NP-MRD: Showing NP-Card for Erysotramidine (NP0069161)

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Record Information

Version

2.0

Created at

2022-04-28 14:28:42 UTC

Updated at

2022-04-28 14:28:42 UTC

NP-MRD ID

NP0069161

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Erysotramidine

Description

Erysotramidine belongs to the class of organic compounds known as erythrinanes. These are erythrina alkaloids possessing either a 6-5-6-6-membered indoloisoquinoline core or a derivative thereof. Erysotramidine is found in Erythrina arborescens Roxb., Erythrina bidwillii, Erythrina herbacea, Erythrina latissima and Erythrina lysistemon. Erysotramidine was first documented in 2014 (PMID: 25601909). Based on a literature review a small amount of articles have been published on Erysotramidine (PMID: 29792153) (PMID: 27076115) (PMID: 26125652) (PMID: 25569446).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 48  0  0  0  0  0  0  0  0999 V2000
    5.2771   -1.3348   -0.7061 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6314   -0.1713   -0.2330 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2301   -0.2379   -0.1241 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5317   -1.3658   -0.4575 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1367   -1.4585   -0.3585 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4238   -0.3634    0.0966 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1124    0.7658    0.4316 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5071    0.8453    0.3280 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1633    2.0025    0.6758 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5479    3.1631    1.1452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0801   -0.4359    0.2125 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7374    0.1510   -0.9834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4872    1.4108   -0.7415 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8496    1.0852   -0.5604 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6220    1.6363   -1.5808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0798    2.2499    0.4007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6472    1.6015    1.5003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6166    0.1334    1.4641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0484   -0.7962    2.3023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8671   -2.1167    1.6897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1330   -3.2529    2.1391 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2998   -1.8795    0.4109 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9033   -2.7507   -0.6762 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5809   -2.7603   -0.7625 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8828   -1.6763   -1.6868 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3635   -1.1543   -0.8652 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1072   -2.1924   -0.0060 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1203   -2.2208   -0.8159 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6543    1.6731    0.7987 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7065    3.4196    0.4435 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0735    3.0542    2.1428 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3041    3.9923    1.1401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4659   -0.6140   -1.3691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0196    0.2539   -1.8555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3897    2.0382   -1.6768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6920    1.4000   -1.4682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5419    2.7395   -1.6294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2612    1.2309   -2.5458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1048    3.3198    0.4112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3402    2.0900    2.4065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4692   -0.6352    3.2938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3576   -2.4425   -1.6410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2502   -3.7864   -0.4842 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9716   -3.1115   -1.7409 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9377   -3.4990    0.0189 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 11 12  1  6
 11 22  1  0
 22 23  1  0
 23 24  1  0
 24  5  1  0
  5  4  2  0
  4  3  1  0
  3  2  1  0
  2  1  1  0
  3  8  2  0
  8  9  1  0
  9 10  1  0
  8  7  1  0
  7  6  2  0
 22 20  1  0
 20 21  2  0
 20 19  1  0
 19 18  2  0
 18 17  1  0
 17 16  2  0
 16 13  1  0
  6 11  1  0
 18 11  1  0
  6  5  1  0
 15 36  1  0
 15 37  1  0
 15 38  1  0
 13 35  1  6
 12 33  1  0
 12 34  1  0
 23 42  1  0
 23 43  1  0
 24 44  1  0
 24 45  1  0
  4 28  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
 10 30  1  0
 10 31  1  0
 10 32  1  0
  7 29  1  0
 19 41  1  0
 17 40  1  0
 16 39  1  0
M  END


  Mrv1652304282216282D          

 24 27  0  0  1  0            999 V2000
    3.3464    1.1333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7415    0.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3119   -0.2952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4871   -0.2752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1532    0.3497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5217    1.1533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2673    0.4690    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8376   -0.2353    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2327   -0.9596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0575   -0.9795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0350   -0.0443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5912   -0.5814    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0313    0.7780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7302    1.0952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0041    1.8734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8149    2.0254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3520    1.3991    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0782    0.6209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1629    1.5511    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4367    2.3293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5663    0.3892    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9614   -0.3351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7761    1.8376    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6009    1.8177    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
  5  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
  7 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  7 18  1  0  0  0  0
 17 19  1  6  0  0  0
 19 20  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  1  0  0  0  0
  1 23  1  0  0  0  0
 23 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0069161

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H]1C[C@@]23N(CCC4=CC(OC)=C(OC)C=C24)C(=O)C=C3C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H21NO4/c1-22-14-5-4-13-9-18(21)20-7-6-12-8-16(23-2)17(24-3)10-15(12)19(13,20)11-14/h4-5,8-10,14H,6-7,11H2,1-3H3/t14-,19-/m0/s1

> <INCHI_KEY>
AUDDBHVKKYSXKU-LIRRHRJNSA-N

> <FORMULA>
C19H21NO4

> <MOLECULAR_WEIGHT>
327.38

> <EXACT_MASS>
327.14705816

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
34.78811506133087

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,16R)-4,5,16-trimethoxy-10-azatetracyclo[8.7.0.0^{1,13}.0^{2,7}]heptadeca-2,4,6,12,14-pentaen-11-one

> <ALOGPS_LOGP>
2.14

> <JCHEM_LOGP>
1.311486750666666

> <ALOGPS_LOGS>
-2.98

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-0.24379540037584857

> <JCHEM_POLAR_SURFACE_AREA>
48.0

> <JCHEM_REFRACTIVITY>
92.19539999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.39e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,16R)-4,5,16-trimethoxy-10-azatetracyclo[8.7.0.0^{1,13}.0^{2,7}]heptadeca-2,4,6,12,14-pentaen-11-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       6.247   2.116   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.984   0.764   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.182  -0.551   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.643  -0.514   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.019   0.653   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.707   2.153   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.366   0.875   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       1.564  -0.439   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       2.301  -1.791   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.841  -1.828   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.065  -0.083   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.104  -1.085   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.059   1.452   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.363   2.044   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.874   3.497   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.388   3.781   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.390   2.612   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.879   1.159   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.904   2.895   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.415   4.348   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.524   0.726   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.261  -0.625   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       7.049   3.430   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.588   3.393   0.000  0.00  0.00           C+0
CONECT    1    2    6   23                                                  
CONECT    2    1    3   21                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8   14   18                                             
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9    4                                                       
CONECT   11    8   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13    7   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17    7                                                       
CONECT   19   17   20                                                       
CONECT   20   19                                                            
CONECT   21    2   22                                                       
CONECT   22   21                                                            
CONECT   23    1   24                                                       
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₁NO₄

Average Mass

327.3800 Da

Monoisotopic Mass

327.14706 Da

IUPAC Name

(1S,16R)-4,5,16-trimethoxy-10-azatetracyclo[8.7.0.0^{1,13}.0^{2,7}]heptadeca-2,4,6,12,14-pentaen-11-one

Traditional Name

(1S,16R)-4,5,16-trimethoxy-10-azatetracyclo[8.7.0.0^{1,13}.0^{2,7}]heptadeca-2,4,6,12,14-pentaen-11-one

CAS Registry Number

Not Available

SMILES

CO[C@@H]1C[C@@]23N(CCC4=CC(OC)=C(OC)C=C24)C(=O)C=C3C=C1

InChI Identifier

InChI=1S/C19H21NO4/c1-22-14-5-4-13-9-18(21)20-7-6-12-8-16(23-2)17(24-3)10-15(12)19(13,20)11-14/h4-5,8-10,14H,6-7,11H2,1-3H3/t14-,19-/m0/s1

InChI Key

AUDDBHVKKYSXKU-LIRRHRJNSA-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
Erythrina arborescens Roxb.	Plant	KNApSAcK
Erythrina bidwillii	LOTUS Database	35616633
Erythrina herbacea	Plant	KNApSAcK
Erythrina latissima	Plant	KNApSAcK
Erythrina lysistemon	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as erythrinanes. These are erythrina alkaloids possessing either a 6-5-6-6-membered indoloisoquinoline core or a derivative thereof.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Erythrina alkaloids

Sub Class

Erythrinanes

Direct Parent

Erythrinanes

Alternative Parents

Substituents

Erythrinane skeleton
Tetrahydroisoquinoline
Indole or derivatives
Anisole
Phenol ether
Alkyl aryl ether
Benzenoid
Tertiary carboxylic acid amide
Pyrroline
Carboxamide group
Lactam
Carboxylic acid derivative
Dialkyl ether
Ether
Azacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxygen compound
Organic nitrogen compound
Carbonyl group
Organic oxide
Organonitrogen compound
Organooxygen 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	2.14	ALOGPS
logP	1.31	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Basic)	-0.24	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	48 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	92.2 m³·mol⁻¹	ChemAxon
Polarizability	34.79 Å³	ChemAxon
Number of Rings	4	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

C00027351

Chemspider ID

9209956

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11034782

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

de Avila JM, Dalcol II, Pereira AO, Santos EW, Ferraz A, Santos MZ, Mostardeiro MA, Morel AF: Antimicrobial Evaluation of Erythrinan Alkaloids from Erythrina cristagalli L. Med Chem. 2018;14(8):784-790. doi: 10.2174/1573406414666180524081650. [PubMed:29792153 ]
Andreev IA, Ratmanova NK, Novoselov AM, Belov DS, Seregina IF, Kurkin AV: Oxidative Dearomatization of 4,5,6,7-Tetrahydro-1H-indoles Obtained by Metal- and Solvent-Free Thermal 5-endo-dig Cyclization: The Route to Erythrina and Lycorine Alkaloids. Chemistry. 2016 May 17;22(21):7262-7. doi: 10.1002/chem.201600273. Epub 2016 Apr 14. [PubMed:27076115 ]
Paladino M, Zaifman J, Ciufolini MA: Total Synthesis of (+)-3-Demethoxyerythratidinone and (+)-Erysotramidine via the Oxidative Amidation of a Phenol. Org Lett. 2015 Jul 17;17(14):3422-5. doi: 10.1021/acs.orglett.5b01423. Epub 2015 Jun 30. [PubMed:26125652 ]
Maertens G, L'Homme C, Canesi S: Total synthesis of natural products using hypervalent iodine reagents. Front Chem. 2015 Jan 5;2:115. doi: 10.3389/fchem.2014.00115. eCollection 2014. [PubMed:25601909 ]
Mostowicz D, Dygas M, Kaluza Z: Heck cyclization strategy for preparation of erythrinan alkaloids: asymmetric synthesis of unnatural (-)-erysotramidine from L-tartaric acid. J Org Chem. 2015 Feb 6;80(3):1957-63. doi: 10.1021/jo5026157. Epub 2015 Jan 20. [PubMed:25569446 ]

Showing NP-Card for Erysotramidine (NP0069161)

MOL for NP0069161 (Erysotramidine)

3D MOL for NP0069161 (Erysotramidine)

3D SDF for NP0069161 (Erysotramidine)

3D-SDF for NP0069161 (Erysotramidine)

PDB for NP0069161 (Erysotramidine)

3D PDB for NP0069161 (Erysotramidine)

SMILES for NP0069161 (Erysotramidine)

INCHI for NP0069161 (Erysotramidine)

Structure for NP0069161 (Erysotramidine)

3D Structure for NP0069161 (Erysotramidine)