NP-MRD: Showing NP-Card for 2-[(23s)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-1(13),2,4(8),9,11,14,16,21-octaen-23-yl]ethanol (NP0320996)

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Record Information

Version

2.0

Created at

2022-09-11 22:57:59 UTC

Updated at

2022-09-11 22:57:59 UTC

NP-MRD ID

NP0320996

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(23s)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-1(13),2,4(8),9,11,14,16,21-octaen-23-yl]ethanol

Description

2-[(23S)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]Tetracosa-1(13),2,4(8),9,11,14(22),15,17(21)-octaen-23-yl]ethan-1-ol belongs to the class of organic compounds known as dihydrobenzophenanthridine alkaloids. These are alkaloids containing a dihydrobenzophenanthridine skeleton, which is a tetracyclic compound containing a benzene fused to a dihydrophenanthridine moiety. Based on a literature review very few articles have been published on 2-[(23S)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]Tetracosa-1(13),2,4(8),9,11,14(22),15,17(21)-octaen-23-yl]ethan-1-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122200582D          

 28 33  0  0  1  0            999 V2000
    4.6854    2.6351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1904    1.9751    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5145    1.2164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0196    0.5564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3437   -0.2023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1628   -0.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6577    0.3592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4768    0.2605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9718    0.9206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6477    1.6792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8286    1.7778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3336    1.1178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2690    2.2219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9772    1.7987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7935    0.9944    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2005    0.6550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7055   -0.0050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8865    0.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5623    0.8523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0573    1.5123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8764    1.4137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3713    2.0737    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0472    2.8324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2281    2.9310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9040    3.6897    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5825    2.1870    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7941    1.9440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7817    1.1191    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  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  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
  3 12  2  0  0  0  0
  7 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  9 15  1  0  0  0  0
  4 16  1  0  0  0  0
 16 17  2  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
 16 21  1  0  0  0  0
 21 22  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 20 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 19 28  1  0  0  0  0
M  END

     RDKit          3D

 47 52  0  0  0  0  0  0  0  0999 V2000
    0.2434    0.4773    2.0285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0221   -0.0898    0.7464 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8454    0.2398   -0.3597 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2376    0.5094   -1.6044 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0187    0.8937   -2.6581 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4032    1.0042   -2.4551 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9775    0.7336   -1.2350 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3373    0.8299   -1.0517 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9058    0.5394    0.1655 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1129    0.1442    1.2198 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7279    0.0360    1.0687 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1949    0.3359   -0.1442 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9794   -0.0720    2.2858 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3197   -0.1686    1.8048 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2289    0.5665    0.5819 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2201    0.3932   -1.6399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8613    1.0480   -2.7091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2119    1.2879   -2.5928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9488    0.9220   -1.4937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2652    0.2655   -0.4558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9454    0.0047   -0.5349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1594   -0.9157    0.3908 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9280   -1.4716    1.5040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9567   -2.4749    1.0330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2284   -3.5969    0.4549 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2329    0.0380    0.4863 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2973    0.9526    0.3116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2888    1.0481   -1.1208 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2456   -0.1752    2.8940 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9020    1.3725    2.0522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7568    1.0439    2.2207 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5714    1.0967   -3.5997 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0013    1.3110   -3.2973 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9260    1.1417   -1.9038 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2248   -0.3390    1.8949 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0536    0.2501    2.4976 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4849   -1.2496    1.5899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3580    1.3640   -3.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7553    1.7953   -3.4026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8158   -1.7251   -0.2796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2114   -2.0677    2.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3597   -0.7337    2.2073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5993   -2.8827    1.7998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5463   -2.1714    0.1575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6886   -3.9893    1.2031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2538    0.5430    0.6902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0309    1.9352    0.7007 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 22 21  1  0
 21 20  2  0
 20 26  1  0
 26 27  1  0
 27 28  1  0
 28 19  1  0
 19 18  2  0
 18 17  1  0
 17 16  2  0
 16  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 15  1  0
 15 14  1  0
 14 13  1  0
 13 10  1  0
 10 11  2  0
 11 12  1  0
 12  3  2  0
  3  2  1  0
 16 21  1  0
  3  4  1  0
 19 20  1  0
 12  7  1  0
 10  9  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 22 40  1  6
 23 41  1  0
 23 42  1  0
 24 43  1  0
 24 44  1  0
 25 45  1  0
 27 46  1  0
 27 47  1  0
 18 39  1  0
 17 38  1  0
  5 32  1  0
  6 33  1  0
  8 34  1  0
 14 36  1  0
 14 37  1  0
 11 35  1  0
M  END


  Mrv1652309122200582D          

 28 33  0  0  1  0            999 V2000
    4.6854    2.6351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1904    1.9751    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5145    1.2164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0196    0.5564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3437   -0.2023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1628   -0.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6577    0.3592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4768    0.2605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9718    0.9206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6477    1.6792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8286    1.7778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3336    1.1178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2690    2.2219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9772    1.7987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7935    0.9944    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2005    0.6550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7055   -0.0050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8865    0.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5623    0.8523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0573    1.5123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8764    1.4137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3713    2.0737    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0472    2.8324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2281    2.9310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9040    3.6897    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5825    2.1870    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7941    1.9440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7817    1.1191    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  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  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
  3 12  2  0  0  0  0
  7 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  9 15  1  0  0  0  0
  4 16  1  0  0  0  0
 16 17  2  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
 16 21  1  0  0  0  0
 21 22  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 20 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 19 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0320996

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1[C@@H](CCO)C2=C3OCOC3=CC=C2C2=CC=C3C=C4OCOC4=CC3=C12

> <INCHI_IDENTIFIER>
InChI=1S/C22H19NO5/c1-23-16(6-7-24)20-13(4-5-17-22(20)28-11-25-17)14-3-2-12-8-18-19(27-10-26-18)9-15(12)21(14)23/h2-5,8-9,16,24H,6-7,10-11H2,1H3/t16-/m0/s1

> <INCHI_KEY>
GSEHWAORUDPHTL-INIZCTEOSA-N

> <FORMULA>
C22H19NO5

> <MOLECULAR_WEIGHT>
377.396

> <EXACT_MASS>
377.126322716

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
40.16755090751026

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(23S)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0^{2,10}.0^{4,8}.0^{14,22}.0^{17,21}]tetracosa-1,3,8,10,12,14,16,21-octaen-23-yl]ethan-1-ol

> <JCHEM_LOGP>
3.1453108269999994

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.911393474480242

> <JCHEM_PKA_STRONGEST_BASIC>
2.167701441434043

> <JCHEM_POLAR_SURFACE_AREA>
60.390000000000015

> <JCHEM_REFRACTIVITY>
102.9893

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2-[(23S)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0^{2,10}.0^{4,8}.0^{14,22}.0^{17,21}]tetracosa-1,3,8,10,12,14,16,21-octaen-23-yl]ethanol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       8.746   4.919   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       7.822   3.687   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       8.427   2.271   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.503   1.039   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.108  -0.378   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.637  -0.562   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.561   0.670   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.090   0.486   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.014   1.718   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.409   3.135   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.880   3.319   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.956   2.087   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      13.569   4.148   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      14.891   3.357   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      14.548   1.856   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.974   1.223   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.050  -0.009   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.521   0.175   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.916   1.591   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.840   2.823   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.369   2.639   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.293   3.871   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.688   5.287   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.159   5.471   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       3.554   6.887   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       2.954   4.082   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       1.482   3.629   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.459   2.089   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4   12                                                  
CONECT    4    3    5   16                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   15                                                  
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11    3    7                                                  
CONECT   13   10   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14    9                                                       
CONECT   16    4   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   28                                                  
CONECT   20   19   21   26                                                  
CONECT   21   20   16   22                                                  
CONECT   22   21    2   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   20   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   19                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₁₉NO₅

Average Mass

377.3960 Da

Monoisotopic Mass

377.12632 Da

IUPAC Name

2-[(23S)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0^{2,10}.0^{4,8}.0^{14,22}.0^{17,21}]tetracosa-1,3,8,10,12,14,16,21-octaen-23-yl]ethan-1-ol

Traditional Name

2-[(23S)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0^{2,10}.0^{4,8}.0^{14,22}.0^{17,21}]tetracosa-1,3,8,10,12,14,16,21-octaen-23-yl]ethanol

CAS Registry Number

Not Available

SMILES

CN1[C@@H](CCO)C2=C3OCOC3=CC=C2C2=CC=C3C=C4OCOC4=CC3=C12

InChI Identifier

InChI=1S/C22H19NO5/c1-23-16(6-7-24)20-13(4-5-17-22(20)28-11-25-17)14-3-2-12-8-18-19(27-10-26-18)9-15(12)21(14)23/h2-5,8-9,16,24H,6-7,10-11H2,1H3/t16-/m0/s1

InChI Key

GSEHWAORUDPHTL-INIZCTEOSA-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 dihydrobenzophenanthridine alkaloids. These are alkaloids containing a dihydrobenzophenanthridine skeleton, which is a tetracyclic compound containing a benzene fused to a dihydrophenanthridine moiety.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Benzophenanthridine alkaloids

Sub Class

Dihydrobenzophenanthridine alkaloids

Direct Parent

Dihydrobenzophenanthridine alkaloids

Alternative Parents

Substituents

Dihydrobenzophenanthridine alkaloid skeleton
Benzoquinoline
Phenanthridine
Naphthalene
Quinoline
Benzodioxole
Dialkylarylamine
Tertiary aliphatic/aromatic amine
Aralkylamine
Benzenoid
1,3-aminoalcohol
Tertiary amine
Acetal
Organoheterocyclic compound
Azacycle
Oxacycle
Primary alcohol
Organopnictogen compound
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organic nitrogen compound
Amine
Alcohol
Hydrocarbon derivative
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	3.15	ChemAxon
pKa (Strongest Acidic)	15.91	ChemAxon
pKa (Strongest Basic)	2.17	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	60.39 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	102.99 m³·mol⁻¹	ChemAxon
Polarizability	40.17 Å³	ChemAxon
Number of Rings	6	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

163188010

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[(23s)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-1(13),2,4(8),9,11,14,16,21-octaen-23-yl]ethanol (NP0320996)

MOL for NP0320996 (2-[(23s)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-1(13),2,4(8),9,11,14,16,21-octaen-23-yl]ethanol)

3D MOL for NP0320996 (2-[(23s)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-1(13),2,4(8),9,11,14,16,21-octaen-23-yl]ethanol)

3D SDF for NP0320996 (2-[(23s)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-1(13),2,4(8),9,11,14,16,21-octaen-23-yl]ethanol)

3D-SDF for NP0320996 (2-[(23s)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-1(13),2,4(8),9,11,14,16,21-octaen-23-yl]ethanol)

PDB for NP0320996 (2-[(23s)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-1(13),2,4(8),9,11,14,16,21-octaen-23-yl]ethanol)

3D PDB for NP0320996 (2-[(23s)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-1(13),2,4(8),9,11,14,16,21-octaen-23-yl]ethanol)

SMILES for NP0320996 (2-[(23s)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-1(13),2,4(8),9,11,14,16,21-octaen-23-yl]ethanol)

INCHI for NP0320996 (2-[(23s)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-1(13),2,4(8),9,11,14,16,21-octaen-23-yl]ethanol)

Structure for NP0320996 (2-[(23s)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-1(13),2,4(8),9,11,14,16,21-octaen-23-yl]ethanol)

3D Structure for NP0320996 (2-[(23s)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-1(13),2,4(8),9,11,14,16,21-octaen-23-yl]ethanol)