NP-MRD: Showing NP-Card for (+)-Discorhabdin A (NP0068721)

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Record Information

Version

2.0

Created at

2022-04-28 13:58:57 UTC

Updated at

2022-04-28 13:58:57 UTC

NP-MRD ID

NP0068721

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Discorhabdin A

Description

(3S,8R,10S)-5-bromo-9-thia-11,15,20-triazahexacyclo[12.6.1.1³,¹⁰.0²,¹².0³,⁸.0¹⁷,²¹]Docosa-1(20),2(12),4,14(21),16-pentaene-6,13-dione belongs to the class of organic compounds known as phenanthrolines. These are aromatic polycyclic compounds containing the phenanthroline skeleton, which is a derivative of phenanthrene, and consists of two pyridine rings non-linearly joined by a benzene ring. (+)-Discorhabdin A is found in Bryopsis pennata, Latrunculia brevis, Latrunculia sp. and Prianos melanos. Based on a literature review very few articles have been published on (3S,8R,10S)-5-bromo-9-thia-11,15,20-triazahexacyclo[12.6.1.1³,¹⁰.0²,¹².0³,⁸.0¹⁷,²¹]Docosa-1(20),2(12),4,14(21),16-pentaene-6,13-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282215592D          

 25 30  0  0  1  0            999 V2000
    3.2066    2.2081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8209    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9964    1.4483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7951    0.4840    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3695   -0.1082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1696    0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3952    0.8867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1360    1.2499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0194    2.0666    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5577    2.1470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9435    2.8762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7679    2.9068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1536    3.6361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4563    3.6061    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5982    3.5198    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6822    2.7741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6576    2.0665    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6625    1.2158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0269    0.7529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7757    1.1176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4512    0.6440    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8620    1.9349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1744    2.3806    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2145    3.2449    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.0300   -0.0701    0.0000 Br  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  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  1  9  1  0  0  0  0
  3 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
  1 12  1  0  0  0  0
 12 13  2  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 17 16  1  1  0  0  0
 10 17  1  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
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  1  0  0  0
 15 24  1  0  0  0  0
 19 25  1  0  0  0  0
M  END

     RDKit          3D

 39 44  0  0  0  0  0  0  0  0999 V2000
    4.4112    2.3977    1.5576 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4540    1.6810    1.2145 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6240    0.7264    0.1051 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3281    0.2512   -0.4656 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7006   -1.3271   -1.2988 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.1919   -2.4375    0.0773 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0464   -1.4566    1.1977 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3603   -0.2449    0.6129 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1727    0.8254    1.5684 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1246    1.6923    1.8267 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7332    3.0713    3.1253 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.0941   -0.7043    0.0013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1139   -1.9354   -0.4304 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9120   -2.9532   -0.3643 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3913   -2.3686   -1.0361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5844   -3.5386   -1.4418 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4801   -1.4016   -1.1725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7416   -1.3805   -1.6502 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2642   -0.1180   -1.4949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3167    0.6991   -0.9012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2361   -0.1245   -0.7186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9914    0.2857   -0.1293 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9202    1.5159    0.2396 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9480    2.4899    0.1264 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2428    2.1134   -0.4760 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2824   -0.0861    0.4649 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1723    1.2496   -0.7041 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8730    0.9665   -1.1464 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9360   -3.2141    0.2489 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0326   -1.2488    1.6130 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4002   -1.8237    2.0208 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2373    0.9089    2.1001 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7820   -3.9304   -0.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2011   -2.2114   -2.0606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2473    0.1988   -1.7827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5313    3.4415   -0.3417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1455    2.8361    1.1950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4384    2.7989   -1.3359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0747    2.3558    0.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 10  1  0
 10  9  2  0
  8  9  1  1
  8  7  1  0
  7  6  1  0
  6 14  1  0
 14 13  1  0
 13 12  2  0
 12 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  1  0
 25 20  1  0
 20 19  2  0
 19 18  1  0
 18 17  1  0
 17 21  2  0
 17 15  1  0
 15 16  2  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  0
  2 10  1  0
 12  8  1  0
 21 22  1  0
  4  8  1  0
 15 13  1  0
 21 20  1  0
  9 32  1  0
  7 30  1  0
  7 31  1  0
  6 29  1  1
 14 33  1  0
 24 36  1  0
 24 37  1  0
 25 38  1  0
 25 39  1  0
 19 35  1  0
 18 34  1  0
  4 28  1  6
  3 26  1  0
  3 27  1  0
M  END


  Mrv1652304282215592D          

 25 30  0  0  1  0            999 V2000
    3.2066    2.2081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8209    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9964    1.4483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7951    0.4840    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3695   -0.1082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1696    0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3952    0.8867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1360    1.2499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0194    2.0666    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5577    2.1470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9435    2.8762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7679    2.9068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1536    3.6361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4563    3.6061    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5982    3.5198    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6822    2.7741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6576    2.0665    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6625    1.2158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0269    0.7529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7757    1.1176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4512    0.6440    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8620    1.9349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1744    2.3806    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2145    3.2449    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.0300   -0.0701    0.0000 Br  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  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  1  9  1  0  0  0  0
  3 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
  1 12  1  0  0  0  0
 12 13  2  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 17 16  1  1  0  0  0
 10 17  1  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
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  1  0  0  0
 15 24  1  0  0  0  0
 19 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0068721

> <DATABASE_NAME>
NP-MRD

> <SMILES>
BrC1=C[C@@]23C[C@@H](NC4=C2C2=NCCC5=CNC(=C25)C4=O)S[C@@H]3CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H14BrN3O2S/c19-8-4-18-5-11(25-10(18)3-9(8)23)22-16-13(18)14-12-7(1-2-20-14)6-21-15(12)17(16)24/h4,6,10-11,21-22H,1-3,5H2/t10-,11+,18+/m1/s1

> <INCHI_KEY>
IMRWMDAHKYBDMQ-DDBGAENHSA-N

> <FORMULA>
C18H14BrN3O2S

> <MOLECULAR_WEIGHT>
416.29

> <EXACT_MASS>
414.999011

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
37.717931479124935

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,8R,10S)-5-bromo-9-thia-11,15,20-triazahexacyclo[12.6.1.1^{3,10}.0^{2,12}.0^{3,8}.0^{17,21}]docosa-1(20),2(12),4,14(21),16-pentaene-6,13-dione

> <ALOGPS_LOGP>
2.49

> <JCHEM_LOGP>
1.2403795233333335

> <ALOGPS_LOGS>
-3.54

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
16.73183493270533

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.297547138304129

> <JCHEM_PKA_STRONGEST_BASIC>
7.691921141995948

> <JCHEM_POLAR_SURFACE_AREA>
74.32

> <JCHEM_REFRACTIVITY>
102.28769999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.21e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,8R,10S)-5-bromo-9-thia-11,15,20-triazahexacyclo[12.6.1.1^{3,10}.0^{2,12}.0^{3,8}.0^{17,21}]docosa-1(20),2(12),4,14(21),16-pentaene-6,13-dione

> <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       5.986   4.122   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.266   2.761   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.727   2.703   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0       3.351   0.903   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       4.423  -0.202   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.917   0.174   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.338   1.655   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.720   2.333   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       7.503   3.858   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       2.908   4.008   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.628   5.369   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.167   5.426   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.887   6.787   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0       2.718   6.731   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       1.117   6.570   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.273   5.178   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.228   3.857   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.237   2.269   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.050   1.405   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.448   2.086   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -2.709   1.202   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -1.609   3.612   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.326   4.444   0.000  0.00  0.00           C+0
HETATM   24  S   UNK     0      -0.400   6.057   0.000  0.00  0.00           S+0
HETATM   25 Br   UNK     0       0.056  -0.131   0.000  0.00  0.00          Br+0
CONECT    1    2    9   12                                                  
CONECT    2    1    3    7                                                  
CONECT    3    2    4   10                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    2    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8    1                                                       
CONECT   10    3   11   17                                                  
CONECT   11   10   12   14                                                  
CONECT   12   11    1   13                                                  
CONECT   13   12                                                            
CONECT   14   11   15                                                       
CONECT   15   14   16   24                                                  
CONECT   16   15   17                                                       
CONECT   17   16   10   18   23                                             
CONECT   18   17   19                                                       
CONECT   19   18   20   25                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   17   24                                                  
CONECT   24   23   15                                                       
CONECT   25   19                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₄BrN₃O₂S

Average Mass

416.2900 Da

Monoisotopic Mass

414.99901 Da

IUPAC Name

(3S,8R,10S)-5-bromo-9-thia-11,15,20-triazahexacyclo[12.6.1.1^{3,10}.0^{2,12}.0^{3,8}.0^{17,21}]docosa-1(20),2(12),4,14(21),16-pentaene-6,13-dione

Traditional Name

(3S,8R,10S)-5-bromo-9-thia-11,15,20-triazahexacyclo[12.6.1.1^{3,10}.0^{2,12}.0^{3,8}.0^{17,21}]docosa-1(20),2(12),4,14(21),16-pentaene-6,13-dione

CAS Registry Number

Not Available

SMILES

BrC1=C[C@@]23C[C@@H](NC4=C2C2=NCCC5=CNC(=C25)C4=O)S[C@@H]3CC1=O

InChI Identifier

InChI=1S/C18H14BrN3O2S/c19-8-4-18-5-11(25-10(18)3-9(8)23)22-16-13(18)14-12-7(1-2-20-14)6-21-15(12)17(16)24/h4,6,10-11,21-22H,1-3,5H2/t10-,11+,18+/m1/s1

InChI Key

IMRWMDAHKYBDMQ-DDBGAENHSA-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
Bryopsis pennata	LOTUS Database	35616633
Latrunculia brevis	LOTUS Database	35616633
Latrunculia sp.	-	KNApSAcK
Prianos melanos	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenanthrolines. These are aromatic polycyclic compounds containing the phenanthroline skeleton, which is a derivative of phenanthrene, and consists of two pyridine rings non-linearly joined by a benzene ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Phenanthrolines

Sub Class

Not Available

Direct Parent

Phenanthrolines

Alternative Parents

Substituents

1,7-phenanthroline
Pyrrolo[4,3,2-de]quinoline
Pyrroloquinoline
Indole or derivatives
Aryl ketone
Cyclohexenone
Tetrahydropyridine
Alpha-haloketone
Heteroaromatic compound
Pyrrole
Thiolane
Ketimine
Ketone
Cyclic ketone
Enamine
Azacycle
Bromoalkene
Haloalkene
Dialkylthioether
Thioether
Hemithioaminal
Organic 1,3-dipolar compound
Vinyl bromide
Vinyl halide
Propargyl-type 1,3-dipolar organic compound
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Amine
Imine
Organic nitrogen compound
Organic oxygen compound
Organic oxide
Organohalogen compound
Organobromide
Organonitrogen 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	2.49	ALOGPS
logP	1.24	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	13.3	ChemAxon
pKa (Strongest Basic)	7.69	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.32 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	102.29 m³·mol⁻¹	ChemAxon
Polarizability	37.72 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

4678152

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5748836

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Discorhabdin A (NP0068721)

MOL for NP0068721 ((+)-Discorhabdin A)

3D MOL for NP0068721 ((+)-Discorhabdin A)

3D SDF for NP0068721 ((+)-Discorhabdin A)

3D-SDF for NP0068721 ((+)-Discorhabdin A)

PDB for NP0068721 ((+)-Discorhabdin A)

3D PDB for NP0068721 ((+)-Discorhabdin A)

SMILES for NP0068721 ((+)-Discorhabdin A)

INCHI for NP0068721 ((+)-Discorhabdin A)

Structure for NP0068721 ((+)-Discorhabdin A)

3D Structure for NP0068721 ((+)-Discorhabdin A)