NP-MRD: Showing NP-Card for methyl 2-(1-hydroxybut-3-en-2-yl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine-3-carboxylate (NP0304818)

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Record Information

Version

2.0

Created at

2022-09-10 20:11:03 UTC

Updated at

2022-09-10 20:11:03 UTC

NP-MRD ID

NP0304818

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-(1-hydroxybut-3-en-2-yl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine-3-carboxylate

Description

Methyl 4-(1-hydroxybut-3-en-2-yl)-12-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-7,17-diazatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]Heptadeca-1(10),5,11(16),12,14-pentaene-5-carboxylate belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. methyl 2-(1-hydroxybut-3-en-2-yl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine-3-carboxylate is found in Cephalanthus occidentalis. Methyl 4-(1-hydroxybut-3-en-2-yl)-12-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-7,17-diazatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]Heptadeca-1(10),5,11(16),12,14-pentaene-5-carboxylate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161506202D          

 38 42  0  0  0  0            999 V2000
    1.1107   -4.1615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6580   -3.4718    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0290   -2.7349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5764   -2.0451    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8527   -2.6877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3053   -3.3775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1290   -3.3303    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5816   -4.0200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4053   -3.9729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7763   -3.2360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3236   -2.5463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8397   -1.9027    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6113   -2.1946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3446   -1.8165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0387   -2.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9995   -3.0866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2662   -3.4647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2270   -4.2887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9210   -4.7347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6543   -4.3566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3484   -4.8026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0816   -4.4245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1208   -3.6005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3092   -5.6267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0032   -6.0727    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5759   -6.0048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5367   -6.8288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8818   -5.5588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.5721   -3.0187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5000   -2.5934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0473   -1.9037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2237   -1.9509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7710   -1.2611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9474   -1.3083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4947   -0.6185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1420   -0.5242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9657   -0.4771    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  2  0  0  0  0
  3  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  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  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
 21 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
 19 28  1  0  0  0  0
 28 29  1  0  0  0  0
 17 30  2  0  0  0  0
 10 30  1  0  0  0  0
 13 30  1  0  0  0  0
 11 31  1  0  0  0  0
  7 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
  5 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 34 37  1  0  0  0  0
 37 38  2  0  0  0  0
M  END

     RDKit          3D

 72 76  0  0  0  0  0  0  0  0999 V2000
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   -4.2662    0.0072   -0.3353 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -1.2345   -1.0532   -1.7342 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.6435   -3.2342   -0.7650 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2257   -0.1554    1.3767 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5034    0.3007    1.6425 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -4.2652    1.4662   -0.5476 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.3294    3.5617   -0.3514 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.2256   -3.4625    1.4355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2724   -1.9442    1.0131 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.3833    0.0827    0.6189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9386    1.4905    1.8708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2933    0.2115    2.9584 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.2996   -0.3717   -0.2419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5796   -1.7172   -1.3427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4341   -0.5513   -2.3896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3794    0.0186   -3.0966 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.9554    0.9195   -2.3973 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.5890    3.5762    0.5678 H   0  0  0  0  0  0  0  0  0  0  0  0
 38 37  1  0
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 29  9  2  0
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  6 46  1  1
  3 42  1  6
  4 43  1  0
  4 44  1  0
  5 45  1  0
  2 41  1  0
  1 39  1  0
  1 40  1  0
M  END


  Mrv1533004161506202D          

 38 42  0  0  0  0            999 V2000
    1.1107   -4.1615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6580   -3.4718    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0290   -2.7349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5764   -2.0451    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8527   -2.6877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3053   -3.3775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1290   -3.3303    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5816   -4.0200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4053   -3.9729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7763   -3.2360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3236   -2.5463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8397   -1.9027    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6113   -2.1946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.9995   -3.0866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.0816   -4.4245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1208   -3.6005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3092   -5.6267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0032   -6.0727    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5759   -6.0048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.8818   -5.5588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1486   -5.9369    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5721   -3.0187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5000   -2.5934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0473   -1.9037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2237   -1.9509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7710   -1.2611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9474   -1.3083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4947   -0.6185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1420   -0.5242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9657   -0.4771    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  2  0  0  0  0
  3  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  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  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
 21 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
 19 28  1  0  0  0  0
 28 29  1  0  0  0  0
 17 30  2  0  0  0  0
 10 30  1  0  0  0  0
 13 30  1  0  0  0  0
 11 31  1  0  0  0  0
  7 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
  5 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 34 37  1  0  0  0  0
 37 38  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0304818

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CN2CCC3=C(NC4=CC=CC(OC5OC(CO)C(O)C(O)C5O)=C34)C2CC1C(CO)C=C

> <INCHI_IDENTIFIER>
InChI=1S/C27H34N2O9/c1-3-13(11-30)15-9-18-22-14(7-8-29(18)10-16(15)26(35)36-2)21-17(28-22)5-4-6-19(21)37-27-25(34)24(33)23(32)20(12-31)38-27/h3-6,10,13,15,18,20,23-25,27-28,30-34H,1,7-9,11-12H2,2H3

> <INCHI_KEY>
USUGTFYUSIJKAR-UHFFFAOYSA-N

> <FORMULA>
C27H34N2O9

> <MOLECULAR_WEIGHT>
530.574

> <EXACT_MASS>
530.226430683

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
72

> <JCHEM_AVERAGE_POLARIZABILITY>
55.17881553443614

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 2-(1-hydroxybut-3-en-2-yl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,2H,6H,7H,12H,12bH-indolo[2,3-a]quinolizine-3-carboxylate

> <ALOGPS_LOGP>
0.15

> <JCHEM_LOGP>
-0.06148305266666507

> <ALOGPS_LOGS>
-2.53

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.195906355016529

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.20009183992389

> <JCHEM_PKA_STRONGEST_BASIC>
-1.4462726330366982

> <JCHEM_POLAR_SURFACE_AREA>
164.94

> <JCHEM_REFRACTIVITY>
135.86819999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.58e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 2-(1-hydroxybut-3-en-2-yl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,2H,6H,7H,12H,12bH-indolo[2,3-a]quinolizine-3-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       2.073  -7.768   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.228  -6.481   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.921  -5.105   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.076  -3.818   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.458  -5.017   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.303  -6.305   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       5.841  -6.217   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       6.686  -7.504   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.223  -7.416   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.916  -6.041   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.071  -4.753   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       9.034  -3.552   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0      10.475  -4.097   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.843  -3.391   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.139  -4.223   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.066  -5.762   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.697  -6.467   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      11.624  -8.006   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      12.919  -8.838   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      14.288  -8.132   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      15.584  -8.965   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      16.952  -8.259   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      17.026  -6.721   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      15.510 -10.503   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      16.806 -11.336   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      14.142 -11.209   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      14.068 -12.747   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      12.846 -10.376   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      11.477 -11.082   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      10.401  -5.635   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.533  -4.841   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.688  -3.554   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.151  -3.642   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       3.306  -2.354   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       1.768  -2.442   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       0.923  -1.155   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       3.998  -0.979   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       5.536  -0.891   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   33                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   31                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   30                                                  
CONECT   11   10   12   31                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   30                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   30                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   28                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   19   29                                                  
CONECT   29   28                                                            
CONECT   30   17   10   13                                                  
CONECT   31   11    7   32                                                  
CONECT   32   31   33                                                       
CONECT   33   32    5   34                                                  
CONECT   34   33   35   37                                                  
CONECT   35   34   36                                                       
CONECT   36   35                                                            
CONECT   37   34   38                                                       
CONECT   38   37                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   84    0
END

View in JSmol

Synonyms

Value	Source
Methyl 4-(1-hydroxybut-3-en-2-yl)-12-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-7,17-diazatetracyclo[8.7.0.0,.0,]heptadeca-1(10),5,11(16),12,14-pentaene-5-carboxylic acid	Generator
Methyl 4-(1-hydroxybut-3-en-2-yl)-12-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-7,17-diazatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-1(10),5,11(16),12,14-pentaene-5-carboxylic acid	Generator

Chemical Formula

C₂₇H₃₄N₂O₉

Average Mass

530.5740 Da

Monoisotopic Mass

530.22643 Da

IUPAC Name

methyl 2-(1-hydroxybut-3-en-2-yl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,2H,6H,7H,12H,12bH-indolo[2,3-a]quinolizine-3-carboxylate

Traditional Name

methyl 2-(1-hydroxybut-3-en-2-yl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,2H,6H,7H,12H,12bH-indolo[2,3-a]quinolizine-3-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CN2CCC3=C(NC4=CC=CC(OC5OC(CO)C(O)C(O)C5O)=C34)C2CC1C(CO)C=C

InChI Identifier

InChI=1S/C27H34N2O9/c1-3-13(11-30)15-9-18-22-14(7-8-29(18)10-16(15)26(35)36-2)21-17(28-22)5-4-6-19(21)37-27-25(34)24(33)23(32)20(12-31)38-27/h3-6,10,13,15,18,20,23-25,27-28,30-34H,1,7-9,11-12H2,2H3

InChI Key

USUGTFYUSIJKAR-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
Cephalanthus occidentalis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
Beta-carboline
Pyridoindole
Hexose monosaccharide
O-glycosyl compound
Quinolizine
3-alkylindole
Indole
Indole or derivatives
Aralkylamine
Tetrahydropyridine
Monosaccharide
Oxane
Benzenoid
Enoate ester
Heteroaromatic compound
Methyl ester
Vinylogous amide
Pyrrole
Alpha,beta-unsaturated carboxylic ester
Tertiary aliphatic amine
Carboxylic acid ester
Tertiary amine
Secondary alcohol
Amino acid or derivatives
Polyol
Azacycle
Allylamine
Carboxylic acid derivative
Oxacycle
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Acetal
Enamine
Hydrocarbon derivative
Organopnictogen compound
Alcohol
Organic oxide
Carbonyl group
Organic nitrogen compound
Organonitrogen compound
Primary alcohol
Amine
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	0.15	ALOGPS
logP	-0.061	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	12.2	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	164.94 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	135.87 m³·mol⁻¹	ChemAxon
Polarizability	55.18 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 methyl 2-(1-hydroxybut-3-en-2-yl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine-3-carboxylate (NP0304818)

MOL for NP0304818 (methyl 2-(1-hydroxybut-3-en-2-yl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine-3-carboxylate)

3D MOL for NP0304818 (methyl 2-(1-hydroxybut-3-en-2-yl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine-3-carboxylate)

3D SDF for NP0304818 (methyl 2-(1-hydroxybut-3-en-2-yl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine-3-carboxylate)

3D-SDF for NP0304818 (methyl 2-(1-hydroxybut-3-en-2-yl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine-3-carboxylate)

PDB for NP0304818 (methyl 2-(1-hydroxybut-3-en-2-yl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine-3-carboxylate)

3D PDB for NP0304818 (methyl 2-(1-hydroxybut-3-en-2-yl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine-3-carboxylate)

SMILES for NP0304818 (methyl 2-(1-hydroxybut-3-en-2-yl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine-3-carboxylate)

INCHI for NP0304818 (methyl 2-(1-hydroxybut-3-en-2-yl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine-3-carboxylate)

Structure for NP0304818 (methyl 2-(1-hydroxybut-3-en-2-yl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine-3-carboxylate)

3D Structure for NP0304818 (methyl 2-(1-hydroxybut-3-en-2-yl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine-3-carboxylate)