NP-MRD: Showing NP-Card for (+)-Arboflorine (NP0076177)

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Record Information

Version

2.0

Created at

2022-04-28 21:20:09 UTC

Updated at

2022-04-28 21:20:09 UTC

NP-MRD ID

NP0076177

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Arboflorine

Description

Arboflorine belongs to the class of organic compounds known as naphthyridines. Naphthyridines are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings. The naphthyridine skeleton can also be described as an assembly two fused pyridine rings, which do not share their nitrogen atom. (+)-Arboflorine is found in Kopsia arborea. (+)-Arboflorine was first documented in 2006 (PMID: 16597153). Based on a literature review very few articles have been published on Arboflorine (PMID: 23020147).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 48  0  0  0  0  0  0  0  0999 V2000
   -4.2917   -1.7495    0.6845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9378   -1.2177    1.0304 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8733   -2.1866    0.7993 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9407   -2.0531   -0.2539 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5790   -3.1194   -0.8567 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3758   -0.7484   -0.6794 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0759   -0.6298   -0.3879 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8599   -1.6779   -0.0849 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1279   -1.2662    0.1303 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2912   -1.9327    0.4639 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4651   -1.2283    0.6211 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5349    0.1497    0.4562 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3727    0.8052    0.1243 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1849    0.1124   -0.0373 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8951    0.4794   -0.3587 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4917    1.8804   -0.6271 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2421    2.1815    0.1742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8584    1.5741   -0.5094 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9411    2.4735   -0.6792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1777    1.8089   -1.2301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5588    0.6251   -0.3991 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5724   -0.0231    0.1896 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1594    0.3261    0.0898 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4218   -2.7159    1.1892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4012   -1.8813   -0.4020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0450   -1.0589    1.1147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9252   -0.9527    2.1181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8221   -2.9950    1.4477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5831   -0.6306   -1.7564 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5506   -2.6943   -0.0177 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2736   -2.9997    0.5993 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3813   -1.7470    0.8830 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4740    0.6903    0.5849 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3767    1.8731   -0.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3144    2.5668   -0.4270 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2033    2.0084   -1.7100 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1181    3.2788    0.2979 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4048    1.7220    1.1833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6441    3.2604   -1.4042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1979    3.0307    0.2685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0064    1.4828   -2.2565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9975    2.5340   -1.1677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5950    0.3692   -0.3263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7327    0.2750    1.1352 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6 23  1  0
 23 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 18 17  1  0
 17 16  1  0
 16 15  1  0
 15  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 22  2  1  0
 14 15  1  0
  7  6  1  0
 14  9  1  0
 22 23  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  1
  3 28  1  0
  6 29  1  6
 23 44  1  1
 19 39  1  0
 19 40  1  0
 20 41  1  0
 20 42  1  0
 21 43  1  0
 17 37  1  0
 17 38  1  0
 16 35  1  0
 16 36  1  0
  8 30  1  0
 10 31  1  0
 11 32  1  0
 12 33  1  0
 13 34  1  0
M  END


  Mrv1652304282223202D          

 23 27  0  0  1  0            999 V2000
    2.2923   -1.0957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0580   -1.4029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1551   -0.3823    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4646    0.0691    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7921   -0.4088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0420   -0.0654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0356    0.7559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6368    1.2338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3870    0.8904    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9807    1.4632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7987    1.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2250    0.6498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9386   -0.1239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5859   -0.6354    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2724   -0.1778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0494    0.6165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6257    1.2068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4251    1.0028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6481    0.2085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0718   -0.3818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8697   -1.2302    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6199   -1.5736    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1973   -1.7081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  3 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 15 20  2  0  0  0  0
  5 21  1  0  0  0  0
 21 22  1  0  0  0  0
  1 22  1  0  0  0  0
 21 23  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0076177

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1NC(=O)[C@H]2[C@H]3N(CCC=C13)CCC1=C2NC2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C19H21N3O/c1-11-12-6-4-9-22-10-8-14-13-5-2-3-7-15(13)21-17(14)16(18(12)22)19(23)20-11/h2-3,5-7,11,16,18,21H,4,8-10H2,1H3,(H,20,23)/t11-,16-,18+/m1/s1

> <INCHI_KEY>
PLEVOJMDNFPZJV-ONUMYQOESA-N

> <FORMULA>
C19H21N3O

> <MOLECULAR_WEIGHT>
307.397

> <EXACT_MASS>
307.168462308

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
34.94898801546738

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,18R,21R)-18-methyl-3,13,19-triazapentacyclo[11.7.1.0^{2,10}.0^{4,9}.0^{17,21}]henicosa-2(10),4,6,8,16-pentaen-20-one

> <ALOGPS_LOGP>
2.45

> <JCHEM_LOGP>
1.6592020496666668

> <ALOGPS_LOGS>
-2.93

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
16.400407726818454

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.389356802351262

> <JCHEM_PKA_STRONGEST_BASIC>
8.317927732621822

> <JCHEM_POLAR_SURFACE_AREA>
48.13

> <JCHEM_REFRACTIVITY>
91.4231

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.65e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,18R,21R)-18-methyl-3,13,19-triazapentacyclo[11.7.1.0^{2,10}.0^{4,9}.0^{17,21}]henicosa-2(10),4,6,8,16-pentaen-20-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       4.279  -2.045   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.708  -2.619   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.023  -0.714   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.734   0.129   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.479  -0.763   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.078  -0.122   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.067   1.411   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.189   2.303   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       2.589   1.662   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       3.697   2.731   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.224   2.531   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.020   1.213   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.485  -0.231   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       6.694  -1.186   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       7.975  -0.332   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.559   1.151   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.635   2.253   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.127   1.872   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.543   0.389   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.467  -0.713   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.624  -2.296   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0       3.024  -2.937   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       0.368  -3.188   0.000  0.00  0.00           C+0
CONECT    1    2    3   22                                                  
CONECT    2    1                                                            
CONECT    3    1    4   13                                                  
CONECT    4    3    5    9                                                  
CONECT    5    4    6   21                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8    4   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   16                                                  
CONECT   13   12    3   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   12   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   15                                                       
CONECT   21    5   22   23                                                  
CONECT   22   21    1                                                       
CONECT   23   21                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₁N₃O

Average Mass

307.3970 Da

Monoisotopic Mass

307.16846 Da

IUPAC Name

(1S,18R,21R)-18-methyl-3,13,19-triazapentacyclo[11.7.1.0^{2,10}.0^{4,9}.0^{17,21}]henicosa-2(10),4,6,8,16-pentaen-20-one

Traditional Name

(1S,18R,21R)-18-methyl-3,13,19-triazapentacyclo[11.7.1.0^{2,10}.0^{4,9}.0^{17,21}]henicosa-2(10),4,6,8,16-pentaen-20-one

CAS Registry Number

Not Available

SMILES

C[C@H]1NC(=O)[C@H]2[C@H]3N(CCC=C13)CCC1=C2NC2=CC=CC=C12

InChI Identifier

InChI=1S/C19H21N3O/c1-11-12-6-4-9-22-10-8-14-13-5-2-3-7-15(13)21-17(14)16(18(12)22)19(23)20-11/h2-3,5-7,11,16,18,21H,4,8-10H2,1H3,(H,20,23)/t11-,16-,18+/m1/s1

InChI Key

PLEVOJMDNFPZJV-ONUMYQOESA-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
Kopsia arborea	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthyridines. Naphthyridines are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings. The naphthyridine skeleton can also be described as an assembly two fused pyridine rings, which do not share their nitrogen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazanaphthalenes

Sub Class

Naphthyridines

Direct Parent

Naphthyridines

Alternative Parents

Substituents

Naphthyridine
Pyrroloazepine
3-alkylindole
Indole
Indole or derivatives
Azepine
Delta-lactam
Piperidinone
Aralkylamine
Benzenoid
Piperidine
Heteroaromatic compound
Pyrrole
Tertiary aliphatic amine
Tertiary amine
Carboxamide group
Amino acid or derivatives
Lactam
Secondary carboxylic acid amide
Carboxylic acid derivative
Azacycle
Carbonyl group
Organic oxygen compound
Organic nitrogen compound
Amine
Organic oxide
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
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	2.45	ALOGPS
logP	1.66	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	14.39	ChemAxon
pKa (Strongest Basic)	8.32	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	48.13 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	91.42 m³·mol⁻¹	ChemAxon
Polarizability	34.95 Å³	ChemAxon
Number of Rings	5	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

C00038487

Chemspider ID

28283314

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102181745

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Lim KH, Kam TS: Arboflorine, an unusual pentacyclic monoterpenoid indole alkaloid incorporating a third nitrogen atom. Org Lett. 2006 Apr 13;8(8):1733-5. doi: 10.1021/ol060348k. [PubMed:16597153 ]
Leal RA, Beaudry DR, Alzghari SK, Sarpong R: Synthesis of the pentacyclic skeleton of the indole alkaloid arboflorine. Org Lett. 2012 Oct 19;14(20):5350-3. doi: 10.1021/ol302535r. Epub 2012 Sep 28. [PubMed:23020147 ]

Showing NP-Card for (+)-Arboflorine (NP0076177)

MOL for NP0076177 ((+)-Arboflorine)

3D MOL for NP0076177 ((+)-Arboflorine)

3D SDF for NP0076177 ((+)-Arboflorine)

3D-SDF for NP0076177 ((+)-Arboflorine)

PDB for NP0076177 ((+)-Arboflorine)

3D PDB for NP0076177 ((+)-Arboflorine)

SMILES for NP0076177 ((+)-Arboflorine)

INCHI for NP0076177 ((+)-Arboflorine)

Structure for NP0076177 ((+)-Arboflorine)

3D Structure for NP0076177 ((+)-Arboflorine)