NP-MRD: Showing NP-Card for (2s,3s,6s)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0²,⁶.0⁶,¹⁰.0¹⁵,¹⁹]icosa-1(20),4,13,15(19)-tetraen-10-ium-10-olate (NP0320228)

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Record Information

Version

2.0

Created at

2022-09-11 21:45:48 UTC

Updated at

2022-09-11 21:45:48 UTC

NP-MRD ID

NP0320228

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3s,6s)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0²,⁶.0⁶,¹⁰.0¹⁵,¹⁹]icosa-1(20),4,13,15(19)-tetraen-10-ium-10-olate

Description

(2S,3S,6S)-3-hydroxy-4-methoxy-16,18-dioxa-10λ⁵-azapentacyclo[11.7.0.0²,⁶.0⁶,¹⁰.0¹⁵,¹⁹]Icosa-1(20),4,13,15(19)-tetraen-10-one belongs to the class of organic compounds known as cephalotaxus alkaloids. These are alkaloids with a structure based on the cephalotaxine skeleton, a tetracyclic 1,3-benzodioxole-containing compound which arises from the skeletal rearrangement of the hydroaromatic component of the Erythrina group. (2s,3s,6s)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0²,⁶.0⁶,¹⁰.0¹⁵,¹⁹]icosa-1(20),4,13,15(19)-tetraen-10-ium-10-olate is found in Cephalotaxus fortunei. Based on a literature review very few articles have been published on (2S,3S,6S)-3-hydroxy-4-methoxy-16,18-dioxa-10λ⁵-azapentacyclo[11.7.0.0²,⁶.0⁶,¹⁰.0¹⁵,¹⁹]Icosa-1(20),4,13,15(19)-tetraen-10-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112223452D          

 24 28  0  0  1  0            999 V2000
   -0.5612   -3.1520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2544   -3.0280    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5548   -2.2596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1316   -1.6796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6329   -0.9270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0411   -1.4028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7018   -0.9088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4362   -0.1277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3887   -0.1390    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    0.0078    0.5928    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    0.8526    0.5432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6752    0.6060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2371    0.0019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0047    0.3043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6504   -0.2092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5285   -1.0252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7609   -1.3276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1152   -0.8140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4013   -1.2275    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3530   -2.0510    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9909   -2.5742    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2668   -1.3932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8450   -0.8048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4641   -0.0730    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
  5  4  1  1  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
  5  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  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  2  0  0  0  0
 13 18  1  0  0  0  0
 19 18  1  6  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
  3 20  1  0  0  0  0
 20 21  1  6  0  0  0
 16 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 15 24  1  0  0  0  0
M  CHG  2   9   1  10  -1
M  END

     RDKit          3D

 45 49  0  0  0  0  0  0  0  0999 V2000
   -3.0132    3.8690   -0.7334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2743    2.5002   -0.6238 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2905    1.5750   -0.3049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5073    0.2830   -0.0904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2321   -0.3313    0.2135 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0771   -0.3516    1.6997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8468   -1.6493    2.0159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0434   -2.3351    0.6531 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0061   -1.6967   -0.0899 N   0  0  2  0  0  4  0  0  0  0  0  0
    0.1527   -2.0234    0.5936 O   0  0  0  0  0  1  0  0  0  0  0  0
   -0.8081   -2.0479   -1.4267 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6914   -2.1741   -1.7334 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4724   -1.0874   -1.0398 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7926   -1.4222   -0.9620 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6985   -0.5521   -0.3549 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2457    0.6416    0.1618 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9145    0.9829    0.0853 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0315    0.1375   -0.5053 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3174    0.5571   -0.5459 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8000    1.8619   -0.1452 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6342    2.3044    1.1152 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3510    1.3020    0.7009 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3315    0.2945    0.9467 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0601   -0.5907   -0.1206 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9514    4.3897   -0.9940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2662    4.0134   -1.5402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6015    4.2394    0.2306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4867   -0.1771   -0.1462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0471   -0.4139    2.0519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6519    0.4775    2.1633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7935   -1.4441    2.5135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1595   -2.3100    2.5805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9122   -3.4313    0.7519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0529   -2.1102    0.2762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2859   -1.4060   -2.1899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2259   -3.0793   -1.6051 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8982   -2.0651   -2.7990 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0394   -3.1247   -1.2868 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1860   -2.3503   -1.3560 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5788    1.9052    0.4869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6774    0.4576   -1.6247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5973    2.6572   -0.8902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3807    3.2664    1.1103 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3607    0.7052    0.8732 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1359   -0.2470    1.8843 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  5  4  1  1
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  1
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 22  1  0
 22 23  1  0
 23 24  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20  3  1  0
  9  5  1  0
 18 13  1  0
 19  5  1  0
 24 15  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
  6 29  1  0
  6 30  1  0
  7 31  1  0
  7 32  1  0
  8 33  1  0
  8 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 14 39  1  0
 23 44  1  0
 23 45  1  0
 17 40  1  0
 19 41  1  6
 20 42  1  6
 21 43  1  0
M  CHG  2   9   1  10  -1
M  END


  Mrv1652309112223452D          

 24 28  0  0  1  0            999 V2000
   -0.5612   -3.1520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2544   -3.0280    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5548   -2.2596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1316   -1.6796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6329   -0.9270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0411   -1.4028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7018   -0.9088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4362   -0.1277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3887   -0.1390    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    0.0078    0.5928    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    0.8526    0.5432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6752    0.6060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2371    0.0019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0047    0.3043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6504   -0.2092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5285   -1.0252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7609   -1.3276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1152   -0.8140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4013   -1.2275    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3530   -2.0510    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9909   -2.5742    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2668   -1.3932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8450   -0.8048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4641   -0.0730    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
  5  4  1  1  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
  5  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  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  2  0  0  0  0
 13 18  1  0  0  0  0
 19 18  1  6  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
  3 20  1  0  0  0  0
 20 21  1  6  0  0  0
 16 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 15 24  1  0  0  0  0
M  CHG  2   9   1  10  -1
M  END
> <DATABASE_ID>
NP0320228

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C[C@@]23CCC[N+]2([O-])CCC2=CC4=C(OCO4)C=C2[C@@H]3[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C18H21NO5/c1-22-15-9-18-4-2-5-19(18,21)6-3-11-7-13-14(24-10-23-13)8-12(11)16(18)17(15)20/h7-9,16-17,20H,2-6,10H2,1H3/t16-,17-,18-,19?/m1/s1

> <INCHI_KEY>
AZWNRVNQMXFTSX-SLZIBOOSSA-N

> <FORMULA>
C18H21NO5

> <MOLECULAR_WEIGHT>
331.368

> <EXACT_MASS>
331.14197278

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
34.563911594308166

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3S,6S)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0^{2,6}.0^{6,10}.0^{15,19}]icosa-1(20),4,13,15(19)-tetraen-10-ium-10-olate

> <JCHEM_LOGP>
-0.0413269440000002

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.34923277743226

> <JCHEM_PKA_STRONGEST_BASIC>
3.2225466326073273

> <JCHEM_POLAR_SURFACE_AREA>
70.98

> <JCHEM_REFRACTIVITY>
88.54270000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S,6S)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0^{2,6}.0^{6,10}.0^{15,19}]icosa-1(20),4,13,15(19)-tetraen-10-ium-10-olate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.048  -5.884   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.475  -5.652   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.036  -4.218   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.246  -3.135   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.181  -1.730   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.077  -2.619   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.310  -1.696   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.814  -0.238   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       0.726  -0.259   0.000  0.00  0.00           N+1
HETATM   10  O   UNK     0       0.014   1.106   0.000  0.00  0.00           O-1
HETATM   11  C   UNK     0       1.591   1.014   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.127   1.131   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.176   0.004   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.609   0.568   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.814  -0.391   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.586  -1.914   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.154  -2.478   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.948  -1.520   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.616  -2.291   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.526  -3.829   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       3.716  -4.805   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       7.965  -2.601   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.044  -1.502   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.333  -0.136   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   20                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    9   19                                             
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8    5   10   11                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   24                                                  
CONECT   16   15   17   22                                                  
CONECT   17   16   18                                                       
CONECT   18   17   13   19                                                  
CONECT   19   18    5   20                                                  
CONECT   20   19    3   21                                                  
CONECT   21   20                                                            
CONECT   22   16   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   15                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₁NO₅

Average Mass

331.3680 Da

Monoisotopic Mass

331.14197 Da

IUPAC Name

(2S,3S,6S)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0^{2,6}.0^{6,10}.0^{15,19}]icosa-1(20),4,13,15(19)-tetraen-10-ium-10-olate

Traditional Name

(2S,3S,6S)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0^{2,6}.0^{6,10}.0^{15,19}]icosa-1(20),4,13,15(19)-tetraen-10-ium-10-olate

CAS Registry Number

Not Available

SMILES

COC1=C[C@@]23CCC[N+]2([O-])CCC2=CC4=C(OCO4)C=C2[C@@H]3[C@@H]1O

InChI Identifier

InChI=1S/C18H21NO5/c1-22-15-9-18-4-2-5-19(18,21)6-3-11-7-13-14(24-10-23-13)8-12(11)16(18)17(15)20/h7-9,16-17,20H,2-6,10H2,1H3/t16-,17-,18-,19?/m1/s1

InChI Key

AZWNRVNQMXFTSX-SLZIBOOSSA-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
Cephalotaxus fortunei	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cephalotaxus alkaloids. These are alkaloids with a structure based on the cephalotaxine skeleton, a tetracyclic 1,3-benzodioxole-containing compound which arises from the skeletal rearrangement of the hydroaromatic component of the Erythrina group.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Cephalotaxus alkaloids

Sub Class

Not Available

Direct Parent

Cephalotaxus alkaloids

Alternative Parents

Substituents

Cephalotaxine
Cephalotaxus alkaloid skeleton
Benzazepine
Benzodioxole
Azepine
Benzenoid
N-alkylpyrrolidine
Trialkyl amine oxide
Pyrrolidine
Secondary alcohol
Oxacycle
Azacycle
Organoheterocyclic compound
Trisubstituted n-oxide
N-oxide
Acetal
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organic zwitterion
Organooxygen compound
Organonitrogen compound
Alcohol
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	-0.041	ChemAxon
pKa (Strongest Acidic)	13.35	ChemAxon
pKa (Strongest Basic)	3.22	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	70.98 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	88.54 m³·mol⁻¹	ChemAxon
Polarizability	34.56 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

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

163187451

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3s,6s)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0²,⁶.0⁶,¹⁰.0¹⁵,¹⁹]icosa-1(20),4,13,15(19)-tetraen-10-ium-10-olate (NP0320228)

MOL for NP0320228 ((2s,3s,6s)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0²,⁶.0⁶,¹⁰.0¹⁵,¹⁹]icosa-1(20),4,13,15(19)-tetraen-10-ium-10-olate)

3D MOL for NP0320228 ((2s,3s,6s)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0²,⁶.0⁶,¹⁰.0¹⁵,¹⁹]icosa-1(20),4,13,15(19)-tetraen-10-ium-10-olate)

3D SDF for NP0320228 ((2s,3s,6s)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0²,⁶.0⁶,¹⁰.0¹⁵,¹⁹]icosa-1(20),4,13,15(19)-tetraen-10-ium-10-olate)

3D-SDF for NP0320228 ((2s,3s,6s)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0²,⁶.0⁶,¹⁰.0¹⁵,¹⁹]icosa-1(20),4,13,15(19)-tetraen-10-ium-10-olate)

PDB for NP0320228 ((2s,3s,6s)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0²,⁶.0⁶,¹⁰.0¹⁵,¹⁹]icosa-1(20),4,13,15(19)-tetraen-10-ium-10-olate)

3D PDB for NP0320228 ((2s,3s,6s)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0²,⁶.0⁶,¹⁰.0¹⁵,¹⁹]icosa-1(20),4,13,15(19)-tetraen-10-ium-10-olate)

SMILES for NP0320228 ((2s,3s,6s)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0²,⁶.0⁶,¹⁰.0¹⁵,¹⁹]icosa-1(20),4,13,15(19)-tetraen-10-ium-10-olate)

INCHI for NP0320228 ((2s,3s,6s)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0²,⁶.0⁶,¹⁰.0¹⁵,¹⁹]icosa-1(20),4,13,15(19)-tetraen-10-ium-10-olate)

Structure for NP0320228 ((2s,3s,6s)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0²,⁶.0⁶,¹⁰.0¹⁵,¹⁹]icosa-1(20),4,13,15(19)-tetraen-10-ium-10-olate)

3D Structure for NP0320228 ((2s,3s,6s)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0²,⁶.0⁶,¹⁰.0¹⁵,¹⁹]icosa-1(20),4,13,15(19)-tetraen-10-ium-10-olate)