Showing NP-Card for Salinipeptin B (NP0019224)
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Version | 2.0 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Created at | 2021-01-06 04:47:48 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||
Updated at | 2021-07-15 17:30:24 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||
NP-MRD ID | NP0019224 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Secondary Accession Numbers | None | |||||||||||||||||||||||||||||||||||||||||||||||||||
Natural Product Identification | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Common Name | Salinipeptin B | |||||||||||||||||||||||||||||||||||||||||||||||||||
Provided By | NPAtlas | |||||||||||||||||||||||||||||||||||||||||||||||||||
Description | Salinipeptin B is found in Streptomyces. Based on a literature review very few articles have been published on Salinipeptin B. | |||||||||||||||||||||||||||||||||||||||||||||||||||
Structure | MOL for NP0019224 (Salinipeptin B)Mrv1652307042107443D 297300 0 0 0 0 999 V2000 3.0770 2.9080 -1.8802 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2955 1.6695 -2.6814 C 0 0 0 0 0 0 0 0 0 0 0 0 3.7100 1.7176 -3.9356 C 0 0 0 0 0 0 0 0 0 0 0 0 3.9300 3.0095 -4.4600 N 0 0 0 0 0 0 0 0 0 0 0 0 3.2176 3.6877 -5.4633 C 0 0 0 0 0 0 0 0 0 0 0 0 2.2447 3.1255 -6.0193 O 0 0 0 0 0 0 0 0 0 0 0 0 3.5733 5.0618 -5.8906 C 0 0 2 0 0 0 0 0 0 0 0 0 4.4357 5.7597 -4.8558 C 0 0 1 0 0 0 0 0 0 0 0 0 3.6958 5.9241 -3.6816 O 0 0 0 0 0 0 0 0 0 0 0 0 2.4408 5.9226 -6.1151 N 0 0 0 0 0 0 0 0 0 0 0 0 2.1098 6.5788 -7.3135 C 0 0 0 0 0 0 0 0 0 0 0 0 2.9021 6.3649 -8.2986 O 0 0 0 0 0 0 0 0 0 0 0 0 0.9656 7.4637 -7.5341 C 0 0 1 0 0 0 0 0 0 0 0 0 0.1341 7.6936 -6.4006 N 0 0 0 0 0 0 0 0 0 0 0 0 -1.0819 8.4973 -6.4035 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.4654 9.0334 -7.4555 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.8375 8.6589 -5.1661 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.4927 9.8855 -4.3530 C 0 0 1 0 0 0 0 0 0 0 0 0 -2.4226 9.8321 -3.1361 C 0 0 1 0 0 0 0 0 0 0 0 0 -2.2434 10.9757 -2.2319 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.0576 11.0411 -1.0685 N 0 0 0 0 0 0 0 0 0 0 0 0 -1.4097 11.9081 -2.4177 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.2840 8.6557 -5.2751 N 0 0 0 0 0 0 0 0 0 0 0 0 -4.0253 7.4850 -5.0088 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.3982 6.4390 -4.7265 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.4905 7.4459 -5.0399 C 0 0 2 0 0 0 0 0 0 0 0 0 -5.9539 6.0579 -4.8419 N 0 0 0 0 0 0 0 0 0 0 0 0 -5.8868 5.4615 -3.5842 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.4147 6.2155 -2.6348 O 0 0 0 0 0 0 0 0 0 0 0 0 -6.2517 4.1139 -3.1228 C 0 0 1 0 0 0 0 0 0 0 0 0 -5.8121 3.9248 -1.7484 N 0 0 0 0 0 0 0 0 0 0 0 0 -4.8553 2.9421 -1.3862 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.3356 2.1354 -2.1728 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.4265 2.8770 0.0741 C 0 0 2 0 0 0 0 0 0 0 0 0 -3.4002 3.9568 0.1572 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.6716 4.2089 1.3574 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.3960 3.6402 1.4854 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.6254 3.8599 2.6050 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.0837 4.6427 3.6277 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.3230 5.2057 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C 0 0 0 0 0 0 0 0 0 0 0 0 8.6036 -0.9844 2.0301 N 0 3 1 0 0 4 0 0 0 0 0 0 9.8097 -1.4690 2.6548 C 0 0 0 0 0 0 0 0 0 0 0 0 7.8230 -2.0513 1.4235 C 0 0 0 0 0 0 0 0 0 0 0 0 9.0279 -0.1798 0.9915 O 0 5 0 0 0 1 0 0 0 0 0 0 -7.7006 3.7499 -3.2926 C 0 0 1 0 0 0 0 0 0 0 0 0 -8.6724 4.6245 -2.5827 C 0 0 0 0 0 0 0 0 0 0 0 0 -8.0753 3.6180 -4.7554 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.2296 8.2554 -5.9876 C 0 0 2 0 0 0 0 0 0 0 0 0 -7.7334 8.0037 -5.7843 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.8571 8.1534 -7.4384 C 0 0 2 0 0 0 0 0 0 0 0 0 -6.7553 9.0780 -8.2459 C 0 0 0 0 0 0 0 0 0 0 0 0 4.0559 0.5316 -4.7501 C 0 0 0 0 0 0 0 0 0 0 0 0 4.4249 0.7660 -5.9497 O 0 0 0 0 0 0 0 0 0 0 0 0 4.0106 -0.7672 -4.2766 N 0 0 0 0 0 0 0 0 0 0 0 0 4.2396 -2.0846 -4.5509 C 0 0 1 0 0 0 0 0 0 0 0 0 3.2239 -2.9821 -5.1620 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5533 -2.5913 -6.1328 O 0 0 0 0 0 0 0 0 0 0 0 0 3.0176 -4.2885 -4.6506 N 0 0 0 0 0 0 0 0 0 0 0 0 2.1542 -5.3222 -5.1422 C 0 0 1 0 0 0 0 0 0 0 0 0 2.6688 -6.6159 -4.5569 C 0 0 2 0 0 0 0 0 0 0 0 0 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144289 1 1 145290 1 0 145291 1 0 145292 1 0 146293 1 0 146294 1 0 147295 1 0 147296 1 0 147297 1 0 M CHG 2 103 1 106 -1 M END 3D SDF for NP0019224 (Salinipeptin B)Mrv1652307042107443D 297300 0 0 0 0 999 V2000 3.0770 2.9080 -1.8802 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2955 1.6695 -2.6814 C 0 0 0 0 0 0 0 0 0 0 0 0 3.7100 1.7176 -3.9356 C 0 0 0 0 0 0 0 0 0 0 0 0 3.9300 3.0095 -4.4600 N 0 0 0 0 0 0 0 0 0 0 0 0 3.2176 3.6877 -5.4633 C 0 0 0 0 0 0 0 0 0 0 0 0 2.2447 3.1255 -6.0193 O 0 0 0 0 0 0 0 0 0 0 0 0 3.5733 5.0618 -5.8906 C 0 0 2 0 0 0 0 0 0 0 0 0 4.4357 5.7597 -4.8558 C 0 0 1 0 0 0 0 0 0 0 0 0 3.6958 5.9241 -3.6816 O 0 0 0 0 0 0 0 0 0 0 0 0 2.4408 5.9226 -6.1151 N 0 0 0 0 0 0 0 0 0 0 0 0 2.1098 6.5788 -7.3135 C 0 0 0 0 0 0 0 0 0 0 0 0 2.9021 6.3649 -8.2986 O 0 0 0 0 0 0 0 0 0 0 0 0 0.9656 7.4637 -7.5341 C 0 0 1 0 0 0 0 0 0 0 0 0 0.1341 7.6936 -6.4006 N 0 0 0 0 0 0 0 0 0 0 0 0 -1.0819 8.4973 -6.4035 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.4654 9.0334 -7.4555 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.8375 8.6589 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0 85 86 1 0 0 0 0 86 87 2 0 0 0 0 86 88 1 0 0 0 0 88 89 1 0 0 0 0 89 90 1 0 0 0 0 90 91 1 0 0 0 0 91 92 1 0 0 0 0 92 93 1 0 0 0 0 93 94 2 0 0 0 0 93 95 1 0 0 0 0 95 96 2 0 0 0 0 96 97 1 0 0 0 0 95 98 1 0 0 0 0 98 99 1 0 0 0 0 99100 2 0 0 0 0 99101 1 0 0 0 0 101102 1 0 0 0 0 101103 1 0 0 0 0 103104 1 0 0 0 0 103105 1 0 0 0 0 103106 1 6 0 0 0 30107 1 0 0 0 0 107108 1 0 0 0 0 107109 1 0 0 0 0 26110 1 0 0 0 0 110111 1 0 0 0 0 110112 1 0 0 0 0 112113 1 0 0 0 0 3114 1 0 0 0 0 114115 2 0 0 0 0 114116 1 0 0 0 0 116117 1 0 0 0 0 117118 1 0 0 0 0 118119 2 0 0 0 0 118120 1 0 0 0 0 120121 1 0 0 0 0 121122 1 0 0 0 0 122123 1 0 0 0 0 123124 1 0 0 0 0 124125 2 0 0 0 0 125126 1 0 0 0 0 126127 1 0 0 0 0 127128 2 0 0 0 0 127129 1 0 0 0 0 129130 1 0 0 0 0 130131 1 0 0 0 0 130132 1 0 0 0 0 129133 1 0 0 0 0 133134 1 0 0 0 0 134135 2 0 0 0 0 134136 1 0 0 0 0 136137 1 0 0 0 0 137138 1 0 0 0 0 138139 1 0 0 0 0 138140 1 0 0 0 0 136141 1 0 0 0 0 141142 1 0 0 0 0 142143 2 0 0 0 0 117144 1 0 0 0 0 144145 1 0 0 0 0 144146 1 0 0 0 0 146147 1 0 0 0 0 41 36 1 0 0 0 0 74 70 1 0 0 0 0 92 88 1 0 0 0 0 142121 1 0 0 0 0 1148 1 0 0 0 0 1149 1 0 0 0 0 1150 1 0 0 0 0 2151 1 0 0 0 0 4152 1 0 0 0 0 7153 1 6 0 0 0 8154 1 0 0 0 0 8155 1 0 0 0 0 9156 1 0 0 0 0 10157 1 0 0 0 0 13158 1 0 0 0 0 13159 1 0 0 0 0 14160 1 0 0 0 0 17161 1 1 0 0 0 18162 1 0 0 0 0 18163 1 0 0 0 0 19164 1 0 0 0 0 19165 1 0 0 0 0 21166 1 0 0 0 0 21167 1 0 0 0 0 23168 1 0 0 0 0 26169 1 1 0 0 0 27170 1 0 0 0 0 30171 1 6 0 0 0 31172 1 0 0 0 0 34173 1 1 0 0 0 35174 1 0 0 0 0 35175 1 0 0 0 0 37176 1 0 0 0 0 38177 1 0 0 0 0 39178 1 0 0 0 0 40179 1 0 0 0 0 41180 1 0 0 0 0 42181 1 0 0 0 0 45182 1 1 0 0 0 46183 1 0 0 0 0 46184 1 0 0 0 0 47185 1 0 0 0 0 47186 1 0 0 0 0 49187 1 0 0 0 0 49188 1 0 0 0 0 51189 1 0 0 0 0 54190 1 6 0 0 0 55191 1 0 0 0 0 55192 1 0 0 0 0 55193 1 0 0 0 0 56194 1 0 0 0 0 59195 1 1 0 0 0 60196 1 0 0 0 0 60197 1 0 0 0 0 60198 1 0 0 0 0 61199 1 0 0 0 0 65200 1 0 0 0 0 66201 1 0 0 0 0 66202 1 0 0 0 0 66203 1 0 0 0 0 67204 1 0 0 0 0 70205 1 6 0 0 0 71206 1 0 0 0 0 71207 1 0 0 0 0 72208 1 0 0 0 0 72209 1 0 0 0 0 73210 1 0 0 0 0 73211 1 0 0 0 0 78212 1 0 0 0 0 79213 1 0 0 0 0 79214 1 0 0 0 0 79215 1 0 0 0 0 80216 1 0 0 0 0 83217 1 6 0 0 0 84218 1 0 0 0 0 84219 1 0 0 0 0 84220 1 0 0 0 0 85221 1 0 0 0 0 88222 1 6 0 0 0 89223 1 0 0 0 0 89224 1 0 0 0 0 90225 1 0 0 0 0 90226 1 0 0 0 0 91227 1 0 0 0 0 91228 1 0 0 0 0 96229 1 0 0 0 0 97230 1 0 0 0 0 97231 1 0 0 0 0 97232 1 0 0 0 0 98233 1 0 0 0 0 101234 1 1 0 0 0 102235 1 0 0 0 0 102236 1 0 0 0 0 102237 1 0 0 0 0 104238 1 0 0 0 0 104239 1 0 0 0 0 104240 1 0 0 0 0 105241 1 0 0 0 0 105242 1 0 0 0 0 105243 1 0 0 0 0 107244 1 1 0 0 0 108245 1 0 0 0 0 108246 1 0 0 0 0 108247 1 0 0 0 0 109248 1 0 0 0 0 109249 1 0 0 0 0 109250 1 0 0 0 0 110251 1 1 0 0 0 111252 1 0 0 0 0 111253 1 0 0 0 0 111254 1 0 0 0 0 112255 1 0 0 0 0 112256 1 0 0 0 0 113257 1 0 0 0 0 113258 1 0 0 0 0 113259 1 0 0 0 0 116260 1 0 0 0 0 117261 1 1 0 0 0 120262 1 0 0 0 0 121263 1 6 0 0 0 122264 1 0 0 0 0 122265 1 0 0 0 0 124266 1 0 0 0 0 125267 1 0 0 0 0 126268 1 0 0 0 0 129269 1 1 0 0 0 130270 1 1 0 0 0 131271 1 0 0 0 0 131272 1 0 0 0 0 131273 1 0 0 0 0 132274 1 0 0 0 0 132275 1 0 0 0 0 132276 1 0 0 0 0 133277 1 0 0 0 0 136278 1 1 0 0 0 137279 1 0 0 0 0 137280 1 0 0 0 0 138281 1 1 0 0 0 139282 1 0 0 0 0 139283 1 0 0 0 0 139284 1 0 0 0 0 140285 1 0 0 0 0 140286 1 0 0 0 0 140287 1 0 0 0 0 141288 1 0 0 0 0 144289 1 1 0 0 0 145290 1 0 0 0 0 145291 1 0 0 0 0 145292 1 0 0 0 0 146293 1 0 0 0 0 146294 1 0 0 0 0 147295 1 0 0 0 0 147296 1 0 0 0 0 147297 1 0 0 0 0 M CHG 2 103 1 106 -1 M END > <DATABASE_ID> NP0019224 > <DATABASE_NAME> NP-MRD > <SMILES> [H]OC([H])([H])[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)[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])(N([H])C(=O)C(\N([H])C(=O)[C@]1([H])N(C(=O)C(\N([H])C(=O)[C@]([H])(N([H])C(=O)[C@]2([H])N(C(=O)C(\N([H])C(=O)[C@]([H])(C([H])([H])[H])[N+]([O-])(C([H])([H])[H])C([H])([H])[H])=C(/[H])C([H])([H])[H])C([H])([H])C([H])([H])C2([H])[H])C([H])([H])[H])=C(/[H])C([H])([H])[H])C([H])([H])C([H])([H])C1([H])[H])=C(/[H])C([H])([H])[H])C([H])([H])[H])C([H])([H])[H])C([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])(C([H])([H])[H])C([H])([H])[H])[C@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])[H])C([H])([H])C([H])([H])C(=O)N([H])[H])C(=O)N([H])C(=C(\[H])C([H])([H])[H])\C(=O)N([H])[C@@]([H])(C(=O)N([H])[C@]1([H])C(=O)N([H])[C@]([H])(C(=O)N([H])[C@]([H])(C(=O)N([H])\C([H])=C([H])/SC1([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])[H])[C@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])[H] > <INCHI_IDENTIFIER> InChI=1S/C97H150N24O25S/c1-21-52(13)76(95(143)114-68-48-147-43-40-100-92(140)74(50(9)10)115-86(134)65(44-49(7)8)112-89(68)137)117-84(132)60(24-4)106-88(136)67(47-122)105-73(125)46-101-82(130)63(36-38-71(98)123)111-94(142)77(53(14)22-2)118-93(141)75(51(11)12)116-87(135)66(45-58-32-28-27-29-33-58)113-85(133)64(37-39-72(99)124)110-80(128)55(16)102-78(126)54(15)103-83(131)59(23-3)107-91(139)70-35-31-42-120(70)96(144)61(25-5)108-79(127)56(17)104-90(138)69-34-30-41-119(69)97(145)62(26-6)109-81(129)57(18)121(19,20)146/h23-29,32-33,40,43,49-57,63-70,74-77,122H,21-22,30-31,34-39,41-42,44-48H2,1-20H3,(H2,98,123)(H2,99,124)(H,100,140)(H,101,130)(H,102,126)(H,103,131)(H,104,138)(H,105,125)(H,106,136)(H,107,139)(H,108,127)(H,109,129)(H,110,128)(H,111,142)(H,112,137)(H,113,133)(H,114,143)(H,115,134)(H,116,135)(H,117,132)(H,118,141)/b43-40-,59-23-,60-24-,61-25-,62-26-/t52-,53-,54-,55-,56-,57+,63-,64-,65+,66+,67+,68+,69-,70-,74+,75+,76-,77-/m1/s1 > <INCHI_KEY> FFDBCIHUUBZMLG-PQCLXWMJSA-N > <FORMULA> C97H150N24O25S > <MOLECULAR_WEIGHT> 2084.47 > <EXACT_MASS> 2083.0924676 > <JCHEM_ACCEPTOR_COUNT> 25 > <JCHEM_ATOM_COUNT> 297 > <JCHEM_AVERAGE_POLARIZABILITY> 219.48739432533944 > <JCHEM_BIOAVAILABILITY> 0 > <JCHEM_DONOR_COUNT> 22 > <JCHEM_FORMAL_CHARGE> 0 > <JCHEM_GHOSE_FILTER> 0 > <JCHEM_IUPAC> {[(1S)-1-{[(2Z)-1-[(2R)-2-{[(1R)-1-{[(2Z)-1-[(2R)-2-{[(1Z)-1-{[(1R)-1-{[(1R)-1-{[(1R)-3-carbamoyl-1-{[(1S)-1-{[(1S)-1-{[(1R,2R)-1-{[(1R)-3-carbamoyl-1-[({[(1S)-2-hydroxy-1-{[(1Z)-1-{[(1R,2R)-2-methyl-1-{[(2Z,6S,9S,12R)-9-(2-methylpropyl)-5,8,11-trioxo-6-(propan-2-yl)-1-thia-4,7,10-triazacyclotridec-2-en-12-yl]carbamoyl}butyl]carbamoyl}prop-1-en-1-yl]carbamoyl}ethyl]carbamoyl}methyl)carbamoyl]propyl]carbamoyl}-2-methylbutyl]carbamoyl}-2-methylpropyl]carbamoyl}-2-phenylethyl]carbamoyl}propyl]carbamoyl}ethyl]carbamoyl}ethyl]carbamoyl}prop-1-en-1-yl]carbamoyl}pyrrolidin-1-yl]-1-oxobut-2-en-2-yl]carbamoyl}ethyl]carbamoyl}pyrrolidin-1-yl]-1-oxobut-2-en-2-yl]carbamoyl}ethyl]dimethylnitroso}-lambda1-oxidanyl > <JCHEM_LOGP> -6.9221973680000035 > <JCHEM_MDDR_LIKE_RULE> 1 > <JCHEM_NUMBER_OF_RINGS> 4 > <JCHEM_PHYSIOLOGICAL_CHARGE> 0 > <JCHEM_PKA> 11.412667666602026 > <JCHEM_PKA_STRONGEST_ACIDIC> 10.81513593636693 > <JCHEM_PKA_STRONGEST_BASIC> 3.237263695017823 > <JCHEM_POLAR_SURFACE_AREA> 722.9899999999999 > <JCHEM_REFRACTIVITY> 540.8055 > <JCHEM_ROTATABLE_BOND_COUNT> 52 > <JCHEM_RULE_OF_FIVE> 0 > <JCHEM_TRADITIONAL_IUPAC> [(1S)-1-{[(2Z)-1-[(2R)-2-{[(1R)-1-{[(2Z)-1-[(2R)-2-{[(1Z)-1-{[(1R)-1-{[(1R)-1-{[(1R)-3-carbamoyl-1-{[(1S)-1-{[(1S)-1-{[(1R,2R)-1-{[(1R)-3-carbamoyl-1-[({[(1S)-2-hydroxy-1-{[(1Z)-1-{[(1R,2R)-1-{[(2Z,6S,9S,12R)-6-isopropyl-9-(2-methylpropyl)-5,8,11-trioxo-1-thia-4,7,10-triazacyclotridec-2-en-12-yl]carbamoyl}-2-methylbutyl]carbamoyl}prop-1-en-1-yl]carbamoyl}ethyl]carbamoyl}methyl)carbamoyl]propyl]carbamoyl}-2-methylbutyl]carbamoyl}-2-methylpropyl]carbamoyl}-2-phenylethyl]carbamoyl}propyl]carbamoyl}ethyl]carbamoyl}ethyl]carbamoyl}prop-1-en-1-yl]carbamoyl}pyrrolidin-1-yl]-1-oxobut-2-en-2-yl]carbamoyl}ethyl]carbamoyl}pyrrolidin-1-yl]-1-oxobut-2-en-2-yl]carbamoyl}ethyldimethylnitroso]-lambda1-oxidanyl > <JCHEM_VEBER_RULE> 0 $$$$ 3D-SDF for NP0019224 (Salinipeptin B)RDKit 3D 297300 0 0 0 0 0 0 0 0999 V2000 3.0770 2.9080 -1.8802 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2955 1.6695 -2.6814 C 0 0 0 0 0 0 0 0 0 0 0 0 3.7100 1.7176 -3.9356 C 0 0 0 0 0 0 0 0 0 0 0 0 3.9300 3.0095 -4.4600 N 0 0 0 0 0 0 0 0 0 0 0 0 3.2176 3.6877 -5.4633 C 0 0 0 0 0 0 0 0 0 0 0 0 2.2447 3.1255 -6.0193 O 0 0 0 0 0 0 0 0 0 0 0 0 3.5733 5.0618 -5.8906 C 0 0 2 0 0 0 0 0 0 0 0 0 4.4357 5.7597 -4.8558 C 0 0 0 0 0 0 0 0 0 0 0 0 3.6958 5.9241 -3.6816 O 0 0 0 0 0 0 0 0 0 0 0 0 2.4408 5.9226 -6.1151 N 0 0 0 0 0 0 0 0 0 0 0 0 2.1098 6.5788 -7.3135 C 0 0 0 0 0 0 0 0 0 0 0 0 2.9021 6.3649 -8.2986 O 0 0 0 0 0 0 0 0 0 0 0 0 0.9656 7.4637 -7.5341 C 0 0 0 0 0 0 0 0 0 0 0 0 0.1341 7.6936 -6.4006 N 0 0 0 0 0 0 0 0 0 0 0 0 -1.0819 8.4973 -6.4035 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.4654 9.0334 -7.4555 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.8375 8.6589 -5.1661 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.4927 9.8855 -4.3530 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4226 9.8321 -3.1361 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.2434 10.9757 -2.2319 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.0576 11.0411 -1.0685 N 0 0 0 0 0 0 0 0 0 0 0 0 -1.4097 11.9081 -2.4177 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.2840 8.6557 -5.2751 N 0 0 0 0 0 0 0 0 0 0 0 0 -4.0253 7.4850 -5.0088 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.3982 6.4390 -4.7265 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.4905 7.4459 -5.0399 C 0 0 2 0 0 0 0 0 0 0 0 0 -5.9539 6.0579 -4.8419 N 0 0 0 0 0 0 0 0 0 0 0 0 -5.8868 5.4615 -3.5842 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.4147 6.2155 -2.6348 O 0 0 0 0 0 0 0 0 0 0 0 0 -6.2517 4.1139 -3.1228 C 0 0 1 0 0 0 0 0 0 0 0 0 -5.8121 3.9248 -1.7484 N 0 0 0 0 0 0 0 0 0 0 0 0 -4.8553 2.9421 -1.3862 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.3356 2.1354 -2.1728 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.4265 2.8770 0.0741 C 0 0 2 0 0 0 0 0 0 0 0 0 -3.4002 3.9568 0.1572 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.6716 4.2089 1.3574 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.3960 3.6402 1.4854 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.6254 3.8599 2.6050 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.0837 4.6427 3.6277 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.3230 5.2057 3.5298 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.1069 4.9790 2.3841 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.9716 1.5995 0.4174 N 0 0 0 0 0 0 0 0 0 0 0 0 -4.4850 0.3383 0.0073 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.4456 0.2895 -0.8382 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.9612 -0.9243 0.5164 C 0 0 1 0 0 0 0 0 0 0 0 0 -5.0893 -1.5935 1.3341 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.6592 -2.9257 1.8954 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.7936 -3.5156 2.6334 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.7010 -4.8470 3.1563 N 0 0 0 0 0 0 0 0 0 0 0 0 -6.8704 -2.9138 2.8442 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.5903 -1.8504 -0.5507 N 0 0 0 0 0 0 0 0 0 0 0 0 -2.2583 -2.3013 -0.4463 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.4855 -1.9054 0.4742 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.6910 -3.2984 -1.4408 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.7086 -2.6443 -2.7536 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.3162 -3.4758 -0.8775 N 0 0 0 0 0 0 0 0 0 0 0 0 -0.2000 -4.1739 0.3566 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.2910 -4.6230 0.8587 O 0 0 0 0 0 0 0 0 0 0 0 0 1.0614 -4.3962 1.0968 C 0 0 1 0 0 0 0 0 0 0 0 0 2.0977 -3.3304 0.7288 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7044 -4.2782 2.5251 N 0 0 0 0 0 0 0 0 0 0 0 0 0.6866 -3.0635 3.2032 C 0 0 0 0 0 0 0 0 0 0 0 0 1.0046 -2.0183 2.5831 O 0 0 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HETATM 7 C UNK 0 3.573 5.062 -5.891 0.00 0.00 C+0 HETATM 8 C UNK 0 4.436 5.760 -4.856 0.00 0.00 C+0 HETATM 9 O UNK 0 3.696 5.924 -3.682 0.00 0.00 O+0 HETATM 10 N UNK 0 2.441 5.923 -6.115 0.00 0.00 N+0 HETATM 11 C UNK 0 2.110 6.579 -7.314 0.00 0.00 C+0 HETATM 12 O UNK 0 2.902 6.365 -8.299 0.00 0.00 O+0 HETATM 13 C UNK 0 0.966 7.464 -7.534 0.00 0.00 C+0 HETATM 14 N UNK 0 0.134 7.694 -6.401 0.00 0.00 N+0 HETATM 15 C UNK 0 -1.082 8.497 -6.404 0.00 0.00 C+0 HETATM 16 O UNK 0 -1.465 9.033 -7.455 0.00 0.00 O+0 HETATM 17 C UNK 0 -1.837 8.659 -5.166 0.00 0.00 C+0 HETATM 18 C UNK 0 -1.493 9.886 -4.353 0.00 0.00 C+0 HETATM 19 C UNK 0 -2.423 9.832 -3.136 0.00 0.00 C+0 HETATM 20 C UNK 0 -2.243 10.976 -2.232 0.00 0.00 C+0 HETATM 21 N UNK 0 -3.058 11.041 -1.069 0.00 0.00 N+0 HETATM 22 O UNK 0 -1.410 11.908 -2.418 0.00 0.00 O+0 HETATM 23 N UNK 0 -3.284 8.656 -5.275 0.00 0.00 N+0 HETATM 24 C UNK 0 -4.025 7.485 -5.009 0.00 0.00 C+0 HETATM 25 O UNK 0 -3.398 6.439 -4.726 0.00 0.00 O+0 HETATM 26 C UNK 0 -5.490 7.446 -5.040 0.00 0.00 C+0 HETATM 27 N UNK 0 -5.954 6.058 -4.842 0.00 0.00 N+0 HETATM 28 C UNK 0 -5.887 5.462 -3.584 0.00 0.00 C+0 HETATM 29 O UNK 0 -5.415 6.215 -2.635 0.00 0.00 O+0 HETATM 30 C UNK 0 -6.252 4.114 -3.123 0.00 0.00 C+0 HETATM 31 N UNK 0 -5.812 3.925 -1.748 0.00 0.00 N+0 HETATM 32 C UNK 0 -4.855 2.942 -1.386 0.00 0.00 C+0 HETATM 33 O UNK 0 -4.336 2.135 -2.173 0.00 0.00 O+0 HETATM 34 C UNK 0 -4.426 2.877 0.074 0.00 0.00 C+0 HETATM 35 C UNK 0 -3.400 3.957 0.157 0.00 0.00 C+0 HETATM 36 C UNK 0 -2.672 4.209 1.357 0.00 0.00 C+0 HETATM 37 C UNK 0 -1.396 3.640 1.485 0.00 0.00 C+0 HETATM 38 C UNK 0 -0.625 3.860 2.605 0.00 0.00 C+0 HETATM 39 C UNK 0 -1.084 4.643 3.628 0.00 0.00 C+0 HETATM 40 C UNK 0 -2.323 5.206 3.530 0.00 0.00 C+0 HETATM 41 C UNK 0 -3.107 4.979 2.384 0.00 0.00 C+0 HETATM 42 N UNK 0 -3.972 1.599 0.417 0.00 0.00 N+0 HETATM 43 C UNK 0 -4.485 0.338 0.007 0.00 0.00 C+0 HETATM 44 O UNK 0 -5.446 0.290 -0.838 0.00 0.00 O+0 HETATM 45 C UNK 0 -3.961 -0.924 0.516 0.00 0.00 C+0 HETATM 46 C UNK 0 -5.089 -1.593 1.334 0.00 0.00 C+0 HETATM 47 C UNK 0 -4.659 -2.926 1.895 0.00 0.00 C+0 HETATM 48 C UNK 0 -5.794 -3.516 2.633 0.00 0.00 C+0 HETATM 49 N UNK 0 -5.701 -4.847 3.156 0.00 0.00 N+0 HETATM 50 O UNK 0 -6.870 -2.914 2.844 0.00 0.00 O+0 HETATM 51 N UNK 0 -3.590 -1.850 -0.551 0.00 0.00 N+0 HETATM 52 C UNK 0 -2.258 -2.301 -0.446 0.00 0.00 C+0 HETATM 53 O UNK 0 -1.486 -1.905 0.474 0.00 0.00 O+0 HETATM 54 C UNK 0 -1.691 -3.298 -1.441 0.00 0.00 C+0 HETATM 55 C UNK 0 -1.709 -2.644 -2.754 0.00 0.00 C+0 HETATM 56 N UNK 0 -0.316 -3.476 -0.878 0.00 0.00 N+0 HETATM 57 C UNK 0 -0.200 -4.174 0.357 0.00 0.00 C+0 HETATM 58 O UNK 0 -1.291 -4.623 0.859 0.00 0.00 O+0 HETATM 59 C UNK 0 1.061 -4.396 1.097 0.00 0.00 C+0 HETATM 60 C UNK 0 2.098 -3.330 0.729 0.00 0.00 C+0 HETATM 61 N UNK 0 0.704 -4.278 2.525 0.00 0.00 N+0 HETATM 62 C UNK 0 0.687 -3.063 3.203 0.00 0.00 C+0 HETATM 63 O UNK 0 1.005 -2.018 2.583 0.00 0.00 O+0 HETATM 64 C UNK 0 0.317 -2.946 4.599 0.00 0.00 C+0 HETATM 65 C UNK 0 -0.010 -3.934 5.397 0.00 0.00 C+0 HETATM 66 C UNK 0 -0.379 -3.742 6.821 0.00 0.00 C+0 HETATM 67 N UNK 0 0.190 -1.601 5.180 0.00 0.00 N+0 HETATM 68 C UNK 0 -0.671 -0.746 4.497 0.00 0.00 C+0 HETATM 69 O UNK 0 -1.273 -1.183 3.430 0.00 0.00 O+0 HETATM 70 C UNK 0 -1.010 0.645 4.816 0.00 0.00 C+0 HETATM 71 C UNK 0 -2.354 0.945 4.210 0.00 0.00 C+0 HETATM 72 C UNK 0 -3.245 1.082 5.381 0.00 0.00 C+0 HETATM 73 C UNK 0 -2.397 1.067 6.626 0.00 0.00 C+0 HETATM 74 N UNK 0 -1.028 0.981 6.209 0.00 0.00 N+0 HETATM 75 C UNK 0 0.110 1.170 7.016 0.00 0.00 C+0 HETATM 76 O UNK 0 1.243 1.146 6.388 0.00 0.00 O+0 HETATM 77 C UNK 0 0.199 1.379 8.415 0.00 0.00 C+0 HETATM 78 C UNK 0 -0.791 1.438 9.275 0.00 0.00 C+0 HETATM 79 C UNK 0 -0.523 1.666 10.737 0.00 0.00 C+0 HETATM 80 N UNK 0 1.502 1.537 9.021 0.00 0.00 N+0 HETATM 81 C UNK 0 2.452 0.496 8.907 0.00 0.00 C+0 HETATM 82 O UNK 0 2.117 -0.535 8.256 0.00 0.00 O+0 HETATM 83 C UNK 0 3.760 0.618 9.534 0.00 0.00 C+0 HETATM 84 C UNK 0 3.497 0.755 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104 C UNK 0 9.810 -1.469 2.655 0.00 0.00 C+0 HETATM 105 C UNK 0 7.823 -2.051 1.424 0.00 0.00 C+0 HETATM 106 O UNK 0 9.028 -0.180 0.992 0.00 0.00 O-1 HETATM 107 C UNK 0 -7.701 3.750 -3.293 0.00 0.00 C+0 HETATM 108 C UNK 0 -8.672 4.625 -2.583 0.00 0.00 C+0 HETATM 109 C UNK 0 -8.075 3.618 -4.755 0.00 0.00 C+0 HETATM 110 C UNK 0 -6.230 8.255 -5.988 0.00 0.00 C+0 HETATM 111 C UNK 0 -7.733 8.004 -5.784 0.00 0.00 C+0 HETATM 112 C UNK 0 -5.857 8.153 -7.438 0.00 0.00 C+0 HETATM 113 C UNK 0 -6.755 9.078 -8.246 0.00 0.00 C+0 HETATM 114 C UNK 0 4.056 0.532 -4.750 0.00 0.00 C+0 HETATM 115 O UNK 0 4.425 0.766 -5.950 0.00 0.00 O+0 HETATM 116 N UNK 0 4.011 -0.767 -4.277 0.00 0.00 N+0 HETATM 117 C UNK 0 4.240 -2.085 -4.551 0.00 0.00 C+0 HETATM 118 C UNK 0 3.224 -2.982 -5.162 0.00 0.00 C+0 HETATM 119 O UNK 0 2.553 -2.591 -6.133 0.00 0.00 O+0 HETATM 120 N UNK 0 3.018 -4.289 -4.651 0.00 0.00 N+0 HETATM 121 C UNK 0 2.154 -5.322 -5.142 0.00 0.00 C+0 HETATM 122 C UNK 0 2.669 -6.616 -4.557 0.00 0.00 C+0 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4.326 0.00 0.00 H+0 HETATM 180 H UNK 0 -4.078 5.474 2.387 0.00 0.00 H+0 HETATM 181 H UNK 0 -3.116 1.532 1.071 0.00 0.00 H+0 HETATM 182 H UNK 0 -3.165 -0.735 1.242 0.00 0.00 H+0 HETATM 183 H UNK 0 -5.901 -1.787 0.614 0.00 0.00 H+0 HETATM 184 H UNK 0 -5.427 -0.919 2.116 0.00 0.00 H+0 HETATM 185 H UNK 0 -4.484 -3.593 0.997 0.00 0.00 H+0 HETATM 186 H UNK 0 -3.769 -2.833 2.512 0.00 0.00 H+0 HETATM 187 H UNK 0 -6.083 -5.105 4.103 0.00 0.00 H+0 HETATM 188 H UNK 0 -5.231 -5.529 2.536 0.00 0.00 H+0 HETATM 189 H UNK 0 -4.193 -2.154 -1.283 0.00 0.00 H+0 HETATM 190 H UNK 0 -2.222 -4.240 -1.319 0.00 0.00 H+0 HETATM 191 H UNK 0 -1.877 -3.362 -3.588 0.00 0.00 H+0 HETATM 192 H UNK 0 -0.815 -2.030 -2.994 0.00 0.00 H+0 HETATM 193 H UNK 0 -2.576 -1.916 -2.885 0.00 0.00 H+0 HETATM 194 H UNK 0 0.427 -3.070 -1.438 0.00 0.00 H+0 HETATM 195 H UNK 0 1.576 -5.345 0.974 0.00 0.00 H+0 HETATM 196 H UNK 0 2.755 -3.128 1.591 0.00 0.00 H+0 HETATM 197 H UNK 0 1.640 -2.402 0.394 0.00 0.00 H+0 HETATM 198 H UNK 0 2.754 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9.277 0.00 0.00 H+0 HETATM 218 H UNK 0 2.455 1.079 11.159 0.00 0.00 H+0 HETATM 219 H UNK 0 3.578 -0.254 11.507 0.00 0.00 H+0 HETATM 220 H UNK 0 4.219 1.448 11.517 0.00 0.00 H+0 HETATM 221 H UNK 0 4.172 -1.434 9.024 0.00 0.00 H+0 HETATM 222 H UNK 0 7.967 -1.233 9.245 0.00 0.00 H+0 HETATM 223 H UNK 0 7.810 -2.975 10.734 0.00 0.00 H+0 HETATM 224 H UNK 0 6.547 -1.883 11.435 0.00 0.00 H+0 HETATM 225 H UNK 0 5.973 -4.475 10.541 0.00 0.00 H+0 HETATM 226 H UNK 0 4.812 -3.138 10.539 0.00 0.00 H+0 HETATM 227 H UNK 0 6.377 -4.482 8.379 0.00 0.00 H+0 HETATM 228 H UNK 0 4.792 -3.574 8.267 0.00 0.00 H+0 HETATM 229 H UNK 0 5.626 -4.231 6.240 0.00 0.00 H+0 HETATM 230 H UNK 0 6.513 -3.802 3.307 0.00 0.00 H+0 HETATM 231 H UNK 0 6.456 -5.358 4.140 0.00 0.00 H+0 HETATM 232 H UNK 0 4.917 -4.396 3.826 0.00 0.00 H+0 HETATM 233 H UNK 0 8.111 -2.753 3.995 0.00 0.00 H+0 HETATM 234 H UNK 0 8.452 0.708 3.210 0.00 0.00 H+0 HETATM 235 H UNK 0 5.801 -0.139 2.107 0.00 0.00 H+0 HETATM 236 H UNK 0 7.003 0.501 0.917 0.00 0.00 H+0 HETATM 237 H UNK 0 6.492 1.486 2.391 0.00 0.00 H+0 HETATM 238 H UNK 0 10.730 -1.007 2.182 0.00 0.00 H+0 HETATM 239 H UNK 0 9.953 -2.551 2.522 0.00 0.00 H+0 HETATM 240 H UNK 0 9.892 -1.143 3.728 0.00 0.00 H+0 HETATM 241 H UNK 0 6.795 -1.949 1.829 0.00 0.00 H+0 HETATM 242 H UNK 0 8.260 -3.049 1.646 0.00 0.00 H+0 HETATM 243 H UNK 0 7.750 -1.848 0.343 0.00 0.00 H+0 HETATM 244 H UNK 0 -7.809 2.702 -2.865 0.00 0.00 H+0 HETATM 245 H UNK 0 -9.282 5.252 -3.255 0.00 0.00 H+0 HETATM 246 H UNK 0 -8.167 5.210 -1.782 0.00 0.00 H+0 HETATM 247 H UNK 0 -9.403 3.978 -2.031 0.00 0.00 H+0 HETATM 248 H UNK 0 -8.501 4.551 -5.137 0.00 0.00 H+0 HETATM 249 H UNK 0 -8.857 2.812 -4.894 0.00 0.00 H+0 HETATM 250 H UNK 0 -7.205 3.336 -5.386 0.00 0.00 H+0 HETATM 251 H UNK 0 -6.132 9.368 -5.744 0.00 0.00 H+0 HETATM 252 H UNK 0 -8.147 7.361 -6.569 0.00 0.00 H+0 HETATM 253 H UNK 0 -7.881 7.585 -4.745 0.00 0.00 H+0 HETATM 254 H UNK 0 -8.314 8.945 -5.795 0.00 0.00 H+0 HETATM 255 H UNK 0 -5.941 7.141 -7.871 0.00 0.00 H+0 HETATM 256 H UNK 0 -4.822 8.518 -7.605 0.00 0.00 H+0 HETATM 257 H UNK 0 -7.274 9.809 -7.577 0.00 0.00 H+0 HETATM 258 H UNK 0 -6.154 9.637 -8.998 0.00 0.00 H+0 HETATM 259 H UNK 0 -7.485 8.495 -8.833 0.00 0.00 H+0 HETATM 260 H UNK 0 3.580 -0.704 -3.186 0.00 0.00 H+0 HETATM 261 H UNK 0 4.627 -2.614 -3.595 0.00 0.00 H+0 HETATM 262 H UNK 0 3.613 -4.479 -3.765 0.00 0.00 H+0 HETATM 263 H UNK 0 2.309 -5.297 -6.275 0.00 0.00 H+0 HETATM 264 H UNK 0 1.946 -6.909 -3.810 0.00 0.00 H+0 HETATM 265 H UNK 0 3.577 -6.319 -3.917 0.00 0.00 H+0 HETATM 266 H UNK 0 1.944 -9.578 -6.736 0.00 0.00 H+0 HETATM 267 H UNK 0 1.753 -11.106 -5.024 0.00 0.00 H+0 HETATM 268 H UNK 0 3.646 -10.724 -3.196 0.00 0.00 H+0 HETATM 269 H UNK 0 0.972 -7.784 -1.725 0.00 0.00 H+0 HETATM 270 H UNK 0 -0.359 -9.353 -0.499 0.00 0.00 H+0 HETATM 271 H UNK 0 1.420 -11.439 -1.694 0.00 0.00 H+0 HETATM 272 H UNK 0 1.264 -11.564 0.075 0.00 0.00 H+0 HETATM 273 H UNK 0 -0.180 -11.559 -0.946 0.00 0.00 H+0 HETATM 274 H UNK 0 0.928 -9.148 1.329 0.00 0.00 H+0 HETATM 275 H UNK 0 2.340 -9.960 0.644 0.00 0.00 H+0 HETATM 276 H UNK 0 2.088 -8.194 0.243 0.00 0.00 H+0 HETATM 277 H UNK 0 -0.276 -10.100 -3.104 0.00 0.00 H+0 HETATM 278 H UNK 0 -0.341 -6.508 -2.606 0.00 0.00 H+0 HETATM 279 H UNK 0 -2.508 -5.557 -3.325 0.00 0.00 H+0 HETATM 280 H UNK 0 -2.742 -6.837 -4.497 0.00 0.00 H+0 HETATM 281 H UNK 0 -2.747 -7.088 -1.420 0.00 0.00 H+0 HETATM 282 H UNK 0 -3.954 -9.398 -2.423 0.00 0.00 H+0 HETATM 283 H UNK 0 -2.627 -9.306 -3.555 0.00 0.00 H+0 HETATM 284 H UNK 0 -2.330 -9.410 -1.773 0.00 0.00 H+0 HETATM 285 H UNK 0 -4.970 -7.060 -1.638 0.00 0.00 H+0 HETATM 286 H UNK 0 -5.024 -7.866 -3.211 0.00 0.00 H+0 HETATM 287 H UNK 0 -4.632 -6.122 -3.155 0.00 0.00 H+0 HETATM 288 H UNK 0 -1.093 -5.923 -5.479 0.00 0.00 H+0 HETATM 289 H UNK 0 6.354 -1.773 -4.984 0.00 0.00 H+0 HETATM 290 H UNK 0 6.029 -0.892 -7.079 0.00 0.00 H+0 HETATM 291 H UNK 0 4.336 -1.500 -7.175 0.00 0.00 H+0 HETATM 292 H UNK 0 5.775 -2.557 -7.544 0.00 0.00 H+0 HETATM 293 H UNK 0 5.048 -4.390 -5.772 0.00 0.00 H+0 HETATM 294 H UNK 0 6.183 -4.026 -4.424 0.00 0.00 H+0 HETATM 295 H UNK 0 7.563 -2.972 -6.561 0.00 0.00 H+0 HETATM 296 H UNK 0 7.812 -4.612 -5.875 0.00 0.00 H+0 HETATM 297 H UNK 0 6.751 -4.344 -7.327 0.00 0.00 H+0 CONECT 1 2 148 149 150 CONECT 2 1 3 151 CONECT 3 2 4 114 CONECT 4 3 5 152 CONECT 5 4 6 7 CONECT 6 5 CONECT 7 5 8 10 153 CONECT 8 7 9 154 155 CONECT 9 8 156 CONECT 10 7 11 157 CONECT 11 10 12 13 CONECT 12 11 CONECT 13 11 14 158 159 CONECT 14 13 15 160 CONECT 15 14 16 17 CONECT 16 15 CONECT 17 15 18 23 161 CONECT 18 17 19 162 163 CONECT 19 18 20 164 165 CONECT 20 19 21 22 CONECT 21 20 166 167 CONECT 22 20 CONECT 23 17 24 168 CONECT 24 23 25 26 CONECT 25 24 CONECT 26 24 27 110 169 CONECT 27 26 28 170 CONECT 28 27 29 30 CONECT 29 28 CONECT 30 28 31 107 171 CONECT 31 30 32 172 CONECT 32 31 33 34 CONECT 33 32 CONECT 34 32 35 42 173 CONECT 35 34 36 174 175 CONECT 36 35 37 41 CONECT 37 36 38 176 CONECT 38 37 39 177 CONECT 39 38 40 178 CONECT 40 39 41 179 CONECT 41 40 36 180 CONECT 42 34 43 181 CONECT 43 42 44 45 CONECT 44 43 CONECT 45 43 46 51 182 CONECT 46 45 47 183 184 CONECT 47 46 48 185 186 CONECT 48 47 49 50 CONECT 49 48 187 188 CONECT 50 48 CONECT 51 45 52 189 CONECT 52 51 53 54 CONECT 53 52 CONECT 54 52 55 56 190 CONECT 55 54 191 192 193 CONECT 56 54 57 194 CONECT 57 56 58 59 CONECT 58 57 CONECT 59 57 60 61 195 CONECT 60 59 196 197 198 CONECT 61 59 62 199 CONECT 62 61 63 64 CONECT 63 62 CONECT 64 62 65 67 CONECT 65 64 66 200 CONECT 66 65 201 202 203 CONECT 67 64 68 204 CONECT 68 67 69 70 CONECT 69 68 CONECT 70 68 71 74 205 CONECT 71 70 72 206 207 CONECT 72 71 73 208 209 CONECT 73 72 74 210 211 CONECT 74 73 75 70 CONECT 75 74 76 77 CONECT 76 75 CONECT 77 75 78 80 CONECT 78 77 79 212 CONECT 79 78 213 214 215 CONECT 80 77 81 216 CONECT 81 80 82 83 CONECT 82 81 CONECT 83 81 84 85 217 CONECT 84 83 218 219 220 CONECT 85 83 86 221 CONECT 86 85 87 88 CONECT 87 86 CONECT 88 86 89 92 222 CONECT 89 88 90 223 224 CONECT 90 89 91 225 226 CONECT 91 90 92 227 228 CONECT 92 91 93 88 CONECT 93 92 94 95 CONECT 94 93 CONECT 95 93 96 98 CONECT 96 95 97 229 CONECT 97 96 230 231 232 CONECT 98 95 99 233 CONECT 99 98 100 101 CONECT 100 99 CONECT 101 99 102 103 234 CONECT 102 101 235 236 237 CONECT 103 101 104 105 106 CONECT 104 103 238 239 240 CONECT 105 103 241 242 243 CONECT 106 103 CONECT 107 30 108 109 244 CONECT 108 107 245 246 247 CONECT 109 107 248 249 250 CONECT 110 26 111 112 251 CONECT 111 110 252 253 254 CONECT 112 110 113 255 256 CONECT 113 112 257 258 259 CONECT 114 3 115 116 CONECT 115 114 CONECT 116 114 117 260 CONECT 117 116 118 144 261 CONECT 118 117 119 120 CONECT 119 118 CONECT 120 118 121 262 CONECT 121 120 122 142 263 CONECT 122 121 123 264 265 CONECT 123 122 124 CONECT 124 123 125 266 CONECT 125 124 126 267 CONECT 126 125 127 268 CONECT 127 126 128 129 CONECT 128 127 CONECT 129 127 130 133 269 CONECT 130 129 131 132 270 CONECT 131 130 271 272 273 CONECT 132 130 274 275 276 CONECT 133 129 134 277 CONECT 134 133 135 136 CONECT 135 134 CONECT 136 134 137 141 278 CONECT 137 136 138 279 280 CONECT 138 137 139 140 281 CONECT 139 138 282 283 284 CONECT 140 138 285 286 287 CONECT 141 136 142 288 CONECT 142 141 143 121 CONECT 143 142 CONECT 144 117 145 146 289 CONECT 145 144 290 291 292 CONECT 146 144 147 293 294 CONECT 147 146 295 296 297 CONECT 148 1 CONECT 149 1 CONECT 150 1 CONECT 151 2 CONECT 152 4 CONECT 153 7 CONECT 154 8 CONECT 155 8 CONECT 156 9 CONECT 157 10 CONECT 158 13 CONECT 159 13 CONECT 160 14 CONECT 161 17 CONECT 162 18 CONECT 163 18 CONECT 164 19 CONECT 165 19 CONECT 166 21 CONECT 167 21 CONECT 168 23 CONECT 169 26 CONECT 170 27 CONECT 171 30 CONECT 172 31 CONECT 173 34 CONECT 174 35 CONECT 175 35 CONECT 176 37 CONECT 177 38 CONECT 178 39 CONECT 179 40 CONECT 180 41 CONECT 181 42 CONECT 182 45 CONECT 183 46 CONECT 184 46 CONECT 185 47 CONECT 186 47 CONECT 187 49 CONECT 188 49 CONECT 189 51 CONECT 190 54 CONECT 191 55 CONECT 192 55 CONECT 193 55 CONECT 194 56 CONECT 195 59 CONECT 196 60 CONECT 197 60 CONECT 198 60 CONECT 199 61 CONECT 200 65 CONECT 201 66 CONECT 202 66 CONECT 203 66 CONECT 204 67 CONECT 205 70 CONECT 206 71 CONECT 207 71 CONECT 208 72 CONECT 209 72 CONECT 210 73 CONECT 211 73 CONECT 212 78 CONECT 213 79 CONECT 214 79 CONECT 215 79 CONECT 216 80 CONECT 217 83 CONECT 218 84 CONECT 219 84 CONECT 220 84 CONECT 221 85 CONECT 222 88 CONECT 223 89 CONECT 224 89 CONECT 225 90 CONECT 226 90 CONECT 227 91 CONECT 228 91 CONECT 229 96 CONECT 230 97 CONECT 231 97 CONECT 232 97 CONECT 233 98 CONECT 234 101 CONECT 235 102 CONECT 236 102 CONECT 237 102 CONECT 238 104 CONECT 239 104 CONECT 240 104 CONECT 241 105 CONECT 242 105 CONECT 243 105 CONECT 244 107 CONECT 245 108 CONECT 246 108 CONECT 247 108 CONECT 248 109 CONECT 249 109 CONECT 250 109 CONECT 251 110 CONECT 252 111 CONECT 253 111 CONECT 254 111 CONECT 255 112 CONECT 256 112 CONECT 257 113 CONECT 258 113 CONECT 259 113 CONECT 260 116 CONECT 261 117 CONECT 262 120 CONECT 263 121 CONECT 264 122 CONECT 265 122 CONECT 266 124 CONECT 267 125 CONECT 268 126 CONECT 269 129 CONECT 270 130 CONECT 271 131 CONECT 272 131 CONECT 273 131 CONECT 274 132 CONECT 275 132 CONECT 276 132 CONECT 277 133 CONECT 278 136 CONECT 279 137 CONECT 280 137 CONECT 281 138 CONECT 282 139 CONECT 283 139 CONECT 284 139 CONECT 285 140 CONECT 286 140 CONECT 287 140 CONECT 288 141 CONECT 289 144 CONECT 290 145 CONECT 291 145 CONECT 292 145 CONECT 293 146 CONECT 294 146 CONECT 295 147 CONECT 296 147 CONECT 297 147 MASTER 0 0 0 0 0 0 0 0 297 0 600 0 END SMILES for NP0019224 (Salinipeptin B)[H]OC([H])([H])[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)[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])(N([H])C(=O)C(\N([H])C(=O)[C@]1([H])N(C(=O)C(\N([H])C(=O)[C@]([H])(N([H])C(=O)[C@]2([H])N(C(=O)C(\N([H])C(=O)[C@]([H])(C([H])([H])[H])[N+]([O-])(C([H])([H])[H])C([H])([H])[H])=C(/[H])C([H])([H])[H])C([H])([H])C([H])([H])C2([H])[H])C([H])([H])[H])=C(/[H])C([H])([H])[H])C([H])([H])C([H])([H])C1([H])[H])=C(/[H])C([H])([H])[H])C([H])([H])[H])C([H])([H])[H])C([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])(C([H])([H])[H])C([H])([H])[H])[C@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])[H])C([H])([H])C([H])([H])C(=O)N([H])[H])C(=O)N([H])C(=C(\[H])C([H])([H])[H])\C(=O)N([H])[C@@]([H])(C(=O)N([H])[C@]1([H])C(=O)N([H])[C@]([H])(C(=O)N([H])[C@]([H])(C(=O)N([H])\C([H])=C([H])/SC1([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])[H])[C@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])[H] INCHI for NP0019224 (Salinipeptin B)InChI=1S/C97H150N24O25S/c1-21-52(13)76(95(143)114-68-48-147-43-40-100-92(140)74(50(9)10)115-86(134)65(44-49(7)8)112-89(68)137)117-84(132)60(24-4)106-88(136)67(47-122)105-73(125)46-101-82(130)63(36-38-71(98)123)111-94(142)77(53(14)22-2)118-93(141)75(51(11)12)116-87(135)66(45-58-32-28-27-29-33-58)113-85(133)64(37-39-72(99)124)110-80(128)55(16)102-78(126)54(15)103-83(131)59(23-3)107-91(139)70-35-31-42-120(70)96(144)61(25-5)108-79(127)56(17)104-90(138)69-34-30-41-119(69)97(145)62(26-6)109-81(129)57(18)121(19,20)146/h23-29,32-33,40,43,49-57,63-70,74-77,122H,21-22,30-31,34-39,41-42,44-48H2,1-20H3,(H2,98,123)(H2,99,124)(H,100,140)(H,101,130)(H,102,126)(H,103,131)(H,104,138)(H,105,125)(H,106,136)(H,107,139)(H,108,127)(H,109,129)(H,110,128)(H,111,142)(H,112,137)(H,113,133)(H,114,143)(H,115,134)(H,116,135)(H,117,132)(H,118,141)/b43-40-,59-23-,60-24-,61-25-,62-26-/t52-,53-,54-,55-,56-,57+,63-,64-,65+,66+,67+,68+,69-,70-,74+,75+,76-,77-/m1/s1 3D Structure for NP0019224 (Salinipeptin B) | |||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
Chemical Formula | C97H150N24O25S | |||||||||||||||||||||||||||||||||||||||||||||||||||
Average Mass | 2084.4700 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||
Monoisotopic Mass | 2083.09247 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||
IUPAC Name | {[(1S)-1-{[(2Z)-1-[(2R)-2-{[(1R)-1-{[(2Z)-1-[(2R)-2-{[(1Z)-1-{[(1R)-1-{[(1R)-1-{[(1R)-3-carbamoyl-1-{[(1S)-1-{[(1S)-1-{[(1R,2R)-1-{[(1R)-3-carbamoyl-1-[({[(1S)-2-hydroxy-1-{[(1Z)-1-{[(1R,2R)-2-methyl-1-{[(2Z,6S,9S,12R)-9-(2-methylpropyl)-5,8,11-trioxo-6-(propan-2-yl)-1-thia-4,7,10-triazacyclotridec-2-en-12-yl]carbamoyl}butyl]carbamoyl}prop-1-en-1-yl]carbamoyl}ethyl]carbamoyl}methyl)carbamoyl]propyl]carbamoyl}-2-methylbutyl]carbamoyl}-2-methylpropyl]carbamoyl}-2-phenylethyl]carbamoyl}propyl]carbamoyl}ethyl]carbamoyl}ethyl]carbamoyl}prop-1-en-1-yl]carbamoyl}pyrrolidin-1-yl]-1-oxobut-2-en-2-yl]carbamoyl}ethyl]carbamoyl}pyrrolidin-1-yl]-1-oxobut-2-en-2-yl]carbamoyl}ethyl]dimethylnitroso}-lambda1-oxidanyl | |||||||||||||||||||||||||||||||||||||||||||||||||||
Traditional Name | [(1S)-1-{[(2Z)-1-[(2R)-2-{[(1R)-1-{[(2Z)-1-[(2R)-2-{[(1Z)-1-{[(1R)-1-{[(1R)-1-{[(1R)-3-carbamoyl-1-{[(1S)-1-{[(1S)-1-{[(1R,2R)-1-{[(1R)-3-carbamoyl-1-[({[(1S)-2-hydroxy-1-{[(1Z)-1-{[(1R,2R)-1-{[(2Z,6S,9S,12R)-6-isopropyl-9-(2-methylpropyl)-5,8,11-trioxo-1-thia-4,7,10-triazacyclotridec-2-en-12-yl]carbamoyl}-2-methylbutyl]carbamoyl}prop-1-en-1-yl]carbamoyl}ethyl]carbamoyl}methyl)carbamoyl]propyl]carbamoyl}-2-methylbutyl]carbamoyl}-2-methylpropyl]carbamoyl}-2-phenylethyl]carbamoyl}propyl]carbamoyl}ethyl]carbamoyl}ethyl]carbamoyl}prop-1-en-1-yl]carbamoyl}pyrrolidin-1-yl]-1-oxobut-2-en-2-yl]carbamoyl}ethyl]carbamoyl}pyrrolidin-1-yl]-1-oxobut-2-en-2-yl]carbamoyl}ethyldimethylnitroso]-lambda1-oxidanyl | |||||||||||||||||||||||||||||||||||||||||||||||||||
CAS Registry Number | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
SMILES | CC[C@@H](C)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@@H](C)NC(=O)[C@@H](C)NC(=O)C(\NC(=O)[C@H]1CCCN1C(=O)C(\NC(=O)[C@@H](C)NC(=O)[C@H]1CCCN1C(=O)C(\NC(=O)[C@H](C)[N+](C)(C)[O-])=C\C)=C\C)=C\C)C(C)C)C(=O)N[C@H](CCC(N)=O)C(=O)NCC(=O)N[C@@H](CO)C(=O)N\C(=C/C)C(=O)N[C@H]([C@H](C)CC)C(=O)N[C@H]1CS\C=C/NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC1=O)C(C)C | |||||||||||||||||||||||||||||||||||||||||||||||||||
InChI Identifier | InChI=1S/C97H150N24O25S/c1-21-52(13)76(95(143)114-68-48-147-43-40-100-92(140)74(50(9)10)115-86(134)65(44-49(7)8)112-89(68)137)117-84(132)60(24-4)106-88(136)67(47-122)105-73(125)46-101-82(130)63(36-38-71(98)123)111-94(142)77(53(14)22-2)118-93(141)75(51(11)12)116-87(135)66(45-58-32-28-27-29-33-58)113-85(133)64(37-39-72(99)124)110-80(128)55(16)102-78(126)54(15)103-83(131)59(23-3)107-91(139)70-35-31-42-120(70)96(144)61(25-5)108-79(127)56(17)104-90(138)69-34-30-41-119(69)97(145)62(26-6)109-81(129)57(18)121(19,20)146/h23-29,32-33,40,43,49-57,63-70,74-77,122H,21-22,30-31,34-39,41-42,44-48H2,1-20H3,(H2,98,123)(H2,99,124)(H,100,140)(H,101,130)(H,102,126)(H,103,131)(H,104,138)(H,105,125)(H,106,136)(H,107,139)(H,108,127)(H,109,129)(H,110,128)(H,111,142)(H,112,137)(H,113,133)(H,114,143)(H,115,134)(H,116,135)(H,117,132)(H,118,141)/b43-40-,59-23-,60-24-,61-25-,62-26-/t52-,53-,54-,55-,56-,57+,63-,64-,65+,66+,67+,68+,69-,70-,74+,75+,76-,77-/m1/s1 | |||||||||||||||||||||||||||||||||||||||||||||||||||
InChI Key | FFDBCIHUUBZMLG-PQCLXWMJSA-N | |||||||||||||||||||||||||||||||||||||||||||||||||||
Experimental Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Predicted Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||
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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 | ||||||||||||||||||||||||||||||||||||||||||||||||||||
NPAtlas ID | NPA025861 | |||||||||||||||||||||||||||||||||||||||||||||||||||
HMDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
DrugBank ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
Phenol Explorer Compound ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
FoodDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
KNApSAcK ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
Chemspider ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
KEGG Compound ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
BioCyc ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
BiGG ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
Wikipedia Link | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
METLIN ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
PubChem Compound | 146682334 | |||||||||||||||||||||||||||||||||||||||||||||||||||
PDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
ChEBI ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
Good Scents ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
References | ||||||||||||||||||||||||||||||||||||||||||||||||||||
General References |