Mrv1652306172222012D
36 39 0 0 1 0 999 V2000
0.7294 -0.4466 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9055 0.6018 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.3895 0.1997 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.3987 0.4304 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.6955 1.7614 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.3784 2.2244 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.9051 -0.2209 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.5297 0.8922 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.7176 0.7470 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.2782 2.2989 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9343 2.7844 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.0934 0.4566 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.4185 0.3176 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
4.4661 2.1537 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8100 1.6682 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.9249 0.9689 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
2.0297 1.7180 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
3.3737 1.2325 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
3.1221 2.6391 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
2.2812 0.3114 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
-1.7223 -0.1081 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.8418 1.8632 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
4.1858 1.3777 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
1.7494 0.9421 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0
6.6221 1.8134 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.5903 3.2699 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.0009 -0.4646 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.2287 -0.7594 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.0332 0.6561 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
-0.0879 -0.3338 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
0.1146 1.1244 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
2.2274 2.5190 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
3.6540 2.0084 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
3.4024 3.4151 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
2.5615 1.0873 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
2.9871 1.0511 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
6 5 1 0 0 0 0
7 4 1 0 0 0 0
9 8 1 0 0 0 0
13 1 1 6 0 0 0
13 4 1 0 0 0 0
14 10 2 0 0 0 0
14 11 1 0 0 0 0
15 8 1 0 0 0 0
15 10 1 0 0 0 0
16 5 1 0 0 0 0
16 13 1 1 0 0 0
17 6 1 0 0 0 0
18 12 1 0 0 0 0
19 11 1 0 0 0 0
20 12 1 0 0 0 0
21 7 1 0 0 0 0
22 17 1 0 0 0 0
22 18 1 0 0 0 0
22 19 1 0 0 0 0
23 2 1 1 0 0 0
23 9 1 0 0 0 0
23 14 1 0 0 0 0
23 18 1 0 0 0 0
24 3 1 1 0 0 0
24 16 1 0 0 0 0
24 17 1 0 0 0 0
24 20 1 0 0 0 0
25 15 2 0 0 0 0
19 26 1 6 0 0 0
20 27 1 1 0 0 0
28 21 2 0 0 0 0
29 21 1 0 0 0 0
13 30 1 1 0 0 0
16 31 1 6 0 0 0
17 32 1 6 0 0 0
18 33 1 6 0 0 0
19 34 1 1 0 0 0
20 35 1 1 0 0 0
22 36 1 1 0 0 0
M CHG 1 29 -1
M END
> <DATABASE_ID>
MMDBc0055641
> <DATABASE_NAME>
MIME
> <SMILES>
[H][C@@](C)(CCC([O-])=O)[C@@]1([H])CC[C@@]2([H])[C@]3([H])[C@]([H])(O)CC4=CC(=O)CC[C@]4(C)[C@@]3([H])C[C@]([H])(O)[C@]12C
> <INCHI_IDENTIFIER>
InChI=1S/C24H36O5/c1-13(4-7-21(28)29)16-5-6-17-22-18(12-20(27)24(16,17)3)23(2)9-8-15(25)10-14(23)11-19(22)26/h10,13,16-20,22,26-27H,4-9,11-12H2,1-3H3,(H,28,29)/p-1/t13-,16-,17+,18+,19-,20+,22+,23+,24-/m1/s1
> <INCHI_KEY>
ZZUMXQCSMJCDDC-DFQOQHGMSA-M
> <FORMULA>
C24H35O5
> <MOLECULAR_WEIGHT>
403.54
> <EXACT_MASS>
403.248997807
> <JCHEM_ACCEPTOR_COUNT>
5
> <JCHEM_ATOM_COUNT>
64
> <JCHEM_AVERAGE_POLARIZABILITY>
45.627750644368334
> <JCHEM_BIOAVAILABILITY>
1
> <JCHEM_DONOR_COUNT>
2
> <JCHEM_FORMAL_CHARGE>
-1
> <JCHEM_GHOSE_FILTER>
1
> <JCHEM_IUPAC>
(4R)-4-[(1S,2R,9R,10R,11S,14R,15R,16S)-9,16-dihydroxy-2,15-dimethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-en-14-yl]pentanoate
> <JCHEM_LOGP>
2.6441609233333345
> <JCHEM_MDDR_LIKE_RULE>
0
> <JCHEM_NUMBER_OF_RINGS>
4
> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1
> <JCHEM_PKA>
17.137674241562625
> <JCHEM_PKA_STRONGEST_ACIDIC>
4.475011880124207
> <JCHEM_PKA_STRONGEST_BASIC>
-0.182516353258798
> <JCHEM_POLAR_SURFACE_AREA>
97.66
> <JCHEM_REFRACTIVITY>
121.42499999999998
> <JCHEM_ROTATABLE_BOND_COUNT>
4
> <JCHEM_RULE_OF_FIVE>
1
> <JCHEM_TRADITIONAL_IUPAC>
(4R)-4-[(1S,2R,9R,10R,11S,14R,15R,16S)-9,16-dihydroxy-2,15-dimethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-en-14-yl]pentanoate
> <JCHEM_VEBER_RULE>
0
$$$$