Showing NP-Card for geranylgeranyl-chlorophyll b (NP0339904)
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| Version | 2.0 | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Created at | 2024-09-12 00:08:37 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Updated at | 2024-09-12 00:08:38 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||
| NP-MRD ID | NP0339904 | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary Accession Numbers | None | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Natural Product Identification | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Common Name | geranylgeranyl-chlorophyll b | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Description | Based on a literature review very few articles have been published on geranylgeranyl-chlorophyll b. | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Structure |  MOL for NP0339904 (geranylgeranyl-chlorophyll b)
Mrv2104 05272302402D
66 74 0 0 0 0 999 V2000
-0.0592 -0.4894 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.7070 -0.8659 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.6109 -0.7572 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.8567 0.0304 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.3672 0.7419 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6816 0.0400 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.4080 0.8287 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1993 1.0619 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.2089 0.2369 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.2692 0.1886 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.9964 -0.0089 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1340 -0.8108 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.9049 -1.5709 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1620 -1.7589 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9166 -0.9859 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.4567 -2.1580 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.7731 -1.6587 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.9034 -1.9716 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.1422 -2.8551 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.9396 -3.0668 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.5602 -3.4397 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.7755 -4.2361 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.1934 -4.8208 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.3960 -4.6091 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.1807 -3.8126 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.1860 -5.1937 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.9834 -4.9820 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.5654 -5.5667 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.3628 -5.3549 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.5781 -4.5585 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.9449 -5.9396 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.7422 -5.7278 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.3243 -6.3125 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.1216 -6.1008 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.7037 -6.6854 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.3370 -5.3044 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.4736 0.6642 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.9809 1.3259 0.0000 N 0 0 0 0 0 5 0 0 0 0 0 0
4.4090 -0.8496 0.0000 Mg 0 0 0 0 0 0 0 0 0 0 0 0
4.0874 -2.4880 0.0000 N 0 0 0 0 0 5 0 0 0 0 0 0
4.5801 -3.1498 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1029 -3.8228 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.4786 -4.6409 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.2153 -5.0659 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.3154 -3.5770 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6485 -4.1667 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.4371 -4.9946 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.3058 -2.7520 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.5170 -2.0257 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.2839 -1.2343 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.9456 -0.7417 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
5.3714 -2.9166 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.0334 -2.2099 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.8407 -2.0396 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.4884 -2.5913 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.9281 -1.2192 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.4810 -0.6069 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.3156 -0.7699 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
7.0696 0.1081 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.4239 0.9125 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.2500 1.1584 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
8.4791 2.0028 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.9910 1.6832 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
6.2624 -0.0622 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.1749 -0.8826 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.6220 -1.4948 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
1 2 2 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
4 6 2 0 0 0 0
6 7 1 0 0 0 0
7 8 2 0 0 0 0
8 9 1 0 0 0 0
9 10 1 0 0 0 0
9 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 2 0 0 0 0
14 16 1 0 0 0 0
16 17 1 0 0 0 0
18 17 1 4 0 0 0
18 19 2 0 0 0 0
19 20 1 0 0 0 0
19 21 1 0 0 0 0
21 22 1 0 0 0 0
23 22 1 4 0 0 0
23 24 2 0 0 0 0
24 25 1 0 0 0 0
24 26 1 0 0 0 0
26 27 1 0 0 0 0
28 27 1 4 0 0 0
28 29 2 0 0 0 0
29 30 1 0 0 0 0
29 31 1 0 0 0 0
31 32 1 0 0 0 0
32 33 1 0 0 0 0
33 34 2 0 0 0 0
34 35 1 0 0 0 0
34 36 1 0 0 0 0
11 37 1 0 0 0 0
37 38 2 0 0 0 0
38 39 1 0 0 0 0
39 40 1 0 0 0 0
40 41 2 0 0 0 0
41 42 1 0 0 0 0
42 43 1 0 0 0 0
43 44 1 0 0 0 0
42 45 2 0 0 0 0
45 46 1 0 0 0 0
46 47 2 0 0 0 0
45 48 1 0 0 0 0
40 48 1 0 0 0 0
48 49 2 0 0 0 0
49 50 1 0 0 0 0
3 50 2 0 0 0 0
50 51 1 0 0 0 0
39 51 1 0 0 0 0
6 51 1 0 0 0 0
41 52 1 0 0 0 0
52 53 2 0 0 0 0
53 54 1 0 0 0 0
54 55 1 0 0 0 0
54 56 2 0 0 0 0
56 57 1 0 0 0 0
57 58 2 0 0 0 0
57 59 1 0 0 0 0
59 60 1 0 0 0 0
60 61 1 0 0 0 0
61 62 1 0 0 0 0
60 63 2 0 0 0 0
59 64 1 0 0 0 0
37 64 1 0 0 0 0
64 65 2 0 0 0 0
65 66 1 0 0 0 0
39 66 1 0 0 0 0
53 66 1 0 0 0 0
56 65 1 0 0 0 0
8 38 1 0 0 0 0
M END
3D SDF for NP0339904 (geranylgeranyl-chlorophyll b)
Mrv2104 05272302402D
66 74 0 0 0 0 999 V2000
-0.0592 -0.4894 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.7070 -0.8659 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.6109 -0.7572 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.8567 0.0304 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.3672 0.7419 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6816 0.0400 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.4080 0.8287 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1993 1.0619 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.2089 0.2369 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.2692 0.1886 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.9964 -0.0089 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1340 -0.8108 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.9049 -1.5709 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1620 -1.7589 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9166 -0.9859 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.4567 -2.1580 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.7731 -1.6587 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.9034 -1.9716 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.1422 -2.8551 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.9396 -3.0668 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.5602 -3.4397 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.7755 -4.2361 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.1934 -4.8208 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.3960 -4.6091 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.1807 -3.8126 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.1860 -5.1937 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.9834 -4.9820 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.5654 -5.5667 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.3628 -5.3549 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.5781 -4.5585 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.9449 -5.9396 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.7422 -5.7278 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.3243 -6.3125 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.1216 -6.1008 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.7037 -6.6854 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.3370 -5.3044 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.4736 0.6642 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.9809 1.3259 0.0000 N 0 0 0 0 0 5 0 0 0 0 0 0
4.4090 -0.8496 0.0000 Mg 0 0 0 0 0 0 0 0 0 0 0 0
4.0874 -2.4880 0.0000 N 0 0 0 0 0 5 0 0 0 0 0 0
4.5801 -3.1498 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1029 -3.8228 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.4786 -4.6409 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.2153 -5.0659 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.3154 -3.5770 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6485 -4.1667 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.4371 -4.9946 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.3058 -2.7520 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.5170 -2.0257 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.2839 -1.2343 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.9456 -0.7417 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
5.3714 -2.9166 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.0334 -2.2099 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.8407 -2.0396 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.4884 -2.5913 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.9281 -1.2192 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.4810 -0.6069 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.3156 -0.7699 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
7.0696 0.1081 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.4239 0.9125 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.2500 1.1584 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
8.4791 2.0028 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.9910 1.6832 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
6.2624 -0.0622 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.1749 -0.8826 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.6220 -1.4948 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
1 2 2 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
4 6 2 0 0 0 0
6 7 1 0 0 0 0
7 8 2 0 0 0 0
8 9 1 0 0 0 0
9 10 1 0 0 0 0
9 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 2 0 0 0 0
14 16 1 0 0 0 0
16 17 1 0 0 0 0
18 17 1 4 0 0 0
18 19 2 0 0 0 0
19 20 1 0 0 0 0
19 21 1 0 0 0 0
21 22 1 0 0 0 0
23 22 1 4 0 0 0
23 24 2 0 0 0 0
24 25 1 0 0 0 0
24 26 1 0 0 0 0
26 27 1 0 0 0 0
28 27 1 4 0 0 0
28 29 2 0 0 0 0
29 30 1 0 0 0 0
29 31 1 0 0 0 0
31 32 1 0 0 0 0
32 33 1 0 0 0 0
33 34 2 0 0 0 0
34 35 1 0 0 0 0
34 36 1 0 0 0 0
11 37 1 0 0 0 0
37 38 2 0 0 0 0
38 39 1 0 0 0 0
39 40 1 0 0 0 0
40 41 2 0 0 0 0
41 42 1 0 0 0 0
42 43 1 0 0 0 0
43 44 1 0 0 0 0
42 45 2 0 0 0 0
45 46 1 0 0 0 0
46 47 2 0 0 0 0
45 48 1 0 0 0 0
40 48 1 0 0 0 0
48 49 2 0 0 0 0
49 50 1 0 0 0 0
3 50 2 0 0 0 0
50 51 1 0 0 0 0
39 51 1 0 0 0 0
6 51 1 0 0 0 0
41 52 1 0 0 0 0
52 53 2 0 0 0 0
53 54 1 0 0 0 0
54 55 1 0 0 0 0
54 56 2 0 0 0 0
56 57 1 0 0 0 0
57 58 2 0 0 0 0
57 59 1 0 0 0 0
59 60 1 0 0 0 0
60 61 1 0 0 0 0
61 62 1 0 0 0 0
60 63 2 0 0 0 0
59 64 1 0 0 0 0
37 64 1 0 0 0 0
64 65 2 0 0 0 0
65 66 1 0 0 0 0
39 66 1 0 0 0 0
53 66 1 0 0 0 0
56 65 1 0 0 0 0
8 38 1 0 0 0 0
M END
> <DATABASE_ID>
NP0339904
> <DATABASE_NAME>
NP-MRD
> <SMILES>
CCC1=C(C=O)C2=CC3=C(C=C)C(C)=C4C=C5C(C)C(CCC(=O)OCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C)C6=[NH]5[Mg]5(N34)N3C(=CC1=[NH]25)C(C)=C1C(=O)C(C(=O)OC)C6=C31
> <INCHI_IDENTIFIER>
InChI=1/C55H65N4O6.Mg/c1-12-38-35(8)42-27-43-36(9)40(23-24-48(61)65-26-25-34(7)22-16-21-33(6)20-15-19-32(5)18-14-17-31(3)4)52(58-43)50-51(55(63)64-11)54(62)49-37(10)44(59-53(49)50)28-46-39(13-2)41(30-60)47(57-46)29-45(38)56-42;/h12,17,19,21,25,27-30,36,40,51H,1,13-16,18,20,22-24,26H2,2-11H3,(H-,56,57,58,59,60,62);/q-1;/p+1
> <INCHI_KEY>
NRLHHMXVBPYZRX-UHFFFAOYNA-O
> <FORMULA>
C55H66MgN4O6
> <MOLECULAR_WEIGHT>
903.46
> <EXACT_MASS>
902.48327756
> <JCHEM_ACCEPTOR_COUNT>
6
> <JCHEM_ATOM_COUNT>
132
> <JCHEM_AVERAGE_POLARIZABILITY>
108.547046236462
> <JCHEM_BIOAVAILABILITY>
0
> <JCHEM_DONOR_COUNT>
2
> <JCHEM_FORMAL_CHARGE>
0
> <JCHEM_GHOSE_FILTER>
0
> <JCHEM_IUPAC>
methyl 17-ethenyl-12-ethyl-13-formyl-8,18,22-trimethyl-6-oxo-23-{3-oxo-3-[(3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl)oxy]propyl}-2,25lambda5,26lambda5,27-tetraaza-1-magnesanonacyclo[12.11.1.1^{1,16}.0^{2,9}.0^{3,7}.0^{4,24}.0^{11,26}.0^{21,25}.0^{19,27}]heptacosa-3,7,9,11(26),12,14,16,18,20,24-decaene-5-carboxylate
> <JCHEM_LOGP>
3.068200000000006
> <JCHEM_MDDR_LIKE_RULE>
1
> <JCHEM_NUMBER_OF_RINGS>
9
> <JCHEM_PHYSIOLOGICAL_CHARGE>
0
> <JCHEM_PKA_STRONGEST_ACIDIC>
11.637601654136471
> <JCHEM_PKA_STRONGEST_BASIC>
-6.666341790047791
> <JCHEM_POLAR_SURFACE_AREA>
147.20000000000002
> <JCHEM_REFRACTIVITY>
284.9415000000001
> <JCHEM_ROTATABLE_BOND_COUNT>
20
> <JCHEM_RULE_OF_FIVE>
0
> <JCHEM_TRADITIONAL_IUPAC>
methyl 17-ethenyl-12-ethyl-13-formyl-8,18,22-trimethyl-6-oxo-23-{3-oxo-3-[(3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl)oxy]propyl}-2,25lambda5,26lambda5,27-tetraaza-1-magnesanonacyclo[12.11.1.1^{1,16}.0^{2,9}.0^{3,7}.0^{4,24}.0^{11,26}.0^{21,25}.0^{19,27}]heptacosa-3,7,9,11(26),12,14,16,18,20,24-decaene-5-carboxylate
> <JCHEM_VEBER_RULE>
0
$$$$
PDB for NP0339904 (geranylgeranyl-chlorophyll b)HEADER PROTEIN 27-MAY-23 NONE TITLE NULL COMPND NULL SOURCE NULL KEYWDS NULL EXPDTA NULL AUTHOR Marvin REVDAT 1 27-MAY-23 0 HETATM 1 C UNK 0 -0.110 -0.913 0.000 0.00 0.00 C+0 HETATM 2 C UNK 0 1.320 -1.616 0.000 0.00 0.00 C+0 HETATM 3 C UNK 0 3.007 -1.413 0.000 0.00 0.00 C+0 HETATM 4 C UNK 0 3.466 0.057 0.000 0.00 0.00 C+0 HETATM 5 C UNK 0 2.552 1.385 0.000 0.00 0.00 C+0 HETATM 6 C UNK 0 5.006 0.075 0.000 0.00 0.00 C+0 HETATM 7 C UNK 0 6.362 1.547 0.000 0.00 0.00 C+0 HETATM 8 C UNK 0 7.839 1.982 0.000 0.00 0.00 C+0 HETATM 9 C UNK 0 7.857 0.442 0.000 0.00 0.00 C+0 HETATM 10 C UNK 0 6.103 0.352 0.000 0.00 0.00 C+0 HETATM 11 C UNK 0 9.327 -0.017 0.000 0.00 0.00 C+0 HETATM 12 C UNK 0 9.583 -1.513 0.000 0.00 0.00 C+0 HETATM 13 C UNK 0 9.156 -2.932 0.000 0.00 0.00 C+0 HETATM 14 C UNK 0 7.769 -3.283 0.000 0.00 0.00 C+0 HETATM 15 O UNK 0 7.311 -1.840 0.000 0.00 0.00 O+0 HETATM 16 O UNK 0 6.453 -4.028 0.000 0.00 0.00 O+0 HETATM 17 C UNK 0 5.176 -3.096 0.000 0.00 0.00 C+0 HETATM 18 C UNK 0 3.553 -3.680 0.000 0.00 0.00 C+0 HETATM 19 C UNK 0 3.999 -5.329 0.000 0.00 0.00 C+0 HETATM 20 C UNK 0 5.487 -5.725 0.000 0.00 0.00 C+0 HETATM 21 C UNK 0 2.912 -6.421 0.000 0.00 0.00 C+0 HETATM 22 C UNK 0 3.314 -7.907 0.000 0.00 0.00 C+0 HETATM 23 C UNK 0 2.228 -8.999 0.000 0.00 0.00 C+0 HETATM 24 C UNK 0 0.739 -8.604 0.000 0.00 0.00 C+0 HETATM 25 C UNK 0 0.337 -7.117 0.000 0.00 0.00 C+0 HETATM 26 C UNK 0 -0.347 -9.695 0.000 0.00 0.00 C+0 HETATM 27 C UNK 0 -1.836 -9.300 0.000 0.00 0.00 C+0 HETATM 28 C UNK 0 -2.922 -10.391 0.000 0.00 0.00 C+0 HETATM 29 C UNK 0 -4.411 -9.996 0.000 0.00 0.00 C+0 HETATM 30 C UNK 0 -4.812 -8.509 0.000 0.00 0.00 C+0 HETATM 31 C UNK 0 -5.497 -11.087 0.000 0.00 0.00 C+0 HETATM 32 C UNK 0 -6.985 -10.692 0.000 0.00 0.00 C+0 HETATM 33 C UNK 0 -8.072 -11.783 0.000 0.00 0.00 C+0 HETATM 34 C UNK 0 -9.560 -11.388 0.000 0.00 0.00 C+0 HETATM 35 C UNK 0 -10.647 -12.479 0.000 0.00 0.00 C+0 HETATM 36 C UNK 0 -9.962 -9.901 0.000 0.00 0.00 C+0 HETATM 37 C UNK 0 10.217 1.240 0.000 0.00 0.00 C+0 HETATM 38 N UNK 0 9.298 2.475 0.000 0.00 0.00 N+0 HETATM 39 Mg UNK 0 8.230 -1.586 0.000 0.00 0.00 Mg+0 HETATM 40 N UNK 0 7.630 -4.644 0.000 0.00 0.00 N+0 HETATM 41 C UNK 0 8.549 -5.880 0.000 0.00 0.00 C+0 HETATM 42 C UNK 0 7.659 -7.136 0.000 0.00 0.00 C+0 HETATM 43 C UNK 0 8.360 -8.663 0.000 0.00 0.00 C+0 HETATM 44 C UNK 0 9.735 -9.456 0.000 0.00 0.00 C+0 HETATM 45 C UNK 0 6.189 -6.677 0.000 0.00 0.00 C+0 HETATM 46 C UNK 0 4.944 -7.778 0.000 0.00 0.00 C+0 HETATM 47 O UNK 0 4.549 -9.323 0.000 0.00 0.00 O+0 HETATM 48 C UNK 0 6.171 -5.137 0.000 0.00 0.00 C+0 HETATM 49 C UNK 0 4.698 -3.781 0.000 0.00 0.00 C+0 HETATM 50 C UNK 0 4.263 -2.304 0.000 0.00 0.00 C+0 HETATM 51 N UNK 0 5.499 -1.384 0.000 0.00 0.00 N+0 HETATM 52 C UNK 0 10.027 -5.444 0.000 0.00 0.00 C+0 HETATM 53 C UNK 0 11.262 -4.125 0.000 0.00 0.00 C+0 HETATM 54 C UNK 0 12.769 -3.807 0.000 0.00 0.00 C+0 HETATM 55 C UNK 0 13.978 -4.837 0.000 0.00 0.00 C+0 HETATM 56 C UNK 0 12.932 -2.276 0.000 0.00 0.00 C+0 HETATM 57 C UNK 0 13.965 -1.133 0.000 0.00 0.00 C+0 HETATM 58 O UNK 0 15.523 -1.437 0.000 0.00 0.00 O+0 HETATM 59 C UNK 0 13.197 0.202 0.000 0.00 0.00 C+0 HETATM 60 C UNK 0 13.858 1.703 0.000 0.00 0.00 C+0 HETATM 61 O UNK 0 15.400 2.162 0.000 0.00 0.00 O+0 HETATM 62 C UNK 0 15.828 3.739 0.000 0.00 0.00 C+0 HETATM 63 O UNK 0 13.050 3.142 0.000 0.00 0.00 O+0 HETATM 64 C UNK 0 11.690 -0.116 0.000 0.00 0.00 C+0 HETATM 65 C UNK 0 11.527 -1.647 0.000 0.00 0.00 C+0 HETATM 66 N UNK 0 10.494 -2.790 0.000 0.00 0.00 N+0 CONECT 1 2 CONECT 2 1 3 CONECT 3 2 4 50 CONECT 4 3 5 6 CONECT 5 4 CONECT 6 4 7 51 CONECT 7 6 8 CONECT 8 7 9 38 CONECT 9 8 10 11 CONECT 10 9 CONECT 11 9 12 37 CONECT 12 11 13 CONECT 13 12 14 CONECT 14 13 15 16 CONECT 15 14 CONECT 16 14 17 CONECT 17 16 18 CONECT 18 17 19 CONECT 19 18 20 21 CONECT 20 19 CONECT 21 19 22 CONECT 22 21 23 CONECT 23 22 24 CONECT 24 23 25 26 CONECT 25 24 CONECT 26 24 27 CONECT 27 26 28 CONECT 28 27 29 CONECT 29 28 30 31 CONECT 30 29 CONECT 31 29 32 CONECT 32 31 33 CONECT 33 32 34 CONECT 34 33 35 36 CONECT 35 34 CONECT 36 34 CONECT 37 11 38 64 CONECT 38 37 39 8 CONECT 39 38 40 51 66 CONECT 40 39 41 48 CONECT 41 40 42 52 CONECT 42 41 43 45 CONECT 43 42 44 CONECT 44 43 CONECT 45 42 46 48 CONECT 46 45 47 CONECT 47 46 CONECT 48 45 40 49 CONECT 49 48 50 CONECT 50 49 3 51 CONECT 51 50 39 6 CONECT 52 41 53 CONECT 53 52 54 66 CONECT 54 53 55 56 CONECT 55 54 CONECT 56 54 57 65 CONECT 57 56 58 59 CONECT 58 57 CONECT 59 57 60 64 CONECT 60 59 61 63 CONECT 61 60 62 CONECT 62 61 CONECT 63 60 CONECT 64 59 37 65 CONECT 65 64 66 56 CONECT 66 65 39 53 MASTER 0 0 0 0 0 0 0 0 66 0 148 0 END SMILES for NP0339904 (geranylgeranyl-chlorophyll b)CCC1=C(C=O)C2=CC3=C(C=C)C(C)=C4C=C5C(C)C(CCC(=O)OCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C)C6=[NH]5[Mg]5(N34)N3C(=CC1=[NH]25)C(C)=C1C(=O)C(C(=O)OC)C6=C31 INCHI for NP0339904 (geranylgeranyl-chlorophyll b)InChI=1/C55H65N4O6.Mg/c1-12-38-35(8)42-27-43-36(9)40(23-24-48(61)65-26-25-34(7)22-16-21-33(6)20-15-19-32(5)18-14-17-31(3)4)52(58-43)50-51(55(63)64-11)54(62)49-37(10)44(59-53(49)50)28-46-39(13-2)41(30-60)47(57-46)29-45(38)56-42;/h12,17,19,21,25,27-30,36,40,51H,1,13-16,18,20,22-24,26H2,2-11H3,(H-,56,57,58,59,60,62);/q-1;/p+1 3D Structure for NP0339904 (geranylgeranyl-chlorophyll b) | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Synonyms | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Chemical Formula | C55H66MgN4O6 | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Average Mass | 903.4600 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Monoisotopic Mass | 902.48328 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||
| IUPAC Name | methyl 17-ethenyl-12-ethyl-13-formyl-8,18,22-trimethyl-6-oxo-23-{3-oxo-3-[(3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl)oxy]propyl}-2,25lambda5,26lambda5,27-tetraaza-1-magnesanonacyclo[12.11.1.1^{1,16}.0^{2,9}.0^{3,7}.0^{4,24}.0^{11,26}.0^{21,25}.0^{19,27}]heptacosa-3,7,9,11(26),12,14,16,18,20,24-decaene-5-carboxylate | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Traditional Name | methyl 17-ethenyl-12-ethyl-13-formyl-8,18,22-trimethyl-6-oxo-23-{3-oxo-3-[(3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl)oxy]propyl}-2,25lambda5,26lambda5,27-tetraaza-1-magnesanonacyclo[12.11.1.1^{1,16}.0^{2,9}.0^{3,7}.0^{4,24}.0^{11,26}.0^{21,25}.0^{19,27}]heptacosa-3,7,9,11(26),12,14,16,18,20,24-decaene-5-carboxylate | |||||||||||||||||||||||||||||||||||||||||||||||||||
| CAS Registry Number | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
| SMILES | CCC1=C(C=O)C2=CC3=C(C=C)C(C)=C4C=C5C(C)C(CCC(=O)OCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C)C6=[NH]5[Mg]5(N34)N3C(=CC1=[NH]25)C(C)=C1C(=O)C(C(=O)OC)C6=C31 | |||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Identifier | InChI=1/C55H65N4O6.Mg/c1-12-38-35(8)42-27-43-36(9)40(23-24-48(61)65-26-25-34(7)22-16-21-33(6)20-15-19-32(5)18-14-17-31(3)4)52(58-43)50-51(55(63)64-11)54(62)49-37(10)44(59-53(49)50)28-46-39(13-2)41(30-60)47(57-46)29-45(38)56-42;/h12,17,19,21,25,27-30,36,40,51H,1,13-16,18,20,22-24,26H2,2-11H3,(H-,56,57,58,59,60,62);/q-1;/p+1 | |||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Key | NRLHHMXVBPYZRX-UHFFFAOYNA-O | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Experimental Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Predicted Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chemical Shift Submissions | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Species | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Species of Origin | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Chemical Taxonomy | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Classification | Not classified | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Physical Properties | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| State | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Experimental Properties |
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| Predicted Properties |
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| External Links | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| 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 | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
| PDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
| ChEBI ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Good Scents ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
| References | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| General References | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
