NP-MRD: Showing NP-Card for methyl (4s,5r,6s)-5-ethenyl-4-{[(1r)-7-hydroxy-2-[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-3,4-dihydro-1h-isoquinolin-1-yl]methyl}-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate (NP0193294)

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Record Information

Version

2.0

Created at

2022-09-04 10:41:56 UTC

Updated at

2022-09-04 10:41:56 UTC

NP-MRD ID

NP0193294

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (4s,5r,6s)-5-ethenyl-4-{[(1r)-7-hydroxy-2-[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-3,4-dihydro-1h-isoquinolin-1-yl]methyl}-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate

Description

Methyl (2S,3R,4S)-3-ethenyl-4-{[(1R)-7-hydroxy-2-[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]methyl}-2-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,4-dihydro-2H-pyran-5-carboxylate belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone. methyl (4s,5r,6s)-5-ethenyl-4-{[(1r)-7-hydroxy-2-[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-3,4-dihydro-1h-isoquinolin-1-yl]methyl}-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate is found in Carapichea ipecacuanha. Based on a literature review very few articles have been published on methyl (2S,3R,4S)-3-ethenyl-4-{[(1R)-7-hydroxy-2-[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]methyl}-2-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,4-dihydro-2H-pyran-5-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042212412D          

 51 55  0  0  1  0            999 V2000
    0.2979    3.2641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9870    2.7291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7260    2.2227    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2781    2.8358    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9943    3.6487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5752    4.2335    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3589    5.0297    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9403    5.6150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7241    6.4112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3055    6.9965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7379    5.4042    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3193    5.9895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9542    4.6080    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7518    4.3972    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3728    4.0227    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5890    3.2265    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0850    2.6643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3400    1.8797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7879    1.2666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1595    0.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2808    0.1419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0149    0.3869    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6330    1.0176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9810    1.4381    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3172    0.8550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4861   -0.0543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.7145   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0484    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2868   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  1  0  0  0
  4 17  1  0  0  0  0
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 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 19 24  1  0  0  0  0
  3 24  1  0  0  0  0
 24 25  1  1  0  0  0
 26 25  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
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 29 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 34  1  0  0  0  0
 34 35  2  0  0  0  0
 27 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
 26 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  0  0  0  0
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 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 48 51  2  0  0  0  0
 43 51  1  0  0  0  0
M  END

     RDKit          3D

 94 98  0  0  0  0  0  0  0  0999 V2000
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 45 89  1  0
 47 90  1  0
 50 91  1  0
 50 92  1  0
 50 93  1  0
 51 94  1  0
M  END


  Mrv1652309042212412D          

 51 55  0  0  1  0            999 V2000
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    2.2781    2.8358    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9943    3.6487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5752    4.2335    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3589    5.0297    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.3055    6.9965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7379    5.4042    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3193    5.9895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9542    4.6080    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7518    4.3972    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3728    4.0227    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5890    3.2265    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0850    2.6643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3400    1.8797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7879    1.2666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1595    0.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2808    0.1419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0149    0.3869    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6330    1.0176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9810    1.4381    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3172    0.8550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4861   -0.0543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3326   -1.7324    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4177   -2.5747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0484    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4154    0.8023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7974   -0.3727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4889    0.1087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  1  0  0  0
  4 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 19 24  1  0  0  0  0
  3 24  1  0  0  0  0
 24 25  1  1  0  0  0
 26 25  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 34  1  0  0  0  0
 34 35  2  0  0  0  0
 27 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
 26 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 48 51  2  0  0  0  0
 43 51  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0193294

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](C=C)[C@@H]1C[C@H]1N(CCC2=CC(OC)=C(O)C=C12)C(=O)\C=C\C1=CC=C(O)C(OC)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C36H43NO14/c1-5-20-22(23(34(45)48-4)17-49-35(20)51-36-33(44)32(43)31(42)29(16-38)50-36)14-24-21-15-26(40)28(47-3)13-19(21)10-11-37(24)30(41)9-7-18-6-8-25(39)27(12-18)46-2/h5-9,12-13,15,17,20,22,24,29,31-33,35-36,38-40,42-44H,1,10-11,14,16H2,2-4H3/b9-7+/t20-,22+,24-,29-,31-,32+,33-,35+,36+/m1/s1

> <INCHI_KEY>
AVWLFUPXDFPXOR-NQDJLKGZSA-N

> <FORMULA>
C36H43NO14

> <MOLECULAR_WEIGHT>
713.733

> <EXACT_MASS>
713.268355069

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
94

> <JCHEM_AVERAGE_POLARIZABILITY>
72.87058530828642

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (2S,3R,4S)-3-ethenyl-4-{[(1R)-7-hydroxy-2-[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]methyl}-2-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,4-dihydro-2H-pyran-5-carboxylate

> <JCHEM_LOGP>
1.5489565663333331

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.147116851441416

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.54307061635317

> <JCHEM_PKA_STRONGEST_BASIC>
-0.3090167601149568

> <JCHEM_POLAR_SURFACE_AREA>
214.13999999999996

> <JCHEM_REFRACTIVITY>
180.60409999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl (4S,5R,6S)-5-ethenyl-4-{[(1R)-7-hydroxy-2-[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-3,4-dihydro-1H-isoquinolin-1-yl]methyl}-6-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4H-pyran-3-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       0.556   6.093   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.842   5.094   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.222   4.149   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.252   5.294   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       3.723   6.811   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.807   7.903   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.403   9.389   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.489  10.481   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.085  11.968   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.170  13.060   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.977  10.088   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.063  11.180   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       7.381   8.602   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       8.870   8.208   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.296   7.509   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.699   6.023   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       5.759   4.973   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.235   3.509   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.204   2.364   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.898   1.062   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.258   0.265   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       7.494   0.722   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       8.648   1.899   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.698   2.684   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.459   1.596   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       8.374  -0.101   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       8.087  -3.234   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       8.246  -4.806   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   38  N   UNK     0       1.334  -0.770   0.000  0.00  0.00           N+0
HETATM   39  C   UNK     0      -0.090   0.031   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -0.775   1.498   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -1.489  -0.696   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -2.779   0.203   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      -8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      -6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      -8.002  -0.000   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      -8.002   1.540   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      -5.335  -0.000   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   24                                                  
CONECT    4    3    5   17                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   15                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    8   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    6   16                                                  
CONECT   16   15                                                            
CONECT   17    4   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   24                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22                                                            
CONECT   24   19    3   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   38                                                  
CONECT   27   26   28   35                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   34                                                  
CONECT   32   31   33                                                       
CONECT   33   32                                                            
CONECT   34   31   35                                                       
CONECT   35   34   27   36                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   26   39                                                  
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44   51                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46   49   51                                                  
CONECT   49   48   50                                                       
CONECT   50   49                                                            
CONECT   51   48   43                                                       
MASTER        0    0    0    0    0    0    0    0   51    0  110    0
END

View in JSmol

Synonyms

Value	Source
Methyl (2S,3R,4S)-3-ethenyl-4-{[(1R)-7-hydroxy-2-[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]methyl}-2-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,4-dihydro-2H-pyran-5-carboxylic acid	Generator

Chemical Formula

C₃₆H₄₃NO₁₄

Average Mass

713.7330 Da

Monoisotopic Mass

713.26836 Da

IUPAC Name

methyl (2S,3R,4S)-3-ethenyl-4-{[(1R)-7-hydroxy-2-[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]methyl}-2-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,4-dihydro-2H-pyran-5-carboxylate

Traditional Name

methyl (4S,5R,6S)-5-ethenyl-4-{[(1R)-7-hydroxy-2-[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-3,4-dihydro-1H-isoquinolin-1-yl]methyl}-6-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4H-pyran-3-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](C=C)[C@@H]1C[C@H]1N(CCC2=CC(OC)=C(O)C=C12)C(=O)\C=C\C1=CC=C(O)C(OC)=C1

InChI Identifier

InChI=1S/C36H43NO14/c1-5-20-22(23(34(45)48-4)17-49-35(20)51-36-33(44)32(43)31(42)29(16-38)50-36)14-24-21-15-26(40)28(47-3)13-19(21)10-11-37(24)30(41)9-7-18-6-8-25(39)27(12-18)46-2/h5-9,12-13,15,17,20,22,24,29,31-33,35-36,38-40,42-44H,1,10-11,14,16H2,2-4H3/b9-7+/t20-,22+,24-,29-,31-,32+,33-,35+,36+/m1/s1

InChI Key

AVWLFUPXDFPXOR-NQDJLKGZSA-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
Cephaelis ipecacuanha	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Terpene glycosides

Alternative Parents

Substituents

Terpene glycoside
Cinnamic acid or derivatives
Hydroxycinnamic acid or derivatives
Glycosyl compound
Secoiridoid-skeleton
O-glycosyl compound
Aromatic monoterpenoid
Bicyclic monoterpenoid
Methoxyphenol
Monoterpenoid
Tetrahydroisoquinoline
Anisole
Phenoxy compound
Phenol ether
Styrene
Methoxybenzene
1-hydroxy-2-unsubstituted benzenoid
Sugar acid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Monosaccharide
Oxane
Benzenoid
Tertiary carboxylic acid amide
Methyl ester
Vinylogous ester
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Carboxamide group
Secondary alcohol
Azacycle
Oxacycle
Ether
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Carboxylic acid derivative
Acetal
Polyol
Primary alcohol
Organic oxygen compound
Organopnictogen compound
Carbonyl group
Alcohol
Organic oxide
Organic nitrogen compound
Hydrocarbon derivative
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	1.55	ChemAxon
pKa (Strongest Acidic)	9.54	ChemAxon
pKa (Strongest Basic)	-0.31	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	214.14 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	180.6 m³·mol⁻¹	ChemAxon
Polarizability	72.87 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

163186331

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (4s,5r,6s)-5-ethenyl-4-{[(1r)-7-hydroxy-2-[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-3,4-dihydro-1h-isoquinolin-1-yl]methyl}-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate (NP0193294)

MOL for NP0193294 (methyl (4s,5r,6s)-5-ethenyl-4-{[(1r)-7-hydroxy-2-[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-3,4-dihydro-1h-isoquinolin-1-yl]methyl}-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate)

3D MOL for NP0193294 (methyl (4s,5r,6s)-5-ethenyl-4-{[(1r)-7-hydroxy-2-[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-3,4-dihydro-1h-isoquinolin-1-yl]methyl}-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate)

3D SDF for NP0193294 (methyl (4s,5r,6s)-5-ethenyl-4-{[(1r)-7-hydroxy-2-[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-3,4-dihydro-1h-isoquinolin-1-yl]methyl}-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate)

3D-SDF for NP0193294 (methyl (4s,5r,6s)-5-ethenyl-4-{[(1r)-7-hydroxy-2-[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-3,4-dihydro-1h-isoquinolin-1-yl]methyl}-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate)

PDB for NP0193294 (methyl (4s,5r,6s)-5-ethenyl-4-{[(1r)-7-hydroxy-2-[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-3,4-dihydro-1h-isoquinolin-1-yl]methyl}-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate)

3D PDB for NP0193294 (methyl (4s,5r,6s)-5-ethenyl-4-{[(1r)-7-hydroxy-2-[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-3,4-dihydro-1h-isoquinolin-1-yl]methyl}-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate)

SMILES for NP0193294 (methyl (4s,5r,6s)-5-ethenyl-4-{[(1r)-7-hydroxy-2-[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-3,4-dihydro-1h-isoquinolin-1-yl]methyl}-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate)

INCHI for NP0193294 (methyl (4s,5r,6s)-5-ethenyl-4-{[(1r)-7-hydroxy-2-[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-3,4-dihydro-1h-isoquinolin-1-yl]methyl}-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate)

Structure for NP0193294 (methyl (4s,5r,6s)-5-ethenyl-4-{[(1r)-7-hydroxy-2-[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-3,4-dihydro-1h-isoquinolin-1-yl]methyl}-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate)

3D Structure for NP0193294 (methyl (4s,5r,6s)-5-ethenyl-4-{[(1r)-7-hydroxy-2-[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]-6-methoxy-3,4-dihydro-1h-isoquinolin-1-yl]methyl}-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate)