NP-MRD: Showing NP-Card for 1,24-Tetracosane dioic acid (NP0073688)

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Record Information

Version

2.0

Created at

2022-04-28 18:54:46 UTC

Updated at

2022-04-28 18:54:46 UTC

NP-MRD ID

NP0073688

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,24-Tetracosane dioic acid

Description

Methyl (1R,4S,12R,13R,21S)-7-methoxy-20-oxo-5,15-diazahexacyclo[11.5.2.1¹,¹².0⁴,¹².0⁶,¹¹.0¹⁵,²¹]Henicosa-6(11),7,9,17-tetraene-4-carboxylate belongs to the class of organic compounds known as aspidofractine alkaloids. These are alkaloids with a structure that is based on the hexacyclic aspidofractine core. These compounds are related to the Aspidosperma group by formation of a C-2 to C-18 bond. 1,24-Tetracosane dioic acid is found in Arabidopsis thaliana and Kopsia arborea. Based on a literature review very few articles have been published on methyl (1R,4S,12R,13R,21S)-7-methoxy-20-oxo-5,15-diazahexacyclo[11.5.2.1¹,¹².0⁴,¹².0⁶,¹¹.0¹⁵,²¹]Henicosa-6(11),7,9,17-tetraene-4-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282220542D          

 28 33  0  0  1  0            999 V2000
    0.7572   -1.6122    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8817   -0.5601    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2363    0.0391    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0508   -0.7013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2951   -1.7769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2799   -1.6803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4477    0.8697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2598    1.0128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7590    0.3523    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4798   -0.4918    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6103   -1.1096    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4766   -1.5894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3901   -1.0199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9554   -1.6208    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5197   -0.1660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2914   -0.7798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9142   -0.2387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5690    0.5078    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6942   -0.5076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8513   -1.3175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2285   -1.8585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4485   -1.5897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3170    0.0335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1598    0.8434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0550    1.1223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8699    1.2510    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5361    1.7637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8321    2.5338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  3  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
  2 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
  1 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  3 15  1  0  0  0  0
 10 16  1  6  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
  9 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 16 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
  9 25  1  1  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

     RDKit          3D

 52 57  0  0  0  0  0  0  0  0999 V2000
    1.7056    1.6610    3.9631 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8227    1.5735    2.8400 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2793    1.3137    1.5659 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5223    1.1594    1.4592 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4507    1.2050    0.3464 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2844    2.4160   -0.0141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3785    2.2789   -1.0219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2135    1.0417   -0.7842 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2701    0.8263   -1.7979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6687   -0.3938   -2.0792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1171   -1.6147   -1.4314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9563   -1.3933   -0.6320 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1415   -1.4740    0.7797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1846   -0.4371    1.4122 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0634    0.7291    1.6924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1792    1.2978    2.7426 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8729    1.2234    0.5445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2860   -0.1131    0.2745 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7772   -1.1105    0.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9630   -2.4295    0.2677 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1245   -3.0937   -0.1118 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1354   -2.4200   -0.7466 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9753   -1.0675   -1.0007 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9763   -0.3630   -1.6384 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1736   -1.0062   -2.0398 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8216   -0.4287   -0.6185 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4296    0.9353   -0.7515 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2941   -0.1273   -0.8742 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5694    2.2852    3.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2432    2.1881    4.7981 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1350    0.6758    4.2158 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4278    3.1844   -0.3966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7225    2.8712    0.9144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9692    2.2055   -2.0498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0462    3.1570   -0.9962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7061    1.6634   -2.2985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4423   -0.5351   -2.8231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8145   -2.2944   -2.2759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8890   -2.1796   -0.8650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2170   -1.1883    0.9808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0214   -2.4703    1.2278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6926   -0.8410    2.2996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0503    2.3061    0.7088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9078    0.7743    0.5646 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2117   -3.0151    0.7625 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2241   -4.1363    0.0955 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0394   -2.9191   -1.0465 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6134   -1.6284   -1.2375 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9055   -1.6073   -2.9490 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9260   -0.2205   -2.3180 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7220    1.6382   -1.4346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7856   -0.1027   -1.8454 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  3  1  1
  5  6  1  0
  6  7  1  0
  8  7  1  6
  8 17  1  0
 17 15  1  0
 15 16  2  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  9  2  0
 12 28  1  0
 28 18  1  0
 18 19  1  6
 19 26  2  0
 26 27  1  0
 26 23  1  0
 23 24  1  0
 24 25  1  0
 23 22  2  0
 22 21  1  0
 21 20  2  0
 18  5  1  0
 20 19  1  0
 27  5  1  0
  8  9  1  0
 28  8  1  0
 18 14  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  6 32  1  0
  6 33  1  0
  7 34  1  0
  7 35  1  0
 17 43  1  0
 17 44  1  0
 14 42  1  1
 13 40  1  0
 13 41  1  0
 11 38  1  0
 11 39  1  0
 10 37  1  0
  9 36  1  0
 28 52  1  6
 27 51  1  0
 25 48  1  0
 25 49  1  0
 25 50  1  0
 22 47  1  0
 21 46  1  0
 20 45  1  0
M  END


  Mrv1652304282220542D          

 28 33  0  0  1  0            999 V2000
    0.7572   -1.6122    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8817   -0.5601    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2363    0.0391    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0508   -0.7013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2951   -1.7769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2799   -1.6803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4477    0.8697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2598    1.0128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7590    0.3523    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4798   -0.4918    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6103   -1.1096    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4766   -1.5894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3901   -1.0199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9554   -1.6208    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5197   -0.1660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2914   -0.7798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9142   -0.2387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5690    0.5078    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6942   -0.5076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8513   -1.3175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2285   -1.8585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4485   -1.5897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3170    0.0335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1598    0.8434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0550    1.1223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8699    1.2510    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5361    1.7637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8321    2.5338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  3  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
  2 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
  1 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  3 15  1  0  0  0  0
 10 16  1  6  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
  9 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 16 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
  9 25  1  1  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0073688

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@]12CC[C@@]34CC(=O)[C@H]5CN(CC=C3)[C@@H]4[C@@]15C1=C(N2)C(OC)=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C22H24N2O4/c1-27-16-6-3-5-13-17(16)23-21(19(26)28-2)9-8-20-7-4-10-24-12-14(15(25)11-20)22(13,21)18(20)24/h3-7,14,18,23H,8-12H2,1-2H3/t14-,18+,20-,21-,22+/m1/s1

> <INCHI_KEY>
XPLYAIRFUUIGPK-TVTJTFRUSA-N

> <FORMULA>
C22H24N2O4

> <MOLECULAR_WEIGHT>
380.444

> <EXACT_MASS>
380.173607261

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
39.56103199551726

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1R,4S,12R,13R,21S)-7-methoxy-20-oxo-5,15-diazahexacyclo[11.5.2.1^{1,12}.0^{4,12}.0^{6,11}.0^{15,21}]henicosa-6(11),7,9,17-tetraene-4-carboxylate

> <ALOGPS_LOGP>
2.37

> <JCHEM_LOGP>
1.4115275120000006

> <ALOGPS_LOGS>
-2.92

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
15.798337688692786

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.720991648158403

> <JCHEM_PKA_STRONGEST_BASIC>
7.354061270322254

> <JCHEM_POLAR_SURFACE_AREA>
67.87

> <JCHEM_REFRACTIVITY>
105.0015

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.55e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1R,4S,12R,13R,21S)-7-methoxy-20-oxo-5,15-diazahexacyclo[11.5.2.1^{1,12}.0^{4,12}.0^{6,11}.0^{15,21}]henicosa-6(11),7,9,17-tetraene-4-carboxylate

> <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  N   UNK     0       1.413  -3.010   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0       1.646  -1.045   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.441   0.073   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.095  -1.309   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.551  -3.317   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.523  -3.137   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.836   1.624   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.352   1.890   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.283   0.658   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.762  -0.918   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.139  -2.071   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.756  -2.967   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.728  -1.904   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -1.783  -3.026   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -0.970  -0.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.277  -1.456   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.440  -0.446   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0       4.796   0.948   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       6.896  -0.947   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.189  -2.459   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.027  -3.469   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.571  -2.967   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.058   0.062   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       7.765   1.574   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.836   2.095   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.357   2.335   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       2.867   3.292   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       3.420   4.730   0.000  0.00  0.00           C+0
CONECT    1    2    6   12                                                  
CONECT    2    1    3   10                                                  
CONECT    3    2    4    7   15                                             
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    1                                                       
CONECT    7    3    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   18   25                                             
CONECT   10    9    2   11   16                                             
CONECT   11   10   12   13                                                  
CONECT   12   11    1                                                       
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    3                                                       
CONECT   16   10   17   22                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17    9                                                       
CONECT   19   17   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   16                                                       
CONECT   23   19   24                                                       
CONECT   24   23                                                            
CONECT   25    9   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   66    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1R,4S,12R,13R,21S)-7-methoxy-20-oxo-5,15-diazahexacyclo[11.5.2.1,.0,.0,.0,]henicosa-6(11),7,9,17-tetraene-4-carboxylic acid	Generator

Chemical Formula

C₂₂H₂₄N₂O₄

Average Mass

380.4440 Da

Monoisotopic Mass

380.17361 Da

IUPAC Name

methyl (1R,4S,12R,13R,21S)-7-methoxy-20-oxo-5,15-diazahexacyclo[11.5.2.1^{1,12}.0^{4,12}.0^{6,11}.0^{15,21}]henicosa-6(11),7,9,17-tetraene-4-carboxylate

Traditional Name

methyl (1R,4S,12R,13R,21S)-7-methoxy-20-oxo-5,15-diazahexacyclo[11.5.2.1^{1,12}.0^{4,12}.0^{6,11}.0^{15,21}]henicosa-6(11),7,9,17-tetraene-4-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@]12CC[C@@]34CC(=O)[C@H]5CN(CC=C3)[C@@H]4[C@@]15C1=C(N2)C(OC)=CC=C1

InChI Identifier

InChI=1S/C22H24N2O4/c1-27-16-6-3-5-13-17(16)23-21(19(26)28-2)9-8-20-7-4-10-24-12-14(15(25)11-20)22(13,21)18(20)24/h3-7,14,18,23H,8-12H2,1-2H3/t14-,18+,20-,21-,22+/m1/s1

InChI Key

XPLYAIRFUUIGPK-TVTJTFRUSA-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
Arabidopsis thaliana	Plant	KNApSAcK
Kopsia arborea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aspidofractine alkaloids. These are alkaloids with a structure that is based on the hexacyclic aspidofractine core. These compounds are related to the Aspidosperma group by formation of a C-2 to C-18 bond.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Aspidofractine alkaloids

Sub Class

Not Available

Direct Parent

Aspidofractine alkaloids

Alternative Parents

Substituents

Aspidofractine skeleton
Carbazole
Alpha-amino acid ester
Indolecarboxylic acid
Indolecarboxylic acid derivative
Alpha-amino acid or derivatives
Dihydroindole
Indole or derivatives
Anisole
Alkyl aryl ether
Azepane
Secondary aliphatic/aromatic amine
Aralkylamine
Benzenoid
N-alkylpyrrolidine
Methyl ester
Pyrrolidine
Carboxylic acid ester
Amino acid or derivatives
Tertiary aliphatic amine
Ketone
Tertiary amine
Organoheterocyclic compound
Ether
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Azacycle
Secondary amine
Organic nitrogen compound
Carbonyl group
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Amine
Organopnictogen compound
Organic oxygen 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	2.37	ALOGPS
logP	1.41	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	11.72	ChemAxon
pKa (Strongest Basic)	7.35	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	67.87 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	105 m³·mol⁻¹	ChemAxon
Polarizability	39.56 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

162971561

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 1,24-Tetracosane dioic acid (NP0073688)

MOL for NP0073688 (1,24-Tetracosane dioic acid)

3D MOL for NP0073688 (1,24-Tetracosane dioic acid)

3D SDF for NP0073688 (1,24-Tetracosane dioic acid)

3D-SDF for NP0073688 (1,24-Tetracosane dioic acid)

PDB for NP0073688 (1,24-Tetracosane dioic acid)

3D PDB for NP0073688 (1,24-Tetracosane dioic acid)

SMILES for NP0073688 (1,24-Tetracosane dioic acid)

INCHI for NP0073688 (1,24-Tetracosane dioic acid)

Structure for NP0073688 (1,24-Tetracosane dioic acid)

3D Structure for NP0073688 (1,24-Tetracosane dioic acid)