PG(16:1(9Z)/28:1(9Z))
Mrv1652306231615392D
63 62 0 0 1 0 999 V2000
14.0374 -24.1595 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
13.3624 -24.5493 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
12.6871 -24.1595 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
14.7126 -24.5493 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
12.0120 -24.5493 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
12.8354 -25.3289 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
15.3878 -24.1595 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0
14.9979 -23.4844 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
15.7775 -24.8347 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
16.0628 -23.7697 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
16.7379 -24.1595 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
17.4131 -23.7697 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
18.0883 -24.1595 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
13.9501 -25.3586 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
18.7261 -23.7330 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
17.9894 -23.0847 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
16.8011 -23.0847 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
11.2975 -24.1369 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.2975 -23.3654 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
10.5834 -24.5500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.8693 -24.1369 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.1551 -24.5500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.4410 -24.1369 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.7268 -24.5500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.0127 -24.1369 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.2985 -24.5500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.5844 -24.1369 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.7594 -24.1369 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.0453 -24.5500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.3311 -24.1369 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6170 -24.5500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.9029 -24.1369 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.1887 -24.5500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.4745 -24.1369 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.1210 -25.7414 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.1210 -26.5128 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
11.4069 -25.3283 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.6928 -25.7414 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.9786 -25.3283 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.2645 -25.7414 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.5504 -25.3283 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.8362 -25.7414 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.1221 -25.3283 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.4079 -25.7414 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.6938 -25.3283 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.8688 -25.3283 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1546 -25.7414 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.4405 -25.3283 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.7264 -25.7414 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.0122 -25.3283 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.2981 -25.7414 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.5839 -25.3283 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.1302 -25.7414 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.8443 -25.3283 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.5585 -25.7414 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.2726 -25.3283 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.9867 -25.7414 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.7009 -25.3283 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.4150 -25.7414 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.1292 -25.3283 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.8433 -25.7414 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-6.5574 -25.3283 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.2716 -25.7414 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2 1 1 0 0 0 0
2 6 1 0 0 0 0
2 14 1 1 0 0 0
3 2 1 0 0 0 0
4 1 1 0 0 0 0
5 3 1 0 0 0 0
5 18 1 0 0 0 0
7 4 1 0 0 0 0
8 7 2 0 0 0 0
9 7 1 0 0 0 0
10 7 1 0 0 0 0
11 10 1 0 0 0 0
12 11 1 0 0 0 0
12 16 1 6 0 0 0
12 17 1 0 0 0 0
13 12 1 0 0 0 0
13 15 1 0 0 0 0
18 19 2 0 0 0 0
18 20 1 0 0 0 0
20 21 1 0 0 0 0
21 22 1 0 0 0 0
22 23 1 0 0 0 0
23 24 1 0 0 0 0
24 25 1 0 0 0 0
25 26 1 0 0 0 0
26 27 1 0 0 0 0
27 28 2 0 0 0 0
28 29 1 0 0 0 0
29 30 1 0 0 0 0
30 31 1 0 0 0 0
31 32 1 0 0 0 0
32 33 1 0 0 0 0
33 34 1 0 0 0 0
35 6 1 0 0 0 0
35 36 2 0 0 0 0
35 37 1 0 0 0 0
37 38 1 0 0 0 0
38 39 1 0 0 0 0
39 40 1 0 0 0 0
40 41 1 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
44 45 1 0 0 0 0
45 46 2 0 0 0 0
46 47 1 0 0 0 0
47 48 1 0 0 0 0
48 49 1 0 0 0 0
49 50 1 0 0 0 0
50 51 1 0 0 0 0
51 52 1 0 0 0 0
52 53 1 0 0 0 0
53 54 1 0 0 0 0
54 55 1 0 0 0 0
55 56 1 0 0 0 0
56 57 1 0 0 0 0
57 58 1 0 0 0 0
58 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
62 63 1 0 0 0 0
M END
> <DATABASE_ID>
MMDBc0046764
> <DATABASE_NAME>
MIME
> <SMILES>
[H][C@](O)(CO)COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCC\C=C/CCCCCC)OC(=O)CCCCCCCC\C=C/CCCCCCCCCCCCCCCCC
> <INCHI_IDENTIFIER>
InChI=1S/C50H95O10P/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-23-24-25-26-27-28-30-32-34-36-38-40-42-50(54)60-48(46-59-61(55,56)58-44-47(52)43-51)45-57-49(53)41-39-37-35-33-31-29-16-14-12-10-8-6-4-2/h14,16,26-27,47-48,51-52H,3-13,15,17-25,28-46H2,1-2H3,(H,55,56)/b16-14-,27-26-/t47-,48+/m0/s1
> <INCHI_KEY>
SNWROHSBROAGLG-OPZFMELOSA-N
> <FORMULA>
C50H95O10P
> <MOLECULAR_WEIGHT>
887.274
> <EXACT_MASS>
886.666286257
> <JCHEM_ACCEPTOR_COUNT>
6
> <JCHEM_ATOM_COUNT>
156
> <JCHEM_AVERAGE_POLARIZABILITY>
110.05526279039239
> <JCHEM_BIOAVAILABILITY>
0
> <JCHEM_DONOR_COUNT>
3
> <JCHEM_FORMAL_CHARGE>
0
> <JCHEM_GHOSE_FILTER>
0
> <JCHEM_IUPAC>
[(2S)-2,3-dihydroxypropoxy][(2R)-3-[(9Z)-hexadec-9-enoyloxy]-2-[(10Z)-octacos-10-enoyloxy]propoxy]phosphinic acid
> <ALOGPS_LOGP>
9.62
> <JCHEM_LOGP>
15.548032186
> <ALOGPS_LOGS>
-7.23
> <JCHEM_MDDR_LIKE_RULE>
0
> <JCHEM_NUMBER_OF_RINGS>
0
> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1
> <JCHEM_PKA>
13.641245576372423
> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8907737771908404
> <JCHEM_PKA_STRONGEST_BASIC>
-2.9689647678483633
> <JCHEM_POLAR_SURFACE_AREA>
148.82000000000002
> <JCHEM_REFRACTIVITY>
252.7541
> <JCHEM_ROTATABLE_BOND_COUNT>
50
> <JCHEM_RULE_OF_FIVE>
0
> <ALOGPS_SOLUBILITY>
5.17e-05 g/l
> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2,3-dihydroxypropoxy((2R)-3-[(9Z)-hexadec-9-enoyloxy]-2-[(10Z)-octacos-10-enoyloxy]propoxy)phosphinic acid
> <JCHEM_VEBER_RULE>
0
$$$$