Showing NP-Card for CL(16:0/18:3(9Z,12Z,15Z)/18:3(9Z,12Z,15Z)/20:1(11Z)) (NP0340345)
| Record Information | ||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Version | 2.0 | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Created at | 2024-09-12 02:57:05 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Updated at | 2024-09-12 02:57:06 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||
| NP-MRD ID | NP0340345 | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary Accession Numbers | None | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Natural Product Identification | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Common Name | CL(16:0/18:3(9Z,12Z,15Z)/18:3(9Z,12Z,15Z)/20:1(11Z)) | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Description | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Structure |  MOL for NP0340345 (CL(16:0/18:3(9Z,12Z,15Z)/18:3(9Z,12Z,15Z)/20:1(11Z)))
CL(16:0/18:3(9Z,12Z,15Z)/18:3(9Z,12Z,15Z)/20:1(11Z))
Mrv2104 05272305292D
103102 0 0 0 0 999 V2000
28.9804 -8.8498 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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102103 1 0 0 0 0
M END
3D SDF for NP0340345 (CL(16:0/18:3(9Z,12Z,15Z)/18:3(9Z,12Z,15Z)/20:1(11Z)))
CL(16:0/18:3(9Z,12Z,15Z)/18:3(9Z,12Z,15Z)/20:1(11Z))
Mrv2104 05272305292D
103102 0 0 0 0 999 V2000
28.9804 -8.8498 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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102103 1 0 0 0 0
M END
> <DATABASE_ID>
NP0340345
> <DATABASE_NAME>
NP-MRD
> <SMILES>
[H]C(O)(COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC)OC(=O)CCCCCCCCC\C=C/CCCCCCCC)COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC
> <INCHI_IDENTIFIER>
InChI=1/C81H144O17P2/c1-5-9-13-17-21-25-29-33-36-37-40-44-48-52-56-60-64-68-81(86)98-77(72-92-79(84)66-62-58-54-50-46-42-38-34-30-26-22-18-14-10-6-2)74-96-100(89,90)94-70-75(82)69-93-99(87,88)95-73-76(71-91-78(83)65-61-57-53-49-45-41-32-28-24-20-16-12-8-4)97-80(85)67-63-59-55-51-47-43-39-35-31-27-23-19-15-11-7-3/h10-11,14-15,22-23,26-27,33-36,38-39,75-77,82H,5-9,12-13,16-21,24-25,28-32,37,40-74H2,1-4H3,(H,87,88)(H,89,90)/b14-10-,15-11-,26-22-,27-23-,36-33-,38-34-,39-35-/t75-,76+,77+/s2
> <INCHI_KEY>
OVRNGLQPVAQKIK-BDSBYBIANA-N
> <FORMULA>
C81H144O17P2
> <MOLECULAR_WEIGHT>
1451.974
> <EXACT_MASS>
1450.987877173
> <JCHEM_ACCEPTOR_COUNT>
9
> <JCHEM_ATOM_COUNT>
244
> <JCHEM_AVERAGE_POLARIZABILITY>
172.28241127565946
> <JCHEM_BIOAVAILABILITY>
0
> <JCHEM_DONOR_COUNT>
3
> <JCHEM_FORMAL_CHARGE>
0
> <JCHEM_GHOSE_FILTER>
0
> <JCHEM_IUPAC>
[(2R)-3-(hexadecanoyloxy)-2-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propoxy][(2R)-2-hydroxy-3-({hydroxy[(2R)-2-[(11Z)-icos-11-enoyloxy]-3-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propoxy]phosphoryl}oxy)propoxy]phosphinic acid
> <JCHEM_LOGP>
24.736214784666657
> <JCHEM_MDDR_LIKE_RULE>
0
> <JCHEM_NUMBER_OF_RINGS>
0
> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2
> <JCHEM_PKA>
2.191804358217231
> <JCHEM_PKA_STRONGEST_ACIDIC>
1.5897376143223727
> <JCHEM_PKA_STRONGEST_BASIC>
-3.41050295233858
> <JCHEM_POLAR_SURFACE_AREA>
236.94999999999996
> <JCHEM_REFRACTIVITY>
414.72589999999985
> <JCHEM_ROTATABLE_BOND_COUNT>
79
> <JCHEM_RULE_OF_FIVE>
0
> <JCHEM_TRADITIONAL_IUPAC>
(2R)-3-(hexadecanoyloxy)-2-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propoxy((2R)-2-hydroxy-3-{[hydroxy((2R)-2-[(11Z)-icos-11-enoyloxy]-3-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propoxy)phosphoryl]oxy}propoxy)phosphinic acid
> <JCHEM_VEBER_RULE>
0
$$$$
PDB for NP0340345 (CL(16:0/18:3(9Z,12Z,15Z)/18:3(9Z,12Z,15Z)/20:1(11Z)))HEADER PROTEIN 27-MAY-23 NONE TITLE NULL COMPND MOLECULE: CL(16:0/18:3(9Z,12Z,15Z)/18:3(9Z,12Z,15Z)/20:1(11Z SOURCE NULL KEYWDS NULL EXPDTA NULL AUTHOR Marvin REVDAT 1 27-MAY-23 0 HETATM 1 C UNK 0 54.097 -16.520 0.000 0.00 0.00 C+0 HETATM 2 C UNK 0 53.011 -14.755 0.000 0.00 0.00 C+0 HETATM 3 C UNK 0 53.995 -12.932 0.000 0.00 0.00 C+0 HETATM 4 O UNK 0 53.112 -18.342 0.000 0.00 0.00 O+0 HETATM 5 O UNK 0 52.909 -11.168 0.000 0.00 0.00 O+0 HETATM 6 O UNK 0 54.554 -14.224 0.000 0.00 0.00 O+0 HETATM 7 H UNK 0 51.453 -14.081 0.000 0.00 0.00 H+0 HETATM 8 C UNK 0 49.765 -8.809 0.000 0.00 0.00 C+0 HETATM 9 C UNK 0 47.971 -9.845 0.000 0.00 0.00 C+0 HETATM 10 C UNK 0 46.177 -8.809 0.000 0.00 0.00 C+0 HETATM 11 O UNK 0 51.560 -9.845 0.000 0.00 0.00 O+0 HETATM 12 O UNK 0 44.383 -9.845 0.000 0.00 0.00 O+0 HETATM 13 O UNK 0 46.467 -11.369 0.000 0.00 0.00 O+0 HETATM 14 H UNK 0 49.429 -11.448 0.000 0.00 0.00 H+0 HETATM 15 P UNK 0 53.849 -9.088 0.000 0.00 0.00 P+0 HETATM 16 O UNK 0 55.955 -9.688 0.000 0.00 0.00 O+0 HETATM 17 O UNK 0 53.849 -6.668 0.000 0.00 0.00 O+0 HETATM 18 C UNK 0 46.557 -17.307 0.000 0.00 0.00 C+0 HETATM 19 C UNK 0 44.763 -18.342 0.000 0.00 0.00 C+0 HETATM 20 C UNK 0 42.968 -17.307 0.000 0.00 0.00 C+0 HETATM 21 O UNK 0 48.351 -18.342 0.000 0.00 0.00 O+0 HETATM 22 O UNK 0 41.174 -18.342 0.000 0.00 0.00 O+0 HETATM 23 O UNK 0 43.206 -19.918 0.000 0.00 0.00 O+0 HETATM 24 H UNK 0 46.168 -19.997 0.000 0.00 0.00 H+0 HETATM 25 P UNK 0 50.640 -17.459 0.000 0.00 0.00 P+0 HETATM 26 O UNK 0 50.640 -15.919 0.000 0.00 0.00 O+0 HETATM 27 O UNK 0 49.857 -19.431 0.000 0.00 0.00 O+0 HETATM 28 C UNK 0 43.049 -9.075 0.000 0.00 0.00 C+0 HETATM 29 O UNK 0 43.049 -7.635 0.000 0.00 0.00 O+0 HETATM 30 C UNK 0 41.716 -9.846 0.000 0.00 0.00 C+0 HETATM 31 C UNK 0 40.383 -9.075 0.000 0.00 0.00 C+0 HETATM 32 C UNK 0 39.050 -9.846 0.000 0.00 0.00 C+0 HETATM 33 C UNK 0 37.717 -9.075 0.000 0.00 0.00 C+0 HETATM 34 C UNK 0 36.384 -9.846 0.000 0.00 0.00 C+0 HETATM 35 C UNK 0 35.051 -9.075 0.000 0.00 0.00 C+0 HETATM 36 C UNK 0 33.718 -9.846 0.000 0.00 0.00 C+0 HETATM 37 C UNK 0 32.385 -9.075 0.000 0.00 0.00 C+0 HETATM 38 C UNK 0 31.052 -9.846 0.000 0.00 0.00 C+0 HETATM 39 C UNK 0 29.719 -9.075 0.000 0.00 0.00 C+0 HETATM 40 C UNK 0 28.386 -9.846 0.000 0.00 0.00 C+0 HETATM 41 C UNK 0 27.052 -9.075 0.000 0.00 0.00 C+0 HETATM 42 C UNK 0 25.719 -9.846 0.000 0.00 0.00 C+0 HETATM 43 C UNK 0 24.387 -9.075 0.000 0.00 0.00 C+0 HETATM 44 C UNK 0 23.054 -9.846 0.000 0.00 0.00 C+0 HETATM 45 C UNK 0 45.133 -12.139 0.000 0.00 0.00 C+0 HETATM 46 O UNK 0 45.133 -13.579 0.000 0.00 0.00 O+0 HETATM 47 C UNK 0 43.800 -11.367 0.000 0.00 0.00 C+0 HETATM 48 C UNK 0 42.467 -12.139 0.000 0.00 0.00 C+0 HETATM 49 C UNK 0 41.134 -11.367 0.000 0.00 0.00 C+0 HETATM 50 C UNK 0 39.801 -12.139 0.000 0.00 0.00 C+0 HETATM 51 C UNK 0 38.468 -11.367 0.000 0.00 0.00 C+0 HETATM 52 C UNK 0 37.135 -12.139 0.000 0.00 0.00 C+0 HETATM 53 C UNK 0 35.802 -11.367 0.000 0.00 0.00 C+0 HETATM 54 C UNK 0 34.469 -12.139 0.000 0.00 0.00 C+0 HETATM 55 C UNK 0 32.929 -12.139 0.000 0.00 0.00 C+0 HETATM 56 C UNK 0 31.596 -11.367 0.000 0.00 0.00 C+0 HETATM 57 C UNK 0 30.263 -12.139 0.000 0.00 0.00 C+0 HETATM 58 C UNK 0 28.723 -12.139 0.000 0.00 0.00 C+0 HETATM 59 C UNK 0 27.390 -11.367 0.000 0.00 0.00 C+0 HETATM 60 C UNK 0 26.057 -12.139 0.000 0.00 0.00 C+0 HETATM 61 C UNK 0 24.517 -12.139 0.000 0.00 0.00 C+0 HETATM 62 C UNK 0 23.184 -11.367 0.000 0.00 0.00 C+0 HETATM 63 C UNK 0 21.851 -12.139 0.000 0.00 0.00 C+0 HETATM 64 C UNK 0 39.840 -17.572 0.000 0.00 0.00 C+0 HETATM 65 O UNK 0 39.840 -16.132 0.000 0.00 0.00 O+0 HETATM 66 C UNK 0 38.507 -18.344 0.000 0.00 0.00 C+0 HETATM 67 C UNK 0 37.174 -17.572 0.000 0.00 0.00 C+0 HETATM 68 C UNK 0 35.841 -18.344 0.000 0.00 0.00 C+0 HETATM 69 C UNK 0 34.508 -17.572 0.000 0.00 0.00 C+0 HETATM 70 C UNK 0 33.175 -18.344 0.000 0.00 0.00 C+0 HETATM 71 C UNK 0 31.842 -17.572 0.000 0.00 0.00 C+0 HETATM 72 C UNK 0 30.509 -18.344 0.000 0.00 0.00 C+0 HETATM 73 C UNK 0 29.176 -17.572 0.000 0.00 0.00 C+0 HETATM 74 C UNK 0 27.636 -17.572 0.000 0.00 0.00 C+0 HETATM 75 C UNK 0 26.303 -18.344 0.000 0.00 0.00 C+0 HETATM 76 C UNK 0 24.970 -17.572 0.000 0.00 0.00 C+0 HETATM 77 C UNK 0 23.430 -17.572 0.000 0.00 0.00 C+0 HETATM 78 C UNK 0 22.097 -18.344 0.000 0.00 0.00 C+0 HETATM 79 C UNK 0 20.764 -17.572 0.000 0.00 0.00 C+0 HETATM 80 C UNK 0 19.224 -17.572 0.000 0.00 0.00 C+0 HETATM 81 C UNK 0 17.891 -18.344 0.000 0.00 0.00 C+0 HETATM 82 C UNK 0 16.558 -17.572 0.000 0.00 0.00 C+0 HETATM 83 C UNK 0 41.872 -20.688 0.000 0.00 0.00 C+0 HETATM 84 O UNK 0 41.872 -22.128 0.000 0.00 0.00 O+0 HETATM 85 C UNK 0 40.539 -19.917 0.000 0.00 0.00 C+0 HETATM 86 C UNK 0 39.206 -20.688 0.000 0.00 0.00 C+0 HETATM 87 C UNK 0 37.873 -19.917 0.000 0.00 0.00 C+0 HETATM 88 C UNK 0 36.540 -20.688 0.000 0.00 0.00 C+0 HETATM 89 C UNK 0 35.207 -19.917 0.000 0.00 0.00 C+0 HETATM 90 C UNK 0 33.874 -20.688 0.000 0.00 0.00 C+0 HETATM 91 C UNK 0 32.541 -19.917 0.000 0.00 0.00 C+0 HETATM 92 C UNK 0 31.208 -20.688 0.000 0.00 0.00 C+0 HETATM 93 C UNK 0 29.875 -19.917 0.000 0.00 0.00 C+0 HETATM 94 C UNK 0 28.542 -20.688 0.000 0.00 0.00 C+0 HETATM 95 C UNK 0 27.002 -20.688 0.000 0.00 0.00 C+0 HETATM 96 C UNK 0 25.669 -19.917 0.000 0.00 0.00 C+0 HETATM 97 C UNK 0 24.336 -20.688 0.000 0.00 0.00 C+0 HETATM 98 C UNK 0 23.003 -19.917 0.000 0.00 0.00 C+0 HETATM 99 C UNK 0 21.670 -20.688 0.000 0.00 0.00 C+0 HETATM 100 C UNK 0 20.337 -19.917 0.000 0.00 0.00 C+0 HETATM 101 C UNK 0 19.004 -20.688 0.000 0.00 0.00 C+0 HETATM 102 C UNK 0 17.671 -19.917 0.000 0.00 0.00 C+0 HETATM 103 C UNK 0 16.338 -20.688 0.000 0.00 0.00 C+0 CONECT 1 2 4 CONECT 2 1 3 6 7 CONECT 3 2 5 CONECT 4 1 25 CONECT 5 3 15 CONECT 6 2 CONECT 7 2 CONECT 8 9 11 CONECT 9 8 10 13 14 CONECT 10 9 12 CONECT 11 8 15 CONECT 12 10 28 CONECT 13 9 45 CONECT 14 9 CONECT 15 16 17 5 11 CONECT 16 15 CONECT 17 15 CONECT 18 19 21 CONECT 19 18 20 23 24 CONECT 20 19 22 CONECT 21 18 25 CONECT 22 20 64 CONECT 23 19 83 CONECT 24 19 CONECT 25 4 26 27 21 CONECT 26 25 CONECT 27 25 CONECT 28 12 29 30 CONECT 29 28 CONECT 30 28 31 CONECT 31 30 32 CONECT 32 31 33 CONECT 33 32 34 CONECT 34 33 35 CONECT 35 34 36 CONECT 36 35 37 CONECT 37 36 38 CONECT 38 37 39 CONECT 39 38 40 CONECT 40 39 41 CONECT 41 40 42 CONECT 42 41 43 CONECT 43 42 44 CONECT 44 43 CONECT 45 13 46 47 CONECT 46 45 CONECT 47 45 48 CONECT 48 47 49 CONECT 49 48 50 CONECT 50 49 51 CONECT 51 50 52 CONECT 52 51 53 CONECT 53 52 54 CONECT 54 53 55 CONECT 55 54 56 CONECT 56 55 57 CONECT 57 56 58 CONECT 58 57 59 CONECT 59 58 60 CONECT 60 59 61 CONECT 61 60 62 CONECT 62 61 63 CONECT 63 62 CONECT 64 22 65 66 CONECT 65 64 CONECT 66 64 67 CONECT 67 66 68 CONECT 68 67 69 CONECT 69 68 70 CONECT 70 69 71 CONECT 71 70 72 CONECT 72 71 73 CONECT 73 72 74 CONECT 74 73 75 CONECT 75 74 76 CONECT 76 75 77 CONECT 77 76 78 CONECT 78 77 79 CONECT 79 78 80 CONECT 80 79 81 CONECT 81 80 82 CONECT 82 81 CONECT 83 23 84 85 CONECT 84 83 CONECT 85 83 86 CONECT 86 85 87 CONECT 87 86 88 CONECT 88 87 89 CONECT 89 88 90 CONECT 90 89 91 CONECT 91 90 92 CONECT 92 91 93 CONECT 93 92 94 CONECT 94 93 95 CONECT 95 94 96 CONECT 96 95 97 CONECT 97 96 98 CONECT 98 97 99 CONECT 99 98 100 CONECT 100 99 101 CONECT 101 100 102 CONECT 102 101 103 CONECT 103 102 MASTER 0 0 0 0 0 0 0 0 103 0 204 0 END SMILES for NP0340345 (CL(16:0/18:3(9Z,12Z,15Z)/18:3(9Z,12Z,15Z)/20:1(11Z)))[H]C(O)(COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC)OC(=O)CCCCCCCCC\C=C/CCCCCCCC)COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC INCHI for NP0340345 (CL(16:0/18:3(9Z,12Z,15Z)/18:3(9Z,12Z,15Z)/20:1(11Z)))InChI=1/C81H144O17P2/c1-5-9-13-17-21-25-29-33-36-37-40-44-48-52-56-60-64-68-81(86)98-77(72-92-79(84)66-62-58-54-50-46-42-38-34-30-26-22-18-14-10-6-2)74-96-100(89,90)94-70-75(82)69-93-99(87,88)95-73-76(71-91-78(83)65-61-57-53-49-45-41-32-28-24-20-16-12-8-4)97-80(85)67-63-59-55-51-47-43-39-35-31-27-23-19-15-11-7-3/h10-11,14-15,22-23,26-27,33-36,38-39,75-77,82H,5-9,12-13,16-21,24-25,28-32,37,40-74H2,1-4H3,(H,87,88)(H,89,90)/b14-10-,15-11-,26-22-,27-23-,36-33-,38-34-,39-35-/t75-,76+,77+/s2 3D Structure for NP0340345 (CL(16:0/18:3(9Z,12Z,15Z)/18:3(9Z,12Z,15Z)/20:1(11Z))) | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Synonyms | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Chemical Formula | C81H144O17P2 | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Average Mass | 1451.9740 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Monoisotopic Mass | 1450.98788 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||
| IUPAC Name | [(2R)-3-(hexadecanoyloxy)-2-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propoxy][(2R)-2-hydroxy-3-({hydroxy[(2R)-2-[(11Z)-icos-11-enoyloxy]-3-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propoxy]phosphoryl}oxy)propoxy]phosphinic acid | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Traditional Name | (2R)-3-(hexadecanoyloxy)-2-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propoxy((2R)-2-hydroxy-3-{[hydroxy((2R)-2-[(11Z)-icos-11-enoyloxy]-3-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propoxy)phosphoryl]oxy}propoxy)phosphinic acid | |||||||||||||||||||||||||||||||||||||||||||||||||||
| CAS Registry Number | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
| SMILES | [H]C(O)(COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC)OC(=O)CCCCCCCCC\C=C/CCCCCCCC)COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC | |||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Identifier | InChI=1/C81H144O17P2/c1-5-9-13-17-21-25-29-33-36-37-40-44-48-52-56-60-64-68-81(86)98-77(72-92-79(84)66-62-58-54-50-46-42-38-34-30-26-22-18-14-10-6-2)74-96-100(89,90)94-70-75(82)69-93-99(87,88)95-73-76(71-91-78(83)65-61-57-53-49-45-41-32-28-24-20-16-12-8-4)97-80(85)67-63-59-55-51-47-43-39-35-31-27-23-19-15-11-7-3/h10-11,14-15,22-23,26-27,33-36,38-39,75-77,82H,5-9,12-13,16-21,24-25,28-32,37,40-74H2,1-4H3,(H,87,88)(H,89,90)/b14-10-,15-11-,26-22-,27-23-,36-33-,38-34-,39-35-/t75-,76+,77+/s2 | |||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Key | OVRNGLQPVAQKIK-BDSBYBIANA-N | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Experimental Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Predicted Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chemical Shift Submissions | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Species | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Species of Origin | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Chemical Taxonomy | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Classification | Not classified | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Physical Properties | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| State | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Experimental Properties |
| |||||||||||||||||||||||||||||||||||||||||||||||||||
| Predicted Properties |
| |||||||||||||||||||||||||||||||||||||||||||||||||||
| External Links | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| External Links | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
| References | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| General References | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
