Showing NP-Card for gamma-eudesmol 11-alpha-L-rhamnoside (NP0025632)
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Version | 1.0 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Created at | 2021-06-19 17:42:35 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Updated at | 2021-06-29 23:50:42 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
NP-MRD ID | NP0025632 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Secondary Accession Numbers | None | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Natural Product Identification | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Common Name | gamma-eudesmol 11-alpha-L-rhamnoside | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Provided By | JEOL Database | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Description | gamma-eudesmol 11-alpha-L-rhamnoside is found in Cananga odorata. It was first documented in 2001 (Hsieh, T.-J., et al.). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structure | MOL for NP0025632 (gamma-eudesmol 11-alpha-L-rhamnoside)Mrv1652306192119423D 62 64 0 0 0 0 999 V2000 0.4415 -3.2031 2.3343 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8507 -3.0285 0.8924 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8474 -1.8523 0.2176 C 0 0 0 0 0 0 0 0 0 0 0 0 0.3347 -0.5429 0.8000 C 0 0 1 0 0 0 0 0 0 0 0 0 1.3877 0.5870 0.7388 C 0 0 2 0 0 0 0 0 0 0 0 0 0.8567 1.9322 1.3599 C 0 0 1 0 0 0 0 0 0 0 0 0 0.5045 1.7284 2.8454 C 0 0 0 0 0 0 0 0 0 0 0 0 1.9449 3.0205 1.2610 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.2844 2.3114 0.5703 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.0648 3.4277 1.0072 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.0069 3.0719 2.0168 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.9738 2.1022 1.5861 C 0 0 1 0 0 0 0 0 0 0 0 0 -3.8767 1.8010 2.7779 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.7811 2.6177 0.3867 C 0 0 2 0 0 0 0 0 0 0 0 0 -4.6879 1.6234 -0.0966 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.8309 3.0199 -0.7415 C 0 0 1 0 0 0 0 0 0 0 0 0 -3.5938 3.6156 -1.8062 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.7812 4.0061 -0.2294 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.8553 4.2802 -1.2956 O 0 0 0 0 0 0 0 0 0 0 0 0 1.8477 0.7573 -0.7267 C 0 0 1 0 0 0 0 0 0 0 0 0 2.3553 -0.5560 -1.3241 C 0 0 2 0 0 0 0 0 0 0 0 0 1.3539 -1.7340 -1.2281 C 0 0 2 0 0 0 0 0 0 0 0 0 0.1598 -1.4952 -2.1816 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1081 -3.0101 -1.6915 C 0 0 2 0 0 0 0 0 0 0 0 0 1.3922 -4.2817 -1.2673 C 0 0 1 0 0 0 0 0 0 0 0 0 1.2738 -4.3344 0.2502 C 0 0 1 0 0 0 0 0 0 0 0 0 1.0966 -3.9303 2.8276 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5187 -2.2885 2.9253 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5857 -3.5766 2.3914 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5655 -0.2477 0.2473 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0007 -0.6765 1.8282 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2605 0.2667 1.3265 H 0 0 0 0 0 0 0 0 0 0 0 0 1.3335 1.2628 3.3892 H 0 0 0 0 0 0 0 0 0 0 0 0 0.2876 2.6827 3.3387 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.3894 1.1115 2.9746 H 0 0 0 0 0 0 0 0 0 0 0 0 1.6955 3.8982 1.8673 H 0 0 0 0 0 0 0 0 0 0 0 0 2.0548 3.3867 0.2349 H 0 0 0 0 0 0 0 0 0 0 0 0 2.9128 2.6501 1.6153 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4110 4.2075 1.4080 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.4602 1.1691 1.3228 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2794 1.4546 3.6285 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.6177 1.0324 2.5394 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.4005 2.7043 3.1098 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.3826 3.4879 0.6789 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.0173 1.9728 -0.9492 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.3577 2.1335 -1.1819 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.9367 4.0622 -2.3775 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.2706 4.9533 0.0262 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.2407 3.5184 -1.3119 H 0 0 0 0 0 0 0 0 0 0 0 0 1.0332 1.1552 -1.3426 H 0 0 0 0 0 0 0 0 0 0 0 0 2.6662 1.4828 -0.7861 H 0 0 0 0 0 0 0 0 0 0 0 0 3.2847 -0.8193 -0.7999 H 0 0 0 0 0 0 0 0 0 0 0 0 2.6344 -0.3856 -2.3720 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.3577 -0.5518 -1.9817 H 0 0 0 0 0 0 0 0 0 0 0 0 0.4933 -1.4591 -3.2252 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5880 -2.2916 -2.0998 H 0 0 0 0 0 0 0 0 0 0 0 0 3.1206 -3.0304 -1.2653 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2376 -3.0055 -2.7811 H 0 0 0 0 0 0 0 0 0 0 0 0 0.3974 -4.3337 -1.7242 H 0 0 0 0 0 0 0 0 0 0 0 0 1.9447 -5.1593 -1.6225 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2410 -4.6289 0.6773 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5568 -5.1232 0.5095 H 0 0 0 0 0 0 0 0 0 0 0 0 18 16 1 0 0 0 0 16 14 1 0 0 0 0 25 24 1 0 0 0 0 26 2 1 0 0 0 0 2 3 2 0 0 0 0 22 24 1 0 0 0 0 22 3 1 0 0 0 0 14 12 1 0 0 0 0 12 11 1 0 0 0 0 11 10 1 0 0 0 0 22 21 1 0 0 0 0 3 4 1 0 0 0 0 4 5 1 0 0 0 0 5 20 1 0 0 0 0 21 20 1 0 0 0 0 18 19 1 0 0 0 0 14 15 1 0 0 0 0 16 17 1 0 0 0 0 22 23 1 6 0 0 0 5 6 1 0 0 0 0 6 9 1 6 0 0 0 25 26 1 0 0 0 0 2 1 1 0 0 0 0 6 7 1 0 0 0 0 10 18 1 0 0 0 0 6 8 1 0 0 0 0 12 13 1 0 0 0 0 10 9 1 0 0 0 0 19 49 1 0 0 0 0 10 39 1 1 0 0 0 14 44 1 1 0 0 0 15 45 1 0 0 0 0 16 46 1 6 0 0 0 17 47 1 0 0 0 0 18 48 1 1 0 0 0 13 41 1 0 0 0 0 13 42 1 0 0 0 0 13 43 1 0 0 0 0 12 40 1 6 0 0 0 25 59 1 0 0 0 0 25 60 1 0 0 0 0 26 61 1 0 0 0 0 26 62 1 0 0 0 0 24 57 1 0 0 0 0 24 58 1 0 0 0 0 4 30 1 0 0 0 0 4 31 1 0 0 0 0 5 32 1 1 0 0 0 21 52 1 0 0 0 0 21 53 1 0 0 0 0 20 50 1 0 0 0 0 20 51 1 0 0 0 0 23 54 1 0 0 0 0 23 55 1 0 0 0 0 23 56 1 0 0 0 0 1 27 1 0 0 0 0 1 28 1 0 0 0 0 1 29 1 0 0 0 0 7 33 1 0 0 0 0 7 34 1 0 0 0 0 7 35 1 0 0 0 0 8 36 1 0 0 0 0 8 37 1 0 0 0 0 8 38 1 0 0 0 0 M END 3D MOL for NP0025632 (gamma-eudesmol 11-alpha-L-rhamnoside)RDKit 3D 62 64 0 0 0 0 0 0 0 0999 V2000 0.4415 -3.2031 2.3343 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8507 -3.0285 0.8924 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8474 -1.8523 0.2176 C 0 0 0 0 0 0 0 0 0 0 0 0 0.3347 -0.5429 0.8000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3877 0.5870 0.7388 C 0 0 2 0 0 0 0 0 0 0 0 0 0.8567 1.9322 1.3599 C 0 0 1 0 0 0 0 0 0 0 0 0 0.5045 1.7284 2.8454 C 0 0 0 0 0 0 0 0 0 0 0 0 1.9449 3.0205 1.2610 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.2844 2.3114 0.5703 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.0648 3.4277 1.0072 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.0069 3.0719 2.0168 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.9738 2.1022 1.5861 C 0 0 1 0 0 0 0 0 0 0 0 0 -3.8767 1.8010 2.7779 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.7811 2.6177 0.3867 C 0 0 2 0 0 0 0 0 0 0 0 0 -4.6879 1.6234 -0.0966 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.8309 3.0199 -0.7415 C 0 0 1 0 0 0 0 0 0 0 0 0 -3.5938 3.6156 -1.8062 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.7812 4.0061 -0.2294 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.8553 4.2802 -1.2956 O 0 0 0 0 0 0 0 0 0 0 0 0 1.8477 0.7573 -0.7267 C 0 0 0 0 0 0 0 0 0 0 0 0 2.3553 -0.5560 -1.3241 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3539 -1.7340 -1.2281 C 0 0 2 0 0 0 0 0 0 0 0 0 0.1598 -1.4952 -2.1816 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1081 -3.0101 -1.6915 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3922 -4.2817 -1.2673 C 0 0 0 0 0 0 0 0 0 0 0 0 1.2738 -4.3344 0.2502 C 0 0 0 0 0 0 0 0 0 0 0 0 1.0966 -3.9303 2.8276 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5187 -2.2885 2.9253 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5857 -3.5766 2.3914 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5655 -0.2477 0.2473 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0007 -0.6765 1.8282 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2605 0.2667 1.3265 H 0 0 0 0 0 0 0 0 0 0 0 0 1.3335 1.2628 3.3892 H 0 0 0 0 0 0 0 0 0 0 0 0 0.2876 2.6827 3.3387 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.3894 1.1115 2.9746 H 0 0 0 0 0 0 0 0 0 0 0 0 1.6955 3.8982 1.8673 H 0 0 0 0 0 0 0 0 0 0 0 0 2.0548 3.3867 0.2349 H 0 0 0 0 0 0 0 0 0 0 0 0 2.9128 2.6501 1.6153 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4110 4.2075 1.4080 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.4602 1.1691 1.3228 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2794 1.4546 3.6285 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.6177 1.0324 2.5394 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.4005 2.7043 3.1098 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.3826 3.4879 0.6789 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.0173 1.9728 -0.9492 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.3577 2.1335 -1.1819 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.9367 4.0622 -2.3775 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.2706 4.9533 0.0262 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.2407 3.5184 -1.3119 H 0 0 0 0 0 0 0 0 0 0 0 0 1.0332 1.1552 -1.3426 H 0 0 0 0 0 0 0 0 0 0 0 0 2.6662 1.4828 -0.7861 H 0 0 0 0 0 0 0 0 0 0 0 0 3.2847 -0.8193 -0.7999 H 0 0 0 0 0 0 0 0 0 0 0 0 2.6344 -0.3856 -2.3720 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.3577 -0.5518 -1.9817 H 0 0 0 0 0 0 0 0 0 0 0 0 0.4933 -1.4591 -3.2252 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5880 -2.2916 -2.0998 H 0 0 0 0 0 0 0 0 0 0 0 0 3.1206 -3.0304 -1.2653 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2376 -3.0055 -2.7811 H 0 0 0 0 0 0 0 0 0 0 0 0 0.3974 -4.3337 -1.7242 H 0 0 0 0 0 0 0 0 0 0 0 0 1.9447 -5.1593 -1.6225 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2410 -4.6289 0.6773 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5568 -5.1232 0.5095 H 0 0 0 0 0 0 0 0 0 0 0 0 18 16 1 0 16 14 1 0 25 24 1 0 26 2 1 0 2 3 2 0 22 24 1 0 22 3 1 0 14 12 1 0 12 11 1 0 11 10 1 0 22 21 1 0 3 4 1 0 4 5 1 0 5 20 1 0 21 20 1 0 18 19 1 0 14 15 1 0 16 17 1 0 22 23 1 6 5 6 1 0 6 9 1 6 25 26 1 0 2 1 1 0 6 7 1 0 10 18 1 0 6 8 1 0 12 13 1 0 10 9 1 0 19 49 1 0 10 39 1 1 14 44 1 1 15 45 1 0 16 46 1 6 17 47 1 0 18 48 1 1 13 41 1 0 13 42 1 0 13 43 1 0 12 40 1 6 25 59 1 0 25 60 1 0 26 61 1 0 26 62 1 0 24 57 1 0 24 58 1 0 4 30 1 0 4 31 1 0 5 32 1 1 21 52 1 0 21 53 1 0 20 50 1 0 20 51 1 0 23 54 1 0 23 55 1 0 23 56 1 0 1 27 1 0 1 28 1 0 1 29 1 0 7 33 1 0 7 34 1 0 7 35 1 0 8 36 1 0 8 37 1 0 8 38 1 0 M END 3D SDF for NP0025632 (gamma-eudesmol 11-alpha-L-rhamnoside)Mrv1652306192119423D 62 64 0 0 0 0 999 V2000 0.4415 -3.2031 2.3343 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8507 -3.0285 0.8924 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8474 -1.8523 0.2176 C 0 0 0 0 0 0 0 0 0 0 0 0 0.3347 -0.5429 0.8000 C 0 0 1 0 0 0 0 0 0 0 0 0 1.3877 0.5870 0.7388 C 0 0 2 0 0 0 0 0 0 0 0 0 0.8567 1.9322 1.3599 C 0 0 1 0 0 0 0 0 0 0 0 0 0.5045 1.7284 2.8454 C 0 0 0 0 0 0 0 0 0 0 0 0 1.9449 3.0205 1.2610 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.2844 2.3114 0.5703 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.0648 3.4277 1.0072 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.0069 3.0719 2.0168 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.9738 2.1022 1.5861 C 0 0 1 0 0 0 0 0 0 0 0 0 -3.8767 1.8010 2.7779 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.7811 2.6177 0.3867 C 0 0 2 0 0 0 0 0 0 0 0 0 -4.6879 1.6234 -0.0966 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.8309 3.0199 -0.7415 C 0 0 1 0 0 0 0 0 0 0 0 0 -3.5938 3.6156 -1.8062 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.7812 4.0061 -0.2294 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.8553 4.2802 -1.2956 O 0 0 0 0 0 0 0 0 0 0 0 0 1.8477 0.7573 -0.7267 C 0 0 1 0 0 0 0 0 0 0 0 0 2.3553 -0.5560 -1.3241 C 0 0 2 0 0 0 0 0 0 0 0 0 1.3539 -1.7340 -1.2281 C 0 0 2 0 0 0 0 0 0 0 0 0 0.1598 -1.4952 -2.1816 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1081 -3.0101 -1.6915 C 0 0 2 0 0 0 0 0 0 0 0 0 1.3922 -4.2817 -1.2673 C 0 0 1 0 0 0 0 0 0 0 0 0 1.2738 -4.3344 0.2502 C 0 0 1 0 0 0 0 0 0 0 0 0 1.0966 -3.9303 2.8276 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5187 -2.2885 2.9253 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5857 -3.5766 2.3914 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5655 -0.2477 0.2473 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0007 -0.6765 1.8282 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2605 0.2667 1.3265 H 0 0 0 0 0 0 0 0 0 0 0 0 1.3335 1.2628 3.3892 H 0 0 0 0 0 0 0 0 0 0 0 0 0.2876 2.6827 3.3387 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.3894 1.1115 2.9746 H 0 0 0 0 0 0 0 0 0 0 0 0 1.6955 3.8982 1.8673 H 0 0 0 0 0 0 0 0 0 0 0 0 2.0548 3.3867 0.2349 H 0 0 0 0 0 0 0 0 0 0 0 0 2.9128 2.6501 1.6153 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4110 4.2075 1.4080 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.4602 1.1691 1.3228 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2794 1.4546 3.6285 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.6177 1.0324 2.5394 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.4005 2.7043 3.1098 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.3826 3.4879 0.6789 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.0173 1.9728 -0.9492 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.3577 2.1335 -1.1819 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.9367 4.0622 -2.3775 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.2706 4.9533 0.0262 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.2407 3.5184 -1.3119 H 0 0 0 0 0 0 0 0 0 0 0 0 1.0332 1.1552 -1.3426 H 0 0 0 0 0 0 0 0 0 0 0 0 2.6662 1.4828 -0.7861 H 0 0 0 0 0 0 0 0 0 0 0 0 3.2847 -0.8193 -0.7999 H 0 0 0 0 0 0 0 0 0 0 0 0 2.6344 -0.3856 -2.3720 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.3577 -0.5518 -1.9817 H 0 0 0 0 0 0 0 0 0 0 0 0 0.4933 -1.4591 -3.2252 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5880 -2.2916 -2.0998 H 0 0 0 0 0 0 0 0 0 0 0 0 3.1206 -3.0304 -1.2653 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2376 -3.0055 -2.7811 H 0 0 0 0 0 0 0 0 0 0 0 0 0.3974 -4.3337 -1.7242 H 0 0 0 0 0 0 0 0 0 0 0 0 1.9447 -5.1593 -1.6225 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2410 -4.6289 0.6773 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5568 -5.1232 0.5095 H 0 0 0 0 0 0 0 0 0 0 0 0 18 16 1 0 0 0 0 16 14 1 0 0 0 0 25 24 1 0 0 0 0 26 2 1 0 0 0 0 2 3 2 0 0 0 0 22 24 1 0 0 0 0 22 3 1 0 0 0 0 14 12 1 0 0 0 0 12 11 1 0 0 0 0 11 10 1 0 0 0 0 22 21 1 0 0 0 0 3 4 1 0 0 0 0 4 5 1 0 0 0 0 5 20 1 0 0 0 0 21 20 1 0 0 0 0 18 19 1 0 0 0 0 14 15 1 0 0 0 0 16 17 1 0 0 0 0 22 23 1 6 0 0 0 5 6 1 0 0 0 0 6 9 1 6 0 0 0 25 26 1 0 0 0 0 2 1 1 0 0 0 0 6 7 1 0 0 0 0 10 18 1 0 0 0 0 6 8 1 0 0 0 0 12 13 1 0 0 0 0 10 9 1 0 0 0 0 19 49 1 0 0 0 0 10 39 1 1 0 0 0 14 44 1 1 0 0 0 15 45 1 0 0 0 0 16 46 1 6 0 0 0 17 47 1 0 0 0 0 18 48 1 1 0 0 0 13 41 1 0 0 0 0 13 42 1 0 0 0 0 13 43 1 0 0 0 0 12 40 1 6 0 0 0 25 59 1 0 0 0 0 25 60 1 0 0 0 0 26 61 1 0 0 0 0 26 62 1 0 0 0 0 24 57 1 0 0 0 0 24 58 1 0 0 0 0 4 30 1 0 0 0 0 4 31 1 0 0 0 0 5 32 1 1 0 0 0 21 52 1 0 0 0 0 21 53 1 0 0 0 0 20 50 1 0 0 0 0 20 51 1 0 0 0 0 23 54 1 0 0 0 0 23 55 1 0 0 0 0 23 56 1 0 0 0 0 1 27 1 0 0 0 0 1 28 1 0 0 0 0 1 29 1 0 0 0 0 7 33 1 0 0 0 0 7 34 1 0 0 0 0 7 35 1 0 0 0 0 8 36 1 0 0 0 0 8 37 1 0 0 0 0 8 38 1 0 0 0 0 M END > <DATABASE_ID> NP0025632 > <DATABASE_NAME> NP-MRD > <SMILES> [H]O[C@]1([H])[C@]([H])(OC(C([H])([H])[H])(C([H])([H])[H])[C@@]2([H])C([H])([H])C3=C(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[C@]3(C([H])([H])[H])C([H])([H])C2([H])[H])O[C@@]([H])(C([H])([H])[H])[C@]([H])(O[H])[C@@]1([H])O[H] > <INCHI_IDENTIFIER> InChI=1S/C21H36O5/c1-12-7-6-9-21(5)10-8-14(11-15(12)21)20(3,4)26-19-18(24)17(23)16(22)13(2)25-19/h13-14,16-19,22-24H,6-11H2,1-5H3/t13-,14+,16-,17+,18-,19-,21+/m0/s1 > <INCHI_KEY> QKXSRJAHTPTJNG-ZBELAPBMSA-N > <FORMULA> C21H36O5 > <MOLECULAR_WEIGHT> 368.514 > <EXACT_MASS> 368.256274259 > <JCHEM_ACCEPTOR_COUNT> 5 > <JCHEM_ATOM_COUNT> 62 > <JCHEM_AVERAGE_POLARIZABILITY> 41.435869898618144 > <JCHEM_BIOAVAILABILITY> 1 > <JCHEM_DONOR_COUNT> 3 > <JCHEM_FORMAL_CHARGE> 0 > <JCHEM_GHOSE_FILTER> 1 > <JCHEM_IUPAC> (2S,3S,4R,5R,6S)-2-({2-[(2R,4aR)-4a,8-dimethyl-1,2,3,4,4a,5,6,7-octahydronaphthalen-2-yl]propan-2-yl}oxy)-6-methyloxane-3,4,5-triol > <ALOGPS_LOGP> 2.65 > <JCHEM_LOGP> 2.7062107439999976 > <ALOGPS_LOGS> -3.00 > <JCHEM_MDDR_LIKE_RULE> 0 > <JCHEM_NUMBER_OF_RINGS> 3 > <JCHEM_PHYSIOLOGICAL_CHARGE> 0 > <JCHEM_PKA> 13.272394123636719 > <JCHEM_PKA_STRONGEST_ACIDIC> 12.22396766331953 > <JCHEM_PKA_STRONGEST_BASIC> -3.61218280102206 > <JCHEM_POLAR_SURFACE_AREA> 79.15 > <JCHEM_REFRACTIVITY> 100.03699999999999 > <JCHEM_ROTATABLE_BOND_COUNT> 3 > <JCHEM_RULE_OF_FIVE> 1 > <ALOGPS_SOLUBILITY> 3.65e-01 g/l > <JCHEM_TRADITIONAL_IUPAC> (2S,3S,4R,5R,6S)-2-({2-[(2R,4aR)-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]propan-2-yl}oxy)-6-methyloxane-3,4,5-triol > <JCHEM_VEBER_RULE> 0 $$$$ 3D-SDF for NP0025632 (gamma-eudesmol 11-alpha-L-rhamnoside)RDKit 3D 62 64 0 0 0 0 0 0 0 0999 V2000 0.4415 -3.2031 2.3343 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8507 -3.0285 0.8924 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8474 -1.8523 0.2176 C 0 0 0 0 0 0 0 0 0 0 0 0 0.3347 -0.5429 0.8000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3877 0.5870 0.7388 C 0 0 2 0 0 0 0 0 0 0 0 0 0.8567 1.9322 1.3599 C 0 0 1 0 0 0 0 0 0 0 0 0 0.5045 1.7284 2.8454 C 0 0 0 0 0 0 0 0 0 0 0 0 1.9449 3.0205 1.2610 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.2844 2.3114 0.5703 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.0648 3.4277 1.0072 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.0069 3.0719 2.0168 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.9738 2.1022 1.5861 C 0 0 1 0 0 0 0 0 0 0 0 0 -3.8767 1.8010 2.7779 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.7811 2.6177 0.3867 C 0 0 2 0 0 0 0 0 0 0 0 0 -4.6879 1.6234 -0.0966 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.8309 3.0199 -0.7415 C 0 0 1 0 0 0 0 0 0 0 0 0 -3.5938 3.6156 -1.8062 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.7812 4.0061 -0.2294 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.8553 4.2802 -1.2956 O 0 0 0 0 0 0 0 0 0 0 0 0 1.8477 0.7573 -0.7267 C 0 0 0 0 0 0 0 0 0 0 0 0 2.3553 -0.5560 -1.3241 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3539 -1.7340 -1.2281 C 0 0 2 0 0 0 0 0 0 0 0 0 0.1598 -1.4952 -2.1816 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1081 -3.0101 -1.6915 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3922 -4.2817 -1.2673 C 0 0 0 0 0 0 0 0 0 0 0 0 1.2738 -4.3344 0.2502 C 0 0 0 0 0 0 0 0 0 0 0 0 1.0966 -3.9303 2.8276 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5187 -2.2885 2.9253 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5857 -3.5766 2.3914 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5655 -0.2477 0.2473 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0007 -0.6765 1.8282 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2605 0.2667 1.3265 H 0 0 0 0 0 0 0 0 0 0 0 0 1.3335 1.2628 3.3892 H 0 0 0 0 0 0 0 0 0 0 0 0 0.2876 2.6827 3.3387 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.3894 1.1115 2.9746 H 0 0 0 0 0 0 0 0 0 0 0 0 1.6955 3.8982 1.8673 H 0 0 0 0 0 0 0 0 0 0 0 0 2.0548 3.3867 0.2349 H 0 0 0 0 0 0 0 0 0 0 0 0 2.9128 2.6501 1.6153 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4110 4.2075 1.4080 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.4602 1.1691 1.3228 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2794 1.4546 3.6285 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.6177 1.0324 2.5394 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.4005 2.7043 3.1098 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.3826 3.4879 0.6789 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.0173 1.9728 -0.9492 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.3577 2.1335 -1.1819 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.9367 4.0622 -2.3775 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.2706 4.9533 0.0262 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.2407 3.5184 -1.3119 H 0 0 0 0 0 0 0 0 0 0 0 0 1.0332 1.1552 -1.3426 H 0 0 0 0 0 0 0 0 0 0 0 0 2.6662 1.4828 -0.7861 H 0 0 0 0 0 0 0 0 0 0 0 0 3.2847 -0.8193 -0.7999 H 0 0 0 0 0 0 0 0 0 0 0 0 2.6344 -0.3856 -2.3720 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.3577 -0.5518 -1.9817 H 0 0 0 0 0 0 0 0 0 0 0 0 0.4933 -1.4591 -3.2252 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5880 -2.2916 -2.0998 H 0 0 0 0 0 0 0 0 0 0 0 0 3.1206 -3.0304 -1.2653 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2376 -3.0055 -2.7811 H 0 0 0 0 0 0 0 0 0 0 0 0 0.3974 -4.3337 -1.7242 H 0 0 0 0 0 0 0 0 0 0 0 0 1.9447 -5.1593 -1.6225 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2410 -4.6289 0.6773 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5568 -5.1232 0.5095 H 0 0 0 0 0 0 0 0 0 0 0 0 18 16 1 0 16 14 1 0 25 24 1 0 26 2 1 0 2 3 2 0 22 24 1 0 22 3 1 0 14 12 1 0 12 11 1 0 11 10 1 0 22 21 1 0 3 4 1 0 4 5 1 0 5 20 1 0 21 20 1 0 18 19 1 0 14 15 1 0 16 17 1 0 22 23 1 6 5 6 1 0 6 9 1 6 25 26 1 0 2 1 1 0 6 7 1 0 10 18 1 0 6 8 1 0 12 13 1 0 10 9 1 0 19 49 1 0 10 39 1 1 14 44 1 1 15 45 1 0 16 46 1 6 17 47 1 0 18 48 1 1 13 41 1 0 13 42 1 0 13 43 1 0 12 40 1 6 25 59 1 0 25 60 1 0 26 61 1 0 26 62 1 0 24 57 1 0 24 58 1 0 4 30 1 0 4 31 1 0 5 32 1 1 21 52 1 0 21 53 1 0 20 50 1 0 20 51 1 0 23 54 1 0 23 55 1 0 23 56 1 0 1 27 1 0 1 28 1 0 1 29 1 0 7 33 1 0 7 34 1 0 7 35 1 0 8 36 1 0 8 37 1 0 8 38 1 0 M END PDB for NP0025632 (gamma-eudesmol 11-alpha-L-rhamnoside)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 0.442 -3.203 2.334 0.00 0.00 C+0 HETATM 2 C UNK 0 0.851 -3.029 0.892 0.00 0.00 C+0 HETATM 3 C UNK 0 0.847 -1.852 0.218 0.00 0.00 C+0 HETATM 4 C UNK 0 0.335 -0.543 0.800 0.00 0.00 C+0 HETATM 5 C UNK 0 1.388 0.587 0.739 0.00 0.00 C+0 HETATM 6 C UNK 0 0.857 1.932 1.360 0.00 0.00 C+0 HETATM 7 C UNK 0 0.504 1.728 2.845 0.00 0.00 C+0 HETATM 8 C UNK 0 1.945 3.021 1.261 0.00 0.00 C+0 HETATM 9 O UNK 0 -0.284 2.311 0.570 0.00 0.00 O+0 HETATM 10 C UNK 0 -1.065 3.428 1.007 0.00 0.00 C+0 HETATM 11 O UNK 0 -2.007 3.072 2.017 0.00 0.00 O+0 HETATM 12 C UNK 0 -2.974 2.102 1.586 0.00 0.00 C+0 HETATM 13 C UNK 0 -3.877 1.801 2.778 0.00 0.00 C+0 HETATM 14 C UNK 0 -3.781 2.618 0.387 0.00 0.00 C+0 HETATM 15 O UNK 0 -4.688 1.623 -0.097 0.00 0.00 O+0 HETATM 16 C UNK 0 -2.831 3.020 -0.742 0.00 0.00 C+0 HETATM 17 O UNK 0 -3.594 3.616 -1.806 0.00 0.00 O+0 HETATM 18 C UNK 0 -1.781 4.006 -0.229 0.00 0.00 C+0 HETATM 19 O UNK 0 -0.855 4.280 -1.296 0.00 0.00 O+0 HETATM 20 C UNK 0 1.848 0.757 -0.727 0.00 0.00 C+0 HETATM 21 C UNK 0 2.355 -0.556 -1.324 0.00 0.00 C+0 HETATM 22 C UNK 0 1.354 -1.734 -1.228 0.00 0.00 C+0 HETATM 23 C UNK 0 0.160 -1.495 -2.182 0.00 0.00 C+0 HETATM 24 C UNK 0 2.108 -3.010 -1.692 0.00 0.00 C+0 HETATM 25 C UNK 0 1.392 -4.282 -1.267 0.00 0.00 C+0 HETATM 26 C UNK 0 1.274 -4.334 0.250 0.00 0.00 C+0 HETATM 27 H UNK 0 1.097 -3.930 2.828 0.00 0.00 H+0 HETATM 28 H UNK 0 0.519 -2.289 2.925 0.00 0.00 H+0 HETATM 29 H UNK 0 -0.586 -3.577 2.391 0.00 0.00 H+0 HETATM 30 H UNK 0 -0.566 -0.248 0.247 0.00 0.00 H+0 HETATM 31 H UNK 0 -0.001 -0.677 1.828 0.00 0.00 H+0 HETATM 32 H UNK 0 2.260 0.267 1.327 0.00 0.00 H+0 HETATM 33 H UNK 0 1.333 1.263 3.389 0.00 0.00 H+0 HETATM 34 H UNK 0 0.288 2.683 3.339 0.00 0.00 H+0 HETATM 35 H UNK 0 -0.389 1.111 2.975 0.00 0.00 H+0 HETATM 36 H UNK 0 1.696 3.898 1.867 0.00 0.00 H+0 HETATM 37 H UNK 0 2.055 3.387 0.235 0.00 0.00 H+0 HETATM 38 H UNK 0 2.913 2.650 1.615 0.00 0.00 H+0 HETATM 39 H UNK 0 -0.411 4.207 1.408 0.00 0.00 H+0 HETATM 40 H UNK 0 -2.460 1.169 1.323 0.00 0.00 H+0 HETATM 41 H UNK 0 -3.279 1.455 3.628 0.00 0.00 H+0 HETATM 42 H UNK 0 -4.618 1.032 2.539 0.00 0.00 H+0 HETATM 43 H UNK 0 -4.401 2.704 3.110 0.00 0.00 H+0 HETATM 44 H UNK 0 -4.383 3.488 0.679 0.00 0.00 H+0 HETATM 45 H UNK 0 -5.017 1.973 -0.949 0.00 0.00 H+0 HETATM 46 H UNK 0 -2.358 2.134 -1.182 0.00 0.00 H+0 HETATM 47 H UNK 0 -2.937 4.062 -2.377 0.00 0.00 H+0 HETATM 48 H UNK 0 -2.271 4.953 0.026 0.00 0.00 H+0 HETATM 49 H UNK 0 -0.241 3.518 -1.312 0.00 0.00 H+0 HETATM 50 H UNK 0 1.033 1.155 -1.343 0.00 0.00 H+0 HETATM 51 H UNK 0 2.666 1.483 -0.786 0.00 0.00 H+0 HETATM 52 H UNK 0 3.285 -0.819 -0.800 0.00 0.00 H+0 HETATM 53 H UNK 0 2.634 -0.386 -2.372 0.00 0.00 H+0 HETATM 54 H UNK 0 -0.358 -0.552 -1.982 0.00 0.00 H+0 HETATM 55 H UNK 0 0.493 -1.459 -3.225 0.00 0.00 H+0 HETATM 56 H UNK 0 -0.588 -2.292 -2.100 0.00 0.00 H+0 HETATM 57 H UNK 0 3.121 -3.030 -1.265 0.00 0.00 H+0 HETATM 58 H UNK 0 2.238 -3.006 -2.781 0.00 0.00 H+0 HETATM 59 H UNK 0 0.397 -4.334 -1.724 0.00 0.00 H+0 HETATM 60 H UNK 0 1.945 -5.159 -1.623 0.00 0.00 H+0 HETATM 61 H UNK 0 2.241 -4.629 0.677 0.00 0.00 H+0 HETATM 62 H UNK 0 0.557 -5.123 0.509 0.00 0.00 H+0 CONECT 1 2 27 28 29 CONECT 2 26 3 1 CONECT 3 2 22 4 CONECT 4 3 5 30 31 CONECT 5 4 20 6 32 CONECT 6 5 9 7 8 CONECT 7 6 33 34 35 CONECT 8 6 36 37 38 CONECT 9 6 10 CONECT 10 11 18 9 39 CONECT 11 12 10 CONECT 12 14 11 13 40 CONECT 13 12 41 42 43 CONECT 14 16 12 15 44 CONECT 15 14 45 CONECT 16 18 14 17 46 CONECT 17 16 47 CONECT 18 16 19 10 48 CONECT 19 18 49 CONECT 20 5 21 50 51 CONECT 21 22 20 52 53 CONECT 22 24 3 21 23 CONECT 23 22 54 55 56 CONECT 24 25 22 57 58 CONECT 25 24 26 59 60 CONECT 26 2 25 61 62 CONECT 27 1 CONECT 28 1 CONECT 29 1 CONECT 30 4 CONECT 31 4 CONECT 32 5 CONECT 33 7 CONECT 34 7 CONECT 35 7 CONECT 36 8 CONECT 37 8 CONECT 38 8 CONECT 39 10 CONECT 40 12 CONECT 41 13 CONECT 42 13 CONECT 43 13 CONECT 44 14 CONECT 45 15 CONECT 46 16 CONECT 47 17 CONECT 48 18 CONECT 49 19 CONECT 50 20 CONECT 51 20 CONECT 52 21 CONECT 53 21 CONECT 54 23 CONECT 55 23 CONECT 56 23 CONECT 57 24 CONECT 58 24 CONECT 59 25 CONECT 60 25 CONECT 61 26 CONECT 62 26 MASTER 0 0 0 0 0 0 0 0 62 0 128 0 END SMILES for NP0025632 (gamma-eudesmol 11-alpha-L-rhamnoside)[H]O[C@]1([H])[C@]([H])(OC(C([H])([H])[H])(C([H])([H])[H])[C@@]2([H])C([H])([H])C3=C(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[C@]3(C([H])([H])[H])C([H])([H])C2([H])[H])O[C@@]([H])(C([H])([H])[H])[C@]([H])(O[H])[C@@]1([H])O[H] INCHI for NP0025632 (gamma-eudesmol 11-alpha-L-rhamnoside)InChI=1S/C21H36O5/c1-12-7-6-9-21(5)10-8-14(11-15(12)21)20(3,4)26-19-18(24)17(23)16(22)13(2)25-19/h13-14,16-19,22-24H,6-11H2,1-5H3/t13-,14+,16-,17+,18-,19-,21+/m0/s1 3D Structure for NP0025632 (gamma-eudesmol 11-alpha-L-rhamnoside) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Chemical Formula | C21H36O5 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Average Mass | 368.5140 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Monoisotopic Mass | 368.25627 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
IUPAC Name | (2S,3S,4R,5R,6S)-2-({2-[(2R,4aR)-4a,8-dimethyl-1,2,3,4,4a,5,6,7-octahydronaphthalen-2-yl]propan-2-yl}oxy)-6-methyloxane-3,4,5-triol | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Traditional Name | (2S,3S,4R,5R,6S)-2-({2-[(2R,4aR)-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]propan-2-yl}oxy)-6-methyloxane-3,4,5-triol | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
CAS Registry Number | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
SMILES | [H]O[C@]1([H])[C@]([H])(OC(C([H])([H])[H])(C([H])([H])[H])[C@@]2([H])C([H])([H])C3=C(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[C@]3(C([H])([H])[H])C([H])([H])C2([H])[H])O[C@@]([H])(C([H])([H])[H])[C@]([H])(O[H])[C@@]1([H])O[H] | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
InChI Identifier | InChI=1S/C21H36O5/c1-12-7-6-9-21(5)10-8-14(11-15(12)21)20(3,4)26-19-18(24)17(23)16(22)13(2)25-19/h13-14,16-19,22-24H,6-11H2,1-5H3/t13-,14+,16-,17+,18-,19-,21+/m0/s1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
InChI Key | QKXSRJAHTPTJNG-ZBELAPBMSA-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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