Showing NP-Card for Asteltoxin D (NP0014364)
| Record Information | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Version | 2.0 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Created at | 2021-01-05 23:33:20 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Updated at | 2021-07-15 17:17:06 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| NP-MRD ID | NP0014364 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary Accession Numbers | None | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Natural Product Identification | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Common Name | Asteltoxin D | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Provided By | NPAtlas![]() | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Description | Asteltoxin D is found in Metapochonia bulbillosa and Pochonia. Based on a literature review very few articles have been published on Asteltoxin D. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structure | MOL for NP0014364 (Asteltoxin D)
Mrv1652306242119553D
58 61 0 0 0 0 999 V2000
9.3865 0.2959 -0.3076 C 0 0 0 0 0 0 0 0 0 0 0 0
8.1476 -0.2972 -0.5804 O 0 0 0 0 0 0 0 0 0 0 0 0
6.9728 0.0193 0.0450 C 0 0 0 0 0 0 0 0 0 0 0 0
6.9192 0.9817 1.0267 C 0 0 0 0 0 0 0 0 0 0 0 0
5.6990 1.2379 1.6034 C 0 0 0 0 0 0 0 0 0 0 0 0
5.6026 2.1164 2.5122 O 0 0 0 0 0 0 0 0 0 0 0 0
4.6049 0.5979 1.2458 O 0 0 0 0 0 0 0 0 0 0 0 0
4.6178 -0.3329 0.3063 C 0 0 0 0 0 0 0 0 0 0 0 0
3.3700 -1.0006 -0.0390 C 0 0 0 0 0 0 0 0 0 0 0 0
2.2400 -0.6991 0.5601 C 0 0 0 0 0 0 0 0 0 0 0 0
0.9727 -1.3410 0.2460 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.1563 -1.0342 0.8501 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.4362 -1.6969 0.5183 C 0 0 1 0 0 0 0 0 0 0 0 0
-2.5276 -0.9531 1.0135 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.4521 0.1887 0.2799 C 0 0 1 0 0 0 0 0 0 0 0 0
-2.1570 -0.2175 -1.1590 C 0 0 2 0 0 0 0 0 0 0 0 0
-3.4164 -0.1537 -1.7559 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.8705 1.0989 -1.3468 C 0 0 1 0 0 0 0 0 0 0 0 0
-5.2157 1.2902 -1.5192 O 0 0 0 0 0 0 0 0 0 0 0 0
-5.8999 0.7789 -0.4474 C 0 0 2 0 0 0 0 0 0 0 0 0
-6.9924 1.7458 -0.0708 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.9214 0.5346 0.6731 C 0 0 2 0 0 0 0 0 0 0 0 0
-5.0213 -0.8769 1.0987 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.3468 1.3397 1.7500 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.6472 1.0193 0.1610 C 0 0 1 0 0 0 0 0 0 0 0 0
-3.3499 2.4068 0.7214 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.6702 -1.6314 -0.9765 C 0 0 2 0 0 0 0 0 0 0 0 0
-2.6744 -2.5599 -1.2639 O 0 0 0 0 0 0 0 0 0 0 0 0
5.8146 -0.6331 -0.3084 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8240 -1.6780 -1.3617 C 0 0 0 0 0 0 0 0 0 0 0 0
9.8754 -0.1304 0.5933 H 0 0 0 0 0 0 0 0 0 0 0 0
10.0922 0.1552 -1.1520 H 0 0 0 0 0 0 0 0 0 0 0 0
9.3181 1.3910 -0.1459 H 0 0 0 0 0 0 0 0 0 0 0 0
7.7811 1.5319 1.3547 H 0 0 0 0 0 0 0 0 0 0 0 0
3.4002 -1.7579 -0.8090 H 0 0 0 0 0 0 0 0 0 0 0 0
2.2584 0.0640 1.3231 H 0 0 0 0 0 0 0 0 0 0 0 0
0.9494 -2.1033 -0.5143 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.1313 -0.2561 1.6267 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.5002 -2.7258 0.9069 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.5643 0.7791 0.6093 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.4245 0.4476 -1.6318 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.2871 1.9292 -1.7934 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.3825 -0.1831 -0.7864 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.5708 1.4255 0.8185 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.6479 1.8550 -0.9557 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.5127 2.7448 0.0919 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.5818 -1.0118 2.1223 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.6725 -1.6177 0.3728 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.1191 -1.1056 1.2522 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.9318 0.8474 2.3575 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.0299 3.1663 0.3244 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.4287 2.3218 1.8201 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.2719 2.6385 0.5167 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.7752 -1.8507 -1.5705 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.7726 -3.2410 -0.5738 H 0 0 0 0 0 0 0 0 0 0 0 0
6.8480 -1.8084 -1.7676 H 0 0 0 0 0 0 0 0 0 0 0 0
5.1854 -1.3919 -2.2270 H 0 0 0 0 0 0 0 0 0 0 0 0
5.4804 -2.6605 -1.0017 H 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 2 0 0 0 0
4 5 1 0 0 0 0
5 6 2 0 0 0 0
5 7 1 0 0 0 0
7 8 1 0 0 0 0
8 9 1 0 0 0 0
9 10 2 0 0 0 0
10 11 1 0 0 0 0
11 12 2 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
15 16 1 0 0 0 0
16 17 1 0 0 0 0
17 18 1 0 0 0 0
18 19 1 0 0 0 0
19 20 1 0 0 0 0
20 21 1 0 0 0 0
20 22 1 0 0 0 0
22 23 1 0 0 0 0
22 24 1 1 0 0 0
22 25 1 0 0 0 0
25 26 1 1 0 0 0
16 27 1 0 0 0 0
27 28 1 0 0 0 0
8 29 2 0 0 0 0
29 30 1 0 0 0 0
29 3 1 0 0 0 0
27 13 1 0 0 0 0
25 15 1 0 0 0 0
25 18 1 0 0 0 0
1 31 1 0 0 0 0
1 32 1 0 0 0 0
1 33 1 0 0 0 0
4 34 1 0 0 0 0
9 35 1 0 0 0 0
10 36 1 0 0 0 0
11 37 1 0 0 0 0
12 38 1 0 0 0 0
13 39 1 1 0 0 0
15 40 1 1 0 0 0
16 41 1 6 0 0 0
18 42 1 6 0 0 0
20 43 1 6 0 0 0
21 44 1 0 0 0 0
21 45 1 0 0 0 0
21 46 1 0 0 0 0
23 47 1 0 0 0 0
23 48 1 0 0 0 0
23 49 1 0 0 0 0
24 50 1 0 0 0 0
26 51 1 0 0 0 0
26 52 1 0 0 0 0
26 53 1 0 0 0 0
27 54 1 6 0 0 0
28 55 1 0 0 0 0
30 56 1 0 0 0 0
30 57 1 0 0 0 0
30 58 1 0 0 0 0
M END
3D MOL for NP0014364 (Asteltoxin D)
RDKit 3D
58 61 0 0 0 0 0 0 0 0999 V2000
9.3865 0.2959 -0.3076 C 0 0 0 0 0 0 0 0 0 0 0 0
8.1476 -0.2972 -0.5804 O 0 0 0 0 0 0 0 0 0 0 0 0
6.9728 0.0193 0.0450 C 0 0 0 0 0 0 0 0 0 0 0 0
6.9192 0.9817 1.0267 C 0 0 0 0 0 0 0 0 0 0 0 0
5.6990 1.2379 1.6034 C 0 0 0 0 0 0 0 0 0 0 0 0
5.6026 2.1164 2.5122 O 0 0 0 0 0 0 0 0 0 0 0 0
4.6049 0.5979 1.2458 O 0 0 0 0 0 0 0 0 0 0 0 0
4.6178 -0.3329 0.3063 C 0 0 0 0 0 0 0 0 0 0 0 0
3.3700 -1.0006 -0.0390 C 0 0 0 0 0 0 0 0 0 0 0 0
2.2400 -0.6991 0.5601 C 0 0 0 0 0 0 0 0 0 0 0 0
0.9727 -1.3410 0.2460 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.1563 -1.0342 0.8501 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.4362 -1.6969 0.5183 C 0 0 1 0 0 0 0 0 0 0 0 0
-2.5276 -0.9531 1.0135 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.4521 0.1887 0.2799 C 0 0 1 0 0 0 0 0 0 0 0 0
-2.1570 -0.2175 -1.1590 C 0 0 2 0 0 0 0 0 0 0 0 0
-3.4164 -0.1537 -1.7559 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.8705 1.0989 -1.3468 C 0 0 1 0 0 0 0 0 0 0 0 0
-5.2157 1.2902 -1.5192 O 0 0 0 0 0 0 0 0 0 0 0 0
-5.8999 0.7789 -0.4474 C 0 0 2 0 0 0 0 0 0 0 0 0
-6.9924 1.7458 -0.0708 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.9214 0.5346 0.6731 C 0 0 2 0 0 0 0 0 0 0 0 0
-5.0213 -0.8769 1.0987 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.3468 1.3397 1.7500 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.6472 1.0193 0.1610 C 0 0 1 0 0 0 0 0 0 0 0 0
-3.3499 2.4068 0.7214 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.6702 -1.6314 -0.9765 C 0 0 2 0 0 0 0 0 0 0 0 0
-2.6744 -2.5599 -1.2639 O 0 0 0 0 0 0 0 0 0 0 0 0
5.8146 -0.6331 -0.3084 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8240 -1.6780 -1.3617 C 0 0 0 0 0 0 0 0 0 0 0 0
9.8754 -0.1304 0.5933 H 0 0 0 0 0 0 0 0 0 0 0 0
10.0922 0.1552 -1.1520 H 0 0 0 0 0 0 0 0 0 0 0 0
9.3181 1.3910 -0.1459 H 0 0 0 0 0 0 0 0 0 0 0 0
7.7811 1.5319 1.3547 H 0 0 0 0 0 0 0 0 0 0 0 0
3.4002 -1.7579 -0.8090 H 0 0 0 0 0 0 0 0 0 0 0 0
2.2584 0.0640 1.3231 H 0 0 0 0 0 0 0 0 0 0 0 0
0.9494 -2.1033 -0.5143 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.1313 -0.2561 1.6267 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.5002 -2.7258 0.9069 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.5643 0.7791 0.6093 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.4245 0.4476 -1.6318 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.2871 1.9292 -1.7934 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.3825 -0.1831 -0.7864 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.5708 1.4255 0.8185 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.6479 1.8550 -0.9557 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.5127 2.7448 0.0919 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.5818 -1.0118 2.1223 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.6725 -1.6177 0.3728 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.1191 -1.1056 1.2522 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.9318 0.8474 2.3575 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.0299 3.1663 0.3244 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.4287 2.3218 1.8201 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.2719 2.6385 0.5167 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.7752 -1.8507 -1.5705 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.7726 -3.2410 -0.5738 H 0 0 0 0 0 0 0 0 0 0 0 0
6.8480 -1.8084 -1.7676 H 0 0 0 0 0 0 0 0 0 0 0 0
5.1854 -1.3919 -2.2270 H 0 0 0 0 0 0 0 0 0 0 0 0
5.4804 -2.6605 -1.0017 H 0 0 0 0 0 0 0 0 0 0 0 0
1 2 1 0
2 3 1 0
3 4 2 0
4 5 1 0
5 6 2 0
5 7 1 0
7 8 1 0
8 9 1 0
9 10 2 0
10 11 1 0
11 12 2 0
12 13 1 0
13 14 1 0
14 15 1 0
15 16 1 0
16 17 1 0
17 18 1 0
18 19 1 0
19 20 1 0
20 21 1 0
20 22 1 0
22 23 1 0
22 24 1 1
22 25 1 0
25 26 1 1
16 27 1 0
27 28 1 0
8 29 2 0
29 30 1 0
29 3 1 0
27 13 1 0
25 15 1 0
25 18 1 0
1 31 1 0
1 32 1 0
1 33 1 0
4 34 1 0
9 35 1 0
10 36 1 0
11 37 1 0
12 38 1 0
13 39 1 1
15 40 1 1
16 41 1 6
18 42 1 6
20 43 1 6
21 44 1 0
21 45 1 0
21 46 1 0
23 47 1 0
23 48 1 0
23 49 1 0
24 50 1 0
26 51 1 0
26 52 1 0
26 53 1 0
27 54 1 6
28 55 1 0
30 56 1 0
30 57 1 0
30 58 1 0
M END
3D SDF for NP0014364 (Asteltoxin D)
Mrv1652306242119553D
58 61 0 0 0 0 999 V2000
9.3865 0.2959 -0.3076 C 0 0 0 0 0 0 0 0 0 0 0 0
8.1476 -0.2972 -0.5804 O 0 0 0 0 0 0 0 0 0 0 0 0
6.9728 0.0193 0.0450 C 0 0 0 0 0 0 0 0 0 0 0 0
6.9192 0.9817 1.0267 C 0 0 0 0 0 0 0 0 0 0 0 0
5.6990 1.2379 1.6034 C 0 0 0 0 0 0 0 0 0 0 0 0
5.6026 2.1164 2.5122 O 0 0 0 0 0 0 0 0 0 0 0 0
4.6049 0.5979 1.2458 O 0 0 0 0 0 0 0 0 0 0 0 0
4.6178 -0.3329 0.3063 C 0 0 0 0 0 0 0 0 0 0 0 0
3.3700 -1.0006 -0.0390 C 0 0 0 0 0 0 0 0 0 0 0 0
2.2400 -0.6991 0.5601 C 0 0 0 0 0 0 0 0 0 0 0 0
0.9727 -1.3410 0.2460 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.1563 -1.0342 0.8501 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.4362 -1.6969 0.5183 C 0 0 1 0 0 0 0 0 0 0 0 0
-2.5276 -0.9531 1.0135 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.4521 0.1887 0.2799 C 0 0 1 0 0 0 0 0 0 0 0 0
-2.1570 -0.2175 -1.1590 C 0 0 2 0 0 0 0 0 0 0 0 0
-3.4164 -0.1537 -1.7559 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.8705 1.0989 -1.3468 C 0 0 1 0 0 0 0 0 0 0 0 0
-5.2157 1.2902 -1.5192 O 0 0 0 0 0 0 0 0 0 0 0 0
-5.8999 0.7789 -0.4474 C 0 0 2 0 0 0 0 0 0 0 0 0
-6.9924 1.7458 -0.0708 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.9214 0.5346 0.6731 C 0 0 2 0 0 0 0 0 0 0 0 0
-5.0213 -0.8769 1.0987 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.3468 1.3397 1.7500 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.6472 1.0193 0.1610 C 0 0 1 0 0 0 0 0 0 0 0 0
-3.3499 2.4068 0.7214 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.6702 -1.6314 -0.9765 C 0 0 2 0 0 0 0 0 0 0 0 0
-2.6744 -2.5599 -1.2639 O 0 0 0 0 0 0 0 0 0 0 0 0
5.8146 -0.6331 -0.3084 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8240 -1.6780 -1.3617 C 0 0 0 0 0 0 0 0 0 0 0 0
9.8754 -0.1304 0.5933 H 0 0 0 0 0 0 0 0 0 0 0 0
10.0922 0.1552 -1.1520 H 0 0 0 0 0 0 0 0 0 0 0 0
9.3181 1.3910 -0.1459 H 0 0 0 0 0 0 0 0 0 0 0 0
7.7811 1.5319 1.3547 H 0 0 0 0 0 0 0 0 0 0 0 0
3.4002 -1.7579 -0.8090 H 0 0 0 0 0 0 0 0 0 0 0 0
2.2584 0.0640 1.3231 H 0 0 0 0 0 0 0 0 0 0 0 0
0.9494 -2.1033 -0.5143 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.1313 -0.2561 1.6267 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.5002 -2.7258 0.9069 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.5643 0.7791 0.6093 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.4245 0.4476 -1.6318 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.2871 1.9292 -1.7934 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.3825 -0.1831 -0.7864 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.5708 1.4255 0.8185 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.6479 1.8550 -0.9557 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.5127 2.7448 0.0919 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.5818 -1.0118 2.1223 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.6725 -1.6177 0.3728 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.1191 -1.1056 1.2522 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.9318 0.8474 2.3575 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.0299 3.1663 0.3244 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.4287 2.3218 1.8201 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.2719 2.6385 0.5167 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.7752 -1.8507 -1.5705 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.7726 -3.2410 -0.5738 H 0 0 0 0 0 0 0 0 0 0 0 0
6.8480 -1.8084 -1.7676 H 0 0 0 0 0 0 0 0 0 0 0 0
5.1854 -1.3919 -2.2270 H 0 0 0 0 0 0 0 0 0 0 0 0
5.4804 -2.6605 -1.0017 H 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 2 0 0 0 0
4 5 1 0 0 0 0
5 6 2 0 0 0 0
5 7 1 0 0 0 0
7 8 1 0 0 0 0
8 9 1 0 0 0 0
9 10 2 0 0 0 0
10 11 1 0 0 0 0
11 12 2 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
15 16 1 0 0 0 0
16 17 1 0 0 0 0
17 18 1 0 0 0 0
18 19 1 0 0 0 0
19 20 1 0 0 0 0
20 21 1 0 0 0 0
20 22 1 0 0 0 0
22 23 1 0 0 0 0
22 24 1 1 0 0 0
22 25 1 0 0 0 0
25 26 1 1 0 0 0
16 27 1 0 0 0 0
27 28 1 0 0 0 0
8 29 2 0 0 0 0
29 30 1 0 0 0 0
29 3 1 0 0 0 0
27 13 1 0 0 0 0
25 15 1 0 0 0 0
25 18 1 0 0 0 0
1 31 1 0 0 0 0
1 32 1 0 0 0 0
1 33 1 0 0 0 0
4 34 1 0 0 0 0
9 35 1 0 0 0 0
10 36 1 0 0 0 0
11 37 1 0 0 0 0
12 38 1 0 0 0 0
13 39 1 1 0 0 0
15 40 1 1 0 0 0
16 41 1 6 0 0 0
18 42 1 6 0 0 0
20 43 1 6 0 0 0
21 44 1 0 0 0 0
21 45 1 0 0 0 0
21 46 1 0 0 0 0
23 47 1 0 0 0 0
23 48 1 0 0 0 0
23 49 1 0 0 0 0
24 50 1 0 0 0 0
26 51 1 0 0 0 0
26 52 1 0 0 0 0
26 53 1 0 0 0 0
27 54 1 6 0 0 0
28 55 1 0 0 0 0
30 56 1 0 0 0 0
30 57 1 0 0 0 0
30 58 1 0 0 0 0
M END
> <DATABASE_ID>
NP0014364
> <DATABASE_NAME>
NP-MRD
> <SMILES>
[H]O[C@]1([H])[C@]([H])(O[C@@]2([H])[C@]1([H])O[C@@]1([H])O[C@]([H])(C([H])([H])[H])[C@@](O[H])(C([H])([H])[H])[C@@]21C([H])([H])[H])C(\[H])=C(/[H])\C(\[H])=C(/[H])C1=C(C(OC([H])([H])[H])=C([H])C(=O)O1)C([H])([H])[H]
> <INCHI_IDENTIFIER>
InChI=1S/C22H28O8/c1-11-13(28-16(23)10-15(11)26-5)8-6-7-9-14-17(24)18-19(29-14)21(3)20(30-18)27-12(2)22(21,4)25/h6-10,12,14,17-20,24-25H,1-5H3/b8-6+,9-7+/t12-,14-,17-,18-,19+,20-,21+,22+/m1/s1
> <INCHI_KEY>
AVOLRKQPXXFPLF-WMBDBGTCSA-N
> <FORMULA>
C22H28O8
> <MOLECULAR_WEIGHT>
420.458
> <EXACT_MASS>
420.178417862
> <JCHEM_ACCEPTOR_COUNT>
7
> <JCHEM_ATOM_COUNT>
58
> <JCHEM_AVERAGE_POLARIZABILITY>
44.43272479029524
> <JCHEM_BIOAVAILABILITY>
1
> <JCHEM_DONOR_COUNT>
2
> <JCHEM_FORMAL_CHARGE>
0
> <JCHEM_GHOSE_FILTER>
1
> <JCHEM_IUPAC>
6-[(1E,3E)-4-[(1R,2R,4R,5R,6R,8S,10R,11R)-5,11-dihydroxy-1,10,11-trimethyl-3,7,9-trioxatricyclo[6.3.0.0^{2,6}]undecan-4-yl]buta-1,3-dien-1-yl]-4-methoxy-5-methyl-2H-pyran-2-one
> <ALOGPS_LOGP>
2.60
> <JCHEM_LOGP>
1.330019173666665
> <ALOGPS_LOGS>
-3.10
> <JCHEM_MDDR_LIKE_RULE>
0
> <JCHEM_NUMBER_OF_RINGS>
4
> <JCHEM_PHYSIOLOGICAL_CHARGE>
0
> <JCHEM_PKA>
13.581022923348954
> <JCHEM_PKA_STRONGEST_ACIDIC>
12.907564763532143
> <JCHEM_PKA_STRONGEST_BASIC>
-3.4888271613942683
> <JCHEM_POLAR_SURFACE_AREA>
103.68000000000002
> <JCHEM_REFRACTIVITY>
109.78950000000003
> <JCHEM_ROTATABLE_BOND_COUNT>
4
> <JCHEM_RULE_OF_FIVE>
1
> <ALOGPS_SOLUBILITY>
3.32e-01 g/l
> <JCHEM_TRADITIONAL_IUPAC>
6-[(1E,3E)-4-[(1R,2R,4R,5R,6R,8S,10R,11R)-5,11-dihydroxy-1,10,11-trimethyl-3,7,9-trioxatricyclo[6.3.0.0^{2,6}]undecan-4-yl]buta-1,3-dien-1-yl]-4-methoxy-5-methylpyran-2-one
> <JCHEM_VEBER_RULE>
0
$$$$
3D-SDF for NP0014364 (Asteltoxin D)
RDKit 3D
58 61 0 0 0 0 0 0 0 0999 V2000
9.3865 0.2959 -0.3076 C 0 0 0 0 0 0 0 0 0 0 0 0
8.1476 -0.2972 -0.5804 O 0 0 0 0 0 0 0 0 0 0 0 0
6.9728 0.0193 0.0450 C 0 0 0 0 0 0 0 0 0 0 0 0
6.9192 0.9817 1.0267 C 0 0 0 0 0 0 0 0 0 0 0 0
5.6990 1.2379 1.6034 C 0 0 0 0 0 0 0 0 0 0 0 0
5.6026 2.1164 2.5122 O 0 0 0 0 0 0 0 0 0 0 0 0
4.6049 0.5979 1.2458 O 0 0 0 0 0 0 0 0 0 0 0 0
4.6178 -0.3329 0.3063 C 0 0 0 0 0 0 0 0 0 0 0 0
3.3700 -1.0006 -0.0390 C 0 0 0 0 0 0 0 0 0 0 0 0
2.2400 -0.6991 0.5601 C 0 0 0 0 0 0 0 0 0 0 0 0
0.9727 -1.3410 0.2460 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.1563 -1.0342 0.8501 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.4362 -1.6969 0.5183 C 0 0 1 0 0 0 0 0 0 0 0 0
-2.5276 -0.9531 1.0135 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.4521 0.1887 0.2799 C 0 0 1 0 0 0 0 0 0 0 0 0
-2.1570 -0.2175 -1.1590 C 0 0 2 0 0 0 0 0 0 0 0 0
-3.4164 -0.1537 -1.7559 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.8705 1.0989 -1.3468 C 0 0 1 0 0 0 0 0 0 0 0 0
-5.2157 1.2902 -1.5192 O 0 0 0 0 0 0 0 0 0 0 0 0
-5.8999 0.7789 -0.4474 C 0 0 2 0 0 0 0 0 0 0 0 0
-6.9924 1.7458 -0.0708 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.9214 0.5346 0.6731 C 0 0 2 0 0 0 0 0 0 0 0 0
-5.0213 -0.8769 1.0987 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.3468 1.3397 1.7500 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.6472 1.0193 0.1610 C 0 0 1 0 0 0 0 0 0 0 0 0
-3.3499 2.4068 0.7214 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.6702 -1.6314 -0.9765 C 0 0 2 0 0 0 0 0 0 0 0 0
-2.6744 -2.5599 -1.2639 O 0 0 0 0 0 0 0 0 0 0 0 0
5.8146 -0.6331 -0.3084 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8240 -1.6780 -1.3617 C 0 0 0 0 0 0 0 0 0 0 0 0
9.8754 -0.1304 0.5933 H 0 0 0 0 0 0 0 0 0 0 0 0
10.0922 0.1552 -1.1520 H 0 0 0 0 0 0 0 0 0 0 0 0
9.3181 1.3910 -0.1459 H 0 0 0 0 0 0 0 0 0 0 0 0
7.7811 1.5319 1.3547 H 0 0 0 0 0 0 0 0 0 0 0 0
3.4002 -1.7579 -0.8090 H 0 0 0 0 0 0 0 0 0 0 0 0
2.2584 0.0640 1.3231 H 0 0 0 0 0 0 0 0 0 0 0 0
0.9494 -2.1033 -0.5143 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.1313 -0.2561 1.6267 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.5002 -2.7258 0.9069 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.5643 0.7791 0.6093 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.4245 0.4476 -1.6318 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.2871 1.9292 -1.7934 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.3825 -0.1831 -0.7864 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.5708 1.4255 0.8185 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.6479 1.8550 -0.9557 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.5127 2.7448 0.0919 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.5818 -1.0118 2.1223 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.6725 -1.6177 0.3728 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.1191 -1.1056 1.2522 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.9318 0.8474 2.3575 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.0299 3.1663 0.3244 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.4287 2.3218 1.8201 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.2719 2.6385 0.5167 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.7752 -1.8507 -1.5705 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.7726 -3.2410 -0.5738 H 0 0 0 0 0 0 0 0 0 0 0 0
6.8480 -1.8084 -1.7676 H 0 0 0 0 0 0 0 0 0 0 0 0
5.1854 -1.3919 -2.2270 H 0 0 0 0 0 0 0 0 0 0 0 0
5.4804 -2.6605 -1.0017 H 0 0 0 0 0 0 0 0 0 0 0 0
1 2 1 0
2 3 1 0
3 4 2 0
4 5 1 0
5 6 2 0
5 7 1 0
7 8 1 0
8 9 1 0
9 10 2 0
10 11 1 0
11 12 2 0
12 13 1 0
13 14 1 0
14 15 1 0
15 16 1 0
16 17 1 0
17 18 1 0
18 19 1 0
19 20 1 0
20 21 1 0
20 22 1 0
22 23 1 0
22 24 1 1
22 25 1 0
25 26 1 1
16 27 1 0
27 28 1 0
8 29 2 0
29 30 1 0
29 3 1 0
27 13 1 0
25 15 1 0
25 18 1 0
1 31 1 0
1 32 1 0
1 33 1 0
4 34 1 0
9 35 1 0
10 36 1 0
11 37 1 0
12 38 1 0
13 39 1 1
15 40 1 1
16 41 1 6
18 42 1 6
20 43 1 6
21 44 1 0
21 45 1 0
21 46 1 0
23 47 1 0
23 48 1 0
23 49 1 0
24 50 1 0
26 51 1 0
26 52 1 0
26 53 1 0
27 54 1 6
28 55 1 0
30 56 1 0
30 57 1 0
30 58 1 0
M END
PDB for NP0014364 (Asteltoxin D)HEADER PROTEIN 24-JUN-21 NONE TITLE NULL COMPND NULL SOURCE NULL KEYWDS NULL EXPDTA NULL AUTHOR Marvin REVDAT 1 24-JUN-21 0 HETATM 1 C UNK 0 9.386 0.296 -0.308 0.00 0.00 C+0 HETATM 2 O UNK 0 8.148 -0.297 -0.580 0.00 0.00 O+0 HETATM 3 C UNK 0 6.973 0.019 0.045 0.00 0.00 C+0 HETATM 4 C UNK 0 6.919 0.982 1.027 0.00 0.00 C+0 HETATM 5 C UNK 0 5.699 1.238 1.603 0.00 0.00 C+0 HETATM 6 O UNK 0 5.603 2.116 2.512 0.00 0.00 O+0 HETATM 7 O UNK 0 4.605 0.598 1.246 0.00 0.00 O+0 HETATM 8 C UNK 0 4.618 -0.333 0.306 0.00 0.00 C+0 HETATM 9 C UNK 0 3.370 -1.001 -0.039 0.00 0.00 C+0 HETATM 10 C UNK 0 2.240 -0.699 0.560 0.00 0.00 C+0 HETATM 11 C UNK 0 0.973 -1.341 0.246 0.00 0.00 C+0 HETATM 12 C UNK 0 -0.156 -1.034 0.850 0.00 0.00 C+0 HETATM 13 C UNK 0 -1.436 -1.697 0.518 0.00 0.00 C+0 HETATM 14 O UNK 0 -2.528 -0.953 1.014 0.00 0.00 O+0 HETATM 15 C UNK 0 -2.452 0.189 0.280 0.00 0.00 C+0 HETATM 16 C UNK 0 -2.157 -0.218 -1.159 0.00 0.00 C+0 HETATM 17 O UNK 0 -3.416 -0.154 -1.756 0.00 0.00 O+0 HETATM 18 C UNK 0 -3.870 1.099 -1.347 0.00 0.00 C+0 HETATM 19 O UNK 0 -5.216 1.290 -1.519 0.00 0.00 O+0 HETATM 20 C UNK 0 -5.900 0.779 -0.447 0.00 0.00 C+0 HETATM 21 C UNK 0 -6.992 1.746 -0.071 0.00 0.00 C+0 HETATM 22 C UNK 0 -4.921 0.535 0.673 0.00 0.00 C+0 HETATM 23 C UNK 0 -5.021 -0.877 1.099 0.00 0.00 C+0 HETATM 24 O UNK 0 -5.347 1.340 1.750 0.00 0.00 O+0 HETATM 25 C UNK 0 -3.647 1.019 0.161 0.00 0.00 C+0 HETATM 26 C UNK 0 -3.350 2.407 0.721 0.00 0.00 C+0 HETATM 27 C UNK 0 -1.670 -1.631 -0.977 0.00 0.00 C+0 HETATM 28 O UNK 0 -2.674 -2.560 -1.264 0.00 0.00 O+0 HETATM 29 C UNK 0 5.815 -0.633 -0.308 0.00 0.00 C+0 HETATM 30 C UNK 0 5.824 -1.678 -1.362 0.00 0.00 C+0 HETATM 31 H UNK 0 9.875 -0.130 0.593 0.00 0.00 H+0 HETATM 32 H UNK 0 10.092 0.155 -1.152 0.00 0.00 H+0 HETATM 33 H UNK 0 9.318 1.391 -0.146 0.00 0.00 H+0 HETATM 34 H UNK 0 7.781 1.532 1.355 0.00 0.00 H+0 HETATM 35 H UNK 0 3.400 -1.758 -0.809 0.00 0.00 H+0 HETATM 36 H UNK 0 2.258 0.064 1.323 0.00 0.00 H+0 HETATM 37 H UNK 0 0.949 -2.103 -0.514 0.00 0.00 H+0 HETATM 38 H UNK 0 -0.131 -0.256 1.627 0.00 0.00 H+0 HETATM 39 H UNK 0 -1.500 -2.726 0.907 0.00 0.00 H+0 HETATM 40 H UNK 0 -1.564 0.779 0.609 0.00 0.00 H+0 HETATM 41 H UNK 0 -1.425 0.448 -1.632 0.00 0.00 H+0 HETATM 42 H UNK 0 -3.287 1.929 -1.793 0.00 0.00 H+0 HETATM 43 H UNK 0 -6.383 -0.183 -0.786 0.00 0.00 H+0 HETATM 44 H UNK 0 -7.571 1.426 0.819 0.00 0.00 H+0 HETATM 45 H UNK 0 -7.648 1.855 -0.956 0.00 0.00 H+0 HETATM 46 H UNK 0 -6.513 2.745 0.092 0.00 0.00 H+0 HETATM 47 H UNK 0 -4.582 -1.012 2.122 0.00 0.00 H+0 HETATM 48 H UNK 0 -4.673 -1.618 0.373 0.00 0.00 H+0 HETATM 49 H UNK 0 -6.119 -1.106 1.252 0.00 0.00 H+0 HETATM 50 H UNK 0 -5.932 0.847 2.357 0.00 0.00 H+0 HETATM 51 H UNK 0 -4.030 3.166 0.324 0.00 0.00 H+0 HETATM 52 H UNK 0 -3.429 2.322 1.820 0.00 0.00 H+0 HETATM 53 H UNK 0 -2.272 2.639 0.517 0.00 0.00 H+0 HETATM 54 H UNK 0 -0.775 -1.851 -1.571 0.00 0.00 H+0 HETATM 55 H UNK 0 -2.773 -3.241 -0.574 0.00 0.00 H+0 HETATM 56 H UNK 0 6.848 -1.808 -1.768 0.00 0.00 H+0 HETATM 57 H UNK 0 5.185 -1.392 -2.227 0.00 0.00 H+0 HETATM 58 H UNK 0 5.480 -2.660 -1.002 0.00 0.00 H+0 CONECT 1 2 31 32 33 CONECT 2 1 3 CONECT 3 2 4 29 CONECT 4 3 5 34 CONECT 5 4 6 7 CONECT 6 5 CONECT 7 5 8 CONECT 8 7 9 29 CONECT 9 8 10 35 CONECT 10 9 11 36 CONECT 11 10 12 37 CONECT 12 11 13 38 CONECT 13 12 14 27 39 CONECT 14 13 15 CONECT 15 14 16 25 40 CONECT 16 15 17 27 41 CONECT 17 16 18 CONECT 18 17 19 25 42 CONECT 19 18 20 CONECT 20 19 21 22 43 CONECT 21 20 44 45 46 CONECT 22 20 23 24 25 CONECT 23 22 47 48 49 CONECT 24 22 50 CONECT 25 22 26 15 18 CONECT 26 25 51 52 53 CONECT 27 16 28 13 54 CONECT 28 27 55 CONECT 29 8 30 3 CONECT 30 29 56 57 58 CONECT 31 1 CONECT 32 1 CONECT 33 1 CONECT 34 4 CONECT 35 9 CONECT 36 10 CONECT 37 11 CONECT 38 12 CONECT 39 13 CONECT 40 15 CONECT 41 16 CONECT 42 18 CONECT 43 20 CONECT 44 21 CONECT 45 21 CONECT 46 21 CONECT 47 23 CONECT 48 23 CONECT 49 23 CONECT 50 24 CONECT 51 26 CONECT 52 26 CONECT 53 26 CONECT 54 27 CONECT 55 28 CONECT 56 30 CONECT 57 30 CONECT 58 30 MASTER 0 0 0 0 0 0 0 0 58 0 122 0 END SMILES for NP0014364 (Asteltoxin D)[H]O[C@]1([H])[C@]([H])(O[C@@]2([H])[C@]1([H])O[C@@]1([H])O[C@]([H])(C([H])([H])[H])[C@@](O[H])(C([H])([H])[H])[C@@]21C([H])([H])[H])C(\[H])=C(/[H])\C(\[H])=C(/[H])C1=C(C(OC([H])([H])[H])=C([H])C(=O)O1)C([H])([H])[H] INCHI for NP0014364 (Asteltoxin D)InChI=1S/C22H28O8/c1-11-13(28-16(23)10-15(11)26-5)8-6-7-9-14-17(24)18-19(29-14)21(3)20(30-18)27-12(2)22(21,4)25/h6-10,12,14,17-20,24-25H,1-5H3/b8-6+,9-7+/t12-,14-,17-,18-,19+,20-,21+,22+/m1/s1 3D Structure for NP0014364 (Asteltoxin D) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Synonyms | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chemical Formula | C22H28O8 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Average Mass | 420.4580 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Monoisotopic Mass | 420.17842 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| IUPAC Name | 6-[(1E,3E)-4-[(1R,2R,4R,5R,6R,8S,10R,11R)-5,11-dihydroxy-1,10,11-trimethyl-3,7,9-trioxatricyclo[6.3.0.0^{2,6}]undecan-4-yl]buta-1,3-dien-1-yl]-4-methoxy-5-methyl-2H-pyran-2-one | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Traditional Name | 6-[(1E,3E)-4-[(1R,2R,4R,5R,6R,8S,10R,11R)-5,11-dihydroxy-1,10,11-trimethyl-3,7,9-trioxatricyclo[6.3.0.0^{2,6}]undecan-4-yl]buta-1,3-dien-1-yl]-4-methoxy-5-methylpyran-2-one | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| CAS Registry Number | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| SMILES | COC1=CC(=O)OC(\C=C\C=C\[C@H]2O[C@H]3[C@H](O[C@H]4O[C@H](C)[C@](C)(O)[C@@]34C)[C@@H]2O)=C1C | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Identifier | InChI=1S/C22H28O8/c1-11-13(28-16(23)10-15(11)26-5)8-6-7-9-14-17(24)18-19(29-14)21(3)20(30-18)27-12(2)22(21,4)25/h6-10,12,14,17-20,24-25H,1-5H3/b8-6+,9-7+/t12-,14-,17-,18-,19+,20-,21+,22+/m1/s1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Key | AVOLRKQPXXFPLF-WMBDBGTCSA-N | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Experimental Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Predicted Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chemical Shift Submissions | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Species | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Species of Origin |
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chemical Taxonomy | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Classification | Not classified | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Physical Properties | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| State | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Experimental Properties |
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Predicted Properties |
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| External Links | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| NPAtlas ID | NPA009345 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HMDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| DrugBank ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Phenol Explorer Compound ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| FoodDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| KNApSAcK ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chemspider ID | 78437358 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| KEGG Compound ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BioCyc ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BiGG ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Wikipedia Link | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| METLIN ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| PubChem Compound | 139585687 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| PDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| ChEBI ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Good Scents ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| References | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| General References | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
