NP-MRD: Showing NP-Card for 4-[(5-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxy-6-methyloxan-2-yl)oxy]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate (NP0146875)

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Record Information

Version

2.0

Created at

2022-09-02 02:21:37 UTC

Updated at

2022-09-02 02:21:37 UTC

NP-MRD ID

NP0146875

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-[(5-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxy-6-methyloxan-2-yl)oxy]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

Description

4-[(5-{[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxy-6-methyloxan-2-yl)oxy]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate belongs to the class of organic compounds known as beta carbolines. Beta carbolines are compounds containing a 9H-pyrido[3,4-b]indole moiety. 4-[(5-{[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxy-6-methyloxan-2-yl)oxy]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241504402D          

 55 59  0  0  0  0            999 V2000
   -3.0388   -6.5910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3744   -5.8374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8895   -5.1699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2250   -4.4163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7401   -3.7488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9196   -3.8351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4347   -3.1676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6142   -3.2538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1293   -2.5864    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6912   -2.6726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0267   -3.4263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8472   -3.5126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1828   -4.2662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6979   -4.9337    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3322   -2.8451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1526   -2.9314    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.9496   -3.9437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7701   -4.0300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1057   -4.7836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9261   -4.8699    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.9563   -6.2048    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.8003   -5.3649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9966   -2.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4815   -1.4240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1460   -0.6703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3255   -0.5841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9899    0.1696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1694    0.2558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4748    0.8370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1393    1.5907    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242    2.2581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4492    2.2581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7041    3.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367    3.5277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4847    4.1408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5887    4.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3338    4.9254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3693    3.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5846    3.2977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2953    0.7508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7802    1.4182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6309   -0.0029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4514   -0.0891    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1761   -2.0052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8406   -1.2515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5841   -4.5887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0690   -5.2562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7334   -6.0098    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  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
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 19 17  1  4  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  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
 27 28  1  0  0  0  0
 26 29  2  0  0  0  0
 21 29  1  0  0  0  0
 15 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
 34 35  1  0  0  0  0
 34 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
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
 41 45  1  0  0  0  0
 38 45  1  0  0  0  0
 45 46  1  0  0  0  0
 36 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
 32 49  1  0  0  0  0
 49 50  1  0  0  0  0
 30 51  1  0  0  0  0
 10 51  1  0  0  0  0
 51 52  1  0  0  0  0
  6 53  1  0  0  0  0
 53 54  2  0  0  0  0
  3 54  1  0  0  0  0
 54 55  1  0  0  0  0
M  END

     RDKit          3D

103107  0  0  0  0  0  0  0  0999 V2000
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    5.4264    2.2640   -1.6453 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8558    2.1588   -0.4236 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0037    2.8720    0.1290 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7754    3.7220   -0.6308 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8600    4.4222   -0.0852 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.2644    1.8776   -3.8771 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.7065    0.8699    1.4266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7538   -4.1927    2.1538 H   0  0  0  0  0  0  0  0  0  0  0  0
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 46 95  1  0
 47 96  1  6
 48 97  1  0
 49 98  1  6
 50 99  1  0
 51100  1  1
 52101  1  0
 53102  1  0
 55103  1  0
M  END


  Mrv1533004241504402D          

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    2.4815   -1.4240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1460   -0.6703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3255   -0.5841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.1694    0.2558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4748    0.8370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1393    1.5907    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.4492    2.2581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7041    3.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367    3.5277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4847    4.1408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5887    4.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3338    4.9254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3693    3.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5846    3.2977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8406   -1.2515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5841   -4.5887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0690   -5.2562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7334   -6.0098    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  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
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 11 12  1  0  0  0  0
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 17 18  2  0  0  0  0
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 22 23  1  0  0  0  0
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 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 29  2  0  0  0  0
 21 29  1  0  0  0  0
 15 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
 34 35  1  0  0  0  0
 34 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
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
 41 45  1  0  0  0  0
 38 45  1  0  0  0  0
 45 46  1  0  0  0  0
 36 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
 32 49  1  0  0  0  0
 49 50  1  0  0  0  0
 30 51  1  0  0  0  0
 10 51  1  0  0  0  0
 51 52  1  0  0  0  0
  6 53  1  0  0  0  0
 53 54  2  0  0  0  0
  3 54  1  0  0  0  0
 54 55  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0146875

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(CCOC2OC(CO)C(OC(=O)C=CC3=CC=C(O)C(OC)=C3)C(OC3OC(C)C(OC4OCC(O)(CO)C4O)C(O)C3O)C2O)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C36H48O19/c1-17-29(54-35-32(45)36(46,15-38)16-50-35)26(42)27(43)34(51-17)55-31-28(44)33(49-11-10-19-5-8-22(47-2)21(40)12-19)52-24(14-37)30(31)53-25(41)9-6-18-4-7-20(39)23(13-18)48-3/h4-9,12-13,17,24,26-35,37-40,42-46H,10-11,14-16H2,1-3H3

> <INCHI_KEY>
VAKFQUUZNDZEHP-UHFFFAOYSA-N

> <FORMULA>
C36H48O19

> <MOLECULAR_WEIGHT>
784.761

> <EXACT_MASS>
784.278979326

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_ATOM_COUNT>
103

> <JCHEM_AVERAGE_POLARIZABILITY>
79.17116141730479

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-[(5-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxy-6-methyloxan-2-yl)oxy]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

> <ALOGPS_LOGP>
0.43

> <JCHEM_LOGP>
-0.16528558766666576

> <ALOGPS_LOGS>
-2.94

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.22756871125801

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.62404599478209

> <JCHEM_PKA_STRONGEST_BASIC>
-3.142379131333633

> <JCHEM_POLAR_SURFACE_AREA>
282.21

> <JCHEM_REFRACTIVITY>
184.0379000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.05e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-[(5-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxy-6-methyloxan-2-yl)oxy]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -5.672 -12.303   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -6.299 -10.896   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -5.394  -9.651   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.020  -8.244   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.115  -6.998   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.583  -7.159   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.678  -5.913   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.147  -6.074   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -0.241  -4.828   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.290  -4.989   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.917  -6.396   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.448  -6.557   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.075  -7.964   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.169  -9.210   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.353  -5.311   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.885  -5.472   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.511  -6.879   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.606  -8.125   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.043  -7.040   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.669  -8.447   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.201  -8.608   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.106  -7.362   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      12.638  -7.523   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      13.264  -8.929   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      14.795  -9.090   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      12.359 -10.175   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      12.985 -11.582   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      12.080 -12.828   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.827 -10.014   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.727  -3.904   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       4.632  -2.658   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       4.006  -1.251   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       2.474  -1.090   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       1.848   0.317   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       0.316   0.478   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       2.753   1.562   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       2.127   2.969   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       3.032   4.215   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       4.572   4.215   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       5.048   5.680   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       3.802   6.585   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       2.771   7.729   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       4.832   7.729   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       4.356   9.194   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       2.556   5.680   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       1.091   6.156   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       4.285   1.401   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       5.190   2.647   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0       4.911  -0.005   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0       6.443  -0.166   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0       2.195  -3.743   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0       1.569  -2.336   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0      -2.957  -8.566   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      -3.862  -9.812   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0      -3.236 -11.218   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   54                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   53                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   51                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12   16   30                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   29                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   29                                                  
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   26   21                                                       
CONECT   30   15   31   51                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   49                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   47                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39   45                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42   43   45                                             
CONECT   42   41                                                            
CONECT   43   41   44                                                       
CONECT   44   43                                                            
CONECT   45   41   38   46                                                  
CONECT   46   45                                                            
CONECT   47   36   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47   32   50                                                  
CONECT   50   49                                                            
CONECT   51   30   10   52                                                  
CONECT   52   51                                                            
CONECT   53    6   54                                                       
CONECT   54   53    3   55                                                  
CONECT   55   54                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  118    0
END

View in JSmol

Synonyms

Value	Source
4-[(5-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxy-6-methyloxan-2-yl)oxy]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoic acid	Generator

Chemical Formula

C₃₆H₄₈O₁₉

Average Mass

784.7610 Da

Monoisotopic Mass

784.27898 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC=C(CCOC2OC(CO)C(OC(=O)C=CC3=CC=C(O)C(OC)=C3)C(OC3OC(C)C(OC4OCC(O)(CO)C4O)C(O)C3O)C2O)C=C1O

InChI Identifier

InChI=1S/C36H48O19/c1-17-29(54-35-32(45)36(46,15-38)16-50-35)26(42)27(43)34(51-17)55-31-28(44)33(49-11-10-19-5-8-22(47-2)21(40)12-19)52-24(14-37)30(31)53-25(41)9-6-18-4-7-20(39)23(13-18)48-3/h4-9,12-13,17,24,26-35,37-40,42-46H,10-11,14-16H2,1-3H3

InChI Key

VAKFQUUZNDZEHP-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as beta carbolines. Beta carbolines are compounds containing a 9H-pyrido[3,4-b]indole moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Pyridoindoles

Direct Parent

Beta carbolines

Alternative Parents

Substituents

Beta-carboline
Carbazole
Quinolizidine
Dialkylarylamine
Aralkylamine
Piperidine
Benzenoid
Methyl ester
Cyclic alcohol
Amino acid or derivatives
Carboxylic acid ester
Tertiary aliphatic amine
Tertiary amine
Azacycle
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Alkanolamine
Organopnictogen compound
Amine
Hydrocarbon derivative
Carbonyl group
Organic oxygen compound
Organic nitrogen compound
Organic oxide
Organonitrogen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	0.43	ALOGPS
logP	-0.17	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	9.62	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	282.21 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	184.04 m³·mol⁻¹	ChemAxon
Polarizability	79.17 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

Not Available

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-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxy-6-methyloxan-2-yl)oxy]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate (NP0146875)

MOL for NP0146875 (4-[(5-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxy-6-methyloxan-2-yl)oxy]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D MOL for NP0146875 (4-[(5-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxy-6-methyloxan-2-yl)oxy]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D SDF for NP0146875 (4-[(5-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxy-6-methyloxan-2-yl)oxy]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D-SDF for NP0146875 (4-[(5-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxy-6-methyloxan-2-yl)oxy]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

PDB for NP0146875 (4-[(5-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxy-6-methyloxan-2-yl)oxy]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D PDB for NP0146875 (4-[(5-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxy-6-methyloxan-2-yl)oxy]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

SMILES for NP0146875 (4-[(5-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxy-6-methyloxan-2-yl)oxy]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

INCHI for NP0146875 (4-[(5-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxy-6-methyloxan-2-yl)oxy]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

Structure for NP0146875 (4-[(5-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxy-6-methyloxan-2-yl)oxy]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D Structure for NP0146875 (4-[(5-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxy-6-methyloxan-2-yl)oxy]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)