Showing NP-Card for MS-271 (NP0018364)
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Version | 1.0 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Created at | 2021-01-06 03:00:36 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||
Updated at | 2021-07-15 17:28:00 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||
NP-MRD ID | NP0018364 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Secondary Accession Numbers | None | |||||||||||||||||||||||||||||||||||||||||||||||||||
Natural Product Identification | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Common Name | MS-271 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Provided By | NPAtlas | |||||||||||||||||||||||||||||||||||||||||||||||||||
Description | MS-271 is found in Streptomyces. It was first documented in 2018 (PMID: 29974638). Based on a literature review very few articles have been published on MS-271 (PMID: 34164024). | |||||||||||||||||||||||||||||||||||||||||||||||||||
Structure | MOL for NP0018364 (MS-271)Mrv1652307042107403D 281288 0 0 0 0 999 V2000 6.8838 6.4879 -4.9699 C 0 0 0 0 0 0 0 0 0 0 0 0 6.3956 6.0233 -3.6446 C 0 0 2 0 0 0 0 0 0 0 0 0 5.0739 5.2241 -3.7491 C 0 0 2 0 0 0 0 0 0 0 0 0 4.0125 6.0740 -4.3684 C 0 0 0 0 0 0 0 0 0 0 0 0 4.7728 4.6578 -2.4127 C 0 0 1 0 0 0 0 0 0 0 0 0 4.5097 5.5225 -1.3193 N 0 0 0 0 0 0 0 0 0 0 0 0 3.7607 6.6925 -1.1593 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5581 6.5620 -0.6836 O 0 0 0 0 0 0 0 0 0 0 0 0 4.0576 8.1111 -1.4220 C 0 0 2 0 0 0 0 0 0 0 0 0 4.3118 8.7023 -0.0134 C 0 0 0 0 0 0 0 0 0 0 0 0 3.0716 8.8438 -2.1546 N 0 0 0 0 0 0 0 0 0 0 0 0 1.7169 8.6958 -2.3708 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3831 8.3564 -3.5894 O 0 0 0 0 0 0 0 0 0 0 0 0 0.5459 8.8459 -1.4970 C 0 0 1 0 0 0 0 0 0 0 0 0 0.6438 9.8449 -0.4022 C 0 0 2 0 0 0 0 0 0 0 0 0 0.9037 11.2511 -0.8791 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1818 11.7376 -0.9699 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4016 13.0183 -1.4165 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3523 13.8273 -1.7762 C 0 0 0 0 0 0 0 0 0 0 0 0 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1 0 71 72 1 0 72 73 1 0 73 74 1 0 74 75 2 0 75 76 1 0 76 77 1 0 77 78 2 0 78 79 1 0 79 80 2 0 80 81 1 0 81 82 2 0 72 83 1 0 83 84 2 0 83 85 1 0 57 86 1 0 86 87 1 0 87 88 2 0 87 89 1 0 89 90 1 0 90 91 1 0 90 92 1 0 89 93 1 0 93 94 1 0 94 95 2 0 52 96 1 0 96 97 1 0 97 98 2 0 97 99 1 0 99100 1 0 100101 1 0 99102 1 0 102103 1 0 103104 2 0 103105 1 0 105106 1 0 106107 1 0 107108 2 0 107109 1 0 109110 1 0 110111 1 0 110112 1 0 109113 1 0 113114 1 0 114115 2 0 114116 1 0 116117 1 0 117118 1 0 118119 2 0 118120 1 0 120121 1 0 121122 1 0 122123 1 0 122124 1 0 120125 1 0 125126 1 0 126127 2 0 40128 1 0 128129 2 0 128130 1 0 130131 1 0 131132 1 0 132133 1 0 133134 2 0 134135 1 0 135136 2 0 136137 1 0 137138 2 0 131139 1 0 139140 2 0 139141 1 0 141142 1 0 142143 1 0 142144 1 0 144145 2 0 144146 1 0 146147 1 0 147148 1 0 148149 2 0 148150 1 0 94 5 1 0 138133 1 0 22 16 1 0 150 30 1 0 126 35 1 0 68 63 1 0 82 74 1 0 82 77 1 0 1151 1 0 1152 1 0 1153 1 0 2154 1 0 2155 1 0 3156 1 6 4157 1 0 4158 1 0 4159 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1 0 123258 1 0 123259 1 0 124260 1 0 124261 1 0 124262 1 0 125263 1 0 130264 1 0 131265 1 1 132266 1 0 132267 1 0 134268 1 0 135269 1 0 136270 1 0 137271 1 0 138272 1 0 141273 1 0 142274 1 6 143275 1 0 143276 1 0 143277 1 0 146278 1 0 147279 1 0 147280 1 0 150281 1 0 M END 3D SDF for NP0018364 (MS-271)Mrv1652307042107403D 281288 0 0 0 0 999 V2000 6.8838 6.4879 -4.9699 C 0 0 0 0 0 0 0 0 0 0 0 0 6.3956 6.0233 -3.6446 C 0 0 2 0 0 0 0 0 0 0 0 0 5.0739 5.2241 -3.7491 C 0 0 2 0 0 0 0 0 0 0 0 0 4.0125 6.0740 -4.3684 C 0 0 0 0 0 0 0 0 0 0 0 0 4.7728 4.6578 -2.4127 C 0 0 1 0 0 0 0 0 0 0 0 0 4.5097 5.5225 -1.3193 N 0 0 0 0 0 0 0 0 0 0 0 0 3.7607 6.6925 -1.1593 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5581 6.5620 -0.6836 O 0 0 0 0 0 0 0 0 0 0 0 0 4.0576 8.1111 -1.4220 C 0 0 2 0 0 0 0 0 0 0 0 0 4.3118 8.7023 -0.0134 C 0 0 0 0 0 0 0 0 0 0 0 0 3.0716 8.8438 -2.1546 N 0 0 0 0 0 0 0 0 0 0 0 0 1.7169 8.6958 -2.3708 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3831 8.3564 -3.5894 O 0 0 0 0 0 0 0 0 0 0 0 0 0.5459 8.8459 -1.4970 C 0 0 1 0 0 0 0 0 0 0 0 0 0.6438 9.8449 -0.4022 C 0 0 2 0 0 0 0 0 0 0 0 0 0.9037 11.2511 -0.8791 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1818 11.7376 -0.9699 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4016 13.0183 -1.4165 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3523 13.8273 -1.7762 C 0 0 0 0 0 0 0 0 0 0 0 0 1.5515 15.1422 -2.2343 O 0 0 0 0 0 0 0 0 0 0 0 0 0.0582 13.3742 -1.6981 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.1421 12.0671 -1.2418 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.6480 9.2125 -2.2900 N 0 0 0 0 0 0 0 0 0 0 0 0 -1.9264 8.7488 -2.0138 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.8693 9.6221 -2.0606 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.3433 7.3718 -1.6683 C 0 0 2 0 0 0 0 0 0 0 0 0 -3.1190 7.2987 -0.4435 N 0 0 0 0 0 0 0 0 0 0 0 0 -4.4975 7.2151 -0.3211 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.0829 8.0597 0.4485 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.3691 6.2524 -0.9863 C 0 0 1 0 0 0 0 0 0 0 0 0 -4.8105 4.8846 -1.2164 C 0 0 2 0 0 0 0 0 0 0 0 0 -6.2454 3.8087 -1.5891 S 0 0 0 0 0 0 0 0 0 0 0 0 -5.6753 1.8049 -1.1914 S 0 0 0 0 0 0 0 0 0 0 0 0 -6.7747 1.0372 0.0218 C 0 0 1 0 0 0 0 0 0 0 0 0 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[H]OC(=O)[C@@]([H])(N([H])C(=O)[C@@]([H])(N([H])C(=O)[C@@]1([H])N([H])C(=O)[C@@]([H])(N([H])C(=O)[C@]([H])(N([H])C(=O)[C@@]([H])(N([H])C(=O)[C@]([H])(N([H])C(=O)C([H])([H])N([H])C(=O)[C@]2([H])N([H])C(=O)C([H])([H])N([H])C(=O)[C@]([H])(N([H])C(=O)[C@@]([H])(N([H])C(=O)[C@@]3([H])N([H])C(=O)[C@@]([H])(N([H])C(=O)[C@]([H])(N([H])C(=O)[C@@]([H])(N([H])C(=O)C([H])([H])N([H])C(=O)[C@@]([H])(N([H])C(=O)C([H])([H])N([H])C(=O)[C@@]([H])(N([H])C(=O)[C@]([H])(N([H])C(=O)C3([H])[H])C([H])([H])SSC2([H])[H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H])C([H])([H])O[H])C([H])([H])SSC1([H])[H])C([H])([H])C(=O)N([H])[H])C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H])C([H])([H])[H])C([H])([H])C1=C([H])C([H])=C(O[H])C([H])=C1[H])C([H])([H])[H])[C@@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H])C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H])C([H])([H])C1=C([H])N([H])C2=C([H])C([H])=C([H])C([H])=C12 > <INCHI_IDENTIFIER> InChI=1S/C97H131N23O26S4/c1-11-50(8)80-96(144)119-79(49(6)7)95(143)117-71(93(141)112-63(32-54-22-16-13-17-23-54)87(135)115-66(97(145)146)34-56-37-99-59-25-19-18-24-58(56)59)46-150-149-45-70-92(140)113-64(35-72(98)123)88(136)114-65-36-73(124)108-69(91(139)110-60(30-47(2)3)83(131)101-41-77(128)118-78(48(4)5)94(142)103-40-75(126)107-67(42-121)90(138)116-70)44-148-147-43-68(109-76(127)38-100-81(129)51(9)104-86(134)62(111-89(65)137)31-53-20-14-12-15-21-53)84(132)102-39-74(125)106-61(33-55-26-28-57(122)29-27-55)85(133)105-52(10)82(130)120-80/h12-29,37,47-52,60-71,78-80,99,121-122H,11,30-36,38-46H2,1-10H3,(H2,98,123)(H,100,129)(H,101,131)(H,102,132)(H,103,142)(H,104,134)(H,105,133)(H,106,125)(H,107,126)(H,108,124)(H,109,127)(H,110,139)(H,111,137)(H,112,141)(H,113,140)(H,114,136)(H,115,135)(H,116,138)(H,117,143)(H,118,128)(H,119,144)(H,120,130)(H,145,146)/t50-,51+,52-,60-,61+,62-,63-,64-,65-,66-,67-,68+,69+,70+,71-,78-,79-,80+/m0/s1 > <INCHI_KEY> TXYRKTDGDMHVHR-POXCZHPVSA-N > <FORMULA> C97H131N23O26S4 > <MOLECULAR_WEIGHT> 2163.49 > <EXACT_MASS> 2161.851846126 > <JCHEM_ACCEPTOR_COUNT> 26 > <JCHEM_ATOM_COUNT> 281 > <JCHEM_AVERAGE_POLARIZABILITY> 224.62275678974794 > <JCHEM_BIOAVAILABILITY> 0 > <JCHEM_DONOR_COUNT> 26 > <JCHEM_FORMAL_CHARGE> 0 > <JCHEM_GHOSE_FILTER> 0 > <JCHEM_IUPAC> (2S)-2-(2-{[(1S,4S,7R,13S,19R,22S,25R,28S,31R,36S,39S,45S,51S,54S,60S)-4-benzyl-25-[(2S)-butan-2-yl]-60-(carbamoylmethyl)-39-(hydroxymethyl)-19-[(4-hydroxyphenyl)methyl]-7,22-dimethyl-51-(2-methylpropyl)-2,5,8,11,14,17,20,23,26,29,38,41,44,47,50,53,56,59,62-nonadecaoxo-28,45-bis(propan-2-yl)-33,34,64,65-tetrathia-3,6,9,12,15,18,21,24,27,30,37,40,43,46,49,52,55,58,61-nonadecaazatricyclo[34.21.5.4^{13,54}]hexahexacontan-31-yl]formamido}-3-phenylpropanamido)-3-(1H-indol-3-yl)propanoic acid > <JCHEM_LOGP> -6.328688749 > <JCHEM_MDDR_LIKE_RULE> 1 > <JCHEM_NUMBER_OF_RINGS> 8 > <JCHEM_PHYSIOLOGICAL_CHARGE> -1 > <JCHEM_PKA> 9.492422036751174 > <JCHEM_PKA_STRONGEST_ACIDIC> 3.9220454293578233 > <JCHEM_PKA_STRONGEST_BASIC> -5.958331586739058 > <JCHEM_POLAR_SURFACE_AREA> 747.74 > <JCHEM_REFRACTIVITY> 545.2657000000002 > <JCHEM_ROTATABLE_BOND_COUNT> 22 > <JCHEM_RULE_OF_FIVE> 0 > <JCHEM_TRADITIONAL_IUPAC> (2S)-2-(2-{[(1S,4S,7R,13S,19R,22S,25R,28S,31R,36S,39S,45S,51S,54S,60S)-4-benzyl-25-[(2S)-butan-2-yl]-60-(carbamoylmethyl)-39-(hydroxymethyl)-19-[(4-hydroxyphenyl)methyl]-28,45-diisopropyl-7,22-dimethyl-51-(2-methylpropyl)-2,5,8,11,14,17,20,23,26,29,38,41,44,47,50,53,56,59,62-nonadecaoxo-33,34,64,65-tetrathia-3,6,9,12,15,18,21,24,27,30,37,40,43,46,49,52,55,58,61-nonadecaazatricyclo[34.21.5.4^{13,54}]hexahexacontan-31-yl]formamido}-3-phenylpropanamido)-3-(1H-indol-3-yl)propanoic acid > <JCHEM_VEBER_RULE> 0 $$$$ 3D-SDF for NP0018364 (MS-271)RDKit 3D 281288 0 0 0 0 0 0 0 0999 V2000 6.8838 6.4879 -4.9699 C 0 0 0 0 0 0 0 0 0 0 0 0 6.3956 6.0233 -3.6446 C 0 0 0 0 0 0 0 0 0 0 0 0 5.0739 5.2241 -3.7491 C 0 0 2 0 0 0 0 0 0 0 0 0 4.0125 6.0740 -4.3684 C 0 0 0 0 0 0 0 0 0 0 0 0 4.7728 4.6578 -2.4127 C 0 0 1 0 0 0 0 0 0 0 0 0 4.5097 5.5225 -1.3193 N 0 0 0 0 0 0 0 0 0 0 0 0 3.7607 6.6925 -1.1593 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5581 6.5620 -0.6836 O 0 0 0 0 0 0 0 0 0 0 0 0 4.0576 8.1111 -1.4220 C 0 0 2 0 0 0 0 0 0 0 0 0 4.3118 8.7023 -0.0134 C 0 0 0 0 0 0 0 0 0 0 0 0 3.0716 8.8438 -2.1546 N 0 0 0 0 0 0 0 0 0 0 0 0 1.7169 8.6958 -2.3708 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3831 8.3564 -3.5894 O 0 0 0 0 0 0 0 0 0 0 0 0 0.5459 8.8459 -1.4970 C 0 0 1 0 0 0 0 0 0 0 0 0 0.6438 9.8449 -0.4022 C 0 0 0 0 0 0 0 0 0 0 0 0 0.9037 11.2511 -0.8791 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1818 11.7376 -0.9699 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4016 13.0183 -1.4165 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3523 13.8273 -1.7762 C 0 0 0 0 0 0 0 0 0 0 0 0 1.5515 15.1422 -2.2343 O 0 0 0 0 0 0 0 0 0 0 0 0 0.0582 13.3742 -1.6981 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.1421 12.0671 -1.2418 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.6480 9.2125 -2.2900 N 0 0 0 0 0 0 0 0 0 0 0 0 -1.9264 8.7488 -2.0138 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.8693 9.6221 -2.0606 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.3433 7.3718 -1.6683 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.1190 7.2987 -0.4435 N 0 0 0 0 0 0 0 0 0 0 0 0 -4.4975 7.2151 -0.3211 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.0829 8.0597 0.4485 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.3691 6.2524 -0.9863 C 0 0 1 0 0 0 0 0 0 0 0 0 -4.8105 4.8846 -1.2164 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.2454 3.8087 -1.5891 S 0 0 0 0 0 0 0 0 0 0 0 0 -5.6753 1.8049 -1.1914 S 0 0 0 0 0 0 0 0 0 0 0 0 -6.7747 1.0372 0.0218 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.0422 -0.4361 -0.2454 C 0 0 1 0 0 0 0 0 0 0 0 0 -6.9025 -1.1986 0.9866 N 0 0 0 0 0 0 0 0 0 0 0 0 -5.7602 -1.8326 1.4793 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.8090 -3.1026 1.7349 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.4674 -1.1837 1.7418 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.1910 -0.7555 3.1485 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.9193 -1.2261 3.6606 N 0 0 0 0 0 0 0 0 0 0 0 0 -2.1795 -2.3595 3.2305 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.9583 -2.1218 2.9197 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.6441 -3.7293 3.1084 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.1482 -4.5960 4.2816 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.7067 -5.9518 4.0469 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.9843 -6.3560 4.5190 N 0 0 0 0 0 0 0 0 0 0 0 0 -2.0237 -6.7847 3.3981 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.4190 -4.3905 1.8431 N 0 0 0 0 0 0 0 0 0 0 0 0 -1.7315 -4.0728 0.7013 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4182 -3.6142 -0.3254 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.2937 -4.1309 0.3232 C 0 0 1 0 0 0 0 0 0 0 0 0 0.6287 -4.7770 1.2665 C 0 0 0 0 0 0 0 0 0 0 0 0 2.3183 -4.2944 1.0734 S 0 0 0 0 0 0 0 0 0 0 0 0 2.8624 -3.1881 -0.6012 S 0 0 0 0 0 0 0 0 0 0 0 0 3.2094 -1.4662 -0.3207 C 0 0 0 0 0 0 0 0 0 0 0 0 4.6964 -1.0699 -0.4180 C 0 0 1 0 0 0 0 0 0 0 0 0 5.5180 -2.0657 0.3678 C 0 0 0 0 0 0 0 0 0 0 0 0 4.9838 -3.1368 0.6893 O 0 0 0 0 0 0 0 0 0 0 0 0 6.8126 -1.7326 0.6963 N 0 0 0 0 0 0 0 0 0 0 0 0 7.8538 -2.3079 1.4961 C 0 0 1 0 0 0 0 0 0 0 0 0 7.4079 -2.8715 2.7921 C 0 0 0 0 0 0 0 0 0 0 0 0 8.4934 -3.2812 3.6963 C 0 0 0 0 0 0 0 0 0 0 0 0 8.8132 -4.5318 4.0373 C 0 0 0 0 0 0 0 0 0 0 0 0 9.9061 -4.7760 4.8794 C 0 0 0 0 0 0 0 0 0 0 0 0 10.6667 -3.7189 5.3669 C 0 0 0 0 0 0 0 0 0 0 0 0 10.3495 -2.4438 5.0259 C 0 0 0 0 0 0 0 0 0 0 0 0 9.2892 -2.2094 4.2099 C 0 0 0 0 0 0 0 0 0 0 0 0 8.8658 -2.9826 0.7060 C 0 0 0 0 0 0 0 0 0 0 0 0 9.2716 -2.2454 -0.3095 O 0 0 0 0 0 0 0 0 0 0 0 0 9.4840 -4.2217 0.7832 N 0 0 0 0 0 0 0 0 0 0 0 0 10.5067 -4.5934 -0.1936 C 0 0 1 0 0 0 0 0 0 0 0 0 11.4182 -5.6722 0.2187 C 0 0 0 0 0 0 0 0 0 0 0 0 12.2337 -5.5518 1.4005 C 0 0 0 0 0 0 0 0 0 0 0 0 11.9091 -6.1909 2.6084 C 0 0 0 0 0 0 0 0 0 0 0 0 12.8386 -5.9139 3.5060 N 0 0 0 0 0 0 0 0 0 0 0 0 13.7730 -5.1160 2.9492 C 0 0 0 0 0 0 0 0 0 0 0 0 14.9260 -4.5642 3.4368 C 0 0 0 0 0 0 0 0 0 0 0 0 15.7396 -3.7831 2.6683 C 0 0 0 0 0 0 0 0 0 0 0 0 15.3693 -3.5564 1.3632 C 0 0 0 0 0 0 0 0 0 0 0 0 14.2212 -4.0937 0.8464 C 0 0 0 0 0 0 0 0 0 0 0 0 13.3931 -4.8877 1.6275 C 0 0 0 0 0 0 0 0 0 0 0 0 9.7670 -5.1102 -1.4313 C 0 0 0 0 0 0 0 0 0 0 0 0 8.5445 -5.1027 -1.4219 O 0 0 0 0 0 0 0 0 0 0 0 0 10.4976 -5.5667 -2.5050 O 0 0 0 0 0 0 0 0 0 0 0 0 5.0716 -0.9399 -1.7837 N 0 0 0 0 0 0 0 0 0 0 0 0 5.7134 0.1901 -2.3821 C 0 0 0 0 0 0 0 0 0 0 0 0 6.3695 -0.0615 -3.4554 O 0 0 0 0 0 0 0 0 0 0 0 0 5.6988 1.6003 -1.9035 C 0 0 2 0 0 0 0 0 0 0 0 0 6.6641 1.7644 -0.7940 C 0 0 1 0 0 0 0 0 0 0 0 0 8.1020 1.4941 -1.2636 C 0 0 0 0 0 0 0 0 0 0 0 0 6.6709 2.9817 0.0510 C 0 0 0 0 0 0 0 0 0 0 0 0 4.4007 2.1810 -1.7828 N 0 0 0 0 0 0 0 0 0 0 0 0 3.9725 3.4153 -2.4124 C 0 0 0 0 0 0 0 0 0 0 0 0 2.8518 3.4406 -2.9947 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.1442 -4.8518 -0.9572 N 0 0 0 0 0 0 0 0 0 0 0 0 -1.0826 -5.7552 -1.4959 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.3492 -5.6036 -2.7387 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.7811 -6.8414 -0.7886 C 0 0 2 0 0 0 0 0 0 0 0 0 -1.0850 -8.1806 -0.8479 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6382 -8.9558 0.1756 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.1977 -6.8977 -0.9926 N 0 0 0 0 0 0 0 0 0 0 0 0 -4.0070 -7.9196 -1.4706 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.9034 -8.3755 -0.6593 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.0011 -8.5786 -2.7925 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.2967 -7.8722 -3.8228 N 0 0 0 0 0 0 0 0 0 0 0 0 -3.8388 -7.1115 -4.8713 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.2754 -7.2631 -6.0115 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.9699 -6.1646 -4.8169 C 0 0 2 0 0 0 0 0 0 0 0 0 -5.6133 -6.1471 -6.2249 C 0 0 1 0 0 0 0 0 0 0 0 0 -6.0940 -7.5051 -6.6325 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.7892 -5.1993 -6.2750 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.4215 -4.8116 -4.6256 N 0 0 0 0 0 0 0 0 0 0 0 0 -4.7744 -3.9193 -3.6063 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.8112 -3.2895 -3.0424 O 0 0 0 0 0 0 0 0 0 0 0 0 -6.1334 -3.6167 -3.0993 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.6480 -2.5227 -3.9157 N 0 0 0 0 0 0 0 0 0 0 0 0 -7.6580 -1.6621 -3.4506 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.5683 -0.4162 -3.6363 O 0 0 0 0 0 0 0 0 0 0 0 0 -8.8281 -2.1941 -2.7484 C 0 0 2 0 0 0 0 0 0 0 0 0 -10.0663 -1.7639 -3.5028 C 0 0 0 0 0 0 0 0 0 0 0 0 -10.0935 -2.2353 -4.8998 C 0 0 1 0 0 0 0 0 0 0 0 0 -10.0748 -3.7159 -5.0157 C 0 0 0 0 0 0 0 0 0 0 0 0 -11.3236 -1.6681 -5.6282 C 0 0 0 0 0 0 0 0 0 0 0 0 -9.0249 -1.6534 -1.4023 N 0 0 0 0 0 0 0 0 0 0 0 0 -8.4410 -0.5836 -0.7481 C 0 0 0 0 0 0 0 0 0 0 0 0 -9.2199 0.4310 -0.5346 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.3070 -0.9195 4.0860 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.8299 -2.0995 4.1261 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.8961 0.0094 4.9477 N 0 0 0 0 0 0 0 0 0 0 0 0 -5.2523 0.8662 5.9138 C 0 0 1 0 0 0 0 0 0 0 0 0 -4.4585 0.1226 6.9640 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.2116 -0.8150 7.8095 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.8168 -0.4723 9.0137 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.4900 -1.4071 9.7825 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.5896 -2.7214 9.3822 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.0109 -3.0893 8.2133 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.3518 -2.1686 7.4643 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.4238 1.9397 5.3251 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.1507 1.8002 5.4766 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.8569 3.0649 4.6406 N 0 0 0 0 0 0 0 0 0 0 0 0 -5.7875 3.1491 3.5368 C 0 0 2 0 0 0 0 0 0 0 0 0 -4.9645 3.3868 2.2739 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.8167 4.1839 3.7233 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.3877 4.1428 4.8868 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.2474 5.1835 2.8442 N 0 0 0 0 0 0 0 0 0 0 0 0 -6.4414 6.2078 2.2130 C 0 0 0 0 0 0 0 0 0 0 0 0 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HETATM 8 O UNK 0 2.558 6.562 -0.684 0.00 0.00 O+0 HETATM 9 C UNK 0 4.058 8.111 -1.422 0.00 0.00 C+0 HETATM 10 C UNK 0 4.312 8.702 -0.013 0.00 0.00 C+0 HETATM 11 N UNK 0 3.072 8.844 -2.155 0.00 0.00 N+0 HETATM 12 C UNK 0 1.717 8.696 -2.371 0.00 0.00 C+0 HETATM 13 O UNK 0 1.383 8.356 -3.589 0.00 0.00 O+0 HETATM 14 C UNK 0 0.546 8.846 -1.497 0.00 0.00 C+0 HETATM 15 C UNK 0 0.644 9.845 -0.402 0.00 0.00 C+0 HETATM 16 C UNK 0 0.904 11.251 -0.879 0.00 0.00 C+0 HETATM 17 C UNK 0 2.182 11.738 -0.970 0.00 0.00 C+0 HETATM 18 C UNK 0 2.402 13.018 -1.417 0.00 0.00 C+0 HETATM 19 C UNK 0 1.352 13.827 -1.776 0.00 0.00 C+0 HETATM 20 O UNK 0 1.552 15.142 -2.234 0.00 0.00 O+0 HETATM 21 C UNK 0 0.058 13.374 -1.698 0.00 0.00 C+0 HETATM 22 C UNK 0 -0.142 12.067 -1.242 0.00 0.00 C+0 HETATM 23 N UNK 0 -0.648 9.213 -2.290 0.00 0.00 N+0 HETATM 24 C UNK 0 -1.926 8.749 -2.014 0.00 0.00 C+0 HETATM 25 O UNK 0 -2.869 9.622 -2.061 0.00 0.00 O+0 HETATM 26 C UNK 0 -2.343 7.372 -1.668 0.00 0.00 C+0 HETATM 27 N UNK 0 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4.047 0.00 0.00 C+0 HETATM 47 N UNK 0 -3.984 -6.356 4.519 0.00 0.00 N+0 HETATM 48 O UNK 0 -2.024 -6.785 3.398 0.00 0.00 O+0 HETATM 49 N UNK 0 -2.419 -4.391 1.843 0.00 0.00 N+0 HETATM 50 C UNK 0 -1.732 -4.073 0.701 0.00 0.00 C+0 HETATM 51 O UNK 0 -2.418 -3.614 -0.325 0.00 0.00 O+0 HETATM 52 C UNK 0 -0.294 -4.131 0.323 0.00 0.00 C+0 HETATM 53 C UNK 0 0.629 -4.777 1.266 0.00 0.00 C+0 HETATM 54 S UNK 0 2.318 -4.294 1.073 0.00 0.00 S+0 HETATM 55 S UNK 0 2.862 -3.188 -0.601 0.00 0.00 S+0 HETATM 56 C UNK 0 3.209 -1.466 -0.321 0.00 0.00 C+0 HETATM 57 C UNK 0 4.696 -1.070 -0.418 0.00 0.00 C+0 HETATM 58 C UNK 0 5.518 -2.066 0.368 0.00 0.00 C+0 HETATM 59 O UNK 0 4.984 -3.137 0.689 0.00 0.00 O+0 HETATM 60 N UNK 0 6.813 -1.733 0.696 0.00 0.00 N+0 HETATM 61 C UNK 0 7.854 -2.308 1.496 0.00 0.00 C+0 HETATM 62 C UNK 0 7.408 -2.872 2.792 0.00 0.00 C+0 HETATM 63 C UNK 0 8.493 -3.281 3.696 0.00 0.00 C+0 HETATM 64 C UNK 0 8.813 -4.532 4.037 0.00 0.00 C+0 HETATM 65 C UNK 0 9.906 -4.776 4.879 0.00 0.00 C+0 HETATM 66 C UNK 0 10.667 -3.719 5.367 0.00 0.00 C+0 HETATM 67 C UNK 0 10.350 -2.444 5.026 0.00 0.00 C+0 HETATM 68 C UNK 0 9.289 -2.209 4.210 0.00 0.00 C+0 HETATM 69 C UNK 0 8.866 -2.983 0.706 0.00 0.00 C+0 HETATM 70 O UNK 0 9.272 -2.245 -0.310 0.00 0.00 O+0 HETATM 71 N UNK 0 9.484 -4.222 0.783 0.00 0.00 N+0 HETATM 72 C UNK 0 10.507 -4.593 -0.194 0.00 0.00 C+0 HETATM 73 C UNK 0 11.418 -5.672 0.219 0.00 0.00 C+0 HETATM 74 C UNK 0 12.234 -5.552 1.401 0.00 0.00 C+0 HETATM 75 C UNK 0 11.909 -6.191 2.608 0.00 0.00 C+0 HETATM 76 N UNK 0 12.839 -5.914 3.506 0.00 0.00 N+0 HETATM 77 C UNK 0 13.773 -5.116 2.949 0.00 0.00 C+0 HETATM 78 C UNK 0 14.926 -4.564 3.437 0.00 0.00 C+0 HETATM 79 C UNK 0 15.740 -3.783 2.668 0.00 0.00 C+0 HETATM 80 C UNK 0 15.369 -3.556 1.363 0.00 0.00 C+0 HETATM 81 C UNK 0 14.221 -4.094 0.846 0.00 0.00 C+0 HETATM 82 C UNK 0 13.393 -4.888 1.628 0.00 0.00 C+0 HETATM 83 C UNK 0 9.767 -5.110 -1.431 0.00 0.00 C+0 HETATM 84 O UNK 0 8.544 -5.103 -1.422 0.00 0.00 O+0 HETATM 85 O UNK 0 10.498 -5.567 -2.505 0.00 0.00 O+0 HETATM 86 N UNK 0 5.072 -0.940 -1.784 0.00 0.00 N+0 HETATM 87 C UNK 0 5.713 0.190 -2.382 0.00 0.00 C+0 HETATM 88 O UNK 0 6.370 -0.062 -3.455 0.00 0.00 O+0 HETATM 89 C UNK 0 5.699 1.600 -1.904 0.00 0.00 C+0 HETATM 90 C UNK 0 6.664 1.764 -0.794 0.00 0.00 C+0 HETATM 91 C UNK 0 8.102 1.494 -1.264 0.00 0.00 C+0 HETATM 92 C UNK 0 6.671 2.982 0.051 0.00 0.00 C+0 HETATM 93 N UNK 0 4.401 2.181 -1.783 0.00 0.00 N+0 HETATM 94 C UNK 0 3.973 3.415 -2.412 0.00 0.00 C+0 HETATM 95 O UNK 0 2.852 3.441 -2.995 0.00 0.00 O+0 HETATM 96 N UNK 0 -0.144 -4.852 -0.957 0.00 0.00 N+0 HETATM 97 C UNK 0 -1.083 -5.755 -1.496 0.00 0.00 C+0 HETATM 98 O UNK 0 -1.349 -5.604 -2.739 0.00 0.00 O+0 HETATM 99 C UNK 0 -1.781 -6.841 -0.789 0.00 0.00 C+0 HETATM 100 C UNK 0 -1.085 -8.181 -0.848 0.00 0.00 C+0 HETATM 101 O UNK 0 -1.638 -8.956 0.176 0.00 0.00 O+0 HETATM 102 N UNK 0 -3.198 -6.898 -0.993 0.00 0.00 N+0 HETATM 103 C UNK 0 -4.007 -7.920 -1.471 0.00 0.00 C+0 HETATM 104 O UNK 0 -4.903 -8.376 -0.659 0.00 0.00 O+0 HETATM 105 C UNK 0 -4.001 -8.579 -2.793 0.00 0.00 C+0 HETATM 106 N UNK 0 -3.297 -7.872 -3.823 0.00 0.00 N+0 HETATM 107 C UNK 0 -3.839 -7.112 -4.871 0.00 0.00 C+0 HETATM 108 O UNK 0 -3.275 -7.263 -6.011 0.00 0.00 O+0 HETATM 109 C UNK 0 -4.970 -6.165 -4.817 0.00 0.00 C+0 HETATM 110 C UNK 0 -5.613 -6.147 -6.225 0.00 0.00 C+0 HETATM 111 C UNK 0 -6.094 -7.505 -6.633 0.00 0.00 C+0 HETATM 112 C UNK 0 -6.789 -5.199 -6.275 0.00 0.00 C+0 HETATM 113 N UNK 0 -4.422 -4.812 -4.626 0.00 0.00 N+0 HETATM 114 C UNK 0 -4.774 -3.919 -3.606 0.00 0.00 C+0 HETATM 115 O UNK 0 -3.811 -3.289 -3.042 0.00 0.00 O+0 HETATM 116 C UNK 0 -6.133 -3.617 -3.099 0.00 0.00 C+0 HETATM 117 N UNK 0 -6.648 -2.523 -3.916 0.00 0.00 N+0 HETATM 118 C UNK 0 -7.658 -1.662 -3.451 0.00 0.00 C+0 HETATM 119 O UNK 0 -7.568 -0.416 -3.636 0.00 0.00 O+0 HETATM 120 C UNK 0 -8.828 -2.194 -2.748 0.00 0.00 C+0 HETATM 121 C UNK 0 -10.066 -1.764 -3.503 0.00 0.00 C+0 HETATM 122 C UNK 0 -10.094 -2.235 -4.900 0.00 0.00 C+0 HETATM 123 C UNK 0 -10.075 -3.716 -5.016 0.00 0.00 C+0 HETATM 124 C UNK 0 -11.324 -1.668 -5.628 0.00 0.00 C+0 HETATM 125 N UNK 0 -9.025 -1.653 -1.402 0.00 0.00 N+0 HETATM 126 C UNK 0 -8.441 -0.584 -0.748 0.00 0.00 C+0 HETATM 127 O UNK 0 -9.220 0.431 -0.535 0.00 0.00 O+0 HETATM 128 C UNK 0 -5.307 -0.920 4.086 0.00 0.00 C+0 HETATM 129 O UNK 0 -5.830 -2.099 4.126 0.00 0.00 O+0 HETATM 130 N UNK 0 -5.896 0.009 4.948 0.00 0.00 N+0 HETATM 131 C UNK 0 -5.252 0.866 5.914 0.00 0.00 C+0 HETATM 132 C UNK 0 -4.458 0.123 6.964 0.00 0.00 C+0 HETATM 133 C UNK 0 -5.212 -0.815 7.809 0.00 0.00 C+0 HETATM 134 C UNK 0 -5.817 -0.472 9.014 0.00 0.00 C+0 HETATM 135 C UNK 0 -6.490 -1.407 9.783 0.00 0.00 C+0 HETATM 136 C UNK 0 -6.590 -2.721 9.382 0.00 0.00 C+0 HETATM 137 C UNK 0 -6.011 -3.089 8.213 0.00 0.00 C+0 HETATM 138 C UNK 0 -5.352 -2.169 7.464 0.00 0.00 C+0 HETATM 139 C UNK 0 -4.424 1.940 5.325 0.00 0.00 C+0 HETATM 140 O UNK 0 -3.151 1.800 5.477 0.00 0.00 O+0 HETATM 141 N UNK 0 -4.857 3.065 4.641 0.00 0.00 N+0 HETATM 142 C UNK 0 -5.787 3.149 3.537 0.00 0.00 C+0 HETATM 143 C UNK 0 -4.965 3.387 2.274 0.00 0.00 C+0 HETATM 144 C UNK 0 -6.817 4.184 3.723 0.00 0.00 C+0 HETATM 145 O UNK 0 -7.388 4.143 4.887 0.00 0.00 O+0 HETATM 146 N UNK 0 -7.247 5.184 2.844 0.00 0.00 N+0 HETATM 147 C UNK 0 -6.441 6.208 2.213 0.00 0.00 C+0 HETATM 148 C UNK 0 -7.063 6.555 0.900 0.00 0.00 C+0 HETATM 149 O UNK 0 -8.074 7.349 0.958 0.00 0.00 O+0 HETATM 150 N UNK 0 -6.665 6.109 -0.354 0.00 0.00 N+0 HETATM 151 H UNK 0 6.778 7.597 -4.986 0.00 0.00 H+0 HETATM 152 H UNK 0 6.408 5.994 -5.819 0.00 0.00 H+0 HETATM 153 H UNK 0 7.989 6.303 -5.095 0.00 0.00 H+0 HETATM 154 H UNK 0 6.391 6.741 -2.831 0.00 0.00 H+0 HETATM 155 H UNK 0 7.139 5.229 -3.310 0.00 0.00 H+0 HETATM 156 H UNK 0 5.304 4.395 -4.431 0.00 0.00 H+0 HETATM 157 H UNK 0 4.299 7.142 -4.122 0.00 0.00 H+0 HETATM 158 H UNK 0 4.087 6.074 -5.496 0.00 0.00 H+0 HETATM 159 H UNK 0 2.983 5.833 -4.118 0.00 0.00 H+0 HETATM 160 H UNK 0 5.854 4.243 -2.160 0.00 0.00 H+0 HETATM 161 H UNK 0 4.959 5.191 -0.386 0.00 0.00 H+0 HETATM 162 H UNK 0 5.088 8.277 -1.884 0.00 0.00 H+0 HETATM 163 H UNK 0 3.402 8.746 0.591 0.00 0.00 H+0 HETATM 164 H UNK 0 4.794 9.672 -0.042 0.00 0.00 H+0 HETATM 165 H UNK 0 5.005 8.013 0.538 0.00 0.00 H+0 HETATM 166 H UNK 0 3.509 9.710 -2.661 0.00 0.00 H+0 HETATM 167 H UNK 0 0.234 7.880 -1.029 0.00 0.00 H+0 HETATM 168 H UNK 0 1.284 9.572 0.431 0.00 0.00 H+0 HETATM 169 H UNK 0 -0.394 9.898 0.057 0.00 0.00 H+0 HETATM 170 H UNK 0 3.030 11.126 -0.679 0.00 0.00 H+0 HETATM 171 H UNK 0 3.445 13.400 -1.485 0.00 0.00 H+0 HETATM 172 H UNK 0 1.678 15.351 -3.214 0.00 0.00 H+0 HETATM 173 H UNK 0 -0.766 14.005 -1.976 0.00 0.00 H+0 HETATM 174 H UNK 0 -1.182 11.745 -1.192 0.00 0.00 H+0 HETATM 175 H UNK 0 -0.466 9.857 -3.097 0.00 0.00 H+0 HETATM 176 H UNK 0 -1.429 6.734 -1.575 0.00 0.00 H+0 HETATM 177 H UNK 0 -2.912 6.972 -2.533 0.00 0.00 H+0 HETATM 178 H UNK 0 -2.529 7.320 0.443 0.00 0.00 H+0 HETATM 179 H UNK 0 -5.532 6.676 -2.033 0.00 0.00 H+0 HETATM 180 H UNK 0 -4.284 4.434 -0.363 0.00 0.00 H+0 HETATM 181 H UNK 0 -4.090 4.853 -2.063 0.00 0.00 H+0 HETATM 182 H UNK 0 -6.408 1.184 1.072 0.00 0.00 H+0 HETATM 183 H UNK 0 -7.737 1.594 -0.011 0.00 0.00 H+0 HETATM 184 H UNK 0 -6.374 -0.751 -1.057 0.00 0.00 H+0 HETATM 185 H UNK 0 -7.789 -1.278 1.575 0.00 0.00 H+0 HETATM 186 H UNK 0 -4.411 -0.333 1.000 0.00 0.00 H+0 HETATM 187 H UNK 0 -3.604 -1.847 1.438 0.00 0.00 H+0 HETATM 188 H UNK 0 -4.069 0.391 3.056 0.00 0.00 H+0 HETATM 189 H UNK 0 -2.511 -0.619 4.452 0.00 0.00 H+0 HETATM 190 H UNK 0 -3.775 -3.735 3.312 0.00 0.00 H+0 HETATM 191 H UNK 0 -1.062 -4.599 4.354 0.00 0.00 H+0 HETATM 192 H UNK 0 -2.665 -4.185 5.191 0.00 0.00 H+0 HETATM 193 H UNK 0 -4.639 -5.748 5.068 0.00 0.00 H+0 HETATM 194 H UNK 0 -4.362 -7.327 4.338 0.00 0.00 H+0 HETATM 195 H UNK 0 -2.946 -5.348 1.828 0.00 0.00 H+0 HETATM 196 H UNK 0 0.045 -3.068 0.176 0.00 0.00 H+0 HETATM 197 H UNK 0 0.581 -5.901 1.238 0.00 0.00 H+0 HETATM 198 H UNK 0 0.312 -4.437 2.312 0.00 0.00 H+0 HETATM 199 H UNK 0 2.729 -0.830 -1.125 0.00 0.00 H+0 HETATM 200 H UNK 0 2.836 -1.088 0.639 0.00 0.00 H+0 HETATM 201 H UNK 0 4.729 -0.136 0.180 0.00 0.00 H+0 HETATM 202 H UNK 0 7.225 -0.856 0.160 0.00 0.00 H+0 HETATM 203 H UNK 0 8.382 -1.295 1.912 0.00 0.00 H+0 HETATM 204 H UNK 0 6.827 -2.087 3.329 0.00 0.00 H+0 HETATM 205 H UNK 0 6.768 -3.780 2.645 0.00 0.00 H+0 HETATM 206 H UNK 0 8.240 -5.391 3.682 0.00 0.00 H+0 HETATM 207 H UNK 0 10.149 -5.795 5.142 0.00 0.00 H+0 HETATM 208 H UNK 0 11.504 -3.982 6.016 0.00 0.00 H+0 HETATM 209 H UNK 0 10.961 -1.624 5.418 0.00 0.00 H+0 HETATM 210 H UNK 0 9.037 -1.198 3.935 0.00 0.00 H+0 HETATM 211 H UNK 0 9.258 -4.921 1.480 0.00 0.00 H+0 HETATM 212 H UNK 0 10.998 -3.693 -0.556 0.00 0.00 H+0 HETATM 213 H UNK 0 10.835 -6.660 0.250 0.00 0.00 H+0 HETATM 214 H UNK 0 12.138 -5.905 -0.652 0.00 0.00 H+0 HETATM 215 H UNK 0 11.042 -6.810 2.787 0.00 0.00 H+0 HETATM 216 H UNK 0 12.873 -6.243 4.492 0.00 0.00 H+0 HETATM 217 H UNK 0 15.184 -4.769 4.471 0.00 0.00 H+0 HETATM 218 H UNK 0 16.649 -3.368 3.101 0.00 0.00 H+0 HETATM 219 H UNK 0 16.001 -2.939 0.724 0.00 0.00 H+0 HETATM 220 H UNK 0 13.896 -3.933 -0.184 0.00 0.00 H+0 HETATM 221 H UNK 0 11.306 -5.076 -2.889 0.00 0.00 H+0 HETATM 222 H UNK 0 4.861 -1.764 -2.415 0.00 0.00 H+0 HETATM 223 H UNK 0 6.233 2.223 -2.767 0.00 0.00 H+0 HETATM 224 H UNK 0 6.513 0.940 -0.011 0.00 0.00 H+0 HETATM 225 H UNK 0 8.073 0.930 -2.215 0.00 0.00 H+0 HETATM 226 H UNK 0 8.630 0.927 -0.500 0.00 0.00 H+0 HETATM 227 H UNK 0 8.621 2.475 -1.432 0.00 0.00 H+0 HETATM 228 H UNK 0 7.283 2.732 0.995 0.00 0.00 H+0 HETATM 229 H UNK 0 5.678 3.260 0.438 0.00 0.00 H+0 HETATM 230 H UNK 0 7.240 3.814 -0.384 0.00 0.00 H+0 HETATM 231 H UNK 0 3.685 1.677 -1.195 0.00 0.00 H+0 HETATM 232 H UNK 0 0.765 -4.627 -1.467 0.00 0.00 H+0 HETATM 233 H UNK 0 -1.668 -6.554 0.319 0.00 0.00 H+0 HETATM 234 H UNK 0 -1.094 -8.675 -1.810 0.00 0.00 H+0 HETATM 235 H UNK 0 -0.023 -8.009 -0.582 0.00 0.00 H+0 HETATM 236 H UNK 0 -0.960 -9.554 0.577 0.00 0.00 H+0 HETATM 237 H UNK 0 -3.705 -5.990 -0.717 0.00 0.00 H+0 HETATM 238 H UNK 0 -5.056 -8.814 -3.135 0.00 0.00 H+0 HETATM 239 H UNK 0 -3.545 -9.609 -2.642 0.00 0.00 H+0 HETATM 240 H UNK 0 -2.228 -7.962 -3.756 0.00 0.00 H+0 HETATM 241 H UNK 0 -5.753 -6.407 -4.101 0.00 0.00 H+0 HETATM 242 H UNK 0 -4.875 -5.791 -6.968 0.00 0.00 H+0 HETATM 243 H UNK 0 -7.116 -7.723 -6.255 0.00 0.00 H+0 HETATM 244 H UNK 0 -5.439 -8.324 -6.255 0.00 0.00 H+0 HETATM 245 H UNK 0 -6.155 -7.569 -7.749 0.00 0.00 H+0 HETATM 246 H UNK 0 -6.538 -4.183 -6.621 0.00 0.00 H+0 HETATM 247 H UNK 0 -7.560 -5.570 -7.015 0.00 0.00 H+0 HETATM 248 H UNK 0 -7.307 -5.151 -5.299 0.00 0.00 H+0 HETATM 249 H UNK 0 -3.698 -4.553 -5.366 0.00 0.00 H+0 HETATM 250 H UNK 0 -6.045 -3.327 -2.020 0.00 0.00 H+0 HETATM 251 H UNK 0 -6.757 -4.509 -3.111 0.00 0.00 H+0 HETATM 252 H UNK 0 -6.258 -2.358 -4.897 0.00 0.00 H+0 HETATM 253 H UNK 0 -8.831 -3.312 -2.705 0.00 0.00 H+0 HETATM 254 H UNK 0 -10.988 -2.073 -2.941 0.00 0.00 H+0 HETATM 255 H UNK 0 -10.123 -0.639 -3.515 0.00 0.00 H+0 HETATM 256 H UNK 0 -9.225 -1.828 -5.495 0.00 0.00 H+0 HETATM 257 H UNK 0 -11.122 -4.034 -5.273 0.00 0.00 H+0 HETATM 258 H UNK 0 -9.374 -4.023 -5.831 0.00 0.00 H+0 HETATM 259 H UNK 0 -9.811 -4.231 -4.086 0.00 0.00 H+0 HETATM 260 H UNK 0 -12.187 -1.704 -4.928 0.00 0.00 H+0 HETATM 261 H UNK 0 -11.086 -0.641 -5.921 0.00 0.00 H+0 HETATM 262 H UNK 0 -11.469 -2.275 -6.529 0.00 0.00 H+0 HETATM 263 H UNK 0 -9.787 -2.223 -0.877 0.00 0.00 H+0 HETATM 264 H UNK 0 -6.976 0.076 4.867 0.00 0.00 H+0 HETATM 265 H UNK 0 -6.060 1.383 6.519 0.00 0.00 H+0 HETATM 266 H UNK 0 -3.858 0.838 7.577 0.00 0.00 H+0 HETATM 267 H UNK 0 -3.714 -0.511 6.414 0.00 0.00 H+0 HETATM 268 H UNK 0 -5.749 0.546 9.348 0.00 0.00 H+0 HETATM 269 H UNK 0 -6.963 -1.159 10.728 0.00 0.00 H+0 HETATM 270 H UNK 0 -7.106 -3.489 9.952 0.00 0.00 H+0 HETATM 271 H UNK 0 -6.060 -4.126 7.836 0.00 0.00 H+0 HETATM 272 H UNK 0 -4.885 -2.492 6.546 0.00 0.00 H+0 HETATM 273 H UNK 0 -4.471 4.025 4.927 0.00 0.00 H+0 HETATM 274 H UNK 0 -6.319 2.191 3.352 0.00 0.00 H+0 HETATM 275 H UNK 0 -4.525 2.403 1.953 0.00 0.00 H+0 HETATM 276 H UNK 0 -5.607 3.693 1.448 0.00 0.00 H+0 HETATM 277 H UNK 0 -4.081 4.025 2.469 0.00 0.00 H+0 HETATM 278 H UNK 0 -8.289 5.208 2.605 0.00 0.00 H+0 HETATM 279 H UNK 0 -6.469 7.156 2.835 0.00 0.00 H+0 HETATM 280 H UNK 0 -5.386 5.960 2.139 0.00 0.00 H+0 HETATM 281 H UNK 0 -7.391 5.595 -0.949 0.00 0.00 H+0 CONECT 1 2 151 152 153 CONECT 2 1 3 154 155 CONECT 3 2 4 5 156 CONECT 4 3 157 158 159 CONECT 5 3 6 94 160 CONECT 6 5 7 161 CONECT 7 6 8 9 CONECT 8 7 CONECT 9 7 10 11 162 CONECT 10 9 163 164 165 CONECT 11 9 12 166 CONECT 12 11 13 14 CONECT 13 12 CONECT 14 12 15 23 167 CONECT 15 14 16 168 169 CONECT 16 15 17 22 CONECT 17 16 18 170 CONECT 18 17 19 171 CONECT 19 18 20 21 CONECT 20 19 172 CONECT 21 19 22 173 CONECT 22 21 16 174 CONECT 23 14 24 175 CONECT 24 23 25 26 CONECT 25 24 CONECT 26 24 27 176 177 CONECT 27 26 28 178 CONECT 28 27 29 30 CONECT 29 28 CONECT 30 28 31 150 179 CONECT 31 30 32 180 181 CONECT 32 31 33 CONECT 33 32 34 CONECT 34 33 35 182 183 CONECT 35 34 36 126 184 CONECT 36 35 37 185 CONECT 37 36 38 39 CONECT 38 37 CONECT 39 37 40 186 187 CONECT 40 39 41 128 188 CONECT 41 40 42 189 CONECT 42 41 43 44 CONECT 43 42 CONECT 44 42 45 49 190 CONECT 45 44 46 191 192 CONECT 46 45 47 48 CONECT 47 46 193 194 CONECT 48 46 CONECT 49 44 50 195 CONECT 50 49 51 52 CONECT 51 50 CONECT 52 50 53 96 196 CONECT 53 52 54 197 198 CONECT 54 53 55 CONECT 55 54 56 CONECT 56 55 57 199 200 CONECT 57 56 58 86 201 CONECT 58 57 59 60 CONECT 59 58 CONECT 60 58 61 202 CONECT 61 60 62 69 203 CONECT 62 61 63 204 205 CONECT 63 62 64 68 CONECT 64 63 65 206 CONECT 65 64 66 207 CONECT 66 65 67 208 CONECT 67 66 68 209 CONECT 68 67 63 210 CONECT 69 61 70 71 CONECT 70 69 CONECT 71 69 72 211 CONECT 72 71 73 83 212 CONECT 73 72 74 213 214 CONECT 74 73 75 82 CONECT 75 74 76 215 CONECT 76 75 77 216 CONECT 77 76 78 82 CONECT 78 77 79 217 CONECT 79 78 80 218 CONECT 80 79 81 219 CONECT 81 80 82 220 CONECT 82 81 74 77 CONECT 83 72 84 85 CONECT 84 83 CONECT 85 83 221 CONECT 86 57 87 222 CONECT 87 86 88 89 CONECT 88 87 CONECT 89 87 90 93 223 CONECT 90 89 91 92 224 CONECT 91 90 225 226 227 CONECT 92 90 228 229 230 CONECT 93 89 94 231 CONECT 94 93 95 5 CONECT 95 94 CONECT 96 52 97 232 CONECT 97 96 98 99 CONECT 98 97 CONECT 99 97 100 102 233 CONECT 100 99 101 234 235 CONECT 101 100 236 CONECT 102 99 103 237 CONECT 103 102 104 105 CONECT 104 103 CONECT 105 103 106 238 239 CONECT 106 105 107 240 CONECT 107 106 108 109 CONECT 108 107 CONECT 109 107 110 113 241 CONECT 110 109 111 112 242 CONECT 111 110 243 244 245 CONECT 112 110 246 247 248 CONECT 113 109 114 249 CONECT 114 113 115 116 CONECT 115 114 CONECT 116 114 117 250 251 CONECT 117 116 118 252 CONECT 118 117 119 120 CONECT 119 118 CONECT 120 118 121 125 253 CONECT 121 120 122 254 255 CONECT 122 121 123 124 256 CONECT 123 122 257 258 259 CONECT 124 122 260 261 262 CONECT 125 120 126 263 CONECT 126 125 127 35 CONECT 127 126 CONECT 128 40 129 130 CONECT 129 128 CONECT 130 128 131 264 CONECT 131 130 132 139 265 CONECT 132 131 133 266 267 CONECT 133 132 134 138 CONECT 134 133 135 268 CONECT 135 134 136 269 CONECT 136 135 137 270 CONECT 137 136 138 271 CONECT 138 137 133 272 CONECT 139 131 140 141 CONECT 140 139 CONECT 141 139 142 273 CONECT 142 141 143 144 274 CONECT 143 142 275 276 277 CONECT 144 142 145 146 CONECT 145 144 CONECT 146 144 147 278 CONECT 147 146 148 279 280 CONECT 148 147 149 150 CONECT 149 148 CONECT 150 148 30 281 CONECT 151 1 CONECT 152 1 CONECT 153 1 CONECT 154 2 CONECT 155 2 CONECT 156 3 CONECT 157 4 CONECT 158 4 CONECT 159 4 CONECT 160 5 CONECT 161 6 CONECT 162 9 CONECT 163 10 CONECT 164 10 CONECT 165 10 CONECT 166 11 CONECT 167 14 CONECT 168 15 CONECT 169 15 CONECT 170 17 CONECT 171 18 CONECT 172 20 CONECT 173 21 CONECT 174 22 CONECT 175 23 CONECT 176 26 CONECT 177 26 CONECT 178 27 CONECT 179 30 CONECT 180 31 CONECT 181 31 CONECT 182 34 CONECT 183 34 CONECT 184 35 CONECT 185 36 CONECT 186 39 CONECT 187 39 CONECT 188 40 CONECT 189 41 CONECT 190 44 CONECT 191 45 CONECT 192 45 CONECT 193 47 CONECT 194 47 CONECT 195 49 CONECT 196 52 CONECT 197 53 CONECT 198 53 CONECT 199 56 CONECT 200 56 CONECT 201 57 CONECT 202 60 CONECT 203 61 CONECT 204 62 CONECT 205 62 CONECT 206 64 CONECT 207 65 CONECT 208 66 CONECT 209 67 CONECT 210 68 CONECT 211 71 CONECT 212 72 CONECT 213 73 CONECT 214 73 CONECT 215 75 CONECT 216 76 CONECT 217 78 CONECT 218 79 CONECT 219 80 CONECT 220 81 CONECT 221 85 CONECT 222 86 CONECT 223 89 CONECT 224 90 CONECT 225 91 CONECT 226 91 CONECT 227 91 CONECT 228 92 CONECT 229 92 CONECT 230 92 CONECT 231 93 CONECT 232 96 CONECT 233 99 CONECT 234 100 CONECT 235 100 CONECT 236 101 CONECT 237 102 CONECT 238 105 CONECT 239 105 CONECT 240 106 CONECT 241 109 CONECT 242 110 CONECT 243 111 CONECT 244 111 CONECT 245 111 CONECT 246 112 CONECT 247 112 CONECT 248 112 CONECT 249 113 CONECT 250 116 CONECT 251 116 CONECT 252 117 CONECT 253 120 CONECT 254 121 CONECT 255 121 CONECT 256 122 CONECT 257 123 CONECT 258 123 CONECT 259 123 CONECT 260 124 CONECT 261 124 CONECT 262 124 CONECT 263 125 CONECT 264 130 CONECT 265 131 CONECT 266 132 CONECT 267 132 CONECT 268 134 CONECT 269 135 CONECT 270 136 CONECT 271 137 CONECT 272 138 CONECT 273 141 CONECT 274 142 CONECT 275 143 CONECT 276 143 CONECT 277 143 CONECT 278 146 CONECT 279 147 CONECT 280 147 CONECT 281 150 MASTER 0 0 0 0 0 0 0 0 281 0 576 0 END SMILES for NP0018364 (MS-271)[H]OC(=O)[C@@]([H])(N([H])C(=O)[C@@]([H])(N([H])C(=O)[C@@]1([H])N([H])C(=O)[C@@]([H])(N([H])C(=O)[C@]([H])(N([H])C(=O)[C@@]([H])(N([H])C(=O)[C@]([H])(N([H])C(=O)C([H])([H])N([H])C(=O)[C@]2([H])N([H])C(=O)C([H])([H])N([H])C(=O)[C@]([H])(N([H])C(=O)[C@@]([H])(N([H])C(=O)[C@@]3([H])N([H])C(=O)[C@@]([H])(N([H])C(=O)[C@]([H])(N([H])C(=O)[C@@]([H])(N([H])C(=O)C([H])([H])N([H])C(=O)[C@@]([H])(N([H])C(=O)C([H])([H])N([H])C(=O)[C@@]([H])(N([H])C(=O)[C@]([H])(N([H])C(=O)C3([H])[H])C([H])([H])SSC2([H])[H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H])C([H])([H])O[H])C([H])([H])SSC1([H])[H])C([H])([H])C(=O)N([H])[H])C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H])C([H])([H])[H])C([H])([H])C1=C([H])C([H])=C(O[H])C([H])=C1[H])C([H])([H])[H])[C@@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H])C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H])C([H])([H])C1=C([H])N([H])C2=C([H])C([H])=C([H])C([H])=C12 INCHI for NP0018364 (MS-271)InChI=1S/C97H131N23O26S4/c1-11-50(8)80-96(144)119-79(49(6)7)95(143)117-71(93(141)112-63(32-54-22-16-13-17-23-54)87(135)115-66(97(145)146)34-56-37-99-59-25-19-18-24-58(56)59)46-150-149-45-70-92(140)113-64(35-72(98)123)88(136)114-65-36-73(124)108-69(91(139)110-60(30-47(2)3)83(131)101-41-77(128)118-78(48(4)5)94(142)103-40-75(126)107-67(42-121)90(138)116-70)44-148-147-43-68(109-76(127)38-100-81(129)51(9)104-86(134)62(111-89(65)137)31-53-20-14-12-15-21-53)84(132)102-39-74(125)106-61(33-55-26-28-57(122)29-27-55)85(133)105-52(10)82(130)120-80/h12-29,37,47-52,60-71,78-80,99,121-122H,11,30-36,38-46H2,1-10H3,(H2,98,123)(H,100,129)(H,101,131)(H,102,132)(H,103,142)(H,104,134)(H,105,133)(H,106,125)(H,107,126)(H,108,124)(H,109,127)(H,110,139)(H,111,137)(H,112,141)(H,113,140)(H,114,136)(H,115,135)(H,116,138)(H,117,143)(H,118,128)(H,119,144)(H,120,130)(H,145,146)/t50-,51+,52-,60-,61+,62-,63-,64-,65-,66-,67-,68+,69+,70+,71-,78-,79-,80+/m0/s1 3D Structure for NP0018364 (MS-271) | 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Synonyms |
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Chemical Formula | C97H131N23O26S4 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Average Mass | 2163.4900 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||
Monoisotopic Mass | 2161.85185 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||
IUPAC Name | (2S)-2-(2-{[(1S,4S,7R,13S,19R,22S,25R,28S,31R,36S,39S,45S,51S,54S,60S)-4-benzyl-25-[(2S)-butan-2-yl]-60-(carbamoylmethyl)-39-(hydroxymethyl)-19-[(4-hydroxyphenyl)methyl]-7,22-dimethyl-51-(2-methylpropyl)-2,5,8,11,14,17,20,23,26,29,38,41,44,47,50,53,56,59,62-nonadecaoxo-28,45-bis(propan-2-yl)-33,34,64,65-tetrathia-3,6,9,12,15,18,21,24,27,30,37,40,43,46,49,52,55,58,61-nonadecaazatricyclo[34.21.5.4^{13,54}]hexahexacontan-31-yl]formamido}-3-phenylpropanamido)-3-(1H-indol-3-yl)propanoic acid | |||||||||||||||||||||||||||||||||||||||||||||||||||
Traditional Name | (2S)-2-(2-{[(1S,4S,7R,13S,19R,22S,25R,28S,31R,36S,39S,45S,51S,54S,60S)-4-benzyl-25-[(2S)-butan-2-yl]-60-(carbamoylmethyl)-39-(hydroxymethyl)-19-[(4-hydroxyphenyl)methyl]-28,45-diisopropyl-7,22-dimethyl-51-(2-methylpropyl)-2,5,8,11,14,17,20,23,26,29,38,41,44,47,50,53,56,59,62-nonadecaoxo-33,34,64,65-tetrathia-3,6,9,12,15,18,21,24,27,30,37,40,43,46,49,52,55,58,61-nonadecaazatricyclo[34.21.5.4^{13,54}]hexahexacontan-31-yl]formamido}-3-phenylpropanamido)-3-(1H-indol-3-yl)propanoic acid | |||||||||||||||||||||||||||||||||||||||||||||||||||
CAS Registry Number | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
SMILES | CC[C@H](C)[C@H]1NC(=O)[C@H](C)NC(=O)[C@@H](CC2=CC=C(O)C=C2)NC(=O)CNC(=O)[C@H]2CSSC[C@H]3NC(=O)C[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](CSSC[C@H](NC(=O)[C@@H](NC1=O)C(C)C)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC1=CNC4=CC=CC=C14)C(O)=O)NC(=O)[C@H](CO)NC(=O)CNC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CC(C)C)NC3=O)C(C)C)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@H](C)C(=O)NCC(=O)N2 | |||||||||||||||||||||||||||||||||||||||||||||||||||
InChI Identifier | InChI=1S/C97H131N23O26S4/c1-11-50(8)80-96(144)119-79(49(6)7)95(143)117-71(93(141)112-63(32-54-22-16-13-17-23-54)87(135)115-66(97(145)146)34-56-37-99-59-25-19-18-24-58(56)59)46-150-149-45-70-92(140)113-64(35-72(98)123)88(136)114-65-36-73(124)108-69(91(139)110-60(30-47(2)3)83(131)101-41-77(128)118-78(48(4)5)94(142)103-40-75(126)107-67(42-121)90(138)116-70)44-148-147-43-68(109-76(127)38-100-81(129)51(9)104-86(134)62(111-89(65)137)31-53-20-14-12-15-21-53)84(132)102-39-74(125)106-61(33-55-26-28-57(122)29-27-55)85(133)105-52(10)82(130)120-80/h12-29,37,47-52,60-71,78-80,99,121-122H,11,30-36,38-46H2,1-10H3,(H2,98,123)(H,100,129)(H,101,131)(H,102,132)(H,103,142)(H,104,134)(H,105,133)(H,106,125)(H,107,126)(H,108,124)(H,109,127)(H,110,139)(H,111,137)(H,112,141)(H,113,140)(H,114,136)(H,115,135)(H,116,138)(H,117,143)(H,118,128)(H,119,144)(H,120,130)(H,145,146)/t50-,51+,52-,60-,61+,62-,63-,64-,65-,66-,67-,68+,69+,70+,71-,78-,79-,80+/m0/s1 | |||||||||||||||||||||||||||||||||||||||||||||||||||
InChI Key | TXYRKTDGDMHVHR-POXCZHPVSA-N | |||||||||||||||||||||||||||||||||||||||||||||||||||
Experimental Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Predicted Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||
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Chemical Shift Submissions | ||||||||||||||||||||||||||||||||||||||||||||||||||||
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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 | ||||||||||||||||||||||||||||||||||||||||||||||||||||
NPAtlas ID | NPA024450 | |||||||||||||||||||||||||||||||||||||||||||||||||||
HMDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
DrugBank ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
Phenol Explorer Compound ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
FoodDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
KNApSAcK ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
Chemspider ID | 78439538 | |||||||||||||||||||||||||||||||||||||||||||||||||||
KEGG Compound ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
BioCyc ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
BiGG ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
Wikipedia Link | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
METLIN ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
PubChem Compound | 139591576 | |||||||||||||||||||||||||||||||||||||||||||||||||||
PDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
ChEBI ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
Good Scents ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
References | ||||||||||||||||||||||||||||||||||||||||||||||||||||
General References |
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