Showing NP-Card for Gelliusterol B (NP0025748)
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Version | 1.0 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Created at | 2021-06-19 17:47:23 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Updated at | 2021-06-29 23:50:53 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
NP-MRD ID | NP0025748 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Secondary Accession Numbers | None | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Natural Product Identification | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Common Name | Gelliusterol B | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Provided By | JEOL Database | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Description | Gelliusterol B is found in Gellius species. It was first documented in 2001 (Gallimore, W. A., et al.). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structure | MOL for NP0025748 (Gelliusterol B)Mrv1652306192119473D 63 66 0 0 0 0 999 V2000 -2.4156 -3.5899 -5.1831 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4320 -2.2319 -4.6399 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4394 -1.1167 -4.1938 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4479 0.2476 -3.6436 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.0691 0.9358 -3.6744 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.6695 1.2164 -5.1363 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0670 0.1836 -2.9226 C 0 0 1 0 0 0 0 0 0 0 0 0 1.4068 0.9729 -2.9731 C 0 0 1 0 0 0 0 0 0 0 0 0 2.1825 0.6309 -1.6952 C 0 0 2 0 0 0 0 0 0 0 0 0 1.3804 -0.4988 -1.0575 C 0 0 1 0 0 0 0 0 0 0 0 0 1.6035 -0.8002 0.4325 C 0 0 2 0 0 0 0 0 0 0 0 0 3.0386 -1.2279 0.7263 C 0 0 0 0 0 0 0 0 0 0 0 0 4.0002 -0.9519 0.0142 O 0 0 0 0 0 0 0 0 0 0 0 0 3.2978 -1.9543 1.9917 C 0 0 0 0 0 0 0 0 0 0 0 0 2.3046 -2.4043 2.7765 C 0 0 0 0 0 0 0 0 0 0 0 0 2.6405 -3.0678 4.0959 C 0 0 2 0 0 0 0 0 0 0 0 0 1.9243 -4.4060 4.2742 C 0 0 1 0 0 0 0 0 0 0 0 0 2.1721 -4.8924 5.5904 O 0 0 0 0 0 0 0 0 0 0 0 0 0.4217 -4.2494 4.0677 C 0 0 2 0 0 0 0 0 0 0 0 0 0.1105 -3.6449 2.6995 C 0 0 1 0 0 0 0 0 0 0 0 0 0.8191 -2.2857 2.4139 C 0 0 1 0 0 0 0 0 0 0 0 0 0.1910 -1.1841 3.2989 C 0 0 0 0 0 0 0 0 0 0 0 0 0.6635 -1.9567 0.8770 C 0 0 1 0 0 0 0 0 0 0 0 0 -0.8016 -1.7493 0.4257 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.9428 -1.3560 -1.0519 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.0886 -0.1276 -1.4016 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.6087 1.1155 -0.6375 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.4334 -3.9721 -5.3064 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.8763 -4.2688 -4.5157 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.9235 -3.6121 -6.1600 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.1630 0.8524 -4.2164 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.8404 0.2357 -2.6232 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2012 1.9185 -3.2022 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.4873 1.7043 -5.6780 H 0 0 0 0 0 0 0 0 0 0 0 0 0.1932 1.8873 -5.1928 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4126 0.2938 -5.6673 H 0 0 0 0 0 0 0 0 0 0 0 0 0.2415 -0.7685 -3.4455 H 0 0 0 0 0 0 0 0 0 0 0 0 1.9809 0.6881 -3.8622 H 0 0 0 0 0 0 0 0 0 0 0 0 1.2458 2.0561 -3.0197 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2421 1.5037 -1.0354 H 0 0 0 0 0 0 0 0 0 0 0 0 3.2060 0.3339 -1.9418 H 0 0 0 0 0 0 0 0 0 0 0 0 1.6493 -1.4144 -1.6107 H 0 0 0 0 0 0 0 0 0 0 0 0 1.4234 0.1059 1.0204 H 0 0 0 0 0 0 0 0 0 0 0 0 4.3457 -2.0656 2.2507 H 0 0 0 0 0 0 0 0 0 0 0 0 2.3764 -2.3929 4.9203 H 0 0 0 0 0 0 0 0 0 0 0 0 3.7212 -3.2307 4.2007 H 0 0 0 0 0 0 0 0 0 0 0 0 2.3281 -5.1384 3.5646 H 0 0 0 0 0 0 0 0 0 0 0 0 1.7311 -5.7557 5.6719 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0088 -3.6361 4.8689 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0656 -5.2282 4.1584 H 0 0 0 0 0 0 0 0 0 0 0 0 0.4017 -4.3781 1.9349 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.9772 -3.5313 2.6196 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8948 -1.1320 3.1711 H 0 0 0 0 0 0 0 0 0 0 0 0 0.6029 -0.1952 3.0739 H 0 0 0 0 0 0 0 0 0 0 0 0 0.3652 -1.3615 4.3657 H 0 0 0 0 0 0 0 0 0 0 0 0 1.0093 -2.8510 0.3314 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2905 -0.9864 1.0384 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.3712 -2.6729 0.5787 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.0022 -1.1761 -1.2508 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.6486 -2.2104 -1.6748 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.6688 1.2883 -0.8507 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5185 1.0137 0.4472 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0731 2.0299 -0.9114 H 0 0 0 0 0 0 0 0 0 0 0 0 26 10 1 0 0 0 0 26 25 1 0 0 0 0 25 24 1 0 0 0 0 10 9 1 0 0 0 0 9 8 1 0 0 0 0 8 7 1 0 0 0 0 26 7 1 0 0 0 0 19 17 1 0 0 0 0 19 20 1 0 0 0 0 21 22 1 1 0 0 0 7 5 1 0 0 0 0 17 16 1 0 0 0 0 5 6 1 0 0 0 0 21 23 1 0 0 0 0 5 4 1 0 0 0 0 15 14 2 0 0 0 0 4 3 1 0 0 0 0 14 12 1 0 0 0 0 10 42 1 6 0 0 0 12 11 1 0 0 0 0 17 18 1 0 0 0 0 23 11 1 0 0 0 0 12 13 2 0 0 0 0 16 15 1 0 0 0 0 23 56 1 6 0 0 0 21 20 1 0 0 0 0 11 43 1 1 0 0 0 21 15 1 0 0 0 0 26 27 1 1 0 0 0 23 24 1 0 0 0 0 3 2 3 0 0 0 0 11 10 1 0 0 0 0 2 1 1 0 0 0 0 19 49 1 0 0 0 0 19 50 1 0 0 0 0 17 47 1 6 0 0 0 16 45 1 0 0 0 0 16 46 1 0 0 0 0 20 51 1 0 0 0 0 20 52 1 0 0 0 0 14 44 1 0 0 0 0 25 59 1 0 0 0 0 25 60 1 0 0 0 0 24 57 1 0 0 0 0 24 58 1 0 0 0 0 22 53 1 0 0 0 0 22 54 1 0 0 0 0 22 55 1 0 0 0 0 9 40 1 0 0 0 0 9 41 1 0 0 0 0 8 38 1 0 0 0 0 8 39 1 0 0 0 0 7 37 1 6 0 0 0 5 33 1 1 0 0 0 6 34 1 0 0 0 0 6 35 1 0 0 0 0 6 36 1 0 0 0 0 4 31 1 0 0 0 0 4 32 1 0 0 0 0 18 48 1 0 0 0 0 27 61 1 0 0 0 0 27 62 1 0 0 0 0 27 63 1 0 0 0 0 1 28 1 0 0 0 0 1 29 1 0 0 0 0 1 30 1 0 0 0 0 M END 3D MOL for NP0025748 (Gelliusterol B)RDKit 3D 63 66 0 0 0 0 0 0 0 0999 V2000 -2.4156 -3.5899 -5.1831 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4320 -2.2319 -4.6399 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4394 -1.1167 -4.1938 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4479 0.2476 -3.6436 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.0691 0.9358 -3.6744 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.6695 1.2164 -5.1363 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0670 0.1836 -2.9226 C 0 0 1 0 0 0 0 0 0 0 0 0 1.4068 0.9729 -2.9731 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1825 0.6309 -1.6952 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3804 -0.4988 -1.0575 C 0 0 1 0 0 0 0 0 0 0 0 0 1.6035 -0.8002 0.4325 C 0 0 2 0 0 0 0 0 0 0 0 0 3.0386 -1.2279 0.7263 C 0 0 0 0 0 0 0 0 0 0 0 0 4.0002 -0.9519 0.0142 O 0 0 0 0 0 0 0 0 0 0 0 0 3.2978 -1.9543 1.9917 C 0 0 0 0 0 0 0 0 0 0 0 0 2.3046 -2.4043 2.7765 C 0 0 0 0 0 0 0 0 0 0 0 0 2.6405 -3.0678 4.0959 C 0 0 0 0 0 0 0 0 0 0 0 0 1.9243 -4.4060 4.2742 C 0 0 1 0 0 0 0 0 0 0 0 0 2.1721 -4.8924 5.5904 O 0 0 0 0 0 0 0 0 0 0 0 0 0.4217 -4.2494 4.0677 C 0 0 0 0 0 0 0 0 0 0 0 0 0.1105 -3.6449 2.6995 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8191 -2.2857 2.4139 C 0 0 1 0 0 0 0 0 0 0 0 0 0.1910 -1.1841 3.2989 C 0 0 0 0 0 0 0 0 0 0 0 0 0.6635 -1.9567 0.8770 C 0 0 1 0 0 0 0 0 0 0 0 0 -0.8016 -1.7493 0.4257 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.9428 -1.3560 -1.0519 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0886 -0.1276 -1.4016 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.6087 1.1155 -0.6375 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.4334 -3.9721 -5.3064 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.8763 -4.2688 -4.5157 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.9235 -3.6121 -6.1600 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.1630 0.8524 -4.2164 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.8404 0.2357 -2.6232 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2012 1.9185 -3.2022 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.4873 1.7043 -5.6780 H 0 0 0 0 0 0 0 0 0 0 0 0 0.1932 1.8873 -5.1928 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4126 0.2938 -5.6673 H 0 0 0 0 0 0 0 0 0 0 0 0 0.2415 -0.7685 -3.4455 H 0 0 0 0 0 0 0 0 0 0 0 0 1.9809 0.6881 -3.8622 H 0 0 0 0 0 0 0 0 0 0 0 0 1.2458 2.0561 -3.0197 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2421 1.5037 -1.0354 H 0 0 0 0 0 0 0 0 0 0 0 0 3.2060 0.3339 -1.9418 H 0 0 0 0 0 0 0 0 0 0 0 0 1.6493 -1.4144 -1.6107 H 0 0 0 0 0 0 0 0 0 0 0 0 1.4234 0.1059 1.0204 H 0 0 0 0 0 0 0 0 0 0 0 0 4.3457 -2.0656 2.2507 H 0 0 0 0 0 0 0 0 0 0 0 0 2.3764 -2.3929 4.9203 H 0 0 0 0 0 0 0 0 0 0 0 0 3.7212 -3.2307 4.2007 H 0 0 0 0 0 0 0 0 0 0 0 0 2.3281 -5.1384 3.5646 H 0 0 0 0 0 0 0 0 0 0 0 0 1.7311 -5.7557 5.6719 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0088 -3.6361 4.8689 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0656 -5.2282 4.1584 H 0 0 0 0 0 0 0 0 0 0 0 0 0.4017 -4.3781 1.9349 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.9772 -3.5313 2.6196 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8948 -1.1320 3.1711 H 0 0 0 0 0 0 0 0 0 0 0 0 0.6029 -0.1952 3.0739 H 0 0 0 0 0 0 0 0 0 0 0 0 0.3652 -1.3615 4.3657 H 0 0 0 0 0 0 0 0 0 0 0 0 1.0093 -2.8510 0.3314 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2905 -0.9864 1.0384 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.3712 -2.6729 0.5787 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.0022 -1.1761 -1.2508 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.6486 -2.2104 -1.6748 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.6688 1.2883 -0.8507 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5185 1.0137 0.4472 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0731 2.0299 -0.9114 H 0 0 0 0 0 0 0 0 0 0 0 0 26 10 1 0 26 25 1 0 25 24 1 0 10 9 1 0 9 8 1 0 8 7 1 0 26 7 1 0 19 17 1 0 19 20 1 0 21 22 1 1 7 5 1 0 17 16 1 0 5 6 1 0 21 23 1 0 5 4 1 0 15 14 2 0 4 3 1 0 14 12 1 0 10 42 1 6 12 11 1 0 17 18 1 0 23 11 1 0 12 13 2 0 16 15 1 0 23 56 1 6 21 20 1 0 11 43 1 1 21 15 1 0 26 27 1 1 23 24 1 0 3 2 3 0 11 10 1 0 2 1 1 0 19 49 1 0 19 50 1 0 17 47 1 6 16 45 1 0 16 46 1 0 20 51 1 0 20 52 1 0 14 44 1 0 25 59 1 0 25 60 1 0 24 57 1 0 24 58 1 0 22 53 1 0 22 54 1 0 22 55 1 0 9 40 1 0 9 41 1 0 8 38 1 0 8 39 1 0 7 37 1 6 5 33 1 1 6 34 1 0 6 35 1 0 6 36 1 0 4 31 1 0 4 32 1 0 18 48 1 0 27 61 1 0 27 62 1 0 27 63 1 0 1 28 1 0 1 29 1 0 1 30 1 0 M END 3D SDF for NP0025748 (Gelliusterol B)Mrv1652306192119473D 63 66 0 0 0 0 999 V2000 -2.4156 -3.5899 -5.1831 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4320 -2.2319 -4.6399 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4394 -1.1167 -4.1938 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4479 0.2476 -3.6436 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.0691 0.9358 -3.6744 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.6695 1.2164 -5.1363 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0670 0.1836 -2.9226 C 0 0 1 0 0 0 0 0 0 0 0 0 1.4068 0.9729 -2.9731 C 0 0 1 0 0 0 0 0 0 0 0 0 2.1825 0.6309 -1.6952 C 0 0 2 0 0 0 0 0 0 0 0 0 1.3804 -0.4988 -1.0575 C 0 0 1 0 0 0 0 0 0 0 0 0 1.6035 -0.8002 0.4325 C 0 0 2 0 0 0 0 0 0 0 0 0 3.0386 -1.2279 0.7263 C 0 0 0 0 0 0 0 0 0 0 0 0 4.0002 -0.9519 0.0142 O 0 0 0 0 0 0 0 0 0 0 0 0 3.2978 -1.9543 1.9917 C 0 0 0 0 0 0 0 0 0 0 0 0 2.3046 -2.4043 2.7765 C 0 0 0 0 0 0 0 0 0 0 0 0 2.6405 -3.0678 4.0959 C 0 0 2 0 0 0 0 0 0 0 0 0 1.9243 -4.4060 4.2742 C 0 0 1 0 0 0 0 0 0 0 0 0 2.1721 -4.8924 5.5904 O 0 0 0 0 0 0 0 0 0 0 0 0 0.4217 -4.2494 4.0677 C 0 0 2 0 0 0 0 0 0 0 0 0 0.1105 -3.6449 2.6995 C 0 0 1 0 0 0 0 0 0 0 0 0 0.8191 -2.2857 2.4139 C 0 0 1 0 0 0 0 0 0 0 0 0 0.1910 -1.1841 3.2989 C 0 0 0 0 0 0 0 0 0 0 0 0 0.6635 -1.9567 0.8770 C 0 0 1 0 0 0 0 0 0 0 0 0 -0.8016 -1.7493 0.4257 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.9428 -1.3560 -1.0519 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.0886 -0.1276 -1.4016 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.6087 1.1155 -0.6375 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.4334 -3.9721 -5.3064 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.8763 -4.2688 -4.5157 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.9235 -3.6121 -6.1600 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.1630 0.8524 -4.2164 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.8404 0.2357 -2.6232 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2012 1.9185 -3.2022 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.4873 1.7043 -5.6780 H 0 0 0 0 0 0 0 0 0 0 0 0 0.1932 1.8873 -5.1928 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4126 0.2938 -5.6673 H 0 0 0 0 0 0 0 0 0 0 0 0 0.2415 -0.7685 -3.4455 H 0 0 0 0 0 0 0 0 0 0 0 0 1.9809 0.6881 -3.8622 H 0 0 0 0 0 0 0 0 0 0 0 0 1.2458 2.0561 -3.0197 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2421 1.5037 -1.0354 H 0 0 0 0 0 0 0 0 0 0 0 0 3.2060 0.3339 -1.9418 H 0 0 0 0 0 0 0 0 0 0 0 0 1.6493 -1.4144 -1.6107 H 0 0 0 0 0 0 0 0 0 0 0 0 1.4234 0.1059 1.0204 H 0 0 0 0 0 0 0 0 0 0 0 0 4.3457 -2.0656 2.2507 H 0 0 0 0 0 0 0 0 0 0 0 0 2.3764 -2.3929 4.9203 H 0 0 0 0 0 0 0 0 0 0 0 0 3.7212 -3.2307 4.2007 H 0 0 0 0 0 0 0 0 0 0 0 0 2.3281 -5.1384 3.5646 H 0 0 0 0 0 0 0 0 0 0 0 0 1.7311 -5.7557 5.6719 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0088 -3.6361 4.8689 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0656 -5.2282 4.1584 H 0 0 0 0 0 0 0 0 0 0 0 0 0.4017 -4.3781 1.9349 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.9772 -3.5313 2.6196 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8948 -1.1320 3.1711 H 0 0 0 0 0 0 0 0 0 0 0 0 0.6029 -0.1952 3.0739 H 0 0 0 0 0 0 0 0 0 0 0 0 0.3652 -1.3615 4.3657 H 0 0 0 0 0 0 0 0 0 0 0 0 1.0093 -2.8510 0.3314 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2905 -0.9864 1.0384 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.3712 -2.6729 0.5787 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.0022 -1.1761 -1.2508 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.6486 -2.2104 -1.6748 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.6688 1.2883 -0.8507 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5185 1.0137 0.4472 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0731 2.0299 -0.9114 H 0 0 0 0 0 0 0 0 0 0 0 0 26 10 1 0 0 0 0 26 25 1 0 0 0 0 25 24 1 0 0 0 0 10 9 1 0 0 0 0 9 8 1 0 0 0 0 8 7 1 0 0 0 0 26 7 1 0 0 0 0 19 17 1 0 0 0 0 19 20 1 0 0 0 0 21 22 1 1 0 0 0 7 5 1 0 0 0 0 17 16 1 0 0 0 0 5 6 1 0 0 0 0 21 23 1 0 0 0 0 5 4 1 0 0 0 0 15 14 2 0 0 0 0 4 3 1 0 0 0 0 14 12 1 0 0 0 0 10 42 1 6 0 0 0 12 11 1 0 0 0 0 17 18 1 0 0 0 0 23 11 1 0 0 0 0 12 13 2 0 0 0 0 16 15 1 0 0 0 0 23 56 1 6 0 0 0 21 20 1 0 0 0 0 11 43 1 1 0 0 0 21 15 1 0 0 0 0 26 27 1 1 0 0 0 23 24 1 0 0 0 0 3 2 3 0 0 0 0 11 10 1 0 0 0 0 2 1 1 0 0 0 0 19 49 1 0 0 0 0 19 50 1 0 0 0 0 17 47 1 6 0 0 0 16 45 1 0 0 0 0 16 46 1 0 0 0 0 20 51 1 0 0 0 0 20 52 1 0 0 0 0 14 44 1 0 0 0 0 25 59 1 0 0 0 0 25 60 1 0 0 0 0 24 57 1 0 0 0 0 24 58 1 0 0 0 0 22 53 1 0 0 0 0 22 54 1 0 0 0 0 22 55 1 0 0 0 0 9 40 1 0 0 0 0 9 41 1 0 0 0 0 8 38 1 0 0 0 0 8 39 1 0 0 0 0 7 37 1 6 0 0 0 5 33 1 1 0 0 0 6 34 1 0 0 0 0 6 35 1 0 0 0 0 6 36 1 0 0 0 0 4 31 1 0 0 0 0 4 32 1 0 0 0 0 18 48 1 0 0 0 0 27 61 1 0 0 0 0 27 62 1 0 0 0 0 27 63 1 0 0 0 0 1 28 1 0 0 0 0 1 29 1 0 0 0 0 1 30 1 0 0 0 0 M END > <DATABASE_ID> NP0025748 > <DATABASE_NAME> NP-MRD > <SMILES> [H]O[C@]1([H])C([H])([H])C2=C([H])C(=O)[C@@]3([H])[C@]4([H])C([H])([H])C([H])([H])[C@]([H])([C@@]([H])(C([H])([H])[H])C([H])([H])C#CC([H])([H])[H])[C@@]4(C([H])([H])[H])C([H])([H])C([H])([H])[C@]3([H])[C@@]2(C([H])([H])[H])C([H])([H])C1([H])[H] > <INCHI_IDENTIFIER> InChI=1S/C25H36O2/c1-5-6-7-16(2)19-8-9-20-23-21(11-13-25(19,20)4)24(3)12-10-18(26)14-17(24)15-22(23)27/h15-16,18-21,23,26H,7-14H2,1-4H3/t16-,18-,19+,20-,21-,23-,24-,25+/m0/s1 > <INCHI_KEY> HHGLFNRDPUBPSI-NOCRRZKMSA-N > <FORMULA> C25H36O2 > <MOLECULAR_WEIGHT> 368.561 > <EXACT_MASS> 368.271530399 > <JCHEM_ACCEPTOR_COUNT> 2 > <JCHEM_ATOM_COUNT> 63 > <JCHEM_AVERAGE_POLARIZABILITY> 44.684496114773175 > <JCHEM_BIOAVAILABILITY> 1 > <JCHEM_DONOR_COUNT> 1 > <JCHEM_FORMAL_CHARGE> 0 > <JCHEM_GHOSE_FILTER> 1 > <JCHEM_IUPAC> (1S,2R,5S,10S,11S,14R,15R)-14-[(2S)-hex-4-yn-2-yl]-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-9-one > <ALOGPS_LOGP> 5.19 > <JCHEM_LOGP> 5.402502537000001 > <ALOGPS_LOGS> -5.56 > <JCHEM_MDDR_LIKE_RULE> 0 > <JCHEM_NUMBER_OF_RINGS> 4 > <JCHEM_PHYSIOLOGICAL_CHARGE> 0 > <JCHEM_PKA> 18.270745923091404 > <JCHEM_PKA_STRONGEST_ACIDIC> 17.388330106574543 > <JCHEM_PKA_STRONGEST_BASIC> -1.3680983533849584 > <JCHEM_POLAR_SURFACE_AREA> 37.3 > <JCHEM_REFRACTIVITY> 111.47229999999998 > <JCHEM_ROTATABLE_BOND_COUNT> 3 > <JCHEM_RULE_OF_FIVE> 0 > <ALOGPS_SOLUBILITY> 1.01e-03 g/l > <JCHEM_TRADITIONAL_IUPAC> (1S,2R,5S,10S,11S,14R,15R)-14-[(2S)-hex-4-yn-2-yl]-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-9-one > <JCHEM_VEBER_RULE> 1 $$$$ 3D-SDF for NP0025748 (Gelliusterol B)RDKit 3D 63 66 0 0 0 0 0 0 0 0999 V2000 -2.4156 -3.5899 -5.1831 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4320 -2.2319 -4.6399 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4394 -1.1167 -4.1938 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4479 0.2476 -3.6436 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.0691 0.9358 -3.6744 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.6695 1.2164 -5.1363 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0670 0.1836 -2.9226 C 0 0 1 0 0 0 0 0 0 0 0 0 1.4068 0.9729 -2.9731 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1825 0.6309 -1.6952 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3804 -0.4988 -1.0575 C 0 0 1 0 0 0 0 0 0 0 0 0 1.6035 -0.8002 0.4325 C 0 0 2 0 0 0 0 0 0 0 0 0 3.0386 -1.2279 0.7263 C 0 0 0 0 0 0 0 0 0 0 0 0 4.0002 -0.9519 0.0142 O 0 0 0 0 0 0 0 0 0 0 0 0 3.2978 -1.9543 1.9917 C 0 0 0 0 0 0 0 0 0 0 0 0 2.3046 -2.4043 2.7765 C 0 0 0 0 0 0 0 0 0 0 0 0 2.6405 -3.0678 4.0959 C 0 0 0 0 0 0 0 0 0 0 0 0 1.9243 -4.4060 4.2742 C 0 0 1 0 0 0 0 0 0 0 0 0 2.1721 -4.8924 5.5904 O 0 0 0 0 0 0 0 0 0 0 0 0 0.4217 -4.2494 4.0677 C 0 0 0 0 0 0 0 0 0 0 0 0 0.1105 -3.6449 2.6995 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8191 -2.2857 2.4139 C 0 0 1 0 0 0 0 0 0 0 0 0 0.1910 -1.1841 3.2989 C 0 0 0 0 0 0 0 0 0 0 0 0 0.6635 -1.9567 0.8770 C 0 0 1 0 0 0 0 0 0 0 0 0 -0.8016 -1.7493 0.4257 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.9428 -1.3560 -1.0519 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0886 -0.1276 -1.4016 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.6087 1.1155 -0.6375 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.4334 -3.9721 -5.3064 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.8763 -4.2688 -4.5157 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.9235 -3.6121 -6.1600 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.1630 0.8524 -4.2164 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.8404 0.2357 -2.6232 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2012 1.9185 -3.2022 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.4873 1.7043 -5.6780 H 0 0 0 0 0 0 0 0 0 0 0 0 0.1932 1.8873 -5.1928 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4126 0.2938 -5.6673 H 0 0 0 0 0 0 0 0 0 0 0 0 0.2415 -0.7685 -3.4455 H 0 0 0 0 0 0 0 0 0 0 0 0 1.9809 0.6881 -3.8622 H 0 0 0 0 0 0 0 0 0 0 0 0 1.2458 2.0561 -3.0197 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2421 1.5037 -1.0354 H 0 0 0 0 0 0 0 0 0 0 0 0 3.2060 0.3339 -1.9418 H 0 0 0 0 0 0 0 0 0 0 0 0 1.6493 -1.4144 -1.6107 H 0 0 0 0 0 0 0 0 0 0 0 0 1.4234 0.1059 1.0204 H 0 0 0 0 0 0 0 0 0 0 0 0 4.3457 -2.0656 2.2507 H 0 0 0 0 0 0 0 0 0 0 0 0 2.3764 -2.3929 4.9203 H 0 0 0 0 0 0 0 0 0 0 0 0 3.7212 -3.2307 4.2007 H 0 0 0 0 0 0 0 0 0 0 0 0 2.3281 -5.1384 3.5646 H 0 0 0 0 0 0 0 0 0 0 0 0 1.7311 -5.7557 5.6719 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0088 -3.6361 4.8689 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0656 -5.2282 4.1584 H 0 0 0 0 0 0 0 0 0 0 0 0 0.4017 -4.3781 1.9349 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.9772 -3.5313 2.6196 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8948 -1.1320 3.1711 H 0 0 0 0 0 0 0 0 0 0 0 0 0.6029 -0.1952 3.0739 H 0 0 0 0 0 0 0 0 0 0 0 0 0.3652 -1.3615 4.3657 H 0 0 0 0 0 0 0 0 0 0 0 0 1.0093 -2.8510 0.3314 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2905 -0.9864 1.0384 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.3712 -2.6729 0.5787 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.0022 -1.1761 -1.2508 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.6486 -2.2104 -1.6748 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.6688 1.2883 -0.8507 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5185 1.0137 0.4472 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0731 2.0299 -0.9114 H 0 0 0 0 0 0 0 0 0 0 0 0 26 10 1 0 26 25 1 0 25 24 1 0 10 9 1 0 9 8 1 0 8 7 1 0 26 7 1 0 19 17 1 0 19 20 1 0 21 22 1 1 7 5 1 0 17 16 1 0 5 6 1 0 21 23 1 0 5 4 1 0 15 14 2 0 4 3 1 0 14 12 1 0 10 42 1 6 12 11 1 0 17 18 1 0 23 11 1 0 12 13 2 0 16 15 1 0 23 56 1 6 21 20 1 0 11 43 1 1 21 15 1 0 26 27 1 1 23 24 1 0 3 2 3 0 11 10 1 0 2 1 1 0 19 49 1 0 19 50 1 0 17 47 1 6 16 45 1 0 16 46 1 0 20 51 1 0 20 52 1 0 14 44 1 0 25 59 1 0 25 60 1 0 24 57 1 0 24 58 1 0 22 53 1 0 22 54 1 0 22 55 1 0 9 40 1 0 9 41 1 0 8 38 1 0 8 39 1 0 7 37 1 6 5 33 1 1 6 34 1 0 6 35 1 0 6 36 1 0 4 31 1 0 4 32 1 0 18 48 1 0 27 61 1 0 27 62 1 0 27 63 1 0 1 28 1 0 1 29 1 0 1 30 1 0 M END PDB for NP0025748 (Gelliusterol B)HEADER PROTEIN 19-JUN-21 NONE TITLE NULL COMPND NULL SOURCE NULL KEYWDS NULL EXPDTA NULL AUTHOR Marvin REVDAT 1 19-JUN-21 0 HETATM 1 C UNK 0 -2.416 -3.590 -5.183 0.00 0.00 C+0 HETATM 2 C UNK 0 -2.432 -2.232 -4.640 0.00 0.00 C+0 HETATM 3 C UNK 0 -2.439 -1.117 -4.194 0.00 0.00 C+0 HETATM 4 C UNK 0 -2.448 0.248 -3.644 0.00 0.00 C+0 HETATM 5 C UNK 0 -1.069 0.936 -3.674 0.00 0.00 C+0 HETATM 6 C UNK 0 -0.670 1.216 -5.136 0.00 0.00 C+0 HETATM 7 C UNK 0 0.067 0.184 -2.923 0.00 0.00 C+0 HETATM 8 C UNK 0 1.407 0.973 -2.973 0.00 0.00 C+0 HETATM 9 C UNK 0 2.183 0.631 -1.695 0.00 0.00 C+0 HETATM 10 C UNK 0 1.380 -0.499 -1.058 0.00 0.00 C+0 HETATM 11 C UNK 0 1.603 -0.800 0.433 0.00 0.00 C+0 HETATM 12 C UNK 0 3.039 -1.228 0.726 0.00 0.00 C+0 HETATM 13 O UNK 0 4.000 -0.952 0.014 0.00 0.00 O+0 HETATM 14 C UNK 0 3.298 -1.954 1.992 0.00 0.00 C+0 HETATM 15 C UNK 0 2.305 -2.404 2.777 0.00 0.00 C+0 HETATM 16 C UNK 0 2.640 -3.068 4.096 0.00 0.00 C+0 HETATM 17 C UNK 0 1.924 -4.406 4.274 0.00 0.00 C+0 HETATM 18 O UNK 0 2.172 -4.892 5.590 0.00 0.00 O+0 HETATM 19 C UNK 0 0.422 -4.249 4.068 0.00 0.00 C+0 HETATM 20 C UNK 0 0.111 -3.645 2.700 0.00 0.00 C+0 HETATM 21 C UNK 0 0.819 -2.286 2.414 0.00 0.00 C+0 HETATM 22 C UNK 0 0.191 -1.184 3.299 0.00 0.00 C+0 HETATM 23 C UNK 0 0.664 -1.957 0.877 0.00 0.00 C+0 HETATM 24 C UNK 0 -0.802 -1.749 0.426 0.00 0.00 C+0 HETATM 25 C UNK 0 -0.943 -1.356 -1.052 0.00 0.00 C+0 HETATM 26 C UNK 0 -0.089 -0.128 -1.402 0.00 0.00 C+0 HETATM 27 C UNK 0 -0.609 1.115 -0.638 0.00 0.00 C+0 HETATM 28 H UNK 0 -3.433 -3.972 -5.306 0.00 0.00 H+0 HETATM 29 H UNK 0 -1.876 -4.269 -4.516 0.00 0.00 H+0 HETATM 30 H UNK 0 -1.924 -3.612 -6.160 0.00 0.00 H+0 HETATM 31 H UNK 0 -3.163 0.852 -4.216 0.00 0.00 H+0 HETATM 32 H UNK 0 -2.840 0.236 -2.623 0.00 0.00 H+0 HETATM 33 H UNK 0 -1.201 1.919 -3.202 0.00 0.00 H+0 HETATM 34 H UNK 0 -1.487 1.704 -5.678 0.00 0.00 H+0 HETATM 35 H UNK 0 0.193 1.887 -5.193 0.00 0.00 H+0 HETATM 36 H UNK 0 -0.413 0.294 -5.667 0.00 0.00 H+0 HETATM 37 H UNK 0 0.242 -0.769 -3.446 0.00 0.00 H+0 HETATM 38 H UNK 0 1.981 0.688 -3.862 0.00 0.00 H+0 HETATM 39 H UNK 0 1.246 2.056 -3.020 0.00 0.00 H+0 HETATM 40 H UNK 0 2.242 1.504 -1.035 0.00 0.00 H+0 HETATM 41 H UNK 0 3.206 0.334 -1.942 0.00 0.00 H+0 HETATM 42 H UNK 0 1.649 -1.414 -1.611 0.00 0.00 H+0 HETATM 43 H UNK 0 1.423 0.106 1.020 0.00 0.00 H+0 HETATM 44 H UNK 0 4.346 -2.066 2.251 0.00 0.00 H+0 HETATM 45 H UNK 0 2.376 -2.393 4.920 0.00 0.00 H+0 HETATM 46 H UNK 0 3.721 -3.231 4.201 0.00 0.00 H+0 HETATM 47 H UNK 0 2.328 -5.138 3.565 0.00 0.00 H+0 HETATM 48 H UNK 0 1.731 -5.756 5.672 0.00 0.00 H+0 HETATM 49 H UNK 0 -0.009 -3.636 4.869 0.00 0.00 H+0 HETATM 50 H UNK 0 -0.066 -5.228 4.158 0.00 0.00 H+0 HETATM 51 H UNK 0 0.402 -4.378 1.935 0.00 0.00 H+0 HETATM 52 H UNK 0 -0.977 -3.531 2.620 0.00 0.00 H+0 HETATM 53 H UNK 0 -0.895 -1.132 3.171 0.00 0.00 H+0 HETATM 54 H UNK 0 0.603 -0.195 3.074 0.00 0.00 H+0 HETATM 55 H UNK 0 0.365 -1.361 4.366 0.00 0.00 H+0 HETATM 56 H UNK 0 1.009 -2.851 0.331 0.00 0.00 H+0 HETATM 57 H UNK 0 -1.291 -0.986 1.038 0.00 0.00 H+0 HETATM 58 H UNK 0 -1.371 -2.673 0.579 0.00 0.00 H+0 HETATM 59 H UNK 0 -2.002 -1.176 -1.251 0.00 0.00 H+0 HETATM 60 H UNK 0 -0.649 -2.210 -1.675 0.00 0.00 H+0 HETATM 61 H UNK 0 -1.669 1.288 -0.851 0.00 0.00 H+0 HETATM 62 H UNK 0 -0.519 1.014 0.447 0.00 0.00 H+0 HETATM 63 H UNK 0 -0.073 2.030 -0.911 0.00 0.00 H+0 CONECT 1 2 28 29 30 CONECT 2 3 1 CONECT 3 4 2 CONECT 4 5 3 31 32 CONECT 5 7 6 4 33 CONECT 6 5 34 35 36 CONECT 7 8 26 5 37 CONECT 8 9 7 38 39 CONECT 9 10 8 40 41 CONECT 10 26 9 42 11 CONECT 11 12 23 43 10 CONECT 12 14 11 13 CONECT 13 12 CONECT 14 15 12 44 CONECT 15 14 16 21 CONECT 16 17 15 45 46 CONECT 17 19 16 18 47 CONECT 18 17 48 CONECT 19 17 20 49 50 CONECT 20 19 21 51 52 CONECT 21 22 23 20 15 CONECT 22 21 53 54 55 CONECT 23 21 11 56 24 CONECT 24 25 23 57 58 CONECT 25 26 24 59 60 CONECT 26 10 25 7 27 CONECT 27 26 61 62 63 CONECT 28 1 CONECT 29 1 CONECT 30 1 CONECT 31 4 CONECT 32 4 CONECT 33 5 CONECT 34 6 CONECT 35 6 CONECT 36 6 CONECT 37 7 CONECT 38 8 CONECT 39 8 CONECT 40 9 CONECT 41 9 CONECT 42 10 CONECT 43 11 CONECT 44 14 CONECT 45 16 CONECT 46 16 CONECT 47 17 CONECT 48 18 CONECT 49 19 CONECT 50 19 CONECT 51 20 CONECT 52 20 CONECT 53 22 CONECT 54 22 CONECT 55 22 CONECT 56 23 CONECT 57 24 CONECT 58 24 CONECT 59 25 CONECT 60 25 CONECT 61 27 CONECT 62 27 CONECT 63 27 MASTER 0 0 0 0 0 0 0 0 63 0 132 0 END SMILES for NP0025748 (Gelliusterol B)[H]O[C@]1([H])C([H])([H])C2=C([H])C(=O)[C@@]3([H])[C@]4([H])C([H])([H])C([H])([H])[C@]([H])([C@@]([H])(C([H])([H])[H])C([H])([H])C#CC([H])([H])[H])[C@@]4(C([H])([H])[H])C([H])([H])C([H])([H])[C@]3([H])[C@@]2(C([H])([H])[H])C([H])([H])C1([H])[H] INCHI for NP0025748 (Gelliusterol B)InChI=1S/C25H36O2/c1-5-6-7-16(2)19-8-9-20-23-21(11-13-25(19,20)4)24(3)12-10-18(26)14-17(24)15-22(23)27/h15-16,18-21,23,26H,7-14H2,1-4H3/t16-,18-,19+,20-,21-,23-,24-,25+/m0/s1 3D Structure for NP0025748 (Gelliusterol B) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Chemical Formula | C25H36O2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Average Mass | 368.5610 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Monoisotopic Mass | 368.27153 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
IUPAC Name | (1S,2R,5S,10S,11S,14R,15R)-14-[(2S)-hex-4-yn-2-yl]-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-9-one | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Traditional Name | (1S,2R,5S,10S,11S,14R,15R)-14-[(2S)-hex-4-yn-2-yl]-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-9-one | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
CAS Registry Number | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
SMILES | [H]O[C@]1([H])C([H])([H])C2=C([H])C(=O)[C@@]3([H])[C@]4([H])C([H])([H])C([H])([H])[C@]([H])([C@@]([H])(C([H])([H])[H])C([H])([H])C#CC([H])([H])[H])[C@@]4(C([H])([H])[H])C([H])([H])C([H])([H])[C@]3([H])[C@@]2(C([H])([H])[H])C([H])([H])C1([H])[H] | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
InChI Identifier | InChI=1S/C25H36O2/c1-5-6-7-16(2)19-8-9-20-23-21(11-13-25(19,20)4)24(3)12-10-18(26)14-17(24)15-22(23)27/h15-16,18-21,23,26H,7-14H2,1-4H3/t16-,18-,19+,20-,21-,23-,24-,25+/m0/s1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
InChI Key | HHGLFNRDPUBPSI-NOCRRZKMSA-N | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Experimental Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Predicted Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Chemical Shift Submissions | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Species | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Species of Origin |
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Chemical Taxonomy | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Classification | Not classified | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Physical Properties | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
State | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Experimental Properties |
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Predicted Properties |
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External Links | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
External Links | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
References | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
General References |
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