NP-MRD: Showing NP-Card for 4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0³,⁸.0¹⁰,¹⁵]tritriacontan-33-yl 2-methylbut-2-enoate (NP0286306)

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Record Information

Version

2.0

Created at

2022-09-09 14:49:29 UTC

Updated at

2022-09-09 14:49:29 UTC

NP-MRD ID

NP0286306

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0³,⁸.0¹⁰,¹⁵]tritriacontan-33-yl 2-methylbut-2-enoate

Description

4,5,11,12-Tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0³,⁸.0¹⁰,¹⁵]Tritriacontan-33-yl 2-methylbut-2-enoate belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds. 4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0³,⁸.0¹⁰,¹⁵]tritriacontan-33-yl 2-methylbut-2-enoate is found in Ipomoea orizabensis. 4,5,11,12-Tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0³,⁸.0¹⁰,¹⁵]Tritriacontan-33-yl 2-methylbut-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171502592D          

 65 69  0  0  0  0            999 V2000
   14.7981    0.1252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2483   -0.4899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4407   -0.3213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8909   -0.9363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0833   -0.7677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5335   -1.3828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7913   -2.1665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2415   -2.7816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4993   -3.5653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9495   -4.1804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1419   -4.0118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8841   -3.2281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0765   -3.0595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8187   -2.2758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0112   -2.1072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7338   -0.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2836   -0.3589    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9458   -1.1549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6880   -0.3712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8804   -0.2026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3306   -0.8177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5230   -0.6491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2653    0.1346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4577    0.3032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1999    1.0869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9079   -0.3119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1003   -0.1433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1656   -1.0956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6158   -1.7106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9732   -1.2642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2310   -2.0479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6227    0.5811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8151    0.7497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1725    1.1962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9800    1.0276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5299    1.6427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3374    1.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8873    2.0892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6295    2.8729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0443    1.9401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2447    2.5356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9722    0.7874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7798    0.6188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3296    1.2339    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4224    0.1723    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9447    0.7100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7523    0.5414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7575    0.0941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4028    0.5218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5952    0.6904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9526    1.1369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6948    1.9206    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7602    0.9683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3100    1.5833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0180    0.1846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4682   -0.4305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7260   -1.2142    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2378    0.2439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0454    0.0753    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3032   -0.7084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7534   -1.3235    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1108   -0.8770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3686   -1.6607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1761   -1.8293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6606   -0.2619    0.0000 C   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
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 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  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 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
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 22 30  1  0  0  0  0
 30 31  1  0  0  0  0
 20 32  1  0  0  0  0
 32 33  1  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
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 37 46  1  0  0  0  0
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 47 48  1  0  0  0  0
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 49 50  1  0  0  0  0
 49 51  1  0  0  0  0
 51 52  1  0  0  0  0
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 53 54  1  0  0  0  0
 53 55  1  0  0  0  0
 55 56  1  0  0  0  0
 48 56  1  0  0  0  0
 56 57  1  0  0  0  0
  6 57  1  0  0  0  0
 35 58  1  0  0  0  0
 19 58  1  0  0  0  0
 58 59  1  0  0  0  0
 59 60  1  0  0  0  0
 60 61  2  0  0  0  0
 60 62  1  0  0  0  0
 62 63  2  0  0  0  0
 63 64  1  4  0  0  0
 62 65  1  0  0  0  0
M  END

     RDKit          3D

141145  0  0  0  0  0  0  0  0999 V2000
    1.3106    0.9004    5.7288 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5380    0.0702    5.6509 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9977   -0.4137    4.5198 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2323   -1.2334    4.5360 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3053   -0.1485    3.2704 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2568    0.5391    3.1998 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8044   -0.6640    2.1043 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2028   -0.4640    0.8226 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9732   -1.7754    0.1012 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7988   -1.9257   -1.0078 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1411   -1.8553   -0.7176 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5697   -3.1113    0.0205 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5105   -0.6040    0.0766 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5380    0.1059   -0.4880 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.7684    3.7453   -0.5041 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.5803   -5.1358   -1.0815 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7284   -6.1331   -2.2104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7006   -6.0578   -3.1198 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3460   -6.5473   -0.8247 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004171502592D          

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M  END
> <DATABASE_ID>
NP0286306

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC1CCCCCCCCCC(=O)OC2C(OC3OC(C)C(O)C(O)C3O)C(C)OC(OC3C(O)C(O)C(CO)OC3OC3C(O)C(O)C(C)OC3O1)C2OC(=O)C(C)=CC

> <INCHI_IDENTIFIER>
InChI=1S/C45H76O20/c1-7-9-15-18-26-19-16-13-11-10-12-14-17-20-28(47)61-39-36(63-42-35(54)32(51)29(48)23(4)56-42)25(6)58-45(40(39)62-41(55)22(3)8-2)65-38-34(53)31(50)27(21-46)60-44(38)64-37-33(52)30(49)24(5)57-43(37)59-26/h8,23-27,29-40,42-46,48-54H,7,9-21H2,1-6H3

> <INCHI_KEY>
MDEMDKARDFUEHH-UHFFFAOYSA-N

> <FORMULA>
C45H76O20

> <MOLECULAR_WEIGHT>
937.083

> <EXACT_MASS>
936.492994847

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_ATOM_COUNT>
141

> <JCHEM_AVERAGE_POLARIZABILITY>
99.01798155761429

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0³,⁸.0¹⁰,¹⁵]tritriacontan-33-yl 2-methylbut-2-enoate

> <ALOGPS_LOGP>
1.92

> <JCHEM_LOGP>
3.804659927333332

> <ALOGPS_LOGS>
-3.27

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.519903217969453

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.012580245069659

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981083802044763

> <JCHEM_POLAR_SURFACE_AREA>
288.28

> <JCHEM_REFRACTIVITY>
224.1128000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.98e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0³,⁸.0¹⁰,¹⁵]tritriacontan-33-yl 2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      27.623   0.234   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      26.597  -0.914   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      25.089  -0.600   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      24.063  -1.748   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      22.556  -1.433   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      21.529  -2.581   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      22.010  -4.044   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      20.984  -5.192   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      21.465  -6.655   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      20.439  -7.803   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      18.932  -7.489   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      18.450  -6.026   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      16.943  -5.711   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      16.462  -4.248   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.954  -3.933   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.436  -1.818   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      15.463  -0.670   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      12.965  -2.156   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      12.484  -0.693   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.977  -0.378   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.950  -1.526   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.443  -1.212   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       7.962   0.251   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.454   0.566   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.973   2.029   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.428  -0.582   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       3.921  -0.267   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       5.909  -2.045   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.883  -3.193   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       7.417  -2.360   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       7.898  -3.823   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      10.496   1.085   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.988   1.399   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      11.522   2.233   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      13.029   1.918   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      14.056   3.066   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      15.563   2.752   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      16.590   3.900   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      16.108   5.363   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      18.749   3.622   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      19.123   4.733   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      18.615   1.470   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      20.122   1.155   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      21.149   2.303   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0      17.588   0.322   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      16.697   1.325   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      18.204   1.011   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      18.214   0.176   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      17.552   0.974   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      16.044   1.289   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0      18.578   2.122   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      18.097   3.585   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0      20.086   1.807   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      21.112   2.956   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0      20.567   0.345   0.000  0.00  0.00           O+0
HETATM   56  C   UNK     0      19.541  -0.804   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0      20.022  -2.267   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0      13.511   0.455   0.000  0.00  0.00           C+0
HETATM   59  O   UNK     0      15.018   0.141   0.000  0.00  0.00           O+0
HETATM   60  C   UNK     0      15.499  -1.322   0.000  0.00  0.00           C+0
HETATM   61  O   UNK     0      14.473  -2.471   0.000  0.00  0.00           O+0
HETATM   62  C   UNK     0      17.007  -1.637   0.000  0.00  0.00           C+0
HETATM   63  C   UNK     0      17.488  -3.100   0.000  0.00  0.00           C+0
HETATM   64  C   UNK     0      18.995  -3.415   0.000  0.00  0.00           C+0
HETATM   65  C   UNK     0      18.033  -0.489   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   57                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   58                                                  
CONECT   20   19   21   32                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   30                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   22   31                                                  
CONECT   31   30                                                            
CONECT   32   20   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36   58                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   46                                                  
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43   45                                                  
CONECT   43   42   44                                                       
CONECT   44   43                                                            
CONECT   45   42   46                                                       
CONECT   46   45   37   47                                                  
CONECT   47   46   48                                                       
CONECT   48   47   49   56                                                  
CONECT   49   48   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49   52   53                                                  
CONECT   52   51                                                            
CONECT   53   51   54   55                                                  
CONECT   54   53                                                            
CONECT   55   53   56                                                       
CONECT   56   55   48   57                                                  
CONECT   57   56    6                                                       
CONECT   58   35   19   59                                                  
CONECT   59   58   60                                                       
CONECT   60   59   61   62                                                  
CONECT   61   60                                                            
CONECT   62   60   63   65                                                  
CONECT   63   62   64                                                       
CONECT   64   63                                                            
CONECT   65   62                                                            
MASTER        0    0    0    0    0    0    0    0   65    0  138    0
END

View in JSmol

Synonyms

Value	Source
4,5,11,12-Tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0,.0,]tritriacontan-33-yl 2-methylbut-2-enoic acid	Generator
4,5,11,12-Tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0³,⁸.0¹⁰,¹⁵]tritriacontan-33-yl 2-methylbut-2-enoic acid	Generator

Chemical Formula

C₄₅H₇₆O₂₀

Average Mass

937.0830 Da

Monoisotopic Mass

936.49299 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CCCCCC1CCCCCCCCCC(=O)OC2C(OC3OC(C)C(O)C(O)C3O)C(C)OC(OC3C(O)C(O)C(CO)OC3OC3C(O)C(O)C(C)OC3O1)C2OC(=O)C(C)=CC

InChI Identifier

InChI=1S/C45H76O20/c1-7-9-15-18-26-19-16-13-11-10-12-14-17-20-28(47)61-39-36(63-42-35(54)32(51)29(48)23(4)56-42)25(6)58-45(40(39)62-41(55)22(3)8-2)65-38-34(53)31(50)27(21-46)60-44(38)64-37-33(52)30(49)24(5)57-43(37)59-26/h8,23-27,29-40,42-46,48-54H,7,9-21H2,1-6H3

InChI Key

MDEMDKARDFUEHH-UHFFFAOYSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Ipomoea orizabensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Oligosaccharides

Alternative Parents

Substituents

Oligosaccharide
Fatty acyl glycoside
Macrolide
Alkyl glycoside
Glycosyl compound
O-glycosyl compound
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Oxane
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Secondary alcohol
Lactone
Carboxylic acid ester
Acetal
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Polyol
Alcohol
Hydrocarbon derivative
Carbonyl group
Organic oxide
Primary alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	1.92	ALOGPS
logP	3.8	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	12.01	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	288.28 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	224.11 m³·mol⁻¹	ChemAxon
Polarizability	99.02 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

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

74392116

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0³,⁸.0¹⁰,¹⁵]tritriacontan-33-yl 2-methylbut-2-enoate (NP0286306)

MOL for NP0286306 (4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0³,⁸.0¹⁰,¹⁵]tritriacontan-33-yl 2-methylbut-2-enoate)

3D MOL for NP0286306 (4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0³,⁸.0¹⁰,¹⁵]tritriacontan-33-yl 2-methylbut-2-enoate)

3D SDF for NP0286306 (4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0³,⁸.0¹⁰,¹⁵]tritriacontan-33-yl 2-methylbut-2-enoate)

3D-SDF for NP0286306 (4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0³,⁸.0¹⁰,¹⁵]tritriacontan-33-yl 2-methylbut-2-enoate)

PDB for NP0286306 (4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0³,⁸.0¹⁰,¹⁵]tritriacontan-33-yl 2-methylbut-2-enoate)

3D PDB for NP0286306 (4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0³,⁸.0¹⁰,¹⁵]tritriacontan-33-yl 2-methylbut-2-enoate)

SMILES for NP0286306 (4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0³,⁸.0¹⁰,¹⁵]tritriacontan-33-yl 2-methylbut-2-enoate)

INCHI for NP0286306 (4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0³,⁸.0¹⁰,¹⁵]tritriacontan-33-yl 2-methylbut-2-enoate)

Structure for NP0286306 (4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0³,⁸.0¹⁰,¹⁵]tritriacontan-33-yl 2-methylbut-2-enoate)

3D Structure for NP0286306 (4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.0³,⁸.0¹⁰,¹⁵]tritriacontan-33-yl 2-methylbut-2-enoate)