NP-MRD: Showing NP-Card for Acanthacerebroside B (NP0072696)

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Record Information

Version

2.0

Created at

2022-04-28 18:00:21 UTC

Updated at

2022-04-28 18:00:21 UTC

NP-MRD ID

NP0072696

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Acanthacerebroside B

Description

Acanthacerebroside B belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol. Acanthacerebroside B is found in Acanthaster planci, Patiria pectinifera, Astropecten latespinosus and Luidia maculata. Acanthacerebroside B was first documented in 2002 (PMID: 12192142). Based on a literature review very few articles have been published on Acanthacerebroside B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282220002D          

 55 55  0  0  1  0            999 V2000
   19.2907   -4.5375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   20.0052   -4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   20.0052   -5.7750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   19.2907   -6.1875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.5762   -5.7750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.5762   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.8618   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.1473   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.4328   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   -2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   21.4341   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.7223   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.4367   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.1512   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.8657   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.5801   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.2946   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.0091   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197   -1.2375    0.0000 O   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  1  0  0  0
  7  8  1  0  0  0  0
  4  9  1  6  0  0  0
  3 10  1  1  0  0  0
  2 11  1  6  0  0  0
  1 12  1  1  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
 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  1  0  0  0  0
 16 29  1  6  0  0  0
 15 30  1  1  0  0  0
 14 31  1  1  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 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  1  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
 34 55  1  6  0  0  0
M  END

     RDKit          3D

142142  0  0  0  0  0  0  0  0999 V2000
   14.9711    1.1288   -2.9514 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5812    1.5055   -1.5347 C   0  0  0  0  0  0  0  0  0  0  0  0
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   13.0560   -0.4254   -1.3000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7981    0.4791   -1.3730 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6809   -0.3112   -1.9570 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3786    0.2587   -2.2399 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5151    0.8876   -1.1961 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9869    2.1587   -0.6181 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1240    2.7725    0.4475 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9421    2.0857    1.7063 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3345    0.8252    2.0279 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8839    0.6143    1.8302 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3476    0.7181    0.4713 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8884    0.5344    0.2754 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2673   -0.7599    0.5161 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2922   -1.4397    1.8142 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7838   -0.7888    3.0085 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4216   -0.3615    3.2873 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3388   -1.3266    3.4296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1935   -2.1032    2.2974 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2068   -2.9835    2.8686 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0355   -1.1321    1.4430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4189   -0.6486    0.5100 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3401   -0.9231    1.8166 N   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.3215    1.8151   -1.7183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1823    0.5915   -2.5679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4184    0.1056   -3.2125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5817   -0.3997   -2.5144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3200    0.4323   -1.5341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5596   -0.3256   -1.0422 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.4696   -2.6993    1.7582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2868   -3.6959    2.1950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6312   -1.5508    2.7346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6277   -0.4914    0.2946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3661    0.1727    3.2645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4032    0.4269    1.8677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8414   -1.6144    0.6115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8666   -2.8433    1.0361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7253   -4.6911    3.1686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2170   -3.5953    3.1243 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.4706   -5.2990    0.7745 H   0  0  0  0  0  0  0  0  0  0  0  0
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 55142  1  0
M  END


  Mrv1652304282220002D          

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  2  3  1  0  0  0  0
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  4  9  1  6  0  0  0
  3 10  1  1  0  0  0
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 12 13  1  0  0  0  0
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 27 28  1  0  0  0  0
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 31 32  1  0  0  0  0
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 35 36  1  0  0  0  0
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 41 42  1  0  0  0  0
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 49 50  1  0  0  0  0
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 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 34 55  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0072696

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCCCCCC[C@@H](O)C(=O)N[C@@H](CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)[C@H](O)[C@H](O)CCCCCCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C44H87NO10/c1-3-5-7-9-11-13-15-16-17-18-19-20-21-22-24-26-28-30-32-37(48)43(53)45-35(34-54-44-42(52)41(51)40(50)38(33-46)55-44)39(49)36(47)31-29-27-25-23-14-12-10-8-6-4-2/h35-42,44,46-52H,3-34H2,1-2H3,(H,45,53)/t35-,36+,37+,38+,39-,40+,41-,42+,44+/m0/s1

> <INCHI_KEY>
KQYMTELMIRHEAQ-GDGDGXLOSA-N

> <FORMULA>
C44H87NO10

> <MOLECULAR_WEIGHT>
790.177

> <EXACT_MASS>
789.632998005

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
142

> <JCHEM_AVERAGE_POLARIZABILITY>
100.29009091743934

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R)-N-[(2S,3S,4R)-3,4-dihydroxy-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hexadecan-2-yl]-2-hydroxydocosanamide

> <ALOGPS_LOGP>
6.82

> <JCHEM_LOGP>
9.132838826999999

> <ALOGPS_LOGS>
-5.49

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.614174299024175

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.045026491109326

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810834177580157

> <JCHEM_POLAR_SURFACE_AREA>
189.17

> <JCHEM_REFRACTIVITY>
218.48409999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
38

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.56e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-N-[(2S,3S,4R)-3,4-dihydroxy-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hexadecan-2-yl]-2-hydroxydocosanamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      36.009  -8.470   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      37.343  -9.240   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      37.343 -10.780   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      36.009 -11.550   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      34.676 -10.780   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      34.676  -9.240   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      33.342 -11.550   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      32.008 -10.780   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      36.009 -13.090   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      38.677 -11.550   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      38.677  -8.470   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      36.009  -6.930   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      34.676  -6.160   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      34.676  -4.620   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      33.342  -3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      32.008  -4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      30.675  -3.850   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      29.341  -4.620   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      28.007  -3.850   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      26.674  -4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      25.340  -3.850   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      24.006  -4.620   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      22.673  -3.850   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      21.339  -4.620   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      20.005  -3.850   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      18.672  -4.620   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      17.338  -3.850   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      16.004  -4.620   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      32.008  -6.160   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      33.342  -2.310   0.000  0.00  0.00           O+0
HETATM   31  N   UNK     0      36.009  -3.850   0.000  0.00  0.00           N+0
HETATM   32  C   UNK     0      37.343  -4.620   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      37.343  -6.160   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      38.677  -3.850   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      40.010  -4.620   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      41.344  -3.850   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      42.678  -4.620   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      44.011  -3.850   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      45.345  -4.620   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      46.679  -3.850   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      48.012  -4.620   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      49.346  -3.850   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      50.680  -4.620   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      52.013  -3.850   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      53.347  -4.620   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      54.681  -3.850   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      56.015  -4.620   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      57.348  -3.850   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      58.682  -4.620   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      60.016  -3.850   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      61.349  -4.620   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      62.683  -3.850   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      64.017  -4.620   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      65.350  -3.850   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0      38.677  -2.310   0.000  0.00  0.00           O+0
CONECT    1    2    6   12                                                  
CONECT    2    1    3   11                                                  
CONECT    3    2    4   10                                                  
CONECT    4    3    5    9                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7                                                            
CONECT    9    4                                                            
CONECT   10    3                                                            
CONECT   11    2                                                            
CONECT   12    1   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   31                                                  
CONECT   15   14   16   30                                                  
CONECT   16   15   17   29                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   16                                                            
CONECT   30   15                                                            
CONECT   31   14   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   55                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52   54                                                       
CONECT   54   53                                                            
CONECT   55   34                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  110    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₄H₈₇NO₁₀

Average Mass

790.1770 Da

Monoisotopic Mass

789.63300 Da

IUPAC Name

(2R)-N-[(2S,3S,4R)-3,4-dihydroxy-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hexadecan-2-yl]-2-hydroxydocosanamide

Traditional Name

(2R)-N-[(2S,3S,4R)-3,4-dihydroxy-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hexadecan-2-yl]-2-hydroxydocosanamide

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCCCCC[C@@H](O)C(=O)N[C@@H](CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)[C@H](O)[C@H](O)CCCCCCCCCCCC

InChI Identifier

InChI=1S/C44H87NO10/c1-3-5-7-9-11-13-15-16-17-18-19-20-21-22-24-26-28-30-32-37(48)43(53)45-35(34-54-44-42(52)41(51)40(50)38(33-46)55-44)39(49)36(47)31-29-27-25-23-14-12-10-8-6-4-2/h35-42,44,46-52H,3-34H2,1-2H3,(H,45,53)/t35-,36+,37+,38+,39-,40+,41-,42+,44+/m0/s1

InChI Key

KQYMTELMIRHEAQ-GDGDGXLOSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Acanthaster planci	LOTUS Database	35616633
Asterina pectinifera	LOTUS Database	35616633
Astropecten latespinosus	LOTUS Database	35616633
Luidia maculata	Animalia	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl glycosides

Direct Parent

Fatty acyl glycosides of mono- and disaccharides

Alternative Parents

Substituents

Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Fatty amide
Monosaccharide
N-acyl-amine
Oxane
Carboxamide group
Secondary carboxylic acid amide
Secondary alcohol
Acetal
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Polyol
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Alcohol
Organic oxygen compound
Organic nitrogen compound
Primary alcohol
Carbonyl group
Organonitrogen compound
Organooxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	6.82	ALOGPS
logP	9.13	ChemAxon
logS	-5.5	ALOGPS
pKa (Strongest Acidic)	12.05	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	189.17 Å²	ChemAxon
Rotatable Bond Count	38	ChemAxon
Refractivity	218.48 m³·mol⁻¹	ChemAxon
Polarizability	100.29 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00032693

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

101188275

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Kawatake S, Nakamura K, Inagaki M, Higuchi R: Isolation and structure determination of six glucocerebrosides from the starfish Luidia maculata. Chem Pharm Bull (Tokyo). 2002 Aug;50(8):1091-6. doi: 10.1248/cpb.50.1091. [PubMed:12192142 ]

Showing NP-Card for Acanthacerebroside B (NP0072696)

MOL for NP0072696 (Acanthacerebroside B)

3D MOL for NP0072696 (Acanthacerebroside B)

3D SDF for NP0072696 (Acanthacerebroside B)

3D-SDF for NP0072696 (Acanthacerebroside B)

PDB for NP0072696 (Acanthacerebroside B)

3D PDB for NP0072696 (Acanthacerebroside B)

SMILES for NP0072696 (Acanthacerebroside B)

INCHI for NP0072696 (Acanthacerebroside B)

Structure for NP0072696 (Acanthacerebroside B)

3D Structure for NP0072696 (Acanthacerebroside B)