NP-MRD: Showing NP-Card for (+)-Fendlerine (NP0066820)

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Record Information

Version

2.0

Created at

2022-04-28 11:03:19 UTC

Updated at

2022-04-28 11:03:19 UTC

NP-MRD ID

NP0066820

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Fendlerine

Description

(+)-Fendlerine belongs to the class of organic compounds known as carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring. (+)-Fendlerine is found in Aspidosperma album and Aspidosperma megalocarpon. Based on a literature review very few articles have been published on (+)-Fendlerine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282213032D          

 29 34  0  0  1  0            999 V2000
    5.3893    1.2081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9692    0.6213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7509   -0.1743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9528   -0.3831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3729    0.2037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5911    0.9993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6356   -0.1665    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7598   -0.9821    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5739   -1.1160    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9441   -1.8532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4906   -2.5425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7677   -1.9013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1378   -2.6386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1156   -1.4974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3472   -1.1972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2230   -0.3816    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8672    0.1338    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8589    0.9365    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9745    1.2496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3303    0.7342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4416   -0.1974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7134    1.1661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1586    0.4716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5761    0.9057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7520    0.8674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5337    0.0718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3308   -0.7611    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7673    0.8301    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9856    1.6257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  7  5  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
  7 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 16 21  1  0  0  0  0
 18 22  1  0  0  0  0
 22 23  1  0  0  0  0
  7 23  1  0  0  0  0
 17 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 16 26  1  6  0  0  0
  3 27  1  0  0  0  0
  2 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END

     RDKit          3D

 59 64  0  0  0  0  0  0  0  0999 V2000
   -2.6990    4.0587    2.4566 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6801    3.1083    1.8923 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3053    1.9650    1.1580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5547    1.9663    1.1204 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4707    0.9865    0.5718 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8453   -0.1407   -0.1678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8086   -1.0594   -0.1314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0351   -2.2533   -0.8034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2036   -2.5418   -1.4770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2163   -1.6166   -1.5012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4258   -1.8833   -2.1836 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5489   -3.1471   -2.8416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0333   -0.4238   -0.8485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0935    0.4930   -0.8999 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2880   -0.4794    0.6285 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2434   -1.0617    2.0227 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5798   -0.7264    2.5692 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4508   -0.6299    1.4514 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1975    0.5720    1.5418 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1654    0.7662    0.4314 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6762    0.2613   -0.8712 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2117   -0.0779   -0.9394 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1357   -1.1483   -2.0423 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4746   -2.3534   -1.1840 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7470   -2.1802   -0.0153 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6838   -0.8057    0.2256 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4572    1.1303   -1.3709 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6325    1.8170   -0.3573 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0196    0.9861    0.6600 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3330    4.4153    3.4399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6903    3.5857    2.6303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9021    4.9113    1.7562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0458    3.6827    1.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0205    2.7503    2.6847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2557   -3.0373   -0.8087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3579   -3.4837   -1.9967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3307   -3.9811   -2.1185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7554   -3.1847   -3.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5418   -3.2913   -3.2653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9441    0.3175   -1.3750 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1255   -2.1640    1.9657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5967   -0.5883    2.5736 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4815    0.2437    3.1315 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9137   -1.5080    3.3040 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6119    1.4986    1.7158 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8129    0.4788    2.4903 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4151    1.8688    0.4002 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1442    0.2742    0.7010 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8559    1.0776   -1.6337 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3342   -0.5654   -1.2216 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9280   -1.0169   -2.7885 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1332   -1.2684   -2.4460 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2267   -3.2916   -1.7142 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5434   -2.4118   -0.9049 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1640    1.8854   -1.8080 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8043    0.8392   -2.2362 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2285    2.6343    0.1218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1777    2.3813   -0.9111 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2248    1.3658    1.6738 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
  3  5  1  0
  5 29  1  0
 29 28  1  0
 28 27  1  0
 22 27  1  6
 22 23  1  0
 23 24  1  0
 24 25  1  0
 26 25  1  6
 26 18  1  0
 18 17  1  0
 17 16  1  0
 15 16  1  1
 15  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 10 13  1  0
 13 14  1  0
 13  6  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
  6  5  1  0
 15 29  1  0
  6  7  1  0
 26 22  1  0
 15 26  1  0
 21 22  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  2 34  1  0
 29 59  1  1
 28 57  1  0
 28 58  1  0
 27 55  1  0
 27 56  1  0
 23 51  1  0
 23 52  1  0
 24 53  1  0
 24 54  1  0
 17 43  1  0
 17 44  1  0
 16 41  1  0
 16 42  1  0
  8 35  1  0
  9 36  1  0
 12 37  1  0
 12 38  1  0
 12 39  1  0
 14 40  1  0
 19 45  1  0
 19 46  1  0
 20 47  1  0
 20 48  1  0
 21 49  1  0
 21 50  1  0
M  END


  Mrv1652304282213032D          

 29 34  0  0  1  0            999 V2000
    5.3893    1.2081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9692    0.6213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7509   -0.1743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9528   -0.3831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3729    0.2037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5911    0.9993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6356   -0.1665    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7598   -0.9821    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5739   -1.1160    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9441   -1.8532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4906   -2.5425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7677   -1.9013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1378   -2.6386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1156   -1.4974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3472   -1.1972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2230   -0.3816    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8672    0.1338    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8589    0.9365    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9745    1.2496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3303    0.7342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4416   -0.1974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7134    1.1661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1586    0.4716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5761    0.9057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7520    0.8674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5337    0.0718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3308   -0.7611    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7673    0.8301    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9856    1.6257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  7  5  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
  7 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 16 21  1  0  0  0  0
 18 22  1  0  0  0  0
 22 23  1  0  0  0  0
  7 23  1  0  0  0  0
 17 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 16 26  1  6  0  0  0
  3 27  1  0  0  0  0
  2 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0066820

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(=O)N1[C@@H]2CC[C@]34CCO[C@@]33N(CC[C@@]23C2=CC=C(OC)C(O)=C12)CCC4

> <INCHI_IDENTIFIER>
InChI=1S/C23H30N2O4/c1-3-18(26)25-17-7-9-21-8-4-12-24-13-10-22(17,23(21,24)29-14-11-21)15-5-6-16(28-2)20(27)19(15)25/h5-6,17,27H,3-4,7-14H2,1-2H3/t17-,21-,22-,23+/m1/s1

> <INCHI_KEY>
BQUQIANAVWLUAX-LUGPXAIHSA-N

> <FORMULA>
C23H30N2O4

> <MOLECULAR_WEIGHT>
398.503

> <EXACT_MASS>
398.220557454

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
43.03733672177509

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-[(1R,4R,12R,16S)-7-hydroxy-8-methoxy-17-oxa-5,15-diazahexacyclo[13.4.3.0^{1,16}.0^{4,12}.0^{6,11}.0^{12,16}]docosa-6,8,10-trien-5-yl]propan-1-one

> <ALOGPS_LOGP>
2.53

> <JCHEM_LOGP>
2.593353688188146

> <ALOGPS_LOGS>
-2.64

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.159907629027598

> <JCHEM_PKA_STRONGEST_BASIC>
7.3701957411803996

> <JCHEM_POLAR_SURFACE_AREA>
62.24000000000001

> <JCHEM_REFRACTIVITY>
108.76549999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.06e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-[(1R,4R,12R,16S)-7-hydroxy-8-methoxy-17-oxa-5,15-diazahexacyclo[13.4.3.0^{1,16}.0^{4,12}.0^{6,11}.0^{12,16}]docosa-6,8,10-trien-5-yl]propan-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      10.060   2.255   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.142   1.160   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.735  -0.325   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.245  -0.715   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.163   0.380   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.570   1.865   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.786  -0.311   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.018  -1.833   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       8.538  -2.083   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       9.229  -3.459   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.383  -4.746   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      10.766  -3.549   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.457  -4.925   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.816  -2.795   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.381  -2.235   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.150  -0.712   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.352   0.250   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0       5.337   1.748   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       3.686   2.333   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.483   1.370   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.691  -0.368   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.932   2.177   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.763   0.880   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       4.809   1.691   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.270   1.619   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.863   0.134   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      11.818  -1.421   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      12.632   1.549   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      13.040   3.035   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   28                                                  
CONECT    3    2    4   27                                                  
CONECT    4    3    5    9                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8   17   23                                             
CONECT    8    7    9   14                                                  
CONECT    9    8    4   10                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12                                                            
CONECT   14    8   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   21   26                                             
CONECT   17   16    7   18   24                                             
CONECT   18   17   19   22                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   16                                                       
CONECT   22   18   23                                                       
CONECT   23   22    7                                                       
CONECT   24   17   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   16                                                       
CONECT   27    3                                                            
CONECT   28    2   29                                                       
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₀N₂O₄

Average Mass

398.5030 Da

Monoisotopic Mass

398.22056 Da

IUPAC Name

1-[(1R,4R,12R,16S)-7-hydroxy-8-methoxy-17-oxa-5,15-diazahexacyclo[13.4.3.0^{1,16}.0^{4,12}.0^{6,11}.0^{12,16}]docosa-6,8,10-trien-5-yl]propan-1-one

Traditional Name

1-[(1R,4R,12R,16S)-7-hydroxy-8-methoxy-17-oxa-5,15-diazahexacyclo[13.4.3.0^{1,16}.0^{4,12}.0^{6,11}.0^{12,16}]docosa-6,8,10-trien-5-yl]propan-1-one

CAS Registry Number

Not Available

SMILES

CCC(=O)N1[C@@H]2CC[C@]34CCO[C@@]33N(CC[C@@]23C2=CC=C(OC)C(O)=C12)CCC4

InChI Identifier

InChI=1S/C23H30N2O4/c1-3-18(26)25-17-7-9-21-8-4-12-24-13-10-22(17,23(21,24)29-14-11-21)15-5-6-16(28-2)20(27)19(15)25/h5-6,17,27H,3-4,7-14H2,1-2H3/t17-,21-,22-,23+/m1/s1

InChI Key

BQUQIANAVWLUAX-LUGPXAIHSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Aspidosperma album	Plant	KNApSAcK
Aspidosperma megalocarpon Muell.Arg.	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Carbazoles

Direct Parent

Carbazoles

Alternative Parents

Substituents

Carbazole
Quinolidine
Indolizidine
Anisole
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
Piperidine
Benzenoid
N-alkylpyrrolidine
Tetrahydrofuran
Tertiary carboxylic acid amide
Pyrrolidine
Carboxamide group
Hemiaminal
Carboxylic acid derivative
Ether
Oxacycle
Azacycle
Hydrocarbon derivative
Organic oxygen compound
Organic nitrogen compound
Organic oxide
Carbonyl group
Organonitrogen compound
Organooxygen compound
Organopnictogen 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	2.53	ALOGPS
logP	2.59	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	9.16	ChemAxon
pKa (Strongest Basic)	7.37	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	62.24 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	108.77 m³·mol⁻¹	ChemAxon
Polarizability	43.04 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

12309862

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Fendlerine (NP0066820)

MOL for NP0066820 ((+)-Fendlerine)

3D MOL for NP0066820 ((+)-Fendlerine)

3D SDF for NP0066820 ((+)-Fendlerine)

3D-SDF for NP0066820 ((+)-Fendlerine)

PDB for NP0066820 ((+)-Fendlerine)

3D PDB for NP0066820 ((+)-Fendlerine)

SMILES for NP0066820 ((+)-Fendlerine)

INCHI for NP0066820 ((+)-Fendlerine)

Structure for NP0066820 ((+)-Fendlerine)

3D Structure for NP0066820 ((+)-Fendlerine)