NP-MRD: Showing NP-Card for (+)-Erythraline (NP0069162)

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Record Information

Version

2.0

Created at

2022-04-28 14:28:44 UTC

Updated at

2022-04-28 14:28:44 UTC

NP-MRD ID

NP0069162

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Erythraline

Description

Erythraline 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. (+)-Erythraline is found in Erythrina abyssinica, Erythrina bidwillii, Erythrina brucei, Erythrina caffra , Erythrina coralloides, Erythrina crista-galli , Erythrina fusca, Erythrina glauca Willd., Erythrina latissima, Erythrina suberosa , Erythrina variegata, Erythrina velutina, Erythrina verna, Erythrina vespertilio and Erythrina x bidwillii. Based on a literature review very few articles have been published on Erythraline.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 41 45  0  0  0  0  0  0  0  0999 V2000
   -4.4322    1.6231   -1.2737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5506    0.7640   -0.6683 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3537    1.3865   -0.2676 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3659    1.3950    1.2075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8492    0.3280    1.8182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3060   -0.7765    1.0163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3025   -2.0821    1.0986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5929   -2.7084   -0.0712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7283   -1.6350   -1.0379 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2127   -1.7936   -2.0717 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6282   -1.9639   -1.6046 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8718   -0.9189   -0.5830 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2081   -0.6310   -0.2204 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5343    0.3189    0.7189 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5370    1.0308    1.3445 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2454    0.7506    0.9922 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8796   -0.2160    0.0342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5699   -0.4192   -0.2565 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2381    0.6983   -0.9398 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1368    1.9224    2.2446 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5223    2.0518    1.8888 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7261    0.7998    1.2589 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7402    2.4651   -0.6163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9192    2.0430   -2.1874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2841    1.0383   -1.6444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4774    2.4627   -0.5771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7693    2.2164    1.7840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    0.2452    2.8874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7754   -2.6049    1.9467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2364   -3.5418   -0.4194 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4222   -2.9971    0.1704 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2111   -0.8342   -2.6732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1250   -2.6194   -2.7307 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2662   -1.8158   -2.5085 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8665   -2.9795   -1.2381 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9668   -1.1935   -0.7167 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4676    1.2947    1.4702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4674    1.4856   -1.1992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6080    0.3761   -1.9599 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1577    2.2134    2.7570 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6527    2.8213    1.0851 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 19  1  0
 18 19  1  6
 18  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 20  1  0
 20 21  1  0
 21 22  1  0
 15 16  1  0
 16 17  2  0
  4  3  1  0
 17 12  1  0
  6 18  1  0
 22 14  1  0
 17 18  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  6
 19 38  1  0
 19 39  1  0
  8 30  1  0
  8 31  1  0
  7 29  1  0
  5 28  1  0
  4 27  1  0
 10 32  1  0
 10 33  1  0
 11 34  1  0
 11 35  1  0
 13 36  1  0
 21 40  1  0
 21 41  1  0
 16 37  1  0
M  END


  Mrv1652304282216282D          

 22 26  0  0  1  0            999 V2000
    3.4305    0.6255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6899   -0.1576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1414   -0.7738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3335   -0.6069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1165    0.0675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6226    0.7925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2661    0.3431    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7176   -0.2731    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9770   -1.0563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7849   -1.2232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0380    0.0581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0436    0.8791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8495    1.0552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2579    1.7721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0829    1.7768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4995    1.0647    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0911    0.3478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3245    1.0694    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7329    1.7862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5149   -0.1529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7654    0.6332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0952    1.1143    0.0000 O   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  1  0  0  0  0
 12 13  2  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  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
 16 18  1  6  0  0  0
 18 19  1  0  0  0  0
  2 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  1 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0069162

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H]1C[C@]23N(CC=C2C=C1)CCC1=CC2=C(OCO2)C=C31

> <INCHI_IDENTIFIER>
InChI=1S/C18H19NO3/c1-20-14-3-2-13-5-7-19-6-4-12-8-16-17(22-11-21-16)9-15(12)18(13,19)10-14/h2-3,5,8-9,14H,4,6-7,10-11H2,1H3/t14-,18-/m0/s1

> <INCHI_KEY>
TVOFUERNMZTYRM-KSSFIOAISA-N

> <FORMULA>
C18H19NO3

> <MOLECULAR_WEIGHT>
297.354

> <EXACT_MASS>
297.136493476

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
31.953108689442217

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,19R)-19-methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.0^{1,16}.0^{2,10}.0^{4,8}]icosa-2,4(8),9,15,17-pentaene

> <ALOGPS_LOGP>
2.01

> <JCHEM_LOGP>
1.998125228333333

> <ALOGPS_LOGS>
-2.45

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
8.924907829931353

> <JCHEM_POLAR_SURFACE_AREA>
30.930000000000003

> <JCHEM_REFRACTIVITY>
85.27970000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.05e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,19R)-19-methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.0^{1,16}.0^{2,10}.0^{4,8}]icosa-2,4(8),9,15,17-pentaene

> <JCHEM_VEBER_RULE>
1

$$$$

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       6.404   1.168   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.888  -0.294   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.864  -1.445   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.356  -1.133   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.951   0.126   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.895   1.479   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.363   0.641   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       1.339  -0.510   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       1.824  -1.972   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.332  -2.283   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.071   0.109   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.081   1.641   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.586   1.970   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.348   3.308   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.888   3.317   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.666   1.987   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.903   0.649   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.206   1.996   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.968   3.334   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.428  -0.285   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       8.895   1.182   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       7.644   2.080   0.000  0.00  0.00           O+0
CONECT    1    2    6   22                                                  
CONECT    2    1    3   20                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8   13   17                                             
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9    4                                                       
CONECT   11    8   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    7   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16    7                                                       
CONECT   18   16   19                                                       
CONECT   19   18                                                            
CONECT   20    2   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    1                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₉NO₃

Average Mass

297.3540 Da

Monoisotopic Mass

297.13649 Da

IUPAC Name

(1S,19R)-19-methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.0^{1,16}.0^{2,10}.0^{4,8}]icosa-2,4(8),9,15,17-pentaene

Traditional Name

(1S,19R)-19-methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.0^{1,16}.0^{2,10}.0^{4,8}]icosa-2,4(8),9,15,17-pentaene

CAS Registry Number

Not Available

SMILES

CO[C@@H]1C[C@]23N(CC=C2C=C1)CCC1=CC2=C(OCO2)C=C31

InChI Identifier

InChI=1S/C18H19NO3/c1-20-14-3-2-13-5-7-19-6-4-12-8-16-17(22-11-21-16)9-15(12)18(13,19)10-14/h2-3,5,8-9,14H,4,6-7,10-11H2,1H3/t14-,18-/m0/s1

InChI Key

TVOFUERNMZTYRM-KSSFIOAISA-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 abyssinica	LOTUS Database	35616633
Erythrina bidwillii	LOTUS Database	35616633
Erythrina brucei	LOTUS Database	35616633
Erythrina caffra	Plant	KNApSAcK
Erythrina coralloides	LOTUS Database	35616633
Erythrina crista-galli	Plant	KNApSAcK
Erythrina fusca	LOTUS Database	35616633
Erythrina glauca Willd.	Plant	KNApSAcK
Erythrina latissima	Plant	KNApSAcK
Erythrina suberosa	Plant	KNApSAcK
Erythrina variegata	LOTUS Database	35616633
Erythrina velutina	LOTUS Database	35616633
Erythrina verna	Plant	KNApSAcK
Erythrina vespertilio	LOTUS Database	35616633
Erythrina x bidwillii	Plant	KNApSAcK

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
Benzodioxole
Indole or derivatives
Aralkylamine
Benzenoid
Pyrroline
Tertiary amine
Tertiary aliphatic amine
Oxacycle
Dialkyl ether
Ether
Azacycle
Acetal
Organoheterocyclic compound
Organopnictogen compound
Organonitrogen compound
Organooxygen compound
Organic nitrogen compound
Amine
Hydrocarbon derivative
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	2.01	ALOGPS
logP	2	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Basic)	8.92	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	30.93 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	85.28 m³·mol⁻¹	ChemAxon
Polarizability	31.95 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

C00027265

Chemspider ID

4476106

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5317205

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Erythraline (NP0069162)

MOL for NP0069162 ((+)-Erythraline)

3D MOL for NP0069162 ((+)-Erythraline)

3D SDF for NP0069162 ((+)-Erythraline)

3D-SDF for NP0069162 ((+)-Erythraline)

PDB for NP0069162 ((+)-Erythraline)

3D PDB for NP0069162 ((+)-Erythraline)

SMILES for NP0069162 ((+)-Erythraline)

INCHI for NP0069162 ((+)-Erythraline)

Structure for NP0069162 ((+)-Erythraline)

3D Structure for NP0069162 ((+)-Erythraline)