Showing NP-Card for Nocacyclomycin E (NP0351856)
| Record Information | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Version | 2.0 | |||||||||||||||
| Created at | 2025-11-12 04:16:14 UTC | |||||||||||||||
| Updated at | 2025-11-13 01:00:56 UTC | |||||||||||||||
| NP-MRD ID | NP0351856 | |||||||||||||||
| Natural Product DOI | https://doi.org/10.57994/4926 | |||||||||||||||
| Secondary Accession Numbers | None | |||||||||||||||
| Natural Product Identification | ||||||||||||||||
| Common Name | Nocacyclomycin E | |||||||||||||||
| Description | Not Available | |||||||||||||||
| Structure |  MOL for NP0351856 (Nocacyclomycin E)
Mrv2104 05182321282D
70 71 0 0 1 0 999 V2000
-6.4128 -7.2348 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.6429 -7.5311 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.0013 -7.0125 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.2314 -7.3088 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.5897 -6.7902 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.8198 -7.0866 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.1782 -6.5680 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.4083 -6.8643 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.7666 -6.3457 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.0033 -6.6421 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.6449 -6.1235 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.4148 -6.4198 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.5432 -7.2348 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.3131 -7.5311 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.9547 -7.0125 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
3.7247 -7.3088 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
3.5963 -6.4939 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
4.2379 -5.9753 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
5.0079 -6.2716 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1362 -7.0866 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
5.7778 -6.5680 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.5478 -6.8643 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.1894 -6.3457 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.6761 -7.6793 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.9061 -7.3829 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
6.0345 -8.1979 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.8044 -8.4942 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
7.4460 -7.9756 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.2159 -8.2720 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.8576 -7.7534 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.6275 -8.0497 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.7558 -8.8647 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.1142 -9.3833 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.3443 -9.0869 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.9327 -9.3092 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
7.7027 -9.6056 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.8310 -10.4205 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
7.1894 -10.9391 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
7.3177 -11.7541 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.6761 -12.2727 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
5.9061 -11.9763 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
5.7778 -11.1614 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.0079 -10.8650 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
4.8796 -10.0501 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
4.1096 -9.7537 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9813 -8.9388 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
3.2114 -8.6424 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
3.0830 -7.8275 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.3907 -8.2762 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.6229 -8.4202 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.4680 -10.2723 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.3663 -11.3836 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.4946 -12.1986 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.2645 -12.4950 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.8530 -12.7172 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.4194 -10.6428 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
6.8044 -13.0876 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.1628 -13.6063 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.2911 -14.4212 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.3928 -13.3099 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.0876 -12.0504 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
8.6009 -10.7169 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.2425 -10.1982 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.6177 -9.4635 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.0125 -10.4946 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.5266 -9.5631 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
5.3928 -8.7165 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
5.6495 -5.7530 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.8264 -6.1975 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.9379 -8.2659 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1 2 1 0 0 0 0
2 3 1 0 0 0 0
3 4 1 0 0 0 0
4 5 1 0 0 0 0
5 6 1 0 0 0 0
6 7 1 0 0 0 0
7 8 1 0 0 0 0
8 9 1 0 0 0 0
9 10 1 0 0 0 0
10 11 1 0 0 0 0
11 12 1 0 0 0 0
12 13 1 0 0 0 0
13 14 1 0 0 0 0
14 15 1 0 0 0 0
16 15 1 6 0 0 0
16 17 1 0 0 0 0
17 18 1 0 0 0 0
18 19 1 0 0 0 0
20 19 1 0 0 0 0
20 21 1 1 0 0 0
21 22 1 0 0 0 0
22 23 1 0 0 0 0
22 24 1 0 0 0 0
20 25 1 6 0 0 0
25 26 1 0 0 0 0
27 26 1 0 0 0 0
27 28 1 6 0 0 0
28 29 1 0 0 0 0
29 30 2 0 0 0 0
30 31 1 0 0 0 0
31 32 2 0 0 0 0
32 33 1 0 0 0 0
33 34 2 0 0 0 0
29 34 1 0 0 0 0
27 35 1 0 0 0 0
35 36 1 0 0 0 0
37 36 1 0 0 0 0
37 38 1 0 0 0 0
38 39 1 0 0 0 0
40 39 1 0 0 0 0
40 41 1 0 0 0 0
41 42 1 0 0 0 0
43 42 1 0 0 0 0
43 44 1 0 0 0 0
44 45 1 0 0 0 0
46 45 1 0 0 0 0
46 47 1 0 0 0 0
47 48 1 0 0 0 0
16 48 1 1 0 0 0
48 49 2 0 0 0 0
46 50 1 6 0 0 0
45 51 2 0 0 0 0
43 52 1 6 0 0 0
52 53 1 0 0 0 0
53 54 1 0 0 0 0
53 55 1 0 0 0 0
42 56 2 0 0 0 0
40 57 1 6 0 0 0
57 58 1 0 0 0 0
58 59 1 0 0 0 0
58 60 1 0 0 0 0
39 61 2 0 0 0 0
37 62 1 6 0 0 0
62 63 1 0 0 0 0
63 64 1 0 0 0 0
63 65 1 0 0 0 0
36 66 2 0 0 0 0
26 67 2 0 0 0 0
19 68 2 0 0 0 0
17 69 1 1 0 0 0
14 70 2 0 0 0 0
M END
3D SDF for NP0351856 (Nocacyclomycin E)
Mrv2104 05182321282D
70 71 0 0 1 0 999 V2000
-6.4128 -7.2348 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.6429 -7.5311 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.0013 -7.0125 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.2314 -7.3088 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.5897 -6.7902 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.8198 -7.0866 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.1782 -6.5680 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.4083 -6.8643 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.7666 -6.3457 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.0033 -6.6421 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.6449 -6.1235 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.4148 -6.4198 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.5432 -7.2348 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.3131 -7.5311 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.9547 -7.0125 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
3.7247 -7.3088 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
3.5963 -6.4939 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
4.2379 -5.9753 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
5.0079 -6.2716 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1362 -7.0866 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
5.7778 -6.5680 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.5478 -6.8643 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.1894 -6.3457 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.6761 -7.6793 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.9061 -7.3829 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
6.0345 -8.1979 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.8044 -8.4942 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
7.4460 -7.9756 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.2159 -8.2720 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.8576 -7.7534 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.6275 -8.0497 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.7558 -8.8647 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.1142 -9.3833 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.3443 -9.0869 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.9327 -9.3092 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
7.7027 -9.6056 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.8310 -10.4205 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
7.1894 -10.9391 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
7.3177 -11.7541 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.6761 -12.2727 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
5.9061 -11.9763 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
5.7778 -11.1614 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.0079 -10.8650 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
4.8796 -10.0501 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
4.1096 -9.7537 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9813 -8.9388 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
3.2114 -8.6424 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
3.0830 -7.8275 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.3907 -8.2762 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.6229 -8.4202 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.4680 -10.2723 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.3663 -11.3836 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.4946 -12.1986 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.2645 -12.4950 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.8530 -12.7172 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.4194 -10.6428 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
6.8044 -13.0876 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.1628 -13.6063 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.2911 -14.4212 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.3928 -13.3099 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.0876 -12.0504 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
8.6009 -10.7169 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.2425 -10.1982 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.6177 -9.4635 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.0125 -10.4946 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.5266 -9.5631 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
5.3928 -8.7165 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
5.6495 -5.7530 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.8264 -6.1975 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.9379 -8.2659 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1 2 1 0 0 0 0
2 3 1 0 0 0 0
3 4 1 0 0 0 0
4 5 1 0 0 0 0
5 6 1 0 0 0 0
6 7 1 0 0 0 0
7 8 1 0 0 0 0
8 9 1 0 0 0 0
9 10 1 0 0 0 0
10 11 1 0 0 0 0
11 12 1 0 0 0 0
12 13 1 0 0 0 0
13 14 1 0 0 0 0
14 15 1 0 0 0 0
16 15 1 6 0 0 0
16 17 1 0 0 0 0
17 18 1 0 0 0 0
18 19 1 0 0 0 0
20 19 1 0 0 0 0
20 21 1 1 0 0 0
21 22 1 0 0 0 0
22 23 1 0 0 0 0
22 24 1 0 0 0 0
20 25 1 6 0 0 0
25 26 1 0 0 0 0
27 26 1 0 0 0 0
27 28 1 6 0 0 0
28 29 1 0 0 0 0
29 30 2 0 0 0 0
30 31 1 0 0 0 0
31 32 2 0 0 0 0
32 33 1 0 0 0 0
33 34 2 0 0 0 0
29 34 1 0 0 0 0
27 35 1 0 0 0 0
35 36 1 0 0 0 0
37 36 1 0 0 0 0
37 38 1 0 0 0 0
38 39 1 0 0 0 0
40 39 1 0 0 0 0
40 41 1 0 0 0 0
41 42 1 0 0 0 0
43 42 1 0 0 0 0
43 44 1 0 0 0 0
44 45 1 0 0 0 0
46 45 1 0 0 0 0
46 47 1 0 0 0 0
47 48 1 0 0 0 0
16 48 1 1 0 0 0
48 49 2 0 0 0 0
46 50 1 6 0 0 0
45 51 2 0 0 0 0
43 52 1 6 0 0 0
52 53 1 0 0 0 0
53 54 1 0 0 0 0
53 55 1 0 0 0 0
42 56 2 0 0 0 0
40 57 1 6 0 0 0
57 58 1 0 0 0 0
58 59 1 0 0 0 0
58 60 1 0 0 0 0
39 61 2 0 0 0 0
37 62 1 6 0 0 0
62 63 1 0 0 0 0
63 64 1 0 0 0 0
63 65 1 0 0 0 0
36 66 2 0 0 0 0
26 67 2 0 0 0 0
19 68 2 0 0 0 0
17 69 1 1 0 0 0
14 70 2 0 0 0 0
M END
> <DATABASE_ID>
NP0351856
> <DATABASE_NAME>
NP-MRD
> <SMILES>
CCCCCCCCCCCCCC(=O)N[C@H]1[C@@H](C)OC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC2=CC=CC=C2)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](C)NC1=O
> <INCHI_IDENTIFIER>
InChI=1S/C54H91N7O9/c1-12-13-14-15-16-17-18-19-20-21-25-28-46(62)61-47-39(11)70-54(69)45(32-37(8)9)60-52(67)44(33-40-26-23-22-24-27-40)59-51(66)43(31-36(6)7)58-50(65)42(30-35(4)5)57-49(64)41(29-34(2)3)56-48(63)38(10)55-53(47)68/h22-24,26-27,34-39,41-45,47H,12-21,25,28-33H2,1-11H3,(H,55,68)(H,56,63)(H,57,64)(H,58,65)(H,59,66)(H,60,67)(H,61,62)/t38-,39-,41+,42+,43+,44+,45?,47?/m1/s1
> <INCHI_KEY>
ZRPOZAPPXKJCQM-JWCKBLPFSA-N
> <FORMULA>
C54H91N7O9
> <MOLECULAR_WEIGHT>
982.362
> <EXACT_MASS>
981.687827538
$$$$
PDB for NP0351856 (Nocacyclomycin E)HEADER PROTEIN 18-MAY-23 NONE TITLE NULL COMPND NULL SOURCE NULL KEYWDS NULL EXPDTA NULL AUTHOR Marvin REVDAT 1 18-MAY-23 0 HETATM 1 C UNK 0 -11.971 -13.505 0.000 0.00 0.00 C+0 HETATM 2 C UNK 0 -10.533 -14.058 0.000 0.00 0.00 C+0 HETATM 3 C UNK 0 -9.336 -13.090 0.000 0.00 0.00 C+0 HETATM 4 C UNK 0 -7.899 -13.643 0.000 0.00 0.00 C+0 HETATM 5 C UNK 0 -6.701 -12.675 0.000 0.00 0.00 C+0 HETATM 6 C UNK 0 -5.264 -13.228 0.000 0.00 0.00 C+0 HETATM 7 C UNK 0 -4.066 -12.260 0.000 0.00 0.00 C+0 HETATM 8 C UNK 0 -2.629 -12.813 0.000 0.00 0.00 C+0 HETATM 9 C UNK 0 -1.431 -11.845 0.000 0.00 0.00 C+0 HETATM 10 C UNK 0 0.006 -12.399 0.000 0.00 0.00 C+0 HETATM 11 C UNK 0 1.204 -11.430 0.000 0.00 0.00 C+0 HETATM 12 C UNK 0 2.641 -11.984 0.000 0.00 0.00 C+0 HETATM 13 C UNK 0 2.881 -13.505 0.000 0.00 0.00 C+0 HETATM 14 C UNK 0 4.318 -14.058 0.000 0.00 0.00 C+0 HETATM 15 N UNK 0 5.515 -13.090 0.000 0.00 0.00 N+0 HETATM 16 C UNK 0 6.953 -13.643 0.000 0.00 0.00 C+0 HETATM 17 C UNK 0 6.713 -12.122 0.000 0.00 0.00 C+0 HETATM 18 O UNK 0 7.911 -11.154 0.000 0.00 0.00 O+0 HETATM 19 C UNK 0 9.348 -11.707 0.000 0.00 0.00 C+0 HETATM 20 C UNK 0 9.588 -13.228 0.000 0.00 0.00 C+0 HETATM 21 C UNK 0 10.785 -12.260 0.000 0.00 0.00 C+0 HETATM 22 C UNK 0 12.222 -12.813 0.000 0.00 0.00 C+0 HETATM 23 C UNK 0 13.420 -11.845 0.000 0.00 0.00 C+0 HETATM 24 C UNK 0 12.462 -14.335 0.000 0.00 0.00 C+0 HETATM 25 N UNK 0 11.025 -13.781 0.000 0.00 0.00 N+0 HETATM 26 C UNK 0 11.264 -15.303 0.000 0.00 0.00 C+0 HETATM 27 C UNK 0 12.702 -15.856 0.000 0.00 0.00 C+0 HETATM 28 C UNK 0 13.899 -14.888 0.000 0.00 0.00 C+0 HETATM 29 C UNK 0 15.336 -15.441 0.000 0.00 0.00 C+0 HETATM 30 C UNK 0 16.534 -14.473 0.000 0.00 0.00 C+0 HETATM 31 C UNK 0 17.971 -15.026 0.000 0.00 0.00 C+0 HETATM 32 C UNK 0 18.211 -16.547 0.000 0.00 0.00 C+0 HETATM 33 C UNK 0 17.013 -17.515 0.000 0.00 0.00 C+0 HETATM 34 C UNK 0 15.576 -16.962 0.000 0.00 0.00 C+0 HETATM 35 N UNK 0 12.941 -17.377 0.000 0.00 0.00 N+0 HETATM 36 C UNK 0 14.378 -17.930 0.000 0.00 0.00 C+0 HETATM 37 C UNK 0 14.618 -19.452 0.000 0.00 0.00 C+0 HETATM 38 N UNK 0 13.420 -20.420 0.000 0.00 0.00 N+0 HETATM 39 C UNK 0 13.660 -21.941 0.000 0.00 0.00 C+0 HETATM 40 C UNK 0 12.462 -22.909 0.000 0.00 0.00 C+0 HETATM 41 N UNK 0 11.025 -22.356 0.000 0.00 0.00 N+0 HETATM 42 C UNK 0 10.785 -20.835 0.000 0.00 0.00 C+0 HETATM 43 C UNK 0 9.348 -20.281 0.000 0.00 0.00 C+0 HETATM 44 N UNK 0 9.109 -18.760 0.000 0.00 0.00 N+0 HETATM 45 C UNK 0 7.671 -18.207 0.000 0.00 0.00 C+0 HETATM 46 C UNK 0 7.432 -16.686 0.000 0.00 0.00 C+0 HETATM 47 N UNK 0 5.995 -16.133 0.000 0.00 0.00 N+0 HETATM 48 C UNK 0 5.755 -14.611 0.000 0.00 0.00 C+0 HETATM 49 O UNK 0 4.463 -15.449 0.000 0.00 0.00 O+0 HETATM 50 C UNK 0 8.629 -15.718 0.000 0.00 0.00 C+0 HETATM 51 O UNK 0 6.474 -19.175 0.000 0.00 0.00 O+0 HETATM 52 C UNK 0 8.150 -21.249 0.000 0.00 0.00 C+0 HETATM 53 C UNK 0 8.390 -22.771 0.000 0.00 0.00 C+0 HETATM 54 C UNK 0 9.827 -23.324 0.000 0.00 0.00 C+0 HETATM 55 C UNK 0 7.192 -23.739 0.000 0.00 0.00 C+0 HETATM 56 O UNK 0 11.983 -19.867 0.000 0.00 0.00 O+0 HETATM 57 C UNK 0 12.702 -24.430 0.000 0.00 0.00 C+0 HETATM 58 C UNK 0 11.504 -25.398 0.000 0.00 0.00 C+0 HETATM 59 C UNK 0 11.743 -26.920 0.000 0.00 0.00 C+0 HETATM 60 C UNK 0 10.067 -24.845 0.000 0.00 0.00 C+0 HETATM 61 O UNK 0 15.097 -22.494 0.000 0.00 0.00 O+0 HETATM 62 C UNK 0 16.055 -20.005 0.000 0.00 0.00 C+0 HETATM 63 C UNK 0 17.253 -19.037 0.000 0.00 0.00 C+0 HETATM 64 C UNK 0 17.953 -17.665 0.000 0.00 0.00 C+0 HETATM 65 C UNK 0 18.690 -19.590 0.000 0.00 0.00 C+0 HETATM 66 O UNK 0 15.916 -17.851 0.000 0.00 0.00 O+0 HETATM 67 O UNK 0 10.067 -16.271 0.000 0.00 0.00 O+0 HETATM 68 O UNK 0 10.546 -10.739 0.000 0.00 0.00 O+0 HETATM 69 C UNK 0 5.276 -11.569 0.000 0.00 0.00 C+0 HETATM 70 O UNK 0 3.617 -15.430 0.000 0.00 0.00 O+0 CONECT 1 2 CONECT 2 1 3 CONECT 3 2 4 CONECT 4 3 5 CONECT 5 4 6 CONECT 6 5 7 CONECT 7 6 8 CONECT 8 7 9 CONECT 9 8 10 CONECT 10 9 11 CONECT 11 10 12 CONECT 12 11 13 CONECT 13 12 14 CONECT 14 13 15 70 CONECT 15 14 16 CONECT 16 15 17 48 CONECT 17 16 18 69 CONECT 18 17 19 CONECT 19 18 20 68 CONECT 20 19 21 25 CONECT 21 20 22 CONECT 22 21 23 24 CONECT 23 22 CONECT 24 22 CONECT 25 20 26 CONECT 26 25 27 67 CONECT 27 26 28 35 CONECT 28 27 29 CONECT 29 28 30 34 CONECT 30 29 31 CONECT 31 30 32 CONECT 32 31 33 CONECT 33 32 34 CONECT 34 33 29 CONECT 35 27 36 CONECT 36 35 37 66 CONECT 37 36 38 62 CONECT 38 37 39 CONECT 39 38 40 61 CONECT 40 39 41 57 CONECT 41 40 42 CONECT 42 41 43 56 CONECT 43 42 44 52 CONECT 44 43 45 CONECT 45 44 46 51 CONECT 46 45 47 50 CONECT 47 46 48 CONECT 48 47 16 49 CONECT 49 48 CONECT 50 46 CONECT 51 45 CONECT 52 43 53 CONECT 53 52 54 55 CONECT 54 53 CONECT 55 53 CONECT 56 42 CONECT 57 40 58 CONECT 58 57 59 60 CONECT 59 58 CONECT 60 58 CONECT 61 39 CONECT 62 37 63 CONECT 63 62 64 65 CONECT 64 63 CONECT 65 63 CONECT 66 36 CONECT 67 26 CONECT 68 19 CONECT 69 17 CONECT 70 14 MASTER 0 0 0 0 0 0 0 0 70 0 142 0 END SMILES for NP0351856 (Nocacyclomycin E)CCCCCCCCCCCCCC(=O)N[C@H]1[C@@H](C)OC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC2=CC=CC=C2)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](C)NC1=O INCHI for NP0351856 (Nocacyclomycin E)InChI=1S/C54H91N7O9/c1-12-13-14-15-16-17-18-19-20-21-25-28-46(62)61-47-39(11)70-54(69)45(32-37(8)9)60-52(67)44(33-40-26-23-22-24-27-40)59-51(66)43(31-36(6)7)58-50(65)42(30-35(4)5)57-49(64)41(29-34(2)3)56-48(63)38(10)55-53(47)68/h22-24,26-27,34-39,41-45,47H,12-21,25,28-33H2,1-11H3,(H,55,68)(H,56,63)(H,57,64)(H,58,65)(H,59,66)(H,60,67)(H,61,62)/t38-,39-,41+,42+,43+,44+,45?,47?/m1/s1 3D Structure for NP0351856 (Nocacyclomycin E) | |||||||||||||||
| Synonyms | Not Available | |||||||||||||||
| Chemical Formula | C54H91N7O9 | |||||||||||||||
| Average Mass | 982.3620 Da | |||||||||||||||
| Monoisotopic Mass | 981.68783 Da | |||||||||||||||
| IUPAC Name | Not Available | |||||||||||||||
| Traditional Name | Not Available | |||||||||||||||
| CAS Registry Number | Not Available | |||||||||||||||
| SMILES | CCCCCCCCCCCCCC(=O)N[C@H]1[C@@H](C)OC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC2=CC=CC=C2)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](C)NC1=O | |||||||||||||||
| InChI Identifier | InChI=1S/C54H91N7O9/c1-12-13-14-15-16-17-18-19-20-21-25-28-46(62)61-47-39(11)70-54(69)45(32-37(8)9)60-52(67)44(33-40-26-23-22-24-27-40)59-51(66)43(31-36(6)7)58-50(65)42(30-35(4)5)57-49(64)41(29-34(2)3)56-48(63)38(10)55-53(47)68/h22-24,26-27,34-39,41-45,47H,12-21,25,28-33H2,1-11H3,(H,55,68)(H,56,63)(H,57,64)(H,58,65)(H,59,66)(H,60,67)(H,61,62)/t38-,39-,41+,42+,43+,44+,45?,47?/m1/s1 | |||||||||||||||
| InChI Key | ZRPOZAPPXKJCQM-JWCKBLPFSA-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 | ||||||||||||||||
