MiMeDB: Showing metabocard for 2-hydroxyanhydroaplysiatoxin (MMDBc0025580)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 15:19:25 UTC

Update Date

2022-08-31 06:50:44 UTC

Metabolite ID

MMDBc0025580

Metabolite Identification

Common Name

2-hydroxyanhydroaplysiatoxin

Description

2-hydroxyanhydroaplysiatoxin belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. Based on a literature review very few articles have been published on 2-hydroxyanhydroaplysiatoxin.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152117192D          

 51 54  0  0  1  0            999 V2000
    3.9189    6.0701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8310    3.4704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6817    3.9209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6711   -0.5392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2212    5.3132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2304    5.0131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4439    6.0701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6814    5.3556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2064    2.4978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0314    2.4978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2689    4.6412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2064    3.9267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2105    0.9680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7399    4.4064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7736    3.2516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5064    5.3556    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0200    3.6215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5067    3.9260    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9785   -0.0910    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2061    3.2122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0314    3.9267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4439    3.2122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4439    4.6412    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0204    0.7330    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9304    3.2114    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6523    1.6034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7662    2.1812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9189    4.6412    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4745    2.9883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5095    1.3771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9120    4.5483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2831    3.9530    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2689    3.2122    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.2440   -0.4667    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0311    3.2122    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8899    1.2880    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5910    2.1968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1808    0.8975    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0314    5.3556    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5989    2.4385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8453    0.8838    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7645    4.6406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6641    3.1895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0939    6.0701    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1005    3.2079    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7130    0.2847    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8564    3.9267    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0623    1.5569    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3215    3.9378    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9413    2.1656    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0939    4.6409    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  2  0  0  0  0
 11  8  1  0  0  0  0
 16  1  1  6  0  0  0
 16  8  1  0  0  0  0
 17  2  1  0  0  0  0
 17 14  1  0  0  0  0
 18  3  1  6  0  0  0
 19  4  1  0  0  0  0
 20  9  1  0  0  0  0
 20 12  2  0  0  0  0
 21 12  1  0  0  0  0
 22 10  1  0  0  0  0
 22 21  2  0  0  0  0
 23 11  1  0  0  0  0
 23 21  1  0  0  0  0
 24 13  1  0  0  0  0
 24 19  1  6  0  0  0
 25 15  1  0  0  0  0
 25 18  1  0  0  0  0
 26 13  1  0  0  0  0
 28 16  1  1  0  0  0
 28 18  1  0  0  0  0
 29 17  2  0  0  0  0
 29 27  1  0  0  0  0
 30 27  1  0  0  0  0
 31  5  1  0  0  0  0
 31  6  1  0  0  0  0
 31 14  1  0  0  0  0
 32 15  1  1  0  0  0
 32 31  1  0  0  0  0
 33 22  1  0  0  0  0
 19 34  1  6  0  0  0
 35 20  1  0  0  0  0
 36 26  2  0  0  0  0
 37 27  1  0  0  0  0
 38 30  2  0  0  0  0
 39  7  1  0  0  0  0
 23 39  1  6  0  0  0
 40 25  1  0  0  0  0
 40 26  1  0  0  0  0
 41 24  1  0  0  0  0
 41 30  1  0  0  0  0
 42 28  1  0  0  0  0
 42 32  1  0  0  0  0
 43 29  1  0  0  0  0
 43 32  1  0  0  0  0
 16 44  1  1  0  0  0
 18 45  1  1  0  0  0
 19 46  1  6  0  0  0
 23 47  1  6  0  0  0
 24 48  1  6  0  0  0
 25 49  1  1  0  0  0
 50 27  1  0  0  0  0
 28 51  1  6  0  0  0
M  END


  Mrv1652305152117192D          

 51 54  0  0  1  0            999 V2000
    3.9189    6.0701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8310    3.4704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6817    3.9209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6711   -0.5392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2212    5.3132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2304    5.0131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4439    6.0701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6814    5.3556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2064    2.4978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0314    2.4978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2689    4.6412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2064    3.9267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2105    0.9680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7399    4.4064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7736    3.2516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5064    5.3556    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0200    3.6215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5067    3.9260    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9785   -0.0910    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2061    3.2122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0314    3.9267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4439    3.2122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4439    4.6412    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0204    0.7330    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9304    3.2114    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6523    1.6034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7662    2.1812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9189    4.6412    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4745    2.9883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5095    1.3771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9120    4.5483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2831    3.9530    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2689    3.2122    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.2440   -0.4667    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0311    3.2122    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8899    1.2880    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5910    2.1968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1808    0.8975    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0314    5.3556    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5989    2.4385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8453    0.8838    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7645    4.6406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6641    3.1895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0939    6.0701    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1005    3.2079    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7130    0.2847    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8564    3.9267    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0623    1.5569    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3215    3.9378    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9413    2.1656    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0939    4.6409    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  2  0  0  0  0
 11  8  1  0  0  0  0
 16  1  1  6  0  0  0
 16  8  1  0  0  0  0
 17  2  1  0  0  0  0
 17 14  1  0  0  0  0
 18  3  1  6  0  0  0
 19  4  1  0  0  0  0
 20  9  1  0  0  0  0
 20 12  2  0  0  0  0
 21 12  1  0  0  0  0
 22 10  1  0  0  0  0
 22 21  2  0  0  0  0
 23 11  1  0  0  0  0
 23 21  1  0  0  0  0
 24 13  1  0  0  0  0
 24 19  1  6  0  0  0
 25 15  1  0  0  0  0
 25 18  1  0  0  0  0
 26 13  1  0  0  0  0
 28 16  1  1  0  0  0
 28 18  1  0  0  0  0
 29 17  2  0  0  0  0
 29 27  1  0  0  0  0
 30 27  1  0  0  0  0
 31  5  1  0  0  0  0
 31  6  1  0  0  0  0
 31 14  1  0  0  0  0
 32 15  1  1  0  0  0
 32 31  1  0  0  0  0
 33 22  1  0  0  0  0
 19 34  1  6  0  0  0
 35 20  1  0  0  0  0
 36 26  2  0  0  0  0
 37 27  1  0  0  0  0
 38 30  2  0  0  0  0
 39  7  1  0  0  0  0
 23 39  1  6  0  0  0
 40 25  1  0  0  0  0
 40 26  1  0  0  0  0
 41 24  1  0  0  0  0
 41 30  1  0  0  0  0
 42 28  1  0  0  0  0
 42 32  1  0  0  0  0
 43 29  1  0  0  0  0
 43 32  1  0  0  0  0
 16 44  1  1  0  0  0
 18 45  1  1  0  0  0
 19 46  1  6  0  0  0
 23 47  1  6  0  0  0
 24 48  1  6  0  0  0
 25 49  1  1  0  0  0
 50 27  1  0  0  0  0
 28 51  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0025580

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@](C)(O)[C@@]1([H])CC(=O)O[C@@]2([H])C[C@@]3(OC(=C(C)CC3(C)C)C([H])(O)C(=O)O1)O[C@]([H])([C@@]([H])(C)CC[C@]([H])(OC)C1=C(Br)C=CC(O)=C1)[C@@]2([H])C

> <INCHI_IDENTIFIER>
InChI=1S/C32H45BrO10/c1-16(8-11-23(39-7)21-12-20(35)9-10-22(21)33)28-18(3)25-15-32(42-28)31(5,6)14-17(2)29(43-32)27(37)30(38)41-24(19(4)34)13-26(36)40-25/h9-10,12,16,18-19,23-25,27-28,34-35,37H,8,11,13-15H2,1-7H3/t16-,18-,19+,23-,24+,25-,27?,28+,32-/m0/s1

> <INCHI_KEY>
DPPGOCHFFSGODO-UIWMMILUSA-N

> <FORMULA>
C32H45BrO10

> <MOLECULAR_WEIGHT>
669.606

> <EXACT_MASS>
668.219611

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
88

> <JCHEM_AVERAGE_POLARIZABILITY>
65.83394097832971

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3R,4S,5S,9R)-3-[(2S,5S)-5-(2-bromo-5-hydroxyphenyl)-5-methoxypentan-2-yl]-12-hydroxy-9-[(1R)-1-hydroxyethyl]-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.1^{1,5}]octadec-13-ene-7,11-dione

> <ALOGPS_LOGP>
4.14

> <JCHEM_LOGP>
5.170218893666665

> <ALOGPS_LOGS>
-4.85

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.456759862208562

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.916841454486628

> <JCHEM_PKA_STRONGEST_BASIC>
-3.034345766122212

> <JCHEM_POLAR_SURFACE_AREA>
140.98000000000002

> <JCHEM_REFRACTIVITY>
160.83280000000008

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.48e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,4S,5S,9R)-3-[(2S,5S)-5-(2-bromo-5-hydroxyphenyl)-5-methoxypentan-2-yl]-12-hydroxy-9-[(1R)-1-hydroxyethyl]-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.1^{1,5}]octadec-13-ene-7,11-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0       7.315  11.331   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.618   6.478   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.006   7.319   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.586  -1.007   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.613   9.918   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.763   9.358   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.695  11.331   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.005   9.997   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.385   4.662   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.925   4.662   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.235   8.664   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.385   7.330   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.860   1.807   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.581   8.225   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.911   6.070   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.545   9.997   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.104   6.760   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.546   7.328   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.293  -0.170   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.385   5.996   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.925   7.330   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.695   5.996   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.695   8.664   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.371   1.368   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.337   5.995   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.818   2.993   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.630   4.072   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.315   8.664   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      12.086   5.578   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      12.151   2.571   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      11.036   8.490   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.862   7.379   0.000  0.00  0.00           C+0
HETATM   33 Br   UNK     0       4.235   5.996   0.000  0.00  0.00          Br+0
HETATM   34  O   UNK     0       7.922  -0.871   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      -1.925   5.996   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       5.395   2.404   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      14.170   4.101   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      13.404   1.675   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       1.925   9.997   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       6.718   4.552   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      10.911   1.650   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       8.894   8.662   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0      10.573   5.954   0.000  0.00  0.00           O+0
HETATM   44  H   UNK     0       5.775  11.331   0.000  0.00  0.00           H+0
HETATM   45  H   UNK     0       5.788   5.988   0.000  0.00  0.00           H+0
HETATM   46  H   UNK     0      10.664   0.531   0.000  0.00  0.00           H+0
HETATM   47  H   UNK     0       3.465   7.330   0.000  0.00  0.00           H+0
HETATM   48  H   UNK     0       9.450   2.906   0.000  0.00  0.00           H+0
HETATM   49  H   UNK     0       8.067   7.350   0.000  0.00  0.00           H+0
HETATM   50  H   UNK     0      11.090   4.042   0.000  0.00  0.00           H+0
HETATM   51  H   UNK     0       5.775   8.663   0.000  0.00  0.00           H+0
CONECT    1   16                                                            
CONECT    2   17                                                            
CONECT    3   18                                                            
CONECT    4   19                                                            
CONECT    5   31                                                            
CONECT    6   31                                                            
CONECT    7   39                                                            
CONECT    8   11   16                                                       
CONECT    9   10   20                                                       
CONECT   10    9   22                                                       
CONECT   11    8   23                                                       
CONECT   12   20   21                                                       
CONECT   13   24   26                                                       
CONECT   14   17   31                                                       
CONECT   15   25   32                                                       
CONECT   16    1    8   28   44                                             
CONECT   17    2   14   29                                                  
CONECT   18    3   25   28   45                                             
CONECT   19    4   24   34   46                                             
CONECT   20    9   12   35                                                  
CONECT   21   12   22   23                                                  
CONECT   22   10   21   33                                                  
CONECT   23   11   21   39   47                                             
CONECT   24   13   19   41   48                                             
CONECT   25   15   18   40   49                                             
CONECT   26   13   36   40                                                  
CONECT   27   29   30   37   50                                             
CONECT   28   16   18   42   51                                             
CONECT   29   17   27   43                                                  
CONECT   30   27   38   41                                                  
CONECT   31    5    6   14   32                                             
CONECT   32   15   31   42   43                                             
CONECT   33   22                                                            
CONECT   34   19                                                            
CONECT   35   20                                                            
CONECT   36   26                                                            
CONECT   37   27                                                            
CONECT   38   30                                                            
CONECT   39    7   23                                                       
CONECT   40   25   26                                                       
CONECT   41   24   30                                                       
CONECT   42   28   32                                                       
CONECT   43   29   32                                                       
CONECT   44   16                                                            
CONECT   45   18                                                            
CONECT   46   19                                                            
CONECT   47   23                                                            
CONECT   48   24                                                            
CONECT   49   25                                                            
CONECT   50   27                                                            
CONECT   51   28                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  108    0
END

Synonyms

Not Available

Molecular Formula

C₃₂H₄₅BrO₁₀

Average Mass

669.606

Monoisotopic Mass

668.219611

IUPAC Name

(1S,3R,4S,5S,9R)-3-[(2S,5S)-5-(2-bromo-5-hydroxyphenyl)-5-methoxypentan-2-yl]-12-hydroxy-9-[(1R)-1-hydroxyethyl]-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.1^{1,5}]octadec-13-ene-7,11-dione

Traditional Name

CAS Registry Number

Not Available

SMILES

[H][C@](C)(O)[C@@]1([H])CC(=O)O[C@@]2([H])C[C@@]3(OC(=C(C)CC3(C)C)C([H])(O)C(=O)O1)O[C@]([H])([C@@]([H])(C)CC[C@]([H])(OC)C1=C(Br)C=CC(O)=C1)[C@@]2([H])C

InChI Identifier

InChI=1S/C32H45BrO10/c1-16(8-11-23(39-7)21-12-20(35)9-10-22(21)33)28-18(3)25-15-32(42-28)31(5,6)14-17(2)29(43-32)27(37)30(38)41-24(19(4)34)13-26(36)40-25/h9-10,12,16,18-19,23-25,27-28,34-35,37H,8,11,13-15H2,1-7H3/t16-,18-,19+,23-,24+,25-,27?,28+,32-/m0/s1

InChI Key

DPPGOCHFFSGODO-UIWMMILUSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Benzylether
4-bromophenol
4-halophenol
1-hydroxy-2-unsubstituted benzenoid
Ketal
Phenol
Halobenzene
Bromobenzene
Benzenoid
Oxane
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Aryl halide
Aryl bromide
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organobromide
Organohalogen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.0095 g/L	ALOGPS
logP	4.14	ALOGPS
logP	5.17	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	8.92	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	140.98 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	160.83 m³·mol⁻¹	ChemAxon
Polarizability	65.83 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Not Available

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria	Cyanobacteria	1	Human feces	Metabolic reconstruction

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

73930324

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

146682205

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for 2-hydroxyanhydroaplysiatoxin (MMDBc0025580)

MOL for #<Metabolite:0x00007f469879d3b8>

3D MOL for #<Metabolite:0x00007f469879d3b8>

3D SDF for #<Metabolite:0x00007f469879d3b8>

3D-SDF for #<Metabolite:0x00007f469879d3b8>

PDB for #<Metabolite:0x00007f469879d3b8>

3D PDB for #<Metabolite:0x00007f469879d3b8>

SMILES for #<Metabolite:0x00007f469879d3b8>

INCHI for #<Metabolite:0x00007f469879d3b8>

Structure for #<Metabolite:0x00007f469879d3b8>

3D Structure for #<Metabolite:0x00007f469879d3b8>