NP-MRD: Showing NP-Card for (15r,16s,18r)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.0⁴,¹².0⁵,¹⁰.0¹⁶,¹⁸]icosa-4(12),5,7,9-tetraene (NP0154535)

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Record Information

Version

2.0

Created at

2022-09-02 11:27:56 UTC

Updated at

2022-09-02 11:27:56 UTC

NP-MRD ID

NP0154535

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(15r,16s,18r)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.0⁴,¹².0⁵,¹⁰.0¹⁶,¹⁸]icosa-4(12),5,7,9-tetraene

Description

Conoflorine belongs to the class of organic compounds known as quebrachamine alkaloids. These are alkaloids with a structure based on the quebrachamine skeleton, a tetracyclic compound that is derived by fission of the 7,21 bond of the aspidospermidine skeleton. Some quebrachamine alkaloids lack the C-16 methoxycarbonyl group. (15r,16s,18r)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.0⁴,¹².0⁵,¹⁰.0¹⁶,¹⁸]icosa-4(12),5,7,9-tetraene is found in Tabernaemontana grandiflora, Tabernanthe iboga and Trachelospermum jasminoides. (15r,16s,18r)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.0⁴,¹².0⁵,¹⁰.0¹⁶,¹⁸]icosa-4(12),5,7,9-tetraene was first documented in 2002 (PMID: 12375951). Based on a literature review very few articles have been published on Conoflorine.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 50  0  0  0  0  0  0  0  0999 V2000
   -3.7129    2.1314   -0.1491 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2601    0.9835    0.6885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2264    0.1016   -0.0042 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0950    0.9633   -0.4152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2252    1.4807    0.6764 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2213    1.1903    0.3634 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1626    1.9806   -0.2137 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3190    1.3428   -0.3099 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5376    1.7234   -0.8124 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6334    0.8523   -0.8019 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4282   -0.4009   -0.2643 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1971   -0.7689    0.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1209    0.0908    0.2252 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7918   -0.0184    0.6566 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0396   -1.1444    1.3058 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2687   -1.9442    0.3284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1125   -2.0445    0.4777 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7306   -2.6993   -0.6141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6722   -1.8863   -1.4176 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8964   -1.4850   -0.8099 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8455   -0.5220   -1.2049 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8868   -0.9916    0.9743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0334    3.0080   -0.1116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9767    1.8156   -1.1683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6793    2.5032    0.3021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1188    0.3478    0.9852 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8064    1.3447    1.6366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4568    0.5165   -1.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5518    1.8663   -0.9237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3167    2.6008    0.8065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4063    1.0669    1.6695 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9643    2.9736   -0.5338 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7295    2.6986   -1.2402 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5986    1.1618   -1.2030 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2629   -1.0877   -0.2475 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0153   -1.7582    0.6672 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4531   -0.7162    2.1449 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8348   -1.7587    1.8274 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5466   -1.5986   -0.7132 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6895   -2.9980    0.3453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9850   -3.1601   -1.3021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3088   -3.5777   -0.2015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8909   -2.3241   -2.4348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1528    0.1599   -2.0182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5659   -0.5776    1.9669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9017   -1.4419    1.2301 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  3  2  1  1
  3 22  1  0
 22 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14  6  2  0
  6  5  1  0
  5  4  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 21  3  1  0
 13 14  1  0
  4  3  1  0
 13  8  1  0
 21 19  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  2 27  1  0
 22 45  1  0
 22 46  1  0
 18 41  1  0
 18 42  1  0
 19 43  1  6
 21 44  1  6
 16 39  1  0
 16 40  1  0
 15 37  1  0
 15 38  1  0
  5 30  1  0
  5 31  1  0
  4 28  1  0
  4 29  1  0
  7 32  1  0
  9 33  1  0
 10 34  1  0
 11 35  1  0
 12 36  1  0
M  END


  Mrv1652309022213272D          

 22 26  0  0  1  0            999 V2000
    1.0323   -0.4619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6075    0.2453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0075    0.9668    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6730    0.3977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5284    0.3028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2172    0.7863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9205    0.3550    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5479    0.8907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3659    0.7828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8682    1.4372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5527    2.1995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7348    2.3074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2324    1.6530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4099    1.5884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0166    2.3344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2115    2.6385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3601    2.4339    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5013    2.6030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1183    2.0133    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6553    1.3870    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1556    1.2351    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2560    1.6830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  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
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
  6 14  2  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
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 21 20  1  6  0  0  0
 19 21  1  0  0  0  0
  3 21  1  0  0  0  0
 17 22  1  0  0  0  0
  3 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0154535

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@]12CN(C[C@H]3O[C@@H]13)CCC1=C(CC2)NC2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C19H24N2O/c1-2-19-9-7-16-14(13-5-3-4-6-15(13)20-16)8-10-21(12-19)11-17-18(19)22-17/h3-6,17-18,20H,2,7-12H2,1H3/t17-,18-,19-/m1/s1

> <INCHI_KEY>
OGDFTQDRHAGLTB-GUDVDZBRSA-N

> <FORMULA>
C19H24N2O

> <MOLECULAR_WEIGHT>
296.414

> <EXACT_MASS>
296.188863401

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
34.14608092381593

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(15R,16S,18R)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.0^{4,12}.0^{5,10}.0^{16,18}]icosa-4(12),5,7,9-tetraene

> <ALOGPS_LOGP>
3.33

> <JCHEM_LOGP>
3.321567222666666

> <ALOGPS_LOGS>
-3.72

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.127770805270718

> <JCHEM_PKA_STRONGEST_BASIC>
7.7260181898179185

> <JCHEM_POLAR_SURFACE_AREA>
31.560000000000002

> <JCHEM_REFRACTIVITY>
88.3843

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.63e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(15R,16S,18R)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.0^{4,12}.0^{5,10}.0^{16,18}]icosa-4(12),5,7,9-tetraene

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       1.927  -0.862   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.134   0.458   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.881   1.805   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.123   0.742   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.720   0.565   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.005   1.468   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       7.318   0.663   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       8.489   1.663   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.016   1.461   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.954   2.683   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.365   4.106   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.838   4.307   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.900   3.086   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.365   2.965   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.631   4.358   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.128   4.925   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       2.539   4.543   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       0.936   4.859   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.221   3.758   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -1.223   2.589   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.290   2.305   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.345   3.142   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   21   22                                             
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   14                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    8   14                                                  
CONECT   14   13    6   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19   21                                                       
CONECT   21   20   19    3                                                  
CONECT   22   17    3                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₄N₂O

Average Mass

296.4140 Da

Monoisotopic Mass

296.18886 Da

IUPAC Name

(15R,16S,18R)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.0^{4,12}.0^{5,10}.0^{16,18}]icosa-4(12),5,7,9-tetraene

Traditional Name

(15R,16S,18R)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.0^{4,12}.0^{5,10}.0^{16,18}]icosa-4(12),5,7,9-tetraene

CAS Registry Number

Not Available

SMILES

CC[C@@]12CN(C[C@H]3O[C@@H]13)CCC1=C(CC2)NC2=CC=CC=C12

InChI Identifier

InChI=1S/C19H24N2O/c1-2-19-9-7-16-14(13-5-3-4-6-15(13)20-16)8-10-21(12-19)11-17-18(19)22-17/h3-6,17-18,20H,2,7-12H2,1H3/t17-,18-,19-/m1/s1

InChI Key

OGDFTQDRHAGLTB-GUDVDZBRSA-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
Stemmadenia grandiflora	LOTUS Database	35616633
Tabernanthe iboga	LOTUS Database	35616633
Trachelospermum jasminoides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quebrachamine alkaloids. These are alkaloids with a structure based on the quebrachamine skeleton, a tetracyclic compound that is derived by fission of the 7,21 bond of the aspidospermidine skeleton. Some quebrachamine alkaloids lack the C-16 methoxycarbonyl group.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Quebrachamine alkaloids

Sub Class

Not Available

Direct Parent

Quebrachamine alkaloids

Alternative Parents

Substituents

Quebrachamine skeleton
3-alkylindole
Indole
Indole or derivatives
Para-oxazepine
Epoxypiperidine
Aralkylamine
Benzenoid
Piperidine
Heteroaromatic compound
Pyrrole
Tertiary aliphatic amine
Tertiary amine
Organoheterocyclic compound
Oxacycle
Azacycle
Dialkyl ether
Oxirane
Ether
Hydrocarbon derivative
Organic nitrogen compound
Organic oxygen compound
Amine
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	3.33	ALOGPS
logP	3.32	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	17.13	ChemAxon
pKa (Strongest Basic)	7.73	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	31.56 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	88.38 m³·mol⁻¹	ChemAxon
Polarizability	34.15 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

C00024619

Chemspider ID

399177

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

453208

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Eles J, Kalaus G, Greiner I, Kajtar-Peredy M, Szabo P, Keseru GM, Szabo L, Szantay C: Synthesis of vinca alkaloids and related compounds. 100. Stereoselective oxidation reactions of compounds with the aspidospermane and quebrachamine ring system. First synthesis of some alkaloids containing the epoxy ring. J Org Chem. 2002 Oct 18;67(21):7255-60. doi: 10.1021/jo020386r. [PubMed:12375951 ]
LOTUS database [Link]

Showing NP-Card for (15r,16s,18r)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.0⁴,¹².0⁵,¹⁰.0¹⁶,¹⁸]icosa-4(12),5,7,9-tetraene (NP0154535)

MOL for NP0154535 ((15r,16s,18r)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.0⁴,¹².0⁵,¹⁰.0¹⁶,¹⁸]icosa-4(12),5,7,9-tetraene)

3D MOL for NP0154535 ((15r,16s,18r)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.0⁴,¹².0⁵,¹⁰.0¹⁶,¹⁸]icosa-4(12),5,7,9-tetraene)

3D SDF for NP0154535 ((15r,16s,18r)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.0⁴,¹².0⁵,¹⁰.0¹⁶,¹⁸]icosa-4(12),5,7,9-tetraene)

3D-SDF for NP0154535 ((15r,16s,18r)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.0⁴,¹².0⁵,¹⁰.0¹⁶,¹⁸]icosa-4(12),5,7,9-tetraene)

PDB for NP0154535 ((15r,16s,18r)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.0⁴,¹².0⁵,¹⁰.0¹⁶,¹⁸]icosa-4(12),5,7,9-tetraene)

3D PDB for NP0154535 ((15r,16s,18r)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.0⁴,¹².0⁵,¹⁰.0¹⁶,¹⁸]icosa-4(12),5,7,9-tetraene)

SMILES for NP0154535 ((15r,16s,18r)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.0⁴,¹².0⁵,¹⁰.0¹⁶,¹⁸]icosa-4(12),5,7,9-tetraene)

INCHI for NP0154535 ((15r,16s,18r)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.0⁴,¹².0⁵,¹⁰.0¹⁶,¹⁸]icosa-4(12),5,7,9-tetraene)

Structure for NP0154535 ((15r,16s,18r)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.0⁴,¹².0⁵,¹⁰.0¹⁶,¹⁸]icosa-4(12),5,7,9-tetraene)

3D Structure for NP0154535 ((15r,16s,18r)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.0⁴,¹².0⁵,¹⁰.0¹⁶,¹⁸]icosa-4(12),5,7,9-tetraene)