NP-MRD: Showing NP-Card for methyl (1r,10s,12r,13e,18r)-13-ethylidene-10-hydroxy-8-methyl-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0⁹,¹⁵]octadeca-2,4,6-triene-18-carboxylate (NP0164148)

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Record Information

Version

2.0

Created at

2022-09-02 22:58:25 UTC

Updated at

2022-09-02 22:58:25 UTC

NP-MRD ID

NP0164148

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1r,10s,12r,13e,18r)-13-ethylidene-10-hydroxy-8-methyl-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0⁹,¹⁵]octadeca-2,4,6-triene-18-carboxylate

Description

Deformylcorymine 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. methyl (1r,10s,12r,13e,18r)-13-ethylidene-10-hydroxy-8-methyl-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0⁹,¹⁵]octadeca-2,4,6-triene-18-carboxylate is found in Hunteria zeylanica. methyl (1r,10s,12r,13e,18r)-13-ethylidene-10-hydroxy-8-methyl-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0⁹,¹⁵]octadeca-2,4,6-triene-18-carboxylate was first documented in 2017 (PMID: 28952737). Based on a literature review very few articles have been published on Deformylcorymine (PMID: 31992040).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032200582D          

 26 30  0  0  1  0            999 V2000
   -1.4530   -0.2565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7325    0.1941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1083    0.4231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7613    1.1035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4871    0.7410    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4414    1.4235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5610    1.3203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4197    0.4890    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2653    0.3217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9218    0.8212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6827    0.5024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7871   -0.3159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1305   -0.8155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3696   -0.4967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5830   -0.7768    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8218   -1.6151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9568   -0.1770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5370   -0.9464    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3063   -1.7580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6989   -0.9823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7187   -0.1419    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5339    0.1710    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1699    1.0639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7889    1.8879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1831    1.2750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3697    0.6626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
  5 17  1  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 21 20  1  1  0  0  0
  3 21  1  0  0  0  0
 21 22  1  0  0  0  0
  8 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END

     RDKit          3D

 52 56  0  0  0  0  0  0  0  0999 V2000
    4.5208   -0.3630   -0.2126 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4648   -0.5839   -1.2230 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1620   -0.4911   -0.8945 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2549   -0.7371   -2.0103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0724   -1.1026   -1.6843 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9774   -0.0896   -2.1981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8236    1.0180   -1.1494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4820    0.2863    0.1559 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6035    0.3360    1.1109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9707    1.2224    2.1290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1007    1.0322    2.8902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8870   -0.0677    2.6334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5311   -0.9432    1.6335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3983   -0.7612    0.8635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8181   -1.5197   -0.2159 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5521   -2.4596   -1.0059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4009   -1.1226   -0.2990 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3895   -2.0424    0.5391 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8753   -3.0908   -0.2652 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5533   -1.4289    1.2469 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9443   -0.1618    0.5137 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8100    0.8141    0.7297 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0887    2.1401    0.1406 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1356    2.4490   -0.4747 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1145    3.1124    0.2824 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2658    4.4174   -0.2375 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5050   -0.5944   -0.6654 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5697    0.7177    0.0702 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4247   -0.9963    0.6787 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7286   -0.8293   -2.2670 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3108    0.1553   -2.6994 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6991   -1.5740   -2.6254 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0102   -0.4211   -2.2888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5948    0.2496   -3.1910 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0404    1.6226   -1.5126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7481    1.5892   -1.0725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3719    2.0820    2.3435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3719    1.7397    3.6850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7789   -0.2151    3.2363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1434   -1.8099    1.4252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7986   -3.3285   -0.3370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0408   -2.7899   -1.9090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5545   -2.0408   -1.2922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2655   -2.5119    1.3105 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3749   -3.1244   -1.1288 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4142   -2.1165    1.3527 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2090   -1.0876    2.2666 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8278    0.2540    1.0249 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7409    0.9675    1.8426 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2994    4.7786   -0.0917 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0807    4.3447   -1.3335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5082    5.0760    0.1798 H   0  0  0  0  0  0  0  0  0  0  0  0
 26 25  1  0
 25 23  1  0
 23 24  2  0
 23 22  1  0
 22 21  1  0
 21 20  1  0
 20 18  1  0
 18 19  1  0
 18 17  1  0
 17  5  1  0
  5  6  1  0
  6  7  1  0
  8  7  1  6
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  8 22  1  0
 14  9  1  0
  3 21  1  0
  8 17  1  0
 17 15  1  6
 26 50  1  0
 26 51  1  0
 26 52  1  0
 22 49  1  1
 21 48  1  1
 20 46  1  0
 20 47  1  0
 18 44  1  1
 19 45  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
 10 37  1  0
 11 38  1  0
 12 39  1  0
 13 40  1  0
 16 41  1  0
 16 42  1  0
 16 43  1  0
  4 31  1  0
  4 32  1  0
  2 30  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
M  END


  Mrv1652309032200582D          

 26 30  0  0  1  0            999 V2000
   -1.4530   -0.2565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7325    0.1941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1083    0.4231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7613    1.1035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4871    0.7410    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4414    1.4235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5610    1.3203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4197    0.4890    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2653    0.3217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9218    0.8212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6827    0.5024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7871   -0.3159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1305   -0.8155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3696   -0.4967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5830   -0.7768    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8218   -1.6151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9568   -0.1770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5370   -0.9464    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3063   -1.7580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6989   -0.9823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7187   -0.1419    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5339    0.1710    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1699    1.0639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7889    1.8879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1831    1.2750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3697    0.6626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
  5 17  1  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 21 20  1  1  0  0  0
  3 21  1  0  0  0  0
 21 22  1  0  0  0  0
  8 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0164148

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@H]1[C@H]2C[C@H](O)C34N(CC[C@]13C1=CC=CC=C1N4C)C\C2=C\C

> <INCHI_IDENTIFIER>
InChI=1S/C21H26N2O3/c1-4-13-12-23-10-9-20-15-7-5-6-8-16(15)22(2)21(20,23)17(24)11-14(13)18(20)19(25)26-3/h4-8,14,17-18,24H,9-12H2,1-3H3/b13-4-/t14-,17-,18-,20-,21?/m0/s1

> <INCHI_KEY>
CFKUJHVLEYIZOQ-TXTHPRGESA-N

> <FORMULA>
C21H26N2O3

> <MOLECULAR_WEIGHT>
354.45

> <EXACT_MASS>
354.194342705

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
38.37062076735816

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1R,10S,12R,13E,18R)-13-ethylidene-10-hydroxy-8-methyl-8,15-diazapentacyclo[10.5.1.0^{1,9}.0^{2,7}.0^{9,15}]octadeca-2,4,6-triene-18-carboxylate

> <ALOGPS_LOGP>
2.75

> <JCHEM_LOGP>
2.4187585646666667

> <ALOGPS_LOGS>
-1.78

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.947992597899688

> <JCHEM_PKA_STRONGEST_BASIC>
7.058423236774721

> <JCHEM_POLAR_SURFACE_AREA>
53.010000000000005

> <JCHEM_REFRACTIVITY>
100.9031

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.84e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1R,10S,12R,13E,18R)-13-ethylidene-10-hydroxy-8-methyl-8,15-diazapentacyclo[10.5.1.0^{1,9}.0^{2,7}.0^{9,15}]octadeca-2,4,6-triene-18-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.712  -0.479   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.367   0.362   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.202   0.790   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.421   2.060   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       2.776   1.383   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       2.691   2.657   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.781   2.465   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.517   0.913   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.095   0.600   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.321   1.533   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.741   0.938   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.936  -0.590   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.710  -1.522   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.290  -0.927   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       4.822  -1.450   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       5.267  -3.015   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.653  -0.330   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.869  -1.767   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.438  -3.282   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.305  -1.834   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.341  -0.265   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.863   0.319   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.184   1.986   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       3.339   3.524   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       0.342   2.380   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -0.690   1.237   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   21                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   17                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   17   22                                             
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9   15                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15    5    8   18                                             
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20    3   22                                                  
CONECT   22   21    8   23                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₆N₂O₃

Average Mass

354.4500 Da

Monoisotopic Mass

354.19434 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@H]1[C@H]2C[C@H](O)C34N(CC[C@]13C1=CC=CC=C1N4C)C\C2=C\C

InChI Identifier

InChI=1S/C21H26N2O3/c1-4-13-12-23-10-9-20-15-7-5-6-8-16(15)22(2)21(20,23)17(24)11-14(13)18(20)19(25)26-3/h4-8,14,17-18,24H,9-12H2,1-3H3/b13-4-/t14-,17-,18-,20-,21?/m0/s1

InChI Key

CFKUJHVLEYIZOQ-TXTHPRGESA-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
Hunteria zeylanica	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
Pyrroloindole
Indole
Dialkylarylamine
Azepane
Benzenoid
N-alkylpyrrolidine
Methyl ester
Pyrrolidine
Pyrrole
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Azacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
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

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

102120632

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhang B, Wang X, Li C: Enantioselective Total Synthesis of (+)-Corymine and (-)-Deformylcorymine. J Am Chem Soc. 2020 Feb 12;142(6):3269-3274. doi: 10.1021/jacs.0c00302. Epub 2020 Jan 31. [PubMed:31992040 ]
Xie X, Wei B, Li G, Zu L: Unified Total Syntheses of Structurally Diverse Akuammiline Alkaloids. Org Lett. 2017 Oct 6;19(19):5430-5433. doi: 10.1021/acs.orglett.7b02698. Epub 2017 Sep 27. [PubMed:28952737 ]
LOTUS database [Link]

Showing NP-Card for methyl (1r,10s,12r,13e,18r)-13-ethylidene-10-hydroxy-8-methyl-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0⁹,¹⁵]octadeca-2,4,6-triene-18-carboxylate (NP0164148)

MOL for NP0164148 (methyl (1r,10s,12r,13e,18r)-13-ethylidene-10-hydroxy-8-methyl-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0⁹,¹⁵]octadeca-2,4,6-triene-18-carboxylate)

3D MOL for NP0164148 (methyl (1r,10s,12r,13e,18r)-13-ethylidene-10-hydroxy-8-methyl-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0⁹,¹⁵]octadeca-2,4,6-triene-18-carboxylate)

3D SDF for NP0164148 (methyl (1r,10s,12r,13e,18r)-13-ethylidene-10-hydroxy-8-methyl-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0⁹,¹⁵]octadeca-2,4,6-triene-18-carboxylate)

3D-SDF for NP0164148 (methyl (1r,10s,12r,13e,18r)-13-ethylidene-10-hydroxy-8-methyl-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0⁹,¹⁵]octadeca-2,4,6-triene-18-carboxylate)

PDB for NP0164148 (methyl (1r,10s,12r,13e,18r)-13-ethylidene-10-hydroxy-8-methyl-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0⁹,¹⁵]octadeca-2,4,6-triene-18-carboxylate)

3D PDB for NP0164148 (methyl (1r,10s,12r,13e,18r)-13-ethylidene-10-hydroxy-8-methyl-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0⁹,¹⁵]octadeca-2,4,6-triene-18-carboxylate)

SMILES for NP0164148 (methyl (1r,10s,12r,13e,18r)-13-ethylidene-10-hydroxy-8-methyl-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0⁹,¹⁵]octadeca-2,4,6-triene-18-carboxylate)

INCHI for NP0164148 (methyl (1r,10s,12r,13e,18r)-13-ethylidene-10-hydroxy-8-methyl-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0⁹,¹⁵]octadeca-2,4,6-triene-18-carboxylate)

Structure for NP0164148 (methyl (1r,10s,12r,13e,18r)-13-ethylidene-10-hydroxy-8-methyl-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0⁹,¹⁵]octadeca-2,4,6-triene-18-carboxylate)

3D Structure for NP0164148 (methyl (1r,10s,12r,13e,18r)-13-ethylidene-10-hydroxy-8-methyl-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0⁹,¹⁵]octadeca-2,4,6-triene-18-carboxylate)