205 CONECT 147 146 CONECT 148 18 149 CONECT 149 148 150 151 CONECT 150 149 CONECT 151 149 152 CONECT 152 151 153 CONECT 153 152 154 CONECT 154 153 155 CONECT 155 154 156 CONECT 156 155 157 CONECT 157 156 158 CONECT 158 157 159 CONECT 159 158 160 CONECT 160 159 161 CONECT 161 160 162 CONECT 162 161 163 CONECT 163 162 164 CONECT 164 163 165 CONECT 165 164 166 CONECT 166 165 167 CONECT 167 166 CONECT 168 16 CONECT 169 18 CONECT 170 21 CONECT 171 23 CONECT 172 26 CONECT 173 28 CONECT 174 30 CONECT 175 33 CONECT 176 35 CONECT 177 37 CONECT 178 40 CONECT 179 42 CONECT 180 44 CONECT 181 46 CONECT 182 49 CONECT 183 51 CONECT 184 55 CONECT 185 57 CONECT 186 64 CONECT 187 66 CONECT 188 73 CONECT 189 75 CONECT 190 80 CONECT 191 84 CONECT 192 86 CONECT 193 93 CONECT 194 95 CONECT 195 101 CONECT 196 103 CONECT 197 110 CONECT 198 112 CONECT 199 118 CONECT 200 120 CONECT 201 127 CONECT 202 129 CONECT 203 142 CONECT 204 144 CONECT 205 146 MASTER 0 0 0 0 0 0 0 0 205 0 424 0 END SMILES for NP0338896 (Ganglioside GQ1c (d18:1/18:1(11Z)))[H][C@@](O)(CO)[C@@]([H])(O)C1O[C@@](C[C@]([H])(O)[C@@]1([H])NC(C)=O)(O[C@]([H])(CO)[C@@]([H])(O)C1O[C@@](C[C@]([H])(O)[C@@]1([H])NC(C)=O)(O[C@]([H])(CO)[C@@]([H])(O)C1O[C@@](C[C@]([H])(O)[C@@]1([H])NC(C)=O)(O[C@]1([H])[C@@]([H])(O)[C@]([H])(O[C@]2([H])[C@@]([H])(CO)O[C@@]([H])(OC[C@]([H])(NC(=O)CCCCCCCCCC=CCCCCCC)[C@]([H])(O)C=CCCCCCCCCCCCCC)[C@]([H])(O)[C@@]2([H])O)O[C@]([H])(CO)[C@]1([H])O[C@]1([H])O[C@]([H])(CO)[C@]([H])(O)[C@]([H])(O[C@]2([H])O[C@]([H])(CO)[C@]([H])(O)[C@]([H])(O[C@@]3(C[C@]([H])(O)[C@@]([H])(NC(C)=O)C(O3)[C@]([H])(O)[C@]([H])(O)CO)C(O)=O)[C@@]2([H])O)[C@@]1([H])CC(C)=O)C(O)=O)C(O)=O)C(O)=O INCHI for NP0338896 (Ganglioside GQ1c (d18:1/18:1(11Z)))InChI=1S/C107H181N5O55/c1-8-10-12-14-16-18-20-22-23-25-27-29-31-33-35-37-72(133)112-58(59(126)36-34-32-30-28-26-24-21-19-17-15-13-11-9-2)51-152-97-84(141)83(140)88(70(49-119)155-97)158-99-86(143)95(89(71(50-120)156-99)159-96-57(38-52(3)121)87(79(136)66(45-115)153-96)157-98-85(142)94(80(137)67(46-116)154-98)166-106(102(148)149)41-62(129)74(109-54(5)123)91(163-106)78(135)65(132)44-114)167-107(103(150)151)42-63(130)76(111-56(7)125)93(165-107)82(139)69(48-118)161-105(101(146)147)40-61(128)75(110-55(6)124)92(164-105)81(138)68(47-117)160-104(100(144)145)39-60(127)73(108-53(4)122)90(162-104)77(134)64(131)43-113/h18,20,34,36,57-71,73-99,113-120,126-132,134-143H,8-17,19,21-33,35,37-51H2,1-7H3,(H,108,122)(H,109,123)(H,110,124)(H,111,125)(H,112,133)(H,144,145)(H,146,147)(H,148,149)(H,150,151)/t57-,58+,59-,60+,61+,62+,63+,64-,65-,66-,67-,68-,69-,70-,71-,73-,74-,75-,76-,77-,78-,79+,80+,81?,82-,83-,84-,85-,86?,87-,88-,89+,90?,91?,92?,93?,94+,95-,96+,97-,98+,99+,104-,105-,106+,107+/m1/s1 3D Structure for NP0338896 (Ganglioside GQ1c (d18:1/18:1(11Z))) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Chemical Formula | C107H181N5O55 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Average Mass | 2417.5825 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Monoisotopic Mass | 2416.15201 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
IUPAC Name | (2S,4S,5R)-2-{[(1S,2R)-1-[(3R,4S,6S)-6-carboxy-6-{[(1S,2R)-1-[(3R,4S,6S)-6-carboxy-6-{[(2R,3S,4R,5R,6S)-3-{[(2S,3R,4R,5R,6R)-4-{[(2R,3R,4S,5S,6R)-4-{[(2S,4S,5R)-2-carboxy-5-acetamido-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxan-2-yl]oxy}-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-hydroxy-6-(hydroxymethyl)-3-(2-oxopropyl)oxan-2-yl]oxy}-6-{[(2R,3S,4R,5R,6R)-4,5-dihydroxy-6-{[(2S,3R)-3-hydroxy-2-(octadec-11-enamido)octadec-4-en-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxy}-5-hydroxy-2-(hydroxymethyl)oxan-4-yl]oxy}-3-acetamido-4-hydroxyoxan-2-yl]-1,3-dihydroxypropan-2-yl]oxy}-3-acetamido-4-hydroxyoxan-2-yl]-1,3-dihydroxypropan-2-yl]oxy}-5-acetamido-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Traditional Name | (2S,4S,5R)-2-{[(1S,2R)-1-[(3R,4S,6S)-6-carboxy-6-{[(1S,2R)-1-[(3R,4S,6S)-6-carboxy-6-{[(2R,3S,4R,5R,6S)-3-{[(2S,3R,4R,5R,6R)-4-{[(2R,3R,4S,5S,6R)-4-{[(2S,4S,5R)-2-carboxy-5-acetamido-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxan-2-yl]oxy}-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-hydroxy-6-(hydroxymethyl)-3-(2-oxopropyl)oxan-2-yl]oxy}-6-{[(2R,3S,4R,5R,6R)-4,5-dihydroxy-6-{[(2S,3R)-3-hydroxy-2-(octadec-11-enamido)octadec-4-en-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxy}-5-hydroxy-2-(hydroxymethyl)oxan-4-yl]oxy}-3-acetamido-4-hydroxyoxan-2-yl]-1,3-dihydroxypropan-2-yl]oxy}-3-acetamido-4-hydroxyoxan-2-yl]-1,3-dihydroxypropan-2-yl]oxy}-5-acetamido-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
CAS Registry Number | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
SMILES | [H][C@@](O)(CO)[C@@]([H])(O)C1O[C@@](C[C@]([H])(O)[C@@]1([H])NC(C)=O)(O[C@]([H])(CO)[C@@]([H])(O)C1O[C@@](C[C@]([H])(O)[C@@]1([H])NC(C)=O)(O[C@]([H])(CO)[C@@]([H])(O)C1O[C@@](C[C@]([H])(O)[C@@]1([H])NC(C)=O)(O[C@]1([H])[C@@]([H])(O)[C@]([H])(O[C@]2([H])[C@@]([H])(CO)O[C@@]([H])(OC[C@]([H])(NC(=O)CCCCCCCCCC=CCCCCCC)[C@]([H])(O)C=CCCCCCCCCCCCCC)[C@]([H])(O)[C@@]2([H])O)O[C@]([H])(CO)[C@]1([H])O[C@]1([H])O[C@]([H])(CO)[C@]([H])(O)[C@]([H])(O[C@]2([H])O[C@]([H])(CO)[C@]([H])(O)[C@]([H])(O[C@@]3(C[C@]([H])(O)[C@@]([H])(NC(C)=O)C(O3)[C@]([H])(O)[C@]([H])(O)CO)C(O)=O)[C@@]2([H])O)[C@@]1([H])CC(C)=O)C(O)=O)C(O)=O)C(O)=O | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
InChI Identifier | InChI=1S/C107H181N5O55/c1-8-10-12-14-16-18-20-22-23-25-27-29-31-33-35-37-72(133)112-58(59(126)36-34-32-30-28-26-24-21-19-17-15-13-11-9-2)51-152-97-84(141)83(140)88(70(49-119)155-97)158-99-86(143)95(89(71(50-120)156-99)159-96-57(38-52(3)121)87(79(136)66(45-115)153-96)157-98-85(142)94(80(137)67(46-116)154-98)166-106(102(148)149)41-62(129)74(109-54(5)123)91(163-106)78(135)65(132)44-114)167-107(103(150)151)42-63(130)76(111-56(7)125)93(165-107)82(139)69(48-118)161-105(101(146)147)40-61(128)75(110-55(6)124)92(164-105)81(138)68(47-117)160-104(100(144)145)39-60(127)73(108-53(4)122)90(162-104)77(134)64(131)43-113/h18,20,34,36,57-71,73-99,113-120,126-132,134-143H,8-17,19,21-33,35,37-51H2,1-7H3,(H,108,122)(H,109,123)(H,110,124)(H,111,125)(H,112,133)(H,144,145)(H,146,147)(H,148,149)(H,150,151)/t57-,58+,59-,60+,61+,62+,63+,64-,65-,66-,67-,68-,69-,70-,71-,73-,74-,75-,76-,77-,78-,79+,80+,81?,82-,83-,84-,85-,86?,87-,88-,89+,90?,91?,92?,93?,94+,95-,96+,97-,98+,99+,104-,105-,106+,107+/m1/s1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
InChI Key | OIQDHZKSBJYFLC-HCRJAZJVSA-N | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Experimental Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Predicted Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Chemical Shift Submissions | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Species | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Species of Origin | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Chemical Taxonomy | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Description | This compound belongs to the class of organic compounds known as gangliosides. These are lipid molecules composed of a glycosphingolipid (ceramide and saccharide) with one or more sialic acids linked on the sugar chain. They are usually oligoglycosylceramides derived from lactosylceramide and containing a sialic acid residue such as N-acetylneuraminic acid. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Kingdom | Organic compounds | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Super Class | Lipids and lipid-like molecules | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Class | Sphingolipids | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sub Class | Glycosphingolipids | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Direct Parent | Gangliosides | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Alternative Parents |
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Substituents |
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Molecular Framework | Aliphatic heteromonocyclic compounds | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
External Descriptors | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Physical Properties | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
State | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Experimental Properties |
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Predicted Properties |
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External Links | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
HMDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
DrugBank ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Phenol Explorer Compound ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
FoodDB ID | FDB028620 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Good Scents ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
References | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
General References | Not Available |