NP-MRD: Showing NP-Card for Arcyriaflavin C (NP0066440)

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Record Information

Version

2.0

Created at

2022-04-28 10:41:39 UTC

Updated at

2022-04-28 10:41:39 UTC

NP-MRD ID

NP0066440

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Arcyriaflavin C

Description

Arcyriaflavin C belongs to the class of organic compounds known as indolocarbazoles. These are polycyclic aromatic compounds containing an indole fused to a carbazole. Arcyriaflavin C is found in Arcyria denudata, Arcyria ferruginea, Arcyria nutans, Metatrichia vesparium and Tubifera casparyi. Arcyriaflavin C is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191515522D          

 27 32  0  0  0  0            999 V2000
    2.0116   -2.7764    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7653   -3.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8515   -3.9325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6052   -4.2680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2726   -3.7831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1864   -2.9626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4327   -2.6271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9401   -2.6271    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4921   -3.2402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3171   -3.2402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8691   -2.6271    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.6228   -2.9626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3765   -2.6271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0439   -3.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7976   -2.7764    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9577   -3.9325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2040   -4.2680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5366   -3.7831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7296   -3.9546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3171   -4.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5721   -5.4537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3567   -5.7087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9046   -5.9387    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2372   -5.4537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4526   -5.7087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4921   -4.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0796   -3.9546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  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
  6  7  1  0  0  0  0
  2  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  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
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
 10 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 20 26  2  0  0  0  0
 26 27  1  0  0  0  0
  5 27  1  0  0  0  0
  9 27  2  0  0  0  0
M  END

     RDKit          3D

 38 43  0  0  0  0  0  0  0  0999 V2000
   -2.5943    3.3481    0.0687 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3858    2.9582    0.0050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2928    3.8594   -0.1112 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9276    3.1073   -0.1588 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0565    3.6415   -0.2603 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5798    1.6984   -0.0695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8283    1.6212    0.0296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4177    0.3733    0.1278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7010   -0.0659    0.2353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9139    0.5627    0.2882 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0685   -0.2110    0.4026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0274   -1.5775    0.4636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2060   -2.3147    0.5779 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8190   -2.2266    0.4119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6654   -1.4392    0.2970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3866   -1.8280    0.2284 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6129   -0.7418    0.1253 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7707   -0.6744    0.0283 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6903   -1.6596    0.0120 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8806   -1.0596   -0.0967 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1341   -1.6147   -0.1558 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2403   -0.8063   -0.2685 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5234   -1.3573   -0.3298 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0818    0.5614   -0.3216 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8267    1.1396   -0.2635 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7243    0.3314   -0.1511 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3653    0.5536   -0.0693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3531    4.8804   -0.1547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0157    1.6346    0.2451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0172    0.3488    0.4408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7151   -2.6369   -0.2493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7611   -3.2880    0.4575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0703   -2.8112    0.2529 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4780   -2.6657    0.0733 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2236   -2.7043   -0.1110 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6550   -2.3473   -0.2925 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9527    1.2207   -0.4114 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7415    2.1896   -0.3068 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 12  1  0
 12 14  2  0
 14 15  1  0
 15  9  2  0
  9 10  1  0
 10 11  2  0
  9  8  1  0
  8 17  2  0
 17 16  1  0
 17 18  1  0
 18 27  2  0
 27 26  1  0
 26 25  2  0
 25 24  1  0
 24 22  2  0
 22 23  1  0
 22 21  1  0
 21 20  2  0
 20 19  1  0
 27  6  1  0
  6  7  2  0
  7  2  1  0
  2  1  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
 11 12  1  0
  7  8  1  0
 16 15  1  0
 19 18  1  0
  4  6  1  0
 20 26  1  0
 13 31  1  0
 14 32  1  0
 10 29  1  0
 11 30  1  0
 16 33  1  0
 25 38  1  0
 24 37  1  0
 23 36  1  0
 21 35  1  0
 19 34  1  0
  3 28  1  0
M  END


  Mrv1533004191515522D          

 27 32  0  0  0  0            999 V2000
    2.0116   -2.7764    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7653   -3.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8515   -3.9325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6052   -4.2680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2726   -3.7831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1864   -2.9626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4327   -2.6271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9401   -2.6271    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4921   -3.2402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3171   -3.2402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8691   -2.6271    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.6228   -2.9626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3765   -2.6271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0439   -3.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7976   -2.7764    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9577   -3.9325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2040   -4.2680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5366   -3.7831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7296   -3.9546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3171   -4.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5721   -5.4537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3567   -5.7087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9046   -5.9387    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2372   -5.4537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4526   -5.7087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4921   -4.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0796   -3.9546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  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
  6  7  1  0  0  0  0
  2  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  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
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
 10 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 20 26  2  0  0  0  0
 26 27  1  0  0  0  0
  5 27  1  0  0  0  0
  9 27  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0066440

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC2=C(C=C1)C1=C(N2)C2=C(C3=CC=C(O)C=C3N2)C2=C1C(=O)NC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H11N3O4/c24-7-1-3-9-11(5-7)21-17-13(9)15-16(20(27)23-19(15)26)14-10-4-2-8(25)6-12(10)22-18(14)17/h1-6,21-22,24-25H,(H,23,26,27)

> <INCHI_KEY>
COUUDSNRXUXNDW-UHFFFAOYSA-N

> <FORMULA>
C20H11N3O4

> <MOLECULAR_WEIGHT>
357.325

> <EXACT_MASS>
357.074955846

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
36.897294736824925

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6,20-dihydroxy-3,13,23-triazahexacyclo[14.7.0.0²,¹⁰.0⁴,⁹.0¹¹,¹⁵.0¹⁷,²²]tricosa-1(16),2(10),4,6,8,11(15),17(22),18,20-nonaene-12,14-dione

> <ALOGPS_LOGP>
2.85

> <JCHEM_LOGP>
2.3215721416666666

> <ALOGPS_LOGS>
-4.13

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.067495759605567

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.07737144253026

> <JCHEM_PKA_STRONGEST_BASIC>
-5.554856594338557

> <JCHEM_POLAR_SURFACE_AREA>
118.20999999999998

> <JCHEM_REFRACTIVITY>
98.10499999999993

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.65e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6,20-dihydroxy-3,13,23-triazahexacyclo[14.7.0.0²,¹⁰.0⁴,⁹.0¹¹,¹⁵.0¹⁷,²²]tricosa-1(16),2(10),4,6,8,11(15),17(22),18,20-nonaene-12,14-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  O   UNK     0       3.755  -5.183   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       5.162  -5.809   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.323  -7.341   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.730  -7.967   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.976  -7.062   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.815  -5.530   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.408  -4.904   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       9.221  -4.904   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0      10.252  -6.048   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.792  -6.048   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      12.822  -4.904   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      14.229  -5.530   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      15.636  -4.904   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      16.882  -5.809   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      18.289  -5.183   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      16.721  -7.341   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      15.314  -7.967   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.068  -7.062   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.562  -7.382   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.792  -8.716   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.268 -10.180   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      13.732 -10.656   0.000  0.00  0.00           O+0
HETATM   23  N   UNK     0      11.022 -11.085   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0       9.776 -10.180   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.311 -10.656   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      10.252  -8.716   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.482  -7.382   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   27                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6    2                                                       
CONECT    8    6    9                                                       
CONECT    9    8   10   27                                                  
CONECT   10    9   11   19                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   12   19                                                  
CONECT   19   18   10   20                                                  
CONECT   20   19   21   26                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   20   27                                                  
CONECT   27   26    5    9                                                  
MASTER        0    0    0    0    0    0    0    0   27    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₁₁N₃O₄

Average Mass

357.3250 Da

Monoisotopic Mass

357.07496 Da

IUPAC Name

6,20-dihydroxy-3,13,23-triazahexacyclo[14.7.0.0²,¹⁰.0⁴,⁹.0¹¹,¹⁵.0¹⁷,²²]tricosa-1(16),2(10),4,6,8,11(15),17(22),18,20-nonaene-12,14-dione

Traditional Name

6,20-dihydroxy-3,13,23-triazahexacyclo[14.7.0.0²,¹⁰.0⁴,⁹.0¹¹,¹⁵.0¹⁷,²²]tricosa-1(16),2(10),4,6,8,11(15),17(22),18,20-nonaene-12,14-dione

CAS Registry Number

Not Available

SMILES

OC1=CC2=C(C=C1)C1=C(N2)C2=C(C3=CC=C(O)C=C3N2)C2=C1C(=O)NC2=O

InChI Identifier

InChI=1S/C20H11N3O4/c24-7-1-3-9-11(5-7)21-17-13(9)15-16(20(27)23-19(15)26)14-10-4-2-8(25)6-12(10)22-18(14)17/h1-6,21-22,24-25H,(H,23,26,27)

InChI Key

COUUDSNRXUXNDW-UHFFFAOYSA-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
Arcyria denudata	Amoebozoa	KNApSAcK
Arcyria ferruginea	Amoebozoa	KNApSAcK
Arcyria nutans	Amoebozoa	KNApSAcK
Metatrichia vesparium	-	KNApSAcK
Tubifera casparyi	Amoebozoa	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indolocarbazoles. These are polycyclic aromatic compounds containing an indole fused to a carbazole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Carbazoles

Direct Parent

Indolocarbazoles

Alternative Parents

Substituents

Indolocarbazole
Pyrrolo[2,3-a]carbazole
Pyrroloindole
Phthalimide
Isoindolone
Hydroxyindole
Indole
Isoindoline
Isoindole or derivatives
Phenol
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Pyrrole
Carboxylic acid imide, n-unsubstituted
Carboxylic acid imide
Heteroaromatic compound
Azacycle
Carboxylic acid derivative
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
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	2.85	ALOGPS
logP	2.32	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	8.08	ChemAxon
pKa (Strongest Basic)	-5.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	118.21 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	98.1 m³·mol⁻¹	ChemAxon
Polarizability	36.9 Å³	ChemAxon
Number of Rings	6	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

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

5482346

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Arcyriaflavin C (NP0066440)

MOL for NP0066440 (Arcyriaflavin C)

3D MOL for NP0066440 (Arcyriaflavin C)

3D SDF for NP0066440 (Arcyriaflavin C)

3D-SDF for NP0066440 (Arcyriaflavin C)

PDB for NP0066440 (Arcyriaflavin C)

3D PDB for NP0066440 (Arcyriaflavin C)

SMILES for NP0066440 (Arcyriaflavin C)

INCHI for NP0066440 (Arcyriaflavin C)

Structure for NP0066440 (Arcyriaflavin C)

3D Structure for NP0066440 (Arcyriaflavin C)